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Isotope-Labeled Compounds
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Isotope-Labeled Compounds Related Products (11097)
Related Products (11097)
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Scutellarein-d6
0 ImagesCat. No.: HY-W754220Synonyms: 6-Hydroxyapigenin-d6; 4',5,6,7-Tetrahydroxyflavone-d6Scutellarein-d6 (6-Hydroxyapigenin-d6) is deuterium labeled Scutellarein. -
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Gamma-6Z-Dodecenolactone-d2
0 ImagesCat. No.: HY-156260SCAS No.: 1082581-86-9Gamma-6Z-Dodecenolactone-d2 is deuterated labeled Gamma-6Z-Dodecenolactone. -
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Ceftiofur-d3 sodium
0 ImagesCat. No.: HY-B0898SCeftiofur-d3 sodium is deuterium labeled Ceftiofur sodium (HY-B0898). Ceftiofur sodium is a cell wall synthesis inhibitor that targets bacterial penicillin-binding proteins (PBPs) and has anti-inflammatory effects in endotoxemia. Ceftiofur sodium exerts bactericidal effects by inhibiting the synthesis of bacterial cell wall peptidoglycan, leading to bacterial cell lysis. Ceftiofur sodium also inhibits the activation of NF-κB and MAPKs, thereby reducing the secretion of pro-inflammatory cytokines such as TNF-α, IL-1β, and IL-6. -
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Ditiocarb-d10
0 ImagesCat. No.: HY-126363SCAS No.: 1261734-83-1Synonyms: Diethyldithiocarbamic acid-d10Ditiocarb-d10 (Diethyldithiocarbamic acid-d10) is the deuterium labeled Ditiocarb (HY-126363). Ditiocarb (Diethyldithiocarbamic acid) is an accelerator of the rate of copper cementation. Ditiocarb (Diethyldithiocarbamic acid) reduces the incidence of HIV infection, and also enhances adjuvant immunoresearch of high risk breast cancer. -
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2-Naphthaldehyde-13C
0 ImagesCat. No.: HY-Y0075S1CAS No.: 116815-49-72-Naphthaldehyde-13C is the 13C-labeled 2-Naphthaldehyde (HY-Y0075). 2-Naphthaldehyde belongs to naphthalene-based bis-aromatic aldehyde compounds. 2-Naphthaldehyde scavenges DPPH and ABTS+ free radicals, and exerts reductive effects by donating hydrogen atoms to interrupt free radical chain reactions. 2-Naphthaldehyde inhibits the growth and proliferation of colon cancer cells. 2-Naphthaldehyde serves as a substrate for NAD+-dependent salicylaldehyde dehydrogenase from Pseudomonas strain C6 and is catalytically oxidized. 2-Naphthaldehyde acts as a precursor material for the chemical synthesis of antioxidant Schiff bases. -
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3-Ethyladenine-d5 hydroiodide
0 ImagesCat. No.: HY-154763S3-Ethyladenine-d5 (hydroiodide) is deuterated labeled 3-Ethyladenine. -
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1-Docosahexaenoyl-sn-glycero-3-phosphocholine-d9
0 ImagesCat. No.: HY-W7702391-Docosahexaenoyl-sn-glycero-3-phosphocholine-d9 is the deuterium labeled 1-Docosahexaenoyl-sn-glycero-3-phosphocholine (HY-W587891). 1-Docosahexaenoyl-sn-glycero-3-phosphocholine is an ester product. -
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rel-Ritonavir-d6
0 ImagesSynonyms: rel-ABT 538-d6; rel-RTV-d6rel-Ritonavir-d6 (rel-ABT 538-d6) is the deuterium labeled rel-Ritonavir. rel-Ritonavir is a relative configuration of Ritonavir (HY-90001). Ritonavir (ABT 538) is an inhibitor of HIV protease used to study of HIV infection and AIDS. Ritonavir is also a SARS-CoV 3CLpro inhibitor with an IC50 of 1.61 μM. -
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Aldosterone-13C3
0 ImagesCat. No.: HY-W751098Aldosterone-13C3 is a 13C-labeled Aldosterone (HY-113313). Aldosterone is a primary mineralocorticoid and steroid hormone. -
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Tebuconazole-d6
0 ImagesCat. No.: HY-B0852S2Tebuconazole-d6 is a deuterium labeled Tebuconazole (HY-B0852). Tebuconazole is an orally active agricultural azole fungicide which can also inhibit CYP51 with IC50s of 0.9 and 1.3 μM for Candida albicans CYP51 (CaCYP51) and truncated Homo sapiens CYP51 (Δ60HsCYP51), respectively. Tebuconazole induces lipid accumulation and oxidative stress in HepG2 Cells. Tebuconazole decreases MAC-T cells viability and proliferation, induces ER-stress-mediated apoptosis and increases oxidative stress levels in MAC-T cells. -
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2,4-Dibromophenol-d3
0 Images2,4-Dibromophenol-d3 is the deuterium labeled 2,4-Dibromophenol. -
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S-(5'-Adenosyl)-L-methionine-13C5 sulfate
0 ImagesCat. No.: HY-W338810SS-(5'-Adenosyl)-L-methionine-13C5 sulfate is a 13C-labeled S-(5'-Adenosyl)-L-methionine. S-(5'-Adenosyl)-L-methionine is a methyl donor and cofactor. -
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3-Bromopropan-1-ol-d6
0 Images3-Bromopropan-1-ol-d6 is the deuterium labeled 3-Bromopropan-1-ol (HY-W007337). 3-Bromopropan-1-ol is an endogenous metabolite. 3-Bromopropan-1-ol is significantly upregulated during the estrus period in buffaloes. 3-Bromopropan-1-ol can be used in buffalo estrus research. -
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Emtricitabine-d2
0 ImagesCat. No.: HY-17427S4Synonyms: BW1592-d2Emtricitabine-d2 (BW1592-d2) is deuterium labeled Emtricitabine. Emtricitabine is a nucleoside reverse transcriptase inhibitor (NRTI) with an EC50 of 0.01 μM in PBMC cell. It is an antiviral agent for the treatment of HIV infection. -
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1β-Hydroxydeoxycholic acid-d5
0 ImagesCat. No.: HY-113482SSynonyms: 1β-OH-DCA-d51β-Hydroxydeoxycholic Acid-d5 is the deuterium labeled 1β-Hydroxydeoxycholic Acid. -
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1-Indanamine-d9 hydrochloride
0 ImagesCat. No.: HY-Y0484SCAS No.: 2012598-74-0Synonyms: 1-Aminoindan-d9 hydrochloride; 1-Aminoindane-d9 hydrochloride; NSC 186227-d9 hydrochloride; 1-Aminoindane-d9 hydrochloride1-Indanamine-d9 (1-Aminoindan-d9; 1-Aminoindane-d9; NSC 186227-d9; 1-Aminoindane-d9) hydrochloride is deuterium-labeled 1-Indanamine hydrochloride (HY-Y0484). -
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Tazobactam-15N,d2
0 ImagesCat. No.: HY-B1418S2Synonyms: CL-298741-15N,d2; YTR-830H-15N,d2Tazobactam-15N,d2 (CL-298741-15N,d2) is 15N and deuterium labeled Tazobactam. Tazobactam (CL-298741) is a potent β-lactamases inhibitor and penicillin antibiotic. Tazobactam has antibacterial activity. Tazobactam can be used for pneumonia research. -
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2-(3-Carbamoyl-1-((6-chloropyridin-3-yl)methyl)ureido)ethane-1-sulfonate (sodium)-d4
0 ImagesCat. No.: HY-165704S2-(3-Carbamoyl-1-((6-chloropyridin-3-yl)methyl)ureido)ethane-1-sulfonate (sodium)-d4 is deuterium labeled 2-(3-Carbamoyl-1-((6-chloropyridin-3-yl)methyl)ureido)ethane-1-sulfonate (sodium). -
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Diclofenamide-13C6
0 ImagesCat. No.: HY-W778555CAS No.: 1391054-76-4Diclofenamide-13C6 is 13C-labeled Diclofenamide (HY-B0397). -
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Milnacipran-d10 hydrochloride
0 ImagesMilnacipran-d10 (hydrochloride) is the deuterium labeled Milnacipran hydrochloride (HY-B0168A). Milnacipran hydrochloride is an orally active Serotonin (HY-B1473A) and Norepinephrine (HY-13715) reuptake inhibitor. Milnacipran hydrochloride inhibits monoamine transporters, especially the norepinephrine transporter and the serotonin transporter (Ki values of 31 and 8.5 nM, respectively). Milnacipran hydrochloride inhibits pERK1/2 activation. Milnacipran hydrochloride has antidepressant, anxiolytic and analgesic properties. Milnacipran hydrochloride inhibits biting behavior in mice. Milnacipran hydrochloride can be used in the study of major depressive disorder, anxiety disorders, and neuropathic pain (e.g., fibromyalgia). -
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