ID: ALA2288285

Max Phase: Preclinical

Molecular Formula: C15H28NO2PS

Molecular Weight: 317.44

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)=CCC/C(C)=C/COP1(=S)N[C@@H](C(C)C)CO1

Standard InChI:  InChI=1S/C15H28NO2PS/c1-12(2)7-6-8-14(5)9-10-17-19(20)16-15(11-18-19)13(3)4/h7,9,13,15H,6,8,10-11H2,1-5H3,(H,16,20)/b14-9+/t15-,19?/m1/s1

Standard InChI Key:  RAFRURNZKZCGCF-GRYPOMHRSA-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: 317.44Molecular Weight (Monoisotopic): 317.1578AlogP: 4.56#Rotatable Bonds: 7
Polar Surface Area: 30.49Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 10.84CX Basic pKa: CX LogP: 4.43CX LogD: 4.43
Aromatic Rings: 0Heavy Atoms: 20QED Weighted: 0.55Np Likeness Score: 1.54

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