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CAS:1794760-38-5|Tazarotenic acid-d6,AGN 190299-d6

CAS:1794760-38-5|Tazarotenic acid-d6,AGN 190299-d6

作者:德尔塔生物 日期:2025-07-08

生物活性:Tazarotenic acid-d6 is deuterium labeled Tazarotenic acid. Tazarotenic acid is the metabolite of Tazarotene. Tazarotenic acid binding to retinoic acid receptors (RARs) is the probable molecular target of retinoid action. Tazarotenic acid has the potential for the research of warty dyskeratoma[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.Tazarotenic acid-d6 相关抗体:FMO3 Antibody (YA1992)分子量:329.45Formula:C19H11D6NO2SCAS 号:1794760-38-5非标记 CAS:118292-41-4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]. Chandraratna RA. Tazarotene--first of a new generation of receptor-selective retinoids. Br J Dermatol. 1996;135 Suppl 49:18-25. [Content Brief][3]. Hsyu PH, et al. Pharmacokinetics of a novel retinoid AGN 190168 and its metabolite AGN 190299 after intravenous administration of AGN 190168 to rats. Biopharm Drug Dispos. 1994;15(5):347-357. [Content

CAS:1881277-29-7|5-OxoETE-d7,5-KETE-d7

CAS:1881277-29-7|5-OxoETE-d7,5-KETE-d7

作者:德尔塔生物 日期:2025-07-08

生物活性:5-OxoETE-d7 is the deuterium labeled 5-OxoETE[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:325.49Formula:C20H23D7O3CAS 号:1881277-29-7非标记 CAS:106154-18-1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 (517 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]

CAS:326495-43-6|1,2-Distearoyl-sn-glycero-3-phosphorylethanolamine-d70,DSPE-d70

CAS:326495-43-6|1,2-Distearoyl-sn-glycero-3-phosphorylethanolamine-d70,DSPE-d70

作者:德尔塔生物 日期:2025-07-08

生物活性:1,2-Distearoyl-sn-glycero-3-phosphorylethanolamine-d70 is deuterium labeled 1,2-Distearoyl-sn-glycero-3-phosphorylethanolamine. 1,2-Distearoyl-sn-glycero-3-phosphorylethanolamine (DSPE) is a phosphoethanolamine (PE) lipid that can be used in the synthesis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[2].德尔塔生物 has not independently confirmed the accuracy of these methods. They are for reference only.1,2-Distearoyl-sn-glycero-3-phosphorylethanolamine-d70 相关抗体:BNSP AntibodyFACL4 AntibodyBrdU Antibody (YA578)GAPDH AntibodyGlucose 6 Phosphate Dehydrogenase AntibodyMETTL3 AntibodyTSG101 AntibodyAlkaline Phosphatase AntibodyCalnexin Antibody (YA573)Lamin A/C AntibodyLamin B1 AntibodyLAMP1 AntibodyLAMP2 Antibody (YA713)LAMP2a AntibodyNQO1 Antibody (YA697)NQO1 Antibody (YA261)OPA1 AntibodyRBM3 AntibodySynaptophysin Antibody (YA043)Laminin beta 1 AntibodyHeme Oxygenase 1 AntibodyKi67 Antibody (YA717)Ki67 Antibody (YA322)Asparagine Synthetase AntibodyCalnexin AntibodyKi67 Antibody (YA001)Osteopontin AntibodySynaptophysin Antibody (YA664)TREM2 AntibodyGAPDH Antibody (YA848)分子量:818.50Formula:C41H12D70NO8PCAS 号:326495-43-6非标记 CAS:1069-79-0性状:固体颜色:White to off-white运输条件:Room temperature in continental US; may vary elsewhere.储存方式:Powder:-20°C:3 yearsIn solvent:-80°C:6 mon

CAS:2123483-49-6|WNK-IN-11-d3

CAS:2123483-49-6|WNK-IN-11-d3

作者:德尔塔生物 日期:2025-07-08

生物活性:WNK-IN-11-d3 is an orally active, selective and potent With-No-Lysine (WNK) kinase inhibitor. WNK-IN-11-d3 is effective at regulating cardiovascular homeostasis[1].IC50 & Target:WNK[1]体内研究(In Vivo)WNK-IN-11 D3 (1.5 mg/kg; p.o.) shows an improved rat PK profile, including lower clearance, improvement in absolute oral exposure, and a 2-fold improvement in oral bioavailability[1].WNK-IN-11 D3 (30 mg/kg; p.o.) shows significant reductions in systolic blood pressure (SBP) vs untreated mice[1].WNK-IN-11 D3 (0~100 mg/kg; p.o.) induces dose dependent diuresis, natriuresis, and kaliuresis, from 10 to 100 mg/kg[1].WNK-IN-11 D3 shows trends toward reduction of blood pressure, stroke volume, and total peripheral resistance, while increasing heart rate. WNK-IN-11 D3 shows efficacy in rodent models of hypertension and volume overload[1].德尔塔生物 has not independently confirmed the accuracy of these methods. They are for reference only.Animal Model:Sprague−Dawley rats[1]Dosage:1.5 mg/kg Administration:P.o.Result:Showed an improved rat PK profile, including lower clearance, improvement in absolute oral exposure, and a 2-fold improvement in oral bioavailability.Animal Model:FVB mice[1]Dosage:30 mg/kg Administration:P.o.Result:Showed significant reductions in systolic blood pressure (SBP) vs untreated mice.Animal Model:FVB mice[1]Dosage:0~100 mg/kg Administration:P.o.Result:Induced dose dependent diuresis, natriuresis, and kaliuresis, from 10 to 100 mg/kg.分子量:465.41Formula:C21H18D3Cl2N5OSCAS 号:2123483-49-6非标记 CAS:2123489-30-3性状:固体颜色:Off-white to light yell

CAS:1346747-38-3|Fingolimod-d4,FTY720 free based-d4

CAS:1346747-38-3|Fingolimod-d4,FTY720 free based-d4

作者:德尔塔生物 日期:2025-07-08

生物活性:Fingolimod-d4 is the deuterium labeled Fingolimod. Fingolimod (FTY720 free base) is a sphingosine 1-phosphate (S1P) antagonist with an IC50 of 0.033 nM in K562 and NK cells. Fingolimod also is a pak1 activator, a immunosuppressant[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.Fingolimod-d4 相关抗体:PAK2 Antibody (YA695)PAK1 Antibody (YA1363)KPNA2 Antibody (YA1415)Phospho-PAK1/2/3 (Ser144/Ser141/Ser154) Antibody (YA1530)SCARB1 Antibody (YA1908)EDG3 Antibody (YA2359)Involucrin Antibody (YA2488)JAB1 Antibody (YA3159)Myelin Basic Protein Antibody (YA3271)Phospho-PAK4/5/6 (Ser474/Ser560/Ser602) Antibody (YA3333)S1PR4 AntibodyJMJD6 Antibody (YA1064)Scavenging Receptor SR-BI Antibody (YA1160)EDG1 Antibody (YA1239)LILRB1 Antibody (YA1261)PAK3 Antibody (YA1367)KSR1 Antibody (YA1391)PKN1 Antibody (YA1664)Lipoamide Dehydrogenase Antibody (YA1694)Intra Acrosomal Protein Antibody (YA1856)Lipin 1 Antibody (YA1909)Lactoferrin Antibody (YA2274)LCAT Antibody (YA2864)PKN2 Antibody (YA2890)ITPA Antibody (YA3104)L1CAM Antibody (YA3149)LAT Antibody (YA3161)Myelin Protein Zero Antibody (YA3278)EDG2 Antibody (YA3375)分子量:311.50Formula:C19H29D4NO2CAS 号:1346747-38-3非标记 CAS:162359-55-9性状:固体颜色:White

CAS:194930-00-2|(S-Rivastigmine-d6 tartrate,酒石酸卡巴拉汀 D6

CAS:194930-00-2|(S-Rivastigmine-d6 tartrate,酒石酸卡巴拉汀 D6

作者:德尔塔生物 日期:2025-07-08

生物活性:(S)-Rivastigmine-d6 (tartrate) is the deuterium labeled (S)-Rivastigmine, which is an cholinesterase inhibitor.分子量:406.46Formula:C18H22D6N2O8CAS 号:194930-00-2性状:固体颜色:White to off-white中文名称:酒石酸卡巴拉汀 d6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)

CAS:1159908-42-5|N-Arachidonyldopamine-d8

CAS:1159908-42-5|N-Arachidonyldopamine-d8

作者:德尔塔生物 日期:2025-07-08

生物活性:N-Arachidonyldopamine-d8 is the deuterium labeled N-Arachidonyldopamine[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.N-Arachidonyldopamine-d8 相关抗体:TRPM8 Antibody (YA1609)Phospho-Cannabinoid Receptor I (Ser316) Antibody (YA2350)TRPM7 Antibody (YA2391)TrpC1 Antibody (YA1814)分子量:447.68Formula:C28H33D8NO3CAS 号:1159908-42-5非标记 CAS:199875-69-9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 (513 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]

CAS:2712126-59-3|Trametinib-13C,d3,曲美替尼-13C,d3; GSK1120212-13C,d3; JTP-74057-13C,d3

CAS:2712126-59-3|Trametinib-13C,d3,曲美替尼-13C,d3; GSK1120212-13C,d3; JTP-74057-13C,d3

作者:德尔塔生物 日期:2025-07-08

生物活性:Trametinib-13C,d3 is the 13C- and deuterium labeled Trametinib. Trametinib (GSK1120212; JTP-74057) is an orally active MEK inhibitor that inhibits MEK1 and MEK2 with IC50s of about 2 nM. Trametinib activates autophagy and induces apoptosis[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[88].德尔塔生物 has not independently confirmed the accuracy of these methods. They are for reference only.Trametinib-13C,d3 相关抗体:MEK1/2 AntibodyERK1/2 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 AntibodyPhospho-MEK1 (Ser298) 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)分子量:619.41Formula:C2513CH20D3FIN5O4CAS 号:2712126-59-3非标记 CAS:871700-17-3中文名称:曲美替尼-13C,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 (535

CAS:2749980-90-1|Oleoyl Serotonin-d17

CAS:2749980-90-1|Oleoyl Serotonin-d17

作者:德尔塔生物 日期:2025-07-08

生物活性:Oleoyl Serotonin-d17 is the deuterium labeled Oleoyl Serotonin[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.Oleoyl Serotonin-d17 相关抗体:TRPM8 Antibody (YA1609)TRPM7 Antibody (YA2391)TrpC1 Antibody (YA1814)分子量:457.77Formula:C28H27D17N2O2CAS 号:2749980-90-1非标记 CAS:1002100-44-8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 (515 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]

CAS:2268785-42-6|Crisaborole-d4,克立硼罗-d4; AN-2728-d4; PF-06930164-d4

CAS:2268785-42-6|Crisaborole-d4,克立硼罗-d4; AN-2728-d4; PF-06930164-d4

作者:德尔塔生物 日期:2025-07-08

生物活性:Crisaborole-d4 is deuterium labeled Crisaborole. Crisaborole (AN-2728) is a potent inhibitor of PDE4 and cytokine release; inhibit PDE4 with an IC50 of 0.49 μM.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.Crisaborole-d4 相关抗体:PDE1B Antibody (YA1553)PDE4B Antibody (YA2932)PDE2A Antibody (YA2989)PDE4D Antibody (YA1714)分子量:255.07Formula:C14H6D4BNO3CAS 号:2268785-42-6非标记 CAS:906673-24-3性状:固体颜色:Off-white to light yellow中文名称:克瑞沙硼-d4;克立硼罗-d4运输条件:Room temperature in continental US; may vary elsewhere.储存方式:-20°C, protect from light*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)纯度 & 产品资料含量: 98.8%参考文献[1]. Nazarian R, et al. AN-2728, a PDE4 inhibitor for the potential topical treatment of psoriasis and atopic dermatitis. Curr Opin Investig Drugs. 2009 Nov;10(11):1236-42. [Content Brief][2]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. [Content Brief][3]. Akama T, et al. Discovery and structure-activity study of a novel benzoxaborole anti-inflammatory agent (AN2728) for the potential topical treatment of psoriasis and atopic dermatitis. Bioor

CAS:1794811-58-7|Niflumic Acid-d5,尼氟灭酸 d5

CAS:1794811-58-7|Niflumic Acid-d5,尼氟灭酸 d5

作者:德尔塔生物 日期:2025-07-08

生物活性:Niflumic Acid-d5 is the deuterium labeled Niflumic acid. Niflumic acid, a Ca2+-activated Cl- channel blocker, is an analgesic and anti-inflammatory agent used in the treatment of rheumatoid arthritis[1][2].细胞效力(Cellular Effect)Bone marrow cellCHOHEK293HEK-293THT-29THP-1U2OSU-937Cell Line TypeValueDescriptionReferencesBone marrow cellEC50> 20 μMCompound: Niflumic acidInduction of bone marrow cell differentiation isolated from ER-HOXA9 fusion protein expressed mouse harboring GFP-lysozyme assessed as upregulation of CD11b/MAC1 after 4 days by flow cytometryInduction of bone marrow cell differentiation isolated from ER-HOXA9 fusion protein expressed mouse harboring GFP-lysozyme assessed as upregulation of CD11b/MAC1 after 4 days by flow cytometry[PMID: 27994748]CHOEC5030.8 μMCompound: 8Agonist activity at C-terminal beta-galactosidase tagged human recombinant GPR35 expressed in CHO cells after 90 mins by beta-arrestin recruitment assayAgonist activity at C-terminal beta-galactosidase tagged human recombinant GPR35 expressed in CHO cells after 90 mins by beta-arrestin recruitment assay[PMID: 23888932]HEK293IC5013 μMCompound: Niflumic acidInhibition of human recombinant UGT1A1 expressed in HEK293 cells assessed as reduction in estradiol 3-glucuronidation by LC-MS/MS methodInhibition of human recombinant UGT1A1 expressed in HEK293 cells assessed as reduction in estradiol 3-glucuronidation by LC-MS/MS method[PMID: 21030469]HEK293IC5053 μMCompound: Niflumic acidInhibition of human recombinant UGT1A1 expressed in HEK293 cells assessed as reduction in bilirubin glucuron

CAS:1189882-28-7|Clomipramine-d6 hydrochloride,Chlorimipramine-d6 (hydrochloride; G-34586-d6 (hydrochloride; NSC-169865-d6 (hydrochloride

CAS:1189882-28-7|Clomipramine-d6 hydrochloride,Chlorimipramine-d6 (hydrochloride; G-34586-d6 (hydrochloride; NSC-169865-d6 (hydrochloride

作者:德尔塔生物 日期:2025-07-08

生物活性:Clomipramine-d6 (hydrochloride) is the deuterium labeled Clomipramine hydrochloride. Clomipramine (Chlorimipramine) hydrochloride is a potent 5-HT reuptake blocker with the IC50 value of 1.5 nM. Clomipramine hydrochloride is a tricyclic antidepressant that can be used for the research of depression and obsessive compulsive disorder (OCD)[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.Clomipramine-d6 hydrochloride 相关抗体:Serotonin Transporter Antibody (YA1638)HTR7 Antibody (YA2796)HTR2C Antibody (YA3364)分子量:357.35Formula:C19H18D6Cl2N2CAS 号:1189882-28-7非标记 CAS:17321-77-6中文名称:盐酸氯米帕明 d6 (盐酸盐)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 (535 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]. Yumi Sugimoto, et al. The tricyclic antidepressant Clomipramine increases plasma glucose levels of mice. J Pharmacol Sci. 2003 Sep;93(1):74-9. [Content Brief][3]. Mushtaq Ahmed, et al. Comparative stud

CAS:136765-29-2|Clomipramine-d3,Chlorimipramine-d3; G-34586-d3; NSC-169865-d3

CAS:136765-29-2|Clomipramine-d3,Chlorimipramine-d3; G-34586-d3; NSC-169865-d3

作者:德尔塔生物 日期:2025-07-08

生物活性:Clomipramine-d3 is the deuterium labeled Clomipramine. Clomipramine is a serotonin transporter (SERT), norepinephrine transporter (NET) dopamine transporter (DAT) blocker with Ki of 0.14, 54 and 3 nM, respectively[1][2].分子量:317.87Formula:C19H20D3ClN2CAS 号:136765-29-2非标记 CAS:303-49-1中文名称:氯米帕明 d3;氯丙咪嗪 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 (530 KB)产品使用指南 (1538 KB)参考文献[1]. McTavish, D. and P. Benfield, Clomipramine. An overview of its pharmacological properties and a review of its therapeutic use in obsessive compulsive disorder and panic disorder. Drugs, 1990. 39(1): p. 136-53. [Content Brief][2]. Owens, M.J., et al., Neurotransmitter receptor and transporter binding profile of antidepressants and their metabolites. J Pharmacol Exp Ther, 1997. 283(3): p. 1305-22. [Content Brief]

CAS:1398065-80-9|Miconazole-d5 nitrate (2,4-Dichlorobenzyloxy-d5,R18134-d5 (nitrate (2,4-Dichlorobenzyloxy-d5

CAS:1398065-80-9|Miconazole-d5 nitrate (2,4-Dichlorobenzyloxy-d5,R18134-d5 (nitrate (2,4-Dichlorobenzyloxy-d5

作者:德尔塔生物 日期:2025-07-08

生物活性:Miconazole-d5 (nitrate) (2,4-Dichlorobenzyloxy-d5) is the deuterium labeled Miconazole nitrate. Miconazole nitrate (R18134 nitrate) is an imidazole antifungal agent. Miconazole nitrate also has antibacterial effects[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.Miconazole-d5 nitrate (2,4-Dichlorobenzyloxy-d5) 相关抗体:SDHA AntibodyMRP2 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:484.17Formula:C18H10D5Cl4N3O4CAS 号:1398065-80-9非标记 CAS:22832-87-7中文名称:硝酸咪康唑 d5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 (531 KB)产品使用指南 (1538 KB)参考文献[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokin

CAS:1794942-12-3|Maprotiline-d5 hydrochloride,盐酸马普替林 d5 (盐酸盐

CAS:1794942-12-3|Maprotiline-d5 hydrochloride,盐酸马普替林 d5 (盐酸盐

作者:德尔塔生物 日期:2025-07-08

生物活性:Maprotiline-d5 (hydrochloride) is the deuterium labeled Maprotiline hydrochloride. Maprotiline hydrochloride is a selective noradrenalin re-uptake inhibitor and a tetracyclic antidepressant[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.Maprotiline-d5 hydrochloride 相关抗体:FOXO1A AntibodyBeclin 1 AntibodyAtg12 AntibodyATG5 AntibodyBmi1 AntibodyFOXO4 AntibodyFOXP3 AntibodyGABARAP AntibodyLAMP2 Antibody (YA713)LAMP2a AntibodyPhospho-FOXO3a(Ser253) AntibodyAPG5L AntibodyATG10 Antibody (YA603)ATG3 AntibodyATG4A AntibodyATG4C AntibodyATG7 AntibodyFOXO1 Antibody (YA430)FOXO3 AntibodyFOXP3 Antibody (YA759)FTO AntibodyPhospho-FOXO3A (Ser253) AntibodyFOXO1 AntibodyATG10 AntibodyGranulin Antibody (YA1162)ATG13 Antibody (YA1650)ATG9A Antibody (YA3081)LAMP2 Antibody (YA310)WIPI1 Antibody (YA1721)ATG16L1 Antibody (YA2187)分子量:318.90Formula:C20H19D5ClNCAS 号:1794942-12-3非标记 CAS:10347-81-6中文名称:盐酸马普替林 d5 (盐酸盐)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 (527 KB)产品使用指南 (1538 KB)参考文献[1]. Russak EM, et al. Impact of Deuterium Subst