A novel set of thiazolylhydrazonothiazoles bearing an indole moiety were synthesized by
subjection reactions of carbothioamide derivative and hydrazonoyl chlorides (or α …

Many literature reports revealed the anticancer activity of pyridine and thiazole derivatives,
especially in lung cancer. Therefore, a new series of thiazolyl pyridines linked with …

Investigating novel compounds that may be useful in designing new, less toxic, selective,
and potent breast anticancer agents is still the main challenge for medicinal chemists. Thus …

The essential enzyme cyclin-dependent kinase 2 (CDK2) is a promising target for anticancer
drug development due to its pivotal role in regulating the cell cycle. This study aimed to …

A new series of coloring compounds (pigments) based on 5-(2-aminothiazol-5-yl) thiazol-2-
amine and 5-(4-aminophenyl) thiazol-2-amine as heterocyclic alternatives for benzidine …

To highlight the importance of thiazole and thiadiazole derivatives in the progression of
cancer and microbial treatments and to aid in drug design, we have synthesized a new …

In this contribution, five Ni (II) complexes have been synthesized from sulfonamide-based
Schiff bases (SB1–SB5) that comprise bromo or iodo substituents in the salicylidene moiety …

A series of transition metal complexes of alloxan monohydrate (H2L1) and ninhydrin (H2L2)
have been prepared where metal ions are Fe (III), Co (II), Ni (II), Cu (II), Zr (IV), and Mo (VI) …

In this study, three new phospho thiadiazole compounds (A, F and W) were investigated as
possible cytotoxic agents. The compounds were synthesised and characterised by using …

The review covers the results of studies published in the literature on the use of hydrazonoyl
halides in the synthesis of five‐(pyrazoles, thiazoles, triazoles, oxa‐and thiadiazoles), six …