3-((((1R,3aS,4R,7aR)-7a-methyl-1-((R)-6-methylheptan-2-yl)octahydro-1H-inden-4-yl)methyl)amino)phenol

ID: ALA4443970

Chembl Id: CHEMBL4443970

PubChem CID: 155516669

Max Phase: Preclinical

Molecular Formula: C25H41NO

Molecular Weight: 371.61

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@H](CNc3cccc(O)c3)CCC[C@]12C

Standard InChI:  InChI=1S/C25H41NO/c1-18(2)8-5-9-19(3)23-13-14-24-20(10-7-15-25(23,24)4)17-26-21-11-6-12-22(27)16-21/h6,11-12,16,18-20,23-24,26-27H,5,7-10,13-15,17H2,1-4H3/t19-,20+,23-,24+,25-/m1/s1

Standard InChI Key:  MOZKGGPPOCHUSV-NBABOCAUSA-N

Alternative Forms

  1. Parent:

    ALA4443970

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Associated Targets(non-human)

Vdr Vitamin D receptor (250 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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

Calculated Properties

Molecular Weight: 371.61Molecular Weight (Monoisotopic): 371.3188AlogP: 7.10#Rotatable Bonds: 8
Polar Surface Area: 32.26Molecular Species: NEUTRALHBA: 2HBD: 2
#RO5 Violations: 1HBA (Lipinski): 2HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 9.80CX Basic pKa: 4.73CX LogP: 7.20CX LogD: 7.19
Aromatic Rings: 1Heavy Atoms: 27QED Weighted: 0.51Np Likeness Score: 1.40

References

1. 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