USRE42152E1 - Aromatic-linked polyamine macrocyclic compounds with anti-HIV activity - Google Patents
Aromatic-linked polyamine macrocyclic compounds with anti-HIV activity Download PDFInfo
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- USRE42152E1 USRE42152E1 US12/192,704 US19270492A USRE42152E US RE42152 E1 USRE42152 E1 US RE42152E1 US 19270492 A US19270492 A US 19270492A US RE42152 E USRE42152 E US RE42152E
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- bis
- methylene
- tetraazacyclotetradecane
- admixture
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Definitions
- This invention concerns improvements in chemical compounds, more especially it concerns compounds and pharmaceutical compositions. In particular it concerns compositions and compounds having activity in in vitro tests on Human Immunodeficiency Virus-infected cells.
- AIDS Acquired Immune Deficiency Syndrome
- chemo-therapeutic treatments have been advocated, and some compounds have emerged as a potential basis for treatment, there is still a need for alternatives.
- most treatments such as the compound known as AZT have a high toxicity to cells, and it would be desirable to find compounds which are less toxic. In man, the development of resistance to AZT has been identified as an additional clinical problem.
- the present invention provides the use of compounds defined below, in phamaceutical compositions for treating HIV-infected patients.
- the invention further provides pharmaceutical compositions comprising a said compound in combination or association with a pharmaceutically acceptable diluent or excipient, for the treatment of HIV-infected patents.
- the invention may also be defined as the use of a said compound for the manufacture of a medicament for the treatment of HIV-infected patients.
- the invention further provides a process for the production of a pharmaceutical composition for the treatment of a HIV-infected patient, comprising the combination of a compound as defined below with a pharmaceutically acceptable diluent or excipient, and formulating said composition into a form suitable far administration to said patient.
- the invention also provides a method of treatment of an HIV-infected patient, comprising administering to said patient an effective dose of a said compound. It is to be understood that treatment includes prophylactic treatment of patients at risk, in view of the protective properties observed.
- the use of the compounds may also be stated as a method of treating HIV-infected or HIV-challenged human cells to prevent or modulate the multiplication of the HIV, comprising administering to said cells an effective dose of a said compound. Whilst this description is especially directed to combating HIV, this invention includes other aspects in which other diseases may be treated, including for example microbial infections.
- U.S. Pat. No. 4,156,683 discloses monocyclic and bicyclic macrocyclic compounds, which axe are said to have biological activity in regulating sodium, potassium and calcium levels in mammals. Additionally, a specific group of N-alkylated monocyclic compounds are said to possess activity against A 2 influenza viruses in a modified Hermann test on chick fibroblast tissue. It is also said that the preferred compounds, which form complexes of greater stability, are those having three bridging chains between bridgehead nitrogen atoms, that is fused bicyclic compounds.
- EP-A-0296522 discloses certain functionally modified cyclic polyamines, including that known as “cyclam”, which complexes with rhodium and may be bound to an antibody or antibody fragment
- cyclam which complexes with rhodium and may be bound to an antibody or antibody fragment
- the aromatic-linked cyclic polyamines which form the subject of the present invention are not disclosed, nor is any anti-vital activity.
- EP-A-0305320 also discloses several modified cyclic polyamines, but does not disclose identical cyclic polyamines linked together.
- WO-A-9105762 discloses polyamines useful for their multi-point chelating activity, but does not disclose linked cyclic polyamines.
- WO-A-9216494 is in the same name as the present applicants, and discloses long-chain polyamines, optionally linked to a cyclic polyamine, as agents active against HIV. No molecules having two cyclic polyamines, linked through an aromatic linker are disclosed in this prior art.
- the present invention provides as active compounds linked cyclic compounds of the general formula I Z-R-A-R′-Y (I) in which Z and Y are identical cyclic polyamine moieties having from 9 to 20 ring members and from 3 to 6 amine nitrogens in the ring spaced by 2 or more carbon atoms from each other,
- the cyclic polyamine moieties may be substituted or unsubstituted, and suitable substituents are alkyl and/or aryl groups, eg of up to 10 carbon atoms, and any other atoms or groups which do not substantially adversely affect the activity or toxicity of the compounds.
- Preferred moieties are those of 10 to 15 ring members, and there are preferably 3 or 4 amine nitrogen atoms.
- the aromatic or heteroaromatic moiety A tethers Y and Z through the linking groups R and R′.
- Moiety A may be phenyl or fused aromatic such as napthyl, heterocyclic such as pyridyl or thiophenyl, fused heterocyclic or joined aromatic and/or joined heteroaromatic, for example biphenyl or bipyridyl respectively.
- the moieties A may also be substituted at single or multiple non-linking positions with electron-donating groups, eg alkyl, thio, thioalkyl, hydroxyl, alkoxyl, amino and derivatives thereof, or electron-withdrawing groups or atoms, eg nitro, halogen, carboxy, carboxamido, sulfonic acid and derivatives thereof.
- electron-donating groups eg alkyl, thio, thioalkyl, hydroxyl, alkoxyl, amino and derivatives thereof
- electron-withdrawing groups or atoms eg nitro, halogen, carboxy, carboxamido, sulfonic acid and derivatives thereof.
- the invention also includes what may be termed “prodrugs”, that is protected forms of the linked cyclic compounds, which release the compound after administration to a patient.
- the compound may carry a protective group which is split off by hydrolysis in body fluids, eg e.g. in the bloodstream, thus releasing active compound.
- a discussion of pro-drugs may be found in “Smith and Williams' Introduction to the Principles of Drug Design”, H. J. Smith, Wright, 2nd Edition, London 1988.
- the invention further provides a method for the production of the compounds of formula la, which method comprises nucleophilic attack by cyclic polyamines Z′ and Y′ each having a single unprotected ring amine nitrogen, all other ring amine nitrogens being protected, on a compound of formula II X-R-A′-R′-X II wherein R, R′ and A′ are as defined above, and
- the reaction is preferably carried out by reacting two equivalents of the protected polyamine with the compound of formula II in a solvent, such as acetonitrile or dimethylformamide, tetrahydrofuran or dioxane and in the presence of a base, for example sodium carbonate or potassium carbonate.
- a solvent such as acetonitrile or dimethylformamide, tetrahydrofuran or dioxane
- a base for example sodium carbonate or potassium carbonate.
- the reaction generally takes place readily at room temperature to elevated temperature, to give a linked molecule having protected amine nitrogen atoms.
- chromatography on silica gel is a particularly convenient method of separation.
- the deprotection step is suitably carried out by refluxing the protected molecule in a mixture of aqueous HBr and acetic acid or in the case of diethylphosphoryl in the presence of hydrogen chloride (gas) in THF or dioxane.
- the compounds are indicated for the treatment of vital infections, especially retrovirus infections and particularly HIV infections, and the compounds of formula I are to he be considered as active compounds for the pharmaceutical compositions, processes for making the same and methods of treatment mentioned above.
- the compounds of formula I are to he be considered as active compounds for the pharmaceutical compositions, processes for making the same and methods of treatment mentioned above.
- meso forms, enantiomers and resolved optically active forms of the compounds of formula I are included.
- compounds of formula I diluted with non-toxic or other active substances.
- Acid addition salts for example hydrochlorides, and non-toxic labile metal complexes of the compounds of formula I are also active compounds according to the present invention.
- Non-toxic in the present context has to be considered with reference to the prognosis for the infected patient without treatment. Copper and zinc complexes are preferred although other metals such as nickel may be considered, whereas less labile metal atoms such as cobalt and rhodium are less preferred because of likely lower selectivity.
- 1,1′-[2,3,5,6-Tetrafluoro-1,4-phenylenebis-(methylene)]-bis-tris-(p-toluenesulfonyl)-1,4,8,11-tetraazacyclotetradecane 200 mg, 0.13 mmol was dissolved in a mixture of acetic acid and hydrobromic acid (48%) in a ratio of approximately 3:2 by volume (10 ml) and heated to 100° C. for 24 hours during which time a white solid precipitated.
- 1,4-Dimethylnaphthalene-4,4′-dibromide gave 1,1′-[1,4-naphthylenebis-(methylene)]-bis-1,4,8,11-tetraazacyclotetradecane octahydrobromide tetrahydrate.
- step b) The mono-deprotected tetraazacyclohexadecane macrocycle described in step b) was used as described in Example 1 steps c) and d), to prepare tetraazacyclohexadecane dimers.
- 4,4′-Dibromo-m-xylene gave 1,1′-[1,3-phenylene-bis-(methylene)]-bis-1,5,9,13-tetraazacyclohexadecane octahydrobromide hexahydrate.
- reaction mixture was allowed to cool to mom temperature and the solid was filtered off, washed with acetic acid followed by ether and dried in vacuo thus affording a white solid which was identified by 1 H NMR, 13 C NMR, FAB-MS and elemental analysis as 1,1′-[2,6-pyridinebis-(methylene)]-bis-1,4,8,11-tetraazacyclotetradecane octahydrobromide tetrahydrate (230 mg, 65%).
- Mass spectrum (FAB); m/e (relative intensity); 591 (M+HBr, 26), 589 (M+HBr, 26), 509 (M+1, 22) 311 (23), 201 (71), 185 (100).
- the compounds of the invention were tested in a screen by the MTT method (I Vixol Methods 120:309-321 [1988]).
- MT-4 cells 2.5 ⁇ 10 4 /well
- HIV-1 HIV-1
- LAV-2 ROD HIV-2
- CCID 50 concentration of 100 CCID 50
- MTT tetrazolium
- Anti-viral activity and cytotoxicity of the compounds are expressed in the table below as IC 50 ( ⁇ g/ml) and CC 50 ( ⁇ g/ml), respectively.
- the potential therapeutic usefulness was assessed by calculating a Selectivity Index (SI) corresponding to the ratio of CC 50 to IC 50 .
- SI Selectivity Index
- the compounds according to the invention are highly active against HIV-1 and -2, with low toxicity, in the in vitro tests used.
- the compound B which is the most preferred compound of the invention, was further tested for antiviral effects on different laboratory strains of HIV-1 in MT-4 cells, using the MIT assay.
- Compound B was found to have an IC 50 in the range of 2-5 ng/ml against IIIb, RF, HE and NDK strains, showing that its high activity is remarkably strain-independent.
- T4-lymphocytes and monocytes are targets for HIV-1 infection in vivo.
- the following test method showed that compound B inhibits virus replication also in primary T4 cells and primary monocytes in culture.
- T4 lymphocytes were purified from human spleens obtained from healthy donors by using a commercial kit (“Lympho-Kwik”) which combines reaction of cells with specific monoclonal antibodies and density gradient centrifugation to separate the cells. Preparations obtained by this procedure contained 60-80% CD4 positive cells as analysed by FACS. Cells were stimulated with 2 ⁇ g/ml PHA for 24 hours. Then they were spun down and infected with HIV-1, strain IIIb, by suspending the cells 10-fold concentrated in virus solution. Adsorption was allowed for 2 hours at 37° C. The inoculum was removed by centrifugation and the cells were re-suspended at their original concentration in fresh culture medium containing IL-2 (40 IE/ml).
- Test compound was added after stimulation and virus adsorption. Every 3 to 4 days post infection half of the supernatant of the infected cultures was removed and replaced by fresh medium containing the test compound at the particular concentration, The concentration of vital p24 antigen was determined in the supernatent by means of a commercial ELISA kit (Coulter) and served as a parameter for virus production. Compound B does not interfere with the p24 Elisa test (highest concentration tested: 100 ⁇ g/ml).
- Mononuclear cells were isolated from healthy, HIV-negative donors using Ficoll density separation. Cells (4 ⁇ 10 6 /ml) were incubated for 5 days in 48 well plates (Costar) in monocyte medium consisting of RPMII640, supplemented with 20% ECS and 10% human serum. On day 5 non-adherent cells were washed out four times with warm PBS containing 2% human serum. Preparations obtained by the procedure were >95% positive for non-specific esterase (Sigma) and cell viability (as determined by trypan blue exclusion) was always >95%.
- the monocytotropic strain of HIV-1, BaL was used for the infection of these monocyte preparations (Pemo et al, 1 Exp Meal, 169, 933, 1989).
- Adherent monocytes were exposed to 50 ⁇ g/well of a 1:30 dilution of HIV-1, BaL for 30 minutes subsequently, monocyte medium was added to 1 ml/well. Adsorption was allowed for 24 hours at 37° C. Then, the wells were washed twice in order to remove excess virus and were cultivated in the presence of different drug concentrations. Thus, test compounds were added after adsorption. Every 3 to 4 days post infection the supernatant of the infected cultures was removed and replaced by fresh medium containing the test compound at the particular concentration. The concentration of viral p24 antigen was determined as described above.
- IC 50 and IC 90 values were calculated by comparing the p24 antigen concentrations in supernatent of treated, infected cells and uncreated, infected cells at days 11 and 14 post infection.
- Table 2 shows that Compound B is a potent inhibitor of HIV-1 replication in both primary cell types, with IC 90 values of 1-2 ng/ml. At the highest concentration tested, 100 ng/ml, no cytotoxicity was observed.
- Compound B was a strong inhibitor of vital replication in primary T4 cells infected with low-passage primary clinical isolates of HIV-1 from three different geographical locations (K31, Zaire, D370, California, and K6/2, Germany).
- the low cytotoxicity of Compound B was also shown by incubation of exponentially growing cells with Compound B or with AZT and determining cell numbers 2, 3 and 4 days after seeding.
- Compound B did not inhibit growth of MT4, MOLT4, HUT78, Jurkat cells (all T cell lines) nor the growth of the monocylic U937 cell line at concentrations below 300 ⁇ g/ml.
- HUT78 cells AZT was in all cases more cytotoxic than Compound B with TC 50 values ( ⁇ g/ml) of 23, 37, 184 and 5 for MT4, MOLT4, Jurkat and U937 respectively.
- the compounds of the invention do not block virus production from chronically infected cells, indicating that the antiviral target is in the early part of the infection process, before, or at, integration of the provirus.
- a time-of-addition experiment was carried out on MT4 cells infected with HIV-1 strain IIIb at high virus multiplicity to ensure that the virus replicative steps would be synchronised in the whole cell populations.
- Test compounds wife added 1, 2, 3, . . . 22, 23, 24 hours after infection, and vital p24 antigen production determined 29 hours after infection.
- TIBO derivative R82913
- Compound B was also found to inhibit fusion, which is the mechanism by which viruses enter cells and by which virus or infectious material is transmitted from cell to cell. Syncytium formation between chronically infected cells and uninfected cells reflects the gp120/41 mediated fusion process of vital entry.
- the syncytium inhibition assay (Baba et al, J AIDS 3 493, 1990)) using HIV-1 IIIb infected HUT78 cells with MOLT4 cells indicates that Compound B is at least as potent as dextran sulphate in inhibition of fusion.
- concentrations required (approximately 1 ⁇ g/ml) are considerably higher than the antiviral IC 50 values, but are well below cytotoxicity levels.
- the compounds of Formula I axe therefore useful for the treatment and/or prophylaxis of HIV infection, alone or in combination with other active agents.
- the appropriate dosage will, of course, vary depending upon, for example, the compound of Formula I employed, the host, the mode of administration and the nature and severity of the conditions being treated. However, in general, satisfactory results in humans are indicated to be obtained at daily dosages from about 0.01-20 mg/kg of body weight.
- An indicated daily dosage in humans is in the range from about 0.7 mg to about 1400 mg of a compound of Formula I conveniently administered for example in divided doses up to four times a day.
- the compounds of Formula I may be administered by any conventional route, particularly enterally, preferably orally, eg in the loan of tablets or capsules or in liquid form, eg as a syrup; or parenterally, eg in the form of solutions or suspensions for iv or sc administration.
- Compound B is the preferred compound of Formula I. In view of its activity in the test methods as described above, it is indicated that Compound B may be administered to humans at daily dosages of from 2 to 200 mg, preferably 10 to 70 mg, by parentexal administration, eg by subcutaneous injection.
- the compounds of Formula I may be administered in free base form or in pharmaceutically acceptable acid addition salt or metal complex form. Such salts and complexes may be prepaxed in conventional manner as described in the Examples, and exhibit the same order of activity as the free bases. Pharmaceutical compositions containing compounds of Formula I may be manufactured in conventional manner. Unit dosage forms contain for example from about 0.5 mg to about 100 mg of a compound of Formula I in free base or pharmaceutically acceptable acid addition salt form.
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- Tropical Medicine & Parasitology (AREA)
- Communicable Diseases (AREA)
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- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- AIDS & HIV (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Liquid Crystal Substances (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
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- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB919126677A GB9126677D0 (en) | 1991-12-16 | 1991-12-16 | Improvements in chemical compounds |
PCT/GB1992/002334 WO1993012096A1 (en) | 1991-12-16 | 1992-12-16 | Linked cyclic polyamines with activity against hiv |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US08/244,863 Reissue US5583131A (en) | 1991-12-16 | 1992-12-16 | Aromatic-linked polyamine macrocyclic compounds with anti-HIV activity |
Publications (1)
Publication Number | Publication Date |
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USRE42152E1 true USRE42152E1 (en) | 2011-02-15 |
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ID=10706343
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US12/192,704 Expired - Lifetime USRE42152E1 (en) | 1991-12-16 | 1992-12-16 | Aromatic-linked polyamine macrocyclic compounds with anti-HIV activity |
US08/244,863 Ceased US5583131A (en) | 1991-12-16 | 1992-12-16 | Aromatic-linked polyamine macrocyclic compounds with anti-HIV activity |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US08/244,863 Ceased US5583131A (en) | 1991-12-16 | 1992-12-16 | Aromatic-linked polyamine macrocyclic compounds with anti-HIV activity |
Country Status (26)
Country | Link |
---|---|
US (2) | USRE42152E1 (ru) |
EP (2) | EP0619813B1 (ru) |
JP (1) | JP3375961B2 (ru) |
KR (1) | KR100286235B1 (ru) |
AT (1) | ATE273964T1 (ru) |
AU (1) | AU661086B2 (ru) |
CA (1) | CA2125978C (ru) |
CZ (1) | CZ286928B6 (ru) |
DE (2) | DE69233401T2 (ru) |
DK (1) | DK0619813T3 (ru) |
ES (1) | ES2224096T3 (ru) |
FI (1) | FI942849A (ru) |
GB (1) | GB9126677D0 (ru) |
HK (2) | HK1014368A1 (ru) |
HU (1) | HU224013B1 (ru) |
IL (1) | IL103984A (ru) |
MX (1) | MX9207316A (ru) |
MY (1) | MY110897A (ru) |
NL (1) | NL300425I1 (ru) |
NO (2) | NO305984B1 (ru) |
NZ (1) | NZ246179A (ru) |
PL (1) | PL173643B1 (ru) |
PT (1) | PT619813E (ru) |
RU (1) | RU94031208A (ru) |
WO (1) | WO1993012096A1 (ru) |
ZA (1) | ZA929632B (ru) |
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US20080300165A1 (en) * | 2004-11-05 | 2008-12-04 | The General Hospital Corporation | Purposeful Movement Of Human Migratory Cells Away From An Agent Source |
WO2012158707A1 (en) | 2011-05-16 | 2012-11-22 | Genzyme Corporation | Use of cxcr4 antagonists |
WO2015031722A1 (en) | 2013-08-30 | 2015-03-05 | Ramot At Tel-Aviv University Ltd. | Method for treating amyotrophic lateral sclerosis by inhibition of cxcr4/cxcl12 signaling |
Families Citing this family (104)
Publication number | Priority date | Publication date | Assignee | Title |
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GB9126677D0 (en) | 1991-12-16 | 1992-02-12 | Johnson Matthey Plc | Improvements in chemical compounds |
GB9318550D0 (en) * | 1993-09-07 | 1993-10-20 | Nycomed Salutar Inc | Chelants |
GB9400411D0 (en) * | 1994-01-11 | 1994-03-09 | Johnson Matthey Plc | Improvements in chemical compounds |
US5663161A (en) * | 1995-02-17 | 1997-09-02 | The Research Foundation Of State University Of New York | Anti-viral triaza compounds |
US5612478A (en) * | 1995-03-30 | 1997-03-18 | Johnson Matthey Plc | Process for preparing 1,1'-[1,4-phenylenebis-(methylene)]-bis-1,4,8,11-tetraazacyclotetradecane |
US5606053A (en) * | 1995-05-02 | 1997-02-25 | Johnson Matthey Plc | Process for preparing 1,1'-[1,4-phenylenebis-(methylene)]-bis-1,4,8,11-tetraazacyclotetradecane |
US6506770B1 (en) | 1996-06-06 | 2003-01-14 | Anormed, Inc. | Antiviral compounds |
GB9511357D0 (en) * | 1995-06-06 | 1995-08-02 | Johnson Matthey Plc | Improved antiviral compounds |
US5608061A (en) * | 1995-08-02 | 1997-03-04 | Johnson Matthey Plc | Process for preparing 1,4,8,11-tetraazacyclotetradecane |
US7087648B1 (en) * | 1997-10-27 | 2006-08-08 | The Regents Of The University Of California | Methods for modulating macrophage proliferation using polyamine analogs |
US6498155B1 (en) | 1998-11-17 | 2002-12-24 | Smithkline Beecham Corporation | Methods of treating thrombocytopenia |
US6365583B1 (en) | 1999-02-02 | 2002-04-02 | Anormed, Inc. | Methods to enhance white blood cell count |
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JP2002543126A (ja) * | 1999-05-03 | 2002-12-17 | スミスクライン・ビーチャム・コーポレイション | Cxcr−4受容体アンタゴニスト−トロンボポエチン模倣物 |
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RU2289581C2 (ru) * | 2000-09-15 | 2006-12-20 | Анормед, Инк. | Гетероциклические соединения, содержащая их фармацевтическая композиция и их применение |
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