
CAS 927871-76-9
:Fórmula:C11H15NOS
InChI:InChI=1S/C11H15NOS/c1-12-5-6-14-11-4-3-10(13-2)7-9(11)8-12/h3-4,7H,5-6,8H2,1-2H3
Clave InChI:BGVCEGVSQDOGSB-UHFFFAOYSA-N
SMILES:CN1CCSC2=C(C1)C=C(C=C2)OC
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Se han encontrado 7 productos.
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7-Methoxy-4-Methyl-2,3,4,5-Tetrahydrobenzo[f][1,4]Thiazepine
CAS:7-Methoxy-4-Methyl-2,3,4,5-Tetrahydrobenzo[f][1,4]Thiazepine
Pureza:95%Peso molecular:209.31g/mol2,3,4,5-Tetrahydro-7-methoxy-4-methyl-1,4-benzothiazepine
CAS:Fórmula:C11H15NOSPureza:98%Forma y color:SolidPeso molecular:209.3079S107
CAS:S107 stabilizes RyR2 by improving calstabin2 binding to mutant/PKA-phosphorylated channels.Fórmula:C11H15NOSPureza:99.90%Forma y color:SolidPeso molecular:209.317-Methoxy-4-methyl-2,3,4,5-tetrahydrobenzo[f][1,4]thiazepine
CAS:Fórmula:C11H15NOSPureza:≥98%Peso molecular:209.312,3,4,5-Tetrahydro-7-methoxy-4-methyl-1,4-benzothiazepine
CAS:Producto controlado2,3,4,5-Tetrahydro-7-methoxy-4-methyl-1,4-benzothiazepine (TMBS) is a natural compound that has been shown to be active against Actinomyces in vitro. TMBS inhibits the calcium release from the sarcoplasmic reticulum by binding to the ryanodine receptor. TMBS also exhibits cytotoxic activity against human cells and can induce cell death by apoptosis. TMBS has no effect on organisms without ryanodine receptors and is only active against Actinomyces when used as a monomer. Comparative studies show that TMBS was more effective than other analogs such as 2,3,4,5-tetrahydrobenzo(b)thiophene and 2-[2-(3H)-dioxo-1,2,3,-benzoxadiazol-4(5H)-yl]pFórmula:C11H15NOSPureza:Min. 95%Peso molecular:209.31 g/mol






