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T60037SR15006growth,inhibit,KLF5,SR 15006,Krüppel-like factor,SR15006,colorectal cancer cells,cycle,Inhibi
SR15006 is Krüppel-like factor 5 (KLF5) inhibitor (IC50 = 41.6 nM).
价 格：￥电议型 号：T60037产 地：中国大陆
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T7203OglufanideM21 human melanoma,anti-angiogenesis,Vascular endothelial growth factor receptor,HCV,inhib
Oglufanide is a naturally occurring thymic immunomodulator,and inhibits vascular endothelial growth factor (VEGF).
价 格：￥电议型 号：T7203产 地：中国大陆
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T8482Ripretinibc-Kit,Inhibitor,DCC2618,Vascular endothelial growth factor receptor,CD135,CD117,Platelet-d
Ripretinib is an orally bioavailable inhibitor of KIT and PDGFRA.
价 格：￥电议型 号：T8482产 地：中国大陆
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T6996SU 5402SU-5402,SU 5402,VEGFR,inhibit,Inhibitor,Fibroblast growth factor receptor,FGFR,Platelet-deriv
SU5402 is a potent multi-targeted receptor tyrosine kinase inhibitor with IC50 of 20 nM, 30 nM, and 510 nM for VEGFR2, FGFR1, and PDGF-Rβ, respectively.
价 格：￥电议型 号：T6996产 地：中国大陆
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T6720Vatalanib dihydrochloridePTK-787,Inhibitor,Vascular endothelial growth factor receptor,VEGFR,PTK 787
Vatalanib (PTK787) (IC50=37 nM) is an inhibitor of VEGFR2/KDR. It exhibits less effective against VEGFR1/Flt-1 and 18-fold against VEGFR3/Flt-4.
价 格：￥电议型 号：T6720产 地：中国大陆
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T6734WZ8040HER1,WZ 8040,mutated,WZ8040,Inhibitor,phosphorylation,EGFR,NSCLC,Epidermal growth factor recep
WZ8040 is a novel mutant-selective irreversible EGFRT790M inhibitor, does not inhibit ERBB2 phosphorylation (T798I).
价 格：￥电议型 号：T6734产 地：中国大陆
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T16766Ro 08-2750growth,MSI,Ro 082750,p75NTR,TRKA,RNA-binding,Nerve,NGF,Inhibitor,leukemia,Apoptosis,AML,Ro
Ro 08-2750 is a non-peptide and reversible nerve growth factor (NGF) inhibitor which binds to NGF, and with an IC50 of ~ 1 ?M. Ro 08-2750 is a selective MSI RNA-binding activity inhibitor, with an IC50 of 2.7 μM. Ro 08-2750 inhibits NGF binding to p75NTR selectively over TRKA.
价 格：￥电议型 号：T16766产 地：中国大陆
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TN2354MethylnissolinMethylnissolin,Astrapterocarpan,ERK,Inhibitor,Platelet-derived growth factor receptor,
3-Hydroxy-9,10-dimethoxyptercarpan is derived from Astragalus and has antibacterial and anti-cancer effects.
价 格：￥电议型 号：TN2354产 地：中国大陆
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T7322TheliatinibATP-competitive,inhibit,EGFR,ERK,cancer,esophageal,Epidermal growth factor receptor,HMPL-
Theliatinib, a potent and highly selective EGFR inhibitor, with anti-tumor activity. Ki of 0.05 nM for wild type EGFR, and IC50s of 3 and 22 nM for EGFR and EGFR T790M/L858R mutant, respectively.
价 格：￥电议型 号：T7322产 地：中国大陆
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T8283(+)-Bornyl Acetateoil,inhibit,growth,Inhibitor,root,(+)-Bornyl,(+) Bornyl Acetate,(+)Bornyl Acetate,
(+)-Bornyl Acetate has a stronger inhibitory effect on root growth of Arabidopsis seedlings.
价 格：￥电议型 号：T8283产 地：中国大陆
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T94734SC-203tumor,antineoplastic,Fms like tyrosine kinase 3,Vascular endothelial growth factor receptor,4
4SC-203 is a multikinase inhibitor with potential antineoplastic activity. 4SC-203 selectively inhibits FMS-related tyrosine kinase 3 (FLT3/STK1), FLT3 mutated forms, and vascular endothelial growth factor receptors (VEGFRs).
价 格：￥电议型 号：T9473产 地：中国大陆
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T6918OlmutinibOlmutinib,ErbB-1,inhibit,HER1,EGFR,Epidermal growth factor receptor,Inhibitor
Olmutinib is an orally available small molecule, a mutant-selective inhibitor of epidermal growth factor receptor (EGFR) with potential antineoplastic activity. Olmutinib binds to and inhibits mutant forms of EGFR, thereby leading to cell death of EGFR-expressing tumor cells. As this agent is selective towards mutant forms of EGFR, its toxicity profile may be reduced as compared to non-selective EGFR inhibitors which also inhibit the EGFR wild-type form.
价 格：￥电议型 号：T6918产 地：中国大陆
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T9724WAY-340935Inhibitor,WAY340935,Vascular endothelial growth factor receptor,WAY 340935,inhibit,VEGFR,A
WAY-340935 has anti-inflammatory and analgesic activities.
价 格：￥电议型 号：T9724产 地：中国大陆
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T7861Flumatinib mesylateHHGV-678,PDGFRβ,HHGV678,c-Abl,Bcr-Abl,Platelet-derived growth factor receptor,PDG
Flumatinib mesylate is a selective inhibitor of c-Abl, PDGFRβ and c-Kit, effectively overcomes drug resistance of certain KIT mutants.
价 格：￥电议型 号：T7861产 地：中国大陆
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T7175Alflutinib mesylatecancer,Epidermal growth factor receptor,AST2818,esistant mutation,Alflutinib,Alfl
AST2818 mesylate,is an irreversible tyrosine kinase inhibitor that selectively inhibits EGFR mutations, especially T790M.
价 格：￥电议型 号：T7175产 地：中国大陆
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T9465ZZW-115 hydrochloridenecroptosis,cell,PDAC,growth,ZZW-115,pancreatic,ZZW115 hydrochloride,ZZW 115 hy
ZZW-115 hydrochloride inhibits the activity of NUPR1.
价 格：￥电议型 号：T9465产 地：中国大陆
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T6517GolvatinibE7050,Golvatinib,c-Met/HGFR,VEGFR,Inhibitor,Vascular endothelial growth factor receptor,E
Golvatinib is an orally bioavailable dual kinase inhibitor of c-Met (hepatocyte growth factor receptor) and VEGFR-2 (vascular endothelial growth factor receptor-2) tyrosine kinases with potential antineoplastic activity. c-Met/VEGFR kinase inhibitor E7050 binds to and inhibits the activities of both c-Met and VEGFR-2, which may inhibit tumor cell growth and survival of tumor cells that overexpress these receptor tyrosine kinases. c-Met and VEGFR-2 are upregulated in a variety of tumor cell types
价 格：￥电议型 号：T6517产 地：中国大陆
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T7186CZC-8004CZC 8004,HER1,Vascular endothelial growth factor receptor,ErbB-1,Epidermal growth factor rec
CZC-8004 is a pan-kinase(ABL kinase) inhibitor and binds a range of tyrosine kinases.
价 格：￥电议型 号：T7186产 地：中国大陆
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T7945SU14813c-Kit,Inhibitor,VEGFR,Vascular endothelial growth factor receptor,SU 14813,PDGFR,CD117,Platel
SU14813 is a multi-receptor tyrosine kinase inhibitor with potent antiangiogenesis and antitumor activity (IC50s of 50, 2, 4, 15 nM for VEGFR2, VEGFR1, PDGFRβ and KIT).
价 格：￥电议型 号：T7945产 地：中国大陆
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T6856Halofuginoneosteoarthritis,collagen-1,Na+ channels,Calcium Channel,Na channels,Transforming growth f
Halofuginone, the competitive inhibitor of prolyl-tRNA synthetase（Ki=18.3 nM）, could also down-regulate Smad3 and blocked TGF-β signaling at 10 ng/ml in the mammal.
价 格：￥电议型 号：T6856产 地：中国大陆
