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T7197Fadrozole(Rac)-FAD286,inhibit,Fadrozole,CGS 16949A,Inhibitor,Aromatase
Fadrozole is a nonsteroidal aromatase inhibitor with potential antineoplastic activity(IC50 : 6.4 nM)
价 格：￥电议型 号：T7197产 地：中国大陆
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T7709(E/Z)-GSK5182(E/Z)GSK5182,(E/Z) GSK5182,(E/Z)-GSK-5182
(E/Z)-GSK5182 is a racemate of (E)-GSK5182 and (Z)-GSK5182 isomers. GSK5182 is a highly selective and orally active inverse agonist of estrogen-related receptor γ (ERRγ) with an IC 50 of 79 nM [1]. GSK5182 also induces reactive oxyen species (ROS) generation in hepatocellular carcinoma [1] [2] [3].
价 格：￥电议型 号：T7709产 地：中国大陆
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T3079GSK1838705ACD246,Anaplastic lymphoma kinase,inhibit,Cluster of differentiation 246,Anaplastic lympho
GSK1838705A is an effective IGF-1R inhibitor (IC50: 2.0 nM), modestly potent to IR (IC50: 1.6 nM) and ALK (IC50: 0.5 nM), respectively, and little inhibition to other protein kinases.
价 格：￥电议型 号：T3079产 地：中国大陆
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T9703LGSK778 hydrochlorideGSK778 hydrochloride
GSK778 hydrochloride hydrochloride is a potent and selective BD1 bromodomain inhibitor of the BET proteins, with IC50s of 75 nM (BRD2 BD1), 41 nM (BRD3 BD1), 41 nM (BRD4 BD1), and 143 nM (BRDT BD1), respectively. GSK778 hydrochloride hydrochloride phenocopies the effects of pan-BET inhibitors in cancer models[1].
价 格：￥电议型 号：T9703L产 地：中国大陆
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T74373-(3-Hydroxyphenyl)propionic Acidaortic,Inhibitor,rings,Endogenous Metabolite,3(3Hydroxyphenyl)propi
3-(3-Hydroxyphenyl)propionic Acid is one of the major metabolites of ingested caffeic acid.it inhibited osteoclastogenesis and bone osteoclastic resorptive activity.
价 格：￥电议型 号：T7437产 地：中国大陆
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T7436CilofexorGS9674,Inhibitor,inhibit,NR1H4,FXR,Cilofexor,PSC,GS 9674,oral,NASH,GS-9674,antifibrotic,non
Cilofexor inhibits binding of a synthetic peptide, Cilofexor is a farnesoid X receptor (FXR) agonist.
价 格：￥电议型 号：T7436产 地：中国大陆
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T6434CCG-50014Regulators of G-protein Signaling,Regulator of G-protein Signaling,RGS Protein,CCG-50014,in
CCG 50014 is a potent and selective inhibitor of RGS4 with IC50 of 30 nM.
价 格：￥电议型 号：T6434产 地：中国大陆
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T6847GSK-J1GSK-J1,inhibit,Inhibitor,Histone Demethylase,GSKJ1,GSK-J-1
GSK-J1 is a highly potent H3K27 histone demethylase inhibitor with IC50 of 28 nM and 53 nM in cell-free assays for JMJD3 (KDM6B) and UTX (KDM6A), respectively, >10-fold selectivity over other tested demethylases.
价 格：￥电议型 号：T6847产 地：中国大陆
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T9178(E/Z)-GSK-3β inhibitor 1Glycogen synthase kinase 3,Inhibitor,Glycogen synthase kinase-3,inhibit,(E/Z
GSK-3β inhibitor 1 is a glycogen synthase kinase 3β (GSK-3β) inhibitor and demonstrates high antidiabetic efficacy.
价 格：￥电议型 号：T9178产 地：中国大陆
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T7397GSK547Inhibitor,RIP kinase,inhibit,GSK-547,GSK547,Receptor-interacting protein kinases,RIPK,GSK 547
GSK547 is a highly selective and potent inhibitor of RIP1 kinase,inhibits macrophage-mediated adaptive immune tolerance in pancreatic cancer.
价 格：￥电议型 号：T7397产 地：中国大陆
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T8703yGsy2p-IN-1diseases,synthase,hGYS1,pyrazole,GSDs,yGsy2p,yGsy2pIN1,yGsy-2p-IN-1,glycogen,storage,yGsy
yGsy2p-IN-1 is a potent yeast glycogen synthase 2 (yGsy2p) and human glycogen synthase 1 (hGYS1) inhibitor. yGsy2p-IN-H23 a pyrazole inhibitor,and is used for glycogen storage diseases (GSDs)
价 格：￥电议型 号：T8703产 地：中国大陆
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T21956GSK3β inhibitor IIGSK3 Inhibitor II,GSK 3 Inhibitor II
GSK3β inhibitor II is a GSK3β inhibitor. GSK3β inhibitor II exhibits the research potential of Alzheimer´s disease (AD).
价 格：￥电议型 号：T21956产 地：中国大陆
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T15438GSK3186899
GSK3186899 is an inhibitor of Cdc2-related kinase 12 with an EC50 of 1.4 μM for L. donovani.
价 格：￥电议型 号：T15438产 地：中国大陆
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T41302Itaconate-alkyneGSN,labeling,bioorthogonal,DDB1,AK2,Itaconatealkyne,Itaconation,LPS,probe,site-speci
Itaconate-alkyne is a bioorthogonal probe for quantitative and site-specific chemoproteomic profiling of itaconate in inflammatory macrophages and enables biochemical evaluation and proteomic analysis of its direct targets.
价 格：￥电议型 号：T41302产 地：中国大陆
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T9003CVT-11127Inhibitor,apoposis,GS 456332,S-phase,monounsaturated fatty acids (MUFA),Stearoyl-CoA Desatu
CVT-11127 is an StearoylCoA Desaturase-1 (SCD1) inhibitor.
价 格：￥电议型 号：T9003产 地：中国大陆
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T7361VerucerfontGSK 561679,Verucerfont,Corticotropin-releasing Factor Receptor,Inhibitor,GSK-561679,CRFR,
Verucerfont is an antagonist of corticotropin-releasing factor receptor 1 (CRF1) .
价 格：￥电议型 号：T7361产 地：中国大陆
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T67843GSK215GSK215
GSK215 is a potent and selective PROTAC focal adhesion kinase (FAK) degrader (pDC50= 8.4). GSK215 is designed by the FAK inhibitor VS-4718 and a binder for the VHL E3 ligase. GSK215 can induce rapid and prolonged FAK degradation.
价 格：￥电议型 号：T67843产 地：中国大陆
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T7079BatefenterolGSK-961081,mAChR,inhibit,TD 5959,Muscarinic acetylcholine receptor,GSK 961081,Adrenergic
Batefenterol (GSK961081, TD-5959) is a muscarinic receptor antagonist and β2-adrenoceptor agonist. It displays high affinity for hM2, hM3 muscarinic and hβ2-adrenoceptor (Ki:1.4/1.3/3.7 nM).
价 格：￥电议型 号：T7079产 地：中国大陆
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T63581-AzakenpaulloneGlycogen synthase kinase-3,1 Azakenpaullone,GSK-3,1-Azakenpaullone,1Azakenpaullone,G
1-Azakenpaullone is a potent and selective GSK-3β inhibitor with IC50 of 18 nM, >100-fold selectivity over CDK1/cyclin B and CDK5/p25.
价 格：￥电议型 号：T6358产 地：中国大陆
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T6846VesatolimodHepatitis B virus,Vesatolimod,HCV,inhibit,Apoptosis,GS9620,Human immunodeficiency virus,G
GS-9620 is an effective and specific orally active agonist of Toll-like receptor 7.
价 格：￥电议型 号：T6846产 地：中国大陆
