Olaparib AZD-2281 CAS 763113-22-0 Mama ≥99.0% API Falegaosi

Fa'amatalaga Puupuu:

Igoa Vailaau: Olaparib (AZD-2281)

CAS: 763113-22-0

Mama: ≥99.0% (e LC-MS)

Fa'aaliga: Pa'epa'e i le Pa'epa'e Pa'epa'e

Ose PARP-Inhibitor sili ona malosi ma filifilia

API Tulaga Maualuga, Gaosiga Fa'apisinisi

Inquiry: alvin@ruifuchem.com


Fa'amatalaga Oloa

Oloa Fa'atatau

Faailoga o oloa

Fa'amatalaga:

Meatotino tau vailaau:

Igoa Vailaau Olaparib
Synonyms AZD-2281;KU0059436;Lynparza;4-(3-(4-(cyclopropanecarbonyl)piperazine-1-carbonyl)-4-fluorobenzyl)phthalazin-1(2H)-tasi;1-(Cyclopropylcarbonyl)-4-[5-[(3,4-dihydro-4-oxo-1-phthalazinyl)Methyl]-2-fluorobenzoyl]piperazin
Numera CAS 763113-22-0
CAT Numera RF-API103
Tulaga Fa'asoa I Fa'atauga, Oloa Fua e O'o i le selau Kilograms
Fuafua mole C24H23FN4O3
Molecular Weight 434.46
Solubility Solu i le DMSO
Fa'ailoga Ruifu Chemical

Fa'amatalaga:

Aitema Fa'amatalaga
Fa'aaliga Pa'epa'e i le Pa'epa'e Pa'epa'e
Fa'ailoaina e le 1H NMR Tausi ma le fausaga
LC-MS Tausi ma le fausaga
Mama / Suʻesuʻega Metotia ≥99.0% (e LC-MS)
Susū (KF) ≤0.50%
Le mama nofofua ≤0.50%
Aofa'i Fa'aleaga ≤1.0%
Metala mamafa (pei o le Pb) ≤20ppm
Tulaga Su'ega Pisinisi Tulaga
Fa'aoga API;PARP Inhibitor

Paket & Teuina:

afifi: Fagu, Ato pepa alumini, Pusa Pusa, 25kg / Paʻu, poʻo e tusa ai ma manaʻoga o tagata faʻatau.

Tulaga teuina:Teu i totonu o pusa faʻamaufaʻailoga i se nofoaga malulu ma mago;Puipui mai le malamalama ma le susu.

Tulaga lelei:

1

FAQ:

Talosaga:

Olaparib (CAS: 763113-22-0), o se PARP-inhibitor sili ona malosi ma filifilia.Ia Tesema 19, 2014, na faamaonia ai e le FDA le tala fou e tetee atu ai i le kanesa o Olaparib (Lynparza) mo le monotherapy i tagata mamaʻi o le kanesa ovarian maʻi ua maeʻa ia le itiiti ifo ma le 3 taamilosaga o le chemotherapy poʻo tagata gasegase masalomia BRCA suiga.I le taimi lava e tasi, na faʻamaonia e le FDA le aofaʻi ma le faʻavasegaina o pusa faʻamaonia mo le suʻeina o suiga ile BRCA1 ma BRCA2, BRACAnalysis CDx.Olaparib o le PARP inhibitor muamua lea ua faʻamaonia e le FDA.Ia Fepuari 2, 2015, na faʻamaonia ai foi e le European Union Food and Drug Administration (EMA) Olaparib e ulufale atu i le maketi i atunuu e 28 o Europa e aofia ai Iceland, Liechtenstein ma Nouei.Ae o faʻailoga a le EMA ma le FDA ua faʻamaonia e fai sina eseesega;o le mea muamua e mo le BRCA gene mutation mataupu, faʻapea foʻi ma le tausiga o togafitiga mo tagata mamaʻi o le epithelial ovarian kanesa o loʻo maua muamua vailaʻau chemotherapy o loʻo i ai le platinum ma faʻaalia tali ma e mafai ona toe foʻi mai.

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