General Information of Drug (ID: DR5437)
Drug Name
Carbenicillin Indanyl Sodium
Synonyms Geocillin
Indication Bacterial infection [ICD11: 1A00-1C4Z] Approved [1]
Structure
3D MOL is unavailable 2D MOL
Pharmaceutical Properties Molecular Weight 516.5 Topological Polar Surface Area 141
Heavy Atom Count 36 Rotatable Bond Count 7
Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 7
Cross-matching ID
PubChem CID
23676503
ChEBI ID
CHEBI:31358
CAS Number
26605-69-6
TTD Drug ID
D0PN1F
Formula
C26H25N2NaO6S
Canonical SMILES
CC1([C@@H](N2[C@H](S1)[C@@H](C2=O)NC(=O)C(C3=CC=CC=C3)C(=O)OC4=CC5=C(CCC5)C=C4)C(=O)[O-])C.[Na+]
InChI
InChI=1S/C26H26N2O6S.Na/c1-26(2)20(24(31)32)28-22(30)19(23(28)35-26)27-21(29)18(15-7-4-3-5-8-15)25(33)34-17-12-11-14-9-6-10-16(14)13-17;/h3-5,7-8,11-13,18-20,23H,6,9-10H2,1-2H3,(H,27,29)(H,31,32);/q;+1/p-1/t18?,19-,20+,23-;/m1./s1
InChIKey
QFWPXOXWAUAYAB-XZVIDJSISA-M
The Metabolic Roadmap of This Drug
The Full List of Drug Metabolites (DM) of This Drug
DM Name DM ID PubChem ID Reaction DM Level REF
Carbenicillin DM014986
20824
Unclear - Unclear 1 [2]
The Full List of Metabolic Reaction (MR) of This Drug
MR ID Reactant Product MR Type DME REF
MR008094 Carbenicillin Indanyl Sodium Carbenicillin Unclear - Unclear ES [2]
Drug-Metabolizing Enzyme(s) (DME) Metabolizing This Drug
DME Name DME Info Species Uniprot ID EC Number REF
Esterases (ES) DMEN229 Homo sapiens Not Available Not Available [2]
References
1 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services. 2015
2 GI absorption of beta-lactam antibiotics I: kinetic assessment of competing absorption and degradation in GI tract

If you find any error in data or bug in web service, please kindly report it to Dr. Yin and Dr. Li.