| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA82809
Max Phase: Preclinical
Molecular Formula: C10H13N5S
Molecular Weight: 235.32
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: C=CCNc1ccc(/C=N/N=C(/N)S)nc1
Standard InChI: InChI=1S/C10H13N5S/c1-2-5-12-8-3-4-9(13-6-8)7-14-15-10(11)16/h2-4,6-7,12H,1,5H2,(H3,11,15,16)/b14-7+
Standard InChI Key: NZQVQMFRRFARHU-VGOFMYFVSA-N
Associated Targets(Human)
Ribonucleoside-diphosphate reductase M2 chain 14 Activities
Associated Targets(non-human)
L1210 27553 Activities
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Mus musculus 284745 Activities
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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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 |
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Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Properties
| Molecular Weight: 235.32 | Molecular Weight (Monoisotopic): 235.0892 | AlogP: 1.26 | #Rotatable Bonds: 5 |
| Polar Surface Area: 75.66 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 3 |
| #RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 6.66 | CX Basic pKa: 3.64 | CX LogP: 1.43 | CX LogD: 0.77 |
| Aromatic Rings: 1 | Heavy Atoms: 16 | QED Weighted: 0.24 | Np Likeness Score: -1.59 |
References
| 1. Liu MC, Lin TS, Cory JG, Cory AH, Sartorelli AC.. (1996) Synthesis and biological activity of 3- and 5-amino derivatives of pyridine-2-carboxaldehyde thiosemicarbazone., 39 (13): [PMID:8691457] [10.1021/jm9600454] |
Source
Source(1):