IL102058A - History of pyrimidine nucleoside as a lipid-lowering agent - Google Patents

History of pyrimidine nucleoside as a lipid-lowering agent

Info

Publication number: IL102058A
Authority: IL; Israel
Prior art keywords: active ingredient; propynyluracil; arabinofuranosyl; pharmaceutically acceptable; formulation
Prior art date: 1991-05-30

Application number

IL10205892A

Other languages

English (en)

Hebrew (he)

Other versions

IL102058A0 (en

Original Assignee

Wellcome Found

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.)

1991-05-30

Filing date

1992-05-29

Publication date

1996-07-23

1992-05-29 Application filed by Wellcome Found filed Critical Wellcome Found

1992-12-30 Publication of IL102058A0 publication Critical patent/IL102058A0/xx

1996-07-23 Publication of IL102058A publication Critical patent/IL102058A/en

Links

150000003833 nucleoside derivatives Chemical class 0.000 title description 3
239000002718 pyrimidine nucleoside Substances 0.000 title description 3
239000003524 antilipemic agent Substances 0.000 title description 2
HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims abstract description 33
150000002148 esters Chemical class 0.000 claims abstract description 14
150000003839 salts Chemical class 0.000 claims abstract description 13
239000002775 capsule Substances 0.000 claims description 9
239000008194 pharmaceutical composition Substances 0.000 claims description 6
239000002552 dosage form Substances 0.000 claims description 5
239000003814 drug Substances 0.000 claims description 5
102000007330 LDL Lipoproteins Human genes 0.000 claims description 4
108010007622 LDL Lipoproteins Proteins 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 3
QLOCVMVCRJOTTM-SDNRWEOFSA-N 1-[(2r,3s,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-prop-1-ynylpyrimidine-2,4-dione Chemical compound O=C1NC(=O)C(C#CC)=CN1[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O1 QLOCVMVCRJOTTM-SDNRWEOFSA-N 0.000 abstract description 3
108010028554 LDL Cholesterol Proteins 0.000 abstract 1
239000000203 mixture Substances 0.000 description 39
239000004480 active ingredient Substances 0.000 description 38
238000009472 formulation Methods 0.000 description 33
HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 18
239000004615 ingredient Substances 0.000 description 12
239000003826 tablet Substances 0.000 description 12
235000019359 magnesium stearate Nutrition 0.000 description 9
229920000036 polyvinylpyrrolidone Polymers 0.000 description 9
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 9
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 8
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 8
239000008101 lactose Substances 0.000 description 8
239000007788 liquid Substances 0.000 description 8
229940069328 povidone Drugs 0.000 description 8
239000000243 solution Substances 0.000 description 8
235000012000 cholesterol Nutrition 0.000 description 7
230000000694 effects Effects 0.000 description 7
239000000725 suspension Substances 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
-1 5-substituted pyrimidine Chemical class 0.000 description 6
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
239000000843 powder Substances 0.000 description 6
238000008214 LDL Cholesterol Methods 0.000 description 4
239000002585 base Substances 0.000 description 4
150000001875 compounds Chemical class 0.000 description 4
238000007906 compression Methods 0.000 description 4
230000006835 compression Effects 0.000 description 4
239000003085 diluting agent Substances 0.000 description 4
229940080313 sodium starch Drugs 0.000 description 4
239000000829 suppository Substances 0.000 description 4
102000015779 HDL Lipoproteins Human genes 0.000 description 3
108010010234 HDL Lipoproteins Proteins 0.000 description 3
241000282567 Macaca fascicularis Species 0.000 description 3
241001465754 Metazoa Species 0.000 description 3
210000004369 blood Anatomy 0.000 description 3
239000008280 blood Substances 0.000 description 3
239000000969 carrier Substances 0.000 description 3
239000001913 cellulose Substances 0.000 description 3
229920002678 cellulose Polymers 0.000 description 3
235000010980 cellulose Nutrition 0.000 description 3
230000007812 deficiency Effects 0.000 description 3
238000007907 direct compression Methods 0.000 description 3
239000007903 gelatin capsule Substances 0.000 description 3
239000008187 granular material Substances 0.000 description 3
238000000034 method Methods 0.000 description 3
239000002245 particle Substances 0.000 description 3
239000008213 purified water Substances 0.000 description 3
238000005550 wet granulation Methods 0.000 description 3
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
239000001856 Ethyl cellulose Substances 0.000 description 2
ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 2
102100024640 Low-density lipoprotein receptor Human genes 0.000 description 2
229920002472 Starch Polymers 0.000 description 2
230000005856 abnormality Effects 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
235000019445 benzyl alcohol Nutrition 0.000 description 2
239000007963 capsule composition Substances 0.000 description 2
238000013270 controlled release Methods 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
239000003937 drug carrier Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
235000019325 ethyl cellulose Nutrition 0.000 description 2
229920001249 ethyl cellulose Polymers 0.000 description 2
239000000796 flavoring agent Substances 0.000 description 2
239000011521 glass Substances 0.000 description 2
239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 2
235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 2
229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 2
UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 2
238000002347 injection Methods 0.000 description 2
239000007924 injection Substances 0.000 description 2
238000007918 intramuscular administration Methods 0.000 description 2
238000007913 intrathecal administration Methods 0.000 description 2
238000001990 intravenous administration Methods 0.000 description 2
239000000155 melt Substances 0.000 description 2
238000000465 moulding Methods 0.000 description 2
239000006072 paste Substances 0.000 description 2
230000001575 pathological effect Effects 0.000 description 2
239000008363 phosphate buffer Substances 0.000 description 2
230000036470 plasma concentration Effects 0.000 description 2
WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 2
235000010234 sodium benzoate Nutrition 0.000 description 2
239000004299 sodium benzoate Substances 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000000600 sorbitol Substances 0.000 description 2
229940032147 starch Drugs 0.000 description 2
239000008107 starch Substances 0.000 description 2
235000019698 starch Nutrition 0.000 description 2
238000007920 subcutaneous administration Methods 0.000 description 2
230000001225 therapeutic effect Effects 0.000 description 2
239000002562 thickening agent Substances 0.000 description 2
230000000699 topical effect Effects 0.000 description 2
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 2
239000008215 water for injection Substances 0.000 description 2
CTPDSKVQLSDPLC-UHFFFAOYSA-N 2-(oxolan-2-ylmethoxy)ethanol Chemical compound OCCOCC1CCCO1 CTPDSKVQLSDPLC-UHFFFAOYSA-N 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
101150102415 Apob gene Proteins 0.000 description 1
241000282693 Cercopithecidae Species 0.000 description 1
208000031288 Combined hyperlipidaemia Diseases 0.000 description 1
241000701022 Cytomegalovirus Species 0.000 description 1
108010010803 Gelatin Proteins 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
241000701085 Human alphaherpesvirus 3 Species 0.000 description 1
208000035150 Hypercholesterolemia Diseases 0.000 description 1
208000001021 Hyperlipoproteinemia Type I Diseases 0.000 description 1
208000000563 Hyperlipoproteinemia Type II Diseases 0.000 description 1
XQFRJNBWHJMXHO-RRKCRQDMSA-N IDUR Chemical group C1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C(I)=C1 XQFRJNBWHJMXHO-RRKCRQDMSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
108010001831 LDL receptors Proteins 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
229920003091 Methocel™ Polymers 0.000 description 1
229920000168 Microcrystalline cellulose Polymers 0.000 description 1
229920000881 Modified starch Polymers 0.000 description 1
240000005809 Prunus persica Species 0.000 description 1
235000006040 Prunus persica var persica Nutrition 0.000 description 1
206010045261 Type IIa hyperlipidaemia Diseases 0.000 description 1
241000700605 Viruses Species 0.000 description 1
DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
125000004183 alkoxy alkyl group Chemical group 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
230000003078 antioxidant effect Effects 0.000 description 1
235000006708 antioxidants Nutrition 0.000 description 1
239000003443 antiviral agent Substances 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
125000005160 aryl oxy alkyl group Chemical group 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
238000012742 biochemical analysis Methods 0.000 description 1
210000004204 blood vessel Anatomy 0.000 description 1
239000000872 buffer Substances 0.000 description 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
125000004181 carboxyalkyl group Chemical group 0.000 description 1
150000001733 carboxylic acid esters Chemical class 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
150000001840 cholesterol esters Chemical class 0.000 description 1
229940110456 cocoa butter Drugs 0.000 description 1
235000019868 cocoa butter Nutrition 0.000 description 1
239000007891 compressed tablet Substances 0.000 description 1
208000029078 coronary artery disease Diseases 0.000 description 1
239000006071 cream Substances 0.000 description 1
230000002939 deleterious effect Effects 0.000 description 1
239000008121 dextrose Substances 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
239000007884 disintegrant Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
238000001035 drying Methods 0.000 description 1
201000001386 familial hypercholesterolemia Diseases 0.000 description 1
201000011110 familial lipoprotein lipase deficiency Diseases 0.000 description 1
235000019634 flavors Nutrition 0.000 description 1
239000006260 foam Substances 0.000 description 1
235000013355 food flavoring agent Nutrition 0.000 description 1
238000003304 gavage Methods 0.000 description 1
239000000499 gel Substances 0.000 description 1
229920000159 gelatin Polymers 0.000 description 1
239000008273 gelatin Substances 0.000 description 1
235000019322 gelatine Nutrition 0.000 description 1
235000011852 gelatine desserts Nutrition 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
229940116364 hard fat Drugs 0.000 description 1
239000003701 inert diluent Substances 0.000 description 1
239000007972 injectable composition Substances 0.000 description 1
238000010255 intramuscular injection Methods 0.000 description 1
239000007927 intramuscular injection Substances 0.000 description 1
229940080428 lactose 200 mg Drugs 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
239000012528 membrane Substances 0.000 description 1
239000002207 metabolite Substances 0.000 description 1
229940016286 microcrystalline cellulose Drugs 0.000 description 1
235000019813 microcrystalline cellulose Nutrition 0.000 description 1
239000008108 microcrystalline cellulose Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000007923 nasal drop Substances 0.000 description 1
229940100662 nasal drops Drugs 0.000 description 1
229940097496 nasal spray Drugs 0.000 description 1
239000007922 nasal spray Substances 0.000 description 1
150000002823 nitrates Chemical class 0.000 description 1
238000007911 parenteral administration Methods 0.000 description 1
239000008188 pellet Substances 0.000 description 1
150000003904 phospholipids Chemical class 0.000 description 1
229940068196 placebo Drugs 0.000 description 1
239000000902 placebo Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
230000003234 polygenic effect Effects 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
229920001592 potato starch Polymers 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
239000002510 pyrogen Substances 0.000 description 1
YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
229960001860 salicylate Drugs 0.000 description 1
238000007493 shaping process Methods 0.000 description 1
238000010008 shearing Methods 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
239000007921 spray Substances 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
239000006188 syrup Substances 0.000 description 1
235000020357 syrup Nutrition 0.000 description 1
239000007916 tablet composition Substances 0.000 description 1
230000008719 thickening Effects 0.000 description 1
UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical class OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
230000002792 vascular Effects 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Veterinary Medicine (AREA)
Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Pharmacology & Pharmacy (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Epidemiology (AREA)
Molecular Biology (AREA)
Engineering & Computer Science (AREA)
Bioinformatics & Cheminformatics (AREA)
Diabetes (AREA)
Hematology (AREA)
Obesity (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Organic Chemistry (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Saccharide Compounds (AREA)

IL10205892A 1991-05-30 1992-05-29 History of pyrimidine nucleoside as a lipid-lowering agent IL102058A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB919111580A GB9111580D0 (en)	1991-05-30	1991-05-30	Nucleoside derivative

Publications (2)

Publication Number	Publication Date
IL102058A0 IL102058A0 (en)	1992-12-30
IL102058A true IL102058A (en)	1996-07-23

Family

ID=10695778

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL10205892A IL102058A (en)	1991-05-30	1992-05-29	History of pyrimidine nucleoside as a lipid-lowering agent

Country Status (14)

Country	Link
US (1)	US5432166A (de)
EP (1)	EP0542952B1 (de)
JP (1)	JPH06500129A (de)
AT (1)	ATE142501T1 (de)
AU (1)	AU657756B2 (de)
CA (1)	CA2088264A1 (de)
DE (1)	DE69213660D1 (de)
GB (1)	GB9111580D0 (de)
HU (1)	HUT63767A (de)
IE (1)	IE921731A1 (de)
IL (1)	IL102058A (de)
MX (1)	MX9202595A (de)
WO (1)	WO1992021352A1 (de)
ZA (1)	ZA923962B (de)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6753006B1 (en)	1993-02-22	2004-06-22	American Bioscience, Inc.	Paclitaxel-containing formulations
US20040033267A1 (en) *	2002-03-20	2004-02-19	Elan Pharma International Ltd.	Nanoparticulate compositions of angiogenesis inhibitors
US20030054042A1 (en) *	2001-09-14	2003-03-20	Elaine Liversidge	Stabilization of chemical compounds using nanoparticulate formulations
KR102072041B1 (ko)	2011-12-22	2020-01-31	앨리오스 바이오파마 인크.	치환된 뉴클레오사이드, 뉴클레오타이드 및 그의 유사체
US9441007B2 (en)	2012-03-21	2016-09-13	Alios Biopharma, Inc.	Substituted nucleosides, nucleotides and analogs thereof
USRE48171E1 (en)	2012-03-21	2020-08-25	Janssen Biopharma, Inc.	Substituted nucleosides, nucleotides and analogs thereof

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2244328A1 (de) *	1972-09-09	1974-03-21	Boehringer Mannheim Gmbh	Neue n(6)-disubstituierte adenosinderivate und verfahren zur herstellung derselben
US4594339A (en) *	1982-04-06	1986-06-10	Sloan-Kettering Institute For Cancer Research	Anti-herpes virus compositions containing 5-substituted 1-2'(deoxy-2-'-substituted-β-d-arabinofuranosyl)pyrimedene nucleosides
IT1196261B (it) *	1984-09-20	1988-11-16	Pierrel Spa	Derivati nucleosidici e purinici 8-sostituiti
US5063233A (en) *	1986-11-14	1991-11-05	Ciba-Geigy Corporation	N9 -cyclopentyl-substituted adenine derivatives useful as adenosine receptor agonists
NL8702926A (nl) *	1986-12-15	1988-07-01	Sandoz Ag	Nieuwe furanuronzuurderivaten en werkwijzen voor het bereiden en toepassen van deze derivaten.
GB8629892D0 (en) *	1986-12-15	1987-01-28	Wellcome Found	Antiviral compounds
PT86660B (pt) *	1987-02-04	1992-02-28	Ciba Geigy Ag	Processo para a preparacao de derivados de adenosina-5'-carboxamida
US4962194A (en) *	1987-04-02	1990-10-09	Warner-Lambert Company	Method of preparing 51,N6-disubstituted adenosines from inosines
US5028596A (en) *	1987-12-14	1991-07-02	Burroughs Wellcome Co.	1-(β-D-arabinofuranosyl)-5-propynyluracil for treatment of VZV infections
GB8729994D0 (en) *	1987-12-23	1988-02-03	Glaxo Group Ltd	Chemical compounds
AU3820989A (en) *	1988-08-02	1990-02-08	Ciba-Geigy Ag	7-amino-3-beta-d-ribofuranosyl-3h-imidazo(4,5-b) pyridin-5-amine derivatives
GB2226027B (en) *	1988-12-13	1992-05-20	Sandoz Ltd	Adenosine derivatives,their production and use
JPH03287537A (ja) *	1990-03-31	1991-12-18	Yamasa Shoyu Co Ltd	抗動脈硬化症剤
FR2665362B1 (fr) *	1990-08-03	1994-12-09	Cepbepe	Substance contenant, comme principe actif, une adenosine substitutee en n6 et son application.

1991
- 1991-05-30 GB GB919111580A patent/GB9111580D0/en active Pending
1992
- 1992-05-29 JP JP4509647A patent/JPH06500129A/ja active Pending
- 1992-05-29 ZA ZA923962A patent/ZA923962B/xx unknown
- 1992-05-29 DE DE69213660T patent/DE69213660D1/de not_active Expired - Lifetime
- 1992-05-29 WO PCT/GB1992/000971 patent/WO1992021352A1/en not_active Ceased
- 1992-05-29 CA CA002088264A patent/CA2088264A1/en not_active Abandoned
- 1992-05-29 HU HU9300243A patent/HUT63767A/hu unknown
- 1992-05-29 IL IL10205892A patent/IL102058A/en active IP Right Grant
- 1992-05-29 AT AT92910638T patent/ATE142501T1/de not_active IP Right Cessation
- 1992-05-29 US US07/988,122 patent/US5432166A/en not_active Expired - Fee Related
- 1992-05-29 EP EP92910638A patent/EP0542952B1/de not_active Expired - Lifetime
- 1992-05-29 MX MX9202595A patent/MX9202595A/es unknown
- 1992-05-29 AU AU17673/92A patent/AU657756B2/en not_active Ceased
- 1992-07-01 IE IE173192A patent/IE921731A1/en not_active Application Discontinuation

Also Published As

Publication number	Publication date
EP0542952B1 (de)	1996-09-11
IE921731A1 (en)	1992-12-02
HUT63767A (en)	1993-10-28
US5432166A (en)	1995-07-11
EP0542952A1 (de)	1993-05-26
CA2088264A1 (en)	1992-12-01
HU9300243D0 (en)	1993-04-28
ATE142501T1 (de)	1996-09-15
MX9202595A (es)	1992-11-01
ZA923962B (en)	1993-11-29
DE69213660D1 (de)	1996-10-17
GB9111580D0 (en)	1991-07-24
AU657756B2 (en)	1995-03-23
JPH06500129A (ja)	1994-01-06
WO1992021352A1 (en)	1992-12-10
AU1767392A (en)	1993-01-08
IL102058A0 (en)	1992-12-30

Legal Events

Date	Code	Title	Description
1996-12-05	FF	Patent granted

Publication	Publication Date	Title
US5079235A (en)	1992-01-07	Antiviral compounds
CA2112239C (en)	2000-05-09	Enantiomeric hydroxylated xanthine compounds
TW201622728A (zh)	2016-07-01	全身紅斑性狼瘡之治療
US5432166A (en)	1995-07-11	Use of 1-(β-D-arabinofuranosyl) -5-propynyluracil for lowering serum cholesterol
EP0253962A2 (de)	1988-01-27	Verwendung von Adenosin-Derivaten als Anti-Dementia-Mittel
US7354906B2 (en)	2008-04-08	Composition of anti-HIV drugs and anti-cortisol compounds and method for decreasing the side effects of anti-HIV drugs in a human
US5432165A (en)	1995-07-11	Methods for the treatment of infection caused by Hepatitis B virus (HBV)
EP1113802B1 (de)	2004-06-30	Antivirale kombinationen von lamivudin und adefovir
WO2007103468A2 (en)	2007-09-13	Use of vx-702 for treating rheumatoid arthritis
US5504093A (en)	1996-04-02	Method for inhibiting nucleoside and nucleobase transport in mammalian cells, and method for inhibition of DNA virus replication
WO2007006544A2 (en)	2007-01-18	Cyclic adenosine monophosphate compounds for the treatment of immune-related disorders
US6432966B2 (en)	2002-08-13	Antiviral combinations
US6372763B1 (en)	2002-04-16	Treatment and prevention of cardiac disorders using selective serotonin re-uptake inhibitors (SSRI)
EP0253517B1 (de)	1992-03-25	Verwendung von 3'azido-3'deoxythymidin zur Herstellung eines Arzneimittels zur Behandlung von Gardiasis
GB2197588A (en)	1988-05-25	Immunoregulator comprising a derivative of estradiol
AU620471B2 (en)	1992-02-20	Antiviral 5-propynyl pyrimidine nucleosides
DE4204108C2 (de)	1998-09-24	Arzneimittel zur Behandlung und/oder Prophylaxe von Störungen des Folat-Stoffwechsels
US5028596A (en)	1991-07-02	1-(β-D-arabinofuranosyl)-5-propynyluracil for treatment of VZV infections
EP0655918A1 (de)	1995-06-07	Behandlung von krebs mit azt und alkylantien oder interkalierenden verbindungen
EP1104301A1 (de)	2001-06-06	Verfahren zur behandlung von krankheiten
WO1998052571A1 (en)	1998-11-26	Antiviral combinations containing the carbocyclic nucleoside 1592u89
HK1035670B (en)	2005-02-18	Antiviral combinations of lamivudine and adefovir
JPS59184147A (ja)	1984-10-19	痙れん防止性を有する化合物