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

Details

Stereochemistry ABSOLUTE
Molecular Formula C20H20N6O7S4
Molecular Weight 584.669
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CEFODIZIME

SMILES

[H][C@]12SCC(CSC3=NC(C)=C(CC(O)=O)S3)=C(N1C(=O)[C@H]2NC(=O)C(=N/OC)\C4=CSC(N)=N4)C(O)=O

InChI

InChIKey=XDZKBRJLTGRPSS-BGZQYGJUSA-N
InChI=1S/C20H20N6O7S4/c1-7-10(3-11(27)28)37-20(22-7)36-5-8-4-34-17-13(16(30)26(17)14(8)18(31)32)24-15(29)12(25-33-2)9-6-35-19(21)23-9/h6,13,17H,3-5H2,1-2H3,(H2,21,23)(H,24,29)(H,27,28)(H,31,32)/b25-12-/t13-,17-/m1/s1

HIDE SMILES / InChI

Molecular Formula C20H20N6O7S4
Molecular Weight 584.669
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 Fri Dec 15 17:12:15 UTC 2023
Edited
by admin
on Fri Dec 15 17:12:15 UTC 2023
Record UNII
Z31298J4HQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CEFODIZIME
INN   MI   WHO-DD  
INN  
Official Name English
THR 221 FREE ACID
Code English
S-77-1221-B FREE ACID
Code English
(6R,7R)-7-(2-(2-AMINO-4-THIAZOLYL)GLYOXYLAMIDO)-3-(((5-(CARBOXYMETHYL)-4-METHYL-2-THIAZOLYL)THIO)METHYL)-8-OXO-5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID 7(SUP 2)-(Z)-(O-METHYLOXIME)
Common Name English
cefodizime [INN]
Common Name English
S 77 1221 B FREE ACID
Code English
HR 221 FREE ACID
Code English
CEFODIZIME SODIUM [JAN]
Common Name English
Cefodizime [WHO-DD]
Common Name English
HR-221 FREE ACID
Code English
THR-221 FREE ACID
Code English
CEFODIZIME [MI]
Common Name English
Classification Tree Code System Code
WHO-VATC QJ01DD09
Created by admin on Fri Dec 15 17:12:15 UTC 2023 , Edited by admin on Fri Dec 15 17:12:15 UTC 2023
NCI_THESAURUS C357
Created by admin on Fri Dec 15 17:12:15 UTC 2023 , Edited by admin on Fri Dec 15 17:12:15 UTC 2023
WHO-ATC J01DD09
Created by admin on Fri Dec 15 17:12:15 UTC 2023 , Edited by admin on Fri Dec 15 17:12:15 UTC 2023
Code System Code Type Description
MERCK INDEX
m3199
Created by admin on Fri Dec 15 17:12:15 UTC 2023 , Edited by admin on Fri Dec 15 17:12:15 UTC 2023
PRIMARY Merck Index
DRUG CENTRAL
541
Created by admin on Fri Dec 15 17:12:15 UTC 2023 , Edited by admin on Fri Dec 15 17:12:15 UTC 2023
PRIMARY
SMS_ID
100000081823
Created by admin on Fri Dec 15 17:12:15 UTC 2023 , Edited by admin on Fri Dec 15 17:12:15 UTC 2023
PRIMARY
INN
4967
Created by admin on Fri Dec 15 17:12:15 UTC 2023 , Edited by admin on Fri Dec 15 17:12:15 UTC 2023
PRIMARY
RXCUI
20485
Created by admin on Fri Dec 15 17:12:15 UTC 2023 , Edited by admin on Fri Dec 15 17:12:15 UTC 2023
PRIMARY RxNorm
NCI_THESAURUS
C98224
Created by admin on Fri Dec 15 17:12:15 UTC 2023 , Edited by admin on Fri Dec 15 17:12:15 UTC 2023
PRIMARY
FDA UNII
Z31298J4HQ
Created by admin on Fri Dec 15 17:12:15 UTC 2023 , Edited by admin on Fri Dec 15 17:12:15 UTC 2023
PRIMARY
ChEMBL
CHEMBL2303613
Created by admin on Fri Dec 15 17:12:15 UTC 2023 , Edited by admin on Fri Dec 15 17:12:15 UTC 2023
PRIMARY
WIKIPEDIA
Cefodizime
Created by admin on Fri Dec 15 17:12:15 UTC 2023 , Edited by admin on Fri Dec 15 17:12:15 UTC 2023
PRIMARY
MESH
C033356
Created by admin on Fri Dec 15 17:12:15 UTC 2023 , Edited by admin on Fri Dec 15 17:12:15 UTC 2023
PRIMARY
EPA CompTox
DTXSID2022757
Created by admin on Fri Dec 15 17:12:15 UTC 2023 , Edited by admin on Fri Dec 15 17:12:15 UTC 2023
PRIMARY
DRUG BANK
DB13470
Created by admin on Fri Dec 15 17:12:15 UTC 2023 , Edited by admin on Fri Dec 15 17:12:15 UTC 2023
PRIMARY
PUBCHEM
5361871
Created by admin on Fri Dec 15 17:12:15 UTC 2023 , Edited by admin on Fri Dec 15 17:12:15 UTC 2023
PRIMARY
CAS
69739-16-8
Created by admin on Fri Dec 15 17:12:15 UTC 2023 , Edited by admin on Fri Dec 15 17:12:15 UTC 2023
PRIMARY
CHEBI
63214
Created by admin on Fri Dec 15 17:12:15 UTC 2023 , Edited by admin on Fri Dec 15 17:12:15 UTC 2023
PRIMARY
EVMPD
SUB07401MIG
Created by admin on Fri Dec 15 17:12:15 UTC 2023 , Edited by admin on Fri Dec 15 17:12:15 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY