Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
ID: ALA2288432
Max Phase: Preclinical
Molecular Formula: C14H18N4
Molecular Weight: 242.33
Molecule Type: Small molecule
Associated Items:
ID: ALA2288432
Max Phase: Preclinical
Molecular Formula: C14H18N4
Molecular Weight: 242.33
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: Cc1cc(C)nc(-n2nc3c(c2C)CCCC3)n1
Standard InChI: InChI=1S/C14H18N4/c1-9-8-10(2)16-14(15-9)18-11(3)12-6-4-5-7-13(12)17-18/h8H,4-7H2,1-3H3
Standard InChI Key: DWZMFYARTYAIOT-UHFFFAOYSA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
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: 242.33 | Molecular Weight (Monoisotopic): 242.1531 | AlogP: 2.47 | #Rotatable Bonds: 1 |
Polar Surface Area: 43.60 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 0 |
#RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: 2.17 | CX LogP: 2.60 | CX LogD: 2.60 |
Aromatic Rings: 2 | Heavy Atoms: 18 | QED Weighted: 0.77 | Np Likeness Score: -1.51 |
1. KONISHI K, KURAGANO T. (1990) Fungicidal Activity of Pyrazolylpyrimidines, 15 (1): [10.1584/jpestics.15.13] |
Source(1):