RS61065B1 - Hidrohloridne soli n-(cijanometil)-4-(2-(4-morfolinofenilamino)pirimidin-4-il)benzamida - Google Patents

Hidrohloridne soli n-(cijanometil)-4-(2-(4-morfolinofenilamino)pirimidin-4-il)benzamida

Info

Publication number
RS61065B1
RS61065B1 RS20201158A RSP20201158A RS61065B1 RS 61065 B1 RS61065 B1 RS 61065B1 RS 20201158 A RS20201158 A RS 20201158A RS P20201158 A RSP20201158 A RS P20201158A RS 61065 B1 RS61065 B1 RS 61065B1
Authority
RS
Serbia
Prior art keywords
morpholinophenylamino
cyanomethyl
pyrimidin
benzamide hydrochloride
hydrochloride salts
Prior art date
Application number
RS20201158A
Other languages
English (en)
Inventor
Brandon H Brown
Ernest A Carra
Jeffrey N Hemenway
Henry Morrison
Troy Reynolds
Bing Shi
Dimitrios Stefanidis
Fang Wang
Matthew Robert Warr
James Andrew Whitney
Yan Xin
Original Assignee
Sierra Oncology Inc
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=53674249&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=RS61065(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Sierra Oncology Inc filed Critical Sierra Oncology Inc
Publication of RS61065B1 publication Critical patent/RS61065B1/sr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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
    • C07D239/32One oxygen, sulfur or nitrogen atom
    • C07D239/42One nitrogen atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D265/00Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D265/281,4-Oxazines; Hydrogenated 1,4-oxazines
    • C07D265/301,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Hematology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Diabetes (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
RS20201158A 2014-06-12 2015-06-11 Hidrohloridne soli n-(cijanometil)-4-(2-(4-morfolinofenilamino)pirimidin-4-il)benzamida RS61065B1 (sr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201462011315P 2014-06-12 2014-06-12
PCT/US2015/035316 WO2015191846A1 (en) 2014-06-12 2015-06-11 N-(cyanomethyl)-4-(2-(4-morpholinophenylamino)pyrimidin-4-yl)benzamide hydrochloride salts
EP15739042.8A EP3154950B1 (en) 2014-06-12 2015-06-11 N-(cyanomethyl)-4-(2-(4-morpholinophenylamino)pyrimidin-4-yl)benzamide hydrochloride salts

Publications (1)

Publication Number Publication Date
RS61065B1 true RS61065B1 (sr) 2020-12-31

Family

ID=53674249

Family Applications (1)

Application Number Title Priority Date Filing Date
RS20201158A RS61065B1 (sr) 2014-06-12 2015-06-11 Hidrohloridne soli n-(cijanometil)-4-(2-(4-morfolinofenilamino)pirimidin-4-il)benzamida

Country Status (33)

Country Link
US (4) US9469613B2 (sr)
EP (3) EP3719005A1 (sr)
JP (5) JP6600649B2 (sr)
KR (1) KR101928225B1 (sr)
CN (2) CN110627728A (sr)
AP (1) AP2016009551A0 (sr)
AR (1) AR100818A1 (sr)
AU (1) AU2015274554B9 (sr)
BR (1) BR112016028749A2 (sr)
CA (1) CA2951883C (sr)
CR (1) CR20160575A (sr)
CU (1) CU20160183A7 (sr)
CY (1) CY1123604T1 (sr)
DK (1) DK3154950T3 (sr)
EA (1) EA032639B1 (sr)
EC (1) ECSP16093323A (sr)
ES (1) ES2822773T3 (sr)
HR (1) HRP20201492T1 (sr)
HU (1) HUE051360T2 (sr)
IL (3) IL249038B (sr)
LT (1) LT3154950T (sr)
MA (1) MA40067A (sr)
MX (3) MX2016016294A (sr)
NZ (1) NZ725966A (sr)
PH (1) PH12016502461A1 (sr)
PL (1) PL3154950T3 (sr)
PT (1) PT3154950T (sr)
RS (1) RS61065B1 (sr)
SG (2) SG10201911925TA (sr)
SI (1) SI3154950T1 (sr)
TW (3) TWI681954B (sr)
UY (1) UY36166A (sr)
WO (1) WO2015191846A1 (sr)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI681954B (zh) 2014-06-12 2020-01-11 美商西爾拉癌症醫學公司 N-(氰基甲基)-4-(2-(4-𠰌啉基苯基胺基)嘧啶-4-基)苯甲醯胺
CN106316964B (zh) * 2015-06-26 2019-06-25 苏州泽璟生物制药股份有限公司 苯基氨基嘧啶化合物或其盐的多晶型物
CN106316963B (zh) * 2015-06-26 2021-06-08 苏州泽璟生物制药股份有限公司 吗啡啉苯基氨基嘧啶化合物或其盐的多晶型物
TWI794171B (zh) 2016-05-11 2023-03-01 美商滬亞生物國際有限公司 Hdac抑制劑與pd-l1抑制劑之組合治療
TWI808055B (zh) 2016-05-11 2023-07-11 美商滬亞生物國際有限公司 Hdac 抑制劑與 pd-1 抑制劑之組合治療
US10245268B2 (en) 2016-08-10 2019-04-02 Sierra Oncology, Inc. Treatment of ACVR1-mediated diseases
AU2019269815A1 (en) * 2018-05-15 2020-10-22 Jiangsu Hansoh Pharmaceutical Group Co., Ltd. Pharmaceutical composition comprising small molecule EGFR inhibitor and preparation method therefor
KR20210047308A (ko) * 2018-08-21 2021-04-29 시에라 온코로지, 인코퍼레이티드 골수섬유증을 치료하는 혈소판 수-불특정 방법
US20230250068A1 (en) * 2019-02-12 2023-08-10 Inpact Biomedicines, Inc. Crystalline forms of a jak2 inhibitor
EP4376849A1 (en) 2021-07-30 2024-06-05 GlaxoSmithKline LLC Biomarker and patient selection in treatment for myelofibrosis
WO2023019095A2 (en) 2021-08-10 2023-02-16 Sierra Oncology, Inc. Momelotinib combination therapy
WO2023023473A1 (en) 2021-08-16 2023-02-23 Sierra Oncology, Inc. Methods of using momelotinib to treat chronic kidney disease
WO2023152773A1 (en) * 2022-02-14 2023-08-17 Dr. Reddy's Institute Of Life Sciences Solid forms of momelotinib salts and improved processes for the preparation of momelotinib

Family Cites Families (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3481932A (en) 1967-09-01 1969-12-02 Searle & Co 2-anilino-5-methyl-6-phenylpyrimidines and congeners
US5021456A (en) 1988-02-25 1991-06-04 Merrell Dow Pharmaceuticals Inc. Inhibitors of lysyl oxidase
US4965288A (en) 1988-02-25 1990-10-23 Merrell Dow Pharmaceuticals Inc. Inhibitors of lysyl oxidase
US5182297A (en) 1988-02-25 1993-01-26 Merrell Dow Pharmaceuticals Inc. Inhibitors of lysyl oxidase
US5252608A (en) 1988-02-25 1993-10-12 Merrell Dow Pharmaceuticals Inc. Inhibitors of lysyl oxidase
US4943593A (en) 1988-02-25 1990-07-24 Merrell Dow Pharmaceuticals Inc. Inhibitors of lysyl oxidase
US5059714A (en) 1988-02-25 1991-10-22 Merrell Dow Pharmaceuticals Inc. Inhibitors of lysyl oxidase
US5120764A (en) 1988-11-01 1992-06-09 Merrell Dow Pharmaceuticals Inc. Inhibitors of lysyl oxidase
US4997854A (en) 1989-08-25 1991-03-05 Trustees Of Boston University Anti-fibrotic agents and methods for inhibiting the activity of lysyl oxidase in-situ using adjacently positioned diamine analogue substrates
US5559714A (en) 1990-10-22 1996-09-24 Hallmark Cards, Incorporated Method and apparatus for display sequencing personalized social occasion products
GB9523675D0 (en) 1995-11-20 1996-01-24 Celltech Therapeutics Ltd Chemical compounds
GB9914258D0 (en) 1999-06-18 1999-08-18 Celltech Therapeutics Ltd Chemical compounds
GB9924862D0 (en) 1999-10-20 1999-12-22 Celltech Therapeutics Ltd Chemical compounds
US7122544B2 (en) 2000-12-06 2006-10-17 Signal Pharmaceuticals, Llc Anilinopyrimidine derivatives as IKK inhibitors and compositions and methods related thereto
CA2436487A1 (en) 2001-01-30 2002-08-08 Cytopia Pty Ltd. Methods of inhibiting kinases
DE60223790D1 (de) 2001-03-29 2008-01-10 Vertex Pharma Hemmer von c-jun-terminal kinase (jnk) und andere protein kinase
FR2828206B1 (fr) 2001-08-03 2004-09-24 Centre Nat Rech Scient Utilisation d'inhibiteurs des lysyl oxydases pour la culture cellulaire et le genie tissulaire
US6433018B1 (en) 2001-08-31 2002-08-13 The Research Foundation Of State University Of New York Method for reducing hypertrophy and ischemia
WO2003022244A1 (en) 2001-09-12 2003-03-20 Virexx Research, Inc. Vascular occlusion solid-phase agent with immobilised platelet binding agent
US7122550B2 (en) 2002-05-23 2006-10-17 Cytopia Pty Ltd Protein kinase inhibitors
BR0313397A (pt) 2002-08-14 2005-06-28 Vertex Pharmaceuticals Incorpo Inibidores de proteina cinase e usos destes
US7312227B2 (en) 2002-11-01 2007-12-25 Vertex Pharmaceuticals Incorporated Compositions useful as inhibitors of JAK and other protein kinases
WO2004041814A1 (en) 2002-11-04 2004-05-21 Vertex Pharmaceuticals Incorporated Heteroaryl-pyramidine derivatives as jak inhibitors
AU2003286895A1 (en) 2002-11-05 2004-06-07 Vertex Pharmaceuticals Incorporated Compounds useful as inhibitors of jak and other protein kinases
GB0317841D0 (en) 2003-07-30 2003-09-03 Cyclacel Ltd Compound
CA2533474A1 (en) 2003-07-30 2005-02-10 Shudong Wang 2-aminophenyl-4-phenylpyrimidines as kinase inhibitors
LT2612862T (lt) 2004-05-13 2017-01-25 Icos Corporation Chinazolinonai kaip žmogaus fosfatidilinozitol-3-kinazės delta inhibitoriai
BRPI0516597A (pt) 2004-10-13 2008-09-16 Wyeth Corp composto da fórmula
US7593820B2 (en) 2005-05-12 2009-09-22 Cytopia Research Pty Ltd Crystal structure of human Janus Kinase 2 (JAK2) and uses thereof
EA200870217A1 (ru) 2006-01-30 2009-02-27 Экселиксис, Инк. 4-арил-2-аминопиримидины или 4-арил-2-аминоалкилпиримидины в качестве модуляторов jak-2 и содержащие их фармацевтические композиции
WO2007101232A2 (en) 2006-02-28 2007-09-07 Cytopia Research Pty, Ltd. Inhibition of jak2 as a treatment of pulmonary arterial hypertension
FR2911139A1 (fr) 2007-01-05 2008-07-11 Sanofi Aventis Sa Nouveaux derives de phenyl-(4-phenyl-pyrimidin-2-yl)amines, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk
EP3023422A1 (en) 2007-03-12 2016-05-25 YM BioSciences Australia Pty Ltd Phenyl amino pyrimidine compounds and uses thereof
AU2016200866B2 (en) 2007-03-12 2017-06-22 Glaxosmithkline Llc Phenyl amino pyrimidine compounds and uses thereof
AU2013201306B2 (en) 2007-03-12 2015-11-12 Glaxosmithkline Llc Phenyl Amino Pyrimidine Compounds and Uses Thereof
EP2200436B1 (en) 2007-09-04 2015-01-21 The Scripps Research Institute Substituted pyrimidinyl-amines as protein kinase inhibitors
WO2009029998A1 (en) 2007-09-06 2009-03-12 Cytopia Research Pty Ltd Retrometabolic compounds
WO2009073575A2 (en) 2007-11-30 2009-06-11 Oregon Health & Science University Methods for treating induced cellular proliferative disorders
WO2010017122A2 (en) 2008-08-05 2010-02-11 Targegen Inc. Methods of treating thalassemia
UA102128C2 (en) * 2008-12-05 2013-06-10 Х. Луннбек А/С Nalmefene hydrochloride dihydrate
US8450321B2 (en) 2008-12-08 2013-05-28 Gilead Connecticut, Inc. 6-(1H-indazol-6-yl)-N-[4-(morpholin-4-yl)phenyl]imidazo-[1,2-A]pyrazin-8-amine, or a pharmaceutically acceptable salt thereof, as a SYK inhibitor
US8580749B2 (en) 2009-06-05 2013-11-12 Cell Targeting, Inc. Peptide-coated cell localization to diseased or damaged tissues and methods related thereto
JP5086385B2 (ja) * 2010-03-08 2012-11-28 日立オートモティブシステムズ株式会社 電動パワーステアリング制御装置
SG185617A1 (en) 2010-05-31 2012-12-28 Ono Pharmaceutical Co Purinone derivative
WO2012071612A1 (en) 2010-12-03 2012-06-07 Ym Biosciences Australia Pty Ltd Treatment of jak2-mediated conditions
AU2012250491A1 (en) * 2011-05-02 2013-05-02 Ym Biosciences Australia Pty Ltd Multiple myeloma treatment
US8809359B2 (en) 2012-06-29 2014-08-19 Ym Biosciences Australia Pty Ltd Phenyl amino pyrimidine bicyclic compounds and uses thereof
WO2014051056A1 (ja) * 2012-09-28 2014-04-03 東レ株式会社 グリシン誘導体の結晶及びその医薬用途
AU2014205472B2 (en) 2013-01-09 2018-05-10 Concert Pharmaceuticals Inc. Deuterated momelotinib
CN103965114B (zh) 2013-01-28 2016-01-06 苏州泽璟生物制药有限公司 氘代的苯基氨基嘧啶化合物以及包含该化合物的药物组合物
TWI681954B (zh) * 2014-06-12 2020-01-11 美商西爾拉癌症醫學公司 N-(氰基甲基)-4-(2-(4-𠰌啉基苯基胺基)嘧啶-4-基)苯甲醯胺

Also Published As

Publication number Publication date
US9809559B2 (en) 2017-11-07
AU2015274554B2 (en) 2018-02-15
EP3719005A1 (en) 2020-10-07
LT3154950T (lt) 2020-11-25
NZ725966A (en) 2018-04-27
CA2951883C (en) 2020-05-05
IL286442A (en) 2021-10-31
JP2018184486A (ja) 2018-11-22
TWI681954B (zh) 2020-01-11
SG11201610079VA (en) 2016-12-29
BR112016028749A2 (pt) 2017-08-22
USRE49445E1 (en) 2023-03-07
JP6600649B2 (ja) 2019-10-30
HUE051360T2 (hu) 2021-03-01
EP3907219A1 (en) 2021-11-10
MX2019009564A (es) 2019-10-02
PT3154950T (pt) 2020-10-09
WO2015191846A1 (en) 2015-12-17
IL276948A (en) 2020-10-29
KR101928225B1 (ko) 2018-12-11
JP2021107465A (ja) 2021-07-29
ES2822773T3 (es) 2021-05-04
KR20170015496A (ko) 2017-02-08
JP2017517535A (ja) 2017-06-29
IL249038A0 (en) 2017-01-31
PH12016502461A1 (en) 2017-03-06
TW201617323A (zh) 2016-05-16
US20160347719A1 (en) 2016-12-01
MX2016016294A (es) 2017-09-01
ECSP16093323A (es) 2017-01-31
HRP20201492T1 (hr) 2021-01-08
EP3154950A1 (en) 2017-04-19
CN106458929A (zh) 2017-02-22
TW202134236A (zh) 2021-09-16
AR100818A1 (es) 2016-11-02
AP2016009551A0 (en) 2016-11-30
SI3154950T1 (sl) 2021-01-29
DK3154950T3 (da) 2020-09-14
JP2020059759A (ja) 2020-04-16
CN110627728A (zh) 2019-12-31
EP3154950B1 (en) 2020-08-05
UY36166A (es) 2016-01-29
JP6840909B2 (ja) 2021-03-10
IL276948B (en) 2021-09-30
AU2015274554B9 (en) 2018-04-19
US9469613B2 (en) 2016-10-18
MA40067A (fr) 2015-12-17
CU20160183A7 (es) 2017-05-10
JP6883560B2 (ja) 2021-06-09
CY1123604T1 (el) 2022-03-24
AU2015274554A1 (en) 2016-11-24
TWI729644B (zh) 2021-06-01
CR20160575A (es) 2017-01-20
EA032639B1 (ru) 2019-06-28
PL3154950T3 (pl) 2021-01-25
EA201692356A1 (ru) 2017-07-31
TW202012378A (zh) 2020-04-01
MX2022015558A (es) 2023-01-30
IL249038B (en) 2020-09-30
USRE48285E1 (en) 2020-10-27
JP7198867B2 (ja) 2023-01-04
JP2023021454A (ja) 2023-02-10
US20150361050A1 (en) 2015-12-17
CA2951883A1 (en) 2015-12-17
SG10201911925TA (en) 2020-01-30

Similar Documents

Publication Publication Date Title
IL286442A (en) n-(cyanomethyl)-4-(2-(4-morpholinophenylamino)pyrimidin-4-yl)benzamide hydrochloride salts
HK1245244A1 (zh) 作爲激酶抑制劑的雜環酰胺
IL259698B (en) Crystalline 2- (3-ethanesulfonylfluoridine-2-yl)-5- (trifluoromethanesulfonyl)benzoxazole
IL257282B (en) Compounds 2-(4-aminocyclohexylamino)-4-(pyrazol-4-yl)pyrimidine
PL3875459T3 (pl) Sole dichlorowodorkowe walbenazyny i ich polimorfy
IL263739B (en) History of n-(converted-phenyl)-sulfonamide as kinase inhibitors
IL304547A (en) 3-substituted benzamide derivatives as kinase inhibitors
AP2015008407A0 (en) N-(2-(cyclic amine)ethyl) benzamide derivatives asP2X7 inhibitors
PL2986593T3 (pl) Herbicydowo aktywne związki 2-(podstawione-fenylo)-cyklopentano-1,3-dionu i ich pochodne
EP3212611A4 (en) Crystal forms of verapamil hydrochloride
IL265893A (en) Crystal forms of 4-(2-((r1(2r,-2-hydroxycyclohexylamino)benzothiazol-6-yloxy)-n-methylpicolinamide
GB201611641D0 (en) Iosartan amine salts
GB201611642D0 (en) Iosartan amine salts 2
TH1501004620A (th) เฮทเทอโรไซคลิก เอไมด์ ในรูปสารยับยั้งไคเนส
TH1601001993A (th) อะมิโนเฮตเทอโรอัลริล เบนซาไมด์ในรูปตัวยับยั้งไคเนส
PT3395818T (pt) 2-(morfolin-4-il)-1,7-naftiridinas