cefdinir
A cephalosporin compound having 7β-2-(2-amino-thiazol-4-yl)-2-[(Z)-hydroxyimino]-acetylamino- and 3-vinyl side groups.
Machine-generated and unreviewed. Identity, structure and cross-references come straight from ChEBI's and CARD's own data; no curator has signed off on this record yet.
Classification
cephalosporinARO:0000032
- cephalosporin
CHEBI:23066 -
CHEBI:24983 - cephalosporin
ARO:0000032
Chemical structure
| Molecular formula | C14H13N5O5S2 |
|---|---|
| Charge | 0 |
| Average mass | 395.422 Da |
| Monoisotopic mass | 395.03581 Da |
| Source | ChEBI |
| InChIKey | RTXOFQZKPXMALH-GHXIOONMSA-N |
C=CC1=C(C(=O)O)N2C(=O)[C@@H](NC(=O)/C(=N\O)c3csc(N)n3)[C@H]2SC1
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-/m1/s1
Also called
- cefdinirum
- (6R,7R)-7-{[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(hydroxyimino)acetyl]amino}-3-ethenyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
- 7β-[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(hydroxyimino)acetamido]-3-ethenyl-3,4-didehydrocepham-4-carboxylic acid
- (6R,7R)-7-{2-(2-Amino-thiazol-4-yl)-2-[(Z)-hydroxyimino]-acetylamino}-8-oxo-3-vinyl-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid
- (6R,7R,Z)-7-(2-(2-aminothiazol-4-yl)-2-(hydroxyimino)acetamido)-8-oxo-3-vinyl-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid
- CFDN
- CDR
Cross-references
- cefdinir
ARO:3000650 - beilstein:6829362
- cas:91832-40-5
- kegg.compound:C08110
- chembl:CHEMBL134561
- pubchem.compound:6915944
Drug registries
Patents and articles
Activity roles
- antimicrobial agent
CHEBI:33281 - antibacterial drug
CHEBI:36047
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| ARO | ARO:3000650 |
cefdinir | antibioticmech:aro-1fb7c4a747 |
2026-08-30 |
| CHEBI | CHEBI:3485 |
cefdinir | antibioticmech:chebi-7560371759 |
2026-08-30 |
Molecular targets
beta-lactam sensitive penicillin-binding protein PROTEIN DIRECT_BINDING_TARGET
Mechanism summary
- Clinical status
- APPROVED
Resistance mechanisms
ANTIBIOTIC_TARGET_ALTERATION 1
| Determinant | ARO ID | Organism | Gene families | Evidence |
|---|---|---|---|---|
| Haemophilus influenzae PBP3 conferring resistance to beta-lactam antibiotics | ARO:3004446 | — |
Curation history
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SEEDED_FROM_SOURCES
Seeded from data/raw/ inventories (ARO, CHEBI)
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RESEEDED_FROM_SOURCES
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories