Yu, Yongguo published the artcileDesign, synthesis and anticancer activity evaluation of diazepinomicin derivatives, Category: chlorides-buliding-blocks, the publication is Letters in Drug Design & Discovery (2013), 10(4), 369-373, 5 pp., database is CAplus.
A series of diazepinomicin derivatives [5,10-dihydro-4,6,8-trihydroxy-10-[(2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrien-1-yl]-11H-dibenzo[b,e][1,4]diazepin-11-one derivatives] were synthesized and evaluated in vitro for their growth inhibitory activity against the human carcinoma cell lines. The results indicated the anticancer selectivity of this kind of compounds Based on the results, preliminary structure-activity relationships were discussed. The synthesis of the target compounds was achieved using 5,10-dihydro-11H-dibenzo[b,e][1,4]diazepin-11-one derivatives and (2E,6E)-1-bromo-3,7,11-trimethyl-2,6,10-dodecatriene (trans,trans-farnesyl bromide) as key intermediates. The title compounds thus formed included a diazepinomicin analog (I) and related substances.
Letters in Drug Design & Discovery published new progress about 60091-87-4. 60091-87-4 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Nitro Compound,Carboxylic acid,Amine,Benzene, name is 2-((4-Chloro-2-nitrophenyl)amino)benzoic acid, and the molecular formula is C5H5ClIN, Category: chlorides-buliding-blocks.
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