Compound ID | 3560

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24,25-Dihydrofusidic acid

Class: Fusidane

Spectrum of activity: Gram-positive
Details of activity: Active against Staphylococcus aureus and Corynebacterium xerosis
Description: Semi-synthetic compound; fusidic acid derivative; activity comparable to fusidic acid (i.e. no improvement in antibacterial potency or spectrum)
Institute where first reported: Leo Pharmaceutical Products, Denmark
Year first mentioned: 1966
Development status: Experimental
Chemical structure(s):
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Molecular weight: 514.78
Iso. SMILES: C[C@@H]1CC[C@]2([C@H]([C@H]1C)CC[C@]3([C@H]2[C@@H](C[C@@H]4[C@@]3(CC(C4=C(CCCC(C)C)C(=O)O)OC(=C)C)C)O)C)C
InChI Key: BFIXKNVQSJCXFB-PNLDEPSKSA-N
Can. SMILES: CC(C)CCCC(=C1[C@@H]2C[C@H]([C@H]3[C@@]4(C)CC[C@@H](C)[C@H](C)[C@@H]4CC[C@]3(C)[C@@]2(C)CC1OC(=C)C)O)C(=O)O
InChI: InChI=1S/C33H54O4/c1-19(2)11-10-12-23(30(35)36)28-25-17-26(34)29-31(7)15-13-21(5)22(6)24(31)14-16-32(29,8)33(25,9)18-27(28)37-20(3)4/h19,21-22,24-27,29,34H,3,10-18H2,1-2,4-9H3,(H,35,36)/t21-,22+,24+,25+,26-,27?,29+,31+,32+,33+/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/129711290
Citation: https://pubs.acs.org/doi/epdf/10.1021/jm00319a004?ref=article_openPDF

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