主要文件

查看所有文档

D0633

7-(2,3-二羟丙基)茶碱

Name: 7-(2,3-二羟丙基)茶碱
Brand: SIGMA

PDE inhibitor, powder

别名:

喘定

登录查看组织和合同定价。

选择尺寸

变更视图

关于此项目

经验公式（希尔记法）:

C₁₀H₁₄N₄O₄

化学文摘社编号:

479-18-5

分子量:

254.24

NACRES:

NA.77

PubChem Substance ID:

24893280

UNSPSC Code:

41106305

EC Number:

207-526-1

MDL number:

MFCD00005759

Beilstein/REAXYS Number:

284563

Form:

powder

Quality level:

200

技术服务

需要帮助？我们经验丰富的科学家团队随时乐意为您服务。

让我们为您提供帮助

属性

产品名称

7-(2,3-二羟丙基)茶碱,

form

powder

Quality Level

200

mp

161-162 °C (lit.)

SMILES string

CN1C(=O)N(C)c2ncn(CC(O)CO)c2C1=O

InChI

1S/C10H14N4O4/c1-12-8-7(9(17)13(2)10(12)18)14(5-11-8)3-6(16)4-15/h5-6,15-16H,3-4H2,1-2H3

InChI key

KSCFJBIXMNOVSH-UHFFFAOYSA-N

Gene Information

human ... PDE3A(5139), PDE4A(5141), PDE4B(5142), PDE4C(5143), PDE4D(5144)

说明

Biochem/physiol Actions

7-(2,3-Dihydroxypropyl)theophylline is also called as dyphylline. Dyphylline serves as a bronchodilator and aids in better air flow through the lungs. It reduces the symptoms of chronic lung disorder such as asthma and bronchitis.

Features and Benefits

This compound is a featured product for Cyclic Nucleotide research. Click here to discover more featured Cyclic Nucleotide products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

pictograms

GHS07

signalword

Warning

hcodes

H302

pcodes

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

存储类别

11 - Combustible Solids

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

新产品

此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本？

如果您需要特殊版本，可通过批号或批次号查找具体证书。

搜索COA

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

商品

Discover Bioactive Molecules for Nucleotides

Cyclic nucleotides like cAMP modulate cell function via PKA activation and ion channels.

The effect of the aqueous solubility of xanthine derivatives on the release mechanism from ethylcellulose matrix tablets.

S H Neau et al.

International journal of pharmaceutics, 179(1), 97-105 (1999-03-04)

Release data from ethylcellulose (EC) matrix tablets was analyzed to determine which release equation provides the best fit to the data and to observe the effect of drug solubility on the release mechanism(s). Tablets were prepared by direct compression of

A comparison of the stability of ertapenem and meropenem in pharmaceutical preparations in solid state.

Judyta Cielecka-Piontek et al.

Journal of pharmaceutical and biomedical analysis, 46(1), 52-57 (2007-10-16)

The following first-order rate constants of the degradation of ertapenem in INVANZ and meropenem in MERONEM were determined: (a) in dry air at 363, 373, 378, 383, 388, 393 K; (b) at increased relative air humidity (76.4% RH) at 313

Therapeutic Drug Monitoring and Toxicology by Liquid Chromatography (2017)

查看所有相关文献

全球贸易项目编号

货号	GTIN
D0633-500G	04061832897783
D0633-1KG	04061826744314