Prediction of stability in pharmaceutical preparations. XXI: The analysis and kinetics of hydrolysis of a cocaine degradation product, ecgonine methyl ester, plus the pharmacokinetics of cocaine in the dog [2]

DOI: 10.1002/jps.2600830233

Source and publish data:

Journal of Pharmaceutical Sciences p. 269 - 272 (1994)

Update date:2022-08-04

Topics:

Authors:

Garrett Garrett

Eberst Eberst

Maruhn Maruhn

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1002/jps.2600830233

Full text of DOI:10.1002/jps.2600830233

Products guided by the article

Product name:(1R-2-exo-3-exo)-2-carbomethoxy-8-methyl-8-azabicyclo<3.2.1>octyl-3-N-phenylcarbamate

Cas No:29364-08-7

R&D Labs maybe for 29364-08-7

Shanghai birch chemical technology co.,ltd

Contact:+86-21-54096810

Address:No.2588,Jungong Road,Shanghai,China
Zhejiang Kaili Industrial Co., Ltd

Contact:+86-571-85241926

Address:lantian business center,No.18 Moganshan Road
ShangHai Soyoung Biotechnology Inc

website:http://www.soyoungbio.com

Contact:+86-21-69893009

Address:shanghai
Goldwills Pharmaceuticals Co., Ltd.

Contact:0916-2237889 13991621155

Address:North Suburb of Hanzhong city, Shaanxi Province
Li's chemicals

Contact:+86-15850770348

Address:51 OF XIANGFANGCUN ROAD, Nanjing 210002, China

Relevant to this article

Visible-Light-Driven Aryl Migration and Cyclization of α-Azido Amides

Doi:10.1021/acs.orglett.1c01120
(2021)
Doi:10.1021/ma60017a013
(1970)
Different ways to distort a tetracapped tetrahedron on route to forming an E₄M₄ cubane: The case of [E₄(Pd(PPh₂Me)₂)₄] [Ph₂EX₂]₂ (E = Sb, X = Cl; E = Bi, X = Br)

Doi:10.1021/ja982902u
(1999)
Synthesis, transition temperatures, and optical properties of compounds with simple phenyl units linked by double bond, triple bond, ester or propiolate linkages

Doi:10.1039/b001164i
(2000)
Lewis acid mediated [1,2]-rearrangement of ammonium ylides

Doi:10.1016/j.tetlet.2007.04.151
(2007)
A new preparative method for the synthesis of diethyl 1-diazo-2,2,2- trifluoroethylphosphonate via an imino phosphonate

Doi:10.1007/s11172-010-0051-1
(2010)

Article Doi