ID: ALA3729794

Max Phase: Preclinical

Molecular Formula: C28H28N2O

Molecular Weight: 408.55

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  N#Cc1cccc(CO[C@@H]2C3CCN(CC3)C2C(c2ccccc2)c2ccccc2)c1

Standard InChI:  InChI=1S/C28H28N2O/c29-19-21-8-7-9-22(18-21)20-31-28-25-14-16-30(17-15-25)27(28)26(23-10-3-1-4-11-23)24-12-5-2-6-13-24/h1-13,18,25-28H,14-17,20H2/t27?,28-/m1/s1

Standard InChI Key:  UTAKSYGAZXEURO-PLYLYKGUSA-N

Associated Targets(Human)

Mas-related G-protein coupled receptor member X1 365 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Mas-related G-protein coupled receptor member X1 44 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: 408.55Molecular Weight (Monoisotopic): 408.2202AlogP: 5.37#Rotatable Bonds: 6
Polar Surface Area: 36.26Molecular Species: NEUTRALHBA: 3HBD: 0
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 7.91CX LogP: 5.65CX LogD: 5.02
Aromatic Rings: 3Heavy Atoms: 31QED Weighted: 0.55Np Likeness Score: -0.11

References

1.  (2012)  Methods and compositions for treating or preventing pruritis, 

Source