Home >> Signaling Pathways >> 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.

Products for  Proteases

  1. Cat.No. 产品名称 Information
  2. 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
  3. GC49159 2-(1-Piperazinyl)pyrimidine

    1-(2-嘧啶基)哌嗪

    An α2-AR antagonist and active metabolite of azapirones
  4. GC49157 rac-5-carboxy Tolterodine

    5-羧基托特罗定

    An inactive metabolite of tolterodine
  5. GC49156 Etodolac Acyl Glucuronide

    依托度酸酰基-Β-D葡糖苷酸

    A phase II metabolite of etodolac
  6. GC49152 Celecoxib Carboxylic Acid

    羧酸塞来昔布

    An inactive metabolite of celecoxib
  7. GC49147 Carboxyphosphamide

    CPCOOH, NSC 145124

    An inactive metabolite of cyclophosphamide
  8. GC49142 Isorhoifolin

    异野漆树苷

    A flavonoid glycoside with diverse biological activities
  9. GC49133 N-hydroxy Riluzole

    N-羟基利鲁唑

    A metabolite of riluzole
  10. GC49131 Dehydro Warfarin

    去羟基华法林

    A metabolite of (±)-warfarin
  11. GC49130 Hydroxy Celecoxib

    羟甲基塞来昔布

    An inactive metabolite of celecoxib
  12. GC49127 4-oxo Cyclophosphamide

    4-keto CP, 4-keto Cyclophosphamide, NSC 139488, 4-oxo CP

    An inactive metabolite of cyclophosphamide
  13. GC49119 5-hydroxy Flunixin

    5-羟基氟尼辛

    A metabolite of flunixin
  14. GC49118 10-hydroxy Warfarin

    10-羟基华法林(非对映体的混合物)

    A metabolite of (R)-warfarin

  15. GC49115 Desacetylcefotaxime (potassium salt)

    des-CTX

    An active metabolite of cefotaxime
  16. GC49111 Carbamazepine 10,11-epoxide

    卡马西平10,11-环氧化物

    An active metabolite of carbamazepine
  17. GC49108 Racecadotril-d5

    消旋卡多曲杂质,Acetorphan-d5

    An internal standard for the quantification of racecadotril
  18. GC49100 Desmethyl Ofloxacin (hydrochloride) A metabolite of ofloxacin
  19. GC49098 Olsalazine-13C6 An internal standard for the quantification of olsalazine
  20. GC49051 7-hydroxy Methotrexate

    7-羟基甲氨蝶呤

    A metabolite of methotrexate
  21. GC49022 Didanosine-d2

    去羟肌苷 d2

    An internal standard for the quantification of didanosine
  22. GC49017 8-hydroxy Amoxapine A metabolite of amoxapine
  23. GC48993 Protectin D1-d5

    Neuroprotectin D1-d5, NPD1-d5, PD1-d5

    An internal standard for the quantification of protectin D1
  24. GC48989 LTX-315 (trifluoroacetate salt) A synthetic cationic amphiphilic peptide
  25. 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
  26. GC48972 Resolvin E2

    (-)-Resolvin E2

    A specialized pro-resolving mediator
  27. 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。
  28. 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。
  29. 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。
  30. 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。
  31. 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。
  32. GC62618 IPN60090 IACS-6274 (IPN60090), is a potent, selective and orally active glutaminase inhibitor with potential antineoplastic and immunostimulating activities.
  33. 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。
  34. 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。
  35. 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。
  36. GC62587 Simvastatin acid ammonium

    辛伐他汀铵盐; Tenivastatin ammonium

    An inhibitor of HMG-CoA reductase
  37. 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。
  38. 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。
  39. 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。
  40. 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。
  41. 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.
  42. GC62464 MLT-943 MLT-943 是一种有效的、选择性的、口服活性的 MALT1 protease 抑制剂。MLT-943 可抑制 PBMC 或全血中 IL-2 的分泌,PBMC 中抑制的 IC50 值为 0.07~0.09 μM,全血中抑制的 IC50 值为 0.6~0.8 μM)。MLT-943具有抗炎活性,可用于 FcgR 介导的炎症研究。
  43. GC62458 Rodatristat ethyl

    KAR5585

    Rodatristat ethyl (KAR5585) 是一种首创的,具有口服活性的 tryptophan hydroxylase 1 (TPH1) 抑制剂,具有体外纳摩尔浓度,可降低 5-hydroxytryptamine (5-HT) 的水平并显着降低肺动脉高压 (PAH),

  44. GC62444 SDZ 224-015 SDZ 224-015 是具有口服活性的、IL-1β 转化酶和 caspase-1 的抑制剂。SDZ 224-015 具有抗COVID-19的活性,靶向 Mpro (IC50 of 30 nM)。
  45. GC62439 Edoxaban impurity 6

    依度沙班杂质F(单体)

    Edoxaban impurity 6 是 Edoxaban 的一种杂质。Edoxaban (DU-176) 是一种选择性,有效和具有口服活性的 factor Xa (FXa) 抑制剂,对游离 FXa 和凝血酶原的 Ki 分别为 0.561 nM 和 2.98 nM。Edoxaban 是一种抗凝剂,可用于预防中风。
  46. GC62428 Ervogastat

    (S)-2-(5-((3-乙氧基吡啶-2-基]氧基]吡啶-3-基)-N-(四氢呋喃-3-基)嘧啶-5-甲酰胺

    Ervogastat (PF-06865571, DGAT2i) is a potent diacylglycerol acyltransferase 2 (DGAT2) inhibitor that reduces steatosis and hepatic triglyceride levels in non-alcoholic steatohepatitis (NASH).
  47. GC62408 CRA-2059 hydrochloride CRA-2059 hydrochloride 是一种特异性、选择性的类胰蛋白酶 (tryptase) 抑制剂,对重组人类胰蛋白酶-β (rHTβ) 的 Ki 为 620 pM。
  48. GC62388 YUM70 YUM70 is a potent inhibitor of glucose-regulated protein 78 (GRP78) inhibitor with an IC50 of 1.5 μM. YUM70 induces endoplasmic reticulum (ER) stress-mediated apoptosis in pancreatic cancer.Although YUM70 inhibits GRP78 enzymatic activity, it increases the expression of GRP78 by increasing the chaperone translation mechanism.
  49. GC62372 Cyclic-di-GMP sodium

    c-di-GMP sodium; cyclic diguanylate sodium; 5GP-5GP sodium

    A bacterial second messenger and cyclic dinucleotide
  50. GC62352 1,3-Butanediol

    1,3-丁二醇

    1,3-丁二醇(1,3-Butanediol)是一种有机化合物,该化合物是一种无色、苦乐参半的水溶性液体。它是丁二醇的四种常见结构异构体之一。1,3-丁二醇可用作降血糖剂。1,3-丁二醇可转化为β-羟基丁酸,作为脑代谢的底物。
  51. GC62347 CMC2.24

    TRB-N0224

    CMC2.24 (TRB-N0224) 是一种口服活性三羰基甲烷制剂,通过抑制 Ras 及其下游效应子 ERK1/2 途径对小鼠胰腺肿瘤有效。CMC2.24 也是一种有效的锌依赖性 MMPs 抑制剂,IC50 范围为 2.0-69 μM。CMC2.24 通过恢复软骨内稳态和通过NF-κB/HIF-2α 轴抑制软骨细胞凋亡来减轻骨关节炎的进展。

Items 1151 to 1200 of 4079 total

per page

Set Descending Direction