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Chemical Hay 28543 productos.
SM-102
ALC-0159 is a lipid conjugate of polyethylene glycol that can be used as an immunosuppressant SM-102 is an ionizable aminolipid with a terminal hydroxyl group in the head group, which reduces the hydration of the head group and improves hydrogen bonding interactions with nucleic acids, thus enhancing transfection.SM-102 can be used for the preparation of...
Dusquetide
Dusquetide (SGX942) is a first-in-class innate defense regulator (IDR). Dusquetide modulates the innate immune response to both PAMPs and DAMPs by binding to p62. Dusquetide shows activity in both reducing inflammation and increasing clearance of bacterial infection.
Dusquetide
Dusquetide (SGX942) is a first-in-class innate defense regulator (IDR). Dusquetide modulates the innate immune response to both PAMPs and DAMPs by binding to p62. Dusquetide shows activity in both reducing inflammation and increasing clearance of bacterial infection.
CTB
CTB is a potent p300 histone acetyltransferase activator. CTB induces time dependence apoptosis of MCF-7 cells.
CTB
CTB is a potent p300 histone acetyltransferase activator. CTB induces time dependence apoptosis of MCF-7 cells.
Apraglutide
Apraglutide (FE 203799) is a potentially best-in-class, potent, synthetic 33-amino acid peptide and long-acting GLP-2 analog that can be used in studies related to short bowel syndrome (SBS).
Apraglutide
Apraglutide (FE 203799) is a potentially best-in-class, potent, synthetic 33-amino acid peptide and long-acting GLP-2 analog that can be used in studies related to short bowel syndrome (SBS).
Theogallin
Theogallin (3-Galloylquinic acid) is an active ingredient in decaffeinated green tea extract. Theogallin has antidepressive and cognition enhancing effect.
IRL 2500
IRL 2500 is a potent Endothelin receptor antagonist. IRL 2500 shows IC50 values of 1.3 and 94 nM for ETB and ETA receptors, respectively. IRL 2500 inhibits ETB receptor-mediated blood pressure increase and renal vascular resistance in rats in vivo.
Migoprotafib
Migoprotafib (GDC-1971) is an orally active allosteric SHP2 inhibitor for studies related to solid tumors.
Migoprotafib
Migoprotafib (GDC-1971) is an orally active allosteric SHP2 inhibitor for studies related to solid tumors.
Imlunestrant
Imlunestrant (LY-3484356) is an orally active, potent and selective estrogen receptor degrader (SERD) with pure antagonistic properties. Imlunestrant results in sustained inhibition of ER-dependent gene transcription and cell growth. Imlunestrant can be used for the research of ER-positive (ER+) advanced breast cancer (aBC) and endometrial endometrioid...