WO2002074309A2 - Verwendung von tryptophan-derivaten zur spezifischen zytostatischen behandlung von serotonin-produzierenden tumoren - Google Patents

Verwendung von tryptophan-derivaten zur spezifischen zytostatischen behandlung von serotonin-produzierenden tumoren Download PDF

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Publication number
WO2002074309A2
WO2002074309A2 PCT/DE2002/000959 DE0200959W WO02074309A2 WO 2002074309 A2 WO2002074309 A2 WO 2002074309A2 DE 0200959 W DE0200959 W DE 0200959W WO 02074309 A2 WO02074309 A2 WO 02074309A2
Authority
WO
WIPO (PCT)
Prior art keywords
tryptophan
serotonin
derivatives
htp
producing
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.)
Ceased
Application number
PCT/DE2002/000959
Other languages
German (de)
English (en)
French (fr)
Other versions
WO2002074309A3 (de
Inventor
Diego Walther
Michael Bader
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Max Delbrueck Centrum fuer Molekulare in der Helmholtz Gemeinschaft
Original Assignee
Max Delbrueck Centrum fuer Molekulare in der Helmholtz Gemeinschaft
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 fuer Molekulare in der Helmholtz Gemeinschaft filed Critical Max Delbrueck Centrum fuer Molekulare in der Helmholtz Gemeinschaft
Priority to US10/471,776 priority Critical patent/US20040097576A1/en
Priority to JP2002573016A priority patent/JP2004519500A/ja
Priority to EP02732330A priority patent/EP1368027B1/de
Priority to DE50200757T priority patent/DE50200757D1/de
Priority to AT02732330T priority patent/ATE272400T1/de
Publication of WO2002074309A2 publication Critical patent/WO2002074309A2/de
Publication of WO2002074309A3 publication Critical patent/WO2002074309A3/de
Anticipated expiration legal-status Critical
Priority to US11/847,970 priority patent/US20070299128A1/en
Ceased legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
    • A61K31/405Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/18Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis

Definitions

  • tryptophan derivatives for the specific cytostatic treatment of serotonin-producing tumors
  • the invention relates to the use of tryptophan derivatives for the specific cytostatic treatment of serotonin-producing tumors, such as carcinoids and others. Areas of application of the invention are medicine and the pharmaceutical industry.
  • Carcinoids are unusual neuroendocrine tumors, which predominantly occur in the gastrointestinal tract and arise from the transformation of chromaffin cells in the Lieberkühn crypts (Neary et al., Dis. Colon Rectum 40: 349-362, 1997), but also occur in the lungs and in Pancreas. Carcinoids can only be removed surgically, since conventional adjuvant therapy, especially advanced serotonin-producing tumors, is unsatisfactory because these tumor cells are resistant to conventional cytostatics (Neary et al, Dis. Colon Rectum 40: 349-362, 1997; Litvak et al, Surgery 124: 1071-1076, 1998).
  • serotonin-producing lung tumor the so-called small cell lung carcinoma, and for mastocytomas.
  • serotonin apparently acts as an autocrine growth hormone, which is why it is desirable on the one hand to reduce the serotonin synthesis, and on the other hand to act on the tumor cells with specific toxins.
  • the object of the invention is therefore to search for and provide substances which enable the treatment of serotonin-producing tumors. These substances are said to act on the one hand as specific cytostatics, but at the same time they are also intended to reduce the serotonin synthesis as such.
  • hydroxylated tryptophan derivatives which are poisoned in particular in the above-mentioned malignant cells by the body's own enzymes tryptophan hydroxylase (TPH) and aromatic amino acid decarboxylase (AAAD) to reduce and / or inhibit the synthesis of serotonin used in tumor cells, whereby these cells are specifically killed.
  • TPH tryptophan hydroxylase
  • AAAD aromatic amino acid decarboxylase
  • the tryptophan derivatives 7-HTP, 6-HTP or 4-HTP, and derivatives which are further substituted on the aromatic system of tryptophan and which are converted into specific toxins are preferably used.
  • the toxins 5,7-DHT and 5,6-DHT e.g. have long been used in research to examine lesions of tissues in which the serotonin transporter is expressed. This leads to the cytotoxic effect of a large number of cells expressing serotonin transporters that are not identical to cells producing serotonin. In addition, these substances are difficult to handle because of their high sensitivity to oxidation.
  • tryptophan hydroxylase is inhibited competitively with hydroxylated tryptophan derivatives since they compete with the actual substrate, tryptophan. This prevents the autocrine growth promotion of the serotonin on these malignant cells.
  • tryptophan derivatives preferably hydroxylated derivatives such as e.g. the 7-HTP, 6-HTP or 4-HTP an effective cytostatic agent for the treatment of serotonin-producing tumors, such as carcinoids.
  • the tryptophan derivatives specifically inhibit tryptophan hydroxylase, thereby protecting against the autocrine growth requirement of serotonin on the escuonin-producing tumors.
  • Primary tumors can therefore be treated and metastases destroyed cytostatically.
  • the cytostatic agents according to the invention for chemotherapy of malignant diseases based on serotonin-producing tumors are characterized in that they contain hydroxylated tryptophan derivatives with conventional carriers and auxiliaries, preferably the derivatives 7-HTP, 6-HTP and 4-HTP.
  • they are used for the therapy of neuroendocrine tumors, which predominantly occur in the gastrotestinal tract, in the lungs and in the pancreas, and in certain other serotonin-producing lung tumors, especially the small cell lung carcinoma and mastocytomas.
  • the agents are preferably in formulations for parenteral and / or oral administration or, if appropriate, also in the form of liposomal complexes.
  • FIG. 1 Reaction scheme for the enzymatic conversion of 7-hydroxy-tryptophan (7-HTP) to 5,7-dihydroxy-tryptamine (5,7-DHT).
  • the rate-determining first step is mediated by the enzyme tryptophan hydroxylase (TPH), followed by rapid decarboxylation by aromatic amino acid decarboxylase (AAAD).
  • TPH tryptophan hydroxylase
  • AAAD aromatic amino acid decarboxylase

Landscapes

  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Oncology (AREA)
  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
PCT/DE2002/000959 2001-03-15 2002-03-15 Verwendung von tryptophan-derivaten zur spezifischen zytostatischen behandlung von serotonin-produzierenden tumoren Ceased WO2002074309A2 (de)

Priority Applications (6)

Application Number Priority Date Filing Date Title
US10/471,776 US20040097576A1 (en) 2001-03-15 2002-03-15 Use of tryptophan derivatives for the specific cytostatic treatment of serotonin-producing tumors
JP2002573016A JP2004519500A (ja) 2001-03-15 2002-03-15 セロトニン生成腫瘍の特異的細胞増殖抑制性治療に関するトリプトファン誘導体の使用法
EP02732330A EP1368027B1 (de) 2001-03-15 2002-03-15 Verwendung von tryptophan-derivaten zur spezifischen zytostatischen behandlung von serotonin-produzierenden tumoren
DE50200757T DE50200757D1 (de) 2001-03-15 2002-03-15 Verwendung von tryptophan-derivaten zur spezifischen zytostatischen behandlung von serotonin-produzierenden tumoren
AT02732330T ATE272400T1 (de) 2001-03-15 2002-03-15 Verwendung von tryptophan-derivaten zur spezifischen zytostatischen behandlung von serotonin-produzierenden tumoren
US11/847,970 US20070299128A1 (en) 2001-03-15 2007-08-30 Use of Tryptophan Derivatives for the Specific Cytostatic Treatment of Serotonin-Producing Tumors

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10112882.7 2001-03-15
DE10112882A DE10112882A1 (de) 2001-03-15 2001-03-15 Verwendung von Tryptophan-Derivaten zur spezifischen zytostatischen Behandlung von Serotonin-produzierenden Tumoren

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US11/847,970 Continuation US20070299128A1 (en) 2001-03-15 2007-08-30 Use of Tryptophan Derivatives for the Specific Cytostatic Treatment of Serotonin-Producing Tumors

Publications (2)

Publication Number Publication Date
WO2002074309A2 true WO2002074309A2 (de) 2002-09-26
WO2002074309A3 WO2002074309A3 (de) 2002-11-21

Family

ID=7677818

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/DE2002/000959 Ceased WO2002074309A2 (de) 2001-03-15 2002-03-15 Verwendung von tryptophan-derivaten zur spezifischen zytostatischen behandlung von serotonin-produzierenden tumoren

Country Status (7)

Country Link
US (2) US20040097576A1 (https=)
EP (1) EP1368027B1 (https=)
JP (1) JP2004519500A (https=)
AT (1) ATE272400T1 (https=)
DE (2) DE10112882A1 (https=)
ES (1) ES2225789T3 (https=)
WO (1) WO2002074309A2 (https=)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7962299B2 (en) 2003-12-09 2011-06-14 One Click (Ip) Limited Electricity metering

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10043124A1 (de) * 2000-08-31 2002-03-14 Max Delbrueck Centrum Verfahren zur Diagnostik von neuronalen Erkrankungen sowie zur Behandlung der defizienten primären Hämostase
US20060264178A1 (en) * 2005-05-20 2006-11-23 Noble Gayle L Wireless diagnostic systems
CN109912489B (zh) * 2019-03-08 2022-05-13 哈尔滨商业大学 非活化烯烃烷基化合成2,3-二氢色胺类化合物的方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2236876C3 (de) * 1971-08-19 1981-02-12 Ajinomoto Co., Inc., Tokio N-Substituierte Aminocarbonsäuren und diese Verbindungen enthaltende Arzneimittel
US4183858A (en) * 1977-07-01 1980-01-15 Merrell Toraude Et Compagnie α-Vinyl tryptophanes
DE3519687A1 (de) * 1985-06-01 1986-12-04 Veit Arend Aminosaeuren enthaltendes arzneimittel
US5631281A (en) * 1989-06-29 1997-05-20 Warner-Lambert Company N-substituted cycloalkyl and polycycloalkyl α-substituted Trp-Phe- and phenethylamine derivatives
US6124263A (en) * 1998-11-16 2000-09-26 Asta Medica Ag Treatment of tumors by administration of growth hormone releasing compounds and their antagonists
WO2003030907A1 (en) * 2001-10-09 2003-04-17 Myriad Genetics, Inc. Reverse-turn mimetics and composition and methods relating thereto

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7962299B2 (en) 2003-12-09 2011-06-14 One Click (Ip) Limited Electricity metering

Also Published As

Publication number Publication date
DE50200757D1 (de) 2004-09-09
ATE272400T1 (de) 2004-08-15
ES2225789T3 (es) 2005-03-16
US20070299128A1 (en) 2007-12-27
US20040097576A1 (en) 2004-05-20
EP1368027B1 (de) 2004-08-04
JP2004519500A (ja) 2004-07-02
EP1368027A2 (de) 2003-12-10
DE10112882A1 (de) 2002-09-19
WO2002074309A3 (de) 2002-11-21

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