5-クロロ-2-[((1S)-1-(5-フルオロピリミジン-2-イル)エチル)]アミノ-4-(5-メチル-1H-ピラゾール-3-イル-アミノ)ピリミジン
5-クロロ-2-[((1S)-1-(5-フルオロピリミジン-2-イル)エチル)]アミノ-4-(5-メチル-1H-ピラゾール-3-イル-アミノ)ピリミジン 物理性質(zhì)
- 融點(diǎn) :
- >205°C (dec.)
- 沸點(diǎn) :
- 575.2±60.0 °C(Predicted)
- 比重(密度) :
- 1.517
- 貯蔵溫度 :
- -20°C
- 溶解性:
- クロロホルム(微熱)、DMSO(微熱)、メタノール(微熱)
- 外見 :
- 粉
- 酸解離定數(shù)(Pka):
- 13.73±0.10(Predicted)
- 色:
- 白からベージュ
- InChI:
- InChI=1S/C14H14ClFN8/c1-7-3-11(24-23-7)21-13-10(15)6-19-14(22-13)20-8(2)12-17-4-9(16)5-18-12/h3-6,8H,1-2H3,(H3,19,20,21,22,23,24)/t8-/m0/s1
- InChIKey:
- PDOQBOJDRPLBQU-QMMMGPOBSA-N
- SMILES:
- C1(N[C@H](C2=NC=C(F)C=N2)C)=NC=C(Cl)C(NC2C=C(C)NN=2)=N1
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 |
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 |
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 |
|
| 注意書き |
|
5-クロロ-2-[((1S)-1-(5-フルオロピリミジン-2-イル)エチル)]アミノ-4-(5-メチル-1H-ピラゾール-3-イル-アミノ)ピリミジン 価格
もっと(3)
| 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 |
購入 |
|
富士フイルム和光純薬株式會(huì)社(wako)
|
W01TOC5617 |
AZD 1480 |
935666-88-9 |
10mg |
￥94000 |
2024-03-01 |
購入 |
|
Sigma-Aldrich Japan
|
SML1505 |
≥98% (HPLC)
AZD1480 ≥98% (HPLC) |
935666-88-9 |
5mg |
￥21900 |
2024-03-01 |
購入 |
|
Sigma-Aldrich Japan
|
SML1505 |
≥98% (HPLC)
AZD1480 ≥98% (HPLC) |
935666-88-9 |
25mg |
￥87000 |
2024-03-01 |
購入 |
5-クロロ-2-[((1S)-1-(5-フルオロピリミジン-2-イル)エチル)]アミノ-4-(5-メチル-1H-ピラゾール-3-イル-アミノ)ピリミジン 化學(xué)特性,用途語,生産方法
使用
AZD1480 has been used as an inhibitor of janus kinase 2 (JAK2) and signal transducer and activator of transcription 3 (STAT3) in an
in vitro cell model of upper gastrointestinal adenocarcinoma. It has also been used in combination with bortezomib to study tumor-associated macrophage-mediated survival of myeloma cells.
生物活性
AZD1480 is a novel small-molecule JAK inhibitor. It is able to block cell proliferation and induce apoptosis of myeloma cell lines. It can effectively inhibit tumor angiogenesis and metastasis mediated by STAT3 in stromal cells as well as tumor cells. AZD1480 has broad efficacy on a wider variety of myeloma cells, such as RPMI 8226, OPM-2, NCI-H929, Kms.18, MM1.S and IM-9, as well as primary myeloma cells. AZD1480 induces cell death of Kms.11 cells grown in the presence of HS-5 bone marrow (BM)-derived stromal cells and inhibits tumor growth in a Kms.11 xenograft mouse model, accompanied with inhibition of phospho-FGFR3, phospho-JAK2, phospho-STAT3 and Cyclin D2 levels. AZD1480 also demonstrates important Jak2 selectivity over Jak3, in particular at high ATP concentrations and marginal selectivity over Jak1 at Km ATP.
Biochem/physiol Actions
AZD1480 is an orally active, potent and selective inhibitor of Janus kinases JAK1 and JAK 2 with selectivity for JAK2 as evidenced by IC50 values of 1.3 nM for JAK1 and <0.4 nM for JAK2 in enzyme assays. AZD1480 inhibits endogenous as well as IL-6 induced STAT3 activation. AZD1480 reduces myeloid cell-mediated angiogenesis and metastasis. AZD1489 is an effective anticancer agent in bot adult and pediatric human tumors.
5-クロロ-2-[((1S)-1-(5-フルオロピリミジン-2-イル)エチル)]アミノ-4-(5-メチル-1H-ピラゾール-3-イル-アミノ)ピリミジン 上流と下流の製品情報(bào)
原材料
準(zhǔn)備製品
5-クロロ-2-[((1S)-1-(5-フルオロピリミジン-2-イル)エチル)]アミノ-4-(5-メチル-1H-ピラゾール-3-イル-アミノ)ピリミジン 生産企業(yè)
Global( 162)Suppliers
5-クロロ-2-[((1S)-1-(5-フルオロピリミジン-2-イル)エチル)]アミノ-4-(5-メチル-1H-ピラゾール-3-イル-アミノ)ピリミジン スペクトルデータ(1HNMR)
935666-88-9(5-クロロ-2-[((1S)-1-(5-フルオロピリミジン-2-イル)エチル)]アミノ-4-(5-メチル-1H-ピラゾール-3-イル-アミノ)ピリミジン)キーワード:
- 935666-88-9
- 5-Chloro-N2-[(1S)-1-(5-fluoro-2-pyrimidinyl)ethyl]-N4-(5-methyl-1H-pyrazol-3-yl)-2,4-pyrimidinediamine
- AZD 1480
- (S)-5-chloro-N4-(5-Methyl-1H-pyrazol-3-yl)-N2-(1-(5-MethylpyriMidin-2-yl)ethyl)pyriMidine-2,4-diaMine
- (S)-5-chloro-N2-(1-(5-fluoropyriMidin-2-yl)ethyl)-N4-(5-Methyl-1H-pyrazol-3-yl)pyriMidine-2,4-diaMine
- 5-Chloro-N2-[(1S)-1-(5-fluoro-2-pyrimidinyl)ethyl]-N4-(5-methyl-1H-pyrazol-3-yl)-2,4-pyrimidinediamine AZD 1480
- AZD 1480 5-Chloro-N2-[(1S)-1-(5-fluoro-2-pyrimidinyl)ethyl]-N4-(5-methyl-1H-pyrazol-3-yl)-2,4-pyrimidinediamine
- AZD1480, >=98%
- AZD1480;AZD1480;AZD 1480
- (S)-5-Chloro-N2-(1-(5-fluoropyrimidin-2-yl)ethyl)-N4-(5-methyl-1H-pyrazol-3-yl)pyrimidine-2,4-
- 5-Chloro-N2-[(1S)-1-(5-fluoro-2-pyrimidinyl)ethyl]-N4-(5-methyl-1H-pyrazol-3-yl)-2,4-pyrimidine-2,4-diamine
- AZD-1480;AZD 1480
- AZD1480, 98%, a novel ATP-competitive JAK2 inhibitor
- 2,4-Pyrimidinediamine, 5-chloro-N2-[(1S)-1-(5-fluoro-2-pyrimidinyl)ethyl]-N4-(5-methyl-1H-pyrazol-3-yl)-
- 5-Chloro-N2-[(1S)-1-(5-fluoro-2-pyrimidinyl)ethyl]-N4-(5-methyl-1H-pyrazol-3-yl)-2,4-pyrimidinediamine USP/EP/BP
- (S)-5-chloro-N2-(1-(5-fluoropyrimidin-2-yl)ethyl)-N4-(5-methyl-1H-pyrazol-3-yl)pyrimidine-2,4-diamin
- AZD-1480, 10 mM in DMSO
- 5-クロロ-N2-[(1S)-1-(5-フルオロピリミジン-2-イル)エチル]-N4-(5-メチル-1H-ピラゾール-3-イル)ピリミジン-2,4-ジアミン
- 5-クロロ-2-[((1S)-1-(5-フルオロピリミジン-2-イル)エチル)]アミノ-4-(5-メチル-1H-ピラゾール-3-イル-アミノ)ピリミジン