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Figure 1. Mono sulfated steroids are derived from marine sources, and their pharmacological profile is shown in Table 1.
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Figure 2. Mono sulfated steroids are derived from marine sources, and their pharmacological profile is shown in Table 2.
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Figure 3. Mono sulfated steroids are derived from marine sources, and their pharmacological profile is shown in Table 3.
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Figure 4. Mono- and poly-sulfated steroids derived from marine sources, and their pharmacological profile, are shown in Table 4.
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Figure 5. Polysulfated steroids derived from marine sources, and their pharmacological profile is shown in Table 4.
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Figure 6. Sulfur-containing steroids and triterpenoids derived from marine invertebrates, sediments, crude oil, and other sources, and their pharmacological profile is shown in Table 5.
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Figure 7. Sulfur-containing steroids and triterpenoids derived from marine sediments, crude oil, and other sources, and their pharmacological profile is shown in Table 6.
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Figure 8. Sulfur-containing steroids and triterpenoids derived from marine sediments, crude oil, and other sources, and their pharmacological profile is shown in Table 7.
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Figure 9. Semi-synthetic and synthetic epithio steroids, and their pharmacological profile is shown in Table 8.
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Figure 10. The 3D graph shows the predicted and calculated antitumor activity of selected sulfated steroids (compound numbers: 28, 29, 40, 42, 43, 44, 45, 48, and 64) showing the highest degree of confidence, more than 91%. These sulfated steroids derived from marine sources can be used in clinical medicine as agents with strong antitumor activity.
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Figure 11. 3D column graph of sulfated steroids derived from marine sources that show anti-hypercholesterolemic activity. The letters represent the steroid numbers shown in Figure 1, Figure 2, Figure 3 and Figure 4 and Table 1, Table 2, Table 3, Table 4 and Table 5: Aâ(1), Bâ(14), Câ(16), Dâ(18), Eâ(19), Fâ(20), Gâ(21), Hâ(23), Iâ(24), Jâ(26), Kâ(31), Lâ(40), Mâ(41), Nâ(42), Oâ(43), and Pâ(52). Steroids that belong to this group, according to the data obtained by the PASS, have confirmed more than 90% of their biological activity.
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Figure 12. The 3D graph shows the predicted and calculated wound-healing activity of selected sulfated steroids (compound numbers: 14 (95.5%), 18 (93.8%), 19 (95.2%), 21 (92.8%), 29 (96.5%), 40 (95.3%), 41 (96.3%), 42 (97.5%), 43 (98.0%), 44 (97.7%), 60 (93.3%), and 61 (94.2%). These sulfated steroids show the highest degree of confidence, more than 92%.
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Figure 13. The 3D graph shows the predicted and calculated antitumor activity of selected sulfur-containing steroids (compound numbers): 98 (94.7%), 99 (94.7%), 100 (92.8%) and 105 (93.3%). These steroids show the highest degree of confidence, more than 92%.
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Figure 14. The 3D Graph (X and Y views) predicted and calculated activities of the spironolactone, which was isolated from the human urine extracts. According to PASS data, this steroid demonstrated seventeen different activities, with five activities having confidence of more than 90%. The main pharmacological properties and activities of spironolactone (73) are diuretic (99.1%), anti-hyperaldosteronism (96.3%), anti-hypertensive (94%), renal disease treatment (93.4%), and heart failure treatment (91.2%). As shown in numerous publications, spironolactone demonstrates properties as a potential diuretic, antihypertensive agent, or agent for the treatment of renal failure and heart failure, as well as an agent in the treatment of hyperaldosteronism (including Connâs syndrome) and female hirsutism (due to additional antiandrogenic actions). All these properties and activities are confirmed by the PASS data as shown in this figure and shown in Table 5.
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Figure 15. The 3D graph shows the predicted and calculated antitumor activity of selected semi- and synthetic epithio steroids (compound numbers): 122 (96.4%), 123 (96.6%), 124 (96.6%), 125 (93.2%), 126 (95.5%), 127 (96.2%), 128 (97.1%), 129 (97.0%), 131 (96.0%), 132 (93.9%), 133 (97.4%), and 138 (91.2%). These steroids show the highest degree of confidence, more than 91%.
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Figure 16. The 3D graph shows the predicted and calculated anti-secretoric activity of some an epithio steroids (compound numbers): 122 (94.8%), 123 (95.2%), 124 (95.2%), 126 (93.8%), 130 (90.6%), 131 (96.5%), and 132 (96.7%). These epithio steroids show the highest degree of confidence, more than 90%.
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