ID: ALA7681

Max Phase: Preclinical

Molecular Formula: C10H13NO3

Molecular Weight: 195.22

Molecule Type: Small molecule

Representations

Canonical SMILES:  Oc1ccc(C2CNCCO2)cc1O

Standard InChI:  InChI=1S/C10H13NO3/c12-8-2-1-7(5-9(8)13)10-6-11-3-4-14-10/h1-2,5,10-13H,3-4,6H2

Standard InChI Key:  GYJRRQRGZZEHEB-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: 195.22

Molecular Weight (Monoisotopic): 195.0895

AlogP: 0.76

#Rotatable Bonds: 1

Polar Surface Area: 61.72

Molecular Species: NEUTRAL

HBA: 4

HBD: 3

#RO5 Violations: 0

HBA (Lipinski): 4

HBD (Lipinski): 3

#RO5 Violations (Lipinski): 0

CX Acidic pKa: 9.24

CX Basic pKa: 8.06

CX LogP: 0.51

CX LogD: -0.01

Aromatic Rings: 1

Heavy Atoms: 14

QED Weighted: 0.58

Np Likeness Score: 0.75

References

1. Macchia B, Balsamo A, Breschi MC, Lapucci A, Lucacchini A, Macchia F, Manera C, Martinelli A, Martini C, Martinotti E..  (1992)  Conformational effects on the activity of drugs. 13. A revision of previously proposed models for the activation of alpha- and beta-adrenergic receptors.,  35  (6): [PMID:1313109] [10.1021/jm00084a006]

2. Macchia B, Balsamo A, Epifani E, Lapucci A, Nencetti S, Macchia F, Breschi MC, Martinotti E, Ceserani R..  (1986)  Conformational effects on the activity of drugs. 11. Stereostructural models for the direct activation of the alpha- and beta-adrenergic receptor.,  29  (5): [PMID:3009812] [10.1021/jm00155a025]

Source

Source(1):

• Scientific Literature