CHEBI:19363 - 2,5-bis(aziridin-1-yl)-1,4-benzoquinone

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ChEBI Name 2,5-bis(aziridin-1-yl)-1,4-benzoquinone
ChEBI ID CHEBI:19363
Definition A member of the class of 1,4-benzoquinones that is p-benzoquinone in which the hydrogens at positions 2 and 5 are replaced by aziridin-1-yl groups.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C10H10N2O2
Net Charge 0
Average Mass 190.19868
Monoisotopic Mass 190.07423
InChI InChI=1S/C10H10N2O2/c13-9-6-8(12-3-4-12)10(14)5-7(9)11-1-2-11/h5-6H,1-4H2
InChIKey RCWJMKCTHJPXJV-UHFFFAOYSA-N
SMILES O=C1C=C(N2CC2)C(=O)C=C1N1CC1
Roles Classification
Biological Role(s): alkylating agent
Highly reactive chemical that introduces alkyl radicals into biologically active molecules and thereby prevents their proper functioning. It could be used as an antineoplastic agent, but it might be very toxic, with carcinogenic, mutagenic, teratogenic, and immunosuppressant actions. It could also be used as a component of poison gases.
mutagen
An agent that increases the frequency of mutations above the normal background level, usually by interacting directly with DNA and causing it damage, including base substitution.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2,5-bis(aziridin-1-yl)-1,4-benzoquinone (CHEBI:19363) has role alkylating agent (CHEBI:22333)
2,5-bis(aziridin-1-yl)-1,4-benzoquinone (CHEBI:19363) has role mutagen (CHEBI:25435)
2,5-bis(aziridin-1-yl)-1,4-benzoquinone (CHEBI:19363) is a 1,4-benzoquinones (CHEBI:132124)
2,5-bis(aziridin-1-yl)-1,4-benzoquinone (CHEBI:19363) is a aziridines (CHEBI:22681)
IUPAC Name
2,5-bis(aziridin-1-yl)cyclohexa-2,5-diene-1,4-dione
Synonyms Sources
2,5,-bis(ethyleneimine)-1,4-benzoquinone ChEBI
2,5,-bisethylene-imine-1,4-benzoquinone ChEBI
2,5-bis(1-aziridinyl)-2,5-cyclohexadiene-1,4-dione ChemIDplus
2,5-bis(1-aziridinyl)-p-benzoquinone ChemIDplus
2,5-bis(1-aziridynyl)benzoquinone ChemIDplus
2,5-bis(aziridino)-1,4-benzoquinone ChemIDplus
2,5-bis(aziridino)benzoquinone ChemIDplus
2,5-bis(ethyleneimino)-1,4-benzoquinone ChemIDplus
2,5-bis-ethyleniminobenzoquinone ChemIDplus
2,5-Bisäthyleniminobenzochinon-1,4 ChEBI
2,5-bisethyleneiminebenzoquinone ChemIDplus
2,5-di(ethyleneimino)-1,4-benzoquinone ChemIDplus
2,5-diaziridinyl-1,4-benzoquinone ChemIDplus
3,6-diaziridinyl-1,4-benzoquinone ChEBI
DZQ ChEBI
ethylenimine quinone ChemIDplus
TW 13 ChemIDplus
Registry Numbers Types Sources
169182 Reaxys Registry Number Reaxys
169182 Beilstein Registry Number Beilstein
526-62-5 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
10373575 PubMed citation Europe PMC
10978162 PubMed citation Europe PMC
11211879 PubMed citation Europe PMC
13415397 PubMed citation Europe PMC
17094478 PubMed citation Europe PMC
1751490 PubMed citation Europe PMC
8137269 PubMed citation Europe PMC
8461296 PubMed citation Europe PMC
9690517 PubMed citation Europe PMC
Last Modified
06 July 2016