16 Results for "

TRPV2

" in MedChemExpress (MCE) Product Catalog:
Products (16)

16 Results for "TRPV2" in MCE Product Catalog:

  • Isoforms Recommended:
49
49 Publications Verification
Cat. No.: HY-B0545
CAS No.: 57-66-9
Target:  

TRP Channel Bacterial HIV

Research Areas:  

Metabolic Disease Cancer

Probenecid is a potent and selective agonist of transient receptor potential vanilloid 2 (TRPV2) channels. Probenecid also inhibits pannexin 1 channels.
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2
2 Cited Publications
Cat. No.: HY-132222
CAS No.: 2313525-20-9
Purity:  99.78%
Target:  

TRP Channel

Research Areas:  

Cancer

SET2 is a selective TRPV2 antagonist (IC50=0.46 μM). SET2 blocks the TRP channel and suppresses prostate cancer cells migration. SET2 reduces the lysophosphatidic acid (LPA, a TRPV2 activator)-induced cytoplasmic calcium increases .
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2
2 Cited Publications
Cat. No.: HY-157131
CAS No.: 2242724-49-6
Purity:  99.84%
Target:  

TRP Channel

Research Areas:  

Neurological Disease

TRPV2-selective blocker 1 is a TRPV2-selective blocker that inhibits calcium influx and ionic currents. TRPV2-selective blocker 1 exhibits an IC50 of 6.3 μM against rat TRPV2, and shows no activity against TRPV1, TRPV3 or TRPV4 channels. TRPV2-selective blocker 1 attenuates macrophage phagocytosis, LPS-induced macrophage migration, and calcium microdomains generated by peripheral TRPV2. TRPV2-selective blocker 1 is non-cytotoxic and can be used to investigate the function of TRPV2 during immune processes .
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1
1 Cited Publications
Cat. No.: HY-N8264
CAS No.: 73255-40-0
Moringin is a potent and selective TRPA1 ion channel natural agonist with an EC50 of 3.14 μM. Moringin does not activate or activates very weakly the vanilloids somatosensory channels TRPV1, TRPV2, TRPV3 and TRPV4, and the melastatin cooling receptor TRPM8. Moringin has hypoglycemic, antimicrobial, anti-inflammatory, anticancer and neuroprotection activities [2].
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1
1 Cited Publications
Cat. No.: HY-B0545R
CAS No.: 57-66-9
Probenecid (Standard) is the analytical standard of Probenecid. This product is intended for research and analytical applications. Probenecid is a potent and selective agonist of transient receptor potential vanilloid 2 (TRPV2) channels. Probenecid also inhibits pannexin 1 channels.
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Cat. No.: HY-RS17234
Research Areas:  

Others

Trpv2 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Trpv2 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS15122
Research Areas:  

Others

TRPV2 Human Pre-designed siRNA Set A contains three designed siRNAs for TRPV2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS23687
Research Areas:  

Others

Trpv2 Rat Pre-designed siRNA Set A contains three designed siRNAs for Trpv2 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-B0545S
CAS No.: 1189657-87-1
Probenecid-d14 is the deuterium labeled Probenecid. Probenecid is a potent and selective agonist of transient receptor potential vanilloid 2 (TRPV2) channels. Probenecid also inhibits pannexin 1 channels [2].
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Cat. No.: HY-N3230
CAS No.: 88478-44-8
Synonyms: Murraxocin
Murpanicin (murraxocin) is a coumarin that is a thermosensitive transient receptor potential vanilloid 2 (TRPV2) channel inhibitor. Murpanicin has significant anti-inflammatory and insecticidal effects.
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Cat. No.: HY-182896
Research Areas:  

Neurological Disease Cancer

HKC54 is a selective TRPV2 antagonist with an IC50 of 0.4 μM. HKC54 binds directly to TRPV2 and inhibits TRPV2-mediated calcium influx. HKC54 inhibits glioblastoma cell migration in vitro and breast cancer metastasis in vivo. HKC54 can be used for the research of breast cancer lung metastasis .
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Cat. No.: HY-186172
CAS No.: 1689577-22-7
Research Areas:  

Metabolic Disease

KS0365 is a selective TRPV3 agonist with an EC50 of 5.08 μM. KS0365 does not activate TRPV2 or TRPV4 channels. KS0365 triggers an increase in [Ca 2+]i and accelerates keratinocyte migration. KS0365 can be used in studies related to impaired skin wound healing .
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Cat. No.: HY-P89618
Synonyms: VRL, TRPV2, Transient receptor potential cation channel subfamily V member 2, TRPV2, Osm-9-like TRP channel 2, Vanilloid receptor-like protein 1, OTRPC2, VRL-1

Host:  

Mouse

Application:  

WB, ICC/IF, IF-Tissue, IP, ELISA

Reactivity:  

human

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Cat. No.: HY-179432
CAS No.: 2699950-81-5
Synonyms: CBDD
Cannabitwinol is a selective thermosensitive TRP modulator and NF-κB inhibitor. Cannabitwinol inhibits TNFα-induced NF-κB-driven transcription and TNFα-induced IL-8 release, and exhibits anti-inflammatory and antioxidant activities. Cannabitwinol shows selectivity for cold-activated TRP channels, activating TRPA1 (EC50 = 3.0 μM) and antagonizing TRPM8 (IC50 = 3.9 μM), but has no significant affinity for heat-activated TRP channels such as TRPV1 and TRPV2. Cannabitwinol can be used in research related to inflammatory skin diseases, cold allodynia, and hyperalgesia [2].
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Cat. No.: HY-P702476
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: Transient receptor potential cation channel subfamily V member 2; Osm-9-like TRP channel 2; OTRPC2; Stretch-activated channel 2B; Vanilloid receptor-like protein 1; VRL-1
Species:  
Rat
Source:  
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Cat. No.: HY-114583
CAS No.: 1041478-78-7
Target:  

TRP Channel

Research Areas:  

Neurological Disease

AMG-8562 is a selective, orally active transient receptor potential vanilloid 1 (TRPV1) modulator that inhibits the activation of rat TRPV1 by Capsaicin (HY-10448), Anandamide (HY-10863) and N-arachidonyldopamine (HY-110018), with IC50 values of 1.75, 9.29 and 3.87 nM, respectively. AMG-8562 blocks capsaicin-induced activation, potentiates pH5-induced activation and has no effect on heat-induced activation of rat TRPV1, whereas it completely blocks capsaicin- and heat-induced activation and partially blocks pH5-induced activation of human TRPV1. AMG-8562 can be used in studies of TRPV1 activation patterns, hyperalgesia and pain-related research .
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