2. Signaling Pathways
  3. Others
  4. Isotope-Labeled Compounds

Isotope-Labeled Compounds

Isotope-labeled compounds are chemical substances in which some atoms in their molecules are replaced by isotope atoms. The range of stable isotope products can cover from gases to complex molecules. Isotope-labeled compounds could provide a site-specific investigation of structures, making molecules easily detectable by mass spectrometry and NMR, and maintaining the physico-chemical properties of the target molecule at the same time. MCE isotope-labeled compounds are all stable isotope-labeled compounds and are non-radioactive labeled substances. MCE isotope-labeled compounds are unique tools for identifying and understanding biological and chemical processes. Stable isotope-labeled products are now getting more and more popular among scientists. The scope of application is gradually penetrating into various scientific fields, such as life sciences, food and medicine, agriculture, environment, geology, etc. Stable isotope-labeled compounds have a wide range of applications in the Life Science areas, such as Metabolomics, Proteomics, Clinical studies, Deuterium drugs, etc.

Isotope-Labeled Compounds Related Products (10876):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-W015339S1
    Octanoate-d3 sodium
    		99.9%
    Octanoate-d3 (sodium) is the deuterium labeled Octanoate.
    Octanoate-d<sub>3</sub> sodium
  • HY-W010750S
    Trioctyl trimellitate-d6
    		98.0%
    Trioctyl trimellitate-d6 is a deuterium labeled trioctyl trimellitate. Trioctyl trimellitate is a plasticizer.
    Trioctyl trimellitate-d<sub>6</sub>
  • HY-139931S
    1-Stearoyl-2-Arachidonoyl-d8-sn-glycero-3-PC
    		99.0%
    1-Stearoyl-2-Arachidonoyl-d8-sn-glycero-3-PC is the deuterium labeled 1-Stearoyl-2-Arachidonoyl-sn-glycero-3-PC.
    1-Stearoyl-2-Arachidonoyl-d<sub>8</sub>-sn-glycero-3-PC
  • HY-50751S
    Linifanib-d4
    Linifanib-d4 (ABT-869-d4; AL-39324-d4) is deuterium-labeled Linifanib (HY-50751).
    Linifanib-d<sub>4</sub>
  • HY-N7819S
    Pristane-d40
    		98.56%
    Pristane-d40 is the deuterium labeled Pristane. Pristane (Norphytane) is a naturally occurring hydrocarbon oil found in small quantities in many plants, in various marine organisms, and as the most active component of mineral oil. Pristane is a non-antigenic adjuvant, and induces MHC class II-restricted, arthritogenic T cells in the rat.
    Pristane-d<sub>40</sub>
  • HY-N5060S
    Estragole-d4
    		99.9%
    Estragole-d4 is deuterated labeled Estragole (HY-N5060). Estragole (4-Allylanisole) is a relatively nontoxic volatile terpenoid ether and major component of the essential oil from many plants. Estragole significantly triggers Apoptosis, suppresses LPS-induced intracellular ROS production. Estragole activats Nrf-2 and regulates NF-κB. Estragole has anti-toxoplasma, anti-inflammatory, anti-edema, antioxidant and immunomodulatory properties. Estragole blocks DRG neuron excitability. Estragole has improves gastric ulcer activity[10].
    Estragole-d<sub>4</sub>
  • HY-N6600S
    Octadecane-d38
    		99.49%
    Octadecane-d38 is the deuterium labeled Octadecane. Octadecane is an alkane used as a phase change material for storing thermal energy at ambient temperature. Octadecane can endow pesticide formulations with environmental responsiveness in the field of agricultural nanomaterials, enabling precise and safe pesticide application.
    Octadecane-d<sub>38</sub>
  • HY-16973S
    Fluralaner-13C2,15N,d3
    		98.35%
    Fluralaner-13C2,15N,d3 is the deuterium, 13C-, and 15-labeled Fluralaner. Fluralaner (INN) is a systemic insecticide and acaricide Fluralaner through potent blockage of GABA and L-glutamate gated chloride channels.
    Fluralaner-<sup>13</sup>C<sub>2</sub>,<sup>15</sup>N,d<sub>3</sub>
  • HY-B1873S
    Methoxychlor-d6
    		98.22%
    Methoxychlor-d6 is the deuterium labeled Methoxychlor.
    Methoxychlor-d<sub>6</sub>
  • HY-17506S1
    Azithromycin-13C,d3
    		99.90%
    Azithromycin-13C,d3 is the deuterium and 13C labeled Azithromycin.
    Azithromycin-<sup>13</sup>C,d<sub>3</sub>
  • HY-33212S
    D-N-Acetylgalactosamine-13C
    		99.95%
    D-N-Acetylgalactosamine-13C is the 13C labeled D-N-Acetylgalactosamine. D-N-Acetylgalactosamine is an endogenous metabolite.
    D-N-Acetylgalactosamine-<sup>13</sup>C
  • HY-W074889S3
    N-Myristoylglycine-13C2
    		99.93%
    N-Myristoylglycine-13C2 is the 13C-labeled N-Myristoylglycine (HY-W074889). N-Myristoylglycine is a glycine derivative.
    N-Myristoylglycine-<sup>13</sup>C<sub>2</sub>
  • HY-143816S
    4-Hydroxy Atorvastatin-d5 hemicalcium
    		99.9%
    4-Hydroxy Atorvastatin-d5 (calcium) is the deuterium labeled 4-Hydroxy Atorvastatin calcium.
    4-Hydroxy Atorvastatin-d<sub>5</sub> hemicalcium
  • HY-W094847S
    N-Eicosane-d42
    		99.54%
    N-Eicosane-d42 is the deuterium labeled N-Eicosane.
    N-Eicosane-d<sub>42</sub>
  • HY-150627S
    Pyrene-d10
    		99.88%
    Pyrene-d10 is the deuterium labeled Pyrene.
    Pyrene-d<sub>10</sub>
  • HY-W088065S1
    Sodium formate-13C,d1
    		98.0%
    Sodium formate-13C,d1 is the deuterium and 13C labeled Sodium formate.Sodium formate is a biochemical assay reagent. Sodium formate can react with zinc sources (such as ZnCl2) on the surface of alpha alumina support to form a zinc oxide layer. Sodium formate acts as a deprotonating agent, promoting the deprotonation of ligands (such as 2-methylimidazole) at high temperatures. Sodium formate provides the required reducing force in the catalytic oxidation of methane to methanol by methane monooxygenase (sMMO) and inhibits further oxidation of methanol.
    Sodium formate-<sup>13</sup>C,d<sub>1</sub>
  • HY-N0168AS1
    (Rac)-Hesperetin-13C,d3
    		99.3%
    (Rac)-Hesperetin-13C,d3 is the 13C- and deuterium labeled (Rac)-Hesperetin. (Rac)-Hesperetin is the racemate of Hesperetin (HY-N0168), an orally active multi-target inhibitor. (Rac)-Hesperetin exhibits significant anti-tumor and anti-inflammatory activities by blocking the TGF-β1-mediated Fyn/RhoA signaling axis and the TLR4-MyD88-NF-κB inflammatory pathway. (Rac)-Hesperetin inhibits the formation of actin stress fibers and the migration and invasion of cancer cells, and is suitable for triple-negative breast cancer research. In inflammation models, (Rac)-Hesperetin effectively alleviates lung injury by reducing the release of pro-inflammatory mediators and regulating the activity of oxidative stress enzymes, and is suitable for acute lung injury research. (Rac)-Hesperetin also interferes with the entry and early replication processes of channel catfish virus, inhibits viral gene expression and progeny virus production, thereby protecting cells from virus-induced cytopathic effects.
    (Rac)-Hesperetin-<sup>13</sup>C,d<sub>3</sub>
  • HY-104077S
    Remdesivir-d5
    		99.86%
    Remdesivir-d5 (GS-5734-d5) is a deuterium labeled Remdesivir (HY-104077). Remdesivir (GS-5734) is a nucleoside analogue with effective antiviral activity. Remdesivir can inhibit the synthesis of viral DNA or RNA. Remdesivir can be used for the research of infection, such as SARS-CoV and MHV infection.
    Remdesivir-d<sub>5</sub>
  • HY-14248S
    Letrozole-d4
    		99.23%
    Letrozole-d4 (CGS 20267-d4) is the deuterium labeled Letrozole. Letrozole (CGS 20267) is a potent, selective, reversible and orally active non-steroidal inhibitor of aromatase, with an IC50 of 11.5 nM. Letrozole selective inhibits estrogen biosynthesis, and can be used for the research of breast cancer.
    Letrozole-d<sub>4</sub>
  • HY-13234S
    Rifaximin-d6
    		≥99.0%
    Rifaximin-d6 is the deuterium labeled Rifaximin. Rifaximin is an orally administered, semi-synthetic, nonsystemic antibiotic derived from rifamycin SV with antibacterial activity.
    Rifaximin-d<sub>6</sub>