CAS 927871-76-9

2,3,4,5-Tetrahydro-7-methoxy-4-methyl-1,4-benzothiazepine

CAS: 927871-76-9

Formula: C₁₁H₁₅NOS

Purity: 98%

Color and Shape: Solid

Molecular weight: 209.3079

Ref: IN-DA00GW95

S107

CAS: 927871-76-9

S107

Purity: ≥98%

Molecular weight: 209.31g/mol

Ref: 54-BUP10061

7-Methoxy-4-Methyl-2,3,4,5-Tetrahydrobenzo[f][1,4]Thiazepine

CAS: 927871-76-9

7-Methoxy-4-Methyl-2,3,4,5-Tetrahydrobenzo[f][1,4]Thiazepine

Purity: 95%

Molecular weight: 209.31g/mol

Ref: 54-OR1025322

Surlorian Impurity 1

CAS: 927871-76-9

Formula: C₁₁H₁₅NOS

Molecular weight: 209.31

Ref: 4Z-S-257002

S107

CAS: 927871-76-9

S107 stabilizes RyR2 by improving calstabin2 binding to mutant/PKA-phosphorylated channels.

Formula: C₁₁H₁₅NOS

Purity: 99.90%

Color and Shape: Solid

Molecular weight: 209.31

Ref: TM-T3438

7-Methoxy-4-methyl-2,3,4,5-tetrahydrobenzo[f][1,4]thiazepine

CAS: 927871-76-9

Formula: C₁₁H₁₅NOS

Purity: ≥98%

Molecular weight: 209.31

Ref: 10-F521444

2,3,4,5-Tetrahydro-7-methoxy-4-methyl-1,4-benzothiazepine

Controlled Product

CAS: 927871-76-9

2,3,4,5-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]p

Formula: C₁₁H₁₅NOS

Purity: Min. 95%

Molecular weight: 209.31 g/mol

Ref: 3D-CMB87176