U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C15H14ClN3O4S
Molecular Weight 367.807
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CEFACLOR ANHYDROUS

SMILES

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

InChI

InChIKey=QYIYFLOTGYLRGG-GPCCPHFNSA-N
InChI=1S/C15H14ClN3O4S/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)/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

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:44:22 UTC 2023
Edited
by admin
on Fri Dec 15 15:44:22 UTC 2023
Record UNII
3Z6FS3IK0K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CEFACLOR ANHYDROUS
Common Name English
Cefaclor [WHO-DD]
Common Name English
CEFACLOR IMPURITY C [EP IMPURITY]
Common Name English
CEFACLOR [MI]
Common Name English
cefaclor [INN]
Common Name English
CEFACLOR [JAN]
Common Name English
5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID, 7-(((2R)-2-AMINO-2-PHENYLACETYL)AMINO)-3-CHLORO-8-OXO-, (6R,7R)-
Common Name English
(6R,7R)-7-(((2R)-2-AMINO-2-PHENYLACETYL)AMINO)-3-CHLORO-8-OXO-5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID
Systematic Name English
Classification Tree Code System Code
NDF-RT N0000175488
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
WHO-ATC J01DC04
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
NCI_THESAURUS C357
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
LIVERTOX NBK548666
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
LIVERTOX NBK548358
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
Code System Code Type Description
SMS_ID
100000092421
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
PRIMARY
CAS
53994-73-3
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
PRIMARY
INN
4086
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
PRIMARY
FDA UNII
3Z6FS3IK0K
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
PRIMARY
NCI_THESAURUS
C76033
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
PRIMARY
CHEBI
3478
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
PRIMARY
DAILYMED
3Z6FS3IK0K
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
PRIMARY
EVMPD
SUB06163MIG
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
PRIMARY
DRUG BANK
DB00833
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
PRIMARY
RXCUI
1450910
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
PRIMARY RxNorm
EPA CompTox
DTXSID3022748
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
PRIMARY
WIKIPEDIA
Cefaclor
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
PRIMARY
MERCK INDEX
m3184
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
258-909-5
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
PRIMARY
PUBCHEM
51039
Created by admin on Fri Dec 15 15:44:22 UTC 2023 , Edited by admin on Fri Dec 15 15:44:22 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SOLVATE->ANHYDROUS
TRANSPORTER -> INHIBITOR
Ki
SALT/SOLVATE -> PARENT
EXCRETED UNCHANGED
Approximately 60% to 85% of the drug is excreted unchanged in the urine within 8 hours, the greater portion being excreted within the first 2 hours.
URINE
SOLVATE->ANHYDROUS
BINDER->LIGAND
BINDING
Related Record Type Details
ACTIVE MOIETY