ID: ALA2147929

Max Phase: Preclinical

Molecular Formula: C26H30ClN3O2

Molecular Weight: 415.54

Molecule Type: Small molecule

Representations

Canonical SMILES:  CN(C)c1ccc2nc3c(cc2c1)C[C@@]1(O)[C@H]2Cc4ccc(O)cc4[C@@]1(CCN2C)C3.Cl

Standard InChI:  InChI=1S/C26H29N3O2.ClH/c1-28(2)19-5-7-22-17(11-19)10-18-14-26(31)24-12-16-4-6-20(30)13-21(16)25(26,8-9-29(24)3)15-23(18)27-22;/h4-7,10-11,13,24,30-31H,8-9,12,14-15H2,1-3H3;1H/t24-,25-,26-;/m1./s1

Standard InChI Key:  YGMBQLZKAOJXNF-PRVDTAJYSA-N

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Small molecule

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Properties

Molecular Weight: 415.54

Molecular Weight (Monoisotopic): 415.2260

AlogP: 3.03

#Rotatable Bonds: 1

Polar Surface Area: 59.83

Molecular Species: NEUTRAL

HBA: 5

HBD: 2

#RO5 Violations: 0

HBA (Lipinski): 5

HBD (Lipinski): 2

#RO5 Violations (Lipinski): 0

CX Acidic pKa: 10.20

CX Basic pKa: 8.11

CX LogP: 3.32

CX LogD: 2.53

Aromatic Rings: 3

Heavy Atoms: 31

QED Weighted: 0.64

Np Likeness Score: 0.54

References

1. Ida Y, Matsubara A, Nemoto T, Saito M, Hirayama S, Fujii H, Nagase H..  (2012)  Synthesis of quinolinomorphinan derivatives as highly selective δ opioid receptor ligands.,  20  (19): [PMID:22967810] [10.1016/j.bmc.2012.08.004]

Source

Source(1):

• Scientific Literature