Chemistry:Rugulovasine

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Rugulovasine
Rugulovasine A and B.svg
Names
IUPAC name
    • A: (4S,5R)-4'-methyl-4-(methylamino)-3,4-dihydro-1H,5'H-spiro[benzo[cd]indole-5,2'-furan]-5'-one
    • B: (4R,5R)-4'-methyl-4-(methylamino)-3,4-dihydro-1H,5'H-spiro[benzo[cd]indole-5,2'-furan]-5'-one
Identifiers
3D model (JSmol)
ChemSpider
Properties
C16H16N2O2
Molar mass 268.316 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


Rugulovasines are bio-active alkaloids made by Penicillium.[1] Rugulovasine A and B bind strongly to the 5-HT1A, 5-HT2A, and 5-HT2C receptors, but lack meaningful binding affinity towards the α1 adrenergic and dopamine receptors.[2] Little is known about the in vivo activity of Rugulovasine A and B, although they have hypotensive effects in cats.[3]

References

  1. Dorner, JW; Cole, RJ; Hill, R; Wicklow, D; Cox, RH (September 1980). "Penicillium rubrum and Penicillium biforme, new sources of rugulovasines A and B.". Applied and Environmental Microbiology 40 (3): 685–7. doi:10.1128/aem.40.3.685-687.1980. PMID 7425621. 
  2. Bartoccini, Francesca; Regni, Alessio; Retini, Michele; Piersanti, Giovanni (6 May 2022). "Asymmetric Total Synthesis of All Rugulovasine Stereoisomers and Preliminary Evaluation of Their Biological Properties" (in en). European Journal of Organic Chemistry 2022 (17). doi:10.1002/ejoc.202200315. ISSN 1434-193X. 
  3. Nagaoka, A; Kikuchi, K (January 1972). "Pharmacological studies of new indole alkaloids, rugulovasine A and B hydrochloride. II. Hypotensive mechanism of both alkaloids in the anesthetized cats.". Arzneimittel-Forschung 22 (1): 143–6. PMID 5066989.