ID: ALA3275462

Max Phase: Preclinical

Molecular Formula: C20H25NO3

Molecular Weight: 327.42

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC[C@@H](C)N1CC[C@]23c4c5ccc(O)c4O[C@H]2[C@@H](O)C=C[C@H]3[C@H]1C5

Standard InChI:  InChI=1S/C20H25NO3/c1-3-11(2)21-9-8-20-13-5-7-16(23)19(20)24-18-15(22)6-4-12(17(18)20)10-14(13)21/h4-7,11,13-14,16,19,22-23H,3,8-10H2,1-2H3/t11-,13+,14-,16+,19+,20+/m1/s1

Standard InChI Key:  DHWOEIFEZNBNSB-QHOWBERBSA-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: 327.42Molecular Weight (Monoisotopic): 327.1834AlogP: 2.37#Rotatable Bonds: 2
Polar Surface Area: 52.93Molecular Species: BASEHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.70CX Basic pKa: 10.48CX LogP: 1.94CX LogD: -0.05
Aromatic Rings: 1Heavy Atoms: 24QED Weighted: 0.82Np Likeness Score: 1.84

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