Carousel Bootstrap First

Home Immunoboosting Vegetables Scientific Name Vernacular Name State Search

Capsicum annuum L.

It is commonly known as Mirch and belongs to the family Solanaceae. The fruit is consumed as vegetable. Capsaicin, Capsiate, Capsiconiate, Nordihydrocapsiate, Nordihydrocapsaicin, Phytol, Phytol, β-Amyrin, Viminalol , α-Tocopherol are some of its bioactive markers. Capsaicin that creates a burning sensation or hotness has anti-inflammatory property. Capsaicin and Nordihydrocapsiate inhibited NF-κB activation in vivo. Also, Capsaicin is reported in reducing TNF-α in an in-vitro cell culture.

Mode of Consumption : Salad, Cooked with other vegetables, Boiled, Pickled
Plant Details Agro-climatic Zone Vernacular Names Pictures
Scientific Name: Capsicum annuum L.
Family: Solanaceae Juss.
Class: Magnoliopsida
Order: Solanales
Genus: Capsicum L.
Fruiting Season: All round the year
Parts: Fruit
  • The Eastern Coastal Region
  • The North-Eastern Hill Region
  • The Middle Ganga Plain Region
  • The Western Coastal Region
  • The Gujarat Region
  • North-Western Mountain Region
  • The Deccan Interior Region & The Western Coastal Region
  • The Maharashtra Plateau Region & The Western Coastal Region
  • The Deccan Interior Region & The Eastern Coastal Region
  • The Upper Ganga Plain Region & The Middle Ganga Plain Region
Andhra Pradesh : Bunga mirapakay
Arunachal Pradesh : Me fit, Jalokia
Assam : Jalakia
Bihar : Shimla mirch
Goa : Donne mirsang
Gujarat : Capsicum
Himachal Pradesh : Shimla mirch
Karnataka : Donne menasinakai
Kerala : Pachamulaku, Vattal mulaku, Kappal mulaku, Chuvanna mulaku
Maharashtra : Dhobli mirchi, bhopli mirchi
Mizoram : Hmarcha
Nagaland : Chusi
Tamil Nadu : Kudai milagai, Kepcikam
Uttar Pradesh : Shimla mirch

Fruits


Fruit

Compound/Extract Activity Mode of Action Marker/References
Capsaicin and NordihydrocapsiateAnti-inflammatoryCapsaicin and nordihydrocapsiate inhibited NF-κB activation in vivo.NF-κB[1]
Capsaicin, T-pellitorine, Nonivamide extractAnti-inflammatoryPrevent the EC-LPS-induced activation of the Mitogen-activated protein kinase (MAPK) pathway and activates Transient Receptor Potential (TRP) channel MAPK pathway, and TRP channel[2]
Capsaicin extractAntioxidantDecrease in the Malondialdehyde (MDA) level and protein carbonyl group content MDA[3]
FlavonoidAntioxidant, Anti-inflammatoryAll the isolated flavonoids exhibited higher radical scavenging activity than ascorbic acid in (DPPH) assay and suppressed production of TNF-α / IL-1β in cultured THP-1 cells.TNF-α / IL-1β[4]
CapsicumanAnti-inflammatoryCapsicuman (pectic polysaccharide) on Diethylaminoethyl cellulose decreased production of TNF-α (2.3 ± 0.4 vs. 4.4 ± 0.5 ng/ml in control). Galacturonanic fragment of Capsicuman decreased TNF-α production (1.4 ± 0.4 vs. 4.4 ± 0.5 ng/ml in control) and improved the survival of mice in response to lipopolysaccharide.TNF-α[5]
Aqueous extractHepatoprotectiveAqueous extract with ethanol co-treatment decreased the TNF-α and IL-6 levels in male albino Wistar ratsIL-6 and TNF-α[6]
Ethanol extract and capsaicinImmunomodulatoryEthanol extract of red pepper and capsaicin directly inhibit T helper cytokine production in cultured PP cells in vitro, whereas oral injection enhanced IL-2 and IFN-γ levels in response to Concanavalin A.IL-2 and IFN-γ[7]
Capsaicin extractAnticancerDecrease the production of all cytokines (TNF-α, IL-1β, IFN-γ, IL-10, and IL-1ra and IL-6) and prevent the growth of colon cancer cells. TNF-α, IL-1β, IFN-γ, IL-10, IL-1ra and IL-6[10]
CapsaicinAnti-inflammatoryCapsaicin reduced TNF-α (21.9%) in an in-vitro model using cell culture.TNF-α[13]
CookedAntioxidantThe highest β-Carotene, vitamin E, and Folate contents were detected in deep fried red pepper, roasted red pepper, and boiled red pepper, respectively.[15]
AntioxidantResults suggested that there is no significant difference in radical-scavenging activity (RSA), total polyphenol (TP), ascorbic acid (AsA) and total carotenoid contents between the cooked and raw peppers when processed for 5 min. However, the cooked peppers showed reduction in the (RSA), total polyphenol content (TP) and ascorbic acid content (AsA) when cooked for 5 min in boiling water.Further reduction of the RSA was observed when the boiling time was prolonged to 30 min. with further reduction observed after boiling for 30 min. It is concluded that microwave heating and stir-frying without using water are more suitable cooking methods for pepper, to ensure the maximum retention of antioxidant molecules.[16]
Capsorubin and Capsanthin[18] [19]
Major Class Metabolites (Content of bioactives: mg/100g Fresh Weight)
Capsicuman: [5]
AlcoholFarnesol: [12]
AldehydeMethyl 9-oxononanoate: , Octadecanal: , Tetradecanal: [12]
AlkaneDocosane: , Eicosane: , Heptacosane: , Hexadecane: , Octadecane: , Pentadecane: , Tetradecane: , Undecane: [12]
AlkanesHeptadecane: [12]
Alkene1-Octadecene: , 1-Pentadecene: , 9-Octadecene: , Neophytadiene: [12]
AmideOctadecanamide: [12]
CapsaicinoidDihydrocapsaicin : 1.38-32.13 mg/100g[17]
Carboxylic AcidPelargonic acid vanillylamide: [12]
CarotenoidLutein: , Zeaxanthin: , α- Carotene: , β- Carotene: , β-carotene : 7.3-85.7, β-Cryptoxanthin : 2-10.6 mg/100g[9]
Fatty acid5,9-Tetradecadienoic acid: , Cyclotetracosane: , Lignoceric acid methyl ester: , Linoleic acid: , Linolenic acid methyl ester: , Myristic acid methyl ester: , Oleic acid: , Oleic acid methyl ester: , Palmitic acid ethyl ester: , Pentadecanoic acid: , Stearic acid: [12]
Fatty acid esterBehenic acid methyl ester: , Heneicosanoic acid methyl ester: , Margaric acid methyl ester: , Nonadecanoic acid methyl ester: , Pentadecanoic acid methyl ester: , Stearic acid methyl ester: , Tricosanoic acid methyl ester: [12]
Flavonoid Kaempferol 3-O-[α-rhamnopyranosyl-(1→4)-O-α-rhamnopyranosyl-(1→6)-O]-β-galactopyranoside (kaempferol 3-O-β-isorhamninoside) : , Kaempferol 3-O-α-[(6-P-coumaroyl galactopyranosyl-O-β-(→4)-O-α-rhamnopyranosyl-(1→4)]-O-α-rhamnopyranoside: , Luteolin: 0.12-1.03 mg/100g, Quercetin 3-O-[(2,3,4-triacetyl-α-rhamnopyranosyl)-(1 → 6)-3-acetyl-β-galactopyranoside: , Quercetin 3-O-[(2,3,4-triacetyl-α-rhamnopyranosyl)-(1 → 6)-β-galactopyranoside: , Quercetin 3-O-[(2,4-diacetyl-α-rhamnopyranosyl)-(1 → 6)]-3,4-diacetyl-β-galactopyranoside: , Rutin : 8.94mg/100g[9]
FlavonolQuercetin: [12]
Hydrocarbon5-Octadecene: [12]
Nitrile3-Phenylpropionitrile: [6]
Palmitic AcidHexadecanamide: [12]
PhenolCapsaicin: 407-540 mg/100g, Capsiate: , Capsiconiate: , Dihydrocapsiate: , Dihydrocapsiconiate: , Nordihydrocapsaicin: , Nordihydrocapsiate: [12]
Phenolic acidOrtho-coumaric acid : 10.28 mg/100g[9]
PhytosterolErgost-5-en-3-ol, (3β ,24R)- : , Stigmast-4-en-3-one: , Stigmast-5,22-dien-3-ol (3β ,22E): , Stigmast-5-en-3-ol, (3 ,24S): [12]
SterolCholest-5-en-3-ol (3β): [12]
TerpeneCapsanthin: , Capsorubin: , Cryptoxanthin: , Phytol: , Viminalol: , β-Amyrin: [12]
VitaminAscorbic acid: 42-168 mg/100g, Tocopherol: , α-Tocopherol: [12]
Effect Observation DOI
Human clinical studiesIncreased count of Akkermansia and Flavonifractor strains DOI: 10.3390/biomedicines9091246
Disease Formulation Reference Author TKDL
Information from Wealth of India Reference
  • Capsicum preparetions are used as emolient in lumbago, neuralagia and rheumatic disorders.
  • It is useful in atonic dyspepsia.
  • It is sometimes added to tannin or rose gargles for pharyngitis and to relax sore throat.
CSIR(1950).The Wealth of India, Raw materials,Vol.-II ,P.69-73, New Delhi, India
4.2, 4.2.1, 4.2.1.1, 4.2.1.2, 4.2.1.3, 4.2.2, 4.2.2.1, 4.2.2.2, 4.2.2.3, 4.2.2.4, 4.2.2.5, 4.2.2.6, 4.2.2.7, 4.2.2.8
CSIR-North East Institute of Science and Technology, Jorhat-6, Assam, India
CSIR-Institute of Himalayan Bioresource Technology, Palampur-61,Himachal Pradesh, India