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Cat. No. | Product Name | ||
---|---|---|---|
LF1000 | 多样性核心预制库 | 50000 compounds | |
For your convenience, there are Diversity Sets of 5,000, 10,000, 15,000, and 20,000 compounds with no structure overlap. | |||
L7820 | 高溶解性微型片段化合物库 | 1081 compounds | |
高溶解性微型片段化合物库由 1081 个低分子量片段组成。 | |||
CB1100 | EXP多样性库 | 50000 compounds | |
For hit finding across different targets, against novel targets, or for the discovery of new chemical series against existing targets, ChemBridge offers up to 150,000 DIVERSet Library compounds in economical, pre-plated format. The DIVERSet Libraries are suitable for biochemical assays, phenotypic and other cell based assays, and assays using model organisms such as bacteria, yeast, c. elegans, zebrafish, or arabidopsis. DIVERSet Libraries have been used across many disease areas resulting in hu... | |||
VM1400 | 多样性核心库Part2 | 25920 compounds | |
分子量<500,主要集中于250-450之间,方便后续的改造优化; | |||
L4520 | 抗菌活性库 | 904 compounds | |
904 种具有抗菌活性的化合物,是抗菌药物研发的有力工具; | |||
L9820 | β-内酰胺类化合物库 | 97 compounds | |
97 种β-内酰胺类化合物的集合,可以用于高通量和高内涵筛选; | |||
L9830 | 抗帕金森病化合物库 | 857 compounds | |
857 种帕金森病相关的化合物集合,可用于高通量和高内涵筛选; | |||
L6020 | 天然产物单体化合物库 | 16627 compounds | |
16627 种精选天然产物集合,结构多样,遍布多种动植物与微生物; | |||
L6800 | 中国药典收录天然产物库 | 2051 compounds | |
2051 种中国药典收录的天然产物,是药物开发、药理研究等领域的有力工具; | |||
DF4500 | 多样性核心库Part1 | 50000 compounds | |
绝大部分分子量<500,主要集中于250-450之间,方便后续的改造优化; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
T9865 |
Almonertinib mesylate
|
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Almonertinib mesylate 是一种不可逆的 EGFR 酪氨酸激酶抑制剂,对 EGFR 敏感突变和 T790M 耐药突变具有高选择性。 它可用于非小细胞肺癌研究。 | |||
T1457 |
Deferasirox
ICL 670,CGP-72670,地拉罗司 |
Others; Ferroptosis; Antibacterial | Apoptosis; Microbiology/Virology; Others |
Deferasirox (CGP-72670) 是一种口服铁螯合剂,用于治疗慢性铁过载。 | |||
T2923 |
Apremilast
阿普斯特,CC-10004,阿普司特 |
Apoptosis; TNF; PDE | Apoptosis; Metabolism |
Apremilast (CC-10004) 是一种口服有效的磷酸二酯酶 4 抑制剂,IC50为 74 nM。它抑制脂多糖释放TNF-α,IC50为 104 nM。 | |||
T16841 |
SAR-260301
|
PI3K | PI3K/Akt/mTOR signaling |
SAR-260301 is an orally available and selective inhibitor of PI3Kβ (IC50: 23 nM). | |||
T15198 |
Edasalonexent
CAT-1004 |
NF-κB | NF-κB |
Edasalonexent (CAT-1004) 是一种可口服的 NF-κB 抑制剂,可用于改善杜氏肌营养不良症。 | |||
T13997 |
AU-224
|
Others | Others |
AU-224 是一种可口服的苯甲酰胺衍生物,是一种强效的胃肠促动力活性。 | |||
T27632 |
Isomazole
|
PDE | Metabolism |
Isomazole 是一种可口服的具有钙敏特性的新型磷酸二酯酶(PDE)抑制剂,对PDE3 和 PDE4 有抑制作用。 | |||
T17226 |
Vericiguat
维利西呱,BAY1021189 |
Guanylate cyclase | GPCR/G Protein |
Vericiguat (BAY1021189) 是一种有效的口服鸟苷酸环化酶刺激剂。 | |||
T31668 |
Eribaxaban
PD 348292,PD0348292,PD-0348292,PD-348292,PD 0348292,PD348292 |
Factor Xa | Metabolism |
Eribaxaban (PD348292) 是一种可口服的 Xa 因子抑制剂,可用于预防和治疗静脉血栓栓塞。 | |||
T3218 |
Napabucasin
BBI608 |
STAT | JAK/STAT signaling; Stem Cells |
Napabucasin (BBI608) 是一种口服的 Stat3 和 Y 干细胞活性抑制剂。 | |||
T6153 |
Icotinib
BPI-2009,埃克替尼,BPI-2009H,Conmana |
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Icotinib (Conmana) 是一种口服的基于喹唑啉的表皮生长因子受体 (EGFR) 抑制剂,IC50值为5 nM,具有潜在的抗肿瘤活性。 | |||
T27812 |
Leminoprazole
|
ATPase | Membrane transporter/Ion channel |
Leminoprazole 是一种可口服的 H+,K(+)-ATPase 抑制剂,可保护胃黏膜细胞免受各种细胞损伤,可用于治疗胃溃疡。 | |||
T68050L |
Dazolicin HCl
Dazolicine HCl,Dazolicine hydrochloride |
Others | Others |
Dazolicin HCl (Dazolicine HCl) 是一种可口服的抗心律失常化合物。 | |||
T6585 |
SAR405838
MI773,MI 773,MI-77301,MI-773 |
Mdm2; E1/E2/E3 Enzyme | Apoptosis; Ubiquitination |
SAR405838 (MI 773) 是 MI-773 的类似物,具有抗肿瘤活性。它是一种高效、选择性的MDM2-p53相互作用抑制剂,与 MDM2 结合的Ki 值为 0.88 nM。 | |||
T33421 |
MK-0686
MK0686 |
Bradykinin Receptor | GPCR/G Protein |
MK-0686 是一种可口服的缓激肽 B1 受体拮抗剂,具有潜在的抗炎活性。 | |||
T5605 |
EZM 2302
GSK3359088 |
Histone Methyltransferase | Chromatin/Epigenetic |
EZM 2302 (GSK3359088) 是选择性口服精氨酸甲基转移酶 CARM1 抑制剂,IC50值为 6 nM。 | |||
T16785 |
Ropidoxuridine
IPdR |
Others | Others |
Ropidoxuridine (IPdR) 是一种新型的、可口服的卤化胸苷类似物,有望成为人类肿瘤的增敏剂。Ropidoxuridine 是一种可口服且具有生物可利用的IUdR(5-碘-2'-脱氧尿苷)前药。 | |||
T15423 |
GSK-7975A
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
GSK-7975A 是具有口服活性的高效CRAC 通道抑制剂。 | |||
T67963 |
Teniloxazine
|
Others | Others |
Teniloxazine 是一种可口服的抗抑郁化合物,具有抗缺氧特性。 | |||
T25006 |
AGI-14100
AGI 14100 |
Dehydrogenase | Metabolism |
AGI-14100 是一种新型且可口服的 mIDH1 抑制剂。AGI-14100 用于治疗原发性人类髓性白血病。 | |||
T28911 |
Tafetinib
SIM-010603,SIM010603,SIM 010603 |
Tyrosine Kinases | Tyrosine Kinase/Adaptors |
Tafetinib (SIM-010603) 是一种新型有效且可口服的酪氨酸激酶抑制剂,具有抗血管生成和抗肿瘤活性。 | |||
T27176 |
Dimethandrolone Undecanoate
DMAU |
Others | Others |
Dimethandrolone Undecanoate (DMAU) 是一种新型可口服的雄激素,具有孕激素活性,是有潜力的男性避孕化合物。 | |||
T67960 |
Recainam
|
Others | Others |
Recainam 是一种可口服的新型且具有有效的 I 类抗心律失常活性的化合物。 | |||
T33836L |
Oxamisole TFA
Oxamisole TFA(99258-56-7 Free base) |
Antiviral | Immunology/Inflammation |
Oxamisole TFA 是一种可口服且具有选择性的 T 细胞免疫调节剂,可用于研究病毒感染。 | |||
T16781 |
Rogaratinib
BAY1163877 |
FGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
Rogaratinib (BAY1163877) 选择性抑制成纤维细胞生长因子受体。 | |||
T17235 |
Voclosporin
ISAtx-247 |
Phosphatase | Metabolism |
Voclosporin (ISAtx-247) 是一种新型且可口服钙调磷酸酶(CN; PP2B)抑制剂和免疫抑制剂,可用于治疗狼疮性肾炎。 | |||
T39707 |
AS-1763
|
BTK | Angiogenesis; Tyrosine Kinase/Adaptors |
AS-1763 是一种有效的、选择性的、非共价的、可口服的抑制剂,IC50 为 0.85 nM。 | |||
T2614 |
GSK2606414
|
Apoptosis; PERK; Autophagy | Apoptosis; Autophagy |
GSK2606414 是可渗透细胞且有口服活性的蛋白激酶 R 样内质网激酶抑制剂,IC50值为 0.4 nM。 | |||
T13111 |
Tegadifur
40497S,FD 1 |
Others | Others |
Tegadifur (40497S) 是一种可口服的抗肿瘤化合物,具有抗新陈代谢作用,常与尿嘧啶林和治疗直肠腺癌。 | |||
TQ0266 |
MSC2530818
|
CDK | Cell Cycle/Checkpoint |
MSC2530818 是一种有效的、选择性的、可口服的 CDK8 抑制剂,IC50值为2.6 nM。 | |||
T68139 |
Scio-323
|
p38 MAPK | MAPK |
Scio-323是一种可口服的 p38丝裂原活化蛋白(MAPK)激酶抑制剂。 | |||
TP1399 |
Fmoc-N-Me-Leu-OH
|
Others | Others |
Fmoc-N-Me-Leu-OH 是 N-Fmoc-N-甲基氨基酸的一种,能够用于肽偶联反应。 | |||
T3723 |
Dioxopromethazine hydrochloride
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Dioxopromethazine hydrochloride 是一种基于目标的药物分类,在全球许多国家都有销售。 | |||
T23297 |
(S)-(+)-Dimethindene maleate
|
AChR; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
(S)-(+)-Dimethindene maleate 是一种可口服且具有选择性毒蕈碱 M2 受体和组胺 H1 受体拮抗剂,抑制毒蕈碱 M1,M3 和 M4 受体。 | |||
T23711 |
WAY-260022
WAY 260022,NRI 022,NRI022,NRI-022,WAY260022 |
Dopamine Receptor; Serotonin Transporter; Norepinephrine | GPCR/G Protein; Neuroscience |
WAY-260022 是一种可口服且具有选择性去甲肾上腺素转运蛋白抑制剂,对血清素和多巴胺转运蛋白显示出抑制作用。 | |||
TQ0042 |
BAY-1436032
|
Dehydrogenase; Isocitrate Dehydrogenase (IDH) | Metabolism |
BAY-1436032 是一种选择性泛突变异柠檬酸脱氢酶 1 新型口服抑制剂。 | |||
T14089 |
AC-261066
AC 261066 |
Retinoid Receptor | Metabolism |
AC-261066是一种口服的RARβ2的同型选择性激动剂,pEC50为8.0。 | |||
T69356 |
Cindunistat
Cindunistat free base,SD6010,SD-6010 |
NOS | Immunology/Inflammation |
Cindunistat (free base) 是一种可口服的选择性 iNOS 抑制剂,可用于研究关节炎。 | |||
T68122L |
Oxmetidine FA
Oxmetidine FA(72830-39-8 Free base) |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Oxmetidine FA 是一种可口服的特异性组胺 H2 受体拮抗剂,具有抗溃疡作用。 | |||
T6076 |
EPZ015666
GSK3235025 |
Histone Methyltransferase | Chromatin/Epigenetic |
EPZ015666 (GSK3235025) 是一种口服有效的 PRMT5 酶活性抑制剂,IC50为 22 nM。 | |||
T27271 |
Enzaplatovir
BTAC585,BTA 585,BTA585,BTA-C585,BTA-585 |
RSV | Microbiology/Virology |
Enzaplatovir (BTA-585) 是一种可口服的融合 (fusion) 抑制剂,具有抗病毒活性,可用于研究呼吸道合胞病毒感染和冠状病毒病 (COVID-19) 感染。 | |||
T6511 |
Ravoxertinib
GDC-0994 |
ERK | MAPK |
Ravoxertinib (GDC-0994) 是可口服的ERK 激酶抑制剂,抑制ERK1和ERK2的IC50分别为 6.1 和 3.1 nM。 | |||
T7547 |
Ralfinamide mesylate
FCE-26742A (mesylate) |
Sodium Channel | Membrane transporter/Ion channel |
Ralfinamide mesylate (FCE-26742A (mesylate)) 是一种口服有效,来源于 α-aminoamide 的钠离子通道阻滞剂, 在缓解疼痛方面有研究价值。 | |||
T30787 |
Cefetamet sodium
Ro 15-8074/001,Ro15-8074/001,Ro-15-8074/001 |
Antibiotic | Microbiology/Virology |
Cefetamet sodium (Ro 15-8074/001) 是一种可口服的头孢类抗生素,具有抗菌活性,可用于研究肝硬化和肺部感染。 | |||
T12717 |
Basimglurant
CTEP Derivative,RG7090 |
GluR | Neuroscience |
Basimglurant (CTEP Derivative) 是一种高效,选择性,可口服的 mGlu5负变构调节剂,Kd 值为1.1 nM。 | |||
T16114 |
Pavinetant
MLE-4901,AZD4901,AZD2624 |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Pavinetant (MLE-4901) 是一种可口服的神经激肽-3 受体 (NK3R) 拮抗剂,可用于改善更年期症状。 | |||
T15575 |
Indeglitazar
PPM 204 |
PPAR | DNA Damage/DNA Repair; Metabolism |
Indeglitazar (PPM 204) 是 PPAR 的泛激动剂,包括亚型 alpha (α)、delta (δ) 和 gamma (γ)。 | |||
T10983L |
DDP-38003 dihydrochloride
|
Histone Demethylase | Chromatin/Epigenetic |
DDP-38003 dihydrochloride 是具有口服活性的KDM1A/LSD1抑制剂,IC50 值为 84 nM。 | |||
T25982 |
Pramiconazole
R-126638,R126638,R 126638,Azoline |
Antifungal | Microbiology/Virology |
Pramiconazole (R126638) 是一种可口服的抗真菌化合物。Pramiconazole 是治疗皮肤癣菌和皮肤酵母菌感染的候选化合物,可用于治疗脂溢性皮炎。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN5073 |
Strophanthidin
毒毛旋花子甙元,Strophanthidine,葡萄球菌素 |
ATPase; Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Strophanthidin (Strophanthidine) 是黄花夹竹桃中的一种类固醇,可增加舒张期和收缩期胞内 Ca2+浓度。它在 0.1 和 1 nmol/L 增加Na+/K+-ATPase 活性,1到100 μ mol/L 抑制Na+/K+-ATPase 活性,10 和 100 nmol/L 对Na+/K+-ATPase 活性无影响。 | |||
T5368 |
Eicosapentaenoic Acid
|
Histone Demethylase; Others; Endogenous Metabolite | Chromatin/Epigenetic; Metabolism; Others |
Eicosapentaenoic Acid 是一种 ω-3 脂肪酸。 | |||
T3428 |
Helicid
Hilicidum,4-formylphenyl-O-β-d-allopyranoside,Helicide,豆腐果苷 |
Others | Others |
Helicid (Helicide) 是 Helicia nilgirica Bedd 的主要组成部分。它被用于精神神经症的相关研究,可用于促进安定、睡眠和缓解疼痛。 | |||
TQ0024 |
3-Hydroxyglutaric acid
|
Endogenous Metabolite | Metabolism |
3-Hydroxyglutaric acid 是一种戊二酸的衍生物。 | |||
T2933 |
Wogonin
Vogonin,汉黄芩素 |
Apoptosis; Wnt/beta-catenin; CDK; Autophagy | Apoptosis; Autophagy; Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
Wogonin (Vogonin) 是一种具有细胞渗透性的口服类黄酮,具有抗炎和抗癌特性,能够抑制 CDK8和 Wnt 的活性。 | |||
T3S2007 |
MRE-269
3-氧代-12-烯-28-乌苏酸,MRE 269,ACT-333679,MRE269 |
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
MRE-269 (ACT-333679) 是一种口服的长效前列环素受体激动剂前药,是 Selexipag 的活性代谢物,用于治疗肺动脉高压。 | |||
T2947 |
Indole-3-carbinol
吲哚-3-甲醇,I3C,3-Indolemethanol,3-吲哚甲醇,Indole-3-Methanol |
E1/E2/E3 Enzyme; NF-κB; Aryl Hydrocarbon Receptor; Endogenous Metabolite; p53 | Apoptosis; Immunology/Inflammation; Metabolism; NF-κB; Ubiquitination |
Indole-3-carbinol (I3C) 是樟子松中的一种天然产物,是可口服的硫代葡萄糖苷葡糖苷酶裂解产物。它是芳烃受体 (AhR) 的激动剂,可抑制 NF-κB 和 IκBα 激酶活化。 | |||
T1045 |
Trimipramine maleate
Surmontil maleate,马来酸三甲丙咪嗪,三甲丙咪嗪马来酸盐 |
Dopamine Receptor; 5-HT Receptor; Antibacterial; Adrenergic Receptor; Norepinephrine; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Trimipramine maleate (Surmontil maleate) 是一种 5-HT 受体拮抗剂,对 5-HT1C、5-HT2和 5-HT1A 受体的 pKi 值分别为 6.39、8.10和 4.66。 | |||
T5253 |
3-Methyladipic acid
|
Others; Endogenous Metabolite | Metabolism; Others |
3-Methyladipic acid 是 ω 氧化途径的终产物。它是植烷酸分解代谢的代谢物。 | |||
T3O2749 |
L-Leucine
(S)-Leucine,Leu,L-亮氨酸,亮氨酸 |
mTOR | PI3K/Akt/mTOR signaling |
L-Leucine ((S)-Leucine) 是必需的支链氨基酸,能够激活 mTOR 信号通路。 | |||
T0978 |
Pantethine
LBF disulfide,Pantosin,Pantetina,Bis-pantethine,泛硫乙胺(维生素B5),泛硫乙胺,Pantomin,D-Pantethine |
Endogenous Metabolite | Metabolism |
D-Pantethine (Pantomin) 是泛酸的二聚体形式, 是生产辅酶 A 的中间体。D-Pantethine 能够作为膳食补充剂,用于改善血液胆固醇和研究痤疮。 | |||
T20643 |
Cefoxitin
Rephoxitin,Cefoxitinum |
Cell wall; Antibacterial; Antibiotic | Immunology/Inflammation; Microbiology/Virology |
Cefoxitin (Rephoxitin) 是一种广谱的、可口服的第二代头孢霉素类抗生素。Cefoxitin 干扰细菌细胞壁的合成。其活性谱包括革兰氏阴性和革兰氏阳性菌,通常用于腹腔感染、盆腔感染和某些类型的妇科感染等腹部,对厌氧菌具有高效性。 | |||
T15248 |
Estetrol
Donesta |
Estrogen Receptor/ERR; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Estetrol(Donesta) 是可口服且具有选择性核雌激素受体 (estrogen receptor) 调节剂,是一种在怀孕期间由人类胎儿肝脏合成的天然雌激素。Estetrol 对子宫内膜或中枢神经系统有作用,但对乳房有拮抗作用。Estetrol 在低浓度时可能有助于降低血栓形成。Estetrol 可用于缓解更年期症状。 | |||
T3746 |
Dimethyl phthalate
邻苯二甲酸二甲酯,Solvanom,Avolin,Fermine,避蚊酯 |
Others | Others |
Dimethyl phthalate (Fermine) 是一种邻苯二甲酸酯 (PAEs),是一种已知的内分泌干扰物,也是一种普遍存在的污染物。它常作为增塑剂,赋予硬质聚氯乙烯 (PVC) 树脂以柔韧性。 | |||
TN1056 |
Mogroside IIe
|
IL Receptor | Immunology/Inflammation |
Mogroside IIe 是一种天然来源的三萜糖苷,作为非糖类甜味剂,Mogroside 比蔗糖更甜。Mogroside 具有抗氧化,抗糖尿病和抗癌活性。 | |||
TN6550 |
New compound 2
|
||
New compound 2 可用于生命科学领域的相关研究,其产品编号为 TN6550。 | |||
TN6578 |
Dihydromarein
|
||
Dihydromarein 可用于生命科学领域的相关研究,其产品编号为 TN6578。 | |||
TN6654 |
cis-Aegineoside
|
||
cis-Aegineoside 可用于生命科学领域的相关研究,其产品编号为 TN6654。 | |||
TN3405 |
Amaronol B
|
Others | Others |
Amaronol B 是在 Pseudolarix amabilis 和 Larix kaempferi 中发现的一种天然产物,有可用的数据。 | |||
TN6479 |
13-Dehydroxyindaconintine
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13-Dehydroxyindaconintine 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 TN6479。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-00369 |
LY6D Protein, Human, Recombinant (mFc)
E48,lymphocyte antigen 6 complex, locus D,Ly-6D |
Human | HEK293 Cells |
LY6D (Lymphocyte Antigen 6 Family Member D) is a Protein Coding gene. It may act as a specification marker at the earliest stage specification of lymphocytes between B- and T-cell development. Marks the earliest stage of B-cell specification. The expression of LY6D is induced in MCF10A cells by X-ray irradiation. The induction of LY6D expression is triggered through a pathway regulated by ATM, CHK2, and p53. This method is a new Ab-directed proteomic strategy for the analysis of membrane protein... | |||
TMPY-02157 |
GST Protein, Schistosoma japonicum, Recombinant
|
Schistosoma japonicum | Baculovirus Insect Cells |
Genetic engineers have used glutathione S-transferase to create the GST gene fusion system. This system is used to purify and detect proteins of interest. In a GST gene fusion system, the GST sequence is incorporated into an expression vector alongside the gene sequence encoding the protein of interest. Induction of protein expression from the vector's promoter results in expression of a fusion protein: the protein of interest fused to the GST protein. This GST-fusion protein can then be purifie... | |||
TMPH-00771 |
Ferritin-2 Protein, Glycine max, Recombinant (His & SUMO)
Ferritin-2, chloroplastic,SFerH-2 |
Glycine max | E. coli |
Stores iron in a soluble, non-toxic, readily available form. Important for iron homeostasis. Has ferroxidase activity. Iron is taken up in the ferrous form and deposited as ferric hydroxides after oxidation. | |||
TMPK-01125 |
FAM19A5 Protein, Mouse, Recombinant (His)
Fam19a5,QLLK5208,Tafa5,Chemokine-like protein TAFA-5,UNQ5208 |
Mouse | E. coli |
FAM19A5 is a secretory protein that is predominantly expressed in the brain. Although the FAM19A5 gene has been found to be associated with neurological and/or psychiatric diseases, only limited information is available on its function in the brain. FAM19A5 plays a role in nervous system development from an early stage and increases its expression in response to pathological conditions in subsets of neurons and OPCs of the brain. FAM19A5 Protein, Mouse, Recombinant (His) is expressed in E. coli ... | |||
TMPK-00906 |
PSCA Protein, Mouse, Recombinant (hFc)
UNQ206,PSCA,PRO232 |
Mouse | HEK293 Cells |
Gastric cancer is a deadly malignancy and is a prognostically unfavorable entity with restricted therapeutic strategies available. Prostate stem cell antigen (PSCA) is a glycosylphosphatidylinositol (GPI)-anchored cell surface protein widely expressed in bladder, prostate, and pancreatic cancers. Existing studies have thoroughly recognized the availability of utilizing anti-PSCA CAR-T cells in the treatment of metastatic prostate cancer and non-small-cell lung cancer. PSCA Protein, Mouse, Recomb... | |||
TMPK-00699 |
FAM19A5 Protein, Human, Recombinant (His)
Chemokine-like protein TAFA-5,UNQ5208,Tafa5,QLLK5208,Fam19a5 |
Human | E. coli |
FAM19A5 is a secretory protein that is predominantly expressed in the brain. Although the FAM19A5 gene has been found to be associated with neurological and/or psychiatric diseases, only limited information is available on its function in the brain. FAM19A5 plays a role in nervous system development from an early stage and increases its expression in response to pathological conditions in subsets of neurons and OPCs of the brain. FAM19A5 Protein, Human, Recombinant (His) is expressed in E. coli ... | |||
TMPK-00728 |
PSCA Protein, Human, Recombinant (hFc)
UNQ206,PRO232,PSCA |
Human | HEK293 Cells |
Gastric cancer is a deadly malignancy and is a prognostically unfavorable entity with restricted therapeutic strategies available. Prostate stem cell antigen (PSCA) is a glycosylphosphatidylinositol (GPI)-anchored cell surface protein widely expressed in bladder, prostate, and pancreatic cancers. Existing studies have thoroughly recognized the availability of utilizing anti-PSCA CAR-T cells in the treatment of metastatic prostate cancer and non-small-cell lung cancer. PSCA Protein, Human, Recomb... | |||
TMPY-00561 |
Neurotensin Protein, Human, Recombinant (hFc)
NMN-125,NTS1,NN,NT/N,neurotensin,NT |
Human | HEK293 Cells |
NTS (Neurotensin) is a Protein Coding gene. This gene encodes a common precursor for two peptides, neuromedin N and neurotensin. NTS is a neuropeptide distributed in the central nervous and digestive systems. It belongs to the neurotensin family. NTS is an endogenous tridecapeptide of the central nervous system and the gastrointestinal tract of different mammalian species including the human. The human gene encoding neurotensin has previously been assigned to chromosome 12 but no regional locali... | |||
TMPJ-00696 |
NOL3 Protein, Human, Recombinant
Apoptosis Repressor With CARD,Nucleolar Protein of 30 kDa,Nu... |
Human | E. coli |
Nucleolar protein 3 is encoded by NOL3 gene. Multiple transcript variants encoding different isoforms have been found for this gene. So far, Nucleolar protein 3 has show to have two Isoforms. Isoform 1 may be involved in RNA splicing. Isoform 2 functions as an apoptosis repressor that blocks multiple modes of cell death. It inhibits extrinsic apoptotic pathways through two different ways. Firstly, it by interacting with FAS and FADD upon FAS activation blocking death-inducing signaling complex ... | |||
TMPJ-00761 |
FTH Protein, Human, Recombinant (His)
FTHL6,Cell proliferation-inducing gene 15 protein,Ferritin h... |
Human | E. coli |
Ferritin heavy polypeptide 1(FTH1), is a ubiquitous intracellular protein which stores iron in a soluble, non-toxic, readily available form. FTH1 has ferroxidase activity and is important for iron homeostasis. Iron is taken up in the ferrous form and deposited as ferric hydroxides after oxidation. Ferritin is composed of 24 subunits of the light and heavy ferritin chains. It plays a role in delivery of iron to cells and mediates iron uptake in capsule cells of the developing kidney. Variation of... | |||
TMPY-02711 |
Ferritin heavy chain 1/FTH1 Protein, Human, Recombinant
FHC,FTHL6,FTH,PIG15,PLIF,ferritin, heavy polypeptide 1,HFE5 |
Human | E. coli |
FTH1 (ferritin, heavy polypeptide 1) is the heavy subunit of ferritin which is the major intracellular iron storage protein in prokaryotes and eukaryotes. It is composed of 24 subunits of the heavy and light ferritin chains. Variation in ferritin subunit composition may affect the rates of iron uptake and release in different tissues. A major function of ferritin is the storage of iron in a soluble and nontoxic state. Defects in ferritin proteins are associated with several neurodegenerative dis... | |||
TMPH-02524 |
Arginase-1/ARG1 Protein, Mouse, Recombinant (His)
Arginase-1,Type I arginase,Liver-type arginase,Arg1 |
Mouse | P. pastoris (Yeast) |
Key element of the urea cycle converting L-arginine to urea and L-ornithine, which is further metabolized into metabolites proline and polyamides that drive collagen synthesis and bioenergetic pathways critical for cell proliferation, respectively; the urea cycle takes place primarily in the liver and, to a lesser extent, in the kidneys.; Functions in L-arginine homeostasis in nonhepatic tissues characterized by the competition between nitric oxide synthase (NOS) and arginase for the available i... | |||
TMPH-00651 |
Lpp Protein, E. coli, Recombinant (His & KSI)
Major outer membrane lipoprotein Lpp,Braun lipoprotein,Murei... |
E. coli | E. coli |
An outer membrane lipoprotein that controls the distance between the inner and outer membranes; adding residues to Lpp increases the width of the periplasm. The only protein known to be covalently linked to the peptidoglycan network (PGN). Also non-covalently binds the PGN. The link between the cell outer membrane and PGN contributes to the maintenance of the structural and functional integrity of the cell envelope, and maintains the correct distance between the PGN and the outer membrane. The m... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T12224 |
Nilotinib-d6
AMN107 D6 |
Others | Others |
Nilotinib D6 is a deuterium labeled Nilotinib which is an orally available inhibitor of Bcr-Abl tyrosine kinase ,and with antineoplastic activity. | |||
T13121 |
Teneligliptin D8
MP-513 D8 |
Others | Others |
Teneligliptin D8 a deuterium labeled Teneligliptin (MP-513). Teneligliptin is a potent, orally available, competitive, and long-lasting inhibitor of DPP-4. | |||
T10350 |
Apremilast-d5
Apremilast D5,CC-10004 D5 |
TNF; PDE | Apoptosis; Metabolism |
Apremilast D5 (CC-10004 D5) is a deuterium-labeled Apremilast. Apremilast is an orally available inhibitor of PDE-4 (IC50: 74 nM). Apremilast inhibits TNF-α release by lipopolysaccharide (IC50: 104 nM). | |||
TMIH-0595 |
Vericiguat-d3
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Vericiguat-d3 是 Vericiguat 的氘代化合物。Vericiguat 的 CAS 号为 1350653-20-1。Vericiguat 是一种有效的口服鸟苷酸环化酶刺激剂。 | |||
TMIJ-0379 |
Eicosapentaenoic Acid-d5
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Eicosapentaenoic Acid-d5 是 Eicosapentaenoic Acid 的氘代化合物。Eicosapentaenoic Acid 的 CAS 号为 10417-94-4。Eicosapentaenoic Acid 是一种 ω-3 脂肪酸。 | |||
TMIJ-0207 |
(S)-Ketoprofen-d3
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(S)-Ketoprofen-d3 是 (S)-Ketoprofen 的氘代化合物。(S)-Ketoprofen 的 CAS 号为 22161-81-5。S-(+)-Ketoprofen 抑制COX-1和COX-2的IC50值分别为 1.9 和 27 nM。 | |||
TMIH-0117 |
Binimetinib-13C-d3
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Binimetinib-13C-d3 是 Binimetinib 的 13C 和氘代化合物。Binimetinib 的 CAS 号为 606143-89-9。Binimetinib 是一种可口服的选择性MEK1/2抑制剂,抑制MEK的IC50为 12 nM。 | |||
TMID-0021 |
Fruquintinib-d3
|
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Fruquintinib-d3 是 Fruquintinib 的氘代化合物。Fruquintinib 的 CAS 号为 1194506-26-7。Fruquintinib 是一种选择性的VEGFR 1/2/3抑制剂,它们的IC50值分别为33 nM、0.5 nM、35 nM。 | |||
TMIH-0609 |
Zafirlukast-d7
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Zafirlukast-d7 是 Zafirlukast 的氘代化合物。Zafirlukast 的 CAS 号为 107753-78-6。Zafirlukast 是一种可口服的白三烯 D4受体拮抗剂,具有平喘、抗炎和抗菌作用。 | |||
TMIJ-0295 |
Flubendazole-d3 (methyl-d3)
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Flubendazole-d3 (methyl-d3) 是 Flubendazole 的氘代化合物。Flubendazole 的 CAS 号为 31430-15-6。Flubendazole 是用于治疗人类蠕虫感染的驱虫药。它通过抑制微管功能等机制发挥抗癌作用。它诱导p53介导的细胞凋亡,抑制 G2/M 细胞周期。 | |||
TMID-0073 |
Alectinib-d8
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Alectinib-d8 是 Alectinib 的氘代化合物。Alectinib 的 CAS 号为 1256580-46-7。Alectinib 是一种有效的、选择性的、口服具有活力的、ATP 竞争性的ALK抑制剂,其IC50=1.9 nM,Kd=2.4 nM,并且还抑制ALK F1174L和ALK R1275Q,其IC50分别为 1 nM 和 3.5 nM。它还有中枢神经系统渗透能力。 | |||
TMIH-0519 |
Selexipag Active Metabolite-d7
|
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Selexipag Active Metabolite-d7 是 Selexipag Active Metabolite 的氘代化合物。Selexipag Active Metabolite 的 CAS 号为 475085-57-5。MRE269 是一种口服的长效前列环素受体激动剂前药,是 Selexipag 的活性代谢物,用于治疗肺动脉高压。 | |||
TMIJ-0329 |
Montelukast-d6
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Montelukast-d6 是 Montelukast 的氘代化合物。Montelukast 的 CAS 号为 158966-92-8。Montelukast 是可口服的半胱氨酸白三烯受体1 选择性拮抗剂,可用于研究预防哮喘和肝损伤。它还可减少心脏损伤,在肠缺血-再灌注损伤中也具有抗氧化作用。 | |||
TMIJ-0374 |
L-Leucine-d3
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L-Leucine-d3 是 L-Leucine 的氘代化合物。L-Leucine 的 CAS 号为 61-90-5。L-Leucine 是必需的支链氨基酸,能够激活mTOR信号通路。 | |||
TMIJ-0081 |
L-Leucine-d10
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L-Leucine-d10 是 L-Leucine 的氘代化合物。L-Leucine 的 CAS 号为 61-90-5。L-Leucine 是必需的支链氨基酸,能够激活mTOR信号通路。 | |||
TMIH-0235 |
Finerenone-d5
|
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Finerenone-d5 是 Finerenone 的氘代化合物。Finerenone 的 CAS 号为 1050477-31-0。Finerenone 是一种选择性、具有口服活性的、非甾体类盐皮质激素受体拮抗剂 (IC50=18 nM)。与糖皮质激素受体、雄激素受体和孕酮受体相比,它表现出良好的选择性 (>500-fold)。它在心肾疾病研究中具有潜在的应用前景,如 2 型糖尿病和慢性肾脏疾病。 | |||
TMIH-0109 |
Bempedoic acid-d4
|
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Bempedoic acid-d4 是 Bempedoic acid 的氘代化合物。Bempedoic acid 的 CAS 号为 738606-46-7。ETC-1002 是一种 ATP-柠檬酸裂解酶抑制剂,可激活AMPK。它是脂质和碳水化合物代谢的调节剂。 | |||
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。 | |||
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。 |