ES446006A1 - Procedimiento de preparacion de una nueva sustancia antitu- moral basica, designada por el numero 32.999 rp. - Google Patents
Procedimiento de preparacion de una nueva sustancia antitu- moral basica, designada por el numero 32.999 rp.Info
- Publication number
- ES446006A1 ES446006A1 ES446006A ES446006A ES446006A1 ES 446006 A1 ES446006 A1 ES 446006A1 ES 446006 A ES446006 A ES 446006A ES 446006 A ES446006 A ES 446006A ES 446006 A1 ES446006 A1 ES 446006A1
- Authority
- ES
- Spain
- Prior art keywords
- atcc
- ethanol
- translation
- designated
- formula
- 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.)
- Expired
Links
- 239000000126 substance Substances 0.000 title abstract 3
- 230000000259 anti-tumor effect Effects 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 abstract 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 abstract 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 abstract 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 abstract 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- 241000187747 Streptomyces Species 0.000 abstract 2
- 238000010521 absorption reaction Methods 0.000 abstract 2
- 244000005700 microbiome Species 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 1
- 241000894006 Bacteria Species 0.000 abstract 1
- 208000007093 Leukemia L1210 Diseases 0.000 abstract 1
- 208000008342 Leukemia P388 Diseases 0.000 abstract 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 abstract 1
- 241000203720 Pimelobacter simplex Species 0.000 abstract 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical group CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 230000001174 ascending effect Effects 0.000 abstract 1
- 229930188550 carminomycin Natural products 0.000 abstract 1
- XREUEWVEMYWFFA-CSKJXFQVSA-N carminomycin 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=C(O)C=CC=C3C3=O)=C3C(O)=C2C[C@@](O)(C(C)=O)C1 XREUEWVEMYWFFA-CSKJXFQVSA-N 0.000 abstract 1
- XREUEWVEMYWFFA-UHFFFAOYSA-N carminomycin I Natural products C1C(N)C(O)C(C)OC1OC1C2=C(O)C(C(=O)C3=C(O)C=CC=C3C3=O)=C3C(O)=C2CC(O)(C(C)=O)C1 XREUEWVEMYWFFA-UHFFFAOYSA-N 0.000 abstract 1
- 229950001725 carubicin Drugs 0.000 abstract 1
- 238000004587 chromatography analysis Methods 0.000 abstract 1
- LYBCHMBMGSZNOA-UHFFFAOYSA-N dichloromethane;formic acid;methanol Chemical compound OC.OC=O.ClCCl LYBCHMBMGSZNOA-UHFFFAOYSA-N 0.000 abstract 1
- 230000002255 enzymatic effect Effects 0.000 abstract 1
- 239000000284 extract Substances 0.000 abstract 1
- 238000002329 infrared spectrum Methods 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 239000000741 silica gel Substances 0.000 abstract 1
- 229910002027 silica gel Inorganic materials 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 238000002211 ultraviolet spectrum Methods 0.000 abstract 1
- 238000001429 visible spectrum Methods 0.000 abstract 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
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)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7507893A FR2303552A1 (fr) | 1975-03-13 | 1975-03-13 | Nouveau derive du naphtacene, sa preparation et les compositions qui le contiennent |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES446006A1 true ES446006A1 (es) | 1977-06-01 |
Family
ID=9152527
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES446006A Expired ES446006A1 (es) | 1975-03-13 | 1976-03-12 | Procedimiento de preparacion de una nueva sustancia antitu- moral basica, designada por el numero 32.999 rp. |
Country Status (6)
| Country | Link |
|---|---|
| AT (1) | AT342767B (enrdf_load_stackoverflow) |
| BE (1) | BE839540A (enrdf_load_stackoverflow) |
| CH (1) | CH615222A5 (enrdf_load_stackoverflow) |
| ES (1) | ES446006A1 (enrdf_load_stackoverflow) |
| FR (1) | FR2303552A1 (enrdf_load_stackoverflow) |
| ZA (1) | ZA761526B (enrdf_load_stackoverflow) |
-
1975
- 1975-03-13 FR FR7507893A patent/FR2303552A1/fr active Granted
-
1976
- 1976-03-12 ZA ZA761526A patent/ZA761526B/xx unknown
- 1976-03-12 CH CH310676A patent/CH615222A5/fr not_active IP Right Cessation
- 1976-03-12 ES ES446006A patent/ES446006A1/es not_active Expired
- 1976-03-12 AT AT185876A patent/AT342767B/de not_active IP Right Cessation
- 1976-03-12 BE BE165145A patent/BE839540A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CH615222A5 (en) | 1980-01-15 |
| ZA761526B (en) | 1977-03-30 |
| BE839540A (fr) | 1976-09-13 |
| ATA185876A (de) | 1977-08-15 |
| FR2303552A1 (fr) | 1976-10-08 |
| AT342767B (de) | 1978-04-25 |
| FR2303552B1 (enrdf_load_stackoverflow) | 1979-08-10 |
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