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产品数：86101
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T24076FzM1
FzM1 is a negative allosteric modulator (NAM) of Frizzled receptor FZD4. FzM1 reduces WNT5A-dependent WNT responsive element (WRE) activity (log EC50inh=?6.2). FzM1 binds to an allosteric binding site located in intracellular loop 3 (ICL3) of FZD4 and alters the conformation of the receptor, ultimately inhibiting the WNT/β-catenin cascade
价 格：￥电议型 号：T24076产 地：中国大陆
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TN2054Periplocymarinproliferation,inhibit,Inhibitor,cardiac,Periplocymarin,U937,anti-cancer,HCT-8,cells,gl
Periplocymarin, a cardiac glycoside, has potential anti-cancer activity.
价 格：￥电议型 号：TN2054产 地：中国大陆
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T23285S 14506 hydrochlorideS 14506 hydrochloride
S 14506 hydrochloride is a 5-HT1A receptor full agonist.
价 格：￥电议型 号：T23285产 地：中国大陆
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T14184Alkynyl myristic acid
Alkynyl myristic acid is an alkyl chain-based PROTAC linker.
价 格：￥电议型 号：T14184产 地：中国大陆
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T94943-(IMIDAZOL-4-YL)PROPIONIC ACID3 (IMIDAZOL 4 YL)PROPIONIC ACID,3(IMIDAZOL4YL)PROPIONIC ACID
3-(IMIDAZOL-4-YL)PROPIONIC ACID is a product of histidine metabolism and may involve oxidation or transamination. 3-(IMIDAZOL-4-YL)PROPIONIC ACID is potent inhibitors of G. candidum histidinol dehydrogenase, showing IC50 values as low as 3.17 microM.
价 格：￥电议型 号：T9494产 地：中国大陆
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T10792LCHK1-IN-4 hydrochloride
CHK1-IN-4 hydrochloride is a potent inhibitor of checkpoint kinase 1 (chk1). CHK1-IN-4 hydrochloride potently inhibits chk1 phosphorylation in the tumor cells. CHK1-IN-4 hydrochloride has anti-tumor activity.
价 格：￥电议型 号：T10792L产 地：中国大陆
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T80154-METHOXYCHALCONE4 METHOXYCHALCONE,4METHOXYCHALCONE
4-METHOXYCHALCONE is a natural compound that enhanced adipocyte differentiation,
价 格：￥电议型 号：T8015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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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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TP1761LHandle region peptide, rat acetateHandle region peptide, rat acetate
Handle region peptide, rat acetate is a prorenin receptor antagonist, suppresses the progression of diabetic nephropathy and has anti-inflammatory in the eye.
价 格：￥电议型 号：TP1761L产 地：中国大陆
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TP1031TetracosactideTetracosactide,adrenal gland,adrenocorticotrophic hormone,Inhibitor,corticosteroids,in
Tetracosactide (INN) is a synthetic peptide that is identical to the 24-amino acid segment (sequence: SYSMEHFRWGKPVGKKRRPVKVYP) at the N-terminal of adrenocorticotropic hormone.
价 格：￥电议型 号：TP1031产 地：中国大陆
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TN11428-Oxocoptisine8-Oxocoptisine,inhibit,Inhibitor,8 Oxocoptisine,8Oxocoptisine
8-Oxycoptisine is a natural product with Anti-inflammatory, analgesic, cooling, antihypertensive, anti-cancer
价 格：￥电议型 号：TN1142产 地：中国大陆
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T16873SERCA2a activator 1Ca channels,phospholamban,Inhibitor,Ca2+ channels,SERCA2a activator 1,SERCA2a,SER
SERCA2a activator 1 is a sarco/endoplasmic reticulum Ca2+-dependent ATPase 2a activator. SERCA2a activator 1 decreases phospholamban inhibition and enhances the systolic and diastolic functions of the heart.
价 格：￥电议型 号：T16873产 地：中国大陆
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T86486-AZATHYMINE6-Azathymine,6AZATHYMINE,antibacterial,nucleobase,Inhibitor,Influenza Virus,DNA,6-nitrog
6-azathymine is a potent inhibitors of D-3-aminoisobutyrate-pyruvate aminotransferase. 6-Azauracil acted as a competitive inhibitor with respect to beta-alanine, and was an uncompetitive inhibitor with respect to pyruvic acid with a Ki of approximately 8.9 mM.
价 格：￥电议型 号：T8648产 地：中国大陆
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T9380LAntide acetateAntide acetate
Antide acetate is an LHRH antagonist and represses LH and FSH release from the pituitary gland.?
价 格：￥电议型 号：T9380L产 地：中国大陆
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TQ00011,4-CineoleTransient receptor potential channels,Inhibitor,1,4-Cineole,Endogenous Metabolite,inhibit
1,4-Cineole is a natural, oxygenated monoterpene. 1,4-Cineole can activate both human TRPM8 and human TRPA1.
价 格：￥电议型 号：TQ0001产 地：中国大陆
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T13368YLF-466D
YLF-466D is a newly developed AMPK activator, which inhibits platelet aggregation.
价 格：￥电议型 号：T13368产 地：中国大陆
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T21967MEG hemisulfate
MEG hemisulfate is a potent and selective inhibitor of the inducible NO synthase (iNOS), with EC50s of 11.5, 110, and 60 μM for iNOS, ecNOS, and bNOS respectively in tissue homogenates. MEG hemisulfate is also a potent scavenger of peroxynitrite and inhibits peroxynitrite-induced oxidative processes. MEG hemisulfate has a protective effect in many experimental models of inflammation, including ischemia/reperfusion injury, periodontitis, hemorrhagic shock, inflammatory bowel disease, and endotoxi
价 格：￥电议型 号：T21967产 地：中国大陆
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T12262L1NPS ALX Compound 4a hydrochloride(1:1)NPSALXCompound4ahydrochloride(299433106Freebase)
NPS ALX Compound 4a hydrochloride(1:1) is a potent and selective 5-hydroxytryptamine6 (5-HT6) receptor antagonist, with an IC50 of 7.2 nM and a Ki of 0.2 nM.
价 格：￥电议型 号：T12262L1产 地：中国大陆
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T7181IDO-IN-1Inhibitor,inhibit,Indoleamine 2,3-Dioxygenase (IDO),IDO IN 1,IDOIN1
IDO-IN-1 is a potent indoleamine 2,3-dioxygenase (IDO) inhibitor( IC50 values of 59 and 12 nM for human IDO enzymatic activity and HeLa cell assays, respectively.)
价 格：￥电议型 号：T7181产 地：中国大陆
