ID: ALA3408016

Max Phase: Preclinical

Molecular Formula: C24H39NO

Molecular Weight: 357.58

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@H](Nc3ccc(O)cc3)CCC[C@]12C

Standard InChI:  InChI=1S/C24H39NO/c1-17(2)7-5-8-18(3)21-14-15-22-23(9-6-16-24(21,22)4)25-19-10-12-20(26)13-11-19/h10-13,17-18,21-23,25-26H,5-9,14-16H2,1-4H3/t18-,21-,22+,23-,24-/m1/s1

Standard InChI Key:  VXFKLMHFYSPAMR-REXJZNOJSA-N

Associated Targets(Human)

Vitamin D receptor 26531 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Vitamin D receptor 250 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: 357.58Molecular Weight (Monoisotopic): 357.3032AlogP: 6.85#Rotatable Bonds: 7
Polar Surface Area: 32.26Molecular Species: NEUTRALHBA: 2HBD: 2
#RO5 Violations: 1HBA (Lipinski): 2HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 10.35CX Basic pKa: 6.37CX LogP: 6.96CX LogD: 6.92
Aromatic Rings: 1Heavy Atoms: 26QED Weighted: 0.52Np Likeness Score: 1.38

References

1. DeBerardinis AM, Raccuia DS, Thompson EN, Maschinot CA, Kyle Hadden M..  (2015)  Vitamin D3 analogues that contain modified A- and seco-B-rings as hedgehog pathway inhibitors.,  93  [PMID:25676864] [10.1016/j.ejmech.2015.01.049]
2. Maschinot CA, Chau LQ, Wechsler-Reya RJ, Hadden MK..  (2019)  Synthesis and evaluation of third generation vitamin D3 analogues as inhibitors of Hedgehog signaling.,  162  [PMID:30471551] [10.1016/j.ejmech.2018.11.028]

Source