WO2002006279A9 - Efficient method of synthesizing combretastatin a-4 prodrugs - Google Patents
Efficient method of synthesizing combretastatin a-4 prodrugsInfo
- Publication number
- WO2002006279A9 WO2002006279A9 PCT/US2001/022403 US0122403W WO0206279A9 WO 2002006279 A9 WO2002006279 A9 WO 2002006279A9 US 0122403 W US0122403 W US 0122403W WO 0206279 A9 WO0206279 A9 WO 0206279A9
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- combretastatin
- solution
- agent
- phosphate
- phosphoric acid
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/12—Esters of phosphoric acids with hydroxyaryl compounds
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Definitions
- the present invention relates generally to the field of compounds with antiangiogenesis effects that may be useful in the treatment of one or more neoplastic diseases.
- the present invention relates to new and efficient methods of synthesizing prodrugs of the known antiangiogenesis compound denominated combretastatin A-4 and its analogs as described in U.S. Patents 4,940,726; 5,409,953; and 5,569,786. More particularly, this invention relates to the improved and efficient phosphorylation and deprotection of phenol combretastatin A-4 in the synthesis of water soluble antiangiogenesis prodrugs of combretastatin A-4.
- Combretastatin A-4 (Formula 1 below) is reported to be an antineoplastic compound inhibiting cancer cell growth and tubulin assembly.
- combretastatin A-4 attacks the lining of blood vessels that grow around tumors, thereby severing the blood supply to the cancerous tumor.
- combretastatin A-4 has exhibited strong anti-cancer activity, its development has been inhibited by extremely poor solubility in water making development and biological distribution impracticable.
- combretastatin A-4P phosphate salts of combretastatin A-4, designated “combretastatin A-4P" (Formula 2 below) have been found to impart the requisite water solubility to the prodrug and are disclosed in US Patent No. 5,561,122 issued to G.R. Pettit et al . on October 1, 1996.
- the phosphate group of the prodrug combretastatin A- 4P reportedly is hydrolyzed in vivo to liberate the active drug combretastatin A-4.
- the currently disclosed methods for synthesizing combretastatin A-4P are difficult, require the use of undesirable solvents or restricted solvents, and are not easily scalable.
- Z Na + , Na + , i + , Mg 2+ , Mn 2+ , Zn 2+ , Ca 2+ , Cs 2+ , imidazole, morpholine, piperazine, piperidine, pyrazole, pyridine, adenosine, cinchonine , glucosamine, quinine, quinidine, tetracycline, verapamil .
- An improved method of preparing prodrugs of combretastatin is/ necessary in order to meet the demand for an efficient and scalable synthesis to produce combretastatin A-4P and isomers thereof for effective use in treating cancer tumors and similar diseases .
- combretastatin A-4 is a potent anticancer agent, its poor water solubility has hindered development of the drug as an anticancer treatment.
- Current methods of synthesizing water soluble derivatives of combretastatin A-4 require the use of undesirable or restricted solvents, such as chloroform, pyridine, dichloromethane or dimethylformamide (“DMF”), require extractions, separations and dilution of the reaction solutions, and heating and cooling of reaction mixtures at temperatures that are not suitable for production of prodrugs of combretastatin A-4 in commercial quantities.
- the subject invention provides a novel and improved method of synthesizing combretastatin A-4P that minimizes or eliminates the use of undesirable solvents, and overcomes many other deficiencies of the prior art using a continuous process.
- a novel process is herein disclosed in which dibenzyl phosphite/carbon tetrabromide is used to phosphorylate phenol combretastatin A-4 forming a phosphate ester of combretastatin A-4 with benzyl protecting groups thereon.
- An improved method of cleaving the benzyl protecting groups from the phosphate ester of combretastatin A-4 is disclosed in which bromotrimethylsilane is reacted with combretastatin A-4 to form phosphoric acid of combretastatin.
- An alternate novel phosphorylation process was concurrently developed and is herein disclosed in which 2,2,2-trichloroethyl phosphorodichloridate phosphorylates combretastatin A-4 to a phosphate ester with trichloroethyl protecting groups thereon.
- trichloroethyl groups are then cleaved from combretastatin A-4 using Zn/Cu amalgam to form a phosphoric acid of combretastatin A-4. Further improvements to the current processes for synthesizing phosphate salts of combretastatin A- 4 are described herein disclosing a continuous process that overcomes many obstacles and limitations to the use and large scale production of combretastatin A-4 prodrugs.
- the invention embraces the provision of combretastatin A-4 prodrug products of the aforesaid novel and improved method.
- the invention contemplates the provision of methods of synthesizing combretastatin A-4 prodrugs including a complete procedure for synthesizing cis combretastatin A-4, to which the foregoing method steps and procedures may then be applied to obtain the prodrug.
- the procedure for synthesizing cis combretastatin A-4 in accordance with this aspect of the invention includes the steps of obtaining a phosphonium salt of 3 ,4, 5-trimethoxybenzyl bromide by mixing a brominating reagent and 3 , 4, 5-trimethoxybenzyl alcohol in toluene to obtain the bromide, and adding triphenylphosphine thereto; obtaining tritylated isovanillin by mixing an amine base, isovanillin, and trityl chloride in an ether solvent, and after quenching, adding heptane and ethyl acetate; mixing a suspension of the phosphonium salt in tetrahydrofuran, an alkyl lithium reagent, and a slurry of the tritylated isovanillin, to obtain a cis/ trans stilbene; and reacting the cis/trans stilbene with an acid to obtain a product consisting essentially
- a combretastatin A-4 prodrug may then be prepared from the latter product by reacting the cis combretastatin A-4 with an activated phosphor- ylating agent having hydroxyl-protecting groups thereon wherein the phosphorylating agent is either dibenzylphosphite/carbon tetrabromide or 2,2,2-trichloroethyl phosphorodichloridate, to form a phosphate ester of combretastatin with protecting groups thereon; deprotecting the hydroxyl-protecting groups with a deprotecting agent to yield a phosphoric acid of combretastatin A-4; and reacting the phosphoric acid with reactive agent to form a phosphate salt of combretastatin A-4.
- an activated phosphor- ylating agent having hydroxyl-protecting groups thereon wherein the phosphorylating agent is either dibenzylphosphite/carbon tetrabromide or 2,2,
- the brominating reagent is phosphorus tribromide
- the triphenylphosphine is unsubstitu- ted triphenylphosphine
- the amine base is triethyl amine
- the ether solvent is tetrahydrofuran
- the trityl chloride is unsubstituted trityl chloride
- the alkyl lithium reagent is n- butyl lithium
- the acid is hydrochloric acid.
- FIG. 1 is a flow chart illustrating the first step in a specific example of the complete synthesis of a combretastatin A-4 prodrug in an embodiment of the method of the invention
- FIG. 2 is a flow chart illustrating the second step in the aforesaid specific example
- FIG. 3 is a flow chart illustrating the third step in the same specific example
- FIG. 4 is a flow chart illustrating the fourth step in the same specific example.
- FIG. 5 is a flow chart illustrating the fifth step in the same specific example.
- the Troc Method requires the use of carcinogenic chloroform in the initial phosphorylation reaction. Moreover, phosphorylation by this method requires the use of dimethyl- formamide having a high boiling point of 153°C. Use of DMF necessitates the additional step of evaporating the solvent during deprotection of the phosphoric ester.
- the Troc Method requires the use of Zn/Cu amalgam to deprotect the intermediate of the Troc group, leaving heavy metal contaminants that are difficult to remove from the final product.
- the first improvement to the existing Troc Method was the replacement of neat pyridine with triethylamine (“TEA”) and a reactive amount of dimethylaminopyridine (“DMAP”) (Table 1, Entry 1) .
- the reaction proceeds much more rapidly with TEA than with pyridine (1.5 hours vs. 16 hours) .
- Replacing the DMF solvent (boiling point of 152.8°C) with acetonitrile (boiling point 82°C) (Table 1, Entry 2) was still a further improvement making isolation of the product from solvent easier to perform.
- the phosphate ester intermediate having Troc protecting groups thereon may then be deprotected without the need for isolation. Deprotection of the intermediate is performed using acetonitrile in Zn/Cu amalgam to form the intermediate phosphate acid of combretastatin A-4P.
- the intermediate phosphate acid is isolated using a DowexTM ion-exchange resin, purchased from Aldrich Chemical Company, Milwaukee, Wisconsin, and thereby eliminating the need for separation by chromatography.
- synthesis may be performed without isolation of the intermediate phosphate acid (Table 1, Entry 3) to produce product with low Zn/Cu levels (130 ppm) thereby limiting the cis/ trans isomerization of intermediates caused by such metals.
- the improvements to the Troc phosphorylation method of the subject invention overcome the problems attributable to the Troc Method disclosed in the prior art, resulting in a new and improved phosphorylation method to synthesize the combretastatin A-4P using Troc as a protecting group to form 3'-0-Bis- 2 , 2 , 2- (trichloroethyl) hosphate combretastatin A-4 (5). See Formula 4.
- Synthesis of combretastatin A-4P was further improved using dibenzyl phosphite/carbon tetrabromide to phosphorylate the phenol combretastatin A-4 (Formula 1) with benzyl protecting groups thereon to form 3 ' -O-Bis (benzyl) phosphate combretastatin A-4. See Formula 6.
- Table 2 summarizes the improvements to the synthetic processes of the prior art by use of the dibenzyl phosphite/carbon tetrabromide phosphorylation method.
- the combretastatin A-4 is phosphorylated using dibenzyl phosphite in presence of triethylamine, carbon tetrabromide, and DMAP, and dibenzylphosphite in acetonitrile to yield crude 3' -O-Bis (benzyl) phosphorylcombretastatin A-4. See (6) in Formula 6. These improvements to the benzyl phosphorylation reaction cause the reaction to go to completion leaving only trace phenol combretastatin (I) . Further improvements to the process resulted in the elimination of the use of DMAP in the reaction, which is a difficult solvent to remove from the product due to its high boiling point.
- crude combretastatin A-4P may be stirred into water/methanol mixture and the solution basified to pH 10-12 resulting in the crude product to become completely dissolved in solution. The mixture is then heated to " approximately 35-40 °C for about one hour.
- a cold solution of a brominating reagent in toluene is added to a cold solution of 3, 4, 5-trimethoxybenzyl alcohol
- TMBA phosphorus tribromide
- examples of alternative brominating reagents include gaseous HBr, triphenylphosphine dibromide and SOBr 2 .
- the resulting bromide (TMBB) is quenched with water and washed. The phases are separated and triphenylphosphine
- triphenylphosphine includes unsubstituted triphenylphosphine, which is currently preferred for this step, and singly or multiply substituted triarylphosphines
- the group (s) attached to the aryl ring(s) in the phosphine may be lower alkyl, lower alkoxy, fluorine and nitro, the substitution pattern on the ring(s) being any location other than the carbon-phosphorus bond; the triphenylphosphine of Formula (7) is unsubstituted when all R are H.
- Step 1 is represented as follows:
- FIG. 1 a flow chart of a specific example is shown in FIG. 1.
- the amine base is preferably triethyl amine (Et 3 N) ; more generally, the amine base may be a trialkyl amine base (lower alkyl or cyclic, including aryl, up to six carbons per alkyl group or ring, examples being Ph 3 N, R 3 N, and cyclic amines such as pyridine, N- methyl morpholine, and DBU) , or an amine resin (such as polyvinyl pyridine or IRA-68 or equivalent) .
- Et 3 N triethyl amine
- trityl chloride includes unsubstituted trityl chloride, which is currently preferred for this step, and singly or multiply (one to five groups) substituted aryl groups on the trityl chloride; the group (s) attached to the aryl ring in the trityl chloride may be lower alkyl, lower alkoxy, fluorine and nitro, the substitution pattern on the ring being any location other than the carbon-carbon bond forming the trityl chloride :
- the trityl chloride is the currently preferred unsubstituted trityl chloride.
- the ether solvent may be lower alkyl or cyclic (including aryl) up to six carbons per alkyl group or ring, the preferred solvent being tetrahydrofuran (THF) , other illustrative examples including
- Step 2 is represented as follows:
- n-butyl lithium (n-BuLi) followed by a slurry of Compound II in THF.
- n-BuLi alkyl amine bases
- alkyl amine bases such as methyl lithium, s-butyl lithium, tert-butyl lithium, other commercially available alkyl lithium reagents such as pentyl, hexyl and octyl lithium (available from FMC LithCo Div)
- hindered amine bases such as lithium diisopropyl or dicyclohexyl amide and lithium hexamethyl disilazane. The resulting mixture is stirred until the reaction is complete.
- Step 3 is represented as follows :
- a mixture of Compound III, acid preferably hydrochloric acid; alternatives include sulfuric acid, hydrobromic acid, methanesulfonic acid, and acid resins such as amberlyst
- toluene is stirred until the reaction is complete.
- the reaction is quenched with water and the mixture is stirred with cooling.
- the product is collected, washed and dried to provide exclusively the cis-isomer of combretastatin A-4 (cis-CA4) ; Compound IV) ; i . e . , only the cis-isomer crystallizes .
- Step 4 is represented as follows :
- FIG. 4 a flow chart of a specific example is shown in FIG. 4.
- a cold mixture of the cis-CA4 (Compound IV) , a trialkyl amine base (preferably Et 3 N) , CBr 4 and acetonitrile (CH 3 CN) is combined with a mixture of dibenzyl phosphite (HPO(OBn) 2 ) and CH 3 CN and the resulting mixture is stirred at room temperature until phosphorylation is complete
- dibenzyl phosphite include, e.g., di-tert butyl phosphite, dibutyl phosphite, diethyl phosphite, diisopropyl phosphite, dimethyl phosphite, diphenyl phosphite, and dipropyl phosphite; together with dibenzyl phosphite, these may be designated phosphites having the formula HPOY 2 where Y is benzyl, tert butyl, butyl,
- TMSBr Bromotrimethylsilane
- TMSCl/NaBr or Nal and higher alkyl silyl bromides up to four carbons per alkyl group
- higher alkyl silyl chlorides in conjunction with NaBr or Nal
- the higher alkyl silyl reagents will react much more slowly in this type of reaction
- NaOMe sodium methoxide
- MeOH methanol
- NaOMe sodium methoxide
- MeOH methanol
- other sodium alkoxides such as sodium ethoxide, isopropoxide, tert-butoxide and tert amyloxide; sodium 2-ethyl hexanoate, sodium acetate or an ion exchange resin that would act as a sodium carrier
- the solid is collected, and washed with acetone to provide a crude product. This crude product is dissolved in a mixture of methanol and water with heat.
- Step 5 is represented as follows:
- FIG. 5 a flow chart of a specific example is shown in FIG. 5.
- Cis-combretastatin A-4 (5 g, 15.8 mmol, leq) was dissolved in acetonitrile (50 ml) under argon atmosphere and dimethylaminopyridine (50 mg, 0.41 mmol) and 2,2,2-trichloroethyl phosphorodichloridate (5.77 g, 21.7, 1.4 eq) were added to the solution forming the phosphate ester of combretastatin A-4.
- Triethylamine (2.3 g, 22.7, 1.44 eq) was added to the mixture portionwise over 20 minutes. After 30 minutes, TLC confirmed the completion of the reaction.
- Zinc/copper amalgam (6.26 g) was added to the solution and the solution was heated to 40°C. After 30 minutes, 2, 4-pentanedione (1.62 g, 16.2 mmol, 1.02 eq) was added in portions while heating at 40°C. After 1.5 hours, heat was removed and the reaction was cooled to room temperature
- the crude combretastatin A-4P (2.42g) was dissolved in ml H 2 0/Methanol 50% (24 ml) and the solution was filtered to remove any undissolved particles. The solution was then heated to 35-40°C for 1 hour. Once the solution cooled down to 30°C acetone was added (12 ml) . Solution was allowed to cool to room temperature and stirred for 2 hours. A second volume of acetone was added and the solution was stirred at room temperature for 12-16 hours and the product was filtered out the next day. The cake was washed with 20% H 2 0/acetone (4.5 ml) twice and then with acetone (4.5 ml). The isolated solid was dried in high-vacuum oven overnight at 40°C.
- Cis-combretastatin A-4 250 g, 791 mmol, leq was dissolved in acetonitrile (1250 ml) .
- Triethylamine 120 g, 1186 mmol, 1.5 eq
- carbon tetrabromide 320 g, 965 mmol, 1.22 eq
- Dibenzylphosphite (249 g, 949 mmol, 1.2 eq) was dissolved in acetonitrile (500 ml). Reaction was cooled to 0°C and the dibenzylphosphite solution was added dropwise to the reaction mixture. After one hour, the completion of the reaction was verified by TLC and HPLC.
- TMS-Br Distilled bromotrimethylsilane
- Crude combretastatin A-4P was isolated in approximately 75% yield (85% w/w assay) .
- the crude combretastatin A-4P (260 g) was suspended in H 2 0 (1300 ml) . Material dissolved as pH was adjusted to 10-12, using sodium methoxide/methanol (25 w%) . Methanol was added to the solution (1300 ml) and the solution was filtered to remove any undissolved particles. The solution was then heated to 35-40°C for 1 hour. Once the solution cooled down to 30 °C acetone was added (1300 ml) . Solution was allowed to cool to room temperature and stirred for 2 hours.
- Process B The Compound V product obtained by the specific process example represented by FIG. 5 (herein “Process B”) was tested and compared with another sample of combretastatin A-4 disodium phosphate prepared by an earlier and different process (herein “Process A”) not embraced within the present invention. It will be noted that Process B (embodying the method of the invention) is also represented by Example 2 above.
- salt forms of combretastatin A-4P may be formed by replacing sodium methoxide solution with reactive amounts of alkaline metals or inorganic salts such as Na 2+ , Na + , Li + , Mg 2+ , Mn 2+ , Zn 2+ , Ca 2+ , Cs 2+ , imid- azole, morpholine, piperazine, piperidine, pyrazole, pyridine, adenosine, cinchonine, glucosamine, quinine, quinidine, tetracycline, or verapamil resulting in salt forms of combretastatin A-4P with varying solubility.
- alkaline metals or inorganic salts such as Na 2+ , Na + , Li + , Mg 2+ , Mn 2+ , Zn 2+ , Ca 2+ , Cs 2+ , imid- azole, morpholine, piperazine, piperidine, pyrazo
- An advantage of the subject invention is the phosphorylation of the combretastatin A-4 in a continuous process, thereby shortening the reaction from three steps to one step eliminating time consuming and costly work-ups, isolations, purifications, and evaporations.
- a further advantage of the subject invention is the development of improved phosphorylation with the benzyl group providing an alternative phosphorylation method to the Troc Method thereby avoiding heavy metal contaminants associated with the deprotection of the Troc group.
- a further advantage of the subject invention is the replacement of the ion exchange chromatographic separation of the phosphate acid with an ion exchange resin.
- a further advantage of the subject invention is the elimination of carbon tetrachloride, chloroform, DMF and pyridine from the phosphorylation reaction.
- a further advantage of the subject invention is the increase in concentration of the reactants thereby allowing increased loading and increasing yield of combretastatin A-4.
- a further advantage of the subject invention is elimination of the evaporation of the solvent after the completion of the reaction.
- a still further advantage of the subject invention is the elimination of the side products and remaining starting materials during the wash.
- the subject invention further provides the advantage of a high throughput, scalable process by eliminating the use of ion exchange chromatography, hazardous and inconvenient solvents and expensive reagents, and by increasing the loading in every step. Consequently, the methods disclosed herein can be scaled up to produce large quantities of combretastatin A-4 prodrugs.
Abstract
Description
Claims
Priority Applications (1)
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AU2001296215A AU2001296215A1 (en) | 2000-07-17 | 2001-07-17 | Efficient method of synthesizing combretastatin a-4 prodrugs |
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US21876600P | 2000-07-17 | 2000-07-17 |
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WO2002006279A1 WO2002006279A1 (en) | 2002-01-24 |
WO2002006279A8 WO2002006279A8 (en) | 2002-02-14 |
WO2002006279A3 WO2002006279A3 (en) | 2002-04-18 |
WO2002006279A9 true WO2002006279A9 (en) | 2003-04-03 |
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US (1) | US6743937B2 (en) |
AU (1) | AU2001296215A1 (en) |
WO (1) | WO2002006279A1 (en) |
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US7576084B2 (en) * | 2001-10-12 | 2009-08-18 | Choongwae Pharma Corporation | Reverse-turn mimetics and method relating thereto |
US7105695B2 (en) | 2001-12-21 | 2006-09-12 | Arizona Board Of Regents, Acting For And On Behalf Of Arizona State University | Synthesis of combretastatin A-2 prodrugs |
US7705188B2 (en) * | 2002-04-10 | 2010-04-27 | Arizona Board of Regents, a body corporate of the State of Arizona, Acting for and on Behalf of the Arizona State University | Structural modification of resveratrol: sodium resverastatin phosphate |
GB0306907D0 (en) * | 2003-03-26 | 2003-04-30 | Angiogene Pharm Ltd | Boireductively-activated prodrugs |
CN100343216C (en) * | 2004-05-25 | 2007-10-17 | 浙江大德药业集团有限公司 | Synthesis of Combretastatin A-4 supported by polymer |
RU2375384C2 (en) | 2004-09-22 | 2009-12-10 | Ниппон Каяку Кабусики Кайся | New block copolymer, micellar preparation and anticarcinogenic agent containing micellar preparation as active component |
CN1312161C (en) * | 2005-04-30 | 2007-04-25 | 中国科学院广州化学研究所 | 3-hydroxy-4,3',4',5'-tetromethoxy bibenzyl phosphate and its composition, prepn and application |
FR2895735B1 (en) | 2005-12-30 | 2008-04-18 | Ecopack France | IMPROVED POCKET VALVE |
WO2007111211A1 (en) | 2006-03-28 | 2007-10-04 | Nippon Kayaku Kabushiki Kaisha | Polymer conjugate of taxane |
RU2447095C2 (en) | 2006-05-18 | 2012-04-10 | Ниппон Каяку Кабусики Кайся | High-molecular weight conjugate of podophyllotoxins |
WO2008010463A1 (en) | 2006-07-19 | 2008-01-24 | Nippon Kayaku Kabushiki Kaisha | Polymer conjugate of combretastatin |
CA2664852A1 (en) * | 2006-10-03 | 2008-04-10 | Nippon Kayaku Kabushiki Kaisha | High-molecular weight conjugate of resorcinol derivatives |
WO2008056596A1 (en) | 2006-11-06 | 2008-05-15 | Nippon Kayaku Kabushiki Kaisha | Polymeric derivative of nucleic acid metabolic antagonist |
EP2090607B1 (en) | 2006-11-08 | 2015-05-20 | Nippon Kayaku Kabushiki Kaisha | Polymeric derivative of nucleic acid metabolic antagonist |
WO2009041570A1 (en) | 2007-09-28 | 2009-04-02 | Nippon Kayaku Kabushiki Kaisha | Polymer conjugate of steroid |
ES2529434T3 (en) * | 2007-11-21 | 2015-02-20 | Oxigene, Inc. | Method to treat hematopoietic neoplasms |
EP2258397B1 (en) | 2008-03-18 | 2017-10-11 | Nippon Kayaku Kabushiki Kaisha | Polymer conjugate of physiologically active substance |
JP5366940B2 (en) | 2008-05-08 | 2013-12-11 | 日本化薬株式会社 | Polymer conjugate of folic acid or folic acid derivative |
JP5544357B2 (en) | 2009-05-15 | 2014-07-09 | 日本化薬株式会社 | Polymer conjugate of a physiologically active substance having a hydroxyl group |
JP2012532113A (en) * | 2009-07-02 | 2012-12-13 | オキシジーン, インコーポレイテッド | Combretastatin to prevent posterior capsule opacification |
WO2011036674A1 (en) * | 2009-09-24 | 2011-03-31 | Inogent Laboratories Private Limited | A new process for the preparation of olmesartan medoxomil |
FR2953518B1 (en) | 2009-12-03 | 2012-01-20 | Sanofi Aventis | PROCESS FOR PREPARING A COMBRETASTATIN DERIVATIVE |
CA2816997A1 (en) | 2010-11-17 | 2012-05-24 | Nippon Kayaku Kabushiki Kaisha | Novel polymer derivative of cytidine metabolic antagonist |
US9346923B2 (en) | 2011-09-11 | 2016-05-24 | Nippon Kayaku Kabushiki Kaisha | Method for manufacturing block copolymer |
CN103102254B (en) * | 2013-02-06 | 2015-08-26 | 浙江新赛科药业有限公司 | The synthetic method of a kind of Pterostilene |
CN104892668B (en) * | 2015-05-12 | 2017-03-29 | 上海大学 | Prodrug and preparation method thereof before combretastatin analog water solublity |
US11419934B2 (en) | 2015-08-18 | 2022-08-23 | Oncotelic Therapeutics, Inc. | Use of VDAS to enhance immunomodulating therapies against tumors |
Family Cites Families (6)
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US4670193A (en) * | 1986-05-12 | 1987-06-02 | E. R. Squibb & Sons, Inc. | Process for preparing phosphonic acids |
US4996237A (en) | 1987-01-06 | 1991-02-26 | Arizona Board Of Regents | Combretastatin A-4 |
CA1338645C (en) | 1987-01-06 | 1996-10-15 | George R. Pettit | Isolation, structural elucidation and synthesis of novel antineoplastic substances denominated "combretastatins" |
GB9106177D0 (en) | 1991-03-22 | 1991-05-08 | Aston Molecules Ltd | Substituted diphenylethylenes and analogues or derivatives thereof |
US5561122A (en) | 1994-12-22 | 1996-10-01 | Arizona Board Of Regents Acting On Behalf Of Arizona State University | Combretastatin A-4 prodrug |
US7018987B1 (en) | 1998-01-09 | 2006-03-28 | Arizona Broad of Regents acting for and on behalf of Arizona State University | Synthesis of combretastatin A-4 prodrugs and trans-isomers thereof |
-
2001
- 2001-07-17 WO PCT/US2001/022403 patent/WO2002006279A1/en active Application Filing
- 2001-07-17 US US09/908,321 patent/US6743937B2/en not_active Expired - Lifetime
- 2001-07-17 AU AU2001296215A patent/AU2001296215A1/en not_active Abandoned
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WO2002006279A3 (en) | 2002-04-18 |
US20020119951A1 (en) | 2002-08-29 |
WO2002006279A1 (en) | 2002-01-24 |
US6743937B2 (en) | 2004-06-01 |
AU2001296215A1 (en) | 2002-01-30 |
WO2002006279A8 (en) | 2002-02-14 |
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