145 Results for "

Anesthetic

" in MedChemExpress (MCE) Product Catalog:
Products (145)

145 Results for "Anesthetic" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-B1240
CAS No.: 548-73-2
Synonyms: Dehydrobenzperidol
Research Areas:  

Neurological Disease

Droperidol (Dehydrobenzperidol) is a butyrophenone pamine-2 receptor antagonist that inhibits the activation of GABA(A) and neuronal nicotinic receptors (nAChR), with IC50 values of 12.6 nM and 5.8 μM. Droperidol has anesthetic and sedative properties .
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4
4 Cited Publications
Cat. No.: HY-B0405
CAS No.: 38396-39-3
Bupivacaine is a NMDA receptor inhibitor. Bupivacaine can block sodium, L-calcium, and potassium channels.Bupivacaine potently blocks SCN5A channels with the IC50 of 69.5 μM. Bupivacaine can be used for the research of chronic pain .
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4
4 Cited Publications
Cat. No.: HY-B0405A
CAS No.: 18010-40-7
Bupivacaine hydrochloride is a NMDA receptor inhibitor.Bupivacaine can block sodium, L-calcium, and potassium channels.Bupivacaine potently blocks SCN5A channels with the IC50 of 69.5 μM. Bupivacaine hydrochloride can be used for the research of chronic pain .
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3
3 Cited Publications
Cat. No.: HY-Y1314
CAS No.: 67-71-0
Dimethyl sulfone (Methyl Sulfonyl Methane) is a metabolic product of endogenous methanethiol metabolism and intestinal bacterial metabolism. Dimethyl sulfone inhibits choriocapillary endothelial (CCE) cell proliferation, also has many biological effects, including antiinflammatory, antioxidant, and local anesthetic effects that could be neuroprotective .
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3
3 Cited Publications
Cat. No.: HY-B0379A
CAS No.: 50-42-0
Target:  

nAChR

Research Areas:  

Neurological Disease

Adiphenine hydrochloride is a non-competitive inhibitor of nicotinic acetylcholine receptor (nAChR), with an IC50s of 1.9, 1.8, 3.7, and 6.3 μM for α1, α3β4, α4β2, and α4β4, respectively. Adiphenine hydrochloride has anticonvulsant effects .
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3
3 Cited Publications
Cat. No.: HY-66012
CAS No.: 5875-06-9
Synonyms: Proxymetacaine hydrochloride
Target:  

Sodium Channel

Research Areas:  

Neurological Disease

Proparacaine (Proxymetacaine) hydrochloride is a local anesthetic. Proparacaine hydrochloride blocks voltage-gated sodium channels on neuronal cell membranes, thereby inhibiting signal conduction and nociceptive signal transmission. Proparacaine hydrochloride blocks nociceptive signals in the eye and induces ocular muscle relaxation to reduce eye movement during surgery. Proparacaine hydrochloride is used in research related to cataracts .
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3
3 Cited Publications
Cat. No.: HY-A0182
CAS No.: 56-59-7
Synonyms: PLV-2
Target:  

Vasopressin Receptor

Research Areas:  

Cardiovascular Disease

Felypressin (PLV-2) is a non-catecholamine vasoconstrictor and a vasopressin 1 agonist. Felypressin is widely used in dental procedures .
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3
3 Cited Publications
Cat. No.: HY-A0182A
CAS No.: 914453-97-7
Synonyms: PLV-2 acetate
Target:  

Vasopressin Receptor

Research Areas:  

Cardiovascular Disease

Felypressin acetate (PLV-2 acetate) is a non-catecholamine vasoconstrictor and a vasopressin 1 agonist. Felypressin acetate is widely used in dental procedures .
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2
2 Cited Publications
Cat. No.: HY-B0985
CAS No.: 136-40-3
Target:  

TRP Channel

Research Areas:  

Neurological Disease

Phenazopyridine hydrochlorideis a competitive SARM1 inhibitor, with IC50 145 μM. Phenazopyridine hydrochlorideis a TRPM8 antagonist. Phenazopyridine hydrochloride has a local anesthetic/analgesic effect. Phenazopyridine hydrochlorideis used to relieve painful symptoms of conditions such as cystitis and urethritis. Phenazopyridine hydrochloridecan promote neuronal differentiation and can also be used in the study of traumatic brain injury, peripheral neuropathy and neurodegenerative diseases .
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2
2 Cited Publications
Cat. No.: HY-B0480
CAS No.: 980-71-2
Synonyms: (±)-Brompheniramine maleate
Brompheniramine ((±)-Brompheniramine) maleate is a potent and orally active antihistamine of the alkylamine class. Brompheniramine maleate is a selective histamine H1 receptor antagonist with a Kd of 6.06 nM. Brompheniramine maleate can block the hERG channels, calcium channels, and sodium channels with IC50s of 0.90 μM, 16.12 μM and 21.26 μM, respectively. Brompheniramine maleate has anticholinergic, antidepressant and anesthetic properties and can be used for allergic rhinitis research .
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2
2 Cited Publications
Cat. No.: HY-B0900
CAS No.: 104-46-1
Synonyms: Anise camphor; p-Propenylanisole; Isoestragole
Anethole is a type of orally active aromatic compound that is widely found in nature and used as a flavoring agent. Anethole possesses anticancer, anti-inflammatory, antioxidant, antibacterial, antifungal, anesthetic, estrogenic, central nervous system depressant, hypnotic, insecticidal, and gastroprotective effects. Anethole can be used in the study of oxidative stress-related skin diseases and prostate cancer .
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2
2 Cited Publications
Cat. No.: HY-B1704
CAS No.: 53179-07-0
Nisoxetine is a potent and selective inhibitor of noradrenaline transporter (NET), with a Kd of 0.76 nM. Nisoxetine is an antidepressant and local anesthetic, it can block voltage-gated sodium channels .
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2
2 Cited Publications
Cat. No.: HY-B1007
CAS No.: 149-16-6
Target:  

Sodium Channel

Research Areas:  

Neurological Disease

Butacaine is a reversible nerve conduction blocker. Butacaine acts on the nervous system and nerve fibers, can cause both sensory and motor paralysis. Butacaine inhibits the NavBh currents. Butacaine can form inclusion complexes with α-cyclodextrin (α-CD) and β-cyclodextrin (β-CD). Butacaine is commonly used as a negative control for other local anesthetics .
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2
2 Cited Publications
Cat. No.: HY-B1704A
CAS No.: 57754-86-6
Nisoxetine hydrochloride is a potent and selective inhibitor of noradrenaline transporter (NET), with a Kd of 0.76 nM. Nisoxetine hydrochloride is an antidepressant and local anesthetic, it can block voltage-gated sodium channels .
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2
2 Cited Publications
Cat. No.: HY-B2080A
CAS No.: 36637-19-1
Synonyms: EDC hydrochloride
Target:  

Sodium Channel

Research Areas:  

Infection Others

Etidocaine (hydrochloride) is a long aminoamide local agent that can suppress or relieve pain .
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2
2 Cited Publications
Cat. No.: HY-B0985A
CAS No.: 94-78-0
Target:  

TRP Channel

Research Areas:  

Neurological Disease

Phenazopyridine is a competitive SARM1 inhibitor, with IC50 145 μM. Phenazopyridine is a TRPM8 antagonist. Phenazopyridine has a local anesthetic/analgesic effect. Phenazopyridine is used to relieve painful symptoms of conditions such as cystitis and urethritis. Phenazopyridine can promote neuronal differentiation and can also be used in the study of traumatic brain injury, peripheral neuropathy and neurodegenerative diseases .
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2
2 Cited Publications
Cat. No.: HY-B0480A
CAS No.: 86-22-6
Synonyms: (±)-Brompheniramine
Brompheniramine ((±)-Brompheniramine) is a potent and orally active antihistamine of the alkylamine class. Brompheniramine is a selective histamine H1 receptor antagonist with a Kd of 6.06 nM. Brompheniramine can block the hERG channels, calcium channels, and sodium channels with IC50s of 0.90 μM, 16.12 μM and 21.26 μM, respectively. Brompheniramine has anticholinergic, antidepressant and anesthetic properties and can be used for allergic rhinitis research .
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1
1 Cited Publications
Cat. No.: HY-Y0258
CAS No.: 94-09-7
Benzocaine is an orally active local anesthetic. Benzocaine non-competitively inhibits the binding of Ca-ATPase to Ca 2+, with an IC50 of 47.1 mM. Benzocaine exerts anesthetic effects by blocking voltage-gated sodium channels. Benzocaine induces methemoglobinemia in various experimental animals .
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1
1 Cited Publications
Cat. No.: HY-B0517
CAS No.: 96-88-8
Target:  

Sodium Channel

Research Areas:  

Neurological Disease

Mepivacaine is an amide-type local anesthetic agent. Mepivacaine binds to specific voltage-gated sodium ion channels in neuronal cell membranes, which inhibits both sodium influx and membrane depolarization .
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1
1 Cited Publications
Cat. No.: HY-Y0258A
CAS No.: 23239-88-5
Research Areas:  

Neurological Disease

Benzocaine hydrochloride is an orally active local anesthetic. Benzocaine hydrochloride non-competitively inhibits the binding of Ca-ATPase to Ca 2+, with an IC50 of 47.1 mM. Benzocaine hydrochloride exerts anesthetic effects by blocking voltage-gated sodium channels. Benzocaine hydrochloride induces methemoglobinemia in various experimental animals .
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