184475-35-2 Gefitinib C22H24ClFN4O3
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Gefitinib Basic information |
Product Name: | Gefitinib |
Synonyms: | IRESSA;GEFITINIB;AKOS 91371;n-(3-chloro-4-fluoro-phenyl)-7-methoxy-6-(3-morpholin-4-ylpropoxy)quinazolin-4-amine;N-(3-Chloro-4-fluorophenyl)-7-methoxy-6-[3-(4-morpholinyl)propoxy]-4-quinazolinamine;ZD 1839;4-Quinazolinamine, N-(3-chloro-4-fluorophenyl)-7-methoxy-6-[3-(4-morpholinyl)propoxy]-;Gefitinib(TINIBS) |
CAS: | 184475-35-2 |
MF: | C22H24ClFN4O3 |
MW: | 446.9 |
EINECS: | |
Product Categories: | Active Pharmaceutical Ingredients;Gefitinib;Molecular Targeted Antineoplastic;Intermediates & Fine Chemicals;Pharmaceuticals;Pharmaceutical intermediate;APIs;IRESSA;Anti-cancer&immunity;API |
Mol File: | 184475-35-2.mol |
Gefitinib Chemical Properties |
mp | 119-1200C |
storage temp. | Store at RT |
CAS DataBase Reference | 184475-35-2(CAS DataBase Reference) |
Safety Information |
Gefitinib Usage And Synthesis |
Chemical Properties | Light-Yellow Crystalline Powder |
Usage | Gefitinib (Iressa, ZD-1839) is an EGFR inhibitor for Tyr1173, Tyr992, Tyr1173 and Tyr992 in the NR6wtEGFR and NR6W cells with IC50 of 37 nM, 37nM, 26 nM and 57 nM, respectively. |
Usage | Gefitinib is an antineoplastic. |
Biological Activity | Orally active, selective inhibitor of EGFR tyrosine kinase (IC 50 = 23-79 nM). Shows minimal activity against ErbB2, KDR, c-flt, PKC, MEK and ERK-2. Blocks EGFR autophosphorylation and inhibits tumor growth in mice bearing a range of human xenografts. |
Gefitinib Preparation Products And Raw materials |
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