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 (11128)
Related Products (11128)
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Acetohydrazide-d3
0 ImagesCat. No.: HY-Y0626SCAS No.: 1028333-41-6Synonyms: Ethanehydrazonic acid-d3Acetohydrazide-d3 (Ethanehydrazonic acid-d3) is deuterium labeled Acetohydrazide. Acethydrazide is an organic building that undergo catalytic hydrogenation to produce N′-methyl acethydrazide (MAH).
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2,4-Dimethylthiazole-13C3
0 ImagesCat. No.: HY-W012932SCAS No.: 1335402-15-72,4-Dimethylthiazole-13C3 is 13C labeled 2,4-Dimethylthiazole.
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Venlafaxine-d10 hydrochloride
0 ImagesCat. No.: HY-B0196ASCAS No.: 1216539-56-8Venlafaxine-d10 (hydrochloride) is the deuterium labeled Venlafaxine hydrochloride. Venlafaxine (Wy 45030) hydrochloride is an orally active, potent serotonin (5-HT)/norepinephrine (NE) reuptake dual inhibitor. Venlafaxine is an antidepressant.
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2,3,6,7-Tetrachloro-naphthalene-13C10
0 ImagesCat. No.: HY-W703429S2,3,6,7-Tetrachloro-naphthalene-13C10 is 13C labeled 2,3,6,7-Tetrachloronaphthalene.
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Linalool-13C3
0 ImagesCat. No.: HY-N0368S1Linalool-13C3 is 13C labeled Linalool (HY-N0368). Linalool is a natural monoterpene which is a competitive NMDA receptor antagonist. Linalool is orally active and crosses the blood-brain barrier. Linalool has anticancer, antibacterial, anti-inflammatory, neuroprotective, anxiolytic, antidepressant, anti-stress, cardioprotective, hepatoprotective, nephroprotective and pulmonary protective activities.
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Tolvaptan-d7
0 ImagesCat. No.: HY-17000SCAS No.: 1246818-18-7Tolvaptan-d7 is the deuterium labeled Tolvaptan. Tolvaptan is a selective, competitive arginine vasopressin receptor 2 antagonist with an IC50 of 1.28μM for the inhibition of AVP-induced platelet aggregation.
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Bendroflumethiazide-d7
0 ImagesCat. No.: HY-B1363S1Synonyms: Bendrofluazide-d7Bendroflumethiazide-d7 (Bendrofluazide-d7) is deuterium labeled Bendroflumethiazide (HY-B1363). Bendroflumethiazide (Bendrofluazide) is an orally available diuretic. Bendroflumethiazide inhibits the electroneutral sodium-chloride symporter located in the apical membrane of the early segment of the distal convoluted tubule and can effectively lower blood pressure. Bendroflumethiazide is used in the study of hypertension and edema. Bendroflumethiazide has an antidiuretic effect in diabetes insipidus.
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Hexabromobenzene-13C6
0 ImagesCat. No.: HY-W140740SCAS No.: 2483735-50-6Synonyms: Perbromobenzene-13C6Hexabromobenzene-13C6 (Perbromobenzene-13C6) is 13C labeled Hexabromobenzene.
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Dibenzo[a,c]anthracene-13C6
![Dibenzo[a,c]anthracene-13C6](https://file.medchemexpress.com/product_pic/hy-w011577s1.gif "Click to View Dibenzo[a,c]anthracene-13C6 Product Detail")
0 ImagesCat. No.: HY-W011577S1Synonyms: 2,3-Benzotriphenylene-13C6Dibenzo[a,c]anthracene-13C6 (2,3-Benzotriphenylene-13C6) is 13C labeled Benzo[f]tetraphene. Benzo[f]tetraphene (Dibenz[a,c]anthracene) is a polycyclic aromatic hydrocarbon with significant antitumor activity. Benzo[f]tetraphene is used as a luminescent probe in cell biology research and can effectively detect reactive oxygen species in biological systems. Benzo[f]tetraphene can also be used as a potential photosensitizer and shows good application prospects in photodynamic inhibition.
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Erlotinib-d4
0 ImagesCat. No.: HY-50896S2CAS No.: 1130852-41-3Synonyms: CP-358774-d4; NSC 718781-d4; OSI-774-d4Erlotinib-d4 (CP-358774-d4) is the deuterated-labeled Erlotinib (HY-50896). Erlotinib (CP-358774) is a selective, orally active EGFR tyrosine kinase inhibitor. Erlotinib also acts as a substrate and inhibitor of OATP2B1, with an IC50 of approximately 0.079 μM for inhibiting OATP2B1-mediated uptake of estrone 3-sulfate. Erlotinib blocks EGFR phosphorylation, downstream signal transduction, as well as the growth and proliferation of cancer cells. Erlotinib inhibits MMP-10-mediated renal injury, fibrotic lesions, the ERK1/2, GSK-3β and β-catenin signaling pathways, fibronectin, α-SMA, collagen deposition, and renal injury markers. Erlotinib is metabolized via CYP3A to produce the active metabolite OSI-420. Erlotinib can be used in research related to non-small cell lung cancer, gastric cancer, papillary renal cell carcinoma, pancreatic cancer, renal fibrosis, and other conditions.
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(Rac)-5-Carboxy desisopropyl tolterodine-d7
0 ImagesCat. No.: HY-132353SCAS No.: 1189868-60-7(Rac)-5-Carboxy desisopropyl tolterodine-d7 is the deuterium labeled (Rac)-5-Carboxy desisopropyl tolterodine.
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Sodium 2-((2,6-bis(methyl-d3)phenyl-3,4,5-d3amino)-2-oxoethane-1-sulfonate
0 ImagesCat. No.: HY-165693SSodium 2-((2,6-bis(methyl-d3)phenyl-3,4,5-d3)amino)-2-oxoethane-1-sulfonate is deuterium labeled Sodium 2-((2,6-dimethylphenyl)amino)-2-oxoethane-1-sulfonate.
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Imiquimod-d7
0 ImagesCat. No.: HY-B0180S2Synonyms: R 837-d7Imiquimod-d7 (R 837-d7) is deuterium labeled Imiquimod. Imiquimod (R 837), an immune response modifier, is a selective toll like receptor 7 (TLR7) agonist. Imiquimod exhibits antiviral and antitumor effects in vivo. Imiquimod can be used for the research of external genital, perianal warts, cancer and COVID-19.
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1,3-Dimethoxybenzene-d3
0 ImagesCat. No.: HY-34487S3CAS No.: 78955-99-4Synonyms: Resorcinol dimethyl ether-d31,3-Dimethoxybenzene-d3 (Resorcinol dimethyl ether-d3) is the deuterium labeled 1,3-Dimethoxybenzene (HY-34487). 1,3-Dimethoxybenzene belongs to the class of organic compounds known as dimethoxybenzenes. 1,3-Dimethoxybenzene is an intermediate in synthesis of organic compounds.
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N-Acetyl-S-(2,5-dimethylbenzene)-L-cysteine-d3
0 ImagesCat. No.: HY-144362SCAS No.: 1331909-07-9N-Acetyl-S-(2,5-dimethylbenzene)-L-cysteine-d3 is the deuterium labeled N-Acetyl-S-(2,5-dimethylbenzene)-L-cysteine.
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1-(5-Fluoropentyl)-1H-indole-3-carboxylic acid-d5
0 ImagesCat. No.: HY-114553SCAS No.: 2703812-55-7Synonyms: 5F-PB-223-Carboxyindolemetabolite-d51-(5-Fluoropentyl)-1H-indole-3-carboxylic acid-d5 (5F-PB-223-Carboxyindolemetabolite-d5) is deuterium labeled 1-(5-Fluoropentyl)-1H-indole-3-carboxylic acid.
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3,4-Dichlorodiphenyl ether-13C12
0 ImagesCat. No.: HY-W617979S3,4-Dichlorodiphenyl ether-13C12 is 13C labeled 3,4-Dichlorodiphenyl ether.
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Omeprazole-d3 sodium
0 ImagesCat. No.: HY-B0113S4Synonyms: H 16868-d3 sodiumOmeprazole-d3 sodium is deuterated labeled Omeprazole (HY-B0113). Omeprazole sodium (H 16868) is an orally active H+,K+-ATPase inhibitor and a proton pump inhibitor. Omeprazole sodium competitively inhibits CYP2C19, CYP3A4, and CYP2C9 activity. Omeprazole sodium inhibits gastric acid secretion and can be used for acid-related gastrointestinal disorders. Omeprazole sodium inhibits pancreatic cancer cell proliferation, induces apoptosis, autophagosome accumulation (elevated LC3-I and LC3-II levels), oxidative stress, and cytogenetic imbalance, modulates lysosomal transport, reduces inflammatory cytokines. Omeprazole sodium alters small intestinal morphology and magnesium absorption, and induces gastric mucosa morphologic changes. Omeprazole sodium also has neuroprotective and antibacterial effects.
