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.
All Product Categories
-
Isotope-Labeled Compounds Produits associés (11102)
Produits associés (11102)
-
4-Nonyl phenol diethoxylate-13C6
0 ImagesCat. No.: HY-W778259CAS No.: 1346602-11-64-Nonyl phenol diethoxylate-13C6 is the 13C-labeled 4-Nonyl phenol diethoxylate.
-
Tetrabromobisphenol A-13C12
0 ImagesCat. No.: HY-W780180CAS No.: 1352876-39-1Tetrabromobisphenol A-13C12 is 13C labeled Tetrabromobisphenol A.
-
CER11-2’S-d9
0 ImagesCat. No.: HY-146937SCAS No.: 2260670-22-0CER11-2’S-d9 is deuterium labeled CER11-2’S.
-
6-Hydroxy Chlorzoxazone-13C6
0 ImagesCat. No.: HY-W777188CAS No.: 475295-90-06-Hydroxy Chlorzoxazone-13C6 is a the 13C-labeled 6-Hydroxy Chlorzoxazone (HY-W016221). 6-Hydroxy Chlorzoxazone is a metabolite of Chlorzoxazone (HY-B1462). Chlorzoxazone is a centrally acting muscle relaxant used to treat muscle spasm and the resulting pain or discomfort.
-
Epinastine-13C,d3 hydrobromide
0 ImagesCat. No.: HY-B0640SSynonyms: WAL801-13C,d3 hydrobromideEpinastine-13C,d3 (hydrobromide) is the 13C- and deuterium labeled Epinastine. Epinastine (WAL801) is an antihistamine and mast cell stabilizer. Epinastine is a potent, selective and orally-active histamine H1 receptor antagonist. Epinastine also inhibits IL-8 release and has an antiallergic action.
-
Ipratropium-d7 bromide
0 ImagesCat. No.: HY-B0241S1Synonyms: Sch 1000-d7 bromideIpratropium-d7 (bromide)eis the deuterium labeled Ipratropium bromide. Ipratropium bromide (Sch 1000) is a muscarinic receptor antagonist, with binding IC50 values of 2.9 nM, 2 nM, and 1.7 nM for M1, M2, and M3 receptors, respectively. Ipratropium bromide can be used in the research for COPD (chronic obstructive pulmonary disease) and asthma.
-
N-Dansyl-d6 1,4-diaminobutane, 97% (CP)
0 ImagesCat. No.: HY-150665SN-Dansyl-d6 1,4-diaminobutane, 97% (CP) is the deuterium labeled N-Dansyl 1,4-diaminobutane, 97% (CP).
-
5-Aminosalicylic Acid-d3 hydrochloride
0 ImagesSynonyms: Mesalamine-D3 hydrochloride; 5-ASA-D3 hydrochloride; Mesalazine-D3 hydrochloride5-Aminosalicylic Acid-d3 (hydrochloride) is the deuterium labeled 5-Aminosalicylic Acid. 5-Aminosalicylic acid (Mesalamine) hydrochloride acts as a specific PPARγ agonist and also inhibits p21-activated kinase 1 (PAK1) and NF-κB.
-
2-(Dodecyloxy)ethanol-d25
0 ImagesCat. No.: HY-W771020CAS No.: 2469007-22-3Synonyms: Ethylene glycol monododecyl ether-d252-(Dodecyloxy)ethanol-d25 (Ethylene glycol monododecyl ether-d25) is the deuterium labeled 2-(Dodecyloxy)ethanol (HY-W250300). 2-(Dodecyloxy)ethanol is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
-
Paroxetine-d6-1
0 ImagesCat. No.: HY-122272S2CAS No.: 1435728-63-4Synonyms: BRL29060-d6-1Paroxetine-d6-1 (BRL29060-d6-1) is the deuterated-labeled Paroxetine (HY-122272). Paroxetine (BRL29060) is an orally active and selective serotonin reuptake inhibitor (SSRI) and apoptosis inducer with blood-brain barrier permeability. Paroxetine inhibits nitric oxide synthase and CYP2D6, induces desensitization of 5-HT1A/1B/1D autoreceptors, downregulates 5-HT2 receptors, and promotes the production of inflammatory cytokines. Paroxetine is a weak norepinephrine (NE) uptake inhibitor and possesses antitumor activity. Paroxetine is widely used in research concerning depression, obsessive-compulsive disorder, panic disorder, social phobia, generalized anxiety disorder, post-traumatic stress disorder, premenstrual dysphoric disorder, hot flashes, and related conditions.
-
Carbamazepine-d2,15N
0 ImagesCat. No.: HY-W653882Synonyms: CBZ-d2,15N; NSC 169864-d2,15NCarbamazepine-d2,15N is a deuterated labeled Carbamazepine-d2,15N.
-
Thyminose-13C
0 ImagesSynonyms: Deoxyribose-13CThyminose-13C is the 13C labeled Thyminose. Thyminose is an endogenous metabolite.
-
17β-Estradiol-13C3
0 Images17β-Estradiol-13C3 is the 13C labeled 17β-Estradiol.
-
Thymidine 5'-monophosphate-d13 dilithium
0 ImagesCat. No.: HY-W392933S5Synonyms: Thymidine-5'-phosphate-d13 dilithium
-
2-Methyl-3-hexanol-d4
0 ImagesCat. No.: HY-W286622SSynonyms: 1-Isopropyl-1-butanol-d4; 5-Methyl-4-hexanol-d42-Methyl-3-hexanol-d4 (1-Isopropyl-1-butanol-d4) is the deuterium labeled 2-Methylhexan-3-ol.
-
Esomeprazole-d3 sodium
0 ImagesCat. No.: HY-17021SSynonyms: (S)-Omeprazole-d3 sodium; (-)-Omeprazole-d3 sodiumEsomeprazole-d3 (sodium) is the deuterium labeled Esomeprazole. Esomeprazole ((S)-Omeprazole) is a potent and orally active proton pump inhibitor and reduces acid secretion through inhibition of the H+, K+-ATPase in gastric parietal cells. Esomeprazole has the potential for symptomatic gastroesophageal reflux disease research.
-
Flurbiprofen-d4
0 ImagesCat. No.: HY-10582S3Synonyms: dl-Flurbiprofen-d4Flurbiprofen-d4 is deuterated labeled Flurbiprofen (HY-10582). Flurbiprofen (dl-Flurbiprofen) is a potent, orally active nonsteroidal anti-inflammatory agent (NSAIA/NSAID), with antipyretic and analgesic activities. Flurbiprofen is commonly used for the research of inflammatory diseases, including osteoarthritis and rheumatoid arthritis. Flurbiprofen is a non-selective cyclooxygenase (COX) inhibitor that can be used for the research of colorectal cancer.
-
2-Oxobutanoic acid-13C,d1 sodium hydrate
0 ImagesCat. No.: HY-150628SCAS No.: 1049741-69-62-Oxobutanoic acid-13C,d1 sodium hydrate is the deuterium and 13C labeled 2-Oxobutanoic acid sodium hydrate.
-
1,2-Dipalmitoyl-sn-glycero-3-phosphoethanolamine-d9
0 ImagesCat. No.: HY-W040268S1CAS No.: 2747990-85-61,2-Dipalmitoyl-sn-glycero-3-phosphoethanolamine-d9 is deuterium labeled 1,2-Dipalmitoyl-sn-glycero-3-phosphoethanolamine. 1,2-Dipalmitoyl-sn-glycero-3-phosphoethanolamine is a phospholipid that is a major component of the lipid bilayer that surrounds cells and provides stability to the membrane.
-
(Rac)-Finerenone-d5
0 ImagesCat. No.: HY-W950003CAS No.: 2917530-31-3Synonyms: (Rac)-BAY 94-8862-d5(Rac)-Finerenone-d5 ((Rac)-BAY 94-8862-d5) is the deuterium labeled (Rac)-Finerenone (HY-111372A). (Rac)-Finerenone ((Rac)-BAY 94-8862) is the racemate of Finerenone. Finerenone is a third-generation, selective, and orally available nonsteroidal mineralocorticoid receptor (MR) antagonist (IC50=18 nM). Finerenone displays excellent selectivity versus glucocorticoid receptor (GR), androgen receptor (AR), and progesterone receptor (>500-fold).
