Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
ID: ALA2315305
Max Phase: Preclinical
Molecular Formula: C11H14N2S2
Molecular Weight: 238.38
Molecule Type: Small molecule
Associated Items:
ID: ALA2315305
Max Phase: Preclinical
Molecular Formula: C11H14N2S2
Molecular Weight: 238.38
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CC(C)(C)SSc1nc2ccccc2[nH]1
Standard InChI: InChI=1S/C11H14N2S2/c1-11(2,3)15-14-10-12-8-6-4-5-7-9(8)13-10/h4-7H,1-3H3,(H,12,13)
Standard InChI Key: JUGXHSUVCKNTAC-UHFFFAOYSA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
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 |
MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
---|
Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
---|
Molecular Weight: 238.38 | Molecular Weight (Monoisotopic): 238.0598 | AlogP: 4.10 | #Rotatable Bonds: 2 |
Polar Surface Area: 28.68 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 1 |
#RO5 Violations: 0 | HBA (Lipinski): 2 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 9.82 | CX Basic pKa: 3.67 | CX LogP: 3.91 | CX LogD: 3.91 |
Aromatic Rings: 2 | Heavy Atoms: 15 | QED Weighted: 0.80 | Np Likeness Score: -1.10 |
1. DiRaimondo TR, Plugis NM, Jin X, Khosla C.. (2013) Selective inhibition of extracellular thioredoxin by asymmetric disulfides., 56 (3): [PMID:23327656] [10.1021/jm301775s] |
Source(1):