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)
- GC73363Antitumor agent-81CAS: 2765180-17-2纯度: >98.00%
Antitumor agent-81(化合物5a)是一种低细胞毒性的P62-RNF168激动剂,可增强P62和RNF168之间的相互作用。
- GC73512Skp2 inhibitor 2CAS: 2760612-77-7纯度: 不显示
Skp2 inhibitor 2(14f)是F-box蛋白S期激酶相关蛋白2(Skp2)的抑制剂,IC50值为10.2μM(Skp2-Cks1)。
- GC73547PROTAC TG2 degrader-2纯度: >99.00%
PROTAC TG2 degrader-2(化合物7)是靶向转谷氨酰胺酶2 (TG2)的选择性竞争性降解物,Kd为100 μM。
- GC73673LeramistatCAS: 1642602-54-7纯度: >98.00%
Leramistat(HMC-C-01-A;MBS2320)是一种线粒体复合物1抑制剂,参与细胞代谢免疫代谢调节。
- GC73677Olgotrelvir sodiumCAS: 2763596-72-9纯度: >95.00%
Olgotrelvir sodium是一种口服活性的冠状病毒主要蛋白酶(Mpro)和人细胞组织蛋白酶(cathepsin L)的双重抑制剂。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC73301 | 5-Aminosalicylic acid-d3 | 1309283-32-6 | >99.00% | |
5-Aminosalicylic acid-d3是氘标记的5-氨基水杨酸。 | ||||
| GC73363 | Antitumor agent-81 | 2765180-17-2 | >98.00% | |
Antitumor agent-81(化合物5a)是一种低细胞毒性的P62-RNF168激动剂,可增强P62和RNF168之间的相互作用。 | ||||
| GC73374 | TD1092 | - | >99.00% | |
TD1092是一种泛IAP降解剂,可降解cIAP1、cIAP2和XIAP。 | ||||
| GC73380 | MMP-1-IN-1 | - | >99.00% | |
MMP-1-IN-1(化合物6)是一种高效的MMP-1抑制剂,IC50为0.034 μM。 | ||||
| GC73388 | GRP78-IN-3 | 2707510-30-1 | >99.00% | |
GRP78-IN-3(化合物8)是一种选择性Grp78(HSPA5)抑制剂,IC50为0.59μM。 | ||||
| GC73412 | BDM-2 | 1643876-33-8 | >99.00% | |
BDM-2是HIV-1整合酶(IN指整合酶)的IN-LEDGF变构抑制剂(INLAI)(IC50=47 nM),具有强效的抗逆转录病毒(ARV)活性。 | ||||
| GC73417 | CASP8-IN-1 | 1956368-39-0 | >98.00% | |
CASP8-IN-1(化合物63-R)是胱天蛋白酶8(CASP8)的选择性抑制剂,IC50为0.7μM。 | ||||
| GC73433 | (S)-BAY 2965501 | 2732902-09-7 | >99.00% | |
(S)-BAY 2965501是BAY 2965501的左旋异构体。 | ||||
| GC73485 | UC-764864 | 278806-03-4 | >99.00% | |
UC-764864是一种UBE2N抑制剂。 | ||||
| GC73512 | Skp2 inhibitor 2 | 2760612-77-7 | 不显示 | |
Skp2 inhibitor 2(14f)是F-box蛋白S期激酶相关蛋白2(Skp2)的抑制剂,IC50值为10.2μM(Skp2-Cks1)。 | ||||
| GC73547 | PROTAC TG2 degrader-2 | - | >99.00% | |
PROTAC TG2 degrader-2(化合物7)是靶向转谷氨酰胺酶2 (TG2)的选择性竞争性降解物,Kd为100 μM。 | ||||
| GC73551 | PF-07247685 | - | >99.00% | |
PF-07247685是BCKDC激酶(BDK)抑制剂(EC50=2.2nM)。 | ||||
| GC73585 | (Rac)-M826 | 2649883-37-2 | 不显示 | |
(Rac)-M826是M826的外消旋体。 | ||||
| GC73589 | GPX4-IN-6 | 2922824-07-3 | >99.00% | |
GPX4-IN-6(化合物C25)是GPX4共价抑制剂,IC50值为0.13 μM。 | ||||
| GC73619 | M190S | 2578300-07-7 | >99.00% | |
M190S是一种新型小分子,在体外和体内保护细胞免受线粒体依赖性凋亡。 | ||||
| GC73626 | PF-07202954 | 2639372-47-5 | >97.00% | |
PF-07202954是一种弱碱性DGAT2抑制剂,对人DGAT2的IC50为10 nM。 | ||||
| GC73641 | MMP-7-IN-3 | 2865097-58-9 | >99.00% | |
MMP-7-IN-3是一种有效的选择性MMP-7抑制剂。 | ||||
| GC73642 | ALK-IN-26 | 2447607-85-2 | >99.00% | |
ALK-IN-26是ALK抑制剂,对ALK酪氨酸激酶的IC50值为7.0 μM。 | ||||
| GC73643 | NBI-961 | 2225902-98-5 | >99.00% | |
NBI-961是一种有效的NEK2抑制剂,可抑制蛋白酶体降解。 | ||||
| GC73645 | YG1702 | 724737-08-0 | >99.00% | |
YG1702是一种有效的aldh18a1特异性抑制剂。 | ||||
| GC73673 | Leramistat | 1642602-54-7 | >98.00% | |
Leramistat(HMC-C-01-A;MBS2320)是一种线粒体复合物1抑制剂,参与细胞代谢免疫代谢调节。 | ||||
| GC73677 | Olgotrelvir sodium | 2763596-72-9 | >95.00% | |
Olgotrelvir sodium是一种口服活性的冠状病毒主要蛋白酶(Mpro)和人细胞组织蛋白酶(cathepsin L)的双重抑制剂。 | ||||
| GC73684 | CHK-336 | 2743436-86-2 | >98.00% | |
CHK-336(实施例1)是一种口服活性LDHA抑制剂(IC50<1nM),其抑制小鼠肝细胞中乳酸的产生。 | ||||
| GC73701 | HSP90-IN-27 | 525577-38-2 | >95.00% | |
HSP90-IN-27(化合物19)是一种HSP90抑制剂。 | ||||
