CHEBI:50138 - lonidamine

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ChEBI Name lonidamine
Definition A member of the class of indazoles that is 1H-indazole that is substituted at positions 1 and 3 by 2,4-dichlorobenzyl and carboxy groups, respectively.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C15H10Cl2N2O2
Net Charge 0
Average Mass 321.15758
Monoisotopic Mass 320.01193
InChI InChI=1S/C15H10Cl2N2O2/c16-10-6-5-9(12(17)7-10)8-19-13-4-2-1-3-11(13)14(18-19)15(20)21/h1-7H,8H2,(H,20,21)
SMILES OC(=O)c1nn(Cc2ccc(Cl)cc2Cl)c2ccccc12
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Application(s): antispermatogenic agent
An agent that destroy spermatozoa in the male genitalia and block spermatogenesis.
antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing lonidamine (CHEBI:50138) has role antineoplastic agent (CHEBI:35610)
lonidamine (CHEBI:50138) has role antispermatogenic agent (CHEBI:145047)
lonidamine (CHEBI:50138) is a dichlorobenzene (CHEBI:23697)
lonidamine (CHEBI:50138) is a indazoles (CHEBI:38769)
lonidamine (CHEBI:50138) is a monocarboxylic acid (CHEBI:25384)
Incoming gamendazole (CHEBI:90703) has functional parent lonidamine (CHEBI:50138)
1-(2,4-dichlorobenzyl)-1H-indazole-3-carboxylic acid
INNs Sources
lonidamina ChemIDplus
lonidamine ChemIDplus
lonidaminum ChemIDplus
Synonyms Sources
1-(2,4-dichlorbenzyl)-indazole-3-carboxylic acid ChemIDplus
DICA ChemIDplus
diclondazolic acid ChemIDplus
Lonidamin ChEBI
Brand Name Source
Doridamina ChemIDplus
Manual Xrefs Databases
1598 DrugCentral
DE2310031 Patent
Lonidamine Wikipedia
US3895026 Patent
View more database links
Registry Numbers Types Sources
50264-69-2 CAS Registry Number ChemIDplus
894483 Beilstein Registry Number Beilstein
Citations Waiting for Citations Types Sources
26831515 PubMed citation Europe PMC
27497601 PubMed citation Europe PMC
Last Modified
08 October 2019