sc-99

SC99 is a selective inhibitor of JAK2-STAT3 activation. SC99 downregulates the expression of STAT3-modulated genes.SC99 inhibits platelet activation, aggregation and displays potent anti-myeloma, anti-thrombotic activities

DL-Phenylalanine, a phenylalanine derivative, exhibits antifungal activity against Aspergillus flavus and antibacterial activity against Bacillus cereus and Escherichia coli.

Equilenin (E 400), a natural estrogen, is a specific fluorescent probe for steroid-protein interactions in sex steroid-binding proteins and has a high binding affinity for sex steroid-binding proteins (SBPs) Equilenin is an endocrine disruptor and can be used in the study of breast cancer.

Valproic Acid-D15 is a deuterated compound of Valproic Acid. Valproic Acid (T7064) has a CAS number of 99-66-1. Valproic Acid (T7064) is a branched chain fatty acid which potentially enhances central GABAergic neurotransmission and inhibits Na+ channels. Currently, the various molecular mechanisms of action of Valproic Acid (T7064) have not been completely elucidated. Valproic Acid (T7064) has been reported to be a potent inhibitor of histone deacetylases (HDACs) in vitro. Valproic Acid (T7064) is also noted to relieve HDAC-dependent transcriptional repression and causes the hyperacetylation of histones in cultured cells. Additionally, Valproic Acid (T7064) is reported to activate Wnt-dependent gene expression and to mimic trichostatin A (sc-3511) in the inhibition of histone deacetylase.

Valproic Acid-D4 is a deuterated compound of Valproic Acid. Valproic Acid (T7064) has a CAS number of 99-66-1. Valproic Acid (T7064) is a branched chain fatty acid which potentially enhances central GABAergic neurotransmission and inhibits Na+ channels. Currently, the various molecular mechanisms of action of Valproic Acid (T7064) have not been completely elucidated. Valproic Acid (T7064) has been reported to be a potent inhibitor of histone deacetylases (HDACs) in vitro. Valproic Acid (T7064) is also noted to relieve HDAC-dependent transcriptional repression and causes the hyperacetylation of histones in cultured cells. Additionally, Valproic Acid (T7064) is reported to activate Wnt-dependent gene expression and to mimic trichostatin A (sc-3511) in the inhibition of histone deacetylase.

2-(Propyl-3,3,3-D3) pentanoic-5,5,5-D3 Acid is a deuterated compound of 2-Propylpentanoic acid (TMSM-3352). 2-pentanoic Acid has a CAS number of 99-66-1. Valproic Acid is a branched chain fatty acid which potentially enhances central GABAergic neurotransmission and inhibits Na+ channels. Currently, the various molecular mechanisms of action of Valproic Acid have not been completely elucidated. Valproic Acid has been reported to be a potent inhibitor of histone deacetylases (HDACs) in vitro. Valproic Acid is also noted to relieve HDAC-dependent transcriptional repression and causes the hyperacetylation of histones in cultured cells. Additionally, Valproic Acid is reported to activate Wnt-dependent gene expression and to mimic trichostatin A (sc-3511) in the inhibition of histone deacetylase.

Valproic Acid-D15 (Standard) is a reference standard of Valproic Acid-D15 intended for quantitative analysis, quality control, and related biochemical research applications. Valproic Acid-d15 is a deuterated compound of Valproic Acid. Valproic Acid has a CAS number of 99-66-1. Valproic Acid is a branched chain fatty acid which potentially enhances central GABAergic neurotransmission and inhibits Na+ channels. Currently, the various molecular mechanisms of action of Valproic Acid have not been completely elucidated. Valproic Acid has been reported to be a potent inhibitor of histone deacetylases (HDACs) in vitro. Valproic Acid is also noted to relieve HDAC-dependent transcriptional repression and causes the hyperacetylation of histones in cultured cells. Additionally, Valproic Acid is reported to activate Wnt-dependent gene expression and to mimic trichostatin A (sc-3511) in the inhibition of histone deacetylase.

Valproic Acid-D4 (Standard) is a reference standard of Valproic Acid-D4 intended for quantitative analysis, quality control, and related biochemical research applications. Valproic Acid-d4 is a deuterated compound of Valproic Acid. Valproic Acid has a CAS number of 99-66-1. Valproic Acid is a branched chain fatty acid which potentially enhances central GABAergic neurotransmission and inhibits Na+ channels. Currently, the various molecular mechanisms of action of Valproic Acid have not been completely elucidated. Valproic Acid has been reported to be a potent inhibitor of histone deacetylases (HDACs) in vitro. Valproic Acid is also noted to relieve HDAC-dependent transcriptional repression and causes the hyperacetylation of histones in cultured cells. Additionally, Valproic Acid is reported to activate Wnt-dependent gene expression and to mimic trichostatin A (sc-3511) in the inhibition of histone deacetylase.

2-(Propyl-3,3,3-D3)Pentanoic-5,5,5-D3 Acid (Standard) is a reference standard of 2-(Propyl-3,3,3-D3)Pentanoic-5,5,5-D3 Acid intended for quantitative analysis, quality control, and related biochemical research applications. 2-(Propyl-3,3,3-d3)pentanoic-5,5,5-d3 Acid is a deuterated compound of 2-pentanoic Acid. 2-pentanoic Acid has a CAS number of 99-66-1. Valproic Acid is a branched chain fatty acid which potentially enhances central GABAergic neurotransmission and inhibits Na+ channels. Currently, the various molecular mechanisms of action of Valproic Acid have not been completely elucidated. Valproic Acid has been reported to be a potent inhibitor of histone deacetylases (HDACs) in vitro. Valproic Acid is also noted to relieve HDAC-dependent transcriptional repression and causes the hyperacetylation of histones in cultured cells. Additionally, Valproic Acid is reported to activate Wnt-dependent gene expression and to mimic trichostatin A (sc-3511) in the inhibition of histone deacetylase.