Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
In addition to treating various diseases, isotopes are used for imaging, diagnosis, and newborn screening.
Small molecule compounds labeled with stable isotopes can be used as chemical reference for chemical identification, qualitative, quantitative, detection, etc. Various types of NMR solvents can be used to study the structure, reaction mechanism and reaction kinetics of compounds.
Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
General Information |
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Catalog: BLP-003789 |
CAS: 1346599-65-2 |
Molecular Formula: C17H16D4ClN3O |
Molecular Weight: 321.84 |
Chemical Structure |
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Description | Phentolamine-[d4] Hydrochloride, is the labelled analogue of Phentolamine. Phentolamine is a reversible nonselective α-adrenergic antagonist. |
Synonyms | 2-[N-(m-Hydroxyphenyl)-p-toluidinomethyl]imidazoline-d4 Hydrochloride; 3-[[(4,5-Dihydro-1H-imidazol-2-yl)methyl](4-methylphenyl)amino]phenol-d4 Hydrochloride; Phentolamine-d4 Hydrochloride |
IUPAC Name | 3-[4-methyl-N-[(4,4,5,5-tetradeuterio-1H-imidazol-2-yl)methyl]anilino]phenol;hydrochloride |
Related CAS | 73-05-2 (unlabelled) 1346746-62-0 (free base) |
Canonical SMILES | CC1=CC=C(C=C1)N(CC2=NCCN2)C3=CC(=CC=C3)O.Cl |
InChI | InChI=1S/C17H19N3O.ClH/c1-13-5-7-14(8-6-13)20(12-17-18-9-10-19-17)15-3-2-4-16(21)11-15;/h2-8,11,21H,9-10,12H2,1H3,(H,18,19);1H/i9D2,10D2; |
InChI Key | TUEJFGFQYKDAPM-PQDNHERISA-N |
Melting Point | >221°C(dec.) |
Purity | 98% by CP; 98% atom D |
Solubility | Soluble in DMSO, Methanol |
Appearance | Light Brown Solid |
Storage | Store at-20°C |
Phentolamine-[d4] Hydrochloride, a pharmacological research tool, has diverse applications in cardiovascular and adrenergic studies. Here are key applications presented with high perplexity and burstiness:
Cardiovascular Research: Widely utilized in cardiovascular research, Phentolamine-[d4] Hydrochloride serves to explore the impact of α-adrenergic blockade on blood pressure and vascular function. By antagonizing α-adrenergic receptors, researchers delve into the regulation of blood vessel tone and cardiac output, shedding light on the intricate mechanisms underpinning hypertension and cardiovascular ailments.
Receptor Binding Studies: As a deuterated variant of Phentolamine, Phentolamine-[d4] Hydrochloride proves invaluable in receptor binding assays, enabling precise quantification of its interactions with adrenergic receptors. The isotopic labeling facilitates detailed mass spectrometric analysis, aiding in the understanding of receptor-ligand dynamics, crucial for the development of more efficacious adrenergic receptor-targeting drugs.
Pheochromocytoma Indication: In clinical contexts, Phentolamine-[d4] Hydrochloride finds utility in the diagnosis of pheochromocytoma, a rare adrenal gland tumor. Rapid and potent α-adrenergic receptor antagonism helps mitigate hypertensive crises linked to this condition, guiding physicians in formulating tailored treatment strategies for affected individuals with precision and care.
Endocrine Function Testing: Delving into endocrine assessments, Phentolamine-[d4] Hydrochloride aids in evaluating adrenal medullary function and catecholamine release. By blocking α-adrenergic receptors, this pharmacological tool offers insights into adrenal gland responses to stimuli, illuminating the complex interplay within the endocrine system. Such meticulous studies assist endocrinologists in diagnosing adrenal disorders and comprehending their systemic manifestations comprehensively.
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