Afatinib CAS 439081-18-2 Puritas >99.5% (HPLC)

Description:

Nomen chemicum: Afatinib

Synonyma: BIBW2992

CAS: 439081-18-2

Puritas: >99.5% (HPLC)

Aspectus: Off-Pulvis alba

E-Mail: alvin@ruifuchem.com


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Descriptio:

Chemical Properties:

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

Specifications:

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 & Repono:

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

commoda:

1

FAQ:

Applicatio:

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.

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