ID: ALA3127648

Max Phase: Preclinical

Molecular Formula: C23H27FN6

Molecular Weight: 406.51

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCn1cc(-c2ccc(N3CCC(N4CCc5ccc(F)cc54)CC3)nn2)cn1

Standard InChI:  InChI=1S/C23H27FN6/c1-2-10-29-16-18(15-25-29)21-5-6-23(27-26-21)28-11-8-20(9-12-28)30-13-7-17-3-4-19(24)14-22(17)30/h3-6,14-16,20H,2,7-13H2,1H3

Standard InChI Key:  YTLFZEMWXNXCHP-UHFFFAOYSA-N

Associated Targets(Human)

Liver microsome 8277 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Acyl-CoA desaturase 1011 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Liver microsome 4459 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Acyl-CoA desaturase 1 506 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: 406.51Molecular Weight (Monoisotopic): 406.2281AlogP: 3.92#Rotatable Bonds: 5
Polar Surface Area: 50.08Molecular Species: NEUTRALHBA: 6HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 3.55CX LogP: 3.92CX LogD: 3.92
Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.64Np Likeness Score: -2.17

References

1. Yang SM, Tang Y, Rano T, Lu H, Kuo GH, Gaul MD, Li Y, Ho G, Lang W, Conway JG, Liang Y, Lenhard JM, Demarest KT, Murray WV..  (2014)  4-Bicyclic heteroaryl-piperidine derivatives as potent, orally bioavailable stearoyl-CoA desaturase-1 (SCD1) inhibitors: part 2. Pyridazine-based analogs.,  24  (5): [PMID:24405703] [10.1016/j.bmcl.2013.12.075]

Source