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词条 Erdafitinib
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  1. References

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| IUPAC_name = N′-(3,5-Dimethoxyphenyl)-N′-[3-(1-methylpyrazol-4-yl)quinoxalin-6-yl]-N-propan-2-ylethane-1,2-diamine
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| CAS_number = 1346242-81-6
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| PubChem = 67462786
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| UNII = 890E37NHMV
| KEGG = D10927
| synonyms = JNJ-42756493
| C=25|H=30|N=6|O=2
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Erdafitinib[1] is an experimental small molecule inhibitor of FGFR being investigated for use in treating cancer. FGFRs are a subset of tyrosine kinases which are unregulated in some tumors and influence tumor cell differentiation, proliferation, angiogenesis, and cell survival.[2] Astex Pharmaceuticals discovered the drug and licensed it to Janssen Pharmaceuticals for further development.

Erdafitinib is being evaluated for safety and efficacy in phase II clinical trials for cholangiocarcinoma, gastric cancer, non-small cell lung cancer, and esophageal cancer.[3]

In March 2018, erdafitinib was granted Breakthrough Therapy Designation by the U.S. Food and Drug Administration for treatment of urothelial cancer, which should expedite its development and regulatory review.[2]

References

1. ^https://searchusan.ama-assn.org/usan/documentDownload?uri=%2Funstructured%2Fbinary%2Fusan%2Ferdafitinib.pdf
2. ^{{cite web|url=https://www.jnj.com/media-center/press-releases/janssen-announces-us-fda-breakthrough-therapy-designation-for-erdafitinib-in-the-treatment-of-metastatic-urothelial-cancer|title=Janssen Announces U.S. FDA Breakthrough Therapy Designation for Erdafitinib in the Treatment of Metastatic Urothelial Cancer - Johnson & Johnson|website=www.jnj.com}}
3. ^{{cite web|url=http://adisinsight.springer.com/drugs/800036975|title=Erdafitinib - Janssen Pharmaceutica - AdisInsight|website=adisinsight.springer.com}}

4 : Experimental cancer drugs|Quinoxalines|Protein kinase inhibitors|Pyrazoles

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