Pepticinnamin E
Pepticinnamin E is a Farnesyltransferase (FTase) inhibitor (IC50=42 µM). Pepticinnamin E can be used in cancer and malaria research.
Nur für Forschungszwecke. Wir verkaufen nicht an Patienten.
- CAS. Nr.: 147317-36-0
- Formel: C49H54ClN5O10
- Molecular Weight:908.43
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Speicherung:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biologische Aktivität
Beschreibung
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] |
Chemical Information
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CAS. Nr. 147317-36-0
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Molecular Weight 908.43
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Formel C49H54ClN5O10
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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
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Versand
Room temperature in continental US; may vary elsewhere.
-
Speicherung
Please store the product under the recommended conditions in the Certificate of Analysis.
Reinheit & Dokumentation
Verweise
[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
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)