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1643260

USP

盐酸坦洛新 盐酸盐

United States Pharmacopeia (USP) Reference Standard

别名:

5-[(2R)-2-[[2-(2-Ethoxyphenoxy)ethyl]amino]propyl]-2-methoxybenzenesulfonamide hydrochloride

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100 MG
¥3,795.88

¥3,795.88

国内现货，预计发货时间2025年4月27日详情

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100 MG
¥3,795.88

About This Item

经验公式（希尔记法）:
C20H28N2O5S · HCl
CAS号:
106463-17-6
分子量:
444.97
MDL编号:
MFCD00922997
UNSPSC代码:
41116107
PubChem化学物质编号:
329751218
NACRES:
NA.24

¥3,795.88

国内现货，预计发货时间2025年4月27日详情

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等级

pharmaceutical primary standard

API类

tamsulosin

制造商/商品名称

USP

应用

pharmaceutical (small molecule)

包装形式

neat

储存温度

2-8°C

SMILES字符串

Cl.CCOc1ccccc1OCCN[C@H](C)Cc2ccc(OC)c(c2)S(N)(=O)=O

InChI

1S/C20H28N2O5S.ClH/c1-4-26-17-7-5-6-8-18(17)27-12-11-22-15(2)13-16-9-10-19(25-3)20(14-16)28(21,23)24;/h5-10,14-15,22H,4,11-13H2,1-3H3,(H2,21,23,24);1H/t15-;/m1./s1

InChI key

ZZIZZTHXZRDOFM-XFULWGLBSA-N

基因信息

human ... ADRA1A(148) , ADRA1B(147) , ADRA1D(146)

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此商品
PHR220908511239802
Curcumin suitable for matrix substance for MALDI-MS, ≥99.5% (HPLC)

78246

Curcumin

Curcumin Pharmaceutical Secondary Standard; Certified Reference Material

PHR2209

Curcumin

Curcumin analytical standard

08511

Curcumin

Curcumin, Curcuma longa L. A cell-permeable and irreversible antitumor and anti-inflammatory agent that acts as an inhibitor of 5-lipoxygenase (IC₅₀ = 8 µM) and cyclooxygenase (IC₅₀ = 52 µM).

239802

Curcumin, Curcuma longa L.

assay

≥99.5% (HPLC)

assay

-

assay

≥98.0% (HPLC)

assay

≥80% (HPLC)

form

powder

form

solid

form

powder

form

solid

Quality Level

100

Quality Level

300

Quality Level

100

Quality Level

100

technique(s)

MALDI-MS: suitable

technique(s)

-

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

-

storage temp.

2-8°C

storage temp.

-10 to -25°C

storage temp.

2-8°C

storage temp.

10-30°C

grade

matrix substance for MALDI-MS

grade

certified reference material, pharmaceutical secondary standard

grade

analytical standard

grade

-

一般描述

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia.

应用

Tamsulosin hydrochloride USP reference standard, intended for use in specified quality tests and assays as specified in the USP compendia. Also, for use with USP monographs such as:
  • Tamsulosin Hydrochloride Capsules
  • Dutasteride and Tamsulosin Hydrochloride Capsules

生化/生理作用

Tamsulosin is a α1A/1D-adrenoceptor antagonist; Used as a treatment of BPH (benign prostatic hypertrophy).
Tamsulosin is an α1A/1D-adrenoceptor antagonist used as a treatment of benign prostatic hypertrophy (BPH). Its activity as an ? blocker also affects the iris, and has led to complications during cataract surgery, a condition called "floppy iris" syndrome.

分析说明

These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.  ​

其他说明

Sales restrictions may apply.

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H302

危险分类

Acute Tox. 4 Oral

储存分类代码

11 - Combustible Solids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

  • 技术规格说明书

    • 历史批次信息供参考:

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    Tamsulosin Hydrochloride Capsules
    United States Pharmacopeia and National Formulary
    United States Pharmacopeia, 46(3) (2022)
    Dutasteride and Tamsulosin Hydrochloride Capsules
    United States Pharmacopeia and National Formulary
    United States Pharmacopeia, 46(5) (2023)
    Tamsulosin Hydrochloride
    United States Pharmacopeia and National Formulary
    United States Pharmacopeia, 42(2), 4211-4211 (2020)
    Shuo Yang et al.
    The AAPS journal, 16(4), 860-871 (2014-05-31)
    Multi-pellet formulations are advantageous for the controlled release of drugs over single-unit dosage forms. To understand the diffusion controlled drug release mechanism, the pellet structure and drug release from a single pellet (not at dose level) were studied using synchrotron
    Nannan Chu et al.
    Clinical therapeutics, 37(2), 462-472 (2014-12-04)
    The primary aim of this study was to evaluate whether there was clinically significant pharmacokinetic (PK) interaction between finasteride and tamsulosin in healthy Chinese male subjects. This was an open-label, randomized, 3-period, crossover study. Subjects received single and multiple doses
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