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M2028

Sigma-Aldrich

Capsaicin

from Capsicum sp., ≥95% (HPLC), powder, TRPV1 agonist

Synonyma:

8-Methyl-N-vanillyl-trans-6-nonenamide

Přihlásitk zobrazení cen stanovených pro organizaci a smluvních cen

Vybrat velikost

50 MG
2 030,00 Kč
250 MG
7 050,00 Kč
1 G
21 300,00 Kč

2 030,00 Kč


Obraťte se na zákaznický servis a vyžádejte si informaci o dostupnosti.

Vyžádat hromadnou objednávku

Vybrat velikost

Změnit zobrazení
50 MG
2 030,00 Kč
250 MG
7 050,00 Kč
1 G
21 300,00 Kč

About This Item

Lineární vzorec:
(CH3)2CHCH=CH(CH2)4CONHCH2C6H3-4-(OH)-3-(OCH3)
Číslo CAS:
Molekulová hmotnost:
305.41
Beilstein/REAXYS Number:
2816484
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77

2 030,00 Kč


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Vyžádat hromadnou objednávku

Název produktu

Capsaicin, ≥95%, from Capsicum sp.

biological source

Capsicum sp.

assay

≥95%

mp

62-65 °C (lit.)

solubility

H2O: insoluble
ethanol: soluble

Storage temp.

2-8°C

SMILES string

COc1cc(CNC(=O)CCCC\C=C\C(C)C)ccc1O

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+

Inchi Key

YKPUWZUDDOIDPM-SOFGYWHQSA-N

Gene Information

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General description

Capsaicin is an alkaloid[1] that is present inthe fruit of the Capsicum genus and is the main reason for the spicy flavor inhot peppers including jalapenos, habaneros, and red chili peppers. It isobserved that capsaicin acts as a chemoprotective agent and can induceapoptosis, inhibit proliferation, and induce cell-cycle arrest in variouscancer cells.[2] Capsaicin activates its receptor transient receptorpotential vanilloid subfamily member 1 (TRPV1) and activates sensory afferentneurons[3] that causes neurogenicinflammation, hypothermia, and pain.

Application

Capsaicin has also been used asa TRPV1 agonist to study the effect of barbamide on capsaicin response indorsal root ganglion sensory neurons.[4]
Capsaicin has been used:
  • to study its effects on chromatin remodeling and gene expression related to synaptic plasticity[5]
  • to study TRPV1 channel signaling in H2C1 cells (which are human embryonic kidney 293 cells expressing TRPV1 channels)[6]

Biochem/physiol Actions

Prototype vanilloid receptor agonist. Neurotoxin; activates sensory neurons that give rise to unmyelinated C-fibers, many of which contain substance P. Topical application desensitizes the sensory nerve endings giving a paradoxical antinociceptive effect; systemic administration can be neurotoxic to capsaicin-sensitive cells, especially in newborn animals. Active component of chili peppers.
Prototype vanilloid receptor agonist; neurotoxin. Active component of chili peppers.

signalword

Danger

Hazard Classifications

Acute Tox. 2 Oral - Eye Dam. 1 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Osvědčení o analýze (COA)

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Zákazníci si také prohlíželi

Slide 1 of 7

1 of 7

Stimulation of TRPV1 channels activates the AP-1 transcription factor.
Backes TM, et al.
Biochemical Pharmacology, 150(3), 160-169 (2018)
Chemical and Pharmacological Aspects of Capsaicin
Maria D, et al.
Molecules (Basel), 16(2), 1253-1270 (2011)
Capsaicin upregulates HDAC2 via TRPV1 and impairs neuronal maturation in mice.
Wang S, et al.
Experimental & Molecular Medicine, 50(3), e455-e455 (2018)
Shao-Gang Lu et al.
Pain, 151(3), 633-643 (2010-10-05)
The impact of persistent inflammation on voltage-activated Ca(2+) channels in cutaneous DRG neurons from adult rats was assessed with whole cell patch clamp techniques, sqRT-PCR and Western blot analysis. Inflammation was induced with a subcutaneous injection of complete Freund's adjuvant
Ann M Bode et al.
Cancer research, 71(8), 2809-2814 (2011-04-14)
Capsaicin (trans-8-methyl-N-vanillyl-6-nonenamide) is the principal pungent component in hot peppers, including red chili peppers, jalapeños, and habaneros. Consumed worldwide, capsaicin has a long and convoluted history of controversy about whether its consumption or topical application is entirely safe. Conflicting epidemiologic

Questions

1–2 of 2 Questions  
  1. Is this food grade? If it is not, is there a food grade option available?

    1 answer
    1. This product is not food grade and intended for research use only. Currently, a food grade product option is not available.

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  2. What is the Department of Transportation shipping information for this product?

    1 answer
    1. Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.

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