MA43580A - L-valinate d'un dérivé d'hydroxypropylthiazolidine carboxamide, sel et forme cristalline polymorphe correspondants - Google Patents

L-valinate d'un dérivé d'hydroxypropylthiazolidine carboxamide, sel et forme cristalline polymorphe correspondants

Info

Publication number
MA43580A
MA43580A MA043580A MA43580A MA43580A MA 43580 A MA43580 A MA 43580A MA 043580 A MA043580 A MA 043580A MA 43580 A MA43580 A MA 43580A MA 43580 A MA43580 A MA 43580A
Authority
MA
Morocco
Prior art keywords
valinate
salt
crystalline form
polymorphic crystalline
corresponding polymorphic
Prior art date
Application number
MA043580A
Other languages
English (en)
Inventor
Catherine Jorand-Lebrun
Page Patrick Naxos
Vincent Pomel
Anna Quattropani
Matthias Schwarz
Original Assignee
Merck Serono Sa
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
Priority claimed from US14/987,586 external-priority patent/US9447055B1/en
Application filed by Merck Serono Sa filed Critical Merck Serono Sa
Publication of MA43580A publication Critical patent/MA43580A/fr

Links

Classifications

    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
    • A61K31/4261,3-Thiazoles
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/44221,4-Dihydropyridines, e.g. nifedipine, nicardipine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/04Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • A61K38/08Peptides having 5 to 11 amino acids
    • A61K38/095Oxytocins; Vasopressins; Related peptides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/04Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • A61K38/12Cyclic peptides, e.g. bacitracins; Polymyxins; Gramicidins S, C; Tyrocidins A, B or C
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • A61P15/06Antiabortive agents; Labour repressants
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/04Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D277/06Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • Organic Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Reproductive Health (AREA)
  • Endocrinology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Immunology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Pregnancy & Childbirth (AREA)
  • Gynecology & Obstetrics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Cephalosporin Compounds (AREA)
  • Rheumatology (AREA)
  • Pyrrole Compounds (AREA)
  • Pain & Pain Management (AREA)
  • Emergency Medicine (AREA)
  • Medicinal Preparation (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Peptides Or Proteins (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
MA043580A 2016-01-04 2017-01-04 L-valinate d'un dérivé d'hydroxypropylthiazolidine carboxamide, sel et forme cristalline polymorphe correspondants MA43580A (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201662274674P 2016-01-04 2016-01-04
US14/987,586 US9447055B1 (en) 2016-01-04 2016-01-04 α-amino esters of hydroxypropylthiazolidine carboxamide derivative and salt form, crystal polymorph thereof
US201662395664P 2016-09-16 2016-09-16
US201662407918P 2016-10-13 2016-10-13

Publications (1)

Publication Number Publication Date
MA43580A true MA43580A (fr) 2021-05-26

Family

ID=57799697

Family Applications (2)

Application Number Title Priority Date Filing Date
MA043580A MA43580A (fr) 2016-01-04 2017-01-04 L-valinate d'un dérivé d'hydroxypropylthiazolidine carboxamide, sel et forme cristalline polymorphe correspondants
MA043549A MA43549A (fr) 2016-01-04 2017-01-04 Alpha-amino esters de dérivé d'hydroxypropylthiazolidine carboxamide, sel et forme cristalline polymorphe correspondants

Family Applications After (1)

Application Number Title Priority Date Filing Date
MA043549A MA43549A (fr) 2016-01-04 2017-01-04 Alpha-amino esters de dérivé d'hydroxypropylthiazolidine carboxamide, sel et forme cristalline polymorphe correspondants

Country Status (25)

Country Link
EP (4) EP3400217B1 (fr)
JP (6) JP6933322B2 (fr)
KR (3) KR20250107965A (fr)
CN (1) CN108779087A (fr)
AU (5) AU2017205670B2 (fr)
CA (2) CA3009576A1 (fr)
CY (2) CY1125231T1 (fr)
DK (2) DK3397622T3 (fr)
EA (1) EA036990B1 (fr)
ES (2) ES2916835T3 (fr)
HR (2) HRP20220674T1 (fr)
HU (2) HUE058872T2 (fr)
IL (5) IL318222A (fr)
LT (2) LT3400217T (fr)
MA (2) MA43580A (fr)
MX (3) MX389261B (fr)
PL (2) PL3400217T3 (fr)
PT (2) PT3400217T (fr)
RS (2) RS63285B1 (fr)
SG (4) SG11201804594YA (fr)
SI (2) SI3400217T1 (fr)
SM (2) SMT202200248T1 (fr)
UA (2) UA125377C2 (fr)
WO (2) WO2017118639A1 (fr)
ZA (1) ZA201903769B (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
LT3400217T (lt) * 2016-01-04 2022-06-27 Merck Serono S.A. Hidroksipropiltiazolidino karboksamido l-valinato darinys, jo druska ir jo kristalinė forma
RU2711615C1 (ru) * 2019-09-12 2020-01-17 Федеральное государственное бюджетное научное учреждение "Научно-исследовательский институт акушерства, гинекологии и репродуктологии имени Д.О. Отта" Способ лечения эндометриоза на основании экспериментальной модели у крыс
CA3152099A1 (fr) * 2019-09-23 2021-04-01 Liang Liang Procedes de traitement de prolongation de la gestation et des complications des menstruations ou de la gestation
US12426782B2 (en) 2020-11-06 2025-09-30 The Board Of Trustees Of The Leland Stanford Junior University Systems and temporal alignment methods for evaluation of gestational age and time to delivery
WO2022125876A1 (fr) * 2020-12-11 2022-06-16 Olsen Elise A Compositions et procédés destinés à inhiber la croissance pileuse

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3835175A (en) 1971-03-15 1974-09-10 Research Corp 9-fluorenylmethanol haloformates, carbonates and thiocarbonates
US3839396A (en) 1971-07-15 1974-10-01 Shionogi & Co 9-lower alkyl-9-fluorenyl carbonates
US4108846A (en) 1977-02-01 1978-08-22 Hoffmann-La Roche Inc. Solid phase synthesis with base N alpha-protecting group cleavage
SE430885B (sv) 1980-03-24 1983-12-19 Ferring Ab Oxytocin-derivat
US4581167A (en) 1982-01-19 1986-04-08 Research Corporation Peptide synthesis and amino acid blocking agents
US4508657A (en) 1982-01-19 1985-04-02 Research Corporation Peptide synthesis and amino acid blocking agents
US4504469A (en) 1982-12-21 1985-03-12 Ferring Ab Vasotocin derivatives
US4460501A (en) 1983-08-30 1984-07-17 Research Corporation Process for the synthesis of peptides utilizing thioxanthylmethyloxycarbonyl dioxides
US5370135A (en) * 1993-10-13 1994-12-06 Biex, Inc. Use of estriol measurement to monitor tocolytic therapy
DE4434488A1 (de) * 1994-09-14 1996-03-21 Schering Ag Steroidester und -amide, Verfahren zu ihrer Herstellung und ihre pharmazeutische Verwendung
SE9604341D0 (sv) 1996-11-26 1996-11-26 Ferring Bv Hepta-peptide oxytocin analogue
IN188411B (fr) * 1997-03-27 2002-09-21 Yuhan Corp
AU2001261161A1 (en) * 2000-05-30 2001-12-11 Ortho-Mcneil Pharmaceutical, Inc. Dihydropyridine compounds for inhibition of calcium-influx
GB0130677D0 (en) 2001-12-21 2002-02-06 Glaxo Group Ltd Medicaments and novel compounds
AU2003211011A1 (en) 2002-02-27 2003-09-09 Ferring Bv Intermediates and methods for making heptapeptide oxytocin analogues
RS81604A (sr) 2002-03-28 2006-12-15 Applied Research Systems Ars Holding N.V. Derivati tijazolidin karboksamida kao modulatori receptora prostaglandina f
GB0208785D0 (en) * 2002-04-17 2002-05-29 Medical Res Council Treatment methtods
US7521530B2 (en) * 2002-06-11 2009-04-21 Universite De Montreal Peptides and peptidomimetics useful for inhibiting the activity of prostaglandin F2α receptor
UA78058C2 (en) 2002-07-05 2007-02-15 Applied Research Systems Pyrrolidine derivative as oxitocin antagonists
MXPA05006230A (es) * 2002-12-12 2005-09-20 Idenix Cayman Ltd Proceso para la produccion de nucleosidos ramificados-2'.
GB0314738D0 (en) 2003-06-24 2003-07-30 Glaxo Group Ltd Novel compounds
GB0414093D0 (en) 2004-06-23 2004-07-28 Glaxo Group Ltd Novel compounds
EP2493874A1 (fr) 2009-10-30 2012-09-05 Glaxo Group Limited Nouvelles formes cristallines de (3r,6r) -3- (2, 3 -dihydro- 1h- inden- 2 -yl) - 1 - [ (1r) - 1 - (2, 6 - diméthyl - 3 - pyridinyl) - 2 - (4 -morpholinyl) -2-oxoéthyl]-6- [(1s) - 1 -méthylpropyl]-2,5- pipérazinedione
EP2845850A1 (fr) 2013-09-10 2015-03-11 ObsEva S.A. Dérivés de pyrrolidine comme antagonistes des récepteurs V1a de vasopressine/oxytocine
EP2886107A1 (fr) 2013-12-17 2015-06-24 ObsEva S.A. Formules orales de dérivés de pyrrolydine
AU2014397706A1 (en) * 2014-06-16 2016-12-22 Glaxosmithkline Intellectual Property Development Limited Retosiban for the treatment of pre-term labour
CN114105851A (zh) 2014-07-02 2022-03-01 奥布赛瓦股份公司 治疗ot-r活性相关的病症的方法中可用的晶体
ES2716862T3 (es) 2014-12-22 2019-06-17 Ferring Bv Terapia con antagonistas del receptor de oxitocina en la fase lútea para la implantación y embarazo en mujeres que se someten a tecnologías de reproducción asistida
US9447055B1 (en) * 2016-01-04 2016-09-20 Merck Serono S.A. α-amino esters of hydroxypropylthiazolidine carboxamide derivative and salt form, crystal polymorph thereof
LT3400217T (lt) * 2016-01-04 2022-06-27 Merck Serono S.A. Hidroksipropiltiazolidino karboksamido l-valinato darinys, jo druska ir jo kristalinė forma

Also Published As

Publication number Publication date
MX389261B (es) 2025-03-20
JP7432284B2 (ja) 2024-02-16
KR102795275B1 (ko) 2025-04-11
IL260286B (en) 2022-02-01
AU2017205670A1 (en) 2018-08-16
PL3397622T3 (pl) 2022-07-04
CA3009576A1 (fr) 2017-07-13
EA036990B1 (ru) 2021-01-25
JP2024012376A (ja) 2024-01-30
AU2023233151A1 (en) 2023-10-12
IL259742A (en) 2018-07-31
SI3397622T1 (sl) 2022-07-29
MX2022000154A (es) 2022-02-21
AU2017205254A1 (en) 2018-08-16
IL260286A (en) 2018-07-31
SI3400217T1 (sl) 2022-07-29
PL3400217T3 (pl) 2022-07-04
SG11201804594YA (en) 2018-06-28
SG10202009723PA (en) 2020-11-27
SG11201804789QA (en) 2018-07-30
SG10202009769WA (en) 2020-11-27
MA43549A (fr) 2021-05-26
EP3397622A1 (fr) 2018-11-07
MX2018008304A (es) 2019-01-24
AU2025256134A1 (en) 2025-11-13
JP7169573B2 (ja) 2022-11-11
JP6933322B2 (ja) 2021-09-08
CN108779087A (zh) 2018-11-09
EP4144351A1 (fr) 2023-03-08
LT3400217T (lt) 2022-06-27
ZA201903769B (en) 2023-03-29
PT3400217T (pt) 2022-06-15
CA3009573A1 (fr) 2017-07-13
MX2018008157A (es) 2018-09-03
AU2021218009A1 (en) 2021-09-09
UA125377C2 (uk) 2022-03-02
EP4140988A1 (fr) 2023-03-01
LT3397622T (lt) 2022-06-27
AU2021218009B2 (en) 2023-06-22
JP2021178858A (ja) 2021-11-18
HRP20220673T1 (hr) 2022-07-08
JP2019500351A (ja) 2019-01-10
WO2017118641A1 (fr) 2017-07-13
DK3397622T3 (en) 2022-06-07
AU2017205254B2 (en) 2021-05-20
JP7377588B2 (ja) 2023-11-10
EP3397622B1 (fr) 2022-03-09
HRP20220674T1 (hr) 2022-07-22
DK3400217T3 (da) 2022-06-07
MX379544B (es) 2025-03-11
EP3400217A1 (fr) 2018-11-14
KR20180099708A (ko) 2018-09-05
IL284912A (en) 2021-08-31
WO2017118639A1 (fr) 2017-07-13
CY1125231T1 (el) 2025-03-28
IL289256A (en) 2022-02-01
RS63285B1 (sr) 2022-06-30
AU2017205670B2 (en) 2021-05-20
AU2021218003A1 (en) 2021-09-02
IL284912B (en) 2022-07-01
KR20180100120A (ko) 2018-09-07
HUE058872T2 (hu) 2022-09-28
JP2019501897A (ja) 2019-01-24
ES2915948T3 (es) 2022-06-27
IL318222A (en) 2025-03-01
ES2916835T3 (es) 2022-07-06
HUE058871T2 (hu) 2022-09-28
PT3397622T (pt) 2022-06-15
SMT202200249T1 (it) 2022-07-21
UA125118C2 (uk) 2022-01-12
KR20250107965A (ko) 2025-07-14
SMT202200248T1 (it) 2022-07-21
EP3400217B1 (fr) 2022-03-09
JP2026000959A (ja) 2026-01-06
CY1125223T1 (el) 2025-03-28
RS63286B1 (sr) 2022-06-30
IL259742B (en) 2021-08-31
EA201891095A1 (ru) 2019-01-31
JP2023002668A (ja) 2023-01-10

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