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  3. 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 (7743):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-12650S
    Mirogabalin-13C2,d1 (Mixture of Diastereomers)
    Mirogabalin-13C2,d1 (Mixture of Diastereomers) is a C13 and deuterium labeled Mirogabalin. Mirogabalin (DS-5565) is a novel, preferentially selective α2δ-1 ligand characterized by high potency and selectivity to the α2δ-1 subunit of voltage-sensitive calcium channel complexes in the CNS.
    Mirogabalin-<sup>13</sup>C<sub>2</sub>,d<sub>1</sub> (Mixture of Diastereomers)
  • HY-13609S
    Deflazacort-d5
    Deflazacort-d5 is the deuterium labeled Deflazacort. Deflazacort, a glucocorticoid, is an inactive proagent and is converted rapidly to the active metabolite 21-desacetyldeflazacort. Deflazacort is used as an anti-inflammatory and immunosuppressant[1].
    Deflazacort-d<sub>5</sub>
  • HY-146635S
    (25RS)-26-Hydroxycholesterol-d4
    (25RS)-26-Hydroxycholesterol-d4 is the deuterium labeled (25RS)-26-Hydroxycholesterol[1].
    (25RS)-26-Hydroxycholesterol-d<sub>4</sub>
  • HY-B0442S1
    Vardenafil-d4
    Vardenafil-d4 is deuterium-labeled Vardenafil (HY-B0442).
    Vardenafil-d<sub>4</sub>
  • HY-W141928S
    N-Isobutyryl-glycine-d7
    ≥99.0%
    N-Isobutyryl-glycine-d7 is the deuterium labeled N-Isobutyryl-glycine[1].
    N-Isobutyryl-glycine-d<sub>7</sub>
  • HY-B0290S1
    Pranlukast-d4
    Pranlukast-d4 is deuterium labeled Pranlukast. Pranlukast is a highly potent, selective and competitive antagonist of peptide leukotrienes. Pranlukast inhibits [3H]LTE4, [3H]LTD4, and [3H]LTC4 bindings to lung membranes with Kis of 0.63±0.11, 0.99±0.19, and 5640±680 nM, respectively.
    Pranlukast-d<sub>4</sub>
  • HY-166924S
    1,2,3,4,6-Pentachloro-dibenzofuran-13C12
    1,2,3,4,6-Pentachloro-dibenzofuran-13C12 is 13C labeled 1,2,3,4,6-Pentachloro-dibenzofuran.
    1,2,3,4,6-Pentachloro-dibenzofuran-<sup>13</sup>C<sub>12</sub>
  • HY-W654190
    Fipronil sulfone-13C2,15N2
    Fipronil sulfone-13C2,15N2 is a deuterated labeled Fipronil sulfone.
    Fipronil sulfone-<sup>13</sup>C<sub>2</sub>,<sup>15</sup>N<sub>2</sub>
  • HY-B0180S1
    Imiquimod-d9
    Imiquimod-d9 is deuterium labeled Imiquimod. Imiquimod (R 837), an immune response modifier, is a selective toll like receptor 7 (TLR7) agonist. Imiquimod exhibits antiviral and antitumor effects in vivo. Imiquimod can be used for the research of external genital, perianal warts, cancer and COVID-19[1][2].
    Imiquimod-d<sub>9</sub>
  • HY-W778336
    Girard's Reagent P-d5
    Girard's Reagent P-d5 is a deuterated labeled Girard's Reagent P-d5.
    Girard's Reagent P-d<sub>5</sub>
  • HY-W025785S
    Methyl yellow-d5
    Methyl yellow-d5 is the deuterium labeled Methyl yellow[1].
    Methyl yellow-d<sub>5</sub>
  • HY-108195S
    2,2′,4,5,5′-Pentachlorobiphenyl-3′,4′,6′-d3
    2,2′,4,5,5′-Pentachlorobiphenyl-3′,4′,6′-d3 is the deuterium labeled 2,2′,4,5,5′-Pentachlorobiphenyl[1].
    2,2′,4,5,5′-Pentachlorobiphenyl-3′,4′,6′-d<sub>3</sub>
  • HY-119485AS
    Dilevalol-d3 hydrochloride
    Dilevalol-d3 (hydrochloride) is the deuterium labeled Dilevalol hydrochloride[1].
    Dilevalol-d<sub>3</sub> hydrochloride
  • HY-B1695S
    Methyl nicotinate-d4
    99.5%
    Methyl nicotinate-d4 is the deuterium labeled Methyl nicotinate[1]. Methyl nicotinate, the methyl ester of Niacin found in alcoholic beverages, that is used as an active ingredient as a rubefacient in over-the-counter topical preparations indicated for muscle and joint pain[2].
    Methyl nicotinate-d<sub>4</sub>
  • HY-W011886S
    N2-(tert-Butyl)-N4-cyclopropyl-6-(methylthio)-1,3,5-triazine-2,4-diamine-d9
    N2-(tert-Butyl)-N4-cyclopropyl-6-(methylthio)-1,3,5-triazine-2,4-diamine-d9 is the deuterium labeled N2-(tert-Butyl)-N4-cyclopropyl-6-(methylthio)-1,3,5-triazine-2,4-diamine[1].
    N2-(tert-Butyl)-N4-cyclopropyl-6-(methylthio)-1,3,5-triazine-2,4-diamine-d<sub>9</sub>
  • HY-W097453S
    6-(Methylthio)purine-13C,d3
    6-(Methylthio)purine-13C,d3 is the 13C labeled 6-(Methylthio)purine.
    6-(Methylthio)purine-<sup>13</sup>C,d<sub>3</sub>
  • HY-132267S
    N-Nitrosodibenzylamine-d4
    N-Nitrosodibenzylamine-d4 is deuterium labeled N-Nitrosodibenzylamine. N-Nitrosodibenzylamine is a potent and orally activity DNA damage inducer. N-Nitrosodibenzylamine induces DNA single-strand breaks (SSBs).
    N-Nitrosodibenzylamine-d<sub>4</sub>
  • HY-101981S4
    Uridine 5'-monophosphate-13C9 dilithium
    Uridine 5'-monophosphate-13C9 (5'- Uridylic acid-13C9) dilithium is 13C-labeled Uridine 5'-monophosphate (HY-101981). Uridine 5'-monophosphate (5'- Uridylic acid), a monophosphate form of UTP, can be acquired either from a de novo pathway or degradation products of nucleotides and nucleic acids in vivo and is a major nucleotide analogue in mammalian milk.
    Uridine 5'-monophosphate-<sup>13</sup>C<sub>9</sub> dilithium
  • HY-W019895S
    Tetradecylphosphocholine-d42
    Tetradecylphosphocholine-d42 is the deuterium labeled Tetradecylphosphocholine[1].
    Tetradecylphosphocholine-d<sub>42</sub>
  • HY-B0010AS
    Formoterol-d3
    Formoterol-d3 is deuterium labeled Arformoterol. Arformoterol ((R,R)-Formoterol), the (R,R)-enantiomer of Formoterol, is a long-acting β2-adrenergic receptor (β2-AR) agonist, with a Kd of 2.9 nM. Arformoterol can be used for the research of chronic obstructive pulmonary disease (COPD)[1][2].
    Formoterol-d<sub>3</sub>