|
|
xiii | |
Editor Biography |
|
xvii | |
Foreword |
|
xxi | |
Preface |
|
xxiii | |
|
1 Therapeutics from natural products against neglected tropical diseases: an overview |
|
|
1 | (6) |
|
|
|
1 | (1) |
|
1.2 An overview of the book |
|
|
2 | (4) |
|
|
6 | (1) |
|
2 Marine natural products as strategic prototypes in the development of a new generation of antimalarial agents |
|
|
7 | (42) |
|
|
|
7 | (2) |
|
2.2 Antimalarial marine natural products |
|
|
9 | (25) |
|
2.2.1 Phenolic compounds and polyketides |
|
|
9 | (5) |
|
|
14 | (2) |
|
2.2.3 Endoperoxides and polyethers |
|
|
16 | (8) |
|
|
24 | (7) |
|
2.2.5 Peptides and depsipeptides |
|
|
31 | (2) |
|
|
33 | (1) |
|
|
34 | (1) |
|
|
35 | (1) |
|
|
36 | (11) |
|
|
47 | (2) |
|
3 Sesquiterpene lactones: a versatile class of structurally diverse natural products and their semisynthetic analogs as potential antimalarials |
|
|
49 | (38) |
|
|
|
49 | (2) |
|
3.2 Antimalarial potential of plant derived sesquiterpene lactones |
|
|
51 | (28) |
|
3.2.1 Artemisinin and its C-12 oxa (ether/ester) derivatives |
|
|
51 | (21) |
|
3.2.2 Germacranolides, guaianolides, and pseudoguiainolides antimalarials SLs |
|
|
72 | (6) |
|
3.2.3 Miscellaneous antimalarial sesquiterpene lactones |
|
|
78 | (1) |
|
3.3 Structural---activity relationships of sesquiterpene lactones |
|
|
79 | (1) |
|
|
79 | (1) |
|
|
80 | (1) |
|
|
80 | (1) |
|
|
81 | (6) |
|
4 Natural and synthetic quinoline molecules against tropical parasitic pathologies: an analysis of activity and structural evolution for developing new quinoline-based antiprotozoal agents |
|
|
87 | (78) |
|
|
|
|
|
|
88 | (1) |
|
4.2 Leishmaniasis, Chagas disease, and African sleeping sickness as protozoan neglected tropical diseases and quinoline-based molecules: background |
|
|
89 | (4) |
|
|
90 | (2) |
|
|
92 | (1) |
|
4.2.3 Human African trypanosomiasis |
|
|
93 | (1) |
|
4.3 Current chemotherapy and drugs on clinical trials |
|
|
93 | (2) |
|
4.4 Recent phytoresearch on alkaloid extracts from plants and marine organisms for drug development against NTDs |
|
|
95 | (4) |
|
4.5 Quinolines: functional and structural diversity |
|
|
99 | (2) |
|
4.6 Natural sources of quinoline alkaloids with antiparasitic activity |
|
|
101 | (4) |
|
4.7 Synthetic efforts for targeted quinoline compounds |
|
|
105 | (22) |
|
4.7.1 Synthesis of polyfunctionalized quinolines from unsubstituted anilines: Route A |
|
|
106 | (13) |
|
4.7.2 Synthesis of polyfunctionalized quinolines from ortho-substituted anilines: Route B |
|
|
119 | (8) |
|
4.8 Quinoline compounds as antitrypanosomal agents |
|
|
127 | (21) |
|
4.8.1 Simple polyfunctionalized quinolines |
|
|
127 | (15) |
|
4.8.2 Polycyclic quinoline molecules |
|
|
142 | (6) |
|
|
148 | (1) |
|
|
148 | (1) |
|
|
149 | (1) |
|
|
150 | (14) |
|
|
164 | (1) |
|
5 Promising trypanocidal heterocyclic compounds of natural origin and their synthetic analogs |
|
|
165 | (54) |
|
Edeildo F. da Silva-Junior |
|
|
|
|
|
166 | (2) |
|
5.2 Trypanosomiasis: Chagas disease and African sleeping sickness |
|
|
168 | (4) |
|
|
168 | (2) |
|
5.2.2 Human African trypanosomiasis or sleeping sickness |
|
|
170 | (2) |
|
5.3 Promising heterocyclic compounds from natural resources |
|
|
172 | (22) |
|
5.3.1 Amaranthaceae family |
|
|
172 | (1) |
|
5.3.2 Amaryllidaceae family |
|
|
173 | (1) |
|
|
174 | (1) |
|
|
175 | (4) |
|
5.3.5 Bignoniaceae family |
|
|
179 | (1) |
|
|
180 | (1) |
|
|
181 | (1) |
|
|
181 | (1) |
|
|
182 | (1) |
|
|
183 | (1) |
|
5.3.11 Menispermaceae family |
|
|
184 | (1) |
|
|
184 | (1) |
|
5.3.13 Podospongiidae family |
|
|
184 | (2) |
|
5.3.14 Ranunculaceae family |
|
|
186 | (1) |
|
|
187 | (1) |
|
|
187 | (3) |
|
|
190 | (2) |
|
5.3.18 Sapindaceae family |
|
|
192 | (1) |
|
5.3.19 Vesiculariidae family |
|
|
193 | (1) |
|
5.3.20 Zygophyllaceae family |
|
|
193 | (1) |
|
5.4 Synthesis of promising active compounds inspired by nature |
|
|
194 | (25) |
|
|
194 | (3) |
|
5.4.2 β-Carboline analogs |
|
|
197 | (1) |
|
5.4.3 Crassiflorone analogs |
|
|
197 | (2) |
|
|
199 | (1) |
|
|
199 | (2) |
|
5.4.6 Epoxy-α-acyloxycarboxamide analogs |
|
|
201 | (2) |
|
5.4.7 Cinchona alkaloids and bile acid hybrids |
|
|
203 | (1) |
|
|
203 | (2) |
|
|
205 | (14) |
5.5 Concluding remarks |
|
206 | (1) |
5.6 List of abbreviations |
|
206 | (1) |
Acnowledgments |
|
207 | (1) |
References |
|
207 | (206) |
|
6 Oxidative stress in schistosomiasis, echinococcosis, and trypanosomiasis: a therapeutic approach |
|
|
219 | (22) |
|
|
|
|
|
|
219 | (2) |
|
6.2 Life cycles of echinococcosis, trypanosomiasis, and schistosomiasis |
|
|
221 | (2) |
|
|
221 | (1) |
|
6.2.2 Trypanosomiasis and Chagas disease |
|
|
221 | (2) |
|
|
223 | (1) |
|
6.3 Role of oxidative stress in the pathogenesis of schistosomiasis, echinococcosis, and trypanosomiasis |
|
|
223 | (1) |
|
6.4 Oxidative stress associated therapeutic strategies |
|
|
224 | (9) |
|
6.4.1 Chagas disease and trypanosomiasis |
|
|
224 | (4) |
|
|
228 | (2) |
|
|
230 | (3) |
|
|
233 | (1) |
|
|
234 | (1) |
|
|
235 | (6) |
|
7 Plant-derived compounds against protozoan neglected diseases: toward sustainable drug development |
|
|
241 | (52) |
|
|
|
|
241 | (3) |
|
7.1.1 Protozoan neglected diseases |
|
|
243 | (1) |
|
7.1.2 Current treatment approaches and limitations |
|
|
244 | (1) |
|
7.2 Natural products as therapeutic agents against protozoan diseases |
|
|
244 | (4) |
|
7.2.1 Plant-derived secondary metabolites as antiprotozoal leads and drugs |
|
|
245 | (1) |
|
7.2.2 Isolation and extraction of plant-derived antiprotozoal agents |
|
|
245 | (3) |
|
7.3 Human African trypanosomiasis |
|
|
248 | (17) |
|
7.3.1 Etiology of the disease |
|
|
248 | (3) |
|
7.3.2 Antitrypanosomal drugs and associated challenges |
|
|
251 | (1) |
|
7.3.3 Plant-derived antihuman trypanosomal products |
|
|
252 | (13) |
|
|
265 | (7) |
|
7.4.1 Etiology of the disease |
|
|
265 | (1) |
|
7.4.2 Antichagasic drugs and associated challenges |
|
|
265 | (1) |
|
7.4.3 Plant-derived antichagasic products |
|
|
266 | (6) |
|
|
272 | (10) |
|
7.5.1 Etiology of the disease |
|
|
272 | (1) |
|
7.5.2 Antileishmanial drugs and associated challenges |
|
|
273 | (1) |
|
7.5.3 Plant-derived antileishmanial products |
|
|
274 | (8) |
|
|
282 | (1) |
|
|
282 | (1) |
|
|
283 | (9) |
|
|
292 | (1) |
|
8 Leishmaniasis control: limitations of current drugs and prospects of natural products |
|
|
293 | (58) |
|
|
|
|
|
|
|
|
|
|
293 | (2) |
|
8.2 Leishmaniasis: etiology and epidemiology |
|
|
295 | (3) |
|
8.3 Parasites' survival mechanisms and possible drug targets |
|
|
298 | (3) |
|
8.4 Current therapeutic options and their limitations |
|
|
301 | (4) |
|
8.4.1 Pentavalent antimonials |
|
|
301 | (2) |
|
|
303 | (1) |
|
8.4.3 Pentamidine and paromomycin |
|
|
303 | (1) |
|
8.4.4 Amphotericin B and its lipid formulation, AmBisome |
|
|
304 | (1) |
|
8.5 Prospects of natural products in antileishmanial drug discovery |
|
|
305 | (27) |
|
|
306 | (8) |
|
|
314 | (8) |
|
|
322 | (1) |
|
|
322 | (8) |
|
|
330 | (1) |
|
|
331 | (1) |
|
8.6 Therapeutic role of natural products in combating multidrug resistance |
|
|
332 | (2) |
|
|
334 | (1) |
|
|
335 | (1) |
|
|
335 | (16) |
|
9 Natural antileprotic agents: a boon for the management of leprosy |
|
|
351 | (22) |
|
|
|
|
|
|
351 | (1) |
|
9.2 Current available treatments and their associated disadvantages |
|
|
352 | (1) |
|
9.3 Role of natural agents in the treatment of leprosy |
|
|
353 | (1) |
|
9.4 Plant-derived antileprotic agents |
|
|
354 | (8) |
|
|
354 | (2) |
|
|
356 | (1) |
|
|
357 | (1) |
|
|
358 | (1) |
|
|
359 | (1) |
|
|
360 | (1) |
|
|
360 | (1) |
|
|
361 | (1) |
|
|
361 | (1) |
|
9.5 Animal/microbe-derived antileprotic agents |
|
|
362 | (2) |
|
|
362 | (1) |
|
|
363 | (1) |
|
9.6 Patents associated with herbal agents in leprosy |
|
|
364 | (1) |
|
|
364 | (5) |
|
|
369 | (1) |
|
|
369 | (4) |
|
10 Aloe vera: a promising hope against Buruli ulcer |
|
|
373 | (12) |
|
|
|
373 | (2) |
|
10.2 Aloe vera: a promising hope against Buruli ulcer |
|
|
375 | (3) |
|
|
375 | (1) |
|
|
376 | (1) |
|
10.2.3 Studies with Aloe vera against Buruli ulcer |
|
|
376 | (2) |
|
10.3 Future hopes and concluding remarks |
|
|
378 | (1) |
|
|
379 | (6) |
|
11 Plant and marine products: a promising hope in the search of therapeutics against dengue |
|
|
385 | (22) |
|
|
|
|
|
385 | (1) |
|
11.1.1 Dengue: a pandemic concern |
|
|
386 | (1) |
|
11.2 Transmission and potential strategies for inhibition of dengue |
|
|
386 | (3) |
|
11.3 Clinical molecules and therapies |
|
|
389 | (1) |
|
11.4 Natural product-based antidengue research |
|
|
389 | (10) |
|
11.4.1 Plant-derived compounds with antidengue potential |
|
|
391 | (6) |
|
11.4.2 Marine natural products for the treatment of dengue |
|
|
397 | (2) |
|
|
399 | (2) |
|
|
401 | (1) |
|
|
401 | (6) |
|
12 Total synthetic approaches for lucidone: a promising natural lead candidate against dengue infection |
|
|
407 | (6) |
|
|
|
407 | (1) |
|
|
408 | (1) |
|
|
408 | (1) |
|
12.2.2 Spectral properties of lucidone |
|
|
409 | (1) |
|
12.3 Total synthetic approaches for lucidone |
|
|
409 | (2) |
|
|
411 | (1) |
|
|
411 | (2) |
Index |
|
413 | |