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 (9980):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-152020S
    Sphingosine-d9 (d18:1)
    Sphingosine-d9 (d18:1) (D-eytho-Sphigosie C18-d9) is deuterium labeled Sphingosine (d18:1).
    Sphingosine-d<sub>9</sub> (d18:1)
  • HY-143712S1
    Allolithocholic Acid-d4
    Allolithocholic Acid-d4 (3α-hydoxy-5α-Cholaoic Acid-d4, allo-LCA-d4) is deuterium labeled Allolithocholic acid. Allolithocholic acid is a steroid acid could found in normal serum and feces. Allolithocholic acid facilitates excretion, absorption, and transport of fats and sterols in the intestine and liver.
    Allolithocholic Acid-d<sub>4</sub>
  • HY-14740S2
    Elvitegravir-13C6
    Elvitegravir-13C6 (GS-9137-13C6) is 13C labeled Elvitegravir. Elvitegravir (GS-9137; JTK-303; D06677) is an HIV integrase inhibitor for HIV-1IIIB, HIV-2EHO and HIV-2ROD with IC50 of 0.7 nM, 2.8 nM and 1.4 nM, respectively.
    Elvitegravir-<sup>13</sup>C<sub>6</sub>
  • HY-B0084S3
    Dienogest-13C2,15N
    Dienogest-13C2,15N (STS 557-13C2,15N) is 13C- and 15N-labeled Dienogest (HY-B0084).
    Dienogest-<sup>13</sup>C<sub>2</sub>,<sup>15</sup>N
  • HY-W188178S
    2-[Methyl(nitroso)amino]acetic acid-d3
    2-[Methyl(nitroso)amino]acetic acid-d3 is the deuterium labeled 2-[methyl(nitroso)amino]acetic acid.
    2-[Methyl(nitroso)amino]acetic acid-d<sub>3</sub>
  • HY-W705479
    Pazopanib-d3 hydrochloride
    Pazopanib-d3 (hydrochloride) (GW786034-d3 (hydrochloride)) is deuterium labeled Pazopanib (Hydrochloride). Pazopanib Hydrochloride (GW786034 Hydrochloride) is a novel multi-target inhibitor of VEGFR1, VEGFR2, VEGFR3, PDGFRβ, c-Kit, FGFR1, and c-Fms with an IC50 of 10, 30, 47, 84, 74, 140 and 146 nM, respectively.
    Pazopanib-d<sub>3</sub> hydrochloride
  • HY-W705485
    N-Methylmethan-d3-amine hydrochloride
    N-Methylmethan-d3-amine (hydrochloride) is deuterium labeled N-Methylmethan-amine (hydrochloride).
    N-Methylmethan-d<sub>3</sub>-amine hydrochloride
  • HY-17007S2
    Saquinavir-13C6
    Saquinavir-13C6 (Ro 31-8959-13C6) is 13C labeled Saquinavir (HY-17007). Saquinavir (Ro 31-8959) is an orally active HIV protease inhibitor that can be used in the research of AIDS. Saquinavir also has anti-inflammatory activity and can induce apoptosis of human red blood cells.
    Saquinavir-<sup>13</sup>C<sub>6</sub>
  • HY-155912S
    2-Allyl-3-methylpyrazine-d3
    2-Allyl-3-methylpyrazine-d3 is deuterated labeled 2-Allyl-3-methylpyrazine.
    2-Allyl-3-methylpyrazine-d<sub>3</sub>
  • HY-15409S1
    Empagliflozin-13C6
    Empagliflozin-13C6 (BI 10773-13C6) is 13C labeled Empagliflozin. Empagliflozin (BI 107730 is a selective sodium glucose cotransporter-2 (SGLT-2) inhibitor with an IC50 of 3.1 nM for human SGLT-2.
    Empagliflozin-<sup>13</sup>C<sub>6</sub>
  • HY-W715198S
    4-Bromo-2,3,7,8-tetrachlorodibenzofuran-13C12
    4-Bromo-2,3,7,8-tetrachlorodibenzofuran-13C12 is 13C labeled 4-Bromo-2,3,7,8-tetrachlorodibenzo[b,d]furan.
    4-Bromo-2,3,7,8-tetrachlorodibenzofuran-<sup>13</sup>C<sub>12</sub>
  • HY-W728761
    Voxelotor-d7
    Voxelotor-d7 is the deuterium labeled Voxelotor (HY-18681). Voxelotor is a potent inhibitor of haemoglobin S (HbS) polymerization.
    Voxelotor-d<sub>7</sub>
  • HY-16774S2
    Vericiguat-d6
    Vericiguat-d6 (BAY1021189-d6) is deuterium labeled Vericiguat. Vericiguat (BAY1021189) is a potent, orally available and soluble guanylate cyclase stimulator.
    Vericiguat-d<sub>6</sub>
  • HY-B1225S
    Promazine-d6 hydrochloride
    Promazine-d6 (hydrochloride) (Romtiazin-d6 (hydrochloride)) is deuterium labeled Promazine (hydrochloride). Promazine (Romtiazin) hydrochloride is an antipsychotic and a dopamine receptor D2 antagonist. Promazine hydrochloride inhibits dopaminergic neurotransmission.
    Promazine-d<sub>6</sub> hydrochloride
  • HY-130547S
    BS2G Crosslinker-d4 disodium
    BS2G Crosslinker-d4 (disodium) is the deuterium labeled BS2G Crosslinker. Radioactive isotopes labeled compounds can be used in metabolic analysis, allowing the movement of individual atoms to be precisely tracked and quantified.
    BS2G Crosslinker-d<sub>4</sub> disodium
  • HY-10285S2
    Saxagliptin-13C2
    Saxagliptin-13C2 (BMS-477118-13C2) is 13C labeled Saxagliptin. Saxagliptin (BMS-477118) is a potent, selective, reversible, competitive and orally active dipeptidyl peptidase-4 (DPP-4) (Ki = 0.6-1.3 nM) inhibitor. Saxagliptin has the peotential for type 2 diabetes mellitus research.
    Saxagliptin-<sup>13</sup>C<sub>2</sub>
  • HY-W783639S
    Bzo-poxizid-d9
    Bzo-poxizid-d9 (5C-MDA-19-d9, Petyl MDA-19-d9) is deuterium labeled Bzo-poxizid. Bzo-poxizid is a synthetic cannabinoid that is a psychoactive substance.
    Bzo-poxizid-d<sub>9</sub>
  • HY-W032022S2
    1-Hexanol-d3
    		99.05%
    1-Hexanol-d3 is the deuterium labeled 1-Hexanol. 1-Hexanol, a primary alcohol, is a surfactant that can be employed in industrial processes to enhance interfacial properties. 1-Hexanol uncouples mitochondrial respiration by a non-protonophoric mechanism.
    1-Hexanol-d<sub>3</sub>
  • HY-W103935S
    2,2-Bis(((2-cyano-3,3-diphenylacryloyl)oxy)methyl)propane-1,3-diyl bis(2-cyano-3,3-diphenylacrylate)-d40
    2,2-Bis(((2-cyano-3,3-diphenylacryloyl)oxy)methyl)propane-1,3-diyl bis(2-cyano-3,3-diphenylacrylate)-d40 (Uvinul 3030-d40) is deuterium labeled 2,2-Bis(((2-cyano-3,3-diphenylacryloyl)oxy)methyl)propane-1,3-diyl bis(2-cyano-3,3-diphenylacrylate).
    2,2-Bis(((2-cyano-3,3-diphenylacryloyl)oxy)methyl)propane-1,3-diyl bis(2-cyano-3,3-diphenylacrylate)-d<sub>40</sub>
  • HY-B0690S
    Fosinopril-d5
    Fosinopril-d5 (SQ28555-d5 (free acid)) is deuterium labeled Fosinopril. Fosinopril (SQ28555 free acid) is the ester proagent of angiotensin-converting enzyme (ACE) inhibitor with an IC50 value of 0.18 μM. Fosinopril demonstrates a non-competitive inhibition effect on ACE activity with an Ki value of 1.675 μM.
    Fosinopril-d<sub>5</sub>