ID: ALA193803

Max Phase: Preclinical

Molecular Formula: C12H20O2S

Molecular Weight: 228.36

Molecule Type: Small molecule

Representations

Canonical SMILES:  CCCCCCC1(C)SC(O)=C(C)C1=O

Standard InChI:  InChI=1S/C12H20O2S/c1-4-5-6-7-8-12(3)10(13)9(2)11(14)15-12/h14H,4-8H2,1-3H3

Standard InChI Key:  LTLIOCSGRMCPCA-UHFFFAOYSA-N

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

Properties

Molecular Weight: 228.36

Molecular Weight (Monoisotopic): 228.1184

AlogP: 3.82

#Rotatable Bonds: 5

Polar Surface Area: 37.30

Molecular Species: NEUTRAL

HBA: 3

HBD: 1

#RO5 Violations: 0

HBA (Lipinski): 2

HBD (Lipinski): 1

#RO5 Violations (Lipinski): 0

CX Acidic pKa: 6.79

CX Basic pKa:

CX LogP: 4.54

CX LogD: 3.84

Aromatic Rings: 0

Heavy Atoms: 15

QED Weighted: 0.73

Np Likeness Score: 0.83

References

1. Jones SM, Urch JE, Kaiser M, Brun R, Harwood JL, Berry C, Gilbert IH..  (2005)  Analogues of thiolactomycin as potential antimalarial agents.,  48  (19): [PMID:16161997] [10.1021/jm049067d]

2. Kim P, Zhang YM, Shenoy G, Nguyen QA, Boshoff HI, Manjunatha UH, Goodwin MB, Lonsdale J, Price AC, Miller DJ, Duncan K, White SW, Rock CO, Barry CE, Dowd CS..  (2006)  Structure-activity relationships at the 5-position of thiolactomycin: an intact (5R)-isoprene unit is required for activity against the condensing enzymes from Mycobacterium tuberculosis and Escherichia coli.,  49  (1): [PMID:16392800] [10.1021/jm050825p]

Source

Source(1):

• Scientific Literature