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
- ¥21900 - ¥94000
- 化學名: 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
- 英語名: AZD 1480
- 別名: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
- CAS番號: 935666-88-9
- 分子式: C14H14ClFN8
- 分子量: 348.77
- EINECS:
- MDL Number:MFCD16038904
3物価
選択條件:
ブランド
- 富士フイルム和光純薬株式會社(wako)
- Sigma-Aldrich Japan
パッケージ
- 5mg
- 10mg
- 25mg
- 生産者富士フイルム和光純薬株式會社(wako)
- 製品番號W01TOC5617
- 製品説明
- 英語製品説明AZD 1480
- 包裝単位10mg
- 価格¥94000
- 更新しました2024-03-01
- 購入
- 生産者Sigma-Aldrich Japan
- 製品番號SML1505
- 製品説明 ≥98% (HPLC)
- 英語製品説明AZD1480 ≥98% (HPLC)
- 包裝単位5mg
- 価格¥21900
- 更新しました2024-03-01
- 購入
- 生産者Sigma-Aldrich Japan
- 製品番號SML1505
- 製品説明 ≥98% (HPLC)
- 英語製品説明AZD1480 ≥98% (HPLC)
- 包裝単位25mg
- 価格¥87000
- 更新しました2024-03-01
- 購入
生産者 | 製品番號 | 製品説明 | 包裝単位 | 価格 | 更新時間 | 購入 |
---|---|---|---|---|---|---|
富士フイルム和光純薬株式會社(wako) | W01TOC5617 | AZD 1480 |
10mg | ¥94000 | 2024-03-01 | 購入 |
Sigma-Aldrich Japan | SML1505 | ≥98% (HPLC) AZD1480 ≥98% (HPLC) |
5mg | ¥21900 | 2024-03-01 | 購入 |
Sigma-Aldrich Japan | SML1505 | ≥98% (HPLC) AZD1480 ≥98% (HPLC) |
25mg | ¥87000 | 2024-03-01 | 購入 |
プロパティ
融點 :>205°C (dec.)
沸點 :575.2±60.0 °C(Predicted)
比重(密度) :1.517
貯蔵溫度 :-20°C
溶解性 :Chloroform (Slightly, Heated), DMSO (Slightly, Heated), Methanol (Slightly, Heat
外見 :powder
酸解離定數(Pka) :13.73±0.10(Predicted)
色 :white to beige
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
沸點 :575.2±60.0 °C(Predicted)
比重(密度) :1.517
貯蔵溫度 :-20°C
溶解性 :Chloroform (Slightly, Heated), DMSO (Slightly, Heated), Methanol (Slightly, Heat
外見 :powder
酸解離定數(Pka) :13.73±0.10(Predicted)
色 :white to beige
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
安全情報
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注意喚起語: | Warning | ||||||||||||||
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注意書き: |
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説明
Janus-associated kinases (JAKs) are cytoplasmic tyrosine kinases that are required for activating the signaling of certain cytokines and growth factor receptors. Many myeloproliferative diseases have been linked to a mutation in JAK2 where a switch from valine to phenylalanine occurs at the 617 position (V617F). AZD1480 is a potent JAK2 inhibitor that blocks signaling (IC50 = 58 nM at 5 mM ATP) and proliferation of JAK2-expressing cell lines (GI50 = 60 nM). It is selective for JAK2 over other JAK family members as well as a panel of related kinases. AZD1480 also inhibits the growth of cells expressing the V617F mutant of JAK2 (GI50 = 60 nM). It reversibly blocks JAK2-mediated phosphorylation of STAT3 and STAT5. AZD1480 displays good pharmacokinetics in vivo, inhibits STAT3 and STAT5 activation in vivo, and suppresses tumorigenesis in mouse xenografts harboring constitutive STAT3 activity. In addition to suppressing myeloma cell growth and survival, AZD1480 reduces angiogenesis and metastasis in vitro and in human xenograft tumor models.供給者とメーカー
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