JPWO2019195513A5 - - Google Patents

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JPWO2019195513A5
JPWO2019195513A5 JP2021503706A JP2021503706A JPWO2019195513A5 JP WO2019195513 A5 JPWO2019195513 A5 JP WO2019195513A5 JP 2021503706 A JP2021503706 A JP 2021503706A JP 2021503706 A JP2021503706 A JP 2021503706A JP WO2019195513 A5 JPWO2019195513 A5 JP WO2019195513A5
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Japan
Prior art keywords
complex according
biologically active
integer
complex
metal
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Pending
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JP2021503706A
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Japanese (ja)
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JP2021521268A (en
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Priority claimed from PCT/US2019/025725 external-priority patent/WO2019195513A1/en
Publication of JP2021521268A publication Critical patent/JP2021521268A/en
Publication of JPWO2019195513A5 publication Critical patent/JPWO2019195513A5/ja
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Claims (24)

式I:
[Mによる超分子金属配位錯体であって、式中、
Mは、金属原子であり、
Dは、二価の金属に配位することができる少なくとも2つの官能基を含む生物学的に活性な部分であり、
Aは、第2の生物学的に活性な部分またはアジュバントであり、
Wは、HOであり、
xは、1~10の整数であり、
oは、1~10の整数であり、
pはゼロまたは1~10の整数であり、
qは、ゼロまたは1~20の整数であり、
nは、2以上の整数である、超分子金属配位錯体。
Formula I:
[M x Do A p W q ] A supramolecular metal coordination complex with n , which is described in the formula.
M is a metal atom,
D is a biologically active moiety containing at least two functional groups capable of coordinating to a divalent metal.
A is a second biologically active moiety or adjuvant,
W is H 2 O,
x is an integer from 1 to 10.
o is an integer from 1 to 10 and
p is zero or an integer from 1 to 10 and
q is zero or an integer from 1 to 20
n is a supramolecular metal coordination complex which is an integer of 2 or more.
水に不溶性である、請求項1に記載の錯体。 The complex according to claim 1, which is insoluble in water. 高分子構造である、請求項1に記載の錯体。 The complex according to claim 1, which has a polymer structure. 前記生物学的に活性な部分が、患者に投与されたときに前記錯体からの放出制御を示す、請求項1に記載の錯体。 The complex according to claim 1, wherein the biologically active moiety exhibits control of release from the complex when administered to a patient. 前記官能基が、金属配位結合を形成するヘテロ原子を含む、請求項1に記載の錯体。 The complex according to claim 1, wherein the functional group contains a heteroatom forming a metal coordination bond. 前記ヘテロ原子が、窒素、酸素、および硫黄から選択される、請求項5に記載の錯体。 The complex according to claim 5, wherein the heteroatom is selected from nitrogen, oxygen, and sulfur. 前記金属が、sブロック元素、遷移金属、pブロック金属、ランタニド、およびアクチニドから選択される、請求項1に記載の錯体。 The complex according to claim 1, wherein the metal is selected from an s-block element, a transition metal, a p-block metal, a lanthanide, and an actinide. 前記金属が、亜鉛、銅、マグネシウム、カルシウム、ストロンチウム、ナトリウム、ニッケル、およびビスマスから選択される、請求項7に記載の錯体。 The complex according to claim 7, wherein the metal is selected from zinc, copper, magnesium, calcium, strontium, sodium, nickel, and bismuth. 前記生物学的に活性な部分が、第1の官能基および第2の官能基を含む、請求項1に記載の錯体。 The complex according to claim 1, wherein the biologically active moiety comprises a first functional group and a second functional group. 前記生物学的に活性な部分が、第1の官能基、第2の官能基、および第3の官能基を含む、請求項1に記載の錯体。 The complex according to claim 1, wherein the biologically active moiety comprises a first functional group, a second functional group, and a third functional group. 前記アジュバントが、芳香族ジカルボン酸、フェノール、およびカテコールから選択される、請求項1に記載の錯体。 The complex according to claim 1, wherein the adjuvant is selected from aromatic dicarboxylic acids, phenols, and catechols. 前記アジュバントが、チロシンである、請求項11に記載の錯体。 The complex according to claim 11, wherein the adjuvant is tyrosine. xおよびoが、同じ値である、請求項1に記載の錯体。 The complex according to claim 1, wherein x and o have the same value. xおよびoが、異なる値である、請求項1に記載の錯体。 The complex according to claim 1, wherein x and o are different values. 前記生物学的に活性な部分が、トリヨードサイロニン(T3)、アモキシシリン、セフォテタン、フロセミド、メトトレキサート、バルサルタン、クロルテトラサイクリン、デメクロサイクリン、ドキシサイクリン、メクロサイクリン、オキシテトラサイクリン、テ
トラサイクリン、シプロフロキサシン、ダノフロキサシン、ジフロキサシン、エノキサシン、エンロフロキサシン、フレロキサシン、ロメフロキサシン、マルボフロキサシン、ノルフロキサシン、ペルフロキサシン、ピペミド酸、オフロキサシン、およびサラフロキサシン、ならびにそれらの組み合わせから選択される、請求項1に記載の錯体。
The biologically active moieties are triiodosilonin (T3), amoxycycline, cefotetan, frosemide, methotrexate, balsartan, chlortetracycline, demeclocycline, doxycycline, meclocycline, oxytetracycline, tetracycline, ciprofloxacin. , Danofloxacin, difloxacin, enoxacin, enlofloxacin, freroxacin, lomefloxacin, malvofloxacin, norfloxacin, perfloxacin, pipemidic acid, ofloxacin, and salafloxacin, and combinations thereof, according to claim 1.
前記生物学的に活性な部分が、トリヨードサイロニン(T3)である、請求項1に記載の錯体。 The complex according to claim 1, wherein the biologically active moiety is triiodothyronine (T3). Zn(T3)(tyr)、[Cu(T3)(HO)]、[Mg(T3)-2HO]、[Ca(T3)-2HO]、および[Sr(T3)-4HO]から選択される、請求項16に記載の錯体。 [ Zn 6 (T3) (tyr) 5 ] n , [Cu (T3) (H 2 O)] n , [Mg (T3) -2H 2 O] n , [Ca (T3) -2H 2 O] n , The complex according to claim 16, which is selected from [Sr (T3) -4H 2 O] n . 請求項1に記載の錯体および薬学的に許容される担体を含む、医薬組成物。 A pharmaceutical composition comprising the complex according to claim 1 and a pharmaceutically acceptable carrier. 前記組成物が、前記生物学的に活性な部分の放出制御を示す、請求項18に記載の組成物。 18. The composition of claim 18, wherein the composition exhibits control of release of the biologically active moiety. 療有効量の請求項1に記載の錯体を含む、疾患を有する患者を治療するための医薬組成物 A pharmaceutical composition for treating a patient with a disease, which comprises the complex according to claim 1 in a therapeutically effective amount. 前記疾患が、甲状腺機能低下症である、請求項20に記載の組成物The composition according to claim 20, wherein the disease is hypothyroidism. 生物学的に活性な部分の粘膜付着特性を増加させる方法であって、式I:
[M(式中、
Mは、金属原子であり、
Dは、二価の金属に配位することができる少なくとも2つの官能基を含む生物学的に活性な部分であり、
Aは、第2の生物学的に活性な部分またはアジュバントであり、
Wは、HOであり、
xは、1~10の整数であり、
oは、1~10の整数であり、
pはゼロまたは1~10の整数であり、
qは、ゼロまたは1~20の整数であり、
nは、2以上の整数である)による金属配位錯体を形成することを含む、方法。
A method of increasing the mucosal adhesion properties of biologically active moieties, according to Formula I :.
[M x Do A p W q ] n (in the formula,
M is a metal atom,
D is a biologically active moiety containing at least two functional groups capable of coordinating to a divalent metal.
A is a second biologically active moiety or adjuvant,
W is H 2 O,
x is an integer from 1 to 10.
o is an integer from 1 to 10 and
p is zero or an integer from 1 to 10 and
q is zero or an integer from 1 to 20
A method comprising forming a metal coordination complex (n is an integer greater than or equal to 2).
前記金属配位錯体が[Zn(T3)(HThe metal coordination complex is [Zn (T3) (H). 2 O)]O)] n である、請求項8に記載の金属配位錯体。The metal coordination complex according to claim 8. 前記金属配位錯体が[Zn(T3)(HThe metal coordination complex is [Zn (T3) (H). 2 O)]O)] n である、請求項22に記載の方法。The method according to claim 22.
JP2021503706A 2018-04-04 2019-04-04 Metallo-Rio Pylonin Pending JP2021521268A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201862652705P 2018-04-04 2018-04-04
US62/652,705 2018-04-04
PCT/US2019/025725 WO2019195513A1 (en) 2018-04-04 2019-04-04 Metallo-liothyronine

Publications (2)

Publication Number Publication Date
JP2021521268A JP2021521268A (en) 2021-08-26
JPWO2019195513A5 true JPWO2019195513A5 (en) 2022-04-27

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JP2021503706A Pending JP2021521268A (en) 2018-04-04 2019-04-04 Metallo-Rio Pylonin

Country Status (9)

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US (2) US11712426B2 (en)
EP (1) EP3773733A4 (en)
JP (1) JP2021521268A (en)
KR (1) KR20200143701A (en)
CN (1) CN112218661A (en)
AU (1) AU2019247217A1 (en)
BR (1) BR112020020403A8 (en)
CA (1) CA3096199A1 (en)
WO (1) WO2019195513A1 (en)

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1298613B1 (en) 1998-03-10 2000-01-12 Bracco Spa HIGH RELAXATION MANGANESE COMPLEX CHELATES IN SERUM
JP2003261683A (en) 2002-03-06 2003-09-19 Nof Corp Neutral (benzene-1,2,4,5-tetrathiolate) metal complex polymer, its production method and use
US7799937B2 (en) * 2004-10-25 2010-09-21 Synthonics, Inc. Metal coordinated compositions
US20060141054A1 (en) 2004-10-25 2006-06-29 Thomas Piccariello Metal coordinated compositions
AU2013205471B2 (en) * 2005-10-24 2016-02-11 Synthonics, Inc. Metal coordinated compositions
EP1990090A4 (en) 2006-03-02 2009-01-21 Kek High Energy Accelerator Microchannel reactor
US10150792B2 (en) * 2010-11-08 2018-12-11 Synthonics, Inc. Bismuth-containing compounds, coordination polymers, methods for modulating pharmacokinetic properties of biologically active agents, and methods for treating patients
JP6183763B2 (en) 2014-05-02 2017-08-23 国立研究開発法人物質・材料研究機構 Organic / heterometallic hybrid polymer, synthesis method thereof, organic / heterometallic hybrid polymer film, organic / multimetallic hybrid polymer, synthesis method thereof, and organic / multimetallic hybrid polymer film
KR20170023061A (en) 2014-06-18 2017-03-02 테티스 파마수티컬스 엘엘씨 Mineral amino-acid complexes of active agents
JP6838268B2 (en) 2015-10-21 2021-03-03 コニカミノルタ株式会社 Light conversion material, light conversion film, and light emitting element

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