An article Identification of a potent heme oxygenase-2 (HO-2) inhibitor by targeting the secondary hydrophobic pocket of the HO-2 western region WOS:000592529800004 published article about ACID PHENETHYL ESTER; DRUG DISCOVERY; DERIVATIVES; IMIDAZOLE; INDUCERS; ANALOGS in [Floresta, Giuseppe; Fallica, Antonino N.; Romeo, Giuseppe; Sorrenti, Valeria; Salerno, Loredana; Rescifina, Antonio; Pittala, Valeria] Univ Catania, Dept Drug Sci, Vle Doria 6, I-95125 Catania, Italy; [Floresta, Giuseppe] Kings Coll London, Dept Analyt Environm & Forens, Stamford St, London SE1 9NH, England in 2020.0, Cited 54.0. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4. SDS of cas: 99-93-4
The enzymatic family of heme oxygenase (HO) is accountable for heme breakdown. Among the two isoforms characterized to date, HO-2 is poorly investigated due to the lack of potent HO-2 chemical modulators and the greater attentiveness towards HO-1 isoform. In the present paper, we report the rational design and synthesis of HO-2 inhibitors achieved by modulating the volume of known HO-1 inhibitors. The inhibition preference has been moved from HO-1 to HO-2 by merely increasing the volume of the substituent in the western region of the inhibitors. Docking studies demonstrated that new derivatives soak differently in the two binding pockets, probably due to the presence of a Tyr187 residue in HO-2. These findings could be useful for the design of new selective HO-2 compounds.
SDS of cas: 99-93-4. About 4′-Hydroxyacetophenone, If you have any questions, you can contact Floresta, G; Fallica, AN; Romeo, G; Sorrenti, V; Salerno, L; Rescifina, A; Pittala, V or concate me.
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Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles