Standard InChI: InChI=1S/C32H56N2O5S/c1-10-30(8)16-24(39-25(36)17-40-29(6,7)18-34-28(38)22(33)15-19(2)3)31(9)20(4)11-13-32(21(5)27(30)37)14-12-23(35)26(31)32/h19-22,24,26-27,37H,10-18,33H2,1-9H3,(H,34,38)/t20-,21+,22-,24-,26+,27+,30-,31+,32+/m1/s1
Standard InChI Key: LDBVKDZWXIIVOD-SYDOLDNLSA-N
Associated Targets(non-human)
Staphylococcus aureus 210822 Activities
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Mycolicibacterium smegmatis 8003 Activities
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Mycobacterium tuberculosis 203094 Activities
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Escherichia coli 133304 Activities
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Vero 26788 Activities
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Acinetobacter baumannii 41033 Activities
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Klebsiella pneumoniae 43867 Activities
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Streptococcus pneumoniae 31063 Activities
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Clostridioides difficile 2968 Activities
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Enterococcus faecalis 29875 Activities
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Streptococcus salivarius 87 Activities
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Bacillus subtilis 32866 Activities
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Molecule Features
Natural Product: No
Oral: No
Chemical Probe: No
Parenteral: No
Molecule Type: Small molecule
Topical: No
First In Class: No
Black Box: No
Chirality: No
Availability: No
Prodrug: No
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Properties
Molecular Weight: 580.88
Molecular Weight (Monoisotopic): 580.3910
AlogP: 5.12
#Rotatable Bonds: 10
Polar Surface Area: 118.72
Molecular Species: NEUTRAL
HBA: 7
HBD: 3
#RO5 Violations: 2
HBA (Lipinski): 7
HBD (Lipinski): 4
#RO5 Violations (Lipinski): 2
CX Acidic pKa:
CX Basic pKa: 8.43
CX LogP: 4.64
CX LogD: 3.57
Aromatic Rings: 0
Heavy Atoms: 40
QED Weighted: 0.31
Np Likeness Score: 1.41
References
1.Lemieux MR, Siricilla S, Mitachi K, Eslamimehr S, Wang Y, Yang D, Pressly JD, Kong Y, Park F, Franzblau SG, Kurosu M.. (2018) An antimycobacterial pleuromutilin analogue effective against dormant bacilli., 26 (17):[PMID:30145051][10.1016/j.bmc.2018.07.034]