CEFACLOR

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C15H14ClN3O4S.H2O
Molecular Weight	385.823
Optical Activity	UNSPECIFIED
Defined Stereocenters	3 / 3
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of CEFACLOR

Structure Search

SMILES

O.[H][C@]12SCC(Cl)=C(N1C(=O)[C@H]2NC(=O)[C@H](N)C3=CC=CC=C3)C(O)=O

InChI

InChIKey=WKJGTOYAEQDNIA-IOOZKYRYSA-N

InChI=1S/C15H14ClN3O4S.H2O/c16-8-6-24-14-10(13(21)19(14)11(8)15(22)23)18-12(20)9(17)7-4-2-1-3-5-7;/h1-5,9-10,14H,6,17H2,(H,18,20)(H,22,23);1H2/t9-,10-,14-;/m1./s1

HIDE SMILES / InChI

Molecular Formula	C15H14ClN3O4S
Molecular Weight	367.807
Charge	0
Count

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

Molecular Formula	H2O
Molecular Weight	18.0153
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:16:39 UTC 2023` Edited by `admin` on `Fri Dec 15 15:16:39 UTC 2023`
Record UNII	69K7K19H4L
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

CEFACLOR

Official Name

English

Cefaclor monohydrate [WHO-DD]

Common Name

English

COMPOUND 99638

Code

English

J01DC04

Code

English

CEFACLOR MONOHYDRATE [VANDF]

Common Name

English

(6R,7R)-7-[(R)-2-Amino-2-phenylacetamido]-3-chloro-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid monohydrate

Systematic Name

English

CEFACLOR [VANDF]

Common Name

English

CECLOR

Brand Name

English

CEFACLOR MONOHYDRATE [MI]

Common Name

English

CEFACLOR MONOHYDRATE

Common Name

English

COMPOUND-99638

Code

English

CEFACLOR [USAN]

Common Name

English

CEFACLOR [USP-RS]

Common Name

English

CEFACLOR [ORANGE BOOK]

Common Name

English

CEFACLOR [MART.]

Common Name

English

CEFACLOR [EP MONOGRAPH]

Common Name

English

3-CHLORO-7-D-(2-PHENYLGLYCINAMIDO)-3-CEPHEM-4-CARBOXYLIC ACID MONOHYDRATE

Common Name

English

NSC-757422

Code

English

5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID, 7-((AMINOPHENYLACETYL)AMINO)-3-CHLORO-8-OXO-, MONOHYDRATE, (6R-(6.ALPHA.,7.BETA.(R*)))-

Common Name

English

CEFACLOR [USP MONOGRAPH]

Common Name

English

RANICLOR

Brand Name

English

Classification Tree Code System Code

WHO-VATC

QJ01DC04

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

NDF-RT

N0000175488

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

NCI_THESAURUS

C357

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

WHO-ATC

J01DC04

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

LIVERTOX

NBK548666

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

LIVERTOX

NBK548358

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

Code System Code Type Description

DRUG BANK

DB00833

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

PRIMARY

RS_ITEM_NUM

1096906

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

PRIMARY

PUBCHEM

51038

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

PRIMARY

EVMPD

SUB13271MIG

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

PRIMARY

EPA CompTox

DTXSID80990551

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

PRIMARY

ChEMBL

CHEMBL680

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

PRIMARY

CHEBI

3478

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

PRIMARY

FDA UNII

69K7K19H4L

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

PRIMARY

NCI_THESAURUS

C28911

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

PRIMARY

DRUG CENTRAL

525

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

PRIMARY

SMS_ID

100000089869

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

PRIMARY

CAS

70356-03-5

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

PRIMARY

LACTMED

Cefaclor

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

PRIMARY

NSC

757422

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

PRIMARY

MERCK INDEX

m3184

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

PRIMARY

Merck Index

DAILYMED

69K7K19H4L

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

PRIMARY

MESH

D002433

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

PRIMARY

RXCUI

2176

Created by admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023

PRIMARY

RxNorm

Related Record Type Details


					3Z6FS3IK0K

CEFACLOR ANHYDROUS

PARENT -> SALT/SOLVATE

Amount:


					3Z6FS3IK0K

CEFACLOR ANHYDROUS

ANHYDROUS->SOLVATE

Amount:

Related Record Type Details


					E131SU560G

3-Phenyl-2(1H)-pyrazinone

IMPURITY -> PARENT

Amount:


					QBD8CQ4TN8

7-[[(2R)-aminophenylacetyl]amino]-3-chloro-8-oxo-5-Thia-1-azabicyclo[4.2.0]oct-3-ene-2-carboxylic acid, (6R,7R)-

IMPURITY -> PARENT

Amount:


					RR9S2A3JZG

2-[[(2R)-2-amino-2-phenylacetyl]amino]-2-(5-chloro-4-oxo-3,4-dihydro-2H-1,3-thiazin-2-yl)acetic acid

IMPURITY -> PARENT

Amount:


					YUK95YEL4R

IMPURITY -> PARENT

Amount:

Related Record Type Details


					3Z6FS3IK0K

CEFACLOR ANHYDROUS

ACTIVE MOIETY

Amount:

Name	Property Type	Amount	Referenced Substance	Defining	Parameters	References
Biological Half-life	PHARMACOKINETIC