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)
- GC35300Aloin(mixture of A&B)CAS: 8015-61-0纯度: >95.00%
An anthroquinone with diverse biological activities
- GC35320Aminoadipic acidCAS: 542-32-5纯度: >98.00% / >97.00%
DL-2-Aminoadipic acid is an excitatory amino acid analogue, which functions as a glutamine synthetase inhibitor.
- GC35321Aminomalonic acidCAS: 1068-84-4纯度: >98.00%
Aminomalonic acid (Aminomalonate, Aminopropanedioic acid) is an amino dicarboxylic acid. It has a role as a human metabolite and a Daphnia magna metabolite.
- GC35339AnandamideCAS: 94421-68-8纯度: >98.00%
Anandamide是一种来源于含花生四烯酸膜脂的内源性大麻素,通过结合并激活CB1和CB2大麻素受体以及香草素瞬时受体电位通道1(TRPV1)受体发挥作用。
- GC35361Antineoplaston A10CAS: 91531-30-5纯度: >98.00%
Antineoplaston A10 is a naturally occurring substance in the human body that that can be potentially used for the treatment of glioma, lymphoma, astrocytoma and breast cancer. The main ingredient active of antineoplaston A10 (Phenylacetylglutamine, PG) inhibits RAS and promotes apoptosis.
- GC35369Apigenin-7-glucuronideCAS: 29741-09-1纯度: >98.50%
Apigenin-7-O-glucuronide (Apigenin-7-glucuronide) is the major flavonoid found in milk thistle. Apigenin 7-o-glucuronide inhibits tumor necrosis factor alpha (TNF-α) and total nitrite release in lipopolysaccharide-activated macrophages.
- GC35377ApratastatCAS: 287405-51-0纯度: >99.00%
Apratastat是一种口服活性、可逆的双重抑制剂,能够抑制肿瘤坏死因子-α转换酶(TACE;IC 50 =81.7ng/mL)和基质金属蛋白酶(MMPs)的活性。
- GC35388Aristolactam ICAS: 13395-02-3纯度: >99.50%
Aristololactam I (AL-I) 是马兜铃酸I (AA-I) 的主要代谢产物,参与导致肾损伤的过程。Aristololactam I (AL-I) 直接损伤肾近端小管细胞,AL-I 的细胞毒性效力高于AA-I,并且这些分子的细胞毒性作用是通过 caspase-3 依赖性细胞凋亡介导。
- GC35476BAY-678 racemateCAS: 675103-35-2
BAY-678 racemate 是 BAY-678 的消旋体。BAY-678 是具有口服生物活性的、高效的、选择性的、人中性粒细胞弹性蛋白酶(HNE) 的细胞渗透性抑制剂,其 IC50 值为 20 nM。BAY-678 也是被基因结构组学联盟 (SGC) 推荐的化学探针。
- GC35494BenzoyloxypaeoniflorinCAS: 72896-40-3
Benzoyloxypaeoniflorin 分离于 Paeonia suffruticosa 的根,是 tyrosinase 抑制剂,对蘑菇 tyrosinase 的 IC50为 0.453 mM。Benzoyloxypaeoniflorin 是 NF-κB 抑制剂,Benzoyloxypaeoniflorin 通过对血小板聚集和凝血的抑制作用,有助于改善血液循环。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC35262 | Afzelin | 482-39-3 | >98.00% | |
A polyphenolic glycoside flavone with diverse biological activities | ||||
| GC35295 | Allopurinol riboside | 16220-07-8 | >98.00% | |
A ribonucleoside | ||||
| GC35300 | Aloin(mixture of A&B) | 8015-61-0 | >95.00% | |
An anthroquinone with diverse biological activities | ||||
| GC35320 | Aminoadipic acid | 542-32-5 | >98.00% / >97.00% | |
DL-2-Aminoadipic acid is an excitatory amino acid analogue, which functions as a glutamine synthetase inhibitor. | ||||
| GC35321 | Aminomalonic acid | 1068-84-4 | >98.00% | |
Aminomalonic acid (Aminomalonate, Aminopropanedioic acid) is an amino dicarboxylic acid. It has a role as a human metabolite and a Daphnia magna metabolite. | ||||
| GC35339 | Anandamide | 94421-68-8 | >98.00% | |
Anandamide是一种来源于含花生四烯酸膜脂的内源性大麻素,通过结合并激活CB1和CB2大麻素受体以及香草素瞬时受体电位通道1(TRPV1)受体发挥作用。 | ||||
| GC35355 | Angiotensin III | 12687-51-3 | - | |
Angiotensin III是血管紧张素1 (AT1) 和 AT2 受体激动剂。 | ||||
| GC35356 | Angiotensin III TFA | - | >99.50% | |
Angiotensin III (TFA) 是血管紧张素1 (AT1) 和 AT2 受体激动剂。 | ||||
| GC35361 | Antineoplaston A10 | 91531-30-5 | >98.00% | |
Antineoplaston A10 is a naturally occurring substance in the human body that that can be potentially used for the treatment of glioma, lymphoma, astrocytoma and breast cancer. The main ingredient active of antineoplaston A10 (Phenylacetylglutamine, PG) inhibits RAS and promotes apoptosis. | ||||
| GC35367 | APG-115 | 1818393-16-6 | >98.00% | |
APG-115 (APG-115) 是一种具有口服活性的 MDM2 蛋白抑制剂,与 MDM2 蛋白结合,IC50 和 Ki 值分别为 3.8 nM 和 1 nM。 APG-115 阻断 MDM2 和 p53 的相互作用,并以 p53 依赖性方式诱导细胞周期停滞和细胞凋亡。 | ||||
| GC35369 | Apigenin-7-glucuronide | 29741-09-1 | >98.50% | |
Apigenin-7-O-glucuronide (Apigenin-7-glucuronide) is the major flavonoid found in milk thistle. Apigenin 7-o-glucuronide inhibits tumor necrosis factor alpha (TNF-α) and total nitrite release in lipopolysaccharide-activated macrophages. | ||||
| GC35377 | Apratastat | 287405-51-0 | >99.00% | |
Apratastat是一种口服活性、可逆的双重抑制剂,能够抑制肿瘤坏死因子-α转换酶(TACE;IC 50 =81.7ng/mL)和基质金属蛋白酶(MMPs)的活性。 | ||||
| GC35379 | Arachidic acid | 506-30-9 | >99.00% | |
A long- chain saturated fatty acid | ||||
| GC35384 | Argatroban monohydrate | 141396-28-3 | >99.50% | |
A thrombin inhibitor | ||||
| GC35388 | Aristolactam I | 13395-02-3 | >99.50% | |
Aristololactam I (AL-I) 是马兜铃酸I (AA-I) 的主要代谢产物,参与导致肾损伤的过程。Aristololactam I (AL-I) 直接损伤肾近端小管细胞,AL-I 的细胞毒性效力高于AA-I,并且这些分子的细胞毒性作用是通过 caspase-3 依赖性细胞凋亡介导。 | ||||
| GC35395 | Arnicolide D | 34532-68-8 | >98.00% | |
A sesquiterpene lactone with anticancer activity | ||||
| GC35420 | ATP | 56-65-5 | >99.50% / >99.00% / >98.00% | |
ATP是代谢反应中底物激活的磷酸基供体,用于生物合成细胞内第二信使环状腺苷酸单磷酸(cAMP),并作为真正的细胞外信使介导细胞间通讯。 | ||||
| GC35425 | Atreleuton | 154355-76-7 | - | |
A 5-LO inhibitor | ||||
| GC35470 | Batimastat sodium salt | 130464-84-5 | - | |
A potent broad spectrum inhibitor of MMPs | ||||
| GC35476 | BAY-678 racemate | 675103-35-2 | - | |
BAY-678 racemate 是 BAY-678 的消旋体。BAY-678 是具有口服生物活性的、高效的、选择性的、人中性粒细胞弹性蛋白酶(HNE) 的细胞渗透性抑制剂,其 IC50 值为 20 nM。BAY-678 也是被基因结构组学联盟 (SGC) 推荐的化学探针。 | ||||
| GC35494 | Benzoyloxypaeoniflorin | 72896-40-3 | - | |
Benzoyloxypaeoniflorin 分离于 Paeonia suffruticosa 的根,是 tyrosinase 抑制剂,对蘑菇 tyrosinase 的 IC50为 0.453 mM。Benzoyloxypaeoniflorin 是 NF-κB 抑制剂,Benzoyloxypaeoniflorin 通过对血小板聚集和凝血的抑制作用,有助于改善血液循环。 | ||||
| GC35499 | Bestatin trifluoroacetate | 223763-80-2 | - | |
An aminopeptidase inhibitor | ||||
| GC35510 | BI 224436 | 1155419-89-8 | >99.50% | |
BI 224436是一种新型的HIV-1非催化性位点整合酶抑制剂,对HIV-1实验室菌株的EC50值小于15 nM。 | ||||
| GC35511 | BI-0252 | 1818291-27-8 | - | |
BI-0252 是一种具有口服活性,选择性的 MDM2-p53 抑制剂,IC50 值为 4 nM。 BI-0252 可诱导异种移植小鼠 SJSA-1 的所有动物肿瘤消退,同时诱导肿瘤蛋白p53 (TP53) 靶基因和凋亡标志物。 | ||||
