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Diacerein D6

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

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Diltiazem D6

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

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Diosmetin D3

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

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Docetaxel D9

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

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Dolutegravir

Dolutegravir is a second generation HIV-1 integrase strand transfer inhibitor. Dolutegravir is currently in Phase III clinical trials for the treatment of HIV infection.

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Efavirenz D5

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

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Erlotinib D6

Labelled Erlotinib. Selective epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor. Antineoplastic.;Labeled Erlotinib, intended for use as an internal standard for the quantification of Erlotinib by GC- or LC-mass spectrometry.

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Erythromycin

Erythromycin is bacteriostatic antibiotic macrolide produced by Streptomyces erythreus. Erythromycin A is considered its major active component. In sensitive organisms, it inhibits protein synthesis by binding to 50S ribosomal subunits. This binding process inhibits peptidyl transferase activity and interferes with translocation of amino acids during translation and assembly of proteins.

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Estradiol D4

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

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Ethylphenidate

Ethylphenidate is a psychostimulant and a close analog of methylphenidate. Ethylphenidate acts as both a dopamine reuptake inhibitor and norepinephrine reuptake inhibitor, meaning it effectively boosts the levels of the norepinephrine and dopamine neurotransmitters in the brain, by binding to, and partially blocking the transporter proteins that normally remove those monoamines from the synaptic cleft.Ethylphenidate formation appears to be more common when large quantities of methylphenidate and alcohol are consumed at the same time, such as in non-medical use or overdose scenarios.

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