ID: ALA2048970

Max Phase: Preclinical

Molecular Formula: C22H29NO5

Molecular Weight: 297.44

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CN(CCOCCCc1ccccc1)CCc1ccccc1.O=C(O)C(=O)O

Standard InChI:  InChI=1S/C20H27NO.C2H2O4/c1-21(15-14-20-11-6-3-7-12-20)16-18-22-17-8-13-19-9-4-2-5-10-19;3-1(4)2(5)6/h2-7,9-12H,8,13-18H2,1H3;(H,3,4)(H,5,6)

Standard InChI Key:  FCOBTRSOPGLUSI-UHFFFAOYSA-N

Associated Targets(non-human)

Mu opioid receptor 6060 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Delta opioid receptor 3911 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Kappa opioid receptor 774 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: 297.44Molecular Weight (Monoisotopic): 297.2093AlogP: 3.81#Rotatable Bonds: 10
Polar Surface Area: 12.47Molecular Species: BASEHBA: 2HBD: 0
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 8.88CX LogP: 4.61CX LogD: 3.13
Aromatic Rings: 2Heavy Atoms: 22QED Weighted: 0.62Np Likeness Score: -0.65

References

1. Stavitskaya L, Shim J, Healy JR, Matsumoto RR, MacKerell AD, Coop A..  (2012)  Deconstructing 14-phenylpropyloxymetopon: minimal requirements for binding to mu opioid receptors.,  20  (14): [PMID:22677527] [10.1016/j.bmc.2012.05.006]

Source