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ID: ALA4086902
Max Phase: Preclinical
Molecular Formula: C19H22N2O2
Molecular Weight: 310.40
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CCc1c(CO)c(CO)c2n1CCc1c-2n(C)c2ccccc12
Standard InChI: InChI=1S/C19H22N2O2/c1-3-16-14(10-22)15(11-23)19-18-13(8-9-21(16)19)12-6-4-5-7-17(12)20(18)2/h4-7,22-23H,3,8-11H2,1-2H3
Standard InChI Key: PJXKYXGXJMUUNA-UHFFFAOYSA-N
Associated Targets(Human)
CCRF-CEM (65223 Activities)
HCT-116 (91556 Activities)
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PC-3 (62116 Activities)
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NCI-H460 (60772 Activities)
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NCI-H526 (216 Activities)
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NCI-H211 (20 Activities)
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TOP1 Tclin DNA topoisomerase I (7553 Activities)
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TOP2A Tclin DNA topoisomerase II alpha (6317 Activities)
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Molecule Features
| 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 |
Drug Indications
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Mechanisms of Action
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Properties
| Molecular Weight: 310.40 | Molecular Weight (Monoisotopic): 310.1681 | AlogP: 2.75 | #Rotatable Bonds: 3 |
| Polar Surface Area: 50.32 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 2 |
| #RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: | CX LogP: 2.31 | CX LogD: 2.31 |
| Aromatic Rings: 3 | Heavy Atoms: 23 | QED Weighted: 0.78 | Np Likeness Score: 0.01 |
References
| 1. Chang SM, Christian W, Wu MH, Chen TL, Lin YW, Suen CS, Pidugu HB, Detroja D, Shah A, Hwang MJ, Su TL, Lee TC.. (2017) Novel indolizino[8,7-b]indole hybrids as anti-small cell lung cancer agents: Regioselective modulation of topoisomerase II inhibitory and DNA crosslinking activities., 127 [PMID:28064078] [10.1016/j.ejmech.2016.12.046] |
Source
Source(1):