NO20071515L - Lerkanidipinsalt - Google Patents

Lerkanidipinsalt

Info

Publication number
NO20071515L
NO20071515L NO20071515A NO20071515A NO20071515L NO 20071515 L NO20071515 L NO 20071515L NO 20071515 A NO20071515 A NO 20071515A NO 20071515 A NO20071515 A NO 20071515A NO 20071515 L NO20071515 L NO 20071515L
Authority
NO
Norway
Prior art keywords
acids
clerididipine
acidic
amorphous
salts
Prior art date
Application number
NO20071515A
Other languages
English (en)
Inventor
Gianni Motta
Amadeo Leonardi
Markus Von Raumer
Original Assignee
Recordati Ireland Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Recordati Ireland Ltd filed Critical Recordati Ireland Ltd
Publication of NO20071515L publication Critical patent/NO20071515L/no

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/80Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D211/84Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen directly attached to ring carbon atoms
    • C07D211/90Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives

Abstract

Oppfinnelsen angår nye addisjonssalter innbefattende lerkanidipin og et syremotion valgt fra gruppen bestående av: (i) uorganiske syrer, (ii) sulfonsyrer, (iii) monokarboksylisyrer, (iv) dikarboksylsyrer, (v) trikarboksylsyrer, og (vi) aromatiske sulfonimider, under forutsetning at syremotionet ikke er saltsyre. Spesielt er beskrevet både amorfe og krystallinske salter av lerkanidipin med benzensulfon og naftalen-1,5-disulfonsyrer, samt amorfe salter av lerkanidipin med flere andre syremotioner.
NO20071515A 2004-08-24 2007-03-23 Lerkanidipinsalt NO20071515L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US60414904P 2004-08-24 2004-08-24
PCT/EP2005/009043 WO2006021397A1 (en) 2004-08-24 2005-08-22 Lercanidipine salts

Publications (1)

Publication Number Publication Date
NO20071515L true NO20071515L (no) 2007-05-22

Family

ID=35159792

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20071515A NO20071515L (no) 2004-08-24 2007-03-23 Lerkanidipinsalt

Country Status (19)

Country Link
US (1) US7683179B2 (no)
EP (1) EP1799644B1 (no)
JP (1) JP2008510754A (no)
KR (1) KR20070045351A (no)
CN (1) CN101048379A (no)
AR (1) AR050467A1 (no)
AU (1) AU2005276619B2 (no)
BR (1) BRPI0514606A (no)
CA (1) CA2575078A1 (no)
EA (1) EA011773B1 (no)
ES (1) ES2462921T3 (no)
IL (1) IL180905A0 (no)
MX (1) MX2007002141A (no)
NO (1) NO20071515L (no)
NZ (1) NZ553127A (no)
PE (1) PE20060629A1 (no)
TW (1) TW200613275A (no)
WO (1) WO2006021397A1 (no)
ZA (1) ZA200702364B (no)

Families Citing this family (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ528216A (en) * 2001-02-24 2006-12-22 Boehringer Ingelheim Pharma Xanthine derivatives, the preparation thereof and their use as pharmaceutical compositions
US7407955B2 (en) 2002-08-21 2008-08-05 Boehringer Ingelheim Pharma Gmbh & Co., Kg 8-[3-amino-piperidin-1-yl]-xanthines, the preparation thereof and their use as pharmaceutical compositions
US7501426B2 (en) 2004-02-18 2009-03-10 Boehringer Ingelheim International Gmbh 8-[3-amino-piperidin-1-yl]-xanthines, their preparation and their use as pharmaceutical compositions
DE102004054054A1 (de) 2004-11-05 2006-05-11 Boehringer Ingelheim Pharma Gmbh & Co. Kg Verfahren zur Herstellung chiraler 8-(3-Amino-piperidin-1-yl)-xanthine
AR052918A1 (es) * 2005-02-25 2007-04-11 Recordati Ireland Ltd Clorhidrato de lercanidipina amorfo
AR053023A1 (es) * 2005-02-25 2007-04-18 Recordati Ireland Ltd Base libre de lercanidipina, metodos para su preparacion y composiciones farmaceuticas que las contienen
DE102005035891A1 (de) * 2005-07-30 2007-02-08 Boehringer Ingelheim Pharma Gmbh & Co. Kg 8-(3-Amino-piperidin-1-yl)-xanthine, deren Herstellung und deren Verwendung als Arzneimittel
EP1852108A1 (en) 2006-05-04 2007-11-07 Boehringer Ingelheim Pharma GmbH & Co.KG DPP IV inhibitor formulations
PE20080251A1 (es) 2006-05-04 2008-04-25 Boehringer Ingelheim Int Usos de inhibidores de dpp iv
EA030606B1 (ru) 2006-05-04 2018-08-31 Бёрингер Ингельхайм Интернациональ Гмбх Способы приготовления лекарственного средства, содержащего полиморфы
JP2009540007A (ja) 2006-06-12 2009-11-19 ノバルティス アクチエンゲゼルシャフト N−ヒドロキシ−3−[4−[[[2−(2−メチル−1h−インドール−3−イル)エチル]アミノ]メチル]フェニル]−2e−2−プロペンアミドの塩の製造方法
WO2008040367A1 (en) * 2006-08-01 2008-04-10 Union Quimico-Farmaceutica S.A. Lercanidipine hydrobromide, a process for its preparation, crystalline forms and compositions thereof
US20080175872A1 (en) * 2006-09-28 2008-07-24 Osmotica Corp. Controlled Release Dosage Form Containing Lercanidipine and a Performance-enhancing Acid
ES2306595B1 (es) * 2007-02-09 2009-09-11 Laboratorios Almirall S.A. Sal de napadisilato de 5-(2-((6-(2,2-difluoro-2-feniletoxi)hexil)amino)-1-hidroxietil)-8-hidroxiquinolin-2(1h)-ona como agonista del receptor adrenergico beta2.
US20080234516A1 (en) * 2007-03-14 2008-09-25 Valerie Niddam-Hildesheim Processes for preparing solid states of O-desmethylvenlafaxine succinate
WO2009017813A1 (en) * 2007-08-02 2009-02-05 Teva Pharmaceutical Industries Ltd. O-desmethyl venlafaxine saccharinate
US8063250B2 (en) 2007-11-26 2011-11-22 Teva Pharmaceutical Industries, Ltd. Crystal forms of O-desmethylvenlafaxine fumarate
PE20140960A1 (es) 2008-04-03 2014-08-15 Boehringer Ingelheim Int Formulaciones que comprenden un inhibidor de dpp4
AU2009276560B2 (en) * 2008-08-01 2015-04-16 Chiesi Farmaceutici S.P.A. Pharmaceutical compositions and methods for producing low impurity concentrations of the same
SI2320739T1 (sl) * 2008-08-01 2020-03-31 Chiesi Farmaceutici S.P.A. Farmacevtski sestavki in postopki za njihovo stabiliziranje
BRPI0916997A2 (pt) 2008-08-06 2020-12-15 Boehringer Ingelheim International Gmbh Inibidor de dpp-4 e seu uso
UY32030A (es) 2008-08-06 2010-03-26 Boehringer Ingelheim Int "tratamiento para diabetes en pacientes inapropiados para terapia con metformina"
EP2344195A2 (en) 2008-09-10 2011-07-20 Boehringer Ingelheim International GmbH Combination therapy for the treatment of diabetes and related conditions
US20200155558A1 (en) 2018-11-20 2020-05-21 Boehringer Ingelheim International Gmbh Treatment for diabetes in patients with insufficient glycemic control despite therapy with an oral antidiabetic drug
BRPI0923121A2 (pt) 2008-12-23 2015-08-11 Boehringer Ingelheim Int Formas salinas de compostos orgânico
TW201036975A (en) 2009-01-07 2010-10-16 Boehringer Ingelheim Int Treatment for diabetes in patients with inadequate glycemic control despite metformin therapy
ES2760917T3 (es) 2009-11-27 2020-05-18 Boehringer Ingelheim Int Tratamiento de pacientes diabéticos genotipificados con inhibidores DPP-IV como la linagliptina
CA2795023A1 (en) * 2010-03-29 2011-10-06 Pliva Hrvatska D.O.O. Crystal forms of o-desmethylvenlafaxine fumarate
JP6034781B2 (ja) 2010-05-05 2016-11-30 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 併用療法
EA201991014A1 (ru) 2010-06-24 2019-09-30 Бёрингер Ингельхайм Интернациональ Гмбх Лечение диабета
US9034883B2 (en) 2010-11-15 2015-05-19 Boehringer Ingelheim International Gmbh Vasoprotective and cardioprotective antidiabetic therapy
MX366629B (es) 2011-07-15 2019-07-17 Boehringer Ingelheim Int Quinazolinas sustituidas, su preparación y su uso en composiciones farmacéuticas.
US9555001B2 (en) 2012-03-07 2017-01-31 Boehringer Ingelheim International Gmbh Pharmaceutical composition and uses thereof
EP3685839A1 (en) 2012-05-14 2020-07-29 Boehringer Ingelheim International GmbH Linagliptin for use in the treatment of albuminuria and kidney related diseases
WO2013174767A1 (en) 2012-05-24 2013-11-28 Boehringer Ingelheim International Gmbh A xanthine derivative as dpp -4 inhibitor for use in modifying food intake and regulating food preference
US9526728B2 (en) 2014-02-28 2016-12-27 Boehringer Ingelheim International Gmbh Medical use of a DPP-4 inhibitor
JP2019517542A (ja) 2016-06-10 2019-06-24 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング リナグリプチンおよびメトホルミンの組合せ
WO2023219106A1 (ja) * 2022-05-10 2023-11-16 Myrodia Therapeutics株式会社 2-メチル-2-チアゾリンの塩

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8403866D0 (en) 1984-02-14 1984-03-21 Recordati Chem Pharm Diphenylalkylaminoalkyl esters
IT1275532B (it) * 1995-07-14 1997-08-07 Recordati Chem Pharm Uso di derivati 1,4-diidropiridinici per la prevenzione e la terapia della degenerazione aterosclerotica della parete arteriosa
US5696139A (en) 1995-05-12 1997-12-09 Recordati S.A., Chemical And Pharmaceutical Company Use of S-enantiomers of 1,4-dihydropyridine derivatives for treating heart failure
US5912351A (en) 1995-05-12 1999-06-15 Recordati, S.A. Chemical And Pharmaceutical Company Anhydrous 1,4-Dihydropyridines and salts thereof
IT1301759B1 (it) * 1998-06-19 2000-07-07 Nicox Sa Sali nitrati di farmaci antiipertensivi
US20030069285A1 (en) 2001-08-06 2003-04-10 Recordati Ireland Limited Novel solvate and crystalline forms of lercanidipine hydrochloride
US6852737B2 (en) 2001-08-06 2005-02-08 Recordati Ireland Limited Crude and crystalline forms of lercanidipine hydrochloride
US6699892B2 (en) * 2002-06-04 2004-03-02 Yung Shin Pharmaceutical Industrial Co., Ltd. Pharmaceutically acceptable salt of amlodipine and method of preparing the same
JP2006504800A (ja) * 2002-10-16 2006-02-09 レコーダチ アイルランド リミテッド リシノプリル/レルカニジピンの組み合わせ治療
US20040198789A1 (en) * 2003-02-28 2004-10-07 Recordati Ireland Limited Lercanidipine/ARB/diuretic therapeutic combinations

Also Published As

Publication number Publication date
PE20060629A1 (es) 2006-08-11
CN101048379A (zh) 2007-10-03
EP1799644A1 (en) 2007-06-27
EP1799644B1 (en) 2014-02-12
CA2575078A1 (en) 2006-03-02
WO2006021397A8 (en) 2006-04-27
ZA200702364B (en) 2008-09-25
EA200700492A1 (ru) 2007-08-31
US20060047125A1 (en) 2006-03-02
KR20070045351A (ko) 2007-05-02
AU2005276619B2 (en) 2009-04-30
AU2005276619A1 (en) 2006-03-02
NZ553127A (en) 2009-07-31
BRPI0514606A (pt) 2008-06-17
MX2007002141A (es) 2007-04-27
TW200613275A (en) 2006-05-01
JP2008510754A (ja) 2008-04-10
ES2462921T3 (es) 2014-05-26
US7683179B2 (en) 2010-03-23
IL180905A0 (en) 2007-07-04
EA011773B1 (ru) 2009-06-30
AR050467A1 (es) 2006-10-25
WO2006021397A1 (en) 2006-03-02

Similar Documents

Publication Publication Date Title
NO20071515L (no) Lerkanidipinsalt
AR121612A2 (es) Inhibidores de glucosilceramida sintasa
CY1118992T1 (el) Μεθοδοι παραγωγης κυκλοαλκυλκαρβοξαμιδο-πυριδινο βενζοϊκων οξεων
CY1118630T1 (el) Στερεες μορφες 3-(6-(1-(2,2-διφθοροβενζο[d][1,3]διοξολ-5-υλο)-κυκλοπροπανοκαρβοξαμ1δο)-3-μεθυλοπυριδιν-3-υλο)-βενζοϊκου οξεος
CY1113029T1 (el) Παραγωγα αζαδικυκλο [3.1.0] εξανιου χρησιμα ως ρυθμιστες υποδοχεων d3 ντοπαμινης
NO20092770L (no) Nye aminopyrimidinderivater som PLK1-inhibitorer
NO20083582L (no) Pyridin-2-karboksamide derivater
NO20091141L (no) Pyrido (2,3-D) pyrimidinonforbindelser og deres anvendelse som P13 inhibitorer
NO20083708L (no) 4-Fenyl-tiazol-5-karboksylsyre og 4-fenyl-tiazol-5-karboksylmider som PLK1-inhibitorer
EA200000804A1 (ru) Мета-азациклические соединения аминобензойной кислоты и их производные, являющиеся ингибиторами интегрина
NO20055694L (no) Fremgangsmate for fremstilling av (4-hydroksy-6-oksotetrahydropyran-2-yl)acetonitril og derivater derav
DE60311869D1 (de) Kristalline cefdinirsalze
MX2010003849A (es) Antagonistas de cgrp.
MX2009005911A (es) Sal de potasio cristalina de analogos de lipoxina a4.
MA34377B1 (fr) Composé de pipéridinyle en tant que modulateur de l'activité des récepteurs des chimiokines
NO20071111L (no) Kynurensyreamidderivater som NR2B-reseptorantagonister
NO20082727L (no) Salter av 9-oksoakridin-10-eddiksyre med 1-alkylamino-1-deoksypolyoler
WO2008001392A3 (en) An improved process for the preparation of pantoprazole and its pharmaceutically acceptable salts
EA200801960A1 (ru) Соли дулоксетина
CY1112714T1 (el) Διαδικασια για την παρασκευη υψηλης-καθαροτητας μελοξικαμης και αλατος καλιου της μελοξικαμης
TH87787B (th) เกลือกลูคูโรเนตของสารประกอบพิเพอราซีน
NO20013000L (no) Nye <beta>-amid- og <beta>-sulfonamidkarboksylsyrederivater, deres fremstilling og anvendelse som endotelinreseptorantagonister
TH1901006588A (th) เกลือโอพิออยด์รีเซพเตอร์(mor)อะโกนิสต์,รูปผลึกiของเกลือฟิวมาเรตของเกลือนั้นและวิธีการเตรียมเกลือนั้น
TH126053A (th) อนุพันธ์อินโดล (indole derivative)ซึ่งเป็น CRTH2 รีเซพเตอร์ แอนทาโกนิสต์ (CRTH2 receptor antagonist)
Ripka Atrofické zmeny v nárečových prejavoch amerických Slovákov

Legal Events

Date Code Title Description
FC2A Withdrawal, rejection or dismissal of laid open patent application