Molecule

Lobosamide B

AlkaPlorer ID: AK030162

Synonym: None

IUPAC Name: (9S,10R,11R,12S,14R,15E,26S)-10,11,12,14-tetrahydroxy-9,19,21,26-tetramethyl-1-azacyclohexacosa-3,5,7,15,17,19,21,23-octaen-2-one

Structure

SMILES: CC1=CC=CC[C@H](C)N=C(O)C=CC=CC=C[C@H](C)[C@@H](O)[C@H](O)[C@@H](O)C[C@@H](O)/C=C/C=CC(C)=C1

InChI: InChI=1S/C29H41NO5/c1-21-13-9-11-16-24(4)30-27(33)18-8-6-5-7-15-23(3)28(34)29(35)26(32)20-25(31)17-12-10-14-22(2)19-21/h5-15,17-19,23-26,28-29,31-32,34-35H,16,20H2,1-4H3,(H,30,33)/b6-5?,11-9?,14-10?,15-7?,17-12+,18-8?,21-13?,22-19?/t23-,24-,25-,26-,28+,29+/m0/s1

InChIKey: OXBKRYKWMRJSMZ-LLGQQDJPSA-N

Reference

Genome-Directed Lead Discovery: Biosynthesis, Structure Elucidation, and Biological Evaluation of Two Families of Polyene Macrolactams against <i>Trypanosoma brucei</i>

PubChem CID: 139587378

LOTUS: LTS0119627

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NPAtlas: NPA015369

Source

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

Properties Information

Molecule Weight: 483.64900000000017

TPSA？: 113.51000000000002

MolLogP？: 4.434700000000003

Number of H-Donors: 5

Number of H-Acceptors: 5

RingCount: 1

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi