(R)-Verapamil hydrochloride(Synonyms: (R)-(+)-Verapamil hydrochloride)

发表于2024年3月2日由上海金畔生物科技有限公司

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，专注于信号通路和疾病研究领域。

(R)-Verapamil hydrochloride (Synonyms: (R)-(+)-Verapamil hydrochloride) 纯度: 98.54%

(R)-Verapamil hydrochloride ((R)-(+)-Verapamil hydrochloride) 是一种 P-糖蛋白 (P-Glycoprotein) 抑制剂。(R)-Verapamil hydrochloride 抑制 MRP1 介导的转运，导致 MRP1 过表达细胞对抗癌药产生化学敏感性。

(R)-Verapamil hydrochloride Chemical Structure

CAS No. : 38176-02-2

规格	价格	是否有货
Free Sample (0.1-0.5 mg)		Apply now
10 mM * 1 mL in DMSO	￥2160	In-stock
5 mg	￥2000	In-stock
10 mg	￥3600	In-stock
50 mg	￥11000	In-stock
100 mg	￥18500	In-stock
200 mg		询价
500 mg		询价

* Please select Quantity before adding items.

(R)-Verapamil hydrochloride 相关产品

•相关化合物库:

Drug Repurposing Compound Library Plus
FDA-Approved Drug Library Plus
Bioactive Compound Library Plus
Apoptosis Compound Library
Membrane Transporter/Ion Channel Compound Library
FDA-Approved Drug Library
Anti-Cancer Compound Library
Drug Repurposing Compound Library
FDA Approved & Pharmacopeial Drug Library

生物活性

(R)-Verapamil hydrochloride ((R)-(+)-Verapamil hydrochloride) is a P-Glycoprotein inhibitor. (R)-Verapamil hydrochloride blocks MRP1 mediated transport, resulting in chemosensitization of MRP1-overexpressing cells to anticancer drugs^[1]^[2].

分子量

491.06

Formula

C₂₇H₃₉ClN₂O₄

CAS 号

38176-02-2

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, stored under nitrogen

*In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)

溶解性数据

In Vitro:

DMSO : 100 mg/mL (203.64 mM; Need ultrasonic)

H₂O : 100 mg/mL (203.64 mM; Need ultrasonic)

配制储备液

浓度溶剂体积质量	1 mg	5 mg	10 mg

1 mM	2.0364 mL	10.1821 mL	20.3641 mL
5 mM	0.4073 mL	2.0364 mL	4.0728 mL
10 mM	0.2036 mL	1.0182 mL	2.0364 mL

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液；一旦配成溶液，请分装保存，避免反复冻融造成的产品失效。
储备液的保存方式和期限：-80°C, 6 months; -20°C, 1 month (stored under nitrogen)。-80°C 储存时，请在 6 个月内使用，-20°C 储存时，请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液，再依次添加助溶剂：

——为保证实验结果的可靠性，澄清的储备液可以根据储存条件，适当保存；体内实验的工作液，建议您现用现配，当天使用；以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比；如在配制过程中出现沉淀、析出现象，可以通过加热和/或超声的方式助溶

1.

请依序添加每种溶剂： 10% DMSO 40% PEG300 5% Tween-80 45% saline

Solubility: ≥ 5 mg/mL (10.18 mM); Clear solution

此方案可获得 ≥ 5 mg/mL (10.18 mM，饱和度未知) 的澄清溶液。

以 1 mL 工作液为例，取 100 μL 50.0 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中，混合均匀；向上述体系中加入50 μL Tween-80，混合均匀；然后继续加入 450 μL生理盐水定容至 1 mL。

将 0.9 g 氯化钠，完全溶解于 100 mL ddH₂O 中，得到澄清透明的生理盐水溶液
2.

请依序添加每种溶剂： 10% DMSO 90% (20% SBE-β-CD in saline)

Solubility: ≥ 5 mg/mL (10.18 mM); Clear solution

此方案可获得 ≥ 5 mg/mL (10.18 mM，饱和度未知) 的澄清溶液。

以 1 mL 工作液为例，取 100 μL 50.0 mg/mL 的澄清 DMSO 储备液加到 900 μL 20% 的 SBE-β-CD 生理盐水水溶液中，混合均匀。

将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中，再用生理盐水定容至 10 mL，完全溶解，澄清透明
3.

请依序添加每种溶剂： 10% DMSO 90% corn oil

Solubility: ≥ 5 mg/mL (10.18 mM); Clear solution

此方案可获得 ≥ 5 mg/mL (10.18 mM，饱和度未知) 的澄清溶液，此方案不适用于实验周期在半个月以上的实验。

以 1 mL 工作液为例，取 100 μL 50.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中，混合均匀。

*以上所有助溶剂都可在上海金畔生物科技有限公司网站选购。

参考文献

[1]. Plumb JA, et al. The activity of verapamil as a resistance modifier in vitro in drug resistant human tumour cell lines is not stereospecific. Biochem Pharmacol. 1990 Feb 15;39(4):787-92.

[2]. Perrotton T, et al. (R)- and (S)-verapamil differentially modulate the multidrug-resistant protein MRP1. J Biol Chem. 2007 Oct 26;282(43):31542-8. Epub 2007 Jul 22.

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(S)-Verapamil hydrochloride(Synonyms: (S)-(-)-Verapamil hydrochloride)

发表于2024年2月24日由上海金畔生物科技有限公司

(S)-Verapamil hydrochloride (Synonyms: (S)-(-)-Verapamil hydrochloride) 纯度: 99.39%

(S)-Verapamil hydrochloride (S(-)-Verapamil hydrochloride) 通过 MRP1 抑制白三烯 C4 (LTC4) 和钙黄绿素的转运。(S)-Verapamil hydrochloride 导致潜在耐药性肿瘤细胞死亡。

(S)-Verapamil hydrochloride Chemical Structure

CAS No. : 36622-28-3

规格	价格	是否有货
Free Sample (0.1-0.5 mg)		Apply now
10 mM * 1 mL in DMSO	￥2700	In-stock
5 mg	￥2500	In-stock
10 mg	￥4500	In-stock
50 mg	￥14000	In-stock
100 mg	￥23500	In-stock
200 mg		询价
500 mg		询价

* Please select Quantity before adding items.

(S)-Verapamil hydrochloride 相关产品

•相关化合物库:

Drug Repurposing Compound Library Plus
FDA-Approved Drug Library Plus
Bioactive Compound Library Plus
Apoptosis Compound Library
GPCR/G Protein Compound Library
Membrane Transporter/Ion Channel Compound Library
Neuronal Signaling Compound Library
FDA-Approved Drug Library
Anti-Cancer Compound Library
Drug Repurposing Compound Library
FDA Approved & Pharmacopeial Drug Library
Neuroprotective Compound Library
Targeted Diversity Library

生物活性

(S)-Verapamil hydrochloride (S(-)-Verapamil hydrochloride) inhibits leukotriene C4 (LTC4) and calcein transport by MRP1. (S)-Verapamil hydrochloride leads to the death of potentially resistant tumor cells^[1]^[2].

IC₅₀ & Target^[1]

LTC₄

Ca²⁺

体外研究
(In Vitro)

(S)-Verapamil hydrochloride (S(-)-Verapamil hydrochloride) not the (R)-Verapamil hydrochloride potently induces the death of MRP1-transfected BHK-21 cells^[1].
(S)-Verapamil hydrochloride is good active form and has the low bioavailability^[1].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

491.06

Formula

C₂₇H₃₉ClN₂O₄

CAS 号

36622-28-3

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, stored under nitrogen

*In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)

溶解性数据

In Vitro:

DMSO : 200 mg/mL (407.28 mM; Need ultrasonic)

H₂O : 100 mg/mL (203.64 mM; Need ultrasonic)

配制储备液

浓度溶剂体积质量	1 mg	5 mg	10 mg

1 mM	2.0364 mL	10.1821 mL	20.3641 mL
5 mM	0.4073 mL	2.0364 mL	4.0728 mL
10 mM	0.2036 mL	1.0182 mL	2.0364 mL

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液，再依次添加助溶剂：

1.

请依序添加每种溶剂： 10% DMSO 40% PEG300 5% Tween-80 45% saline

Solubility: ≥ 5 mg/mL (10.18 mM); Clear solution

此方案可获得 ≥ 5 mg/mL (10.18 mM，饱和度未知) 的澄清溶液。

以 1 mL 工作液为例，取 100 μL 50.0 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中，混合均匀；向上述体系中加入50 μL Tween-80，混合均匀；然后继续加入 450 μL生理盐水定容至 1 mL。

将 0.9 g 氯化钠，完全溶解于 100 mL ddH₂O 中，得到澄清透明的生理盐水溶液
2.

请依序添加每种溶剂： 10% DMSO 90% (20% SBE-β-CD in saline)

Solubility: ≥ 5 mg/mL (10.18 mM); Clear solution

此方案可获得 ≥ 5 mg/mL (10.18 mM，饱和度未知) 的澄清溶液。

以 1 mL 工作液为例，取 100 μL 50.0 mg/mL 的澄清 DMSO 储备液加到 900 μL 20% 的 SBE-β-CD 生理盐水水溶液中，混合均匀。

将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中，再用生理盐水定容至 10 mL，完全溶解，澄清透明
3.

请依序添加每种溶剂： 10% DMSO 90% corn oil

Solubility: ≥ 5 mg/mL (10.18 mM); Clear solution

此方案可获得 ≥ 5 mg/mL (10.18 mM，饱和度未知) 的澄清溶液，此方案不适用于实验周期在半个月以上的实验。

以 1 mL 工作液为例，取 100 μL 50.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中，混合均匀。

*以上所有助溶剂都可在上海金畔生物科技有限公司网站选购。

参考文献

[1]. Perrotton T, et al. (R)- and (S)-verapamil differentially modulate the multidrug-resistant protein MRP1. J Biol Chem. 2007 Oct 26;282(43):31542-8. Epub 2007 Jul 22.

[2]. Tannergren C, et al. St John’s wort decreases the bioavailability of R- and S-verapamil through induction of the first-pass metabolism. Clin Pharmacol Ther. 2004 Apr;75(4):298-309.

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(S)-Verapamil D7 hydrochloride(Synonyms: (S)-(-)-Verapamil D7 hydrochloride)

发表于2024年1月27日由上海金畔生物科技有限公司

(S)-Verapamil D7 hydrochloride (Synonyms: (S)-(-)-Verapamil D7 hydrochloride)

(S)-Verapamil D7 hydrochloride ((S)-(-)-Verapamil D7 hydrochloride) 是 (S)-Verapamil hydrochloride 的一种氘代化合物。(S)-Verapamil hydrochloride (S(-)-Verapamil hydrochloride) 通过 MRP1 抑制白三烯 C4 (LTC4) 和钙黄绿素的转运。(S)-Verapamil hydrochloride 导致潜在耐药性肿瘤细胞死亡。

(S)-Verapamil D7 hydrochloride Chemical Structure

规格	价格	是否有货
1 mg	￥2300	询问价格 & 货期

* Please select Quantity before adding items.

生物活性	(S)-Verapamil D7 hydrochloride ((S)-(-)-Verapamil D7 hydrochloride) is a deuterium labeled (S)-Verapamil hydrochloride. (S)-Verapamil hydrochloride (S(-)-Verapamil hydrochloride) inhibits leukotriene C4 (LTC4) and calcein transport by MRP1. (S)-Verapamil hydrochloride leads to the death of potentially resistant tumor cells^[1]^[2].
分子量	498.11
Formula	C₂₇H₃₂D₇ClN₂O₄
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]. Perrotton T, et al. (R)- and (S)-verapamil differentially modulate the multidrug-resistant protein MRP1. J Biol Chem. 2007 Oct 26;282(43):31542-8. Epub 2007 Jul 22. [2]. Tannergren C, et al. St John’s wort decreases the bioavailability of R- and S-verapamil through induction of the first-pass metabolism. Clin Pharmacol Ther. 2004 Apr;75(4):298-309.

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

(R)-Verapamil D7 hydrochloride(Synonyms: (R)-(+)-Verapamil D7 hydrochloride)

发表于2024年1月27日由上海金畔生物科技有限公司

(R)-Verapamil D7 hydrochloride (Synonyms: (R)-(+)-Verapamil D7 hydrochloride)

(R)-Verapamil D7 hydrochloride ((R)-(+)-Verapamil D7 hydrochloride) 是 (R)-Verapamil hydrochloride 的一种氘代化合物。(R)-Verapamil hydrochloride ((R)-(+)-Verapamil hydrochloride) 是一种 P-糖蛋白抑制剂。(R)-Verapamil hydrochloride 抑制 MRP1 介导的转运，导致 MRP1 过表达细胞对抗癌药产生化学敏感性。

(R)-Verapamil D7 hydrochloride Chemical Structure

规格	价格	是否有货
1 mg	￥2300	询问价格 & 货期

* Please select Quantity before adding items.

生物活性	(R)-Verapamil D7 hydrochloride ((R)-(+)-Verapamil D7 hydrochloride) is a deuterium labeled (R)-Verapamil hydrochloride. (R)-Verapamil hydrochloride ((R)-(+)-Verapamil hydrochloride) is a P-Glycoprotein inhibitor. (R)-Verapamil hydrochloride blocks MRP1 mediated transport, resulting in chemosensitization of MRP1-overexpressing cells to anticancer drugs^[1]^[2].
分子量	498.11
Formula	C₂₇H₃₂D₇ClN₂O₄
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]. Plumb JA, et al. The activity of verapamil as a resistance modifier in vitro in drug resistant human tumour cell lines is not stereospecific. Biochem Pharmacol. 1990 Feb 15;39(4):787-92. [2]. Perrotton T, et al. (R)- and (S)-verapamil differentially modulate the multidrug-resistant protein MRP1. J Biol Chem. 2007 Oct 26;282(43):31542-8. Epub 2007 Jul 22.

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

(S)-Verapamil D7 hydrochloride(Synonyms: (S)-(-)-Verapamil D7 hydrochloride)

发表于2024年1月27日由上海金畔生物科技有限公司

(S)-Verapamil D7 hydrochloride (Synonyms: (S)-(-)-Verapamil D7 hydrochloride)

(S)-Verapamil D7 hydrochloride Chemical Structure

规格	价格	是否有货
1 mg	￥2300	询问价格 & 货期

* Please select Quantity before adding items.

生物活性	(S)-Verapamil D7 hydrochloride ((S)-(-)-Verapamil D7 hydrochloride) is a deuterium labeled (S)-Verapamil hydrochloride. (S)-Verapamil hydrochloride (S(-)-Verapamil hydrochloride) inhibits leukotriene C4 (LTC4) and calcein transport by MRP1. (S)-Verapamil hydrochloride leads to the death of potentially resistant tumor cells^[1]^[2].
分子量	498.11
Formula	C₂₇H₃₂D₇ClN₂O₄
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]. Perrotton T, et al. (R)- and (S)-verapamil differentially modulate the multidrug-resistant protein MRP1. J Biol Chem. 2007 Oct 26;282(43):31542-8. Epub 2007 Jul 22. [2]. Tannergren C, et al. St John’s wort decreases the bioavailability of R- and S-verapamil through induction of the first-pass metabolism. Clin Pharmacol Ther. 2004 Apr;75(4):298-309.

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

(S)-Verapamil D7 hydrochloride(Synonyms: (S)-(-)-Verapamil D7 hydrochloride)

发表于2024年1月27日由上海金畔生物科技有限公司

(S)-Verapamil D7 hydrochloride (Synonyms: (S)-(-)-Verapamil D7 hydrochloride)

(S)-Verapamil D7 hydrochloride Chemical Structure

规格	价格	是否有货
1 mg	￥2300	询问价格 & 货期

* Please select Quantity before adding items.

生物活性	(S)-Verapamil D7 hydrochloride ((S)-(-)-Verapamil D7 hydrochloride) is a deuterium labeled (S)-Verapamil hydrochloride. (S)-Verapamil hydrochloride (S(-)-Verapamil hydrochloride) inhibits leukotriene C4 (LTC4) and calcein transport by MRP1. (S)-Verapamil hydrochloride leads to the death of potentially resistant tumor cells^[1]^[2].
分子量	498.11
Formula	C₂₇H₃₂D₇ClN₂O₄
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]. Perrotton T, et al. (R)- and (S)-verapamil differentially modulate the multidrug-resistant protein MRP1. J Biol Chem. 2007 Oct 26;282(43):31542-8. Epub 2007 Jul 22. [2]. Tannergren C, et al. St John’s wort decreases the bioavailability of R- and S-verapamil through induction of the first-pass metabolism. Clin Pharmacol Ther. 2004 Apr;75(4):298-309.

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

(R)-Verapamil D7 hydrochloride(Synonyms: (R)-(+)-Verapamil D7 hydrochloride)

发表于2024年1月27日由上海金畔生物科技有限公司

(R)-Verapamil D7 hydrochloride (Synonyms: (R)-(+)-Verapamil D7 hydrochloride)

(R)-Verapamil D7 hydrochloride Chemical Structure

规格	价格	是否有货
1 mg	￥2300	询问价格 & 货期

* Please select Quantity before adding items.

生物活性	(R)-Verapamil D7 hydrochloride ((R)-(+)-Verapamil D7 hydrochloride) is a deuterium labeled (R)-Verapamil hydrochloride. (R)-Verapamil hydrochloride ((R)-(+)-Verapamil hydrochloride) is a P-Glycoprotein inhibitor. (R)-Verapamil hydrochloride blocks MRP1 mediated transport, resulting in chemosensitization of MRP1-overexpressing cells to anticancer drugs^[1]^[2].
分子量	498.11
Formula	C₂₇H₃₂D₇ClN₂O₄
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]. Plumb JA, et al. The activity of verapamil as a resistance modifier in vitro in drug resistant human tumour cell lines is not stereospecific. Biochem Pharmacol. 1990 Feb 15;39(4):787-92. [2]. Perrotton T, et al. (R)- and (S)-verapamil differentially modulate the multidrug-resistant protein MRP1. J Biol Chem. 2007 Oct 26;282(43):31542-8. Epub 2007 Jul 22.

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

(R)-Verapamil D7 hydrochloride(Synonyms: (R)-(+)-Verapamil D7 hydrochloride)

发表于2024年1月27日由上海金畔生物科技有限公司

(R)-Verapamil D7 hydrochloride (Synonyms: (R)-(+)-Verapamil D7 hydrochloride)

(R)-Verapamil D7 hydrochloride Chemical Structure

规格	价格	是否有货
1 mg	￥2300	询问价格 & 货期

* Please select Quantity before adding items.

生物活性	(R)-Verapamil D7 hydrochloride ((R)-(+)-Verapamil D7 hydrochloride) is a deuterium labeled (R)-Verapamil hydrochloride. (R)-Verapamil hydrochloride ((R)-(+)-Verapamil hydrochloride) is a P-Glycoprotein inhibitor. (R)-Verapamil hydrochloride blocks MRP1 mediated transport, resulting in chemosensitization of MRP1-overexpressing cells to anticancer drugs^[1]^[2].
分子量	498.11
Formula	C₂₇H₃₂D₇ClN₂O₄
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]. Plumb JA, et al. The activity of verapamil as a resistance modifier in vitro in drug resistant human tumour cell lines is not stereospecific. Biochem Pharmacol. 1990 Feb 15;39(4):787-92. [2]. Perrotton T, et al. (R)- and (S)-verapamil differentially modulate the multidrug-resistant protein MRP1. J Biol Chem. 2007 Oct 26;282(43):31542-8. Epub 2007 Jul 22.

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

(S)-Verapamil-d6 hydrochloride(Synonyms: (S)-(-)-Verapamil-d6 hydrochloride)

发表于2023年11月2日由上海金畔生物科技有限公司

(S)-Verapamil-d6 hydrochloride (Synonyms: (S)-(-)-Verapamil-d6 hydrochloride)

(S)-Verapamil-d6 ((S)-(-)-Verapamil-d6) hydrochloride 是 (S)-Verapamil hydrochloride 的氘代物。(S)-Verapamil hydrochloride (S(-)-Verapamil hydrochloride) 通过 MRP1 抑制白三烯 C4 (LTC4) 和钙黄绿素的转运。(S)-Verapamil hydrochloride 导致潜在耐药性肿瘤细胞死亡。

(S)-Verapamil-d6 hydrochloride Chemical Structure

CAS No. : 1329611-24-6

规格		是否有货
1 mg		Check price and availability
10 mg		Check price and availability

* Please select Quantity before adding items.

生物活性	(S)-Verapamil-d6 ((S)-(-)-Verapamil-d6) hydrochloride is the deuterium labeled (S)-Verapamil hydrochloride. (S)-Verapamil hydrochloride (S(-)-Verapamil hydrochloride) inhibits leukotriene C4 (LTC4) and calcein transport by MRP1. (S)-Verapamil hydrochloride leads to the death of potentially resistant tumor cells^[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]. Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.
分子量	497.10
Formula	C₂₇H₃₃D₆ClN₂O₄
CAS 号	1329611-24-6
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]. Perrotton T, et al. (R)- and (S)-verapamil differentially modulate the multidrug-resistant protein MRP1. J Biol Chem. 2007 Oct 26;282(43):31542-8. Epub 2007 Jul 22. [3]. Tannergren C, et al. St John’s wort decreases the bioavailability of R- and S-verapamil through induction of the first-pass metabolism. Clin Pharmacol Ther. 2004 Apr;75(4):298-309.

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标签归档：verapamil

(R)-Verapamil hydrochloride(Synonyms: (R)-(+)-Verapamil hydrochloride)

(R)-Verapamil hydrochloride 相关产品

•相关化合物库:

(S)-Verapamil hydrochloride(Synonyms: (S)-(-)-Verapamil hydrochloride)

(S)-Verapamil hydrochloride 相关产品

•相关化合物库:

(S)-Verapamil D7 hydrochloride(Synonyms: (S)-(-)-Verapamil D7 hydrochloride)

(R)-Verapamil D7 hydrochloride(Synonyms: (R)-(+)-Verapamil D7 hydrochloride)

(S)-Verapamil D7 hydrochloride(Synonyms: (S)-(-)-Verapamil D7 hydrochloride)

(S)-Verapamil D7 hydrochloride(Synonyms: (S)-(-)-Verapamil D7 hydrochloride)

(R)-Verapamil D7 hydrochloride(Synonyms: (R)-(+)-Verapamil D7 hydrochloride)

(R)-Verapamil D7 hydrochloride(Synonyms: (R)-(+)-Verapamil D7 hydrochloride)

(S)-Verapamil-d6 hydrochloride(Synonyms: (S)-(-)-Verapamil-d6 hydrochloride)

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