83 Results for "

Capsaicin

" in MedChemExpress (MCE) Product Catalog:
Products (83)

83 Results for "Capsaicin" in MCE Product Catalog:

Cat. No.: HY-W931056
CAS No.: 862269-93-0
Target:  

TRP Channel

Research Areas:  

Neurological Disease

AMG-628 is an orally active inhibitor for TRPV1, that inhibits Capsaicin (HY-10448) or acid (pH 5)-induced Ca 2+ influx into TRPV1- expressing CHO cell with IC50 of 4.9 and 3.1 nM. AMG-628 exhibits analgesic activity in Capsaicin (HY-10448)-induced rat model, and exhibits a half-life of 2.4 h in rats .
loading...
    loading...
Cat. No.: HY-108576
CAS No.: 113168-57-3
Synonyms: DuP 996 dihydrochloride
Target:  

TRP Channel

Research Areas:  

Neurological Disease

Linopirdine dihydrochloride is a agonist of capsaicin receptor TRPV1. Linopirdine increases the intracellular calcium concentration in HEK293 cells. Linopirdine dihydrochloride exerts an excitatory action on mammalian nociceptors .
loading...
    loading...
Cat. No.: HY-137459A
CAS No.: 1931116-92-5
Synonyms: CA-008 hydrochloride
Target:  

TRP Channel

Research Areas:  

Neurological Disease

Vocacapsaicin (CA-008) hydrochloride, a proagent of Capsaicin, is a first-in-class non-opioid TRPV1 agonist. Vocacapsaicin hydrochloride can provide meaningful and long-lasting pain relief .
loading...
    loading...
Cat. No.: HY-169780
CAS No.: 862269-92-9
Target:  

TRP Channel

(S)-AMG-628 (Compound 16q) is the S-isomer of AMG-628 (HY-123374). (S)-AMG-628 is the orally active antagonist for TRPV1, that inhibits the Capsaicin (HY-10448)- and acid-induced Ca 2+-influx with IC50 of 7 nM and 5 nM in CHO cell. (S)-AMG-628 ameliorates Capsaicin-induced rats flinching, and reverses the thermal hypersensitivity in CFA-(HY-153808) induced inflammatory pain models .
loading...
    loading...
Cat. No.: HY-148751
CAS No.: 1803181-80-7
Target:  

TRP Channel

Research Areas:  

Cancer

TRPV1 activator-1 (compound 8), a capsaicin analog, has an altered neck structure. TRPV1 activator-1 interacts specifically with T551 residue .
loading...
    loading...
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 .
loading...
    loading...
Cat. No.: HY-121080
CAS No.: 659731-59-6
Target:  

TRP Channel

Research Areas:  

Neurological Disease

AMG8163 is an orally active antagonist for TRPV1. AMG8163 inhibits Capsaicin (HY-10448)-induced flinch in rats models, and exhibits anti-hyperalgesia effects in multiple pain models .
loading...
    loading...
Cat. No.: HY-110209
CAS No.: 1459809-09-6
Target:  

TRP Channel

Research Areas:  

Others

AC4 is a trans antagonist upon voltageactivation of TRPV1 and as cis antagonist of TRPV1 currents upon stimulation with Capsaicin (HY-10448). AC4 demonstrates that a photoswitchable antagonist and an agonist can be used in concert .
loading...
    loading...
Cat. No.: HY-149855
Target:  

Sigma Receptor

Research Areas:  

Others

AB10 is a selective S1R antagonist. AB10 with Ki of 10, 165 nM for S1R and S2R, respectively. AB10 reverses the effect of Capsaicin (HY-10448) caused pain in model .
loading...
    loading...
Cat. No.: HY-111036
CAS No.: 946615-43-6
Target:  

TRP Channel

Research Areas:  

Others

AMG0347 is a transient receptor potential type V1 receptor antagonist. AMG0347 inhibits activation of the rat TRPV1 channel by heat (IC50 = 0.2 nm), protons (IC50= 0.8 nm), or capsaicin (IC50 = 0.7 nm) .
loading...
    loading...
Cat. No.: HY-161273
Target:  

TRP Channel

Research Areas:  

Neurological Disease

TRPV1 antagonist 6 (compound 51) is a mode-selective antagonist for transient receptor potential vanilloid member 1 (TRPV1), which shows antagonism with IC50 of 2.85 nM to capsaicin activation and 28.48 % inhibition against proton activation at a 3 µM concentration .
loading...
    loading...
Cat. No.: HY-113654A
Target:  

TRP Channel

Research Areas:  

Cardiovascular Disease

AMG 7905 TFA is a hypothermia-inducing transient receptor potential vanilloid type 1 (TRPV1) antagonist. AMG 7905 TFA potentiates TRPV1 channels activation by protons and drives the reflectory inhibition of thermogenesis and tail-skin vasoconstriction, while potently blocking channel activation by capsaicin .
loading...
    loading...
Cat. No.: HY-121122
CAS No.: 808756-64-1
Target:  

TRP Channel

Research Areas:  

Others

A778317 is a TRPV1 antagonists. A778317 can block changes in intracellular calcium levels mediated by TRPV1 receptors, with a pIC50 value of 8.31. A-778317 can also block the activation of natural rat TRPV1 receptors in dorsal root ganglion neurons by capsaicin and acid .
loading...
    loading...
Cat. No.: HY-159997
Target:  

Sigma Receptor

Research Areas:  

Neurological Disease

AD353 is a selective sigma-1 receptor ligand with antiallodynic activity. AD353 exhibits high potency both in a model of Capsaicin (HY-10448)-induced allodynia and in PGE2-induced mechanical hyperalgesia. AD353 exhibits a favorable pharmacokinetic profile .
loading...
    loading...
Cat. No.: HY-131986
CAS No.: 852453-71-5
Purity:  99.05%
Target:  

TRP Channel

LASSBio-1135 (Compound 3a) is an orally active TRPV1 antagonist. LASSBio-1135 is an anti-inflammatory and analgesic compound. LASSBio-1135 inhibits moderately the human PGHS-2 enzyme activity (IC50 = 18.5 μM). LASSBio-1135 reverts the Capsaicin (HY-10448)-induced thermal hyperalgesia and reduces the carrageenan-induced rat paw edem .
loading...
    loading...
Cat. No.: HY-170444
CAS No.: 1383657-36-0
Research Areas:  

Neurological Disease

ADS1017 is the antagonist for histamine receptor and muscarinic receptor, that exhibits good affinities to hH3R, hH4R, hM2R and hM4R with pKi of 6.8, 5.5, 7.4 and 7.2. ADS1017 exhibits analgesic and anti-allodynic efficacy in mice Capsaicin (HY-10448)-or Oxaliplatin (HY-17371)-induced pain models .
loading...
    loading...
Cat. No.: HY-16935S
Synonyms: JNJ-39439335-d6
Mavatrep-d6 (JNJ-39439335-d6) is a deuterated labeled Mavatrep (HY-16935). Mavatrep (JNJ-39439335) is an orally active, selective and potent TRPV1 antagonist with high affinity for hTRPV1 channels (Ki=6.5 nM). Mavatrep antagonizes capsaicin-induced Ca 2+ influx with an IC50 value of 4.6 nM. Mavatrep can be used in some studies of neuropathic pain .
loading...
    loading...
Cat. No.: HY-AF10448X2
Synonyms: Capsaicin in Maintenance Diet (100ppm)
Target:  

TRP Channel

Research Areas:  

Inflammation/Immunology

Capsaicin Customized Diet-2 is a diet containing capsaicin, with the substrate being a maintenance diet at a concentration of 100 ppm. Capsaicin Customized Diet-2 can be used to study the effects of capsaicin on animal organisms. Capsaicin Customized Diet-2 does not include a control diet and is recommended for use in conjunction with the control diet, Standard Chow Diet (Maintenance Diet) (HY-AF0007) .
loading...
    loading...
Cat. No.: HY-135487
CAS No.: 154189-40-9
Synonyms: AR-C68397AA free base; AR-C68397XX
Sibenadet (AR-C68397AA free base) is a dual dopamine D2/β2-adrenoceptor agonist with selective β2-adrenoceptor agonism. Sibenadet inhibits capsaicin-induced plasma protein extravasation in rat trachea. Sibenadet suppresses edema from sensory nerve fiber activation by activating β2-adrenoceptor. Sibenadet is promising for research of chronic obstructive pulmonary disease (COPD) .
loading...
    loading...
Cat. No.: HY-N0361S
CAS No.: 1330261-21-6
Dihydrocapsaicin-d3 is the deuterium labeled Dihydrocapsaicin (HY-N0361) . 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 .
loading...
    loading...