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Isotope-Labeled Compounds Related Products (11050)
Related Products (11050)
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N-Nitrosonornicotine-d4
0 ImagesCat. No.: HY-W743781CAS No.: 1426174-36-8Synonyms: (2S)-N'-Nitrosonornicotine-d4N-Nitrosonornicotine-d4 ((2S)-N'-Nitrosonornicotine-d4) is deuterium labeled N-Nitrosonornicotine. N-Nitrosonornicotine is a tobacco-specific nitrosamine that has carcinogenic and mutagenic activity, and it can induce micronuclei in C3A cells. N-Nitrosonornicotine can form DNA adducts. -
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3-Chloro-2-(stearoyloxy)propyl-1,1,2,3,3-d5 oleate
0 ImagesCat. No.: HY-W701859CAS No.: 2489621-82-9Synonyms: 1-Oleoyl-2-Stearoyl-3-chloropropanediol-d53-Chloro-2-(stearoyloxy)propyl-1,1,2,3,3-d5 oleate (1-Oleoyl-2-Stearoyl-3-chloropropanediol-d5) is deuterium labeled 3-Chloro-2-(stearoyloxy)propyl-1,1,2,3,3 oleate. -
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Octinoxate-13C,d3
0 ImagesCat. No.: HY-B1234SOctinoxate-13C,d3 is the deuterium labeled Octinoxate (HY-W245806). Octinoxate (Octyl methoxycinnamate) is a thyroid hormone receptor agonist, reducing the levels of triiodothyronine (T3) and thyroxine (T4) and transcription levels of genes related to type II deiodinase (deio2) in Japanese Medaka. Octinoxate is commonly used as a safe ultraviolet (UV) filter used in the aquatic environment. Octinoxate inhibits CYP1A1 and CYP1B1 to regulate hyaluronan (HA) (HY-B0633A) metabolism in a PI3K pathway-dependent manner in human keratinocytes. Octinoxate also exhibits an anti-estrogenic and anti-androgenic effect in vitro and in vivo. -
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Carfentrazon-ethyl-d5
0 ImagesCat. No.: HY-W725480CAS No.: 2140327-60-0 -
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TC-N 1752-d5
0 ImagesCat. No.: HY-107405S -
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Hydroxy Torsemide-d7
0 ImagesCat. No.: HY-132466SCAS No.: 1329613-35-5Hydroxy Torsemide-d7 is the deuterium labeled Hydroxy Torsemide. -
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Pamapimod-d4
0 ImagesCat. No.: HY-10405SCAS No.: 1246814-57-2Pamapimod-d4 (Ro4402257-d4) is the deuterium labeled Pamapimod. Pamapimod (Ro4402257) is a potent, selective and orally active p38 MAPK inhibitor with IC50s of 14 nM and 480 nM and Kis of 1.3 nM and 120 nM for p38α and p38β, respectively. Pamapimod has no activity against p38δ or p38γ isoforms. Pamapimod has the potential for rheumatoid arthritis and other autoimmune diseases treatment. -
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Granisetron-d6 (Standard)
0 ImagesCat. No.: HY-B0071S2CAS No.: 1224925-80-7Synonyms: BRL 43694-d6 (Standard)Granisetron-d6 (BRL 43694-d6) is deuterium labeled Granisetron. Granisetron (BRL 43694) is a serotonin 5-HT3 receptor antagonist used as an antiemetic to treat nausea and vomiting following chemotherapy. -
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Haloperidol-d4 N-Oxide
0 ImagesCat. No.: HY-14538S2CAS No.: 1246815-56-4Haloperidol-d4 N-Oxide is the deuterium labeled Haloperidol. Haloperidol is a potent dopamine D2 receptor antagonist, widely used as an antipsychotic. -
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2'-Deoxyadenosine monohydrate-15N5
0 ImagesCat. No.: HY-W011683S72'-Deoxyadenosine monohydrate-15N5 is the 15N labeled 2'-Deoxyadenosine monohydrate (HY-W011683). 2′-Deoxyadenosine monohydrate is an adenine nucleoside that inhibits glucose-stimulated insulin release. 2′-Deoxyadenosine monohydrate inhibits glucose-stimulated increases seen in islet cyclic AMP (cAMP) accumulation. 2'-Deoxyadenosine monohydrate activates caspase-3 and promotes apoptosis. 2'-Deoxyadenosine monohydrate inhibits the activity of S-adenosyl-L-homocysteine hydrolase (SAHH). 2'-Deoxyadenosine monohydrate inhibits the growth of various cells. 2'-Deoxyadenosine monohydrate has an anticancer effect on colon cancer. -
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Cefalonium-d4 hydrate
0 ImagesCat. No.: HY-B1252ASCefalonium-d4 hydrate is the deuterated-labeled Cefalonium hydrate (HY-B1252A). Cefalonium hydrate is a first-generation cephalosporin bactericidal antimicrobial agent. Cefalonium hydrate can be used in studies related to bovine mastitis, Staphylococcus aureus-induced mastitis and intramammary infections. -
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rel-(1S,2R)-Dihydro bupropion-d9
0 ImagesCat. No.: HY-W777138CAS No.: 1217684-77-9rel-(1S,2R)-Dihydro bupropion-d9 is the deuterium labeled rel-(1S,2R)-Dihydro bupropion (HY-178240). rel-(1S,2R)-Dihydro bupropion is a metabolite of bupropion. rel-(1S,2R)-Dihydro bupropion can promote endogenous IL-10 production and inhibit Th1 cytokines (IL-12 and TNF-α). rel-(1S,2R)-Dihydro bupropion can induce immune response transition from Th1 to Th2. rel-(1S,2R)-Dihydro bupropion can be used for research on inflammatory conditions. -
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6-Hydroxy Bentazon-d7
0 ImagesCat. No.: HY-132437SCAS No.: 1330180-76-16-Hydroxy Bentazon-d7 is the deuterium labeled 6-Hydroxy Bentazon. -
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S 8849-1-d4 free base
0 ImagesCat. No.: HY-166341SCAS No.: 1330822-91-7Synonyms: Tianeptine metabolite MC5-d4S 8849-1-d4 (free base) (Tianeptine metabolite MC5-d4) is deuterium labeled S 8849-1 (free base). S 8849-1 (free base) (Tianeptine metabolite MC5) is a Tianeptine (HY-90003) metabolite that is found in plasma. The mean elimination half-lives of S 8849-1 (free base) is 7.53 h in rats. S 8849-1 (free base) is promising for research of antidepressants. -
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Lovastatin-d3 hydroxy acid sodium
0 ImagesCat. No.: HY-123672SCAS No.: 1217528-38-5Lovastatin-d3 hydroxy acid (sodium) is the deuterium labeled Lovastatin hydroxy acid sodium. Lovastatin hydroxy acid sodium (Mevinolinic acid sodium) is a highly potent inhibitor of HMG-CoA reductase with a Ki of 0.6 nM. -
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RL71-d6
0 ImagesCat. No.: HY-121605SRL71-d6 is a deuterium labeled RL71 (HY-121605). RL71 is a curcuminoid anticancer agent that exhibits potent cytotoxicity against a variety of ER-negative breast cancer cells. RL71 (1 μM) induces cell cycle arrest in the G2/M phase and induces apoptosis in SKBr3 cells. RL7 also decreases HER2/neu phosphorylation and increases p27. RL71 also significantly reduced the phosphorylation of Akt and transiently increased the stress kinases JNK1/2 and p38 MAPK. Furthermore, RL71 exhibited anti-angiogenic potential in vitro, inhibiting the migration of HUVEC cells and the ability of these cells to form tubular networks. -
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Enalapril-d3
0 ImagesCat. No.: HY-B0331S1CAS No.: 1356847-94-3Synonyms: MK-421-d3Enalapril-d3 (MK-421-d3) is the deuterated-labeled Enalapril (HY-B0331). Enalapril is an orally active angiotensin-converting enzyme inhibitor. Enalapril blocks the conversion of angiotensin I to angiotensin II, regulates the renin-angiotensin system, reduces preload and afterload, and decreases plasma angiotensin II levels. Enalapril inhibits apoptosis, reduces nitric oxide metabolite levels, stabilizes endothelial cells, enhances endothelial antioxidant defense, scavenges reactive oxygen species (ROS), and alleviates neuronal damage. Enalapril attenuates glutathione depletion, protein/lipid oxidation, tissue damage, and type III collagen immunolabeling in organs of diabetic rats. Enalapril reduces systolic blood pressure and urinary albumin excretion, and delays the progression of diabetic cardiac/renal injury. Enalapril is used in research related to asymptomatic left ventricular dysfunction, congestive heart failure, Alzheimer's disease, diabetes mellitus, acute myocardial infarction, atrial fibrillation, hypertension, cerebral ischemia, chronic heart failure, and single-ventricle physiology. -
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- Mephenytoin-d3
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Indole-3-acetyl glutamate-d4
0 ImagesCat. No.: HY-W588263S1Synonyms: IAGlu-d4Indole-3-acetyl glutamate-d4 (IAGlu-d4) is deuterium labeled Indole-3-acetyl glutamate. Indole-3-acetyl glutamate (IAGlu) is a derivative of the plant hormone indole-3-acetic acid (IAA). As a conjugated form of IAA, Indole-3-acetyl glutamate involves in the transport, storage, and homeostatic regulation of IAA within the plant. Indole-3-acetyl glutamate can be used for research into the effects of plant hormones on the growth and development of plants. -
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Isosorbide mononitrate-13C6
0 ImagesCat. No.: HY-W777418CAS No.: 1217604-00-6Synonyms: Isosorbide-5-mononitrate-13C6Isosorbide mononitrate-13C6 (Isosorbide-5-mononitrate-13C6) is 13C-labeled Isosorbide mononitrate (HY-B0642). -
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