CHEBI:3606 - Chloramphenicol succinate

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name Chloramphenicol succinate
ChEBI ID CHEBI:3606
Stars This entity has been manually annotated by a third party.
Supplier Information
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Formula C15H16Cl2N2O8
Net Charge 0
Average Mass 423.20200
InChI InChI=1S/C15H16Cl2N2O8/c16-14(17)15(24)18-10(7-27-12(22)6-5-11(20)21)13(23)8-1-3-9(4-2-8)19(25)26/h1-4,10,13-14,23H,5-7H2,(H,18,24)(H,20,21)/t10-,13-/m1/s1
InChIKey LIRCDOVJWUGTMW-ZWNOBZJWSA-N
SMILES C1([C@H]([C@](NC(C(Cl)Cl)=O)(COC(=O)CCC(O)=O)[H])O)=CC=C([N+](=O)[O-])C=C1
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Application(s): central nervous system stimulant
Any drug that enhances the activity of the central nervous system.
(via amphetamines )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing Chloramphenicol succinate (CHEBI:3606) is a amphetamines (CHEBI:35338)
Chloramphenicol succinate (CHEBI:3606) is a hemisuccinate (CHEBI:138979)
Synonyms Sources
chloramphenicol monosuccinate sodium salt DrugCentral
chloramphenicol sodium succinate DrugCentral
Chloramphenicol succinate KEGG COMPOUND
chloramphenicol succinate sodium DrugCentral
levomycetin sodium succinate DrugCentral
sodium chloramphenicol succinate DrugCentral
Manual Xrefs Databases
4653 DrugCentral
C11727 KEGG COMPOUND
C13962 KEGG COMPOUND
CL8 PDBeChem
D02185 KEGG DRUG
D07675 KEGG DRUG
View more database links
Registry Number Type Source
3544-94-3 CAS Registry Number KEGG COMPOUND
Last Modified
09 November 2017