JPH11507364A5 - - Google Patents

Info

Publication number
JPH11507364A5
JPH11507364A5 JP1997501990A JP50199097A JPH11507364A5 JP H11507364 A5 JPH11507364 A5 JP H11507364A5 JP 1997501990 A JP1997501990 A JP 1997501990A JP 50199097 A JP50199097 A JP 50199097A JP H11507364 A5 JPH11507364 A5 JP H11507364A5
Authority
JP
Japan
Legal status (The legal status 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 status listed.)
Ceased
Application number
JP1997501990A
Other languages
English (en)
Japanese (ja)
Other versions
JPH11507364A (ja
Filing date
Publication date
Priority claimed from US08/476,296 external-priority patent/US5750088A/en
Application filed filed Critical
Publication of JPH11507364A publication Critical patent/JPH11507364A/ja
Publication of JPH11507364A5 publication Critical patent/JPH11507364A5/ja
Ceased legal-status Critical Current

Links

JP9501990A 1995-06-07 1996-06-07 放射性医薬製造用の安定試薬 Ceased JPH11507364A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US08/476,296 US5750088A (en) 1993-03-30 1995-06-07 Stable hydrazones linked to a peptide moiety as reagents for the preparation of radiopharmaceuticals
US08/476,296 1995-06-07
PCT/US1996/009766 WO1996040637A1 (en) 1995-06-07 1996-06-07 Stable reagents for the preparation of radiopharmaceuticals

Publications (2)

Publication Number Publication Date
JPH11507364A JPH11507364A (ja) 1999-06-29
JPH11507364A5 true JPH11507364A5 (enExample) 2004-07-29

Family

ID=23891282

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9501990A Ceased JPH11507364A (ja) 1995-06-07 1996-06-07 放射性医薬製造用の安定試薬

Country Status (29)

Country Link
US (2) US5750088A (enExample)
EP (1) EP0832068B1 (enExample)
JP (1) JPH11507364A (enExample)
KR (1) KR19990022573A (enExample)
CN (1) CN1192733A (enExample)
AR (1) AR003959A1 (enExample)
AT (1) ATE233241T1 (enExample)
AU (1) AU718683B2 (enExample)
BR (1) BR9609003A (enExample)
CA (1) CA2222183A1 (enExample)
CZ (1) CZ380197A3 (enExample)
DE (1) DE69626392T2 (enExample)
EA (1) EA000742B1 (enExample)
EE (1) EE9700313A (enExample)
ES (1) ES2193245T3 (enExample)
HR (1) HRP960250A2 (enExample)
HU (1) HUP9901469A3 (enExample)
IL (1) IL118468A0 (enExample)
LT (1) LT4380B (enExample)
LV (1) LV12044B (enExample)
MX (1) MX9709126A (enExample)
MY (1) MY133974A (enExample)
NO (1) NO975678L (enExample)
NZ (1) NZ310799A (enExample)
PL (1) PL323995A1 (enExample)
SI (1) SI9620076B (enExample)
SK (1) SK163497A3 (enExample)
WO (1) WO1996040637A1 (enExample)
ZA (1) ZA964854B (enExample)

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US6403054B1 (en) 1997-05-28 2002-06-11 Bristol-Myers Squibb Pharma Company Ternary ligand complexes useful as radiopharmaceuticals
US6524553B2 (en) 1998-03-31 2003-02-25 Bristol-Myers Squibb Pharma Company Quinolone vitronectin receptor antagonist pharmaceuticals
US6537520B1 (en) * 1998-03-31 2003-03-25 Bristol-Myers Squibb Pharma Company Pharmaceuticals for the imaging of angiogenic disorders
WO1999051628A1 (en) * 1998-04-03 1999-10-14 Du Pont Pharmaceuticals Company Radiopharmaceuticals for imaging infection and inflammation and for imaging and treatment of cancer
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US6794518B1 (en) * 1998-12-18 2004-09-21 Bristol-Myers Squibb Pharma Company Vitronectin receptor antagonist pharmaceuticals
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CA2727746A1 (en) 1998-12-18 2000-06-22 Bristol-Myers Squibb Pharma Company Quinolone vitronectin receptor antagonist pharmaceuticals
US6511649B1 (en) 1998-12-18 2003-01-28 Thomas D. Harris Vitronectin receptor antagonist pharmaceuticals
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US6808698B1 (en) 1999-03-26 2004-10-26 Bristol-Myers Squibb Pharma Company Method for localization of blood clots
US6656448B1 (en) * 2000-02-15 2003-12-02 Bristol-Myers Squibb Pharma Company Matrix metalloproteinase inhibitors
US20030220646A1 (en) * 2002-05-23 2003-11-27 Thelen Sarah L. Method and apparatus for reducing femoral fractures
US6534038B2 (en) 2000-04-07 2003-03-18 Bristol-Myers Squibb Pharma Company Ternary ligand complexes useful as radiopharmaceuticals
JP2004512382A (ja) 2000-11-03 2004-04-22 ブリストル−マイヤーズ・スクイブ・ファーマ・カンパニー 心臓灌流および心臓炎症の２核種同時イメージング
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HUP0401904A3 (en) * 2001-08-08 2009-01-28 Bristol Myers Squibb Pharma Co Simultaneous imaging of cardiac perfusion and a vitronectin receptor targeted imaging agent
US6838074B2 (en) 2001-08-08 2005-01-04 Bristol-Myers Squibb Company Simultaneous imaging of cardiac perfusion and a vitronectin receptor targeted imaging agent
US7297709B2 (en) 2003-05-22 2007-11-20 Abbott Laboratories Indazole, benzisoxazole, and benzisothiazole kinase inhibitors
US7317104B2 (en) 2003-06-13 2008-01-08 Bristol-Myers Squibb Pharma Company Chelants and macrocyclic metal complex radiopharmaceuticals thereof
US7319149B2 (en) * 2003-06-13 2008-01-15 Bristol-Myers Squibb Pharma Company Chelants and macrocyclic metal complex radiopharmaceuticals thereof
BRPI0412824A (pt) * 2003-07-24 2006-09-26 Bracco Imaging Spa composições radiofarmacêuticas estáveis e métodos para suas preparações
US20050106100A1 (en) * 2003-09-03 2005-05-19 Harris Thomas D. Compounds containing matrix metalloproteinase substrates and methods of their use
EP1896086A1 (en) * 2005-06-30 2008-03-12 Bristol-Myers Squibb Pharma Company Hydrazide conjugates as imaging agents
EP1950205A4 (en) * 2005-10-19 2010-07-07 Dainippon Sumitomo Pharma Co METHOD FOR STABILIZING AN ISOXAZOLE COMPOUND
US7465795B2 (en) * 2005-12-20 2008-12-16 Astrazeneca Ab Compounds and uses thereof
RU2008122405A (ru) * 2005-12-20 2010-01-27 Астразенека Аб (Se) Замещенные производные циннолина в качестве модуляторов гамма-рецепторов и способ их синтеза
US8034815B2 (en) 2007-01-11 2011-10-11 Critical Outcome Technologies, Inc. Compounds and method for treatment of cancer
TW200911760A (en) * 2007-06-19 2009-03-16 Astrazeneca Ab Compounds and uses thereof
CA2710039C (en) 2007-12-26 2018-07-03 Critical Outcome Technologies, Inc. Semicarbazones, thiosemicarbazones and related compounds and methods for treatment of cancer
EP2318406B1 (en) 2008-07-17 2016-01-27 Critical Outcome Technologies, Inc. Thiosemicarbazone inhibitor compounds and cancer treatment methods
ES2481042T3 (es) 2008-12-29 2014-07-29 Sanofi Derivados de 2-piridin-2-il-pirazol-3(2H)-ona, su preparación y uso terapéutico como activadores de HIF
FR2949468B1 (fr) * 2009-08-28 2011-09-30 Sanofi Aventis Derives de 2-pyridin-2-yl-pyrazol-3(2h)-one, leur preparation et leur application en therapeutique
AU2009334570B2 (en) * 2008-12-29 2016-06-09 Sanofi Derivatives of 2-pyridin-2-yl-pyrazol-3(2h)-one, preparation and therapeutic use thereof
FR2940652B1 (fr) * 2008-12-29 2011-02-11 Sanofi Aventis Derives de 2-pyridin-2-yl-pyrazol-3(2h)-one,leur preparation et leur application en therapeutique
CA2999435A1 (en) 2010-04-01 2011-10-06 Critical Outcome Technologies Inc. Compounds and method for treatment of hiv
FR2967671A1 (fr) * 2010-11-24 2012-05-25 Pf Medicament Complexe de technetium 99m en tant qu'outil de diagnostic in vivo des tumeurs cancereuses
CN110818624B (zh) * 2019-11-22 2022-11-22 华东理工大学 吡啶季铵盐腙类化合物及制备方法与在抗菌或香料缓释中的应用
CN112999369B (zh) * 2021-03-03 2022-02-25 江苏元本生物科技有限公司 一种her2亲合体放射性核素标记物组合物及其应用

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