Molecule

Epoxyquinomicin D

AlkaPlorer ID: AK060626

Synonym: None

IUPAC Name: 3-chloro-2-hydroxy-N-[(1R,2S,6R)-2-hydroxy-6-(hydroxymethyl)-5-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]benzamide

Structure

SMILES: O=C1C=C(N=C(O)C2=CC=CC(Cl)=C2O)[C@H](O)[C@H]2O[C@@]12CO

InChI: InChI=1S/C14H12ClNO6/c15-7-3-1-2-6(10(7)19)13(21)16-8-4-9(18)14(5-17)12(22-14)11(8)20/h1-4,11-12,17,19-20H,5H2,(H,16,21)/t11-,12+,14-/m0/s1

InChIKey: CQWDZNQKJPNNJB-SCRDCRAPSA-N

Reference

Epoxyquinomicins A, B, C and D, New Antibiotics from Amycolatopsis. I. Taxonomy, Fermentation, Isolation and Antimicrobial Activities.

PubChem CID: 3075749

CAS: 200496-86-2

LOTUS: LTS0009728

SuperNatural Ⅲ: SN0053178-02

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NPAtlas: NPA010345

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Amycolatopsis sulphurea	Amycolatopsis	Pseudonocardiaceae	Pseudonocardiales	Actinomycetes	Actinomycetota	None	Bacteria

Properties Information

Molecule Weight: 325.7040000000001

TPSA？: 122.88

MolLogP？: 0.3075999999999997

Number of H-Donors: 4

Number of H-Acceptors: 6

RingCount: 3

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi