US2023313204A1PendingUtilityA1

Anti-chymase aptamer and use for same

63
Assignee: RIBOMIC INCPriority: Nov 30, 2017Filed: Apr 3, 2023Published: Oct 5, 2023
Est. expiryNov 30, 2037(~11.4 yrs left)· nominal 20-yr term from priority
C12N 15/115A61K 31/7088C12N 2310/16A61P 1/04A61P 1/16A61P 1/18A61P 3/10A61P 9/00A61P 9/04A61P 9/10A61P 9/12A61P 9/14A61P 11/00A61P 13/08A61P 13/12A61P 15/00A61P 17/00A61P 17/02A61P 17/04A61P 17/06A61P 19/08A61P 19/10A61P 21/00A61P 25/00A61P 27/02A61P 35/00A61P 37/08A61P 43/00C12N 2310/321C12N 2310/322C12N 2310/531C12N 2310/333C12N 2310/343C12N 2310/317C12N 2310/3513C12Q 1/6806
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Claims

Abstract

The present invention provides an aptamer that binds to chymase, and contains a common sequence represented by UAACR 1 N 1 R 2 GGGG wherein R 1 and R 2 are each any one base, and N 1 shows 3 to 30 bases (uracil is optionally thymine).

Claims

exact text as granted — not AI-modified
1 . An aptamer that binds to chymase, and comprises a potential secondary structure represented by the formula (1), wherein uracil is optionally thymine:
                       wherein                         in the formula (1) is a stem-loop partial structure, and R   1  and R 2  are each any one base,
 wherein a base length of the aptamer is not less than 28, the stem-loop partial structure of (1′) has a base length of 3 21, and at least two bases at the 5′ end of the UAAC sequence and at least two bases at the 3′ end of the GGGG sequence form base pairs, and 
 wherein the aptamer comprises a nucleotide sequence selected from any of SEQ ID NOs: 1-11, 14-33, and 42-84, wherein uracil is optionally thymine, and wherein one to several nucleotides are substituted, deleted, inserted or added in the nucleotide sequence other than the sequence UAAC and GGGG in the formula (1). 
 
     
     
         2 . The aptamer according to  claim 1 , wherein a hydroxyl group at the 2′-position of ribose of each pyrimidine nucleotide contained in the aptamer is the same or different and unsubstituted or substituted by an atom or a group selected from the group consisting of a hydrogen atom, a fluorine atom and a methoxy group. 
     
     
         3 . The aptamer according to  claim 1 , wherein a hydroxyl group at the 2′-position of ribose of each purine nucleotide contained in the aptamer is the same or different and unsubstituted or substituted by an atom or a group selected from the group consisting of a hydrogen atom, a fluorine atom and a methoxy group. 
     
     
         4 . A complex comprising the aptamer and the functional substance according to  claim 1 . 
     
     
         5 . A medicament comprising the aptamer according to  claim 1 . 
     
     
         6 . The medicament according to  claim 5  that is a therapeutic drug for a disease involving organ or tissue fibrosis, or a circulatory disease. 
     
     
         7 . The medicament according to  claim 5  that is a therapeutic drug for fibrosis. 
     
     
         8 . A method for detecting chymase, comprising using the aptamer according to  claim 1 .

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