ID: ALA3263683

Max Phase: Preclinical

Molecular Formula: C29H33N5O4

Molecular Weight: 515.61

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1ccccc1N1CCN(c2ccc(C(=O)NCCN3CCCC3=O)cc2NC(=O)c2ccco2)CC1

Standard InChI:  InChI=1S/C29H33N5O4/c1-21-6-2-3-7-24(21)32-15-17-33(18-16-32)25-11-10-22(20-23(25)31-29(37)26-8-5-19-38-26)28(36)30-12-14-34-13-4-9-27(34)35/h2-3,5-8,10-11,19-20H,4,9,12-18H2,1H3,(H,30,36)(H,31,37)

Standard InChI Key:  QSHWUFNCXFOONQ-UHFFFAOYSA-N

Associated Targets(Human)

Follicle stimulating hormone receptor 234 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: 515.61Molecular Weight (Monoisotopic): 515.2533AlogP: 3.52#Rotatable Bonds: 8
Polar Surface Area: 98.13Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 1HBA (Lipinski): 9HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.52CX Basic pKa: 3.48CX LogP: 3.03CX LogD: 3.03
Aromatic Rings: 3Heavy Atoms: 38QED Weighted: 0.48Np Likeness Score: -1.77

References

1. Yu HN, Richardson TE, Nataraja S, Fischer DJ, Sriraman V, Jiang X, Bharathi P, Foglesong RJ, Haxell TF, Heasley BH, Jenks M, Li J, Dugas MS, Collis R, Tian H, Palmer S, Goutopoulos A..  (2014)  Discovery of substituted benzamides as follicle stimulating hormone receptor allosteric modulators.,  24  (9): [PMID:24685543] [10.1016/j.bmcl.2014.03.018]

Source