Olpadronic acid

Honokiol DCA (Honokiol dichloroacetate) is a dichloroacetate analog of Honokiol. Honokiol DCA can inhibit the growth of human prostate cancer cells in vitro and suppress the androgen receptor (AR) protein level.In VitroHonokiol DCA (20-40 μM: 24-48

Honokiol DCA (Honokiol dichloroacetate) is a dichloroacetate analog of Honokiol. Honokiol DCA can inhibit the growth of human prostate cancer cells in vitro and suppress the androgen receptor (AR) protein level.In VitroHonokiol DCA (20-40 μM: 24-48

Honokiol DCA (Honokiol dichloroacetate) is a dichloroacetate analog of Honokiol. Honokiol DCA can inhibit the growth of human prostate cancer cells in vitro and suppress the androgen receptor (AR) protein level.In VitroHonokiol DCA (20-40 μM: 24-48

Cell Line Origin Human Caucasian prostate carcinoma Cell Line Description Derived from a metastasis at the left supraclavicular lymph node of a 50 year old patient with a confirmed diagnosis of metastatic prostate carcinoma. Growth and acid

Biochem/physiol Actions Morroniside is a bioactive natural product with antioxidant and anti-inflammatory activity. Its activities have included protecttion against cerebral ischemia/reperfusion injury by inhibiting neuron apoptosis and MMP2/9

Biochem/physiol Actions Morroniside is a bioactive natural product with antioxidant and anti-inflammatory activity. Its activities have included protecttion against cerebral ischemia/reperfusion injury by inhibiting neuron apoptosis and MMP2/9

Biochem/physiol Actions Olomoucine is a purine derivative which inhibits cyclin-dependent kinases and induces G arrest. Features and Benefits This compound is featured on the CDKs page of the Handbook of Receptor Classification and Signal

Biochem/physiol Actions Olomoucine is a purine derivative which inhibits cyclin-dependent kinases and induces G arrest. Features and Benefits This compound is featured on the CDKs page of the Handbook of Receptor Classification and Signal

ONDANSETRON RELATED COMPOUND G

Rosmarinic acid is a naturally-occurring phenolic compound with antioxidant and anti-inflammatory properties. This compound inhibits lipid peroxidation of rat liver microsomes by 90% at a concentration of 25 &microg/ml.

Application SCH 58261 was used to block A2&#945: adenosine receptor to study the signaling by prostatic acid phosphatase in neurons. 4 Biochem/physiol Actions SCH 58261 reduces the levels of TNF-&#945:, Fas-L, Bax expression and activation of

Amino Acid Sequence Thr-Asn-Glu-Ile-Val-Glu-Glu-Gln-Tyr-Thr-Pro-Gln-Ser-Leu-Ala-Thr-Leu-Glu-Ser-Val-Phe-Gln-Glu-Leu-Gly-Lys-Leu-Thr-Gly-Pro-Ser-Asn-Gln Biochem/physiol Actions Neuropeptide generated in brain, adrenal medulla and other endocrine