NL193318C - N-[N'-gesubstitueerde carbamoylmethyl]iminodiazijnzuren en preparaten die deze verbindingen bevatten. - Google Patents
N-[N'-gesubstitueerde carbamoylmethyl]iminodiazijnzuren en preparaten die deze verbindingen bevatten. Download PDFInfo
- Publication number
- NL193318C NL193318C NL8105845A NL8105845A NL193318C NL 193318 C NL193318 C NL 193318C NL 8105845 A NL8105845 A NL 8105845A NL 8105845 A NL8105845 A NL 8105845A NL 193318 C NL193318 C NL 193318C
- Authority
- NL
- Netherlands
- Prior art keywords
- acid
- solution
- formula
- oxoethyl
- compounds
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims description 23
- NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical class OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 title claims description 7
- 238000002360 preparation method Methods 0.000 title description 3
- -1 3-Iodo-4-methylphenyl Chemical group 0.000 claims description 17
- 125000001424 substituent group Chemical group 0.000 claims description 13
- 150000003839 salts Chemical class 0.000 claims description 11
- 210000004185 liver Anatomy 0.000 claims description 10
- 210000000941 bile Anatomy 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 239000003638 chemical reducing agent Substances 0.000 claims description 7
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 6
- 229910052794 bromium Inorganic materials 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 4
- 239000003446 ligand Substances 0.000 claims description 4
- 241000124008 Mammalia Species 0.000 claims description 3
- 125000001246 bromo group Chemical group Br* 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 229910052740 iodine Chemical group 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 229910052713 technetium Inorganic materials 0.000 claims description 3
- GKLVYJBZJHMRIY-UHFFFAOYSA-N technetium atom Chemical compound [Tc] GKLVYJBZJHMRIY-UHFFFAOYSA-N 0.000 claims description 3
- 238000002347 injection Methods 0.000 claims description 2
- 239000007924 injection Substances 0.000 claims description 2
- FATAVLOOLIRUNA-UHFFFAOYSA-N formylmethyl Chemical group [CH2]C=O FATAVLOOLIRUNA-UHFFFAOYSA-N 0.000 claims 2
- 239000000243 solution Substances 0.000 description 30
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 22
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical class CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 21
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 21
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- GKLVYJBZJHMRIY-OUBTZVSYSA-N Technetium-99 Chemical compound [99Tc] GKLVYJBZJHMRIY-OUBTZVSYSA-N 0.000 description 14
- 239000012153 distilled water Substances 0.000 description 14
- 229940056501 technetium 99m Drugs 0.000 description 14
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 11
- 239000011541 reaction mixture Substances 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 9
- 239000012043 crude product Substances 0.000 description 9
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical class OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 7
- 239000002002 slurry Substances 0.000 description 7
- 238000001035 drying Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 230000029142 excretion Effects 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 239000002808 molecular sieve Substances 0.000 description 5
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 5
- 238000001816 cooling Methods 0.000 description 4
- ANOBYBYXJXCGBS-UHFFFAOYSA-L stannous fluoride Chemical compound F[Sn]F ANOBYBYXJXCGBS-UHFFFAOYSA-L 0.000 description 4
- 229960002799 stannous fluoride Drugs 0.000 description 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- 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 3
- 239000000908 ammonium hydroxide Substances 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 210000003445 biliary tract Anatomy 0.000 description 3
- 230000002440 hepatic effect Effects 0.000 description 3
- 238000003384 imaging method Methods 0.000 description 3
- 125000001841 imino group Chemical group [H]N=* 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 2
- PNDPGZBMCMUPRI-HVTJNCQCSA-N 10043-66-0 Chemical compound [131I][131I] PNDPGZBMCMUPRI-HVTJNCQCSA-N 0.000 description 2
- MVLMPTBHZPYDBZ-UHFFFAOYSA-N 3-bromo-2,4,6-trimethylaniline Chemical compound CC1=CC(C)=C(Br)C(C)=C1N MVLMPTBHZPYDBZ-UHFFFAOYSA-N 0.000 description 2
- FCFLPZAAPZHJKJ-UHFFFAOYSA-N 3-bromo-2,6-diethyl-4-methylaniline Chemical compound CCC1=CC(C)=C(Br)C(CC)=C1N FCFLPZAAPZHJKJ-UHFFFAOYSA-N 0.000 description 2
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000003745 diagnosis Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- 210000003734 kidney Anatomy 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229960003330 pentetic acid Drugs 0.000 description 2
- 230000002285 radioactive effect Effects 0.000 description 2
- 239000012217 radiopharmaceutical Substances 0.000 description 2
- 229940121896 radiopharmaceutical Drugs 0.000 description 2
- 230000002799 radiopharmaceutical effect Effects 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 239000001119 stannous chloride Substances 0.000 description 2
- 235000011150 stannous chloride Nutrition 0.000 description 2
- 150000003495 technetium Chemical class 0.000 description 2
- LJRDOKAZOAKLDU-UDXJMMFXSA-N (2s,3s,4r,5r,6r)-5-amino-2-(aminomethyl)-6-[(2r,3s,4r,5s)-5-[(1r,2r,3s,5r,6s)-3,5-diamino-2-[(2s,3r,4r,5s,6r)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-hydroxycyclohexyl]oxy-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl]oxyoxane-3,4-diol;sulfuric ac Chemical compound OS(O)(=O)=O.N[C@@H]1[C@@H](O)[C@H](O)[C@H](CN)O[C@@H]1O[C@H]1[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](N)C[C@@H](N)[C@@H]2O)O[C@@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)N)O[C@@H]1CO LJRDOKAZOAKLDU-UDXJMMFXSA-N 0.000 description 1
- YKYIFUROKBDHCY-ONEGZZNKSA-N (e)-4-ethoxy-1,1,1-trifluorobut-3-en-2-one Chemical group CCO\C=C\C(=O)C(F)(F)F YKYIFUROKBDHCY-ONEGZZNKSA-N 0.000 description 1
- OIXUMNZGNCAOKY-UHFFFAOYSA-N 2,6-diethyl-4-methylaniline Chemical compound CCC1=CC(C)=CC(CC)=C1N OIXUMNZGNCAOKY-UHFFFAOYSA-N 0.000 description 1
- UDLJWHHLPYMPPJ-UHFFFAOYSA-N 2-[[2-(3-bromo-2,6-diethyl-4-methylanilino)-2-oxoethyl]-(carboxymethyl)amino]acetic acid Chemical compound CCC1=CC(C)=C(Br)C(CC)=C1NC(=O)CN(CC(O)=O)CC(O)=O UDLJWHHLPYMPPJ-UHFFFAOYSA-N 0.000 description 1
- SFPXBXKUJFHQQY-UHFFFAOYSA-N 2-[carboxymethyl-[2-(3-iodo-4-methylanilino)-2-oxoethyl]amino]acetic acid Chemical compound CC1=CC=C(NC(=O)CN(CC(O)=O)CC(O)=O)C=C1I SFPXBXKUJFHQQY-UHFFFAOYSA-N 0.000 description 1
- MLMHOTOHNNVYHN-UHFFFAOYSA-N 2-[carboxymethyl-[2-oxo-2-(2-phenylethylamino)ethyl]amino]acetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(=O)NCCC1=CC=CC=C1 MLMHOTOHNNVYHN-UHFFFAOYSA-N 0.000 description 1
- GRXMMIBZRMKADT-UHFFFAOYSA-N 3-bromo-4-methylaniline Chemical compound CC1=CC=C(N)C=C1Br GRXMMIBZRMKADT-UHFFFAOYSA-N 0.000 description 1
- RRUDMHNAMZFNEK-UHFFFAOYSA-N 3-iodo-4-methylaniline Chemical compound CC1=CC=C(N)C=C1I RRUDMHNAMZFNEK-UHFFFAOYSA-N 0.000 description 1
- ZLIRJJJHZCGEDV-UHFFFAOYSA-N CC1=C(C=C(C(=C1)C)C)NC(=O)CN(CC(=O)O)CC(=O)O Chemical compound CC1=C(C=C(C(=C1)C)C)NC(=O)CN(CC(=O)O)CC(=O)O ZLIRJJJHZCGEDV-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-AKLPVKDBSA-N Molybdenum Mo-99 Chemical compound [99Mo] ZOKXTWBITQBERF-AKLPVKDBSA-N 0.000 description 1
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 1
- 210000000013 bile duct Anatomy 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 230000009918 complex formation Effects 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- DJQJFMSHHYAZJD-UHFFFAOYSA-N lidofenin Chemical class CC1=CC=CC(C)=C1NC(=O)CN(CC(O)=O)CC(O)=O DJQJFMSHHYAZJD-UHFFFAOYSA-N 0.000 description 1
- 210000005229 liver cell Anatomy 0.000 description 1
- 230000003908 liver function Effects 0.000 description 1
- MHPZZZZLAQGTHT-UHFFFAOYSA-N mebrofenin Chemical compound CC1=CC(C)=C(NC(=O)CN(CC(O)=O)CC(O)=O)C(C)=C1Br MHPZZZZLAQGTHT-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229950009740 molybdenum mo-99 Drugs 0.000 description 1
- JDEJGVSZUIJWBM-UHFFFAOYSA-N n,n,2-trimethylaniline Chemical compound CN(C)C1=CC=CC=C1C JDEJGVSZUIJWBM-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 238000009206 nuclear medicine Methods 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 229960001639 penicillamine Drugs 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000000163 radioactive labelling Methods 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 230000003335 steric effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- IUTCEZPPWBHGIX-UHFFFAOYSA-N tin(2+) Chemical compound [Sn+2] IUTCEZPPWBHGIX-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 239000008215 water for injection Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K51/00—Preparations containing radioactive substances for use in therapy or testing in vivo
- A61K51/02—Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus
- A61K51/04—Organic compounds
- A61K51/0474—Organic compounds complexes or complex-forming compounds, i.e. wherein a radioactive metal (e.g. 111In3+) is complexed or chelated by, e.g. a N2S2, N3S, NS3, N4 chelating group
- A61K51/0478—Organic compounds complexes or complex-forming compounds, i.e. wherein a radioactive metal (e.g. 111In3+) is complexed or chelated by, e.g. a N2S2, N3S, NS3, N4 chelating group complexes from non-cyclic ligands, e.g. EDTA, MAG3
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2123/00—Preparations for testing in vivo
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Optics & Photonics (AREA)
- Pharmacology & Pharmacy (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Physics & Mathematics (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US22115580A | 1980-12-29 | 1980-12-29 | |
| US22115580 | 1980-12-29 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NL8105845A NL8105845A (nl) | 1982-07-16 |
| NL193318B NL193318B (nl) | 1999-02-01 |
| NL193318C true NL193318C (nl) | 1999-06-02 |
Family
ID=22826582
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL8105845A NL193318C (nl) | 1980-12-29 | 1981-12-24 | N-[N'-gesubstitueerde carbamoylmethyl]iminodiazijnzuren en preparaten die deze verbindingen bevatten. |
Country Status (15)
| Country | Link |
|---|---|
| JP (2) | JPS58948A (fr) |
| AT (1) | AT377975B (fr) |
| AU (1) | AU539726B2 (fr) |
| BE (1) | BE891534A (fr) |
| CA (1) | CA1187897A (fr) |
| CH (1) | CH649761A5 (fr) |
| DE (1) | DE3151686A1 (fr) |
| FR (1) | FR2497197B1 (fr) |
| GB (1) | GB2090252B (fr) |
| IE (1) | IE52900B1 (fr) |
| IT (1) | IT1140400B (fr) |
| LU (1) | LU83856A1 (fr) |
| NL (1) | NL193318C (fr) |
| SE (2) | SE461015B (fr) |
| ZA (1) | ZA818943B (fr) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4454107A (en) * | 1982-08-30 | 1984-06-12 | Merck & Co., Inc. | Tc99m-Phenida, radioscintigraphic agent for diagnosis of hepatoniliary disease |
| GB8413772D0 (en) * | 1984-05-30 | 1984-07-04 | Nyegaard & Co As | Chemical compounds |
| JPH0331486Y2 (fr) * | 1985-06-24 | 1991-07-04 | ||
| JPH01143751A (ja) * | 1987-11-18 | 1989-06-06 | Corns & Co Ltd | 低圧鋳造装置とその鋳造方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3725295A (en) * | 1971-07-20 | 1973-04-03 | Atomic Energy Commission | Technetium labeling |
| US4017596A (en) * | 1975-03-03 | 1977-04-12 | Research Corporation | Radiopharmaceutical chelates and method of external imaging |
| CA1070695A (fr) * | 1975-09-02 | 1980-01-29 | Michael D. Loberg | Produit pharmaceutique a base d'acide iminodiacetique |
| CH607920A5 (fr) * | 1976-05-31 | 1978-12-15 | Solco Basel Ag | |
| PL115524B1 (en) * | 1978-04-10 | 1981-04-30 | Uniwersytet Warszawski | Process for manufacturing scintigraphic agent |
| DE2855334A1 (de) * | 1978-12-21 | 1980-07-10 | Hoechst Ag | Technetium-99m-markiertes (2,4,5-trimethylacetanilido)-iminodiacetat zur leberfunktionsdiagnostik und verfahren zur herstellung |
| DE2920174A1 (de) * | 1979-05-18 | 1980-11-20 | Hoechst Ag | Technetium-99m-markierte acetanilidoiminodiacetate zur leberfunktionsdiagnostik |
-
1981
- 1981-12-10 CA CA000392015A patent/CA1187897A/fr not_active Expired
- 1981-12-17 GB GB8138054A patent/GB2090252B/en not_active Expired
- 1981-12-18 BE BE0/206879A patent/BE891534A/fr not_active IP Right Cessation
- 1981-12-18 IE IE3110/81A patent/IE52900B1/en not_active IP Right Cessation
- 1981-12-21 FR FR8123803A patent/FR2497197B1/fr not_active Expired
- 1981-12-22 CH CH8210/81A patent/CH649761A5/fr not_active IP Right Cessation
- 1981-12-23 JP JP56216075A patent/JPS58948A/ja active Granted
- 1981-12-23 AU AU78808/81A patent/AU539726B2/en not_active Expired
- 1981-12-24 LU LU83856A patent/LU83856A1/fr unknown
- 1981-12-24 NL NL8105845A patent/NL193318C/nl not_active IP Right Cessation
- 1981-12-28 SE SE8107806A patent/SE461015B/sv not_active IP Right Cessation
- 1981-12-28 DE DE19813151686 patent/DE3151686A1/de active Granted
- 1981-12-28 ZA ZA818943A patent/ZA818943B/xx unknown
- 1981-12-28 IT IT25861/81A patent/IT1140400B/it active
- 1981-12-29 AT AT0561381A patent/AT377975B/de active
-
1987
- 1987-09-18 SE SE8703623A patent/SE466788B/sv not_active IP Right Cessation
-
1989
- 1989-09-28 JP JP1256895A patent/JPH02160727A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| SE8703623D0 (sv) | 1987-09-18 |
| DE3151686A1 (de) | 1982-07-08 |
| SE466788B (sv) | 1992-04-06 |
| ZA818943B (en) | 1982-11-24 |
| IT1140400B (it) | 1986-09-24 |
| SE8703623L (sv) | 1987-09-18 |
| BE891534A (fr) | 1982-04-16 |
| CA1187897A (fr) | 1985-05-28 |
| ATA561381A (de) | 1984-10-15 |
| SE461015B (sv) | 1989-12-18 |
| IE813110L (en) | 1982-06-29 |
| JPH0237345B2 (fr) | 1990-08-23 |
| DE3151686C2 (fr) | 1990-12-20 |
| SE8107806L (sv) | 1982-06-30 |
| IT8125861A0 (it) | 1981-12-28 |
| AT377975B (de) | 1985-05-28 |
| JPH02160727A (ja) | 1990-06-20 |
| GB2090252B (en) | 1985-01-03 |
| NL8105845A (nl) | 1982-07-16 |
| FR2497197B1 (fr) | 1986-04-11 |
| JPH0316327B2 (fr) | 1991-03-05 |
| NL193318B (nl) | 1999-02-01 |
| CH649761A5 (fr) | 1985-06-14 |
| AU7880881A (en) | 1982-07-08 |
| GB2090252A (en) | 1982-07-07 |
| FR2497197A1 (fr) | 1982-07-02 |
| JPS58948A (ja) | 1983-01-06 |
| LU83856A1 (fr) | 1982-07-07 |
| IE52900B1 (en) | 1988-04-13 |
| AU539726B2 (en) | 1984-10-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4017596A (en) | Radiopharmaceutical chelates and method of external imaging | |
| JP3129431B2 (ja) | 腎機能検査のためのテクネチウム―９９ｍ錯化合物 | |
| DE68925034T2 (de) | Konjugate zur knochenbilddarstellung und therapie von knochenkrebs. | |
| EP0292689A2 (fr) | 1,4,7-Triscarboxyméthyl-1,4,7,10-tétraazacyclododécane substitué et analogues | |
| EP0426759B1 (fr) | NOUVEAUX COMPLEXES Tc-99m | |
| EP0213945B1 (fr) | Complexes de radionucléide et d'isonitrile substitué par des groupes carboxy, carbalcoxy et carbamide | |
| US4418208A (en) | N-Substituted iminodiacetic acids | |
| NL193318C (nl) | N-[N'-gesubstitueerde carbamoylmethyl]iminodiazijnzuren en preparaten die deze verbindingen bevatten. | |
| US4885100A (en) | Tris(isonitrile)copper(I) adducts for preparing radionuclide complexes | |
| US4454107A (en) | Tc99m-Phenida, radioscintigraphic agent for diagnosis of hepatoniliary disease | |
| USRE31463E (en) | Radiopharmaceutical chelates and method of external imaging | |
| US5336482A (en) | Technetium-99m complexes with N-substituted 3-hydroxy-4-pyridinones | |
| US5008418A (en) | Tris(isonitrile)copper(I) adducts for preparing radionuclide complexes | |
| US5028699A (en) | Process for preparing Tc-99m tris(isonitrile) copper complexes | |
| AT393357B (de) | Zusammensetzung fuer die herstellung eines tc-99m enthaltenden radiodiagnostikums | |
| CA1096399A (fr) | Acide iminodiacetique a usage pharcacologique | |
| JPH05508162A (ja) | イソニトリルリガンド含有金属―放射性核種錯化合物 | |
| Nunn et al. | N-substituted iminodiacetic acids | |
| Patel et al. | Hepatobiliary Kinetics of 113mIn-Phenolphthalexon |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A85 | Still pending on 85-01-01 | ||
| BA | A request for search or an international-type search has been filed | ||
| BB | A search report has been drawn up | ||
| BC | A request for examination has been filed | ||
| V4 | Discontinued because of reaching the maximum lifetime of a patent |
Free format text: 20011224 |