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1.
公开(公告)号:US20220000971A1
公开(公告)日:2022-01-06
申请号:US17270787
申请日:2019-08-26
Applicant: TRANSFERT PLUS, S.E.C.
Inventor: Richard BÉLIVEAU , Borhane ANNABI , Michel DEMEULE , Alain LAROCQUE , Jean-Christophe CURRIE , Alain ZGHEIB
Abstract: The present disclosure relates to peptide compounds and conjugate compounds, processes, methods and uses thereof for treatment of cancer or aggressive cancer. For example, the compounds can comprise compounds of formula X1X2X3X4X5GVX6AKAGVX7NX8FKSESY (I) (SEQ ID NO: 1) (X9)nGVX10AKAGVX11NX12FKSESY (II) (SEQ ID NO: 2) YKX13LRRX14APRWDX15PLRDPALRX16X17L (III) (SEQ ID NO: 3) YKX18LRR(X19)nPLRDPALRX20X21L (IV) (SEQ ID NO: 4) IKLSGGVQAKAGVINMDKSESM (V) (SEQ ID NO: 5) IKLSGGVQAKAGVINMFKSESY (VI) (SEQ ID NO: 6) IKLSGGVQAKAGVINMFKSESYK (VII) (SEQ ID NO: 7) GVQAKAGVINMFKSESY (VIII) (SEQ ID NO: 8) GVRAKAGVRNMFKSESY (IX) (SEQ ID NO: 9) GVRAKAGVRN(Nle)FKSESY (X) (SEQ ID NO: 10) YKSLRRKAPRWDAPLRDPALRQLL (XI) (SEQ ID NO: 11) YKSLRRKAPRWDAYLRDPALRQLL (XII) (SEQ ID NO: 12) YKSLRRKAPRWDAYLRDPALRPLL (XIII) (SEQ ID NO: 13) wherein X1 to X21 and n can have various different values and wherein at least one protecting group and/or at least one labelling agent is optionally connected to said peptide compound at an N- and/or C-terminal end, for use in inhibiting vasculogenic mimicry and/or for treating a cancer.
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2.
公开(公告)号:US20240199695A1
公开(公告)日:2024-06-20
申请号:US18240295
申请日:2023-08-30
Applicant: TRANSFERT PLUS, S.E.C.
Inventor: Richard BÉLIVEAU , Borhane ANNABI , Michel DEMEULE , Alain LAROCQUE , Jean-Christophe CURRIE , Cyndia CHARFI
CPC classification number: C07K7/08 , A61K31/337 , A61K47/64 , A61P35/00 , C07K1/061 , C07K14/001 , A61K38/00
Abstract: The present disclosure relates to peptide compounds and conjugate compounds, processes, methods and uses thereof for treating cancer. For example, the compounds can comprise compounds of formula
(SEQ ID NO: 1)
X1X2X3X4X5GVX6AKAGVX7NX8FKSESY
(I)
(SEQ ID NO: 2)
(X9)nGVX10AKAGVX11NX12FKSESY
(II)
(SEQ ID NO: 3)
YKX13LRRX14APRWDX15PLRDPALRX16X17L
(III)
(SEQ ID NO: 4)
YKX18LRR(X19)nPLRDPALRX20X21L
(IV)
(SEQ ID NO: 5)
IKLSGGVQAKAGVINMDKSESM
(V)
(SEQ ID NO: 6)
IKLSGGVQAKAGVINMFKSESY
(VI)
(SEQ ID NO: 7)
IKLSGGVQAKAGVINMFKSESYK
(VII)
(SEQ ID NO: 8)
GVQAKAGVINMFKSESY
(VIII)
(SEQ ID NO: 9)
GVRAKAGVRNMFKSESY
(IX)
(SEQ ID NO: 10)
GVRAKAGVRN(Nle)FKSESY
(X)
(SEQ ID NO: 11)
YKSLRRKAPRWDAPLRDPALRQLL
(XI)
(SEQ ID NO: 12)
YKSLRRKAPRWDAYLRDPALRQLL
(XII)
(SEQ ID NO: 13)
YKSLRRKAPRWDAYLRDPALRPLL
(XIII)
wherein X1 to X21 and n can have various different values
and wherein at least one protecting group and/or at least one labelling agent is optionally connected to said peptide compound at an N- and/or C-terminal end.-
公开(公告)号:US20220356209A1
公开(公告)日:2022-11-10
申请号:US17239544
申请日:2021-04-23
Applicant: TRANSFERT PLUS, S.E.C.
Inventor: Richard BÉLIVEAU , Borhane ANNABI , Michel DEMEULE , Alain LAROCQUE , Jean-Christophe CURRIE , Cyndia CHARFI
Abstract: The present disclosure relates to peptide compounds and conjugate compounds, processes, methods and uses thereof for treating cancer. For example, the compounds can comprise compounds of formula X1X2X3X4X5GVX6AKAGVX7NX8FKSESY
(I)
(SEQ ID NO: 1) (X9)nGVX10AKAGVX11NX12FKSESY
(II)
(SEQ ID NO: 2) YKX13LRRX14APRWDX15PLRDPALRX16X17L
(III)
(SEQ ID NO: 3) YKX18LRR(X19)nPLRDPALRX20X21L
(IV)
(SEQ ID NO: 4) IKLSGGVQAKAGVINMDKSESM
(V)
(SEQ ID NO: 5) IKLSGGVQAKAGVINMFKSESY
(VI)
(SEQ ID NO: 6) IKLSGGVQAKAGVINMFKSESYK
(VII)
(SEQ ID NO: 7) GVQAKAGVINMFKSESY
(VIII)
(SEQ ID NO: 8) GVRAKAGVRNMFKSESY
(IX)
(SEQ ID NO: 9) GVRAKAGVRN(Nle)FKSESY
(X)
(SEQ ID NO: 10) YKSLRRKAPRWDAPLRDPALRQLL
(XI)
(SEQ ID NO: 11) YKSLRRKAPRWDAYLRDPALRQLL
(XII)
(SEQ ID NO: 12) YKSLRRKAPRWDAYLRDPALRPLL
(XIII)
(SEQ ID NO: 13) wherein X1 to X21 and n can have various different values and wherein at least one protecting group and/or at least one labelling agent is optionally connected to said peptide compound at an N- and/or C-terminal end.-
4.
公开(公告)号:US20200157151A1
公开(公告)日:2020-05-21
申请号:US16616098
申请日:2018-05-24
Applicant: TRANSFERT PLUS, S.E.C.
Inventor: Richard BÉLIVEAU , Borhane ANNABI , Michel DEMEULE , Alain LAROCQUE , Jean-Christophe CURRIE , Sylvie LAMY
Abstract: The present disclosure relates to peptide compounds and conjugate compounds, processes, methods and uses thereof for treating inflammation. For example, the compounds can comprise compounds; IKLSGGVQAKAGVINMDKSESM, formula (V) as set forth in SEQ ID NO: 5, GVRAKAGVRN(Nle)FKSESY, formula (X) as set forth in SEQ ID NO: 10 and YKSLRRK.APRWDAPLRDPALRQLL, formula (XI) as set forth in SEQ ID NO: 11 wherein at least one protecting group and/or at least one labelling agent is connected to said peptide compound at an N- and/or C-terminal end, for use in inhibiting or decreasing TNF-alpha-induced COX-2 expression in cells expression sortilin.
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