| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4095092
Max Phase: Preclinical
Molecular Formula: C21H12N3NaO9S
Molecular Weight: 483.41
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: Nc1c(S(=O)(=O)[O-])cc(Nc2ccc([N+](=O)[O-])cc2C(=O)O)c2c1C(=O)c1ccccc1C2=O.[Na+]
Standard InChI: InChI=1S/C21H13N3O9S.Na/c22-18-15(34(31,32)33)8-14(23-13-6-5-9(24(29)30)7-12(13)21(27)28)16-17(18)20(26)11-4-2-1-3-10(11)19(16)25;/h1-8,23H,22H2,(H,27,28)(H,31,32,33);/q;+1/p-1
Standard InChI Key: SBHOYZHCJOZKIP-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: 483.41 | Molecular Weight (Monoisotopic): 483.0372 | AlogP: 2.64 | #Rotatable Bonds: 5 |
| Polar Surface Area: 207.00 | Molecular Species: ACID | HBA: 9 | HBD: 4 |
| #RO5 Violations: 0 | HBA (Lipinski): 12 | HBD (Lipinski): 5 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: -2.57 | CX Basic pKa: | CX LogP: 2.10 | CX LogD: -1.57 |
| Aromatic Rings: 3 | Heavy Atoms: 34 | QED Weighted: 0.14 | Np Likeness Score: -0.59 |
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):