Molecule

Chondramide A

AlkaPlorer ID: AK020323

Synonym: None

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

Structure

SMILES: CO[C@@H]1C(=O)O[C@H](C)[C@@H](C)C=C(C)C[C@H](C)C(=O)N[C@@H](C)C(=O)N(C)[C@H](CC2=CNC3=CC=CC=C23)C(=O)NC1C1=CC=C(O)C=C1

InChI: InChI=1S/C36H46N4O7/c1-20-16-21(2)24(5)47-36(45)32(46-7)31(25-12-14-27(41)15-13-25)39-34(43)30(18-26-19-37-29-11-9-8-10-28(26)29)40(6)35(44)23(4)38-33(42)22(3)17-20/h8-16,19,21-24,30-32,37,41H,17-18H2,1-7H3,(H,38,42)(H,39,43)/t21-,22-,23-,24+,30+,31?,32-/m0/s1

InChIKey: IEKCRWAFVYJECW-TYVWEWQESA-N

Reference

Molecular and Biochemical Studies of Chondramide Formation—Highly Cytotoxic Natural Products from Chondromyces crocatus Cm c5

PubChem CID: 139585315

LOTUS: LTS0072628

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NPAtlas: NPA007953

Source

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

Properties Information

Molecule Weight: 646.7850000000002

TPSA？: 150.05999999999997

MolLogP？: 4.174100000000002

Number of H-Donors: 4

Number of H-Acceptors: 7

RingCount: 4

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi