ID: ALA3350848

Max Phase: Preclinical

Molecular Formula: C27H43NO5

Molecular Weight: 461.64

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C=C1/C(=C\C=C2/CCC[C@]3(C)[C@@H]([C@H](C)CC[C@H](O)C(C)(C)[N+](=O)[O-])CC[C@@H]23)C[C@@H](O)C[C@@H]1O

Standard InChI:  InChI=1S/C27H43NO5/c1-17(8-13-25(31)26(3,4)28(32)33)22-11-12-23-19(7-6-14-27(22,23)5)9-10-20-15-21(29)16-24(30)18(20)2/h9-10,17,21-25,29-31H,2,6-8,11-16H2,1,3-5H3/b19-9+,20-10-/t17-,21-,22-,23+,24+,25+,27-/m1/s1

Standard InChI Key:  UFVJSMFUFKQHTE-NABJBPAWSA-N

Associated Targets(Human)

HL-60 67320 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Vitamin D receptor 183 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: 461.64Molecular Weight (Monoisotopic): 461.3141AlogP: 4.96#Rotatable Bonds: 7
Polar Surface Area: 103.83Molecular Species: NEUTRALHBA: 5HBD: 3
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.54CX Basic pKa: CX LogP: 3.82CX LogD: 3.82
Aromatic Rings: 0Heavy Atoms: 33QED Weighted: 0.37Np Likeness Score: 2.31

References

1. Oshida J, Okamoto M, Ishizuka S, Azuma S..  (1999)  Synthesis and biological evaluation of 1alpha,24-dihydroxy-25-nitrovitamin D3.,  (3): [PMID:10091688] [10.1016/s0960-894x(99)00013-x]

Source