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Cat. No. | Product Name | ||
---|---|---|---|
L9850 | 口服活性化合物库 | 2427 compounds | |
2427 种口服活性化合物独特集合,可用于高通量筛选和高内涵筛选 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5405 |
BI-1347
|
CDK | Cell Cycle/Checkpoint |
BI-1347 是一种有效的、选择性的 CDK8/cyclinC 抑制剂,IC50值为 1 nM,可抑制肿瘤生存。 | |||
T3465 |
Vesnarinone
维司力农,OPC-8212,Arkin,Piteranometozine |
HIV Protease; PDE | Metabolism; Microbiology/Virology; Proteases/Proteasome |
Vesnarinone (Arkin) 是一种喹啉酮衍生物,可抑制磷酸二酯酶III 活性,增加钙通量和减小钾通量。 | |||
T67991 |
Iliparcil
|
Others | Others |
Iliparcil 是一种具有口服活性的抗血栓化合物。 | |||
T26914 |
BTA-9881
BTA9881,AZD9639,AZD-9639,BTA 9881,MEDI-564 |
RSV | Microbiology/Virology |
BTA-9881 是一种具有口服活性的新型 RSV 融合抑制剂,具有抗病毒活性,可用于研究呼吸道合胞病毒感染。 | |||
T23449 |
TCS 46b
|
NMDAR | Neuroscience |
TCS 46b 是一种具有口服活性的 NR1A/NR2B NMDA 受体拮抗剂。 | |||
T7120 |
Cefetamet pivoxil hydrochloride
盐酸头孢他美酯,Ro 15-8075 |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefetamet pivoxil hydrochloride (Ro 15-8075) 是一种可口服的头孢类抗生素。 | |||
T34616 |
Seridopidine
ACR-343,ACR 343,ACR343 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Seridopidine (ACR343) 是一种多巴胺能活性调节剂,可作为精神分裂症、帕金森病和抽动秽语综合征的口服疗法。 | |||
T12894 |
SGN-2FF
|
Others | Others |
SGN-2FF 是一种岩藻糖基化抑制剂,具有口服活性,能够抑制岩藻糖基转移酶的活性,具有抗肿瘤活性。 | |||
T9593 |
Senaparib
IMP4297 |
PARP | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Senaparib (IMP4297) 是一种选择性和口服有效的PARP1/2抑制剂,具有强效的抗肿瘤活性。 | |||
T67875 |
DHODH-IN-23
|
Dehydrogenase | Metabolism |
DHODH-IN-23是一种 DHODH 抑制剂,具有口服活性。DHODH-IN-23常用于对癌症的研究。 | |||
T2492 |
Perifosine
NSC 639966,D21266,KRX-0401,哌立福新 |
Apoptosis; Akt; Autophagy | Apoptosis; Autophagy; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
Perifosine (KRX-0401) 是一种具有口服活性的烷基磷酸胆碱 Akt 抑制剂,具有抗肿瘤活性。 | |||
T33711L |
Nolomirole HCl
CHF 1035 HCl,CHF 1035,CHF1035,CHF1035 HCl,CHF-1035 HCl,CHF-1035,Nolomirole Hydrochloride |
Dopamine Receptor; Norepinephrine | GPCR/G Protein; Neuroscience |
Nolomirole HCl(CHF 1035) 是一种具有口服活性的新型选择性多巴胺激动剂,对去甲肾上腺素的释放有抑制作用,可用于研究轻度慢性心力衰竭。 | |||
T16366 |
NVR 3-778
|
HBV | Microbiology/Virology |
NVR 3-778 是一种 SBA 类的口服有效HBV CAM 衣壳组装调制剂,具有抗 HBV 活性。 | |||
T11410L |
GLPG0492
|
Androgen Receptor | Endocrinology/Hormones |
GLPG0492 是一种非甾体选择性雄激素受体 (androgen receptor) 调节剂。GLPG0492 在肌肉骨骼疾病如肌萎缩和恶病质的研究方面具有潜在的潜力。 | |||
T2383 |
Panobinostat
帕比司他,NVP-LBH589,LBH589 |
Apoptosis; HIV Protease; HDAC; Autophagy | Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; Microbiology/Virology; Proteases/Proteasome |
Panobinostat (NVP-LBH589) 是一种广谱的 HDAC 抑制剂 (IC50=5 nM),具有口服活性和非选择性。Panobinostat 具有抗肿瘤活性,可以诱导细胞凋亡和自噬。 | |||
T40287 |
FATP1-IN-2
|
Others | Others |
FATP1-IN-2 是一种脂肪酸转运蛋白1 (FATP1) 抑制剂,具有口服活性,可用于研究肥胖和代谢疾病。 | |||
T60187 |
RP-6685
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
RP-6685, a highly potent and selective inhibitor of DNA polymerase theta (Polθ), manifests remarkable oral activity. With an IC 50 value of 5.8 nM in the PicoGreen assay, RP-6685 effectively hinders the enzymatic activity of Polθ. In addition, it demonstrates significant antitumor efficacy as observed in a mouse tumor xenograft model [1]. | |||
T19705 |
JTE-907
JTE 907 |
Cannabinoid Receptor | GPCR/G Protein |
JTE-907 是一种具有高度选择性和口服活性的 CB2 受体反向激动剂。JTE-907在体内展现出抗炎活性。 | |||
T13331 |
WAY127093B racemate
|
PDE | Metabolism |
WAY127093B racemate 是WAY127093 B 的外消旋体。WAY127093B 是一种磷酸二酯酶IV 抑制剂,在大鼠和豚鼠中具有口服活性。 | |||
T1920 |
Capivasertib
AZD5363 |
Akt; PKA; mTOR; Autophagy | Autophagy; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors |
Capivasertib (AZD5363) 是一种广谱的 AKT 抑制剂,对 Akt1、Akt2 和 Akt3 均有抑制活性 (IC50=3/7/7 nM),具有口服活性。Capivasertib 具有抗肿瘤活性,可以用于治疗乳腺癌。 | |||
T7897 |
PK150
|
Others; Antibacterial | Microbiology/Virology; Others |
PK150 是一种 Sorafenib 类似物,具有抗菌活性。它抑制甲氧西林敏感金黄色葡萄球菌,耐甲氧西林金黄色葡萄球菌,万古霉素中介金黄色葡萄球菌的 MIC 分别为 0.3,0.3-1,0.3 µM。 | |||
T6189 |
Mirdametinib
PD325901,PD0325901 |
Apoptosis; MEK; Autophagy | Apoptosis; Autophagy; MAPK |
Mirdametinib (PD325901) 是一种 MEK 抑制剂 (IC50=0.33 nM),具有选择性、非 ATP 竞争性和口服活性。Mirdametinib 具有抗肿瘤活性,可以抑制 p-ERK1/2 的表达并诱导细胞凋亡。 | |||
T2101 |
Navitoclax
ABT-263 |
BCL | Apoptosis |
Navitoclax (ABT-263) 是一种 Bcl-2 抑制剂,可与 Bcl-xL、Bcl-2、Bcl-w 等蛋白结合 (Ki<1 nM),具有有效性和口服活性。Navitoclax 具有抗肿瘤活性,可以诱导细胞凋亡。 | |||
T15756 |
Lidorestat
IDD-676 |
Reductase | Endocrinology/Hormones; Metabolism |
Lidorestat (IDD-676) 是一种醛糖还原酶抑制剂(IC50: 5 nM),具有有效性,选择性和口服活性。Lidorestat 改善神经传导,减少白内障的形成。Lidorestat 可用于治疗慢性糖尿病并发症。 | |||
TQ0138 |
K145 hydrochloride
K145盐酸盐 |
Apoptosis; S1P Receptor | Apoptosis; GPCR/G Protein |
K145 hydrochloride 是选择性的,底物竞争性的和口服有效的SphK2抑制剂,IC50为 4.3 µM,Ki 为 6.4 µM。它可诱导细胞凋亡,显示出强大的抗肿瘤活性。 | |||
T30252 |
AZD1940
UNII-0J0035E9FT,AZD-1940,AZD 1940 |
Cannabinoid Receptor | GPCR/G Protein |
AZD1940 (UNII-0J0035E9FT)是一种高亲和力的大麻素CB(1)/CB(2)受体激动剂,具有口服活性,应用于口面疼痛的研究。 | |||
T36802L |
Bisubstrate Inhibitor 78 HCl
Bisubstrate Inhibitor 78 HCl(2368247-39-4 Free base) |
Others | Others |
Bisubstrate Inhibitor 78 HCl 是一种 NNMT 抑制剂(IC50 = 1.41 μM),具有潜在的抗癌活性,在 100μM 时抑制HSC-2口腔癌细胞增殖。 | |||
T21686 |
CD 1530
CD-1530,CD1530 |
Retinoid Receptor | Metabolism |
CD 1530 是一种具有选择性和有效性的 RARγ激动剂(Kd:150 nM),具有潜在的抗癌活性,对秀丽隐杆线虫显示出杀虫活性,可用于研究口腔癌变。 | |||
T0078 |
Lapatinib
GSK572016,GW572016,拉帕替尼 |
EGFR; Ferroptosis; Autophagy | Angiogenesis; Apoptosis; Autophagy; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Lapatinib (GW572016) 是一种 ErbB2 和 EGFR 的抑制剂 (IC50=9.2/10.8 nM),具有口服活性。Lapatinib 具有抗肿瘤活性,可以用于治疗 HER2 过表达的晚期或转移性乳腺癌。 | |||
T67872 |
VT104
|
YAP | Stem Cells |
VT104是一种有效的YAP/TAZ 抑制剂,具有口服活性,可用于癌症研究。VT104阻止内源性TEAD1和TEAD3蛋白棕榈酰化。 | |||
T2125 |
Trametinib
GSK1120212,曲美替尼,JTP-74057 |
Apoptosis; MEK; Autophagy | Apoptosis; Autophagy; MAPK |
Trametinib (GSK1120212) 是一种 MEK 抑制剂,抑制 MEK1 和 MEK2 (IC50=0.7/0.9 nM),具有 ATP 非竞争性和口服活性。Trametinib 可以激活自噬,诱导凋亡。 | |||
T0334 |
Rosiglitazone
BRL49653,罗格列酮 |
Ferroptosis; TRP/TRPV Channel; PPAR; Autophagy | Apoptosis; Autophagy; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism |
Rosiglitazone (BRL49653) 是一种 PPARγ 激动剂、TRPC5 激活剂和 TRPM3 抑制剂,具有口服活性。Rosiglitazone 也是一种降糖剂,是噻唑烷二酮类胰岛素增敏剂。 | |||
T11265 |
Faropenem daloxate
法罗培南酯,Faropenem medoxil |
Antibacterial; Antibiotic | Microbiology/Virology |
Faropenem daloxate (Faropenem medoxil) 是β-内酰胺类口服抗生素。 | |||
T35862 |
Cucurbit[8]uril
|
Others | Others |
Cucurbit[8]uril is a highly effective and safe supramolecular compound that promotes protein heterodimerization. It selectively induces the heterodimerization of methylviologen and naphthalene functionalized proteins, demonstrating its specificity and versatility. Additionally, Cucurbit[8]uril shows exceptional oral activity and low toxicity, making it a promising candidate for various pharmaceutical and biotechnological applications. | |||
T12174 |
Naphthoquine phosphate
|
Parasite | Microbiology/Virology |
Naphthoquine phosphate 是一种具有口服活性的广谱4-氨基喹啉类抗疟化合物,可能影响病毒进入和进入后复制。Naphthoquine phosphate 具有肝血管中心毒性,常与青蒿素一起使用来治疗疟疾。 | |||
T6106 |
Selinexor (KPT-330)
Selinexor,KPT-330,塞利尼索 |
CRM1 | Membrane transporter/Ion channel |
Selinexor (KPT-330) 是一种 CRM1 的小分子抑制剂,具有选择性和口服活性。Selinexor 可以阻滞细胞周期、诱导细胞凋亡,具有抗肿瘤活性,可以用于治疗多发性骨髓瘤。 | |||
T1921 |
Alpelisib
BYL-719 |
PI3K | PI3K/Akt/mTOR signaling |
Alpelisib (BYL-719) 是一种 PI3Kα 抑制剂 (IC50=5 nM),具有选择性、有效性和口服活性。Alpelisib 以较低活性抑制 PI3Kβ/γ/δ (IC50=250/290/1200 nM)。Alpelisib 具有抗肿瘤活性,对 PIK3CA 突变肿瘤具有靶向性。 | |||
T61318 |
BRD4 Inhibitor-20
|
Epigenetic Reader Domain | Chromatin/Epigenetic |
BRD4 Inhibitor-20是一种有效的溴结构域蛋白4(BRD4)抑制剂,具有口服活性。BRD4 Inhibitor-20在癌细胞系中具有抗增殖活性,并被用于各种癌症的研究,如结肠癌。 | |||
T0520 |
Lenvatinib
仑伐替尼,E7080 |
VEGFR; FGFR; c-RET; PDGFR; c-Kit | Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors |
Lenvatinib (E7080) 是一种多靶点受体酪氨酸激酶抑制剂,抑制 VEGFR1-3、FGFR1-4、KIT、PDGFR 和 RET 等,具有口服活性。Lenvatinib 对 VEGFR2 和 VEGFR3 的抑制活性最强 (IC50=4/5.2 nM)。Lenvatinib 具有强效抗肿瘤活性。 | |||
T61972 |
Pomaglumetad methionil hydrochloride
LY2140023 hydrochloride |
GluR | Neuroscience |
Pomaglumetad methionil hydrochloride (LY2140023 hydrochloride) (LY2140023 hydrochloride) 是的 LY404039 的蛋氨酸前药,具有口服活性。LY404039是一种选择性 mGlu2/3 受体激动剂。Pomaglumetad methionil hydrochloride 可用于精神分裂症的研究。 | |||
T21463 |
Temozolomide Acid
TMZA,3,4-二氢-3-甲基-4-氧代咪唑并[5,1-D]-1,2,3,5-四嗪-8-甲酰胺酸 |
Others | Others |
Temozolomide Acid (TMZA) 是 temozolomide (TMZ) 的代谢物。TMZ 在体外具有抗癌活性。TMZ 是一种口服烷化剂,用于治疗多形性胶质母细胞瘤 (GBM) 和星形细胞瘤。 | |||
T8850 |
sbp-7455
|
Autophagy | Autophagy |
SBP-7455 是一种高亲和力,可口服的双重ULK1/ULK2自噬抑制剂,可有效抑制ULK1/2酶活性,可研究三阴性乳腺癌,在 ADP-Glo 分析中的IC50分别为 13 nM 和 476 nM。 | |||
T2490 |
Osimertinib
AZD-9291,Mereletinib,奥希替尼 |
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Osimertinib (AZD-9291) 是一种 EGFR 三代抑制剂,抑制二代 EGFR 抑制剂产生的 T790M 耐药突变,具有不可逆性和口服活性。Osimertinib 具有抗肿瘤活性,用于治疗 EGFR 突变的非小细胞肺癌。 | |||
T4990 |
Cefcapene pivoxil hydrochloride hydrate
Cefcapene Pivoxil Hydrochloride,盐酸头孢卡品酯 |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefcapene pivoxil hydrochloride hydrate 是一种头孢菌素的前药,具有口服活性和广谱抗菌活性。它可研究掌跖脓疱病等感染性疾病。 | |||
T11339 |
Furegrelate sodium
U-63557A |
PPAR | DNA Damage/DNA Repair; Metabolism |
Furegrelate sodium (U-63557A) 是口服有效的、血栓素合酶选择性抑制剂,抑制人血小板微粒体血栓素 A2 (TxA2) 合酶的 IC50为 15 nM。它正在开发作为抗血小板药物。 | |||
T70692 |
ST7612AA1
|
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
ST7612AA1 是一种新型有效且可口服的 HDAC 抑制剂,作为作为HIV-1潜伏期再激活剂。ST7612AA1 在体内外实验中低浓度显示出显著的抗肿瘤活性。ST7612AA1 具有潜在的抗癌活性,可用于研究疟疾。 | |||
T6961 |
PX-478
PX-478 2HCl |
HIF/HIF Prolyl-Hydroxylase; HIF; Autophagy | Angiogenesis; Autophagy; Chromatin/Epigenetic; Metabolism |
PX-478 是一种 HIF-1α 抑制剂,具有选择性、口服活性和血脑屏障渗透性。PX-478 具有抗肿瘤活性,还可以保护糖尿病中的胰腺 β 细胞功能,用于 2 型糖尿病的研究。 | |||
T72029 |
CDK8-IN-13
|
Apoptosis; CDK | Apoptosis; Cell Cycle/Checkpoint |
CDK8-IN-13是一种 CDK8抑制剂(IC50:51.9 nM),具有强效性、选择性和口服活性。CDK8-IN-13能诱导细胞凋亡,降低了 p-STAT1 S727和p-STAT5 S726的表达。CDK8-IN-13表现出抗肿瘤活性。 | |||
T67776 |
PCSK9-IN-11
|
Others | Others |
PCSK9-IN-11 (compound 5r) 是口服有效的 PCSK9 抑制剂。 PCSK9-IN-11 在 HepG2 细胞中抑制 PCSK9 转录活性 (IC50= 5.7 μM)。 PCSK9-IN-11 可以增加 LDL 受体 (LDLR) 蛋白水平,可用于动脉粥样硬化研究。 | |||
T22263 |
Bavdegalutamide
ARV-110 |
Androgen Receptor | Endocrinology/Hormones |
Bavdegalutamide (ARV-110) 是一种雄激素受体 (AR) 的 PROTAC 降解剂。 Bavdegalutamide 可用于前列腺癌的研究。 Bavdegalutamide 具有口服活性和选择性,并促进 AR 的泛素化和降解。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7938 |
Quinidine
奎尼丁,奎宁树 |
Parasite | Microbiology/Virology |
Quinidine 是一种抗心律失常剂,也是 K+通道的有效阻断剂,其 IC50值为 19.9 μM。它是一种选择性细胞色素 P450db 的有效抑制剂,也可研究疟疾。 | |||
T0687 |
Simvastatin
辛伐他汀,MK-0733,MK 733 |
Apoptosis; Mitophagy; Ferroptosis; HMG-CoA Reductase; Autophagy | Apoptosis; Autophagy; Metabolism |
Simvastatin (MK 733) 是一种 HMG-CoA 还原酶抑制剂 (Ki=0.2 nM),具有口服活性。Simvastatin 具有降血脂活性,可以抑制肝脏产生胆固醇,还可以用于预防心血管疾病。 | |||
T8125 |
Quinidine sulfate dihydrate
硫酸奎尼宁,硫酸奎尼丁二水合物,Chinidin Sodium,β-quinine Sodium,Pitayine Sodium,Quinidine sulfate |
P450 | Metabolism |
Quinidine sulfate dihydrate (Pitayine Sodium) 是抗心律失常剂,能够阻断 K+通道(IC50:19.9 μM)。它是细胞色素 P450db 的选择性抑制剂,可用于研究疟疾。 | |||
T20198 |
Potassium gluconate
Kalium-beta,Kalium Gluconate,Kaon elixir,Kaon,Potassium D-gluconate,HSDB 3165,K-Iao |
Endogenous Metabolite; Antifungal | Metabolism; Microbiology/Virology |
Potassium gluconate (Potassium D-gluconate) 是一种具有口服活性和螯合性质的氧化型羧酸,具有杀菌活性。 | |||
T8263 |
3,4'-Dihydroxyflavone
|
Influenza Virus | Microbiology/Virology |
3,4'-Dihydroxyflavone 是一种口服活性黄酮类化合物,具有抗甲型流感病毒的抗病毒活性。 | |||
T1687 |
Doxycycline
Vibramycin,多西环素,Doxiciclina,Doxytetracycline,Doxycyclinum,强力霉素 |
MMP; ribosome; Antibacterial; Antibiotic; Parasite | Microbiology/Virology; Proteases/Proteasome |
Doxycycline (Doxiciclina) 属于四环素类抗生素,是一种广谱的金属蛋白酶 (MMP) 抑制剂,具有口服活性。Doxycycline 具有抗菌活性和抗肿瘤活性。 | |||
T1687L |
Doxycycline (hyclate)
Doxycycline hydrochloride hemiethanolate hemihydrate,盐酸强力霉素,WC2031,Doxycycline hyclate |
MMP; ribosome; Antibacterial; Antibiotic | Microbiology/Virology; Proteases/Proteasome |
Doxycycline hyclate (WC2031) 属于四环素类抗生素,是一种广谱的金属蛋白酶 (MMP) 抑制剂,具有口服活性。Doxycycline hyclate 具有抗菌活性和抗肿瘤活性。 | |||
T1508 |
Decitabine
Dacogen,NSC 127716,地西他滨,Deoxycytidine,5-Aza-2'-deoxycytidine |
Apoptosis; Nucleoside Antimetabolite/Analog; DNA Methyltransferase | Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; DNA Damage/DNA Repair |
Decitabine (Deoxycytidine) 是脱氧胞苷类似物,一种 DNA 甲基转移酶抑制剂,具有口服活性。Decitabine 具有抗肿瘤活性和抗代谢活性。Decitabine 诱导细胞周期阻滞和凋亡。 | |||
T3400 |
Bakuchiol
|
p38 MAPK; DNA/RNA Synthesis; Autophagy | Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; MAPK |
Bakuchiol 是一种从补骨脂种子中提取的植物雌激素,具有抗肿瘤和抗蠕虫特性,以及细胞毒活性和抗菌活性。 | |||
T5S2245 |
Alisol C 23-acetate
泽泻醇 C-23-醋酸酯,Alisol C monoacetate |
Others | Others |
Alisol C 23-acetate (Alisol C monoacetate) 是一种提取自东方泽泻中的天然产物,可以显著减少迟发型超敏反应。 | |||
T5746 |
Dictamine
Dictamnine,Dectamine,白鲜碱 |
Apoptosis; Anti-infection; Antibacterial; Antifungal | Apoptosis; Microbiology/Virology |
Dictamine (Dectamine) 显示抗胆碱酯酶、抗炎、致突变、抗菌和抗真菌活性。 它具有在人子宫颈、结肠和口腔癌细胞中发挥细胞毒性的能力。 | |||
T6564 |
Leupeptin Hemisulfate
亮肽素 |
Serine Protease; Cysteine Protease | Proteases/Proteasome |
Leupeptin hemisulfate 是一种蛋白酶抑制剂,具有细胞膜渗透性、可逆性、竞争性和口服活性。Leupeptin hemisulfate 可以抑制 Cathepsin B、Cathepsin H、Cathepsin L 的活性,阻断两性溶酶体的融合。Leupeptin hemisulfate 还具有抗炎活性。 | |||
TN7238L |
Sanguinarine citrate
Sanguinarium citrate,Sanguinarin citrate,Pseudochelerythrine citrate |
Antibiotic | Microbiology/Virology |
Sanguinarine citrate (Pseudochelerythrine chloride) 是一种来源于 Sanguinaria Canadensis 的生物碱,具有抗菌、抗炎和镇痛活性,可用于治疗口腔炎、牙龈出血和喉炎等口腔炎症疾病 。 | |||
T1181 |
Gefitinib
ZD1839,吉非替尼 |
EGFR; Tyrosine Kinases; Autophagy | Angiogenesis; Autophagy; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Gefitinib (ZD1839) 是一种 EGFR 一代抑制剂,具有口服活性,抑制 EGFR 19 Del 和 L858R 突变。Gefitinib 具有抗肿瘤活性,用于治疗 EGFR 突变的非小细胞肺癌。Gefitinib 用药会产生 EGFR C797S 耐药突变。 | |||
T1678 |
Nystatin
Stamycin,Fungicidin,制霉菌素,Nystavescent |
Apoptosis; Antibiotic; Antifungal | Apoptosis; Microbiology/Virology |
Nystatin (Fungicidin) 属于多烯类抗真菌抗生素,对酵母和支原体有效,具有口服活性。Nystatin 可以用于治疗皮肤和口咽念珠菌感染。 | |||
TN4234 |
Hydrangenol
|
NOS; NF-κB; Nrf2; NO Synthase; Antifection; Autophagy | Autophagy; Immunology/Inflammation; Microbiology/Virology; NF-κB |
Hydrangenol 是一种天然产物,可从绣球花 (Hydrangea serrata) 的叶中分离。Hydrangenol 是口服有效的抗光老化化合物,可以预防皱纹的形成。Hydrangenol 可以降低 MMP 和炎症细胞因子的表达,增加保湿因子和抗氧化基因的水平。 | |||
T3834 |
8-Epideoxyloganic acid
8-表去氧马钱酸 |
ROS; Immunology/Inflammation related | Immunology/Inflammation |
8-Epideoxyloganic acid 是从 Incarvillea delavayi 中分离得到的一种环烯醚萜苷。它具有微弱的缓解疼痛活性。 | |||
T3S1612 |
kuwanon G
桑黄酮G,Moracenin B,桑黄酮 G,Kuwanone G |
Phosphatase; Antibacterial; Bombesin Receptor; AChR; AChE; Glucosidase | GPCR/G Protein; Metabolism; Microbiology/Virology; Neuroscience |
Kuwanon G (Moracenin B) 是一种从桑树中得到的黄酮类蛙皮素受体拮抗剂,具有杀菌作用。 | |||
T1326 |
Gentamicin sulfate
SCH9724,Gentamycin sulfate,NSC-82261,硫酸庆大霉素 |
ribosome; DHFR; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Gentamicin sulfate (SCH9724) 是一种广谱的氨基糖苷类抗生素,具有口服活性。Gentamicin sulfate 可以用于抑制敏感生物体中的蛋白质合成。 | |||
T1079 |
Metronidazole
Flagyl,Metronidazol,甲硝唑,Anagiardil |
Apoptosis; NADPH; Hydrogenase; Antibacterial; Antibiotic; Parasite; Antifection | Apoptosis; Metabolism; Microbiology/Virology |
Metronidazole (Metronidazol) 是一种合成的硝基咪唑衍生物,一种抗生素和抗原虫剂,具有口服活性和血脑屏障渗透性。Metronidazole 可用于治疗或预防厌氧菌引起的系统或局部感染。 | |||
T1011 |
Itraconazole
伊曲康唑,R51211 |
P450; Hedgehog/Smoothened; Antibiotic; Autophagy; Antifungal | Autophagy; GPCR/G Protein; Metabolism; Microbiology/Virology; Stem Cells |
Itraconazole (R51211) 属于三唑类天然产物,是一种抗真菌剂,具有口服活性。Itraconazole 是一种 Hedgehog 信号通路拮抗剂,一种 oxysterol-binding protein (OSBP) 抑制剂,也是一种细胞色素 P-450 依赖性酶的抑制剂。 | |||
TMA0955 |
Thunberginol C
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Antifection | Microbiology/Virology |
Thunberginol C exhibits antimicrobial activity against oral bacteria. It shows antiallergic activity in the in vitro bioassay using the Schults-Dale reaction in sensitized guinea pig bronchial muscle. | |||
TN3726 |
Cudraflavone B
|
IκB/IKK; MAO; ROS; Akt; COX; PI3K; Nrf2; Autophagy | Autophagy; Cytoskeletal Signaling; Immunology/Inflammation; Metabolism; Neuroscience; NF-κB; PI3K/Akt/mTOR signaling |
Cudraflavone B has anti-proliferative activity, mouse brain monoamine oxidase (MAO) inhibitory effects, apoptotic actions in human gastric carcinoma cells and mouse melanoma cells, and hepatoprotective activity. It may be a lead for the development of a potential candidate for human oral squamous cell carcinoma cells. | |||
TN2738 |
2,6-Dimethoxy-1-acetonylquinol
|
Antifection | Microbiology/Virology |
2,6-Dimethoxy-1-acetonylquinol shows varying degrees of in vitro antimalarial activity against Plasmodium falciparum. It is devoid of significant cytotoxicity to the human oral epidermoid KB cancer cell line. | |||
T82737 |
Chitobiose
|
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Chitobiose为壳寡糖,为β-1,4-氨基葡萄糖二聚体,具备口服活性及较高的抗氧化活性。 | |||
TN3686 |
Coccinic acid
|
Others | Others |
Coccinic acid shows inhibitory effects against colorectal carcinoma HCT-15 and oral epithelial cell line KB-3-1.Mixture of coccinic acid and anwuweizonic acid shows significant inhibitory activity against human decidual cells and rat luteal cells in vitro | |||
TN1526 |
Corydalmine
|
P450; Antifection | Metabolism; Microbiology/Virology |
Corydalmine exhibits antibacterial activities against Staphylococcus aureus and methicillin-resistant S. aureus strains.1-Corydalmine significantly inhibits spore germination of all the fungi at 100 to 1500 ppm. l-Corydalmine also exhibits potent analgesic activity in preclinical models, it is under development as an oral analgesic agent. | |||
TN4194 |
Heliangin
|
IL Receptor; TNF; NF-κB; MAPK; Prostaglandin Receptor | Apoptosis; GPCR/G Protein; Immunology/Inflammation; MAPK; NF-κB |
Heliangin shows anti-inflammatory effects, it can inhibit lipopolysaccharide-induced inflammation through signaling NF-κB pathway on LPS-induced RAW 264.7 cells. Heliangin has anti-cancer activity, it exhibits cytotoxicity against human oral epidermoid ( | |||
T83407 |
2',3'-Dihydroxy-4',6'-dimethoxychalcone
|
||
2',3'-Dihydroxy-4',6'-dimethoxychalcone 能够抑制β淀粉样蛋白(Aβ42)的纤维化与聚集,并具有口服活性,在大脑中可进行检测。 | |||
T73653 |
Pexiganan
|
Others | Others |
Pexiganan(MSI 78 free base),maganin 2 的合成类似物,是一种具有口服活性的广谱强效抗菌肽,主要用于研究糖尿病足溃疡等相关感染。 | |||
TN4519 |
Mesuaxanthone A
胡桐,海棠木 |
Others | Others |
Mesuaxanthone A and mesuaxanthone B are two yellow pigments.They produce varying degrees of C.N.S. depression characterised by ptosis, sedation, decreased spontaneous motor activity, loss of muscle tone, potentiation of pentobarbitone sleeping time and et | |||
TN4585 |
Moronic acid
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HIV Protease; Antifection; HSV | Microbiology/Virology; Proteases/Proteasome |
Moronic acid shows oral therapeutic efficacy in HSV-infected mice and possessed novel anti-HSV activity. It also shows significant anti-HIV activity (EC(50) 186) and was modified to develop more potent anti-AIDS agents. Moronic acid is a new structural lead for anti-EBV drug development, can substantially reduce the numbers of EBV particles produced by the cells after lytic induction. Morolic and moronic acids have shown sustained antidiabetic and antihyperglycemic action possibly mediated by an... | |||
T82773 |
Catechin 7-O-β-D-glucopyranoside
|
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Catechin 7-O-beta-D-glucopyranoside 是发现于Ulmus davidiana和Paeonia obovata的具有口服活性的天然化合物。该化合物显示出明显的抗氧化与抗炎活性,能改善线粒体功能障碍,有望成为肠道炎症性疾病研究中的潜在用途。 | |||
TN4437 |
Licorisoflavan A
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MMP; IL Receptor; NF-κB; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Immunology/Inflammation; NF-κB; Proteases/Proteasome |
Licorisoflavan A shows weak scavenging activity against superoxide anion radical, it and licoricidin have potential for the development of novel host-modulating strategies for the treatment of cytokine and/or MMP-mediated disorders such as periodontitis.L |
Cat. No. | Product Name | Species | Expression System |
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TMPY-01061 |
FGF-10 Protein, Human, Recombinant
fibroblast growth factor 10,KGF2 |
Human | E. coli |
Fibroblast growth factor 10 (FGF10) is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. FGF10 exhibits mitogenic activity for keratinizing epidermal cells, but essentially no activity for fibroblasts, which is similar to the biological activity of FGF7. FGF10 pla... | |||
TMPJ-00042 |
TSLP Protein, Human, Recombinant
TSLP,Thymic stromal lymphopoietin |
Human | E. coli |
Thymic stromal lymphopoietin (TSLP) is a novel member of the hemopoietic cytokine family that promotes the development of B cells and shares overlapping activity with IL-7. The human TSLP protein comprises a 28 amino acids (aa) signal sequence and 131 aa mature region. Human TSLP has two isoforms lfTSLP and sfTSLP produced by alternative splicing . lfTSLP is expressed in a number of tissues including heart, liver and prostate, and sfTSLP (63aa) is predominantly expressed in keratinocytes of oral... | |||
TMPJ-00764 |
Catalase/CAT Protein, Human, Recombinant
CAT,Catalase |
Human | E. coli |
Catalase (CAT) is a member of the catalase family. It exists as a homotetramer that occurs in almost all aerobically respiring organisms and serves to protect cells from the toxic effects of hydrogen peroxide. Catalase is localized in the peroxisome. Catalase promotes growth of cells including T-cells, B-cells, myeloid leukemia cells, melanoma cells, mastocytoma cells, and normal and transformed fibroblast cells. Defects in CAT are the cause of acatalasemia which is characterized by absence of ... | |||
TMPY-03332 |
PRTFDC1 Protein, Human, Recombinant (His)
HHGP,PRTFDC1,phosphoribosyl transferase domain containing 1 |
Human | E. coli |
PRTFDC1 is a member of the purine/pyrimidine phosphoribosyltransferase family. It can bind GMP, IMP and alpha-D-5-phosphoribosyl 1-pyrophosphate (PRPP). The epigenetic silencing of PRTFDC1 by hypermethylation of the CpG island leads to a loss of PRTFDC1 function, which might be involved in squamous cell oral carcinogenesis. PRTFDC1 is a genetic modifier of HPRT-deficiency in the mouse and has important implications for unraveling the molecular etiology of lesch-Nyhan disease(LND). LND is a sever... | |||
TMPJ-01207 |
UPP1 Protein, Human, Recombinant (His)
UPP1,Uridine Phosphorylase 1,UPP1 Protein |
Human | E. coli |
Uridinephosphorylase 1 (UPP1) is a member of the family of pentosyltransferase. UPP1 catalyses the reversible phosphorolysis of uridine to uracil. The expression levels and the enzymatic activity of UPP1 are higher in human solid tumors than in adjacent normal tissues. The high level of UPP1 expression in some tumors makes it a potential prognosticfactor for some cancers, such as oral squamous cell carcinoma. UPP1 is important for the homeostatic regulation of intracellular and plasma uridine c... | |||
TMPY-02391 |
SUMO1 Protein, Human, Recombinant (His)
small ubiquitin-like modifier 1,SMT3C,SMT3,SMT3H3,UBL1,SENP2... |
Human | E. coli |
Small ubiquitin-like modifier protein (SUMO) modification is a highly dynamic process, catalyzed by SUMO-specific activating (E1), conjugating (E2) and ligating (E3) enzymes, and reversed by a family of SUMO-specific proteases (SENPs). Small ubiquitin-like modifier 1 (SUMO1) is a member of the superfamily of ubiquitin-like proteins. Despite its structural similarity with ubiquitin, SUMO1 does not seem to play any role in protein degradation. SUMO1 plays an important role in modulation of NOX act... | |||
TMPY-02220 |
HRAS Protein, Human, Recombinant (His)
HAMSV,Harvey rat sarcoma viral oncogene homolog,C-H-RAS,C-HA... |
Human | Baculovirus Insect Cells |
HRas, also known as HRAS, belongs to the small GTPase superfamily, Ras family, and is widely expressed. It functions in signal transduction pathways. HRas can bind GTP and GDP, and they have intrinsic GTPase activity. It undergoes a continuous cycle of de- and re-palmitoylation, which regulates its rapid exchange between the plasma membrane and the Golgi apparatus. Defects in HRAS are the cause of faciocutaneoskeletal syndrome (FCSS). FCSS is a rare condition characterized by prenatally increase... |
Cat. No. | Product Name | Target | Signaling Pathways |
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TMID-0003 |
Ribociclib-d6
|
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Ribociclib-d6 是 Ribociclib 的氘代化合物。Ribociclib 的 CAS 号为 1211441-98-3。Ribociclib (LEE011) 是一种细胞周期蛋白依赖性激酶 CDK4/6 抑制剂 (IC50=10/39 nM),具有特异性和口服活性。Ribociclib 具有抗肿瘤活性,可以阻滞细胞周期,抑制肿瘤细胞增殖。 | |||
TMIJ-0272 |
Sarpogrelate-d3 HCl
|
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Sarpogrelate-d3 HCl 是 Sarpogrelate HCl 的氘代化合物。Sarpogrelate HCl 的 CAS 号为 135159-51-2。Sarpogrelate hydrochloride 是一种选择性5-HT2R拮抗剂,可用于研究与血栓形成有关的血管疾病,对 5-HT2A、5-HT2B 和 5-HT2C 受体的pKi值分别为 8.52、6.57 和 7.43。 | |||
T35698 |
Octanoic Acid-13C
|
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Octanoic acid-13C is intended for use as an internal standard for the quantification of octanoic acid by GC- or LC-MS. Octanoic acid is a medium-chain saturated fatty acid. It has been found in Teleme cheeses made from goat, ovine, or bovine milk.1 Octanoic acid is active against the bacteria S. mutans, S. gordonii, F. nucleatum, and P. gingivalis (IC80s = <125, <125, 1,403, and 2,294 μM, respectively).2 Levels of octanoic acid are increased in the plasma of patients with medium-chain acyl-CoA d... |