Capsaicin

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Capsaicin
Names
Pronunciation /kæpˈseɪsɪn/ or /kæpˈseɪəsɪn/
Preferred IUPAC name
(6E)-N-[(4-Hydroxy-3-methoxyphenyl)methyl]-8-methylnon-6-enamide
Other names
(E)-N-(4-Hydroxy-3-methoxybenzyl)-8-methylnon-6-enamide
8-Methyl-N-vanillyl-trans-6-nonenamide
trans-8-Methyl-N-vanillylnon-6-enamide
(E)-Capsaicin
Capsicine
Capsicin
CPS
Identifiers
3D model (JSmol)
2816484
ChEBI
ChEMBL
ChemSpider
DrugBank
EC Number
  • 206-969-8
KEGG
UNII
  • InChI=1S/C18H27NO3/c1-14(2)8-6-4-5-7-9-18(21)19-13-15-10-11-16(20)17(12-15)22-3/h6,8,10-12,14,20H,4-5,7,9,13H2,1-3H3,(H,19,21)/b8-6+ checkY
    Key: YKPUWZUDDOIDPM-SOFGYWHQSA-N checkY
  • InChI=1/C18H27NO3/c1-14(2)8-6-4-5-7-9-18(21)19-13-15-10-11-16(20)17(12-15)22-3/h6,8,10-12,14,20H,4-5,7,9,13H2,1-3H3,(H,19,21)/b8-6+
    Key: YKPUWZUDDOIDPM-SOFGYWHQBQ
  • O=C(NCc1cc(OC)c(O)cc1)CCCC/C=C/C(C)C
Properties
C18H27NO3
Molar mass 305.418 g·mol−1
Appearance Crystalline white powder[1]
Odor Highly volatile and pungent
Melting point 62 to 65 °C (144 to 149 °F; 335 to 338 K)
Boiling point 210 to 220 °C (410 to 428 °F; 483 to 493 K) 0.01 Torr
0.0013 g/100 mL
Solubility
Vapor pressure 1.32×10−8 mm Hg at 25 °C[2]
UV-vis (λmax) 280 nm
Structure
Monoclinic
Pharmacology
M02AB01 (WHO) N01BX04 (WHO)
License data
Hazards
Safety data sheet [2]
GHS pictograms GHS05: CorrosiveGHS06: ToxicGHS07: Harmful
GHS Signal word Danger
H301, H302, H315, H318
P264, P270, P280, P301+310, P301+312, P302+352, P305+351+338, P310, P321, P330, P332+313, P362, P405, P501
NFPA 704 (fire diamond)
2
1
0
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Infobox references
Capsaicin
HeatAbove peak
(pure Capsaicin is toxic)[2]
Scoville scale16,000,000[3] SHU

Capsaicin (8-methyl-N-vanillyl-6-nonenamide) (/kæpˈseɪsɪn/ or /kæpˈseɪəsɪn/) is an active component of chili peppers, which are plants belonging to the genus Capsicum. It is a chemical irritant for mammals, including humans, and produces a sensation of burning in any tissue with which it comes into contact. Capsaicin and several related alkaloids are called capsaicinoids and are produced as secondary metabolites by chili peppers, probably as deterrents against certain mammals and fungi.[4] Pure capsaicin is a hydrophobic, colorless, highly pungent,[2] crystalline to waxy solid compound.

Uses

Food

Curry dishes

Because of the burning sensation caused by capsaicin when it comes in contact with mucous membranes, it is commonly used in food products to provide added spiciness or "heat" (piquancy), usually in the form of spices such as chili powder and paprika.[5] In high concentrations, capsaicin will also cause a burning effect on other sensitive areas, such as skin or eyes.[6] The degree of heat found within a food is often measured on the Scoville scale.[5]

There has long been a demand for capsaicin-spiced products like chili pepper, and hot sauces such as Tabasco sauce and Mexican salsa.[5] It is common for people to experience pleasurable and even euphoric effects from ingesting capsaicin.[5] Folklore among self-described "chiliheads" attribute this to pain-stimulated release of endorphins, a different mechanism from the local receptor overload that makes capsaicin effective as a topical analgesic.[6]

Medical use

Capsaicin cream

Capsaicin is used as a pain medication in topical ointments and dermal patches, typically in concentrations between 0.025% and 0.1%.[7] Evidence of benefit in neuropathic pain and osteoarthritis; however is unclear as of 2018.[8] It may be applied for minor aches and pains of muscles and joints associated with arthritis, backache, strains and sprains, often in compounds with other rubefacients.[7] It is also used in peripheral neuropathy, such as post-herpetic neuralgia caused by shingles.[7] A capsaicin transdermal patch for pain due to post-herpetic neuralgia was approved in 2009 in the United States.[9][10] and the European Union.[11] Use for HIV neuralgia was declined.[12] One 2017 review found that high-dose topical capsaicin (8%) compared with 0.4% capsaicin provided moderate to substantial pain relief from post-herpetic neuralgia, HIV-neuropathy, and diabetic neuropathy.[13]

Although capsaicin creams have been used to treat psoriasis for reduction of itching,[7][14][15] a review of topical capsaicin for treatment of pruritus concluded there was insufficient evidence of effect.[16] Capsaicin decreases LDL cholesterol levels moderately.[17]

There is insufficient evidence to determine the role of ingested capsaicin on several human disorders, including obesity, diabetes, cancer and cardiovascular diseases.[7]

Pepper spray and pests

Capsaicinoids are also an active ingredient in riot control and personal defense pepper spray agents.[18][19][20] When the spray comes in contact with skin, especially eyes or mucous membranes, it produces pain and breathing difficulty in the affected individual.

Capsaicin is also used to deter pests, specifically mammalian pests. Targets of capsaicin repellants include voles, deer, rabbits, squirrels, bears, insects, and attacking dogs.[21] Ground or crushed dried chili pods may be used in birdseed to deter rodents,[22] taking advantage of the insensitivity of birds to capsaicin. The Elephant Pepper Development Trust claims that using chili peppers as a barrier crop can be a sustainable means for rural African farmers to deter elephants from eating their crops.[23]

An article published in the Journal of Environmental Science and Health Part B in 2006 states that "Although hot chili pepper extract is commonly used as a component of household and garden insect-repellent formulas, it is not clear that the capsaicinoid elements of the extract are responsible for its repellency."[24]

The first pesticide product using solely capsaicin as the active ingredient was registered with the U.S. Department of Agriculture in 1962.[21]

Horse sports

Capsaicin is a banned substance in equestrian sports because of its hypersensitizing and pain-relieving properties. At the show jumping events of the 2008 Summer Olympics, four horses tested positive for capsaicin, which resulted in disqualification.[25]

Toxicity

Acute health effects

Capsaicin is a strong irritant requiring proper protective goggles, respirators, and proper hazardous material-handling procedures. Capsaicin takes effect upon skin contact (irritant, sensitizer), eye contact (irritant), ingestion, and inhalation (lung irritant, lung sensitizer). LD50 in mice is 47.2 mg/kg.[26][27]

Painful exposures to capsaicin-containing peppers are among the most common plant-related exposures presented to poison centers.[28] They cause burning or stinging pain to the skin and, if ingested in large amounts by adults or small amounts by children, can produce nausea, vomiting, abdominal pain, and burning diarrhea. Eye exposure produces intense tearing, pain, conjunctivitis, and blepharospasm.[29]

Treatment after exposure

The primary treatment is removal from exposure. Contaminated clothing should be removed and placed in airtight bags before incineration to prevent secondary exposure.

For external exposure, bathing the mucous membrane surfaces that have contacted capsaicin with oily compounds such as vegetable oil, paraffin oil, petroleum jelly (Vaseline), creams, or polyethylene glycol is the most effective way to attenuate the associated discomfort; since oil and capsaicin are both hydrophobic hydrocarbons, the capsaicin that has not already been absorbed into tissues will be picked up into solution and easily removed. Capsaicin can also be washed off the skin using soap, shampoo, or other detergents. Plain water is ineffective at removing capsaicin.[26] Capsaicin is soluble in alcohol, which can be used to clean contaminated items.[26]

When capsaicin is ingested, cold milk is an effective way to relieve the burning sensation (due to caseins, a protein found in milk, having a detergent effect on capsaicin[30]), and sugar solution (10%) at 20 °C (68 °F) is almost as effective.[31] The burning sensation will slowly fade away over several hours if no actions are taken.

Capsaicin-induced asthma might be treated with oral antihistamines or corticosteroids.[29]

Weight loss and regain

As of 2007, there was no evidence showing that weight loss is directly correlated with ingesting capsaicin. Well-designed clinical research had not been performed because the pungency of capsaicin in prescribed doses under research prevented subjects from complying in the study.[32] A 2014 meta-analysis of further trials found weak evidence that consuming capsaicin before a meal might slightly reduce the amount of food consumed, and might drive food preference toward carbohydrates.[33]

Peptic ulcer

One 2006 review concluded that capsaicin may relieve symptoms of a peptic ulcer rather than being a cause of it.[34]

Mechanism of action

The burning and painful sensations associated with capsaicin result from its chemical interaction with sensory neurons. Capsaicin, as a member of the vanilloid family, binds to a receptor called the vanilloid receptor subtype 1 (TRPV1).[35] First cloned in 1997, TRPV1 is an ion channel-type receptor.[36] TRPV1, which can also be stimulated with heat, protons and physical abrasion, permits cations to pass through the cell membrane when activated. The resulting depolarization of the neuron stimulates it to signal the brain. By binding to the TRPV1 receptor, the capsaicin molecule produces similar sensations to those of excessive heat or abrasive damage, explaining why the spiciness of capsaicin is described as a burning sensation.

Early research showed capsaicin to evoke a long-onset current in comparison to other chemical agonists, suggesting the involvement of a significant rate-limiting factor.[37] Subsequent to this, the TRPV1 ion channel has been shown to be a member of the superfamily of TRP ion channels, and as such is now referred to as TRPV1. There are a number of different TRP ion channels that have been shown to be sensitive to different ranges of temperature and probably are responsible for the human range of temperature sensation. Thus, capsaicin does not actually cause a chemical burn, or indeed any direct tissue damage at all, when chili peppers are the source of exposure. The inflammation resulting from exposure to capsaicin is believed to be the result of the body's reaction to nerve excitement. For example, the mode of action of capsaicin in inducing bronchoconstriction is thought to involve stimulation of C fibers[38] culminating in the release of neuropeptides. In essence, the body inflames tissues as if it has undergone a burn or abrasion and the resulting inflammation can cause tissue damage in cases of extreme exposure, as is the case for many substances that cause the body to trigger an inflammatory response.

Capsaicin was instrumental in the 2021 Nobel Prize in Physiology or Medicine, as it had led to the discovery of receptors for temperature and touch.[39][40]

Natural function

Capsaicin is present in large quantities in the placental tissue (which holds the seeds), the internal membranes and, to a lesser extent, the other fleshy parts of the fruits of plants in the genus Capsicum. The seeds themselves do not produce any capsaicin, although the highest concentration of capsaicin can be found in the white pith of the inner wall, where the seeds are attached.[41]

The seeds of Capsicum plants are dispersed predominantly by birds. In birds, the TRPV1 channel does not respond to capsaicin or related chemicals (avian vs. mammalian TRPV1 show functional diversity and selective sensitivity). This is advantageous to the plant, as chili pepper seeds consumed by birds pass through the digestive tract and can germinate later, whereas mammals have molar teeth which destroy such seeds and prevent them from germinating. Thus, natural selection may have led to increasing capsaicin production because it makes the plant less likely to be eaten by animals that do not help it disperse.[42] There is also evidence that capsaicin may have evolved as an anti-fungal agent.[43] The fungal pathogen Fusarium, which is known to infect wild chilies and thereby reduce seed viability, is deterred by capsaicin, which thus limits this form of predispersal seed mortality.

The vanillotoxin-containing venom of a certain tarantula species (Psalmopoeus cambridgei,[44] also known as the Trinidad chevron tarantula) activates the same pathway of pain as is activated by capsaicin, an example of a shared pathway in both plant and animal anti-mammalian defense.[44]

History

The compound was first extracted in impure form in 1816 by Christian Friedrich Bucholz (1770–1818).[45][lower-alpha 1] He called it "capsicin", after the genus Capsicum from which it was extracted. John Clough Thresh (1850–1932), who had isolated capsaicin in almost pure form,[46][47] gave it the name "capsaicin" in 1876.[48] Karl Micko isolated capsaicin in its pure form in 1898.[49][50] Capsaicin's chemical composition was first determined in 1919 by E. K. Nelson, who also partially elucidated capsaicin's chemical structure.[51] Capsaicin was first synthesized in 1930 by Ernst Spath and Stephen F. Darling.[52] In 1961, similar substances were isolated from chili peppers by the Japanese chemists S. Kosuge and Y. Inagaki, who named them capsaicinoids.[53][54]

In 1873 German pharmacologist Rudolf Buchheim[55] (1820–1879) and in 1878 the Hungarian doctor Endre Hőgyes[56] stated that "capsicol" (partially purified capsaicin[57]) caused the burning feeling when in contact with mucous membranes and increased secretion of gastric acid.

Capsaicinoids

See also: Capsinoids

The most commonly occurring capsaicinoids are capsaicin (69%), dihydrocapsaicin (22%), nordihydrocapsaicin (7%), homocapsaicin (1%), and homodihydrocapsaicin (1%).[58]

Capsaicin and dihydrocapsaicin (both 16.0 million SHU) are the most pungent capsaicinoids. Nordihydrocapsaicin (9.1 million SHU), homocapsaicin and homodihydrocapsaicin (both 8.6 million SHU) are about half as hot.[3]

There are six natural capsaicinoids (table below). Although vanillylamide of n-nonanoic acid (Nonivamide, VNA, also PAVA) is produced synthetically for most applications, it does occur naturally in Capsicum species.[59]

Capsaicinoid name Abbrev. Typical
relative
amount 		Scoville
heat units 		Chemical structure
Capsaicin C 69% 16,000,000 Chemical structure of capsaicin
Dihydrocapsaicin DHC 22% 16,000,000 Chemical structure of dihydrocapsaicin
Nordihydrocapsaicin NDHC 7% 9,100,000 Chemical structure of nordihydrocapsaicin
Homocapsaicin HC 1% 8,600,000 Chemical structure of homocapsaicin
Homodihydrocapsaicin HDHC 1% 8,600,000 Chemical structure of homodihydrocapsaicin
Nonivamide PAVA 9,200,000 Chemical structure of nonivamide

Biosynthesis

Chili peppers
Vanillamine is a product of the phenylpropanoid pathway
Valine enters the branched fatty acid pathway to produce 8-methyl-6-nonenoyl-CoA
Capsaicin synthase condenses vanillamine and 8-methyl-6-nonenoyl-CoA to produce capsaicin

History

The general biosynthetic pathway of capsaicin and other capsaicinoids was elucidated in the 1960s by Bennett and Kirby, and Leete and Louden. Radiolabeling studies identified phenylalanine and valine as the precursors to capsaicin.[60][61] Enzymes of the phenylpropanoid pathway, phenylalanine ammonia lyase (PAL), cinnamate 4-hydroxylase (C4H), caffeic acid O-methyltransferase (COMT) and their function in capsaicinoid biosynthesis were identified later by Fujiwake et al.,[62][63] and Sukrasno and Yeoman.[64] Suzuki et al. are responsible for identifying leucine as another precursor to the branched-chain fatty acid pathway.[65] It was discovered in 1999 that pungency of chili peppers is related to higher transcription levels of key enzymes of the phenylpropanoid pathway, phenylalanine ammonia lyase, cinnamate 4-hydroxylase, caffeic acid O-methyltransferase. Similar studies showed high transcription levels in the placenta of chili peppers with high pungency of genes responsible for branched-chain fatty acid pathway.[66]

Biosynthetic pathway

Plants exclusively of the genus Capsicum produce capsaicinoids, which are alkaloids.[67] Capsaicin is believed to be synthesized in the interlocular septum of chili peppers and depends on the gene AT3, which resides at the pun1 locus, and which encodes a putative acyltransferase.[68]

Biosynthesis of the capsaicinoids occurs in the glands of the pepper fruit where capsaicin synthase condenses vanillylamine from the phenylpropanoid pathway with an acyl-CoA moiety produced by the branched-chain fatty acid pathway.[69][70][71][72]

Capsaicin is the most abundant capsaicinoid found in the genus Capsicum, but at least ten other capsaicinoid variants exist.[73] Phenylalanine supplies the precursor to the phenylpropanoid pathway while leucine or valine provide the precursor for the branched-chain fatty acid pathway.[69][70] To produce capsaicin, 8-methyl-6-nonenoyl-CoA is produced by the branched-chain fatty acid pathway and condensed with vanillamine. Other capsaicinoids are produced by the condensation of vanillamine with various acyl-CoA products from the branched-chain fatty acid pathway, which is capable of producing a variety of acyl-CoA moieties of different chain length and degrees of unsaturation.[74] All condensation reactions between the products of the phenylpropanoid and branched-chain fatty acid pathway are mediated by capsaicin synthase to produce the final capsacinoid product.[69][70]

See also

References

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  2. ↑ 2.0 2.1 2.2 2.3 "Capsaicin, Experimental Properties". PubChem, US National Library of Medicine. 2 June 2018. Archived from the original on 12 June 2018. Retrieved 9 June 2018.
  3. ↑ 3.0 3.1 Govindarajan, V. S.; Sathyanarayana, M. N. (1991). "Capsicum—production, technology, chemistry, and quality. Part V. Impact on physiology, pharmacology, nutrition, and metabolism; structure, pungency, pain, and desensitization sequences". Critical Reviews in Food Science and Nutrition. 29 (6): 435–74. doi:10.1080/10408399109527536. PMID 2039598.
  4. ↑ What Made Chili Peppers So Spicy? Archived 12 May 2021 at the Wayback Machine Talk of the Nation, 15 August 2008.
  5. ↑ 5.0 5.1 5.2 5.3 Gorman J (20 September 2010). "A Perk of Our Evolution: Pleasure in Pain of Chilies". New York Times. Archived from the original on 2 April 2015. Retrieved 16 March 2015.
  6. ↑ 6.0 6.1 Rollyson WD, et al. (2014). "Bioavailability of capsaicin and its implications for drug delivery". J Control Release. 196: 96–105. doi:10.1016/j.jconrel.2014.09.027. PMC 4267963. PMID 25307998.
  7. ↑ 7.0 7.1 7.2 7.3 7.4 Fattori, V; Hohmann, M. S.; Rossaneis, A. C.; Pinho Ribeiro, F. A.; Verri, W. A. (2016). "Capsaicin: Current Understanding of Its Mechanisms and Therapy of Pain and Other Pre-Clinical and Clinical Uses". Molecules. 21 (7): 844. doi:10.3390/molecules21070844. PMC 6273101. PMID 27367653.
  8. ↑ Ton, Joey (10 December 2018). "#225 Topical Capsaicin for Neuropathic and Osteoarthritis Pain: Maybe not so hot?". CFPCLearn. Archived from the original on 30 January 2023. Retrieved 16 June 2023.
  9. ↑ "FDA Approves New Drug Treatment for Long-Term Pain Relief after Shingles Attacks" (Press release). U.S. Food and Drug Administration. 17 November 2009. Archived from the original on 23 November 2015. Retrieved 5 January 2016.
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  37. ↑ Geppetti, Pierangelo & Holzer, Peter (1996). Neurogenic Inflammation. CRC Press, 1996.
  38. ↑ Fuller, R. W., Dixon, C. M. S. & Barnes, P. J. (1985). "Bronchoconstrictor response to inhaled capsaicin in humans" J. Appl. Physiol 58, 1080–1084. PubMed, CAS, Web of Science® Times Cited: 174
  39. ↑ "The Nobel Prize in Physiology or Medicine 2021". NobelPrize.org. Archived from the original on 4 October 2021. Retrieved 9 December 2022.
  40. ↑ Santora, Marc; Engelbrecht, Cora (4 October 2021). "Nobel Prize Awarded to Scientists for Research About Temperature and Touch". The New York Times. Archived from the original on 3 December 2022. Retrieved 9 December 2022.
  41. ↑ New Mexico State University – College of Agriculture and Home Economics (2005). "Chile Information – Frequently Asked Questions". Archived from the original on 4 May 2007. Retrieved 17 May 2007.
  42. ↑ Tewksbury, J. J.; Nabhan, G. P. (2001). "Seed dispersal. Directed deterrence by capsaicin in chilies". Nature. 412 (6845): 403–404. doi:10.1038/35086653. PMID 11473305. S2CID 4389051.
  43. ↑ Joshua J. Tewksbury; Karen M. Reagan; Noelle J. Machnicki; Tomás A. Carlo; David C. Haak; Alejandra Lorena Calderón Peñaloza; Douglas J. Levey (19 August 2008), "Evolutionary ecology of pungency in wild chilies", Proceedings of the National Academy of Sciences, 105 (33): 11808–11811, Bibcode:2008PNAS..10511808T, doi:10.1073/pnas.0802691105, PMC 2575311, PMID 18695236
  44. ↑ 44.0 44.1 Siemens J, Zhou S, Piskorowski R, et al. (November 2006). "Spider toxins activate the capsaicin receptor to produce inflammatory pain". Nature. 444 (7116): 208–12. Bibcode:2006Natur.444..208S. doi:10.1038/nature05285. PMID 17093448. S2CID 4387600.
  45. ↑ Bucholz, C. F. (1816). "Chemische Untersuchung der trockenen reifen spanischen Pfeffers" [Chemical investigation of dry, ripe Spanish peppers]. Almanach oder Taschenbuch für Scheidekünstler und Apotheker [Almanac or Pocketbook for Analysts and Apothecaries]. Vol. 37. Weimar. pp. 1–30. [Note: Christian Friedrich Bucholz's surname has been variously spelled as "Bucholz", "Bucholtz", or "Buchholz".]
  46. ↑ In a series of articles, J. C. Thresh obtained capsaicin in almost pure form:
    • J. C. Thresh (1876) "Isolation of capsaicin," The Pharmaceutical Journal and Transactions, 3rd series, vol. 6, pages 941–947;
    • J. C. Thresh (8 July 1876) "Capsaicin, the active principle in Capsicum fruits," The Pharmaceutical Journal and Transactions, 3rd series, vol. 7, no. 315, pages 21 ff. [Note: This article is summarized in: "Capsaicin, the active principle in Capsicum fruits," The Analyst, vol. 1, no. 8, pages 148–149 Archived 20 September 2020 at the Wayback Machine, (1876).]. In The Pharmaceutical Journal and Transactions, volume 7, see also pages 259ff and 473 ff and in vol. 8, see pages 187ff;
    • Year Book of Pharmacy… (1876), pages 250 and 543;
    • J. C. Thresh (1877) "Note on Capsaicin," Year Book of Pharmacy…, pages 24–25;
    • J. C. Thresh (1877) "Report on the active principle of Cayenne pepper," Year Book of Pharmacy..., pages 485–488.
  47. ↑ Obituary notice of J. C. Thresh: "John Clough Thresh, M.D., D. Sc., and D.P.H". The British Medical Journal. 1 (3726): 1057–1058. 1932. doi:10.1136/bmj.1.3726.1057-c. PMC 2521090. PMID 20776886.
  48. ↑ J King, H Wickes Felter, J Uri Lloyd (1905) A King's American Dispensatory. Eclectic Medical Publications (ISBN 1888483024)
  49. ↑ Micko K (1898). "Zur Kenntniss des Capsaïcins" [On our knowledge of capsaicin]. Zeitschrift für Untersuchung der Nahrungs- und Genussmittel (Journal for the Investigation of Necessities and Luxuries) (in Deutsch). 1 (12): 818–829. doi:10.1007/bf02529190.
  50. ↑ Karl Micko (1899). "Über den wirksamen Bestandtheil des Cayennespfeffers" [On the active component of Cayenne pepper]. Zeitschrift für Untersuchung der Nahrungs- und Genussmittel (in Deutsch). 2 (5): 411–412. doi:10.1007/bf02529197.
  51. ↑ Nelson EK (1919). "The constitution of capsaicin, the pungent principle of capsicum". J. Am. Chem. Soc. 41 (7): 1115–1121. doi:10.1021/ja02228a011. Archived from the original on 26 December 2022. Retrieved 9 December 2022.
  52. ↑ Späth E, Darling SF (1930). "Synthese des Capsaicins". Chem. Ber. 63B (3): 737–743. doi:10.1002/cber.19300630331.
  53. ↑ S Kosuge, Y Inagaki, H Okumura (1961). Studies on the pungent principles of red pepper. Part VIII. On the chemical constitutions of the pungent principles. Nippon Nogei Kagaku Kaishi (J. Agric. Chem. Soc.), 35, 923–927; (en) Chem. Abstr. 1964; 60, 9827g.
  54. ↑ (ja) S Kosuge, Y Inagaki (1962) Studies on the pungent principles of red pepper. Part XI. Determination and contents of the two pungent principles. Nippon Nogei Kagaku Kaishi J. Agric. Chem. Soc., 36, pp. 251
  55. ↑ Rudolf Buchheim (1873) "Über die 'scharfen' Stoffe" (On the "hot" substance), Archiv der Heilkunde (Archive of Medicine), vol. 14, pages 1ff. See also: R. Buchheim (1872) "Fructus Capsici," Vierteljahresschrift für praktische Pharmazie (Quarterly Journal for Practical Pharmacy), vol. 4, pages 507ff.; reprinted (in English) in: Proceedings of the American Pharmaceutical Association, vol. 22, pages 106ff (1873).
  56. ↑ Endre Hőgyes, "Adatok a paprika (Capsicum annuum) élettani hatásához" [Data on the physiological effects of the pepper (Capsicum annuum)], Orvos-természettudumányi társulatot Értesítője [Bulletin of the Medical Science Association] (1877); reprinted in: Orvosi Hetilap [Medical Journal] (1878), 10 pages. Published in German as: "Beitrage zur physiologischen Wirkung der Bestandtheile des Capiscum annuum (Spanischer Pfeffer)" [Contributions on the physiological effects of components of Capsicum annuum (Spanish pepper)], Archiv für Experimentelle Pathologie und Pharmakologie, vol. 9, pages 117–130 (1878). See springerlink.com Archived 26 December 2022 at the Wayback Machine
  57. ↑ F.A. Flückiger, Pharmakognosie des Pflanzenreiches ( Berlin, Germany: Gaertner's Verlagsbuchhandlung, 1891).
  58. ↑ Bennett DJ, Kirby GW (1968). "Constitution and biosynthesis of capsaicin". J. Chem. Soc. C: 442. doi:10.1039/j39680000442.
  59. ↑ Howard L. Constant, Geoffrey A. Cordell and Dennis P. West (1996). "Nonivamide, a Constituent of Capsicum oleoresin". J. Nat. Prod. 59 (4): 425–426. doi:10.1021/np9600816.
  60. ↑ Bennett DJ, Kirby GW (1968) Constitution and biosynthesis of capsaicin. J Chem Soc C 4:442–446
  61. ↑ Leete E, Louden MC (1968). "Biosynthesis of capsaicin and dihydrocapsaicin in Capsicum frutescens". J Am Chem Soc. 90 (24): 6837–6841. doi:10.1021/ja01026a049. PMID 5687710.
  62. ↑ Fujiwake H, Suzuki T, Iwai K (1982a) Intracellular distribution of enzymes and intermediates involved in biosynthesis of capsaicin and its analogues in Capsicum fruits. Agric Biol Chem 46:2685–2689
  63. ↑ Fujiwake H, Suzuki T, Iwai K (1982b) Capsaicinoid formation in the protoplast from placenta of Capsicum fruits. Agric Biol Chem 46:2591–2592
  64. ↑ Sukrasno N, Yeoman MM (1993). "Phenylpropanoid metabolism during growth and development of Capsicum frutescens fruits". Phytochemistry. 32 (4): 839–844. doi:10.1016/0031-9422(93)85217-f.
  65. ↑ Suzuki, T; Kawada, T; Iwai, K (1981). "Formation and metabolism of pungent principle of Capsicum fruits. 9. Biosynthesis of acyl moieties of capsaicin and its analogs from valine and leucine in Capsicum fruits". Plant Cell Physiol. 22: 23–32.
  66. ↑ Curry, J; Aluru, M; Mendoza, M; Nevarez, J; Melendrez, M; O'Connell, MA (1999). "Transcripts for possible capsaicinoid biosynthetic genes are differentially accumulated in pungent and non-pungent Capsicum spp". Plant Sci. 148: 47–57. doi:10.1016/s0168-9452(99)00118-1. S2CID 86735106.
  67. ↑ Nelson EK, Dawson LE (1923). "Constitution of capsaicin, the pungent principle of Capsicum. III". J Am Chem Soc. 45 (9): 2179–2181. doi:10.1021/ja01662a023.
  68. ↑ Stewart C, Kang BC, Liu K, et al. (June 2005). "The Pun1 gene for pungency in pepper encodes a putative acyltransferase". Plant J. 42 (5): 675–88. doi:10.1111/j.1365-313X.2005.02410.x. PMID 15918882.
  69. ↑ 69.0 69.1 69.2 Leete E, Louden MC (1968). "Biosynthesis of capsaicin and dihydrocapsaicin in Capsicum frutescens". J. Am. Chem. Soc. 90 (24): 6837–6841. doi:10.1021/ja01026a049. PMID 5687710.
  70. ↑ 70.0 70.1 70.2 Bennett DJ, Kirby GW (1968). "Constitution and biosynthesis of capsaicin". J. Chem. Soc. C. 1968: 442–446. doi:10.1039/j39680000442.
  71. ↑ Fujiwake H.; Suzuki T.; Oka S.; Iwai K. (1980). "Enzymatic formation of capsaicinoid from vanillylamine and iso-type fatty acids by cell-free extracts of Capsicum annuum var. annuum cv. Karayatsubusa". Agricultural and Biological Chemistry. 44 (12): 2907–2912. doi:10.1271/bbb1961.44.2907.
  72. ↑ I. Guzman, P.W. Bosland, and M.A. O'Connell, "Chapter 8: Heat, Color, and Flavor Compounds in Capsicum Fruit" in David R. Gang, ed., Recent Advances in Phytochemistry 41: The Biological Activity of Phytochemicals (New York, New York: Springer, 2011), pages 117–118.
  73. ↑ Kozukue N, Han JS, Kozukue E, Lee SJ, Kim JA, Lee KR, Levin CE, Friedman M (2005). "Analysis of eight capsaicinoids in peppers and pepper-containing foods by high-performance liquid chromatography and liquid chromatography-mass spectrometry". J Agric Food Chem. 53 (23): 9172–9181. doi:10.1021/jf050469j. PMID 16277419.
  74. ↑ Thiele R, Mueller-Seitz E, Petz M (2008). "Chili pepper fruits: presumed precursors of fatty acids characteristic for capsaicinoids". J Agric Food Chem. 56 (11): 4219–4224. doi:10.1021/jf073420h. PMID 18489121.

Notes

  1. ↑ History of early research on capsaicin:
    1. Benjamin Maurach (1816) "Pharmaceutisch-chemische Untersuchung des spanischen Pfeffers" (Pharmaceutical-chemical investigation of Spanish peppers), Berlinisches Jahrbuch für die Pharmacie, vol. 17, pages 63–73. Abstracts of Maurach's paper appear in: (i) Repertorium für die Pharmacie, vol. 6, page 117-119 (1819); (ii) Allgemeine Literatur-Zeitung, vol. 4, no. 18, page 146 (Feb. 1821); (iii) "Spanischer oder indischer Pfeffer", System der Materia medica ..., vol. 6, pages 381–386 (1821) (this reference also contains an abstract of Bucholz's analysis of peppers).
    2. French chemist Henri Braconnot (1817) "Examen chemique du Piment, de son principe âcre, et de celui des plantes de la famille des renonculacées" (Chemical investigation of the chili pepper, of its pungent principle [constituent, component], and of that of plants of the family Ranunculus), Annales de Chemie et de Physique, vol. 6, pages 122- 131.
    3. Danish geologist Johann Georg Forchhammer in: Hans C. Oersted (1820) "Sur la découverte de deux nouveaux alcalis végétaux" (On the discovery of two new plant alkalis), Journal de physique, de chemie, d'histoire naturelle et des arts, vol. 90, pages 173–174.
    4. German apothecary Ernst Witting (1822) "Considerations sur les bases vegetales en general, sous le point de vue pharmaceutique et descriptif de deux substances, la capsicine et la nicotianine" (Thoughts on the plant bases in general from a pharmaceutical viewpoint, and description of two substances, capsicin and nicotine), Beiträge für die pharmaceutische und analytische Chemie, vol. 3, pages 43ff.

Further reading

External links

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