
CAS 927871-76-9
:Formula: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
InChI key:BGVCEGVSQDOGSB-UHFFFAOYSA-N
SMILES:CN1CCSC2=C(C1)C=C(C=C2)OC
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2,3,4,5-Tetrahydro-7-methoxy-4-methyl-1,4-benzothiazepine
CAS:Formula:C11H15NOSPurity:98%Color and Shape:SolidMolecular weight:209.30797-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
Purity:95%Molecular weight:209.31g/molS107
CAS:S107 stabilizes RyR2 by improving calstabin2 binding to mutant/PKA-phosphorylated channels.Formula:C11H15NOSPurity:99.90%Color and Shape:SolidMolecular weight:209.317-Methoxy-4-methyl-2,3,4,5-tetrahydrobenzo[f][1,4]thiazepine
CAS:Formula:C11H15NOSPurity:≥98%Molecular weight:209.312,3,4,5-Tetrahydro-7-methoxy-4-methyl-1,4-benzothiazepine
CAS:Controlled Product2,3,4,5-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]pFormula:C11H15NOSPurity:Min. 95%Molecular weight:209.31 g/mol






