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(498)
- E1/E2/E3 Enzyme(92)
- Endogenous Metabolite(1712)
- FABP(8)
- Farnesyl Transferase(20)
- Glutaminase(17)
- Glutathione Peroxidase(34)
- Isocitrate Dehydrogenase (IDH)(28)
- Lactate Dehydrogenase(19)
- Lipoxygenase(254)
- Mitochondrial Metabolism(243)
- NEDD8-activating Enzyme(6)
- Neprilysin(12)
- PAI-1(13)
- Ser/Thr Protease(49)
- Tryptophan Hydroxylase(12)
- Xanthine Oxidase(18)
- MALT1(10)
- Caspase(113)
- PCSK9(13)
- ADAMTS(1)
- TrxR(1)
- DGK(3)
- Cat.No. 产品名称 Information
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GC39327
3,4-Dimethoxyphenol
3,4-二甲氧基苯酚
3,4-Dimethoxyphenol 是植物来源的苯基丙烷化合物,可在化妆品中用作增白剂。3,4-Dimethoxyphenol 具有酪氨酸酶 (tyrosinase) 抑制活性。从细菌发酵液中分离出的 3,4-Dimethoxyphenol 具有有效的抗氧化作用。
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GC50613
673 A
ALDH1A inhibitor; depletes CD133+ cancer stem cells (CSC)
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GC50570
ST 045849
ST 045849是一种O-GlcNAc转移酶(OGT)抑制剂,IC50值为53μM。
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GC50447
Pep 2-8
TVFTSWEEYLDWV-NH2
Pep 2-8是一种由13个氨基酸组成的线性肽,可抑制PCSK9活性(KD=0.7μM),并抑制LDL受体及EGF(A)结构域与PCSK9的结合,IC50值分别为0.8μM和0.4μM。
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GC50373
Retrobradykinin
逆缓激肽具有与缓激肽相反的序列。
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GC50368
INF 4E
INF 4E 是一种有效的 NLRP3 炎性体抑制剂。
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GC50353
T 26c disodium salt
A selective inhibitor of MMP-13
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GC50283
HM 50316
High affinity FABP4 inhibitor
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GC50251
PF 3084014 hydrobromide
PF-3084014 dihydrobromide; PF-03084014 dihydrobromide
PF 3084014 hydrobromide是一种高效且高选择性的γ-分泌酶抑制剂,属于氮杂环类化合物,其IC₅₀为1.2nM。
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GC50225
ONO 6818
ONO-6818; ONO-PO-736
ONO 6818 (ONO-6818) 是一种有效且具有口服活性的中性粒细胞弹性蛋白酶抑制剂,Ki 为 12.2 nM。
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GC50189
TAPI 0
TAPI 0 是一种 TACE(TNF-α 转化酶;ADAM17)抑制剂,IC50 为 100 nM。
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GC50153
BIX
硫氰酸2-(3,4-二羟基苯基)-2-氧代乙酯
An inducer of GRP78
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GC50151
NHI 2
An inhibitor of LDHA
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GC50134
Bengamide B
Potent inhibitor of NF-κB activation
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GC50129
TC-E 5008
Selective mutant isocitrate dehydrogenase 1 (mIDH1) inhibitor; phenotypically lethal
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GC50113
Noradrenaline bitartrate
L-去甲肾上腺素酒石酸氢盐(酯),Levarterenol tartrate; L-Noradrenaline tartrate
Noradrenaline bitartrate是一种β1选择性肾上腺素受体激动剂,EC50值为5.37μM。
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GC50089
PEAQX tetrasodium salt
Potent and GluN2A-selective NMDA antagonist
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GC50060
Cerestat
阿替加奈,CNS 1102
An NMDA receptor antagonist
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GC39307
4-Methylamino antipyrine
4-(甲氨基)安替比林
An active metabolite of metamizole
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GC39306
D-Glucose 6-phosphate disodium salt
D-葡萄糖-6-磷酸二钠
D-Glucose-6-phosphate disodium salt 称 6-磷酸葡萄糖,是葡萄糖经过磷酸化 (在第 6 号碳) 之后生成的分子。它是生物细胞中的常见分子,参与磷酸戊糖途径与糖酵解等生化途径。
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GC39296
1G244
1G244 是一种有效的 DPP8/9 抑制剂,IC50 分别为 12 nM 和 84 nM,但不抑制 DPPIV 和 DPPII。1G244 可诱导多发性骨髓瘤细胞凋亡,并具有抗骨髓瘤作用。
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GC39279
hDHODH-IN-1
hDHODH-IN-1 is a potent inhibitor of human dihydroorotate dehydrogenase (hDHODH) with anti-inflammatory effect.
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GC39271
(±)-Naringenin
(±)-柚皮素
A citrus-derived flavonoid
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GC39256
LP-935509
LP-935509 是一种小分子衔接蛋白-2 相关激酶1 (AAK1) 选择性和脑渗透抑制剂 (IC50=3.3 nM),一种 ATP 竞争性抑制剂,其 Ki 为 0.9 nM。 LP-935509 是 BIKE 的有效抑制剂 (IC50=14 nM) 和适度的 GAK 抑制剂 (IC50=320 nM)。 LP-935509 可逆转 SNL 手术后的疼痛。
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GC39251
Cinacalcet metabolite M4
Cinacalcet metabolite M4 是 Cinacalcet 的代谢物。Cinacalcet 是一种可口服的 Ca receptor (CaR) 激动剂,用于心血管疾病。
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GC39245
4-Diethylaminobenzaldehyde
N,N-二乙基-4-氨基苯甲醛; DEAB
4-Diethylaminobenzaldehyde 是一种可逆的醛脱氢酶 (ALDHs) 抑制剂,对 ALDH1 的 Ki 为 4 nM。4-Diethylaminobenzaldehyde 具有较强的抗雄激素作用 (IC50= 1.71 μM)。
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GC39223
11-Beta-hydroxyandrostenedione
4-雄烯-11β-醇-3,17-二酮,4-Androsten-11β-ol-3,17-dione
11β-Hydroxyandrostenedione是一种内源性、天然存在的?类固醇和雄激素原,主要(如果不是完全)在肾上腺中产生。它与肾上腺产生的肾上腺素(11-ketoandrostenedione; 11-KA4)、11-ketotestosterone?(11-KT) 和11-ketodihydrotestosterone?(11-KDHT)密切相关。可用作指导肾上腺静脉取样中原发性醛固酮增多症亚型的生物标志物,其中从两个肾上腺采集血样以比较每个腺体产生的激素量。
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GC39215
CM10
A pan-ALDH1A inhibitor
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GC39199
Thymopentin acetate
胸腺五肽醋酸盐
A pentapeptide fragment of thymopoietin
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GC46234
Tropolone
环庚三烯酚酮
A terpene with diverse biological activities
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GC46220
SD 2590 (hydrochloride)
SC-78080
An MMP inhibitor
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GC46105
Butyrolactone II
A fungal metabolite
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GC46078
5-Methoxyindole-3-acetic acid
5-甲氧基吲哚-3-乙酸
A methoxyindole
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GC46057
2,5-Dihydroxycinnamic Acid phenethyl ester
An inhibitor of 5-LO
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GC46048
17(S)-HDHA-d5
17(S)-Hydroxy docosahexaenoic acid-d5, 17(S)-HDoHE-d5
A neuropeptide with diverse biological activities
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GC46041
1,2,3-Trilinoleoyl-rac-glycerol
甘油三亚油酸酯
A triacylglycerol
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GC39185
Pregnanediol
孕二醇; NSC 1612; NSC 47462
Pregnanediol是孕酮的主要代谢产物,通过尿液排出体外。
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GC39173
Phosphorylcholine chloride calcium salt tetrahydrate
胆碱磷酸氯化钙四水
Phosphocholine (Phosphorylcholine) chloride calcium salt tetrahydrate is an active endogenous metabolite.
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GC39169
CC-92480
CC-92480
CC-92480(Mezigdomide)是一种新型的Cereblon(CRBN)E3连接酶调节剂(CELMoD),常以分子胶的方式发挥作用,具有增强的肿瘤和免疫调节活性。
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GC39157
DS-1001b
An inhibitor of mutant IDH1
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GC39134
Isofraxidin
异嗪皮啶
Isofraxidin (6,8-Dimethoxyumbelliferone), a bioactive coumarin compound isolated from the functional foods Siberian ginseng and Apium graveolens, is an anti-bacterial, anti-oxidant, and anti-inflammatory agent.
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GC39119
Isonicotinic acid
异烟酸
Isonicotinic acid (Isoniazid, 4-pyridinecarboxylic acid, p-pyridinecarboxylic acid, 4-Picolinic acid) is a metabolite of isoniazid. It is an isomer of nicotinic acid.
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GC39115
Terpinen-4-ol
4-萜烯醇; 4-Carvomenthenol
Terpinen-4-ol, a naturally occurring monoterpene, is the main bioactive component of tea-tree oil and has been shown to have many biological activities such as antifungal properties.
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GC39095
Isoliquiritin apioside
芹糖异甘草苷
Isoliquiritin apioside (ISLA, ILA), a component isolated from Glycyrrhizae radix rhizome (GR), significantly decreases PMA-induced increases in matrix metalloproteinase (MMP) activities and suppresses PMA-induced activation of mitogen-activated protein kinase (MAPK) and NF-κB. Isoliquiritin apioside possesses anti-metastatic and anti-angiogenic abilities in malignant cancer cells and ECs, with no cytotoxicity.
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GC39068
Rosamultin
罗莎白素
Rosamultin is a 19 α-hydroxyursane-type triterpenoid isolated from Potentilla anserina L. that inhibits HIV-1 protease. Rosamultin has protective effects on H2O2-induced oxidative damage and apoptosis.
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GC39050
Prudomestin
3,5,7-三羟基-8,4'-二甲氧基黄酮
Prudomestin,从 Prunus domestica 心材中分离得到,具有很强的黄嘌呤氧化酶 (XO) 抑制活性(IC50≈6?µM)。
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GC39013
FPL 62064
N-(4-甲氧苯基)-1-苯基-1H-吡唑-3-胺
FPL 62064 is a potent dual inhibitor of 5-lipoxygenase (5-LOX) and prostaglandin synthetase (cyclooxygenase, COX) with IC50 of 3.5 μM and 3.1 μM for RBL-1 cytosolic 5-lipoxygenase and seminal vesicle prostaglandin synthetase, respectively. FPL 62064 has potent anti-inflammatory activity.
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GC38971
Toddalolactone
毛两面针素
Toddalolactone, a natural coumarin, inhibits the activity of recombinant human Plasminogen activator inhibitor-1 (PAI-1) in a dose-dependent manner, yielding an IC50 value of 37.31 ± 3.23 μM.
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GC38958
Sorbic acid
山梨酸
Sorbic acid (2,4-Hexadienoic acid) is a naturally occurring compound that originated from the unripe berries of the Rowan Tree. It inhibits various bacteria, including sporeformers, at various stages of their life cycle (germination, outgrowth and cell division).
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GC38931
N-Desmethyltamoxifen hydrochloride
N-去甲基三苯氧胺盐酸盐
N-Desmethyltamoxifen hydrochloride (N-Desmethyl tamoxifen HCl), the primary metabolite of tamoxifen, is an estrogen response modifer and protein kinase C inhibitor with IC50 of 25 ?M.