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beta-adrenoceptor

" in MedChemExpress (MCE) Product Catalog:

By Targets:	5-HT Receptor (18) Adrenergic Receptor (60) Akt (2) Angiotensin Receptor (2) Angiotensin-converting Enzyme (ACE) (1) Bcl-2 Family (1) Calcium Channel (1) Caspase (1) Cholinesterase (ChE) (1) Cytochrome P450 (1) Drug Derivative (1) Drug Isomer (2) Drug Metabolite (4) Endogenous Metabolite (1) GABA Receptor (2) Isotope-Labeled Compounds (5) mAChR (1) Ornithine decarboxylase (ODC) (1) PI3K (2) Potassium Channel (1) Reference Standards (8) Renin (3) Sodium Channel (1)
By Research Areas:	Cancer (7) Cardiovascular Disease (42) Endocrinology (24) Inflammation/Immunology (4) Metabolic Disease (5) Neurological Disease (24)
Click Chemistry:	Alkynes (1)

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Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-17380

(S)-Timolol maleate 5 Publications Verification (S)-L-714,465 maleate; MK 950	Adrenergic Receptor	Cardiovascular Disease Neurological Disease Cancer
(S)-Timolol Maleate (L-714,465 Maleate) is a non-cardioselective hydrophilic *β-adrenoceptor* blocker. (S)-Timolol Maleate is widely used as standard medication for intraocular pressure (glaucoma) by preventing the production of aqueous humor. (S)-Timolol Maleate can be used for hypertension, angina pectoris and myocardial infarction .

HY-B1517

Alprenolol 5+ Cited Publications (RS)-Alprenolol; dl-Alprenolol	5-HT Receptor	Cardiovascular Disease Cancer
Alprenolol ((RS)-Alprenolol; dl-Alprenolol) is an orally active non-selective *β-adrenoceptor* antagonist and an antagonist of 5-HT1A and 5-HT1B receptors. Alprenolol is used as an anti-hypertensive, anti-anginal and anti-arrhythmic agent .

HY-B1517A

Alprenolol hydrochloride 5+ Cited Publications (RS)-Alprenolol hydrochloride; dl-Alprenolol hydrochloride	5-HT Receptor	Cardiovascular Disease Cancer
Alprenolol ((RS)-Alprenolol; dl-Alprenolol) hydrochloride is an orally active non-selective *β-adrenoceptor* antagonist and an antagonist of 5-HT1A and 5-HT1B receptors. Alprenolol hydrochloride is used as an anti-hypertensive, anti-anginal and anti-arrhythmic agent .

HY-A0295

(R)-Propranolol hydrochloride 1 Publications Verification	Adrenergic Receptor	Cardiovascular Disease Neurological Disease Endocrinology
(R)-Propranolol hydrochloride is a less active enantiomer of the β-adrenoceptor antagonist propranolol (HY-B0573). Propranolol is a nonselective β-adrenergic receptor (βAR) antagonist, has high affinity for the β₁AR and β₂AR with K_i values of 1.8 nM and 0.8 nM, respectively .

HY-103207

Amibegron hydrochloride SR 58611A	Adrenergic Receptor	Neurological Disease Endocrinology
Amibegron hydrochloride is a selective *β3-adrenoceptor* agonist, with an EC₅₀ of 3.5 nM for *β-adrenoceptor* in rat colon; Amibegron hydrochloride has anxiolytic and antidepressant activity.

HY-B1154

Penbutolol sulfate 1 Publications Verification (-)-Terbuclomine	Adrenergic Receptor 5-HT Receptor	Neurological Disease
Penbutolol sulfate ((-)-Terbuclomine) is a potent *β-adrenoceptor* and 5-HT receptor antagonist with K_i of 11.6 nM and 11.9 nM for 5-HT in rat cornu ammonis 1 (CA1) and human CA3 .

HY-15477

YS-49 Maximum Cited Publications 15 Publications Verification	Akt PI3K Angiotensin Receptor Adrenergic Receptor	Cardiovascular Disease Endocrinology
YS-49 is a PI3K/Akt (a downstream target of RhoA) activator, to reduce RhoA/PTEN activation in the 3-methylcholanthrene-treated cells. YS-49 inhibits angiotensin II (Ang II)-stimulated proliferation of VSMCs via induction of heme oxygenase (HO)-1. YS-49 is also an isoquinoline compound alkaloid, has a strong positive inotropic action through activation of cardiac *β-adrenoceptors* .

HY-100606

l-Pindolol (-)-Pindolol; (S)-(-)-Pindolol; S-Pindolol	5-HT Receptor Adrenergic Receptor	Neurological Disease
l-Pindolol ((-)-pindolol) is a reversible, competitive and orally active 5-HT1A/1B antagonist. l-Pindolol is a partial *β-adrenoceptor* agonist. l-Pindolol can be used for the research of neurological disease .

HY-17501A

Bambuterol hydrochloride 1 Publications Verification (±)-Bambuterol hydrochloride; KWD-2183 hydrochloride	Adrenergic Receptor	Endocrinology
Bambuterol hydrochloride ((±)-Bambuterol hydrochloride; KWD-2183 hydrochloride) is a long acting beta-adrenoceptor agonist (LABA) used in the treatment of asthma; it also is a proagent of terbutaline.

HY-101325

(S,S)-BRL-37344 sodium	Drug Isomer Adrenergic Receptor	Cardiovascular Disease Metabolic Disease
(S,S)-BRL-37344 sodium is an isomer of BRL-37344 (HY-101325B). BRL-37344 is a *β-adrenoceptor* agonist with EC₅₀ values of 5.3, 18 and 570 nM for β3, β2 and β1. BRL-37344 induces concentration-dependent increases in atria1 rate, relaxation of guinea pig trachea and lipolysis of brown adipocytes .

HY-100991

FG 7142 ZK 39106; LSU-65	GABA Receptor	Neurological Disease
FG 7142 (ZK 39106; LSU-65), a non-selectively benzodiazepine inverse agonist, has high affinity for the α1 subunit-containing GABAA receptor (K_i=91 nM). FG 7142 (ZK 39106; LSU-65) also modulates GABA-induced chloride flux at GABAA receptors expressing the α1 subunit (EC₅₀= 137 nM). FG 7142 (ZK 39106; LSU-65) can increase tyrosine hydroxylation and cause upregulation of β-adrenoceptors in mouse cerebral cortex .

HY-B0010B

Formoterol-1 1 Publications Verification (±)Formoterol	Adrenergic Receptor	Inflammation/Immunology
Formoterol ((±)Formoterol) is an orally active β2-selective agonist. Formoterol potently relaxes the peripheral airways through stimulating the beta 2-adrenoceptors selectively as is the case in the central airways and that it significantly inhibits IgE-mediated slow reactive substance of anaphylaxis (SRS-A) release through beta-adrenoceptor stimulation .

HY-100635

Diacetolol	Drug Metabolite	Cardiovascular Disease Endocrinology
Diacetolol is an active metabolite of the beta-adrenoceptor blocking agent Acebutolol (HY-17497) .

HY-P5189A

*His-D-beta-Nal-Ala-Trp-D-Phe-Lys-NH2 TFA*	Endogenous Metabolite Cholinesterase (ChE)	Others
His-D-beta-Nal-Ala-Trp-D-Phe-Lys-NH2 TFA, is a growth hormone releasing peptide, as well as a metabolite of GHRP-1. GHRP-1, or Ala-His-D-beta Nal-Ala-Trp-D-Phe-Lys-NH2, has the effect of promoting the release of growth hormone (GH). GHRP-1 increases GH release and increases [Ca2+]i levels in static monolayer cells of rat pituitary gland, but does not affect cAMP levels .

HY-116790A

(+)-Penbutolol (R)-Penbutolol; (+)-Isopenbutolol	Adrenergic Receptor	Metabolic Disease Endocrinology
(+)-Penbutolol is a β-adrenoceptor antagonist, with an IC₅₀ of 0.74 μM . (+)-Penbutolol is an optical isomer of l-penbutolol with Na ⁺ channel-blocking action .

HY-116790

(-)-Penbutolol 1 Publications Verification (S)-Penbutolol; (-)-Isopenbutolol	Adrenergic Receptor 5-HT Receptor	Neurological Disease
(-)-Penbutolol ((S)-Penbutolol) is a potent *β-adrenoceptor* and 5-HT receptor antagonist with K_i values of 11.6 nM and 11.9 nM for 5-HT in rat cornu ammonis 1 (CA1) and human CA3 .

HY-111013

VK-II-86	Drug Derivative Adrenergic Receptor	Cardiovascular Disease
VK-II-86 is a Carvedilol (HY-B0006) analogue lacking antagonist activity at β-adrenoceptors, in hypokalaemia. VK-II-86 prevents hypokalaemia-induced ventricular arrhythmia through multi-channel effects. VK-II-86 prevents all hypokalaemia-induced changes in ion channel activity and oxidative stress .

HY-17380R

(S)-Timolol maleate (Standard) (S)-L-714,465 maleate (Standard); MK 950 (Standard)	Reference Standards Adrenergic Receptor	Cardiovascular Disease Neurological Disease
(S)-Timolol (maleate) (Standard) is the analytical standard of (S)-Timolol (maleate). This product is intended for research and analytical applications. (S)-Timolol Maleate (L-714,465 Maleate) is a non-cardioselective hydrophilic *β-adrenoceptor* blocker. (S)-Timolol Maleate is widely used as standard medication for intraocular pressure (glaucoma) by preventing the production of aqueous humor. (S)-Timolol Maleate can be used for hypertension, angina pectoris and myocardial infarction .

HY-15477A

YS-49 monohydrate Maximum Cited Publications 15 Publications Verification	Akt PI3K Angiotensin Receptor Adrenergic Receptor	Cardiovascular Disease Endocrinology
YS-49 (monohydrate) is a PI3K/Akt (a downstream target of RhoA) activator, to reduce RhoA/PTEN activation in the 3-methylcholanthrene-treated cells. YS-49 inhibits angiotensin II (Ang II)-stimulated proliferation of VSMCs via induction of heme oxygenase (HO)-1. YS-49 is also an isoquinoline compound alkaloid, has a strong positive inotropic action through activation of cardiac *β-adrenoceptors* .

HY-B1562B

Bopindolol malonate (±)-Bopindolol malonate	Adrenergic Receptor Renin 5-HT Receptor	Cardiovascular Disease Neurological Disease
Bopindolol ((±)-Bopindolol) malonate is an orally active antagonist of β-adrenoceptors (ARs) with partial agonist activity. Bopindolol malonate is non-selective for β1- and β2-ARs and has low affinity for β3-AR subtype. Bopindolol malonate has intrinsic sympathomimetic as well as membrane stabilizing actions, inhibits renin secretion, and interacts with 5-HT receptors. Bopindolol malonate is a proagent of Pindolol (HY-B0982). Bopindolol malonate can be used for essential and renovascular hypertension research.

HY-101325A

(S,S)-BRL-37344	Drug Isomer Adrenergic Receptor	Cardiovascular Disease Metabolic Disease
(S,S)-BRL-37344 is an isomer of BRL-37344 (HY-101325B). BRL-37344 is a *β-adrenoceptor* agonist with EC₅₀ values of 5.3, 18 and 570 nM for β3, β2 and β1. BRL-37344 induces concentration-dependent increases in atria1 rate, relaxation of guinea pig trachea and lipolysis of brown adipocytes .

HY-17501S

Bambuterol-d9 hydrochloride (±)-Bambuterol-d9 hydrochloride; KWD-2183-d9 hydrochloride	Adrenergic Receptor	Endocrinology
Bambuterol-d₉ (hydrochloride) is the deuterium labeled Bambuterol. Bambuterol ((±)-Bambuterol) hydrochloride is a long acting beta-adrenoceptor agonist (LABA) used in the treatment of asthma; it also is a prodrug of terbutaline.

HY-19578B

Isamoltane hemifumarate (±)-Isamoltane hemifumarate	5-HT Receptor Adrenergic Receptor	Neurological Disease
Isamoltane hemifumarate is a selective antagonist of 5-HT_1B receptor, with an IC₅₀ of 39 nM for inhibits the binding of [ ¹²⁵I]ICYP to 5-HT_1B recognition sites in rat brain membranes. Isamoltane hemifumarate is also a *β-adrenoceptor* ligand, with an IC₅₀ of 8.4 nM. Isamoltane hemifumarate shows anxiolytic activity .

HY-101752

(±)-Befunolol	Adrenergic Receptor	Cardiovascular Disease Endocrinology
(±)-Befunolol is a *β-adrenoceptor* blocking agent.

HY-A0252

Bupranolol	Adrenergic Receptor	Inflammation/Immunology Cancer
Bupranolol is an orally active, competitive and non-selective *β-adrenoceptor* antagonist without intrinsic sympathomimetic activity .

HY-A0252R

Bupranolol (Standard)	Reference Standards Adrenergic Receptor	Inflammation/Immunology Cancer
Bupranolol (Standard) is the analytical standard of Bupranolol. This product is intended for research and analytical applications. Bupranolol is an orally active, competitive and non-selective *β-adrenoceptor* antagonist without intrinsic sympathomimetic activity .

HY-16056

Arbutamine	Adrenergic Receptor	Cardiovascular Disease
Arbutamine is a short-acting, potent and nonselective *β-adrenoceptor* agonist. Arbutamine stimulates cardiac β₁-, tracheal β₂-, and adiopocyte β₃- adrenergic receptors. Arbutamine provides cardiac stress increases heart rate, cardiac contractility, and systolic blood pressure. Arbutamine can be used for cardiac stress agent .

HY-16056A

Arbutamine hydrochloride	Adrenergic Receptor	Cardiovascular Disease
Arbutamine hydrochloride is a short-acting, potent and nonselective *β-adrenoceptor* agonist. Arbutamine hydrochloride stimulates cardiac β₁-, tracheal β₂-, and adiopocyte β₃- adrenergic receptors. Arbutamine hydrochloride provides cardiac stress increases heart rate, cardiac contractility, and systolic blood pressure. Arbutamine hydrochloride can be used for cardiac stress agent .

HY-B1517AR

Alprenolol hydrochloride (Standard) (RS)-Alprenolol hydrochloride (Standard); dl-Alprenolol hydrochloride (Standard)	Reference Standards 5-HT Receptor	Cancer
Alprenolol (hydrochloride) (Standard) is the analytical standard of Alprenolol (hydrochloride). This product is intended for research and analytical applications. Alprenolol ((RS)-Alprenolol; dl-Alprenolol) hydrochloride is an orally active non-selective *β-adrenoceptor* antagonist and an antagonist of 5-HT1A and 5-HT1B receptors. Alprenolol hydrochloride is used as an anti-hypertensive, anti-anginal and anti-arrhythmic agent .

HY-U00019

Pamatolol	Adrenergic Receptor	Cardiovascular Disease Endocrinology
Pamatolol is a cardioselective *beta-adrenoceptor* antagonist without sympathomimetic activity.

HY-17501

Bambuterol (±)-Bambuterol; KWD-2183	Adrenergic Receptor	Endocrinology
Bambuterol ((±)-Bambuterol; KWD-2183) is a long acting beta-adrenoceptor agonist (LABA) used in the treatment of asthma; it also is a proagent of terbutaline.

HY-128379

Labetalone hydrochloride	Drug Metabolite	Others
Labetalone hydrochloride is an impurity of Labetalol. Labetalol is an orally active adrenoceptor blocking agent which is a competitive antagonist at both alpha- and beta-adrenoceptor sites .

HY-17495

Carteolol OPC-1085	Adrenergic Receptor Caspase Bcl-2 Family	Neurological Disease
Carteolol is a non-selective *β-adrenoceptor* antagonist. Carteolol induces apoptosis via a caspase activated and mitochondrial-dependent pathway. Carteolol can be used for glaucoma research .

HY-P1376

G-Protein antagonist peptide	mAChR Adrenergic Receptor	Endocrinology
G-Protein antagonist peptide is the substance P-related peptide that inhibits binding of G proteins to their receptors. G-Protein antagonist peptide competitively and reversibly inhibits M2 muscarinic receptor activation of G_i or G_o and inhibits G_s activation by β-adrenoceptors.

HY-W703936

Cloranolol	Adrenergic Receptor Cytochrome P450	Cardiovascular Disease
Cloranolol is an orally active nonselective *β-adrenoceptor* blocker. Cloranolol can reduce the content of cytochrome P-450 in rat hepatocytes, prolong hexobarbital anesthesia time, and inhibit aminopyrine-N-demethylation activity. Cloranolol can be used in the research of cardiovascular diseases such as hypertension .

HY-B1517B

Alprenolol benzoate	5-HT Receptor	Cardiovascular Disease Cancer
Alprenolol benzoate is an orally active non-selective *β-adrenoceptor* antagonist and an antagonist of 5-HT1A and 5-HT1B receptors. Alprenolol benzoate is used as an anti-hypertensive, anti-anginal and anti-arrhythmic agent .

HY-106361A

Flerobuterol hydrochloride CRL 40827 hydrochloride	Adrenergic Receptor	Neurological Disease
Flerobuterol hydrochloride is a *beta-adrenoceptor* agonist with antidepressant activity. Flerobuterol hydrochloride enhances serotonergic neurotransmission .

HY-U00356

Tertatolol (±)-Tertatolol; Racemic Tertatolol; dl-Tertatolol	Adrenergic Receptor 5-HT Receptor	Cardiovascular Disease Endocrinology
Tertatolol is a potent antagonist of *beta-adrenoceptor* and 5-HT receptor, with unique renal vasodilatatory effects.

HY-17501AR

Bambuterol hydrochloride (Standard) (±)-Bambuterol hydrochloride (Standard); KWD-2183 hydrochloride (Standard)	Reference Standards Adrenergic Receptor	Endocrinology
Bambuterol hydrochloride (Standard) is the analytical standard of Bambuterol hydrochloride. This product is intended for research and analytical applications. Bambuterol hydrochloride ((±)-Bambuterol hydrochloride; KWD-2183 hydrochloride) is a long acting beta-adrenoceptor agonist (LABA) used in the treatment of asthma; it also is a proagent of terbutaline.

HY-19578A

Isamoltan hydrochloride (±)-Isamoltane hydrochloride	Adrenergic Receptor 5-HT Receptor	Neurological Disease
Isamoltan ((±)-Isamoltane) hydrochloride is a selective antagonist of 5-HT_1B receptor, with an IC₅₀ of 39 nM for inhibits the binding of [ ¹²⁵I]ICYP to 5-HT_1B recognition sites in rat brain membranes. Isamoltan hydrochloride is also a *β-adrenoceptor* ligand, with an IC₅₀ of 8.4 nM. Isamoltan hydrochloride shows anxiolytic activity .

HY-128379R

Labetalone hydrochloride (Standard)	Drug Metabolite Reference Standards	Others
Labetalone (hydrochloride) (Standard) is the analytical standard of Labetalone (hydrochloride). This product is intended for research and analytical applications. Labetalone hydrochloride is an impurity of Labetalol. Labetalol is an orally active adrenoceptor blocking agent which is a competitive antagonist at both alpha- and beta-adrenoceptor sites .

HY-101431

Xibenolol hydrochloride D32 hydrochloride	Adrenergic Receptor	Cardiovascular Disease
Xibenolol hydrochloride (D32 hydrochloride) is an orally active *beta-adrenoceptor* blocking agent. Xibenolol hydrochloride can be used in the research of tachycardia and hypotension .

HY-101752A

(±)-Befunolol hydrochloride	Adrenergic Receptor	Cardiovascular Disease Endocrinology
(±)-Befunolol hydrochloride is a *β-adrenoceptor* blocking agent.

HY-19673

KUL-7211	Adrenergic Receptor	Endocrinology
KUL 7211 is a selective *β-adrenoceptor* agonist.

HY-121692A

(S)-Alprenolol L-tartrate	Adrenergic Receptor	Cardiovascular Disease
(S)-Alprenolol is a potent and nonselective *β-adrenoceptor* antagonist .

HY-121843

Ronactolol	Adrenergic Receptor	Endocrinology
Ronactolol, an aminopropanol derivative with β-adrenoceptor blocking activity .

HY-106499

Sulfinalol	Adrenergic Receptor	Cardiovascular Disease
Sulfinalol is an orally active *β-adrenoceptor* antagonist with direct vasodilator activity .

HY-106499A

Sulfinalol hydrochloride	Adrenergic Receptor	Cardiovascular Disease
Sulfinalol hydrochloride is an orally active *β-adrenoceptor* antagonist with direct vasodilator activity. Sulfinalol hydrochloride is an antihypertensive agent .

HY-19673A

KUL-7211 racemate	Adrenergic Receptor	Endocrinology
KUL-7211 racemate is the racemate of KUL-7211. KUL-7211 is a selective *β-adrenoceptor* agonist .

HY-W181626

Tiprenolol DU 21445	5-HT Receptor	Cardiovascular Disease
Tiprenolol is a *β-adrenoceptor* blocker. Tiprenolol can abolish the ventricular arrhythmias produced by adrenaline in dogs respired with halothane .

Cat. No.	Product Name	Target	Research Area

HY-P5189A

*His-D-beta-Nal-Ala-Trp-D-Phe-Lys-NH2 TFA*	Endogenous Metabolite Cholinesterase (ChE)	Others
His-D-beta-Nal-Ala-Trp-D-Phe-Lys-NH2 TFA, is a growth hormone releasing peptide, as well as a metabolite of GHRP-1. GHRP-1, or Ala-His-D-beta Nal-Ala-Trp-D-Phe-Lys-NH2, has the effect of promoting the release of growth hormone (GH). GHRP-1 increases GH release and increases [Ca2+]i levels in static monolayer cells of rat pituitary gland, but does not affect cAMP levels .

HY-P1376

G-Protein antagonist peptide	mAChR Adrenergic Receptor	Endocrinology
G-Protein antagonist peptide is the substance P-related peptide that inhibits binding of G proteins to their receptors. G-Protein antagonist peptide competitively and reversibly inhibits M2 muscarinic receptor activation of G_i or G_o and inhibits G_s activation by β-adrenoceptors.

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-17501

Bambuterol (±)-Bambuterol; KWD-2183	Classification of Application Fields Disease Research Fields Endocrinology	Adrenergic Receptor
Bambuterol ((±)-Bambuterol; KWD-2183) is a long acting beta-adrenoceptor agonist (LABA) used in the treatment of asthma; it also is a proagent of terbutaline.

Cat. No.	Product Name	Chemical Structure

HY-17501S

Bambuterol-d9 hydrochloride
Bambuterol-d₉ (hydrochloride) is the deuterium labeled Bambuterol. Bambuterol ((±)-Bambuterol) hydrochloride is a long acting beta-adrenoceptor agonist (LABA) used in the treatment of asthma; it also is a prodrug of terbutaline.

HY-116790BSA

(±)-Penbutolol-d9 hydrochloride
(±)-Penbutolol-d₉ (hydrochloride) is a deuterium labeled (±)-Penbutolol hydrochloride. (+)-Penbutolol hydrochloride is a β-adrenoceptor antagonist, with an IC₅₀ of 0.74 μM .

HY-100635S

Diacetolol-d7
Diacetolol-d₇ is a deuterium labeled Diacetolol. Diacetolol is the major metabolite of Acebutolol. Diacetolol is a β-adrenoceptor blocking and anti-arrhythmic agent .

HY-17494S

(Rac)-Timolol-d5 maleate

rac Timolol-d₅ (maleate) is a labelled racemic (S)-Timolol maleate. (S)-Timolol Maleate (L-714,465 Maleate) is a non-cardioselective hydrophilic β-adrenoceptor blocker. (S)-Timolol Maleate is widely used as standard medication for intraocular pressure (glaucoma) by preventing the production of aqueous humor. (S)-Timolol Maleate can be used for hypertension, angina pectoris and myocardial infarction .

HY-17380S

(S)-Timolol-d9 maleate

(S)-Timolol-d₉ (maleate) is deuterium labeled (S)-Timolol (Maleate). (S)-Timolol Maleate (L-714,465 Maleate) is a non-cardioselective hydrophilic β-adrenoceptor blocker. (S)-Timolol Maleate is widely used as standard medication for intraocular pressure (glaucoma) by preventing the production of aqueous humor. (S)-Timolol Maleate can be used for hypertension, angina pectoris and myocardial infarction .

HY-W742404

Bopindolol-d9

Bopindolol-d₉ ((±)-Bopindolol-d₉) is the deuterium labeled Bopindolol (HY-B1562). Bopindolol ((±)-Bopindolol) is an orally active antagonist of β-adrenoceptors (ARs) with partial agonist activity. Bopindolol is non-selective for β1- and β2-ARs and has low affinity for β3-AR subtype. Bopindolol has intrinsic sympathomimetic as well as membrane stabilizing actions, inhibits renin secretion, and interacts with 5-HT receptors. Bopindolol is a proagent of Pindolol (HY-B0982). Bopindolol can be used for essential and renovascular hypertension research.

Cat. No.	Product Name		Classification

HY-101721

Ko-3290		Alkynes
Ko-3290 is an antagonist of *β-adrenoceptor*, with cardioselectivity and antilipolytic effects in animals. Ko-3290 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

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