(4-chlorophenyl)(2-methyl-3,4-dihydroquinolin-1(2H)-yl)methanone

ID: ALA2286415

Chembl Id: CHEMBL2286415

PubChem CID: 12360473

Max Phase: Preclinical

Molecular Formula: C17H16ClNO

Molecular Weight: 285.77

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CC1CCc2ccccc2N1C(=O)c1ccc(Cl)cc1

Standard InChI:  InChI=1S/C17H16ClNO/c1-12-6-7-13-4-2-3-5-16(13)19(12)17(20)14-8-10-15(18)11-9-14/h2-5,8-12H,6-7H2,1H3

Standard InChI Key:  ZSDFNOZRKMPXSL-UHFFFAOYSA-N

Associated Targets(Human)

SL-2 (16 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Ecdysone receptor (90 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EcR Ecdysone receptor (281 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EcR Ecdysone receptor (183 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: 285.77Molecular Weight (Monoisotopic): 285.0920AlogP: 4.32#Rotatable Bonds: 1
Polar Surface Area: 20.31Molecular Species: NEUTRALHBA: 1HBD:
#RO5 Violations: HBA (Lipinski): 2HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: 4.43CX LogD: 4.43
Aromatic Rings: 2Heavy Atoms: 20QED Weighted: 0.76Np Likeness Score: -1.23

References

1. Soin T, De Geyter E, Mosallanejad H, Iga M, Martín D, Ozaki S, Kitsuda S, Harada T, Miyagawa H, Stefanou D, Kotzia G, Efrose R, Labropoulou V, Geelen D, Iatrou K, Nakagawa Y, Janssen CR, Smagghe G, Swevers L..  (2010)  Assessment of species specificity of moulting accelerating compounds in Lepidoptera: comparison of activity between Bombyx mori and Spodoptera littoralis by in vitro reporter and in vivo toxicity assays.,  66  (5): [PMID:20069627] [10.1002/ps.1903]
2. Soin T, Swevers L, Kotzia G, Iatrou K, Janssen CR, Rougé P, Harada T, Nakagawa Y, Smagghe G..  (2010)  Comparison of the activity of non-steroidal ecdysone agonists between dipteran and lepidopteran insects, using cell-based EcR reporter assays.,  66  (11): [PMID:20672340] [10.1002/ps.1998]

Source