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 (10679):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-W011297S2
    Methyl arachidonate-13C4
    Methyl arachidonate-13C4 (Arachidonic acid methyl ester-13C4) is 13C labeled Methyl arachidonate. Methyl arachidonate (Arachidonic acid methyl ester) is a fatty acid methyl ester resulting from the formal condensation of the carboxy group of arachidonic acid with methanol. Methyl arachidonate has activity of human blood serum metabolite.
    Methyl arachidonate-13</sup>C<sub>4</sub>
  • HY-118861S1
    Enclomiphene-d4
    		99.85%
    Enclomiphene-d4 ((E)-Clomiphene-d4) is a deuterium labeled Enclomiphene. Enclomiphen?is a potent and orally active?estrogen receptor?antagonist with antioestrogenic property.
    Enclomiphene-d<sub>4</sub>
  • HY-70057S4
    Safinamide-d5
    Safinamide-d5 (FCE 26743-d5) is deuterium labeled Safinamide. Safinamide is a potent, selective, and reversible monoamine oxidase B (MAO-B) inhibitor (IC50=0.098 μM) over MAO-A (IC50=580 μM). Safinamide also blocks sodium channels and modulates glutamate (Glu) release, showing a greater affinity at depolarized (IC50=8?μM) than at resting (IC50=262?μM) potentials. Safinamide has neuroprotective and neurorescuing effects and can be used for the study of parkinson disease, ischemia stroke etc.al.
    Safinamide-d<sub>5</sub>
  • HY-131332S1
    N-Desmethyl ulipristal acetate-d3
    N-Desmethyl ulipristal-d3 ((11β)-11-[4-(Methylamino)phenyl]-3,20-dioxo-19-norpregna-4,9-dien-17-yl-d3) acetate is deuterium labeled N-Desmethyl ulipristal acetate ((11β)-11-[4-(Methylamino)phenyl]-3,20-dioxo-19-norpregna-4,9-dien-17-yl).
    N-Desmethyl ulipristal acetate-d<sub>3</sub>
  • HY-B0688S3
    Dapsone-15N2
    Dapsone-15N2 (4,4′-Diaminodiphenyl sulfone-15N2) is 15N labeled Dapsone. Dapsone (4,4′-Diaminodiphenyl sulfone) is an orally active and blood-brain penetrant sulfonamide antibiotic with bacteriostatic, antimycobacterial and antiprotozoal activities. Dapsone?exerts effective antileprosy activity?and inhibits folate synthesis in cell extracts of?M. leprae. Dapsone is used for dermatologic disorder research, including leprosy, dermatitis herpetiformis, acne vulgaris et al.
    Dapsone-<sup>15</sup>N<sub>2</sub>
  • HY-166670S
    Ketoconazole carbonyl-13C
    Ketoconazole carbonyl-13C (Ketoconazol-13C) is 13C labeled Ketoconazole. Ketoconazole (R-41400) is an imidazole anti-fungal agent, a CYP3A4 and CYP24A1 inhibitor.
    Ketoconazole carbonyl-<sup>13</sup>C
  • HY-132441S
    (rac)-Mepindolol-d7
    (rac)-Mepindolol-d7 is the deuterium labeled (rac)-Mepindolol.
    (rac)-Mepindolol-d<sub>7</sub>
  • HY-W009362S
    DL-Isocitric acid-13C4 trisodium salt
    DL-Isocitric acid-13C4 (trisodium salt) is a 13C labeled DL-Isocitric acid (trisodium salt) (HY-W009362). DL-Isocitric acid trisodium salt is an endogenous metabolite. DL-Isocitric acid trisodium salt is a substrate in the citric acid cycle. DL-Isocitric acid trisodium salt can be used as a marker for determining the composition of isocitrates in fruit products, including fruit juices.
    DL-Isocitric acid-<sup>13</sup>C<sub>4</sub> trisodium salt
  • HY-121124S
    Fluindione-d4
    Fluindione-d4 is the deuterium labeled Fluindione.
    Fluindione-d<sub>4</sub>
  • HY-165645
    Protectin D1-d5
    Protectin D1-d5 (Neuopotecti D1-d5) is deuterium labeled Protectin D1.
    Protectin D1-d<sub>5</sub>
  • HY-119980BS
    Fluphenazine-d6 hydrochloride
    Fluphenazine-d6 (hydrochloride) is deuterium labeled Fluphenazine (hydrochloride). Fluphenazine hydrochloride is a potent, orally active phenothiazine-based dopamine receptor antagonist. Fluphenazine hydrochloride blocks neuronal voltage-gated sodium channels. Fluphenazine hydrochloride acts primarily through antagonism of postsynaptic dopamine-2 receptors in mesolimbic, nigrostriatal, and tuberoinfundibular neural pathways. Fluphenazine hydrochloride can antagonize Methylphenidate-induced stereotyped gnawing and inhibit climbing behaviour in mice. Fluphenazine hydrochloride can be used for researching psychosis and painful peripheral neuropathy associated with diabetes and has potential to inhibit SARS-CoV-2.
    Fluphenazine-d<sub>6</sub> hydrochloride
  • HY-108685S
    Alendronate-d4 sodium
    Alendronate-d4 (sodium) (Alendronic acid-d4 (monosodium salt)) is deuterium labeled Alendronate sodium. Alendronate sodium is an orally active nitrogen-containing bisphosphonate. Alendronate sodium potently inhibits bone resorption. Alendronate sodium is used for the research of postmenopausal osteoporosis.
    Alendronate-d<sub>4</sub> sodium
  • HY-B0510S3
    Trimethoprim-13C3
    Trimethoprim-13C3 is the deuterium labeled Trimethoprim (HY-B0510). Trimethoprim is a bacteriostatic antibiotic and an orally active dihydrofolate reductase inhibitor. Trimethoprim is active against a wide range of Gram-positive and Gram-negative aerobic bacteria. Trimethoprim has the potential for the research of urinary tract infections, Shigellosis and Pneumocystis pneumonia. Trimethoprim can inhibit infection of Influenza A virus in chick embryo when combinated with zinc.
    Trimethoprim-<sup>13</sup>C<sub>3</sub>
  • HY-101479S
    Iclaprim-d6
    Iclaprim-d6 (AR-100-d6) is the deuterium labeled Iclaprim. Iclaprim is a new selective bacterial Dihydrofolate inhibitor, which can inhibit the growth of S. aureus (MRSA) with an MIC90 of 0.06 μg/mL.
    Iclaprim-d<sub>6</sub>
  • HY-W010529S
    2-Methylfuran-3-thiol-d3
    2-Methylfuran-3-thiol-d3 is deuterated labeled 2-Methylfuran-3-thiol.
    2-Methylfuran-3-thiol-d<sub>3</sub>
  • HY-143784S
    C14 Benzalkonium-1 acid-13C2,d11 chloride
    C14 Benzalkonium-1 acid-13C2,d11 (chloride) is the deuterium and 13C labeled C14 Benzalkonium-1 acid chloride.
    C14 Benzalkonium-1 acid-<sup>13</sup>C<sub>2</sub>,d<sub>11</sub> chloride
  • HY-14959S
    Ulipristal-d3
    Ulipristal-d3 (CDB-3236-d3) is deuterium labeled Ulipristal. Ulipristal (CDB 3236) is a selective progesterone receptor modulator (SPRM). Ulipristal binds to the progesteron receptor, thereby inhibiting PR-mediated gene expression, and interfering with progesterone activity in the reproductive system.
    Ulipristal-d<sub>3</sub>
  • HY-W007692S
    Acetylpyrazine-d3
    Acetylpyrazine-d3 is deuterated labeled Acetylpyrazine (HY-W007692). Acetylpyrazine (2-Acetylpyrazine) is used to form many polycyclic compounds, as useful structures in pharmaceuticals and perfumes. Acetylpyrazine is a component of the folates (vitamin B compounds).
    Acetylpyrazine-d<sub>3</sub>
  • HY-W750297
    p,p'-DDD-13C12
    p,p'-DDD-13C12 is 13C labeled p,p'-DDD. p,p'-DDD is a major metabolite of p,p'-DDT. p,p'-DDD occurs in the feces and livers of rats, that are given p,p'-DDT by stomach tube, but not of rats injected intraperitoneally with p,p'-DDT.
    p,p'-DDD-<sup>13</sup>C<sub>12</sub>
  • HY-W705589
    Rimeporide-15N3 hydrochloride
    Rimeporide-15N3 (hydrochloride) (EMD-87580-15N3 (hydrochloride)) is 15N labeled Rimeporide hydrochloride. Rimeporide hydrochloride (EMD-87580 hydrochloride) is a potent and selective inhibitor of the Na+/H+ exchanger (NHE-1).
    Rimeporide-<sup>15</sup>N<sub>3</sub> hydrochloride