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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: 4/8/2024
|
Inventor(s):
John Beutler
,
Jian-kang 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
Novel ACRV1/ALK2 Inhibitors and Methods for Inhibiting BMP Signaling for the Treatment of Fibrodysplasia Ossificans Progressiva (FOP)
This technology includes the identification and use of novel ACRV1/ALK2 inhibitors for the treatment of fibrodysplasia ossificans progressiva (FOP), an autosomal-dominant rare disease that affects one person in every 1-2 million. FOP is characterized by malformation of the great (big) toes during embryonic development and by progressive heterotopic...
Published: 10/28/2024
|
Inventor(s):
Jian-kang Jiang
,
Khalida Shamim
,
Philip Sanderson
,
Wei Zheng
,
Xiuli Huang
,
Gregory Tawa
,
Asaf Alimardanov
,
Arthur Lee
,
Junfeng Huang
,
Wenwei Huang
Keywords(s):
ALK2
,
BMP
,
INHIBITING
,
Inhibitors
,
Methods
,
Novel
,
SIGNALING
,
VGXXXX
,
WIXXXX
,
WKXXXX
,
XEXXXX
Category(s):
TherapeuticArea > Endocrinology
,
Application > Therapeutics
,
Application > Research Materials
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
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
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