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￥ 0.00 “kinase inhibitor”的搜索结果
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AKT Kinase Inhibitor
Catalog No. A11285 Akt kinase inhibitorAKT Kinase Inhibitor is an Akt kinase inhibitor with anti-tumor activity. 了解更多 -
Multi-kinase inhibitor 1
Catalog No. A22645 multi-kinase inhibitorMulti-kinase inhibitor 1 is a potent multi-kinase inhibitor. Multi-kinase inhibitor 1 has the potential for diseases or disorders associated with abnormal or deregulated tyrosine kinase activity, particularly diseases associated with the activity of PDGF-R, c-Kit and Bcr-abl. 了解更多 -
Src Inhibitor 1
Catalog No. A12299 Src tyrosine kinase inhibitorSrc Inhibitor 1 is a potent and selective dual site Src tyrosine kinase inhibitor with IC50 values of 44 nM for Src and 88nM for Lck. 了解更多 -
RIP1 kinase inhibitor 1
Catalog No. A20154 RIP1 kinase inhibitorRIP1 kinase inhibitor 1 (compound 22) is a highly potent, orally available, and brain-penetrating RIP1 kinase inhibitor (pKi=9.04). 了解更多 -
PDGFRα kinase inhibitor 1
Catalog No. A19632 type II PDGFRα kinase inhibitorPDGFRα kinase inhibitor 1 is a highly selective type II PDGFRα kinase inhibitor with IC50s of 132 nM and 6115 nM for PDGFRα and PDGFRβ, respectively. 了解更多 -
Aurora Kinase Inhibitor 3
Catalog No. A19448 Aurora A kinase inhibitorAurora Kinase Inhibitor 3 is a strong and selective Aurora A kinase inhibitor with an IC50 of 42 nM, and weakly inhibits EGFR with an IC50>10 μM. 了解更多 -
Tie2 kinase inhibitor
Catalog No. A10932 -
Histone Acetyltransferase Inhibitor II
Catalog No. A12331 cell permeable p300 inhibitorHistone Acetyltransferase Inhibitor II is a potent and cell permeable p300 inhibitor, with an IC50 of 5 ?M; Histone Acetyltransferase Inhibitor II can be used in cancer research. 了解更多 -
CPA inhibitor
Catalog No. A11369 -
IRAK inhibitor 2
Catalog No. A11456 interleukin-1 receptor associated kinase inhibitorIRAK inhibitor 2 is interleukin-1 receptor associated kinase inhibitor . 了解更多 -
RIP2 Kinase Inhibitor 3
Catalog No. A20109 RIP2 inhibitorRIP2 Kinase Inhibitor 3 is a highly potent and selective inhibitor of receptor interacting protein-2 (RIP2) Kinase with an IC50 of 1 nM . 了解更多 -
Btk inhibitor 1 R enantiomer hydrochloride
Catalog No. A21865 BTK inhibitorBtk inhibitor 1 R enantiomer hydrochloride (Ibrutinib analog hydrochloride) (Compound 14) is a covalent and irreversible Bruton??s tyrosine kinase (BTK) inhibitor and can be used in synthesis of Ibrutinib and ibrutinib-based activity-based probes (ABPs). 了解更多 -
Btk inhibitor 1 (R enantiomer)
Catalog No. A21861 BTK inhibitorBtk inhibitor 1 R enantiomer (Ibrutinib analog) (Compound 14) is a covalent and irreversible Bruton??s tyrosine kinase (BTK) inhibitor and can be used in synthesis of Ibrutinib and ibrutinib-based activity-based probes (ABPs). 了解更多 -
IRAK inhibitor 4
Catalog No. A11458 IRAK4 inhibitorIRAK inhibitor 4 is an interleukin-1 receptor associated kinase 4(IRAK4) inhibitor. 了解更多 -
MARK4 inhibitor 1
Catalog No. A18695 (MARK4 inhibitorMARK4 inhibitor 1 is a potent microtubule affinity-regulating kinase 4 (MARK4) inhibitor, with an IC50 of 1.54 μM. MARK4 inhibitor 1 inhibits cancer cell proliferation, metastasis and induces apoptosis. 了解更多 -
Casein Kinase II Inhibitor IV
Catalog No. A12624 Epidermal keratinocyte differentiation inducerCasein Kinase II Inhibitor IV is a small-molecule inducer of epidermal keratinocyte differentiation. 了解更多 -
RIP2 kinase inhibitor 2
Catalog No. A16313 RIP2 kinase 抑制剂RIP2 kinase inhibitor 2 是从专利WO/2014043437 A1（化合物实施例9）中提取的受体相互作用蛋白2（RIP2）激酶抑制剂。 了解更多 -
RIP2 kinase inhibitor 1
Catalog No. A16312 RIP2 kinase 抑制剂RIP2 kinase inhibitor 1 是从专利WO/2014043446 A1（化合物实施例1）中提取的受体相互作用蛋白2（RIP2）激酶抑制剂。 了解更多 -
GSK3 Inhibitor XIII
Catalog No. A22128 ATP-binding site inhibitor of GSK-3GSK3 Inhibitor XIII (GSK3i XIII) is an ATP-binding site inhibitor of GSK-3. 了解更多 -
ATR inhibitor 2
Catalog No. A22162 ATR inhibitorATR inhibitor 2 is an ATP-competitive, orally active, and selective ATR inhibitor, with a Ki of <150 pM. 了解更多 -
LMPTP INHIBITOR 1 dihydrochloride
Catalog No. A22227 LMPTP inhibitorLMPTP INHIBITOR 1 (dihydrochloride) is a selective inhibitor of low molecular weight protein tyrosine phosphatase (LMPTP), with an IC50 of 0.8 μM LMPTP-A. 了解更多 -
VPS34 inhibitor 1 (Compound 19)
Catalog No. A22378 VPS34 inhibitorVPS34 inhibitor 1 (Compound 19, PIK-III analogue) is a potent and selective inhibitor of VPS34 with an IC50 of 15 nM. 了解更多 -
Selective PI3Kδ Inhibitor 1 (compound 7n)
Catalog No. A22381 PI3Kδ inhibitorSelective PI3Kδ Inhibitor 1 (compound 7n) is an inhibitor of PI3Kδ with an IC50 of 0.9 nM and >1000-fold selectivity against other class I PI3K isoforms [PI3K α/γ/β=3670/1460/21300 nM]. 了解更多 -
BTK inhibitor 1 (Compound 27)
Catalog No. A22445 BTK inhibitorBTK inhibitor 1 (compound 27) is an inhibitor of BTK with an IC50 of 0.11 nM for Btk and inhibits B cell activation in hWB with an IC50 of 2 nM. 了解更多 -
Diacylglycerol acyltransferase inhibitor-1
Catalog No. A20315 DGAT1 inhibitorDiacylglycerol acyltransferase inhibitor-1 is a diacylglycerol acyltransferase (DGAT1) inhibitor. 了解更多 -
MAT2A inhibitor 2
Catalog No. A20171 MAT2A inhibitorMAT2A inhibitor 2 is a methionine adenosyltransferase 2A (MAT2A) inhibitor. 了解更多 -
DAAO inhibitor-1
Catalog No. A20117 DAAO inhibitorDAAO inhibitor-1 is a potent D-amino acid oxidase (DAAO) inhibitor with an IC50 of 0.12 μM. 了解更多 -
Grp94 Inhibitor-1
Catalog No. A20073 Grp94 inhibitorGrp94 Inhibitor-1 is a potent, selective Grp94 inhibitor with an IC50 value of 2 nM, and over 1000-fold selectivity to Grp94 against Hsp90α. 了解更多 -
mTOR inhibitor-1
Catalog No. A20029 mTOR inhibitormTOR inhibitor-1 is a novel mTOR pathway inhibitor which can suppress cells proliferation and inducing autophagy. 了解更多 -
Tubulin inhibitor 1
Catalog No. A19998 tubulin inhibitorTubulin inhibitor 1 is a tubulin inhibitor, inhibits tubulin polymerization. 了解更多 -
YAP/TAZ inhibitor-1
Catalog No. A19976 YAP/TAZ inhibitorYAP/TAZ inhibitor-1 is a YAP/TAZ inhibitor extracted from patent WO2017058716A1, Compound 1, has an IC50 of <0.100 μμ in firefly luciferase assay. 了解更多 -
SIRT5 inhibitor 1
Catalog No. A19841 SIRT5 inhibitorSIRT5 inhibitor 1 is a potent Human Sirtuin 5 deacylase inhibitor, with an IC50 of 0.11 μM. 了解更多 -
BET bromodomain inhibitor
Catalog No. A19831 BET inhibitorBET bromodomain inhibitor is a potent BET inhibitor extracted from patent WO/2015/153871A2, compound example 11. 了解更多 -
TRAF-STOP inhibitor 6877002
Catalog No. A19758 CD40-TRAF6 interaction inhibitorTRAF-STOP inhibitor 6877002, is a selective inhibitor of CD40-TRAF6 interaction, compound VII, shows inhibition of NF-κB activation in RAW cells, extracted from patent WO2014033122A1. 了解更多 -
Glutaminyl Cyclase Inhibitor 1
Catalog No. A19723 glutaminyl cyclase inhibitorGlutaminyl Cyclase Inhibitor 1 is a glutaminyl cyclase inhibitor with an IC50 of 0.5 μM. 了解更多 -
PKC-theta inhibitor
Catalog No. A19712 PKC-θ inhibitorPKC-theta inhibitor is a selective PKC-θinhibitor, with an IC50 of 12 nM. 了解更多 -
LRRK2 inhibitor 1
Catalog No. A19701 LRRK2 inhibitorLRRK2 inhibitor 1 is a potent, selective and oral LRRK2 inhibitor with an pIC50 of 6.8 nM. 了解更多 -
HIV-1 integrase inhibitor 3
Catalog No. A19628 INST inhibitorHIV-1 integrase inhibitor 3 is a HIV-1 integrase strand transfer (INST) inhibitor with an IC50 of 2.7 nM. 了解更多 -
PI3K/mTOR Inhibitor-2
Catalog No. A19621 dual pan-PI3K/mTOR inhibitorPI3K/mTOR Inhibitor-2 is a potent dual pan-PI3K/mTOR inhibitor with IC50s of 3.4/34/16/1 nM for PI3Kα/PI3Kβ/PI3Kδ/PI3Kγ and 4.7 nM for mTOR. Antitumor activity. 了解更多 -
HIV-1 integrase inhibitor 4
Catalog No. A19617 INST inhibitorHIV-1 integrase inhibitor 4 is a HIV-1 integrase strand transfer (INST) inhibitor with an IC50 of 3.7 nM. 了解更多 -
Neurotoxin Inhibitor
Catalog No. A19507 -
p38α inhibitor 1
Catalog No. A19182 p38α inhibitorp38α inhibitor 1 is a p38α inhibitor extracted from patent WO 2008076265 A1. 了解更多 -
Bromodomain inhibitor-8
Catalog No. A19161 BET bromodomain inhibitorBromodomain inhibitor-8 (Intermediate 21) is a BET bromodomain inhibitor for treating autoimmune and inflammatory diseases. 了解更多 -
FAAH inhibitor 1
Catalog No. A21841 FAAH inhibitorFAAH inhibitor 1 (Benzothiazole analog 3) is a potent fatty acid amide hydrolase (FAAH) inhibitor with an IC50 of 18??8 nM. 了解更多 -
Notch inhibitor 1
Catalog No. A21591 Notch inhibitorNotch inhibitor 1 is a potent Notch inhibitor, with IC50s of 7.8 and 8.5 nM for Notch 1 and Notch 3, respectively. Used in the research of cancer. 了解更多 -
β-Secretase Inhibitor IV
Catalog No. A21346 BACE-1 inhibitorβ-Secretase Inhibitor IV is a potent, cell-active BACE-1 inhibitor with IC50s of 15.6 and 16.3nM under BACE-1 concentrations of 2 nM and 100 pM, respectively. 了解更多 -
HIV-1 integrase inhibitor 2
Catalog No. A11447 HIV-1 integrase inhibitorHIV-1 integrase inhibitor 2, in the treatment of human immunodeficiency virus (HIV) infection. 了解更多 -
HIV-1 integrase inhibitor
Catalog No. A11446 -
P-gp inhibitor 1
Catalog No. A13384 P-gp inhibitorP-gp inhibitor 1 is a novel inhibitor reversing P-glycoprotein-mediated multidrug resistance. 了解更多
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