Compound ID | 1466

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Macfarlandin G

Class: Natural product antibiotic

Details of activity: Antimycobacterial activity against Mycobacterium tuberculosis
Description: Natural product from Samoan marine sponge Chelonaplysilla sp.
Institute where first reported: University of British Columbia, CA
Year first mentioned: 2020
Highest developmental phase: Preclinical
Chemical structure(s):
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Molecular weight: 362.5
Iso. SMILES: O=C1C[C@@H](COC(C)=O)[C@](CO1)([H])[C@]2(C)CC[C@@]3([H])C(C)(C)CCC=C3[C@H]2C
InChI Key: NWFYTQREGAPBOY-HTFSQMSJSA-N
Can. SMILES: C[C@@H]1C2=CCCC(C)(C)[C@]2([H])CC[C@@]1(C)[C@]3([H])COC(=O)C[C@H]3COC(=O)C
InChI: InChI=1S/C22H34O4/c1-14-17-7-6-9-21(3,4)18(17)8-10-22(14,5)19-13-26-20(24)11-16(19)12-25-15(2)23/h7,14,16,18-19H,6,8-13H2,1-5H3/t14-,16+,18-,19-,22-/m1/s1
External links:
Citation: https://www.nature.com/articles/s41429-020-0315-4

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