44270

trans,trans-Farnesyl pyrophosphate ammonium salt

≥95.0% (HPLC)

• Synonyme(s) : (E,E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-yl pyrophosphate ammonium salt, Farnesyl diphosphate ammonium salt
• Formule empirique (notation de Hill): C₁₅H₂₈O₇P₂ · xNH₃
• Poids moléculaire : 382.33 (free acid basis)
• Beilstein: 2482197
• Code UNSPSC : 12352212
• ID de substance PubChem : 329756482
• Nomenclature NACRES : NA.25
• Essai: ≥95.0% (HPLC)
• Forme: solid

Propriétés

• Niveau de qualité: 100
• Essai: ≥95.0% (HPLC)
• Forme: solid
• Température de stockage: −20°C
• Chaîne SMILES: N.C\C(C)=C\CC\C(C)=C\CC\C(C)=C\COP(O)(=O)OP(O)(O)=O
• InChI: 1S/C15H28O7P2.H3N/c1-13(2)7-5-8-14(3)9-6-10-15(4)11-12-21-24(19,20)22-23(16,17)18;/h7,9,11H,5-6,8,10,12H2,1-4H3,(H,19,20)(H2,16,17,18);1H3/b14-9+,15-11+;
• Clé InChI: CPYJTMLHKIWGDF-NDHHSALASA-N

Description

Application

Farnesyl diphosphate ammonium salt may be used to study the posttranslational process known as farnesylation that is used to modify important proteins such as the Ras oncogene.

Actions biochimiques/physiologiques

Farnesyl pyrophosphate is a key intermediate in the biosynthesis of more complex sesquiterpenoids, higher terpenoids, and steroids[1] and different biological functions have been discovered for FPP and the corresponding alcohol farnesol[2][3][4][5][6][7]. FPP plays an important role in the posttranslational processing of Ras proteins. Mutated forms of Ras are associated with human cancer and are therefore investigated in cancer research[5][6].

Conditionnement

Bottomless glass bottle. Contents are inside inserted fused cone.

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable