ID: ALA3402684

Max Phase: Preclinical

Molecular Formula: C18H21Cl2N

Molecular Weight: 285.82

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CN(C)[C@@H]1Cc2ccccc2[C@@H](c2ccccc2Cl)C1.Cl

Standard InChI:  InChI=1S/C18H20ClN.ClH/c1-20(2)14-11-13-7-3-4-8-15(13)17(12-14)16-9-5-6-10-18(16)19;/h3-10,14,17H,11-12H2,1-2H3;1H/t14-,17+;/m1./s1

Standard InChI Key:  HZEWBMLAXFVPPT-CVLQQERVSA-N

Associated Targets(Human)

Serotonin 2b (5-HT2b) receptor 10323 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Serotonin 2a (5-HT2a) receptor 14758 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Serotonin 2c (5-HT2c) receptor 11471 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Histamine H3 receptor 10389 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Serotonin 2 receptors; 5-HT2a & 5-HT2c 792 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: 285.82Molecular Weight (Monoisotopic): 285.1284AlogP: 4.35#Rotatable Bonds: 2
Polar Surface Area: 3.24Molecular Species: BASEHBA: 1HBD: 0
#RO5 Violations: 0HBA (Lipinski): 1HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 9.61CX LogP: 4.77CX LogD: 2.58
Aromatic Rings: 2Heavy Atoms: 20QED Weighted: 0.79Np Likeness Score: -0.59

References

1. Sakhuja R, Kondabolu K, Córdova-Sintjago T, Travers S, Vincek AS, Kim MS, Abboud KA, Fang L, Sun Z, Canal CE, Booth RG..  (2015)  Novel 4-substituted-N,N-dimethyltetrahydronaphthalen-2-amines: synthesis, affinity, and in silico docking studies at serotonin 5-HT2-type and histamine H1 G protein-coupled receptors.,  23  (7): [PMID:25703249] [10.1016/j.bmc.2015.01.060]

Source