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 관련 제품 (10878):

Cat. No. 상품명 효과 Purity Chemical Structure
  • HY-Y0740S2
    4-Methoxybenzaldehyde-d2
    4-Methoxybenzaldehyde-d2 is the deuterium labeled 4-Methoxybenzaldehyde (HY-W041300). 4-Methoxybenzaldehyde (p-anisaldehyde) is a fragrant phenolic compound. 4-Methoxybenzaldehyde has been found in many plant species including horseradish, anise, star anise. 4-Methoxybenzaldehyde is a possible neurotoxicant and it has shown effects that include mortality, attractancy, and interference with host seeking .
    4-Methoxybenzaldehyde-d<sub>2</sub>
  • HY-W709203S
    2-(N-(1-Carboxyethyl)-2-(methoxy-d3)acetamido)-3-methylbenzoic acid
    2-(N-(1-Carboxyethyl)-2-(methoxy-d3)acetamido)-3-methylbenzoic acid is deuterium labeled 2-(N-(1-Carboxyethyl)-2-methoxyacetamido)-3-methylbenzoic acid.
    2-(N-(1-Carboxyethyl)-2-(methoxy-d<sub>3</sub>)acetamido)-3-methylbenzoic acid
  • HY-B0192S3
    Alfuzosin-d6
    Alfuzosin-d6 (SL 77499-d6) is deuterium labeled Alfuzosin. Alfuzosin (SL 77499-10) is an orally active, selective and competitive α1-adrenoceptor antagonist. Alfuzosin relaxes the muscles of the prostate and bladder neck, aiding in urination. Alfuzosin can be used in study of benign prostatic hyperplasia (BPH).
    Alfuzosin-d<sub>6</sub>
  • HY-157062S
    7-O-Desmethylprazosin-d8 hydrochloride
    7-O-Desmethylprazosin-d8 (hydrochloride) is deuterium-labeled 7-O-Desmethylprazosin.
    7-O-Desmethylprazosin-d<sub>8</sub> hydrochloride
  • HY-Y1309S1
    1-Naphthol-d7
    		99.44%
    1-Naphthol-d7 (Furro ER-d7) is the deuterium labeled Naphthol (HY-Y1309). 1-Naphthol (Furro ER) is an excited state proton transfer (ESPT) fluorescent molecular probe. 1-naphthol can sense the hydrophobic domains in micellar aggregation and accurately sense the sol-gel transition. 1-naphthol can be used to study the thermally induced microenvironmental changes and hydration levels of Pluronic F127 (PF127) in different microenvironments in aqueous media.
    1-Naphthol-d<sub>7</sub>
  • HY-W588292S
    6α-Methylprednisolone 17-propionate-d6
    6α-Methylprednisolone 17-propionate-d6 is the deuterium labeled 6α-Methylprednisolone 17-propionate.
    6α-Methylprednisolone 17-propionate-d<sub>6</sub>
  • HY-34428S1
    4-Fluorobenzonitrile-d4
    4-Fluorobenzonitrile-d4 is the deuterium labeled 4-Fluorobenzonitrile.
    4-Fluorobenzonitrile-d<sub>4</sub>
  • HY-W715180S
    2,3-Dibromo-7,8-dichloro dibenzo-p-dioxin-13C12
    2,3-Dibromo-7,8-dichloro dibenzo-p-dioxin-13C12 is 13C labeled 2,3-Dibromo-7,8-dichlorodibenzo[b,E][1,4]dioxine.
    2,3-Dibromo-7,8-dichloro dibenzo-p-dioxin-<sup>13</sup>C<sub>12</sub>
  • HY-B0398S
    Nalidixic Acid-d5
    Nalidixic Acid-d5 is the deuterium labeled Nalidixic acid. Nalidixic acid, a quinolone antibiotic, is effective against both gram-positive and gram-negative bacteria. Nalidixic acid acts in a bacteriostatic manner in lower concentrations and is bactericidal in higher concentrations. Nalidixic acid inhibits a subunit of DNA gyrase and topoisomerase IV and reversibly blocks DNA replication in susceptible bacteria.
    Nalidixic Acid-d<sub>5</sub>
  • HY-B0477AS2
    Quinapril-d4
    Quinapril-d4 (CI-906-d4) is deuterium labeled Quinapril. Quinapril is a potent, orally active, non-peptide and nonsulfhydryl inhibitor of angiotensin-converting enzyme (ACE). Quinapril specifically interrupts the conversion of angiotensin I to angiotensin II in both plasma and tissue. Quinapril is enzymatically hydrolyzed to a pharmacologically active diacid form quinaprilat. Quinapril is efficacious in hypertensive models.
    Quinapril-d<sub>4</sub>
  • HY-76938AS1
    Actarit-d6 sodium
    Actarit-d6 sodium is deuterated labeled Actarit.
    Actarit-d<sub>6</sub> sodium
  • HY-W131352S
    N-Hexacosane-d54
    		99.5%
    N-Hexacosane-d54 is the deuterium labeled N-hexacosane.
    N-Hexacosane-d<sub>54</sub>
  • HY-B0696S
    Tiagabine-d6
    Tiagabine-d6 (NO050328-d6) is deuterium labeled Tiagabine. Tiagabine (NO050328; NO328; TGB) is an orally active, highly selective, and reversible GAT-1 inhibitor and anticonvulsant that crosses the blood-brain barrier. By blocking the reuptake of GABA in neurons and glial cells, tiagabine increases extracellular GABA levels to enhance inhibitory signal transduction, thereby exerting multiple activities such as anticonvulsant, neuroprotective, and antioxidant effects. Tiagabine exhibits linear pharmacokinetic properties. Although it is metabolized by CYP3A and has a high protein binding rate, it carries a low risk of cognitive impairment. Tiagabine is widely used in research on related diseases including epilepsy (including refractory partial seizures), alcohol withdrawal symptoms, and Huntington's disease.
    Tiagabine-d<sub>6</sub>
  • HY-100713S
    Temocapril-d5
    Temocapril-d5 is the deuterium labeled Temocapril. Temocapril is an angiotensin-converting enzyme (ACE) inhibitor. Temocapril hydrochloride can be used for the research of hypertension, congestive heart failure, acute myocardial infarction, insulin resistance, and renal diseases.
    Temocapril-d<sub>5</sub>
  • HY-B0512S
    Sulfamerazine-d4
    		99.00%
    Sulfamerazine-d4 is a deuterium labeled Sulfamerazine. Sulfamerazine (RP2632) is a brain-penetrant and orally active sulfonamide antibiotic and α-synuclein inhibitor with human α-synuclein KD of 352 μM. Sulfamerazine inhibits the synthesis of dihydrofolate by bacteria, thereby inhibiting bacterial growth. Sulfamerazine inhibits α-synuclein fibrillation, reduces α-synuclein aggregation-associated toxicity and α-synuclein aggregate accumulation. Sulfamerazine can be used for the research of Parkinson’s disease and bacterial infection.
    Sulfamerazine-d<sub>4</sub>
  • HY-W023443S
    2-Isopropyl-5-methylpyrazine-d3
    2-Isopropyl-5-methylpyrazine-d3 is deuterated labeled 2-Isopropyl-5-methylpyrazine.
    2-Isopropyl-5-methylpyrazine-d<sub>3</sub>
  • HY-15030S1
    Naproxen-d3
    		99.14%
    Naproxen-d3 ((S)-Naproxen-d3) is the deuterium labeled Naproxen (HY-15030). Naproxen is a COX-1 and COX-2 inhibitor with IC50s of 8.72 and 5.15 μM, respectively in cell assay.
    Naproxen-d<sub>3</sub>
  • HY-106617AS
    Etoperidone-d8 hydrochloride
    Etoperidone-d8 (hydrochloride) is the deuterium labeled Etoperidone hydrochloride.
    Etoperidone-d<sub>8</sub> hydrochloride
  • HY-W654258
    6-Mercaptopurine-13C,15N2 hydrochloride
    		99.85%
    6-Mercaptopurine-13C,15N2 (hydrochloride) is 13C and 15N labeled 3,7-Dihydro-6h-purine-6-thione hydrochloride.
    6-Mercaptopurine-<sup>13</sup>C,<sup>15</sup>N<sub>2</sub> hydrochloride
  • HY-132442S
    ∆8,9-Dehydro Estrone-d2
    ?8,9-Dehydro Estrone-d2 is the deuterium labeled ?8,9-Dehydro Estrone.
    ∆8,9-Dehydro Estrone-d<sub>2</sub>