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 (11046)
Related Products (11046)
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9-([1,1'-Biphenyl]-4-yl)-10-bromoanthracene-d17
![9-([1,1'-Biphenyl]-4-yl)-10-bromoanthracene-d17](https://file.medchemexpress.com/product_pic/hy-w039433s1.gif "Click to View 9-([1,1'-Biphenyl]-4-yl)-10-bromoanthracene-d17 Product Detail")
0 ImagesCat. No.: HY-W039433S1CAS No.: 2770790-77-59-([1,1'-Biphenyl]-4-yl)-10-bromoanthracene-d17 is the deuterium labeled 9-([1,1'-Biphenyl]-4-yl)-10-bromoanthracene.
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Zimeldine-d6
0 ImagesCat. No.: HY-118835SCAS No.: 1185239-75-1Zimeldine-d6 is the deuterium labeled Zimeldine (HY-118835). Zimelidine is an orally active selective serotonin reuptake inhibitor. Zimelidine competitively inhibits central 5-HT uptake and desensitizes 5-HT autoreceptors in dorsal raphe nucleus. Zimelidine time-dependently modulates 5-HT neuronal firing and hippocampal CA3 responses. Zimelidine strengthens central serotonergic neurotransmission and produces related behavioral changes. Zimelidine exerts anxiolytic, analgesic, feeding-suppressive and tolerance-attenuating effects. Zimelidine is used for the study of depressive disorders and analgesic tolerance.
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1,3,6,8-Tetrachloro-dibenzofuran-13C12
0 ImagesCat. No.: HY-166917SCAS No.: 1236286-05-71,3,6,8-Tetrachloro-dibenzofuran-13C12 is 13C labeled 1,3,6,8-Tetrachlorodibenzofuran.
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Fmoc-Gln(Trt)-OH-13C5,15N2
0 ImagesCat. No.: HY-W013081SCAS No.: 1217462-20-8Fmoc-Gln(Trt)-OH-13C5,15N2 is the 13C-labeled and 15N-labeled Fmoc-Gln(Trt)-OH (HY-W013081). Fmoc-Gln(Trt)-OH is a glutamine derivative containing amine protecting group Fmoc. Fmoc-Gln(Trt)-OH can be used in solid-phase peptide synthesis.
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N-Acetyl-L-phenylalanine-13C2
0 ImagesCat. No.: HY-Y0068SSynonyms: N-Acetylphenylalanine-13C2N-Acetyl-L-phenylalanine-13C2 (N-Acetylphenylalanine-13C2) is the 13C-labeled N-Acetyl-L-phenylalanine (HY-Y0068). N-Acetyl-L-phenylalanine (N-Acetylphenylalanine) is a principal acylamino acid. N-Acetyl-L-phenylalanine can be synthesized from L-phenylalanine and acetyl-CoA. N-Acetyl-L-phenylalanine can be used in kidney research.
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(E)-But-2-enal-13C
0 ImagesCat. No.: HY-Y0787S1CAS No.: 127136-17-8(E)-But-2-enal-13C is the 13C-labeled (E)-But-2-enal.
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Lactyl-CoA-d3
0 ImagesCat. No.: HY-141540S1Lactyl-CoA-d3 is the deuterium labeled Lactyl-CoA (HY-141540). Lactyl-CoA is an acyl-CoA formally condensed from the sulfhydryl group of CoA and the carboxyl group of lactic acid, also known as lactyl-CoA. Lactyl-CoA is essential for the biosynthesis of biodegradable and biocompatible lactic acid-based copolymers.
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3-Methyl-4-nitrophenol-d3
0 ImagesCat. No.: HY-W042337S3-Methyl-4-nitrophenol-d3 is the deuterium labeled 3-Methyl-4-nitrophenol (HY-W042337). 3-Methyl-4-nitrophenol, an environmental contaminant, is a well-known constituent of diesel exhaust particles and degradation products of insecticide fenitrothion. 3-Methyl-4-nitrophenol can induce nasal epithelial cell apoptosis and increase the permeability of the nasal epithelial barrier. 3-Methyl-4-nitrophenol is also toxic to the female reproductive system.
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Octreotide-d8 TFA
0 ImagesCat. No.: HY-P0036SSynonyms: SMS 201-995-d8 TFAOctreotide-d8 (SMS 201-995-d8) TFA is the deuterium labeled Octreotide TFA. Octreotide (SMS 201-995) is a somatostatin receptor agonist and synthetic octapeptide endogenous somatostatin analogue. Octreotide (SMS 201-995) can bind to the somatostatin receptor and mainly subtypes 2, 3, and 5, increases Gi activity, and reduces intracellular cAMP production. Octreotide (SMS 201-995) has antitumor activity, mediates apoptosis and may also be used in disease studies in acromegaly.
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Dihydroartemisinin-d
0 ImagesCat. No.: HY-N0176S6CAS No.: 252043-36-0Synonyms: Dihydroqinghaosu-d; β-Dihydroartemisinin-d; Artenimol-dDihydroartemisinin-d (Dihydroqinghaosu-d) is the d-labeled Dihydroartemisinin (HY-N0176). Dihydroartemisinin is an orally active metabolite of rtemisinin (HY-B0094) and antimalarial agent. Dihydroartemisinin induces Autophagy by inhibiting NF-κB activation. Dihydroartemisinin promotes ROS accumulation. Dihydroartemisinin exhibits anticancer activity in esophageal cancer cells. Dihydroartemisinin shows schistosomicidal activity against juvenile and adult worms of Schistosoma japonicum, reduces worm burden, and displays antiparasitic activity. Dihydroartemisinin can be used in research related to multiple myeloma, promyelocytic leukemia, esophageal cancer, and Schistosoma japonicum infection.
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DPA-714-d10
0 ImagesCat. No.: HY-122607SDPA-714-d10 is the deuterium labeled DPA-714 (HY-122607). DPA-714 is a high affinity translocator protein (TSPO) ligand (Ki=7 nM), which is designed with a fluorine atom in its structure, allowing labelling with fluorine -18 and in vivo imaging using positron emission tomography. 18FDPA-714 successfully evaluates for the specific imaging of inflammation in various models of neuroinflammation and in a brain tumor model.
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Pegcetacoplan-13C3,15N TFA
0 ImagesCat. No.: HY-P3252ASPegcetacoplan-13C3,15N TFA is the 13C- and 15N-labeled Pegcetacoplan TFA. Pegcetacoplan is a pegylated complement C3/C3b inhibitor. Pegcetacoplan acts by specifically binding to and inhibiting C3 and C3b, thereby suppressing the complement cascade at its proximal stage. Pegcetacoplan is not a known inhibitor or inducer of CYP450 isoenzymes. Pegcetacoplan can be used for the research of complement-mediated diseases, including paroxysmal nocturnal hemoglobinuria (PNH) and age-related macular degeneration (AMD).
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GDC-0575-d4
0 ImagesCat. No.: HY-112167SSynonyms: ARRY-575-d4; RG7741-d4GDC-0575-d4 (ARRY-575-d4) is the deuterium labeled GDC-0575 (HY-112167). GDC-0575 (ARRY-575, RG7741) is a highly-selective oral small-molecule Chk1 inhibitor with an IC50 of 1.2 nM.
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3-(1-Nitrosopyrrolidin-2-yl)pyridine-13C6
0 ImagesCat. No.: HY-W768044CAS No.: 2726380-44-33-(1-Nitrosopyrrolidin-2-yl)pyridine-13C6 is the 13C-labeled 3-(1-Nitrosopyrrolidin-2-yl)pyridine (HY-W189682). 3-(1-Nitrosopyrrolidin-2-yl)pyridine is a major tobacco-specific nitrosamine.
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(((9H-Fluoren-9-yl)methoxy)carbonyl)-L-aspartic acid-15N
0 ImagesCat. No.: HY-W837593CAS No.: 287484-33-7(((9H-Fluoren-9-yl)methoxy)carbonyl)-L-aspartic acid-15N is the 15N-labeled (((9H-Fluoren-9-yl)methoxy)carbonyl)-L-aspartic acid (HY-W013182). (((9H-Fluoren-9-yl)methoxy)carbonyl)-L-aspartic acid is an aspartic acid derivative.
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Leucic acid-13C
0 ImagesCat. No.: HY-30216ASSynonyms: α-Hydroxyisocaproic acid-13CLeucic acid-13C (α-Hydroxyisocaproic acid-13C) is the 13C-labeled Leucic acid (HY-30216A). Leucic acid is an amino acid metabolite.
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Exatecan Intermediate 1-d2
0 ImagesCat. No.: HY-42487S1CAS No.: 3061737-78-5Exatecan Intermediate 1-d2 is the deuterium labeled Exatecan Intermediate 1 (HY-42487). Exatecan Intermediate 1 (compound 6) is an intermediate of Exatecan (HY-13631). Exatecan is a DNA topoisomerase I inhibitor with anticancer effects.
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Tuvusertib-d3
0 ImagesCat. No.: HY-111451SSynonyms: M1774-d3; ATR inhibitor 1-d3Tuvusertib-d3 (M1774-d3) is the deuterium labeled Tuvusertib (HY-111451). Tuvusertib (M1774; ATR inhibitor 1) is a selective and orally active ATR inhibitor with a Ki value below 1 μΜ.
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Decanoyl-L-carnitine-d19
0 ImagesCat. No.: HY-135035S1Synonyms: (-)-Decanoylcarnitine-d19Decanoyl-L-carnitine-d19 ((-)-Decanoylcarnitine-d19> is the deuterium labeled Decanoyl-L-carnitine (HY-135035). Decanoyl-L-carnitine ((-)-Decanoylcarnitine) is an endogenous metabolite. Decanoyl-L-carnitine can be used as a serum metabolic biomarkers as indicators in the progression of intravenous leiomyomatosis.
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DPPC-13C
0 ImagesCat. No.: HY-109506S10Synonyms: 129Y83-13CDPPC-13C3 (129Y83-13C) is the 13C-labeled DPPC (HY-109506). DPPC (129Y83) is a phosphoglyceride that can be used to prepare lipid monolayers, bilayers, and liposomes. DPPC is the main lipid component of pulmonary surfactant. Dppc-liposome can be effectively used as a delivery vector to induce an immune response against GSL antigen in mice.
