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 (11099)
Related Products (11099)
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18β-Glycyrrhetyl-3-O-sulfate-d3
0 ImagesCat. No.: HY-148682S2Synonyms: Glycyrrhetic acid 3-O-hydrogen sulfate-d3
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DL-Lysine-d4 dihydrochloride
0 ImagesSynonyms: (±)-2,6-Diaminocaproic acid-d4 dihydrochlorideDL-Lysine-4,4,5,5-d4 (dihydrochloride) is the deuterium labeled DL-Lysine. DL-Lysine is a racemic mixture of the D-Lysine and L-Lysine. Lysine is an α-amino acid that is used in the biosynthesis of proteins.
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Octan-1-amine-d17
0 ImagesCat. No.: HY-W032014SCAS No.: 1173022-14-4Octan-1-amine-d17 is the deuterium labeled Octan-1-amine.
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γ-CEHC-d5
0 ImagesCat. No.: HY-113095Sγ-CEHC-d5 is the deuterium labeled γ-CEHC.
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15-Keto Bimatoprost-d5
0 ImagesCat. No.: HY-132277S15-Keto Bimatoprost-d5 is the deuterium labeled 15-Keto Bimatoprost. 15-Keto Bimatoprost is a prostaglandin F2α (PGF2α) analog that can be used for the research of ocular hypotensive.
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Ellagic acid-13C12
0 ImagesCat. No.: HY-B0183SEllagic acid-13C12 is 13 C-labeled Ellagic acid (HY-B0183). Ellagic acid is a natural antioxidant and acts as a potent and ATP-competitive inhibitor of CK2 and SHP2, with an IC50 of 40 nM and a Ki of 20 nM.
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Proguanil-d6 hydrochloride
0 ImagesCat. No.: HY-B0806AS1Purity: 98.73%Proguanil-d6 hydrochloride is the deuterium labeled Proguanil hydrochloride (HY-B0806A). Proguanil hydrochloride, an antimalarial proagent, is metabolized to the active metabolite Cycloguanil (HY-12784). Proguanil hydrochloride is a dihydrofolate reductase (DHFR) inhibitor.
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Cinnamic acid-13C3
0 ImagesSynonyms: 3-Phenylacrylic acid-13C3; β-Phenylacrylic acid-13C3Cinnamic acid-13C3 (3-Phenylacrylic acid-13C3) is the 13C labeled Cinnamic acid (HY-N0610A). Cinnamic acid has potential use in cancer intervention, with IC50s of 1-4.5 mM in glioblastoma, melanoma, prostate and lung carcinoma cells.
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Thiabendazole-13C6
0 ImagesSynonyms: 2-(4-Thiazolyl)benzimidazole-13C6Thiabendazole-13C6 is the 13C6 labeled Thiabendazole. Thiabendazole inhibites the mitochondrial helminth-specific enzyme, fumarate reductase, with anthelminthic property.
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p-Tolualdehyde-d7
0 Imagesp-Tolualdehyde-d7 is the deuterium labeled p-Tolualdehyde (HY-W012860). p-Tolualdehyde is the active small molecule, that could used as drug intermediate.
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7α,25-Dihydroxycholesterol-d6
0 ImagesCat. No.: HY-113962SCAS No.: 2260669-11-0Synonyms: 7α,25-OHC-d67α,25-Dihydroxycholesterol-d6 is deuterium labeled 7α,25-Dihydroxycholesterol. 7α, 25-dihydroxycholesterol (7α,25-OHC) is a potent and selective agonist and endogenous ligand of the orphan GPCR receptor EBI2 (GPR183). 7α, 25-dihydroxycholesterol is highly
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Betahistine-13C,d3 dihydrochloride
0 ImagesCat. No.: HY-B0524AS1Betahistine-13C,d3 (dihydrochloride) is the 13C- and deuterium labeled Betahistine (dihydrochloride). Betahistine dihydrochloride is an orally active histamine H1 receptor agonist and a H3 receptor antagonist. Betahistine dihydrochloride is used for the study of rheumatoid arthritis (RA).
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Azithromycin-13C,d3-1
0 ImagesCat. No.: HY-W654064Purity: 99.9%Synonyms: CP 62993-13C,d3-1Azithromycin-13C,d3-1 is a deuterated labeled Azithromycin.
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L-Glutamine-d4
0 ImagesCat. No.: HY-N0390S15Synonyms: L-Glutamic acid 5-amide-d4L-Glutamine-d4 (L-Glutamic acid 5-amide-d4) is the deuterium labeled L-Glutamine (HY-N0390). L-Glutamine is a non-essential amino acid present abundantly throughout the body and involved in many metabolic processes. L-Glutamine provides a source of carbons for oxidation in some cells.
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Finasteride-d9
0 ImagesCat. No.: HY-13635SCAS No.: 1131342-85-2Synonyms: MK-906-d9Finasteride-d9 is deuterium labeled Finasteride. Finasteride (MK-906) is a potent and competitive 5α-reductase inhibitor, with an IC50 of 4.2 nM for type II 5α-reductase. Finasteride has approximately a 100-fold greater affinity for type II 5α-reductase enzyme than for the type I enzyme. Finasteride can be used for the research of benign prostatic hyperplasia (BPH) and androgenic alopecia.
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Stearoylethanolamide-d3
0 ImagesCat. No.: HY-113015SCAS No.: 2749393-37-9Synonyms: Ceamid-d3; Steaic Acid Ethaolamide-d3Stearoylethanolamide-d3 (Ceamid-d3) is deuterium labeled Stearoylethanolamide. Stearoylethanolamide is an endocannabinoid-like compound with pro-apoptotic activity.
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Ercalcidiol-d3
0 ImagesSynonyms: 25-Hydroxy Vitamin D2-d3
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Febuxostat-d9
0 ImagesFebuxostat-d9 is deuterium labeled Febuxostat, which is a selective xanthine oxidase inhibitor with a Ki of 0.6 nM.
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Tamoxifen-d3
0 ImagesCat. No.: HY-13757AS1CAS No.: 508201-30-7Synonyms: ICI 47699-d3; (Z)-Tamoxifen-d3; trans-Tamoxifen-d3Tamoxifen-d3 is the deuterium labeled Tamoxifen. Tamoxifen (ICI 47699) is an orally active, selective estrogen receptor modulator (SERM) which blocks estrogen action in breast cells and can activate estrogen activity in other cells, such as bone, liver, and uterine cells. Tamoxifen is a potent Hsp90 activator and enhances the Hsp90 molecular chaperone ATPase activity. Tamoxifen also potent inhibits infectious EBOV Zaire and Marburg (MARV) with IC50 of 0.1 μM and 1.8 μM, respectively. Tamoxifen activates autophagy and induces apoptosis. Tamoxifen also can induce gene knockout of CreER(T2) transgenic mouse.
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Dacomitinib-d10 dihydrochloride
0 ImagesCat. No.: HY-13272S2Synonyms: PF-00299804-d10 dihydrochloride; PF-299804-d10 dihydrochloride
