Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA1161297
Max Phase: Preclinical
Molecular Formula: C4H12N2O2S2
Molecular Weight: 184.29
Molecule Type: Small molecule
Associated Items:
ID: ALA1161297
Max Phase: Preclinical
Molecular Formula: C4H12N2O2S2
Molecular Weight: 184.29
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: N[C@@H](CS)CCS(N)(=O)=O
Standard InChI: InChI=1S/C4H12N2O2S2/c5-4(3-9)1-2-10(6,7)8/h4,9H,1-3,5H2,(H2,6,7,8)/t4-/m1/s1
Standard InChI Key: VJPTURNLUNYYNU-SCSAIBSYSA-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: 184.29 | Molecular Weight (Monoisotopic): 184.0340 | AlogP: -1.08 | #Rotatable Bonds: 4 |
Polar Surface Area: 86.18 | Molecular Species: BASE | HBA: 4 | HBD: 3 |
#RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 4 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 10.26 | CX Basic pKa: 9.33 | CX LogP: -1.88 | CX LogD: -3.55 |
Aromatic Rings: 0 | Heavy Atoms: 10 | QED Weighted: 0.49 | Np Likeness Score: -0.62 |
1. Martin L, Cornille F, Turcaud S, Meudal H, Roques BP, Fournié-Zaluski MC.. (1999) Metallopeptidase inhibitors of tetanus toxin: A combinatorial approach., 42 (3): [PMID:9986722] [10.1021/jm981066w] |
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