Abstract: Small molecule disruptors of Beclin-1/Bc1-2 protein-protein interactions induce autophagy and hence are useful for treating a variety of indications where stimulation of autophagy is therapeutically useful, including cancer, infection immunity, neurodegeneration, longevity.
Type:
Grant
Filed:
April 5, 2022
Date of Patent:
February 28, 2023
Assignee:
Board of Regents, The University of Texas System
Inventors:
Jef De Brabander, Qiren Liang, Beth Levine, Wei-Chung Chiang
Abstract: Disclosed are a new composition of lipoamino acids and alkanediols, a process for the preparation thereof, and a cosmetic or pharmaceutical composition resulting therefrom.
Type:
Grant
Filed:
December 12, 2018
Date of Patent:
February 28, 2023
Assignee:
SOCIETE D'EXPLOITATION DE PRODUITS POUR LES INDUSTRIES CHIMIQUES SEPPIC
Inventors:
Jérôme Guilbot, Georges Dacosta, Virginie Barthe
Abstract: The present invention relates to a CSF1R inhibitor, and in particular to a highly active CSF1R inhibitor compound having the structure of formula (I). Said compound of the present invention has high inhibitory activity on CSF1R.
Abstract: Compounds are provided for stabilizing protein transthyretin (TTR) and inhibiting amyloid fibril formation, for example, transthyretin-mediated amyloid fibril formation, and for treating, preventing, or ameliorating one or more symptoms of amyloid diseases, for example, transthyretin-related amyloidosis (ATTR).
Type:
Grant
Filed:
August 18, 2021
Date of Patent:
February 21, 2023
Assignee:
BSIM Therapeutics, S.A.
Inventors:
Rui Manuel Pontes Meireles Ferreira de Brito, Carlos José Vieira Simões, Teresa Margarida Vasconcelos Dias de Pinho e Melo, Bruno Lourenço da Silva Victor, Zaida Catarina Lourenço de Almeida, Ana Lúcia Cabral Cardoso Lopes, Bruno Filipe Oliveira Nascimento
Abstract: The present application is directed to compounds of Formula (I)-(VIII): compositions comprising these compounds and their uses, for example as medicaments and/or diagnostics.
Type:
Grant
Filed:
December 6, 2018
Date of Patent:
February 14, 2023
Assignee:
ONTARIO INSTITUTE FOR CANCER RESEARCH (OICR)
Inventors:
Rima Al-awar, Andrew Zhang, Ahmed Mamai
Abstract: Disclosed herein, inter alia, are acyclic nucleotide analogs and methods of using an acyclic nucleotide analog for treating and/or ameliorating a papillomavirus infection.
Type:
Grant
Filed:
April 21, 2021
Date of Patent:
February 7, 2023
Assignee:
The Regents of the University of California
Inventors:
Karl Y. Hostetler, James R. Beadle, Nadejda Valiaeva
Abstract: This disclosure relates to compositions and methods for inhibiting mutant IDH1, useful in treatment of mIDH1 cancers including AML, as well as mIDH1-positive solid tumors such as glioma.
Abstract: The present invention is directed to a combination comprising a proteasome inhibitor and a compound of formula I or a pharmaceutically acceptable salt thereof: to a pharmaceutical composition and to a kit both comprising said combination, to the combination, composition or kit for use in the treatment of cancer, and to a method of treatment of cancer in a patient in need thereof comprising administering to said patient an effective amount of said combination, composition or kit.
Type:
Grant
Filed:
March 25, 2021
Date of Patent:
January 24, 2023
Assignee:
Purdue Pharmaceutical Products L.P.
Inventors:
Thomas Jorg Mehrling, Enrique Maria Ocio
Abstract: The invention relates to compounds and methods for restoring or preserving cholesterol efflux in a cell infected with Human Immunodeficiency Virus (HIV) by preventing or decreasing an interaction between Negative Regulatory Factor (Nef) protein and Calnexin protein, and methods for screening for such compounds.
Type:
Grant
Filed:
August 24, 2021
Date of Patent:
January 24, 2023
Assignee:
THE GEORGE WASHINGTON UNIVERSITY
Inventors:
Alexei Adzhubei, Michael Bukrinsky, Ruth Hunegnaw
Abstract: Phosphoramidate derivatives of 5-fluoro-2?-deoxyuridine are disclosed for use in the treatment of cancer, especially in the treatment of cancer where the patient shows resistance, for example, in a patient with cells with a lowered level of nucleoside transporter proteins and/or with nucleoside kinase-deficient cells and/or with Mycoplasma-infected cells and/or with cells with a raised level of thymidylate synthase.
Type:
Grant
Filed:
April 6, 2021
Date of Patent:
January 24, 2023
Assignee:
NuCana plc
Inventors:
Christopher McGuigan, Jan Balzarini, Magdalena Slusarczyk, Blanka Gonczy, Paola Murziani
Abstract: The present disclosure relates to a novel crystalline form of L-glufosinate ammonium salt and a process for preparation thereof. The present disclosure also provides compositions comprising said form and a method for the control of undesired plant growth using said compositions.
Abstract: Disclosed are a near-infrared absorbing composition, an optical structure, and a camera module and an electronic device including the same. The near-infrared absorbing composition includes a copper complex represented by Chemical Formula 1. Definitions of Chemical Formula 1 are the same as described in the detailed description.
Type:
Grant
Filed:
November 22, 2019
Date of Patent:
January 17, 2023
Assignee:
Samsung Electronics Co., Ltd.
Inventors:
Yong Joo Lee, Mi Jeong Kim, Changki Kim, Hyung Jun Kim, Hye Ran Kim, Jong Hoon Won, Jae Jun Lee
Abstract: The present disclosure provides fused 1,4-oxazepines and related analogs represented by Formula (I) and the pharmaceutically acceptable salts, hydrates, and solvates thereof, wherein R1, R2a, R2b, R3a, R3b, R4, R5, A, and Y are as defined as set forth in the specification. The present disclosure is also directed to the use of compounds of Formula (I) to treat a condition or disorder responsive to inhibition of BET bromodomains such as cancer.
Type:
Grant
Filed:
February 15, 2017
Date of Patent:
January 10, 2023
Assignee:
THE REGENTS OF THE UNIVERSITY OF MICHIGAN
Abstract: The present invention relates to nitro-vinyl-pyrazole compounds of formula (B) wherein ring A, RB2 and RB3 are as defined in claim 1, as well as the manufacture of such compounds and their subsequent use in the production of agrochemicals and/or pharmaceuticals.
Type:
Grant
Filed:
December 1, 2020
Date of Patent:
January 10, 2023
Assignee:
SYNGENTA CROP PROTECTION AG
Inventors:
James Alan Morris, Sally Elizabeth Russell, Sean Ng
Abstract: The described invention provides small molecule anti-cancer compounds for treating tumors that respond to cholesterol biosynthesis inhibition. The compounds selectively inhibit the cholesterol biosynthetic pathway in tumor-derived cancer cells, but do not affect normally dividing cells.
Type:
Grant
Filed:
September 24, 2018
Date of Patent:
January 10, 2023
Assignee:
The Board of Regents of The University of Texas System
Abstract: The present embodiment provides a compound represented by the formula (1): Q-CHR2??(1) (Q is a nitrogen-containing aliphatic group containing two or more tertiary nitrogens but no oxygen, and R is an aliphatic group containing a biodegradable group). From the compound in combination with other lipids such as a lipid capable of reducing aggregation, lipid particles can be formed. Further, the compound can be used for a pharmaceutical composition to deliver an activator into cells.
Abstract: The present disclosure relates to Emetine Auristatin compounds, pharmaceutical compositions and kits comprising such compounds, and methods for using such compounds or pharmaceutical compositions.
Type:
Grant
Filed:
October 2, 2020
Date of Patent:
January 10, 2023
Assignee:
Arizona Board of Regents on behalf of Arizona State University
Abstract: Provided are a novel amine composition and a novel amine compound. Also provided are a method for producing the amine composition and amine compound, and an epoxy resin curing agent, an epoxy resin composition, a cured product, a urethane prepolymer curing agent, a polyurethane urea resin composition, a polyamide varnish, and a polyamide, each obtained using the amine composition and amine compound. The amine composition contains a compound represented by Formula (1), wherein A is a cyclic alkylene group, and B is a group containing an aryl group or a heteroaryl group.
Abstract: The present invention relates to a pharmaceutical aqueous formulation comprising 1-(4-{[4-(dimethylamino)piperidin-1-yl]carbonyl}phenyl)-3-[4-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl)phenyl]urea, or a pharmaceutically acceptable alkanesulphonate salt thereof, that is a clear solution. Such a formulation is particularly suitable for intravenous or parenteral administration to a patient.
Type:
Grant
Filed:
August 20, 2018
Date of Patent:
January 3, 2023
Assignee:
PFIZER INC.
Inventors:
James Joseph Hussey, Andrew Gilbert Bright
Abstract: The present disclosure provides oral pharmaceutical compositions comprising: 1) metronidazole or a pharmaceutically acceptable salt thereof; and magnesium aluminum silicate; or 2) metronidazole or a pharmaceutically acceptable salt thereof; magnesium aluminum silicate; and a flavoring agent. Methods of treating infection utilizing the oral pharmaceutical compositions are also provided.
Type:
Grant
Filed:
January 16, 2019
Date of Patent:
January 3, 2023
Assignee:
Appili Therapeutics Inc.
Inventors:
Bernard J. Guarino, Jr., Jamie L. Doran, Zorana Radovic, Kevin Sullivan