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T9597H2S Donor 5aEndogenous Metabolite,H2S donor,biological systems,H2S Donor 5a,cysteine-activated,Inhib
H2S Donor 5a is a H2S donor that could mimic the slow and continuous H(2)S generation process.
价 格：￥电议型 号：T9597产 地：中国大陆
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T8588Buramateneuroprotective,Buramate,inhibit,Inhibitor,anticonvulsant
Buramate is an antipsychotic and anticonvulsant.
价 格：￥电议型 号：T8588产 地：中国大陆
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TP1554LHPV16 E7 (86-93) acetateHPV16 E7 (86 93) acetate,HPV16 E7 (8693) acetate
HPV16 E7 (86-93) acetate is a derived peptide of human leukocyte antigen A2.1 restricted HPV16 E7 with immunogenic property in cervical carcinomas.
价 格：￥电议型 号：TP1554L产 地：中国大陆
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TP1263Fz7-21lipid-binding groove,FZD7,Wnt,Fz7 21,Wnt–β-catenin,Fz-7-21,conformation,FZD7 CRD,intestinal or
Fz7-21 is a peptide antagonist of FZD7 . It antagonises WNT3A-induced Wnt-β-catenin signalling in HEK293 expressing FZD7. Fz7-21 impairs Wnt/β-catenin signaling in HEK293 cells stimulated with exogenous WNT3A (IC50=100 nM) or transfected with a construct expressing WNT3A or WNT1. Fz7-21 also blocks WNT3A-mediated stabilization of β-catenin in mouse L cells (IC50=50 nM).
价 格：￥电议型 号：TP1263产 地：中国大陆
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T0151EfloxateEfloxate,inhibit,Inhibitor
Efloxate, a vasodilator, is utilized in the treatment of chronic coronary insufficiency.
价 格：￥电议型 号：T0151产 地：中国大陆
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T8867RO2959 HydrochlorideIP3,SOCE,Ca2+ release-activated Ca2+ channels,RO2959 Hydrochloride,Interleukin R
RO2959 hydrochloride is a potent and selective inhibitor of CRAC channel(IC50: 402 nM). It is also a potent inhibitor of human IL-2.
价 格：￥电议型 号：T8867产 地：中国大陆
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T20692LSchistoflrfamide acetateSchistoflrfamide acetate
Schistoflrfamide acetate is isolated from the grasshopper, Schistocerca gregaria. Schistoflrfamide acetate elicited an immediate effect on the basal membrane potential of the opalescent tubule gland cells in insects.
价 格：￥电议型 号：T20692L产 地：中国大陆
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T67836AT-533Benzamide,2[(trans4hydroxycyclohexyl)amino]4(4,5,6,7tetrahydro3,6,6trimethyl4oxo1Hindazol1yl)
AT-533 is a potent inhibitor of Hsp90 and HSV. AT-533 blocks the HIF-1α/VEGF/VEGFR-2 signaling pathway, leading to suppress tumor growth and angiogenesis. AT-533 also inhibits the activation of the downstream pathways, including Erk1/2, FAK, Akt/mTOR/p70S6K,. AT-533 inhibits the cell migration, invasion, and the tube formation of human umbilical vein endothelial cells (HUVECs).
价 格：￥电议型 号：T67836产 地：中国大陆
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TMS2182trans-Zeatinribosideinhibit,trans Zeatinriboside,trans-Zeatinriboside,transZeatinriboside,Inhibitor
Zeatin Riboside is the most active and ubiquitous form of the naturally occurring cytokinins that promote cell division, stimulate shoot proliferation, inhibit root formation, slow the aging process, and activate gene expression and metabolic activity.
价 格：￥电议型 号：TMS2182产 地：中国大陆
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T40781L(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl dihydrogen diphosphate,tetrabutylam
(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl dihydrogen diphosphate,tetrabutylammonium(1:1.5) is a common precursor of taxadiene such as Paclitaxel.
价 格：￥电议型 号：T40781L产 地：中国大陆
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T8365Methenamine Hippurateantiseptic,Inhibitor,Methenamine Hippurate,pathogens,urinary,tract,Hexamine,Bac
Methenamine Hippurate is a component of Hiprex, with antibacterial activity.
价 格：￥电议型 号：T8365产 地：中国大陆
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TN1403Arjunolic acidhepatocyte injury,hyperglycemia,Inhibitor,type 1 diabetes,antimicrobial,antioxidant,Re
Arjunolic acid has antioxidant, anti-inflammatory, antinociceptive and anticholinesterasic (AChE and BuChE) activities, it may as promising targets for the development of innovative multi-functional medicines for Alzheimer desease treatment.
价 格：￥电议型 号：TN1403产 地：中国大陆
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TQ0009UCB9608Phosphatidylinositol 4 kinases,UCB-9608,Inhibitor,UCB 9608,UCB9608,PI4 kinases,PI4K,inhibit
UCB9608 is a selective and orally active PI4KIIIβ inhibitor (IC50: 11 nM), selective over PI3KC2 α, β, and γ lipid kinases.
价 格：￥电议型 号：TQ0009产 地：中国大陆
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T8457NPS2390Inhibitor,NPS2390,Calcium-sensing receptor,NPS-2390,mGluR,inhibit,Metabotropic glutamate rece
NPS2390 is a first generation quinoxaline derivative that acts as a noncompetitive antagonist of mGluR1 and mGluR5 (IC50 of 5.2 and 82 nM, respectively)
价 格：￥电议型 号：T8457产 地：中国大陆
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T9235GW604714XInhibitor,mitochondrial respiration,Mitochondrial Metabolism,Parkinson’s Disease,MCT1,GW604
GW604714X were found to be potent inhibitors of mitochondrial respiration supported by pyruvate
价 格：￥电议型 号：T9235产 地：中国大陆
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T9593Senaparibinhibit,poly ADP ribose polymerase,IMP 4297,Inhibitor,breast,pancreatic,IMP-4297,Senaparib,
Senaparib is a novel highly potent and selective oral PARP1/2 inhibitor with strong antitumor activity.
价 格：￥电议型 号：T9593产 地：中国大陆
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T8742G5-7antiangiogenic,inhibit,Apoptosis,JAK,Glioma,G-5-7,cycle,G5 7,phase,G57,STAT3,cell,Inhibitor,EGFR
JAK2 inhibitor G5-7 is an orally active JAK2 inhibitor, selectively inhibits JAK2–mediated phosphorylation and activation of EGFR (Tyr1068) and STAT3 by binding to JAK2. G5-7 has the potential for glioma study
价 格：￥电议型 号：T8742产 地：中国大陆
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T8750LX-4211 intermediateLX 4211 intermediate,LX4211 intermediate
LX-4211 intermediate a chemical compound.
价 格：￥电议型 号：T8750产 地：中国大陆
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T8471VonafexorNR1H4,HBV,FXR,EYP 001,Inhibitor,Vonafexor,EYP-001,inhibit,Hepatitis B virus
Vonafexor is a farnesoid X receptor (FXR, NR1H4) agonist, with anti-HBV effects
价 格：￥电议型 号：T8471产 地：中国大陆
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T7299β-Estradiol 17-acetateβ Estradiol 17 acetate,Estrogen Receptor/ERR,Inhibitor,βEstradiol 17acetate,in
beta-estradiol 17-acetate is a metabolite of estradiol.
价 格：￥电议型 号：T7299产 地：中国大陆
