CEPHRADINE ANHYDROUS

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C16H19N3O4S
Molecular Weight	349.405
Optical Activity	UNSPECIFIED
Defined Stereocenters	3 / 3
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of CEPHRADINE ANHYDROUS

Structure Search

SMILES

[H][C@]12SCC(C)=C(N1C(=O)[C@H]2NC(=O)[C@H](N)C3=CCC=CC3)C(O)=O

InChI

InChIKey=RDLPVSKMFDYCOR-UEKVPHQBSA-N

InChI=1S/C16H19N3O4S/c1-8-7-24-15-11(14(21)19(15)12(8)16(22)23)18-13(20)10(17)9-5-3-2-4-6-9/h2-3,6,10-11,15H,4-5,7,17H2,1H3,(H,18,20)(H,22,23)/t10-,11-,15-/m1/s1

HIDE SMILES / InChI

Molecular Formula	C16H19N3O4S
Molecular Weight	349.405
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	3 / 3
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Sat Dec 16 17:07:46 UTC 2023` Edited by `admin` on `Sat Dec 16 17:07:46 UTC 2023`
Record UNII	9YA6SX5S4D
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

CEPHRADINE ANHYDROUS

Common Name

English

Cefradine [WHO-DD]

Common Name

English

cefradine [INN]

Common Name

English

CEFRADINE [EP MONOGRAPH]

Common Name

English

CEFRADINE [JAN]

Common Name

English

5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID, 7-((AMINO-1,4-CYCLOHEXADIEN-1-YLACETYL)AMINO)-3-METHYL-8-OXO-, (6R-(6.ALPHA.,7.BETA.(R*)))-

Common Name

English

CEFRADINE

Official Name

English

(6R,7R)-7-(((2R)-2-AMINO-2-CYCLOHEXA-1,4-DIEN-1-YLACETYL)AMINO)-3-METHYL-8-OXO-5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID

Systematic Name

English

NSC-756672

Code

English

CEFRADINE [MART.]

Common Name

English

(6R,7R)-7-((R)-2-AMINO-2-(1,4-CYCLOHEXADIEN-1-YL)ACETAMIDO)-3-METHYL-8-OXO-5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID

Systematic Name

English

CEPHRADINE [MI]

Common Name

English

CEPHRADINE [HSDB]

Common Name

English

Classification Tree Code System Code

NDF-RT

N0000011161

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

NDF-RT

N0000011161

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

NDF-RT

N0000011161

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

WHO-VATC

QJ01DB09

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

NDF-RT

N0000011161

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

LIVERTOX

NBK547862

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

NDF-RT

N0000011161

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

NCI_THESAURUS

C357

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

NDF-RT

N0000011161

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

NDF-RT

N0000011161

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

LIVERTOX

NBK548666

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

NDF-RT

N0000175488

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

WHO-ATC

J01DB09

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

LIVERTOX

NBK548358

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

NDF-RT

N0000011161

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

NDF-RT

N0000011161

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

NDF-RT

N0000011161

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

NDF-RT

N0000011161

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

NDF-RT

N0000011161

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

Code System Code Type Description

EPA CompTox

DTXSID4022785

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

PRIMARY

ECHA (EC/EINECS)

254-137-8

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

PRIMARY

FDA UNII

9YA6SX5S4D

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

PRIMARY

DRUG CENTRAL

576

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

PRIMARY

INN

3119

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

PRIMARY

SMS_ID

100000092817

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

PRIMARY

CHEBI

3547

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

PRIMARY

MERCK INDEX

m3255

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

PRIMARY

Merck Index

HSDB

3216

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

PRIMARY

NCI_THESAURUS

C76181

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

PRIMARY

WIKIPEDIA

CEFRADINE

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

PRIMARY

PUBCHEM

38103

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

PRIMARY

DRUG BANK

DB01333

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

PRIMARY

ChEMBL

CHEMBL1604

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

PRIMARY

NSC

756672

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

PRIMARY

CAS

38821-53-3

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

PRIMARY

EVMPD

SUB07417MIG

Created by admin on Sat Dec 16 17:07:48 UTC 2023 , Edited by admin on Sat Dec 16 17:07:48 UTC 2023

PRIMARY

Related Record Type Details


					FUC0D71IZN

CEPHRADINE MONOHYDRATE

SALT/SOLVATE -> PARENT

Amount:


					FUC0D71IZN

CEPHRADINE MONOHYDRATE

SOLVATE->ANHYDROUS

Amount:


					41BJN3H129

CEPHRADINE LYSINATE

SALT/SOLVATE -> PARENT

Amount:


					56PPJ9MMPE

CEPHRADINE DIHYDRATE

SOLVATE->ANHYDROUS

Amount:


					04FRJ20XNF

CEPHRADINE SODIUM

SALT/SOLVATE -> PARENT


					56PPJ9MMPE

CEPHRADINE DIHYDRATE

SALT/SOLVATE -> PARENT

Amount:

Related Record Type Details


					451NQ27TG5

2,5-DIHYDROPHENYLGLYCINE, D-

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					EKZ86TVS3U

2-HYDROXYCEPHALEXIN

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					ANM3MSM8TN

7-AMINODESACETOXYCEPHALOSPORANIC ACID

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					82S555S2NY

3-HYDROXY-4-METHYLTHIOPHEN-2(5H)-ONE

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					QXP69Z5JWA

CEFRADINE OXIDE D

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					MDO0VUD5WQ

N-PIVALOYL 7-AMINODESACETOXYCEPHALOSPORANIC ACID

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:

Related Record Type Details


					9YA6SX5S4D

CEPHRADINE ANHYDROUS

ACTIVE MOIETY

Amount: