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Thus, these candidate selections represent potential molecules for further drug design.
Hence, we claim the lead molecules for further development in anticancer drug discovery.
Taken together, our results suggest that compounds A and B represent promising lead molecules for further anti-HSV drug design.
These results suggest that 1,2,3-triazolyl-4-oxoquinolines 1,2,3-triazolyl-4-oxoquinolines 1,2,3-triazolyl-4-oxoquinolines 1,2,3-triazolyl-4-oxoquinolines
The 4- N-dodecyl) pyridinium moiety-containing compounds can be considered as prototype molecules for further chemical modifications and studies as cardioprotective/neuroprotective agents.
These results indicate autohydrolysis as a valuable alternative for the sustainable extraction of high value-added molecules for further use in industrial, food, cosmetic and health applications.
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These results suggest 9d as a promising candidate molecule for further preclinical evaluation against resistant TB strains.
These findings may render 6-MSITC as a promising molecule for further pharmacological studies on the investigation for disease-modifying treatment in PD.
Thus, 4-piperazinylquinoline linked isatin analog can serve as the prototype molecule for further development of a new class of anti-breast cancer agents.
We conclude that the isatin-linked benzothiazole analog can serve as a prototype molecule for further development of a new class of anti-breast cancer agents.
The total of these effects can be expressed in the form of an expanded energy expression for the rotational-vibrational energy of the diatomic molecule; for further discussion, see the texts listed in the Bibliography.
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