Olivacine

Olivacine
Names
Preferred IUPAC name
1,5-Dimethyl-6H-indolo[2,3-g]isoquinoline
Identifiers
CAS Number
  • 484-49-1 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 4444757
KEGG
  • C09230
PubChem CID
  • 5281407
UNII
  • 5WSL5LL2C3 checkY
CompTox Dashboard (EPA)
  • DTXSID10197511 Edit this at Wikidata
InChI
  • InChI=1S/C17H14N2/c1-10-12-7-8-18-11(2)14(12)9-15-13-5-3-4-6-16(13)19-17(10)15/h3-9,19H,1-2H3
    Key: ZIXGXMMUKPLXBB-UHFFFAOYSA-N
  • InChI=1/C17H14N2/c1-10-12-7-8-18-11(2)14(12)9-15-13-5-3-4-6-16(13)19-17(10)15/h3-9,19H,1-2H3
    Key: ZIXGXMMUKPLXBB-UHFFFAOYAZ
  • Cc1c2ccnc(c2cc3c1[nH]c4c3cccc4)C
Properties
Chemical formula
C17H14N2
Molar mass 246.313 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound

Olivacine is an antimalarial alkaloid.[1]

External links

  1. ^ Rocha e Silva, L. F.; Montoia, A.; Amorim, R. C.; Melo, M. R.; Henrique, M. C.; Nunomura, S. M.; Costa, M. R.; Andrade Neto, V. F.; Costa, D. S.; Dantas, G.; Lavrado, J.; Moreira, R.; Paulo, A.; Pinto, A. C.; Tadei, W. P.; Zacardi, R. S.; Eberlin, M. N.; Pohlit, A. M. (2012). "Comparative in vitro and in vivo antimalarial activity of the indole alkaloids ellipticine, olivacine, cryptolepine and a synthetic cryptolepine analog". Phytomedicine. 20 (1): 71–76. doi:10.1016/j.phymed.2012.09.008. PMID 23092722.


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