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

ID: ALA2286419

Chembl Id: CHEMBL2286419

PubChem CID: 76312873

Max Phase: Preclinical

Molecular Formula: C23H21ClN2O

Molecular Weight: 376.89

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1ccc(NC2CCN(C(=O)c3ccc(Cl)cc3)c3ccccc32)cc1

Standard InChI:  InChI=1S/C23H21ClN2O/c1-16-6-12-19(13-7-16)25-21-14-15-26(22-5-3-2-4-20(21)22)23(27)17-8-10-18(24)11-9-17/h2-13,21,25H,14-15H2,1H3

Standard InChI Key:  CXTWGQVBMOBBNS-UHFFFAOYSA-N

Associated Targets(Human)

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

Associated Targets(non-human)

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: 376.89Molecular Weight (Monoisotopic): 376.1342AlogP: 5.85#Rotatable Bonds: 3
Polar Surface Area: 32.34Molecular Species: NEUTRALHBA: 2HBD: 1
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 4.08CX LogP: 5.19CX LogD: 5.19
Aromatic Rings: 3Heavy Atoms: 27QED Weighted: 0.62Np Likeness Score: -1.38

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