25 Results for "

VR1

" in MedChemExpress (MCE) Product Catalog:
Products (25)

25 Results for "VR1" in MCE Product Catalog:

8
8 Cited Publications
Cat. No.: HY-12245
CAS No.: 472981-92-3
Purity:  98.11%
Target:  

TRP Channel

Research Areas:  

Inflammation/Immunology

SB-366791 is a potent and selective vanilloid receptor (VR1/TRPV1) antagonist (IC50=5.7 nM). SB-366791 can be used for the research of inflammation [1] .
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5
5 Cited Publications
Cat. No.: HY-19960
CAS No.: 393514-24-4
BCTC is an orally active current inhibitor of vanilloid receptor type 1 (VR1). BCTC is a transient receptor potential cation channel subfamily M member 8 (TRPM8) and transient receptor potential vanilloid 1 (TRPV1) antagonist. BCTC is an insulin sensitizer and secretor. BCTC has anticancer and analgesic effects [1] .
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Cat. No.: HY-110018
CAS No.: 199875-69-9
Purity:  98.36%
N-Arachidonyldopamine acts as an Anandamide (HY-10863) membrane transport inhibitor, a selective CB1 cannabinoid receptor agonist, and a VR1 receptor activator. It exhibits an EC50 value of 48 nM for rat VR1 and a Ki value of 0.25 μM for CB1. N-Arachidonyldopamine exists in mammalian neural tissues. It stimulates intracellular Ca 2+ mobilization, mediates cannabinoid-like effects, and induces hypothermia, hypomotility, catalepsy, analgesia, and hyperalgesia to heat. N-Arachidonyldopamine possesses anticancer activity against breast cancer. It can be used in research related to breast cancer and heat hyperalgesia [1] .
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Cat. No.: HY-P1175
CAS No.: 206350-79-0
Target:  

TRP Channel

Research Areas:  

Neurological Disease

L-R4W2 is a potent antagonist of vanilloid receptor 1 (VR1, TRPV1), with an IC50 of 0.1 μM. L-R4W2 may act as a potent analgesic [1] .
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Cat. No.: HY-RS15121
Research Areas:  

Others

TRPV1 Human Pre-designed siRNA Set A contains three designed siRNAs for TRPV1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P1175A
Target:  

TRP Channel

Research Areas:  

Neurological Disease

L-R4W2 TFA is a potent antagonist of vanilloid receptor 1 (VR1, TRPV1), with an IC50 of 0.1 μM. L-R4W2 TFA may act as a potent analgesic [1] .
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Cat. No.: HY-118299
CAS No.: 623166-14-3
Target:  

TRP Channel

Research Areas:  

Inflammation/Immunology

JYL 1511 is a partial agonist of vanilloid receptor VR1 [1].
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Cat. No.: HY-130358
CAS No.: 179469-40-0
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

PDDHV is a calcium absorption inducer and may achieve 45Ca 2+ influx by stimulating vanillic acid receptor VR1. PDDHV induces 45Ca 2+ uptake (EC50: 70 nM) in rat dorsal root ganglion neurons (expressing native vanilloid receptors) and calcium mobilization (EC50: 125 nM) in VR1-transfected CHO cells. PDDHV also inhibits [3H]-resiniferatoxin (RTX) binding to the dorsal root ganglion membrane in rats [1].
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Cat. No.: HY-135882
CAS No.: 616884-67-4
OMDM-6 is a hybrid agonist of vanilloid receptor type 1 (VR1, TRPV1) (EC50=75 nM) and cannabinoid receptor type 1 (CB1) (Ki=3.2 μM). OMDM-6 inhibits anandamide cellular uptake (ACU) with a Ki of 7.0 μM [1].
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Cat. No.: HY-135881
CAS No.: 616884-66-3
OMDM-5 is a selective inhibitor of anandamide cellular uptake (ACU), with a Ki of 4.8 μM. OMDM-5 is also a potent vanilloid receptor type 1 (VR1, TRPV1) agonist, with an EC50 of 75 nM, and shows weakly active as cannabinoid receptor type 1 (CB1) ligand (Ki=4.9 μM) [1].
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Cat. No.: HY-P3702
Target:  

TRP Channel

Research Areas:  

Others

CEDAEVFKDSMVPGEK is the rat vanilloid receptor subtype 1 (VR1) peptides sequence, can be used to determine the presence and distribution of VR1 [1].
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Cat. No.: HY-D3097
Target:  

Fluorescent Dye

Research Areas:  

Others

Lyso-VR1 is a fluorescent probe for lysosomal viscosity detection. The detection mechanism of Lyso-VR1 relies on intramolecular rotation restriction. Due to the protonation of its indole moiety in lysosomes, this probe can specifically target lysosomes, thereby localizing to this suborganelle for viscosity monitoring. Its excitation wavelength ranges from 400-500 nm, and its emission peak under excitation at 488 nm is located at ~550 nm to ~560 nm [1].
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Cat. No.: HY-19960R
CAS No.: 393514-24-4
BCTC (Standard) is the analytical standard of BCTC. This product is intended for research and analytical applications. BCTC is an orally active current inhibitor of vanilloid receptor type 1 (VR1). BCTC is a transient receptor potential cation channel subfamily M member 8 (TRPM8) and transient receptor potential vanilloid 1 (TRPV1) antagonist. BCTC is an insulin sensitizer and secretor. BCTC has anticancer and analgesic effects [1] .
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Cat. No.: HY-P1175B
Target:  

TRP Channel

Research Areas:  

Neurological Disease

L-R4W2 acetate is a potent antagonist of vanilloid receptor 1 (VR1, TRPV1), with an IC50 of 0.1 μM. L-R4W2 acetate may act as a potent analgesic [1] .
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Cat. No.: HY-183857
CAS No.: 410080-55-6
Target:  

TRP Channel

Research Areas:  

Neurological Disease

DD-161515 is a TRPV1/VR1 inhibitor with an IC50 of 0.7 μM in rats. DD-161515 binds to an allosteric site of TRPV1 distinct from that of capsaicin, blocks channel opening, inhibits receptor-mediated calcium ion influx, reduces the excitability of peripheral sensory nerve fibers, and thereby inhibits nociception induced by heat and transmission of chemically induced pain signals. DD-161515 can be used in studies related to inflammatory pain [1] .
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Cat. No.: HY-RS16501
Research Areas:  

Others

Trpv1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Trpv1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-121557
CAS No.: 616884-62-9
Purity:  98.05%
OMDM-1 is a potent, selective and metabolically stable inhibitor of anandamide cellular uptake (ACU), with a Ki of 2.4 μM [1].
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Cat. No.: HY-103342
CAS No.: 616884-63-0
OMDM-2 is a potent, selective and metabolically stable inhibitor of anandamide cellular uptake (ACU), with a Ki of 3.0 μM [1].
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Cat. No.: HY-135880
CAS No.: 616884-64-1
OMDM-3 is a selective and metabolically stable inhibitor of anandamide cellular uptake (ACU), with a Ki of 16.6 μM [1].
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Cat. No.: HY-135880A
CAS No.: 616884-65-2
OMDM-4 is a selective and metabolically stable inhibitor of anandamide cellular uptake (ACU), with a Ki 17.7 μM [1].
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