The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
May. 23, 2023

Filed:

Mar. 11, 2021
Applicant:

3+2 Pharma, Llc, Lewes, DE (US);

Inventor:

Fuqiang Ruan, Bellevue, WA (US);

Assignee:

3+2 PHARMA, LLC, Lewes, DE (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C07D 487/04 (2006.01); A61P 17/08 (2006.01); A61P 1/16 (2006.01); A61P 11/00 (2006.01); A61K 8/49 (2006.01); A61K 9/00 (2006.01); A61K 39/39 (2006.01); A61K 45/06 (2006.01); A61Q 19/08 (2006.01);
U.S. Cl.
CPC ...
C07D 487/04 (2013.01); A61K 8/4966 (2013.01); A61K 9/0014 (2013.01); A61K 39/39 (2013.01); A61K 45/06 (2013.01); A61P 1/16 (2018.01); A61P 11/00 (2018.01); A61P 17/08 (2018.01); A61Q 19/08 (2013.01);
Abstract

Provided are compounds of formula (Ia), (Ib) and (IIa), and pharmaceutically acceptable salts thereof. Additionally provided are compositions and pharmaceutical compositions comprising the compounds, therapeutic methods using same for modulating (e.g., inhibiting) CREB binding protein (CBP)/β-catenin mediated signaling in treating a condition, disease or disorder (e.g., fibrosis, cancer, neurological conditions, metabolic disorders (e.g., diabetes, etc.), and skin conditions (dermatitis, psoriasis, scarring, alopecia, etc.) mediated by aberrant CBP/β-catenin signaling, and cosmetic methods for treating skin conditions (e.g., aging, etc.). Additionally, provided are methods for enhancing vaccine efficacy using the compounds and compositions. Further provided are methods for efficiently synthesizing a clinical grade drug, comprising use, in a penultimate, or last reaction step under GMP conditions, of an intermediate 2-propynyl-compound to form a clinical grade isoxazole derivative (e.g., via 3+2 cycloaddition).


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