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Search Results for " hyperalgesia "

20

Compounds

Cat No. Product Name Synonyms Targets
T22518 5-BDBD P2X Receptor
5-BDBD is a potent and selective P2X4 receptor antagonist. 5-BDBD inhibits rP2X4R-mediated currents with an IC50 of 0.75 μM. 5-BDBD completely blocked the basal and acute hyperalgesia induced by NTG.
T9685 DS-1971a Sodium Channel
DS-1971a is a highly potent and selective NaV1.7 inhibitor. DS-1971a exhibits a favorable toxicological profile and analgesic effects.
T3S2312 Poncirin Isosakuranetin-7-neohesperidoside Apoptosis , Others
1. Poncirin (Isosakuranetin-7-neohesperidoside) shows a significant in vitro inhibitory effect on the growth of the human gastric cancer cells, SGC-791, in a dose-dependent manner. 2. Poncirin prevents adipogenesis, enha...
T23498 UNC3230 UNC 3230 Others
UNC3230 is a potent, selective and ATP-competitive PIP5K1C inhibitor with an IC50 of ~41 nM. UNC3230(UNC 3230) also inhibits PIP4K2C.
T21543 AP 18 TRP/TRPV Channel
AP-18 is a potent and selective TRPA1 inhibitor. AP-18 inhibits activation of TRPA1 induced by 50 μM Cinnamaldehyde with an IC50 of 3.1 μM and 4.5 μM for human and mouse TRPA1, respectively. AP-18 could reverse complete ...
T21976 ONO-8130 Prostaglandin Receptor
ONO-8130 is an orally available antagonist of EP1 receptor.
T6950 PNU-120596 NSC 216666 AChR
PNU-120596 (NSC-216666) is a positive allosteric modulator of α7 nAChR with EC50 of 216 nM.
T21983L PKI 14-22 amide, myristoylated Acetate PKI 14-22 amide, myristoylated Acetate(201422-03-9 Free base) PKA
PKI 14-22 amide, myristoylated Acetate inhibit cAMP-dependent protein kinase (PKA) and blocks hyperalgesia produced by spinal administration of 8-bromo-cAMP.
T12632 (R)-Mirtazapine (R)-Org3770,(R)-6-Azamianserin 5-HT Receptor
(R)-Mirtazapine ((R)-Org3770) is the R(-)-enantiomer of Mirtazapine, which has anti-injury sensory properties in an animal model of acute thermal hyperalgesia. (R)-Mirtazapine is an antagonist of 5-HT3 receptors and a po...
T23076L Nociceptin (1-7) acetate Opioid Receptor
Nociceptin (1-7) acetate is a potent agonist of opioid receptor-like 1 (ORL1) receptor. Nociceptin (1-7) combines with nociceptin reduces hyperalgesia and has antinociceptive activity.
T4236 AR-M 1000390 hydrochloride ARM390 Hydrochloride,ARM-390 HCl Opioid Receptor
AR-M 1000390 hydrochloride (ARM-390 HCl) , also known as ARM-390, is a low-internalizing nonpeptidic δ-selective opioid receptor agonist; derivative of SNC 80. Does not trigger acute desensitization of the analgesic resp...
TP1904L FSLLRY-NH2 TFA(245329-02-6 free base) Protease-activated Receptor
FSLLRY-NH2 TFA is a is a protease-activated receptor 2 (PAR2) inhibitor. Reverses taxol-induced mechanical allodynia, heat hyperalgesia and PKC activation in ICR mice. Blocks ERK activation and collagen production in iso...
T3S2259 Methyl eugenol 4-allylveratrole,eugenyl methyl ether,O-methyleugenol,Eugenol Methyl ether GABA Receptor
1. Methyl eugenol (4-allylveratrole) is a natural constituent of the essential oils of a number of plants widely used in foodstuffs as flavouring agents, in view of the carcinogenic potential of ME, the need to check its...
T37610 AT-121 Opioid Receptor
AT-121 is a dual μ-opioid and neuropeptide receptor partial agonist (Kis 16.49 and 3.67 nM, respectively). It stimulates [35S]GTPγS binding to cell membranes expressing either μ-opioid receptors or neuropeptide receptors...
TP2277 Nocistatin(human) Nocistatin (human) Others
Blocker of nociceptin-induced allodynia and hyperalgesia
T23076 Nociceptin(1-7) Nociceptin (1-7) Others
Bioactive metabolite of nociceptin, antagonist of nociceptin-induced hyperalgesia
T15167 Draflazine R-75231 Others
Draflazine is an ENT1 inhibitor. It completely reverses the hypersensitivity in the complete Freund’s adjuvant (CFA) model of mechanical hyperalgesia. Draflazine also completely reverses the hypersensitivity of the carra...
T80500 Jingzhaotoxin-X JZTX-X Potassium Channel
Jingzhaotoxin-X (JZTX-X) selectively inhibits Kv4.2 and Kv4.3 potassium channels, resulting in prolonged mechanical hyperalgesia [1].
T21393 Ethopropazine Hydrochloride Lysivane,Parphezein,Dibutil,Parfezin,Profenamine HCl,Pardisol
Ethoproprazine hydrochloride is an butyrylcholinesterase inhibitor. It reduces extrapyramidal motor effects and used as an antidyskinetic, characteristic of Parkinson′s disease. It also alleviates thermal hyperalgesia in...
TP2276 Nocistatin (bovine) Others
endogenous peptide used to block nociceptin-induced allodynia and hyperalgesia
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TargetMol