Affinisine - Misplaced Pages

Affinisine
Names

IUPAC name 1-Methylsarpagan-17-ol
Systematic IUPAC name quinolizin-11-yl]methanol
Other names De(hydroxymethyl)voachalotinol
Identifiers
CAS Number	2912-11-0
3D model (JSmol)	Interactive image
ChemSpider	10172574
PubChem CID	12000107
UNII	J96TYR7CHG
CompTox Dashboard (EPA)	DTXSID201045726
InChI 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/s1Key: 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/s1Key: UVWQYWHKTZABSO-ILADVTTDSA-N
SMILES CN1C2=C(C=CC=C2)C3=C1(C4()/C(C5)=C\C)()5(()4CO)()C3
Properties
Chemical formula	C₂₀H₂₄N₂O
Molar mass	308.425 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references

Chemical compound

Affinisine is a monoterpenoid indole alkaloid which can be isolated from plants of the genus Tabernaemontana. Structurally, it can be considered a member of the sarpagine alkaloid family and may be synthesized from tryptophan via a Pictet-Spengler reaction.

Pharmacology

Limited pharmacological testing has indicated that affinisine may effectively inhibit acetylcholinesterase and butyrylcholinesterase.

References

^ Andrade, 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.
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. doi:10.1016/0031-9422(91)80111-D.
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.
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.
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.