| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4079524
Max Phase: Preclinical
Molecular Formula: C21H12FN2NaO7S
Molecular Weight: 456.41
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: Nc1c(S(=O)(=O)[O-])cc(Nc2cccc(F)c2C(=O)O)c2c1C(=O)c1ccccc1C2=O.[Na+]
Standard InChI: InChI=1S/C21H13FN2O7S.Na/c22-11-6-3-7-12(15(11)21(27)28)24-13-8-14(32(29,30)31)18(23)17-16(13)19(25)9-4-1-2-5-10(9)20(17)26;/h1-8,24H,23H2,(H,27,28)(H,29,30,31);/q;+1/p-1
Standard InChI Key: JGZSYCIWBWGHPW-UHFFFAOYSA-M
Associated Targets(Human)
Pyrimidinergic receptor P2Y4 598 Activities
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 |
Drug Indications
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Properties
| Molecular Weight: 456.41 | Molecular Weight (Monoisotopic): 456.0427 | AlogP: 2.87 | #Rotatable Bonds: 4 |
| Polar Surface Area: 163.86 | Molecular Species: ACID | HBA: 7 | HBD: 4 |
| #RO5 Violations: 0 | HBA (Lipinski): 9 | HBD (Lipinski): 5 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: -2.53 | CX Basic pKa: | CX LogP: 2.31 | CX LogD: -1.38 |
| Aromatic Rings: 3 | Heavy Atoms: 32 | QED Weighted: 0.27 | Np Likeness Score: -0.41 |
References
| 1. Rafehi M, Malik EM, Neumann A, Abdelrahman A, Hanck T, Namasivayam V, Müller CE, Baqi Y.. (2017) Development of Potent and Selective Antagonists for the UTP-Activated P2Y4 Receptor., 60 (7): [PMID:28306255] [10.1021/acs.jmedchem.7b00030] |
Source
Source(1):