ID: ALA4213107

Max Phase: Preclinical

Molecular Formula: C30H50O3

Molecular Weight: 458.73

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C[C@H](CCCC(C)(C)O)[C@H]1CC[C@@]2(C)C3=C(C(=O)C[C@]12C)[C@@]1(C)CC[C@H](O)C(C)(C)[C@@H]1CC3

Standard InChI:  InChI=1S/C30H50O3/c1-19(10-9-15-26(2,3)33)20-13-17-29(7)21-11-12-23-27(4,5)24(32)14-16-28(23,6)25(21)22(31)18-30(20,29)8/h19-20,23-24,32-33H,9-18H2,1-8H3/t19-,20-,23+,24+,28+,29+,30-/m1/s1

Standard InChI Key:  CKIBFNNRGLOKHA-OCBIZMEBSA-N

Associated Targets(Human)

Alpha-crystallin B chain 132 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: 458.73Molecular Weight (Monoisotopic): 458.3760AlogP: 6.85#Rotatable Bonds: 5
Polar Surface Area: 57.53Molecular Species: NEUTRALHBA: 3HBD: 2
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 5.97CX LogD: 5.97
Aromatic Rings: 0Heavy Atoms: 33QED Weighted: 0.47Np Likeness Score: 2.99

References

1. Yang X, Chen XJ, Yang Z, Xi YB, Wang L, Wu Y, Yan YB, Rao Y..  (2018)  Synthesis, Evaluation, and Structure-Activity Relationship Study of Lanosterol Derivatives To Reverse Mutant-Crystallin-Induced Protein Aggregation.,  61  (19): [PMID:30153006] [10.1021/acs.jmedchem.8b00705]

Source