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ID: ALA199292
Max Phase: Preclinical
Molecular Formula: C24H31NO3
Molecular Weight: 381.52
Molecule Type: Small molecule
Associated Items:
ID: ALA199292
Max Phase: Preclinical
Molecular Formula: C24H31NO3
Molecular Weight: 381.52
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: COc1ccc(/C(=C\c2ccc(OC)c(OC)c2)CN2CCCC[C@H]2C)cc1
Standard InChI: InChI=1S/C24H31NO3/c1-18-7-5-6-14-25(18)17-21(20-9-11-22(26-2)12-10-20)15-19-8-13-23(27-3)24(16-19)28-4/h8-13,15-16,18H,5-7,14,17H2,1-4H3/b21-15-/t18-/m1/s1
Standard InChI Key: AEFWBVCUQVUPMF-AFDUHFSSSA-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: 381.52 | Molecular Weight (Monoisotopic): 381.2304 | AlogP: 5.13 | #Rotatable Bonds: 7 |
Polar Surface Area: 30.93 | Molecular Species: BASE | HBA: 4 | HBD: 0 |
#RO5 Violations: 1 | HBA (Lipinski): 4 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: | CX Basic pKa: 8.83 | CX LogP: 4.83 | CX LogD: 3.39 |
Aromatic Rings: 2 | Heavy Atoms: 28 | QED Weighted: 0.62 | Np Likeness Score: -0.52 |
1. Banwell MG, Bezos A, Burns C, Kruszelnicki I, Parish CR, Su S, Sydnes MO.. (2006) C8c-C15 monoseco-analogues of the phenanthroquinolizidine alkaloids julandine and cryptopleurine exhibiting potent anti-angiogenic properties., 16 (1): [PMID:16236503] [10.1016/j.bmcl.2005.09.032] |
Source(1):