IL242493B - Pharmaceutical formulations relieve radioactivity - Google Patents

Pharmaceutical formulations relieve radioactivity

Info

Publication number
IL242493B
IL242493B IL242493A IL24249315A IL242493B IL 242493 B IL242493 B IL 242493B IL 242493 A IL242493 A IL 242493A IL 24249315 A IL24249315 A IL 24249315A IL 242493 B IL242493 B IL 242493B
Authority
IL
Israel
Prior art keywords
radiomitigating
phamaceutical
formulations
phamaceutical formulations
radiomitigating phamaceutical
Prior art date
Application number
IL242493A
Other languages
English (en)
Hebrew (he)
Other versions
IL242493A0 (en
Original Assignee
Univ California
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 Univ California filed Critical Univ California
Publication of IL242493A0 publication Critical patent/IL242493A0/en
Publication of IL242493B publication Critical patent/IL242493B/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/22Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with hetero atoms directly attached to ring nitrogen atoms
    • C07D295/26Sulfur atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P39/00General protective or antinoxious agents
    • A61P39/06Free radical scavengers or antioxidants
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/15Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/16Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
    • 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
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/54Sulfur atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/92Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with a hetero atom directly attached to the ring nitrogen atom
    • C07D211/96Sulfur atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/48Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C07D215/54Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D333/30Hetero atoms other than halogen
    • C07D333/34Sulfur atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Toxicology (AREA)
  • Biochemistry (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Epidemiology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Hydrogenated Pyridines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
IL242493A 2013-05-07 2015-11-08 Pharmaceutical formulations relieve radioactivity IL242493B (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201361820447P 2013-05-07 2013-05-07
PCT/US2014/037110 WO2014182789A2 (en) 2013-05-07 2014-05-07 Radiomitigating pharmaceutical formulations

Publications (2)

Publication Number Publication Date
IL242493A0 IL242493A0 (en) 2016-02-01
IL242493B true IL242493B (en) 2020-08-31

Family

ID=51867859

Family Applications (1)

Application Number Title Priority Date Filing Date
IL242493A IL242493B (en) 2013-05-07 2015-11-08 Pharmaceutical formulations relieve radioactivity

Country Status (11)

Country Link
US (3) US9783515B2 (enExample)
EP (1) EP2994457B1 (enExample)
JP (1) JP2016523830A (enExample)
KR (1) KR20160005356A (enExample)
CN (1) CN105579439B (enExample)
AU (1) AU2014262764B2 (enExample)
CA (1) CA2911902A1 (enExample)
ES (1) ES2860949T3 (enExample)
IL (1) IL242493B (enExample)
SG (1) SG11201509194SA (enExample)
WO (1) WO2014182789A2 (enExample)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130203722A1 (en) 2006-09-26 2013-08-08 Rhonda R. Voskuhl Estriol therapy for autoimmune and neurodegenerative disease and disorders
KR20160005356A (ko) * 2013-05-07 2016-01-14 더 리젠츠 오브 더 유니버시티 오브 캘리포니아 방사선완화 약제학적 제형
WO2017156222A1 (en) * 2016-03-09 2017-09-14 The Regents Of The University Of California Radiomitigating compounds, compositions and methods related thereto
AU2017342551B2 (en) * 2016-10-16 2022-10-20 BCN Biosciences L.L.C. Methods of treatment and pharmaceutical compositions using BCN057 or BCN512
AU2018316185A1 (en) * 2017-08-08 2020-03-26 BCN Biosciences L.L.C. Methods of treating radiation induced gastrointestinal syndrome (RIGS) and related disease states using compound 512
WO2023122723A1 (en) 2021-12-23 2023-06-29 The Broad Institute, Inc. Panels and methods for diagnosing and treating lung cancer

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4159331A (en) * 1978-05-05 1979-06-26 The Upjohn Company Antihypertensive 4-aminoquinolines
SI20324A (sl) 1997-10-27 2001-02-28 Agouron Pharmaceuticals, Inc. Substituirane 4-amino-tiazol-2-il spojine kot cdk inhibitorji
US6407120B1 (en) * 1999-02-18 2002-06-18 Pfizer Inc. Neuropeptide Y antagonists
IT1313594B1 (it) * 1999-08-03 2002-09-09 Novuspharma Spa Bisplatino complessi attivi per via orale.
JP4365102B2 (ja) * 2001-04-26 2009-11-18 コーロン ライフ サイエンス インク 新規なスルホンアミド誘導体、その中間体化合物、及びその製造方法、並びにスルホンアミド誘導体を含む薬剤学的組成物
HUE032523T2 (en) * 2003-11-14 2017-09-28 Temple Univ - Of The Commonwealth System Of Higher Education Alpha, beta-unsaturated sulfoxides for the treatment of proliferative disorders
JP2005232101A (ja) * 2004-02-20 2005-09-02 Rikogaku Shinkokai セレコキシブアミノアルキル誘導体
US7345043B2 (en) 2004-04-01 2008-03-18 Miikana Therapeutics Inhibitors of histone deacetylase
MY140912A (en) 2004-07-26 2010-01-29 Du Pont Mixtures of anthranilamide invertebrate pest control agents
US7615570B2 (en) * 2004-12-13 2009-11-10 Abbott Laboratories Antagonists to the vanilloid receptor subtype 1 (VR1) and uses thereof
WO2007029078A2 (en) * 2005-09-05 2007-03-15 Ranbaxy Laboratories Limited Succinimide and glutarimide derivatives as adrenergic receptor antagonists
WO2007143745A2 (en) 2006-06-09 2007-12-13 Icos Corporation Substituted phenyl acetic acids as dp-2 antagonists
EA200900496A1 (ru) 2006-09-28 2009-08-28 Эрет Терэпьютикс, Инк. Сульфонамидные соединения (варианты), содержащая их фармацевтическая композиция, способ ингибирования растворимой эпоксидгидролазы и способ лечения заболеваний, опосредованных растворимой эпоксидгидролазой
JP2011526925A (ja) 2008-07-01 2011-10-20 ザカロン ファーマシューティカルズ,インク. ヘパラン硫酸阻害剤
GB0815781D0 (en) * 2008-08-29 2008-10-08 Xention Ltd Novel potassium channel blockers
WO2010111713A2 (en) * 2009-03-27 2010-09-30 Zacharon Pharmaceuticals, Inc. N-linked glycan biosynthesis modulators
WO2012087889A2 (en) * 2010-12-20 2012-06-28 The Ohio State University Research Foundation Dna methylation inhibitors
US9217000B2 (en) * 2011-02-18 2015-12-22 Univerisyt of Pittsburgh—of the Commonwealth System of Higher Education Targeted nitroxide agents
KR20160005356A (ko) * 2013-05-07 2016-01-14 더 리젠츠 오브 더 유니버시티 오브 캘리포니아 방사선완화 약제학적 제형

Also Published As

Publication number Publication date
US20160221976A1 (en) 2016-08-04
CN105579439B (zh) 2018-10-19
US9840483B2 (en) 2017-12-12
ES2860949T3 (es) 2021-10-05
KR20160005356A (ko) 2016-01-14
EP2994457B1 (en) 2021-01-06
US20160090369A1 (en) 2016-03-31
IL242493A0 (en) 2016-02-01
AU2014262764A1 (en) 2015-12-17
US9783515B2 (en) 2017-10-10
WO2014182789A2 (en) 2014-11-13
CN105579439A (zh) 2016-05-11
AU2014262764B2 (en) 2018-11-15
US20180162827A1 (en) 2018-06-14
JP2016523830A (ja) 2016-08-12
WO2014182789A3 (en) 2014-12-11
CA2911902A1 (en) 2014-11-13
EP2994457A2 (en) 2016-03-16
SG11201509194SA (en) 2015-12-30
EP2994457A4 (en) 2016-09-28

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