Proteases
Proteases(蛋白酶)
Proteases, also known as peptidases or proteolytic enzymes, consists of a large number of enzymes catalyzing the hydrolysis of peptide bonds and subsequently resulting in the degradation of protein substrates into amino acids. Proteases are involved in a wide range of human diseases, including cancer, neurodegenerative disorders, inflammatory diseases and cardiovascular diseases. Thus numerous proteases inhibitors (small molecules and proteins) have been identified to block activity of proteases. Proteases inhibitors can be classified into different types based on the class of proteases they inhibit through two general mechanisms, irreversible “trapping” reactions and reversible tight-binding reactions. Proteases inhibitors have been used as diagnostic or therapeutic agents for the treatment of proteases-related diseases.
- Aminopeptidase(21)
- ACE(75)
- Calpains(11)
- Carboxypeptidase(9)
- Cathepsin(65)
- DPP-4(18)
- Elastase(25)
- Gamma Secretase(50)
- HCV Protease(39)
- HSP(105)
- HIV Integrase(30)
- HIV Protease(35)
- MMP(195)
- NS3/4a protease(4)
- Serine Protease(19)
- Thrombin(47)
- Urokinase(2)
- Cysteine Protease
- Tyrosinases(50)
- Other Proteases(15)
- 15-PGDH(1)
- Acetyl-CoA Carboxylase(14)
- Acyltransferase(64)
- Aldehyde Dehydrogenase (ALDH)(30)
- Aminoacyl-tRNA Synthetase(9)
- ATGL(1)
- Dipeptidyl Peptidase(49)
- Drug Metabolite(513)
- E1/E2/E3 Enzyme(92)
- Endogenous Metabolite(1768)
- FABP(9)
- Farnesyl Transferase(20)
- Glutaminase(17)
- Glutathione Peroxidase(35)
- Isocitrate Dehydrogenase (IDH)(28)
- Lactate Dehydrogenase(19)
- Lipoxygenase(274)
- Mitochondrial Metabolism(260)
- NEDD8-activating Enzyme(6)
- Neprilysin(12)
- PAI-1(14)
- Ser/Thr Protease(49)
- Tryptophan Hydroxylase(12)
- Xanthine Oxidase(18)
- MALT1(10)
- Caspase(117)
- PCSK9(13)
- ADAMTS(1)
- Density Lipoprotein
- TrxR(1)
- DGK(3)
Proteases 相关产品(4079)
- GC326085-Amino-4-oxopentanoic acidCAS: 106-60-5纯度: >98.00%
5-Amino-4-oxopentanoic acid是一种天然存在的非蛋白原性氨基酸,是光敏剂原卟啉IX(PpIX)的前药。5-Amino-4-oxopentanoic acid可以被波长约为635nm(580至740nm)的激光激活,发出红色荧光(620至710nm),作为多种癌症的光诊断剂。
- GC32613RP-64477CAS: 135239-65-5纯度: >99.50%
RP-64477 is a potent inhibitor of the cholesterol esterifying enzyme Acyl-coenzyme A:cholesterol O-acyltransferase (ACAT). RP-64477 inhibits ACAT activity with IC50 of 113 nM, 503 nM, and 180 nM in human intestinal (CaCo-2), hepatic (HepG2) and monocytic (THP-1) cell assays, respectively.
- GC32694GNE-140 racemateCAS: 1802977-61-2纯度: >98.00%
GNE-140racemate是(R)-GNE-140和(S)-GNE-140的外消旋混合物。(R)-GNE-140是有效的乳酸脱氢酶A(LDHA)抑制剂。
- GC32732Hyaluronic acidCAS: 9004-61-9纯度: >97.00%
透明质酸 (HA) 是由双糖的重复单元组成的生物聚合物,其中包括通过 β- (1 4) 和 β- (1 3) 糖苷连接的 D- 葡萄糖醛酸分子和 N- 乙酰氨基葡萄糖分子。
- GC32737TAK-243 (MLN7243)CAS: 1450833-55-2纯度: >98.00%
TAK-243 (MLN7243)是一种选择性泛素活化酶(UBA1)抑制剂,IC 50 值为1nM。
- GC32758IsoginkgetinCAS: 548-19-6纯度: >99.50% / >98.00%
Isoginkgetin是一种双黄酮类化合物,可抑制胰脂肪酶活性,IC 50 值为2.9µM。
- GC32759L-778123 hydrochloride (L-778,123 hydrochloride)CAS: 253863-00-2纯度: >98.50%
A dual inhibitor of FTase and GGTase I
- GC32823Incyclinide (CMT-3)CAS: 15866-90-7纯度: >98.00%
Incyclinide (CMT-3)是一种非抗生素,由四环素衍生的基质金属蛋白酶(MMP)抑制剂。
- GC32858ER-000444793CAS: 792957-74-5纯度: >98.00%
ER-000444793 is a potent inhibitor of mitochondrial permeability transition pore (mPTP) opening with IC50 of 2.8 μM.
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC32608 | 5-Amino-4-oxopentanoic acid | 106-60-5 | >98.00% | |
5-Amino-4-oxopentanoic acid是一种天然存在的非蛋白原性氨基酸,是光敏剂原卟啉IX(PpIX)的前药。5-Amino-4-oxopentanoic acid可以被波长约为635nm(580至740nm)的激光激活,发出红色荧光(620至710nm),作为多种癌症的光诊断剂。 | ||||
| GC32611 | H-Ile-Pro-Pro-OH | 26001-32-1 | - | |
A peptide ACE inhibitor | ||||
| GC32613 | RP-64477 | 135239-65-5 | >99.50% | |
RP-64477 is a potent inhibitor of the cholesterol esterifying enzyme Acyl-coenzyme A:cholesterol O-acyltransferase (ACAT). RP-64477 inhibits ACAT activity with IC50 of 113 nM, 503 nM, and 180 nM in human intestinal (CaCo-2), hepatic (HepG2) and monocytic (THP-1) cell assays, respectively. | ||||
| GC32619 | OM-189 | 55381-18-5 | - | |
OM-189是一种人工合成且有选择性的凝血酶抑制剂。 | ||||
| GC32620 | Bimoclomol | 130493-03-7 | >99.00% | |
Bimoclomol是一种heatshockprotein(HSP)辅诱导剂,可用于心血管疾病的研究。 | ||||
| GC32628 | ZD-0892 | 171964-73-1 | - | |
ZD-0892是选择性和有效的中性粒细胞弹性蛋白酶(neutrophilelastase)抑制剂,对于人嗜中性粒细胞弹性蛋白酶和猪胰弹性蛋白酶的Ki值分别为6.7和200nM。 | ||||
| GC32639 | Thrombin inhibitor 1 | 855998-46-8 | - | |
Thrombininhibitor1是一种有效的凝血酶抑制剂(Ki=0.66nM,2xaPTT=0.43μM)。 | ||||
| GC32663 | Desethyl KBT-3022 | 101001-72-3 | - | |
DesethylKBT-3022是新型抗血小板药物KBT-3022的主要活性代谢物。 | ||||
| GC32671 | NEP-IN-2 | 145775-14-0 | - | |
NEP-IN-2是一种neutralendopeptidase抑制剂,主要用于研究动脉粥样硬化、再狭窄症的扩散等症状。 | ||||
| GC32694 | GNE-140 racemate | 1802977-61-2 | >98.00% | |
GNE-140racemate是(R)-GNE-140和(S)-GNE-140的外消旋混合物。(R)-GNE-140是有效的乳酸脱氢酶A(LDHA)抑制剂。 | ||||
| GC32695 | Ac-DEVD-CHO | 169332-60-9 | >98.00% | |
Ac-DEVD-CHO是一种Caspase-3抑制剂,IC 50 值为0.016μM。 | ||||
| GC32706 | ND-646 | 1434639-57-2 | >98.50% | |
An ACC inhibitor | ||||
| GC32715 | TOFA (RMI14514) | 54857-86-2 | >99.50% / >98.00% | |
TOFA (RMI14514)是乙酰辅酶A羧化酶-α (ACCA)的变构抑制剂。 | ||||
| GC32721 | NSC232003 | 1905453-18-0 | >98.50% / >98.00% | |
NSC232003是一种靶向UHRF1的小分子抑制剂。 | ||||
| GC32732 | Hyaluronic acid | 9004-61-9 | >97.00% | |
透明质酸 (HA) 是由双糖的重复单元组成的生物聚合物,其中包括通过 β- (1 4) 和 β- (1 3) 糖苷连接的 D- 葡萄糖醛酸分子和 N- 乙酰氨基葡萄糖分子。 | ||||
| GC32737 | TAK-243 (MLN7243) | 1450833-55-2 | >98.00% | |
TAK-243 (MLN7243)是一种选择性泛素活化酶(UBA1)抑制剂,IC 50 值为1nM。 | ||||
| GC32758 | Isoginkgetin | 548-19-6 | >99.50% / >98.00% | |
Isoginkgetin是一种双黄酮类化合物,可抑制胰脂肪酶活性,IC 50 值为2.9µM。 | ||||
| GC32759 | L-778123 hydrochloride (L-778,123 hydrochloride) | 253863-00-2 | >98.50% | |
A dual inhibitor of FTase and GGTase I | ||||
| GC32792 | JNJ0966 | 315705-75-0 | >99.00% | |
An inhibitor of MMP-9 zymogen activation | ||||
| GC32814 | DKM 2-93 | 65836-72-8 | >98.00% | |
DKM2-93是相对选择性的UBA5抑制剂,IC50值为430μM。 | ||||
| GC32823 | Incyclinide (CMT-3) | 15866-90-7 | >98.00% | |
Incyclinide (CMT-3)是一种非抗生素,由四环素衍生的基质金属蛋白酶(MMP)抑制剂。 | ||||
| GC32838 | BAY-2402234 | 2225819-06-5 | >99.00% | |
A DHODH inhibitor | ||||
| GC32858 | ER-000444793 | 792957-74-5 | >98.00% | |
ER-000444793 is a potent inhibitor of mitochondrial permeability transition pore (mPTP) opening with IC50 of 2.8 μM. | ||||
| GC32865 | BMS-214662 | 195987-41-8 | >99.50% | |
A potent FTase inhibitor | ||||
