JPS58189196A - 4−デメトキシ−13−ジヒドロダウノルビシンおよびその製法 - Google Patents
4−デメトキシ−13−ジヒドロダウノルビシンおよびその製法Info
- Publication number
- JPS58189196A JPS58189196A JP58069322A JP6932283A JPS58189196A JP S58189196 A JPS58189196 A JP S58189196A JP 58069322 A JP58069322 A JP 58069322A JP 6932283 A JP6932283 A JP 6932283A JP S58189196 A JPS58189196 A JP S58189196A
- Authority
- JP
- Japan
- Prior art keywords
- leukemia
- methanol
- extracted
- anthracycline
- cross
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
Links
- KMIBSUUWQWSRQV-UHFFFAOYSA-N Idarubicinol Natural products C12=C(O)C=3C(=O)C4=CC=CC=C4C(=O)C=3C(O)=C2CC(C(O)C)(O)CC1OC1CC(N)C(O)C(C)O1 KMIBSUUWQWSRQV-UHFFFAOYSA-N 0.000 title description 2
- 238000004519 manufacturing process Methods 0.000 title description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 12
- 229960000908 idarubicin Drugs 0.000 claims description 6
- 208000032839 leukemia Diseases 0.000 claims description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 5
- XDXDZDZNSLXDNA-TZNDIEGXSA-N Idarubicin Chemical compound C1[C@H](N)[C@H](O)[C@H](C)O[C@H]1O[C@@H]1C2=C(O)C(C(=O)C3=CC=CC=C3C3=O)=C3C(O)=C2C[C@@](O)(C(C)=O)C1 XDXDZDZNSLXDNA-TZNDIEGXSA-N 0.000 claims description 5
- XDXDZDZNSLXDNA-UHFFFAOYSA-N Idarubicin Natural products C1C(N)C(O)C(C)OC1OC1C2=C(O)C(C(=O)C3=CC=CC=C3C3=O)=C3C(O)=C2CC(O)(C(C)=O)C1 XDXDZDZNSLXDNA-UHFFFAOYSA-N 0.000 claims description 5
- 229930182470 glycoside Natural products 0.000 claims description 5
- 150000002338 glycosides Chemical class 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 4
- 229940045799 anthracyclines and related substance Drugs 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 3
- 239000008194 pharmaceutical composition Substances 0.000 claims description 3
- 238000004587 chromatography analysis Methods 0.000 claims description 2
- 239000003480 eluent Substances 0.000 claims description 2
- 239000000741 silica gel Substances 0.000 claims description 2
- 229910002027 silica gel Inorganic materials 0.000 claims description 2
- 206010028980 Neoplasm Diseases 0.000 claims 2
- 201000011510 cancer Diseases 0.000 claims 2
- 241000124008 Mammalia Species 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 239000012458 free base Substances 0.000 claims 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 claims 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- NASFKTWZWDYFER-UHFFFAOYSA-N sodium;hydrate Chemical compound O.[Na] NASFKTWZWDYFER-UHFFFAOYSA-N 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- STQGQHZAVUOBTE-UHFFFAOYSA-N 7-Cyan-hept-2t-en-4,6-diinsaeure Natural products C1=2C(O)=C3C(=O)C=4C(OC)=CC=CC=4C(=O)C3=C(O)C=2CC(O)(C(C)=O)CC1OC1CC(N)C(O)C(C)O1 STQGQHZAVUOBTE-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 241000699670 Mus sp. Species 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229960000975 daunorubicin Drugs 0.000 description 3
- STQGQHZAVUOBTE-VGBVRHCVSA-N daunorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(C)=O)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 STQGQHZAVUOBTE-VGBVRHCVSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 241000699666 Mus <mouse, genus> Species 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 206010003445 Ascites Diseases 0.000 description 1
- 238000011735 C3H mouse Methods 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 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
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000003972 antineoplastic antibiotic Substances 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 230000003013 cytotoxicity Effects 0.000 description 1
- 231100000135 cytotoxicity Toxicity 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 210000003754 fetus Anatomy 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- -1 methylene nitride Chemical class 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/20—Carbocyclic rings
- C07H15/24—Condensed ring systems having three or more rings
- C07H15/252—Naphthacene radicals, e.g. daunomycins, adriamycins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Biochemistry (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8211692 | 1982-04-22 | ||
GB8211692 | 1982-04-22 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58189196A true JPS58189196A (ja) | 1983-11-04 |
JPS6260397B2 JPS6260397B2 (enrdf_load_stackoverflow) | 1987-12-16 |
Family
ID=10529872
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58069322A Granted JPS58189196A (ja) | 1982-04-22 | 1983-04-21 | 4−デメトキシ−13−ジヒドロダウノルビシンおよびその製法 |
Country Status (3)
Country | Link |
---|---|
JP (1) | JPS58189196A (enrdf_load_stackoverflow) |
BE (1) | BE896522A (enrdf_load_stackoverflow) |
DE (1) | DE3306505C2 (enrdf_load_stackoverflow) |
-
1983
- 1983-02-24 DE DE3306505A patent/DE3306505C2/de not_active Expired
- 1983-04-21 JP JP58069322A patent/JPS58189196A/ja active Granted
- 1983-04-21 BE BE0/210597A patent/BE896522A/fr not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
JPS6260397B2 (enrdf_load_stackoverflow) | 1987-12-16 |
DE3306505A1 (de) | 1983-10-27 |
DE3306505C2 (de) | 1986-06-05 |
BE896522A (fr) | 1983-08-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
BG60535B2 (bg) | Нови морфолинови производни на даунорубицина и на доксорубицина | |
JPS6260395B2 (enrdf_load_stackoverflow) | ||
US5532218A (en) | 3'-aziridino-anthracycline derivatives | |
DE3719377A1 (de) | Anthracyclinglykoside, verfahren zu deren herstellung, arzneimittel, welche diese enthalten und deren verwendung als antitumormittel | |
SU797583A3 (ru) | Способ получени антрациклин-глико-зидОВ | |
US4254110A (en) | Pentofuranosyl anthracyclines, intermediates in and method for their preparation and compositions and use thereof | |
JPS58189196A (ja) | 4−デメトキシ−13−ジヒドロダウノルビシンおよびその製法 | |
US4146616A (en) | Antitumor compounds, their preparation and use | |
US5510469A (en) | 2-acyloxy-4-morpholinyl anthracyclines | |
EP0128670A1 (en) | 4-Demethoxy-3'-deamino-3'(4-morpholinyl) derivatives of anthracycline anticancer antibiotics | |
FR2554450A1 (fr) | Glycosides de 4'-halo-anthracycline, procede pour les preparer et leur emploi comme medicament | |
US4604381A (en) | 4-demethoxy-13-dihydrodaunorubicin and use thereof | |
BE1001688A5 (fr) | Nouveaux derives de demethoxy-4 anthracycline. | |
RU2081878C1 (ru) | Антрациклин гликозид и способ его получения | |
WO1985001049A1 (fr) | 7erives de safracine | |
US4576945A (en) | Hexaalkylmelamine-amino-oxy compounds | |
JPH04247096A (ja) | 13−ジヒドロ−3′−(2−アルコキシ−4−モルホリニル)アンスラサイクリン | |
HU195834B (en) | Process for production of antibiotics with antitumor effect and medical compositions containing such active substances | |
GB2118932A (en) | A daunorubicin derivative | |
FI70414B (fi) | Foerfarande foer framstaellning av nya 4'-jododerivater av antracyklinglykosider | |
CA3143914A1 (en) | Carbonate compound having pyrrolopyrimidine skeleton or pharmaceutically acceptable salt thereof | |
DE3912867A1 (de) | 4-desmethoxy-4'-desoxy-4'-jodoanthracyclinglycoside und verfahren zu deren herstellung | |
KR20010013772A (ko) | 13-디하이드로-3' 아지리디노 안트라사이클린 | |
GB2287463A (en) | Bis-anthracycline derivatives | |
CS227686B2 (cs) | Způsob výroby protinádorově účinné antracyklinové glykosidové sloučeniny |