JP2010507722A - 標的化リガンドを固定化するための改良型リンカー - Google Patents
標的化リガンドを固定化するための改良型リンカー Download PDFInfo
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- JP2010507722A JP2010507722A JP2009534770A JP2009534770A JP2010507722A JP 2010507722 A JP2010507722 A JP 2010507722A JP 2009534770 A JP2009534770 A JP 2009534770A JP 2009534770 A JP2009534770 A JP 2009534770A JP 2010507722 A JP2010507722 A JP 2010507722A
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- 201000008383 nephritis Diseases 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000002405 nuclear magnetic resonance imaging agent Substances 0.000 description 1
- 230000005298 paramagnetic effect Effects 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000001959 radiotherapy Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 238000001226 reprecipitation Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000002151 riboflavin Substances 0.000 description 1
- 238000013341 scale-up Methods 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 239000012321 sodium triacetoxyborohydride Substances 0.000 description 1
- 238000000527 sonication Methods 0.000 description 1
- WWUZIQQURGPMPG-KRWOKUGFSA-N sphingosine Chemical compound CCCCCCCCCCCCC\C=C\[C@@H](O)[C@@H](N)CO WWUZIQQURGPMPG-KRWOKUGFSA-N 0.000 description 1
- 150000003410 sphingosines Chemical class 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical class ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 230000007675 toxicity by organ Effects 0.000 description 1
- 231100000155 toxicity by organ Toxicity 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- JBWKIWSBJXDJDT-UHFFFAOYSA-N triphenylmethyl chloride Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 JBWKIWSBJXDJDT-UHFFFAOYSA-N 0.000 description 1
- DCXXMTOCNZCJGO-UHFFFAOYSA-N tristearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
- 238000005866 tritylation reaction Methods 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
- 238000012285 ultrasound imaging Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical class [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
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Abstract
Description
本願は、2006年10月24日出願の米国仮特許出願第60/853,824号及び2007年10月16日出願の米国特許出願第11/872,984号の利益を主張するものであり、それらの内容は参照により本明細書に組み込まれる。
従って、一態様において、本発明は式
式中、各nは独立して1〜4であり、
xは20〜60の整数であり、
Zは=NH又は=Oであり、
フェニレンは必要に応じて、アルキル、アルケニル又はアルキニルによって置換されていてもよく、
標的化剤は、分子の残りの部分と結合するためのアミノ基又は水酸基を含有する部分であり、及び
アンカーは、化合物を脂質/界面活性剤ベースの粒子状組成物中に包埋するための親油性化合物であり、該アンカーも分子の残りの部分と結合するためのアミノ基又は水酸基を含有する。
特に好ましい本発明の化合物は、式(2)
本発明の乳剤は、本発明の方法において直接調製及び使用してもよく、又は乳剤の成分がキットの形態で供給されてもよい。キットは、全ての所望の補助的物質を緩衝液中に又は凍結乾燥の状態で含有する予め調製された標的化組成物を含んでいてもよい。或いはキットは、別個に供給される、標的リガンドを含まない乳剤を含んでいてもよい。これらの場合、典型的には乳剤はマレイミド基などの反応基をリンカーのうちアンカーの遠位にある末端に有し、それにより乳剤が標的化剤と混合された時に、乳剤自体と標的化剤とを結合させる。結合を生じさせるのに有用な追加的な試薬を別個の容器として提供してもよい。或いは、別個に供給される、反応基を有する所望の成分に結合したリンカーと結合する反応基を乳剤が有していてもよい。適したキットを作成するための、様々な手法を想定することができる。従って、最終的な乳剤を構成する個々の成分は個別の容器で供給されてもよく、又はキットは単に、キットそれ自体とは別個に提供される他の材料と組み合わせるための試薬を含むだけでもよい。
乳剤及びその調製用キットは、高発現レベルの標的を含有する組織の造影、及び、かかる発現レベルの組織が望ましくない場合はその治療を含む、本発明の方法において有用である。
実施例1
式(2)の化合物の調製
αvβ3標的化リガンド中間体12の合成経路:
2−アミノイミダゾールヘミスルフェート(化合物1、30g、227mmol)(アルドリッチ)を水(216mL)に溶解し、炭酸ナトリウム(24.1g、227mmol)を添加した。溶液を室温で15分間撹拌した。水を真空中で除去し、残留物を無水エタノール(85mL)中で粉砕し、混合物をろ過して溶媒を真空中で除去した。残留物を直ちに使用した。
生成物I.D.:1H NMR、FT−IR、LC/MS
粗製2−[(ジメチルアミノ)メチレン]アミノイミダゾール(2)に塩化メチレン(750mL)、トリエチルアミン(98mL、700mmol)及び塩化トリチル(62.98g、226mmol)(アルドリッチ)を添加した。反応混合物を室温で3時間撹拌した。溶媒を真空中で除去し、粗製の化合物3をメタノールから結晶化させた。
プロセス中のアッセイ:HPLC
生成物I.D.:1H NMR、FT−IR、LC/MS
化合物3(44.64g、117mmol)に、試薬級エタノール(1200mL)、氷酢酸(20.65mL)及びヒドラジン(26mL)を添加した。反応混合物を50℃で5時間撹拌した。溶媒を除去し、粗生成物に塩化メチレン(1,500ml)及び1Nの水酸化ナトリウム(67ml)を室温で15分間撹拌しながら添加した。得られた2つの層を分離して有機層をブライン(2×300mL)で洗浄し、無水硫酸ナトリウムで乾燥させてろ過し、溶媒を真空中で除去して、1−トリチル−2−アミノイミダゾール、化合物4(37.2g、97%)を得た。融点196〜199℃。
プロセス中のアッセイ:HPLC
生成物I.D.:1H NMR、FT−IR及びLC/MS
化合物5(アルファ・エイサー)と化合物6(アルドリッチ)との混合物を、ディーンスタークトラップが取り付けられた100mLの一口丸底フラスコ中で115℃まで一晩加熱し、その後室温まで放冷した。回転蒸発(1時間/40℃)により残留エタノールのほとんどを除去した。生成物7(20.30g、定量的収率)は濃厚な油であり、これは時間が経ったり、フリーザーに入れたり、又は乳鉢で激しく破砕したりすることで凝固する。分析(1H NMR)により、そのまま次のステップで使用するために十分純度が高いことが確認される。
プロセス中のアッセイ:HPLC
生成物I.D.:1H NMR
化合物7を、1Lの三口丸底フラスコ中の250℃に予熱された300mLのジフェニルエーテル(アルドリッチ)に添加した。温度を少しの間(1〜2分間)約240℃まで下げ、その後257℃まで上げて255〜260℃で15分間維持し、色が暗くなること、エタノール蒸気の発生を確認した。室温に冷却すると、いくらかの沈殿物が分離したが、混合物は極めて濃かった。混合物をヘキサンで1:4希釈し、さらに沈殿物を分離した。沈殿物をろ過し、ヘキサンで3回洗浄して乾燥させ、19.02gの生成物8(84%)を得た。分析(1H NMR)により、この生成物の純度がそのまま次のステップで使用するのに十分な高さであることが示された。
プロセス中のアッセイ:HPLC
生成物I.D.:1H NMR、FT−IR、LC/MS
化合物8を、500mLの一口丸底フラスコ中の無水DMF(アルドリッチ)に溶解した。無水炭酸カリウム(EMサイエンス)を添加し、混合物を15分間撹拌した。ヨードメタン(アルドリッチ)を添加した後、混合物を室温で一晩撹拌し、その後濃縮してCH2Cl2と含水チオ硫酸ナトリウムとに分離した。CH2Cl2層をブラインで洗浄し、無水硫酸ナトリウムで乾燥させ、ろ過して濃縮し、19.30gの粗製物9(褐色様の固体)を得た。1H NMRスペクトルは十分なものであったが、TLC(MeOH:DCM 1:9)は、少量のより極性の低い不純物と、いくらかの極性の高い不純物(おそらくは大部分が無機物)を示した。THF/水又はCH2Cl2/ヘキサンからの再沈殿により精製しようとしたが、不十分であった。シリカゲルプラグ(勾配はCH2Cl2中1〜2〜4〜6〜10%メタノール)でのクロマトグラフィーによって精製された生成物(17.93g、収率95%)を得た。
プロセス中のアッセイ:HPLC
生成物I.D.:1H NMR、FT−IR、LC/MS
化合物9を1Lの一口丸底フラスコ中でアセトン(EMCO)に60℃で溶解した。予め洗浄したアンバーライトIR−120樹脂(アルドリッチ)を水と共に添加し、混合物を60℃で40分間撹拌し、20分(MCLS0995−078−1)及び40分の時点で一定量を取り出した。取り出した部分のHPLC分析から、アルデヒドの脱保護が20分で完了していたことが明らかとなった。混合物を熱浴槽から取り出してろ過し、初期量の約40%になるまで回転蒸発下で濃縮した(アセトンの除去)。得られた含水懸濁液をCH2Cl2と飽和含水重炭酸ナトリウムで分離した。水層を2×CH2Cl2で抽出した。集めた有機層をブラインで洗浄し、無水硫酸ナトリウムで乾燥させ、ろ過して濃縮し、生成物10(4.20g、収率81%)を得た。
プロセス中のアッセイ:HPLC
生成物I.D.:1H NMR、FT−IR、LC/MS
トルエン中の化合物4及び化合物10を、復水器及びディーンスタークトラップが取り付けられた1Lの一口丸底フラスコ中、窒素下110℃で一晩撹拌した。室温に冷却した後、中間体であるイミン(11)を含有する混合物を濃縮し、分析した(1H NMR、FT−IR、UV)。
プロセス中のアッセイ:HPLC
生成物I.D.:1H NMR、13C NMR、FT−IR、LC/MS、残留溶媒分析、元素分析、乾燥減量
この中間体について作成されたCofA
化合物12をTHFに溶解した。含水LiOHを添加し、混合物を室温で3時間撹拌し、その後水で希釈して、THFが除去されるまで(起泡及び沈殿物の出現)濃縮し、HClでpH4まで酸性化させた(激しい起泡;より多くの沈殿物)。沈殿物を分離し、水で洗浄して乾燥させ、化合物13(生成物、3.40g、HPLC、LC−MSによって純度96.5%、収率81.7%)を得た。1H NMR分析から、遊離アミン型より、過度にプロトン化された種であるTr−Im−N(H2)+−CH2−Arとの整合性が高い。元素分析から、アミン部位のいくつかにおける塩化アルキルアンモニウム塩の部分的な形成が確認される。(材料はステップ17でそのまま使用した)
プロセス中のアッセイ:HPLC
生成物I.D.:1H NMR、FT−IR、LC/MS
500mLの三口フラスコに化合物14及びNaOHを窒素パージ下で充填した。機械で撹拌しながら混合物を加熱してフェノールを融解させ、次に100mLのDMSOを添加した。溶液を125℃に加熱し、次に100℃に冷却した。100℃で化合物15(アルドリッチ)を3分間かけて添加し(8℃の発熱)、次に温度を30分間で125℃まで上昇させた。反応物を90℃まで放冷し、100mLのH2Oを添加した。混合物を60℃まで放冷し、18mLの50%NaOH(含水)を70℃まで発熱させながら添加し、その温度で反応物を15分間保持した。反応物を40℃に冷却し、250mLの水を添加した後、pHが8に達するまで濃HClを添加した。反応物を周囲温度まで冷却し、次に4×50mLのMTBEで抽出した。濃HCl(約20mL)を用いて水層を結晶化が始まるpH1まで酸性化させた。
プロセス中のアッセイ:HPLC
生成物I.D.:1H NMR、FT−IR、LC/MS
500mLの三口フラスコに、3,5−ジメチルフェノキシブタン酸(17)(25g、120mmol)及びCH2Cl2(100mL)を充填した。この溶液を機械により撹拌しながら−27℃まで冷却し、次にクロロスルホン酸(42g、360mmol)を30分間かけて滴下により添加した(温度は最高で−20℃に達した)。材料をさらに1時間、−25℃で撹拌し、次にNaHCO3(20g、238mmol)を反応混合物に添加した。次に反応混合物を150gの氷に添加した。次に反応混合物をEtOAc(750mL)で抽出し、Na2SO4(10g)で乾燥させてろ過し、次に真空中で濃縮した。粗生成物を5℃で2回、MTBEと共に(50mL、次に25mL)粉砕し、20.0gの化合物18(収率54%)を得た。
プロセス中のアッセイ:HPLC
生成物I.D.:1H NMR、FT−IR、LC/MS
4−(クロロスルホニル)−3,5−ジメチルフェノキシブタン酸、化合物18(2.50g、8.1mmol)のジオキサン(60.0g)溶液を、室温で水(20.0g)中のH−Dap(Boc)−OMe・HCl(化合物19)(1.66g、6.5mmol)(バケム社)とNaHCO3(8.21g、97.7mmol)の混合物に約45分間の時間をかけて滴下により加えた。添加完了2時間後、反応混合物を真空中で濃縮し、次に水及びクエン酸(12.50g、10.0等量)を添加した。粗生成物をEtOAcで抽出し、EtOAc層を水で1回洗浄した。EtOAc層を濃縮し、2.75gの化合物20(化合物19を基準として収率87%、化合物18を基準として収率69%)を得た。
140mLのジオキサン/28mLのH2O中のH−Dap(Boc)−OMe・HCl(化合物19)(8.0g、31.4mmol)とNaHCO3(38.6g、460mmol)とのスラリーを氷浴で5℃まで冷却した。このスラリーに、4−(クロロスルホニル)−3,5−ジメチルフェノキシブタン酸、化合物18(14.0g、46mmol)のジオキサン(140mL)溶液を、75分間の時間をかけて滴下により加えた。さらに2時間後、反応混合物をろ過し、ろ液を真空中で濃縮した。残留物に水を添加し(総量420mL)、次にこれを75mLのMTBEで抽出した。水相を3NのHCl(含水)を用いて酸性(pH=4)にし、次にEtOAc(300mL)で抽出した。EtOAc抽出物をNa2SO4で乾燥させ、ろ過して真空中で濃縮し、10.2gの所望の生成物20(20.9mmol、化合物19を基準として66.5%、化合物18を基準として45%)が残った。
プロセス中のアッセイ:HPLC
生成物I.D.:1H NMR、FT−IR、LC/MS、旋光度、キラルHPLC
氷水浴で冷却したCH2Cl2(150mL)に溶解させた前記反応物からの粗フェノキシブタン酸(化合物20)(2.75g)溶液に、4−メチルモルホリン(0.89g、8.8mmol)を加え、次にトリメチルアセチルクロリド(1.06g、8.8mmol)を添加した。反応混合物を室温まで温めた。1時間後、反応混合物を真空中で濃縮し、DMF(100mL)を添加して、さらにこれを真空中で除去した(反応しなかった一切のトリメチルアセチルクロリド(沸点105〜106℃)を除去するため)。粗生成物をCH2Cl2(150mL)中に再溶解し、DMF中のベンジルN−(2−アミノエチル)カルバメートヒドロクロリド、化合物21(1.52g、6.6mmol)及び4−メチルモルホリン(1.11g、11.0mmol)の溶液を加えた。1時間後、反応混合物を真空中で濃縮し、EtOAcと水で分離した。層の分離後、EtOAc溶液を希NaHCO3及び水で洗浄した。EtOAc溶液を真空中で濃縮し、粗生成物を得た。この物質をクロマトグラフィー(97:3 EtOAc/MeOH)により精製し、2.80gの生成物22を得た。
化合物20(8.20g、16.8mmol)をDMF(70mL、3A分子篩で乾燥)に溶解した。ジイソプロピルエチルアミン(8.68g、67.1mmol)を添加し、混合物を窒素下で撹拌した。混合物を冷水浴中で冷却し、次にHBTU、O−ベンゾトリアゾール−1−イル−N,N,N’,N’−テトラメチルウロニウムヘキサフルオロホスファート(7.64g、20.1mmol)を17℃未満の温度で少しずつ添加した。混合物をさらに20分間撹拌した。DMF(21mL、3A分子篩で乾燥)中のベンジルN−(2−アミノエチル)カルバメートヒドロクロリド、化合物21(4.65g、20.1mmol)の溶液を17℃未満の温度で滴下により添加した。溶液をさらに30分間撹拌し、周囲温度まで温めた。次に反応溶液を60℃、10mbarで蒸発させた。これにより、33.8gの残留物を得た。この残留物をジクロロメタン(120mL)に溶解した。混合物を0.1MのHCl(含水)各20mLで2回洗浄した。次に混合物を10%NaHCO3各20mLで3回洗浄した。50℃、10mbarで蒸発させ、13.8gの残留物を得た。
プロセス中のアッセイ:HPLC
生成物I.D.:1H NMR、13C NMR、FT−IR、LC/MS、残留溶媒分析、元素分析、乾燥減量、旋光度
この中間体について作成されたCofA
化合物22をCH2Cl2:トリフルオロ酢酸に溶解し、室温、窒素下で30分間撹拌し、その後濃縮して6のCH2Cl2を蒸発させ、高真空下で乾燥させて、化合物23(薄黄色の油、3.14g)を得た。これはそのままステップ17で使用した。
プロセス中のアッセイ:HPLC
生成物I.D.:1H NMR、LC/MS、旋光度
ガラス器具を110℃のオーブンで乾燥させて、加熱、窒素下で組み立てた。
窒素雰囲気下、磁気攪拌した、無水N−メチルピロリジノン(50mL)中のジイソプロピルエチルアミン(16.5mL;94.7mmol)中の酸性のスラリー13(5.15g;9.5mmol)をO−ベンゾトリアゾール−1−イル−N,N−N’,N’−テトラメチルウロニウムテトラフルオロボレート(3.65g;11.4mmol)の1分量で処理し、続いて無水NMP(15mL)で処理した。スラリーを窒素下、周囲温度(25℃)で15分間撹拌した。無水NMP(100mL)中、いくらかの残留トリフルオロ酢酸(計算上、約21.9mmol)を含有したアミン23(8.9g;72%アッセイ;9.5mmol)の粗トリフルオロ酢酸塩の溶液を62分間かけて滴下により添加した。このとき温度が25℃から28℃に上昇する少しの発熱を伴った。添加用漏斗を無水NMP(10mL)で洗浄し、反応混合物に添加した。透明で明るい琥珀色の溶液を周囲温度、窒素下(3:55pm)で一晩撹拌した。pH紙を反応混合物に浸漬し、次に水に浸漬すると、pH≧8を示した。
量=9.6g。≧94% アッセイでほんの痕跡量の不純物。
収率=92.9%
2.5LのParrボトル中、Degussa E101 NE/W 10%パラジウム炭素(2.0g)を含有する905mLメタノール中のN−カルボベンゾキシ中間体24(9.05g;8.3mmol)の溶液を水素で6回、加圧及び減圧して、大きいParrシェーカーの残留空気を除去した。ボトルを水素で44.5psigに加圧し、Parr水素化反応器で振盪した。
量=7.75g。≧94% DADによるアッセイ。
収率=97.3%
化合物25、210mg(0.22mmol)を6mLの5:1(v:v)THF/H2Oに溶解した。この溶液に200μLの3N LiOH(含水)を添加し、得られた2相系をアルゴン下、周囲温度で3.5時間撹拌した。3.5時間後、反応混合物のpHを1N HCl(含水)を用いて約6に調整した。反応混合物をアルゴンでパージすることによってTHFを除去し、白色のスラリーを得た(真空中で除去しようとすると、激しく起泡した)。このスラリーに5mLのH2Oを添加し、得られたスラリーを、高純度焼結ガラス漏斗を通じてろ過した(緩速ろ過)。固体を10mLのH2Oで洗浄して空気乾燥させ、134mg(0.14mmol、65%)の化合物26が得られた。
化合物26(132mg、0.14mmol)を5mLのTFA(シグマ−アルドリッチ)に溶解した。この溶液に、アルゴン下、0.5mLのEt3SiH(アルファ・エイサー)を添加した。反応混合物をアルゴン下1時間、70℃に加熱した。次に反応物を周囲温度まで放冷した(反応物から白色固体の沈殿物)。粗反応混合物を0.45ミクロンのシリンジフィルタを通じてろ過した。ろ液に25mLのCH2Cl2を添加し、得られた溶液を真空中35℃で濃縮した。得られた油に2回目の25mLのCH2Cl2を添加し、この溶液を真空中35℃で濃縮した。残留物に25mLのヘキサンを添加し、40℃に加温し、得られた液体層をデカンテーションして取り除き、残留物が残った。2回目の25mLのヘキサンを添加し、上記の手順を繰り返した。残った残留物を真空中40℃で乾燥させ、117mgの化合物27(bis−TFA塩としての生成物を基準に90%)を得た。
1)CHCl3:MeOH 3:1(v:v)−3カラム容量
2)CHCl3:MeOH:H2O 75:24:1(v:v:v)−4カラム容量
3)CHCl3:MeOH:H2O 75:23:2(v:v:v)−4カラム容量
4)CHCl3:MeOH:H2O 75:22:3(v:v:v)−4カラム容量
Claims (13)
- 前記標的化剤がインテグリンを標的とする、請求項1に記載の化合物。
- 前記標的化剤が抗体又はその免疫反応性断片であるか、又は、前記標的化剤が受容体のリガンドである、請求項1に記載の化合物。
- 前記アンカーがホスファチジル脂質の残基である、請求項1に記載の化合物。
- 前記アンカーがホスファチジルエタノールアミン基である、請求項4に記載の化合物。
- xが40〜50の整数である、請求項1に記載の化合物。
- 多数の請求項1に記載の化合物の分子を含む、脂質ベースの粒子製剤。
- 前記粒子が治療剤又は診断剤をさらに含んでなる、請求項7に記載の製剤。
- 前記治療剤が医薬であり、及び/又は
前記診断剤がMRI造影用のキレート化金属であり、又は
前記治療剤若しくは診断剤が放射性核種である、請求項8に記載の粒子製剤。 - 前記脂質ベースの粒子が、リポソーム、ミセル、又は脂質/界面活性剤で被膜された液体フッ化炭素からなるコアを含有するナノ粒子である、請求項8に記載の粒子製剤。
- 前記脂質ベースの粒子が、脂質/界面活性剤で被膜された液体フッ化炭素からなるコアを含有するナノ粒子である、請求項10に記載の粒子製剤。
- 対象における所望の目標箇所を標的化する方法であって、請求項8に記載の製剤を前記対象に投与することを含む方法。
- 対象における所望の目標箇所を標的化する方法における請求項8に記載の製剤の使用。
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US11/872,984 US7998462B2 (en) | 2006-10-24 | 2007-10-16 | Linkers for anchoring targeting ligands |
PCT/US2007/081540 WO2008070291A2 (en) | 2006-10-24 | 2007-10-16 | Improved linkers for anchoring targeting ligands |
US11/872,984 | 2007-10-16 |
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WO2014148378A1 (ja) * | 2013-03-19 | 2014-09-25 | 公立大学法人首都大学東京 | 界面活性剤様化合物 |
JPWO2016148125A1 (ja) * | 2015-03-16 | 2017-07-13 | 国立大学法人大阪大学 | 新規蛍光標識スフィンゴミエリン及びその利用 |
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US20100291013A1 (en) * | 2009-05-18 | 2010-11-18 | L'oreal | Comfortable, transfer-resistant colored compositions |
WO2014080251A1 (en) * | 2012-11-24 | 2014-05-30 | Hangzhou Dac Biotech Co., Ltd. | Hydrophilic linkers and their uses for conjugation of drugs to cell binding molecules |
ES2960619T3 (es) * | 2014-02-28 | 2024-03-05 | Hangzhou Dac Biotech Co Ltd | Enlazadores cargados y sus usos para la conjugación |
EP3598983A1 (en) | 2014-10-03 | 2020-01-29 | Synaffix B.V. | Sulfamide linker, conjugates thereof, and methods of preparation |
CN112125929A (zh) * | 2015-06-15 | 2020-12-25 | 杭州多禧生物科技有限公司 | 用于偶联的亲水链接体 |
JP2019507741A (ja) | 2016-02-08 | 2019-03-22 | シンアフィックス ビー.ブイ. | 治療において使用するためのスルファミドリンカーを含むバイオコンジュゲート |
EP3413915A1 (en) | 2016-02-08 | 2018-12-19 | Synaffix B.V. | Antibody-conjugates with improved therapeutic index for targeting her2 tumours and method for improving therapeutic index of antibody-conjugates |
WO2017137457A1 (en) | 2016-02-08 | 2017-08-17 | Synaffix B.V. | Antibody-conjugates with improved therapeutic index for targeting cd30 tumours and method for improving therapeutic index of antibody-conjugates |
EP3413916A1 (en) | 2016-02-08 | 2018-12-19 | Synaffix B.V. | Antibody-conjugates with improved therapeutic index for targeting cd30 tumours and method for improving therapeutic index of antibody-conjugates |
US10874746B2 (en) | 2016-02-08 | 2020-12-29 | Synaffix B.V. | Sulfamide linkers for use in bioconjugates |
WO2019185586A1 (en) | 2018-03-26 | 2019-10-03 | Universidad Complutense De Madrid | Ligands for enhanced imaging and drug delivery to neuroblastoma cells |
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WO2014148378A1 (ja) * | 2013-03-19 | 2014-09-25 | 公立大学法人首都大学東京 | 界面活性剤様化合物 |
JPWO2014148378A1 (ja) * | 2013-03-19 | 2017-02-16 | 公立大学法人首都大学東京 | 界面活性剤様化合物 |
JPWO2016148125A1 (ja) * | 2015-03-16 | 2017-07-13 | 国立大学法人大阪大学 | 新規蛍光標識スフィンゴミエリン及びその利用 |
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EP2094311A2 (en) | 2009-09-02 |
AU2007329793A2 (en) | 2009-06-04 |
WO2008070291A3 (en) | 2008-10-23 |
AU2007329793A1 (en) | 2008-06-12 |
EP2094311A4 (en) | 2013-04-10 |
JP5271912B2 (ja) | 2013-08-21 |
AU2007329793B2 (en) | 2013-01-10 |
US20080305037A1 (en) | 2008-12-11 |
CA2667209A1 (en) | 2008-06-12 |
US7998462B2 (en) | 2011-08-16 |
WO2008070291A2 (en) | 2008-06-12 |
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