Compound ID | 638

Update compound information

Napsamycin B

Class: Peptidylnucleoside

Spectrum of activity: Gram-negative
Details of activity: Anti-pseudomonal activity
Description: Ganguli BN, Nadarni SR, Patel MV, et al. Napsamycins new anti-pseudomonas antibiotics. 32nd-Intersci-Conf-Antimicrobial-Agents-Chemother 1992; 195
Year first mentioned: 1992
Highest developmental phase: Preclinical
Development status: Inactive
Chemical structure(s):
Click here for structure editor
Molecular weight: 866.94
Iso. SMILES: CC1C2=C(CC(N1)C(=O)N(C)C(C)C(C(=O)NC=C3CC(C(O3)N4C=CC(=O)NC4=O)O)NC(=O)C(CCSC)NC(=O)NC(CC5=CC(=CC=C5)O)C(=O)O)C=C(C=C2)O
InChI Key: UTIFRWPUJPPZEZ-UHFFFAOYSA-N
Can. SMILES: CC1C2=CC=C(C=C2CC(C(=O)N(C)C(C)C(C(=O)NC=C3CC(C(N4C=CC(=O)NC4=O)O3)O)NC(=O)C(CCSC)NC(=O)NC(CC5=CC=CC(=C5)O)C(=O)O)N1)O
InChI: InChI=1S/C40H50N8O12S/c1-20-27-9-8-25(50)16-23(27)17-29(42-20)36(55)47(3)21(2)33(35(54)41-19-26-18-31(51)37(60-26)48-12-10-32(52)45-40(48)59)46-34(53)28(11-13-61-4)43-39(58)44-30(38(56)57)15-22-6-5-7-24(49)14-22/h5-10,12,14,16,19-21,28-31,33,37,42,49-51H,11,13,15,17-18H2,1-4H3,(H,41,54)(H,46,53)(H,56,57)(H2,43,44,58)(H,45,52,59)
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/145720601
Citation: https://www.jstage.jst.go.jp/article/antibiotics1968/47/5/47_5_595/_article

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.