ID: ALA2441552

Max Phase: Preclinical

Molecular Formula: C20H34ClNO2

Molecular Weight: 319.49

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCCCCCCc1ccc(CO[C@@H]2CN[C@H](CO)C2)cc1.Cl

Standard InChI:  InChI=1S/C20H33NO2.ClH/c1-2-3-4-5-6-7-8-17-9-11-18(12-10-17)16-23-20-13-19(15-22)21-14-20;/h9-12,19-22H,2-8,13-16H2,1H3;1H/t19-,20-;/m0./s1

Standard InChI Key:  ICGWLOCGXMULOL-FKLPMGAJSA-N

Associated Targets(Human)

CCRF-CEM 65223 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

BV-173 173 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: 319.49Molecular Weight (Monoisotopic): 319.2511AlogP: 3.83#Rotatable Bonds: 11
Polar Surface Area: 41.49Molecular Species: BASEHBA: 3HBD: 2
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 9.97CX LogP: 4.43CX LogD: 1.94
Aromatic Rings: 1Heavy Atoms: 23QED Weighted: 0.61Np Likeness Score: 0.79

References

1. Fransson R, McCracken AN, Chen B, McMonigle RJ, Edinger AL, Hanessian S..  (2013)  Design, Synthesis, and Anti-leukemic Activity of Stereochemically Defined Constrained Analogs of FTY720 (Gilenya).,  (10): [PMID:24273632] [10.1021/ml4002425]

Source