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.
Products for Proteases
- Aminopeptidase(20)
- ACE(73)
- Calpains(11)
- Carboxypeptidase(9)
- Cathepsin(65)
- DPP-4(18)
- Elastase(24)
- Gamma Secretase(42)
- HCV Protease(35)
- HSP(102)
- HIV Integrase(28)
- HIV Protease(34)
- MMP(191)
- NS3/4a protease(4)
- Serine Protease(15)
- Thrombin(44)
- Urokinase(2)
- Tyrosinases(50)
- Other Proteases(15)
- 15-PGDH(1)
- Acetyl-CoA Carboxylase(14)
- Acyltransferase(63)
- Aldehyde Dehydrogenase (ALDH)(30)
- Aminoacyl-tRNA Synthetase(9)
- ATGL(1)
- Dipeptidyl Peptidase(49)
- Drug Metabolite(505)
- E1/E2/E3 Enzyme(92)
- Endogenous Metabolite(1719)
- FABP(9)
- Farnesyl Transferase(20)
- Glutaminase(17)
- Glutathione Peroxidase(34)
- Isocitrate Dehydrogenase (IDH)(28)
- Lactate Dehydrogenase(19)
- Lipoxygenase(262)
- Mitochondrial Metabolism(248)
- NEDD8-activating Enzyme(6)
- Neprilysin(12)
- PAI-1(13)
- Ser/Thr Protease(49)
- Tryptophan Hydroxylase(12)
- Xanthine Oxidase(18)
- MALT1(10)
- Caspase(115)
- PCSK9(13)
- ADAMTS(1)
- TrxR(1)
- DGK(3)
- Cat.No. 产品名称 Information
-
GC49203
rac-Desethyl Oxybutynin (hydrochloride)
(R,S)-DEOB
An active metabolite of oxybutynin -
GC49202
Desmethyl Mirtazapine (hydrochloride)
盐酸去甲基米氮平
A metabolite of mirtazapine -
GC49192
Piracetam-d6
UCB-6215-d6
An internal standard for the quantification of piracetam -
GC49189
(E/Z)-4-hydroxy Tamoxifen-d5
Afimoxifene-d5, 4-OHT-d5
An internal standard for the quantification of (E/Z)-4-hydroxy tamoxifen -
GC49186
O-Demethyl Apremilast
阿普斯特杂质
An active metabolite of apremilast -
GC49185
Mirtazapine N-oxide
米氮平杂质A
A metabolite of mirtazapine -
GC49184
Palonosetron N-oxide
帕洛诺司琼N氧化物
A metabolite of palonosetron -
GC49179
(S)-O-Desmethyl Naproxen
萘普生杂质A
A metabolite of (S)-naproxen -
GC49174
Desmethyl Bosentan
波生坦O-去甲基杂质
An active metabolite of bosentan -
GC49173
N-Despropyl Ropinirole
1,3-二氢-4-[2-(丙基氨基)乙基]-2H-吲哚-2-酮
An active metabolite of ropinirole -
GC49159
2-(1-Piperazinyl)pyrimidine
1-(2-嘧啶基)哌嗪
An α2-AR antagonist and active metabolite of azapirones -
GC49157
rac-5-carboxy Tolterodine
5-羧基托特罗定
An inactive metabolite of tolterodine -
GC49156
Etodolac Acyl Glucuronide
依托度酸酰基-Β-D葡糖苷酸
A phase II metabolite of etodolac -
GC49152
Celecoxib Carboxylic Acid
羧酸塞来昔布
An inactive metabolite of celecoxib -
GC49147
Carboxyphosphamide
CPCOOH, NSC 145124
An inactive metabolite of cyclophosphamide -
GC49142
Isorhoifolin
异野漆树苷
A flavonoid glycoside with diverse biological activities -
GC49133
N-hydroxy Riluzole
N-羟基利鲁唑
A metabolite of riluzole -
GC49131
Dehydro Warfarin
去羟基华法林
A metabolite of (±)-warfarin -
GC49130
Hydroxy Celecoxib
羟甲基塞来昔布
An inactive metabolite of celecoxib -
GC49127
4-oxo Cyclophosphamide
4-keto CP, 4-keto Cyclophosphamide, NSC 139488, 4-oxo CP
An inactive metabolite of cyclophosphamide -
GC49119
5-hydroxy Flunixin
5-羟基氟尼辛
A metabolite of flunixin -
GC49118
10-hydroxy Warfarin
10-羟基华法林(非对映体的混合物)
A metabolite of (R)-warfarin
-
GC49115
Desacetylcefotaxime (potassium salt)
des-CTX
An active metabolite of cefotaxime -
GC49111
Carbamazepine 10,11-epoxide
卡马西平10,11-环氧化物
An active metabolite of carbamazepine -
GC49108
Racecadotril-d5
消旋卡多曲杂质,Acetorphan-d5
An internal standard for the quantification of racecadotril -
GC49100
Desmethyl Ofloxacin (hydrochloride)
A metabolite of ofloxacin
-
GC49098
Olsalazine-13C6
An internal standard for the quantification of olsalazine
-
GC49051
7-hydroxy Methotrexate
7-羟基甲氨蝶呤
A metabolite of methotrexate -
GC49022
Didanosine-d2
去羟肌苷 d2
An internal standard for the quantification of didanosine -
GC49017
8-hydroxy Amoxapine
A metabolite of amoxapine
-
GC48993
Protectin D1-d5
Neuroprotectin D1-d5, NPD1-d5, PD1-d5
An internal standard for the quantification of protectin D1 -
GC48989
LTX-315 (trifluoroacetate salt)
A synthetic cationic amphiphilic peptide
-
GC48979
Estradiol 17-(β-D-Glucuronide) (sodium salt hydrate)
E217G, βEstradiol 17(βDGlucuronide), 17βEstradiol 17(βDGlucuronide), 17βOestradiol 17(βDGlucuronide)
A substrate of multidrug resistance protein 2 -
GC48972
Resolvin E2
(-)-Resolvin E2
A specialized pro-resolving mediator -
GC62721
DI-591
DI-591 是一种有效,高亲和力和细胞渗透性的 DCN1-UBC12 相互作用的抑制剂。DI-591 分别以 Ki 值为 12 nM 和 10.4 nM 与 DCN1 和 DCN2 结合,并且几乎不与 DCN3,DCN4 和 DCN5 蛋白结合。DI-591 选择性抑制 cullin 3 的二烯化,但对其他 cullin 家族成员的二烯化没有影响或影响很小。
-
GC62716
MD-222
MD-222 是一种首创的高效的基于 PROTAC 的 MDM2 降解剂。MD-222 诱导 MDM2 蛋白快速降解并激活细胞中的野生型 p53。MD-222 具有抗癌作用。
-
GC62662
WNK-IN-11 D3
WNK-IN-11 D3 是一种具有口服活性、选择性和强效的 With-No-Lysine (WNK) 激酶抑制剂。WNK-IN-11 D3 有效调节心血管稳态。
-
GC62634
GSK-2793660
GSK-2793660(游离碱)是一种口服的、不可逆的组织蛋白酶 C (CTSC) 抑制剂。
-
GC62621
Milademetan tosylate hydrate
DS-3032b; DS-3032 tosylate hydrate
Milademetan (DS-3032) tosylate hydrate 是特异性的、具有口服活性的 MDM2 抑制剂,用于急性髓系白血病和实体肿瘤的研究。Milademetan (DS-3032) tosylate hydrate 可诱导 G1 细胞周期阻滞、衰老和凋亡。 -
GC62618
IPN60090
IACS-6274 (IPN60090), is a potent, selective and orally active glutaminase inhibitor with potential antineoplastic and immunostimulating activities.
-
GC62617
FABP-IN-1
FABP-IN-1(Compounds 4b) 是一种高亲和力脂肪酸结合蛋白 (FABP) 抑制剂。FABP-IN-1 抑制 FABP3,FABP5 和 FABP7 的 Ki 值分别为 0.69 μM,0.55 μM 和 0.67 μM,并具有有效的镇痛作用。
-
GC62611
MLT-231
MLT-231 是一种高效、高选择性的变构 MALT1 抑制剂,IC50 为 9 nM。MLT-231 特异性地阻止内源性 BCL10 断裂,IC50 为 160 nM。MLT-23 在 ABC-DLBCL 型异种移植模型中具有抗肿瘤活性。
-
GC62598
MI-1061 TFA
MI-1061 TFA 是一种有效的,口服可生物利用的,化学稳定性的 MDM2 (MDM2-p53 互作) 抑制剂 (IC50=4.4 nM; Ki=0.16 nM)。MI-1061 TFA 激活小鼠 SJSA-1 异种移植瘤组织中 p53 并诱导凋亡,具有抗肿瘤活性。
-
GC62587
Simvastatin acid ammonium
辛伐他汀铵盐; Tenivastatin ammonium
An inhibitor of HMG-CoA reductase -
GC62568
Cbl-b-IN-1
Cbl-b-IN-1 (example 519) 是 Cbl-b 的抑制剂,信息来自专利 WO2019148005A1,其 IC50 值 <100 nM。
-
GC62567
Pralnacasan
VX-740; HMR 3480
Pralnacasan (VX-740) 是一种有效的,选择性的,非肽型,具有口服活性白介素 1β 转化酶 (ICE, caspase 1) 抑制剂,Ki 为 1.4 nM。Pralnacasan 抑制促炎细胞因子 IL-18,IL-1β 和 IFN-γ。Pralnacasan 有潜力用于骨关节炎和类风湿关节炎的研究。 -
GC62564
Mito-LND
Mito-Lonidamine
Mito-LND (Mito-Lonidamine) 是一种具有口服活性的且靶向线粒体的氧化磷酸化 (oxidative phosphorylation (OXPHOS)) 抑制剂。Mito-LND 抑制线粒体生物能,刺激活性氧 (reactive oxygen species) 的形成,并诱导肺癌细胞自噬细胞死亡。 -
GC62537
Demethylcantharidate disodium
内氧草索钠盐
Demethylcantharidate disodium 是一种内源性代谢产物,通过内质网应激诱导肝癌细胞凋亡。Demethylcantharidate disodium 对多种类型的癌症具有良好的抗癌活性。 -
GC62518
FABP5-IN-1
FABP5-IN-1 是一种选择性,高亲和力脂肪酸结合蛋白 5 (FABP5) 抑制剂,Ki 值为 1.7 μM。FABP5-IN-1 与 FABP3 和 FABP7 均不结合,并具有有效的镇痛作用。
-
GC62481
AST5902 trimesylate
AST5902 is the principal metabolite of alflutinib both in vitro and in vivo, which exerts remarkable antineoplastic activity similar to alflutinib. AST5902 exhibits much weak CYP3A4 induction potential compared to alflutinib.