ID: ALA2289562

Max Phase: Preclinical

Molecular Formula: C10H17NO2S2

Molecular Weight: 247.38

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(=O)C1(C(C)=O)SCC(N(C)C)CS1

Standard InChI:  InChI=1S/C10H17NO2S2/c1-7(12)10(8(2)13)14-5-9(6-15-10)11(3)4/h9H,5-6H2,1-4H3

Standard InChI Key:  KCVSKXMAEGHUSL-UHFFFAOYSA-N

Associated Targets(non-human)

Henosepilachna vigintioctopunctata 143 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Tetranychus urticae 2600 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Chilo suppressalis 440 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: 247.38Molecular Weight (Monoisotopic): 247.0701AlogP: 1.27#Rotatable Bonds: 3
Polar Surface Area: 37.38Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 7.26CX LogP: 1.82CX LogD: 1.59
Aromatic Rings: 0Heavy Atoms: 15QED Weighted: 0.70Np Likeness Score: 0.06

References

1. MITSUDERA H, KONISHI K.  (1991)  Synthesis and Insecticidal Activity of 1, 3-Dithianes,  16  (3): [10.1584/jpestics.16.387]

Source