21 research outputs found
SELECTIVE ESTROGEN RECEPTOR MODULATORS; ROLE OF SIDE CHAIN IN ACTIVITY MODULATION
Selective estrogen receptor modulators (SERMs) are a class of molecules that activate estrogen receptors (ER), impacting differently on differenttissues. Upon binding to ER, the ligand-receptor complex may present various conformations due to the presence of two different kinds of ERs. Fewof these ligands show estrogenic effects, whereas others will inhibit the action of estrogens. Researchers are working in the direction to generatethe SERMs that have a desirable estrogen-like effects on the various sites i.e., bones, improving lipid profile, reduce hot flushes, but do not act likeestrogens in unwanted ways i.e., causing breast cancer, uterine endometrial proliferation. Given the comprehensive nature of this article, it is not ourintention to revisit many of the issues relating to SERMs, which have already been covered in detail. Rather this article focuses on the aspect thatligand-mediated structural perturbations in and around the ligand binding pocket, contributed by the side chain effects lead to receptor antagonism.Adjusting the balance of these effects may provide a novel strategy for designing of improved SERMs. In the light of this, the article will provide anoverview of the SERMs and their structural diversity.Keywords: Ligand and estrogen receptor, Side chain of selective estrogen receptor modulators, Selective estrogen receptor modulators, Mechanismof action
1,2-addition of ∝-amino acid derivatives to conjugated aldehydes: synthesis of β -substituted serines
Aza variant of intramolecular nucleophile-catalyzed aldol lactonization (NCAL): formal synthesis of (3S,4R) and (3R,4S) 4-(hydroxymethyl)pyrrolidin-3-ol
Use of <i>S</i>-proline as chiral auxiliary in α-alkylations of carboxylic acids<sup>†</sup>
2628-2631Use of S-proline as auxiliary in α-alkylations
of carboxylic acids results in Se-face approach of the electrophile
Thio-claisen rearrangement on pyroglutamates
S-allyl/propargyl/methallyl thioimminium salts derived from methyl 1-benzyl-5-thioxoprolinate (1) undergoes a facile thio-Claisen rearrangement which provides an easy access to 4-substituted thioxoprolinates (2-4)
Pharmacokinetic Studies of 4, 5 CIS-5-STYRYL-2-OXOOxazolidine-4-Carboxylic Acid from its Prodrug
Mechanism of reduction of 3,4,5-triphenylfuran-2(5H)-ones by lithium aluminium hydride
A detailed study of the reduction of 3,4,5-triphenylfuran-2(5H)-ones with lithium aluminium hydride, with deuterium as a marker, has been performed. On the basis of the results it is proposed that 1,4-hydride attack is followed by regiospecific hydridoalumination of the enolate double bond only in those cases where the resulting complex can be stabilised
