ID: ALA3272387

Max Phase: Preclinical

Molecular Formula: C22H27NO3

Molecular Weight: 353.46

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Oc1ccc2c3c1O[C@H]1[C@@H](O)C=C[C@H]4[C@@H](C2)N(C2CCCCC2)CC[C@@]341

Standard InChI:  InChI=1S/C22H27NO3/c24-17-8-6-13-12-16-15-7-9-18(25)21-22(15,19(13)20(17)26-21)10-11-23(16)14-4-2-1-3-5-14/h6-9,14-16,18,21,24-25H,1-5,10-12H2/t15-,16+,18-,21-,22-/m0/s1

Standard InChI Key:  NTRNFOZMJHPTHK-HIFDQRORSA-N

Associated Targets(non-human)

Opioid receptor 994 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mus musculus 284745 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: 353.46Molecular Weight (Monoisotopic): 353.1991AlogP: 2.90#Rotatable Bonds: 1
Polar Surface Area: 52.93Molecular Species: BASEHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.86CX Basic pKa: 10.72CX LogP: 2.21CX LogD: 0.14
Aromatic Rings: 1Heavy Atoms: 26QED Weighted: 0.76Np Likeness Score: 1.97

References

1. DeGraw JI, Lawson JA, Crase JL, Johnson HL, Ellis M, Uyeno ET, Loew GH, Berkowitz DS..  (1978)  Analgesics. 1. Synthesis and analgesic properties of N-sec-alkyl- and N-tert-alkylnormorphines.,  21  (5): [PMID:207868] [10.1021/jm00203a002]

Source