Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and unique chemicals. Sigma-Aldrich does not collect analytical data for this product.
Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and unique chemicals. Sigma-Aldrich does not collect analytical data for this product.
Application S15535 has been used as a serotonin 1A receptor (5-HT1A) agonist in zebrafish. S15535 may be used in histamine 5-HT 1A -medaited cell signaling studies.
Application S15535 has been used as a serotonin 1A receptor (5-HT1A) agonist in zebrafish. S15535 may be used in histamine 5-HT 1A -medaited cell signaling studies.
General description Squamous cell carcinoma of the head and neck (HNSCC) represents 90% of all head and neck cancers (1). HNSCC is the 9th-most common cancer worldwide and is characterized by a high rate of recurrence after therapy, with a median
General description Squamous cell carcinoma of the head and neck (HNSCC) represents 90% of all head and neck cancers (1). HNSCC is the 9th-most common cancer worldwide and is characterized by a high rate of recurrence after therapy, with a median
Application S 17092 may be used in prolyl endopeptidase-mediated cell signaling studies. Biochem/physiol Actions S-17092 is a potent, selective inhibitor of Prolyl oligopeptidase (POP), also known as prolyl endopeptidase (PEP or PE).
Application S 17092 may be used in prolyl endopeptidase-mediated cell signaling studies. Biochem/physiol Actions S-17092 is a potent, selective inhibitor of Prolyl oligopeptidase (POP), also known as prolyl endopeptidase (PEP or PE).
Biochem/physiol Actions Qc1 is a reversible inhibitor of threonine dehydroxygenase (TDH). The IC 50 value for inhibition of TDH by Qc1 is 500 nM, with no detectable inhibition of other dehydroxygenase enzymes at concentrations up to 10 mM.
Biochem/physiol Actions Qc1 is a reversible inhibitor of threonine dehydroxygenase (TDH). The IC 50 value for inhibition of TDH by Qc1 is 500 nM, with no detectable inhibition of other dehydroxygenase enzymes at concentrations up to 10 mM.
Biochem/physiol Actions GNF-5 is a BRC-Abl inhibitor. Features and Benefits This compound is a featured product for Kinase Phosphatase Biology research.
Biochem/physiol Actions GNF-5 is a BRC-Abl inhibitor. Features and Benefits This compound is a featured product for Kinase Phosphatase Biology research.
Biochem/physiol Actions Cu-ATSM is an orally bioavailable, blood-brain barrier permeable complex that specifically inhibits the action of peroxynitrite on Cu,Zn superoxide dismutase (SOD1) and subsequent nitration of cellular proteins. Cu II
Biochem/physiol Actions Cu-ATSM is an orally bioavailable, blood-brain barrier permeable complex that specifically inhibits the action of peroxynitrite on Cu,Zn superoxide dismutase (SOD1) and subsequent nitration of cellular proteins. Cu II
Biochem/physiol Actions Cu-ATSM is an orally bioavailable, blood-brain barrier permeable complex that specifically inhibits the action of peroxynitrite on Cu,Zn superoxide dismutase (SOD1) and subsequent nitration of cellular proteins. Cu II
Biochem/physiol Actions Cu-ATSM is an orally bioavailable, blood-brain barrier permeable complex that specifically inhibits the action of peroxynitrite on Cu,Zn superoxide dismutase (SOD1) and subsequent nitration of cellular proteins. Cu II
Application GI254023X has been used to inhibit ADAM10 (ADAM metallopeptidase domain 10). Biochem/physiol Actions GI254023X blocks ADAM10 (ADAM metallopeptidase domain 10) activity and decreases human leukocyte antigen (HLA)-mediated
Application GI254023X has been used to inhibit ADAM10 (ADAM metallopeptidase domain 10). Biochem/physiol Actions GI254023X blocks ADAM10 (ADAM metallopeptidase domain 10) activity and decreases human leukocyte antigen (HLA)-mediated
Application GI254023X has been used to inhibit ADAM10 (ADAM metallopeptidase domain 10). Biochem/physiol Actions GI254023X blocks ADAM10 (ADAM metallopeptidase domain 10) activity and decreases human leukocyte antigen (HLA)-mediated
Application GI254023X has been used to inhibit ADAM10 (ADAM metallopeptidase domain 10). Biochem/physiol Actions GI254023X blocks ADAM10 (ADAM metallopeptidase domain 10) activity and decreases human leukocyte antigen (HLA)-mediated
Biochem/physiol Actions EGA is a small molecule that blocks the entry of anthrax lethal toxin by inhibiting trafficking pathways in acidified endosomes, without affecting endosome pH. EGA blocks trafficking of other toxins, including diphtheria
Biochem/physiol Actions EGA is a small molecule that blocks the entry of anthrax lethal toxin by inhibiting trafficking pathways in acidified endosomes, without affecting endosome pH. EGA blocks trafficking of other toxins, including diphtheria