1. Neuronal Signaling Membrane Transporter/Ion Channel Metabolic Enzyme/Protease
  2. TRP Channel Endogenous Metabolite
  3. Farnesyl pyrophosphate

Farnesyl pyrophosphate  (Synonyms: Farnesyl diphosphate)

Cat. No.: HY-113037
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Farnesyl pyrophosphate (Farnesyl diphosphate), a 15-carbon isoprenoid, is a metabolic intermediate of the mevalonate (MVA) pathway. Farnesyl pyrophosphate is a TRPM2 (TRP Channel) agonist, activates TRPM2 opening for ion influx. Farnesyl pyrophosphate is a key branch substrate for cholesterol synthesis, ubiquinones synthesis, protein farnesylation decoration, and geranyl-geranyl pyrophosphate (GGPP) synthesis.

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Farnesyl pyrophosphate Chemical Structure

Farnesyl pyrophosphate Chemical Structure

CAS No. : 13058-04-3

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Description

Farnesyl pyrophosphate (Farnesyl diphosphate), a 15-carbon isoprenoid, is a metabolic intermediate of the mevalonate (MVA) pathway. Farnesyl pyrophosphate is a TRPM2 (TRP Channel) agonist, activates TRPM2 opening for ion influx. Farnesyl pyrophosphate is a key branch substrate for cholesterol synthesis, ubiquinones synthesis, protein farnesylation decoration, and geranyl-geranyl pyrophosphate (GGPP) synthesis[1].

In Vitro

Farnesyl pyrophosphate functions as an identified danger signal to trigger acute cell death leading to neuron loss in stroke. Harboring both a hydrophobic 15-carbon isoprenyl chain and a heavily charged pyrophosphate head, Farnesyl pyrophosphate leads to acute cell death independent of its downstream metabolic pathways. Mechanistically, extracellular calcium influx and the cation channel transient receptor potential melastatin 2 (TRPM2) exhibit essential roles in Farnesyl pyrophosphate-induced cell death. Farnesyl pyrophosphate activates TRPM2 opening for ion influx[1].

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

In Vivo

In terms of a mouse model constructing by middle cerebral artery occlusion (MCAO), Farnesyl pyrophosphate accumulates in the brain, which indicates the function of the Farnesyl pyrophosphate and TRPM2 danger signal axis in ischemic injury. Farnesyl pyrophosphate/TRPM2 signaling axis and the MVA pathway exhibit important roles in brain ischemia and potentially neurodegenerative diseases[1].

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

Molecular Weight

382.33

Formula

C15H28O7P2

CAS No.
SMILES

O=P(O)(OP(O)(O)=O)OC/C=C(C)/CC/C=C(C)/CC/C=C(C)/C

Structure Classification
Initial Source
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Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Farnesyl pyrophosphate
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