Molecule

Abyssomicin B

AlkaPlorer ID: AK009075

Synonym: None

IUPAC Name: (1R,2R,3R,7S,8S,10R,15R,17R)-2,7-dihydroxy-8,10,17-trimethyl-6,14,18-trioxa-5-azapentacyclo[10.5.2.14,7.03,15.015,19]icosa-4,12(19)-diene-11,13-dione

Structure

SMILES: C[C@@H]1C[C@H](C)[C@]2(O)CC(=NO2)[C@@H]2[C@@H](O)[C@@H]3OC4=C(C(=O)O[C@@]42C[C@H]3C)C1=O

InChI: InChI=1S/C19H23NO7/c1-7-4-9(3)19(24)6-10(20-27-19)12-14(22)15-8(2)5-18(12)16(25-15)11(13(7)21)17(23)26-18/h7-9,12,14-15,22,24H,4-6H2,1-3H3/t7-,8-,9+,12-,14-,15-,18-,19+/m1/s1

InChIKey: JKMXMRTVIHXWDO-MTONHXPSSA-N

Reference

Abyssomicin C—A Polycyclic Antibiotic from a Marine <i>Verrucosispora</i> Strain as an Inhibitor of the <i>p</i>‐Aminobenzoic Acid/Tetrahydrofolate Biosynthesis Pathway

PubChem CID: 11337879

LOTUS: LTS0079381

SuperNatural Ⅲ: SN0167910-03

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NPAtlas: NPA001891

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Verrucosispora sp.	Micromonospora	Micromonosporaceae	Micromonosporales	Actinomycetes	Actinomycetota	None	Bacteria

Properties Information

Molecule Weight: 377.3930000000002

TPSA？: 114.65000000000003

MolLogP？: 0.6617000000000001

Number of H-Donors: 2

Number of H-Acceptors: 8

RingCount: 6

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi