ID: ALA2419939

Max Phase: Preclinical

Molecular Formula: C18H11NO3

Molecular Weight: 289.29

Molecule Type: Small molecule

Representations

Canonical SMILES:  O=c1cc(-c2ccc3ccccc3n2)oc2cc(O)ccc12

Standard InChI:  InChI=1S/C18H11NO3/c20-12-6-7-13-16(21)10-18(22-17(13)9-12)15-8-5-11-3-1-2-4-14(11)19-15/h1-10,20H

Standard InChI Key:  XBPQUNTVVXEWNB-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: 289.29

Molecular Weight (Monoisotopic): 289.0739

AlogP: 3.71

#Rotatable Bonds: 1

Polar Surface Area: 63.33

Molecular Species: ACID

HBA: 4

HBD: 1

#RO5 Violations: 0

HBA (Lipinski): 4

HBD (Lipinski): 1

#RO5 Violations (Lipinski): 0

CX Acidic pKa: 6.50

CX Basic pKa: 2.09

CX LogP: 3.21

CX LogD: 2.28

Aromatic Rings: 4

Heavy Atoms: 22

QED Weighted: 0.58

Np Likeness Score: 0.10

References

1. Hu Y, Yang Y, Yu Y, Wen G, Shang N, Zhuang W, Lu D, Zhou B, Liang B, Yue X, Li F, Du J, Bu X..  (2013)  Synthesis and identification of new flavonoids targeting liver X receptor β involved pathway as potential facilitators of Aβ clearance with reduced lipid accumulation.,  56  (15): [PMID:23844653] [10.1021/jm301913k]

2. Chen M, Yang F, Kang J, Gan H, Lai X, Gao Y..  (2018)  Discovery of molecular mechanism of a clinical herbal formula upregulating serum HDL-c levels in treatment of metabolic syndrome by in vivo and computational studies.,  28  (2): [PMID:29196136] [10.1016/j.bmcl.2017.11.033]

Source

Source(1):

• Scientific Literature