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ツカチニブ

ツカチニブ 化學(xué)構(gòu)造式
937263-43-9
CAS番號.
937263-43-9
化學(xué)名:
ツカチニブ
別名:
ツカチニブ;N6-(4,4-ジメチル-4,5-ジヒドロ-1,3-オキサゾール-2-イル)-N4-(3-メチル-4-{[1,2,4]トリアゾロ[1,5-a]ピリジン-7-イルオキシ}フェニル)キナゾリン-4,6-ジアミン
英語名:
Tucatinib
英語別名:
Tucatinib;N4-(4-([1,2,4]triazolo[1,5-α]pyridin-7-yloxy)-3-methylphenyl)-N6-(4,4-dimethyl-4,5-dihydrooxazol-2-yl)quinazoline-4,6-diamine;4,6-QuinazolinediaMine, N6-(4,5-dihydro-4,4-diMethyl-2-oxazolyl)-N4-[3-Methyl-4-([1,2,4]triazolo[1,5-a]pyridin-7-yloxy)phenyl]-;CS-1710;ONT-380);6-diaMine;N4-(4-([1;Tacatinib;Tocatinib;Ttucatinib
CBNumber:
CB32616075
化學(xué)式:
C26H24N8O2
分子量:
480.52
MOL File:
937263-43-9.mol

ツカチニブ 物理性質(zhì)

比重(密度) :
1.41±0.1 g/cm3(Predicted)
貯蔵溫度 :
Store at -20°C
溶解性:
DMF:1.0(Max Conc. mg/mL);2.08(Max Conc. mM)
DMSO:49.0(Max Conc. mg/mL);101.97(Max Conc. mM)
DMSO:PBS (pH 7.2) (1:2):0.33(Max Conc. mg/mL);0.69(Max Conc. mM)
外見 :
A crystalline solid
酸解離定數(shù)(Pka):
6.61±0.70(Predicted)
色:
White to yellow
InChIKey:
SDEAXTCZPQIFQM-UHFFFAOYSA-N
SMILES:
N1=C2C(C=C(NC3=NC(C)(C)CO3)C=C2)=C(NC2=CC=C(OC3C=CN4N=CN=C4C=3)C(C)=C2)N=C1
安全性情報
  • リスクと安全性に関する聲明
  • 危険有害性情報のコード(GHS)
絵表示(GHS) GHS hazard pictograms
注意喚起語 警告
危険有害性情報
コード 危険有害性情報 危険有害性クラス 區(qū)分 注意喚起語 シンボル P コード
H315 皮膚刺激 皮膚腐食性/刺激性 2 警告 GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 強い眼刺激 眼に対する重篤な損傷性/眼刺激 性 2A 警告 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 呼吸器への刺激のおそれ 特定標(biāo)的臓器毒性、単回暴露; 気道刺激性 3 警告 GHS hazard pictograms
注意書き
P261 粉じん/煙/ガス/ミスト/蒸気/スプレーの吸入を避ける こと。
P280 保護(hù)手袋/保護(hù)衣/保護(hù)眼鏡/保護(hù)面を著用するこ と。
P304+P340 吸入した場合:空気の新鮮な場所に移し、呼吸しやすい 姿勢で休息させること。
P305+P351+P338 眼に入った場合:水で數(shù)分間注意深く洗うこと。次にコ ンタクトレンズを著用していて容易に外せる場合は外す こと。その後も洗浄を続けること。
P405 施錠して保管すること。

ツカチニブ 価格 もっと(2)

メーカー 製品番號 製品説明 CAS番號 包裝 価格 更新時間 購入
富士フイルム和光純薬株式會社(wako) W01TRCD449790
ARRY-380
937263-43-9 2.5mg ¥77600 2023-06-01 購入
富士フイルム和光純薬株式會社(wako) W01TRCD449790
ARRY-380
937263-43-9 25mg ¥603100 2023-06-01 購入

ツカチニブ 化學(xué)特性,用途語,生産方法

効能

抗悪性腫瘍薬

説明

Tucatinib is also known as ARRY-380 or Irbinitinib. ARRY-380 is an orally inhibitor of human epidermal growth factor receptor tyrosine kinase ErbB-2 (also called HER2) with potential antineoplastic activity. It selectively binds to and inhibits the phosphorylation of ErbB-2, which may prevent the activation of ErbB-2 signal transduction pathways, resulting in growth inhibition and death of ErbB-2-expressing tumor cells. ErbB-2 is overexpressed in a variety of cancers and plays an important role in cellular proliferation and differentiation. Therefore, ARRY-380 may be an alternative treatmentmethod for the treatment of HER2+ cancers.

特性

Year of discovery: 2006
Year of introduction: 2020
Discovered by: Array BioPharma
Developed by: Array BioPharma
Primary targets: HER2
Binding type: I/II
Class: receptor tyrosine kinase
Treatment: HER2-positive breast cancer
Other names: ONT-380, ARRY-380
Oral bioavailability = not reported
Elimination half-life = 5.4 hours
Protein binding = 97%

使用

Tucatinib, a highly selective HER2 inhibitor, was approved in 2020 as a combination therapy with trastuzumab and capecitabine for the treatment of patients with advanced unresectable or metastatic HER2-positive breast cancer, including patients with brain metastases, who have received one or more prior anti-HER2-based regimens in the metastatic setting.

brand name

TukysaTM

副作用

Tukysa (tucatinib) is a brand-name prescription medication. The Active ingredient is tucatinib. Serious side effects can include diarrhoea, liver damage, and allergic reactions. Mild side effects can occur with Tukysa use. This list doesn’t include all possible mild side effects of the drug. Mild side effects that have been reported with Tukysa include nausea and vomiting, fatigue, reduced appetite, weight loss, joint pain; peripheral neuropathy (nerve damage that causes tingling, numbness, or weakness in your arms, hands, legs, or feet); abdominal pain; headache; skin rash; nosebleeds; anemia (low level of red blood cells); stomatitis; hand-foot syndrome.

Mode of action

Tucatinib binds to tyrosine kinase (an enzyme) of HER2, reducing PI3-kinase and MAP-kinase signaling. In vitro, tucatinib inhibits phosphorylation of HER2 and HER3, resulting in inhibition of downstream MAPK and AKT signaling and cell proliferation, and showed anti-tumor activity in HER2 expressing tumor cells. In vivo, tucatinib inhibited the growth of HER2 expressing tumors. The combination of tucatinib and trastuzumab showed increased anti-tumor activity in vitro and in vivo compared to either drug alone.

參考文獻(xiàn)

[1] PATRICE A LEE. In VivoActivity of ARRY-380, a Potent, Small Molecule Inhibitor of ErbB2 in Combination with Trastuzumab, Docetaxel or Bevacizumab.[J]. Cancer research, 2009, 69 1: 5104-5104. DOI:10.1158/0008-5472.SABCS-09-5104.
[2] S. MOULDER. Abstract A143: ARRY-380, a selective HER2 inhibitor: From drug design to clinical evaluation.[J]. Molecular Cancer Therapeutics, 2011, 10 1. DOI:10.1158/1535-7163.TARG-11-A143.
[3] V. DINKEL. Abstract 852: ARRY-380, a potent, small molecule inhibitor of ErbB2, increases survival in intracranial ErbB2+ xenograft models in mice[J]. Cancer research, 2012, 72 1: 852-852. DOI:10.1158/1538-7445.AM2012-852.
[4] KOCIE?SKI P. Synthesis of Tucatinib[J]. Synfacts, 2019, 24 1: 0965. DOI:10.1055/s-0039-1690496.
[5] RASHMI K MURTHY. Tucatinib, Trastuzumab, and Capecitabine for HER2-Positive Metastatic Breast Cancer.[J]. New England Journal of Medicine, 2020, 382 7: 597-609. DOI:10.1056/NEJMoa1914609.
[6] RASHMI MURTHY. Tucatinib with capecitabine and trastuzumab in advanced HER2-positive metastatic breast cancer with and without brain metastases: a non-randomised, open-label, phase 1b study.[J]. Lancet Oncology, 2018: 880-888. DOI:10.1016/S1470-2045(18)30256-0.

ツカチニブ 上流と下流の製品情報

原材料

準(zhǔn)備製品


ツカチニブ 生産企業(yè)

Global( 214)Suppliers
名前 電話番號 電子メール 國籍 製品カタログ 優(yōu)位度
Zhengzhou Anhuida Chemical Co., Ltd
+8615903659408
admin@ahdchem.com China 286 58
BEIJING SJAR TECHNOLOGY DEVELOPMENT CO., LTD.
+86-18600796368 +86-18600796368
sales@sjar-tech.com China 484 58
Hebei Mujin Biotechnology Co.,Ltd
+86 13288715578 +8613288715578
sales@hbmojin.com China 12825 58
HangZhou RunYan Pharma Technology Co.,LTD.
+8618882027439
sales2@runyanpharma.com China 302 58
Zhengzhou Anbu Chem Co.,Ltd
+86-0371-88006763; +8615988602810
sales@anbuchem.com China 2998 58
Hangzhou Hyper Chemicals Limited
+86-0086-57187702781 +8613675893055
info@hyper-chem.com China 295 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21632 55
Nanjing Finetech Chemical Co., Ltd.
025-85710122 17714198479
sales@fine-chemtech.com CHINA 885 55
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795
ivan@atkchemical.com China 32965 60
TianYuan Pharmaceutical CO.,LTD
+86-755-23284190 13684996853
sales@tianpharm.com CHINA 304 58

ツカチニブ  スペクトルデータ(1HNMR)


937263-43-9(ツカチニブ)キーワード:


  • 937263-43-9
  • ONT-380)
  • N4-(4-([1
  • N6-(4,5-Dihydro-4,4-dimethyl-2-oxazolyl)-N4-[3-methyl-4-([1,2,4]triazolo[1,5-a]pyridin-7-yloxy)phenyl]-4,6-quinazolinediamine
  • Irbinitinib
  • Irbinitinib(ARRY380)
  • (R)-N6-(4-Methyl-4
  • 5-dihydrooxazol-2-yl)-N4-(3-Methyl-4-(thiazol-2-ylMethoxy)phenyl)quinazoline-4
  • 6-diaMine
  • 4-diMethyl-4
  • 5-a]pyridin-7-yloxy)-3-Methylphenyl)-N6-(4
  • 5-dihydrooxazol-2-yl)quinazoline-4
  • ARRY-380;IRBINITINIB [INN]; SCHEMBL1193050; ONT-380;
  • Irbinitinib [INN]
  • Tucatinib(ARRY-380, ONT-380)
  • Irbinitinib (Tucatinib)
  • Tucatinib (Irbinitinib,ARRY-380)
  • Tacatinib
  • N6-(4,5-Dihydro-4,4-dimethyl-2-oxazolyl)Chemicalbook-N4-[3-methyl-4-([1,2,4]triazolo[1,5-a]pyridin-7-yloxy)phenyl]-4,6-quinazolinediamine
  • Irbinitirnib(ARRY-380)
  • Tukysa/Tucatinib/ONT-380
  • Tocatinib
  • SCHEMBL1193050
  • CS-1710
  • IRBINITINIB (ARRY-380; ONT-380)
  • Irbinitinib (ARRY-380,Tucatinib,ONT 380)
  • N4-(4-([1,2,4]triazolo[1,5-α]pyridin-7-yloxy)-3-methylphenyl)-N6-(4,4-dimethyl-4,5-dihydrooxazol-2-yl)quinazoline-4,6-diamine
  • Tucatinib
  • 4,6-QuinazolinediaMine, N6-(4,5-dihydro-4,4-diMethyl-2-oxazolyl)-N4-[3-Methyl-4-([1,2,4]triazolo[1,5-a]pyridin-7-yloxy)phenyl]-
  • Ttucatinib
  • 13C6]-Tucatinib
  • ツカチニブ
  • N6-(4,4-ジメチル-4,5-ジヒドロ-1,3-オキサゾール-2-イル)-N4-(3-メチル-4-{[1,2,4]トリアゾロ[1,5-a]ピリジン-7-イルオキシ}フェニル)キナゾリン-4,6-ジアミン
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