NA

ID: ALA4566357

PubChem CID: 155561099

Max Phase: Preclinical

Molecular Formula: C36H50ClNO3

Molecular Weight: 580.25

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  CC1(C)CCC[C@](C)([C@H]2CC[C@]3(C)[C@@H]2[C@H](O)C[C@@H]2[C@@]4(C)Cc5c([nH]c6ccc(Cl)cc56)C(C)(C)[C@@H]4C(=O)C[C@]23C)O1

Standard InChI:  InChI=1S/C36H50ClNO3/c1-31(2)13-9-14-36(8,41-31)23-12-15-34(6)28(23)25(39)17-27-33(5)18-22-21-16-20(37)10-11-24(21)38-30(22)32(3,4)29(33)26(40)19-35(27,34)7/h10-11,16,23,25,27-29,38-39H,9,12-15,17-19H2,1-8H3/t23-,25+,27+,28-,29-,33+,34+,35+,36+/m0/s1

Standard InChI Key:  VYOASZMCYJJXFL-ZUVMCECZSA-N

Molfile:  

 
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M  END

Alternative Forms

  1. Parent:

    ALA4566357

    ---

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

Biocomponents

Calculated Properties

Molecular Weight: 580.25Molecular Weight (Monoisotopic): 579.3479AlogP: 8.41#Rotatable Bonds: 1
Polar Surface Area: 62.32Molecular Species: NEUTRALHBA: 3HBD: 2
#RO5 Violations: 2HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: CX LogP: 7.32CX LogD: 7.32
Aromatic Rings: 2Heavy Atoms: 41QED Weighted: 0.36Np Likeness Score: 2.04

References

1. Wu Q, Wang R, Shi Y, Li W, Li M, Chen P, Pan B, Wang Q, Li C, Wang J, Sun G, Sun X, Fu H..  (2020)  Synthesis and biological evaluation of panaxatriol derivatives against myocardial ischemia/reperfusion injury in the rat.,  185  [PMID:31655431] [10.1016/j.ejmech.2019.111729]

Source