ID: ALA3355591

Max Phase: Preclinical

Molecular Formula: C28H44O2

Molecular Weight: 412.66

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C=C1CC(=C)[C@H](O)C/C1=C/C=C1\CCC[C@]2(C)[C@@H]([C@@H](C)CCCC(C)(C)O)CC[C@@H]12

Standard InChI:  InChI=1S/C28H44O2/c1-19(9-7-15-27(4,5)30)24-13-14-25-22(10-8-16-28(24,25)6)11-12-23-18-26(29)21(3)17-20(23)2/h11-12,19,24-26,29-30H,2-3,7-10,13-18H2,1,4-6H3/b22-11+,23-12-/t19-,24+,25-,26+,28+/m0/s1

Standard InChI Key:  AZNYOYSCSXVRJD-HMEXIFNWSA-N

Associated Targets(Human)

HL-60 67320 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Vitamin D receptor 379 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Rattus norvegicus 775804 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

25-hydroxyvitamin D-1 alpha hydroxylase, mitochondrial 60 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: 412.66Molecular Weight (Monoisotopic): 412.3341AlogP: 6.90#Rotatable Bonds: 6
Polar Surface Area: 40.46Molecular Species: NEUTRALHBA: 2HBD: 2
#RO5 Violations: 1HBA (Lipinski): 2HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 5.75CX LogD: 5.75
Aromatic Rings: 0Heavy Atoms: 30QED Weighted: 0.47Np Likeness Score: 2.33

References

1. Sibilska IK, Sicinski RR, Ochalek JT, Plum LA, DeLuca HF..  (2014)  Synthesis and Biological Activity of 25-Hydroxy-2-methylene-vitamin D3 analogues monohydroxylated in the A-ring.,  57  (20): [PMID:25221942] [10.1021/jm500750b]

Source