
CAS 1316652-41-1
:Fórmula:C16H14N4O2S
InChI:InChI=1S/C16H14N4O2S/c21-16(18-22)13-6-4-5-12(9-13)15-10-20(19-17-15)11-23-14-7-2-1-3-8-14/h1-10,22H,11H2,(H,18,21)
Chave InChI:DORPIZJGSLWDIY-UHFFFAOYSA-N
SMILES:C1=CC=C(C=C1)SCN2C=C(N=N2)C3=CC(=CC=C3)C(=O)NO
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100
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50
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90
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95
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100
Foram encontrados 6 produtos.
N-Hydroxy-3-[1-(phenylthio)methyl-1H-1,2,3-triazol-4-yl]benzamide
CAS:Fórmula:C16H14N4O2SPureza:>96.0%(HPLC)(qNMR)Cor e Forma:Light yellow to Brown powder to crystalPeso molecular:326.37N-Hydroxy-3-[1-(phenylthio)methyl-1H-1,2,3-triazol-4-yl]benzamide
CAS:N-Hydroxy-3-[1-(phenylthio)methyl-1H-1,2,3-triazol-4-yl]benzamideFórmula:C16H14N4O2SPureza:>96.0%Peso molecular:326.37Benzamide, N-hydroxy-3-[1-[(phenylthio)methyl]-1H-1,2,3-triazol-4-yl]-
CAS:Fórmula:C16H14N4O2SPureza:96.0%Cor e Forma:SolidPeso molecular:326.3730N-Hydroxy-3-[1-(phenylthio)methyl-1H-1,2,3-triazol-4-yl]benzamide
CAS:N-Hydroxy-3-[1-(phenylthio)methyl-1H-1,2,3-triazol-4-yl]benzamide (NHTB) is a histone deacetylase inhibitor that binds to the active site of the enzyme and inhibits its activity. It is selective for class I HDACs over class II HDACs. NHTB has been shown to inhibit acetylation of α-tubulin in vitro and in vivo. The compound also inhibits proliferation of T cells from patients with cutaneous T cell lymphoma and promotes apoptosis. NHTB also has antiangiogenic effects by inhibiting proliferation of endothelial cells.Fórmula:C16H14N4O2SPureza:Min. 95%Peso molecular:326.37 g/molN-HYDROXY-3-[1-(PHENYLTHIO)METHYL-1H-1,2,3-TRIAZOL-4-YL]BENZAMIDE
CAS:Pureza:99.02%Peso molecular:326.3699951Ref: 10-F842716
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