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(504)
- 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
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GC12339
Ivermectin
伊维菌素; MK-933
A mixture of ivermectin B1a and ivermectin B1b -
GC15618
Melatonin
褪黑素; N-Acetyl-5-methoxytryptamine
An indoleamine neurohormone that entrains circadian rhythms
-
GC12838
Edaravone
依达拉奉; MCI-186
A free radical scavenger -
GC15917
CA-074 Me
L-TRANS-环氧琥珀酸-ILE-PRO-OME丙醛,CA-074Me
CA-074 Me(CA-074甲酯)是组织蛋白酶B(CB)的特异性抑制剂。 -
GC12725
VX-765
Belnacasan; N-(4-氨基-3-氯苯甲酰基)-3-甲基-L-缬氨酰-N-[(2R,3S)-2-乙氧基四氢-5-氧代-3-呋喃基]-L-脯氨酰胺; VX-765
VX-765 是一种新开发的选择性小分子 caspase-1 抑制剂,可通过血脑屏障并在体外和体内减少炎症。
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GC11065
Pifithrin-μ
NSC 303580
Inhibitor of p53-mediated apoptosis -
GC12604
Fumonisin B1
伏马菌素B1
A mycotoxin
-
GC13590
SJ 172550
MDMX Inhibitor II
A small molecule inhibitor of MDMX -
GC16844
BC 11 hydrobromide
Selective urokinase inhibitor
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GC13337
4-Chlorophenylguanidine hydrochloride
洗必泰二乙酸杂质
Urokinase inhibitor, potent and specific -
GC15954
UK 356618
An inhibitor of MMP-3
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GC14578
GI 254023X
(ALPHAR)-N-[(1S)-2,2-二甲基-1-[(甲基氨基)羰基]丙基]-ALPHA-[(1S)-1-(甲酰基羟基氨基)乙基]苯戊酰胺,GI4023; SRI028594
GI 254023X是一种选择性抑制剂,针对MMP9(Matrix Metalloproteinase 9)的IC50 值为5.3nM,GI 254023X对ADAM10(A Disintegrin and Metalloproteinase 10)的选择性是ADAM17的100倍,IC50 值为2.5nM。GI 254023X主要用于免疫学、炎症和神经退行性疾病的研究。 -
GC14126
NVP DPP 728 dihydrochloride
NVP DPP 728 dihydrochloride 是一种有效的、可逆的和腈依赖性二肽基肽酶 IV (DPP-IV) 抑制剂。
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GC10258
Ac-IEPD-AFC
Ac-IEPD-AFC 是颗粒酶 B 的底物。
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GC12659
Begacestat
GSI-953
An inhibitor of γ-secretase -
GC10064
Flurizan
R-氟比洛芬; (R)-Flurbiprofen; MPC7869
A COX-inactive enantiomer of flurbiprofen -
GC18065
ZJ 43
ZJ 43 是一种有效的 NAAG 肽酶抑制剂,IC50 为 2.4 nM,Ki 为 0.8 nM。
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GC13707
WAY 170523
WAY 170523 是一种有效的选择性 MMP-13(基质金属蛋白酶 13)抑制剂,IC50 为 17 nM。 WAY 170523 可以直接减弱 ERK1/2 磷酸化。 WAY 170523抑制PC-3细胞的侵袭,可用于前列腺癌研究。
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GC16579
UK 370106
UK 370106 是一种有效且高度选择性的 MMP-3(IC50 为 23 nM)和 MMP-12(IC50 为 42 nM)抑制剂,其效力比 MMP-1、MMP-2、MMP-9 和 MMP 高 1200 倍以上-14,大约是 MMP-13 和 MMP-8 的 100 倍。
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GC10672
SSR 69071
A potent inhibitor of neutrophil elastase
-
GC16894
Spinorphin
LVV-hemorphin-4
A peptide inhibitor of enkephalin-degrading enzymes -
GC17247
Sivelestat sodium salt
西维来司钠; ONO5046-Na; Sodium sivelestat; EI546 sodium; LY544349 sodium
An inhibitor of neutrophil elastase -
GC10377
SID 26681509
SID 26681509 是一种有效的、可逆的、竞争性的、选择性的人组织蛋白酶 L 抑制剂,IC50 为 56 nM。
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GC18011
SC 57461A
N-甲基-N-[3-[4-(苯甲基)苯氧基]丙基Β-丙氨酸盐酸盐
A potent, orally active inhibitor of LTA4 hydrolase -
GC10805
Ro 32-3555
Ro 32-3555
Ro 32-3555 是一种有效的、竞争性的人类胶原酶 1、2 和 3 抑制剂,Kis 分别为 3.0、4.4 和 3.4 nM。 -
GC13467
PMPA (NAALADase inhibitor)
2-(Phosphonomethyl)pentanedioic acid
A potent inhibitor of GCP II/NAALADase -
GC14201
PK 44 phosphate
DPP-IV inhibitor
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GC14886
PETCM
Α-(三氯甲基)-4-吡啶乙醇
PETCM 是 caspase-3 的激活剂,并以细胞色素 c (细胞 c) 依赖性方式发挥作用。 PETCM 促进 Apaf-1 寡聚化并诱导 HeLa 细胞中的细胞凋亡。 -
GC12111
PD 166793
N-[(4'-溴[1,1'-联苯]-4-基)磺酰基]-L-缬氨酸
An broad-spectrum MMP inhibitor -
GC16912
PD 150606
An inhibitor of calpains
-
GC15005
ONO 4817
MMP Inhibitor V
An inhibitor of MMP-2 and MMP-9 -
GC16431
MRK 560
A potent inhibitor of γ-secretase
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GC11640
MDL 28170
Calpain Inhibitor III
A cell permeable, selective calpain inhibitor -
GC15364
L-685,458
L-685,458
A γ-secretase inhibitor -
GC17989
L 006235
L-235
An inibitor of cathepsin K -
GC10802
K 579
K 579 是一种有效且具有口服活性的二肽基肽酶 IV 抑制剂。
-
GC13619
JLK 6
7-Amino-4-chloro-3-methoxy-1H-2-benzopyran
A protease inhibitor -
GC18137
Ivachtin
Caspase-3 Inhibitor VII
A reversible caspase-3 inhibitor -
GC12358
Fumagillin
烟曲霉素; Amebacilin; NSC9168
A fungal metabolite with diverse biological activities -
GC12603
DPPI 1c hydrochloride
A DPP-4 inhibitor
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GC12157
CP 471474
2-[[[4-(4-氟苯氧基)苯基]磺酰基]氨基]-N-羟基-2-甲基丙酰胺
A broad-spectrum MMP inhibitor -
GC15645
Compound W
3,5-二(4-硝基苯氧基)苯甲酸,CW3,5-Bis(4-nitrophenoxy)benzoic acid
A Notch1 signaling modulator -
GC15952
CL 82198 hydrochloride
An inhibitor of MMP-13
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GC10342
Calpeptin
A calpain inhibitor
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GC13099
BMS 299897
2-[(1R)-1-[[(4-氯苯基)磺酰基](2,5-二氟苯基)氨基]乙基]-5-氟苯丁酸
A γ-secretase inhibitor -
GC13171
AZ 10417808
Caspase-3 inhibitor,selective non-peptide
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GC12465
ARP 101
ARP 101 是一种有效的选择性抑制剂基质金属蛋白酶 2 (MMP-2)。 ARP 101 在癌细胞中诱导自噬相关的细胞死亡。 ARP 101 可有效诱导自噬体的形成和 LC3I 转化为 LC3II。
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GC13487
ARP 100
CAY10609
A selective inhibitor of MMP-2 -
GC10968
Ac-LEHD-AFC
A caspase-4, -5, and -9 fluorogenic substrate
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GC12152
Acetyl-Calpastatin (184-210) (human)
乙酰钙蛋白酶抑制蛋白(184-210)(人)
Acetyl-Calpastatin (184-210) (human) 是一种有效、选择性和可逆的钙蛋白酶抑制剂,对 µ-calpain 和组织蛋白酶 L 的 Ki 值分别为 0.2 nM 和 6 μM。