JTE-013

JTE-013 化学構造式
383150-41-2
CAS番号.
383150-41-2
化学名:
JTE-013
别名:
N-(2,6-ジクロロ-4-ピリジル)-2-[1,3-ジメチル-4-(1-メチルエチル)-1H-ピラゾロ[3,4-b]ピリジン-6-イル]ヒドラジンカルボアミド;JTE-013;1-(2,6-ジクロロピリジン-4-イル)-3-{[1,3-ジメチル-4-(プロパン-2-イル)-1H-ピラゾロ[3,4-b]ピリジン-6-イル]アミノ}尿素
英語名:
JTE-013
英語别名:
CS-2553;JTE-013 HCl;JTE-013;JTE 013;JTE013;LPL Receptor,Apoptosis,JTE-013,Inhibitor,Lysophospholipid Receptor,JTE 013,inhibit,JTE013;1-(2,6-dichloro-4-pyridyl)-3-[(4-isopropyl-1,3-dimethyl-pyrazolo[3,4-b]pyridin-6-yl)amino]urea;1-(2,6-dichloropyridin-4-yl)-3-[(1,3-dimethyl-4-propan-2-ylpyrazolo[3,4-b]pyridin-6-yl)amino]urea;1-[1,3-Dimethyl-4-(2-methylethyl)-1H-pyrazolo[3,4-b]pyridin-6-yl]-4-(3,5-dichloro-4-pyridinyl)-semicarbazide;1-[1,3-Dimethyl-4-(2-methylethyl)-1H-pyrazolo[3,4-b]pyridin-6-yl]-4-(2,6-dichloro-4-pyridinyl)-semicarbazide;N-(2,6-Dichloropyridin-4-yl)-2-(4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)hydrazine-1-carboxamide;N-(2,6-Dichloro-4-pyridinyl)-2-[1,3-dimethyl-4-(1-methylethyl)-1H-pyrazolo[3,4-b]pyridin-6-yl]hydrazinecarboxamide
CBNumber:
CB52591408
化学式:
C17H19Cl2N7O
分子量:
408.29
MOL File:
383150-41-2.mol
MSDS File:
SDS

JTE-013 物理性質

比重(密度) :
1.50±0.1 g/cm3(Predicted)
貯蔵温度 :
2-8°C
溶解性:
DMSO:20mg/mL以上
酸解離定数(Pka):
9.32±0.43(Predicted)
外見 :
色:
ホワイトからオフホワイト
安全性情報
  • リスクと安全性に関する声明
  • 危険有害性情報のコード(GHS)
主な危険性  T
Rフレーズ  25
Sフレーズ  45
RIDADR  UN 2811 6.1 / PGIII
WGK Germany  3
絵表示(GHS) GHS hazard pictograms
注意喚起語 危険
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 区分 注意喚起語 シンボル P コード
H301 飲み込むと有毒 急性毒性、経口 3 危険 GHS hazard pictograms P264, P270, P301+P310, P321, P330,P405, P501
注意書き
P301+P310 飲み込んだ場合:直ちに医師に連絡すること。

JTE-013 価格 もっと(3)

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入
Sigma-Aldrich Japan J4080 ≥98% (HPLC)
JTE-013 ≥98% (HPLC)
383150-41-2 5mg ¥29800 2024-03-01 購入
Sigma-Aldrich Japan J4080 ≥98% (HPLC)
JTE-013 ≥98% (HPLC)
383150-41-2 25mg ¥113000 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01TOC2392
JTE 013
383150-41-2 10mg ¥82000 2023-06-01 購入

JTE-013 化学特性,用途語,生産方法

説明

Sphingosine-1-phosphate (S1P) is a bioactive lipid that exhibits a broad spectrum of biological activities including cell proliferation, survival, migration, cytoskeletal organization, and morphogenesis. It exerts its activity by binding to five distinct G protein-coupled receptors, S1P1/EDG-1, S1P2/EDG-5, S1P3/EDG-3, S1P4/EDG-6, and S1P5/EDG-8. JTE-013 is a potent, selective sphingosine-1-phosphate 2 (S1P2) receptor antagonist that binds to the human and rat receptors with IC50 values of 17 and 22 nM, respectively, (IC50 values >10 μM for human S1P1 and S1P3). It reverses the inhibitory effects of S1P on cell migration of vascular endothelial cells and smooth muscle cells. Similarly, JTE-013 reverses the inhibition of S1P on invasion and migration of B16 melanoma cells. JTE-013 inhibits S1P-induced contraction of, as well as cyclic AMP accumulation in, coronary artery smooth muscle cells.

使用

JTE-013 has been used in in vitro blood?brain barrier (BBB) and blood?tumor barrier (BTB) assays.

Biochem/physiol Actions

JTE-013 can enhance the excitability of small-diameter sensory neurons. It has the ability to repress sphingosine 1-phosphate (S1P)-mediated cellular migration.

JTE-013 上流と下流の製品情報

原材料

準備製品


JTE-013 生産企業

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JTE-013  スペクトルデータ(1HNMR)



  • 383150-41-2
  • 1-[1,3-Dimethyl-4-(2-methylethyl)-1H-pyrazolo[3,4-b]pyridin-6-yl]-4-(2,6-dichloro-4-pyridinyl)-semicarbazide
  • 1-(2,6-dichloro-4-pyridyl)-3-[(4-isopropyl-1,3-dimethyl-pyrazolo[3,4-b]pyridin-6-yl)amino]urea
  • 1-[1,3-Dimethyl-4-(2-methylethyl)-1H-pyrazolo[3,4-b]pyridin-6-yl]-4-(3,5-dichloro-4-pyridinyl)-semicarbazide
  • CS-2553
  • N-(2,6-Dichloro-4-pyridinyl)-2-[1,3-dimethyl-4-(1-methylethyl)-1H-pyrazolo[3,4-b]pyridin-6-yl]hydrazinecarboxamide
  • JTE-013;JTE 013;JTE013
  • 1-(2,6-dichloropyridin-4-yl)-3-[(1,3-dimethyl-4-propan-2-ylpyrazolo[3,4-b]pyridin-6-yl)amino]urea
  • Hydrazinecarboxamide, N-(2,6-dichloro-4-pyridinyl)-2-[1,3-dimethyl-4-(1-methylethyl)-1H-pyrazolo[3,4-b]pyridin-6-yl]-
  • N-(2,6-Dichloropyridin-4-yl)-2-(4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)hydrazine-1-carboxamide
  • JTE-013 HCl
  • LPL Receptor,Apoptosis,JTE-013,Inhibitor,Lysophospholipid Receptor,JTE 013,inhibit,JTE013
  • N-(2,6-ジクロロ-4-ピリジル)-2-[1,3-ジメチル-4-(1-メチルエチル)-1H-ピラゾロ[3,4-b]ピリジン-6-イル]ヒドラジンカルボアミド
  • JTE-013
  • 1-(2,6-ジクロロピリジン-4-イル)-3-{[1,3-ジメチル-4-(プロパン-2-イル)-1H-ピラゾロ[3,4-b]ピリジン-6-イル]アミノ}尿素
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