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 Inhibitor (1)

Isotope-Labeled Compounds Related Products (7645):

Cat. No.	Product Name	Effect	Purity	Chemical Structure

HY-111326S

Naphazoline-d₄ hydrochloride
Naphazoline-d₄ (hydrochloride) is the deuterium labeled Naphazoline hydrochloride[1].

HY-Y0287AS

Calcium carbonate,99.8%,PT-¹³C		98.00%
Calcium carbonate,99.8%,PT-¹³C is the ¹³C labeled Calcium carbonate,99.95-100.05%,PT[1].

HY-14588S

(rel)-Lopinavir-d₈
(rel)-Lopinavir-d₈ ((rel)-ABT-378-d₈) is the deuterium labeled Lopinavir (HY-14588). Lopinavir (ABT-378) is a highly potent, selective peptidomimetic inhibitor of the HIV-1 protease, with K_is of 1.3 to 3.6 pM for wild-type and mutant HIV protease. Lopinavir acts by arresting maturation of HIV-1 thereby blocking its infectivity. Lopinavir is also a SARS-CoV 3CL^pro inhibitor with an IC₅₀ of 14.2 μM.

HY-W009749AS

DL-Cystathionine-d₄
DL-Cystathionine-d₄ is the deuterium labeled Pencycuron[1].

HY-W010037S

2-(tert-Butyl)-4-methoxyphenol-d₃
2-(tert-Butyl)-4-methoxyphenol-d₃ is deuterium labeled 2-(tert-Butyl)-4-methoxyphenol.

HY-129948S

Ipratropium-d₃ iodide
Ipratropium-d₃ (iodide) is the deuterium labeled Ipratropium iodide[1].

HY-Y0251S

3-Nitrophthalic acid-d₃
NSC 3120-d₃ is the deuterium labeled NSC 3120[1].

HY-116152S2

Cipepofol-d₆-2
Cipepofol-d₆-2 (Ciprofol-d₆-2; HSK3486-d₆-2) is deuterium labeled Cipepofol (HY-116152). Cipepofol (HSK3486), a psychomotor stabilizing agent, is a gamma-aminobutyric acid (GABA) receptor potentiator.

HY-109523S

Cerivastatin-d₃ sodium
Cerivastatin-d₃ sodium is deuterated labeled Cerivastatin sodium (HY-109523). Cerivastatin sodium is a synthetic lipid-lowering agent and a highly potent, well-tolerated and orally active HMG-CoA reductase inhibitor, with a Ki of 1.3 nM/L. Cerivastatin sodium reduces low-density lipoprotein cholesterol levels. Cerivastatin sodium also inhibits proliferation and invasiveness of MDA-MB-231 cells, mainly by RhoA inhibition, and has anti-cancer effect.

HY-W069721S1

N-Acetylsulfanilamide-¹³C₆
N-Acetylsulfanilamide-¹³C₆ is the ¹³C₆ labeled N-Acetylsulfanilamide.

HY-Y0658S

Tetramethyl-ammonium Bromide-d₁₂
Tetramethyl-ammonium Bromide-d₁₂ is the deuterium labeled TMAB[1].

HY-146891S

16:0-16:0 PC-d₃₁
16:0-16:0 PC-d₃₁ is deuterium labeled 16:0-16:0 PC.

HY-143963S

Irbesartan impurity 20-d₄
Irbesartan impurity 20-d₄ is the deuterium labeled Irbesartan impurity 20[1]. Irbesartan impurity 20-d4 is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.

HY-151068S

2,3′,4′,5-Tetrachlorobiphenyl-3,4,6-d₃
2,3′,4′,5-Tetrachlorobiphenyl-3,4,6-d₃ is the deuterium labeled 2,3′,4′,5-Tetrachlorobiphenyl[1].

HY-Y1275S1

N-Methylpyrrolidone-d₃
N-Methylpyrrolidone-d₃ is the deuterium labeled N-Methylpyrrolidone [1]. N-Methylpyrrolidone (1-Methyl-2-pyrrolidinone), a five-membered cyclic amide, is an organic polar solvent. N-Methylpyrrolidone is extensively used in the manufacture of adhesives, paints, fuels, and pharmaceuticals[2][3].

HY-166889S

2,4,5-Trichloro-4'-methoxy-biphenyl-C¹³C₁₂
2,4,5-Trichloro-4'-methoxy-biphenyl-¹³C₁₂ is ¹³C labeled 2,4,5-Trichloro-4'-methoxy-biphenyl.

HY-143980S

Losartan impurity 21-d₄
Losartan impurity 21-d₄ is the deuterium labeled Losartan impurity 21[1]. Losartan impurity 21-d4 is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.

HY-B1658CS

ent-Frovatriptan-d₃ succinate
ent-Frovatriptan-d₃ (succinate) is deuterium labeled ent-Frovatriptan.

HY-W013068S3

DMT-dT Phosphoramidite-d₁₁
DMT-dT Phosphoramidite-d₁₁ is deuterium labeled DMT-dT Phosphoramidite (HY-W013068). DMT-dT Phosphoramidite is typically used in the synthesis of DNA.

HY-B0250S1

Lamivudine-¹³C,¹⁵N₂,d₂
Lamivudine-13C,15N2,d2 (BCH-189-13C,15N2,d2) is a 13C, 15N, and deuterium labeled Lamivudine (HY-B0250). Lamivudine is an orally active and blood-brain barrier permeable nucleoside reverse transcriptase inhibitor (NRTI). Lamivudine inhibits HIV reverse transcriptase 1 and 2 and hepatitis B virus (HBV) reverse transcriptase.

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