ID: ALA58644

Max Phase: Preclinical

Molecular Formula: C25H25FN2O

Molecular Weight: 388.49

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1ccc(N[C@H]2C[C@@H](C)N(C(=O)c3cccc(F)c3)c3ccc(C)cc32)cc1

Standard InChI:  InChI=1S/C25H25FN2O/c1-16-7-10-21(11-8-16)27-23-14-18(3)28(24-12-9-17(2)13-22(23)24)25(29)19-5-4-6-20(26)15-19/h4-13,15,18,23,27H,14H2,1-3H3/t18-,23+/m1/s1

Standard InChI Key:  AAKMQRFRNKSENC-JPYJTQIMSA-N

Associated Targets(non-human)

Ecdysone receptor 102 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: 388.49Molecular Weight (Monoisotopic): 388.1951AlogP: 6.03#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: 4.14CX LogP: 5.66CX LogD: 5.66
Aromatic Rings: 3Heavy Atoms: 29QED Weighted: 0.59Np Likeness Score: -1.22

References

1. Smith HC, Cavanaugh CK, Friz JL, Thompson CS, Saggers JA, Michelotti EL, Garcia J, Tice CM..  (2003)  Synthesis and SAR of cis-1-benzoyl-1,2,3,4-tetrahydroquinoline ligands for control of gene expression in ecdysone responsive systems.,  13  (11): [PMID:12749904] [10.1016/s0960-894x(03)00317-2]

Source