The present study aimed to enhance salicin and direct regeneration inwillow (Salix safsaf Forssk) using the sodium nitroprusside (SNP) regulation of nitric oxide (NO) and vinasse for its nutrition effect in culture medium. Internodes of Salix safsaf were cultured on Murashige and Skoog (MS) medium supplemented with benzyl adenine (BA) (0.25 mg L-1) and different concentrations of SNP (0, 5, 10, 15, and 20 mg L-1) or vinasse (0, 5, 10, and 20%) to examine shoot regeneration, antioxidant defense enzyme activity, total phenolic compounds, flavonoids, and salicine contents. The reported data revealed that application of SNP at15 mg L-1 and vinasse at10% induced asignificant effectin vitro Salix safsaf shoot regeneration. To confirm that, nitric oxide is required for auxin-mediated activation of cell division in a dose-dependent manner. A concentration of 15 mg L-1 SNP promotes regeneration and salicin accumulation (3162.16mg/100g) during signaling action. On the other hand, the cross talk effect of nitric oxide and vinasse combination inSalix safsaf significantly induced a synergistic effect on direct propagation more than vinasse alone. SNP significantly stimulates salicylate accumulation in a dose-dependent manner, but the data on the association of vinasse and SNP on salicylate up-regulation showed a significant reduction in salicin accumulation when SNP was combined with 10% vinasse, which directly affected the signaling action of SNP as secondary product stimulators. Vinasse's phenolic compounds affect directly on thereduction activity ofSNP to suppress its signaling action, or indirectly by inhibiting the sequence cascade of the SNP signaling transduction process to decrease the accumulation of salicin contents. Data confirmed that vinasse andSNP stimulatedtheantioxidant enzymes activity throw quenching thestimulated reactive oxygen species that produced via SNP. Results show that modified media with SNP administration at 15 mg L-1 and the combination of vinasse at 10% and SNP at 15 mg L-1 are recommended for modifying tissue culture media for induced direct regeneration and salicin accumulation in tissue culture applications, which will be very useful for commercial salicin overproduction as a biological active ingredient in willows.