151 Results for "

angina

" in MedChemExpress (MCE) Product Catalog:
Products (151)

151 Results for "angina" in MCE Product Catalog:

91
91 Publications Verification
Referencia número: HY-14275
No. CAS: 52-53-9
Pureza:  98.96%
Synonyms: (±)-Verapamil; CP-16533-1
Verapamil ((±)-Verapamil) is a calcium channel blocker and a potent and orally active first-generation P-glycoprotein (P-gp) inhibitor. Verapamil also inhibits CYP3A4. Verapamil has the potential for high blood pressure, heart arrhythmias and angina research .
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91
91 Publications Verification
Referencia número: HY-A0064
No. CAS: 152-11-4
Synonyms: (±)-Verapamil hydrochloride; CP-16533-1 hydrochloride
Áreas de investigación:  

Cardiovascular Disease Cancer

Verapamil hydrochloride ((±)-Verapamil hydrochloride) is a calcium channel blocker and a potent and orally active first-generation P-glycoprotein (P-gp) inhibitor. Verapamil hydrochloride also inhibits CYP3A4. Verapamil hydrochloride has the potential for high blood pressure, heart arrhythmias and angina research .
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50
50 Cited Publications
Referencia número: HY-B0573
No. CAS: 318-98-9
Propranolol hydrochloride is a nonselective and BBB-permeableβ-adrenergic receptor (βAR) antagonist, has high affinity for the β1AR and β2AR with Ki values of 1.8 nM and 0.8 nM, respectively. Propranolol hydrochloride inhibits [ 3H]-DHA binding to rat brain membrane preparation with an IC50 of 12 nM. Propranolol hydrochloride is used for study of hypertension, pheochromocytoma, myocardial infarction, cardiac arrhythmias, angina pectoris, and hypertrophic cardiomyopathy .
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50
50 Cited Publications
Referencia número: HY-B0573B
No. CAS: 525-66-6
Propranolol is a nonselective and BBB-permeable β-adrenergic receptor (βAR) antagonist, has high affinity for the β1AR and β2AR with Ki values of 1.8 nM and 0.8 nM, respectively . Propranolol inhibits [ 3H]-DHA binding to rat brain membrane preparation with an IC50 of 12 nM . Propranolol is used for the study of hypertension, pheochromocytoma, myocardial infarction, cardiac arrhythmias, angina pectoris, and hypertrophic cardiomyopathy .
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21
21 Cited Publications
Referencia número: HY-17498
No. CAS: 29122-68-7
Synonyms: (RS)-Atenolol
Atenolol ((RS)-Atenolol) is a cardioselective β1-adrenergic receptor blocker, with a Ki of 697 nM at β1-adrenoceptor in guine pig left ventricle membrane. Atenolol can be used for the research of hypertension and angina pectoris .
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16
16 Cited Publications
Referencia número: HY-17503
No. CAS: 51384-51-1
Metoprolol is an orally active, selective β1-adrenoceptor antagonist. Metoprolol shows anti-inflammation, antitumor and anti-angiogenic properties .
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16
16 Cited Publications
Referencia número: HY-17503A
No. CAS: 98418-47-4
Áreas de investigación:  

Cardiovascular Disease Endocrinology Cancer

Metoprolol succinate is an orally active, selective β1-adrenoceptor antagonist. Metoprolol succinate shows anti-inflammation, antitumor and anti-angiogenic properties .
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16
16 Cited Publications
Referencia número: HY-17503B
No. CAS: 56392-17-7
Metoprolol tartrate is an orally active, selective β1-adrenoceptor antagonist. Metoprolol tartrate shows anti-inflammation, antitumor and anti-angiogenic properties .
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14
14 Cited Publications
Referencia número: HY-B0006
No. CAS: 72956-09-3
Synonyms: BM 14190
Carvedilol (BM 14190) is a non-selective β/α-1 blocker . Carvedilol inhibits lipid peroxidation in a dose-dependent manner with an IC50 of 5 μM. Carvedilol is a multiple action antihypertensive agent with potential use in angina and congestive heart failure . Carvedilol is an autophagy inducer that inhibits the NLRP3 inflammasome .
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14
14 Cited Publications
Referencia número: HY-B0006A
No. CAS: 610309-89-2
Synonyms: BM 14190 phosphate hemihydrate
Carvedilol phosphate hemihydrate (BM 14190 phosphate hemihydrate) is a non-selective β/α-1 blocker . Carvedilol phosphate hemihydrate inhibits lipid peroxidation with an IC50 of 5 μM. Carvedilol phosphate hemihydrate is a multiple action antihypertensive agent with potential use in angina and congestive heart failure . Carvedilol phosphate hemihydrate is an autophagy inducer that inhibits the NLRP3 inflammasome .
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10
10 Cited Publications
Referencia número: HY-B0632
No. CAS: 42399-41-7
Target:  

Calcium Channel

Áreas de investigación:  

Cardiovascular Disease Cancer

Diltiazem is an orally active L-type Ca 2+ channel blocker. Diltiazem shows antihypertensive and antiarrhythmic effects. Diltiazem can be used for the research of cardiac arrhythmia, hypertension, and angina pectoris .
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7
7 Cited Publications
Referencia número: HY-B1334A
No. CAS: 6724-53-4
Perhexiline maleate is an orally active CPT1 and CPT2 inhibitor that reduces fatty acid metabolism. Perhexiline maleate induces mitochondrial dysfunction and apoptosis in hepatic cells. Perhexiline maleate can cross the blood brain barrier (BBB) and shows anti-tumor activity. Perhexiline maleate can be used in the research of cancers, and cardiovascular disease like angina .
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7
7 Cited Publications
Referencia número: HY-B1334
No. CAS: 6621-47-2
Perhexiline is an orally active CPT1 and CPT2 inhibitor that reduces fatty acid metabolism. Perhexiline induces mitochondrial dysfunction and apoptosis in hepatic cells. Perhexiline can cross the blood brain barrier (BBB) and shows anti-tumor activity. Perhexiline can be used in the research of cancers, and cardiovascular disease like angina .
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6
6 Cited Publications
Referencia número: HY-17380
No. CAS: 26921-17-5
Synonyms: (S)-L-714,465 maleate; MK 950
Target:  

Adrenergic Receptor

Áreas de investigación:  

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 .
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6
6 Cited Publications
Referencia número: HY-12515
No. CAS: 55985-32-5
Pureza:  99.09%
Synonyms: YC-93 free base
Target:  

Calcium Channel

Áreas de investigación:  

Cardiovascular Disease Neurological Disease Cancer

Nicardipine (YC-93 free base) is a calcium channel blocker with an IC50 of 1 μM for blocking cardiac calcium channels. Nicardipine acts as an agent for chronic stable angina and for controlling blood pressure .
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6
6 Cited Publications
Referencia número: HY-12515A
No. CAS: 54527-84-3
Pureza:  99.73%
Synonyms: YC-93
Áreas de investigación:  

Cardiovascular Disease Neurological Disease Cancer

Nicardipine hydrochloride (YC-93) is a calcium channel blocker with an IC50 of 1 μM for blocking cardiac calcium channels. Nicardipine hydrochloride acts as an agent for chronic stable angina and for controlling blood pressure .
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5
5 Cited Publications
Referencia número: HY-B0280
No. CAS: 95635-55-5
Synonyms: CVT 303; RS 43285-003
Áreas de investigación:  

Cardiovascular Disease Cancer

Ranolazine (CVT 303) is an anti-angina drug that achieves its effects by inhibiting the late phase of inward sodium current (INa and IKr with IC50 values of 6 μM and 12 μM, respectively) without affecting heart rate or blood pressure (BP) . Ranolazine is also a partial fatty acid oxidation (FAO) inhibitor . Antianginal agent.
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5
5 Cited Publications
Referencia número: HY-B0804
No. CAS: 42200-33-9
Synonyms: SQ-11725
Target:  

Adrenergic Receptor

Áreas de investigación:  

Cardiovascular Disease

Nadolol (SQ-11725) is a non-selective and orally active β-adrenergic receptors blocker and is a substrate of organic anion transporting polypeptide 1A2 (OATP1A2). Nadolol has the the potential for high blood pressure, angina pectoris and vascular headaches research .
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5
5 Cited Publications
Referencia número: HY-B0642
No. CAS: 16051-77-7
Synonyms: Isosorbide-5-mononitrate
Isosorbide mononitrate (Isosorbide-5-mononitrate) is an orally active nitric acid compound used for angina pectoris by dilating blood vessels and lowering blood pressure. Isosorbide mononitrate increases the viability and proliferation of HUVECs by decreasing Apoptosis and elevated the expressions of vedf, kdrl, pdgfr in zebrafish embryos. Isosorbide mononitrate is promising for research of heart failure and coronary heart disease .
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5
5 Cited Publications
Referencia número: HY-17401
No. CAS: 95635-56-6
Synonyms: CVT 303 dihydrochloride; RS 43285
Áreas de investigación:  

Cardiovascular Disease Cancer

Ranolazine dihydrochloride (CVT 303 dihydrochloride) is an anti-angina agent that achieves its effects by inhibiting the late phase of inward sodium current (INa and IKr with IC50 values of 6 μM and 12 μM, respectively) without affecting heart rate or blood pressure (BP) . Ranolazine dihydrochloride is also a partial fatty acid oxidation inhibitor .
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