7-MAC

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C24H24N6O4S2
Molecular Weight	524.615
Optical Activity	UNSPECIFIED
Defined Stereocenters	2 / 2
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CO[C@]1(N)[C@H]2SCC(CSC3=NN=NN3C)=C(N2C1=O)C(=O)OC(C4=CC=CC=C4)C5=CC=CC=C5

InChI

InChIKey=QGXKMJVEULWQSB-VWNXMTODSA-N

InChI=1S/C24H24N6O4S2/c1-29-23(26-27-28-29)36-14-17-13-35-22-24(25,33-2)21(32)30(22)18(17)20(31)34-19(15-9-5-3-6-10-15)16-11-7-4-8-12-16/h3-12,19,22H,13-14,25H2,1-2H3/t22-,24+/m1/s1

HIDE SMILES / InChI

Molecular Formula	C24H24N6O4S2
Molecular Weight	524.615
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	2 / 2
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Tue Apr 01 16:23:56 GMT 2025` Edited by `admin` on `Tue Apr 01 16:23:56 GMT 2025`
Record UNII	7SSG9SDN2A
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID, 7-AMINO-7-METHOXY-3-(((1-METHYL-1H-TETRAZOL-5-YL)THIO)METHYL)-8-OXO-, DIPHENYLMETHYL ESTER, (6R-CIS)-

Preferred Name

English

7-MAC

Common Name

English

5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID, 7-AMINO-7-METHOXY-3-(((1-METHYL-1H-TETRAZOL-5-YL)THIO)METHYL)-8-OXO-, DIPHENYLMETHYL ESTER, (6R,7S)-

Systematic Name

English

DIPHENYLMETHYL 7.BETA.-AMINO-7.ALPHA.-METHOXY-3-(((1-METHYL-1H-TETRAZOL-5-YL)THIO)METHYL)-3-CEPHEM-4-CARBOXYLATE

Common Name

English

Code System Code Type Description

EPA CompTox

DTXSID50512224

Created by admin on Tue Apr 01 16:23:56 GMT 2025 , Edited by admin on Tue Apr 01 16:23:56 GMT 2025

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PUBCHEM

12882026

Created by admin on Tue Apr 01 16:23:56 GMT 2025 , Edited by admin on Tue Apr 01 16:23:56 GMT 2025

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CAS

56610-72-1

Created by admin on Tue Apr 01 16:23:56 GMT 2025 , Edited by admin on Tue Apr 01 16:23:56 GMT 2025

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FDA UNII

7SSG9SDN2A

Created by admin on Tue Apr 01 16:23:56 GMT 2025 , Edited by admin on Tue Apr 01 16:23:56 GMT 2025

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