15 Results for "

Transient Receptor Potential Vanilloid 1

" in MedChemExpress (MCE) Product Catalog:
Products (15)

15 Results for "Transient Receptor Potential Vanilloid 1" in MCE Product Catalog:

13
13 Publications Verification
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 .
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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.
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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 .
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3
3 Cited Publications
Cat. No.: HY-N6825
CAS No.: 83883-10-7
Hydroxy-α-sanshool is a transient receptor potential ankyrin 1 (TRPA1) and TRP vanilloid 1 (TRPV1) agonist with EC50s of 69 and 1.1 μM, respectively. Hydroxy-α-sanshool can be used for pain research .
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Cat. No.: HY-N6962
CAS No.: 481-18-5
α-Spinasterol is an orally taken antagonist of transient receptor potential vanilloid 1 ( TRPV1), and it's also an inhibitor of COX-1 and COX-2, with IC50 values of 16.17 μM and 7.76 μM, respectively. α-Spinasterol exhibits antibacterial, anti-inflammatory, antidepressant, and antioxidant effects, has the ability to cross the blood-brain barrier, and can improve diabetes in mice .
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Cat. No.: HY-136363
CAS No.: 1933528-96-1
Purity:  99.02%
Target:  

TRP Channel

Research Areas:  

Neurological Disease

MDR-652 is a highly specific and efficacious transient receptor potential vanilloid 1 (TRPV1) ligand with agonist activity. The Kis are 11.4 and 23.8 nM for hTRPV1 and rTRPV1, respectively. The EC50s are 5.05 and 93 nM for hTRPV1 and rTRPV1, respectively. Potent topical analgesic activity .
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Cat. No.: HY-N6825R
CAS No.: 83883-10-7
Hydroxy-α-sanshool (Standard) is the analytical standard of Hydroxy-α-sanshool. This product is intended for research and analytical applications. Hydroxy-α-sanshool is a transient receptor potential ankyrin 1 (TRPA1) and TRP vanilloid 1 (TRPV1) agonist with EC50s of 69 and 1.1 μM, respectively. Hydroxy-α-sanshool can be used for pain research .
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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 .
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Cat. No.: HY-19589
CAS No.: 942614-99-5
Target:  

TRP Channel

JTS-653 is a highly potent and selective transient receptor potential vanilloid 1 (TRPV1) antagonist in vitro and in vivo. JTS-653 attenuates chronic pain refractory to non-steroidal anti-inflammatory agents .
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Cat. No.: HY-110091
CAS No.: 939040-79-6
Target:  

TRP Channel

Research Areas:  

Neurological Disease

TRPV1 antagonist 9 (compound 13c) is an orally active transient receptor potential vanilloid 1 (TRPV1) channel antagonist. TRPV1 antagonist 9 blocks Ca 2+ uptake by CHO cells expressing TRPV1 receptors with IC50 values are 0.6 and 0.8 nM for Capsaicin (HY-10448) and acid-induced Ca 2+ uptake, respectively. TRPV1 antagonist 9 blocks Capsaicin (HY-10448)-induced flinch response and causes hyperthermia in rats .
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Cat. No.: HY-120476
CAS No.: 1160606-90-5
Target:  

TRP Channel

JNJ-39729209 is an antagonist for transient receptor potential vanilloid 1 (TRPV1) with pIC50 of 7.9, 8.5, 7.9 and 7.7 for TRPV1 from human, rat, canine and guinea pig. JNJ-39729209 inhibits Capsaicin (HY-10448)-induced hypotension and inhibit thereby hypothermia. JNJ-39729209 exhibits anti-inflammatory and analgesic activities in Carrageenan (HY-125474)- and CFA (HY-153808)-induced thermal hyperalgesia rat models. JNJ-39729209 exhibits anti-cough effects in guinea pigs .
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Cat. No.: HY-P705530
Purity:  ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: TRPV1; VR1; Transient Receptor Potential cation channel subfamily V member 1; TrpV1; Capsaicin Receptor; Osm-9-like TRP channel 1; OTRPC1; Vanilloid Receptor 1; TrpV1; Transient Receptor Potential Vanilloid 1a; Transient Receptor Potential Vanilloid 1b; T
Species:  
Source:  
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Cat. No.: HY-118253
CAS No.: 1177195-52-6
Target:  

Drug Derivative

Research Areas:  

Others

CAY10448 is a 6-Iodonordihydrocapsaicin analogue. 6-Iodonordihydrocapsaicin is a selective transient receptor potential vanilloid 1 (TRPV1) modulator.
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Cat. No.: HY-10633R
CAS No.: 501951-42-4
Research Areas:  

Neurological Disease

SB-705498 (Standard) is the analytical standard of SB-705498 (HY-10633). This product is intended for research and analytical applications. SB-705498 is a potent, selective and orally bioavailable transient receptor potential vanilloid 1 (TRPV1) receptor antagonist with a pIC50 of 7.1.
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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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