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African cobras (Naja species) represent one of the most encountered medically important snakes in Africa. They are classified as African spitting (Afronaja subgenus) and non-spitting cobras (Uraeus and Boulengerina subgenera) with similar and different characteristics. Snake venom toxins including three-finger toxin (3FTx), phospholipase A2 (PLA 2), and snake venom metalloproteinase (SVMP) cause snakebite envenomation leading to morbidity and mortality. The profile of the proteome of African cobra venoms will help to develop safer and more effective antivenoms. The approval of Captopril by the US Food and Drug Administration (FDA) for the treatment of cardiovascular diseases, has led to intensified research towards possible use of venom toxins as therapeutics. In this review, we compare the venom proteome profile of 3 African Naja subgenera. In both Afronaja and Boulengerina subgenera, 3FTx (Afronaja –69.79%; Boulengerina –60.56%) followed by PLA 2 (Afronaja –21.15%; Boulengerina –20.21%) dominated the venoms compared to the Uraeus subgenus dominated by 3FTx (84.55%) with little to no PLA 2 abundance (0.8%). The venom of subgenus Uraeus was distinct from the other two subgenera by the almost total absence of PLA 2 , thus indicating little or no contribution of PLA 2 in the envenomation caused by Uraeus compared to Afronaja and Boulengerina. Furthermore, we report studies on the experimental testing of African cobra venoms and toxins against diseases including anti-cancer properties. [Display omitted] • African spitting and non-spitting cobra venoms cause severe envenomation. • 3FTxs are the most dominant toxin of spitting and non-spitting cobras venoms. • African non-spiting cobra venom of the Uraeus genus constitutes little or no PLA 2. • African cobras have potential therapeutic applications against diseases including cancer. [ABSTRACT FROM AUTHOR]