| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4745667
Max Phase: Preclinical
Molecular Formula: C21H25N3O3S3
Molecular Weight: 463.65
Molecule Type: Unknown
Associated Items:
Representations
Canonical SMILES: CCSCc1csc(/C=C/S(=O)(=O)NC(=O)Nc2c3c(cc4c2CCC4)CCC3)n1
Standard InChI: InChI=1S/C21H25N3O3S3/c1-2-28-12-16-13-29-19(22-16)9-10-30(26,27)24-21(25)23-20-17-7-3-5-14(17)11-15-6-4-8-18(15)20/h9-11,13H,2-8,12H2,1H3,(H2,23,24,25)/b10-9+
Standard InChI Key: OYITZGHTIKFAHB-MDZDMXLPSA-N
Associated Targets(Human)
NACHT, LRR and PYD domains-containing protein 3 908 Activities
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 |
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: 463.65 | Molecular Weight (Monoisotopic): 463.1058 | AlogP: 4.50 | #Rotatable Bonds: 7 |
| Polar Surface Area: 88.16 | Molecular Species: ACID | HBA: 6 | HBD: 2 |
| #RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 3.64 | CX Basic pKa: 1.90 | CX LogP: 4.48 | CX LogD: 3.65 |
| Aromatic Rings: 2 | Heavy Atoms: 30 | QED Weighted: 0.63 | Np Likeness Score: -1.30 |
References
| 1. Agarwal S,Pethani JP,Shah HA,Vyas V,Sasane S,Bhavsar H,Bandyopadhyay D,Giri P,Viswanathan K,Jain MR,Sharma R. (2020) Identification of a novel orally bioavailable NLRP3 inflammasome inhibitor., 30 (21.0): [PMID:32980515] [10.1016/j.bmcl.2020.127571] |
Source
Source(1):