ID: ALA1609153

Max Phase: Preclinical

Molecular Formula: C17H25N3O3

Molecular Weight: 319.40

Molecule Type: Small molecule

Representations

Canonical SMILES:  CCOC(=O)N1CCC(NCCNC(=O)c2ccccc2)CC1

Standard InChI:  InChI=1S/C17H25N3O3/c1-2-23-17(22)20-12-8-15(9-13-20)18-10-11-19-16(21)14-6-4-3-5-7-14/h3-7,15,18H,2,8-13H2,1H3,(H,19,21)

Standard InChI Key:  VNRSRVXFGIQMBW-UHFFFAOYSA-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: 319.40

Molecular Weight (Monoisotopic): 319.1896

AlogP: 1.63

#Rotatable Bonds: 6

Polar Surface Area: 70.67

Molecular Species: BASE

HBA: 4

HBD: 2

#RO5 Violations: 0

HBA (Lipinski): 6

HBD (Lipinski): 2

#RO5 Violations (Lipinski): 0

CX Acidic pKa:

CX Basic pKa: 9.65

CX LogP: 0.91

CX LogD: -1.29

Aromatic Rings: 1

Heavy Atoms: 23

QED Weighted: 0.78

Np Likeness Score: -1.21

References

1. PubChem BioAssay data set, 

2. Sheffler DJ, Sevel C, Le U, Lovell KM, Tarr JC, Carrington SJ, Cho HP, Digby GJ, Niswender CM, Conn PJ, Hopkins CR, Wood MR, Lindsley CW..  (2013)  Further exploration of M₁ allosteric agonists: subtle structural changes abolish M₁ allosteric agonism and result in pan-mAChR orthosteric antagonism.,  23  (1): [PMID:23200253] [10.1016/j.bmcl.2012.10.132]

Source

Source(2):

• Scientific Literature
• PubChem BioAssays