EA200200109A1 - Кристаллы динуклеотида - Google Patents
Кристаллы динуклеотидаInfo
- Publication number
- EA200200109A1 EA200200109A1 EA200200109A EA200200109A EA200200109A1 EA 200200109 A1 EA200200109 A1 EA 200200109A1 EA 200200109 A EA200200109 A EA 200200109A EA 200200109 A EA200200109 A EA 200200109A EA 200200109 A1 EA200200109 A1 EA 200200109A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- dcp4u
- crystals
- present
- deoxycytidine
- uridine
- Prior art date
Links
- 239000013078 crystal Substances 0.000 title abstract 4
- DJJCXFVJDGTHFX-UHFFFAOYSA-N Uridinemonophosphate Natural products OC1C(O)C(COP(O)(O)=O)OC1N1C(=O)NC(=O)C=C1 DJJCXFVJDGTHFX-UHFFFAOYSA-N 0.000 abstract 3
- 238000000034 method Methods 0.000 abstract 3
- DJJCXFVJDGTHFX-ZAKLUEHWSA-N uridine-5'-monophosphate Chemical compound O[C@@H]1[C@@H](O)[C@H](COP(O)(O)=O)O[C@H]1N1C(=O)NC(=O)C=C1 DJJCXFVJDGTHFX-ZAKLUEHWSA-N 0.000 abstract 3
- NCMVOABPESMRCP-SHYZEUOFSA-N 2'-deoxycytosine 5'-monophosphate Chemical compound O=C1N=C(N)C=CN1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)C1 NCMVOABPESMRCP-SHYZEUOFSA-N 0.000 abstract 2
- DRTQHJPVMGBUCF-XVFCMESISA-N Uridine Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C=C1 DRTQHJPVMGBUCF-XVFCMESISA-N 0.000 abstract 2
- BHIIGRBMZRSDRI-UHFFFAOYSA-N [chloro(phenoxy)phosphoryl]oxybenzene Chemical compound C=1C=CC=CC=1OP(=O)(Cl)OC1=CC=CC=C1 BHIIGRBMZRSDRI-UHFFFAOYSA-N 0.000 abstract 2
- 238000004519 manufacturing process Methods 0.000 abstract 2
- 239000002994 raw material Substances 0.000 abstract 2
- CKTSBUTUHBMZGZ-SHYZEUOFSA-N 2'‐deoxycytidine Chemical compound O=C1N=C(N)C=CN1[C@@H]1O[C@H](CO)[C@@H](O)C1 CKTSBUTUHBMZGZ-SHYZEUOFSA-N 0.000 abstract 1
- CKTSBUTUHBMZGZ-UHFFFAOYSA-N Deoxycytidine Natural products O=C1N=C(N)C=CN1C1OC(CO)C(O)C1 CKTSBUTUHBMZGZ-UHFFFAOYSA-N 0.000 abstract 1
- YDHWWBZFRZWVHO-UHFFFAOYSA-H [oxido-[oxido(phosphonatooxy)phosphoryl]oxyphosphoryl] phosphate Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O YDHWWBZFRZWVHO-UHFFFAOYSA-H 0.000 abstract 1
- DRTQHJPVMGBUCF-PSQAKQOGSA-N beta-L-uridine Natural products O[C@H]1[C@@H](O)[C@H](CO)O[C@@H]1N1C(=O)NC(=O)C=C1 DRTQHJPVMGBUCF-PSQAKQOGSA-N 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 abstract 1
- 235000011180 diphosphates Nutrition 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- DRTQHJPVMGBUCF-UHFFFAOYSA-N uracil arabinoside Natural products OC1C(O)C(CO)OC1N1C(=O)NC(=O)C=C1 DRTQHJPVMGBUCF-UHFFFAOYSA-N 0.000 abstract 1
- 229940045145 uridine Drugs 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
- C07H19/10—Pyrimidine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H1/00—Processes for the preparation of sugar derivatives
- C07H1/06—Separation; Purification
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Biochemistry (AREA)
- Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Saccharide Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Настоящее изобретение относится к кристаллам P-(2'-дезоксицитидин 5'-)Р-(уридин 5'-) тетрафосфата (dCP4U) или его солей и к способу получения кристаллов. Настоящее изобретение предоставляет также способ получения dCP4U, включающий реакцию уридин 5'-монофосфата (UMP), 2'-дезоксицитидин 5'-монофосфата (dCMP), дифенилфосфохлоридата (DPC) и пирофосфата (PPi). Кристаллы dCP4U по способу настоящего изобретения имеют высокую чистоту и высокую стабильность, а также не гигроскопичны по сравнению с продуктом, высушенным вымораживанием, и поэтому служат в качестве полезного сырьевого материала для получения лекарств. Способ получения dCP4U в соответствии с настоящим изобретением позволяет использовать в качестве сырьевого материала недорогой UMP и обеспечивает высокий выход. Таким образом, процесс является подходящим для крупномасштабного синтеза dCP4U.Международная заявка была опубликована вместе с отчетом о международном поиске.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18495099 | 1999-06-30 | ||
PCT/JP2000/004336 WO2001002416A1 (fr) | 1999-06-30 | 2000-06-30 | Cristaux dinucleotidiques |
Publications (2)
Publication Number | Publication Date |
---|---|
EA200200109A1 true EA200200109A1 (ru) | 2002-06-27 |
EA004707B1 EA004707B1 (ru) | 2004-06-24 |
Family
ID=16162200
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA200200109A EA004707B1 (ru) | 1999-06-30 | 2000-06-30 | Кристаллы динуклеотида |
Country Status (22)
Country | Link |
---|---|
US (1) | US6617444B1 (ru) |
EP (2) | EP1191032B1 (ru) |
JP (1) | JP3421666B2 (ru) |
KR (1) | KR100593723B1 (ru) |
CN (1) | CN1144811C (ru) |
AT (2) | ATE300551T1 (ru) |
AU (1) | AU767136B2 (ru) |
BR (1) | BR0012205A (ru) |
CA (1) | CA2376860C (ru) |
CZ (1) | CZ303172B6 (ru) |
DE (2) | DE60006814T2 (ru) |
EA (1) | EA004707B1 (ru) |
ES (2) | ES2211566T3 (ru) |
HU (1) | HU229225B1 (ru) |
IL (1) | IL147163A (ru) |
MX (1) | MXPA02000035A (ru) |
NO (1) | NO321169B1 (ru) |
NZ (1) | NZ516301A (ru) |
PL (2) | PL202200B1 (ru) |
SK (1) | SK284178B6 (ru) |
WO (1) | WO2001002416A1 (ru) |
ZA (1) | ZA200110468B (ru) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7223744B2 (en) | 1997-02-10 | 2007-05-29 | Inspire Pharmaceuticals, Inc. | Pharmaceutical formulation comprising dinucleoside polyphosphates and salts thereof |
US7078391B2 (en) | 1997-02-10 | 2006-07-18 | Inspire Pharmaceuticals, Inc. | Method of treating edematous retinal disorders |
US6818629B2 (en) | 1997-02-10 | 2004-11-16 | Inspire Pharmaceuticals, Inc. | Pharmaceutical formulation comprising P1-(2'-deoxycytidine 5'-)P4-(uridine 5'-) tetraphosphate |
US6548658B2 (en) * | 1997-07-25 | 2003-04-15 | Inspire Pharmaceuticals, Inc. | Di-(uridine 5′)-tetraphosphate and salts thereof |
US6872710B2 (en) | 1997-07-25 | 2005-03-29 | Inspire Pharmaceuticals, Inc. | Di(uridine 5′)-tetraphosphate and salts thereof |
SK284178B6 (sk) * | 1999-06-30 | 2004-10-05 | Yamasa Corporation | Kryštalická forma P1-(2'-deoxycytidín-5'-)P4-(uridín-5'- )tetrafosfátu a spôsob ich prípravy |
US6867199B2 (en) | 2000-08-21 | 2005-03-15 | Inspire Pharmaceuticals, Inc. | Dinucleoside polyphosphate compositions and their therapeutic use |
US7161029B2 (en) * | 2003-12-17 | 2007-01-09 | Ajinomoto Co., Inc. | DiL-lysine monosulfate trihydrate crystal and method of making |
CN100363376C (zh) * | 2006-06-12 | 2008-01-23 | 南京工业大学 | 一种5’-核苷三磷酸钠盐的结晶方法 |
JPWO2017002827A1 (ja) * | 2015-06-29 | 2018-04-26 | ヤマサ醤油株式会社 | P1,p4−ビス(5’−ウリジル)テトラホスフェート結晶の保管方法 |
CN109843901B (zh) * | 2016-10-25 | 2022-04-26 | Yamasa 酱油株式会社 | P1,p4-二(尿苷5’-)四磷酸的纯化方法 |
CN111253456B (zh) * | 2020-03-13 | 2021-05-11 | 广东先强药业有限公司 | 一种地纽福索钠的制备方法 |
CN111704637A (zh) * | 2020-06-28 | 2020-09-25 | 南京工业大学 | 一种采用膜蒸馏结晶精制核苷酸的方法 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH07242685A (ja) * | 1994-01-12 | 1995-09-19 | Unitika Ltd | ジアデノシン四リン酸水和物の製造方法 |
US5837861A (en) * | 1997-02-10 | 1998-11-17 | Inspire Pharmaceuticals, Inc. | Dinucleotides and their use as modulators of mucociliary clearance and ciliary beat frequency |
US5900407A (en) * | 1997-02-06 | 1999-05-04 | Inspire Pharmaceuticals, Inc. | Method of treating dry eye disease with uridine triphosphates and related compounds |
CN1262556C (zh) * | 1997-02-06 | 2006-07-05 | 印斯拜尔药品股份有限公司 | 特定的二核苷酸和它们作为粘膜纤毛清除和纤毛颤动频率调节剂的应用 |
US6596725B2 (en) * | 1997-02-10 | 2003-07-22 | Inspire Pharmaceuticals, Inc. | Use of certain dinucleotides to stimulate removal of fluid in retinal detachment and retinal edema |
TW593331B (en) * | 1997-07-25 | 2004-06-21 | Inspire Pharmaceuticals Inc | Method for large-scale production of di(uridine 5')-tetraphosphate and salts thereof |
DK1012154T3 (da) * | 1997-07-25 | 2004-07-26 | Inspire Pharmaceuticals Inc | Salte af di(uridin-5'-tetraphosphat), fremgangsmåde til fremstilling og anvendelser deraf |
WO1999061012A2 (en) * | 1998-05-22 | 1999-12-02 | Inspire Pharmaceuticals, Inc. | Therapeutic dinucleotide and derivatives |
SK283729B6 (sk) * | 1998-10-02 | 2003-12-02 | Yamasa Corporation | Kryštály P1, P4-di(uridín-5')-tetrafosfátu alebo kryštály jeho soli, spôsob ich výroby, kryštály tetrasodnej soli P1, P4-di(uridín-5')-tetrafosfátu a kryštály jej hydrátov |
WO2000039145A1 (en) * | 1998-12-23 | 2000-07-06 | The University Of North Carolina At Chapel Hill | Targeted gene transfer using g protein coupled receptors |
SK284178B6 (sk) * | 1999-06-30 | 2004-10-05 | Yamasa Corporation | Kryštalická forma P1-(2'-deoxycytidín-5'-)P4-(uridín-5'- )tetrafosfátu a spôsob ich prípravy |
-
2000
- 2000-06-30 SK SK1870-2001A patent/SK284178B6/sk not_active IP Right Cessation
- 2000-06-30 MX MXPA02000035A patent/MXPA02000035A/es active IP Right Grant
- 2000-06-30 WO PCT/JP2000/004336 patent/WO2001002416A1/ja not_active Application Discontinuation
- 2000-06-30 AT AT03018399T patent/ATE300551T1/de not_active IP Right Cessation
- 2000-06-30 US US09/700,728 patent/US6617444B1/en not_active Expired - Lifetime
- 2000-06-30 PL PL352363A patent/PL202200B1/pl unknown
- 2000-06-30 ES ES00942412T patent/ES2211566T3/es not_active Expired - Lifetime
- 2000-06-30 NZ NZ516301A patent/NZ516301A/en not_active IP Right Cessation
- 2000-06-30 DE DE60006814T patent/DE60006814T2/de not_active Expired - Lifetime
- 2000-06-30 JP JP2001507852A patent/JP3421666B2/ja not_active Expired - Fee Related
- 2000-06-30 EP EP00942412A patent/EP1191032B1/en not_active Expired - Lifetime
- 2000-06-30 BR BR0012205-0A patent/BR0012205A/pt not_active Application Discontinuation
- 2000-06-30 CZ CZ20014502A patent/CZ303172B6/cs not_active IP Right Cessation
- 2000-06-30 CA CA002376860A patent/CA2376860C/en not_active Expired - Fee Related
- 2000-06-30 IL IL14716300A patent/IL147163A/xx not_active IP Right Cessation
- 2000-06-30 PL PL384307A patent/PL202176B1/pl unknown
- 2000-06-30 CN CNB008097356A patent/CN1144811C/zh not_active Expired - Fee Related
- 2000-06-30 EP EP03018399A patent/EP1362862B1/en not_active Expired - Lifetime
- 2000-06-30 AT AT00942412T patent/ATE255123T1/de not_active IP Right Cessation
- 2000-06-30 DE DE60021629T patent/DE60021629T2/de not_active Expired - Lifetime
- 2000-06-30 ES ES03018399T patent/ES2245431T3/es not_active Expired - Lifetime
- 2000-06-30 EA EA200200109A patent/EA004707B1/ru not_active IP Right Cessation
- 2000-06-30 KR KR1020017016184A patent/KR100593723B1/ko not_active IP Right Cessation
- 2000-06-30 AU AU57067/00A patent/AU767136B2/en not_active Ceased
- 2000-06-30 HU HU0201531A patent/HU229225B1/hu not_active IP Right Cessation
-
2001
- 2001-12-20 ZA ZA200110468A patent/ZA200110468B/en unknown
- 2001-12-27 NO NO20016381A patent/NO321169B1/no not_active IP Right Cessation
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EA200200109A1 (ru) | Кристаллы динуклеотида | |
Storer et al. | The resolution and absolute stereochemistry of the enantiomers of cis-1-[2-(hydroxymethyl)-1, 3-oxathiolan-5-yl) cytosine (BCH189): equipotent anti-HIV agents | |
US5831075A (en) | Amino acid ester of nucleoside analogues | |
EP0285884A3 (en) | process to produce 2', 3'-dideoxynucleosides | |
NO20011634D0 (no) | Krystall av diuridintetrafosfat eller salter derav, og fremgangsmåte for fremstilling av samme og fremgangsmåte for fremstilling av nevnte forbindelse | |
CA2135853A1 (en) | Process for large-scale preparation of 2',3'-didehydro-2',3'-dideoxynucleosides | |
CN102827902A (zh) | 一种化学-生物酶法组合制备2′-脱氧尿苷的方法 | |
BG105426A (bg) | Метод за пречистване на амониев сулфат | |
RU95108553A (ru) | Способ получения нуклеозидных аналогов с использованием бициклических промежуточных продуктов | |
Kanai et al. | Pyrimidine nucleosides. 5. Synthesis of carcinostatic halogenocyclonucleosides | |
GB2218417A (en) | Preparation of diacyl derivatives of 2'-deoxy-5 fluorourdine via novel intermediate compound | |
JPH01246297A (ja) | ベータ―2’,2’―ジフルオロヌクレオシド類の製造方法 | |
Matsuzaki et al. | Self-complementary tetradeoxyribonucleoside triphosphates convenient chemical preparation and spectroscopic studies in solution | |
KR100325682B1 (ko) | 2',3'-디디하이드로-2',3'-디데옥시시티딘 유도체의 제조방법 | |
Millo et al. | Simple Synthesis of P1P2-Diadenosine 5′-Pyrophosphate | |
US3773755A (en) | Conversion of cytidylic acid into aracytidine-3'-phosphate | |
Kondo et al. | Synthesis of Q base (queuine) | |
CN114456169A (zh) | 3′-脱氧-3′,4′-二脱氢核糖核苷类似物及其制备方法 | |
JPS62114954A (ja) | N−ベンゾイル−dl−メチオニンの光学分割方法 | |
RU95103392A (ru) | Способ получения 1-гидроксиадамантана | |
Fahr et al. | UV Irradiation of Nucleic Acids and Their Components in the Presence of Air | |
LV12664A (lv) | Synthesis of 4-substituted 2-oxobutenic acid sodium salts | |
JPS6490161A (en) | Production of optically active cyanohydrin or its enantiomer | |
DE3874291T2 (de) | Reines kristallines methyl-2-acryl-amino-2-methoxy-acetat und verfahren zu dessen herstellung. | |
JPH0667940B2 (ja) | 2’,3’‐ジデオキシプリンヌクレオシド類の製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PC4A | Registration of transfer of a eurasian patent by assignment | ||
PC4A | Registration of transfer of a eurasian patent by assignment | ||
MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): RU |