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产品数：86101
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T9784Docosanedioic acid?Antibody-drug conjugates linkers,Docosanedioic acid,inhibit,Docosanedioic acid?,I
BEHENIC ACID is a alkyl-chain-based PROTAC linker. BEHENIC ACID is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T9784产 地：中国大陆
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T6741SPDPSPDP,ADC Linkers,Antibody-drug conjugates linkers,inhibit,Inhibitor
SPDP is a short-chain crosslinker, which is used for amine-to-sulfhydryl conjugation via NHS-ester and pyridyldithiol reactive groups that form cleavable (reducible) disulfide bonds with cysteine sulfhydryls. SPDP could activate equal amounts of anti-CD11c and anti-CTLA-4 Abs (in borate buffered saline; pH 8.5).
价 格：￥电议型 号：T6741产 地：中国大陆
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T27026LCJ-13,610 hydrochlorideCJ 13,610 hydrochloride,CJ13,610 hydrochloride
CJ-13,610 hydrochloride is an orally active nonredox-type inhibitor of 5-LOX and can be used in studies about the prevention of untoward pathophysiological effects of LTs.
价 格：￥电议型 号：T27026L产 地：中国大陆
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T15612JH-VIII-157-02CD246,Cluster of differentiation 246,inhibit,Anaplastic lymphoma kinase,Anaplastic lym
JH-VIII-157-02 is an inhibitor of ALK and inhibits echinoderm microtubule-associated protein-like 4-ALK (EML4-ALK) with IC50s of 2 nM for EML4-ALK G1202R, EML4-ALKwt, EML4-ALK C1156Y, EML4-ALK F1174L, and EML4-ALK F1174L.
价 格：￥电议型 号：T15612产 地：中国大陆
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T9085JFD01307SCJFD-01307SC,Inhibitor,Bacterial,JFD01307SC,inhibit
JFD01307SC is a glutamine synthetase inhibitor. It is anti-tuberculosis agent and acts as a mimic of L-Glutamate and thus target enzymes involved in glutamine biosynthesis.
价 格：￥电议型 号：T9085产 地：中国大陆
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T15608Jarin-1Jarin 1,Jarin1
Jarin-1 is a jasmonic acid-amido synthetase (JAR1) inhibitor (IC50: 3.8 μM). Jarin-1 specific suppresses bioactive JA biosynthesis in Arabidopsis and other plants.
价 格：￥电议型 号：T15608产 地：中国大陆
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T8484JSH-150CDK,inhibit,Cyclin dependent kinase,Inhibitor,JSH150,JSH-150,JSH 150
JSH-150 is a highly selective CDK9 inhibitor(IC50 : 1 nM).
价 格：￥电议型 号：T8484产 地：中国大陆
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T6784BI-78D3BI-78D3,BI-78D-3,inhibit,BI 78D3,Inhibitor,BI78D3,JNK
BI-78D3, a competitive JNK inhibitor. IC50 of BI-78D3 is 280 nM that displays > 100 fold selectivity over p38α, and have no activity at mTOR and PI-3K.
价 格：￥电议型 号：T6784产 地：中国大陆
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T15615JND3229JND-3229,JND3229
JND3229 is a reversible EGFRC797S inhibitor with IC50 values of 5.8, 6.8 and 30.5 nM for EGFRL858R/T790M/C797S, EGFRWT and EGFRL858R/T790M, respectively. JND3229 has good anti-proliferative activity and can effectively inhibit tumour growth in vivo. JND3229 can be used in cancer research, especially in non-small cell carcinoma.
价 格：￥电议型 号：T15615产 地：中国大陆
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T6878LJI308viability,Ribosomal S6 Kinase (RSK),LJI-308,stimulation,phosphorylation,LJI308,inhibit,mutatio
LJI308 is a potent, and pan-RSK (p90 ribosomal S6 kinase) inhibitor with IC50 of 6 nM, 4 nM, and 13 nM for RSK1, RSK2, and RSK3, respectively.
价 格：￥电议型 号：T6878产 地：中国大陆
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T8884hSMG-1 inhibitor 11jhSMG 1 inhibitor 11j,hSMG1 inhibitor 11j
hSMG-1 inhibitor 11j is a pyrimidine derivative. hSMG-1 inhibitor 11j is a potent and selective inhibitor of hSMG-1, IC50 = 0.11 nM. hSMG-1 inhibitor 11j exhibits >455-fold selectivity for hSMG-1 over mTOR (IC50=50 nM), PI3Kα/γ (IC50=92/60 nM) and CDK1/CDK2 (IC50=32/7.1 μM). hSMG-1 inhibitor 11j can be used for the research of cancer.
价 格：￥电议型 号：T8884产 地：中国大陆
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T9382Thalidomide-NH-C2-PEG3-OHinhibit,Inhibitor,Thalidomide-NH-C-2-PEG3-OH,E3 Ligase Ligand-Linker Conjug
Thalidomide-NH-C2-PEG3-OH is an E3 ligase ligand-linker conjugate.
价 格：￥电议型 号：T9382产 地：中国大陆
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T9218AndrograpaninInhibitor,chemotaxis,p38 MAPK,leukocyte,SDF-1α,Andrograpanin,PBL,inhibit,Jurkat,anti-in
Andrograpanin is a bioactive compound from Andrographis paniculata. Andrograpanin has anti-inflammatory and anti-infectious properties.
价 格：￥电议型 号：T9218产 地：中国大陆
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T6S1371Isovitexininhibit,Isovitexin,Nuclear factor-kappaB,Inhibitor,Nuclear factor-κB,NF-κB,JNK
1. Isovitexin exhibits a potential antioxidant activity. 2. Isovitexin shows a strong antihyperglycemic action, inhibits α-glucosidase in vivo.
价 格：￥电议型 号：T6S1371产 地：中国大陆
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T17255WJ460WJ-460,WJ460
WJ460 is an effective inhibitor of myoferlin. WJ460 exerts anti-metastatic activity in breast cancer cells.
价 格：￥电议型 号：T17255产 地：中国大陆
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T7305JQEZ5S-adenosyl,EZH2,JQEZ5,antitumor,methionine,JQEZ 5,H3K27me3,PRC2,inhibit,Inhibitor,JQEZ-5,Histon
JQEZ5 is an inhibitor of EZH2 lysine methyltransferase (IC50 = 11.1 nM).
价 格：￥电议型 号：T7305产 地：中国大陆
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TQ0081JPH203JPH203,JPH-203
JPH203 is an effective and specific L-type amino acid transporter 1 (LAT-1) inhibitor.
价 格：￥电议型 号：TQ0081产 地：中国大陆
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T9010IMM-H007JNK,Nuclear factor-κB,WS 070117,IMM H007,AP-1,inflammatory,WS070117,inhibit,AMPK,atheroscler
IMM-H007 is a novel lipid-lowering agent, increasing abca1 protein expression
价 格：￥电议型 号：T9010产 地：中国大陆
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T22879JNJ 10191584 maleate
JNJ 10191584 maleate is an orally active and selective antagonist of H4 receptor (Ki = 26 nM). JNJ 10191584 maleate inhibits chemotaxis of eosinophils and mast cells (IC50 = 530 nM and 138 nM).
价 格：￥电议型 号：T22879产 地：中国大陆
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T9688CC-90001CC90001,kinase,IPF,JNK,c-Jun,idiopathic,JNK1,Inhibitor,N-terminal,inhibit,CC-90001,CC 90001,
CC-90001 is an orally administered c-Jun N-terminal kinase (JNK) inhibitor with bias for JNK1 over JNK2.
价 格：￥电议型 号：T9688产 地：中国大陆
