Molecule

chondramide C

AlkaPlorer ID: AK037380

Synonym: '', 'Chondramide C'

IUPAC Name: (4R,7S,10R,13S,15Z,17S,18R)-4-(4-hydroxyphenyl)-7-(1H-indol-3-ylmethyl)-8,10,13,15,17,18-hexamethyl-1-oxa-5,8,11-triazacyclooctadec-15-ene-2,6,9,12-tetrone

Structure

SMILES: C/C1=C/[C@H](C)[C@@H](C)OC(=O)C[C@H](C2=CC=C(O)C=C2)N=C(O)[C@H](CC2=CNC3=CC=CC=C23)N(C)C(=O)[C@@H](C)N=C(O)[C@@H](C)C1

InChI: InChI=1S/C35H44N4O6/c1-20-15-21(2)24(5)45-32(41)18-30(25-11-13-27(40)14-12-25)38-34(43)31(17-26-19-36-29-10-8-7-9-28(26)29)39(6)35(44)23(4)37-33(42)22(3)16-20/h7-15,19,21-24,30-31,36,40H,16-18H2,1-6H3,(H,37,42)(H,38,43)/b20-15-/t21-,22-,23+,24+,30+,31-/m0/s1

InChIKey: NCRSWJPOFRASIF-JMVWPIOVSA-N

Reference

Chondramides A - D, New Antifungal and Cytostatic Depsipeptides from Chondromyces crocatus (Myxobacteria). Production, Physico-chemical and Biological Properties.

PubChem CID: 162943439

LOTUS: LTS0037667

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Chondromyces crocatus	Chondromyces	Polyangiaceae	Polyangiales	None	Myxococcota	None	Bacteria

Properties Information

Molecule Weight: 616.7590000000001

TPSA？: 147.81

MolLogP？: 6.229800000000005

Number of H-Donors: 4

Number of H-Acceptors: 6

RingCount: 4

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi