Compound ID | 3241

Update compound information

Angiolam A

Class: Protein synthesis inhibitor

Spectrum of activity: Gram-positive
Details of activity: Active against Bacillus thuringiensis and Clostridium pasteurianum
Description: Natural product from Angiococcus disciformis; lactone-lactam
Year first mentioned: 1985
Development status: Experimental
Chemical structure(s):
Click here for structure editor
Molecular weight: 587.79
Iso. SMILES: CC1CCC(OC(=O)/C(=C/C(C(C(C(=O)CCC(NC(=O)CC1=O)C)C)O)C)/C)/C=C/C(C)CCC(/C(=C\C=C)/C)O
InChI Key: GRCRWFPQJFBHLG-ZXXIUXGKSA-N
Can. SMILES: C=C/C=C(/C)\C(CCC(C)/C=C/C1CCC(C)C(=O)CC(=O)NC(C)CCC(=O)C(C)C(C(C)/C=C(\C)/C(=O)O1)O)O
InChI: InChI=1S/C34H53NO7/c1-9-10-22(3)29(36)17-12-21(2)11-15-28-16-13-23(4)31(38)20-32(39)35-26(7)14-18-30(37)27(8)33(40)24(5)19-25(6)34(41)42-28/h9-11,15,19,21,23-24,26-29,33,36,40H,1,12-14,16-18,20H2,2-8H3,(H,35,39)/b15-11+,22-10-,25-19+
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/6438827
Citation: https://www.jstage.jst.go.jp/article/antibiotics1968/38/12/38_12_1649/_article/-char/en

AntibioticDB is supported by GARDP.

If you have feedback, experience problems, or are interested in a collaboration, please contact us. | Terms and conditions

The content of this site is intended for educational and scientific research purposes only and not as a source of medical advice or consultation.