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Anti-Viral Compounds that Inhibit HIV Activity
Abstract: Several novel tropolone derivatives have been identified that inhibit HIV-1 RNase H function and have potential for anti-viral activity due to reduced cellular toxicity. Inhibiting RNase H function is a potential treatment for many viral infections, since RNase H function is essential for viral replication for many pathogenic retroviruses...
Published: 8/6/2025
|
Inventor(s):
John Beutler
,
Jiankang Jiang
,
Suhman Chung
,
Craig Thomas
,
Stuart LeGrice
,
Jennifer Wilson
Keywords(s):
AIDS
,
HIV
,
ribonuclease H
,
RNase H
,
tropolone derivative
,
viral replication
Category(s):
Collaboration Sought > Licensing
,
Collaboration Sought > Collaboration
,
Application > Therapeutics
,
TherapeuticArea > Infectious Disease
Development and Use of O-linked beta-N-acetylglucosamine (O-GlcNAc) Transferase (OGT) Inhibitors for Multiple Conditions, Including Cancer
This technology includes the development and use of small molecules that inhibit O-linked beta-N-acetylglucosamine (O-GlcNAc) transferase (OGT) for a variety of pathologies, including Alzheimer's disease, cancer, cancer, diabetes, and neurodegenerative disorders the treatment of cancer and as a potential antiviral. OGT is a ubiquitous enzyme that catalyzes...
Published: 10/28/2024
|
Inventor(s):
Sara Martin Schwanger
,
Craig Thomas
,
Damien Duveau
,
Suzanne Walker
Keywords(s):
0-GlcNAc
,
Development
,
Developmtent
,
Inhibitors
,
OGT
,
THEREOF
,
TRANSFERASE
,
USES
,
VEXXXX
,
WIXXXX
,
WKXXXX
Category(s):
Application > Research Materials
,
TherapeuticArea > Neurology
,
Application > Therapeutics
Treatment of Acute Myeloid Leukemia (AML) with the Multi-kinase FLT3-IRAK1/4 Inhibitor, NCGC1481, to Avoid Adaptive Resistance
This technology includes the identification and use of a novel small molecule, NCGC1481, to inhibit both the FLT3 and IRAK1/4 kinase pathways for treating acute myeloid leukemia (AML). An activating mutation of the FMS-like receptor kinase 3 (FMT3) occurs in approximately 25% of AML cases. Consequently, FLT3 inhibitors (FLT3i) have a good initial clinical...
Published: 10/28/2024
|
Inventor(s):
Jian-kang Jiang
,
Craig Thomas
Keywords(s):
FTL3/IRAK
,
Inhibitors
,
MOLECULE
,
Small
,
VCXXXX
,
WIXXXX
,
WKXXXX
,
XEXXXX
Category(s):
Application > Therapeutics
,
TherapeuticArea > Oncology
,
Application > Research Materials
Discovery of imidazo[1,2-b]pyridazines with Anticancer Properties
This technology includes a series of imidazo[1,2-b]pyridazines that display potent inhibition of FLT3, as well as potent binding and activity against FLT3 tyrosine kinase domain and gatekeeper mutations. This chemotype exhibits superior anti-leukemic activity against the common clinically-relevant FLT3-mutant acute myeloid leukemia (AML) in vitro and...
Published: 10/28/2024
|
Inventor(s):
Scott Hoyt
,
Patrick Sutter
,
Chris Finocchio
,
Daniel Starczynowski
,
Gregory Tawa
,
Craig Thomas
Keywords(s):
2-b]pyridazines
,
ANTICANCER
,
Discovery
,
Imidazo[1
,
PROPERTIES
,
VCXXXX
,
WIXXXX
,
WKXXXX
Category(s):
Application > Therapeutics
,
Application > Research Materials
,
TherapeuticArea > Oncology
Use of the Ketamine Metabolite (R,6R)-hydroxynorketamine in Depression
This technology includes the identification and use of a ketamine metabolite, (2R,6R)-2-amino-2-(2-chlorophenyl)-6-hydroxycyclohexanone (HNK), for the treatment of depression. Ketamine is an NMDA receptor antagonist that exerts a rapid and sustained antidepressant and anti-suicidal effect. However, even low doses of ketamine has addictive and psychomimetic...
Published: 4/23/2025
|
Inventor(s):
Todd Gould
,
Irving Wainer
,
Carlos Zarate
,
Ruin Moaddel
,
Patrick Morris
,
Panos Zanos
,
Craig Thomas
Keywords(s):
2R
,
6R-hydroxynorketamine
,
depression
,
Ketamine
,
METABOLITE
,
VEXXXX
,
VNXXXX
,
WIXXXX
,
WKXXXX
Category(s):
TherapeuticArea > Neurology
,
TherapeuticArea > Psychiatry/Mental Health
,
Application > Therapeutics
,
Application > Research Materials
Pyruvate Kinase M2 Activators for the Treatment of Cancer
This technology describes a series of small-molecule activators of the pyruvate kinase M2 isoform (PK-M2). Pyruvate kinase (PK) is a critical metabolic enzyme that catalyzes the last step of the glycolytic pathway. It exists in several isoforms with different patterns of tissue expression. One isoform, PK-M2, is expressed in cells with a high rate...
Published: 11/5/2024
|
Inventor(s):
Jian-kang Jiang
,
Matthew Boxer
,
Min Shen
,
Douglas Auld
,
Craig Thomas
Keywords(s):
Activator
,
ACTIVATORS
,
CANCER
,
CBXXXX
,
CXXXXX
,
Dimer
,
IBXXXX
,
ISOFORM
,
IXXXXX
,
M2
,
METABOLIC
,
METABOLITE
,
PK
,
PKM2
,
PK-M2
,
Proliferation
,
PYRUVATE
,
pyruvate kinase
,
small molecule
,
Tetramer
,
tumor
Category(s):
Collaboration Sought > Collaboration
,
Application > Therapeutics
,
TherapeuticArea > Oncology
,
Application > Diagnostics
,
Application > Research Materials
Pyruvate Kinase M2 Activators for the Treatment of Cancer
NIH investigators have discovered a series of small compounds with the potential to treat a variety of cancers as well as hemolytic anemia. Contrary to most cancer medications, these molecules can be non-toxic to normal cells because they target a protein specific to the metabolic pathways in tumors, thus representing a significant clinical advantage...
Published: 8/13/2025
|
Inventor(s):
Min Shen
,
Craig Thomas
,
Douglas Auld
,
Matthew Boxer
Keywords(s):
[1
,
[b]
,
2
,
2-oxo-1
,
3
,
3-oxo-3
,
4]
,
4-dihydroquinoline-2H-benzo
,
4-tetrahydroquinoline-6-sulfonamides
,
ACTIVATORS
,
CB3CXX
,
CB3XXX
,
CBXXXX
,
CXXXXX
,
Human
,
Kinase
,
MOLECULE
,
Oxazine-7-sulfonamides
,
Patent Category - Chemistry
,
PYRUVATE
,
Small
,
Substituted
Category(s):
Collaboration Sought > Collaboration
,
Application > Therapeutics
,
TherapeuticArea > Oncology
Caspase Inhibitors Useful for the Study of Autoimmune or Inflammatory Diseases
Novel and potent caspase 1 inhibitors are available for licensing. In particular, this technology discloses potent and selective caspase 1 inhibitors that target the active site of the enzyme. Caspase 1 is known to play a pro-inflammatory role in numerous autoimmune and inflammatory diseases and therefore represents an excellent target for treatment...
Published: 8/13/2025
|
Inventor(s):
Matthew Boxer
,
Craig Thomas
Keywords(s):
1
,
Amyotrophic lateral sclerosis
,
Amyotrophic lateral sclerosis 1; Amyotrophic lateral scleros
,
Amyotrophic lateral sclerosis 6
,
Caspase
,
IB3XXX
,
IBXXXX
,
Inflammatory bowel disease 1
,
inhibitor
,
IXXXXX
,
Lou Gehrig's disease
,
Patent Category - Chemistry
Category(s):
Collaboration Sought > Collaboration
,
Collaboration Sought > Licensing
,
Application > Diagnostics
,
Application > Research Materials
,
Application > Therapeutics
,
TherapeuticArea > Immunology
Small Molecule Activators of Human Pyruvate Kinase for Treatment of Cancer and Enzyme-Deficient Hemolytic Anemia
NIH investigators have discovered a series of small compounds with the potential to treat a variety of cancers as well as hemolytic anemia. Contrary to most cancer medications, these molecules can be non-toxic to normal cells because they target a protein specific to the metabolic pathways in tumors, thus representing a significant clinical advantage...
Published: 8/13/2025
|
Inventor(s):
Craig Thomas
Keywords(s):
3-@hydroxyacyl-coa dehydrogenase deficiency
,
ACTIVATORS
,
CB3CXX
,
CB3XXX
,
CBXXXX
,
CXXXXX
,
HAD deficiency
,
HIS deficiency
,
Histidinemia
,
Human
,
Kinase
,
MOLECULE
,
Patent Category - Chemistry
,
PYRUVATE
,
Small
Category(s):
Collaboration Sought > Collaboration
,
Collaboration Sought > Licensing
,
Application > Therapeutics
,
TherapeuticArea > Oncology
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