Molecule

Albogrisin E

AlkaPlorer ID: AK123759

Synonym: None

IUPAC Name: (4S)-4-[(1-methoxy-4-methyl-3-oxobenzo[f][1,7]naphthyridine-5-carbonyl)amino]-7-methyl-5-oxooct-6-enoic acid

Structure

SMILES: COC1=CC(=O)N(C)C2=C(C(=O)N[C@@H](CCC(=O)O)C(=O)C=C(C)C)N=C3C=CC=CC3=C12

InChI: InChI=1S/C24H25N3O6/c1-13(2)11-17(28)16(9-10-20(30)31)26-24(32)22-23-21(14-7-5-6-8-15(14)25-22)18(33-4)12-19(29)27(23)3/h5-8,11-12,16H,9-10H2,1-4H3,(H,26,32)(H,30,31)/t16-/m0/s1

InChIKey: ZPPUCOCARALBOO-INIZCTEOSA-N

Reference

Characterization and Nonenzymatic Transformation of Three Types of Alkaloids from <i>Streptomyces albogriseolus</i> MGR072 and Discovery of Inhibitors of Indoleamine 2,3-Dioxygenase

PubChem CID: 146683279

LOTUS: LTS0056622

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NPAtlas: NPA026862

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Streptomyces albogriseolus	Streptomyces	Streptomycetaceae	Kitasatosporales	Actinomycetes	Actinomycetota	None	Bacteria

Properties Information

Molecule Weight: 451.4790000000002

TPSA？: 127.59000000000002

MolLogP？: 2.5938

Number of H-Donors: 2

Number of H-Acceptors: 7

RingCount: 3

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi