<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2020-04-17 19:21:35 UTC</creation_date>
  <update_date>2020-12-07 19:11:47 UTC</update_date>
  <accession>CDB005222</accession>
  <secondary_accessions>
  </secondary_accessions>
  <name>Dimethylallylpyrophosphate</name>
  <description>Dimethylallylpyrophosphate, also known as 2-isopentenyl diphosphate or delta-prenyl diphosphoric acid, belongs to the class of organic compounds known as isoprenoid phosphates. These are prenol lipids containing a phosphate group linked to an isoprene (2-methylbuta-1,3-diene) unit. Dimethylallylpyrophosphate is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Dimethylallylpyrophosphate is expected to be in Cannabis as all living plants are known to produce and metabolize it.</description>
  <synonyms>
    <synonym>2-Isopentenyl diphosphate</synonym>
    <synonym>3,3-Dimethylallyl pyrophosphate</synonym>
    <synonym>3-Methylbut-2-enyl phosphono hydrogen phosphate</synonym>
    <synonym>delta-Prenyl diphosphate</synonym>
    <synonym>delta2-Isopentenyl diphosphate</synonym>
    <synonym>Dimethylallyl diphosphate</synonym>
    <synonym>Dimethylallyl pyrophosphate</synonym>
    <synonym>DMAPP</synonym>
    <synonym>Monoprenyl diphosphate</synonym>
    <synonym>Prenol pyrophosphate</synonym>
    <synonym>Prenyl diphosphate</synonym>
    <synonym>2-Isopentenyl diphosphoric acid</synonym>
    <synonym>3,3-Dimethylallyl pyrophosphoric acid</synonym>
    <synonym>3-Methylbut-2-enyl phosphono hydrogen phosphoric acid</synonym>
    <synonym>delta-Prenyl diphosphoric acid</synonym>
    <synonym>Δ-prenyl diphosphate</synonym>
    <synonym>Δ-prenyl diphosphoric acid</synonym>
    <synonym>delta2-Isopentenyl diphosphoric acid</synonym>
    <synonym>Δ2-isopentenyl diphosphate</synonym>
    <synonym>Δ2-isopentenyl diphosphoric acid</synonym>
    <synonym>Dimethylallyl diphosphoric acid</synonym>
    <synonym>Dimethylallyl pyrophosphoric acid</synonym>
    <synonym>Monoprenyl diphosphoric acid</synonym>
    <synonym>Prenol pyrophosphoric acid</synonym>
    <synonym>Prenyl diphosphoric acid</synonym>
    <synonym>Dimethylallylpyrophosphoric acid</synonym>
    <synonym>1,1-Dimethyl-4-phenylpiperazinium iodide</synonym>
    <synonym>3-Methyl-2-buten-1-ol pyrophosphate</synonym>
    <synonym>3-Methyl-2-buten-1-ol trihydrogen pyrophosphate</synonym>
    <synonym>3-Methyl-2-butenyl pyrophosphate</synonym>
    <synonym>3-Methylbut-2-enyl pyrophosphate</synonym>
    <synonym>Delta2-Isopentenyl-diphosphate</synonym>
    <synonym>Dimethylallyl-diphosphate</synonym>
    <synonym>Dimethylallyl-PP</synonym>
    <synonym>Dimethylallyl-ppi</synonym>
    <synonym>Dimethylallyl-pyrophosphate</synonym>
    <synonym>Diphosphoric acid mono(3-methyl-2-butenyl) ester</synonym>
    <synonym>DMPP</synonym>
    <synonym>IPE</synonym>
    <synonym>Prenyl-diphosphate</synonym>
    <synonym>3,3-Dimethylallyl pyrophosphate, (14)C-labeled</synonym>
    <synonym>DMADP CPD</synonym>
    <synonym>3-Methyl-2-butenyl trihydrogen diphosphate</synonym>
    <synonym>Dimethylallylpyrophosphate</synonym>
    <synonym>gamma,gamma-Dimethylallyl pyrophosphate</synonym>
    <synonym>γ,γ-Dimethylallyl pyrophosphate</synonym>
  </synonyms>
  <chemical_formula>C5H12O7P2</chemical_formula>
  <average_molecular_weight>246.09</average_molecular_weight>
  <monisotopic_molecular_weight>246.0058</monisotopic_molecular_weight>
  <iupac_name>({hydroxy[(3-methylbut-2-en-1-yl)oxy]phosphoryl}oxy)phosphonic acid</iupac_name>
  <traditional_iupac>dimethylallyl diphosphate</traditional_iupac>
  <cas_registry_number>358-72-5</cas_registry_number>
  <smiles>CC(C)=CCO[P@](O)(=O)OP(O)(O)=O</smiles>
  <inchi>InChI=1S/C5H12O7P2/c1-5(2)3-4-11-14(9,10)12-13(6,7)8/h3H,4H2,1-2H3,(H,9,10)(H2,6,7,8)</inchi>
  <inchikey>CBIDRCWHNCKSTO-UHFFFAOYSA-N</inchikey>
  <taxonomy>
    <description> belongs to the class of organic compounds known as isoprenoid phosphates. These are prenol lipids containing a phosphate group linked to an isoprene (2-methylbuta-1,3-diene) unit.</description>
    <direct_parent>Isoprenoid phosphates</direct_parent>
    <kingdom>Organic compounds</kingdom>
    <super_class>Lipids and lipid-like molecules</super_class>
    <class>Prenol lipids</class>
    <sub_class>Isoprenoid phosphates</sub_class>
    <molecular_framework>Aliphatic acyclic compounds</molecular_framework>
    <alternative_parents>
      <alternative_parent>Hydrocarbon derivatives</alternative_parent>
      <alternative_parent>Monoalkyl phosphates</alternative_parent>
      <alternative_parent>Organic oxides</alternative_parent>
      <alternative_parent>Organic pyrophosphates</alternative_parent>
      <alternative_parent>Organooxygen compounds</alternative_parent>
    </alternative_parents>
    <substituents>
      <substituent>Aliphatic acyclic compound</substituent>
      <substituent>Alkyl phosphate</substituent>
      <substituent>Hydrocarbon derivative</substituent>
      <substituent>Isoprenoid phosphate</substituent>
      <substituent>Monoalkyl phosphate</substituent>
      <substituent>Organic oxide</substituent>
      <substituent>Organic oxygen compound</substituent>
      <substituent>Organic phosphoric acid derivative</substituent>
      <substituent>Organic pyrophosphate</substituent>
      <substituent>Organooxygen compound</substituent>
      <substituent>Phosphoric acid ester</substituent>
    </substituents>
    <external_descriptors>
      <external_descriptor>C5 isoprenoids (hemiterpenes)</external_descriptor>
      <external_descriptor>C5 isoprenoids (hemiterpenes)</external_descriptor>
      <external_descriptor>prenol phosphate</external_descriptor>
    </external_descriptors>
  </taxonomy>
  <experimental_properties>
    <property>
      <kind>melting_point</kind>
      <value>234 - 238 °C</value>
      <source/>
    </property>
  </experimental_properties>
  <predicted_properties>
    <property>
      <kind>logp</kind>
      <value>0.30</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logs</kind>
      <value>-1.58</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logp</kind>
      <value>0.3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>pka_strongest_acidic</kind>
      <value>1.77</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>iupac</kind>
      <value>({hydroxy[(3-methylbut-2-en-1-yl)oxy]phosphoryl}oxy)phosphonic acid</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>average_mass</kind>
      <value>246.09</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>246.0058</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>CC(C)=CCO[P@](O)(=O)OP(O)(O)=O</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C5H12O7P2</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C5H12O7P2/c1-5(2)3-4-11-14(9,10)12-13(6,7)8/h3H,4H2,1-2H3,(H,9,10)(H2,6,7,8)</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>CBIDRCWHNCKSTO-UHFFFAOYSA-N</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polar_surface_area</kind>
      <value>113.29</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>refractivity</kind>
      <value>49.13</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polarizability</kind>
      <value>19.19</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>rotatable_bond_count</kind>
      <value>5</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>acceptor_count</kind>
      <value>5</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>donor_count</kind>
      <value>3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>physiological_charge</kind>
      <value>-2</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formal_charge</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>number_of_rings</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>bioavailability</kind>
      <value>1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>rule_of_five</kind>
      <value>Yes</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>ghose_filter</kind>
      <value>Yes</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>veber_rule</kind>
      <value>Yes</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mddr_like_rule</kind>
      <value>Yes</value>
      <source>ChemAxon</source>
    </property>
  </predicted_properties>
  <kegg_id>C00235</kegg_id>
  <drugbank_id>DB01785</drugbank_id>
  <foodb_id>FDB022434</foodb_id>
  <chemspider_id>627</chemspider_id>
  <pubchem_compound_id>647</pubchem_compound_id>
  <chebi_id>16057</chebi_id>
  <pdb_id/>
  <knapsack_id>C00007294</knapsack_id>
  <biocyc_id>CPD-4211</biocyc_id>
  <phenol_explorer_compound_id/>
  <bigg_id>131960</bigg_id>
  <wikipedia_id>Dimethylallyl pyrophosphate</wikipedia_id>
  <metlin_id>6016</metlin_id>
  <general_references>
  </general_references>
</compound>

