Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA5219414
Max Phase: Preclinical
Molecular Formula: C20H24N6
Molecular Weight: 348.45
Associated Items:
ID: ALA5219414
Max Phase: Preclinical
Molecular Formula: C20H24N6
Molecular Weight: 348.45
Associated Items:
Canonical SMILES: CN(C)CCCNC(=N)Nc1nc(-c2ccccc2)c2ccccc2n1
Standard InChI: InChI=1S/C20H24N6/c1-26(2)14-8-13-22-19(21)25-20-23-17-12-7-6-11-16(17)18(24-20)15-9-4-3-5-10-15/h3-7,9-12H,8,13-14H2,1-2H3,(H3,21,22,23,24,25)
Standard InChI Key: OEFBGDBCFUDDKE-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: | 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: 348.45 | Molecular Weight (Monoisotopic): 348.2062 | AlogP: 3.18 | #Rotatable Bonds: 6 |
Polar Surface Area: 76.93 | Molecular Species: BASE | HBA: 4 | HBD: 3 |
#RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: 8.81 | CX LogP: 3.47 | CX LogD: 1.80 |
Aromatic Rings: 3 | Heavy Atoms: 26 | QED Weighted: 0.36 | Np Likeness Score: -1.02 |
1. Morrill C, Friesen WJ, Babu S, Baiazitov RY, Du W, Karloff DB, Lee CS, Moon YC, Ren H, Sierra J, Tomizawa Y, Vazirani P, Welch EM, Xue X, Zhuo J.. (2022) Guanidino quinazolines and pyrimidines promote readthrough of premature termination codons in cells with native nonsense mutations., 76 [PMID:36150638] [10.1016/j.bmcl.2022.128989] |
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