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 (11126)
Related Products (11126)
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2-Phenoxy-1-phenylethanol-d2
0 Images2-Phenoxy-1-phenylethanol-d2 is the deuterium labeled 2-Phenoxy-1-phenylethanol (HY-W006550).
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Cetrimonium-d33 bromide
0 ImagesCat. No.: HY-B1260S1CAS No.: 347841-42-3Synonyms: CTAB-d33; Cetyltrimethylammonium-d33 bromide; Hexadecyltrimethylammonium-d33 bromideCetrimonium-d33 bromide is the deuterium labeled Cetrimonium bromide. Cetrimonium bromide (CTAB) is an amine based cationic quaternary surfactant, is one of the components of the topical antiseptic Cetrimide.
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N-Demethyl Ivabradine-d6 hydrochloride
0 ImagesSynonyms: Ivabradine metabolite N-demethyl Ivabradine-d6 hydrochlorideN-Demethyl Ivabradine-d6 (hydrochloride) is the deuterium labeled N-Demethyl Ivabradine, which is a metabolite of Ivabradine.
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Sulfamerazine-13C6
0 ImagesSynonyms: RP2632-13C6Sulfamerazine-13C6 (RP2632-13C6) is 13C labeled Sulfamerazine (HY-B0512). 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.
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4-Fluorobenzoyl-2,3,5,6-d4 chloride
0 Images4-Fluorobenzoyl-2,3,5,6-d4 chloride is the deuterium labeled 4-Fluorobenzoyl chloride.
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Taurochenodeoxycholic acid-d4
0 ImagesCat. No.: HY-165651SCAS No.: 1207294-24-3Synonyms: 12-Deoxycholyltaurine-d4Taurochenodeoxycholic acid-d4 (TCDCA-d4) is the deuterium labeled Taurochenodeoxycholic acid. Taurochenodeoxycholic acid (12-Deoxycholyltaurine) is one of the main bioactive substances of animals' bile acid. Taurochenodeoxycholic acid induces apoptosis and shows obvious anti-inflammatory and immune regulation properties.
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Hydroxyurea-15N
0 ImagesCat. No.: HY-W698472CAS No.: 214331-53-0Synonyms: Hydroxycarbamide-15NHydroxyurea-15N (Hydroxycarbamide-15N) is the 15N labeled Hydroxyurea (HY-B0313). Hydroxyurea is a cell apoptosis inducer that inhibit DNA synthesis through inhibition of ribonucleotide reductase. Hydroxyurea shows anti-orthopoxvirus activity.
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Dabigatran-d4
0 ImagesCat. No.: HY-10163SCAS No.: 1618637-32-3Synonyms: BIBR 953-d4; BIBR 953ZW-d4Dabigatran-d4 is deuterium labeled Dabigatran. Dabigatran (BIBR 953), an oral anticoagulant, is a reversible, potent, competitive direct thrombin inhibitor (Ki=4.5 nM). Dabigatran (BIBR 953) also inhibits thrombin-induced platelet aggregation (IC50=10 nM).
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Danicamtiv-d6
0 ImagesCat. No.: HY-109128SCAS No.: 1970975-54-2Synonyms: MYK-491-d6Danicamtiv-d6 (MYK-491-d6) is a deuterated labeled Danicamtiv (HY-109128). Danicamtiv (MYK-491), an inotropic agent, is a selective allosteric activator of cardiac myosin. Danicamtiv increases cardiac systolic function and preserves mechanical efficiency.
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Chlorhexidine-d8 dihydrochloride
0 ImagesCat. No.: HY-B1145SCAS No.: 2012598-75-1Chlorhexidine-d8 (dihydrochloride) is the deuterium labeled Chlorhexidine dihydrochloride (HY-B1145). Chlorhexidine dihydrochloride is a orally active cationic antimicrobial agent that targets microbial cell membranes. Chlorhexidine dihydrochloride binds to cell membrane phospholipids non-specifically, destroys membrane structure and induces leakage of cell contents. Chlorhexidine dihydrochloride has broad-spectrum bactericidal activity against both Gram-positive and Gram-negative bacteria. Chlorhexidine dihydrochloride can interfere with membrane permeability, cause protein precipitation and energy metabolism disorders, such as rapid inhibition of microbial growth and induction of cell death (necrosis or apoptosis).
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C18 Dihydroceramide-d3-1
0 ImagesSynonyms: N-octadecaoyl-D-eytho-Dihydosphigosie-d3; Ce(d18:0/18:0)-d3; Ceamide-d3 (d18:0/18:0-d3)C18 Dihydroceramide-d3-1 (N-octadecaoyl-D-eytho-Dihydosphigosie-d3) is deuterium labeled C18 Dihydroceramide. C18 Dihydroceramide is an ester product.
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D-Xylulose-1-13C
0 ImagesD-Xylulose-1-13C is the 13C-labeled D-Xylulose (HY-W010256). D-Xylulose is a toxic pentose. D-Xylulose does not induce pentitol production in cells. D-Xylulose can induce ATP and intracellular Pi depletion through the accumulation of Sedoheptulose 7-P.
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Acetylvaline-15N
0 ImagesAcetylvaline-15N is the 15N-labeled Acetylvaline (HY-W015466). Acetylvaline is a class of amino acid derivative metabolites. The expression abundance of Acetylvaline is upregulated under heat stress conditions; it participates in the regulation of amino acid biosynthesis, cysteine and methionine metabolic pathways, and mediates the physiological processes of antioxidant defense and energy metabolism reprogramming in Magallana sikamea. Acetylvaline can be released from acetylvalyl-RNA of Turnip Yellow Mosaic Virus (TYMV) by N‑acylaminoacyl‑tRNA hydrolase. Acetylvaline can be used in metabolism-related research.
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Glycerol-13C
0 ImagesSynonyms: Trihydroxypropane-13CGlycerol-13C is the 13C labeled Glycerol. Glycerol is used in sample preparation and gel formation for polyacrylamide gel electrophoresis.
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Zuclomiphene-d4 citrate
0 ImagesZuclomiphene-d4 citrate is a deuterium labeled Zuclomiphene citrate (HY-B1617A). Zuclomiphene citrate is a cis isomer of Clomiphene citrate (HY-B0463). Zuclomiphene citrate is orally active and has an antiestrogenic effect. Zuclomiphene can reduce cholesterol levels. Zuclomiphene citrate can be for the researches of endocrinology and metabolic disease.
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Boc-L-Valine-d8
0 ImagesBoc-L-Valine-d8 is the deuterium labeled Boc-L-Valine.
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Thymidine-13C
0 ImagesSynonyms: DThyd-13C; NSC 21548-13C-
Harman-13C2,15N
0 ImagesCat. No.: HY-W777360CAS No.: 1189461-56-0Harman-13C2,15N is 13C and 15N labeled Harmane. Harmane is a benzodiazepine receptor inhibitor (IC50=7 μM), with IC50 values for mACh, Opioid Receptor, MAO-A/B, and α2-adrenergic receptor of 24 μM, 2.8 μM, 0.5 μM, 5 μM, and 18 μM, respectively. Harmane also inhibits haloperidol and serotonin, with IC50 values of 163 μM and 101 μM, respectively. Harmane inhibits the I1 imidazoline receptor (IC50=30 nM) to reduce blood pressure and has antidepressant, anti-anxiety, anticonvulsant, and analgesic effects. Harmane inhibits dopamine biosynthesis by decreasing tyrosine hydroxylase (TH) activity and enhancing L-DOPA-induced cytotoxicity in PC12 cells. Additionally, Harmane can increase the mutagenic effect induced by 2-acetylaminofluorene (AAF).
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Dimethyl adipate-d8
0 ImagesSynonyms: Hexanedioic acid dimethyl ester-d8Dimethyl adipate-d8 (Hexanedioic acid dimethyl ester-d8) is the deuterium labeled Dimethyl adipate (HY-W015301). Dimethyl adipate is an aliphatic dicarboxylate compound. Dimethyl adipate is mainly used as a plasticizer and an intermediate in organic synthesis.
