[미국특허]
Compositions comprising multivalent synthetic ligands of surface nucleolin and glycosaminoglycans
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
A61K-031/7068
C07K-007/08
A61K-031/726
A61K-036/00
A61K-036/02
A61K-036/10
A61K-038/06
A61K-031/727
A61K-038/16
출원번호
US-0877490
(2011-10-04)
등록번호
US-9487559
(2016-11-08)
국제출원번호
PCT/EP2011/067337
(2011-10-04)
§371/§102 date
20130618
(20130618)
국제공개번호
WO2012/045750
(2012-04-12)
발명자
/ 주소
Zimmer, Robert
Courty, José
출원인 / 주소
ELRO PHARMA SARL
대리인 / 주소
Zerhusen, Bryan D.
인용정보
피인용 횟수 :
0인용 특허 :
13
초록▼
The present invention relates to a composition comprising a Nucant multivalent synthetic compound and a glycosaminoglycan, the admixture of both compounds forming microspheres comprising both compounds, as well as their use for the treatment or prevention of diseases associated with deregulation of
The present invention relates to a composition comprising a Nucant multivalent synthetic compound and a glycosaminoglycan, the admixture of both compounds forming microspheres comprising both compounds, as well as their use for the treatment or prevention of diseases associated with deregulation of proliferation and/or angiogenesis, such as cancer, inflammatory disease, or for promoting wound healing.
대표청구항▼
1. A composition comprising: a) a polyvalent synthetic compound comprising a linear peptide support on which at least 3 pseudopeptide units are grafted, said pseudopeptide units being of formula: Y1-ψ-Z—Y2,wherein: Y1 and Y2 are selected independently from amino acids having a basic side chain;Z is
1. A composition comprising: a) a polyvalent synthetic compound comprising a linear peptide support on which at least 3 pseudopeptide units are grafted, said pseudopeptide units being of formula: Y1-ψ-Z—Y2,wherein: Y1 and Y2 are selected independently from amino acids having a basic side chain;Z is selected from: proline or derivatives thereof; andψ represents a reduced bond (—CH2NH—), a retro-inverso bond (—NHCO—), a methyleneoxy bond (—CH2O—), a thiomethylene bond (—CH2—S—), a carba bond (—CH2CH2—), a ketomethylene bond (—CO—CH2—), a hydroxyethylene bond (—CHOH—CH2—), a (—N—N) bond, an E-alkene bond or a (—CH═CH—) bond; andb) a glycosaminoglycan (GAG). 2. The composition of claim 1, wherein said support comprises: a) a cyclic hexapeptide consisting of alternating alkaline (A) residues of configuration D and Lysine (K) residues of configuration L; orb) 5 lysine residues linked by amide bonds at the c amino group of each Lysine residue orc) a linear peptide of sequence SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 22 and SEQ ID NO: 24. 3. The composition of claim 1, wherein said pseudopeptide units are grafted directly on said support. 4. The composition of claim 1, wherein the compound comprises between 3 and 15 pseudopeptide units. 5. The composition of claim 1, wherein Z is proline (P). 6. The composition of claim 1, wherein Y1 and Y2 are independently selected from arginine (R) and lysine (K). 7. The composition of claim 1, wherein the compound is selected from compounds of formula: 8. The composition of claim 1, wherein the lysine residues in the pseudopeptide units are all in D configuration or all in L configuration. 9. The composition of claim 1 or 7, wherein the GAG is selected from heparin, chondroitin sulfate A, chondroitin sulfate B, chondroitin sulfate C, and combinations thereof. 10. The composition of claim 1, wherein the composition comprises at least 1 μM of the polyvalent synthetic compound. 11. The composition of claim 1, wherein the weight ratio of the polyvalent synthetic compound to the GAG is comprised between 0.01 and 24. 12. The composition of claim 1, wherein the polyvalent synthetic compound is admixed with the GAG. 13. The composition of claim 12, wherein another active compound such as but not limited to a cytotoxic agent is admix to it. 14. A method of treating a disease involving deregulation of cell proliferation and/or angiogenesis, comprising administering the composition of claim 1 to a patient in need thereof. 15. A method of treating an inflammatory disease, comprising administering the composition of claim 1 to a patient in need thereof. 16. A method of improving wound healing, comprising administering the composition of claim 1 to a patient in need thereof. 17. A method of inhibiting proliferation, comprising administering the composition of claim 1 to a patient in need thereof, wherein the inhibition is mediated by inhibiting nucleolin through nucleolin binding.
Voisin Guy (Paris FRX) Jansen Franz (Saint Gely Du Fesc FRX) Gros Pierre (Montpellier FRX), Cytotoxic products formed by covalent bonding of the A chain of ricin with an antibody and the process for their prepara.
Gansow Otto A. (3003 Van Ness ; NW. ; W 524 Washington DC 20008) Strand Mette (807 Harper House ; Village of Cross Keys Baltimore MD 21210), Metal chelate conjugated monoclonal antibodies.
Guichard, Gilles François Roger; Fournel, Sylvie Victorine Lucienne; Bianco, Alberto; Heobeke, Johan Félicien; Muller, Sylviane, Multimeric molecules, the preparation method thereof and use of same for the preparation of medicaments.
Courty, José; Hovanessian, Ara; Briand, Jean Paul; Guichard, Gilles; Hamma, Yamina, Use of multivalent synthetic ligands of surface nucleolin for treating cancer or inflammation.
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