Structure via PubChem · Public domain (PubChem)
cefixime
Sign in to saveAlso known as CL-284635, FK-027, FR-17027, cefixime anhydrous, (−)-cefixime, suprax
chemische verbinding
In the Vinony graph
Within Vinony's link graph, cefixime is referenced by 213 other articles, and connects out to antibiotic, ceftolozane/tazobactam and penicillin binding proteins.
Vinony files it under Cephalosporin antibiotics, Dermatoxins and Drugboxes which contain changes to verified fields.
Its subject is documented across 30 Wikipedia language editions.
Key facts
- Drug.Verifiedfields
- changed
- Drug.Watchedfields
- changed
- Drug.verifiedrevid
- 460023156
- Drug.image
- Cefixime skeletal structure.svg
- Drug.image_class
- skin-invert-image
- Drug.image2
- Cefixime ball-and-stick model from xtal 2013.png
- Drug.image_class2
- bg-transparent
- Drug.tradename
- Suprax, others
- Drug.MedlinePlus
- a690007
- Drug.DailyMedID
- Cefixime
- Drug.routes_of_administration
- By mouth
- Drug.ATC_prefix
- J01
- Drug.ATC_suffix
- DD08
- Drug.legal_CA
- Rx-only
- Drug.legal_UK
- POM
- Drug.legal_US
- Rx-only
- Drug.legal_status
- Rx-only
- Drug.bioavailability
- 30 to 50%
via Wikipedia infobox
Chemical data
- Formula
- C16H15N5O7S2
- Molecular weight
- 453.5 g/mol
- IUPAC name
- (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(carboxymethoxyimino)acetyl]amino]-3-ethenyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
- SMILES
- C=CC1=C(N2[C@@H]([C@@H](C2=O)NC(=O)/C(=N\OCC(=O)O)/C3=CSC(=N3)N)SC1)C(=O)O
- InChIKey
- OKBVVJOGVLARMR-QSWIMTSFSA-N
- XLogP
- -0.7
- Polar surface area
- 238 Ų
- H-bond donors
- 4
- H-bond acceptors
- 12
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Approved
- Molecule type
- Small molecule
- First approval
- 1989
- Admin. routes
- oral
- Indications
- Otitis media, infection, neoplasm, osteomyelitis
via ChEMBL · EBI
Wikidata facts
- Subclass of
- cephalosporin antibiotic
- Mass
- 453.04128982000003
- Has use
- medication
Show 9 more facts
- chemical formula
- C₁₆H₁₅N₅O₇S₂
- subject has role
- enzyme inhibitor
- medical condition treated
- otitis media
- canonical SMILES
- C=CC1=C(N2C(C(C2=O)NC(=O)C(=NOCC(=O)O)C3=CSC(=N3)N)SC1)C(=O)O
- isomeric SMILES
- C=CC1=C(N2[C@@H]([C@@H](C2=O)NC(=O)/C(=N\OCC(=O)O)/C3=CSC(=N3)N)SC1)C(=O)O
- World Health Organisation international non-proprietary name
- cefixime
- NCI Thesaurus ID
- C1100
- defined daily dose
- 0.4
- Commons category
- Cefixime
Sources (7)
via Wikidata · CC0
Connections
antibiotic
Entity
ceftolozane/tazobactam
Entity
penicillin binding proteins
Entity
World Health Organization
Entity
human pregnancy
Entity
kidney
Entity
International Standard Book Number
Entity
pneumonia
Entity
urine
Entity
diarrhea
Entity
allergy
Entity
penicillin
Entity
digital object identifier
Entity
chemical formula
Entity
typhoid fever
Entity
gonorrhea
Entity
patent
Entity
Escherichia coli
Entity
bile
Entity
veterinary medicine
Entity