1. JAK/STAT Signaling
    Autophagy
    Apoptosis
  2. Pim
    Autophagy
    Apoptosis
  3. AZD1208

AZD1208 

製品番号: HY-15604 純度: 99.90%
取扱説明書

AZD1208 is an orally bioavailable, highly selective PIM kinases inhibitor.

商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。

AZD1208 構造式

AZD1208 構造式

CAS 番号 : 1204144-28-4

容量 価格(税別) 在庫状況 数量
Solution
10 mM * 1 mL in DMSO USD 66 在庫あり
Estimated Time of Arrival: December 31
Solid + Solvent
10 mM * 1 mL
ready for reconstitution
USD 66 在庫あり
Estimated Time of Arrival: December 31
Solid
5 mg USD 60 在庫あり
Estimated Time of Arrival: December 31
10 mg USD 86 在庫あり
Estimated Time of Arrival: December 31
50 mg USD 300 在庫あり
Estimated Time of Arrival: December 31
100 mg USD 480 在庫あり
Estimated Time of Arrival: December 31
200 mg USD 630 在庫あり
Estimated Time of Arrival: December 31
500 mg   お問い合わせ  
1 g   お問い合わせ  

* アイテムを追加する前、数量をご選択ください

カスタマーレビュー

Based on 9 publication(s) in Google Scholar

Other Forms of AZD1208:

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製品説明

AZD1208 is an orally bioavailable, highly selective PIM kinases inhibitor[1].

体外実験

AZD1208 shows good antiproliferative activity in a megakaryoblastic leukemia cell line, MOLM-16, with GI50 values less than 100 nM[1]. AZD1208 (10 μM) inhibits the growth of Ramos cells, and at 1 μM, strongly inhibits PIM kinases in all cell at 1 μM. AZD1208 induces apoptosis, and PIM2 knockdown is mainly associated with an alteration of the cell cycle[2]. The combination of AZD1208 and AZD2014 rapidly activates AMPKα, a negative regulator of translation machinery through mTORC1/2 signaling in AML cells; profoundly inhibits AKT and 4EBP1 activation; and suppresses polysome formation[3].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

臨床実験
分子量

379.48

分子式

C21H21N3O2S

CAS 番号
SMILES

O=C(NC/1=O)SC1=C/C2=C(N3C[[email protected]](N)CCC3)C(C4=CC=CC=C4)=CC=C2

輸送条件

Room temperature in continental US; may vary elsewhere.

保管条件
Powder -20°C 3 years
  4°C 2 years
In solvent -80°C 6 months
  -20°C 1 month
溶剤 & 溶解度
体外: 

DMSO : 66.67 mg/mL (175.69 mM; Need ultrasonic)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.6352 mL 13.1759 mL 26.3519 mL
5 mM 0.5270 mL 2.6352 mL 5.2704 mL
10 mM 0.2635 mL 1.3176 mL 2.6352 mL
*Please refer to the solubility information to select the appropriate solvent.
体内:
  • 1.

    Add each solvent one by one:  10% DMSO    40% PEG300    5% Tween-80    45% saline

    Solubility: ≥ 5 mg/mL (13.18 mM); Clear solution

  • 2.

    Add each solvent one by one:  10% DMSO    90% (20% SBE-β-CD in saline)

    Solubility: 5 mg/mL (13.18 mM); Suspended solution; Need ultrasonic

  • 3.

    Add each solvent one by one:  10% DMSO    90% corn oil

    Solubility: ≥ 2.5 mg/mL (6.59 mM); Clear solution

*All of the co-solvents are available by MCE.
参考文献
細胞実験
[1]

MOLM-16 cells, purchased from DSMZ and cultured in RPMI containing 10% fetal bovine serum (FBS) and 1% L-glutamine, are plated at 20,000 cells per well in 96 well plates overnight. Cells are treated for 72 hours with compound or control vehicle (dimethyl sulfoxide) and cell viability is measured after the addition of Cell Titer-Blue for 4 hours at 37°C and reading of fluorescence on a Tecan Infinite® 200. The GI50 is determined by calculating growth at each dose relative to vehicle treated cells and cell viability at the time of treatment.

MCE はこれらの方法の精度を確認していません。 こちらは参照専用です。

参考文献

純度: 99.90%

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The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass   Concentration   Volume   Molecular Weight *
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The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
× = ×
C1   V1   C2   V2

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製品名:
AZD1208
製品番号:
HY-15604
数量:
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