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 (11047)
Related Products (11047)
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Atazanavir-d15
0 ImagesCat. No.: HY-17367SCAS No.: 1092540-56-1Synonyms: BMS-232632-d15Atazanavir-d15 is the d15 labled Atazanavir (HY-17367). Atazanavir is a selective HIV-1 protease inhibitor.
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Pleconaril-d4
0 ImagesCat. No.: HY-19952SCAS No.: 2749329-20-0Synonyms: VP 63843-d4; Win 63843-d4Pleconaril-d4 is deuterium labeled Pleconaril.
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L-Hyoscyamine-d3-1
0 ImagesCat. No.: HY-N0471S1Synonyms: Hyoscyamine-d3L-Hyoscyamine-d3-1 (Hyoscyamine-d3) is the deuterium labeled L-Hyoscyamine (HY-N0471). L-Hyoscyamine (Daturine), a natural plant tropane alkaloid, is a potent and competitive muscarinic receptor (MR) antagonist. L-Hyoscyamine is a levo-isomer to Atropine (HY-B1205).
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1-Palmitoyl-sn-glycero-3-phosphocholine-d3
0 ImagesCat. No.: HY-W590534SCAS No.: 2692624-19-2Synonyms: 16:0 Lyso PC-d31-Palmitoyl-sn-glycero-3-phosphocholine-d3 is a deuterated phosphocholine.
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Nifurtimox-d4
0 ImagesCat. No.: HY-W040073SNifurtimox-d4 is deuterium labeled Nifurtimox. Nifurtimox, an antiprotozoal agent, which is generally used for the treatment of infections with Trypanosoma cruzi, has been used in the therapy of neuroblastoma. Nifurtimox affects enzyme activity of lactate dehydrogenase (LDH).
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9-Dihydroestradiol-d3
0 ImagesCat. No.: HY-143952SSynonyms: delta9,11-Estradiol-d39-Dihydroestradiol-d3 is the deuterium labeled 9-Dihydroestradiol.
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Acetamide-d5
0 ImagesAcetamide-d5 is the deuterium labeled Acetamide. Acetamide is used as an intermediate in the synthesis of methylamine, thioacetamide, and insecticides, and as a plasticizer in leather, cloth and coatings. Acetamide has carcinogenicity.
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1-Octanoyl-2-decanoyl-3-chloropropanediol-d5
0 ImagesCat. No.: HY-W749780CAS No.: 2692623-33-71-Octanoyl-2-decanoyl-3-chloropropanediol-d5 is a deuterated 3-monochloropropanediol (3-MCPD) glycidyl ester.
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(R,S)-Norcotinine-d4
0 ImagesCat. No.: HY-W010143SCAS No.: 1020719-70-3Synonyms: (Rac)-Norcotinine-d4(R,S)-Norcotinine-d4 is a deuterium labeled compound.
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Ioxitalamic acid-d4
0 ImagesCat. No.: HY-125695SCAS No.: 1185156-82-4Ioxitalamic acid-d4 is the deuterium labeled Loxitalamic acid (HY-125695). Ioxitalamic acid is a water-soluble, nephrophilic, highly permeable X-ray iodinated contrast media.
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Proadifen-d2
0 ImagesCat. No.: HY-121789SCAS No.: 151412-33-8
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Ac-D-Ala-OH-d3
0 ImagesCat. No.: HY-W012713S1CAS No.: 2714437-93-9Ac-D-Ala-OH-d3 is the deuterium labeled Ac-D-Ala-OH (HY-W012713). Ac-D-Ala-OH is an alanine derivative.
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D-Arabinose-d2
0 ImagesCat. No.: HY-N0059S4CAS No.: 2419933-20-1D-Arabinose-d2 is the deuterium labeled D-Arabinose (HY-N0059). D-Arabinose is is an orally active antidepressant and a growth inhibitor of C. elegans (IC50 is 7.5 mM). D-Arabinose can penetrate the blood-brain barrier, selectively interfere with the metabolism of D-ribose and D-fructose, and inhibit the growth of nematodes. D-Arabinose can also inhibit the synthesis of cell biofilm and exert antibacterial activity. D-Arabinose activates the ACSS2-PPARγ/TFEB-CRTC1 axis through the lysosomal AXIN-LKB1-AMPK pathway, inducing CRTC1 transcription, exerts antidepressant-like activity. D-Arabinose is the ring-opened form of the aldopentose D-?Arabinose (HY-N7082).
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Thio-TEPA-d12
0 ImagesCat. No.: HY-W701673CAS No.: 1276372-62-3
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NSC 90469-d4
0 ImagesCat. No.: HY-114557SSynonyms: 3,5-Diiodo-L-thyronine-d4NSC 90469-d4 (3,5-Diiodo-L-thyronine-d4) is the deuterium labeled NSC 90469 (HY-114557). NSC 90469 is an endogenous metabolite.
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5-(4-Hydroxyphenyl)-5-phenyl hydantoin-15N2,d5
0 ImagesCat. No.: HY-132948SCAS No.: 369656-71-35-(4-Hydroxyphenyl)-5-phenyl hydantoin-15N2,d5 is the deuterium and 15N labeled 5-(4-Hydroxyphenyl)-5-phenyl hydantoin.
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Cephalexin-d5 monohydrate
0 ImagesCat. No.: HY-B0200BSSynonyms: Cefalexin hydrate-d5; Cephacillin hydrate-d5Cephalexin-d5 (monohydrate) is the deuterium labeled Cephalexin monohydrate. Cephalexin monohydrate is a potent, orally active and the first-generation?cephalosporin antibiotic. Cephalexin monohydrate kills?gram-positive?and some?gram-negative bacteria?by disrupting the growth of the bacterial cell wall. Cephalexin monohydrate is used for the research of?pneumonia,?strep throat, and bacterial endocarditis, et al.
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Flibanserin-d4 hydrochloride
0 ImagesCat. No.: HY-A0095ASCAS No.: 2748630-46-6Synonyms: BIMT-17-d4 hydrochloride; BIMT-17BS-d4 hydrochlorideFlibanserin-d4 (BIMT-17-d4; BIMT-17BS-d4) hydrochloride is the d4-labeled Flibanserin hydrochloride (HY-A0095B). Flibanserin hydrochloride is an orally active serotonin 5-HT1A receptor agonist and 5-HT2A receptor antagonist with Ki values of 1 nM and 49 nM, respectively. Flibanserin hydrochloride binds to dopamine D4 receptors with an Ki value of 4-24 nM. Flibanserin hydrochloride shows anti-depression and anti-anxiety effect, can be used to hypoactive sexual desire disorder (HSDD) research-.
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5-Hydroxymebendazole-d3
0 ImagesCat. No.: HY-123305SCAS No.: 1173020-86-45-Hydroxymebendazole-d3 is a deuterium labeled 5-Hydroxymebendazole. 5-Hydroxymebendazole is the one metabolite of Benzimidazoles.
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eCF506-d5
0 ImagesCat. No.: HY-112096SSynonyms: NXP900-d5eCF506-d5 (NXP900-d5) is deuterated labeled eCF506 (HY-112096). eCF506 is a highly potent and orally active YES1/SRC kinase inhibitor with an IC50 of 0.47 nM. eCF506 locks its target into its native “closed” conformation, thereby inhibiting both kinase activity and complex formation with protein partners. eCF506 can be used for the study of esophageal squamous cancer and breast cancer.
