ID: ALA200803

Max Phase: Preclinical

Molecular Formula: C19H34O2S

Molecular Weight: 326.55

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCCCCCCCCCCCC1(C)SC(O)=C(C)C1=O

Standard InChI:  InChI=1S/C19H34O2S/c1-4-5-6-7-8-9-10-11-12-13-14-15-19(3)17(20)16(2)18(21)22-19/h21H,4-15H2,1-3H3

Standard InChI Key:  FSSQCANEVVTLQF-UHFFFAOYSA-N

Associated Targets(non-human)

3-oxoacyl-[acyl-carrier-protein] synthase III 179 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Escherichia coli 133304 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mycobacterium tuberculosis 203094 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

3-oxoacyl-[acyl-carrier-protein] synthase 2 72 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

3-oxoacyl-[acyl-carrier-protein] synthase 1 34 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

3-oxoacyl-[acyl-carrier-protein] synthase 1 75 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

3-oxoacyl-[acyl-carrier-protein] synthase 3 287 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 326.55Molecular Weight (Monoisotopic): 326.2280AlogP: 6.55#Rotatable Bonds: 12
Polar Surface Area: 37.30Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 1HBA (Lipinski): 2HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 6.65CX Basic pKa: CX LogP: 7.65CX LogD: 6.83
Aromatic Rings: 0Heavy Atoms: 22QED Weighted: 0.41Np Likeness Score: 0.57

References

1. 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