4-Chloro-2-(2,6-difluoro-benzylsulfanyl)-6-trifluoromethyl-benzothiazole

ID: ALA2289713

Chembl Id: CHEMBL2289713

PubChem CID: 76323964

Max Phase: Preclinical

Molecular Formula: C15H7ClF5NS2

Molecular Weight: 395.81

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Fc1cccc(F)c1CSc1nc2c(Cl)cc(C(F)(F)F)cc2s1

Standard InChI:  InChI=1S/C15H7ClF5NS2/c16-9-4-7(15(19,20)21)5-12-13(9)22-14(24-12)23-6-8-10(17)2-1-3-11(8)18/h1-5H,6H2

Standard InChI Key:  DNIFFJDWLQZOCT-UHFFFAOYSA-N

Associated Targets(non-human)

Colletotrichum gossypii (62 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Dothiorella gregaria (66 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Botrytis cinerea (4183 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rhizoctonia solani (2251 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

Calculated Properties

Molecular Weight: 395.81Molecular Weight (Monoisotopic): 394.9629AlogP: 6.54#Rotatable Bonds: 3
Polar Surface Area: 12.89Molecular Species: NEUTRALHBA: 3HBD:
#RO5 Violations: 1HBA (Lipinski): 1HBD (Lipinski): #RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 0.19CX LogP: 6.81CX LogD: 6.81
Aromatic Rings: 3Heavy Atoms: 24QED Weighted: 0.37Np Likeness Score: -2.15

References

1. Huang W, Yang GF..  (2006)  Microwave-assisted, one-pot syntheses and fungicidal activity of polyfluorinated 2-benzylthiobenzothiazoles.,  14  (24): [PMID:17008103] [10.1016/j.bmc.2006.09.016]

Source