Compound ID | 568

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Balhimycin

Class: Glycopeptide

Spectrum of activity: Gram-positive
Details of activity: The activity of balhimycin is similar to that of vancomycin. Against S. epidermidis, S. faecalis, and S. aureus are in the range of 0.39-0.78mcg/ml.
Description: Ganguli BN, Nadkarni SR, Patel MV, et al. Balhimycin- a new glycopeptide from Nocardia sp. Y-8621022. 33rd-Intersci-Conf-Antimicrobial-Agents-Chemother 1993; 223.
Institute where first reported: Hoechst AG. Frankfurt
Year first mentioned: 1993
Highest developmental phase: Preclinical
Development status: Inactive
Chemical structure(s):
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Molecular weight: 1447.24
Iso. SMILES: CC1C(=O)C(CC(O1)OC2C3C(=O)NC(C4=C(C(=CC(=C4)O)O)C5=C(C=CC(=C5)C(C(=O)N3)NC(=O)C6C7=CC(=C(C(=C7)OC8=C(C=C2C=C8)Cl)OC9C(C(C(C(O9)CO)O)O)O)OC%10=C(C=C(C=C%10)C(C(C(=O)NC(C(=O)N6)CC(=O)N)NC(=O)C(CC(C)C)NC)O)Cl)O)C(=O)O)(C)N
InChI Key: WKNFBFHAYANQHF-UHFFFAOYSA-N
Can. SMILES: CC(C)CC(C(=O)NC1C(C2=CC=C(C(=C2)Cl)OC3=CC4=CC(=C3OC5C(C(C(C(CO)O5)O)O)O)OC6=CC=C(C=C6Cl)C(C7C(=O)NC(C8=CC(=CC(=C8C9=CC(=CC=C9O)C(C(=O)N7)NC(=O)C4NC(=O)C(CC(=O)N)NC1=O)O)O)C(=O)O)OC%10CC(C)(C(=O)C(C)O%10)N)O)NC
InChI: InChI=1S/C66H73Cl2N9O24/c1-23(2)12-34(71-5)58(88)76-49-51(83)26-7-10-38(32(67)14-26)97-40-16-28-17-41(56(40)101-65-54(86)53(85)52(84)42(22-78)99-65)98-39-11-8-27(15-33(39)68)55(100-44-21-66(4,70)57(87)24(3)96-44)50-63(93)75-48(64(94)95)31-18-29(79)19-37(81)45(31)30-13-25(6-9-36(30)80)46(60(90)77-50)74-61(91)47(28)73-59(89)35(20-43(69)82)72-62(49)92/h6-11,13-19,23-24,34-35,42,44,46-55,65,71,78-81,83-86H,12,20-22,70H2,1-5H3,(H2,69,82)(H,72,92)(H,73,89)(H,74,91)(H,75,93)(H,76,88)(H,77,90)(H,94,95)
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/16131414
Citation: https://www.jstage.jst.go.jp/article/antibiotics1968/47/3/47_3_334/_article

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