LU87071A1 - Nouveaux derives de l'acide furannuronique,leur preparation et leur utilisation comme medicaments - Google Patents

Nouveaux derives de l'acide furannuronique,leur preparation et leur utilisation comme medicaments Download PDF

Info

Publication number: LU87071A1
Authority: LU; Luxembourg
Prior art keywords: group; optionally; hydroxy; alkyl; phenyl
Prior art date: 1986-12-15

Application number

LU87071A

Other languages

English (en)

French (fr)

Original Assignee

Sandoz 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.)

1986-12-15

Filing date

1987-12-14

Publication date

1988-07-14

1987-12-14 Application filed by Sandoz Sa filed Critical Sandoz Sa

1988-07-14 Publication of LU87071A1 publication Critical patent/LU87071A1/fr

Links

239000002253 acid Substances 0.000 title claims description 16
239000003814 drug Substances 0.000 title claims description 10
238000002360 preparation method Methods 0.000 title claims description 9
150000001875 compounds Chemical class 0.000 claims description 41
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 38
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 21
229910052739 hydrogen Inorganic materials 0.000 claims description 20
239000001257 hydrogen Substances 0.000 claims description 16
125000001424 substituent group Chemical group 0.000 claims description 16
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 15
229910052736 halogen Inorganic materials 0.000 claims description 13
150000002367 halogens Chemical class 0.000 claims description 13
125000000753 cycloalkyl group Chemical group 0.000 claims description 12
-1 -SH Chemical group 0.000 claims description 11
125000000217 alkyl group Chemical group 0.000 claims description 11
125000004414 alkyl thio group Chemical group 0.000 claims description 11
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
238000000034 method Methods 0.000 claims description 9
125000004433 nitrogen atom Chemical group N* 0.000 claims description 9
125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 7
125000002947 alkylene group Chemical group 0.000 claims description 7
150000002431 hydrogen Chemical class 0.000 claims description 7
125000003545 alkoxy group Chemical group 0.000 claims description 6
125000001072 heteroaryl group Chemical group 0.000 claims description 6
229910052757 nitrogen Inorganic materials 0.000 claims description 6
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 5
230000008569 process Effects 0.000 claims description 5
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 4
230000036772 blood pressure Effects 0.000 claims description 4
125000000654 isopropylidene group Chemical group C(C)(C)=* 0.000 claims description 4
125000002950 monocyclic group Chemical group 0.000 claims description 4
229910052760 oxygen Inorganic materials 0.000 claims description 4
239000001301 oxygen Substances 0.000 claims description 4
WDSFCZDGCAXRDY-UHFFFAOYSA-N s-ethylthiohydroxylamine Chemical compound CCSN WDSFCZDGCAXRDY-UHFFFAOYSA-N 0.000 claims description 4
229910052717 sulfur Inorganic materials 0.000 claims description 4
125000004434 sulfur atom Chemical group 0.000 claims description 4
125000003342 alkenyl group Chemical group 0.000 claims description 3
125000000304 alkynyl group Chemical group 0.000 claims description 3
125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims description 2
239000013543 active substance Substances 0.000 claims description 2
239000003085 diluting agent Substances 0.000 claims description 2
AEOCXXJPGCBFJA-UHFFFAOYSA-N ethionamide Chemical compound CCC1=CC(C(N)=S)=CC=N1 AEOCXXJPGCBFJA-UHFFFAOYSA-N 0.000 claims description 2
239000008194 pharmaceutical composition Substances 0.000 claims description 2
150000003556 thioamides Chemical class 0.000 claims description 2
125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 2
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 1
125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 1
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims 1
125000006239 protecting group Chemical group 0.000 claims 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 15
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
239000003795 chemical substances by application Substances 0.000 description 7
229910052799 carbon Inorganic materials 0.000 description 6
239000000243 solution Substances 0.000 description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 4
125000004432 carbon atom Chemical group C* 0.000 description 4
CFHGBZLNZZVTAY-UHFFFAOYSA-N lawesson's reagent Chemical compound C1=CC(OC)=CC=C1P1(=S)SP(=S)(C=2C=CC(OC)=CC=2)S1 CFHGBZLNZZVTAY-UHFFFAOYSA-N 0.000 description 4
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
125000000229 (C1-C4)alkoxy group Chemical group 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
102100028255 Renin Human genes 0.000 description 3
108090000783 Renin Proteins 0.000 description 3
229940030600 antihypertensive agent Drugs 0.000 description 3
239000002220 antihypertensive agent Substances 0.000 description 3
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 3
230000000694 effects Effects 0.000 description 3
229910052731 fluorine Inorganic materials 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
239000007858 starting material Substances 0.000 description 3
230000024883 vasodilation Effects 0.000 description 3
SFLSHLFXELFNJZ-QMMMGPOBSA-N (-)-norepinephrine Chemical compound NC[C@H](O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-QMMMGPOBSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
241000700159 Rattus Species 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
OIRDTQYFTABQOQ-KQYNXXCUSA-N adenosine Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O OIRDTQYFTABQOQ-KQYNXXCUSA-N 0.000 description 2
230000003276 anti-hypertensive effect Effects 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
238000004587 chromatography analysis Methods 0.000 description 2
229940079593 drug Drugs 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
239000011737 fluorine Substances 0.000 description 2
239000006260 foam Substances 0.000 description 2
230000005764 inhibitory process Effects 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
210000001640 nerve ending Anatomy 0.000 description 2
229960002748 norepinephrine Drugs 0.000 description 2
SFLSHLFXELFNJZ-UHFFFAOYSA-N norepinephrine Natural products NCC(O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-UHFFFAOYSA-N 0.000 description 2
239000000047 product Substances 0.000 description 2
230000028327 secretion Effects 0.000 description 2
239000000741 silica gel Substances 0.000 description 2
229910002027 silica gel Inorganic materials 0.000 description 2
229910052938 sodium sulfate Inorganic materials 0.000 description 2
235000011152 sodium sulphate Nutrition 0.000 description 2
238000007280 thionation reaction Methods 0.000 description 2
QPIYPWGWBLCOPY-AVRIJYDRSA-N (2s,3s,4r,5r)-3,4,5-trihydroxyoxolane-2-carboxylic acid Chemical compound O[C@@H]1O[C@H](C(O)=O)[C@@H](O)[C@H]1O QPIYPWGWBLCOPY-AVRIJYDRSA-N 0.000 description 1
ADJUCUMUERSRHL-UHFFFAOYSA-N (4-methoxyphenyl)sulfanylphosphane Chemical compound COC1=CC=C(SP)C=C1 ADJUCUMUERSRHL-UHFFFAOYSA-N 0.000 description 1
125000006273 (C1-C3) alkyl group Chemical group 0.000 description 1
125000003161 (C1-C6) alkylene group Chemical group 0.000 description 1
125000003006 2-dimethylaminoethyl group Chemical group [H]C([H])([H])N(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
239000002126 C01EB10 - Adenosine Substances 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 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
CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical class Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
206010020772 Hypertension Diseases 0.000 description 1
125000002066 L-histidyl group Chemical group [H]N1C([H])=NC(C([H])([H])[C@](C(=O)[*])([H])N([H])[H])=C1[H] 0.000 description 1
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
240000007313 Tilia cordata Species 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
230000003213 activating effect Effects 0.000 description 1
229960005305 adenosine Drugs 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
210000000702 aorta abdominal Anatomy 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
238000013475 authorization Methods 0.000 description 1
210000004369 blood Anatomy 0.000 description 1
239000008280 blood Substances 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
210000003710 cerebral cortex Anatomy 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
238000003776 cleavage reaction Methods 0.000 description 1
238000004440 column chromatography Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
125000001316 cycloalkyl alkyl group Chemical group 0.000 description 1
125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
239000003480 eluent Substances 0.000 description 1
210000003989 endothelium vascular Anatomy 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000012467 final product Substances 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
VZCYOOQTPOCHFL-OWOJBTEDSA-L fumarate(2-) Chemical class [O-]C(=O)\C=C\C([O-])=O VZCYOOQTPOCHFL-OWOJBTEDSA-L 0.000 description 1
239000008103 glucose Substances 0.000 description 1
230000000004 hemodynamic effect Effects 0.000 description 1
125000005980 hexynyl group Chemical group 0.000 description 1
150000003840 hydrochlorides Chemical class 0.000 description 1
229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
230000006872 improvement Effects 0.000 description 1
238000001802 infusion Methods 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
238000001990 intravenous administration Methods 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
210000003734 kidney Anatomy 0.000 description 1
210000000265 leukocyte Anatomy 0.000 description 1
150000002632 lipids Chemical class 0.000 description 1
239000007788 liquid Substances 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
125000005394 methallyl group Chemical group 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
239000000203 mixture Substances 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001298 n-hexoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
125000003935 n-pentoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
210000001577 neostriatum Anatomy 0.000 description 1
210000005036 nerve Anatomy 0.000 description 1
125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
125000005981 pentynyl group Chemical group 0.000 description 1
230000010412 perfusion Effects 0.000 description 1
230000000144 pharmacologic effect Effects 0.000 description 1
125000003884 phenylalkyl group Chemical group 0.000 description 1
CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
230000009467 reduction Effects 0.000 description 1
230000007017 scission Effects 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
208000010110 spontaneous platelet aggregation Diseases 0.000 description 1
238000011699 spontaneously hypertensive rat Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
239000012730 sustained-release form Substances 0.000 description 1
230000009466 transformation Effects 0.000 description 1
210000002700 urine Anatomy 0.000 description 1
238000005406 washing Methods 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- 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
- C07H19/16—Purine radicals

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Biochemistry (AREA)
Biotechnology (AREA)
General Health & Medical Sciences (AREA)
Genetics & Genomics (AREA)
Molecular Biology (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Plural Heterocyclic Compounds (AREA)

LU87071A 1986-12-15 1987-12-14 Nouveaux derives de l'acide furannuronique,leur preparation et leur utilisation comme medicaments LU87071A1 (fr)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
DE3642748		1986-12-15
DE3642748		1986-12-15
DE3729768		1987-09-05
DE3729768		1987-09-05

Publications (1)

Publication Number	Publication Date
LU87071A1 true LU87071A1 (fr)	1988-07-14

Family

ID=25850352

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LU87071A LU87071A1 (fr)	1986-12-15	1987-12-14	Nouveaux derives de l'acide furannuronique,leur preparation et leur utilisation comme medicaments

Country Status (22)

Country	Link
US (1)	US4855288A (de)
KR (1)	KR880007533A (de)
AT (1)	AT393506B (de)
AU (1)	AU601247B2 (de)
BE (1)	BE1001621A3 (de)
CA (1)	CA1291752C (de)
CH (1)	CH676851A5 (de)
DK (1)	DK655487A (de)
ES (1)	ES2010736A6 (de)
FI (1)	FI86431C (de)
FR (1)	FR2608159B1 (de)
GB (1)	GB2199036B (de)
GR (1)	GR871895B (de)
HU (1)	HU198950B (de)
IL (1)	IL84808A (de)
IT (1)	IT1230116B (de)
LU (1)	LU87071A1 (de)
MY (1)	MY102270A (de)
NL (1)	NL8702926A (de)
NZ (1)	NZ222897A (de)
PH (1)	PH25421A (de)
SE (1)	SE8704979L (de)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
LU87181A1 (fr) *	1987-04-06	1988-11-17	Sandoz Sa	Nouveaux derives de l'acide furannuronique,leur preparation et leur utilisation comme medicaments
US5219840A (en) *	1987-04-06	1993-06-15	Sandoz Ltd.	Antihypertensive 9-(2,N6 -disubstituted adenyl) ribofuranuronic acid derivatives
CA2092305C (en) *	1990-09-25	2003-02-11	Alfred P. Spada	Compounds having antihypertensive and anti-ischemic properties
US5561134A (en) *	1990-09-25	1996-10-01	Rhone-Poulenc Rorer Pharmaceuticals Inc.	Compounds having antihypertensive, cardioprotective, anti-ischemic and antilipolytic properties
GB9111580D0 (en) *	1991-05-30	1991-07-24	Wellcome Found	Nucleoside derivative
FR2687678B1 (fr) *	1992-01-31	1995-03-31	Union Pharma Scient Appl	Nouveaux derives de l'adenosine, leurs procedes de preparation, compositions pharmaceutiques les contenant.
TW528755B (en)	1996-12-24	2003-04-21	Glaxo Group Ltd	2-(purin-9-yl)-tetrahydrofuran-3,4-diol derivatives
YU44900A (sh)	1998-01-31	2003-01-31	Glaxo Group Limited	Derivati 2-(purin-9-il)tetrahidrofuran-3,4-diola
EA200001224A1 (ru)	1998-06-23	2001-08-27	Глаксо Груп Лимитед	Производные 2-(пурин-9-ил)-тетрагидрофуран-3,4-диола
PE20060272A1 (es)	2004-05-24	2006-05-22	Glaxo Group Ltd	(2r,3r,4s,5r,2'r,3'r,4's,5's)-2,2'-{trans-1,4-ciclohexanodiilbis-[imino(2-{[2-(1-metil-1h-imidazol-4-il)etil]amino}-9h-purin-6,9-diil)]}bis[5-(2-etil-2h-tetrazol-5-il)tetrahidro-3,4-furanodiol] como agonista a2a
GB0514809D0 (en) *	2005-07-19	2005-08-24	Glaxo Group Ltd	Compounds

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL6717061A (de) *	1966-12-21	1968-06-24
US4029884A (en) *	1971-03-18	1977-06-14	Abbott Laboratories	Adenosine-5'-carboxylic acid amides
CA1082695A (en) *	1972-04-10	1980-07-29	Francis E. Fischer	Process for preparing adenosine-5'-carboxamides
US3966917A (en) *	1974-07-30	1976-06-29	Abbott Laboratories	Platelet aggregation inhibitors
DE2610985A1 (de) *	1976-03-16	1977-09-29	Byk Gulden Lomberg Chem Fab	Arzneimittel enthaltend beta-d-1 (6-amino-9h-purin-9-yl)-1-deoxyribofuranuronsaeurederivate
LU75374A1 (de) *	1976-07-13	1978-02-08
US4167565A (en) *	1976-11-08	1979-09-11	Abbott Laboratories	Adenosine-5'-carboxamides and method of use
US5310731A (en) *	1984-06-28	1994-05-10	Whitby Research, Inc.	N-6 substituted-5'-(N-substitutedcarboxamido)adenosines as cardiac vasodilators and antihypertensive agents
LU87181A1 (fr) *	1987-04-06	1988-11-17	Sandoz Sa	Nouveaux derives de l'acide furannuronique,leur preparation et leur utilisation comme medicaments

1987
- 1987-12-04 NL NL8702926A patent/NL8702926A/nl not_active Application Discontinuation
- 1987-12-04 HU HU875452A patent/HU198950B/hu not_active IP Right Cessation
- 1987-12-07 CH CH4763/87A patent/CH676851A5/de not_active IP Right Cessation
- 1987-12-11 BE BE8701420A patent/BE1001621A3/fr not_active IP Right Cessation
- 1987-12-12 MY MYPI87003187A patent/MY102270A/en unknown
- 1987-12-14 AU AU82523/87A patent/AU601247B2/en not_active Ceased
- 1987-12-14 LU LU87071A patent/LU87071A1/fr unknown
- 1987-12-14 CA CA000554261A patent/CA1291752C/en not_active Expired - Lifetime
- 1987-12-14 PH PH36210A patent/PH25421A/en unknown
- 1987-12-14 KR KR870014412A patent/KR880007533A/ko not_active Ceased
- 1987-12-14 SE SE8704979A patent/SE8704979L/xx not_active Application Discontinuation
- 1987-12-14 GB GB8729116A patent/GB2199036B/en not_active Expired - Lifetime
- 1987-12-14 NZ NZ222897A patent/NZ222897A/xx unknown
- 1987-12-14 DK DK655487A patent/DK655487A/da not_active Application Discontinuation
- 1987-12-14 FR FR878717542A patent/FR2608159B1/fr not_active Expired - Lifetime
- 1987-12-14 AT AT3285/87A patent/AT393506B/de not_active IP Right Cessation
- 1987-12-14 FI FI875491A patent/FI86431C/fi not_active IP Right Cessation
- 1987-12-14 GR GR871895A patent/GR871895B/el unknown
- 1987-12-14 IL IL84808A patent/IL84808A/xx not_active IP Right Cessation
- 1987-12-14 US US07/132,492 patent/US4855288A/en not_active Expired - Fee Related
- 1987-12-15 ES ES8703585A patent/ES2010736A6/es not_active Expired
- 1987-12-15 IT IT8748709A patent/IT1230116B/it active

Also Published As

Publication number	Publication date
BE1001621A3 (fr)	1989-12-19
AT393506B (de)	1991-11-11
SE8704979L (sv)	1988-06-16
KR880007533A (ko)	1988-08-27
CH676851A5 (de)	1991-03-15
SE8704979D0 (sv)	1987-12-14
GB2199036B (en)	1990-07-18
NL8702926A (nl)	1988-07-01
GR871895B (en)	1988-04-04
DK655487D0 (da)	1987-12-14
ES2010736A6 (es)	1989-12-01
IL84808A (en)	1991-07-18
IT8748709A0 (it)	1987-12-15
ATA328587A (de)	1991-04-15
MY102270A (en)	1992-05-15
AU8252387A (en)	1988-06-16
PH25421A (en)	1991-07-01
US4855288A (en)	1989-08-08
FR2608159A1 (fr)	1988-06-17
GB8729116D0 (en)	1988-01-27
CA1291752C (en)	1991-11-05
FI86431B (fi)	1992-05-15
GB2199036A (en)	1988-06-29
NZ222897A (en)	1990-02-26
HUT47594A (en)	1989-03-28
FI875491A0 (fi)	1987-12-14
HU198950B (en)	1989-12-28
FI875491L (fi)	1988-06-16
IT1230116B (it)	1991-10-07
AU601247B2 (en)	1990-09-06
FR2608159B1 (fr)	1990-06-08
FI86431C (fi)	1992-08-25
DK655487A (da)	1988-06-16
IL84808A0 (en)	1988-06-30

Publication	Publication Date	Title
LU87181A1 (fr)	1988-11-17	Nouveaux derives de l'acide furannuronique,leur preparation et leur utilisation comme medicaments
EP0370901A1 (de)	1990-05-30	Zentralnervensystem wirksame Chromanderivate, Verfahren zu deren Herstellung und diese enthaltende pharmazeutische Zusammenstellungen
EP0116494B1 (de)	1988-01-27	Pyridazin-Derivate mit psychotroper Wirkung, Verfahren zur Herstellung, Zwischenprodukte und Heilmittel die sie enthalten
BE1001621A3 (fr)	1989-12-19	Nouveaux derives de l'acide furannuronique, leur preparation et leur utilisation comme medicaments.
EP0306408B1 (de)	1992-03-18	Imidazo[1,2-b]pyridazine, Verfahren zu ihrer Herstellung und diese enthaltende pharmazeutische Zubereitungen
LU85473A1 (fr)	1985-04-17	Nouvelles 1,5-benzothiazepines d'utilite cardiovasculaire,procedes pour leur preparation et compositions pharmaceutiques en contenant
EP0136198B1 (de)	1988-02-10	Triazolopyrimidinderivate, Verfahren zu ihrer Herstellung und ihre therapeutische Anwendung als Kardiotonika
FR2672892A1 (fr)	1992-08-21	Derives de 4-pyrimidinones, leur preparation et leur application en therapeutique.
FR2612517A1 (fr)	1988-09-23	Derives de benzoxazine, procedes de preparation de ces derives et compositions pharmaceutiques les contenant
FR2640271A1 (fr)	1990-06-15	Nouveaux derives de l'adenosine, leur preparation et leur utilisation comme medicaments
MC1600A1 (fr)	1985-05-09	Nouveaux derives de pyrimidone
MC1845A1 (fr)	1988-09-30	Derives de pyrimidine
MC1183A1 (fr)	1978-12-22	Derives d'oxadiazolopyrimidine
EP0382635B1 (de)	1994-11-30	Verwendung von 5-Alkylpyridazin-Derivaten als Medikamente zur Beeinflussung des cholinergen Systems
EP0323325B1 (de)	1991-10-16	Trizyklische Derivate, Agonistn von cholinergetischen Rezeptoren und diese enthaltende Arzneimittel
FR2878524A1 (fr)	2006-06-02	Nouveaux derives d'arylpiperazine
CH637930A5 (fr)	1983-08-31	Analogues de la prostaglandine i(2) et compositions pharmaceutiques les contenant.
EP1659112B1 (de)	2007-06-20	Arylpiperazinderivate als selektive Liganden für den Dopamin D3 Rezeptor
EP0183577A1 (de)	1986-06-04	Auf das Zentralnervensystem wirksame Thiadiazolderivate, Verfahren zu ihrer Herstellung und sie enthaltende Arzneimittel
BE900003A (fr)	1984-12-27	Derives du spirosuccinimide utilisables comme medicaments.
EP0233804A1 (de)	1987-08-26	In Stellung 2 substituierte Monoaryl-5 as-Triazinone, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
EP0424214A1 (de)	1991-04-24	5-[2-[[2-Amino-2-oxoethyl]methylamino]ethyl]-2,3-dihydro-3-hydroxy-2-(4-methoxyphenyl)-1,5(5H)-benzothiazepin-4-on-Derivate, ihre Herstellung und ihre Verwendung in der Therapie
CA1155117A (fr)	1983-10-11	Derives de l'isoquinoleine, leur preparation et les medicaments qui les contiennent
JPH0376289B2 (de)	1991-12-05
FR2539739A1 (fr)	1984-07-27	Nouveaux derives de la naphtyl pyridazine actifs sur le systeme nerveux central, procede de preparation de ces derives et medicaments en contenant