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Affinisine

From Wikipedia, the free encyclopedia
Affinisine
Names
IUPAC name
1-Methylsarpagan-17-ol
Systematic IUPAC name
[(6S,9E,10R,11R,12S)-9-Ethylidene-5-methyl-5,6,7,8,9,10,11,11a,12-decahydro-6,10-methanoindolo[2,3-g]quinolizin-11-yl]methanol
Other names
De(hydroxymethyl)voachalotinol
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C20H24N2O/c1-3-12-10-22-18-9-15-13-6-4-5-7-17(13)21(2)20(15)19(22)8-14(12)16(18)11-23/h3-7,14,16,18-19,23H,8-11H2,1-2H3/b12-3-/t14-,16+,18-,19-/m0/s1
    Key: UVWQYWHKTZABSO-ILADVTTDSA-N
  • InChI=1S/C20H24N2O/c1-3-12-10-22-18-9-15-13-6-4-5-7-17(13)21(2)20(15)19(22)8-14(12)16(18)11-23/h3-7,14,16,18-19,23H,8-11H2,1-2H3/b12-3-/t14-,16+,18-,19-/m0/s1
    Key: UVWQYWHKTZABSO-ILADVTTDSA-N
  • CN1C2=C(C=CC=C2)C3=C1[C@@](C[C@@]4([H])/C(C5)=C\C)([H])[N@]5[C@@]([C@@]([H])4CO)([H])C3
Properties
C20H24N2O
Molar mass308.425 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Affinisine is amonoterpenoidindolealkaloid which can be isolated from plants of the genusTabernaemontana.[1][2] Structurally, it can be considered a member of thesarpagine alkaloid family and may be synthesized fromtryptophan via aPictet-Spengler reaction.[3][4]

Pharmacology

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Limited pharmacological testing has indicated that affinisine may effectively inhibitacetylcholinesterase andbutyrylcholinesterase.[1][5]

See also

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References

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  1. ^abAndrade, Marcelo T.; Lima, Josélia A.; Pinto, Angelo C.; Rezende, Claudia M.; Carvalho, Meriane P.; Epifanio, Rosângela A. (June 2005). "Indole alkaloids from Tabernaemontana australis (Müell. Arg) Miers that inhibit acetylcholinesterase enzyme".Bioorganic & Medicinal Chemistry.13 (12):4092–4095.doi:10.1016/j.bmc.2005.03.045.PMID 15911323.
  2. ^Clivio, Pascale; Richard, Bernard; Deverre, Jean-Robert; Sevenet, Thierry; Zeches, Monique; Le Men-Oliver, Louisette (January 1991). "Alkaloids from leaves and root bark ofErvatamia hirta".Phytochemistry.30 (11):3785–3792.Bibcode:1991PChem..30.3785C.doi:10.1016/0031-9422(91)80111-D.
  3. ^Liu, Xiaoxiang; Wang, Tao; Xu, Qingge; Ma, Chunrong; Cook, James M (August 2000). "Enantiospecific total synthesis of the enantiomer of the indole alkaloid affinisine".Tetrahedron Letters.41 (33):6299–6303.doi:10.1016/S0040-4039(00)01061-3.
  4. ^Liao, Xuebin; Zhou, Hao; Yu, Jianming; Cook, James M. (November 2006). "An Improved Total Synthesis of (+)-Macroline and Alstonerine as Well as the Formal Total Synthesis of (−)-Talcarpine and (−)-Anhydromacrosalhine−methine".The Journal of Organic Chemistry.71 (23):8884–8890.doi:10.1021/jo061652u.PMID 17081019.
  5. ^Vieira, Ivo J.C.; Medeiros, Walter L.B.; Monnerat, Cecilia S.; Souza, Jucimar J.; Mathias, Leda; Braz-Filho, Raimundo; Pinto, Angelo C.; Sousa, Priscila M.; Rezende, Claudia M.; Epifanio, Rosângela De A. (September 2008)."Two fast screening methods (GC-MS and TLC-ChEI assay) for rapid evaluation of potential anticholinesterasic indole alkaloids in complex mixtures".Anais da Academia Brasileira de Ciências.80 (3):419–426.doi:10.1590/S0001-37652008000300003.PMID 18797794.
Enzyme
(modulators)
ChATTooltip Choline acetyltransferase
AChETooltip Acetylcholinesterase
BChETooltip Butyrylcholinesterase
Transporter
(modulators)
CHTTooltip Choline transporter
VAChTTooltip Vesicular acetylcholine transporter
Release
(modulators)
Inhibitors
Enhancers


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