Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA2315316
Max Phase: Preclinical
Molecular Formula: C7H11NS3
Molecular Weight: 205.37
Molecule Type: Small molecule
Associated Items:
ID: ALA2315316
Max Phase: Preclinical
Molecular Formula: C7H11NS3
Molecular Weight: 205.37
Molecule Type: Small molecule
Associated Items:
Synonyms (1): 2-(Sec-Butyldisulfanyl)Thiazole
Synonyms from Alternative Forms(1):
Canonical SMILES: CCC(C)SSc1nccs1
Standard InChI: InChI=1S/C7H11NS3/c1-3-6(2)10-11-7-8-4-5-9-7/h4-6H,3H2,1-2H3
Standard InChI Key: NLEPKZJPFCAMTO-UHFFFAOYSA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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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 |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Molecular Weight: 205.37 | Molecular Weight (Monoisotopic): 205.0054 | AlogP: 3.68 | #Rotatable Bonds: 4 |
Polar Surface Area: 12.89 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 0 |
#RO5 Violations: 0 | HBA (Lipinski): 1 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: 1.15 | CX LogP: 3.55 | CX LogD: 3.55 |
Aromatic Rings: 1 | Heavy Atoms: 11 | QED Weighted: 0.70 | Np Likeness Score: -0.99 |
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):