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ID: ALA380570
Max Phase: Preclinical
Molecular Formula: C23H27NO3
Molecular Weight: 365.47
Molecule Type: Small molecule
Associated Items:
ID: ALA380570
Max Phase: Preclinical
Molecular Formula: C23H27NO3
Molecular Weight: 365.47
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: COc1cc2cc(CN3CCCC[C@H]3C)c3ccc(O)cc3c2cc1OC
Standard InChI: InChI=1S/C23H27NO3/c1-15-6-4-5-9-24(15)14-17-10-16-11-22(26-2)23(27-3)13-20(16)21-12-18(25)7-8-19(17)21/h7-8,10-13,15,25H,4-6,9,14H2,1-3H3/t15-/m1/s1
Standard InChI Key: LGGSFSLBLIQBAZ-OAHLLOKOSA-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: 365.47 | Molecular Weight (Monoisotopic): 365.1991 | AlogP: 5.09 | #Rotatable Bonds: 4 |
Polar Surface Area: 41.93 | Molecular Species: BASE | HBA: 4 | HBD: 1 |
#RO5 Violations: 1 | HBA (Lipinski): 4 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: 9.30 | CX Basic pKa: 10.16 | CX LogP: 3.88 | CX LogD: 2.27 |
Aromatic Rings: 3 | Heavy Atoms: 27 | QED Weighted: 0.65 | Np Likeness Score: 0.00 |
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] |
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