CHEBI:84985 - (2E,6E,10E)-ω-hydroxyfarnesyl diphosphate

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ChEBI Name (2E,6E,10E)-ω-hydroxyfarnesyl diphosphate ChEBI ID CHEBI:84985 ChEBI ASCII Name (2E,6E,10E)-omega-hydroxyfarnesyl diphosphate Definition A terpenyl phosphate obtained by hydroxylation of one of the terminal methyl groups of (2E,6E)-farnesyl diphosphate Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C15H28O8P2 Net Charge 0 Average Mass 398.32550 Monoisotopic Mass 398.12594 InChI InChI=1S/C15H28O8P2/c1-13(7-5-9-15(3)12-16)6-4-8-14(2)10-11-22-25(20,21)23-24(17,18)19/h6,9-10,16H,4-5,7-8,11-12H2,1-3H3,(H,20,21)(H2,17,18,19)/b13-6+,14-10+,15-9+ InChIKey SYIRLGLBHJFFBK-RDUMTQBOSA-N SMILES C\C(CO)=C/CC\C(C)=C\CC\C(C)=C\COP(O)(=O)OP(O)(O)=O ChEBI Ontology Outgoing (2E,6E,10E)-ω-hydroxyfarnesyl diphosphate (CHEBI:84985) has functional parent 2-trans,6-trans-farnesyl diphosphate (CHEBI:17407) (2E,6E,10E)-ω-hydroxyfarnesyl diphosphate (CHEBI:84985) is a olefinic compound (CHEBI:78840) (2E,6E,10E)-ω-hydroxyfarnesyl diphosphate (CHEBI:84985) is a polyprenyl diphosphate (CHEBI:37531) (2E,6E,10E)-ω-hydroxyfarnesyl diphosphate (CHEBI:84985) is a primary alcohol (CHEBI:15734) (2E,6E,10E)-ω-hydroxyfarnesyl diphosphate (CHEBI:84985) is a terpenyl phosphate (CHEBI:26875) (2E,6E,10E)-ω-hydroxyfarnesyl diphosphate (CHEBI:84985) is conjugate acid of (2E,6E,10E)-ω-hydroxyfarnesyl diphosphate(3−) (CHEBI:83958) Incoming (2E,6E,10E)-ω-hydroxyfarnesyl diphosphate(3−) (CHEBI:83958) is conjugate base of (2E,6E,10E)-ω-hydroxyfarnesyl diphosphate (CHEBI:84985) IUPAC Name (2E,6E,10E)-12-hydroxy-3,7,11-trimethyldodeca-2,6,10-trien-1-yl trihydrogen diphosphate Synonyms Sources (2E,6E,10E)-12-hydroxyfarnesyl diphosphate ChEBI (2E,6E,10E)-12-hydroxyfarnesyl pyrophosphate ChEBI (2E,6E,10E)-ω-hydroxyfarnesyl pyrophosphate ChEBI 12-hydroxyfarnesyl diphosphate ChEBI 12-hydroxyfarnesyl pyrophosphate ChEBI Registry Number Type Source 11108289 Reaxys Registry Number Reaxys Citation Type Source 19933331 PubMed citation Europe PMC Last Modified 23 February 2015