ISOVALERYL ISOTHIOCYANATE

ID: ALA2251723

Max Phase: Preclinical

Molecular Formula: C6H9NOS

Molecular Weight: 143.21

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)CC(=O)N=C=S

Standard InChI:  InChI=1S/C6H9NOS/c1-5(2)3-6(8)7-4-9/h5H,3H2,1-2H3

Standard InChI Key:  LAJGSTFFYMRWDX-UHFFFAOYSA-N

Associated Targets(non-human)

Meloidogyne javanica 98 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: 143.21Molecular Weight (Monoisotopic): 143.0405AlogP: 1.66#Rotatable Bonds: 2
Polar Surface Area: 29.43Molecular Species: NEUTRALHBA: 2HBD: 0
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 1.81CX LogD: 1.81
Aromatic Rings: 0Heavy Atoms: 9QED Weighted: 0.43Np Likeness Score: -0.28

References

1. Wu H, Wang CJ, Bian XW, Zeng SY, Lin KC, Wu B, Zhang G, Zhang X..  (2011)  Nematicidal efficacy of isothiocyanates against root-knot nematode Meloidogyne javanica in cucumber,  30  (1): [10.1016/j.cropro.2010.09.004]

Source