ID: ALA4748522

Max Phase: Preclinical

Molecular Formula: C20H16N2O7S

Molecular Weight: 428.42

Molecule Type: Unknown

Representations

Canonical SMILES:  COc1cccc(C(=O)Nc2ccc(S(=O)(=O)Oc3cccc([N+](=O)[O-])c3)cc2)c1

Standard InChI:  InChI=1S/C20H16N2O7S/c1-28-17-6-2-4-14(12-17)20(23)21-15-8-10-19(11-9-15)30(26,27)29-18-7-3-5-16(13-18)22(24)25/h2-13H,1H3,(H,21,23)

Standard InChI Key:  NXFMFXLMEUSPOH-UHFFFAOYSA-N

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Unknown

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Properties

Molecular Weight: 428.42

Molecular Weight (Monoisotopic): 428.0678

AlogP: 3.62

#Rotatable Bonds: 7

Polar Surface Area: 124.84

Molecular Species: NEUTRAL

HBA: 7

HBD: 1

#RO5 Violations: 0

HBA (Lipinski): 9

HBD (Lipinski): 1

#RO5 Violations (Lipinski): 0

CX Acidic pKa:

CX Basic pKa:

CX LogP: 4.06

CX LogD: 4.06

Aromatic Rings: 3

Heavy Atoms: 30

QED Weighted: 0.35

Np Likeness Score: -1.51

References

1. Pillaiyar T,Funke M,Al-Hroub H,Weyler S,Ivanova S,Schlegel J,Abdelrahman A,Müller CE.  (2020)  Design, synthesis and biological evaluation of suramin-derived dual antagonists of the proinflammatory G protein-coupled receptors P2Y and GPR17.,  186  [PMID:31727469] [10.1016/j.ejmech.2019.111789]

Source

Source(1):

• Scientific Literature