CHEBI:7933 - paromamine

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ChEBI Name paromamine
ChEBI ID CHEBI:7933
Definition An aminoglycoside that is 4α,6α-diaminocyclohexane-1β,2α,3β-triol in which the pro-R hydroxy group has been converted into its 2-amino-α-D-glucoside derivative.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C12H25N3O7
Net Charge 0
Average Mass 323.34280
Monoisotopic Mass 323.16925
InChI InChI=1S/C12H25N3O7/c13-3-1-4(14)11(10(20)7(3)17)22-12-6(15)9(19)8(18)5(2-16)21-12/h3-12,16-20H,1-2,13-15H2/t3-,4+,5-,6-,7+,8-,9-,10-,11-,12-/m1/s1
InChIKey JGSMDVGTXBPWIM-HKEUSBCWSA-N
SMILES N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@H]1O
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing paromamine (CHEBI:7933) has functional parent α-D-glucose (CHEBI:17925)
paromamine (CHEBI:7933) has functional parent 2-deoxystreptamine (CHEBI:28295)
paromamine (CHEBI:7933) is a aminoglycoside (CHEBI:47779)
paromamine (CHEBI:7933) is a primary amino compound (CHEBI:50994)
paromamine (CHEBI:7933) is a triamine (CHEBI:38751)
paromamine (CHEBI:7933) is conjugate base of paromamine(3+) (CHEBI:65015)
Incoming 6'-oxoparomamine (CHEBI:65008) has functional parent paromamine (CHEBI:7933)
paromamine(3+) (CHEBI:65015) is conjugate acid of paromamine (CHEBI:7933)
IUPAC Name
(1R,2R,3S,4R,6S)-4,6-diamino-2,3-dihydroxycyclohexyl 2-amino-2-deoxy-α-D-glucopyranoside
Synonyms Sources
(1R)-O4-(2-amino-2-deoxy-α-D-glucopyranosyl)-2-deoxy-streptamine ChEBI
4-O-(2-amino-2-deoxy-α-D-glucopyranosyl)-2-deoxy-D-streptamine ChEBI
Neomycin D KEGG COMPOUND
Paromamine KEGG COMPOUND
Manual Xrefs Databases
C01743 KEGG COMPOUND
CPD-14125 MetaCyc
View more database links
Registry Numbers Types Sources
26713 Reaxys Registry Number Reaxys
534-47-4 CAS Registry Number KEGG COMPOUND
534-47-4 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
17206729 PubMed citation Europe PMC
19466609 PubMed citation Europe PMC
4645948 PubMed citation Europe PMC
5459627 PubMed citation Europe PMC
6698890 PubMed citation Europe PMC
Last Modified
28 April 2020