WO1997001336A1 - Use of lamellarin-class alkaloids in methods of treatment - Google Patents

Use of lamellarin-class alkaloids in methods of treatment Download PDF

Info

Publication number
WO1997001336A1
WO1997001336A1 PCT/IB1996/000742 IB9600742W WO9701336A1 WO 1997001336 A1 WO1997001336 A1 WO 1997001336A1 IB 9600742 W IB9600742 W IB 9600742W WO 9701336 A1 WO9701336 A1 WO 9701336A1
Authority
WO
WIPO (PCT)
Prior art keywords
mdr
lamellarin
compound
group
ocome
Prior art date
Application number
PCT/IB1996/000742
Other languages
French (fr)
Inventor
Jose Luis Fernandez Puentes
Delores Garcia Gravalos
Ana Rodriguez Quesada
Original Assignee
Pharma Mar, S.A.
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 Pharma Mar, S.A. filed Critical Pharma Mar, S.A.
Priority to AU63167/96A priority Critical patent/AU700420B2/en
Priority to PL96324282A priority patent/PL184667B1/en
Priority to CA002225807A priority patent/CA2225807C/en
Priority to DK96922197T priority patent/DK0835108T3/en
Priority to JP50428597A priority patent/JP4153992B2/en
Priority to AT96922197T priority patent/ATE208196T1/en
Priority to EP96922197A priority patent/EP0835108B1/en
Priority to DE69616792T priority patent/DE69616792T2/en
Priority to HU9900186A priority patent/HU225588B1/en
Publication of WO1997001336A1 publication Critical patent/WO1997001336A1/en

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/475—Quinolines; Isoquinolines having an indole ring, e.g. yohimbine, reserpine, strychnine, vinblastine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • 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
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Definitions

  • Marine ascidians have proven to be rich sources of structurally diverse alkaloids, many of which exhibit a broad spectrum of biological activity.
  • Members from the family Didemnidae are generally highly colored, encrusting organisms, colonial by habit, and characteristically contain chemical constituents which are derived from amino acids.
  • the polyaromatic lamellarin alkaloids for example, are probably derived from three tyrosine residues.
  • the lamellarin skeleton was first identified in an isolate from a prosobranch mollusc, Lamellaria sp. , from Palau, but has more recently been found in the didemnid ascidian Didemnum chartaceum from the Seychelles. It has also been suggested that the lamellarins may be distantly related to the tunichromes, reducing blood pigments isolated from the ascidian Ascidia nigra.
  • lamellarin E was determined by spectroscopic and X-ray crystallographic methods.
  • lamellarins F-H were elucidated by interpretation of NMR spectral data. The disclosure of this publication :3 hereby incorporated herein by reference.
  • the lamellarin compounds disclosed herein have been found to be non-toxic inhibitors of acquired multidrug resistance (MDR), which has become a major problem in the treatment of various human tumors.
  • MDR acquired multidrug resistance
  • the lamellarin compounds have also been found to be cytotoxic to MDR cells. Both of these activities are useful in the treatment of MDR tumors.
  • Drugs of proven antitumor chemotherapeutic value to which multidrug resistance has been observed include vinblastine, vincristine, etoposide, teniposide, doxorubicin (adriamycin), daunorubicin, plicamycin (mithramycin) and actinomycin D.
  • Many tumors are intrinsically multidrug resistant (e.g., adenocarcinomas of the colon and kidney) while other tumors acquire multidrug-resistance during therapy (e.g., neuroblastomas and childhood leukemias). While not wishing to be bound by theory, it is believed that the mct gene encodes a glycoprotein (P-1 70 or P-glycoprotein) .
  • This protein is though to act as an energy dependent efflux pump that is utilized in normal cells, as well as in cancer cells, for their detoxification. But, when the latter are able to over express the gene, the effect of an antitumor drug " in such cells is highly reduced and therefore the MDR phenotype appears. See, for instance, Deuchars et al., Seminars in Oncology, 16: 1 56-1 65 ( 1 989) and Gottes an et al., Ann. Rev. Biochem. , 62: 385-427 ( 1 993) .
  • Two ways to overcome MDR are ( 1 ) find inhibitors of P-1 70 or (2) find drugs which are as active against the
  • MDR cancer cell line as they are to said cell line's normal counterpart.
  • MDR inhibitors are agents that are used to restore drug sensitivity to some multidrug resistant tumor cells.
  • agents known to possess this property are certain calcium transport blockers (e.g., verapamil) and certain calmodulin inhibitors (e.g., trifluoperazine) .
  • certain calcium transport blockers e.g., verapamil
  • certain calmodulin inhibitors e.g., trifluoperazine
  • clinical use of these compounds has been limited by their toxic side effects. See, Ozols et al., J. Clin. Oncol. , 5: 541 -547 ( 1 987); see also, Twentyman et al., Int. J. Radiat. Oncol. Biol. Phys. , 12: 1 355 ( 1 986) . The minimization (or elimination) of such toxic side effects is thus an important factor in the selection of a MDR inhibitor.
  • the lamellarin compounds disclosed herein have been found to be non-toxic inhibitors of acquired multidrug resistance (MDR), which has become a major problem in the treatment of various human tumors.
  • MDR acquired multidrug resistance
  • the lamellarin compounds have also been found to be cytotoxic to MDR cells. Both of these activities are useful in the treatment of MDR tumors.
  • MDR is believed to be associated with certain alterations in tumor cells, including an over-expression of a certain high molecular weight membrane glycoprotein and a decrease in the ability of the tumor cell to accumulate and retain chemotherapeutic agents.
  • the present invention is thus directed to methods of treating selected tumors with an effective anti-MDR amount, i.e., either an inhibitory amount, a cytotoxic amount, or both, of one or more lamellarin compounds, which compounds have been found to be effective antitumoral agents against MDR cells.
  • an effective anti-MDR amount i.e., either an inhibitory amount, a cytotoxic amount, or both, of one or more lamellarin compounds, which compounds have been found to be effective antitumoral agents against MDR cells.
  • a method of treating i.e., by slowing the growth or arresting the growth
  • MDR tumors comprising administration of an effective MDR inhibitory amount of a compound having the one (or both) of the following formulae:
  • R 1 to R 17 (in Formula A) or R 1 to R 15 (in Formula B) may be the same or may be different and are selected from the group consisting of - H, -OH, -Me, -Et, -Pro, -OMe, -COMe, and -OCOMe.
  • a method of treating i.e., by slowing the growth or stopping the growth
  • MDR tumors comprising administration of an effective MDR cell cytotoxic amount of an anti-MDR lamellarin compound, particularly of Formula A or B as shown above.
  • the present invention is directed to methods of treatment using the lamellarin compounds embraced in the two general Formulas A and B, and more particularly to methods of treatment utilizing the lamellarins shown below Table I as especially preferred examples of compounds useful in the presently claimed invention.
  • the present invention is directed to novel methods of treating tumors in mammals, comprising administering to a patient in need of such treatment, lamellarins as either inhibitors of MDR activity, or as MDR cytotoxic compounds.
  • lamellarins may be employed either alone against MDP. tumors, or in combination with other anti-tumor drugs, as effective treatments against MDR cells.
  • the present invention is also directed to pharmaceutical compositions comprising one or more lamellarin compounds useful as specified herein.
  • such pharmaceutical compositions can further comprise one or more other antitumor drug, particularly those in which multidrug resistance has been observed; including for example vinblastine, vincristine, etoposide, teniposide, doxorubicin (adriamycin), daunorubicin, plicamycin (mithramycin) and actinomycin D.
  • the present invention is also directed to a method of improving the antitumor chemotherapeutic effect of MDR affected drugs in patients in need of such treatment, comprising coadministerinc
  • the MDR affected antitumor drug with an effective anti-MDR effective amount of a lamellarin compound.
  • the compounds of the present invention have been found to possess MDR antitumor activity both in vitro and in vivo, and as such it is believed that these cytotoxic compounds will be useful as MDR antitumor compounds in animals and preferably in humans.
  • the compounds of the present invention can be prepared and administered in various dosage forms, especially parenteral dosage forms.
  • the dosage forms may comprise as the active ingredient, one or more of the compounds of the present invention.
  • the skilled artisan will likewise recognize that the dosages and routes of administration will vary according to the needs of the patient and the specific activity of the active ingredient(s). The determination of these parameters is within the ordinary skill of the practicing physician.
  • Tables II and III below provide additional data regarding the MDR inhibitory activity of the lamellarins. These data were generated by the procedures described below.
  • Verapamil (Standard) 1 0.15 8.0 0.2 15.0 3 0.06 20.0 0.1 30.0
  • Lamellarin A 0.1 0.7 1.7 2.0 1.5 0.3 0.2 6.0 1.0 3.0
  • Lamellarin I 0.1 0.4 3.0 0.6 5.0
  • Lamellarin 1 0.25 4.8 0.4 7.5 l-acetate 3 0.07 17.1 0.08 37.5
  • Lamellarin J 0.1 0.9 1.3 2.5 1.2 0.3 0.7 1.7 2.0 1.5
  • Lamellarin K 0.03 0.9 1.3 2.0 1.5 0.1 0.3 4.0 0.9 3.3
  • Lamellarin M 0.03 1.0 1.2 1.2 2.5
  • Sensitive and MDR cells were maintained, in logarithmic phase of growth, in Eagle's Minimum Essential Medium, with Earle's Balanced Salts, with non-essential amino acids, with 2.0 mM L-glutamine, without sodium bicarbonate (EMEM/neaa), supplemented with 5% Fetal Calf Serum (FCS), 10 '2 M sodium bicarbonate and 0.1 g/l penicillin G + 0.1 g/l streptomycin sulfate.
  • EMEM/neaa sodium bicarbonate
  • FCS Fetal Calf Serum
  • the tumor cell lines employed have been: P-388 (ATCC CCL 46), suspension culture of a lymphoid neoplasm from a DBA/2 mouse and its corresponding MDR cell line P-388/SCHABEL; CHOB1 (ATCC CCL 1 6), monolayer culture of Chinese hamster ovary and its corresponding MDR cell line CHOC5. See, Rauscher III, et al., "Characterization of Auromycin-Resistant Hamster Cell Mutants that Display a Multidrug Resistance Phenotype," Molecular Pharmacology, 38: 1 98-206 ( 1 990).
  • This form of assay employs 96-well cell culture plates 99 mm diameter. Cells were seeded into wells at 1 X 10 3 cells per well in 100 ⁇ aliquots of EMEM 5% FCS containing different concentrations of the corresponding lamellarins and other compounds (standards) to be tested. Two separate sets of cultures without drugs were seeded, one as control of growth to ensure that cells remained in exponential phase of growth, and another without cells as control of medium. All determinations were carried out in duplicate.
  • the lamellarin compounds also possess immunomodulation activity, and will thus be useful as immunomodulator compounds.
  • Immunomodulator compounds and compositions are useful for modulating or regulating immunological functions in warm blooded animals.
  • Immunomodulators may be immunostimulants for building up immunities to or initiate healing of certain diseases and disorders. Conversely, they may be immunoinhibitors or immunosuppressors for preventing undesirable immune reactions of the body to foreign materials and autoimmune diseases.
  • Immunomodulators have been found to be useful for treating systemic autoimmune diseases, such as lupus erythematosus, as well as immunodeficiency diseases. Further, immunomodulators may be useful for immunotherapy of cancer or to prevent rejections of foreign organs or other tissues in transplants, e.g., kidney, heart or bone marrow.
  • the lamellarin compounds M, J and N triacetate have surprisingly been found to have in vitro antitumor activities which are significantly better, particularly against A549 cells, than the lamellarins I, K and L.
  • lamellarin K As shown below in Table V, the in vivo antitumor activity of lamellarin K is consistent with the in vitro activity demonstrated above. Based upon these data, it is believed that the lamellarin compounds disclosed herein will be useful as antitumor compounds, particularly against the following tumor cell types; leukemia (P388), human lung carcinoma (A549), human colon carcinoma (HT-29), human melanoma (MEL-28) .
  • Lamellarin I 1 1 2 Lamellarin I 1 1 2 —
  • Lamellarin L 0.25 0.25 2
  • Lamellarin M 0.05 0.025 0.5 0.5
  • P388 cells (10 6 ) were implanted i.p. into female CD2F1 mice on day 0. Compounds were administered in saline vehicle i.p. days 1-5 or 1 -9 in a volume of 0.5 mL/animal. Mice were weighed on days 0 and 5 and deaths were recorded daily.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Molecular Biology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Steroid Compounds (AREA)
  • Coating Apparatus (AREA)

Abstract

The lamellarin compounds disclosed herein have been found to be inhibitors of MDR, i.e., acquired multidrug resistance, which has become a major problem in the treatment of various cancers. The lamellarin compounds disclosed herein have also been found to be cytotoxic to MDR cells. MDR is believed to be associated with certain alterations in tumor cells, including an over-expression of a certain high molecular weight membrane glycoprotein and a decrease in the ability of the tumor cell to accumulate and retain chemotherapeutic agents. The present invention is thus directed to methods of treating MDR-type tumors with an effective anti-MDR amount (either inhibitory or cytotoxic) of one or more lamellarin compounds, which compounds have been found to be effective antitumoral agents against MDR cells.

Description

USE OF LAMELLARIN -CUSS ALKALOIDS IN METHODS OF TREATMENT
BACKGROUND OF THE INVENTION
Marine ascidians have proven to be rich sources of structurally diverse alkaloids, many of which exhibit a broad spectrum of biological activity. Members from the family Didemnidae are generally highly colored, encrusting organisms, colonial by habit, and characteristically contain chemical constituents which are derived from amino acids. The polyaromatic lamellarin alkaloids, for example, are probably derived from three tyrosine residues. The lamellarin skeleton was first identified in an isolate from a prosobranch mollusc, Lamellaria sp. , from Palau, but has more recently been found in the didemnid ascidian Didemnum chartaceum from the Seychelles. It has also been suggested that the lamellarins may be distantly related to the tunichromes, reducing blood pigments isolated from the ascidian Ascidia nigra.
Anderson et al., J. Am. Chem. Soc , 107: 5492-5495 ( 1 985), describe the isolation and characterization of four polyaromatic metabolites, the lamellarins A-D, obtained from a marine prosobranch mollusc, Lamellaria sp. The structure of lamellarin A was determined by an X-ray crystallographic study and the structures of lamellarins B-D were assigned by interpretation of spectral data. The disclosure of this publication is hereby incorporated herein by reference. Lindquist et al., J. Org. Chem. , 53: 4570-4574 (1 988) describes the isolation and characterization of four new alkaloids of the lamellarin class from the marine ascidian Didemnum chartaceum obtained from the Indian Ocean. The structure of lamellarin E was determined by spectroscopic and X-ray crystallographic methods. The structure of lamellarins F-H were elucidated by interpretation of NMR spectral data. The disclosure of this publication :3 hereby incorporated herein by reference.
Carroll et al., Aust. J. Chem. , 46: 489-501 ( 1 993) describes six new polyaromatic alkaloids, the lamellarins I, J, K, L, M and the triacetate of lamellarin N, and four known alkaloids of this type, lamellarin A, B, C and the triacetate of lamellarin D, isolated from a marine ascidian Didemnum sp. The disclosure of this publication is hereby incorporated herein by reference.
The lamellarin compounds disclosed herein have been found to be non-toxic inhibitors of acquired multidrug resistance (MDR), which has become a major problem in the treatment of various human tumors. The lamellarin compounds have also been found to be cytotoxic to MDR cells. Both of these activities are useful in the treatment of MDR tumors.
Drugs of proven antitumor chemotherapeutic value to which multidrug resistance has been observed include vinblastine, vincristine, etoposide, teniposide, doxorubicin (adriamycin), daunorubicin, plicamycin (mithramycin) and actinomycin D. Many tumors are intrinsically multidrug resistant (e.g., adenocarcinomas of the colon and kidney) while other tumors acquire multidrug-resistance during therapy (e.g., neuroblastomas and childhood leukemias). While not wishing to be bound by theory, it is believed that the mct gene encodes a glycoprotein (P-1 70 or P-glycoprotein) . This protein is though to act as an energy dependent efflux pump that is utilized in normal cells, as well as in cancer cells, for their detoxification. But, when the latter are able to over express the gene, the effect of an antitumor drug" in such cells is highly reduced and therefore the MDR phenotype appears. See, for instance, Deuchars et al., Seminars in Oncology, 16: 1 56-1 65 ( 1 989) and Gottes an et al., Ann. Rev. Biochem. , 62: 385-427 ( 1 993) . Two ways to overcome MDR are ( 1 ) find inhibitors of P-1 70 or (2) find drugs which are as active against the
MDR cancer cell line as they are to said cell line's normal counterpart.
MDR inhibitors are agents that are used to restore drug sensitivity to some multidrug resistant tumor cells. Among the agents known to possess this property are certain calcium transport blockers (e.g., verapamil) and certain calmodulin inhibitors (e.g., trifluoperazine) . However, clinical use of these compounds has been limited by their toxic side effects. See, Ozols et al., J. Clin. Oncol. , 5: 541 -547 ( 1 987); see also, Twentyman et al., Int. J. Radiat. Oncol. Biol. Phys. , 12: 1 355 ( 1 986) . The minimization (or elimination) of such toxic side effects is thus an important factor in the selection of a MDR inhibitor.
Since verapamil was firstly described, several natural product compounds have been reported to overcome or inhibit MDR. Examples include the plant alkaloid thailblastine (see, Chen et al., Cancer Res. , 53:
2544-2547 ( 1 993)), and the marine natural product patellaminde D (see, Williams et al., Cancer Letters, 71 : 97-102 ( 1 993)) . Other examples of compounds active against MDR cells are the peptide cyclosporin A (see, Beck et al., Biochem. Pharmacol. , 43: 89-93 ( 1 992)), a heterocyclic compound (5-N-acetylardeemin - see, Karwowsky et al., J. Antibiotics, 46: 374-379 ( 1 993)), Geodiamolide A, jaspamide, and glaciasterol A (see, Stingi et al., Cancer Chemother. Pharmacol. , 30: 401 -406 (1992)). Thus, the search for new MDR inhibitors and compounds active agianst MDR cells continues.
SUMMARY OF THE INVENTION
The lamellarin compounds disclosed herein have been found to be non-toxic inhibitors of acquired multidrug resistance (MDR), which has become a major problem in the treatment of various human tumors. The lamellarin compounds have also been found to be cytotoxic to MDR cells. Both of these activities are useful in the treatment of MDR tumors. As discussed above, MDR is believed to be associated with certain alterations in tumor cells, including an over-expression of a certain high molecular weight membrane glycoprotein and a decrease in the ability of the tumor cell to accumulate and retain chemotherapeutic agents.
The present invention is thus directed to methods of treating selected tumors with an effective anti-MDR amount, i.e., either an inhibitory amount, a cytotoxic amount, or both, of one or more lamellarin compounds, which compounds have been found to be effective antitumoral agents against MDR cells.
Thus, in one preferred embodiment of the present invention, there is provided a method of treating (i.e., by slowing the growth or arresting the growth) MDR tumors comprising administration of an effective MDR inhibitory amount of a compound having the one (or both) of the following formulae:
Figure imgf000007_0001
B
wherein R1 to R17 (in Formula A) or R1 to R15 (in Formula B) may be the same or may be different and are selected from the group consisting of - H, -OH, -Me, -Et, -Pro, -OMe, -COMe, and -OCOMe.
Thus, in another preferred embodiment of the present invention, there is provided a method of treating (i.e., by slowing the growth or stopping the growth) MDR tumors comprising administration of an effective MDR cell cytotoxic amount of an anti-MDR lamellarin compound, particularly of Formula A or B as shown above.
Thus, the present invention is directed to methods of treatment using the lamellarin compounds embraced in the two general Formulas A and B, and more particularly to methods of treatment utilizing the lamellarins shown below Table I as especially preferred examples of compounds useful in the presently claimed invention.
Figure imgf000008_0001
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
As described above, the present invention is directed to novel methods of treating tumors in mammals, comprising administering to a patient in need of such treatment, lamellarins as either inhibitors of MDR activity, or as MDR cytotoxic compounds. Thus, the lamellarins may be employed either alone against MDP. tumors, or in combination with other anti-tumor drugs, as effective treatments against MDR cells.
The present invention is also directed to pharmaceutical compositions comprising one or more lamellarin compounds useful as specified herein. Moreover, such pharmaceutical compositions can further comprise one or more other antitumor drug, particularly those in which multidrug resistance has been observed; including for example vinblastine, vincristine, etoposide, teniposide, doxorubicin (adriamycin), daunorubicin, plicamycin (mithramycin) and actinomycin D.
Thus, the present invention is also directed to a method of improving the antitumor chemotherapeutic effect of MDR affected drugs in patients in need of such treatment, comprising coadministerinc
(simultaneously or sequentially) the MDR affected antitumor drug with an effective anti-MDR effective amount of a lamellarin compound.
As demonstrated herein, the compounds of the present invention have been found to possess MDR antitumor activity both in vitro and in vivo, and as such it is believed that these cytotoxic compounds will be useful as MDR antitumor compounds in animals and preferably in humans.
When being used as cytotoxic or antitumor inhibitory MDR agents, the compounds of the present invention can be prepared and administered in various dosage forms, especially parenteral dosage forms. It will be clear to those having ordinary skill in this art that the dosage forms may comprise as the active ingredient, one or more of the compounds of the present invention. The skilled artisan will likewise recognize that the dosages and routes of administration will vary according to the needs of the patient and the specific activity of the active ingredient(s). The determination of these parameters is within the ordinary skill of the practicing physician.
Tables II and III below provide additional data regarding the MDR inhibitory activity of the lamellarins. These data were generated by the procedures described below.
TABLE II
LAMELLARINS TOXICITY TO SENSITIVE AND RESISTANT TUMOR CELL LINES
ACTIVITY: IC50 (μglm\)
Mouse Lymphoma Chinese Hamster Ovary
LAMELLARIN STANDARD P-388 P-388. SCHABEL CH0B1 CH0C5 (MDR) (MDR)
A 0.5 0.5 0.2 0.4
B 5.5 5.5 3.0 10.0
D-triacetate 0.07 0.09 0.03 0.04
1 2.5 2.5 0.2 1 .0 l-acetate 5.5 5.5 2.5 5.0 l-methylate 2.5 3.0 0.5 2.5
J 1 .5 2.0 0.3 0.6
K 0.1 0.1 0.1 0.4
K-triacetate 0.06 0.1 0.1 0.1
L 0.6 0.7 0.4 0.6
L-triacetate 1 .5 1 .5 1 .5 1 .5
M 0.08 0.09 0.04 0.09
M-triacetate 0.6 0.7 0.5 2.0
N-triacetate 0.09 0.2 0.06 0.1
Adriamyclin 0.15 1 .2 0.15 3.0
Verapamil 10.0 10.0 9.0 4.0
PSC833 0.02 0.05 0.04 0.1 TABLE
Adriamycin Toxicity to Resistant Cells (MDR) in Presence or in Absence of Reversing Agents (R.A.) Gain of Sensitivity (G.S.) = IC50 Control/IC50 R.A.
Mouse Lymphoma Chinese Hamster (MDR) Ovary (MDR)
REVERSING AGENT R.A. P-388/SCHABEL CHOC5 (R.A.) (μg/ml) IC50 (//g/ml) G.S. IC50 (μg/ml) G.S.
CONTROL 0 1.2 3.0 (Adriamycin only)
Verapamil (Standard) 1 0.15 8.0 0.2 15.0 3 0.06 20.0 0.1 30.0
Lamellarin A 0.1 0.7 1.7 2.0 1.5 0.3 0.2 6.0 1.0 3.0
Lamellarin B 1 0.3 4.0 0.7 4.3 3 0.15 8.0 0.003 1,000
Lamellarin 0.01 0.7 1.7 2.5 1.2 D-triacetate 0.03 0.12 10.0 0.003 1,000
Lamellarin I 0.1 0.4 3.0 0.6 5.0
0.3 0.15 8.0 0.15 20.0
1 0.04 30.0 0.01 300
Lamellarin 1 0.25 4.8 0.4 7.5 l-acetate 3 0.07 17.1 0.08 37.5
Lamellarin 0.3 0.2 6.0 0.4 7.5 l-Methylate 1 0.04 30.0 0.12 25.0
Lamellarin J 0.1 0.9 1.3 2.5 1.2 0.3 0.7 1.7 2.0 1.5
Lamellarin K 0.03 0.9 1.3 2.0 1.5 0.1 0.3 4.0 0.9 3.3
Lamellarin 0.03 0.4 3.0 1.0 3.0 K-triacetate
Lamellarin L 0.1 0.4 3.0 2.5 1.2 0.3 0.003 400 2.0 1.5
Lamellarin 0.3 0.2 6.0 0.1 30.0 L-triacetate 1 < 0.003 >400 0.003 1,000
Lamellarin M 0.03 1.0 1.2 1.2 2.5
Lamellarin 0.1 0.6 2.0 2.0 1.5 M-triacetate 0.3 0.4 3.0 1.0 3.0
Lamellarin 0.01 0.8 1.5 2.0 1.5 N-triacetate 0.03 0.3 4.0 0.4 7.5 Determination of MDR Activity:
Sensitive and MDR cells were maintained, in logarithmic phase of growth, in Eagle's Minimum Essential Medium, with Earle's Balanced Salts, with non-essential amino acids, with 2.0 mM L-glutamine, without sodium bicarbonate (EMEM/neaa), supplemented with 5% Fetal Calf Serum (FCS), 10'2M sodium bicarbonate and 0.1 g/l penicillin G + 0.1 g/l streptomycin sulfate.
In Vitro cell cytotoxicity was determined using the 3-[4,5- dimethylthiazol-2-yl]-2,5-dipheniltetrazolium bromide (MTT), from Sigma Ref:M-21 28, for quantitative measurement of cell growth and viability. See, T. Mosmann, "Rapid Colorimetric Assay for Cellular Growth and Survival: Application to Proliferation and Cytotoxicity Assays, " Journal of Immunological Methods, 65: 55-63 ( 1 983).
The tumor cell lines employed have been: P-388 (ATCC CCL 46), suspension culture of a lymphoid neoplasm from a DBA/2 mouse and its corresponding MDR cell line P-388/SCHABEL; CHOB1 (ATCC CCL 1 6), monolayer culture of Chinese hamster ovary and its corresponding MDR cell line CHOC5. See, Rauscher III, et al., "Characterization of Auromycin-Resistant Hamster Cell Mutants that Display a Multidrug Resistance Phenotype," Molecular Pharmacology, 38: 1 98-206 ( 1 990).
This form of assay employs 96-well cell culture plates 99 mm diameter. Cells were seeded into wells at 1 X 103 cells per well in 100 μ\ aliquots of EMEM 5% FCS containing different concentrations of the corresponding lamellarins and other compounds (standards) to be tested. Two separate sets of cultures without drugs were seeded, one as control of growth to ensure that cells remained in exponential phase of growth, and another without cells as control of medium. All determinations were carried out in duplicate.
After three days of incubation at 37°C, 10% CO2 in a 98% humid atmosphere, 1 50 μg of MTT is added to each well in 50 μl aliquots of assay medium" Plates were incubated for an additional 4 hours and 100 μ\ aliquots of isopropanol were added to each well. The broad absorption spectrum for the isopropanol solution of this crystal is optimal at 570 nm. Optical density values were obtained with the help of a Dynatech microplate reader and the results of the assay were used to generate graphics from which IC50 was calculated; i.e., wherein the IC50 is the test concentration which produces 50% cell growth inhibition.
Other Biological Properties:
The lamellarin compounds also possess immunomodulation activity, and will thus be useful as immunomodulator compounds. Immunomodulator compounds and compositions, as the name implies, are useful for modulating or regulating immunological functions in warm blooded animals. Immunomodulators may be immunostimulants for building up immunities to or initiate healing of certain diseases and disorders. Conversely, they may be immunoinhibitors or immunosuppressors for preventing undesirable immune reactions of the body to foreign materials and autoimmune diseases.
Immunomodulators have been found to be useful for treating systemic autoimmune diseases, such as lupus erythematosus, as well as immunodeficiency diseases. Further, immunomodulators may be useful for immunotherapy of cancer or to prevent rejections of foreign organs or other tissues in transplants, e.g., kidney, heart or bone marrow. Lamellarins I, K and L all exhibit comparable and significant cytotoxicity against P388 and A549 cell lines in culture (IC50 = 0.25 /yg/ml against each cell line) . Lamellarins K and L also exhibited moderate immunomodulatory activity (LcV:MLR 147 and 98 respectively), and as such, have specific art recognized utilities related thereto.
As shown below in Table IV, the lamellarin compounds M, J and N triacetate, have surprisingly been found to have in vitro antitumor activities which are significantly better, particularly against A549 cells, than the lamellarins I, K and L.
As shown below in Table V, the in vivo antitumor activity of lamellarin K is consistent with the in vitro activity demonstrated above. Based upon these data, it is believed that the lamellarin compounds disclosed herein will be useful as antitumor compounds, particularly against the following tumor cell types; leukemia (P388), human lung carcinoma (A549), human colon carcinoma (HT-29), human melanoma (MEL-28) .
TABLE IV
Lamellarin In Vitro Activity vs. Tumor Cell lines (ICS0 //g/mL)
P388 A549 HT-29 MEI
Lamellarin I 1 1 2 —
Lamellarin K 0.25 0.25 1 —
Lamellarin L 0.25 0.25 2 —
Lamellarin M 0.05 0.025 0.5 0.5
Lamellarin J 0.1 0.025 2.5 2.5
Lamellarin N triacetate 0.1 0.012
TABLE V In Vivo Anti-Tumor Activity vs. P388 Lymphocytic Leukemia
compound Dose (mg/kg) Schedule & Body Body Weight Body Mean Survival % T/C inject. Total Route Weight Day 5 Weight Time
Day 0 (gm) + SD Change
(gm) + SD (gm) Day
5
LAM K 1 5.000 75.000 QD 1 -5 1 9.5 i θ.5 20.7 ± 0.5 1 .2 28.3 i 5.9 > 135.0° (7) iP
I
P388 cells (106) were implanted i.p. into female CD2F1 mice on day 0. Compounds were administered in saline vehicle i.p. days 1-5 or 1 -9 in a volume of 0.5 mL/animal. Mice were weighed on days 0 and 5 and deaths were recorded daily.
Figure imgf000017_0001
* Significant activity (moderate): T/C >_ 125%
Figure imgf000017_0002
Th e present invention has been described in detail, including the preferred embodiments thereof. However, it will be a preciated that those skilled in the art, upon consideration of the present disclosure, may make modifications and/or improvements on this invention and still be within the scope and spirit of this invention as set forth in the following claims.

Claims

WHAT IS CLAIMED IS:
1 . A method of treating multidrug resistant tumors in mammals, comprising administering to a patient in need of such treatment, an effective MDR inhibiting amount of an anti-MDR lamellarin compound.
2. The method of claim 1 , wherein the anti-MDR lamellarin compound has the following formula:
Figure imgf000019_0001
wherein each of R1 to R17 may be the same or may be different and are selected from the group consisting of -H, -OH, -Me, -Et, -Pro, -OMe, - COMe, and -OCOMe.
3. The method of claim 1 , wherein the anti-MDR lamellarin compound has the following formula:
Figure imgf000019_0002
wherein each of R1 to R15 may be the same or may be different and are selected from the group consisting of -H, -OH, -Me, -Et, -Pro, -OMe, - COMe, and -OCOMe.
4. A method of treating multidrug resistant tumors in mammals, comprising administering to a patient in need of such treatment, an effective MDR cell cytotoxic amount of an anti-MDR lamellarin compound.
5. The method of claim 4, wherein the anti-MDR lamellarin compound has the following formula:
Figure imgf000020_0001
wherein each of R1 to R17 may be the same or may be different and are selected from the group consisting of -H, -OH, -Me, -Et, -Pro, -OMe, - COMe, and -OCOMe.
6. The method of claim 4, wherein the anti-MDR lamellarin compound has the following formula:
Figure imgf000020_0002
wherein each of R1 to R15 may be the same or may be different and are selected from the group consisting of -H, -OH, -Me, -Et, -Pro, -OMe, - COMe, and -OCOMe.
7. A pharmaceutical composition comprising one or more anti- MDR lamellarin compounds in combination with one or more MDR affected antitumor drugs.
8. The pharmaceutical composition of claim 7, wherein the MDR affected antitumor drug is selected from the group consisting of vinblastine, vincristine, etoposide, teniposide, doxorubicin (adriamycin), daunorubicin, plicamycin (mithramycin) and actinomycin D.
9. The pharmaceutical composition of claim 7, wherein the anti-MDR lamellarin compound has the following formula:
Figure imgf000021_0001
wherein each of R1 to R17 may be the same or may be different and are selected from the group consisting of -H, -OH, -Me, -Et, -Pro, -OMe, - COMe, and -OCOMe.
10. The pharmaceutical composition of claim 7, wherein the anti-MDR lamellarin compound has the following formula:
Figure imgf000022_0001
wherein each of R1 to R15 may be the same or may be different and are selected from the group consisting of -H, -OH, -Me, -Et, -Pro, -OMe, - COMe, and -OCOMe.
1 1 . A method of improving the antitumor chemotherapeutic effect of MDR affected drugs in patients in need of such treatment, comprising coadministering the MDR affected antitumor drug with an effective amount of an anti-MDR lamellarin compound.
12. The method of claim 1 1 , wherein the anti-MDR lamellarin compound has the following formula:
Figure imgf000022_0002
/01336 PCMB96/00742
- 21 - wherein each of R1 to R17 may be the same or may be different and are selected from the group consisting of -H, -OH, -Me, -Et, -Pro, -OMe, - COMe, and -OCOMe.
13. The method of claim 1 1 , wherein the anti-MDR lamellarin compound has the following formula:
Figure imgf000023_0001
wherein each of R1 to R15 may be the same or may be different and are selected from the group consisting of -H, -OH, -Me, -Et, -Pro, -OMe, - COMe, and -OCOMe.
14. The method of claim 1 1 , wherein the MDR affected antitumor drug and the anti-MDR lamellarin compound are administered simultaneously.
15. The method of claim 1 1 , wherein the MDR affected antitumor drug and the anti-MDR lamellarin compound are administered sequentially.
PCT/IB1996/000742 1995-06-29 1996-06-26 Use of lamellarin-class alkaloids in methods of treatment WO1997001336A1 (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
AU63167/96A AU700420B2 (en) 1995-06-29 1996-06-26 Use of lamellarin-class alkaloids in methods of treatment
PL96324282A PL184667B1 (en) 1995-06-29 1996-06-26 Use of lamellarin - a class of alkaloids - in various treating processes
CA002225807A CA2225807C (en) 1995-06-29 1996-06-26 Use of lamellarin-class alkaloids in methods of treatment
DK96922197T DK0835108T3 (en) 1995-06-29 1996-06-26 Use of lamellarine class alkaloids for treatment methods
JP50428597A JP4153992B2 (en) 1995-06-29 1996-06-26 Use of lamellarin-class alkaloids in therapeutic methods
AT96922197T ATE208196T1 (en) 1995-06-29 1996-06-26 USE OF LEMELLARIN ALKALOIDS IN THERAPEUTIC PROCEDURES
EP96922197A EP0835108B1 (en) 1995-06-29 1996-06-26 Use of lamellarin-class alkaloids in methods of treatment
DE69616792T DE69616792T2 (en) 1995-06-29 1996-06-26 USE OF LEMELLARINE ALKALOIDS IN THERAPEUTIC PROCEDURES
HU9900186A HU225588B1 (en) 1995-06-29 1996-06-26 Use of lamellarin alkaloids in therapy and pharmaceutical compositions containing them

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US08/496,465 US5852033A (en) 1995-06-29 1995-06-29 Methods of treatment using lamellarin-class alkaloids
US08/496,465 1995-06-29

Publications (1)

Publication Number Publication Date
WO1997001336A1 true WO1997001336A1 (en) 1997-01-16

Family

ID=23972747

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB1996/000742 WO1997001336A1 (en) 1995-06-29 1996-06-26 Use of lamellarin-class alkaloids in methods of treatment

Country Status (15)

Country Link
US (2) US5852033A (en)
EP (1) EP0835108B1 (en)
JP (1) JP4153992B2 (en)
AT (1) ATE208196T1 (en)
AU (1) AU700420B2 (en)
CA (1) CA2225807C (en)
DE (1) DE69616792T2 (en)
DK (1) DK0835108T3 (en)
ES (1) ES2164899T3 (en)
HU (1) HU225588B1 (en)
MX (1) MX9800248A (en)
PL (1) PL184667B1 (en)
PT (1) PT835108E (en)
RU (1) RU2188637C2 (en)
WO (1) WO1997001336A1 (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998050365A1 (en) * 1997-05-02 1998-11-12 The Australian National University Preparation of fused polycyclic alkaloids by ring closure of azomethine ylides, novel compounds thereof and their use as chemotherapeutic agents
EP1090008A1 (en) * 1998-06-25 2001-04-11 The Australian National University Syntheses of a variety of lamellarin compounds and analogues
WO2002083669A1 (en) * 2001-04-12 2002-10-24 The Board Of Trustees Of The University Of Illinois Tropane alkaloid multidrug resistance inhibitors from erythroxylum pervillei and use of the same
EP1263723A1 (en) * 2000-03-01 2002-12-11 The Scripps Research Institute Ningalin b analogs employable for reversing multidrug resistance
WO2004014917A2 (en) * 2002-08-13 2004-02-19 Pharma Mar, S.A.U. Antitumoral analogs of lamellarins
JP5888702B2 (en) * 2011-01-17 2016-03-22 国立大学法人 長崎大学 Anticancer active compound

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5852033A (en) * 1995-06-29 1998-12-22 Pharma Mar, S.A. Methods of treatment using lamellarin-class alkaloids
US6248752B1 (en) * 1998-02-27 2001-06-19 Charles Duane Smith Azabicyclooctane compositions and methods for enhancing chemotherapy
GB9920912D0 (en) * 1999-09-03 1999-11-10 Indena Spa Novel derivatives of flavones,xanthones and coumarins
US20030109448A1 (en) * 2001-11-07 2003-06-12 Crowley Kathleen S. Methods of promoting uptake and nuclear accumulation of polyamides in eukaryotic cells
PT1505964E (en) * 2002-05-17 2008-02-28 Merckle Gmbh Annelated pyrrole compounds as proton pump inhibitors for treating ulcer
US20060040945A1 (en) * 2002-05-17 2006-02-23 Merckle Gmbh Annellated pyrrole compounds as proton pump inhibitors for treating ulcer
US8138170B2 (en) * 2004-08-27 2012-03-20 Memorial Sloan-Kettering Cancer Center Immunosuppressive Ningalin compounds
WO2018181777A1 (en) * 2017-03-29 2018-10-04 国立大学法人 長崎大学 Fourth-generation egfr tyrosine kinase inhibitor
JOP20190254A1 (en) 2017-04-27 2019-10-27 Pharma Mar Sa Antitumoral compounds
RU2745401C1 (en) * 2020-07-13 2021-03-24 Федеральное государственное бюджетное учреждение науки Федеральный исследовательский центр "Институт биологии южных морей имени А.О. Ковалевского РАН" (ФИЦ ИнБЮМ) Method for inducing the secretion of biologically active compounds in sea snail rapana venosa val.
CN112300232B (en) * 2020-11-03 2021-11-09 浙江大学 Lamelarin D glycosylated derivative and preparation and application thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5852033A (en) * 1995-06-29 1998-12-22 Pharma Mar, S.A. Methods of treatment using lamellarin-class alkaloids

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
ANDERSEN ET AL: "Metabolites of the Marine Prosobranch Mollusc Lamellaria sp.", JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, vol. 107, 1985, USA, pages 5492 - 5495, XP000602056 *
CARROLL ET AL: "Studies of Australian Ascidians. I, Six New Lamellarin-Class Alkaloids from a Colonial Ascidian, Didemnum sp.", AUSTRALIAN JOURNAL OF CHEMISTRY, vol. 46, no. 4, 1993, AUSTRALIA, pages 489 - 501, XP000602402 *
LINDQUIST ET AL: "New Alkaloids of the Lamellarin class from the marine Ascidian Didemnum chartaceum", JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, vol. 53, 1988, USA, pages 4570 - 4574, XP000602058 *

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6521757B1 (en) 1997-05-02 2003-02-18 The Australian National University Preparation of fused polycyclic alkaloids by ring closure of azomethine ylides, novel compounds thereof and their use as chemotherapeutic agents
US7122673B2 (en) 1997-05-02 2006-10-17 The Australian National University Preparation of fused polycyclic alkaloids by ring closure of azomethine ylides, novel compounds thereof and their use as chemotherapeutic agents
JP2002501504A (en) * 1997-05-02 2002-01-15 ジ・オーストラリアン・ナショナル・ユニバーシティー Process for producing condensed polycyclic alkaloids by ring closure of azomethine ylide, novel compounds by the process and use of the compounds as chemotherapeutic agents
EP1621533A1 (en) * 1997-05-02 2006-02-01 The Australian National University Preparation of fused polycyclic alkaloids by ring closure of azomethine ylides, novel compounds thereof and their use as chemotherapeutic agents
CN1325476C (en) * 1997-05-02 2007-07-11 澳大利亚国立大学 Preparation of fused polycyclic alkaloids by ring closure of azomethine ylides, noval compounds thereof and their use as chemotherapeutic agents
WO1998050365A1 (en) * 1997-05-02 1998-11-12 The Australian National University Preparation of fused polycyclic alkaloids by ring closure of azomethine ylides, novel compounds thereof and their use as chemotherapeutic agents
US7557118B2 (en) 1997-05-02 2009-07-07 The Australian National University Preparation of fused polycyclic alkaloids by ring closure of azomethine ylides, novel compounds thereof and their use as chemotherapeutic agents
JP2002518503A (en) * 1998-06-25 2002-06-25 ジ・オーストラリアン・ナショナル・ユニバーシティー Synthesis of various lamellar compounds and analogs
EP1090008A4 (en) * 1998-06-25 2003-01-02 Univ Australian Syntheses of a variety of lamellarin compounds and analogues
US6469171B1 (en) 1998-06-25 2002-10-22 The Australian National University Syntheses of a variety of lamellarin compounds and analogues
EP1090008A1 (en) * 1998-06-25 2001-04-11 The Australian National University Syntheses of a variety of lamellarin compounds and analogues
EP1263723A1 (en) * 2000-03-01 2002-12-11 The Scripps Research Institute Ningalin b analogs employable for reversing multidrug resistance
EP1263723A4 (en) * 2000-03-01 2004-12-29 Scripps Research Inst Ningalin b analogs employable for reversing multidrug resistance
WO2002083669A1 (en) * 2001-04-12 2002-10-24 The Board Of Trustees Of The University Of Illinois Tropane alkaloid multidrug resistance inhibitors from erythroxylum pervillei and use of the same
US6989396B2 (en) 2001-04-12 2006-01-24 The Board Of Trustees Of The University Of Illinois Tropane alkaloid multidrug resistance inhibitors from Erythroxylum pervillei and use of the same
WO2004014917A3 (en) * 2002-08-13 2004-05-13 Pharma Mar Sau Antitumoral analogs of lamellarins
US7396837B2 (en) 2002-08-13 2008-07-08 Pharma Mar, S.A.U. Antitumoral analogs of lamellarins
WO2004014917A2 (en) * 2002-08-13 2004-02-19 Pharma Mar, S.A.U. Antitumoral analogs of lamellarins
EP2138496A1 (en) 2002-08-13 2009-12-30 Pharma Mar, S.A.U. Antitumoral analogs of lamellarins
JP5888702B2 (en) * 2011-01-17 2016-03-22 国立大学法人 長崎大学 Anticancer active compound

Also Published As

Publication number Publication date
AU6316796A (en) 1997-01-30
CA2225807C (en) 2008-04-22
DE69616792T2 (en) 2002-06-20
HUP9900186A3 (en) 2001-08-28
PL324282A1 (en) 1998-05-11
RU2188637C2 (en) 2002-09-10
AU700420B2 (en) 1999-01-07
MX9800248A (en) 1998-11-30
DK0835108T3 (en) 2002-03-18
ES2164899T3 (en) 2002-03-01
EP0835108A1 (en) 1998-04-15
HUP9900186A2 (en) 1999-06-28
EP0835108B1 (en) 2001-11-07
PL184667B1 (en) 2002-11-29
JPH11508882A (en) 1999-08-03
US5852033A (en) 1998-12-22
US6087370A (en) 2000-07-11
CA2225807A1 (en) 1997-01-16
ATE208196T1 (en) 2001-11-15
HU225588B1 (en) 2007-03-28
DE69616792D1 (en) 2001-12-13
PT835108E (en) 2002-03-28
JP4153992B2 (en) 2008-09-24

Similar Documents

Publication Publication Date Title
US6087370A (en) Methods of treatment using lamellarin-class alkaloids
Eng et al. Activity of rapamycin (AY-22, 989) against transplanted tumors
JP5777562B2 (en) Use of compositions and ET743 for treating cancer
Burke et al. Imidazole carboxamide therapy in advanced malignant melanoma
AU687555B2 (en) Medicinal composition as a remedy for non-small cell lung cancer
Lazaro et al. Antimalarial activity of crambescidin 800 and synthetic analogues against liver and blood stage of Plasmodium sp.
EP3212176B1 (en) Panicein compounds, compositions and their use in the treatment of cancer
JP2003523383A (en) Novel compositions and uses of dictyostatin compounds
Machoñ et al. Immunotropic activity of vratizolin (ITCL, Denotivir)
Lelieveld et al. Effectiveness of P-aminobenzyol-O-phenylenediamine (Goe 1734) against mouse, rat, and human tumour cells
Thadepalli et al. Antitumor activity of trovafloxacin in an animal model
US6011041A (en) Use of anhydrovinblastine
JPS6185320A (en) Enhancer for effect of antitumor agent
CN112402425B (en) Application of 3, 5-dinitrophenyl-pyrazolo [3,4-d ] [1,3] oxazine as tumor drug resistance reversal agent
US6121244A (en) Antitumoral method by administration of partricin derivatives
CN115381956B (en) Pharmaceutical composition for treating cancer and application thereof
Catalona Effects of chemotherapy for prostatic carcinoma on T lymphocyte levels
JP2002255821A (en) Medicine for treating cancer resistant to anticancer medicine
EP1070067B1 (en) Cytotoxic alkaloid derivatives including asmarine a and b isolated from a sponge
Tibell et al. Cyclosporine A in fat emulsion carrier: immunosuppressive effect in vitro
AU745225B2 (en) Cytotoxic pyridoacridine alkaloids
JP2002525316A (en) Pharmaceutical composition having antitumor activity
US20070203113A1 (en) Use of manzamine compounds in anti-cancer therapeutic regimens
Mansour et al. Effect of methotrexate on the response of rat lymphocytes to phytohaemagglutinin
AU2003204339B2 (en) Cytotoxic Alkaloid Derivatives Including Asmarine A and B Isolated from a Sponge

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AL AM AT AU AZ BB BG BR BY CA CH CN CZ DE DK EE ES FI GB GE HU IL IS JP KE KG KP KR KZ LK LR LS LT LU LV MD MG MK MN MW MX NO NZ PL PT RO RU SD SE SG SI SK TJ TM TR TT UA UG UZ VN AM AZ BY KG KZ MD RU TJ TM

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): KE LS MW SD SZ UG AT BE CH DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
121 Ep: the epo has been informed by wipo that ep was designated in this application
ENP Entry into the national phase

Ref document number: 2225807

Country of ref document: CA

Ref country code: CA

Ref document number: 2225807

Kind code of ref document: A

Format of ref document f/p: F

ENP Entry into the national phase

Ref country code: JP

Ref document number: 1997 504285

Kind code of ref document: A

Format of ref document f/p: F

WWE Wipo information: entry into national phase

Ref document number: 1996922197

Country of ref document: EP

WWP Wipo information: published in national office

Ref document number: 1996922197

Country of ref document: EP

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

NENP Non-entry into the national phase

Ref country code: JP

Ref document number: 97504285

Format of ref document f/p: F

NENP Non-entry into the national phase

Ref country code: JP

Ref document number: 97504285

Format of ref document f/p: F

WWG Wipo information: grant in national office

Ref document number: 1996922197

Country of ref document: EP