beta-Carboline

β-Carboline
The prototype of a class of compounds known as β-carbolines
Names
IUPAC name
9H-β-carboline
Other names
9H-pyrido[3,4-b]indole
Identifiers
244-63-3 YesY
3D model (Jmol) Interactive image
ChEBI CHEBI:109895 YesY
ChEMBL ChEMBL275224 YesY
ChemSpider 58486 YesY
ECHA InfoCard 100.005.418
8222
MeSH norharman
PubChem 64961
Properties
C11H8N2
Molar mass 168.20 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

β-Carboline (9H-pyrido[3,4-b]indole), also known as norharmane, is a nitrogen containing heterocycle. It is also the prototype of a class of compounds known as β-carbolines.

Pharmacology

β-Carboline alkaloids are widespread in plants and animals, and frequently act as benzodiazepine inverse agonists. As components of the liana Banisteriopsis caapi, the β-carbolines harmine, harmaline, and tetrahydroharmine play a pivotal role in the pharmacology of the indigenous psychedelic drug ayahuasca by preventing the breakdown of dimethyltryptamine in the gut by reversibly inhibiting monoamine oxidase, thus making it psychoactive upon oral administration. Some β-carbolines, notably tryptoline and pinoline, may be formed naturally in the human body. The latter is possibly implicated along with melatonin in the role of the pineal gland in regulating the sleep-wake cycle. β-carboline is a benzodiazepine receptor inverse agonist and can therefore have convulsive, anxiogenic and memory enhancing effects.[1] 9-methyl-β-carbolines appear to induce DNA damage when exposed to ultra-violet light.[2]

Structure

β-Carboline belongs to the group of indole alkaloids and consist of pyridine ring that is fused to an indole skeleton.[3] The structure of β-carboline is similar to that of tryptamine, with the ethylamine chain re-connected to the indole ring via an extra carbon atom, to produce a three-ringed structure. The biosynthesis of β-carbolines is believed to follow this route from analogous tryptamines.[4] Different levels of saturation are possible in the third ring, which is indicated here in the structural formula by colouring the optionally double bonds red and blue:

Examples of β-carbolines

Some of the more important β-carbolines are tabulated by structure below.

Short Name
Red Bond
Blue Bond
 R1 R6 R7 Structure
β-Carboline
×
×
H
H
H
Tryptoline    
H
H
H
Pinoline    
H
OCH3
H
Harmane
×
 
CH3
H
H
Harmine
×
×
CH3
H
OCH3
Harmaline
×
 
CH3
H
OCH3
Tetrahydroharmine    
CH3
H
OCH3

Occurrence in nature

Eight plant families are known to express 64 different kinds of β-carboline alkaloids. By dry weight, the seeds of Peganum harmala (Syrian Rue) contain between 0.16%[5] and 5.9%[6] β-carboline alkaloids.

As a result of the presence of β-carbolines in the cuticle of scorpions, their skin is known to fluoresce when exposed to certain wavelengths of ultraviolet light such as that produced by a blacklight.[7]

A group of β-carboline derivatives, termed eudistomins were extracted from ascidians (marine tunicates of the family Ascidiacea), like Ritterella sigillinoides,[8] Lissoclinum fragile [9] or Pseudodistoma aureum.[10] Nostocarboline was isolated from freshwater cyanobacterium.

See also

References

  1. ↑ Venault P, Chapouthier G (2007). "From the behavioral pharmacology of beta-carbolines to seizures, anxiety, and memory". ScientificWorldJournal. 7: 204–23. doi:10.1100/tsw.2007.48. PMID 17334612.
  2. ↑ Vignoni M, Rasse-Suriani FA, Butzbach K, Erra-Balsells R, Epe B, Cabrerizo FM (2013). "Mechanisms of DNA damage by photoexcited 9-methyl-β-carbolines". Org Biomol Chem. 11: 5300–9. doi:10.1039/c3ob40344k. PMID 23842892.
  3. ↑ The Encyclopedia of Psychoactive Plants: Ethnopharmacology and its Applications. Ratsch, Christian. Park Street Press c. 2005
  4. ↑ Baiget, Jessica; Llona-Minguez, Sabin; Lang, Stuart; MacKay, Simon P; Suckling, Colin J; Sutcliffe, Oliver B (2011). "Manganese dioxide mediated one-pot synthesis of methyl 9H-pyrido[3,4-b]indole-1-carboxylate: Concise synthesis of alangiobussinine". Beilstein Journal of Organic Chemistry. 7: 1407–11. doi:10.3762/bjoc.7.164. PMC 3201054Freely accessible. PMID 22043251.
  5. ↑ Hemmateenejad B, Abbaspour A, Maghami H, Miri R, Panjehshahin MR (Aug 2006). "Partial least squares-based multivariate spectral calibration method for simultaneous determination of beta-carboline derivatives in Peganum harmala seed extracts". Anal Chim Acta. 575 (2): 290–9. doi:10.1016/j.aca.2006.05.093. PMID 17723604.
  6. ↑ Herraiz T, González D, Ancín-Azpilicueta C, Arán VJ, Guillén H (2010). "beta-Carboline alkaloids in Peganum harmala and inhibition of human monoamine oxidase (MAO)". Food Chem Toxicol. 48 (3): 839–43. doi:10.1016/j.fct.2009.12.019. PMID 20036304.
  7. ↑ Stachel SJ, Stockwell SA, van Vranken DL (August 1999). "The fluorescence of scorpions and cataractogenesis". Chem. Biol. 6 (8): 531–9. doi:10.1016/S1074-5521(99)80085-4. PMID 10421760.
  8. ↑ Lake RJ, Blunt JW, Munro MH (1989). "Eudistomins From the New Zealand Ascidian Ritterella sigillinoides". Aust. J. Chem. 42 (7): 1201–1206. doi:10.1071/CH9891201.
  9. ↑ Badre A, Boulanger A, Abou-Mansour E, Banaigs B, Combaut G, Francisco C (April 1994). "Eudistomin U and Isoeudistomin U, New Alkaloids from the Caribbean Ascidian Lissoclinum fragile". J. Nat. Prod. 57 (4): 528–533. doi:10.1021/np50106a016.
  10. ↑ Davis RA, Carroll AR, Quinn RJ (June 1998). "Eudistomin V, a New β-Carboline from the Australian Ascidian Pseudodistoma aureum". J. Nat. Prod. 61 (7): 959–960. doi:10.1021/np9800452.

External links

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