288 Results for "

trpv

" in MedChemExpress (MCE) Product Catalog:
Products (288)

288 Results for "trpv" in MCE Product Catalog:

81
81 Publications Verification
Cat. No.: HY-10448
CAS No.: 404-86-4
Purity:  99.79%
Synonyms: (E)-Capsaicin
Capsaicin ((E)-Capsaicin), an active component of chili peppers, is a TRPV1 agonist. Capsaicin induces a nociceptive response by binding to its receptors. Capsaicin has analgesic effects on neurological disorders. Capsaicin has antioxidant, anti-inflammatory, anti-cancer effects .
81
81 Publications Verification
Cat. No.: HY-10448R
CAS No.: 404-86-4
Purity:  99.38%
Synonyms: (E)-Capsaicin (Standard)
Capsaicin (Standard) is the analytical standard of Capsaicin. This product is intended for research and analytical applications. Capsaicin ((E)-Capsaicin), an active component of chili peppers, is a TRPV1 agonist. Capsaicin induces a nociceptive response by binding to its receptors. Capsaicin has analgesic effects on neurological disorders. Capsaicin has antioxidant, anti-inflammatory, anti-cancer effects .
58
58 Cited Publications
Cat. No.: HY-15640
CAS No.: 138977-28-3
Purity:  98.14%
Target:  

TRP Channel Apoptosis

Research Areas:  

Cancer

Capsazepine is a synthetic analogue of the sensory neurone excitotoxin, and an antagonist of TRPV1 receptor with an IC50 of 562 nM.
44
44 Cited Publications
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.
44
44 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.
41
41 Cited Publications
Cat. No.: HY-100208
CAS No.: 883031-03-6
Purity:  99.89%
Target:  

TRP Channel

Research Areas:  

Cancer

HC-067047 is a potent and selective TRPV4 antagonist and reversibly inhibits currents through the human, rat, and mouse TRPV4 orthologs with IC50 values of 48 nM, 133 nM, and 17 nM, respectively .
38
38 Cited Publications
Cat. No.: HY-19608
CAS No.: 942206-85-1
GSK1016790A is a potent and selective transient receptor potential vanilloid 4 (TRPV4) channel agonist. GSK1016790A can elicit Ca 2+ influx and elevate intracellular Ca 2+ in HEK cells .
21
21 Cited Publications
Cat. No.: HY-10448A
CAS No.: 404-86-4
Purity:  99.20%
Capsaicin (Purity 65%) is a mixture of Capsaicin and Dihydrocapsaicin (Ratio >2:1). Capsaicin (Purity 65%) is an orally active capsaicin receptor (TRPV1) agonist .
18
18 Cited Publications
Cat. No.: HY-100720
CAS No.: 1336960-13-4
Purity:  99.91%
Target:  

TRP Channel

Research Areas:  

Cardiovascular Disease

GSK2193874 is an orally active, potent, and selective TRPV4 antagonist with IC50s of 2 nM and 40 nM for rTRPV4 and hTRPV4 .
14
14 Cited Publications
Cat. No.: HY-N0637
CAS No.: 552-58-9
Synonyms: Huazhongilexone
Eriodictyol ((±)-Huazhongilexone; Dihydroluteolin) is an orally active TRPV1 receptor antagonist (IC50=44-47 nM, rTRPV1) with antioxidant and anti-inflammatory activities. Eriodictyol effectively inhibits lipid peroxidation and the release of proinflammatory cytokines by specifically antagonizing the TRPV1 receptor and activating the Nrf2 signaling pathway. Eriodictyol reduces the levels of ICAM-1, VEGF, eNOS and TNF-α in the retina and maintains the integrity of the blood-retinal barrier. Eriodictyol alleviates oxidative stress-induced apoptosis and hyperalgesia, enhances the activity and cytotoxicity of immune cells (such as B lymphocytes, NK cells and macrophages), and increases the levels of antioxidant enzymes simultaneously. Eriodictyol can be used in the research of diabetic retinopathy, acute lung injury and various pain-related diseases .
13
13 Cited Publications
Cat. No.: HY-120691A
CAS No.: 1263068-83-2
Purity:  99.47%
Target:  

TRP Channel

GSK205 is a potent, selective TRPV4 antagonist with an IC50 of 4.19  μM for inhibiting TRPV4-mediated Ca 2+ influx .
13
13 Cited Publications
Cat. No.: HY-101507
CAS No.: 1628287-16-0
Purity:  99.47%
Synonyms: Pico145; HC-608
Target:  

TRP Channel

Research Areas:  

Cancer

Pico145 (HC-608) is a remarkable inhibitor of TRPC1/4/5 channels, inhibits (-)-englerin A-activated TRPC4/TRPC5 channels, with IC50s of 0.349 and 1.3 nM in cells, and shows no effect on TRPC3, TRPC6, TRPV1, TRPV4, TRPA1, TRPM2, TRPM8 .
11
11 Cited Publications
Cat. No.: HY-N2333
CAS No.: 57444-62-9
Synonyms: (+)-Resiniferatoxin
Resiniferatoxin ((+)-Resiniferatoxin), is a selective agonist of transient receptor potential vanilloid 1 (TRPV1) receptor agonist. Resiniferatoxin can be isolated from the Euphorbia resinifera plant. Resiniferatoxin eliminates TRPV1+ primary sensory afferents and blunt cardiac sympathetic afferent reflex for a relatively long period .
11
11 Cited Publications
Cat. No.: HY-101736
CAS No.: 545395-94-6
Purity:  99.76%
Target:  

TRP Channel

Research Areas:  

Neurological Disease

AMG9810 is a selective and competitive vanilloid receptor 1 (TRPV1) antagonist with IC50 values of 24.5 and 85.6 nM for human and rat TRPV1, repectively.
9
9 Cited Publications
Cat. No.: HY-18662
CAS No.: 1254205-52-1
Target:  

TRP Channel

Research Areas:  

Neurological Disease Cancer

RQ-00203078 is a highly selective, potent and orally active TRPM8 antagonist with IC50s of 5.3 nM and 8.3 nM for rat and human TRPM8 channels, respectively. RQ-00203078 shows little inhibitory action against TRPV1, TRPA1, TRPV4, or TRPM2 channels .
9
9 Cited Publications
Cat. No.: HY-19975
CAS No.: 946387-07-1
Target:  

TRP Channel

Research Areas:  

Neurological Disease Cancer

RN-1734 is selective antagonist of the TRPV4 channel, completely antagonizes 4αPDD-mediated activation of TRPV4 with comparable, low micromolar IC50s for all three species (hTRPV4: 2.3 μM, mTRPV4: 5.9 μM, rTRPV4: 3.2 μM) . RN-1734 clearly decreases the production of tumor necrosis factor α (TNF-α) and interleukin 1β (IL-1β) without altering the number of olig2-positive cells .
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 .
8
8 Cited Publications
Cat. No.: HY-10633
CAS No.: 501951-42-4
Purity:  99.98%
Target:  

TRP Channel

Research Areas:  

Neurological Disease

SB-705498 is a potent, selective and orally bioavailable transient receptor potential vanilloid 1 (TRPV1) receptor antagonist with a pIC50 of 7.1.
8
8 Cited Publications
Cat. No.: HY-19765
CAS No.: 1419609-94-1
Target:  

TRP Channel

Research Areas:  

Cardiovascular Disease

GSK2798745 is a potent, selective, and orally active transient receptor potential vanilloid 4 (TRPV4) ion channel blocker with IC50s of 1.8 and 1.6 nM for hTRPV4 and rTRPV4, respectively. GSK2798745 can be used in cardiac and respiratory diseases research .