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.
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Isotope-Labeled Compounds Related Products (11128)
Related Products (11128)
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Estradiol-13C6
0 ImagesCat. No.: HY-B0141S4Synonyms: β-Estradiol-13C6; E2-13C6; 17β-Estradiol-13C6; 17β-Oestradiol-13C6Estradiol-13C6 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.
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(−)-11-Hydroxy-Δ8-THC-d3
0 ImagesCat. No.: HY-139429SSynonyms: (−)-11-Hydoxy-Δ8-Tetahydocaabiol-d3; (−)-tas-Δ8-THC-d3; 7-hydoxy-Δ6-THC-d3(?)-11-Hydroxy-Δ8-THC-d3 ((?)-11-Hydoxy-Δ8-Tetahydocaabiol-d3) is deuterium labeled (?)-11-hydroxy-Δ8-THC.
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KRAS 2B G13D mutant, Arg-13C6,15N4, Lys-13C6,15N2
0 ImagesCat. No.: HY-176341SKRAS 2B G13D mutant, Arg-Arg-13C36, 15N4, Lys-13C6, 15N2 is the 13C- and 15N-labeled KRAS 2B G13D mutant.
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18:0-18:0 PC-d35
0 ImagesCat. No.: HY-146893SCAS No.: 327178-88-118:0-18:0 PC-d35 is deuterium labeled 18:0-18:0 PC.
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(-)-Menthol-d4
0 ImagesCat. No.: HY-W711474CAS No.: 1450828-98-4(-)-Menthol-d4 is the deuterium labeled (-)-Menthol (HY-75161). (-)-Menthol is a key component of peppermint oil that binds and activates transient receptor potential melastatin 8 (TRPM8), a Ca2+-permeable nonselective cation channel, to increase [Ca2+]i. Antitumor activity.
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Alkyl diphenyl phosphate-d10
0 ImagesCat. No.: HY-W717687Synonyms: Phosphoric acid, dodecyl diphenyl ester-d10Alkyl diphenyl phosphate-d10 (Phosphoric acid, dodecyl diphenyl ester-d10) is the deuterium labeled Alkyl diphenyl phosphate.
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(S)-2-Hydroxy-3-phenylpropanoic acid-13C9
0 ImagesCat. No.: HY-W753181Synonyms: L-(-)-3-Phenyllactic Acid-13C9(S)-2-Hydroxy-3-phenylpropanoic acid-13C9 (L-(-)-3-Phenyllactic Acid-13C9) is the 13C-labeled (S)-2-Hydroxy-3-phenylpropanoic acid (HY-30220). (S)-2-Hydroxy-3-phenylpropanoic acid is the L-configuration of 2-Hydroxy-3-phenylpropanoic acid, and its level is closely related to some diseases, such as phenylketonuria.
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Momelotinib-d4 dihydrochloride hydrate
0 ImagesCat. No.: HY-10961S8CAS No.: 2056097-81-3Synonyms: CYT387-d4 hydrochloride hydrateMomelotinib-d4 (CYT387-d4) dihydrochloride hydrate is a deuterium labeled Momelotinib (HY-10961). Momelotinib (CYT387) is an ATP-competitive inhibitor of JAK1/JAK2 with IC50s of 11 nM and 18 nM,respectively. CYT387 shows much less activity against JAK3.
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D-Galactosyl-ß-1,1' N-nervonoyl-D-erythro-sphingosine-d7
0 ImagesCat. No.: HY-146922SCAS No.: 2770684-23-4D-Galactosyl-ß-1,1' N-nervonoyl-D-erythro-sphingosine-d7 is deuterium labeled D-Galactosyl-ß-1,1' N-nervonoyl-D-erythro-sphingosine.
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(R)-4-Benzyl-3-propionyloxazolidin-2-one-d3
0 ImagesCat. No.: HY-W750774CAS No.: 1352449-25-2Synonyms: N-3-propionyl-(4R)-benzyl-2-oxazolidinone-d3(R)-4-Benzyl-3-propionyloxazolidin-2-one-d3 (N-3-propionyl-(4R)-benzyl-2-oxazolidinone-d3) is the deuterium labeled (R)-4-Benzyl-3-propionyloxazolidin-2-one (HY-W008773).
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Trihydroxycoprostane-d7
0 ImagesCat. No.: HY-W744525
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Disulfiram impurity 1-d10
0 ImagesCat. No.: HY-143951SCAS No.: 2749799-73-1Disulfiram impurity 1-d10 is the deuterium labeled Disulfiram impurity 1.
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Salbutamol-d4
0 ImagesCat. No.: HY-W707640CAS No.: 2517375-34-5Synonyms: Albuterol-d4; AH-3365-d4Salbutamol-d4 (Albuterol-d4; AH-3365-d4) is the deuterium labeled Salbutamol (HY-B1037). Salbutamol (Albuterol) is a short-acting beta-2 adrenergic receptor agonist with oral activity. Salbutamol promotes tumorigenesis of gastric cancer cells through the β2-AR/ERK/EMT pathway. Salbutamol is used to study bronchospasms caused by asthma and chronic obstructive pulmonary disease (COPD).
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Clindamycin Hydrochloride-13C,d3
0 ImagesCat. No.: HY-W749665CAS No.: 2140264-64-6Clindamycin Hydrochloride-13C,d3 is the deuterium and 13C-labeled Clindamycin hydrochloride (HY-B0408A). Clindamycin hydrochloride is a semisynthetic lincosamide antibiotic, which inhibits protein synthesis by acting on the 50S ribosomal.
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(Rac)-Tolterodine-d14 tartrate
0 ImagesCat. No.: HY-A0024ASCAS No.: 1191280-48-4Synonyms: (Rac)-PNU-200583-d14 tartrate(Rac)-Tolterodine-d14 (tartrate) is the deuterium labeled (Rac)-Tolterodine tartrate.
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Tolcapone-d7
0 ImagesCat. No.: HY-17406SCAS No.: 2749285-04-7Synonyms: Ro 40-7592-d7Tolcapone-d7 (Ro 40-7592-d7) is the deuterium labeled Tolcapone (HY-17406). Tolcapone (Ro 40-7592) is a selective, potent and orally active COMT inhibitor with an IC50of 773 nM. Tolcapone can inhibits α-syn and Aβ42 oligomerization and fibrillogenesis. Tolcapone can cause oxidative stress and induce cancer cells apoptosis and ROS production. Tolcapone can be used for the researches of cancer and neurological disease, such as Parkinson disease and neuroblastoma.
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Cholesteryl linoleate-d11
0 ImagesCat. No.: HY-W010697SCholesteryl linoleate-d11 is the d11-labeled Cholesteryl linoleate (HY-W010697). Cholesteryl linoleate is a cholesteryl ester with antibacterial activity that is present in low-density lipoprotein (LDL) particles, human nasal fluid, and respiratory epithelial secretions. Cholesteryl linoleate is oxidized by 12/15-lipoxygenase in macrophages and participates in selective uptake and efflux via LDL receptor-related protein. Cholesteryl linoleate does not induce endothelial adhesion molecule expression, nor does it induce monocyte binding to endothelial cells. Cholesteryl linoleate liposomal formulations inhibit the growth of multiple bacteria at physiological nasal fluid concentrations and act synergistically with antimicrobial peptides. Cholesteryl linoleate is useful for research related to atherosclerosis and bacterial infections.
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Di(ethylene glycol) dimethacrylate-d8
0 ImagesCat. No.: HY-W743351CAS No.: 2733000-78-5Di(ethylene glycol) dimethacrylate-d8 is the deuterium labeled Di(ethylene glycol) dimethacrylate (HY-W009560). Di(ethylene glycol) dimethacrylate is a biochemical reagent.
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Piracetam-d6
0 ImagesCat. No.: HY-B0585S1CAS No.: 2907016-93-5Synonyms: UCB-6215-d6Piracetam-d6 is deuterium labeled Piracetam. Piracetam (UCB-6215) is a cyclic derivative of the neurotransmitter gamma-aminobutyric acid (GABA), used in treatment of a wide range of cognitive disorders.
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4-Methoxybenzylamine-d3
0 ImagesCat. No.: HY-Y0869SCAS No.: 2289707-21-54-Methoxybenzylamine-d3 is the deuterium labeled 4-Methoxybenzylamine.
