1639
464
13
73
160
22
Cat. No. | Product Name | ||
---|---|---|---|
L9410 | 共价抑制剂库 | 1920 compounds | |
1920 种小分子的独特集合,包含已发现的共价抑制剂以及包含某些共价反应基团常见弹头的分子,如氯乙酰基,2-氯丙酰基,丙烯酰基,1-丙-2-炔基,1-丁-2-炔基,酮羰基,二硫键等,可以用于共价抑制剂药物研发; | |||
L7300 | 钾通道分子库 | 152 compounds | |
152 种钾通道相关化合物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L2160 | 抗癌活性化合物库 | 3188 compounds | |
3188 种具有抗肿瘤活性的化合物的特有集合,用于高通量、高内涵筛选; | |||
L2150 | 抗癌药物库 | 3080 compounds | |
3080 个具有抗癌活性小分子的独特集合,生物活性已经临床前实验证实,可用于高通量、高内涵筛选; | |||
L2100 | 抗癌化合物库 | 7234 compounds | |
7234 种肿瘤相关的生物活性小分子化合物的特有集合,用于高通量、高内涵筛选; | |||
L2120 | 抗癌临床化合物库 | 2545 compounds | |
2545 个具有抗癌活性小分子的独特集合,可用于高通量高内涵筛选。 | |||
L2110 | 抗癌上市药物库 | 1779 compounds | |
1779 个具有抗癌活性小分子的独特集合,所有化合物都经过了严格的临床前研究和临床试验,由FDA、EMA 或NMPA 批准上市,可用于高通量、高内涵筛选。 | |||
L8100 | 细胞周期化合物库 | 677 compounds | |
677 种细胞周期相关的生物活性小分子化合物的特有集合,用于高通量、高内涵筛选; | |||
L2180 | 抗肿瘤库Plus | 1468 compounds | |
1468 种抗肿瘤相关、结构新颖的化合物; | |||
L9000 | 细胞凋亡化合物库 | 1760 compounds | |
1760 种与凋亡相关的生物活性小分子化合物的特有集合,多用于研究肿瘤发生发展机制和抗癌药物筛选等。可用于高通量筛选和高内涵筛选; | |||
L5300 | 线粒体靶向库 | 812 compounds | |
812 种具有潜在或确定线粒体靶向活性的化合物,以促进针对线粒体的药物研究; | |||
L8500 | HIF-1化合物库 | 1336 compounds | |
1336 个HIF-1相关小分子的独特集合,可用于缺血性疾病、癌症等相关领域的药物开发和药理研究; | |||
L7110 | 抗高血压化合物库 | 678 compounds | |
678 种高血压相关的小分子,用于高通量和高内涵筛选; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5637 |
Triflumuron
|
Others | Others |
Triflumuron 是一种杀虫剂,属于所谓的昆虫生长调节剂。它抑制昆虫幼虫合成甲壳素,导致死亡。 | |||
T8794 |
4-MMPB
15-Lipoxygenase Inhibitor 1 |
Apoptosis; Others; Lipoxygenase | Apoptosis; Metabolism; Others |
4-MMPB (15-Lipoxygenase Inhibitor 1) 是一种选择性15-脂氧合酶抑制剂,其 IC50值为 18 μM,具有前列腺癌的研究潜力。它对大豆 15-脂氧合酶和人 15-脂氧合酶-1 的 IC50 分别为 19.5 μM 和 19.1 μM。 | |||
T14496 |
BAMB-4
ITPKA-IN-C14 |
Others | Others |
BAMB-4 (ITPKA-IN-C14) 是一种新型的膜渗透型ITPKA 抑制剂,在ADP-Glo 实验中的IC50值为37uM。 | |||
T22733 |
DL-AP5
DL-2-氨基-5-膦酰基缬草酸 |
NMDAR | Neuroscience |
DL-AP5 是选择性 N-甲基-D-天冬氨酸 (NMDA) 受体拮抗剂的外消旋形式,具有抗惊厥作用。 | |||
T60080 |
TMPH
2,2,6,6-Tetramethylpiperidin-4-yl heptanoate |
AChR | Neuroscience |
TMPH 是一种 nAChR 抑制剂,可抑制缺乏 α5、α6 或 β3 亚基的 nAChR。 TMPH 可用于关于 nAChR 功能障碍或神经系统疾病的研究。 | |||
T2691 |
Oritavancin diphosphate
奥利万星二磷酸盐,LY333328 diphosphate |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Oritavancin diphosphate (LY333328 diphosphate) 是一种新型半合成的糖肽抗生素, 可研究革兰氏阳性菌感染。 | |||
T2051 |
SKLB4771
FLT3-IN-1,FLT3-IN-1 |
FLT | Angiogenesis; Tyrosine Kinase/Adaptors |
SKLB4771 (FLT3-IN-1) 是一种新型的、高效的 Flt3 抑制剂 (IC50:10nM)。 | |||
T7476 |
AS057278
3-Methylpyrazole-5-carboxylic acid,5-甲基-1H-吡唑-3-羧酸 |
Others | Others |
AS057278 (3-Methylpyrazole-5-carboxylic acid) 是一种 D-氨基酸氧化酶 (DAAO) 抑制剂。 | |||
T0171 |
Norethynodrel
Lynestrol,异炔诺酮 |
Estrogen/progestogen Receptor | Endocrinology/Hormones |
Norethynodrel (Lynestrol) 是一种合成的孕激素,其作用和用途类似于孕酮。它已被用于治疗功能性子宫出血和子宫内膜异位症。它作为避孕药,通常与 MESTRANOL 联合使用。 | |||
T23284 |
Ryuvidine
|
Histone Demethylase; Histone Methyltransferase; CDK | Cell Cycle/Checkpoint; Chromatin/Epigenetic |
Ryuvidine 是一种 KDM5A 和 SETD8 双重抑制剂,是一种 DNA 损伤反应的诱导剂,具有潜在的抗癌活性,抑制 H4K20 甲基化,抑制 CDK4,可用于研究乳腺癌和红斑病。 | |||
T14034 |
3CAI
|
Akt | Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
3CAI 是特异性的AKT1和AKT2抑制剂。 | |||
T11226 |
ERK1/2 inhibitor 1
|
ERK | MAPK |
ERK1/2 inhibitor 1 is a potent, orally bioavailable ERK1/2 inhibitor, showing 60% inhibition at 1 nM and an IC50 of 3.0 nM against ERK1 and ERK2, respectively. | |||
T2576 |
Brivanib (alaninate)
丙氨酸布立尼布,BMS-582664,Brivanib Alaninate |
VEGFR; FGFR; Autophagy | Angiogenesis; Autophagy; Tyrosine Kinase/Adaptors |
Brivanib Alaninate (BMS-582664) 是一种血管内皮生长因子受体 2 (VEGFR2) 抑制剂的丙氨酸盐,IC50值为 25 nM,具有潜在的抗肿瘤活性。它对 VEGFR1 和 FGFR1 适度抑制,对 VEGFR2 的选择性是对 PDGFRβ 的 240 倍。 | |||
T68163 |
Timcodar
|
Antibacterial | Microbiology/Virology |
timcodar 是一种非 FKBP12 结合大环内酯衍生物,是外排泵抑制剂,具有抗菌活性,抑制脂质积累,抑制结核杆菌,可用于研究肥胖。 | |||
T25770 |
116-9e
MAL-2-11B,MAL2-11B,MAL211B,MAL 2 11B,MAL2 11B |
Virus Protease | Microbiology/Virology |
116-9e (MAL2-11B) 是一种有效的 Hsp70 共伴侣 DNAJA1 抑制剂,具有抗病毒,抑制猿猴病毒40 (SV40) 的复制,抑制肿瘤抗原 (TAg) 内源性 ATP 酶活性和 TAg 介导的 Hsp70 激活。116-9e 可用于研究癌症耐药性。 | |||
T6686 |
Sulconazole mononitrate
Exelderm,Sulconazole Nitrate,RS 44872,硝酸硫康唑 |
Antibacterial; Antibiotic; Antifungal | Microbiology/Virology |
Sulconazole mononitrate (Exelderm) 是一种咪唑类广谱杀菌剂。它可研究皮肤真菌病,花斑糠疹病,皮肤念珠菌病。 | |||
T12430 |
PF-06821497
|
Histone Methyltransferase | Chromatin/Epigenetic |
PF-06821497 是一种特异性的 EZH2 抑制剂,具有显着的肿瘤生长抑制作用。 | |||
T1348 |
Diphenyl phosphate
磷酸二苯酯,Phenyl hydrogen phosphate |
Others | Others |
Diphenyl Phosphate 能够性别特异性的抑制斑马鱼的生长和能量代谢。 | |||
T15044 |
D609
|
Apoptosis; Antioxidant | Apoptosis; oxidation-reduction |
D609 (Tricyclodecan-9-yl-Xanthogenate) 具有广泛的生物活性,包括抗氧化、抗凋亡、抗胆碱能、抗肿瘤、抗炎、抗病毒、抗增殖和神经保护活性。D609 通过引起磷脂酰胆碱 (PC) 特异性磷脂酶 C (PC-PLC) 和鞘磷脂合酶 (SMS) 的竞争性抑制来发挥作用。 | |||
T6244 |
Cidofovir
HPMPC,GS 0504,西多福韦,(S)-HPMPC |
Others; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Others |
Cidofovir ((S)-HPMPC) 通过特异性抑制病毒 DNA 合成来抑制病毒复制。 | |||
T1428 |
Trifluridine
曲氟尿苷,NSC 529182,Trifluorothymidine,5-Trifluorothymidine,NSC 75520,曲氟胸苷,Viroptic,Trifluridina |
Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis; HSV | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Trifluridine (NSC-75520) 是一种氟化胸苷类似物,具有潜在的抗肿瘤活性,还具有抗病毒活性。它掺入 DNA 并抑制胸苷酸合酶,从而抑制 DNA 合成、抑制蛋白质合成和细胞凋亡。 | |||
T15581 |
Inolitazone
RS5444,Efatutazone,CS-7017,伊诺他酮 |
PPAR | DNA Damage/DNA Repair; Metabolism |
Inolitazone (RS5444) 是一种高亲和力PPARγ激动剂。在体外,Inotazone 显示生长抑制的IC50约为0.8 nM。 | |||
T60019 |
VPC-70063
Thiourea, N-[3,5-bis(trifluoromethyl)phenyl]-N'-(phenylmethyl)- |
Apoptosis; PARP; c-Myc | Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; DNA Damage/DNA Repair |
VPC-70063 (Thiourea, N-[3,5-bis(trifluoromethyl)phenyl]-N'-(phenylmethyl)-) 是 c-Myc-MAX 的抑制剂。 VPC-70063 的 Myc-Max 转录活性抑制率为 106%,IC50 为 8.9 μM,Myc-Max/UBE2C 下游通路抑制率为 94%。 VPC-70063 可用于抗癌研究。 | |||
T5101 |
BW-A 78U
BW-A78U |
PDE | Metabolism |
BW-A 78U 抑制 PDE4,其 IC50值为 3 μM。 | |||
T6536 |
HJC0350
|
cAMP | GPCR/G Protein |
HJC0350 是一种有效地、选择性的EPAC2拮抗剂(IC50:0.3 µM)。 | |||
T14997 |
Conteltinib
SY-707,CT-707 |
FAK; PYK2; ALK | Angiogenesis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors |
Conteltinib (CT-707) 是一种靶向FAK、ALK 和 Pyk2 的酶抑制剂,具有抗肿瘤活性。Conteltinib 对 FAK 有明显的抑制作用,通过抑制 YAP 信号传导来克服肝细胞癌中缺氧介导的索拉非尼耐药性,可用于晚期 ALK 阳性非小细胞肺癌和淋巴癌。 | |||
T6831 |
Etretinate
Retinoid,Tegison,Etretinato,Ethyl etrinoate,Ro 10-9359,依曲替酯 |
Apoptosis; Others | Apoptosis; Others |
Etretinate (Ro 10-9359) 是一种口服芳香族维甲酸,对牛皮癣和其他皮肤病综合征有效。 它激活类视黄醇受体,引起细胞分化的诱导、细胞增殖的抑制和炎症细胞对组织浸润的抑制。 | |||
T9360 |
CRBN ligand-9
2-(2,6-dioxopiperidin-3-yl)-5-nitroisoindoline-1,3-dione |
Ligand for E3 Ligase | PROTAC |
CRBN ligand-9 (2-(2,6-dioxopiperidin-3-yl)-5-nitroisoindoline-1,3-dione) 表现出对 CRBN 的抑制作用。 | |||
T27102 |
CV-6209
CV6209,CV 6209 |
PAFR; AChE | GPCR/G Protein; Neuroscience |
CV-6209 是一种具有选择性和高效性的血小板活化因子 (PAF) 拮抗剂,具有抗增殖作用,部分抑制乙酰胆碱诱导的低血压,抑制 Paf 诱导的 PMN 或血小板聚集。CV-6209 具有抗幽门螺杆菌作用,可以抑制 PAF 引起的大鼠低血压。 | |||
T1849 |
Momelotinib
CYT11387,CYT387,LM-1149 |
Apoptosis; JAK; Autophagy | Angiogenesis; Apoptosis; Autophagy; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells |
Momelotinib (LM-1149) 是一种 ATP 竞争性的 JAK1/JAK2抑制剂,IC50值分别为 11 nM/18 nM。 | |||
T0676 |
Hydroxyurea
Hydroxycarbamide,羟基脲,nsc32065,nci-c04831 |
Apoptosis; HIV Protease; DNA/RNA Synthesis; Autophagy | Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Proteases/Proteasome |
Hydroxyurea (Hydroxycarbamide) 是一种抗肿瘤剂,通过抑制核糖核苷二磷酸还原酶来抑制 DNA 合成。 | |||
T3352 |
XL413
|
cholecystokinin; Casein Kinase; Pim; CDK | Cell Cycle/Checkpoint; Chromatin/Epigenetic; GPCR/G Protein; JAK/STAT signaling; Metabolism; Stem Cells |
XL413 是一种口服生物可利用的细胞分裂周期 7 同源物 (CDC7) 激酶抑制剂,具有潜在的抗肿瘤活性,IC50值为 3.4 nM。它对 pMCM 的 EC50值为 118 nM,对 CK2 和 PIM1 的 IC50值分别为 215 和 42 nM。 | |||
T9015 |
LY900009
|
Gamma-secretase | Neuroscience; Proteases/Proteasome; Stem Cells |
LY900009 是一种通过选择性抑制 γ-分泌酶蛋白来抑制 Notch 信号传导的小分子抑制剂。 | |||
T6632 |
Raltitrexed
ZD1694,雷替曲塞,D1694,ICI-D1694,Tomudex |
Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Raltitrexed (D1694) 是一种抗代谢药物,通过抑制胸苷酸合成酶起作用,可用于化疗。 | |||
T9345 |
Aminopeptidase M
|
Others | Others |
Aminopeptidase M 抑制对多种疾病(例如高度血管化的癌症类型)具有重要意义。 | |||
T8694 |
ML406
|
Antibacterial; Antibiotic | Microbiology/Virology |
ML406 是一种小分子探针,通过抑制M.tuberculosisBioA(DAPA 合酶) 显示出抗结核活性,IC50为 30 nM。 | |||
T24444 |
Medifoxamine
LG 152,Medifoxamina,LG-152,LG152 |
Dopamine Receptor; Monoamine Oxidase | GPCR/G Protein; Neuroscience |
Medifoxamine (LG 152) 是一种选择性非单胺氧化酶抑制剂,通过对5 HT 再摄取的抑制展现其抗抑郁活性。Medifoxamine 优先抑制多巴胺再摄取 (dopamine reuptake)。 | |||
T7690 |
2-hydroxy Flutamide
|
Androgen Receptor | Endocrinology/Hormones |
2-hydroxy Flutamide 是 Flutamide 的活性代谢物,是雄激素受体拮抗剂,其 IC50值为700 nM。它可用于研究前列腺癌。 | |||
T24214 |
Phenamacril
JS39919,苯那普利,JS399 19 |
Myosin; Antifungal | Cytoskeletal Signaling; Microbiology/Virology |
Phenamacril (JS39919) 是一种氰基丙烯酸酯类杀菌剂,对镰刀菌,特别是禾谷镰刀菌有很强的抑制作用。它是一种特异性镰刀菌肌球蛋白 I 抑制剂。 | |||
T2627 |
Nolatrexed dihydrochloride
盐酸诺拉曲塞,Thymitaq,AG 337 |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Nolatrexed dihydrochloride (Thymitaq) 是一种非竞争性的胸苷酸合酶抑制剂,能够在癌细胞 S 期诱导细胞周期停滞,具有抗癌活性。它与该酶的叶酸辅因子结合位点相互作用,对人胸苷酸合酶的Ki 值为 11 nM。 | |||
T14673 |
BMS 299897
|
Beta Amyloid; Gamma-secretase | Neuroscience; Proteases/Proteasome; Stem Cells |
BMS 299897 是一种磺胺类 γ 分泌酶抑制剂。它在稳定过表达淀粉样前体蛋白(APP)的 HEK293 细胞中抑制 Aβ 生成的 IC50 值为 7 nM。 | |||
T33795 |
3-OMFP Cyclohexylammonium salt
OMFP Cyclohexylammonium salt |
Others | Others |
3-OMFP Cyclohexylammonium salt (OMFP Cyclohexylammonium salt) 是 PTEN 抑制研究的底物,可用来测定CDC25B催化结构域的酶活性。 | |||
TNU0022 |
6-Azauridine
6-Azuridine |
Apoptosis | Apoptosis |
6-Azauridine (6-Azuridine) is a purine nucleoside analog with a broad spectrum of antitumor activity, targeting malignant tumors of the inert lymphatic system and inducing apoptosis.6-Azuridine's anticancer mechanism is dependent on the inhibition of DNA synthesis. | |||
T5455 |
HT-2157
SNAP37889,SNAP-37889 |
Neuropeptide Y Receptor | GPCR/G Protein; Neuroscience |
HT-2157 (SNAP-37889) 是一种高亲和力、选择性和竞争性的甘丙肽 3 受体 (Gal3) 拮抗剂。 | |||
T29170 |
XU1
Benzo[c][1,8]naphthyridin-6(5h)-One |
Aurora Kinase | Cell Cycle/Checkpoint; Chromatin/Epigenetic |
XU1(Benzo[c][1,8]naphthyridin-6(5h)-One) 是一种 Aurora 蛋白激酶抑制剂,用于治疗适合激酶信号转导抑制、调节或调节的疾病。 | |||
T10671 |
Candoxatril
UK 79300 |
Neprilysin | Metabolism |
Candoxatril (UK 79300) 是具有口服活性的中性肽链内切酶 (NEP,EC 3.4.24.11) 抑制剂,可改善接受血管紧张素转换酶抑制的慢性心力衰竭患者的运动能力。 | |||
T2267 |
BQU57
|
GTPase; Ras | GPCR/G Protein; MAPK |
BQU57 能够选择性抑制 Ral,且对 Ral 的选择性高于 Ras、Rho,能够作用于 H2122(IC50:2.0 μM)和 H358(IC50:1.3 μM)。 | |||
T29135 |
VU0422288
VU-0422288,ML-396,ML396,VU 0422288,ML 396 |
GluR | Neuroscience |
VU0422288 (ML396) 是一种有效的 III 型 mGlu 受体 (mGlus) 正变构调节剂。VU0422288在钙动员试验中对 mGluR4、mGluR7 和 mGluR8 显示出抑制作用。VU0422288 可用于研究 Rett 综合症 (RTT)。 | |||
T12831L |
SAR405
|
PI3K; Autophagy | Autophagy; PI3K/Akt/mTOR signaling |
SAR-405 是一种选择性 PIK3C3/Vps34 抑制剂,IC50为1.2 nM,Kd 为1.5 nM,可防止自噬并与肿瘤细胞中的 MTOR 抑制协同作用。它抑制饥饿或 mTOR 抑制诱导的自噬,具有抗癌活性。 | |||
T63119 |
NF-κB/MAPK-IN-1
|
NF-κB; MAPK | MAPK; NF-κB |
NF-κB/MAPK-IN-1 是一种有效的 NF-κB 和 MAPK 通路双重抑制剂,具有潜在的抗炎活性,抑制 NO 生成,对 LPS 诱导的iNOS,COX-2,ERΚ和P38激活有抑制作用。 NF-κB/MAPK-IN-1 可用于预防和治疗类风湿关节炎 (RA) 。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5722 |
Nevadensin
Pedunculin,石吊兰素,5,7-二羟基-6,8,4'-三甲氧基黄酮 |
Anti-infection; Antibacterial | Microbiology/Virology |
Nevadensin 是一种重要的草本成分,可抑制雌二醇的生物活化。 它具有抗结核分枝杆菌、镇咳、抗炎、抗高血压等多种药理作用。 | |||
T5S0384 |
Rhapontin
Ponticin,土大黄苷,Rhaponiticin,Rhaponticin,Rhapontigenin glucoside |
Apoptosis; Others | Apoptosis; Others |
Rhapontin (Ponticin) 是药用大黄的一种成分,可减轻KK/Ay 糖尿病小鼠肝脏脂肪变性,改善血糖和血脂,表明其具有显着的降糖作用,有望成为治疗2型糖尿病及其并发症的新药。 | |||
T1465 |
Mupirocin
Pseudomonic acid,莫匹罗星,BRL-4910A |
DNA/RNA Synthesis; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Mupirocin (BRL-4910A) 是从Pseudomonas fluorescens 中分离得到的一种有口服活性的抗生素。它可逆地抑制异亮氨酸转移RNA,并抑制细菌蛋白和RNA 的合成起抗菌作用。 | |||
T8148 |
Mupirocin calcium hydrate
莫匹罗星钙,Mupirocin calcium |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Mupirocin calcium hydrate 是从Pseudomonas fluorescens 中分离得到的,一种有口服活性的抗生素。它可逆地抑制异亮氨酸转移RNA,并抑制细菌蛋白和RNA 的合成起到抗菌作用。 | |||
T3880 |
Silydianin
水飞蓟宁,Silidianin |
Phosphatase | Metabolism |
Silydianin (Silidianin) 是一种水飞蓟的活性成分,具有抗胶原酶和抗弹性酶作用,对氧化产物的体外产生和释放具有抑制作用 。它是一种天然蛋白酪氨酸磷酸酶 1B 抑制剂,其IC50=17.38 μM。 | |||
T10886 |
Crocetine dimethyl ester
Dimethylcrocetin |
Antioxidant | oxidation-reduction |
Crocetine dimethyl ester (Dimethylcrocetin) 是一种藏红花素衍生物,具有抗氧化活性,抑制 AChE 活性,抑制细胞生长分化。 | |||
T3401 |
Ginsenoside F1
人参皂苷 F1,20(S)-Ginsenoside F1 |
P450; Endogenous Metabolite | Metabolism |
Ginsenoside F1 (20(S)-Ginsenoside F1) 是一种 Ginsenoside Rg1 的酶促修饰衍生物,它竞争性抑制CYP3A4,对 CYP2D6 具有较弱的抑制作用。 | |||
T3817 |
Darutigenol
|
Others | Others |
Darutigenol 是一种戊二萜,从Siegesbecikia orientalis L.中分离得到。 | |||
T3899 |
Calceolarioside B
Desrhamnosyl isoacteoside,木通苯乙醇苷 B,Nuomioside A,木通苯乙醇苷B |
Aromatase | Endocrinology/Hormones |
Calceolarioside B (Desrhamnosyl isoacteoside) 是一种分离自Stauntonia hexaphylla 叶片中的天然产物。它抑制 DPPH 自由基清除活性(IC50:94.60 μM)。它显著抑制大鼠晶状体醛糖还原酶(RLAR)活性(C50:23.99 μM。 | |||
TN3460 |
Asebogenin
|
Antifungal | Microbiology/Virology |
Asebogenin 是从丹参中分离出来的化合物,具有抗真菌活性,对GPVI 诱导的血小板反应有抑制作用,抑制促炎刺激诱导的 NET 形成。 | |||
T3S1850 |
Bayogenin
|
Others | Others |
Bayogenin 是紫花苜蓿皂苷,一定程度上能够抑制糖原磷酸化酶的活性。 | |||
TN1057 |
Veratrosine
藜芦托素,Veratramine 3-glycoside,Veratramine-beta-D-glucoside |
Platelet aggregation | Others |
Veratrosine (Veratramine-beta-D-glucoside) 是一种从藜芦草本植物中分离出来的生物碱。 Veratrosine 对血小板聚集表现出微弱的抑制活性。 | |||
T2S0973 |
2-Methoxycinnamic acid
AI3-11206,o-Methoxycinnamic acid,2-甲氧基肉桂酸 |
Tyrosinase | Proteases/Proteasome |
2-Methoxycinnamic acid (o-Methoxycinnamic acid) 是非竞争性的酪氨酸酶抑制剂。 | |||
TN2343 |
Pseudojervine
Jervin-3-glucoside,O-beta-D-Glucopyranosyljervine,假白藜芦碱 |
Platelet aggregation | Others |
Pseudojervine (O-beta-D-Glucopyranosyljervine) 来源于 Veratrum nigrum L. Pseudojervine 对血小板聚集表现出微弱的抑制活性。 | |||
T19931 |
Gentisein
NSC 329491,NSC329491,NSC-329491 |
Serotonin Transporter | Neuroscience |
Gentisein (NSC-329491) 是 Mangiferin 的主要代谢物,有效抑制 5-HT 的摄取,IC50为 4.7 µM。 | |||
TN2202 |
Sempervirine
常绿钩吻碱 |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Sempervirine 可以解开环状 DNA,它显示出选择性抑制癌症 DNA 的体外合成。 | |||
T3668 |
Galangin
Norizalpinin,高良姜素,3,5,7-Trihydroxyflavone |
ERK; P450; NF-κB; Autophagy | Autophagy; MAPK; Metabolism; NF-κB |
Galangin (Norizalpinin) 是芳烃受体的激动剂/拮抗剂,并且还显示对 CYP1A1 活性的抑制作用。 | |||
TN1733 |
Hesperetin 7-O-glucoside
|
Anti-infection; Antibacterial; HMG-CoA Reductase | Metabolism; Microbiology/Virology |
Hesperetin 7-O-glucoside 是通过 Hesperidin 的酶促转化产生的一种人 HMG-CoA 还原酶抑制剂,具有降压作用,可抑制幽门螺杆菌的生长。 | |||
TN3548 |
Bulleyanin
|
Others | Others |
Bulleyanin 是从 isodon species (Labiatae) 中分离出来的一种物质。 | |||
T1441 |
Capreomycin sulfate
Capastat sulfate,硫酸卷曲霉素 |
ribosome; Antibacterial; Antibiotic | Microbiology/Virology |
Capreomycin sulfate (Capastat sulfate) 是一种多肽类抗生素,与其它抗生素结合用于MDR-肺结核。 | |||
TN7125 |
2-Propen-1-one, 1-(2,6-dimethoxyphenyl)-3-(4-hydroxyphenyl)-
|
Others | Others |
2-Propen-1-one, 1-(2,6-dimethoxyphenyl)-3-(4-hydroxyphenyl)- 可用于对 L-苯丙氨酸解氨酶的抑制作用的研究。 | |||
TN1021 |
Secologanic acid
|
NO Synthase | Immunology/Inflammation |
Secologanic acid 是裂环烯醚萜苷的一种。 | |||
T2S2018 |
7beta-Hydroxylathyrol
7β-Hydroxylathyrol,7-Hydroxylathyrol,7-beta-Hydroxylathyrol,7-羟基千金子二萜醇 |
P-gp | Membrane transporter/Ion channel; Neuroscience |
7β-Hydroxylathyrol 是天然萜类化合物的一种。 | |||
T8187 |
Tetrahydroepiberberine
|
Others; Influenza Virus; Antifungal | Microbiology/Virology; Others |
Tetrahydroepiberberine 是从Corydalis impatiens(Pall) 中分离得到的一种异喹啉生物碱,具有抗真菌和选择性抑制 PI-3 病毒活性的作用。 | |||
T6213 |
Vinorelbine ditartrate
Vinorelbine Tartrate,Nor-5'-anhydrovinblastine ditartrate,KW-2307,Navelbine tartrate,长春瑞滨酒石酸盐,酒石酸长春瑞滨 |
Microtubule Associated; Autophagy | Autophagy; Cytoskeletal Signaling |
Vinorelbine ditartrate (KW-2307)是一种抗有丝分裂剂,能够抑制 Hela 细胞的增殖,IC50值为 1.25 nM。 | |||
T3682 |
(-)-Catechin gallate
(-)-Catechin 3-O-gallate,儿茶素没食子酸酯,几茶素没食子酸酯,(-)-Catechin 3-gallate |
Others; COX | Immunology/Inflammation; Neuroscience; Others |
(-)-Catechin gallate ((-)-Catechin 3-O-gallate) 是绿茶儿茶素中的微量组分,可抑制COX-1和COX-2活性。它抑制人 Beta-secretase,对氯喹敏感的恶性疟原虫 NF54 和耐氯喹的恶性疟原虫 K1 具有抗疟原虫活性。 | |||
TQ0070 |
Luteolin-3-O-beta-D-glucuronide
|
Others | Others |
Luteolin-3-O-beta-D-glucuronide 是木犀草素葡萄糖醛酸,木犀草素的 3’ 端位置有 β-d-葡萄糖苷酸残基。 | |||
T1276 |
Danofloxacin mesylate
甲磺酸达氟沙星,CP 76136-27 |
DNA/RNA Synthesis; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Danofloxacin mesylate (CP 76136-27) 是一种兽医用氟喹诺酮类抗菌素。 | |||
T2S1181 |
Aloenin
Aloenin A,Aloearbonaside,芦荟宁 |
Beta-Secretase; AChR | Neuroscience |
Aloenin (Aloenin A) A 是一种具有清除过氧自由基作用的天然产物,对 β-分泌酶 (BACE) 具有中等抑制活性。 | |||
TN1995 |
5,7,8-Trimethoxyflavone
Norwogonin 5,7,8-trimethyl ether |
NO Synthase | Immunology/Inflammation |
5,7,8-Trimethoxyflavone (Norwogonin 5,7,8-trimethyl ether) 是从穿心莲中提取的化合物,具有抗炎活性,对 NO 有抑制作用。 | |||
TN7126 |
N-Vanillyloctanamide
|
Others | Others |
N-Vanillyloctanamide 是一种来自 Capsicum annuum L. var. 果实的辣椒素。年鉴。 N-Vanillyloctanamide 减少 Lactuca sativa 幼苗的自由基长度,这种抑制是剂量依赖性的。 | |||
TN1137 |
Isobutylshikonin
|
Others | Others |
Isobutylshikonin 是分离自Lithospermum canescens 毛状根培养的一种紫草素色素。 | |||
T12651 |
Rabdosiin
(+)-Rabdosiin |
Others | Others |
Rabdosiin ((+)-Rabdosiin) 是一种分离自 Rabdosia japonicaHara 中的咖啡酸四聚体,具有抗过敏、抗 HIV 和抑制 DNA 拓扑异构酶作用。 | |||
TN2008 |
Okanin
|
NF-κB; TLR | Immunology/Inflammation; NF-κB |
Okanin 是鬼针草中的一种有效成分,可通过抑制TLR4/NF-κB 信号通路减弱 LPS 诱导的小胶质细胞活化。 | |||
T3S1967 |
(S)-Indoximod
N-ME-Tryptophan,Abrine,相思豆碱,L-Abrine |
Others; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism; Others |
(S)-Indoximod (L-Abrine) 是一种吲哚胺-2,3-双加氧酶 (IDO) 抑制剂,可用于研究癌症。 | |||
T6413 |
Bindarit
宾达利,AF2838 |
CCR | Immunology/Inflammation; Microbiology/Virology |
Bindarit (AF2838) 是单核细胞趋化蛋白MCP-1/CCL2,MCP-3/CCL7和MCP-2/CCL8的选择性抑制剂,具有抗炎作用。 | |||
T6S1529 |
Cynarin
Cyclohexanecarboxylic acid, 1,3-bis[[3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-4,5-dihydroxy-, (1R,3R,4S,5R)-,Cynarine,1,5-Dicaffeoylquinic acid,洋蓟素,金银花 |
Antioxidant; Antiviral; Influenza Virus; Reactive Oxygen Species | Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB; oxidation-reduction |
Cynarin (1,5-Dicaffeoylquinic acid) 是一种抗窒息剂,具有抗氧化、抗组胺和抗病毒等多种生物活性。 | |||
T6S0444 |
Salvianolic acid A
丹酚酸 A,Dan Phenolic Acid A |
MMP | Proteases/Proteasome |
Salvianolic acid A (Dan Phenolic Acid A) 能够提高抑制基质金属钛酶 9 和抗炎作用,进而保护血脑屏障。 | |||
T8244 |
Raspberry ketone glucoside
覆盆子酮葡糖苷,树莓苷,覆盆子酮葡萄糖甙 |
Others | Others |
Raspberry ketone glucoside 是一种山莓果实中的天然产物。它能够抑制黑色素的合成。 | |||
T4S0111 |
Hupehenine
湖贝甲素,梭砂贝母碱 |
AChR | Neuroscience |
Hupehenine 是 Fritillariae Bulbus 中主要的止咳成分,是具有生物活性的异甾类生物碱。 | |||
TWS1977 |
Kamebakaurin
尾叶香茶菜丙素,Kamebakaurine |
NF-κB | NF-κB |
Kamebakaurin (Kamebakaurine) 是一种提取自Isodon japonicus 中的天然产物,是一种NF-κB 的抑制剂,能够抑制 p50 的 DNA 结合活性。 | |||
T2S1086 |
Nepitrin
假荆芥属苷,Nepetin-7-glucoside |
Antioxidant | oxidation-reduction |
Nepitrin (Nepetin-7-glucoside) 分离自Scrophularia striata 中,具有强大的抗炎、抗关节炎作用。 | |||
TN6710 |
Methyl acetylsalicylate
ACETYLSALICYLIC ACID METHYL ESTER,乙酰水杨酸甲酯 |
Others | Others |
Methyl acetylsalicylate (ACETYLSALICYLIC ACID METHYL ESTER) 是一种从豌豆中分离出来的天然产物。抑制胶原蛋白诱导的人富含血小板的血浆聚集。 | |||
T5S1952 |
9-Methoxycamptothecin
|
Apoptosis; Topoisomerase | Apoptosis; DNA Damage/DNA Repair |
9-Methoxycamptothecin 是从臭味假柴龙树中分离得到的一种天然产物,通过抑制拓扑异构酶起到抗肿瘤作用,具有强效的诱导 G2/M 期细胞和癌细胞凋亡的作用。 | |||
TN1975 |
Neosmitilbin
Neoastilbin,新落新妇苷 |
Others | Others |
Neosmitilbin (Neoastilbin) 分离于 Garcinia mangostana。它能够有效抑制晶状体醛糖还原酶的活性,可能具有抗氧化和抗炎作用。 | |||
T3S2340 |
Usaramine
(15E)-Retrorsine,Mucronatine,光萼野百合碱,NISTC15503874 |
Others; Antibacterial | Microbiology/Virology; Others |
Usaramine (Mucronatine) 是从 Crolatalaria pallida 种子中分离得到的一种吡咯里嗪类生物碱。它对 Lactuca sativa var 具有植物毒性。 | |||
TN5503 |
Linaroside
|
Antibacterial | Microbiology/Virology |
Linaroside 在 6.25 microg mL(-1) 浓度下对结核分枝杆菌、菌株 H(37)Rv 的抗分枝杆菌活性表现出 30%的抑制作用。 | |||
T3796 |
Betulinaldehyde
Betulinic aldehyde,Betulinal,Betunal,白桦脂醛 |
Apoptosis; Antibacterial | Apoptosis; Microbiology/Virology |
Betulinaldehyde (Betunal) 是五环三萜,有抗金黄色葡萄球菌等细菌和真菌作用。 | |||
T3819 |
Ursolic acid acetate
熊果酸乙酸酯,Acetylursolic acid,3-Acetylursolic Acid |
AChE | Neuroscience |
Ursolic acid acetate (Acetylursolic acid) 分离于 Ficus microcarpa 的气根中,对 KB 细胞显示细胞毒性(IC50:8.4 μM)。 | |||
T6S2115 |
Ginkgolide J
BN 52024,7-beta-Hydroxyginkgolide A,银杏内酯 J,银杏内酯J |
PDE | Metabolism |
Ginkgolide J (BN 52024) 是一种银杏叶中非黄酮部分的主要成分(IC50:12-54 µM),具有神经保护和抗神经元凋亡功能。 | |||
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Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPK-00782 |
PLAU/uPA Protein, Mouse, Recombinant (His & Avi)
PLAU,UPA,BDPLT5,ATF,u-PA,QPD,Urokinase,URK |
Mouse | HEK293 Cells |
Plasminogen activator, urokinase (uPA) is a secreted serine protease whose Dysregulation is often accompanied by various cancers. PLAU inhibition could suppress tumor growth. Collectively, PLAU is necessary for tumor progression and can be a diagnostic and prognostic biomarker in HNSCC. PLAU/uPA Protein, Mouse, Recombinant (His & Avi) is expressed in HEK293 mammalian cells with C-His-Avi tag. The predicted molecular weight is 49.00 kDa and the accession number is P06869. | |||
TMPK-00022 |
Galectin-1 Protein, Human, Recombinant (hFc)
GAL1,LGALS1,Galectin-1,S-Lac lectin 1,DKFZp686E23103,GBP,Gal... |
Human | HEK293 Cells |
Galectin 1 (Gal-1), a β-galactoside binding mammalian lectin of 14KDa, is implicated in many signalling pathways, immune responses associated with cancer progression and immune disorders. Inhibition of human Gal-1 has been regarded as one of the potential therapeutic approaches for the treatment of cancer, as it plays a major role in tumour development and metastasis by modulating various biological functions viz. apoptosis, angiogenesis, migration, cell immune escape. | |||
TMPY-02078 |
HtrA2/Omi Protein, Human, Recombinant (His)
PARK13,OMI,HtrA serine peptidase 2,PRSS25 |
Human | E. coli |
Serine protease HTRA2, also known as high-temperature requirement protein A2, Omi stress-regulated endoprotease, Serine protease 25, Serine proteinase OMI and HTRA2, is a single-pass membrane protein that belongs to the peptidase S1B family. HTRA2 contains one PDZ (DHR) domain. HTRA2 is a serine protease that shows proteolytic activity against a non-specific substrate beta-casein. It promotes or induces cell death either by direct binding to and inhibition of BIRC proteins (also called inhibitor... | |||
TMPY-02483 |
ATP citrate lyase/ACLY Protein, Human, Recombinant (His)
ATPCL,ACL,ATP citrate lyase,CLATP |
Human | Baculovirus Insect Cells |
ATP citrate lyase, also known as Acly or Acl, is the primary enzyme responsible for the synthesis of cytosolic acetyl-CoA in many tissues. The enzyme is composed of two polymer chains which are polypeptides in human. ATP citrate lyase is responsible for catalyzing the conversion of citrate and CoA into acetyl-CoA and oxaloacetate, along with the hydrolysis of ATP. A definitive role for ATP citrate lyase in tumorigenesis has emerged from ATP citrate lyase RNAi and chemical inhibitor studies, show... | |||
TMPJ-01172 |
IL-17 Protein, Mouse, Recombinant (His)
CTLA8,IL-17,IL-17A,Interleukin-17A,CTLA-8,Cytotoxic T-Lympho... |
Mouse | HEK293 Cells |
Interleukin-17 is a potent pro-inflammatory cytokine produced by activated memory T cells. There are at least six members of the IL-17 family in humans and in mice. Mature mouse IL-17A shares 61% and 89% amino acid sequence identity with human and rat IL-17A, respectively. As IL-17 shares properties with IL-1 and TNF-alpha, it may induce joint inflammation and bone and cartilage destruction. This cytokine is found in synovial fluids of patients with rheumatoid arthritis, and produced by rheumato... | |||
TMPY-05176 |
AMH Protein, Human, Recombinant (His)
MIS,anti-Mullerian hormone,MIF |
Human | HEK293 Cells |
Anti-Mullerian hormone (AMH), a member of the TGF-beta superfamily, is produced by granulosa cells (GCs) of preantral and small antral follicles and plays a role in regulating the recruitment of primordial follicles and the FSH-dependent development of follicles. BMP15 up-regulates the transcription of AMH and that the inhibition of p38 MAPK decreases the BMP15-induced expression of AMH and SOX9, suggesting that BMP15 up-regulates the expression of AMH via the p38 MAPK signaling pathway, and thi... | |||
TMPY-04830 |
GAS6 Protein, Mouse, Recombinant (His)
growth arrest-specific 6,Gas-6 |
Mouse | HEK293 Cells |
The growth arrest-specific 6 gene (GAS6) is a member of the family of plasma vitamin K-dependent proteins, which are able to bind to phospholipids using an N-terminal gamma-carboxyglutamic acid domain. GAS6 is a vitamin K-dependent protein, plays a role in the survival, proliferation, migration, differentiation, adhesion, and apoptosis of cells. The growth arrest-specific 6 (GAS6) has been implicated in systemic inflammation and coagulation. Growth arrest-specific 6 (GAS6), plays a role in tumor... | |||
TMPY-02219 |
Influenza A H1N1 (A/Puerto Rico/8/34/Mount Sinai) Non-structural/NS1 Protein (His)
NS1 Protein |
H1N1 | E. coli |
The NS1 Influenza protein is created by the internal protein-encoding, linear negative-sense, single-stranded RNA, NS gene segment and which also codes for the nuclear export protein or NEP, formerly referred to as the NS2 protein, which mediates the export of vRNPs. The non-structural (NS1) protein is found in Influenzavirus A, Influenzavirus B, and Influenzavirus C. The non-structural (NS1) protein of the highly pathogenic avian H5N1 viruses circulating in poultry and waterfowl in Southeast As... | |||
TMPH-00554 |
Trypsin inhibitor DE-3 Protein, Erythrina caffra, Recombinant (His)
Trypsin inhibitor DE-3 |
Erythrina caffra | P. pastoris (Yeast) |
Inhibition of trypsin. | |||
TMPH-02886 |
SOST Protein, Mouse, Recombinant (hFc)
Sost,Sclerostin |
Mouse | HEK293 Cells |
Negative regulator of bone growth that acts through inhibition of Wnt signaling and bone formation. | |||
TMPH-01658 |
MAGEA4 Protein, Human, Recombinant (His)
MAGEA4,Melanoma-associated antigen 4,MAGE-4 antigen,MAGE-41 ... |
Human | HEK293 Cells |
Regulates cell proliferation through the inhibition of cell cycle arrest at the G1 phase. Also negatively regulates p53-mediated apoptosis. | |||
TMPH-01659 |
MAGEA4 Protein, Human, Recombinant (A173T, His & Myc)
MAGE-41 antigen,MAGE-4 antigen,Melanoma-associated antigen 4... |
Human | E. coli |
Regulates cell proliferation through the inhibition of cell cycle arrest at the G1 phase. Also negatively regulates p53-mediated apoptosis. | |||
TMPK-01485 |
HLA-A*01:01&B2M&DSG3 (YTDNWLAVY) Monomer Protein, Human, MHC (His & Avi)
CDHF6,DG3,DSG3,PVA,DSG-3,Desmoglein-3 |
Human | HEK293 Cells |
DSG3 is overexpressed in head neck cancer and is a potential molecular target for inhibition of oncogenesis. DSG3 is identified overexpressed in HNC, with the degree of overexpression associated with clinicopathologic features of the tumor. Inhibition of DSG3 significantly suppresses carcinogenic potential in cellular and in vivo animal studies. These findings suggest that DSG3 is a potential molecular target in the development of adjuvant therapy for HNC. | |||
TMPH-01715 |
CHRM2 Protein, Human, Recombinant (His)
CHRM2,Muscarinic acetylcholine receptor M2 |
Human | E. coli |
The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Primary transducing effect is adenylate cyclase inhibition. Signaling promotes phospholipase C activity, leading to the release of inositol trisphosphate (IP3); this then triggers calcium ion release into the cytosol. CHRM2 Protein, Human, Recombinant (His) is expressed in E. col... | |||
TMPY-00729 |
Cystatin D Protein, Human, Recombinant (His)
CST5,MGC71922,cystatin D |
Human | HEK293 Cells |
Cystatins are natural inhibitors of papain-like (family C1) and legumain-related (family C13) cysteine peptidases. The mammalian cystatin superfamily members are of three major types, including the type 1 cystatins (stefins), type 2 cystatins and the kininogens. As a member of type 2 cystatin, cystatin D is a single-domain protein and also has cysteine residues that form disulfide bridges. In contrast with the wider distribution of all the other family 2 cystatins, cystatin D is tissue-restricte... | |||
TMPY-02425 |
Serpin B4, Protein, Human, Recombinant (His)
SCCA-2,LEUPIN,SCCA1,serpin peptidase inhibitor, clade B (ova... |
Human | Baculovirus Insect Cells |
Overexpression of SERPINB4 in tumor cells inhibited recombinant GrM-induced as well as NK cell-mediated cell death and this inhibition depended on the reactive center loop of the serpin. | |||
TMPJ-00604 |
KIR2DL4 Protein, Human, Recombinant (His)
CD158 Antigen-Like Family Member D,KIR2DL4,MHC Class I NK Ce... |
Human | HEK293 Cells |
Killer cell immunoglobulin-like receptor 2DL4(KIR2DL4) is a Single-pass type I membrane protein and contains 2 Ig-like C2-type (immunoglobulin-like) domains.It belongs to the immunoglobulin superfamily. KIR2DL4 is expressed in all NK cells and some T cells. KIR2DL4 activates the cytotoxicity of NK cells, despite the presence of an immunoreceptor tyrosine-based inhibition motif (ITIM) in its cytoplasmic tail. The ITIM was not necessary for activation of lysis by KIR2DL4. The activation signal of ... | |||
TMPH-03338 |
CHRM1 Protein, Rat, Recombinant (His)
Muscarinic acetylcholine receptor M1,CHRM1 |
Rat | E. coli |
The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Primary transducing effect is Pi turnover. CHRM1 Protein, Rat, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 21.1 kDa and the accession number is P08482. | |||
TMPH-01714 |
CHRM1 Protein, Human, Recombinant (His)
Muscarinic acetylcholine receptor M1,CHRM1 |
Human | E. coli |
The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Primary transducing effect is Pi turnover. CHRM1 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 20.8 kDa and the accession number is P11229. | |||
TMPK-00553 |
ADAM9 Protein, Cynomolgus, Recombinant (His)
Adam9,CORD9,mKIAA0021,Meltrin-γ,Meltrin-gamma,ADAM 9,Mltng,M... |
Cynomolgus | HEK293 Cells |
A disintegrin and metalloproteinase 9 (ADAM9) is a member of the transmembrane ADAM family. It is expressed in different types of solid cancer and promotes tumor invasiveness. ADAM9 may be a prognostic marker for vestibular schwannomas (VS), and ADAM9 inhibition might have the potential as a systemic approach for the treatment of VS. | |||
TMPH-01717 |
CHRM5 Protein, Human, Recombinant (His)
CHRM5,Muscarinic acetylcholine receptor M5 |
Human | E. coli |
The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Primary transducing effect is Pi turnover. CHRM5 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 31.5 kDa and the accession number is P08912. | |||
TMPJ-00008 |
CXCL10 Protein, Human, Recombinant (hFc & His)
INP10,10 kDa Interferon Gamma-Induced Protein,C-X-C Motif Ch... |
Human | HEK293 Cells |
Human C-X-C Motif Chemokine Ligand 10 (CXCL10) is a non-ELR chemokine secreted by various cell types, such as monocytes, endothelial cells and fibroblasts, in response to IFN-γ. CXCL10 functions via chemokine receptor CXCR3. CXCL10 has been attributed to several roles, such as chemoattraction for activated T-lymphocytes, inhibition of angiogenesis, and antitumor activity. | |||
TMPH-01341 |
FILIP1L Protein, Human, Recombinant (His)
FILIP1L,Protein down-regulated in ovarian cancer 1,130 kDa G... |
Human | E. coli |
Acts as a regulator of the antiangiogenic activity on endothelial cells. When overexpressed in endothelial cells, leads to inhibition of cell proliferation and migration and an increase in apoptosis. Inhibits melanoma growth When expressed in tumor-associated vasculature. FILIP1L Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 27.6 kDa and the accession number is Q4L180. | |||
TMPK-00103 |
SOST Protein, Human, Recombinant (His & Avi), Biotinylated
VBCH,DAND6,VBCHsclerosteosis,sclerostin,SOST1,CDD,SOST |
Human | HEK293 Cells |
SOST, also known as sclerostin, is a member of the cerberus/DAN family, a group of secreted glycoproteins characterized by a cysteine-knot motif. SOST is negative regulator of bone growth that acts through inhibition of Wnt signaling and bone formation. SOST Protein, Human, Recombinant (His & Avi), Biotinylated is expressed in HEK293 mammalian cells with N-His-Avi tag. The predicted molecular weight is 24.2 kDa and the accession number is Q9BQB4-1. | |||
TMPK-00539 |
PLAU/uPA Protein (active form), Cynomolgus, Recombinant (His)
URK,ATF,UPA,u-PA,Urokinase,QPD,PLAU,BDPLT5 |
Cynomolgus | HEK293 Cells |
Plasminogen activator, urokinase (uPA) is a secreted serine protease whose Dysregulation is often accompanied by various cancers. PLAU inhibition could suppress tumor growth. Collectively, PLAU is necessary for tumor progression and can be a diagnostic and prognostic biomarker in HNSCC. PLAU/uPA Protein (active form), Cynomolgus, Recombinant (His) is expressed in HEK293 mammalian cells with C-His tag. The predicted molecular weight is 47.23 kDa and the accession number is A0A2K5WND1. | |||
TMPK-01293 |
SOST Protein, Cynomolgus, Recombinant (His)
VBCH,SOST1,sclerostin,DAND6,SOST,CDD,VBCHsclerosteosis |
Cynomolgus | HEK293 Cells |
SOST, also known as sclerostin, is a member of the cerberus/DAN family, a group of secreted glycoproteins characterized by a cysteine-knot motif. SOST is negative regulator of bone growth that acts through inhibition of Wnt signaling and bone formation. SOST Protein, Cynomolgus, Recombinant (His) is expressed in HEK293 mammalian cells with C-His tag. The predicted molecular weight is 22.58 kDa and the accession number is XP_005584428.2. | |||
TMPH-01610 |
LINGO1 Protein, Human, Recombinant (His)
Leucine-rich repeat neuronal protein 6A,LINGO1,Leucine-rich ... |
Human | E. coli |
Functional component of the Nogo receptor signaling complex (RTN4R/NGFR) in RhoA activation responsible for some inhibition of axonal regeneration by myelin-associated factors. Is also an important negative regulator of oligodentrocyte differentiation and axonal myelination. Acts in conjunction with RTN4 and RTN4R in regulating neuronal precursor cell motility during cortical development. | |||
TMPH-01642 |
MELK Protein, Human, Recombinant (His & Myc)
Protein kinase Eg3,Tyrosine-protein kinase MELK,Protein kina... |
Human | E. coli |
Serine/threonine-protein kinase involved in various processes such as cell cycle regulation, self-renewal of stem cells, apoptosis and splicing regulation. Has a broad substrate specificity; phosphorylates BCL2L14, CDC25B, MAP3K5/ASK1 and ZNF622. Acts as an activator of apoptosis by phosphorylating and activating MAP3K5/ASK1. Acts as a regulator of cell cycle, notably by mediating phosphorylation of CDC25B, promoting localization of CDC25B to the centrosome and the spindle poles during mitosis. ... | |||
TMPH-01716 |
CHRM3 Protein, Human, Recombinant (B2M & His)
Muscarinic acetylcholine receptor M3,CHRM3 |
Human | E. coli |
The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Primary transducing effect is Pi turnover. CHRM3 Protein, Human, Recombinant (B2M & His) is expressed in E. coli expression system with N-6xHis-B2M tag. The predicted molecular weight is 40.7 kDa and the accession number is P20309. | |||
TMPJ-01052 |
DYNLL1 Protein, Human, Recombinant (His)
DNCL1,PIN,DLC8,Protein Inhibitor of Neuronal Nitric Oxide Sy... |
Human | E. coli |
Human Dynein Cytoplasmic Light Chain 1 (DYNLL1) has been identified as a protein that interacts with NOS1, leading to NOS1 inhibition. NOS1 dimer is destabilized after binding DYNLL1 a conformation necessary activity, and it regulate numerous biologic processes throughits effects on nitric oxide synthase activity. DYNLL1 is widely expressed, with higher expression in testis and moderate expression in brain. | |||
TMPK-01095 |
MEPE Protein, Mouse, Recombinant (His)
Osteoregulin,MEPE,OF45 |
Mouse | HEK293 Cells |
Matrix extracellular phosphoglycoprotein (MEPE) is expressed in bone and teeth where it has multiple functions. The C-terminus of MEPE contains a mineral-binding, acidic serine- and aspartate-rich motif (ASARM) that is also present in other noncollagenous proteins of mineralized tissues.MEPE-derived ASARM peptides function in phosphate homeostasis and direct inhibition of bone mineralization in a phosphorylation-dependent manner. | |||
TMPH-03733 |
Zaire ebolavirus (strain Kikwit-95) VP35 Protein (His & Myc)
Polymerase cofactor VP35,VP35,Ebola VP35 |
ZEBOV | HEK293 Cells |
Plays an essential role in viral RNA synthesis and also a role in suppressing innate immune signaling. Acts as a polymerase cofactor in the RNA polymerase transcription and replication complexes. Serves as nucleoprotein/NP monomer chaperone prior to the formation of the large oligomeric RNA-bound complexes. Regulates RNA synthesis by modulating NP-RNA interactions and interacting with DYNLL1. VP35-NP interaction controls the switch between RNA-bound NP and free NP and thus the switch between gen... | |||
TMPK-00783 |
PLAU/uPA Protein, Mouse, Recombinant (His & Avi), Biotinylated
ATF,URK,Urokinase,PLAU,u-PA,UPA,QPD,BDPLT5 |
Mouse | HEK293 Cells |
Plasminogen activator, urokinase (uPA) is a secreted serine protease whose Dysregulation is often accompanied by various cancers. PLAU inhibition could suppress tumor growth. Collectively, PLAU is necessary for tumor progression and can be a diagnostic and prognostic biomarker in HNSCC. PLAU/uPA Protein, Mouse, Recombinant (His & Avi), Biotinylated is expressed in HEK293 mammalian cells with C-His-Avi tag. The predicted molecular weight is 49.00 kDa and the accession number is P06869. | |||
TMPK-00102 |
SOST Protein, Human, Recombinant (His & Avi)
VBCHsclerosteosis,SOST1,sclerostin,SOST,CDD,DAND6,VBCH |
Human | HEK293 Cells |
SOST, also known as sclerostin, is a member of the cerberus/DAN family, a group of secreted glycoproteins characterized by a cysteine-knot motif. SOST is negative regulator of bone growth that acts through inhibition of Wnt signaling and bone formation. SOST Protein, Human, Recombinant (His & Avi) is expressed in HEK293 mammalian cells with N-His-Avi tag. The predicted molecular weight is 24.2 kDa and the accession number is Q9BQB4-1. | |||
TMPK-00564 |
TNFR1/CD120a/TNFRSF1A Protein, Cynomolgus, Recombinant (His)
TBP1,TNF-RI,TNFAR,p55,p60,p55-R,TNF-R55,FPF,TNF-R1,TNFR1-d2,... |
Cynomolgus | HEK293 Cells |
Tumour necrosis factor alpha (TNF-α) is a pleiotropic cytokine with both injurious and protective functions, which are thought to diverge at the level of its two cell surface receptors, TNFR1 and TNFR2. In the setting of acute injury, selective inhibition of TNFR1 is predicted to attenuate the cell death and inflammation associated with TNF-α, while sparing or potentiating the protective effects of TNFR2 signalling. | |||
TMPH-03732 |
Zaire ebolavirus (strain Kikwit-95) VP35 Protein (E. col, His & Myc)
Polymerase cofactor VP35,Ebola VP35,VP35 |
ZEBOV | E. coli |
Plays an essential role in viral RNA synthesis and also a role in suppressing innate immune signaling. Acts as a polymerase cofactor in the RNA polymerase transcription and replication complexes. Serves as nucleoprotein/NP monomer chaperone prior to the formation of the large oligomeric RNA-bound complexes. Regulates RNA synthesis by modulating NP-RNA interactions and interacting with DYNLL1. VP35-NP interaction controls the switch between RNA-bound NP and free NP and thus the switch between gen... | |||
TMPJ-00407 |
ROBO4 Protein, Human, Recombinant (hFc)
Magic roundabout,Roundabout homolog 4,UNQ421/PRO3674,ROBO4 |
Human | HEK293 Cells |
Roundabout homolog 4(ROBO4) contains 2 fibronectin type-III domains, 2 Ig-like C2-type (immunoglobulin-like) domains and belongs to the immunoglobulin superfamily.The protein is a receptor for slit proteins, at least for SLIT2, and seems to be involved in angiogenesis and vascular patterning. ROBO4 may mediate the inhibition of primary endothelial cell migration by Slit proteins. | |||
TMPK-01045 |
IL-20RA Protein, Mouse, Recombinant (hFc)
IL-20R1,CRF2-8,IL-20R-alpha,IL-20RA,IL-20R-α,FLJ40993,ZcytoR... |
Mouse | HEK293 Cells |
IL-20RA was highly expressed in the tumor tissue of CRC and related to the advanced stage.IL-20RA was involved in regulating oncogenic and immune pathways and affecting the expression of genes related to cell proliferation and immune evasion in CRC.Super-enhancer inhibition by JQ-1 or iBET-151 suppressed the growth of tumor cells and inhibited the expression of IL-20RA. | |||
TMPJ-00855 |
GLUL Protein, Human, Recombinant (His)
GLUL,GS,Glutamine Synthetase,Glutamate-Ammonia Ligase,GLNS,G... |
Human | E. coli |
Glutamine Synthetase reglutes intracellular concentration of glutamate. Glutamine Synthetase catalyzes the synthesis of glutamine from glutamate and ammonia. Glutamine is an important source of energy and that takes part in cell prolifetation, inhibition of apoptosis, and cell signaling. Glutamine Synthetase is expressed during early fetal stages, and has a role in maintaining body PH by removing ammonia from circulation. Mutations in the GLUL gene are related to congenital glutamine deficiency. | |||
TMPK-00428 |
HER2/ErbB2 Protein, Human, Recombinant (His & Avi)
MLN 19,HER2,HER-2,HERVW,EGFR2,ENV,ERBB2,NEU,HERV7Q,ERVWE1,EN... |
Human | HEK293 Cells |
ErbB2, also called Neu and Her2 (human epidermal growth factor receptor 2), is a type I membrane glycoprotein that is a member of the ErbB family of tyrosine kinase receptors. ErbB family members serve as receptors for the epidermal growth factor (EGF) family of growth factors.Upon ERBB2 activation, the MEMO1-RHOA-DIAPH1 signaling pathway elicits the phosphorylation and thus the inhibition of GSK3B at cell membrane. | |||
TMPK-00893 |
PGF Protein, Human, Recombinant (hFc)
PlGF,SHGC-10760,PGFL,PGF,D12S1900,PlGF-2 |
Human | HEK293 Cells |
Placental growth factor (PGF) is another member of the VEGF family of cytokines with pro-angiogenic and pro-inflammatory effects. Retinal inhibition of PGF in combination with VEGF-A prevents vascular leakage and CNV possibly via modulating their own expression in mononuclear phagocytes. PGF-related, optimized strategies to target inflammation-mediated angiogenesis may help to increase efficacy and reduce non-responders in the treatment of wet AMD patients. | |||
TMPY-04409 |
GRK6 Protein, Human, Recombinant (His & GST)
G protein-coupled receptor kinase 6,GPRK6 |
Human | Baculovirus Insect Cells |
G protein-coupled receptor kinase 6, also known as G protein-coupled receptor kinase GRK6, GRK6, and GPRK6, is a lipid-anchor protein that belongs to the protein kinase superfamily, AGC Ser/Thr protein kinase family, and GPRK subfamily. GRK6 / GPRK6 contains one AGC-kinase C-terminal domain, one protein kinase domain, and one RGS domain. This protein phosphorylates the activated forms of G protein-coupled receptors thus initiating their deactivation. Several transcript variants encoding differen... | |||
TMPK-00274 |
PLAU/uPA Protein (active form), Human, Recombinant (His & Avi), Biotinylated
QPD,Urokinase,BDPLT5,UPA,ATF,URK,u-PA,PLAU |
Human | HEK293 Cells |
Plasminogen activator, urokinase (uPA) is a secreted serine protease whose Dysregulation is often accompanied by various cancers. PLAU inhibition could suppress tumor growth. Collectively, PLAU is necessary for tumor progression and can be a diagnostic and prognostic biomarker in HNSCC. PLAU/uPA Protein (active form), Human, Recombinant (His & Avi), Biotinylated is expressed in HEK293 mammalian cells with C-His-Avi tag. The predicted molecular weight is 49.3 kDa and the accession number is P0074... | |||
TMPH-01428 |
TRAP1 Protein, Human, Recombinant (GST)
TNFR-associated protein 1,Tumor necrosis factor type 1 recep... |
Human | E. coli |
Chaperone that expresses an ATPase activity. Involved in maintaining mitochondrial function and polarization, downstream of PINK1 and mitochondrial complex I. Is a negative regulator of mitochondrial respiration able to modulate the balance between oxidative phosphorylation and aerobic glycolysis. The impact of TRAP1 on mitochondrial respiration is probably mediated by modulation of mitochondrial SRC and inhibition of SDHA. TRAP1 Protein, Human, Recombinant (GST) is expressed in E. coli expressi... | |||
TMPH-02753 |
LINGO1 Protein, Mouse, Recombinant (His)
Leucine-rich repeat neuronal protein 6A,Leucine-rich repeat ... |
Mouse | E. coli |
Functional component of the Nogo receptor signaling complex (RTN4R/NGFR) in RhoA activation responsible for some inhibition of axonal regeneration by myelin-associated factors. Is also an important negative regulator of oligodentrocyte differentiation and axonal myelination. Acts in conjunction with RTN4 and RTN4R in regulating neuronal precursor cell motility during cortical development. LINGO1 Protein, Mouse, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The pre... | |||
TMPY-06179 |
IdeS Protein, Streptococcus pyogenes, Recombinant (His & GST)
|
Streptococcus pyogenes | E. coli |
IdeS (IgG-degrading enzyme of Streptococcus pyogenes) is a secreted cysteine endopeptidase from the human pathogen S. pyogenes with an extraordinarily high degree of substrate specificity, catalyzing a single proteolytic cleavage at the lower hinge of human IgG. This proteolytic degradation promotes inhibition of opsonophagocytosis and interferes with the killing of group A Streptococcus. IdeS Protein, Streptococcus pyogenes, Recombinant (His & GST) is expressed in E. coli expression system with... | |||
TMPH-03599 |
Streptopain Protein, S. pyogenes, Recombinant (His & SUMO)
Group A streptococcal cysteine protease,SPE B,Streptococcus ... |
Streptococcus pyogenes | E. coli |
Important streptococcal virulence factor which cleaves human fibronectin and degrades vitronectin. Also cleaves human IL1B precursor to form biologically active IL1B. Can induce apoptosis in human monocytes and epithelial cells in vitro, and reduces phagocytic activity in monocytic cells. Thus, may play a role in bacterial colonization, invasion, and inhibition of wound healing. Streptopain Protein, S. pyogenes, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO... | |||
TMPJ-00708 |
CST7 Protein, Mouse, Recombinant (His)
CMAP,Cystatin-7,Leukocystatin,Cystatin-like Metastasis-Assoc... |
Mouse | HEK293 Cells |
Mouse Cystatin F belongs to cystatin superfamily, which encompasses proteins that contain multiple cystatin-like sequences. It has been shown that Cystatin F is selectively expressed by hematopoietic cells and may be a biomarker for both liver metastasis and inflammatory lung disorders. Mouse Cystatin F inhibits papain and cathepsin L but with affinities lower than other cystatins. It may play a role in immune regulation through inhibition of a unique target in the hematopoietic system. | |||
TMPK-00829 |
Galectin-1 Protein, Mouse, Recombinant (hFc)
GBP,DKFZp686E23103,S-Lac lectin 1,GAL1,Galectin-1,HLBP14,LGA... |
Mouse | HEK293 Cells |
Galectin 1(Gal-1), a β-galactoside binding mammalian lectin of 14KDa, is implicated in many signalling pathways, immune responses associated with cancer progression and immune disorders. Inhibition of human Gal-1 has been regarded as one of the potential therapeutic approaches for the treatment of cancer, as it plays a major role in tumour development and metastasis by modulating various biological functions viz. apoptosis, angiogenesis, migration, cell immune escape. | |||
TMPJ-00692 |
GAS7 Protein, Human, Recombinant (His)
GAS-7,GAS7,Growth Arrest-Specific Protein 7,KIAA0394 |
Human | E. coli |
Growth Arrest-Specific Protein 7 (GAS7) is expressed primarily in terminalaly differentiated brain cells and predominantly in mature cerebellar Purkinje neurons. GAS7 may play a role in neuronal development by promoting maturation and morphological differentiation of cerebellar neurons. Inhibition of GAS7 production in terminally differentiating cultures of embryonic murine cerebullum impedes neurite outgrowth. The hyper-expression of GAS7 may play an major role in the initiation and development... | |||
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Cat. No. | Product Name | Target | Signaling Pathways |
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TMIH-0124 |
Brivanib Alaninate-d4
|
||
Brivanib Alaninate-d4 是 Brivanib Alaninate 的氘代化合物。Brivanib Alaninate 的 CAS 号为 649735-63-7。Brivanib alaninate 是一种血管内皮生长因子受体 2 (VEGFR2) 抑制剂的丙氨酸盐,IC50值为 25 nM,具有潜在的抗肿瘤活性。它对 VEGFR1 和 FGFR1 适度抑制,对 VEGFR2 的选择性是对 PDGFRβ 的 240 倍。 | |||
T70808 |
Cabazitaxel-d6
|
||
Cabazitaxel-d6 is a deuterium labeled cabazitaxel. Cabazitaxel is a semi-synthetic derivative of the natural taxoid 10-deacetylbaccatin III with potential antineoplastic activity. Cabazitaxel binds to and stabilizes tubulin, resulting in the inhibition of microtubule depolymerization and cell division, cell cycle arrest in the G2/M phase, and the inhibition of tumor cell proliferation. Unlike other taxane compounds, this agent is a poor substrate for the membrane-associated, multidrug resistance... | |||
T73711 |
Atomoxetine-d3 hydrochloride
|
||
Atomoxetine-d3 hydrochloride 是氘代标记的Atomoxetine hydrochloride。Atomoxetine hydrochloride 是去甲肾上腺素重吸收抑制剂,与人NET,SERT 和DAT 的放射性配体结合的 Ki 分别为5,77和1451 nM。 | |||
TMIH-0190 |
Difamilast-d5
|
||
Difamilast-d5 是 Difamilast 的氘代化合物。Difamilast 的 CAS 号为 937782-05-3。Difamilast 是局部的、选择性的非甾体磷酸二酯酶 4 抑制剂,对 B 亚型抑制作用较好 (IC50=11.2 nM)。它在研究轻度至中度特应性皮炎方面有研究的价值。 | |||
TMID-0227 |
Rifabutin-d7
|
||
Rifabutin-d7 是 Rifabutin 的氘代化合物。Rifabutin 的 CAS 号为 72559-06-9。Rifabutin是半合成的安莎霉素抗生素,抑制 DNA 依赖性 RNA 聚合酶,有抗分枝杆菌作用。 | |||
TMIJ-0317 |
Nadolol-d9 (Mixture of Diastereomers)
|
||
Nadolol-d9 (Mixture of Diastereomers) 是 Nadolol 的氘代化合物。Nadolol 的 CAS 号为 42200-33-9。Nadolol 是一种有机阴离子转运多肽 1A2 (OATP1A2) 的底物,是一种非选择性的、具有口服活性的 β-肾上腺素受体 (β-adrenergic receptors) 阻滞剂,可用于高血压,心绞痛和血管性头痛的研究。 | |||
TMID-0037 |
Tadalafil-d3
|
||
Tadalafil-d3 是 Tadalafil 的氘代化合物。Tadalafil 的 CAS 号为 171596-29-5。Tadalafil 是一种PDE5抑制剂,IC50为 1.8 nM。 | |||
TMIH-0222 |
Esomeprazole sodium-d6
|
||
Esomeprazole sodium-d6 是 Esomeprazole sodium 的氘代化合物。Esomeprazole sodium 的 CAS 号为 161796-78-7。Esomeprazole sodium 是一种口服有效的活性质子泵抑制剂。Esomeprazole sodium通过抑制胃壁细胞中的H+, K+-ATPase来降低酸分泌,在胃食管反流疾病中有研究价值。Esomeprazole 是一种外泌体抑制剂,通过抑制 V-H+-ATPases 来阻断外泌体的释放。 | |||
TMIJ-0208 |
Beclomethasone Dipropionate-d6
|
||
Beclomethasone Dipropionate-d6 是 Beclomethasone Dipropionate 的氘代化合物。Beclomethasone Dipropionate 的 CAS 号为 5534-09-8。Betamethasone dipropionate是具有口服活性的糖皮质激素,具有抗炎和免疫抑制作用。它是Betamethasone 的前体药物,Betamethasone 是 LPS 诱导的炎症及 MMP 释放的抑制剂。 | |||
TMIJ-0274 |
Sulindac-d3
|
||
Sulindac-d3 是 Sulindac 的氘代化合物。Sulindac 的 CAS 号为 38194-50-2。Sulindac 是一种非甾体类抗炎剂,可抑制COX-2的活性,也可抑制 COX-2 的过表达。它是一种亚磺酰基茚衍生物前药,具有潜在的抗肿瘤活性。 | |||
TMID-0076 |
Busulfan-d8
|
||
Busulfan-d8 是 Busulfan 的氘代化合物。Busulfan 的 CAS 号为 55-98-1。Busulfan 是二甲磺酸盐的合成衍生物,具有抗肿瘤和细胞毒特性。是一种烷化剂,对骨髓具有选择性免疫抑制作用。 | |||
TMID-0072 |
Imipenem-d4
|
||
Imipenem-d4 是 Imipenem 的氘代化合物。Imipenem 的 CAS 号为 64221-86-9。Imipenem (MK0787) 是一种噻吩霉素衍生物,属于抗生素类,具有抗菌活性,对革兰氏阳性和革兰氏阴性菌具有部分的抑制作用。Imipenem 可用于研究碳青霉烯类非易感性感染和铜绿假单胞菌生物膜感染。 | |||
TMID-0209 |
Tadalafil-13C-d3
|
||
Tadalafil-13C-d3 是 Tadalafil 的 13C 和氘代化合物。Tadalafil 的 CAS 号为 171596-29-5。Tadalafil 是一种PDE5抑制剂,IC50为 1.8 nM。 | |||
T71141 |
Fenspiride-d5
|
||
Fenspiride-d5 is intended for use as an internal standard for the quantification of fenspiride by GC- or LC-MS. Fenspiride is an antagonist of histamine H1 receptors and a non-steroidal anti-inflammatory drug (NSAID). It inhibits histamine-induced contraction of isolated guinea pig trachea but not histamine-induced inotropy of isolated guinea pig heart. It also inhibits phosphodiesterase 4 (PDE4), PDE5, and PDE3 (IC50s = 69, ~158, and 363 µM, respectively, in isolated human bronchi derived from ... | |||
TMIJ-0163 |
Valproic Acid-d4
|
||
Valproic Acid-d4 是 Valproic Acid 的氘代化合物。Valproic Acid 的 CAS 号为 99-66-1。Valproic acid是一种 HDAC 抑制剂,可抑制HDAC1的活性,同时可诱导HDAC2的降解。它激活Notch1信号并抑制小细胞肺癌细胞的增殖。它可研究癫痫、双相情感障碍和偏头痛等。 | |||
TMIJ-0431 |
2-(Propyl-3,3,3-d3)pentanoic-5,5,5-d3 Acid
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2-(Propyl-3,3,3-d3)pentanoic-5,5,5-d3 Acid 是 2-pentanoic Acid 的氘代化合物。2-pentanoic Acid 的 CAS 号为 99-66-1。Valproic acid是一种 HDAC 抑制剂,可抑制HDAC1的活性,同时可诱导HDAC2的降解。它激活Notch1信号并抑制小细胞肺癌细胞的增殖。它可研究癫痫、双相情感障碍和偏头痛等。 | |||
TMID-0120 |
Valproic Acid-d15
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Valproic Acid-d15 是 Valproic Acid 的氘代化合物。Valproic Acid 的 CAS 号为 99-66-1。Valproic acid是一种 HDAC 抑制剂,可抑制HDAC1的活性,同时可诱导HDAC2的降解。它激活Notch1信号并抑制小细胞肺癌细胞的增殖。它可研究癫痫、双相情感障碍和偏头痛等。 | |||
TMIJ-0268 |
Relugolix-d6
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Relugolix-d6 是 Relugolix 的氘代化合物。Relugolix 的 CAS 号为 737789-87-6。Relugolix 是口服有活性的非肽性促性腺激素释放激素的拮抗剂。同 TAK-013 相比,它对人和猴子的受体具有高亲和力和强拮抗活性,它们的IC50值分别为0.33 nM和0.32 nM。它可用于研究性激素依赖性疾病,如子宫肌瘤、子宫内膜异位症、前列腺癌等。 | |||
TMIH-0065 |
Acalabrutinib-d4
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Acalabrutinib-d4 是 Acalabrutinib 的氘代化合物。Acalabrutinib 的 CAS 号为 1420477-60-6。Acalabrutinib 是一种不可逆的、高效的、具有口服活性、选择性的第二代BTK抑制剂。它与 BTK 的 ATP 结合口袋中的 Cys481 共价结合。它在慢性淋巴细胞性白血病 (CLL) 小鼠模型中显示出强大的靶向作用和功效。 | |||
TMID-0254 |
Linalool-d3
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Linalool-d3 是 Linalool 的氘代化合物。Linalool 的 CAS 号为 78-70-6。Linalool 是存在芫荽等植物中的单萜类天然产物,是竞争性NMDA受体拮抗剂,具有抗肿瘤和抗心脏毒性的作用。它通过激活 Nrf2 诱导抗氧化防御和通过抑制 NF-κB 减少炎症反应来保护其免受 LPS/GalN 诱导的肝损伤,具有镇痛、抗菌和抗炎的特性。 | |||
TMIJ-0114 |
Vardenafil-d5
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Vardenafil-d5 是 Vardenafil 的氘代化合物。Vardenafil 的 CAS 号为 224785-90-4。Vardenafil 是选择性、高效的、具有口服活性的磷酸二酯酶5抑制剂,IC50=0.7 nM。它能够非竞争性地抑制环磷酸鸟苷水解,从而提高 cGMP 水平。它对 PDE1 (180 nM),PDE6 (11 nM),PDE2,PDE3,PDE4 (>1000 nM) 具有选择性。它可用于研究勃起功能障碍。 | |||
T37847 |
Zonisamide-13C2,15N
Zonisamide-13C2,15N |
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Zonisamide-13C2,15N is intended for use as an internal standard for the quantification of zonisamide by GC- or LC-MS. Zonisamide is an antiepileptic agent.1 It selectively inhibits the repeated firing of sodium channels (IC50 = 2 μg/ml) in mouse embryo spinal cord neurons and inhibits spontaneous channel firing when used at concentrations greater than 10 μg/ml.2 In rat cerebral cortex neurons, zonisamide (1-1,000 μM) inhibits T-type calcium channels with a maximum reduction of 60% of the calcium... |