Cefdinir, 7(S)-

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C14H13N5O5S2
Molecular Weight	395.414
Optical Activity	UNSPECIFIED
Defined Stereocenters	2 / 2
E/Z Centers	1
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

NC1=NC(=CS1)C(=N\O)\C(=O)N[C@@H]2[C@H]3SCC(C=C)=C(N3C2=O)C(O)=O

InChI

InChIKey=RTXOFQZKPXMALH-JQISMDCNSA-N

InChI=1S/C14H13N5O5S2/c1-2-5-3-25-12-8(11(21)19(12)9(5)13(22)23)17-10(20)7(18-24)6-4-26-14(15)16-6/h2,4,8,12,24H,1,3H2,(H2,15,16)(H,17,20)(H,22,23)/b18-7-/t8-,12+/m0/s1

HIDE SMILES / InChI

Molecular Formula	C14H13N5O5S2
Molecular Weight	395.414
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	2 / 2
E/Z Centers	1
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Wed Apr 02 17:09:19 GMT 2025` Edited by `admin` on `Wed Apr 02 17:09:19 GMT 2025`
Record UNII	S9QB3QE3HT
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

Cefdinir, 7(S)-

Common Name

English

7(S)-Cefdinir

Preferred Name

English

5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2-amino-4-thiazolyl)(hydroxyimino)acetyl]amino]-3-ethenyl-8-oxo-, [6R-[6?,7?(Z)]]-

Systematic Name

English

5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(hydroxyimino)acetyl]amino]-3-ethenyl-8-oxo-, (6R,7S)-

Systematic Name

English

(6R,7S)-7-[[(2Z)-2-(2-Amino-4-thiazolyl)-2-(hydroxyimino)acetyl]amino]-3-ethenyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

Systematic Name

English

Code System Code Type Description

EPA CompTox

DTXSID001101178

Created by admin on Wed Apr 02 17:09:19 GMT 2025 , Edited by admin on Wed Apr 02 17:09:19 GMT 2025

PRIMARY

PUBCHEM

87792518

Created by admin on Wed Apr 02 17:09:19 GMT 2025 , Edited by admin on Wed Apr 02 17:09:19 GMT 2025

PRIMARY

FDA UNII

S9QB3QE3HT

Created by admin on Wed Apr 02 17:09:19 GMT 2025 , Edited by admin on Wed Apr 02 17:09:19 GMT 2025

PRIMARY

CAS

178601-89-3

Created by admin on Wed Apr 02 17:09:19 GMT 2025 , Edited by admin on Wed Apr 02 17:09:19 GMT 2025

PRIMARY