WO2000016753A3 - Verwendung von nucleosiden, nucleobasen und deren derivaten zum herabsetzen thrombocytopenischer nebenwirkungen von cytostatika - Google Patents

Verwendung von nucleosiden, nucleobasen und deren derivaten zum herabsetzen thrombocytopenischer nebenwirkungen von cytostatika Download PDF

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Publication number
WO2000016753A3
WO2000016753A3 PCT/DE1999/002944 DE9902944W WO0016753A3 WO 2000016753 A3 WO2000016753 A3 WO 2000016753A3 DE 9902944 W DE9902944 W DE 9902944W WO 0016753 A3 WO0016753 A3 WO 0016753A3
Authority
WO
WIPO (PCT)
Prior art keywords
nucleobases
nucleosides
derivatives
reducing
cytostatic agents
Prior art date
Application number
PCT/DE1999/002944
Other languages
English (en)
French (fr)
Other versions
WO2000016753A2 (de
Inventor
Iduna Fichtner
Peter Langen
Original Assignee
Max Delbrueck Centrum
Iduna Fichtner
Peter Langen
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.)
Filing date
Publication date
Application filed by Max Delbrueck Centrum, Iduna Fichtner, Peter Langen filed Critical Max Delbrueck Centrum
Priority to EP99969331A priority Critical patent/EP1037618A1/de
Publication of WO2000016753A2 publication Critical patent/WO2000016753A2/de
Publication of WO2000016753A3 publication Critical patent/WO2000016753A3/de

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7042Compounds having saccharide radicals and heterocyclic rings
    • A61K31/7052Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
    • A61K31/706Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
    • A61K31/7064Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
    • A61K31/7068Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
    • A61K31/7072Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid having two oxo groups directly attached to the pyrimidine ring, e.g. uridine, uridylic acid, thymidine, zidovudine

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Molecular Biology (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Die Erfindung betrifft die Verwendung von Nucleosiden, Nucleobasen und deren Derivaten, insbesondere von 6-Methyluracil, zum Herabsetzen thrombocytopenischer Nebenwirkungen von Cytostatika sowie Kombinationspräparate von Nucleosiden, Nucleobasen und deren Derivaten und Cytostatika, insbesondere Carboplatin.
PCT/DE1999/002944 1998-09-17 1999-09-16 Verwendung von nucleosiden, nucleobasen und deren derivaten zum herabsetzen thrombocytopenischer nebenwirkungen von cytostatika WO2000016753A2 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP99969331A EP1037618A1 (de) 1998-09-17 1999-09-16 Verwendung von nucleosiden, nucleobasen und deren derivaten zum herabsetzen thrombocytopenischer nebenwirkungen von cytostatika

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19842578.3 1998-09-17
DE1998142578 DE19842578A1 (de) 1998-09-17 1998-09-17 Verwendung von Nucleosiden, Nucleobasen und deren Derivaten zum Herabsetzen thrombocytopenischer Nebenwirkungen von Cytostatika

Publications (2)

Publication Number Publication Date
WO2000016753A2 WO2000016753A2 (de) 2000-03-30
WO2000016753A3 true WO2000016753A3 (de) 2000-09-14

Family

ID=7881265

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/DE1999/002944 WO2000016753A2 (de) 1998-09-17 1999-09-16 Verwendung von nucleosiden, nucleobasen und deren derivaten zum herabsetzen thrombocytopenischer nebenwirkungen von cytostatika

Country Status (3)

Country Link
EP (1) EP1037618A1 (de)
DE (1) DE19842578A1 (de)
WO (1) WO2000016753A2 (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10117615A1 (de) * 2001-04-07 2002-10-10 Max Delbrueck Centrum Verwendung von Nucleosiden, Nucleobasen und deren Derivaten zur verbesserten Gewinnung von adulten Stammzellen

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996023506A1 (de) * 1995-02-01 1996-08-08 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Verwendung von 5' substituierten nukleosiden zur hemmung von resistenzbildung bei der zytostatikabehandlung und arzneimittel, enthaltend diese nukleoside

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996023506A1 (de) * 1995-02-01 1996-08-08 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Verwendung von 5' substituierten nukleosiden zur hemmung von resistenzbildung bei der zytostatikabehandlung und arzneimittel, enthaltend diese nukleoside

Non-Patent Citations (7)

* Cited by examiner, † Cited by third party
Title
FELIU, J. ET AL: "Treatment of patients with advanced gastric carcinoma with the combination of etoposide plus oral tegafur modulated by uracil and leucovorin: A phase II study of the ONCOPAZ cooperative group", CANCER (N. Y.) (1996), 78(2), 211-216, 1996, XP000913477 *
HOFS, H. P. ET AL: "Potentiation of cisplatin antitumor activity by ethyldeshydroxysparsomycin in L1210 leukemia", ANTICANCER RES. (1992), 12(1), 167-70, 1992, XP000910656 *
IVANOVA, R. K.: "Effect of orotic acid on thrombocytopoiesis in guinea pigs with acute posthemorrhagic anemia", PATOL. FIZIOL. EKSP. TER. (1969), 13(2), 71-2, 1969, XP000910557 *
SUGA, SHOJI ET AL: "Neoadjuvant chemotherapy in scirrhous cancer of the stomach using uracil and tegafur and cisplatin", INTERN. MED. (TOKYO) (1996), 35(12), 930-936, 1996, XP000910645 *
TSUNODA, AKIRA ET AL: "Repeated administration of low-dose cisplatin simultaneous with uracil and tegafur against autochthonous colon cancer in rats", SHOWA UNIV. J. MED. SCI. (1998), 10(1), 41-49, 1998, XP000910628 *
VILLALON, ANTONIO H. ET AL: "A comparative, randomized trial of UFT and 5-fluorouracil and combination with cyclophosphamide and doxorubicin in the treatment of advanced breast cancer patients at the Philippines General Hospital", ONCOLOGY (1996), VOLUME DATE 1997, 54(SUPPL. 1), 2-6, 1996, XP000910623 *
ZYLICZ, Z. ET AL: "Potentiation of cisplatin antitumor activity on L1210 leukemia s.c. by sparsomycin and three of its analogs", CANCER LETT. (SHANNON, IREL.) (1989), 46(2), 153-7, 1989, XP000910681 *

Also Published As

Publication number Publication date
WO2000016753A2 (de) 2000-03-30
EP1037618A1 (de) 2000-09-27
DE19842578A1 (de) 2000-03-23

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