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T60032BRM/BRG1 ATP Inhibitor-2Epigenetic Reader Domain,Inhibitor,BRM/BRG1 ATP Inhibitor 2,inhibit,BRM/BRG1
BRM/BRG1 ATP Inhibitor-2 is an inhibitor of BRG1/BRM ATPase and can be used in studies about the treatment of BAF-related disorders.
价 格：￥电议型 号：T60032产 地：中国大陆
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T7083GLPG1837GLPG-1837,ABBV 974,Cystic fibrosis transmembrane conductance regulator,Inhibitor,CFTR,Autoph
GLPG1837 is an effective CFTR potentiator, with EC50s of 3 nM and 339 nM for F508del and G551D CFTR, respectively.
价 格：￥电议型 号：T7083产 地：中国大陆
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T36711FM19G11
FM19G11 is an inhibitor of hypoxia inducible factor (HIF) α-subunit (IC50 = 80 nM in hypoxia induced luciferase assay).
价 格：￥电议型 号：T36711产 地：中国大陆
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T9226CCG-143140CCG143140,CCG 143140
CCG-143140 is a GLP-1 receptor inverse agonists.
价 格：￥电议型 号：T9226产 地：中国大陆
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T6700TenatoprazoleProton Pump,Inhibitor,gastric,ATPase,Tsg101,inhibit,virus,TU199,oral,TU 199,Tenatoprazo
Tenatoprazole, a prodrug of the proton pump inhibitor (PPI) class, can inhibit proton transport (IC50: 3.2 μM).
价 格：￥电议型 号：T6700产 地：中国大陆
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T8336OGG1-IN-08Inhibitor,inhibit,OGG1,FapyGua,OGG1IN08,glycosylase,AP site,OGG1 IN 08,lyase,OGG-1-IN-08
OGG1-IN-O8 is an inhibitor of 8-oxoguanine DNA glycosylase 1 (OGG1;IC50 : 0.35 μM)
价 格：￥电议型 号：T8336产 地：中国大陆
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T6584MG 149HAT,Inhibitor,MG 149,Epigenetic Reader Domain,Apoptosis,HATs,inhibit,Histone Acetyltransferase
MG149 is a selective and potent Tip60 inhibitor with IC50 of 74 uM, similar potentcy for MOF(IC50= 47 uM).
价 格：￥电议型 号：T6584产 地：中国大陆
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T8684SotorasibAMG 510,Ras,KRAS,covalent,Sotorasib,regression,mutation,Inhibitor,G12C,anti-tumour,inhibit,
AMG-510 is a selective and orally bioavailable KRAS G12C covalent inhibitor.
价 格：￥电议型 号：T8684产 地：中国大陆
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T9401Thalidomide-NH-PEG1-NH2 hydrochlorideinhibit,Thalidomide-NH-PEG-1-NH2 hydrochloride,ThalidomideNHPEG
Thalidomide-NH-PEG1-NH2 hydrochloride is a synthetic E3 ligase ligand-linker conjugate that incorporates the Thalidomide-based cereblon ligand and a linker[1].
价 格：￥电议型 号：T9401产 地：中国大陆
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TN1074GL3inhibit,GL 3,GL-3,Inhibitor,GL3
GL3 encodes a bHLH protein that regulates trichome development in arabidopsis through interaction with GL1 and TTG1.
价 格：￥电议型 号：TN1074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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TP1931L1[D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P acetate[D Arg1,D Phe5,D Trp7,9,Leu11] Substance P acetate
Broad spectrum neuropeptide inverse agonist and antagonist. Potent full inverse agonist for the ghrelin receptor (EC50 = 5.2 nM); diminishes constitutive ghrelin receptor signaling. Also antagonist at tachykinin, bradykinin, CCK and bombesin receptors. Induces apoptosis and inhibits cancer cell growth in vitro.
价 格：￥电议型 号：TP1931L1产 地：中国大陆
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T9213G140Inhibitor,cGAS,anti-inflammatory,G 140,Cyclic GMP-AMP Synthase,G140,synthase,G-140,GMP-AMP,cycli
G140 is a potent and selective inhibitor of cyclic GMP-AMP synthase (cGAS).
价 格：￥电议型 号：T9213产 地：中国大陆
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T30998LCOG-1410 acetateCOG1410 acetate,COG 1410 acetate
COG-1410 acetate is an apolipoprotein E-derived peptide and can be used in studies about neurological diseases.
价 格：￥电议型 号：T30998L产 地：中国大陆
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T7821DG172 dihydrochlorideDG-172,DG172,DG172 dihydrochloride,PPAR,inhibit,DG 172,Inhibitor,Peroxisome pro
DG172 (dihydrochloride) is an antagonist of PPARβ/δ(IC50 : 27 nM).
价 格：￥电议型 号：T7821产 地：中国大陆
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T7796TUG-1375Free Fatty Acid Receptor,inhibit,FFAR,TUG 1375,TUG-1375,Inhibitor,TUG1375
TUG-1375 is an Agonist of Thiazolidine Free Fatty Acid Receptor 2
价 格：￥电议型 号：T7796产 地：中国大陆
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T60034TH1085Inhibitor,DNA glycosylase 1 (OGG1),TH-10785,TH 10785,DNA oxidative lesions,TH1085,enzyme,pheny
TH1085 is an enhancer of OGG1. TH1085 stimulates DNA repair and protects cells from the environmental hazard paraquat (PQ).
价 格：￥电议型 号：T60034产 地：中国大陆
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T7493AG-13958Vascular endothelial growth factor receptor,AG 013958,AG 13958,inhibit,VEGFR,AG13958,AG-1395
AG-13958 (AG-013958), a potent VEGFR tyrosine kinase inhibitor, for the treatment of age-related macular degeneration.
价 格：￥电议型 号：T7493产 地：中国大陆
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T9961L82-G17L82 G17,L82G17
L82-G17 is an uncompetitive LigI-selective inhibitor in human cells with utility as a probe of the catalytic activity and cellular functions of LigI.
价 格：￥电议型 号：T9961产 地：中国大陆
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T9303MRTX1133KRAS,Ras,MRTX 1133,G12D,cells,active,wild-type,phosphorylation,mutant,MRTX1133,inactive,ERK,
MRTX1133 is a potent, selective, and noncovalent inhibitor of KRAS G12D. MRTX1133 exhibits an estimated KD against KRAS G12D of 0.2 pM. MRTX1133 inhibits mutant KRAS-dependent signal transduction by preventing SOS1-catalyzed nucleotide exchange and/or formation of the KRAS G12D/GTP/RAF1 complex. MRTX1133 selectively inhibits KRAS G12D mutant tumor cells with no effect on KRAS wild-type. MRTX1133 exhibits single digit nanomolar activity in cellular assays and marked in vivo efficacy in tumor mode
价 格：￥电议型 号：T9303产 地：中国大陆
