82 Results for "

vanilloid

" in MedChemExpress (MCE) Product Catalog:
Products (82)

82 Results for "vanilloid" in MCE Product Catalog:

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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39
39 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 .
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13
13 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 .
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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.
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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 .
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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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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 .
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6
6 Cited Publications
Cat. No.: HY-10634
CAS No.: 659730-32-2
Purity:  99.97%
Target:  

TRP Channel

Research Areas:  

Neurological Disease

AMG 517 is a potent and selective vanilloid receptor-1 (TRPV1) antagonist with an IC50 of 0.5 nM.
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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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4
4 Cited Publications
Cat. No.: HY-N0361
CAS No.: 19408-84-5
Dihydrocapsaicin, a capsaicin, is a potent and selective TRPV1 (transient receptor potential vanilloid channel 1) agonist. Dihydrocapsaicin reduces AIF, Bax, and Caspase-3 expressions, and increased Bcl-2, Bcl-xL and p-Akt levels. Dihydrocapsaicin enhances the hypothermia-induced neuroprotection following ischemic stroke via PI3K/Akt regulation in rat .
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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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2
2 Cited Publications
Cat. No.: HY-12195
CAS No.: 460746-46-7
Purity:  99.23%
ABT-239 is a novel, highly efficacious, non-imidazole class of H3R antagonist and a transient receptor potential vanilloid type 1 (TRPV1) antagonist.
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1
1 Cited Publications
Cat. No.: HY-12777
CAS No.: 1005168-10-4
Purity:  95.76%
Synonyms: PAC-14028
Target:  

TRP Channel

Research Areas:  

Inflammation/Immunology

Asivatrep (PAC-14028) is a potent and selective transient receptor potential vanilloid type I (TRPV1) antagonist.
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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 .
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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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1
1 Cited Publications
Cat. No.: HY-P1651B
Target:  

TRP Channel

Research Areas:  

Cancer

SOR-C13 acetate is the acetate salt form of SOR-C13 (HY-P1651). SOR-C13 acetate is an antagonist for transient receptor potential vanilloid 6 (TRPV 6), with an IC50 of 14 nM. SOR-C13 acetate inhibits tumor growth in SKOV-3 xenograft mouse model .
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Cat. No.: HY-116291
CAS No.: 27536-56-7
Purity:  ≥98.0%
Synonyms: 4αPDD
Target:  

TRP Channel CHIKV

Research Areas:  

Infection Inflammation/Immunology

4α-Phorbol 12,13-didecanoate (4αPDD) is a transient receptor potential vanilloid 4 (TRPV4) agonist. 4α-Phorbol 12,13-didecanoate can promote Ca 2+ influx, induce ATP release and function as an osmoreceptor. 4α-Phorbol 12,13-didecanoate can inhibit water intake and increase maximal micturition pressure in rats. 4α-Phorbol 12,13-didecanoate can be used for the researches of inflammation and infection, such as chikungunya virus (CHIKV) .
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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-A0191
CAS No.: 132-21-8
Synonyms: (+)-Brompheniramine; (S)-Brompheniramine
Dexbrompheniramine ((+)-Brompheniramine; (S)-Brompheniramine) is a dual inhibitor of histamine H1 receptor and TRPV1 receptor that can cross the blood-brain barrier. Dexbrompheniramine exerts its effects by functionally blocking H1 receptor activity and dose-dependently inhibiting TRPV1-mediated calcium responses, including Capsaicin (HY-10448)-induced responses. The combination of Dexbrompheniramine with Cimetidine (HY-14289) eliminates histamine-induced and sham-feeding-induced drinking behavior, whereas Dexbrompheniramine alone does not induce thirst or alter sham-feeding behavior in rats. Dexbrompheniramine can be used in the research of chronic cough and related pathological mechanisms .
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Cat. No.: HY-132596A
CAS No.: 1848239-71-3
Purity:  96.85%
Synonyms: SYL1001 sodium
Tivanisiran sodium (SYL1001 sodium) is a small interfering RNA (siRNA) targeting TRPV1 . Tivanisiran sodium induces the degradation of TRPV1 mRNA, thereby inhibiting protein synthesis. Tivanisiran sodium alleviates ocular discomfort and pain, and improves ocular hyperemia and tear quality. Tivanisiran sodium is applicable to research related to dry eye disease .
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