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￥ 0.00 “Akt Inhibitor”的搜索结果
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JFD00244
Catalog No. A19517 -
Pralsetinib
Catalog No. A19526 -
BMS-816336
Catalog No. A19528 11β-HSD1 inhibitorBMS-816336 is a novel, potent and orally bioavailable inhibitor against human 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) enzyme with an IC50 of 3.0 nM. 了解更多 -
GSTO1-IN-1
Catalog No. A19530 GSTO1 inhibitorGSTO1-IN-1 is a potent glutathione S-transferase omega 1 (GSTO1) inhibitor with an IC50 of 31 nM. 了解更多 -
ERK2 IN-1
Catalog No. A19533 -
EHMT2-IN-2
Catalog No. A19534 EHMT inhibitorEHMT2-IN-2 is a potent EHMT inhibitor, with IC50s of all <100 nM for EHMT1 peptide, EHMT2 peptide and cellular EHMT2. Used in the research of blood disease or cancer. 了解更多 -
Salicyl-AMS
Catalog No. A19535 mycobactin biosynthesis inhibitorSalicyl-AMS is a mycobactin biosynthesis inhibitor which can also inhibit M. tuberculosis growth in vitro under iron-limited conditions. 了解更多 -
N-alpha-Tosyl-L-lysine chloromethyl ketone hydrochloride
Catalog No. A19540 protease inhibitorN-alpha-Tosyl-L-lysine chloromethyl ketone (TLCK), a trypsin like protease inhibitor, sensitizes HeLa cells to Fas-mediated cell death. 了解更多 -
GlyRS-IN-1
Catalog No. A19543 GlyRS inhibitorGlyRS-IN-1 is a glycyl-tRNA synthase (GlyRS) inhibitor extracted from patent WO 2017066459 A1. GlyRS-IN-1 can also inhibit the growth of bacteria. 了解更多 -
KDM4D-IN-1
Catalog No. A19545 KDM4D inhibitorKDM4D-IN-1 is a new histone lysine demethylase 4D (KDM4D) inhibitor with an IC50 value of 0.41±0.03 μM. 了解更多 -
DS88790512
Catalog No. A19551 TRPC6 inhibitorDS88790512 is a potent, selective, and orally bioavailable TRPC6 inhibitor with an IC50 of 11 nM. 了解更多 -
BAY-678 racemate
Catalog No. A19564 HNE inhibitorBAY-678 racemate is a racemate of BAY-678. BAY-678 is an orally bioavailable, highly potent, selective and cell-permeable inhibitor of human neutrophil elastase (HNE), with an IC50 of 20 nM. BAY-678 is also nominated as a chemical probe to the public via the Structural Genomics Consortium (SGC). 了解更多 -
RAD51-IN-2
Catalog No. A19570 RAD51 inhibitorRAD51-IN-2 (compound example 67A) is a RAD51 inhibitor extracted from patent WO2019/051465A1. 了解更多 -
IRAK4-IN-1
Catalog No. A19572 IRAK4 inhibitorIRAK4-IN-1 is an interleukin-1 receptor associated kinase 4 (IRAK4) inhibitor with an IC50 of 7 nM. 了解更多 -
SNIPER(BRD)-1
Catalog No. A19579 SNIPER inhibitorSNIPER(BRD4)-1 is a specific and nongenetic inhibitor of apoptosis protein (IAP)-dependent protein eraser (SNIPER) which acts as a protein degradation inducer of bromodomain-containing protein 4 (BRD4). 了解更多 -
PI3Kδ-IN-1
Catalog No. A19582 PI3Kδ inhibitorPI3Kδ-IN-1 is a potent, selective, and efficacious PI3Kδ inhibitor with an IC50 of 1.7 nM. 了解更多 -
PF-06795071
Catalog No. A19592 covalent MAGL inhibitorPF-06795071 is a potent and selective covalent MAGL inhibitor with an IC50 of 3 nM. 了解更多 -
5,6,7-Trimethoxyflavone
Catalog No. A19612 p38-α MAPK inhibitor5,6,7-Trimethoxyflavone is a novel p38-α MAPK inhibitor with an anti-inflammatory effect. 5,6,7-Trimethoxyflavone is isolated from several plants including Zeyhera tuberculosa, Callicarpa japonica, and Kickxia lanigera. 了解更多 -
KP-457
Catalog No. A19622 ADAM17 inhibitorKP-457 is a selective a disintegrin and metalloproteinase 17 (ADAM17) inhibitor, with higher selectivity for ADAM17 than for other MMPs and ADAM10, and IC50s are 11.1 nM (ADAM17), 748 nM (ADAM10), 717 nM (MMP2), 9760 nM (MMP3), 2200 nM (MMP8), 5410 nM (MMP9), 930 nM (MMP13), 2140 nM (MMP14), and 7100 nM (MMP17), respectively. 了解更多 -
ABT-702 dihydrochloride
Catalog No. A19624 AK inhibitorABT-702 dihydrochloride is a potent adenosine kinase (AK) inhibitor (IC50=1.7 nM). 了解更多 -
PDE5-IN-2
Catalog No. A19625 PDE5 inhibitorPDE5-IN-2 is a potent, highly selective, and orally active PDE5 inhibitor, with an IC50 of 0.31 nM, less potently inhibits PDE2A, PDE10A, PDE4D2, and PDE6C, with IC50s of 106, 46, 43, 1.2 nM, respectively. Anti-pulmonary arterial hypertension activity. 了解更多 -
Melinamide
Catalog No. A19631 cholesterol absorption inhibitorMelinamide, an amide derivative of an unsaturated long-chain fatty acid, is an inhibitor of cholesterol absorption with an IC50 of 20.9 μM. 了解更多 -
inS3-54A18
Catalog No. A19639 STAT3 inhibitorinS3-54A18 is a potent STAT3 inhibitor, with anti-cancer properties. 了解更多 -
SHIP2-IN-1
Catalog No. A19650 SHIP2 inhibitorSHIP2-IN-1 is a potent SHIP2 inhibitor, inhibits SHIP2 activity, with an IC50 of 2 ?M. SHIP2-IN-1 blocks GSK3β activation by phosphorylation at the Ser9 residue. SHIP2-IN-1 is used in the research of Alzheimer??s disease. 了解更多
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