Benproperine trihydrogen phosphate

Apicidin is a cyclic tetrapeptide that inhibits histone deacetylase (HDAC) and exhibits anticancer benefit. In oral squamous cell carcinoma cells, apicidin upregulates expression of p21, inducing G2/M phase cell cycle arrest, apoptosis, and

Apicidin is a cyclic tetrapeptide that inhibits histone deacetylase (HDAC) and exhibits anticancer benefit. In oral squamous cell carcinoma cells, apicidin upregulates expression of p21, inducing G2/M phase cell cycle arrest, apoptosis, and

General description IGFBPs (insulin-like growth factor-binding proteins) are mainly required to regulate IGFs (insulin like growth factors) activities. IGFBP3 is a multifunctional protein and is secreted by various cells.

IMT1B (LDC203974) is an orally active, noncompetitive and specific allosteric inhibitor of mitochondrial RNA polymerase (POLRMT) and inhibits mitochondrial DNA (mtDNA) expression. IMT1B has anti-tumour effectsIn VitroIMT1B is a noncompetitive

IMT1B (LDC203974) is an orally active, noncompetitive and specific allosteric inhibitor of mitochondrial RNA polymerase (POLRMT) and inhibits mitochondrial DNA (mtDNA) expression. IMT1B has anti-tumour effectsIn VitroIMT1B is a noncompetitive

IMT1B (LDC203974) is an orally active, noncompetitive and specific allosteric inhibitor of mitochondrial RNA polymerase (POLRMT) and inhibits mitochondrial DNA (mtDNA) expression. IMT1B has anti-tumour effectsIn VitroIMT1B is a noncompetitive

IMT1B (LDC203974) is an orally active, noncompetitive and specific allosteric inhibitor of mitochondrial RNA polymerase (POLRMT) and inhibits mitochondrial DNA (mtDNA) expression. IMT1B has anti-tumour effectsIn VitroIMT1B is a noncompetitive

IMT1B (LDC203974) is an orally active, noncompetitive and specific allosteric inhibitor of mitochondrial RNA polymerase (POLRMT) and inhibits mitochondrial DNA (mtDNA) expression. IMT1B has anti-tumour effectsIn VitroIMT1B is a noncompetitive

Biochem/physiol Actions INF39 is an orally active acrylate derivative and a non-cytotoxic INF4E analog (no toxicity at 100 &#956:M in THP-1 cultures vs. TC50 = 65 &#956:M with INF4E) that acts as an irreversible inhibitor against NLRP3 (NACHT, LRR

Biochem/physiol Actions INF39 is an orally active acrylate derivative and a non-cytotoxic INF4E analog (no toxicity at 100 &#956:M in THP-1 cultures vs. TC50 = 65 &#956:M with INF4E) that acts as an irreversible inhibitor against NLRP3 (NACHT, LRR

Application Inosine 5&#8242-triphosphate (ITP) is used in studies on the impact of deamination of ATP and GTP by various enzymes and chemical processes. ITP may be used as a substrate to study the specificity and kinetics of

Application Inosine 5&#8242-triphosphate (ITP) is used in studies on the impact of deamination of ATP and GTP by various enzymes and chemical processes. ITP may be used as a substrate to study the specificity and kinetics of