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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Dacomitinib-d10
0 ImagesCat. No.: HY-13272S3Synonyms: PF-00299804-d10; PF-299804-d10
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3-(Methylthio)propylamine-d3
0 ImagesCat. No.: HY-W142881SSynonyms: Methylmercaptopropylamine-d33-(Methylthio)propylamine-d3 (Methylmercaptopropylamine-d3) is the deuterium labeled 3-(Methylthio)propylamine.
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p-Azoxyanisole-d6
0 ImagesCat. No.: HY-W283596SCAS No.: 34172-21-9p-Azoxyanisole-d6 is the deuterium labeled p-Azoxyanisole.
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Cimaterol-d7
0 ImagesSynonyms: CL 263780-d7Cimaterol-d7 is the deuterium labeled Cimaterol. Cimaterol is a potent agonist of β-adrenergic receptors (pEC50s=8.13, 8.78, and 6.62 for human β1, β2, and β3, respectively). Cimaterol has been used in farmed animals to increase carcass mass and to alter muscle and fat deposition.
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16α-Hydroxyprednisolone-d5
0 ImagesCat. No.: HY-117580S2Synonyms: OH-PRED-d516α-Hydroxyprednisolone-d5 (OH-PRED-d5) is the deuterium labeled 16α-Hydroxyprednisolone (HY-117580). 16α-Hydroxyprednisolone (OH-PRED) is a stereoselective metabolite of the 22(R) epimer of the glucocorticoid Budesonide (HY-13580). 16α-Hydroxyprednisolone formation is catalyzed by isoenzymes within the cytochrome P450 3A (CYP3A) subfamily. 16α-Hydroxyprednisolone formation can be inhibited by antibodies targeting the CYP3A subfamily.
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(Rac)-Tolterodine-d5
0 ImagesCat. No.: HY-A0024AS1CAS No.: 2747918-62-1(Rac)-Tolterodine-d5 is deuterium labeled (rac)-Tolterodine.
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Tryptamine-d2-1 hydrochloride
0 ImagesCat. No.: HY-W014971SCAS No.: 362049-49-8Tryptamine-d2-1 hydrochloride is the deuterium labeled Tryptamine hydrochloride (HY-W014971). Tryptamine hydrochloride belongs to the class of indole alkaloids and is a derivative of the amino acid tryptophan. Tryptamine hydrochloride is psychoactive and acts as a neurotransmitter in the body, affecting mood, perception and cognition. In its hydrochloride form, Tryptamine hydrochloride hydrochloride, it is commonly used as a research chemical and as a starting material for the synthesis of other organic compounds. It can also occur naturally in certain plants and animals, including fungi and mammals. Due to the psychoactive properties of Tryptamine hydrochloride and its derivatives, its use and possession are controlled substances in many countries.
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CER6-2’S-d9
0 ImagesCat. No.: HY-146905SCAS No.: 2260670-11-7CER6-2’S-d9 is deuterium labeled CER6-2’S.
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Carazolol-d6 hydrochloride
0 ImagesCat. No.: HY-W777156CAS No.: 1184973-07-6Carazolol-d6 (hydrochloride) is deuterium labeled Carazolol hydrochloride (HY-W517264). Carazolol hydrochloride is a highly potent antagonist of β1/β2 adrenoceptor. Carazolol hydrochloride is also a potent, selective β3-adrenoceptor agonist. Carazolol hydrochloride can be used in the research of hypertension.
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Sulfasalazine-d3,15N
0 ImagesCat. No.: HY-14655S1Synonyms: NSC 667219-d3,15N; Salicylazosulfapyridine-d3,15NSulfasalazine-d3,15N is 15N and deuterated labeled Sulfasalazine (HY-14655). Sulfasalazine (NSC 667219) is an anti-rheumatic agent for the research of rheumatoid arthritis and ulcerative colitis. Sulfasalazine can suppress NF-κB activity. Sulfasalazine is a type 1 ferroptosis inducer.
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Cyproheptadine-d3
0 ImagesCat. No.: HY-B1622SCAS No.: 2712455-05-3Cyproheptadine-d3 is the d3-labeled Cyproheptadine (HY-B1622). Cyproheptadine acts as a p38 MAP kinase activator, CHK2 activator, histamine H1 receptor inhibitor and serotonin receptor inhibitor. Cyproheptadine mediates cell cycle arrest via G1 phase arrest, G1/S transition arrest, G0/G1 phase arrest, reduced expression of cyclins D1/D2/D3, upregulated expression of HBP1, p16, p21, p27, and decreased phosphorylation of retinoblastoma protein. Cyproheptadine induces Apoptosis by increasing PARP and cleaved PARP, as well as activating the mitochondrial caspase pathway. Cyproheptadine inhibits tumor growth with extremely low toxicity to normal cells. Cyproheptadine can be used in research related to hepatocellular carcinoma, multiple myeloma and acute myeloid leukemia.
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D-Fructose-d2-1
0 ImagesCat. No.: HY-N7092S18CAS No.: 478518-48-8Synonyms: D(-)-Fructose-d2-1D-Fructose-d2-1 is the deuterium labeled D-Fructose. D-Fructose (D(-)-Fructose) is a naturally occurring monosaccharide found in many plants.
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CVT-2738-d8
0 ImagesCat. No.: HY-W009512SCAS No.: 2749349-06-0Synonyms: RS-94287-d8N-(2,6-Dimethylphenyl)-2-(piperazin-1-yl)acetamide-d8 is the deuterium labeled N-(2,6-Dimethylphenyl)-2-(piperazin-1-yl)acetamide.
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Simeprevir-13C,d3
0 ImagesCat. No.: HY-10241SSynonyms: TMC435-13C,d3; TMC435350-13C,d3Simeprevir-13C,d3 is the 13C- and deuterium labeled Simeprevir. Simeprevir is an oral, potent and highly specific hepatitis C virus (HCV) NS3/4A protease inhibitor with a Ki of 0.36 nM. Simeprevir inhibits HCV replication with an EC50 of 7.8 nM. Simeprevir also potently suppresses SARS-CoV-2 replication and synergizes with Remdesivir. Simeprevir inhibits the main protease (Mpro) and the RNA-dependent RNA polymerase (RdRp) of SARS-CoV-2, and also modulates host immune responses.
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(S)-Carvedilol-d4
0 ImagesCat. No.: HY-B0006BSCAS No.: 2747915-23-5Synonyms: (S)-BM 14190-d4(S)-Carvedilol-d4 is deuterium labeled (S)-Carvedilol. (S)-Carvedilol, the S-enantiomer of Carvedilol, is a non-selective β/α-1 blocker. (S)-Carvedilol exerts protection against the vascular or cardiac toxicity of Doxorubicin (DOX).
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Etofylline-d6
0 ImagesCat. No.: HY-165670SSynonyms: 7-(β-Hydroxyethyl)theophylline-d67-(β-Hydroxyethyl)theophylline-d6 (Etophyllie-d6, Hydoxyethyltheophyllie-d6) is deuterium labeled 7-(β-Hydroxyethyl)theophylline.
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Diacetylsulfanilamide-13C6
0 ImagesCat. No.: HY-W156511SDiacetylsulfanilamide-13C6 is the 13C6 labeled Diacetylsulfanilamide.
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DL-Methionine-d3
0 ImagesCat. No.: HY-N0325S3CAS No.: 284665-20-9DL-Methionine-d3 is the deuterium labeled DL-Methionine. DL-Methionine is an essential amino acid containing sulfur with oxidative stress defense effects. DL-Methionine can be used for animal natural feed. DL-Methionine also kills H. rostochiensis on potato plants.
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(1R,3r,5S)-Camonsertib-d3
0 ImagesCat. No.: HY-139609ASSynonyms: (1R,3r,5S)-RP-3500-d3 (1R,3r,5S)-ATR inhibitor 4-d3(1R,3r,5S)-Camonsertib-d3 ((1R,3r,5S)-RP-3500-d3) is the deuterated-labeled (1R,3r,5S)-Camonsertib.
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Minodronic acid-d4
0 ImagesCat. No.: HY-16322SCAS No.: 1807367-80-1Synonyms: YM-529-d4Minodronic acid-d4 (YM-529-d4) is deuterium labeled Minodronic acid (HY-16322). Minodronic acid (YM-529) is an FPP synthase inhibitor with an IC50 of 3 nM, and also an antagonist of P2X2/3 receptors with an IC50 of 62.7 μM. Minodronic acid induces tumor cell apoptosis and inhibits cell growth. Minodronic acid also suppresses bone resorption. Minodronic acid can be used in research related to osteoporosis and cancer.
