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ID: ALA4215589
Max Phase: Preclinical
Molecular Formula: C16H17N5O2
Molecular Weight: 311.35
Molecule Type: Small molecule
Associated Items:
ID: ALA4215589
Max Phase: Preclinical
Molecular Formula: C16H17N5O2
Molecular Weight: 311.35
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: COc1ccc2[nH]c(C(=O)NC/C=C/c3c[nH]c(N)n3)cc2c1
Standard InChI: InChI=1S/C16H17N5O2/c1-23-12-4-5-13-10(7-12)8-14(21-13)15(22)18-6-2-3-11-9-19-16(17)20-11/h2-5,7-9,21H,6H2,1H3,(H,18,22)(H3,17,19,20)/b3-2+
Standard InChI Key: KMZOBLJWCCZDOL-NSCUHMNNSA-N
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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: 311.35 | Molecular Weight (Monoisotopic): 311.1382 | AlogP: 1.93 | #Rotatable Bonds: 5 |
Polar Surface Area: 108.82 | Molecular Species: BASE | HBA: 4 | HBD: 4 |
#RO5 Violations: 0 | HBA (Lipinski): 7 | HBD (Lipinski): 5 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: 8.52 | CX LogP: 1.21 | CX LogD: 0.20 |
Aromatic Rings: 3 | Heavy Atoms: 23 | QED Weighted: 0.58 | Np Likeness Score: -0.03 |
1. Zidar N, Žula A, Tomašič T, Rogers M, Kirby RW, Tytgat J, Peigneur S, Kikelj D, Ilaš J, Mašič LP.. (2017) Clathrodin, hymenidin and oroidin, and their synthetic analogues as inhibitors of the voltage-gated potassium channels., 139 [PMID:28802123] [10.1016/j.ejmech.2017.08.015] |
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