Afatinib CAS 439081-18-2 Puritas >99.5% (HPLC)
Ruifu Chemical Supple intermedia de Afatinib
Afatinib CAS 439081-18-2
Afatinib Dimaleate CAS 850140-73-7
(S)-(+)-3-Hydroxytetrahydrofuran CAS 86087-23-2
acetaldehyda Diethyl acetalis CAS 3616-56-6
trans-4-dimethylaminocrotonic Acidum hydrochloridum CAS 848133-35-75
Diethylphosphonoaceticum acidum CAS 3095-95-2
7-Fluoro-6-Nitroquinazolin-4(1H)-one CAS 162012-69-3
7-Chloro-6-Nitro-4-Hydroxyquinazoline CAS 53449-14-2
N-(3-Chloro-4-Fluorophenyl)-7-Fluoro-6-Nitroquinazolin-4-Amine CAS 162012-67-1
(S)-N4-(3-Chloro-4-Fluorophenyl) -7-((Tetrahydrofuran-3-yl)oxy)quinazoline-4,6-DiamineCAS 314771-76-1
(S)-N-(3-Chloro-4-Fluorophenyl)-6-Nitro-7-((Tetrahydrofuran-3-yl)oxy)quinazolin-4-AmineCAS 314771-88-5
Nomen chemicum | Afatinib |
Synonyma | BIBW2992;BIBW-2992;BIBW2992 Free Base;Tomtovok;(S, E)-N-(4-(3-Chloro-4-Fluorophenylamino)-7-(Tetrahydrofuran-3-yloxy)quinazolin-6-yl)-4-(Dimethylamino)but-2-Enamide |
CAS Number | 439081-18-2 |
CATTUS Number | RF-PI2033 |
Stock Status | In Stock, Productio Ascendite ad Tons |
Formulae hypotheticae | C24H25ClFN5O3 |
M. Pondus | 485.94 |
Solubilitas | Solutum in DMSO |
Density | 1.380 |
Brand | Ruifu Chemical |
Item | Specifications |
Aspectus | Off-Pulvis alba |
Lepidium sativum | HPL, NMR |
Puritas / Analysis Methodus | >99.5% (HPLC) |
Liquescens punctum | 1000~102.0℃ |
Damnum in Siccatio | <0.50% |
Residere in Ignition | <0.20% |
Totalis immunditias | <0.50% |
Metalla gravis | ≤20ppm |
NMR Imaginum | Conformat ut Structure |
Test Standard | Enterprise Standard |
Fasciae vita | XXIV menses si proprie Repono |
Consuetudinem | API;Afatinib;Afatinib Dimaleate;NSCLC |
sarcina: Utrem, aluminium foil, sacculum, 25kg/cardboard Drum, vel secundum exigentiam emptoris
Repono Condition:Repone in vasis signatis in loco frigido et sicco;Protege a lumine et humore
Afatinib, etiam ut BIW-2992, (CAS: 439081-18-2) est secunda generatio potens et immedicabilis dualis inhibitor incrementi epidermalis factoris receptoris (EGFR) et incrementi epidermalis humani factoris receptoris 2 (ER2) tyrosini kinasi; evoluta Boehringer Ingelheim, Germania.Capax est irreversibiliter inhibere activitates tyrosinae kinasi Michaelem reactionem cum thiol coetus cysteini in positione 797 EGFR subeundo.Die 12 mensis Iulii anno 2013 novum medicamentum pro anti-parva cellula pulmonis cancri ab US FDA probatum sub artis Gilotrif nomine factum est.Hoc medicamentum tabula est.Ponitur pro curatione aegrorum praecogniti cum cancro metastatico non-parvo cellae pulmonis (NSCLC) cum amissione 19th exon vel L858R mutationem in 21 exon tumoris epidermalis factoris receptoris (EGFR) confirmati utens ornamentum approbatum. apud FDA.Medicamentum etiam efficax est in curatione aegrorum HER2-positivorum cum carcinomate carcinomatis provectis.Afatinib ad genus medicamentorum quae inhibitores tyrosini kinase vocantur.Inhibitores tyrosini kinasi designantur ad impediendam actionem enzyme specificae kinasi vocati tyrosini.Hoc enzyme magnum munus in cellularum munere agit, et agit in incremento et progressu promovendo.Afatinib operatur munus duorum generum kinasium tyrosinorum inhibere: factor incrementi epidermalis receptoris (EGFR) et Her2, quae pluribus generibus cancri "expressae" sunt.Munus harum tyrosinae kinases impediendo, Afatinib impediat cellulas cancer a dividendo et crescendo.