SB-1518

SB-1518 化学構造式
937272-79-2
CAS番号.
937272-79-2
化学名:
SB-1518
别名:
11-[2-(ピロリジン-1-イル)エトキシ]-14,19-ジオキサ-5,7,27-トリアザテトラシクロ[19.3.1.12,6.18,12]ヘプタコサン-1(25),2,4,6(27),8,10,12(26),16,21,23-デカエン;11-[2-(ピロリジン-1-イル)エトキシ]-14,19-ジオキサ-5,7,27-トリアザテトラシクロ[19.3.1.12,6.18,12]ヘプタコサ-1(24),2(27),3,5,8,10,12(26),16,21(25),22-デカエン;パクリチニブ;SB-1518
英語名:
PACRITINIB
英語别名:
CS-914;SB1518;PACRITINIB;2H8]-Pacritinib;Pacritinib, >=98%;SB1518(Pacritinib);Pacritinib (SB1518);PACRITINIB USP/EP/BP;SB1518; SB 1518; SB-1518;Pacritinib SB1518 SB-1518
CBNumber:
CB82628224
化学式:
C28H32N4O3
分子量:
472.58
MOL File:
937272-79-2.mol

SB-1518 物理性質

沸点 :
694.3±65.0 °C(Predicted)
比重(密度) :
1.22±0.1 g/cm3(Predicted)
貯蔵温度 :
Store at -20°C
溶解性:
DMSO:5.0(Max Conc. mg/mL);10.6(Max Conc. mM)
外見 :
A crystalline solid
酸解離定数(Pka):
9.56±0.20(Predicted)
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)
絵表示(GHS) GHS hazard pictogramsGHS hazard pictograms
注意喚起語
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
H373 長期にわたる、または反復暴露により臓器の障 害のおそれ 特定標的臓器有害性、単回暴露 2 警告 P260, P314, P501
H400 水生生物に強い毒性 水生環境有害性、急性毒性 1 警告 GHS hazard pictograms P273, P391, P501
H411 長期的影響により水生生物に毒性 水生環境有害性、慢性毒性 2
注意書き
P260 粉じん/煙/ガス/ミスト/蒸気/スプレーを吸入しないこ と。
P273 環境への放出を避けること。
P314 気分が悪い時は、医師の診断/手当てを受けること。
P391 漏出物を回収すること。
P501 内容物/容器を...に廃棄すること。

SB-1518 価格

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

SB-1518 化学特性,用途語,生産方法

特性

Class: non-receptor tyrosine kinase (JAK3)
Treatment: myelofibrosis
Elimination half-life = 40 h
Protein binding = 99%

使用

Pacritinib is a JAK2/FLT3 inhibitor used in the treatment of acute myeloid leukemia showing significant tumor growth inhibition and lung metastasis.

作用機序

Pacritinib competes  with JAK2 for ATP binding, which may result in inhibition of JAK2  activation, inhibition of the JAK-STAT signaling pathway, and so  caspase-dependent apoptosis.

酵素阻害剤

This pyrimidine-based macrocycle and potent protein kinase inhibitor (FW = 472.59 g/mol; CAS 937272-79-2; Solubility: 11 mg/mL DMSO), also known as SB1518, selectively targets Janus Kinase 2 (or JAK2; IC50 = 23 nM) and Fms-Like Tyrosine Kinase-3 (or FLT3; IC50 = 22 nM), with values of 1280 and 522 nM for JAK1 and JAK3. FLT3 is genetically altered in up to 35% of acute myeloblastic leukemias, making it an attractive target for AML patients. Pacritinib has potent anti-proliferative effects on myeloid and lymphoid cell lines driven by mutant or wild-type JAK2 or FLT3, resulting from cell cycle arrest and induction of apoptosis. SB1518 has favorable pharmacokinetic properties after oral dosing in mice, is well tolerated and significantly reduces splenomegaly and hepatomegaly in a JAK2(Val-617-Phe)-driven disease model. Primary Mode of Inhibitory Action: Upregulation of JAK2 in FLT3-TKI-resistant AML cells was identified as a potential mechanism of resistance to selective FLT3 inhibition. This resistance could be overcome by pacritinib’s combined inhibition of FLT3 and JAK2 in this cellular model. Pacritinib potently inhibits FLT3 auto-phosphorylation and downstream STAT5, MAPK and PI3K signaling pathways in AML cell lines with highest potency against cells harboring FLT3-ITD mutations. Blockade of FLT3 signaling was also demonstrated in primary AML blasts treated ex vivo with pacritinib. In both cell lines and primary blasts, pacritinib treatment led to the induction of G1 arrest, inhibition of cell proliferation, as well as caspase-dependent apoptosis. The anti-proliferative effects of pacritinib on the FLT3-ITD harboring cell lines MV4-11 (IC50 = 47 nM) and MOLM-13 (IC50 = 67 nM), which have been reported previously,16 are in the same range as the inhibition of intracellular FLT3 signalling.

SB-1518 上流と下流の製品情報

原材料

準備製品


SB-1518 生産企業

Global( 138)Suppliers
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Henan Tianfu Chemical Co.,Ltd.
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career henan chemical co
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AFINE CHEMICALS LIMITED
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Zhejiang J&C Biological Technology Co.,Limited
+1-2135480471 +1-2135480471
sales@sarms4muscle.com China 10523 58
InvivoChem
+1-708-310-1919 +1-13798911105
sales@invivochem.cn United States 6393 58

SB-1518  スペクトルデータ(1HNMR)


937272-79-2(SB-1518)キーワード:


  • 937272-79-2
  • 14,19-Dioxa-5,7,27-triazatetracyclo[19.3.1.12,6.18,12]heptacosa-1(25),2,4,6(27),8,10,12(26),16,21,23-decaene, 11-[2-(1-pyrrolidinyl)ethoxy]-, (16E)-
  • 16E)-11-[2-(1-Pyrrolidinyl)ethoxy]-14,19-dioxa-5,7,27-triazatetracyclo[19.3.1.1(2,6).1(8,12)]heptacosa-1(25),2,4,6(27),8,10,12(26),16,21,23-decaene Pacritinib (SB1518)
  • Pacritinib, >=98%
  • PACRITINIB
  • SB1518
  • Pacritinib (SB1518)
  • (16E)-11-[2-(1-Pyrrolidinyl)ethoxy]-14,19-dioxa-5,7,27-triazatetracyclo[19.3.1.1(2,6).1(8,12)]heptacosa-1(25),2,4,6(27),8,10,12(26),16,21,23-decaene
  • SB1518(Pacritinib)
  • SB1518; SB 1518; SB-1518; PACRITINIB.
  • CS-914
  • SB1518; SB 1518; SB-1518
  • PACRITINIB USP/EP/BP
  • 2H8]-Pacritinib
  • Pacritinib SB1518 SB-1518
  • *Dimethylacetamide Impurity 1 (Dimethylacetamide EP Impurity A Potassium Salt)(Acetic Acid Potassium Salt)
  • 11-[2-(ピロリジン-1-イル)エトキシ]-14,19-ジオキサ-5,7,27-トリアザテトラシクロ[19.3.1.12,6.18,12]ヘプタコサン-1(25),2,4,6(27),8,10,12(26),16,21,23-デカエン
  • 11-[2-(ピロリジン-1-イル)エトキシ]-14,19-ジオキサ-5,7,27-トリアザテトラシクロ[19.3.1.12,6.18,12]ヘプタコサ-1(24),2(27),3,5,8,10,12(26),16,21(25),22-デカエン
  • パクリチニブ
  • SB-1518
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