ID: ALA2288291

Max Phase: Preclinical

Molecular Formula: C16H32NO2PS

Molecular Weight: 333.48

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)=CCCC(C)CCOP1(=S)N[C@@H](CC(C)C)CO1

Standard InChI:  InChI=1S/C16H32NO2PS/c1-13(2)7-6-8-15(5)9-10-18-20(21)17-16(12-19-20)11-14(3)4/h7,14-16H,6,8-12H2,1-5H3,(H,17,21)/t15?,16-,20?/m0/s1

Standard InChI Key:  LYGOJAIMAQBLLD-NGEICVOHSA-N

Associated Targets(non-human)

Corticium 78 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Pythium 470 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: 333.48Molecular Weight (Monoisotopic): 333.1891AlogP: 5.03#Rotatable Bonds: 9
Polar Surface Area: 30.49Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 10.93CX Basic pKa: CX LogP: 5.04CX LogD: 5.04
Aromatic Rings: 0Heavy Atoms: 21QED Weighted: 0.47Np Likeness Score: 1.30

References

1. TAIRA S, TAWATA S, KOBAMOTO N, TOYAMA S, YASUDA M.  (1994)  Synthesis and Fungicidal Activity of New 1, 3, 2-Oxazaphospholidine 2-Sulfides,  19  (4): [10.1584/jpestics.19.4_299]

Source