6-Chloro-2,4-dimethoxy-quinoline

ID: ALA194017

Chembl Id: CHEMBL194017

PubChem CID: 9942638

Max Phase: Preclinical

Molecular Formula: C11H10ClNO2

Molecular Weight: 223.66

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1cc(OC)c2cc(Cl)ccc2n1

Standard InChI:  InChI=1S/C11H10ClNO2/c1-14-10-6-11(15-2)13-9-4-3-7(12)5-8(9)10/h3-6H,1-2H3

Standard InChI Key:  PJBXMXPVFBWZRX-UHFFFAOYSA-N

Alternative Forms

Associated Targets(non-human)

Haemonchus contortus (724 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trichostrongylus colubriformis (210 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Teladorsagia circumcincta (67 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: 223.66Molecular Weight (Monoisotopic): 223.0400AlogP: 2.91#Rotatable Bonds: 2
Polar Surface Area: 31.35Molecular Species: NEUTRALHBA: 3HBD: 0
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 2.92CX LogP: 3.01CX LogD: 3.01
Aromatic Rings: 2Heavy Atoms: 15QED Weighted: 0.78Np Likeness Score: -0.95

References

1. Rossiter S, Péron JM, Whitfield PJ, Jones K..  (2005)  Synthesis and anthelmintic properties of arylquinolines with activity against drug-resistant nematodes.,  15  (21): [PMID:16165359] [10.1016/j.bmcl.2005.07.044]

Source