JPWO2021055833A5 - - Google Patents

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JPWO2021055833A5
JPWO2021055833A5 JP2022517722A JP2022517722A JPWO2021055833A5 JP WO2021055833 A5 JPWO2021055833 A5 JP WO2021055833A5 JP 2022517722 A JP2022517722 A JP 2022517722A JP 2022517722 A JP2022517722 A JP 2022517722A JP WO2021055833 A5 JPWO2021055833 A5 JP WO2021055833A5
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alkyl
group
glycero
alkenyl
phosphocholine
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JP2022548304A (ja
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Priority claimed from PCT/US2020/051609 external-priority patent/WO2021055833A1/en
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Claims (27)

  1. 式(A):

    の化合物またはその塩であって、
    式中、R’が、R’分岐状またはR’環式であり、
    R’分岐状が、

    であり、R’環式が、

    であり、

    が、結合点を示し、
    aαが、Hであり、Raβ、Raγ、及びRaδ、独立して、H、C2-12アルキル、及びC2-12アルケニルからなる群から選択され、Raβ、Raγ、及びRaδのうちの少なくとも1つが、C2-12アルキル及びC2-12アルケニルからなる群から選択され、
    及びRが、各々独立して1-14アルキルであり、
    が、-(CHOH、-(CHOH、-(CHOH、-(CHOH、及び

    からなる群から選択され、R10が、N(R)であり、各Rが、独立して、C1-6アルキル、C2-3アルケニル、及びHからなる群から選択され、n2が、1、2、3、4、5、6、7、8、9、及び10からなる群から選択され、
    各Rが、独立して、OH、C1-3アルキル、C2-3アルケニル、及びHからなる群から選択され、
    各Rが、独立して、OH、C1~3アルキル、C2-3アルケニル、及びHからなる群から選択され、
    が、Hであり、
    M及びM’が、独立して、-C(O)O-及び-OC(O)-からなる群から選択され、
    R’が、C1-12アルキルまたはC2-12アルケニルであり、
    が、C3-6炭素環であり、
    が、C1-15アルキル及びC2-15アルケニルからなる群から選択され、
    lが、1、2、3、4、及び5からなる群から選択され、
    sが、2または3であり、
    mが、5、6、7、8、9、10、11、12、及び13からなる群から選択される、化物またはその塩。
  2. 式(B):

    の化合物またはその塩であって、
    式中、R’が、R’分岐状またはR’環式であり、
    R’分岐状が、

    であり、R’環式が、

    であり、

    が、結合点を示し、
    aα及びRaβが、各々Hであり、Raγ及びRaδ、独立して、H、C2-12アルキル、及びC2-12アルケニルからなる群から選択され、Raγ及びRaδのうちの少なくとも1つが、C2-12アルキル及びC2-12アルケニルからなる群から選択され、
    bα、Rbβ、Rbγ、及びRbδが、各々独立して、H、C2-30アルキル、及びC5-20アルケニルからなる群から選択され、Rbα、Rbβ、Rbγ、及びRbδのうちの少なくとも1つが、C2-30アルキル及びC5-20アルケニルからなる群から選択され、
    が、-(CHOH、-(CHOH、-(CHOH、-(CHOH、及び

    からなる群から選択され、

    が、結合点を示し、
    10が、N(R)であり、各Rが、独立して、C1-6アルキル、C2-3アルケニル、及びHからなる群から選択され、n2が、1、2、3、4、5、6、7、8、9、及び10からなる群から選択され、
    各Rが、独立して、OH、C1-3アルキル、C2-3アルケニル、及びHからなる群から選択され、
    各Rが、独立して、OH、C1~3アルキル、C2~3アルケニル、及びHからなる群から選択され、
    M及びM’が、独立して、-C(O)O-及び-OC(O)-からなる群から選択され、
    R’が、C1-12アルキルまたはC2-12アルケニルであり、
    が、C3-6炭素環であり、
    が、C1-15アルキル及びC2-15アルケニルからなる群から選択され、
    lが、1、2、3、4、及び5からなる群から選択され、
    sが、2または3であり、
    mが、5、6、7、8、9、10、11、12、及び13からなる群から選択される、化物またはその塩。
  3. 式(1-1):

    の化合物またはその塩であって、
    式中、R’が、R’分岐状またはR’環式であり、
    R’分岐状が、

    であり、R’環式が、

    であり、
    R’が、

    であり、

    が、結合点を示し、
    aγ及びRbγが、各々独立して、C2-12アルキルまたはC2-12アルケニルであり、
    及びRが、各々独立して、C1-14アルキル及びC2-14アルケニルからなる群から選択され、
    が、-(CHOHであり、
    各R’が、独立して、C1-12アルキルまたはC2-12アルケニルであり、
    が、C3-6炭素環であり、
    が、C1-15アルキル及びC2-15アルケニルからなる群から選択され、
    sが、2または3である、化物またはその塩。
  4. 以下の構造:

    のうちの1つを有する、請求項1~3のいずれか1項に記載の化合物。
  5. aγが、C2-6アルキルである、請求項1~3のいずれか1項に記載の化合物。
  6. bγが、C2-6アルキルである、請求項1~3のいずれか1項に記載の化合物。
  7. aγ及びRbγが、各々独立して、C2-6アルキルである、請求項1~3のいずれか1項に記載の化合物。
  8. bγが、C4-6アルキルである、請求項1~3のいずれか1項に記載の化合物。
  9. 及びRが、各々Cアルキルである、請求項1~3のいずれか1項に記載の化合物。
  10. が、シクロヘキシルまたはシクロペンチルである、請求項1~3のいずれか1項に記載の化合物。
  11. は、C-アルキルまたはC-アルキルである、請求項1~3のいずれか1項に記載の化合物。
  12. 各Rが、独立して、C2-5アルキルである、請求項1~3のいずれか1項に記載の化合物。
  13. 以下から選択される、化合物またはその薬学的に許容される塩
  14. 以下から選択される、化合物またはその薬学的に許容される塩
  15. 求項1~3のいずれか1項に記載の化合物と、リン脂質と、構造的脂質と、PEG脂質と、を含む、空の脂質ナノ粒子(空のLNP)。
  16. (a)約40mol%~約60mol%の前記化合物と、約0mol%~約20mol%のリン脂質と、約30mol%~約50mol%の構造的脂質と、約0mol%~約5mol%のPEG脂質と、を含み、
    (b)前記リン脂質は、
    1,2-ジリノレオイル-sn-グリセロ-3-ホスホコリン(DLPC)、
    1,2-ジミリストイル-sn-グリセロ-ホスホコリン(DMPC)、
    1,2-ジオレオイル-sn-グリセロ-3-ホスホコリン(DOPC)、
    1,2-ジパルミトイル-sn-グリセロ-3-ホスホコリン(DPPC)、
    1,2-ジステアロイル-sn-グリセロ-3-ホスホコリン(DSPC)、
    1,2-ジウンデカノイル-sn-グリセロ-ホスホコリン(DUPC)、
    1-パルミトイル-2-オレオイル-sn-グリセロ-3-ホスホコリン(POPC)、
    1,2-ジ-O-オクタデセニル-sn-グリセロ-3-ホスホコリン(18:0ジエーテルPC)、
    1-オレオイル-2-コレステリルヘミスクシノイル-sn-グリセロ-3-ホスホコリン(OChemsPC)、
    1-ヘキサデシル-sn-グリセロ-3-ホスホコリン(C16 Lyso PC)、
    1,2-ジリノレノイル-sn-グリセロ-3-ホスホコリン、
    1,2-ジアラキドノイル-sn-グリセロ-3-ホスホコリン、
    1,2-ジドコサヘキサエノイル-sn-グリセロ-3-ホスホコリン、
    1,2-ジオレオイル-sn-グリセロ-3-ホスホエタノールアミン(DOPE)、
    1,2-ジフィタノイル-sn-グリセロ-3-ホスホエタノールアミン(ME 16.0 PE)、
    1,2-ジステアロイル-sn-グリセロ-3-ホスホエタノールアミン、
    1,2-ジリノレオイル-sn-グリセロ-3-ホスホエタノールアミン、
    1,2-ジリノレノイル-sn-グリセロ-3-ホスホエタノールアミン、
    1,2-ジアラキドノイル-sn-グリセロ-3-ホスホエタノールアミン、
    1,2-ジドコサヘキサエノイル-sn-グリセロ-3-ホスホエタノールアミン、
    1,2-ジオレオイル-sn-グリセロ-3-ホスホ-rac-(1-グリセロール)ナトリウム塩(DOPG)、
    スフィンゴミエリン、及びそれらの混合物
    からなる群から選択され、
    (c)前記構造的脂質が、コレステロール、フェコステロール、シトステロール、エルゴステロール、カンペステロール、スチグマステロール、ブラジカステロール、及びそれらの混合物からなる群から選択され、
    (d)前記PEG脂質が、PEG修飾ホスファチジルエタノールアミン、PEG修飾ホスファチジン酸、PEG修飾セラミド、PEG修飾ジアルキルアミン、PEG修飾ジアシルグリセロール、PEG修飾ジアルキルグリセロール、及びそれらの混合物からなる群から選択され、および/または
    (e)前記PEG脂質が、PEG 2k -DMG及びPEG-1:

    及びそれらの混合物から選択される、
    請求項15に記載の空のLNP。
  17. 求項15に記載の空のLNPと、1つ以上の治療薬及び/または予防薬と、を含む、充填された脂質ナノ粒子(充填されたLNP)。
  18. 前記1つ以上の治療薬及び/または予防薬が、核酸である、請求項17に記載の充填されたLNP。
  19. 前記核酸が、RNAであり、前記RNAが、短干渉RNA(siRNA)、非対称干渉RNA(aiRNA)、RNA干渉(RNAi)分子、マイクロRNA(miRNA)、アンタゴミル、アンチセンスRNA、リボザイム、ダイサー基質RNA(dsRNA)、小さいヘアピンRNA(shRNA)、メッセンジャーRNA(mRNA)、及びそれらの混合物からなる群から選択される、請求項18に記載の充填されたLNP。
  20. 前記RNAが、mRNAである、請求項19に記載の充填されたLNP。
  21. 求項17に記載の充填されたLNPと、薬学的に許容される担体と、を含む、薬学的組成物。
  22. 対象内の細胞に治療薬及び/または予防薬を送達するための薬学的組成物であって、請求項17に記載の充填されたLNPを含む、薬学的組成物
  23. 対象の臓器に治療薬及び/または予防薬を特異的に送達するための薬学的組成物であって、請求項17に記載の充填されたLNPを含む、薬学的組成物
  24. 対象内の細胞において目的のポリペプチドを生成するための薬学的組成物であって、請求項17に記載の充填されたLNPを含む、薬学的組成物
  25. 疾患または障害を治療することを、それを必要とする対象において行うための薬学的組成物であって、請求項17に記載の充填されたLNPを含む、薬学的組成物
  26. 前記臓器が、肝臓、腎臓、肺、及び脾臓からなる群から選択される、請求項23に記載の薬学的組成物
  27. 前記薬学的組成物が、非経口、筋肉内、皮内、皮下、及び/または静脈内で前記対象に投与される、請求項22~26のいずれか1項に記載の薬学的組成物
JP2022517722A 2019-09-19 2020-09-18 治療薬の細胞内送達のための分岐状尾部脂質化合物及び組成物 Pending JP2022548304A (ja)

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CN (1) CN114728887A (ja)
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AU (1) AU2020350759A1 (ja)
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CA (1) CA3154618A1 (ja)
IL (1) IL291219A (ja)
MX (1) MX2022003269A (ja)
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