| Field | Specification |
|---|---|
| Alternative names | Geranyl pyrophosphate |
| CAS no. | |
| Applications | |
| Source | Endogenous metabolite |
| Molecular weight | |
| Molecular formula | C10H20O7P2 |
| Activity | |
| SMILES | |
| Storage | |
| Shipping | |
| Catalog no. (Mfr.) | |
| Main SKU |
Compound Overview
Geranyl diphosphate is a key intermediate in the isoprenoid biosynthesis pathway (IBP) that plays key roles in cellular metabolism and is responsible for producing both sterol and non-sterol isoprenoids[1][2].
It is also known as Geranyl pyrophosphate (C10H20O7P2, MW 314.21).
Physical & Chemical Properties
| CAS Number | 763-10-0 |
|---|---|
| Molecular Formula | C10H20O7P2 |
| Molecular Weight | 314.21 g/mol |
| Structure Classification | Others |
| SMILES | O=P(O)(O)OP(OC/C=C(C)/CC/C=C(C)/C)(O)=O |
| Signaling Pathway | Metabolic Enzyme/Protease |
| Bioactivity Class | Human Endogenous Metabolite |
| Initial Source | Endogenous metabolite |
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
| Shipping | Room temperature in continental US; may vary elsewhere. |
Literature Cited
Sources cited in this description and in the In Vitro & In Vivo Data tab. Peer-reviewed publications that used this product are listed under References.
Safety
For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with your institution's chemical hygiene plan.
In Vitro
Geranyl diphosphate, an isoprenoid (IsoP), is involved in many different cellular processes, including cholesterol synthesis[1].
Data provided by the manufacturer. Numbered citations refer to the Literature Cited list in the product description.
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