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BioWorld - Sunday, May 3, 2026
Home » Korea Research Institute of Chemical Technology

Articles Tagged with ''Korea Research Institute of Chemical Technology''

Cancer

Korean Research Institute scientists prepare IKZF2 degradation inducers for cancer

Aug. 29, 2024
Korean Research Institute of Bioscience and Biotechnology and Korea Research Institute of Chemical Technology have jointly developed molecular glue degraders acting as zinc finger protein Helios (IKZF2) degradation inducers. They are described as potentially useful for the treatment of cancer.
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Woman with blanket on couch blowing her nose with a tissue
Infection

New antirhinoviral compound with broad-spectrum activity described

Aug. 20, 2024
Human rhinoviruses (hRVs) are associated with upper respiratory tract infections such as the common cold, otitis media or sinusitis. In immunocompromised individuals or older people, hRVs can exacerbate existing pulmonary conditions such as asthma or chronic obstructive pulmonary disease.
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Cancer

Korean scientists discover new GSPT1 degradation inducers

June 6, 2024
Scientists at Korea Research Institute of Chemical Technology and Oncord Bio Inc. have divulged molecular glue degraders targeting protein cereblon (CRBN) and acting as eukaryotic peptide chain release factor GTP-binding subunit ERF3A (GSPT1) degradation inducers reported to be useful for the treatment of cancer, graft-vs.-host disease, leprosy and inflammatory disorders.
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Cancer

BD1-selective BET inhibitor exhibits strong antileukemic activity

Feb. 8, 2024
The bromodomain and extraterminal domain (BET) family of proteins are involved in cell cycle regulation and for this reason are considered therapeutic targets in cancer therapeutics.
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Cancer

Korean researchers divulge new inhibitors of PERK, GCN2 and HRI for cancer

Jan. 3, 2024
Researchers at Aston Science Co. Ltd. and Korea Research Institute of Chemical Technology have synthesized phenylsulfonamide derivatives acting as eukaryotic translation initiation factor 2-α kinase 1 (HRI) and/or translation initiation factor 2-α kinase 3 (PERK) and/or eukaryotic translation initiation factor 2-α kinase 4 (GCN2) inhibitors reported to be useful for the treatment of cancer.
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Woman and 3D brain
Substance Use & Poisoning

Novel AChE reactivator to reverse acetylcholine accumulation in the brain

Dec. 4, 2023
Organophosphorus compounds (OPs) include several types of chemical compounds used as pesticides, herbicides or nerve agents in chemical warfare that, once in the body, act by inhibiting acetylcholinesterase (AChE) functions leading to an excessive increase of acetylcholine that ultimately causes death after respiratory failure.
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Cancer

Korea Research Institute of Chemical Technology patents new HPK1 and MLK3 inhibitors

Nov. 29, 2023
Korea Research Institute of Chemical Technology has disclosed mitogen-activated protein kinase kinase kinase kinase 1 (MAP4K1; HPK1; MEKKK1) and mitogen-activated protein kinase kinase kinase 11 (MAP3K11; MLK3) inhibitors reported to be useful for the treatment of Parkinson's disease, viral infection, cancer, tuberculosis and non-alcoholic steatohepatitis.
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Cancer

Korean researchers patent new prostanoid EP2 and EP4 receptor dual antagonists for cancer

Sep. 19, 2023
Researchers from Kanaph Therapeutics Inc. and Korea Research Institute of Chemical Technology have disclosed prostanoid EP2 and/or EP4 receptor subtype dual antagonists reported to be useful for the treatment of cancer.
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Cancer cell
Cancer

KRICT patents MPS1 inhibitors for the treatment of cancer

July 31, 2023
Research at Korea Research Institute of Chemical Technology (KRICT) has led to the identification of pyrazolopyrimidine-containing compounds acting as dual specificity protein kinase TTK (MPS1; MPS1L1) inhibitors and reported to be useful for the treatment of cancer.
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Cancer

Korea Research Institute of Chemical Technology divulges new EGFR mutant inhibitors for cancer

Feb. 8, 2023
Korea Research Institute of Chemical Technology (KRICT) has synthesized novel pyrimidine-2,4-diamine derivatives acting as EGFR (HER1; erbB1) and/or HER2 (erbB2) (mutant) inhibitors reported to be useful for the treatment of cancer.
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