スニチニブ
スニチニブ 物理性質(zhì)
- 融點(diǎn) :
- 189-191°C
- 沸點(diǎn) :
- 572.1±50.0 °C(Predicted)
- 比重(密度) :
- 1.2
- 閃點(diǎn) :
- 299.8℃
- 貯蔵溫度 :
- 2-8°C
- 溶解性:
- クロロホルム(微量)、メタノール(微量)
- 酸解離定數(shù)(Pka):
- 8.5(at 25℃)
- 外見(jiàn) :
- 個(gè)體
- 色:
- 黃色から濃いオレンジ
- CAS データベース:
- 557795-19-4(CAS DataBase Reference)
安全性情報(bào)
- リスクと安全性に関する聲明
- 危険有害性情報(bào)のコード(GHS)
絵表示(GHS) |
|
注意喚起語(yǔ) |
警告 |
危険有害性情報(bào) |
コード |
危険有害性情報(bào) |
危険有害性クラス |
區(qū)分 |
注意喚起語(yǔ) |
シンボル |
P コード |
H302 |
飲み込むと有害 |
急性毒性、経口 |
4 |
警告 |
 |
P264, P270, P301+P312, P330, P501 |
H315 |
皮膚刺激 |
皮膚腐食性/刺激性 |
2 |
警告 |
 |
P264, P280, P302+P352, P321,P332+P313, P362 |
H319 |
強(qiáng)い眼刺激 |
眼に対する重篤な損傷性/眼刺激 性 |
2A |
警告 |
 |
P264, P280, P305+P351+P338,P337+P313P |
H332 |
吸入すると有害 |
急性毒性、吸入 |
4 |
警告 |
 |
P261, P271, P304+P340, P312 |
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 |
 |
|
|
注意書(shū)き |
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。 |
P305+P351+P338 |
眼に入った場(chǎng)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(chǎng)合は外す こと。その後も洗浄を続けること。 |
P310 |
ただちに醫(yī)師に連絡(luò)すること。 |
|
スニチニブ 価格
メーカー |
製品番號(hào) |
製品説明 |
CAS番號(hào) |
包裝 |
価格 |
更新時(shí)間 |
購(gòu)入 |
スニチニブ 化學(xué)特性,用途語(yǔ),生産方法
効能
抗悪性腫瘍薬, 血管新生阻害薬, 受容體チロシンキナーゼ阻害薬
説明
Sunitinib is an inhibitor of multiple receptor tyrosine kinases (RTKs) involved
in tumor proliferation and angiogenesis, including platelet-derived growth factor
receptors (PDGFR), vascular endothelial growth factor receptors (VEGFR), and
stem cell factor receptor (KIT). It was launched as an oral treatment for
gastrointestinal stromal tumors (GIST) and advanced renal-cell carcinoma (RCC).
In vitro, sunitib inhibits VEGFR2, PDGFRα, PDGFRβ, KIT, and FLT3 receptors
with IC
50 values in the 4–14nM range, and the ligand-dependent autophosphorylation
of VEGFR2 and PDGFRb with IC
50s of approximately 10 nM.
In addition, it inhibits the growth of tumor cells expressing dysregulated target RTKs in vitro and inhibits PDGFRb- and VEGFR2-dependent tumor angiogenesis
in vivo. Sunitinib exhibits broad and potent antitumor activity, causing regression
in murine models of human epidermal (A431), colon (Colo205 and HT-29), lung
(NCI-H226 and H460), breast (MDA-MB-435), prostate (PC3-3M-luc), and renal
(786-O) cancers, and suppressing or delaying the growth of many others,
including the C6 rat and SF763 T human glioma xenografts and B16 melanoma
lung cancer.
化學(xué)的特性
Yellow Solid
使用
Sunitinib Malate (Sutent, SU11248) is a multi-targeted RTK inhibitor targeting VEGFR2 (Flk-1) and PDGFRβ with IC50 of 80 nM and 2 nM, and also inhibits c-Kit.
特性
Class: receptor tyrosine kinase
Treatment: RCC, GIST
Elimination half-life = 70 h
Protein binding = 95%
スニチニブ 上流と下流の製品情報(bào)
原材料
準(zhǔn)備製品
スニチニブ 生産企業(yè)
Global( 430)Suppliers
557795-19-4(スニチニブ)キーワード:
- 557795-19-4
- SU-11248
- N-[2-(Diethylamino)ethyl]-5-[(Z)-(5-fluoro-2-oxo-1,2- dihydro-3H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide
- N-[2-(Diethylamino)ethyl]-5-[(Z)-(5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide Malate
- N-[2-DiethylaMino(ethyl-d4)]-5-[(Z)-(5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)Methyl]-2,4-diMethyl-1H-pyrrole-3-carboxaMide
- SU-11248-d4
- Sutent-d4
- (Z)-N-(2-(DiethylaMino)ethyl)-5-((5-fluoro-2-oxoindolin-3-ylidene)Methyl)-2,4-diMethyl-1H-pyrrole-3-carboxaMide
- Sunitinib (Mixture of E and Z IsoMer)
- Sunitinib N-(2-(Diethylamino)ethyl)-5-((Z)-(5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxamide
- Sunitinib, >=99%
- sunitinib
- SUNITINIB-D4
- n-(2-(diethylamino)ethyl)-5-((z)-(5-fluoro-1,2-dihydro-2-oxo-3h-indol-3-ylidene)methyl)-2,4-dimethyl-1h-pyrrole-3-carboxamide
- 1H-Pyrrole-3-carboxamide, N-[2-(diethylamino)ethyl]-5-[(Z)-(5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4-dimethyl-
- SUNITINIBMALEATE(FORR&DONLY)
- Sunitinib--- free base
- Sunitinib,Sutent
- 5-(5-Fluoro-2-oxo-1,2-dihydroindol-3-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid N-(2-diethylaminoethyl)amide
- Suniti
- N-[2-(diethylaMino)ethyl]-5-{[(3Z)-5-fluoro-2-oxo-2,3-dihydro-1H-indol-3-ylidene]Methyl}-2,4-diMethyl-1H-pyrrole-3-carboxaMide
- SUTENT SUNITINIB
- N-(2-diethylaminoethyl)-5-[(Z)-(5-fluoro-2-oxo-1H-indol-3-ylidene)meth yl]-2,4-dimethyl-1H-pyrrole-3-carboxamide
- Sunitinib malate(TINIBS)
- Sunitinib malate for research
- N-[2-(Diethylamino)ethyl]-5-[(Z)-(5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide Maleate
- SUNITINIB (SU 11248)
- SU-11248;SU11248
- Sunitinib (Sutent, SU11248)
- SNTI
- (Z)-N-[2-(Diethylamino)ethyl]-5-[(5-fluoro-2-oxo-3-indolinylidene)methyl]-2,4-dimethylpyrrole-3-carboxamide
- スニチニブ
- N-[2-(ジエチルアミノ)エチル]-2,4-ジメチル-5-[(Z)-(2-オキソ-5-フルオロインドリン-3-イリデン)メチル]-1H-ピロール-3-カルボアミド
- N-[2-(ジエチルアミノ)エチル]-5-{[(3Z)-5-フルオロ-2-オキソ-2,3-ジヒドロ-1H-インドール-3-イリデン]メチル}-2,4-ジメチル-1H-ピロール-3-カルボキサミド
- N-[2-(ジエチルアミノ)エチル]-5-[(Z)-[5-フルオロ-2-オキソ-1H-インドール-3(2H)-イリデン]メチル]-2,4-ジメチル-1H-ピロール-3-カルボアミド
- N-[2-(ジエチルアミノ)エチル]-5-[(Z)-(5-フルオロ-1,2-ジヒドロ-2-オキソ-3H-インドール-3-イリデン)メチル]-2,4-ジメチル-1H-ピロール-3-カルボアミド
- N-[2-(ジエチルアミノ)エチル]-5-[(Z)-(5-フルオロ-2-オキソ-1,2-ジヒドロ-3H-インドール-3-イリデン)メチル]-2,4-ジメチル-1H-ピロール-3-カルボアミド