Mebendazole-amine-13C6

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白、同位素标记物,专注于信号通路和疾病研究领域。
Mebendazole-amine-13C6 

Mebendazole-amine-13C6 是 13C6 标记的 Mebendazole-amine。Mebendazole-amine 是 Mebendazole 的代谢产物。Mebendazole 是广谱苯并咪唑抗蠕虫药。

Mebendazole-amine-13C6

Mebendazole-amine-13C6 Chemical Structure

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生物活性

Mebendazole-amine-13C6 is the 13C6 labeled Mebendazole-amine. Mebendazole-amine is a metabolite of Mebendazole. Mebendazole is a broad-spectrum benzimidazole anti-helminthic drug.

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].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

243.21

Formula

C813C6H11N3O

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 (476 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):211-223.

    [2]. Majewsky M, et al. Systematic identification of suspected anthelmintic benzimidazole metabolites using LC-MS/MS. J Pharm Biomed Anal. 2018;151:151-158.

    [3]. Pantziarka P, et al. Repurposing Drugs in Oncology (ReDO)-mebendazole as an anti-cancer agent. Ecancermedicalscience. 2014;8:443. Published 2014 Jul 10.

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Propan-2-amine-d7 hydrochloride

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白、同位素标记物,专注于信号通路和疾病研究领域。
Propan-2-amine-d7 hydrochloride 

Propan-2-amine-d7 hydrochloride 是 Propan-2-amine hydrochloride 的氘代物。

Propan-2-amine-d7 hydrochloride

Propan-2-amine-d7 hydrochloride Chemical Structure

CAS No. : 106658-10-0

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250 mg   询价  
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生物活性

Propan-2-amine-d7 hydrochloride is the deuterium labeled Propan-2-amine hydrochloride[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].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

102.61

Formula

C3H3D7ClN

CAS 号

106658-10-0

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.

参考文献
  • [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216.

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Propan-2-amine-d6 hydrochloride

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白、同位素标记物,专注于信号通路和疾病研究领域。
Propan-2-amine-d6 hydrochloride 

Propan-2-amine-d6 (hydrochloride) 是 H-Lys-OH.2HCl 氘代物。

Propan-2-amine-d6 hydrochloride

Propan-2-amine-d6 hydrochloride Chemical Structure

CAS No. : 126794-59-0

规格 是否有货
100 mg   询价  
250 mg   询价  
500 mg   询价  

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生物活性

Propan-2-amine-d6 (hydrochloride) is the deuterium labeled H-Lys-OH.2HCl[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[75].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

101.61

Formula

C3H4D6ClN

CAS 号

126794-59-0

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.

参考文献
  • [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-223.

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N-Phenylnaphthalen-1-amine-13C6

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白、同位素标记物,专注于信号通路和疾病研究领域。
N-Phenylnaphthalen-1-amine-13C6 

N-Phenylnaphthalen-1-amine-13C6

N-Phenylnaphthalen-1-amine-13C6 Chemical Structure

CAS No. : 2300178-77-0

规格 是否有货
100 mg   询价  
250 mg   询价  
500 mg   询价  

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分子量

220.20

Formula

C1013C6H8N

CAS 号

2300178-77-0

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.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

ent-Florfenicol Amine-d3

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白、同位素标记物,专注于信号通路和疾病研究领域。
ent-Florfenicol Amine-d3 

ent-Florfenicol Amine-d3 是 Florfenicol amine 的氘代物。Florfenicol amine 是 Florfenicol (HY-B1374) 的一个代谢产物。Florfenicol 是一种兽用抗生素,在水产养殖业中可以用来控制敏感细菌疾病。

ent-Florfenicol Amine-d3

ent-Florfenicol Amine-d3 Chemical Structure

CAS No. : 1217625-88-1

规格 是否有货
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生物活性

ent-Florfenicol Amine-d3 is the deuterium labeled Florfenicol amine. Florfenicol amine is a metabolite of Florfenicol (HY-B1374). Florfenicol, a veterinary antibiotic, can be used in aquaculture to control susceptible bacterial diseases[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].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

250.30

Formula

C10H11D3FNO3S

CAS 号

1217625-88-1

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.

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.

    [2]. B-K Park, et al. Pharmacokinetics of florfenicol and its metabolite, florfenicol amine, in the Korean catfish (Silurus asotus). J Vet Pharmacol Ther. 2006 Feb;29(1):37-40.

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Bis(2-chloroethyl)amine-d4 hydrochloride

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白、同位素标记物,专注于信号通路和疾病研究领域。
Bis(2-chloroethyl)amine-d4 hydrochloride 

Bis(2-chloroethyl)amine-d4 hydrochloride

Bis(2-chloroethyl)amine-d4 hydrochloride Chemical Structure

CAS No. : 58880-33-4

规格 是否有货
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分子量

182.51

Formula

C4H6D4Cl3N

CAS 号

58880-33-4

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.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Bis(2-chloroethyl)amine-1,1,2,2-d4 hydrochloride

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白、同位素标记物,专注于信号通路和疾病研究领域。
Bis(2-chloroethyl)amine-1,1,2,2-d4 hydrochloride 

Bis(2-chloroethyl)amine-1,1,2,2-d4 hydrochloride

Bis(2-chloroethyl)amine-1,1,2,2-d4 hydrochloride Chemical Structure

CAS No. : 352431-06-2

规格 是否有货
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100 mg Check price and availability

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分子量

182.51

Formula

C4H6D4Cl3N

CAS 号

352431-06-2

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.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务