57775-29-8
57775-29-8
Chemical Structure
Carazolol
Synonym(s): (±)-Carazolol; DL-Carazolol; Suacron
- CAS No.: 57775-29-8
- Formula:C18H22N2O2
- Molecular Weight:298.38
IUPAC Name: 1-((9H-carbazol-4-yl)oxy)-3-(isopropylamino)propan-2-ol
InChIKey: BQXQGZPYHWWCEB-UHFFFAOYSA-N
SMILES: CC(C)NCC(O)COC1=CC=CC2=C1C3=CC=CC=C3N2
Biological Activity: Carazolol is a β1/β2 adrenoceptor antagonist of high potency used in the research of hypertension. Carazolol is also a potent, selective β3-adrenoceptor agonist[1].
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Carazolol | 99.78% | Carazolol is a β1/β2 adrenoceptor antagonist of high potency used in the research of hypertension. Carazolol is also a potent, selective β3-adrenoceptor agonist. | ||||||||||||||||||||
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Carazolol (Standard) | ≥98% | Carazolol (Standard) is the analytical standard of Carazolol. This product is intended for research and analytical applications. Carazolol is a β1/β2 adrenoceptor antagonist of high potency used in the research of hypertension. Carazolol is also a potent, selective β3-adrenoceptor agonist. | ||||||||||||||||||||
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Carazolol-d7 hydrochloride | Carazolol-d7 (hydrochloride) is the deuterium labeled Carazolol hydrochloride (HY-W517264). Carazolol hydrochloride is a highly potent antagonist of β1/β2 adrenoceptor. Carazolol hydrochloride is also a potent, selective β3-adrenoceptor agonist. Carazolol hydrochloride can be used in the research of hypertension. | |||||||||||||||||||||
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Carazolol-d7 | 99.0% | Carazolol-d7 is the deuterium labeled Carazolol (HY-107327). Carazolol is a highly potent antagonist of β1/β2 adrenoceptor. Carazolol is also a potent, selective β3-adrenoceptor agonist. Carazolol can be used in the research of hypertension. | ||||||||||||||||||||
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Espindolol | 99.89% | Espindolol ((-)-pindolol) is a reversible, competitive and orally active 5-HT1A/1B antagonist. lEspindolol is a partial β-adrenoceptor agonist. Espindolol can be used for the research of neurological disease. | ||||||||||||||||||||
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(R)-Propranolol hydrochloride | 99.32% | (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 Ki values of 1.8 nM and 0.8 nM, respectively. | ||||||||||||||||||||
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(S)-(-)-Propranolol hydrochloride | 99.97% | (S)-(-)-Propranolol hydrochloride is the active isomer of Propranolol (HY-B0573B), with 98-fold greater activity than (R)-(+)-Propranolol. (S)-(-)-Propranolol hydrochloride produces antinociception-related phenotypes in mouse models, accompanied by sedative and ataxic side effects. (S)-(-)-Propranolol hydrochloride can be used in research related to hypertension, myocardial infarction, and pain. | ||||||||||||||||||||
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Propranolol | 99.91% | 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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Propranolol hydrochloride (Standard) | 99.93% | Propranolol (hydrochloride) (Standard) is the analytical standard of Propranolol (hydrochloride). This product is intended for research and analytical applications. Propranolol hydrochloride is a nonselective 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 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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Pindolol | 99.92% | Pindolol (LB-46) is the antagonist for 5-HT 1A (Ki=33 nM) and 5-HT 1B. Pindolol is the antagonist for β1/β2-adrenergic receptor. Pindolol exhibits anti-anxiety and antidepressant effects. | ||||||||||||||||||||
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Carazolol hydrochloride | 99.90% | Carazolol (BM 51052) hydrochloride is a highly potent antagonist of β1/β2 adrenoceptor. Carazolol hydrochloride is also a potent, selective β3-adrenoceptor agonist. Carazolol hydrochloride can be used in the research of hypertension. | ||||||||||||||||||||
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Carazolol-d6 hydrochloride | Carazolol-d6 (hydrochloride) is deuterium labeled Carazolol hydrochloride (HY-W517264). Carazolol hydrochloride is a highly potent antagonist of β1/β2 adrenoceptor. Carazolol hydrochloride is also a potent, selective β3-adrenoceptor agonist. Carazolol hydrochloride can be used in the research of hypertension. | |||||||||||||||||||||
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Carvedilol impurity 13 | Carvedilol impurity 13 is an impurity of Carvedilol. | |||||||||||||||||||||
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