ID: ALA4857247

Max Phase: Preclinical

Molecular Formula: C20H22ClNO2

Molecular Weight: 343.85

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COc1ccc(CNC2CC23CCc2ccccc23)c(Cl)c1OC

Standard InChI:  InChI=1S/C20H22ClNO2/c1-23-16-8-7-14(18(21)19(16)24-2)12-22-17-11-20(17)10-9-13-5-3-4-6-15(13)20/h3-8,17,22H,9-12H2,1-2H3

Standard InChI Key:  OSDYMFLVMKNLNC-UHFFFAOYSA-N

Associated Targets(Human)

Lysine-specific histone demethylase 1 3916 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Monoamine oxidase A 11911 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Monoamine oxidase B 8835 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Lysine-specific histone demethylase 1B 147 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

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

Properties

Molecular Weight: 343.85Molecular Weight (Monoisotopic): 343.1339AlogP: 4.10#Rotatable Bonds: 5
Polar Surface Area: 30.49Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 8.22CX LogP: 4.21CX LogD: 3.33
Aromatic Rings: 2Heavy Atoms: 24QED Weighted: 0.89Np Likeness Score: 0.22

References

1. Dai XJ, Liu Y, Xiong XP, Xue LP, Zheng YC, Liu HM..  (2020)  Tranylcypromine Based Lysine-Specific Demethylase 1 Inhibitor: Summary and Perspective.,  63  (23.0): [PMID:32931269] [10.1021/acs.jmedchem.0c00919]

Source