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 (9621):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-W769200
    Asenapine-13C,d3 Maleate
    Asenapine-13C,d3 Maleate is the deuterium labeled and 13C-Asenapine Maleate.
    Asenapine-<sup>13</sup>C,d<sub>3</sub> Maleate
  • HY-B0262S
    Methocarbamol-d5
    Methocarbamol-d5 is deuterium labeled Methocarbamol. Methocarbamol is an orally active central muscle relaxant and blocks muscular Nav1.4 channel.
    Methocarbamol-d<sub>5</sub>
  • HY-Y1010S
    Oxiran-2-ylmethanol-d5
    Oxiran-2-ylmethanol-d5 is the deuterium labeled Oxiran-2-ylmethanol.
    Oxiran-2-ylmethanol-d<sub>5</sub>
  • HY-W743417
    (-)-Norgestrel-d6
    (-)-Norgestrel-d6 is the deuterium labeled Levonorgestrel (HY-B0257). Levonorgestrel is an orally active inhibitor of progesterone (HY-N0437). Levonorgestrel has anticancer activity and can induce Apoptosis. Levonorgestrel can be used as a contraceptive and in combination with other medications. Levonorgestrel can be used in the study of osteoporosis and uterine leiomyoma.
    (-)-Norgestrel-d<sub>6</sub>
  • HY-W756607
    6-Acetyl-1,1,2,4,4,7-hexamethyltetraline-d11
    6-Acetyl-1,1,2,4,4,7-hexamethyltetraline-d11 is the deuterium labeled 6-Acetyl-1,1,2,4,4,7-hexamethyltetraline (HY-W011817). 6-Acetyl-1,1,2,4,4,7-hexamethyltetraline (AHTN) is a synthetic fragrance ingredient that is not significantly genotoxic in mammalian systems.
    6-Acetyl-1,1,2,4,4,7-hexamethyltetraline-d<sub>11</sub>
  • HY-W719355
    N-(Methyl-d3)-1H-imidazole-1-carboxamide
    N-(Methyl-d3)-1H-imidazole-1-carboxamide is the deuterium labeled N-Methyl-1H-imidazole-1-carboxamide (HY-W077637).
    N-(Methyl-d<sub>3</sub>)-1H-imidazole-1-carboxamide
  • HY-Y0399S
    L-Norvaline-d5
    L-Norvaline-d5 is the deuterium labeled L-Norvaline. L-Norvaline is the inhibitor for arginase, that promotes the production of NO, reduces oxidative stress, improves insulin resistance, and exhibits antioxidant and anti-hyperglycemic effects. L-Norvaline can be used in research of Alzheimer’s disease.
    L-Norvaline-d<sub>5</sub>
  • HY-B0141S5
    Estradiol-13C2
    Estradiol-13C2 is the 13C-labeled Estradiol. Estradiol is a steroid sex hormone vital to the maintenance of fertility and secondary sexual characteristics in females. Estradiol upregulates IL-6 expression through the estrogen receptor β (ERβ) pathway.
    Estradiol-<sup>13</sup>C<sub>2</sub>
  • HY-17356S
    Fenofibrate-d6
    		99.70%
    Fenofibrate-d6 is the deuterium labeled Fenofibrate. Fenofibrate is a selective PPARα agonist with an EC50 of 30 μM. Fenofibrate also inhibits human cytochrome P450 isoforms, with IC50s of 0.2, 0.7, 9.7, 4.8 and 142.1 μM for CYP2C19, CYP2B6, CYP2C9, CYP2C8, and CYP3A4, respectively.
    Fenofibrate-d<sub>6</sub>
  • HY-A0016S
    Dronedarone-d6 hydrochloride
    Dronedarone-d6 (hydrochloride) is the deuterium labeled Dronedarone. Dronedarone hydrochloride, a derivative of Amiodarone (HY-14187), is a class III antiarrhythmic agent for the study of atrial fibrillation (AF) and atrial flutter. Dronedarone hydrochloride is a potent blocker of multiple ion currents, including potassium current, sodium current, and L-type calcium current, and exhibits antiadrenergic effects by noncompetitive binding to β-adrenergic receptors. Dronedarone hydrochloride is a substrate for and a moderate inhibitor of CYP3A4.
    Dronedarone-d<sub>6</sub> hydrochloride
  • HY-W105860S
    Guanidine-15N3 hydrobromide
    Guanidine Hydrobromide-15N3 is the 15N labeled Guanidine Hydrobromide[1].
    Guanidine-<sup>15</sup>N<sub>3</sub> hydrobromide
  • HY-12516S2
    Desogestrel-13C2,d2-1
    Desogestrel-13C2,d2-1 (Org-2969-13C2,d2-1) is the deuterium labeled and 13C-labeled Desogestrel (HY-12516). Desogestrel (Org-2969) is a third-generation progesterone analogue contained in many oral contraceptive preparations. Desogestrel is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    Desogestrel-<sup>13</sup>C<sub>2</sub>,d<sub>2</sub>-1
  • HY-W754054
    Propionylglycine (Standard)-13C2,15N
    Propionylglycine (Standard)-13C2,15N is the 13C- and 15N-labeled Propionylglycine (HY-W587803). Propionylglycine is a peptide.
    Propionylglycine (Standard)-<sup>13</sup>C<sub>2</sub>,<sup>15</sup>N
  • HY-A0118AS
    Naloxegol-d5 oxalate
    Naloxegol-d5 (oxalate) is deuterium labeled Naloxegol (oxalate). Naloxegol oxalate (NKTR-118 oxalate; AZ-13337019 oxalate) is a μ-opioid-receptor antagonist. Naloxegol oxalate inhibits opioid binding in μ-opioid receptors in the gastrointestinal tract and effective for alleviating opioid-induced constipation.
    Naloxegol-d<sub>5</sub> oxalate
  • HY-W749327
    2,4-Di-tert-butylphenol-d21
    2,4-Di-tert-butylphenol-d21 (2,4-DTBP-d21) is the deuterium labeled 2,4-Di-tert-butylphenol (HY-W014589). 2,4-Di-tert-butylphenol (2,4-DTBP) is an orally active RXRα activator and a human estrogen receptor ligand with anti-inflammatory and antioxidant activities, which can induce apoptosis in tumor cells. 2,4-Di-tert-butylphenol can activate the RXRα subtype in LXRα/RXRα, PPARγ/RXRα, and hormone receptor β/RXRα. 2,4-Di-tert-butylphenol also has antiviral and antifungal activities and has the potential to inhibit Aβ-induced neurotoxicity. 2,4-Di-tert-butylphenol can be used as an intermediate in the preparation of antioxidants and UV stabilizers, and is also used in the manufacture of drugs and fragrances.
    2,4-Di-tert-butylphenol-d<sub>21</sub>
  • HY-13570S
    Betamethasone-d5
    Betamethasone-d5 is the deuterium labeled Betamethasone. Betamethasone is a synthetic glucocorticoid with anti-inflammatory and immunosuppressive activities. Betamethasone accelerates fetal lung maturation and induces gene expression and apoptosis.
    Betamethasone-d<sub>5</sub>
  • HY-W127329S
    12-Hydroxystearic acid-d5
    12-Hydroxystearic acid-d5 is the deuterium labeled 12-Hydroxystearic acid.
    12-Hydroxystearic acid-d<sub>5</sub>
  • HY-B0621S1
    Triclabendazole-13C,d3
    Triclabendazole-13C,d3 is the 13C- and deuterium labeled Triclabendazole.
    Triclabendazole-<sup>13</sup>C,d<sub>3</sub>
  • HY-146931S
    20:1 SM (d18:1/20:1)-d9
    20:1 SM (d18:1/20:1)-d9 is deuterium labeled 20:1 SM (d18:1/20:1).
    20:1 SM (d18:1/20:1)-d<sub>9</sub>
  • HY-W653296S
    (2,3,4,5-Tetrafluoro-6-methylphenyl)methanol-d5
    (2,3,4,5-Tetrafluoro-6-methylphenyl)methanol-d5 is the deuterium labeled (2,3,4,5-Tetrafluoro-6-methylphenyl)methanol (HY-W653296).
    (2,3,4,5-Tetrafluoro-6-methylphenyl)methanol-d<sub>5</sub>