ID: ALA3361414

Max Phase: Preclinical

Molecular Formula: C37H48N6O5

Molecular Weight: 656.83

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)(C)OC(=O)/N=C(\NC(=O)OC(C)(C)C)Nc1ccc(C(=O)NCC2(Nc3ccccc3)CCN(Cc3ccccc3)CC2)cc1

Standard InChI:  InChI=1S/C37H48N6O5/c1-35(2,3)47-33(45)40-32(41-34(46)48-36(4,5)6)39-29-19-17-28(18-20-29)31(44)38-26-37(42-30-15-11-8-12-16-30)21-23-43(24-22-37)25-27-13-9-7-10-14-27/h7-20,42H,21-26H2,1-6H3,(H,38,44)(H2,39,40,41,45,46)

Standard InChI Key:  DSFGLFLTYKTPCG-UHFFFAOYSA-N

Associated Targets(Human)

Neuropeptide FF receptor 2 533 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Neuropeptide FF receptor 1 514 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: 656.83Molecular Weight (Monoisotopic): 656.3686AlogP: 6.79#Rotatable Bonds: 8
Polar Surface Area: 133.39Molecular Species: BASEHBA: 7HBD: 4
#RO5 Violations: 2HBA (Lipinski): 11HBD (Lipinski): 4#RO5 Violations (Lipinski): 3
CX Acidic pKa: 9.76CX Basic pKa: 8.60CX LogP: 5.57CX LogD: 4.53
Aromatic Rings: 3Heavy Atoms: 48QED Weighted: 0.15Np Likeness Score: -0.84

References

1. Journigan VB, Mésangeau C, Vyas N, Eans SO, Cutler SJ, McLaughlin JP, Mollereau C, McCurdy CR..  (2014)  Nonpeptide small molecule agonist and antagonist original leads for neuropeptide FF1 and FF2 receptors.,  57  (21): [PMID:25268943] [10.1021/jm500989n]

Source