ID: ALA5278225

Max Phase: Preclinical

Molecular Formula: C23H29FN2O3

Molecular Weight: 400.49

Associated Items:

Representations

Canonical SMILES:  COc1cccc(C2(O)CCN(C(=O)Cc3cccc(F)c3)CC2CN(C)C)c1

Standard InChI:  InChI=1S/C23H29FN2O3/c1-25(2)15-19-16-26(22(27)13-17-6-4-8-20(24)12-17)11-10-23(19,28)18-7-5-9-21(14-18)29-3/h4-9,12,14,19,28H,10-11,13,15-16H2,1-3H3

Standard InChI Key:  FRHHUJHFLPXGFM-UHFFFAOYSA-N

Associated Targets(Human)

Delta opioid receptor 15096 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Kappa opioid receptor 16155 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Mu opioid receptor 1674 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: Topical: 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: 400.49Molecular Weight (Monoisotopic): 400.2162AlogP: 2.67#Rotatable Bonds: 6
Polar Surface Area: 53.01Molecular Species: BASEHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.71CX Basic pKa: 8.76CX LogP: 2.22CX LogD: 0.84
Aromatic Rings: 2Heavy Atoms: 29QED Weighted: 0.81Np Likeness Score: -0.82

References

1. Huang H, Li X, Xie P, Li X, Xu X, Qian Y, Yuan C, Meng X, Chai J, Chen J, Liu J, Wang W, Li W, Wang Y, Fu W, Liu J..  (2021)  Discovery, Structure-Activity Relationship, and Mechanistic Studies of 1-((3R,4S)-3-((Dimethylamino)methyl)-4-hydroxy-4-(3-methoxyphenyl)piperidin-1-yl)-2-(2,4,5-trifluorophenyl)ethan-1-one as a Novel Potent Analgesic.,  64  (13.0): [PMID:34152138] [10.1021/acs.jmedchem.1c00722]

Source