Short description: Chemical compound
Lucitanib |
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| Other names | CO-3810, E-3810 |
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Routes of administration | By mouth |
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| Elimination half-life | 31–40 hrs |
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IUPAC name
6-({7-[(1-Aminocyclopropyl)methoxy]-6-methoxy-4-quinolinyl}oxy)-N-methyl-1-naphthamide
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| Chemical and physical data |
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| Formula | C26H25N3O4 |
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| Molar mass | 443.503 g·mol−1 |
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SMILES
CNC(=O)c1cccc2c1ccc(c2)Oc3ccnc4c3cc(c(c4)OCC5(CC5)N)OC
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InChI
InChI=1S/C26H25N3O4/c1-28-25(30)19-5-3-4-16-12-17(6-7-18(16)19)33-22-8-11-29-21-14-24(23(31-2)13-20(21)22)32-15-26(27)9-10-26/h3-8,11-14H,9-10,15,27H2,1-2H3,(H,28,30) Key:CUDVHEFYRIWYQD-UHFFFAOYSA-N
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Lucitanib (INN) is a drug that is being investigated by Clovis Oncology in clinical trials for the treatment of advanced solid tumours[1] including metastatic breast cancer.[2] It is a protein kinase inhibitor that blocks the VEGF receptors 1, 2 and 3, as well as the fibroblast growth factor receptors 1 and 2, and the platelet-derived growth factor receptors alpha and beta.[1]
References
- ↑ 1.0 1.1 "Phase I/IIa study evaluating the safety, efficacy, pharmacokinetics, and pharmacodynamics of lucitanib in advanced solid tumors". Annals of Oncology 25 (11): 2244–51. November 2014. doi:10.1093/annonc/mdu390. PMID 25193991.
- ↑ Clinical trial number NCT02053636 for "A Phase II Trial Testing Oral Administration of Lucitanib in Patients With Fibroblast Growth Factor Receptor (FGFR)1-amplified or Non-amplified Estrogen Receptor Positive Metastatic Breast Cancer (FINESSE)" at ClinicalTrials.gov
 | Original source: https://en.wikipedia.org/wiki/Lucitanib. Read more |