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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Fingolimod phosphate-d4
0 ImagesCat. No.: HY-15381SCAS No.: 1794828-93-5Synonyms: FTY720 phosphate-d4Fingolimod phosphate-d4 is deuterium labeled FTY720 Phosphate.
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1,2-Dioleoyl-sn-glycero-3-phosphocholine-d62
0 ImagesCat. No.: HY-178735SSynonyms: DOPC-d621,2-Dioleoyl-sn-glycero-3-phosphocholine-d62 (DOPC-d62) is the deuterium labeled 1,2-Dioleoyl-sn-glycero-3-phosphocholine.
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4-Chlorodiphenyl ether-d5
0 ImagesSynonyms: 4-CDE-d54-Chlorodiphenyl ether-d5 (4-CDE-d5) is the deuterium labeled 4-Chlorodiphenyl ether. 4-Chlorodiphenyl ether is an estrogen-mimicking active compound. 4-Chlorodiphenyl ether maintains the survival of endometriotic cysts and exhibits estrogenic activity associated with the growth of endometriotic implants. 4-Chlorodiphenyl ether can be used in research related to endometriosis.
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Terizidone-15N2,d6
0 ImagesCat. No.: HY-W702303Terizidone-15N2,d6 is the deuterium and 15N-labeled Terizidone (HY-112324). Terizidone is an antibacterial agent, and shows bacteriostatic activity. Terizidone can be used in tuberculosis (TB) research.
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Sofpironium-13C,d3 bromide
0 ImagesCat. No.: HY-109013SSynonyms: BBI 4000-13C,d3Sofpironium-13C,d3 bromide (BBI 4000-13C,d3) is the deuterium and 13C-labeled Sofpironium bromide (HY-109013). Sofpironium bromide (BBI 4000) is an anticholinergic agent used in the study of primary axillary hyperhidrosis (PAH). Sofpironium bromide reduces sweating by inhibiting M3 muscarinic receptors in eccrine glands at the application site. Sofpironium bromide also has a high afnity for the M1, M2, M4 and M5 subtypes.
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8,12-iso-iPF2α-VI-d11
0 ImagesCat. No.: HY-137119ASCAS No.: 1616977-85-58,12-iso-iPF2α-VI-d11 is the deuterium labeled 8,12-iso-iPF2α-VI.
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16-Hydroxyhexadecanoic acid-13C2
0 ImagesCat. No.: HY-W068212SSynonyms: Juniperic acid-13C216-Hydroxyhexadecanoic acid-13C2 (Juniperic acid-13C2) is the 13C-labeled 16-Hydroxyhexadecanoic acid (HY-W068212). 16-Hydroxyhexadecanoic acid (Juniperic acid) is one of the main monomers of cutin in Vicia faba flower petals. 16-Hydroxyhexadecanoic acid can be used as an internal standard for the measurement of hydroxy and hydroperoxy fatty acids in plasma
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Muscarine-d9 iodide
0 ImagesCat. No.: HY-107654SSynonyms: (+)-Muscarine-d9 iodideMuscarine-d9 (iodide) is the deuterium labeled Muscarine iodide. Muscarine ((+)-Muscarine) iodide is a toxin that can stimulate the parasympathetic nervous system. Muscarine iodide is a prototype muscarinic acetylcholine receptor agonist.
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N-(2-Iodophenyl)-4-methylbenzenesulfonamide-d4
0 ImagesCat. No.: HY-W711137Synonyms: N-Tosyl-2-iodoaniline-d4N-(2-Iodophenyl)-4-methylbenzenesulfonamide-d4 (N-Tosyl-2-iodoaniline-d4) is the deuterium labeled N-(2-Iodophenyl)-4-methylbenzenesulfonamide (HY-W024801).
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L-Tyrosine-d1
0 ImagesCat. No.: HY-178277SCAS No.: 63570-47-8L-Tyrosine-d1 is the deuterium labeled L-Tyrosine (HY-N0473). L-Tyrosine is a non-essential amino acid which can inhibit citrate synthase activity in the posterior cortex.
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rac-trans-N-Desmethyl sertraline-d3 (hydrochloride)
0 ImagesCat. No.: HY-139689Srac-trans-N-Desmethyl sertraline-d3 (hydrochloride) is the deuterium labeled rac-trans-N-Desmethyl sertraline hydrochloride.
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Hydroflumethiazide-13C,d2
0 ImagesCat. No.: HY-W011240SCAS No.: 1189877-11-9Synonyms: Methforylthiazidine-13C,d2; Rontyl-13C,d2Hydroflumethiazide-13C,d2 is the deuterium and 13C labeled Hydroflumethiazide.
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7β-Tibolone-d5
0 ImagesCat. No.: HY-W701410S7β-Tibolone-d5 is the deuterium labeled 7β-Tibolone.
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Pregnenolone monosulfate sodium-13C2,d2
0 ImagesCat. No.: HY-110189SCAS No.: 2483824-22-0Synonyms: 3β-Hydroxy-5-pregnen-20-one monosulfate sodium-13C2,d2Pregnenolone monosulfate (sodium)-13C2,d2 is the 13C- and deuterium labeled Pregnenolone monosulfate sodium. Pregnenolone monosulfate sodium (3β-Hydroxy-5-pregnen-20-one monosulfate sodium) is a powerful neurosteroid, the main precursor of various steroid hormones including steroid ketones. Pregnenolone monosulfate sodium salt acts as a signaling-specific inhibitor of cannabinoid CB1 receptor, inhibits the effects of tetrahydrocannabinol (THC) that are mediated by the CB1 receptors. Pregnenolone monosulfate sodium salt can protect the brain from cannabis intoxication. Pregnenolone monosulfate sodium salt is also a TRPM3 channel activator, and also can weakly activate TRPM1 channels.
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3-O-Methyl-D-glucopyranose-13C6
0 ImagesCat. No.: HY-W145482S13-O-Methyl-D-glucopyranose-13C6 is 13C-labeled 3-O-Methyl-D-glucopyranose (HY-W145482). 3-O-Methyl-D-glucopyranose is a non-metabolizable glucose analog. 3-O-Methyl-D-glucopyranose exerts a protective effect against alloxan-induced damage to rat pancreatic islet β cells. 3-O-Methyl-D-glucopyranose can be used in diabetes research.
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Relugolix-d6
0 ImagesCat. No.: HY-16474SPurity: 98.02%Synonyms: TAK-385-d6Relugolix-d6 is deuterium labeled Relugolix. Relugolix (TAK-385)?is a potent, orally active, nonpeptidic gonadotropin-releasing hormone (GnRH) antagonist. Relugolix possesses high affinity and potent antagonistic activity for human receptor (binding IC50=0.33 nM) and monkey receptor (IC50=0.32 nM) compared with TAK-013 (HY-100209). Relugolix is used for the study of sex-hormone-dependent diseases, such as including endometriosis, uterine fibroids and prostate cancer et al.
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N-Desmethyl-Atomoxetine labeled-d5 hydrochloride
0 ImagesCat. No.: HY-157207SCAS No.: 2712570-39-1N-Desmethyl-Atomoxetine labeled-d5 hydrochloride is the deuterium labeled N-Desmethyl-Atomoxetine labeled hydrochloride.
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5α-Cholesta-7,24-dien-3β-ol-d6
0 Images5α-Cholesta-7,24-dien-3β-ol-d6 is deuterium labeled 5α-Cholesta-7,24-dien-3β-ol. 5α-Cholesta-7,24-dien-3β-ol, a sterol, can be found in hamster cauda epididymal mature spermatozoa.
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Sulindac sulfone-d3
0 ImagesCat. No.: HY-B1787SCAS No.: 250608-67-4Sulindac sulfone-d3 is deuterium labeled Sulindac sulfone.
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Nifuraldezone-15N3
0 ImagesCat. No.: HY-146976SNifuraldezone-15N3 is the 15N3 labeled Nifuraldezone.
