Olaparib AZD-2281 CAS 763113-22-0 Purity ≥99.0% API Factory

Tsanangudzo Pfupi

Zita reKemikari: Olaparib (AZD-2281)

CAS: 763113-22-0

Kuchena: ≥99.0% (neLC-MS)

Chitarisiko: Muchena kusvika Kuchena-Upfu

A Yakanyanya Simba uye Inosarudza PARP-Inhibitor

API High Quality, Commercial Production

Inquiry: alvin@ruifuchem.com


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Tsanangudzo:

Chemical Properties:

Chemical Name Olaparib
Mashoko anoreva zvakafanana AZD-2281;KU0059436;Lynparza;4-(3-(4-(cyclopropanecarbonyl)piperazine-1-carbonyl)-4-fluorobenzyl)phthalazin-1(2H)-imwe;1-(Cyclopropylcarbonyl) -4-[5-[(3,4-dihydro-4-oxo-1-phthalazinyl)Methyl]-2-fluorobenzoyl]piperazin
Nhamba yeCAS 763113-22-0
Nhamba yeCAT RF-API103
Stock Status MuStock, Kugadzirwa Kunokwira Kusvika Mazana emaKilogram
Molecular Formula C24H23FN4O3
Molecular Weight 434.46
Solubility Soluble muDMSO
Brand Ruifu Chemical

Zvinotsanangurwa:

Item Zvinotsanangurwa
Chitarisiko Ichena kusvika kuOff-White Powder
Kuzivikanwa ne1H NMR Teerera nechimiro
LC-MS Teerera nechimiro
Kuchena / Analysis Method ≥99.0% (neLC-MS)
Kunyorova (KF) ≤0.50%
Kusachena Kumwechete ≤0.50%
Zvose Zvisina Kuchena ≤1.0%
Heavy Metals (as Pb) ≤20ppm
Test Standard Enterprise Standard
Usage API;PARP Inhibitor

Package & Kuchengeta:

Package: Bhodhoro, Aluminium foil bag, Cardboard Drum, 25kg/Drum, kana zvinoenderana nezvinodiwa nemutengi.

Storage Condition:Chengetedza mumidziyo yakavharwa panzvimbo inotonhorera uye yakaoma;Dzivirira kubva kuchiedza uye unyoro.

Zvakanakira:

1

FAQ:

Application:

Olaparib (CAS: 763113-22-0), ine simba uye inosarudza PARP-inhibitor.Muna Zvita 19, 2014, iyo FDA yakabvumidza riini rinopesana negomarara mushonga Olaparib (Lynparza) we monotherapy kune varwere vekenza yepamusoro ye ovarian avo vakaita kanenge katatu kutenderera kwechemotherapy kana varwere vanofungidzirwa kuti BRCA shanduko.Panguva imwecheteyo, FDA yakabvumidza kuwanda uye kupatsanurwa kwemakiti ekuongorora kuti aonekwe shanduko muBRCA1 uye BRCA2, BRCAanalysis CDx.Olaparib ndiyo yekutanga PARP inhibitor mishonga yakatenderwa neFDA.Muna Kukadzi 2, 2015, European Union Food and Drug Administration (EMA) yakatenderawo Olaparib kuti ipinde mumusika munyika makumi maviri nesere dzeEuropean Union dzinosanganisira Iceland, Liechtenstein neNorway.Asi zviratidzo zveEMA neFDA zvakatenderwa zvakasiyana zvishoma;yekutanga ndeye BRCA gene mutation kesi, uye zvakare yekurapa kwekurapa kwevarwere vepamusoro epithelial ovarian cancer vakambogamuchira platinum-ine chemotherapy mishonga uye kuratidza mhinduro uye zvichienderana nekudzoka.

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