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Script assisted update of chemical identifiers from ChemSpider for the Chem/Drugbox validation project.
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| ImageName = Chemical structure of cuscohygrine
| ImageName = Chemical structure of cuscohygrine
| Section1 = {{Chembox Identifiers
| Section1 = {{Chembox Identifiers
| CASNo = 454-14-8
| ChemSpiderID = 389876
| InChI = 1/C13H24N2O/c1-14-7-3-5-11(14)9-13(16)10-12-6-4-8-15(12)2/h11-12H,3-10H2,1-2H3
| SMILES = CN1CCCC1CC(CC2CCCN2C)=O
| InChIKey = ZEBIACKKLGVLFZ-UHFFFAOYAQ
}}
| CASNo = 454-14-8
| SMILES = O=C(CC1N(C)CCC1)CC2N(C)CCC2
}}
| Section2 = {{Chembox Properties
| Section2 = {{Chembox Properties
| Formula = C<sub>13</sub>H<sub>24</sub>N<sub>2</sub>O
| Formula = C<sub>13</sub>H<sub>24</sub>N<sub>2</sub>O

Revision as of 09:54, 27 January 2010

Cuscohygrine
Chemical structure of cuscohygrine
Names
IUPAC name
1,3-bis- (1-methylpyrrolidin- 2-yl) -propan- 2-one
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1/C13H24N2O/c1-14-7-3-5-11(14)9-13(16)10-12-6-4-8-15(12)2/h11-12H,3-10H2,1-2H3
    Key: ZEBIACKKLGVLFZ-UHFFFAOYAQ
  • O=C(CC1N(C)CCC1)CC2N(C)CCC2
Properties
C13H24N2O
Molar mass 224.34 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Cuscohygrine is a pyrrolidine alkaloid found in coca. It can be extracted from plants of the family Solanaceae as well, including Atropa belladonna (deadly nightshade), Datura inoxia and Datura stramonium (jimson weed). Cuscohygrine usually comes with other, more potent alkaloids like atropine or cocaine.

Cuscohygrine (along with the related metabolite hygrine) was first isolated by Carl Liebermann in 1889 as an alkaloid accompanying cocaine in coca leaves (also known as Cusco-leaves).

Cuscohygrine is an oil, which can be distilled without decomposition only in vacuum. It is easily soluble in water and forms an optically inactive crystalline hydrate C13H24N2O·3H2O, which melts at 40-41 °C.

References

  • "PubChem Substance Summary". Retrieved July 14, 2005.
  • "USDA, ARS, National Genetic Resources Program. Phytochemical and Ethnobotanical Databases.[Online Database] National Germplasm Resources Laboratory, Beltsville, Maryland". Retrieved July 14, 2005.
  • Dr. Ame Pictet (1904). The Vegetable Alkaloids. With particular reference to their chemical constitution. London: Chapman & Hall.