Molecule

Zoaramine

AlkaPlorer ID: AK318155

Synonym: None

IUPAC Name: 5-hydroxy-8-(6-hydroxy-4-methylazepan-2-ylidene)-3,4b,6a,10a-tetramethyl-4,4a,5,7,10,10b,12,12a-octahydrochrysene-1,6,9,11-tetrone

Structure

SMILES: CC1=CC(=O)C2CC(=O)C3C(C)(C(O)C(=O)C4(C)CC(=C5CC(C)CC(O)CN5)C(=O)CC34C)C2C1

InChI: InChI=1S/C29H39NO6/c1-14-6-16(31)13-30-20(8-14)18-11-28(4)25(35)26(36)29(5)19-7-15(2)9-21(32)17(19)10-22(33)24(29)27(28,3)12-23(18)34/h9,14,16-17,19,24,26,30-31,36H,6-8,10-13H2,1-5H3

InChIKey: BWCIQIZEMRYCND-UHFFFAOYSA-N

Reference

Efficient Preparation of Streptochlorin from Marine Streptomyces sp. SYYLWHS-1-4 by Combination of Response Surface Methodology and High-Speed Counter-Current Chromatography

An efficient synthesis and antifungal evaluation of natural product streptochlorin and its analogues

Interaction of marine Streptomyces compounds with selected cancer drug target proteins by in silico molecular docking studies

Purification of antibiotics from the biocontrol agent Streptomyces anulatus S37 by centrifugal partition chromatography

Statistical optimization and anticancer activity of a red pigment isolated from Streptomyces sp. PM4

Marine actinobacteria: An important source of bioactive natural products

PubChem CID: 163107698

COCONUT: CNP0427727.1

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Zoanthus sp.	Zoanthus	Zoanthidae	Zoantharia	Anthozoa	Cnidaria	Metazoa	Eukaryota

Properties Information

Molecule Weight: 497.6320000000004

TPSA？: 120.77

MolLogP？: 2.6868000000000007

Number of H-Donors: 3

Number of H-Acceptors: 7

RingCount: 5

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi