9 Results for "

α2C-adrenoceptor

" in MedChemExpress (MCE) Product Catalog:
Products (9)

9 Results for "α2C-adrenoceptor" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-103213
CAS No.: 1259314-65-2
Purity:  99.62%
Target:  

Adrenergic Receptor

Research Areas:  

Neurological Disease Endocrinology

JP1302 dihydrochloride is a potent, selective, high affinity antagonist of the α2C-adrenoceptor, with a Kb of 16 nM and a Ki of 28 nM for the human α2C-receptor. JP1302 dihydrochloride shows antidepressant and antipsychotic-like effects. JP1302 dihydrochloride can be used for neuropsychiatric disorders and renal dysfunction research [2] .
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2
2 Cited Publications
Cat. No.: HY-103213A
CAS No.: 80259-18-3
Target:  

Adrenergic Receptor

Research Areas:  

Neurological Disease

JP1302 is a potent, selective, high affinity antagonist of the α2C-adrenoceptor, with a Kb of 16 nM and a Ki of 28 nM for the human α2C-receptor. JP1302 shows antidepressant and antipsychotic-like effects. JP1302 can be used for neuropsychiatric disorders and renal dysfunction research [2] .
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Cat. No.: HY-101198
CAS No.: 145231-35-2
Purity:  98.99%
Research Areas:  

Neurological Disease Cancer

Clobenpropit dihydrobromide is a potent histamine H3R antagonist/inverse agonist with a pEC50 of 8.07 for histamine H3LR . Clobenpropit dihydrobromide acts as partial agonist at histamine H4 receptors (Ki 13 nM). Clobenpropit dihydrobromide also binds to serotonin 5-HT3 receptors (Ki 7.4 nM) and α2A/α2C adrenoceptors (Ki 17.4/7.8 nM) [2]. Clobenpropit dihydrobromide increases apoptosis .
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Cat. No.: HY-103212A
CAS No.: 147663-20-5
Purity:  95.35%
Synonyms: B-HT 933 hydrochloride; Oxazoloazepin hydrochloride
Target:  

Adrenergic Receptor

Research Areas:  

Cardiovascular Disease

Azepexole hydrochloride (B-HT 933 dihydrochloride; Oxazoloazepin dihydrochloride) is a selective agonist for α 2-adrenoceptor, with pKi of 8.3, 7.6, and 7.5 for α2A-, α2B- and α2C-adrenoceptor subtypes, resepctively. Azepexole dihydrochloride causes concentration-dependent inhibition of peristaltic contractions with IC50 of 78.72 nM. Azepexole hydrochloride exhibits antitussive and analgesic efficacy [2].
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Cat. No.: HY-B0371D
CAS No.: 109351-33-9
Target:  

Adrenergic Receptor

Research Areas:  

Endocrinology

(S)-Terazosin is an active S-enantiomer of Terazosin. (S)-Terazosin is a potent and high-affinity α-adrenoceptor antagonist with Ki values of 3.91 nM, 0.79 nM and 1.16 nM for α1a, α1b and α1d-adrenoceptor, respectively. (S)-Terazosin also has high-affinity for α2a, α2B and α2c-adrenoceptor with Ki values of 729 nM, 3.5 nM and 46.4 nM, respectively .
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Cat. No.: HY-101610
CAS No.: 167626-17-7
Target:  

Adrenergic Receptor

OPC-28326 is a selective peripheral vasodilator and an angatonist of α2-adrenergic receptor, with Ki of 2040, 285, and 55 nM for α2A-, α2B- and α2C-adrenoceptors, respectively.
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Cat. No.: HY-158194
CAS No.: 928115-79-1
Target:  

Adrenergic Receptor

Research Areas:  

Cancer

α2C adrenoceptor agonist 1 (Compound A) is an orally active, highly selective, and non-central nervous system penetrating agonist for the α2C-adrenoceptor, with EC50 and Ki values of 108 nM and 12 nM, respectively. α2C adrenoceptor agonist 1 can be used in the study of nasal congestion .
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Cat. No.: HY-103213R
CAS No.: 1259314-65-2
JP1302 dihydrochloride (Standard) is the analytical standard of JP1302 dihydrochloride. This product is intended for research and analytical applications. JP1302 dihydrochloride is a potent, selective, high affinity antagonist of the α2C-adrenoceptor, with a Kb of 16 nM and a Ki of 28 nM for the human α2C-receptor. JP1302 dihydrochloride shows antidepressant and antipsychotic-like effects. JP1302 dihydrochloride can be used for neuropsychiatric disorders and renal dysfunction research [2] .
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Cat. No.: HY-103212
CAS No.: 36067-72-8
Synonyms: B-HT 933 dihydrochloride; Oxazoloazepin dihydrochloride
Target:  

Adrenergic Receptor

Azepexole (B-HT 933) dihydrochloride is a potent and selective alpha 2-adrenoceptor agonist with pKis of 8.3, 7.6, and 7.5 for α2A-, α2B- and α2C-adrenoceptor subtypes, resepctively . Azepexole dihydrochloride causes concentration-dependent inhibition of peristaltic contractions (IC50= 78.72 nM) [2].
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