Pepticinnamin E
Pepticinnamin E is a Farnesyltransferase (FTase) inhibitor (IC50=42 µM). Pepticinnamin E can be used in cancer and malaria research.
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。
- CAS 番号: 147317-36-0
- 分子式: C49H54ClN5O10
- 分子量:908.43
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性
製品説明
IC50 & Target
IC50: 42 µM (Farnesyltransferase)[1].
Cellular Effect
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| LNCaP | IC50 |
>10 μM
Compound: 1
|
Cytotoxicity against drug resistant human LNCaP cells assessed as inhibition of cell growth incubated for 72 hrs by CellTox Green cytotoxicity assay
Cytotoxicity against drug resistant human LNCaP cells assessed as inhibition of cell growth incubated for 72 hrs by CellTox Green cytotoxicity assay
|
[PMID: 38591246] |
| LNCaP | IC50 |
>10 μM
Compound: 1
|
Cytotoxicity against human LNCaP cells assessed as inhibition of cell growth incubated for 72 hrs by CellTox Green cytotoxicity assay
Cytotoxicity against human LNCaP cells assessed as inhibition of cell growth incubated for 72 hrs by CellTox Green cytotoxicity assay
|
[PMID: 38591246] |
| LNCaP C4-2B | IC50 |
>10 μM
Compound: 1
|
Cytotoxicity against drug resistant human LNCaP C4-2B cells assessed as inhibition of cell growth incubated for 72 hrs by CellTox Green cytotoxicity assay
Cytotoxicity against drug resistant human LNCaP C4-2B cells assessed as inhibition of cell growth incubated for 72 hrs by CellTox Green cytotoxicity assay
|
[PMID: 38591246] |
| LNCaP C4-2B | IC50 |
>10 μM
Compound: 1
|
Cytotoxicity against human LNCaP C4-2B cells assessed as inhibition of cell growth incubated for 72 hrs by CellTox Green cytotoxicity assay
Cytotoxicity against human LNCaP C4-2B cells assessed as inhibition of cell growth incubated for 72 hrs by CellTox Green cytotoxicity assay
|
[PMID: 38591246] |
化学情報
-
CAS 番号 147317-36-0
-
分子量 908.43
-
分子式 C49H54ClN5O10
-
SMILES
O=C([C@@H](N(C)C([C@@H](N(C([C@H](NC(/C=C/C1=CC=CC=C1/C=C\CCC)=O)CC2=CC=C(C=C2)O)=O)C)CC3=CC=C(C(O)=C3Cl)OC)=O)CC4=CC=CC=C4)OC[C@@H](N5)C(NCC5=O)=O
-
輸送条件
Room temperature in continental US; may vary elsewhere.
-
保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
[1]. Hinterding K, et al. Synthesis and In Vitro Evaluation of the Ras Farnesyltransferase Inhibitor Pepticinnamin E. Angew Chem Int Ed Engl. 1998 May 18;37(9):1236-1239. [Content Brief]
[2]. Santa Maria KC, et al. Targeted Rediscovery and Biosynthesis of the Farnesyl-Transferase Inhibitor Pepticinnamin E. Chembiochem. 2019 Jun 3;20(11):1387-1393. [Content Brief]
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)