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Verlukast-d6,MK-679-d6; L 668019-d6「同位素标记抑制剂」

Verlukast-d6,MK-679-d6; L 668019-d6「同位素标记抑制剂」

作者:德尔塔生物 日期:2025-08-13

生物活性:Verlukast-d6 is a deuterium labeled Verlukast. Verlukast is a potent, selective, and orally active antagonist of leukotriene receptor. Verlukast has the potential for the research of asthma[1].IC50 & Target:leukotriene receptor[1]分子量:521.12Formula:C26H21D6ClN2O3S2CAS 号:153698-86-3非标记 CAS:120443-16-5运输条件:Room temperature in continental US; may vary elsewhere.储存方式:Please store the product under the recommended conditions in the Certificate of Analysis.纯度 & 产品资料Data Sheet (526 KB)产品使用指南 (1538 KB)参考文献[1]. Dahlén B, et al. Effect of the leukotriene receptor antagonist MK-0679 on baseline pulmonary function in aspirin sensitive asthmatic subjects. Thorax. 1993;48(12):1205-1210. [Content Brief]

Galanthamine-O-methyl-d3,加兰他敏 d3「同位素标记抑制剂」

Galanthamine-O-methyl-d3,加兰他敏 d3「同位素标记抑制剂」

作者:德尔塔生物 日期:2025-08-13

生物活性:Galanthamine-O-methyl-d3 is the deuterium labeled Galanthamine. Galanthamine is a potent acetylcholinesterase (AChE) inhibitor with an IC50 of 500 nM.体外研究(In Vitro):Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].德尔塔生物 has not independently confirmed the accuracy of these methods. They are for reference only.Galanthamine-O-methyl-d3 相关抗体:ERK1/2 AntibodyE-Cadherin Antibody (YA470)Fatty Acid Synthase Antibody (YA766)DYKDDDDK Tag (FLAG) AntibodyGAPDH AntibodyGFP Antibodyp53 Antibody (YA250)RUNX2 AntibodyFerritin Heavy Chain AntibodyCOX2 AntibodyCtip2 AntibodyCyclin D1 Antibody (YA485)Cytochrome C Antibodyc-Myc AntibodyCyclin E1 AntibodyAIF Antibody (YA636)ALIX AntibodyCNPase AntibodyCortactin AntibodyCOX IV AntibodyCOX2/Cyclooxygenase 2 AntibodyCyclin A2 AntibodyCyclin B1 Antibody (YA486)DR5 AntibodyDrosha AntibodyE-Cadherin Antibody (YA778)EEA1 AntibodyEpCAM Antibody (YA772)Fatty Acid Synthase AntibodyFIP200 Antibody分子量:290.37Formula:C17H18D3NO3CAS 号:1279031-09-2非标记 CAS:357-70-0中文名称:加兰他敏 d3运输条件:Room temperature in continental US; may vary elsewhere.储存方式:Please store the product under the recommended conditions in the Certificate of Analysis.纯度 & 产品资料Data Sheet (528 KB)产品使用指南 (1538 KB)参考文献[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmaco

(rac-Etodolac-d3,依托度酸 d3「同位素标记抑制剂」

(rac-Etodolac-d3,依托度酸 d3「同位素标记抑制剂」

作者:德尔塔生物 日期:2025-08-13

生物活性:(rac)-Etodolac-d3 is a labelled racemic Etodolac. Etodolac (AY-24236) is a non-steroidal anti-inflammatory compound that is a non-selective inhibitor of COX (IC50=53.5 nM)体外研究(In Vitro):Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].德尔塔生物 has not independently confirmed the accuracy of these methods. They are for reference only.(rac)-Etodolac-d3 相关抗体:COX2 AntibodyCOX IV AntibodyCOX2/Cyclooxygenase 2 AntibodyCOX IV Antibody (YA867)Cyclooxygenase 1 Antibody (YA2537)Cyclooxygenase 2 Antibody (YA2541)分子量:290.37Formula:C17H18D3NO3CAS 号:1276197-46-6非标记 CAS:41340-25-4中文名称:依托度酸 d3运输条件:Room temperature in continental US; may vary elsewhere.储存方式:Please store the product under the recommended conditions in the Certificate of Analysis.纯度 & 产品资料Data Sheet (529 KB)产品使用指南 (1538 KB)参考文献[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. [Content Brief][2]. Riendeau D, et al. Biochemical and pharmacological profile of a tetrasubstituted furanone as a highly selective COX-2 inhibitor. Br J Pharmacol. 1997 May;121(1):105-17. [Content Brief][3]. Ito S, Tajima K, Nogawa M et al. Etodolac, a cyclooxygenase-2 inhibitor, attenuates paclitaxel-induced peripheral neuropathy in a mouse model of me

Alosetron-d3 hydrochloride,GR-68755C d3「同位素标记抑制剂」

Alosetron-d3 hydrochloride,GR-68755C d3「同位素标记抑制剂」

作者:德尔塔生物 日期:2025-08-13

生物活性:Alosetron-d3 (hydrochloride) is deuterium labeled Alosetron, which is a serotonin 5HT3-receptor antagonist.分子量:333.83Formula:C17H16D3ClN4OCAS 号:1189919-71-8非标记 CAS:122852-69-1性状:固体颜色:Off-white to light yellow中文名称:阿洛司琼盐酸盐 d3运输条件:Room temperature in continental US; may vary elsewhere.储存方式:-20°C, sealed storage, away from moisture*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

Nintedanib-d3,BIBF 1120-d3「同位素标记抑制剂」

Nintedanib-d3,BIBF 1120-d3「同位素标记抑制剂」

作者:德尔塔生物 日期:2025-08-13

生物活性:Nintedanib-d3 is the deuterium labeled Nintedanib. Nintedanib (BIBF 1120) is a potent triple angiokinase inhibitor for VEGFR1/2/3, FGFR1/2/3 and PDGFRα/β with IC50s of 34 nM/13 nM/13 nM, 69 nM/37 nM/108 nM and 59 nM/65 nM, respectively.体外研究(In Vitro):Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].德尔塔生物 has not independently confirmed the accuracy of these methods. They are for reference only.Nintedanib-d3 相关抗体:FGFR2/CD332 AntibodyPhospho-PDGFR beta (Y740) AntibodyVEGF Receptor 2 Antibody (YA014)FGFR1 AntibodyFGFR1 Oncogene Partner AntibodyFGFR2 AntibodyFGFR3 AntibodyPDGFR alpha AntibodyFGF2 AntibodyVEGF Receptor 1 AntibodyVEGFA AntibodyVEGF Receptor2 Antibody FGF1 Antibody (YA1430)PDGF B Antibody (YA1556)FGFR4 Antibody (YA1588)PLGF Antibody (YA1812)PDGFR beta Antibody (YA1925)VEGFD Antibody (YA2385)FGF19 Antibody (YA2672)TACC3 Antibody (YA2921)Phospho-PDGFR beta (Tyr740) Antibody (YA3062)FGF21 Antibody (YA3276)PGF Antibody (YA1434)Neuropilin 1 Antibody (YA1831)VEGFB Antibody (YA2627)分子量:542.64Formula:C31H30D3N5O4CAS 号:1624587-84-3非标记 CAS:656247-17-5中文名称:尼达尼布 d3运输条件:Room temperature in continental US; may vary elsewhere.储存方式:Please store the product under the recommended conditions in the Certificate of Analysis.纯度 & 产品资料Data Sheet (528 KB)产品使用指南 (1538 KB)参考

Vandetanib-d6,ZD6474-d6「同位素标记抑制剂」

Vandetanib-d6,ZD6474-d6「同位素标记抑制剂」

作者:德尔塔生物 日期:2025-08-13

生物活性:Vandetanib-d6 is the deuterium labeled Vandetanib. Vandetanib (D6474) is a potent, orally active inhibitor of VEGFR2/KDR tyrosine kinase activity (IC50=40 nM). Vandetanib also has activity versus the tyrosine kinase activity of VEGFR3/FLT4 (IC50=110 nM) and EGFR/HER1 (IC50=500 nM)[1].体外研究(In Vitro):Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].德尔塔生物 has not independently confirmed the accuracy of these methods. They are for reference only.Vandetanib-d6 相关抗体:ERK1/2 AntibodyE-Cadherin Antibody (YA470)Fatty Acid Synthase Antibody (YA766)DYKDDDDK Tag (FLAG) AntibodyGAPDH AntibodyGFP Antibodyp53 Antibody (YA250)RUNX2 AntibodyFerritin Heavy Chain AntibodyCOX2 AntibodyCtip2 AntibodyCyclin D1 Antibody (YA485)Cytochrome C Antibodyc-Myc AntibodyCyclin E1 AntibodyAIF Antibody (YA636)ALIX AntibodyCNPase AntibodyCortactin AntibodyCOX IV AntibodyCOX2/Cyclooxygenase 2 AntibodyCyclin A2 AntibodyCyclin B1 Antibody (YA486)DR5 AntibodyDrosha AntibodyE-Cadherin Antibody (YA778)EEA1 AntibodyEpCAM Antibody (YA772)Fatty Acid Synthase AntibodyFIP200 Antibody分子量:481.39Formula:C22H18D6BrFN4O2CAS 号:1174683-49-8非标记 CAS:443913-73-3中文名称:凡德他尼 d6运输条件:Room temperature in continental US; may vary elsewhere.储存方式:Please store the product under the recommended conditions in the Certificate of Analysis.纯度

Clofibric acid-d4,Chlorofibrinic acid-d4「同位素标记抑制剂」

Clofibric acid-d4,Chlorofibrinic acid-d4「同位素标记抑制剂」

作者:德尔塔生物 日期:2025-08-13

生物活性:Clofibric acid-d4 is the deuterium labeled Clofibric acid (HY-B1415). Clofibric acid also is an herbicideClofibric acid (Chlorofibrinic acid) is an orally active PPARα agonist. Clofibric acid inhibits the fimbriation of Escherichia coli. Clofibric acid increases SOD activity. Clofibric acid lowers blood lipids and prevents experimental pyelonephritis. Clofibric acid has anticancer activity against ovarian cancer. Clofibric acid is also a herbicide. Clofibric acid is used in ovarian cancer, liver cancer, obesity, and urinary tract infection research[1][2][3][4][5][6][7][8][9].体外研究(In Vitro):Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].德尔塔生物 has not independently confirmed the accuracy of these methods. They are for reference only.Clofibric acid-d4 相关抗体:PPAR alpha AntibodyPPAR gamma AntibodySOD2 Antibody (YA071)PPAR gamma Antibody (YA122)SOD2 Antibody (YA670)MRP2 AntibodySOD1 AntibodyElongation factor 2 Antibody (YA962)Elongation factor 2 Antibody (YA964)PU.1/SPI1 Antibody (YA1116)Sulfadimidine Antibody (YA906)Elongation factor 2 Antibody (YA963)Anthrax Protective gen Antibody (YA1060)PGC1 beta Antibody (YA1411)Elongation factor 1 gamma Antibody (YA2004)Pulmonary Surfactant Associated Protein D Antibody (YA2107)Cathelicidin Antibody (YA2380)Superoxide Dismutase 3 Antibody (YA2420)Elongation Factor Ts

Primidone-d5,扑痫酮 d5「同位素标记抑制剂」

Primidone-d5,扑痫酮 d5「同位素标记抑制剂」

作者:德尔塔生物 日期:2025-08-13

生物活性:Primidone-d5 is the deuterium labeled Primidone. Primidone is the orally active inhibitor for TRPM3 (IC50 = 0.6 μM), RIP kinase and voltage-gated sodium channel, and the antagonist for GABA receptor. Primidone can be used as the analgesic and anticonvulsant agent[1][2][3].体外研究(In Vitro):Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].德尔塔生物 has not independently confirmed the accuracy of these methods. They are for reference only.Primidone-d5 相关抗体:xCT Antibody (YA006)GABARAP AntibodyRIP AntibodyxCT Antibody (YA652)Alpha-ENaC Antibodyp-RIPK1(S166) Antibody (YA1284)IP3 Receptor Antibody (YA1596)TRPM8 Antibody (YA1609)GABA B Receptor 2 Antibody (YA1733)TRPM7 Antibody (YA2391)GABA B Receptor 1 Antibody (YA2418)CRMP2 Antibody (YA3370)GAD65 Antibody (YA758)GABA A Receptor alpha 1 Antibody (YA1315)SLC12A1 Antibody (YA1403)GABA A Receptor beta 2 Antibody (YA1758)GABA Transporter 1 Antibody (YA1795)GAD67 Antibody (YA1807)TrpC1 Antibody (YA1814)CRMP1 Antibody (YA1941)ABAT Antibody (YA1964)GABA A Receptor alpha 5 Antibody (YA2249)GABA A Receptor beta 1 Antibody (YA2261)CRMP5 Antibody (YA2497)CRMP3 Antibody (YA2563)BGAT Antibody (YA2741)CRMP4 Antibody (YA2777)GABARAPL2 Antibody (YA2882)分子量:223.28Formula:C12H9D5N2O2CAS 号:73738-06-4非标记 CAS:125-33-7性状:固体颜色:White to off-white中文名称:扑痫酮 d5运输

Nomifensine-d3 maleate,诺米芬新-d3 (马来酸盐; (±-Nomifensine-d3 maleate; Nomifensin-d3 maleate「同位素标记抑制剂」

Nomifensine-d3 maleate,诺米芬新-d3 (马来酸盐; (±-Nomifensine-d3 maleate; Nomifensin-d3 maleate「同位素标记抑制剂」

作者:德尔塔生物 日期:2025-08-13

生物活性:Nomifensine-d3 ((±)-Nomifensine-d3) maleate is the deuterium labeled Nomifensine maleate (HY-B1110A). Nomifensine ((±)-Nomifensine) maleate is a potent norepinephrine (NE) and dopamine (DA) reuptake inhibitor. Nomifensine maleate inhibits uptake of NE, DA and 5-HT in rat brain synaptosomes, with IC50 values of 6.6 nM, 48 nM and 830 nM, and Ki values of 4.7 nM, 26 nM and 4000 nM, respectively. Nomifensine maleate has antidepressant and analgesic effects. Nomifensine maleate is used in neurodegenerative diseases, compound addiction, and pain research[1][2][3][4][5][6][7].IC50 & Target:D3 Receptor体外研究(In Vitro):氢、碳和其他元素的稳定重同位素已被掺入药物分子中,主要用作药物开发过程中定量的示踪剂。氘化因其可能影响药物的药代动力学和代谢特征而受到关注。德尔塔生物 has not independently confirmed the accuracy of these methods. They are for reference only.Nomifensine-d3 maleate 相关抗体:ADRB2 AntibodyDRD2 AntibodyDopamine Receptor D3 Antibody (YA1742)DOPA Decarboxylase Antibody (YA2428)Dopamine Receptor D1 Antibody (YA3270)Salbutamol Antibody (YA901)Clenbuterol Antibody (YA904)alpha 1a Adrenergic Receptor Antibody (YA2059)Torsin 1A Antibody (YA2935)PITX3 Antibody (YA2974)HMBS Antibody (YA3061)分子量:357.42Formula:C20H19D3N2O4CAS 号:1795140-41-8非标记 CAS:24526-64-5中文名称:诺米芬新-d3 (马来酸盐)运输条件:Room temperature in continental US; may vary elsewhere.储存方式:Please store the product under the recommended conditions in the Certificate of Analysis.纯度 & 产品资料Data Sheet (542 KB)产品使用指南 (1538 KB)参考文献[1]. Russak EM, et al. Impact of Deuterium Su

(R-Ofloxacin-d3,(R-氧氟沙星-d3「同位素标记抑制剂」

(R-Ofloxacin-d3,(R-氧氟沙星-d3「同位素标记抑制剂」

作者:德尔塔生物 日期:2025-08-13

生物活性:(R)-Ofloxacin-d3 is the deuterium labeled (R)-Ofloxacin. (R)-Ofloxacin is the dextrorotatory enantiomer of Ofloxacin (HY-B0125) and is an orally effective fluoroquinolone antibiotic. (R)-Ofloxacin can inhibit the activity of bacterial DNA topoisomerase II, interfere with bacterial DNA replication and repair, and exert a bactericidal effect. (R)-Ofloxacin has a broad-spectrum antibacterial activity and has inhibitory effects on both Gram-negative and Gram-positive bacteria[1][2][3].分子量:364.39Formula:C18H17D3FN3O4CAS 号:1346617-10-4非标记 CAS:100986-86-5中文名称:(R) -氧氟沙星-d3运输条件:Room temperature in continental US; may vary elsewhere.储存方式:Please store the product under the recommended conditions in the Certificate of Analysis.纯度 & 产品资料Data Sheet (529 KB)产品使用指南 (1538 KB)参考文献[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-236. [Content Brief][2]. Zhang, et al. Stereoselective effects and its potential mechanism of ofloxacin on the growth and development of Rana nigromaculata: mainly liver lipid metabolism. Frontiers of Environmental Science & Engineering 19.4 (2025): 50.[3]. Nahla N. Salama, et al. Thin-Layer Chromatographic Enantioseparation of Ofloxacin and Zopiclone using Hydroxy-Propyl-BetaCyclodextrin as Chiral Selector and Thermodynamic Studies of Complexation. Journal of Planar Chromatography. 27 (2014) 3, 166-173.

Pioglitazone-d4 (alkyl,吡格列酮 d4 (alkyl「同位素标记抑制剂」

Pioglitazone-d4 (alkyl,吡格列酮 d4 (alkyl「同位素标记抑制剂」

作者:德尔塔生物 日期:2025-08-13

生物活性:Pioglitazone-d4 (alkyl) (U 72107-d4 (alkyl)) is the deuterium labeled Pioglitazone. Pioglitazone (U 72107) is a potent and selective PPARγ agonist with high affinity binding to the PPARγ ligand-binding domain with EC50 of 0.93 and 0.99 μM for human and mouse PPARγ, respectively[1][2].体外研究(In Vitro):Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].德尔塔生物 has not independently confirmed the accuracy of these methods. They are for reference only.Pioglitazone-d4 (alkyl) 相关抗体:Ferritin Heavy Chain AntibodyPPAR alpha AntibodyPPAR gamma AntibodyPPAR gamma Antibody (YA122)AMID/FSP1 AntibodyPeroxiredoxin 1 Antibody (YA692)PRDX3 Antibody (YA909)Ferritin Light Chain Antibody (YA971)Ferritin Light Chain Antibody (YA972)PGC1 beta Antibody (YA1411)分子量:360.46Formula:C19H16D4N2O3SCAS 号:1134163-31-7非标记 CAS:111025-46-8性状:固体颜色:White to off-white中文名称:吡格列酮 d4 (alkyl)运输条件:Room temperature in continental US; may vary elsewhere.储存方式:-20°C, protect from light, stored under nitrogen*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light, stored under nitrogen)

Dothiepin-d3,度硫平-d3「同位素标记抑制剂」

Dothiepin-d3,度硫平-d3「同位素标记抑制剂」

作者:德尔塔生物 日期:2025-08-13

生物活性:Dothiepin-d3 is the deuterium labeled Dothiepin[1].体外研究(In Vitro):Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].德尔塔生物 has not independently confirmed the accuracy of these methods. They are for reference only.分子量:298.46Formula:C19H18D3NSCAS 号:136765-31-6非标记 CAS:113-53-1性状:固体颜色:Off-white to light yellow中文名称:度硫平-d3运输条件:Room temperature in continental US; may vary elsewhere.储存方式:Please store the product under the recommended conditions in the Certificate of Analysis.纯度 & 产品资料Data Sheet (522 KB)产品使用指南 (1538 KB)参考文献[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. [Content Brief]

Gepirone-d8,吉哌隆-d8「同位素标记抑制剂」

Gepirone-d8,吉哌隆-d8「同位素标记抑制剂」

作者:德尔塔生物 日期:2025-08-13

生物活性:Gepirone-d8 is deuterium labeled Gepirone.体外研究(In Vitro):Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].德尔塔生物 has not independently confirmed the accuracy of these methods. They are for reference only.Gepirone-d8 相关抗体:MTNR1A Antibody分子量:367.52Formula:C19H21D8N5O2CAS 号:2749331-28-8非标记 CAS:83928-76-1性状:固体颜色:White to off-white中文名称:吉哌隆-d8运输条件:Room temperature in continental US; may vary elsewhere.储存方式:4°C, protect from light*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

3-Phenoxybenzoic acid-13C6,3-苯氧基苯甲酸-13C6; 3-PBA-13C6「同位素标记抑制剂」

3-Phenoxybenzoic acid-13C6,3-苯氧基苯甲酸-13C6; 3-PBA-13C6「同位素标记抑制剂」

作者:德尔塔生物 日期:2025-08-13

生物活性:3-Phenoxybenzoic acid-13C6 is the 13C6 labeled 3-Phenoxybenzoic acid. 3-Phenoxybenzoic acid is the metabolite of pyrethroid insecticides. 3-Phenoxybenzoic acid induces immunotoxicity and oxidative stress, and inhibits the phagocytic ability of macrophages[1].体外研究(In Vitro):Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].德尔塔生物 has not independently confirmed the accuracy of these methods. They are for reference only.3-Phenoxybenzoic acid-13C6 相关抗体:ERK1/2 AntibodyE-Cadherin Antibody (YA470)Fatty Acid Synthase Antibody (YA766)DYKDDDDK Tag (FLAG) AntibodyGAPDH AntibodyGFP Antibodyp53 Antibody (YA250)RUNX2 AntibodyFerritin Heavy Chain AntibodyCOX2 AntibodyCtip2 AntibodyCyclin D1 Antibody (YA485)Cytochrome C Antibodyc-Myc AntibodyCyclin E1 AntibodyAIF Antibody (YA636)ALIX AntibodyCatalase Antibody (YA552)Catalase Antibody (YA811)CNPase AntibodyCortactin AntibodyCOX IV AntibodyCOX2/Cyclooxygenase 2 AntibodyCyclin A2 AntibodyCyclin B1 Antibody (YA486)DR5 AntibodyDrosha AntibodyE-Cadherin Antibody (YA778)EEA1 AntibodyEpCAM Antibody (YA772)分子量:220.17Formula:C713C6H10O3CAS 号:1793055-05-6非标记 CAS:3739-38-6性状:固体颜色:White to off-white中文名称:3-苯氧基苯甲酸-13C6运输条件:Room temperature in continental US; may vary elsewhere.储存方式:Powder:-20°C:3 years,4°C:2 yearsIn solvent:-80°C:6 months

Aflatoxin G2-13C17,黄曲霉毒素 G2-13C17「同位素标记抑制剂」

Aflatoxin G2-13C17,黄曲霉毒素 G2-13C17「同位素标记抑制剂」

作者:德尔塔生物 日期:2025-08-13

生物活性:Aflatoxin G2-13C17 is the 13C labeled Aflatoxin G2 (HY-N6698)[1]. Aflatoxin G2 is a major naturally produced aflatoxin that can be produced by the fungi Aspergillus flavus and Aspergillus parasiticus[1].体外研究(In Vitro):氢、碳和其他元素的稳定重同位素已被纳入药物分子中,主要作为药物开发过程中定量的示踪剂。氘化引起了人们的关注,因为它可能影响药物的药代动力学和代谢谱[1]。德尔塔生物 has not independently confirmed the accuracy of these methods. They are for reference only.Aflatoxin G2-13C17 相关抗体:MRP2 AntibodyElongation factor 2 Antibody (YA962)Elongation factor 2 Antibody (YA964)PU.1/SPI1 Antibody (YA1116)Sulfadimidine Antibody (YA906)Elongation factor 2 Antibody (YA963)Anthrax Protective gen Antibody (YA1060)Elongation factor 1 gamma Antibody (YA2004)Pulmonary Surfactant Associated Protein D Antibody (YA2107)Cathelicidin Antibody (YA2380)Elongation Factor Ts Antibody (YA2524)Elongation Factor 1A2 Antibody (YA2879)BPI Antibody (YA3068)MetRS Antibody (YA3196)分子量:347.16Formula:13C17H14O7CAS 号:1217462-49-1非标记 CAS:7241-98-7性状:液体颜色:Colorless to light yellow中文名称:黄曲霉毒素 G2-13C17运输条件:Room temperature in continental US; may vary elsewhere.储存方式:Please store the product under the recommended conditions in the Certificate of Analysis.纯度 & 产品资料纯度: ≥98.0%参考文献[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-220. [Content Brief][2]. Kumar P, et al. Aflatoxins: A Global Concern for Food Safety, Human Health and Their Management. Front Microb