CHEBI:75319 - 3,3'-neotrehalosadiamine

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ChEBI Name 3,3'-neotrehalosadiamine
ChEBI ID CHEBI:75319
Definition An amino disaccharide consisting of α- and β-D-kanosaminyl residues joined by a (1↔1)-linkage.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C12H24N2O9
Net Charge 0
Average Mass 340.32700
Monoisotopic Mass 340.14818
InChI InChI=1S/C12H24N2O9/c13-5-7(17)3(1-15)21-11(9(5)19)23-12-10(20)6(14)8(18)4(2-16)22-12/h3-12,15-20H,1-2,13-14H2/t3-,4-,5+,6+,7-,8-,9-,10-,11-,12+/m1/s1
InChIKey ZPEFXARQZVAHGO-DCSYEGIMSA-N
SMILES N[C@H]1[C@H](O)[C@@H](CO)O[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](N)[C@H]2O)[C@@H]1O
Roles Classification
Biological Role(s): antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 3,3'-neotrehalosadiamine (CHEBI:75319) has role antimicrobial agent (CHEBI:33281)
3,3'-neotrehalosadiamine (CHEBI:75319) has role metabolite (CHEBI:25212)
3,3'-neotrehalosadiamine (CHEBI:75319) is a amino disaccharide (CHEBI:22480)
3,3'-neotrehalosadiamine (CHEBI:75319) is a glycosyl glycoside derivative (CHEBI:63356)
3,3'-neotrehalosadiamine (CHEBI:75319) is conjugate base of 3,3'-neotrehalosadiamine(2+) (CHEBI:75053)
Incoming 3,3'-neotrehalosadiamine(2+) (CHEBI:75053) is conjugate acid of 3,3'-neotrehalosadiamine (CHEBI:75319)
IUPAC Name
3-amino-3-deoxy-β-D-glucopyranosyl 3-amino-3-deoxy-α-D-glucopyranoside
Synonyms Sources
3,3'-Diamino-3,3'-dideoxy-alpha,beta-trehalose ChemIDplus
β-D-Glc3N-(1↔1)-α-D-Gl3N ChEBI
β-D-kanosaminyl-(1↔1)-α-D-kanosamine ChEBI
Registry Numbers Types Sources
104196-14-7 CAS Registry Number ChemIDplus
23730595 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
19342798 PubMed citation Europe PMC
23586652 PubMed citation Europe PMC
Last Modified
22 August 2013