CAS 447459-51-0

Formel: C23H25NO8S3

InChl: InChI=1S/C23H25NO8S3/c1-16(24-33(4,25)26)17-5-10-20(11-6-17)34(27,28)22-14-9-19(32-3)15-23(22)35(29,30)21-12-7-18(31-2)8-13-21/h5-16,24H,1-4H3/t16-/m0/s1

InChI Key: NXODIUKWAVUFGF-INIZCTEOSA-N

SMILES: C[C@@H](C1=CC=C(C=C1)S(=O)(=O)C2=C(C=C(C=C2)OC)S(=O)(=O)C3=CC=C(C=C3)OC)NS(=O)(=O)C

SCH-336

CAS: 447459-51-0

SCH-336

Formel: C₂₃H₂₅NO₈S₃

Reinheit: ≥95%

Molekulargewicht: 539.64

Ref: 54-BUP10592

SCH 336

CAS: 447459-51-0

Formel: C₂₃H₂₅NO₈S₃

Reinheit: 96%

Molekulargewicht: 539.6415

Ref: IN-DA01ENIE

SCH 336

CAS: 447459-51-0

SCH 336 is an antibiotic compound derived from a type of fungus. This compound is characterized by its potent ability to disrupt the synthesis of bacterial cell walls. Its mechanism of action involves the inhibition of transpeptidase enzymes, which are essential for forming cross-links in the peptidoglycan layer of bacterial cell walls. This disruption leads to cell lysis and ultimately, the death of the bacterial cell.

Formel: C₂₃H₂₅NO₈S₃

Reinheit: Min. 95%

Molekulargewicht: 539.6 g/mol

Ref: 3D-XSA45951

SCH-336

CAS: 447459-51-0

SCH-336: potent, selective CB2 agonist (Ki=1.8 nM, EC50=2 nM), orally active, 100x CB2 vs. CB1 preference, reduces leukocyte migration and eosinophilia.

Formel: C₂₃H₂₅NO₈S₃

Reinheit: 97.00%

Farbe und Form: Solid

Molekulargewicht: 539.642

Ref: TM-T24771