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 (11097)
Related Products (11097)
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(R)-Norfluoxetine phthalimide-d5
0 ImagesCat. No.: HY-133171AS1CAS No.: 1346617-46-6(R)-Norfluoxetine-d5 Phthalimide (Phenyl-d5) is the deuterium labeled (R)-Norfluoxetine Phthalimide (Phenyl).
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2-Hydroxycinnamic acid-d4
0 ImagesCat. No.: HY-W012531S22-Hydroxycinnamic acid-d4 is deuterium labeled 2-Hydroxycinnamic acid. 2-Hydroxycinnamic acid is a phenolic acid with antimicrobial and antioxidant properties. 2-Hydroxycinnamic acid has antimicrobial activity against Staphylococcus aureus and is not susceptible to drug resistance. 2-Hydroxycinnamic acid shows inhibitory effects on infection of HIV/SARS-CoV S pseudovirus with an IC50 of 0.3 mM. In addition, 2-Hydroxycinnamic acid has neuroprotective and antitumor activity.
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5-Octyldihydrofuran-2(3H)-one-d7
0 ImagesCat. No.: HY-W275481S2CAS No.: 1104979-35-2Synonyms: γ-Laurolactone-d75-Octyldihydrofuran-2(3H)-one-d7 is deuterated labeled 5-Octyldihydrofuran-2(3H)-one.
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Acotiamide-d4
0 ImagesCat. No.: HY-121467S1Synonyms: Z-338 free base-d4; YM443 free base-d4Acotiamide-d4 (Z-338 (free base)-d4) is deuterium labeled Acotiamide. Acotiamide is an orally active, selective and reversible acetylcholinesterase (AChE) inhibitor, with an IC50 of 1.79 μM. Acotiamide can enhance gastric contractility and accelerate delayed gastric emptying. Acotiamide has the potential for the research of functional dyspepsia involving gastric motility dysfunction and intestinal inflammatory.
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Lisinopril-13C5,15N
0 ImagesCat. No.: HY-18206S2Synonyms: MK-521-13C5,15NLisinopril-13C5,15N (MK-521-13C5,15N) is 13C and 15N labeled Lisinopril. Lisinopril (MK-521) is angiotensin-converting enzyme inhibitor, used in treatment of hypertension, congestive heart failure, and heart attacks.
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Vonedrine-d3 hydrochloride
0 ImagesCat. No.: HY-W701918CAS No.: 1246820-88-1Synonyms: Phenpromethamine-d3 hydrochloride; Methyl-(2-phenyl-propyl)-amine-d3 hydrochlorideVonedrine-d3 (Phenpromethamine-d3 ) hydrochloride is the deuterium labeled Vonedrine hydrochloride.
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Lacidipine-d10
0 ImagesCat. No.: HY-B0347SCAS No.: 1185245-62-8Lacidipine-d10 is the deuterium labeled Lacidipine. Lacidipine (Lacipil, Motens) is a L-type calcium channel blocker.
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Mianserin-d3 (hydrochloride)
0 ImagesCat. No.: HY-B0188ASCAS No.: 1219804-97-3Synonyms: Org GB 94-d3Mianserin-d3 hydrochloride is the deuterium labeled Mianserin. Mianserin (Mianserine) is an orally active H1 receptor antagonist. Mianserin can activate κ-opioid receptor and octopamine receptor. Mianserin increases ERK1/2 and CREB phosphorylation, and antagonizes full κ-opioid agonist and Dynorphin A (HY-P1333)-induced MAPK phosphorylation. Mianserin modulates social and exploratory behaviour, raises electroconvulsive thresholds. Mianserin can be used for the research of neurological disease, such as depression and epilepsy.
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1-Oleoyl-2-hydroxy-sn-glycero-3-phosphatidylethanolamine-d7
0 Images1-Oleoyl-2-hydroxy-sn-glycero-3-phosphatidylethanolamine-d7 is deuterium labeled 1-Oleoyl-2-hydroxy-sn-glycero-3-phosphatidylethanolamine.
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Oseltamivir-13C,d3 phosphate
0 ImagesCat. No.: HY-17016S3Synonyms: GS 4104-13C,d3 phosphateOseltamivir-13C,d3 (phosphate) (GS 4104-13C,d3 (phosphate)) is 13C labeled Oseltamivir (phosphate). Oseltamivir phosphate (GS 4104) is a neuraminidase inhibitor recommended for the treatment and prophylaxis of influenza A and B.
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Diphenidol-d10 hydrochloride
0 ImagesCat. No.: HY-A0082SSynonyms: Difenidol hydrochloride-d10Diphenidol-d10 (hydrochloride) (Difenidol hydrochloride-d10) is deuterium labeled Diphenidol (hydrochloride). Diphenidol hydrochloride (Difenidol hydrochloride) is a non-selective muscarinic M1-M4 receptor antagonist, has anti-arrhythmic activity. Diphenidol hydrochloride is also a potent non-specific blocker of voltage-gated ion channels (Na+, K+, and Ca2+) in neuronal cells. Diphenidol hydrochloride can be used in the study of antivertigo and antinausea.
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Nonanoyl-CoA-d17
0 ImagesCat. No.: HY-W706234Synonyms: Pelargonoyl-CoA-d17; S-Nonanoate coenzyme A-d17Nonanoyl-CoA-d17 (Pelargonoyl-CoA-d17) is the deuterium labeled Nonanoyl-CoA (HY-E70246). Nonanoyl-CoA is a medium-chain fatty acyl-CoA that can be used as substrate for the medium-chain hydrolase.
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(±)-Butyrylcarnitine-d9
0 ImagesCat. No.: HY-113168ASCAS No.: 2936622-23-8(±)-Butyrylcarnitine-d9 is deuterium labeled (±)-Butyrylcarnitine.
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2-Methylbutyl acetate-13C2
0 ImagesCat. No.: HY-W343292SCAS No.: 1335402-10-2Synonyms: Methyl-2-butyl-acetate fcc-13C22-Methylbutyl acetate-13C2 is 13C labeled 2-Methylbutyl acetate.
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Fmoc-His(Trt)-OH-15N3
0 ImagesCat. No.: HY-W010712S1CAS No.: 1217696-12-2Fmoc-His(Trt)-OH-15N3 is the 15N labeled Fmoc-His(Trt)-OH (HY-W010712). Fmoc-His (Trt)-OH is a histidine derivative. Fmoc-His(Trt)-OH has trityl (Trt) group to protect the side-chain of His. Fmoc-His(Trt)-OH has Fmoc group to protect -αNH2. Fmoc-His(Trt)-OH can be used for solid phase synthesis of peptides, providing protection against racemization and by-product formation.
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Posaconazole-d3
0 ImagesCat. No.: HY-17373S2Synonyms: SCH 56592-d3Posaconazole-d3 (SCH 56592-d3) is deuterium labeled Posaconazole. Posaconazole is a broad-spectrum, second generation, triazole compound with antifungal activity.
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Linagliptin-d5
0 ImagesCat. No.: HY-10284S4Synonyms: BI 1356-d5Linagliptin-d5 (BI 1356-d5) is deuterium labeled Linagliptin. Linagliptin is a highly potent, selective DPP-4 inhibitor with IC50 of 1 nM.
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Naloxone-d5
0 ImagesNaloxone-d5 is the deuterated-labeled Naloxone (HY-17417A). Naloxone is an orally active opioid receptor antagonist. Naloxone attenuates spinal cord stimulation‑associated anti‑hyperalgesic effects, antagonizes physiologic effects of endogenous opioid peptides linked to central nervous system injury sequelae, functions as a pressor agent to induce modest elevations in mean arterial blood pressure, exerts neuroprotective effects to improve post‑traumatic neurologic motor function, blocks opioid receptor‑mediated amnesic pathways, enhances memory consolidation, reverses Adrenocorticotropic hormone (ACTH) (HY-106373)‑ and epinephrine‑induced amnesia, and potentiates the memory‑facilitatory effects of ACTH and epinephrine.
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Asenapine-d3,13C
0 ImagesCat. No.: HY-10121S4CAS No.: 1217729-73-1Synonyms: Org 5222-d3,13CAsenapine-d3,13C (Org 5222-d3,13C) is deuterium and 13C labeled Asenapine. Asenapine (Org 5222), an atypical antipsychotic, is an antagonist of serotonin receptors (pKi: 8.4-10.5), adrenoceptors (pKi: 8.9-9.5), dopamine receptors (pKi: 8.9-9.4) and histamine receptors (pKi: 8.2-9.0). Asenapine can be used in the research of schizophrenia and bipolar disorder.
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L-Ornithine-1,2-13C2 hydrochloride
0 ImagesCat. No.: HY-W017018S1CAS No.: 224054-19-7L-Ornithine-1,2-13C2 hydrochloride is the 13C-labeled L-Ornithine hydrochloride (HY-W017018). L-Ornithine hydrochloride is an orally active CaSR and p38 activator. L-Ornithine hydrochloride inhibits ROS and supports urea cycle function. L-Ornithine hydrochloride can be used to study kidney diseases involving proximal tubular cell damage caused by oxidative stress or crystallopathy, as well as research related to anxiety disorders.
