Cat. No.: HY-10448A

Capsaicin (Purity 65%)

21 Cited Publications

고객리뷰

Based on 21 publication(s) in Google Scholar

Capsaicin (Purity 65%) is a mixture of Capsaicin and Dihydrocapsaicin (Ratio >2:1). Capsaicin (Purity 65%) is an orally active capsaicin receptor (TRPV1) agonist.

연구목적의 판매만을 진행합니다. 환자를 대상으로 한 판매는 하지 않습니다.

Purity: 99.20%
CAS No.: 404-86-4
화학식: C₁₈H₂₇NO₃
분자량:305.41

보관:

4°C, protect from light

* In solvent : -80°C, 2 years; -20°C, 1 year (protect from light)

Capsaicin (Purity 65%) Chemical Structure

CAS No.: 404-86-4

사이즈

가격

재고

수량

Sample (0.1mg)

In-stock

(In Japan)

Apply Now

견적 받기 Ask For Quote & Lead Time Consult sales personnel for more information Check price and availability 견적 받기 Ask For Quote & Lead Time Consult sales personnel for more information Check price and availability

대량구매 문의

Amount: USD 0.00

* 장바구니에 담기 전 물품의 수량을 선택해 주십시오.

Top Publications Citing

Use of MCE Products

Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity
- 제품 설명
- Cellular Effect
- In Vitro
- In Vivo
Chemical Information
Publications (21)
용액&용해도
- In Vitro
- In Vivo
순도&문서
References
Help & FAQs
Bioz

Biological Activity

제품 설명

Capsaicin (Purity 65%) is a mixture of Capsaicin and Dihydrocapsaicin (Ratio >2:1). Capsaicin (Purity 65%) is an orally active capsaicin receptor (TRPV1) agonist^[1]^[2].

All TRP Channel Isoforms :

All Endogenous Metabolite Isoforms :

Cellular Effect

Cell Line	Type	Value	Description	References
A2058	IC₅₀	>100 μM Compound: Capsaicin	Cytotoxicity against human A2058 cells assessed as decrease in cell viability incubated for 24 hrs by MTT assay Cytotoxicity against human A2058 cells assessed as decrease in cell viability incubated for 24 hrs by MTT assay	[PMID: 31104785]
B16-F10	IC₅₀	>100 μM Compound: Capsaicin	Cytotoxicity against mouse B16F10 cells assessed as decrease in cell viability incubated for 24 hrs by MTT assay Cytotoxicity against mouse B16F10 cells assessed as decrease in cell viability incubated for 24 hrs by MTT assay	[PMID: 31104785]
B16-F10	IC₅₀	117 μM Compound: 1	Antiproliferative activity against B16-F10 cells assessed as inhibition of cell growth measured after 24 hrs by MTT assay Antiproliferative activity against B16-F10 cells assessed as inhibition of cell growth measured after 24 hrs by MTT assay	[PMID: 37000154]
BGC-823	IC₅₀	4.659 μM Compound: 1	Antiproliferative activity against human BGC-823 cells assessed as reduction in cell viability incubated for 5 days by MTS assay Antiproliferative activity against human BGC-823 cells assessed as reduction in cell viability incubated for 5 days by MTS assay	[PMID: 33581557]
CHO	EC₅₀	25.9 nM Compound: 1; CAP	Agonist activity at human TRPV1 expressed in CHO cells assessed as increase in 45Ca2+ uptake incubated for 5 mins by liquid scintillation counting method Agonist activity at human TRPV1 expressed in CHO cells assessed as increase in 45Ca2+ uptake incubated for 5 mins by liquid scintillation counting method	[PMID: 31702924]
CHO	EC₅₀	44.8 nM Compound: 1; CAP	Agonist activity at rat TRPV1 expressed in CHO cells assessed as increase in 45Ca2+ uptake incubated for 5 mins by liquid scintillation counting method Agonist activity at rat TRPV1 expressed in CHO cells assessed as increase in 45Ca2+ uptake incubated for 5 mins by liquid scintillation counting method	[PMID: 31702924]
CHO	EC₅₀	44.8 nM Compound: Capsaicin	In vitro [Ca2+] influx relative to capsaicin by Rat Vanilloid receptor (VR1) expressing CHO cells In vitro [Ca2+] influx relative to capsaicin by Rat Vanilloid receptor (VR1) expressing CHO cells	[PMID: 12825950]
CHO	EC₅₀	44.8 nM Compound: Capsaicin	Agonist activity at rat TRPV1 receptor expressed in CHO cells assessed as calcium uptake Agonist activity at rat TRPV1 receptor expressed in CHO cells assessed as calcium uptake	[PMID: 19135377]
HBMEC-2	EC₅₀	16.37 μM Compound: Capsaicin	Neuroprotective activity against H2O2-induced cell damage in human HBMEC2 cells assessed as increase in cell viability preincubated for 24 hrs followed by H2O2 addition and measured after 4 hrs by MTT assay Neuroprotective activity against H2O2-induced cell damage in human HBMEC2 cells assessed as increase in cell viability preincubated for 24 hrs followed by H2O2 addition and measured after 4 hrs by MTT assay	[PMID: 31541868]
HCT-116	IC₅₀	40.16 μM Compound: Capsaicin	Antiproliferative activity against human HCT-116 cells assessed as cell growth inhibition measured after 72 hrs by crystal violet staining based assay Antiproliferative activity against human HCT-116 cells assessed as cell growth inhibition measured after 72 hrs by crystal violet staining based assay	[PMID: 34795858]
HEK293	EC₅₀	0.0039 μM Compound: Capsaicin	Agonist activity at human TRPV1 ion channel expressed in HEK293 cells assessed as calcium influx by fluo-4-Am-based fluorimetry Agonist activity at human TRPV1 ion channel expressed in HEK293 cells assessed as calcium influx by fluo-4-Am-based fluorimetry	[PMID: 22257892]
HEK293	EC₅₀	0.0053 μM Compound: 1a	Agonist activity at human recombinant TRPV1 expressed in HEK293 cells assessed as Ca2+ influx by Fluo-4 dye based assay Agonist activity at human recombinant TRPV1 expressed in HEK293 cells assessed as Ca2+ influx by Fluo-4 dye based assay	[PMID: 25666822]
HEK293	EC₅₀	0.02 μM Compound: capsaicin	Agonist activity at human recombinant TRPV1 expressed in HEK293 cells assessed as increase in intracellular calcium level Agonist activity at human recombinant TRPV1 expressed in HEK293 cells assessed as increase in intracellular calcium level	[PMID: 19361197]
HEK293	EC₅₀	40 nM Compound: 1a	Agonist activity at human TRPV1 expressed in HEK293 cells assessed as increase in intracellular calcium level Agonist activity at human TRPV1 expressed in HEK293 cells assessed as increase in intracellular calcium level	[PMID: 19951840]
HEK293	EC₅₀	40 nM Compound: capsaicin	Agonist activity at human recombinant TRPV1 expressed in human HEK293 cells Agonist activity at human recombinant TRPV1 expressed in human HEK293 cells	[PMID: 17046253]
HEK293	IC₅₀	0.008 μM Compound: 1a	Antagonist activity against human recombinant TRPV1 expressed in HEK293 cells assessed as inhibition of capsaicin-induced Ca2+ influx pre-treated 5 mins before capsaicin addition by Fluo-4 dye based assay Antagonist activity against human recombinant TRPV1 expressed in HEK293 cells assessed as inhibition of capsaicin-induced Ca2+ influx pre-treated 5 mins before capsaicin addition by Fluo-4 dye based assay	[PMID: 25666822]
HeLa	IC₅₀	>50 μM Compound: CAP	Antiproliferative activity against human HeLa cells after 48 hrs by MTT assay Antiproliferative activity against human HeLa cells after 48 hrs by MTT assay	[PMID: 29685681]
Jurkat	IC₅₀	~ 128 μM Compound: 1	Induction of apoptosis in human Jurkat cells assessed as increase in apoptotic cells by propidium iodide staining based flow cytometry Induction of apoptosis in human Jurkat cells assessed as increase in apoptotic cells by propidium iodide staining based flow cytometry	[PMID: 37000154]
K562	IC₅₀	49.41 μM Compound: CAP	Antiproliferative activity against human K562 cells after 48 hrs by MTT assay Antiproliferative activity against human K562 cells after 48 hrs by MTT assay	[PMID: 29685681]
MCF7	IC₅₀	~ 53 μM Compound: 1	Antiproliferative activity against human MCF7 cells assessed as inhibition of cell growth incubated for 24 hrs by MTT assay Antiproliferative activity against human MCF7 cells assessed as inhibition of cell growth incubated for 24 hrs by MTT assay	[PMID: 37000154]
MCF7	IC₅₀	100 μM Compound: Capsaicin	Antiproliferative activity in human MCF7 cells assessed as cell growth inhibition by MTT assay Antiproliferative activity in human MCF7 cells assessed as cell growth inhibition by MTT assay	[PMID: 33508189]
MCF7	IC₅₀	49.97 μM Compound: CAP	Antiproliferative activity against human MCF7 cells after 48 hrs by MTT assay Antiproliferative activity against human MCF7 cells after 48 hrs by MTT assay	[PMID: 29685681]
MDA-MB-231	IC₅₀	120 μM Compound: 24	Antiproliferative activity against human MDA-MB-231 cells incubated for 24 hrs by MTT assay Antiproliferative activity against human MDA-MB-231 cells incubated for 24 hrs by MTT assay	[PMID: 32686940]
NCI-H1299	IC₅₀	>=200 μM Compound: 1	Antiproliferative activity against human NCI-H1299 cells assessed as inhibition of cell growth measured after 24 hrs by MTT assay Antiproliferative activity against human NCI-H1299 cells assessed as inhibition of cell growth measured after 24 hrs by MTT assay	[PMID: 37000154]
NCI-H460	IC₅₀	30.66 μM Compound: Capsaicin	Antiproliferative activity against human NCI-H460 cells assessed as cell growth inhibition measured after 72 hrs by crystal violet staining based assay Antiproliferative activity against human NCI-H460 cells assessed as cell growth inhibition measured after 72 hrs by crystal violet staining based assay	[PMID: 34795858]
SH-SY5Y	EC₅₀	14.02 μM Compound: Capsaicin	Neuroprotective activity against H2O2-induced cell damage in human SH-SY5Y cells assessed as increase in cell viability preincubated for 24 hrs followed by H2O2 addition and measured after 4 hrs by MTT assay Neuroprotective activity against H2O2-induced cell damage in human SH-SY5Y cells assessed as increase in cell viability preincubated for 24 hrs followed by H2O2 addition and measured after 4 hrs by MTT assay	[PMID: 31541868]
SH-SY5Y	EC₅₀	2.32 μM Compound: Capsaicin	Agonist activity at rat TRPV1 expressed in human SH-SY5Y cells assessed as intracellular calcium accumulation by Fluo-4 NW dye based fluorescence assay Agonist activity at rat TRPV1 expressed in human SH-SY5Y cells assessed as intracellular calcium accumulation by Fluo-4 NW dye based fluorescence assay	[PMID: 30783490]
SK-MEL-25	IC₅₀	>100 μM Compound: Capsaicin	Cytotoxicity against human SK-MEL-25 cells assessed as decrease in cell viability incubated for 24 hrs by MTT assay Cytotoxicity against human SK-MEL-25 cells assessed as decrease in cell viability incubated for 24 hrs by MTT assay	[PMID: 31104785]
SK-OV-3	IC₅₀	22.03 μM Compound: Capsaicin	Antiproliferative activity against human SK-OV-3 cells assessed as cell growth inhibition measured after 72 hrs by crystal violet staining based assay Antiproliferative activity against human SK-OV-3 cells assessed as cell growth inhibition measured after 72 hrs by crystal violet staining based assay	[PMID: 34795858]
T47D	IC₅₀	100 μM Compound: Capsaicin	Antiproliferative activity in human T47D cells assessed as cell growth inhibition by MTT assay Antiproliferative activity in human T47D cells assessed as cell growth inhibition by MTT assay	[PMID: 33508189]
U-87MG ATCC	IC₅₀	>100 μM Compound: Capsaicin	Cytotoxicity against human U87 cells assessed as decrease in cell viability incubated for 24 hrs by MTT assay Cytotoxicity against human U87 cells assessed as decrease in cell viability incubated for 24 hrs by MTT assay	[PMID: 31104785]

In Vitro

Capsaicin is the main Capsaicinoid in chili peppers, followed by Dihydrocapsaicin. These two compounds provide about twice hotness to the taste and nerves as the minor capsaicinoids^[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Note:
Please do not refer to only one article to determine the experimental conditions. It is recommended to determine the optimal experimental conditions (animal strain, age, dosage, frequency and cycle, detection time and indicators, etc.) through preliminary experiments before the formal experiment.

Note:
Please do not refer to only one article to determine the experimental conditions. It is recommended to determine the optimal experimental conditions (animal strain, age, dosage, frequency and cycle, detection time and indicators, etc.) through preliminary experiments before the formal experiment.

Capsaicin (Purity 65%) (1-10 mg/kg, oral gavage) increases chlorzoxazone 6-hydroxylase activity and the expression of CYP2E1 in liver microsomes of rats^[4].
Capsaicin (Purity 65%) (10 mg/kg, s.c.) shows the C_max of 104.9 ng/mL for Capsaicin and 54.3 ng/mL for Dihydrocapsaicin, the T_max of 5 h for Capsaicin and 4 h for Dihydrocapsaicin^[5].
Capsaicin is more pungent than Dihydrocapsaicin (HY-N0361)^[6].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Chemical Information

CAS No. 404-86-4
Appearance Solid
분자량 305.41
화학식 C₁₈H₂₇NO₃
Color White to light yellow
SMILES

CC(C)/C=C/CCCCC(NCC1=CC=C(O)C(OC)=C1)=O
Structure Classification
- Phenols
- Monophenols
Initial Source
선적

Room temperature in continental US; may vary elsewhere.
보관

4°C, protect from light

* In solvent : -80°C, 2 years; -20°C, 1 year (protect from light)

Publications (21)

All

Sort by:

Journal Impact Factor

Neuron

Sensory Glia Detect Repulsive Odorants and Drive Olfactory Adaptation. [Abstract]

2020 Nov 25;108(4):707-721.e8. PMID: 32970991
Theranostics

Therapeutic potential of targeting MKK3-p38 axis with Capsaicin for Nasopharyngeal Carcinoma. [Abstract]

2020 Jun 24;10(17):7906-7920. PMID: 32685028
J Transl Med

Increased nerve density adversely affects outcome in colorectal cancer and denervation suppresses tumor growth. [Abstract]

2025 Jan 23;23(1):112. PMID: 39849539
Curr Biol

Molecular sensors for temperature detection during behavioral thermoregulation in turtle embryos. [Abstract]

2021 Jul 26;31(14):2995-3003.e4. PMID: 34015251
Neurosci Bull

Angiotensin Type 1 Receptors and Superoxide Anion Production in Hypothalamic Paraventricular Nucleus Contribute to Capsaicin-Induced Excitatory Renal Reflex and Sympathetic Activation. [Abstract]

2020 May;36(5):463-474. PMID: 31989424
Neurosci Bull

Chemical Stimulation of Renal Tissue Induces Sympathetic Activation and a Pressor Response via the Paraventricular Nucleus in Rats. [Abstract]

2020 Feb;36(2):143-152. PMID: 31392556
J Ethnopharmacol

SZAP exerts analgesic effects on rheumatalgia in CIA rats by suppressing pain hyperalgesia and inhibiting TRPV1 and P2X3. [Abstract]

2022 Feb 10:284:114780. PMID: 34728318
Drug Des Devel Ther

Capsaicin Inhibits Proliferation and Induces Apoptosis in Breast Cancer by Down-Regulating FBI-1-Mediated NF-κB Pathway. [Abstract]

2021 Jan 12:15:125-140. PMID: 33469265
Int Immunopharmacol

Paeoniflorin alleviates CFA-induced inflammatory pain by inhibiting TRPV1 and succinate/SUCNR1-HIF-1α/NLPR3 pathway. [Abstract]

2021 Dec;101(Pt B):108364. PMID: 34844873
Stem Cell Rev Rep

Satellite Glial Cells Give Rise to Nociceptive Sensory Neurons. [Abstract]

2021 Jun;17(3):999-1013. PMID: 33389681
J Inflamm Res

Capsaicin Protects Against Lipopolysaccharide-Induced Acute Lung Injury Through the HMGB1/NF-κB and PI3K/AKT/mTOR Pathways. [Abstract]

2021 Oct 14;14:5291-5304. PMID: 34703269
Clin Immunol

Capsaicin alleviates acetaminophen-induced acute liver injury in mice. [Abstract]

2020 Nov;220:108578. PMID: 32861810
Brain Res Bull

Projecting neurons in spinal dorsal horn send collateral projections to dorsal midline/intralaminar thalamic complex and parabrachial nucleus. [Abstract]

2021 Apr:169:184-195. PMID: 33508400
J Endod

Activation of Transient Receptor Potential Ankyrin 1 and Vanilloid 1 Channels Promotes Odontogenic Differentiation of Human Dental Pulp Cells. [Abstract]

2021 Sep;47(9):1409-1416. PMID: 34126160
Front Physiol

Dysregulation of the Excitatory Renal Reflex in the Sympathetic Activation of Spontaneously Hypertensive Rat. [Abstract]

2021 Jun 3;12:673950. PMID: 34149454
Pflugers Arch

Interleukin-1β in hypothalamic paraventricular nucleus mediates excitatory renal reflex. [Abstract]

2020 Nov;472(11):1577-1586. PMID: 32915316
Clin Exp Pharmacol Physiol

Anti-inflammatory and retinal protective effects of capsaicin on ischaemia-induced injuries through the release of endogenous somatostatin. [Abstract]

2017 Jul;44(7):803-814. PMID: 28429852
J Mol Histol

Functional expression of TRPA1 channel, TRPV1 channel and TMEM100 in human odontoblasts. [Abstract]

2021 Oct;52(5):1105-1114. PMID: 34514518
Biochem Biophys Res Commun

A distinct structural mechanism underlies TRPV1 activation by piperine. [Abstract]

2019 Aug 20;516(2):365-372. PMID: 31213294
Eur Rev Med Pharmacol Sci

Involvement of nNOS in the antinociceptive activity of melatonin in inflammatory pain at the level of sensory neurons. [Abstract]

2020 Jul;24(13):7399-7411. PMID: 32706079
SSRN

2020 Jun 25.

용액&용해도

In Vitro:

DMSO : 100 mg/mL (327.43 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

View the Complete Stock Solution Preparation Table

Preparing Stock Solutions

View the Complete Stock Solution Preparation Table

Concentration Solvent Mass

1 mg

5 mg

10 mg

Concentration

Solvent

Mass

1 mM

3.2743 mL

16.3714 mL

32.7429 mL

5 mM

0.6549 mL

3.2743 mL

6.5486 mL

10 mM

0.3274 mL

1.6371 mL

3.2743 mL

Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.

Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year (protect from light). When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

몰농도 계산기

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Concentration Concentration

Volume Volume

Molecular Weight Molecular Weight

농도 희석 계산기

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

Concentration _(start) Concentration _(start)

Volume _(start) Volume _(start)

Concentration _(final) Concentration _(final)

Volume _(final) Volume _(final)

In Vivo:

Select the appropriate dissolution method based on your experimental animal and administration route.

Stock Solution Working Solution

For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

Protocol 1

Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline

Solubility: ≥ 2.5 mg/mL (8.19 mM); Clear solution

This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

Protocol 2

Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)

Solubility: ≥ 2.5 mg/mL (8.19 mM); Clear solution

This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.

Protocol 3

Add each solvent one by one: 10% DMSO 90% Corn Oil

Solubility: ≥ 2.5 mg/mL (8.19 mM); Clear solution

This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown). If the continuous dosing period exceeds half a month, please choose this protocol carefully.

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL Corn oil, and mix evenly.

In Vivo Dissolution Calculator

Please enter the basic information of animal experiments:

Dosage Dosage
mg/kg
Animal Weight (Per Animal) Animal Weight (Per Animal)
g
Dosing Volume (Per Animal) Dosing Volume (Per Animal)
μL
Number of Animals Number of Animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Please enter your animal formula composition:

%
DMSO +

Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
%
+
+
%
Tween-80 + +
%
Saline +

The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).

Working solution concentration: 0.22 mg/mL

순도&문서

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (273 KB)
SDS (806 KB)
- English - EN (806 KB)
- Français - FR (806 KB)
- Deutsch - DE (806 KB)
- Norwegian - NO (806 KB)
- Español - ES (806 KB)
- Swedish - SV (806 KB)
- Italian - IT (806 KB)
- Portuguese - PT (806 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Hoyoun Cho, et al. Development of a database of capsaicinoid contents in foods commonly consumed in Korea. Food Sci Nutr. 2020 Jul 16;8(8):4611-4624. [Content Brief]

[2]. Krishnapura Srinivasan. Biological Activities of Red Pepper (Capsicum annuum) and Its Pungent Principle Capsaicin: A Review. Crit Rev Food Sci Nutr. 2016 Jul 3;56(9):1488-500. [Content Brief]

[3]. Zhang QH, et al. Effects of capsaicin and dihydrocapsaicin on human and rat liver microsomal CYP450 enzyme activities in vitro and in vivo. J Asian Nat Prod Res. 2012;14(4):382-95. [Content Brief]

[4]. Zhang Q, et al. Simultaneous quantification of capsaicin and dihydrocapsaicin in rat plasma using HPLC coupled with tandem mass spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci. 2010 Aug 15;878(24):2292-7. [Content Brief]

[5]. Joshi SK, et al Comparison of antinociceptive actions of standard analgesics in attenuating capsaicin and nerve-injury-induced mechanical hypersensitivity. Neuroscience. 2006 Dec 1;143(2):587-96. [Content Brief]

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Complete Stock Solution Preparation Table

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg
DMSO	1 mM	3.2743 mL	16.3714 mL	32.7429 mL	81.8572 mL
	5 mM	0.6549 mL	3.2743 mL	6.5486 mL	16.3714 mL
	10 mM	0.3274 mL	1.6371 mL	3.2743 mL	8.1857 mL
	15 mM	0.2183 mL	1.0914 mL	2.1829 mL	5.4571 mL
	20 mM	0.1637 mL	0.8186 mL	1.6371 mL	4.0929 mL
	25 mM	0.1310 mL	0.6549 mL	1.3097 mL	3.2743 mL
	30 mM	0.1091 mL	0.5457 mL	1.0914 mL	2.7286 mL
	40 mM	0.0819 mL	0.4093 mL	0.8186 mL	2.0464 mL
	50 mM	0.0655 mL	0.3274 mL	0.6549 mL	1.6371 mL
	60 mM	0.0546 mL	0.2729 mL	0.5457 mL	1.3643 mL
	80 mM	0.0409 mL	0.2046 mL	0.4093 mL	1.0232 mL
	100 mM	0.0327 mL	0.1637 mL	0.3274 mL	0.8186 mL

Keywords

Capsaicin (Purity 65%)

21 Cited Publications

100 mg 견적 받기

Subscribe to the

MedChemExpress

Newsletter

상품명:
Cat. No.:
수량:
MCE Japan Authorized Agent:

상품명:
CAS No.:
Species:
Purity:
수량:

Capsaicin (Purity 65%)

Publications Citing Use of MedChemExpress (MCE) Capsaicin (Purity 65%)

All TRP Channel Isoforms

All Endogenous Metabolite Isoforms

Biological Activity

Chemical Information

Publications (21)

용액&용해도

순도&문서

References

Help & FAQs

Complete Stock Solution Preparation Table

Capsaicin (Purity 65%) Related Classifications

Cat. No.: HY-10448A