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Merck
CN

H9006

Sigma-Aldrich

7-(β-Hydroxyethyl)theophylline

solid

别名:

1,3-Dimethyl-7-(2-hydroxyethyl)xanthine

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关于此项目

经验公式(希尔记法):
C9H12N4O3
化学文摘社编号:
分子量:
224.22
EC 号:
MDL编号:
UNSPSC代码:
41106305
PubChem化学物质编号:
NACRES:
NA.77
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表单

solid

颜色

white

溶解性

H2O: soluble (Solutions may be stored for several days at 4°C.)
ethanol: moderately soluble (Solutions may be stored for several days at 4°C.)

SMILES字符串

CN1C(=O)N(C)c2ncn(CCO)c2C1=O

InChI

1S/C9H12N4O3/c1-11-7-6(8(15)12(2)9(11)16)13(3-4-14)5-10-7/h5,14H,3-4H2,1-2H3

InChI key

NWPRCRWQMGIBOT-UHFFFAOYSA-N

基因信息

human ... ADORA2B(136)

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应用

Useful synthetic intermediate in the preparation of 7-substituted xanthines.

生化/生理作用

Pharmacological profile similar to theophylline.

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A Lagana et al.
Biomedical chromatography : BMC, 4(5), 205-207 (1990-09-01)
A sensitive and selective high performance liquid chromatographic doxophylline assay with ultraviolet detection has been developed for plasma samples. The drug is isolated from biological samples with a reversed phase C18 disposable extraction column. Plasma standard curves are linear for
Diurnal variation in the pharmacokinetics of intravenous theophylline and etophylline in healthy subjects.
B L Chauhan et al.
European journal of clinical pharmacology, 30(5), 635-636 (1986-01-01)
J W Daly et al.
Journal of medicinal chemistry, 29(7), 1305-1308 (1986-07-01)
A variety of analogues of caffeine and theophylline in which the 1-,3-, and 7-methyl substituents have been replaced with n-propyl, allyl, propargyl, and isobutyl and, in a few cases, with chloroethyl, hydroxyethyl, or benzyl were assessed for potency and selectivity
Etophylline as a proconvulsant.
K Girish et al.
Convulsive therapy, 12(3), 196-198 (1996-09-01)
A Apicella et al.
Biomaterials, 14(2), 83-90 (1993-01-01)
An interpretation of the drug release from monolithic water-swellable and soluble polymer tablets is presented. A convenient parameter, alpha, which compares the drug-diffusive conductance in the gel layer with the swelling and dissolving characteristics of the unpenetrated polymer was used

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