| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA3249523
Max Phase: Preclinical
Molecular Formula: C14H10N4S
Molecular Weight: 266.33
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: Cc1cccc(-c2nc3cc(N=C=S)ccc3[nH]2)n1
Standard InChI: InChI=1S/C14H10N4S/c1-9-3-2-4-12(16-9)14-17-11-6-5-10(15-8-19)7-13(11)18-14/h2-7H,1H3,(H,17,18)
Standard InChI Key: QUHFOMNKVPXTMX-UHFFFAOYSA-N
Associated Targets(non-human)
Heligmosomoides polygyrus 261 Activities
Rodentolepis nana 555 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: 266.33 | Molecular Weight (Monoisotopic): 266.0626 | AlogP: 3.67 | #Rotatable Bonds: 2 |
| Polar Surface Area: 53.93 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 10.26 | CX Basic pKa: 2.12 | CX LogP: 3.61 | CX LogD: 3.61 |
| Aromatic Rings: 3 | Heavy Atoms: 19 | QED Weighted: 0.57 | Np Likeness Score: -1.53 |
References
| 1. Haugwitz RD, Maurer BV, Jacobs GA, Narayanan VL, Cruthers L, Szanto J.. (1979) Antiparasitic agents. 3. Synthesis and anthelmintic activities of novel 2-pyridinyl-5-isothiocyanatobenzimidazoles., 22 (9): [PMID:490558] [10.1021/jm00195a021] |
Source
Source(1):