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Results for "

relieving pain

" in MedChemExpress (MCE) Product Catalog:

91

Inhibitors & Agonists

1

Screening Libraries

1

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1

Peptides

12

Natural
Products

7

Isotope-Labeled Compounds

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-B2080A
    Etidocaine hydrochloride
    1 Publications Verification

    EDC hydrochloride

    Others Infection Others
    Etidocaine (hydrochloride) is a long aminoamide local agent that can suppress or relieve pain .
    Etidocaine hydrochloride
  • HY-108068

    Alfadolone acetate; GR 2/1574

    Others Neurological Disease
    Alphadolone acetate (Alfadolone acetate) is a steroid agent that can suppress or relieve pain, with antinociception .
    Alphadolone acetate
  • HY-145558

    Sodium Channel Neurological Disease
    Bliretrigine is a sodium channel blocker. Bliretrigine has the effect of relieving pain .
    Bliretrigine
  • HY-W016083

    β-Naphthoxyethanol

    Others Others
    Anavenol (β-Naphthoxyethanol) is an agent that can suppress or relieve pain, used for horses .
    Anavenol
  • HY-W694291

    Others Others
    Clibucaine is a piperidine derivative possessing local agent that can suppress or relieve pain. Clibucaine can be used as a local agent that can suppress or relieve pain .
    Clibucaine
  • HY-105613

    Others Others
    Metabutoxycaine is a local agent that can suppress or relieve pain .
    Metabutoxycaine
  • HY-105631

    Salicaine

    Others Neurological Disease
    Hydroxytetracaine is a local agent that can suppress or relieve pain .
    Hydroxytetracaine
  • HY-17481

    Others Inflammation/Immunology
    Bumadizone is a non-steroidal anti-inflammatory drug (NSAID) and can relieve pain .
    Bumadizone
  • HY-156061

    GABA Receptor Neurological Disease Inflammation/Immunology
    NAP-1 is a compound with agent that can suppress or relieve pain. effects. NAP-1 enhances the inhibitory current by binding to a specific site of GABAaR, resulting in a narcotic effect. NAP-1 can be used in research to develop clinical agent that can suppress or relieve pain .
    NAP-1
  • HY-117979

    Alfadolone

    Others Cancer
    Alphadolone is an intravenous agent that can suppress or relieve pain. Alphadolone causes general anaesthesia .
    Alphadolone
  • HY-W275039

    2-Phenylbenzoquinone

    Others Neurological Disease
    Phenylquinone (2-Phenylbenzoquinone) causes pain and induces writhing in mice, and is often used in experiments to test the effectiveness of analgesics or agent that can suppress or relieve pain .
    Phenylquinone
  • HY-W005637

    Others Neurological Disease
    Orthocaine is a local agent that can suppress or relieve pain (extracted from patent WO2002089849A1) .
    Orthocaine
  • HY-105584

    Others Neurological Disease
    Tolycaine is a local agent that can suppress or relieve pain. Tolycaine also induces a convulsive response in experimental animals .
    Tolycaine
  • HY-N8290

    Lactucopicrin

    Others Neurological Disease Metabolic Disease
    Lactupicrin (Lactucopicrin) is a characteristic bitter sesquiterpene lactone that can relieve pain. Lactupicrin exhibits atheroprotective effect .
    Lactupicrin
  • HY-106495

    OR K-242

    Others Neurological Disease
    Vadocaine (OR K-242), an orally active antitussive compound, is a local agent that can suppress or relieve pain .
    Vadocaine
  • HY-B1656

    P 652

    Others Cardiovascular Disease Neurological Disease
    Fomocaine (P 652) is an orally active local agent that can suppress or relieve pain. Fomocaine shows antiarrhythmic activity .
    Fomocaine
  • HY-W011777S

    MS-222-d5

    Isotope-Labeled Compounds Neurological Disease
    Tricaine-d5 (methanesulfonate) is the deuterium labeled Tricaine-d5 methanesulfonate. Tricaine methanesulfonate (MS-222) is a commonly used agent that can suppress or relieve pain. agent for immobilization of aquatic species. Tricaine methanesulfonate, the most widely used agent that can suppress or relieve pain. in fish, has been shown to induce embryotoxic effects in zebrafish .
    Tricaine-d5 methanesulfonate
  • HY-13681

    Glucocorticoid Receptor Inflammation/Immunology
    Methylprednisolone acetate, a prednisolone derivative, is a corticosteroid?hormone. Methylprednisolone acetate can relieve pain and swelling that occurs with arthritis and other joint disorders in vivo .
    Methylprednisolone acetate
  • HY-B0193
    Prazosin
    10+ Cited Publications

    Adrenergic Receptor Cardiovascular Disease Endocrinology
    Prazosin is an α-adrenergic receptor antagonist. Prazosin can reduce inflammation, relieve anxiety, alleviate panic, prevent memory decline, and modulate the pain-relieving effects of opioids. Prazosin can be used in the study of hypertension and Alzheimer’s disease .
    Prazosin
  • HY-155236

    Sodium Channel Inflammation/Immunology
    Ancistrotecine B (Compound 2) is a Nav1.7 channel inhibitor (IC50: 0.73 μM). Ancistrotecine B relieves inflammatory pain in mice .
    Ancistrotecine B
  • HY-106965

    GABA Receptor Neurological Disease
    Org 21465 is an agent that can relieve pain. Org 21465 causes no cardiovascular or respiratory depression. Org 21465 can inhibit GABAA receptor in vivo .
    Org 21465
  • HY-129246

    DNA/RNA Synthesis Cancer
    Cytembena is inhibitor for replicative DNA synthesis, purine synthesis and tetrahydrofolate formylase activity. Cytembena ameliorates ovarian or breast cancer, relieves the pain from skeletal metastases .
    Cytembena
  • HY-109547

    Diclofenac hydroxyethylpyrrolidine

    COX Inflammation/Immunology
    Flector Patch (Diclofenac epolamine) is a non-steroidal anti-inflammatory drug (NSAID) . Flector Patch is used for relieving arthritis Pain, acute Pain, osteoarthritis, and actinic Keratosis. Flector Patch has good skin absorption characteristics without local adverse reactions and allergies .
    Diclofenac epolamine
  • HY-107915

    (-)-Cobefrin; (-)-α-Methylnoradrenaline; (-)-Nordefrin

    Adrenergic Receptor Others
    Levonordefrin, a common alternative to levoepinephrine as a vasoconstrictor in dental local agent that can suppress or relieve pain, is usually used in fivefold higher concentrations. Levonordefrin is generally considered equivalent to epinephrine .
    Levonordefrin
  • HY-148157

    Others Others
    Amylocaine is a local agent that can suppress or relieve pain of the ester type. Amylocaine can cause reversible insensitization near the area where it is administered. Amylocaine is used mostly in spinal anesthesia .
    Amylocaine
  • HY-A0057S

    Calcium Channel Neurological Disease
    Gabapentin-d4 is the deuterium labeled Gabapentin. Gabapentin (Neurontin) is a pharmaceutical agent, specifically a GABA analog. It was originally developed to treat epilepsy, and currently is also used to relieve neuropathic pain.
    Gabapentin-d4
  • HY-13283
    MF63
    1 Publications Verification

    PGE synthase Inflammation/Immunology
    MF63 is a selective and orally active inhibitor of mPGES-1. MF63 reduces the accumulation of PGE2, relieves pyresis, hyperalgesia, and inflammatory pain by inhibiting mPGES-1 .
    MF63
  • HY-N0688

    Cytochrome P450 Inflammation/Immunology
    Linderane, isolated from the root of Lindera aggregata, is an irreversible inhibitor cytochrome P450 2C9 (CYP2C9). Linderane has the potential to relieve pain and cramp .
    Linderane
  • HY-107040

    NSC 288020; CL-1848C

    Others Others
    Etoxadrol (CL-1848C) is a potent, high-affinity N-methyl-D-aspartic acid (NMDA) antagonist. Etoxadrol is used in the anaesthetic and anaesthesia research community to suppress or relieve pain .
    Etoxadrol
  • HY-N8290R

    Others Neurological Disease Metabolic Disease
    Lactupicrin (Standard) is the analytical standard of Lactupicrin. This product is intended for research and analytical applications. Lactupicrin (Lactucopicrin) is a characteristic bitter sesquiterpene lactone that can relieve pain. Lactupicrin exhibits atheroprotective effect .
    Lactupicrin (Standard)
  • HY-108562

    Prostaglandin Receptor Neurological Disease
    SC-51322 is a potent and selective antagonist of prostaglandin E2 (PGE2) receptor (EP 1), with a pA2 of 8.1. SC-51322 has the pain-relieving effect .
    SC-51322
  • HY-116457

    Sombrevin; Fabantol

    GABA Receptor Cardiovascular Disease Neurological Disease
    Propanidid (Sombrevin; Fabantol) is a γ-aminobutyric acid type A (GABAA) receptor agonist and a short-acting non-barbiturate general agent that can suppress or relieve pain. Propanidid can decrease the arterial pressure .
    Propanidid
  • HY-B1726

    Holocaine

    Phosphodiesterase (PDE) Metabolic Disease
    Phenacaine (Holocaine) is a local agent that can suppress or relieve pain. Phenacaine inhibits the specific calmodulin-dependent stimulation of erythrocyte Ca 2+-ATPase and cyclic nucleotide phosphodiesterases from brain and heart .
    Phenacaine
  • HY-B0714
    Dexketoprofen (trometamol)
    1 Publications Verification

    Dexketoprofen tromethamine salt

    COX Neurological Disease Inflammation/Immunology Cancer
    Dexketoprofen trometamol (Dexketoprofen tromethamine salt) is an orally active non-selective COX inhibitor. Dexketoprofen trometamol has a pain-relieving effect, anti-inflammatory effect and anti-cancer effect .
    Dexketoprofen (trometamol)
  • HY-B1126

    iGluR Neurological Disease
    Orphenadrine hydrochloride is an orally active and non-competitive NMDA receptor antagonist (crosses the blood-brain barrier) with a Ki of 6.0 μM. Orphenadrine hydrochloride relieves stiffness, pain and discomfort due to muscle strains, sprains or other injuries. Orphenadrine hydrochloride is also used to relieve tremors associated with parkinson's disease. Orphenadrine citrate has good neuroprotective properties, can be used in studies of neurodegenerative diseases .
    Orphenadrine hydrochloride
  • HY-13681R

    Glucocorticoid Receptor Inflammation/Immunology
    Methylprednisolone acetate (Standard) is the analytical standard of Methylprednisolone acetate. This product is intended for research and analytical applications. Methylprednisolone acetate, a prednisolone derivative, is a corticosteroid hormone. Methylprednisolone acetate can relieve pain and swelling that occurs with arthritis and other joint disorders in vivo .
    Methylprednisolone acetate (Standard)
  • HY-13681S

    Glucocorticoid Receptor Isotope-Labeled Compounds Inflammation/Immunology
    Methylprednisolone acetate-d6 is the deuterium labeled Methylprednisolone acetate (HY-13681). Methylprednisolone acetate, a prednisolone derivative, is a corticosteroid hormone. Methylprednisolone acetate can relieve pain and swelling that occurs with arthritis and other joint disorders in vivo .
    Methylprednisolone acetate-d6
  • HY-108707
    LY3130481
    1 Publications Verification

    iGluR Neurological Disease
    LY3130481 is an orally available AMPA receptor antagonist, selectively inhibiting the IC50 value of AMPA/TARP γ-8 at 65 nM. LY3130481 has anticonvulsant, antiepileptic, and pain-relieving effects .
    LY3130481
  • HY-107150

    ADX-102; NS-2

    Others Neurological Disease Inflammation/Immunology
    Reproxalap (ADX-102) is an active aldehyde sequestering agent that's being researched for dry eye syndrome, allergic conjunctivitis, and non-infectious anterior uveitis. Reproxalap has anti-inflammatory and pain-relieving effects .
    Reproxalap
  • HY-B0714R

    COX Neurological Disease
    Dexketoprofen (trometamol) (Standard) is the analytical standard of Dexketoprofen (trometamol). This product is intended for research and analytical applications. Dexketoprofen trometamol (Dexketoprofen tromethamine salt) is an orally active non-selective COX inhibitor. Dexketoprofen trometamol has a pain-relieving effect .
    Dexketoprofen (trometamol) (Standard)
  • HY-121103

    Others Inflammation/Immunology
    Aclantate is a nonsteroidal anti-inflammatory drug with anti-inflammatory and analgesic activity. Aclantate is mainly used to relieve various types of pain and reduce inflammatory responses. Aclantate can be used to suppress rheumatoid arthritis and other related diseases .
    Aclantate
  • HY-B0653A
    Levobupivacaine hydrochloride
    2 Publications Verification

    (S)-(-)-Bupivacaine monohydrochloride

    Sodium Channel Ferroptosis Cardiovascular Disease Neurological Disease Cancer
    Levobupivacaine hydrochloride ((S)-(-)-Bupivacaine monohydrochloride) is a long-acting amide local agent that can suppress or relieve pain. Levobupivacaine hydrochloride exerts agent that can suppress or relieve pain. and analgesic effects through reversible blockade of neuronal sodium channel. Levobupivacaine hydrochloride can inhibit impulse transmission and conduction in cardiovascular and other tissues, possessing certain cardiac and CNS toxicity. Levobupivacaine hydrochloride is metabolized by hepatic cytochrome P450 (CYP450) enzymes in vivo. Levobupivacaine hydrochloride can also induce ferroptosis by miR-489-3p/SLC7A11 signaling in gastric cancer .
    Levobupivacaine hydrochloride
  • HY-B0653

    (S)-(-)-Bupivacaine

    Sodium Channel Ferroptosis Neurological Disease Cancer
    Levobupivacaine ((S)-(-)-Bupivacaine) is a long-acting amide local agent that can suppress or relieve pain. Levobupivacaine exerts agent that can suppress or relieve pain. and analgesic effects through reversible blockade of neuronal sodium channel. Levobupivacaine can inhibit impulse transmission and conduction in cardiovascular and other tissues, possessing certain cardiac and CNS toxicity. Levobupivacaine is metabolized by hepatic cytochrome P450 (CYP450) enzymes in vivo. Levobupivacaine can also induce ferroptosis by miR-489-3p/SLC7A11 signaling in gastric cancer .
    Levobupivacaine
  • HY-B0369A

    iGluR Neurological Disease
    Orphenadrine citrate is an orally active and non-competitive NMDA receptor antagonist (crosses the blood-brain barrier) with a Ki of 6.0 μM. Orphenadrine citrate relieves stiffness, pain and discomfort due to muscle strains, sprains or other injuries. Orphenadrine citrate is also used to relieve tremors associated with parkinson's disease. Orphenadrine citrate has good neuroprotective properties, can be used in studies of neurodegenerative diseases .
    Orphenadrine citrate
  • HY-111613
    Pinaverium bromide
    3 Publications Verification

    Calcium Channel Cancer
    Pinaverium bromide is an L-type calcium channel blocker with selectivity for the gastrointestinal tract, effectively relieves pain, diarrhea and intestinal discomfort, provides good therapeutic efficacies without significant adverse effects on Irritable bowel syndrome (IBS) patients .
    Pinaverium bromide
  • HY-W121901

    (S)-Naproxen-β-D-glucuronide

    COX Inflammation/Immunology
    Naproxen glucuronide ((S)-Naproxen-β-D-glucuronide) is a non-selective COX inhibitor. Naproxen glucuronide, a metabolite of naproxen, is a nonsteroidal anti-inflammatory drug (NSAID) of the propionic acid class (the same as ibuprofen) that relieves pain, fever, swelling, and stiffness .
    Naproxen glucuronide
  • HY-150270

    P2X Receptor Neurological Disease Inflammation/Immunology
    NP-1815-PX is a potent and selective P2X4R antagonist. NP-1815-PX has anti-inflammatory activity, and can relieve pain in chronic pain models. NP-1815-PX also inhibits guinea pig tracheal/bronchial smooth muscle (TSM and BSM) contractions .
    NP-1815-PX
  • HY-150270A

    P2X Receptor Neurological Disease Inflammation/Immunology
    NP-1815-PX sodium is a potent and selective P2X4R antagonist. NP-1815-PX sodium has anti-inflammatory activity, and can relieve pain in chronic pain models. NP-1815-PX sodium also inhibits guinea pig tracheal/bronchial smooth muscle (TSM and BSM) contractions .
    NP-1815-PX sodium
  • HY-A0057
    Gabapentin
    5+ Cited Publications

    Calcium Channel Neurological Disease Cancer
    Gabapentin is a potent, orally active P/Q type Ca 2+ channel blocker. Gabapentin inhibits neuronal Ca 2+ influx and reduction of neurotransmitter release. Gabapentin is a GABA analog that can be used to relieve neuropathic pain .
    Gabapentin
  • HY-A0057A
    Gabapentin hydrochloride
    5+ Cited Publications

    Calcium Channel Neurological Disease Cancer
    Gabapentin hydrochloride is a potent, orally active P/Q type Ca 2+ channel blocker. Gabapentin hydrochloride inhibits neuronal Ca 2+ influx and reduction of neurotransmitter release. Gabapentin hydrochloride is a GABA analog that can be used to relieve neuropathic pain .
    Gabapentin hydrochloride

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