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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 (7658):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-10268S2
    Betrixaban-13C6
    Betrixaban-13C6 (PRT054021-13C6) is 13C labeled Betrixaban. Betrixaban (PRT054021) is a highly potent, selective, and orally efficacious factor Xa (fXa) inhibitor with an IC50 of 1.5 nM. Betrixaban shows antithrombotic effect.
    Betrixaban-<sup>13</sup>C<sub>6</sub>
  • HY-W654100
    Cefepime-d3(sulfate)
    Cefepime-d3 (sulfate) is deuterium labeled Cefepime (sulfate).
    Cefepime-d<sub>3</sub>(sulfate)
  • HY-W778183
    3,5,6-Trichloro-2-pyridinol-13C5
    3,5,6-Trichloro-2-pyridinol-13C5 (TCPy-13C5) is 13C labeled 3,5,6-Trichloro-2-pyridinol.
    3,5,6-Trichloro-2-pyridinol-<sup>13</sup>C<sub>5</sub>
  • HY-B0656S1
    Rabeprazole-13C,d3
    Rabeprazole-13C,d3 is a deuterated labeled Rabeprazole. Rabeprazole (LY307640) is a second-generation proton pump inhibitor (PPI) that irreversibly inactivates gastric H+/K+-ATPase. Rabeprazole induces apoptosis. Rabeprazole acts as an uridine nucleoside ribohydrolase (UNH) inhibitor with an IC50 of 0.3 μM. Rabeprazole can be used for the research of gastric ulcerations and gastroesophageal reflux.
    Rabeprazole-<sup>13</sup>C,d<sub>3</sub>
  • HY-W777599
    (±)-Naproxen-13C,d3-1
    (±)-Naproxen-13C,d3-1 ((Rac)-Naproxen-13C,d3-1) is 13C and deuterium labeled (±)-Naproxen.
    (±)-Naproxen-<sup>13</sup>C,d<sub>3</sub>-1
  • HY-100347S
    SRI-011381-d5
    SRI-011381-d5 is the deuterium labeled SRI-011381 (HY-100347). SRI-011381 is an orally active TGF-β signaling agonist, exhibits neuroprotective effects.
    SRI-011381-d<sub>5</sub>
  • HY-124303S
    4(Z),7(Z),10(Z),13(Z),16(Z)-Nonadecapentaenoic acid-d5
    4(Z),7(Z),10(Z),13(Z),16(Z)-Nonadecapentaenoic acid-d5 (FA 19:5-d5) is deuterium labeled 4(Z),7(Z),10(Z),13(Z),16(Z)-Nonadecapentaenoic acid.
    4(Z),7(Z),10(Z),13(Z),16(Z)-Nonadecapentaenoic acid-d<sub>5</sub>
  • HY-13673S2
    Goserelin-d7 TFA
    Goserelin-d7 (TFA) is deuterium labeled Goserelin. Goserelin (ICI 118630), a decapeptide analogue of gonadotropin-releasing hormone (GnRH/LHRH), functions as a GnRH agonist. Goserelin can be used for the research of breast cancer, epithelial ovarian cancer and prostate cancer.
    Goserelin-d<sub>7</sub> TFA
  • HY-W654301
    Oseltamivir-d5 Phosphate
    Oseltamivir-d5 Phosphate is deuterium labeled Oseltamivir Phosphate.
    Oseltamivir-d<sub>5</sub> Phosphate
  • HY-W020576S
    Rivastigmine metabolite-d6
    (S)-3-(1-(Dimethylamino)ethyl)phenol-d6 is the deuterium labeled Rivastigmine metabolite(HY-W020576).
    Rivastigmine metabolite-d<sub>6</sub>
  • HY-165662S
    Pranoprofen-13C-d3
    Pranoprofen-13C-d3 (Pyaopofe-13C-d3) is 13C and deuterium labeled Pranoprofen.
    Pranoprofen-<sup>13</sup>C-d<sub>3</sub>
  • HY-151993S
    2-Hydroxypropane-1,3-diyl distearate-d75
    2-Hydroxypropane-1,3-diyl distearate-d75 is deuterium labeled Glyceryl 1,3-distearate.
    2-Hydroxypropane-1,3-diyl distearate-d<sub>75</sub>
  • HY-W759845
    Aficamten-d3
    Aficamten-d3 (CK-274-d3) is deuterium labeled Aficamten. Aficamten (CK-274) is a potent cardiac myosin inhibitor with an IC50 of 1.4 μM. Aficamten can be used for the research of hypertrophic cardiomyopathy (HCM).
    Aficamten-d<sub>3</sub>
  • HY-100805S1
    D-Glutamic acid-13C5,15N
    D-Glutamic acid-13C5,15N ((R)-Glutamic acid-13C5,15N) is 13C and 15N labeled D-Glutamic acid. D-glutamic acid, an enantiomer of L- glutamic acid, is widely used in pharmaceuticals and foods.
    D-Glutamic acid-<sup>13</sup>C<sub>5</sub>,<sup>15</sup>N
  • HY-66006S1
    4-Acetaminophen sulfate-d4
    4-Acetaminophen sulfate-d4 is deuterated labeled 4-Acetaminophen sulfate.
    4-Acetaminophen sulfate-d<sub>4</sub>
  • HY-173090S
    VAVVR(pT)PPK(pS)PSSAK-(Lys-13C6,15N2) TFA
    VAVVR(pT)PPK(pS)PSSAK-(Lys-13C6,15N2) TFA is the 13C- and 15N-labeled VAVVR(pT)PPK(pS)PSSAK-(Lys) TFA.
    VAVVR(pT)PPK(pS)PSSAK-(Lys-<sup>13</sup>C<sub>6</sub>,<sup>15</sup>N<sub>2</sub>) TFA
  • HY-69188S
    3,4-Dihydro-2H-benzo[b][1,4]thiazine-d2
    3,4-Dihydro-2H-benzo[b][1,4]thiazine-d2 (3,4-Dihydro-2H-1,4-benzothiazine-d2) is the deuterium labeled 3,4-Dihydro-2H-benzo[b][1,4]thiazine.
    3,4-Dihydro-2H-benzo[b][1,4]thiazine-d<sub>2</sub>
  • HY-154757S
    Iloperidone metabolite P88-d3
    Iloperidone metabolite P88-d3 is deuterated labeled Iloperidone metabolite P88.
    Iloperidone metabolite P88-d<sub>3</sub>
  • HY-W654091
    (R)-Butyryl carnitine-d5 chloride
    (R)-Butyryl carnitine-d5 chloride is deuterium labeled Butyryl-L-carnitine (chloride). Butyryl-L-carnitine chloride is an acylcarnitine that can be isolated from Plasma/Serum.
    (R)-Butyryl carnitine-d<sub>5</sub> chloride
  • HY-14539S3
    Clozapine-d3
    Clozapine-d3 (HF 1854-d3) is deuterium labeled Clozapine. Clozapine (HF 1854) is an antipsychotic used for the research of schizophrenia. Clozapine has high affinity for a number of neuroreceptors. Clozapine is a potent antagonist of dopamine D2 with a Ki of 75 nM. Clozapine inhibits the muscarinic M1 receptor and serotonin 5HT2A receptor with Kis of 9.5 nM and 4 nM, respectively. Clozapine is also a potent and selective agonist at the muscarinic M4 receptor (EC50=11 nM).
    Clozapine-d<sub>3</sub>