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Quinapril D5 Hydrochloride

A deuterium-labeled salt of quinapril. Quinapril-d5, Hydrochloride is deuterium-labeled Quinapril. Quinapril-d5, Hydrochloride acts as an angiotensin converting enzyme (ACE) inhibitor. This compound has potential to be used in kinetic isotope studies and ;Labeled Quinapril, intended for use as an internal standard for the quantification of Quinapril by GC- or LC-mass spectrometry.

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Quinaprilat D5

A labelled metabolite of Quinapril, an angiotensin converting enzyme (ACE) inhibitor.

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Quinic acid

ProductName: Quinic acid

CAS Number: 77-95-2

Synonyms: D-(-)-Quinic acid

ChemicalName: (1?,3?,4?,5?)-1,3,4,5-Tetrahydroxy-cyclohexanecarboxylic acid

ChemicalFormula: C7H12O6

MolecularWeight: 192.17

Chemotaxonomic Group: Phenolic Compounds

Product Number: PS0713-0020

Grade:98.0% (LC&T) Size: 20mg

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Quinidine 13C D2 Hydrochloride

Labeled Quinidine, intended for use as an internal standard for the quantification of Quinidine by GC- or LC-mass spectrometry.

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Quinine Hydrochloride Dihydrate

Quinidine Hydrochloride Dihydrate is a salt of Quinidine ,a dextrorotatory stereoisomer of Quinine. Antiarrhythmic (class IA). Antimalarial.

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R(-)-Lercanidipine D3 Hydrochloride

A dihydropyridine calcium channel blocker. ;Labeled Lercanidipine, intended for use as an internal standard for the quantification of Lercanidipine by GC- or LC-mass spectrometry.

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R-(+)-Warfarin-d5

Labeled Warfarin, intended for use as an internal standard for the quantification of Warfarin by GC- or LC-mass spectrometry.

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R-(-)-O-DesMethyl-Venlafaxine-d6

Labeled Venlafaxine, intended for use as an internal standard for the quantification of Venlafaxine by GC- or LC-mass spectrometry.

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R-Amlodipine D4

Labeled isomer of Amlodipine;Application of Labeled APIs: Labeled Amlodipine, intended for use as an internal standard for the quantification of Amlodipine by GC- or LC-mass spectrometry.

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R-Citalopram Oxalate

An inhibitor of serotonin (5-HT) uptake. Antidepressant.;(R)-Citalopram Oxalate is a derivative of Citalopram. Citalopram is a selective inhibitor of the 5-hydroxytryptamine transporter (serotonin) and therefore is a potent and selective serotonin reuptake inhibitor. Additional studies in indicate that Citalopram may be a weak, allosteric modulator of serotonin in a cross-species chimeric study. Studies also indicate that Citalopram is useful for studying gene expression patterns in circulating lymphocytes. In zebrafish, Citalopram is noted to reduce the frequency of NMDA-induced locomotor rhythm involved in swimming behavor.
An inhibitor of serotonin (5-HT) uptake. Antidepressant.;(R)-Citalopram Oxalate is a derivative of Citalopram. Citalopram is a selective inhibitor of the 5-hydroxytryptamine transporter (serotonin) and therefore is a potent and selective serotonin reuptake inhibitor. Additional studies in indicate that Citalopram may be a weak, allosteric modulator of serotonin in a cross-species chimeric study. Studies also indicate that Citalopram is useful for studying gene expression patterns in circulating lymphocytes. In zebrafish, Citalopram is noted to reduce the frequency of NMDA-induced locomotor rhythm involved in swimming behavor.

 

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