Triptorelin

A rotenoid compound with chemopreventive and chemosensitizing effects in models of skin, mammary, colon, and lung carcinogenesis inhibits cell growth (IC50 = 8 M), blocks PI3K/Akt signaling, suppresses COX-2 expression, and induces apoptosis of

A lipophilic analog of 17-trifluoromethylphenyl trinor PGF2&alpha.

An internal standard for the quantification of PGB2 by GC- or LC-MS.

A lipophilic analog of 16-phenoxy tetranor PGF2&alpha.

A potential prodrug analog of PGE2 with enhanced lipid solubility.

Derived from 17-phenyl trinor PGE2, a synthetic analog of PGE2 that acts as an agonist of EP1 and EP3 in mice (Ki = 14 and 3.7 nM, respectively) and EP1, EP3, and EP4 in rats (Ki = 25, 4.

A lipophilic analog of 16-phenoxy tetranor PGF2&alpha.

A lipophilic analog of 16-phenoxy tetranor PGF2&alpha.

Diethylstilbestrol (DES) is a synthetic estrogen receptor agonist that was prescribed to pregnant women in the late 1930s. It was banned in 1971 because of possible links to increased risk of breast cancer in mothers along with congenital

16,16-dimethyl PGA2 is a metabolism resistant analog of PGA2 with a prolonged in vivo half-life. It inhibits the proliferation of Sendai virus in cultured African green monkey kidney cells by &gt90% at a concentration of 4 &microg/ml.

16,16-dimethyl PGD2 is a metabolically stable synthetic analog of PGD2. It enhances ADP-induced human platelet aggregation and increases systemic blood pressure in rats.

A competitive inhibitor of 15-hydroxy PGDH acts as an agonist on most EP receptor subtypes (Kd d~ 1 nM for isolated EP2 receptors) preserves the self-renewal properties while preventing the differentiation of hematopoietic stem cells during