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 (11092)
Related Products (11092)
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Duloxetine-d7 hydrochloride
0 ImagesCat. No.: HY-B0161AS1Synonyms: (S)-Duloxetine-d7 hydrochloride; LY248686-d7 hydrochlorideDuloxetine-d7 hydrochloride ((S)-Duloxetine-d7 hydrochloride) is the deuterium labeled Duloxetine hydrochloride (HY-B0161A). Duloxetine hydrochloride ((S)-Duloxetine hydrochloride) is a serotonin-norepinephrine reuptake inhibitor (SNRI) with a Ki of 4.6 nM, used for treatment of major depressive disorder and generalized anxiety disorder (GAD).
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Deulumateperone
0 ImagesCat. No.: HY-172425CAS No.: 2102683-75-8Deulumateperone is a deuterium labeled Lumateperone (HY-17637). Lumateperone is the orally active 5-HT2A receptor antagonist (Ki = 0.54 nM) and the modulator for dopamine receptor that exhibits antipsychotic and antineoplastic activities.
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2-Chloro-1,3-propanediol-13C3
0 Images2-Chloro-1,3-propanediol-13C3 is the 13C-labeled 2-Chloro-1,3-propanediol. 2-Chloro-1,3-propanediol is an ester product.
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Bazedoxifene-d4
0 ImagesCat. No.: HY-A0031SCAS No.: 1133695-49-4Synonyms: TSE-424-d4Bazedoxifene-d4 is deuterium labeled Bazedoxifene. Bazedoxifene (TSE-424) is an oral, BBB-penetrant nonsteroidal selective estrogen receptor modulator (SERM), with IC50s of 23 nM and 99 nM for ERα and ERβ, respectively. Bazedoxifene can be used for the research of osteoporosis. Bazedoxifene also acts as an inhibitor of IL-6/GP130 protein-protein interactions and can be used for the research of pancreatic cancer[1][2].
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Dienestrol-d8
0 ImagesCat. No.: HY-B1403S2Dienestrol-d8 is the deuterated-labeled Dienestrol (HY-B1403). Dienestrol is an orally active nonsteroidal estrogen. Dienestrol prevents the formation of implantation swellings in the uterus by inhibiting ovum discharge.
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N-Octyl 4-hydroxybenzoate-d4
0 ImagesCat. No.: HY-W150053SCAS No.: 2708282-26-0Synonyms: Octyl 4-hydroxybenzoate-d4N-Octyl 4-hydroxybenzoate-d4 is the deuterium labeled N-Octyl 4-hydroxybenzoate.
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Cytidine diphosphate-13C9,15N3 dilithium
0 ImagesCat. No.: HY-113400S2Purity: 99.7%
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Acetaminophen-13C6
0 ImagesCat. No.: HY-66005S3CAS No.: 2132405-57-1Synonyms: Paracetamol-13C6; 4-Acetamidophenol-13C6; 4'-Hydroxyacetanilide-13C6Acetaminophen-13C6 (Paracetamol-13C6) is the 13C-labeled Acetaminophen. Acetaminophen (Paracetamol) is a selective cyclooxygenase-2 (COX-2) inhibitor with an IC50 of 25.8 μM; is a widely used antipyretic and analgesic agent. Acetaminophen is a potent hepatic N-acetyltransferase 2 (NAT2) inhibitor.
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L-Serine-2-13C
0 ImagesSynonyms: (-)-Serine-2-13C; (S)-Serine-2-13CL-Serine-2-13C is the 13C-labeled L-Serine. L-Serine ((-)-Serine; (S)-Serine), one of the so-called non-essential amino acids, plays a central role in cellular proliferation.
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Tri-n-octyl trimellitate-d51
0 ImagesCat. No.: HY-W705545Tri-n-octyl trimellitate-d51 is the deuterium labeled Tri-n-octyl trimellitate.
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D-Erythrose-2-13C
0 ImagesCat. No.: HY-116956S1CAS No.: 83434-88-2D-Erythrose-2-13C is the 13C labeled D-Erythrose.
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Cholesteryl arachidonate-d8
0 ImagesCat. No.: HY-113369SPurity: 98.1%Cholesteryl arachidonate-d8 is deuterium labeled Cholesteryl arachidonate (HY-113369). Cholesteryl arachidonate, a lipid, is an endogenous metabolite. Cholesteryl arachidonate has antibacterial activity.
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2,3,4,5-Tetrachlorodiphenyl ether-13C12
0 ImagesCat. No.: HY-166903S2,3,4,5-Tetrachlorodiphenyl ether-13C12 is 13C labeled 2,3,4,5-Tetrachlorodiphenyl ether.
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Milrinone-d3
0 ImagesCat. No.: HY-14252SCAS No.: 2749393-50-6Milrinone-d3 is deuterium labeled Milrinone. Milrinone is a PDE3 inhibitor, and also an inotrope and vasodilator.
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Toceranib-d8
0 ImagesToceranib-d8 is the deuterium labeled Toceranib. Toceranib (SU11654) is an orally active receptor tyrosine kinase (RTK) inhibitor, and it potently inhibits PDGFR, VEGFR, and Kit with Kis of 5 and 6 nM for PDGFRβ and Flk-1/KDR, respectively. Toceranib (SU11654) has antitumor and antiangiogenic activity, and used in the treatment of canine mast cell tumors.
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(R)-2-Acetamidobutanoic acid-d5
0 ImagesCat. No.: HY-W718706CAS No.: 2714431-49-7Synonyms: Acetyl-D-2-aminobutyric acid-d5(R)-2-Acetamidobutanoic acid-d5 (Acetyl-D-2-aminobutyric acid-d5) is the deuterium labeled (R)-2-Acetamidobutanoic acid (HY-W101286).
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Tetrahydrofuran-2-carboxylic acid-d7
0 ImagesCat. No.: HY-W017763SCAS No.: 1219798-42-1Tetrahydrofuran-2-carboxylic acid-d7 is the deuterium labeled Tetrahydrofuran-2-carboxylic acid.
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Tenoxicam-d3
0 ImagesCat. No.: HY-B0440SCAS No.: 2140327-41-7Synonyms: Ro-12-0068-d3Tenoxicam-d3 is the deuterium labeled Tenoxicam. Tenoxicam (Ro-12-0068), an antiinflammatory agent with analgesic and antipyretic properties.
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1-(2-Chloropyridin-3-yl)ethanol-d3
0 ImagesCat. No.: HY-W051547S1Synonyms: 2-Chloro-3-(1-hydroxyethyl)pyridin-d31-(2-Chloropyridin-3-yl)ethanol-d3 (2-Chloro-3-(1-hydroxyethyl)pyridin-d3) is the deuterium labeled 1-(2-Chloropyridin-3-yl)ethanol.
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D-Allose-13C-1
0 ImagesCat. No.: HY-128741S1D-Allose-13C-1 is the 13C labeled D-Allose (HY-128741). D-Allose exhibits antitumor activity against various cancer cells. D-Allose scavenges reactive oxygen species (ROS) and reduces oxidative stress damage. D-Allose exhibits anti-inflammatory and neuroprotective through inhibition of TLR4/PI3K/AKT signaling pathway. D-Allose exhibits antihypertensive, cryoprotective, and anti-osteoporotic activities.
