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TABLE 12.1 (Continued)
Source of Natural Products Bioactive Compound Mode of Action Reference
Ficus benghalensis Morus alba
Ilex paraguariensis 3,5-O-dicaffeoylquinic acid Zingiber officinale Nymphaea stellata
Pelargonidin and leucocyanidin Methyl ursolate, betulinic acid,
kuwanon E, morusin, and cyclomorusin
Gingerol • Increasing insulin sensitivity Said et al. (2007) Nymphayol • Improving the generation of pancreatic β cells Semwal et al. (2021)
• Stimulating pancreatic β cells for secreting insulin Kadam et al. (2019)
• Reducing lipid peroxidation and protecting pancreatic β cells Sharma et al. (2022)
• Elevation in the level of serum GLP-1 Semwal et al. (2021)
 273
274 
investigations and the mechanisms of action of natural products as agents for antidiabetic treatment. To summarize, natural products, particularly those derived from plants, are significant reservoirs of chemical compounds with diverse structures that may provide a therapeutic option for managing type 2 diabetes through various mechanisms.
TABLE 12.2 Antidiabetic Natural Products and Their Chemical Structures
Natural Products Derived from Medicinal Plants Chemical Structures
Carthamus tinctorius (serotonin derivatives: N-p-coumaryl serotonin, N-feruloyl serotonin)
Laminaria japonica (butyl-isobutylphthalate)
Allium sativum (allicin)
Capsicum sp. (capsaicin: 8-methyl-N-vanillyl-
6-nonenamide)
Blueberry (anthocyanins: Malvidin-3-glucoside, malvidin-3-galactoside)
⏎
Various plant species (resveratrol: 3,5,40-trihydroxy-trans-stilbene)
Zingiber officinale (gingerol)
 275
TABLE 12.2 (Continued)
Natural Products Derived from Medicinal Plants Chemical Structures
Pterocarpus marsupium (marsupsin, pterostilbene)
Curcuma longa (curcumin)

12.7 FUTURE SCOPE

Studies of naturally occurring chemicals have shown promising results in combating diabetes. The rising prevalence of diabetes and the limitations of present treatments underscore the need for innovative and effective therapeutic strategies. Finding effective natural remedies for diabetes could proceed down various avenues. New antidiabetic compounds will likely be discovered in as-yet-undiscovered natural deposits. In this regard, metagenomics offers a potential approach. When it comes to creating safe and effective medications, knowledge about the mechanism of action of natural products is essential. Metabolomics, transcriptomics, and proteomics are needed to learn about the mechanisms of action of these drugs. It has been discovered that natural component combination therapy with antidiabetic medicines can boost the efficacy of both therapies while decreasing the likelihood of unwanted side effects. Natural product efficacy and safety must be established through clinical research. In the future, these substances will be evaluated in carefully planned clinical trials. The potential exists in the field of precision medicine for the use of natural products for tailored treatment approaches in patients with diabetes. Natural compounds with antidiabetic properties have great potential as research subjects for the discovery of new and improved treatments for diabetes.

KEYWORDS

• diabetes mellitus
• natural products
• antidiabetic properties
• herbal remedies
• hypoglycemic agents
• medicinal plants
276 

REFERENCES

Abdel Raoof, G. F.; Mohamed, K. Y. Natural products for the management of diabetes. In: Studies in Natural
Products Chemistry. 1st edn. Elsevier B.V. 2018, Vol. 59. doi: 10.1016/B978-0-444-64179-3.00010-4
Aderonke Otunola, G.; Jide Afolayan, A. A review of the antidiabetic activities of ginger. In: Ginger Cultivation
and its Antimicrobial and Pharmacological Potentials. 2020, pp. 1–13. doi: 10.5772/intechopen.88899
Ahmad, A.; Ahmad, N.; Anis, M.; Faisal, M.; Alatar, A. A.; Abdel-Salam, E. M.; Meena, R. P.; Sivanesan, I.
Biotechnological advances in pharmacognosy and in vitro manipulation of pterocarpus marsupium roxb. Plants. 2022, 11(3), 1–39. doi: 10.3390/plants11030247
Ajuwon, O. R.; Ayeleso, A. O.; Adefolaju, G. A. The potential of South African herbal tisanes, rooibos and
honeybush in the management of type 2 diabetes mellitus. Molecules. 2018, 23(12), 3207. doi: 10.3390/ molecules23123207
Akar, F.; Pektas, M. B.; Tufan, C.; Soylemez, S.; Sepici, A.; Ulus, A. T.; Gokalp, B.; Ozturk, K.; Surucu, H. S.
Resveratrol shows vasoprotective effect reducing oxidative stress without affecting metabolic disturbances in insulin-dependent diabetes of rabbits. Cardiovasc. Drugs Ther. 2011, 25(2), 119–131. doi: 10.1007/ s10557-010-6255-7
Anand, A.; Chawla, J.; Mahajan, A.; Sharma, N.; Khurana, N. Therapeutic potential of epigallocatechin gallate.
Int. J. Green Pharm. 2017, 11(3), S364–S370.
Anand, V.; Manikandan, Kumar, V.; Kumar, S.; Pushpa; Hedina, A. Phytopharmacological overview of Psidium
guajava linn. Pharmacogn. J. 2016, 8(4), 314–320. doi: 10.5530/pj.2016.4.3
Arif, A.; Jia, J.; Willard, B.; Li, X.; Fox, P. L. Multisite phosphorylation of S6K1 directs a kinase phospho-code
that determines substrate selection. Mol. Cell. 2019, 73(3), 446-457.e6. doi: 10.1016/j.molcel.2018.11.017
Campos-Florián, J.; Bardales-Valdivia, J.; Caruajulca-Guevara, L.; Cueva-Llanos, D. Anti-diabetic effect of
Coffea arabica, in alloxan-induced diabetic rats. Emirates J. Sci. Food Agric. 2013, 25(10), 772–777. doi:
10.9755/ejfa.v25i10.16409
Cano-Marquina, A.; Tarín, J. J.; Cano, A. The impact of coffee on health. Maturitas. 2013, 75(1), 7–21. doi:
10.1016/j.maturitas.2013.02.002
Christiansen, C. B.; Gabe, M. B. N.; Svendsen, B.; Dragsted, L. O.; Rosenkilde, M. M.; Holst, J. J. The impact
of short-chain fatty acids on glp-1 and pyy secretion from the isolated perfused rat colon. Am. J. Physiol. Gastrointest. Liver Physiol. 2018, 315(1), G53–G65. doi: 10.1152/ajpgi.00346.2017
Couturier, K.; Qin, B.; Batandier, C.; Awada, M.; Hininger-Favier, I.; Canini, F.; Leverve, X.; Roussel, A. M.;
Anderson, R. A. Cinnamon increases liver glycogen in an animal model of insulin resistance. Metab.: Clin. Exp. 2011, 60(11), 1590–1597. doi: 10.1016/j.metabol.2011.03.016
Deokate, U.; Upadhye, M. Antioxidant potential of phytoconstituents with special emphasis on curcumin.
Ginger—Cultivation and Use. 2023, doi: 10.5772/intechopen.103982
Deyno, S.; Eneyew, K.; Seyfe, S.; Tuyiringire, N.; Peter, E. L.; Muluye, R. A.; Tolo, C. U.; Ogwang, P. E.
Efficacy and safety of cinnamon in type 2 diabetes mellitus and pre-diabetes patients: A meta-analysis and meta-regression. Diabetes Res. Clin. Pract. 2019, 156, 107815. doi: 10.1016/j.diabres.2019.107815
Dhanabal, S. P.; Kumaradoss, M.; Maruga, M. Pharmacognostical, Antidiabetic and Antioxidant Studies on.
December. 2018.
Duarte, A. M.; Guarino, M. P.; Barroso, S.; Gil, M. M. Phytopharmacological strategies in the management of
type 2 diabetes mellitus. In: Foods (Vol. 9, Issue 3). 2020, doi: 10.3390/foods9030271
Eidi, A.; Eidi, M.; Esmaeili, E. Antidiabetic effect of garlic (Allium sativum L.) in normal and streptozotocin-
induced diabetic rats. Phytomedicine. 2006, 13(9–10), 624–629. doi: 10.1016/j.phymed.2005.09.010
El Gayar, M. H.; Aboromia, M. M. M.; Ibrahim, N. A.; Abdel Hafiz, M. H. Effects of ginger powder
supplementation on glycemic status and lipid profile in newly diagnosed obese patients with type 2 diabetes mellitus. Obes. Med. 2019, 14(2018), 100094. doi: 10.1016/j.obmed.2019.100094
El-Abhar, H. S.; Schaalan, M. F. Phytotherapy in diabetes: Review on potential mechanistic perspectives.
World J. Diabetes. 2014, 5(2), 176. doi: 10.4239/wjd.v5.i2.176
Elshater, A.-E. A.; Mohammed, H. A.; Al-Amgad, Z.; Ali, R. A. Potential of Aloe vera and amaryl in
amelioration of hyperglycemia correlated with streptozotocin induced diabetes. SVU- Int. J. Vet. Sci. Res. 2022, 5(4), 41–52. doi: 10.21608/svu.2022.149203.1213
 277
Escandón-Rivera, S. M.; Mata, R.; Andrade-Cetto, A. Molecules isolated from Mexican hypoglycemic plants:
A review. Molecules 2020, 25(18), 1–33. doi: 10.3390/molecules25184145
Gao, X.; Li, B.; Jiang, H.; Liu, F.; Xu, D.; Liu, Z. Dioscorea opposita reverses dexamethasone induced insulin
resistance. Fitoterapia. 2007, 78(1), 12–15. doi: 10.1016/j.fitote.2006.09.015
Gautam, S.; Paithankar, V .; Vyas, J.; Wankhade, A. Berberine and its Relevance IN anti-Diabetic Activity. 2021,
11(2), 242–251. https://www.academia.edu/download/65858283/36.pdf
Ghosh, S.; Saha, S. Tinospora cordifolia: One plant, many roles. Anc. Sci. Life. 2012, 31(4), 151. doi: 10.4103/
0257-7941.107344
Goel, R.;Bhatia, D.; Gilani, S. J.; Katiyar, D. Medicinal plants as antidiabetics: A review. Int. Bull. Drug Res.
2012, 1(2), 100–107.
Golovinskaia, O.; Wang, C. K. The hypoglycemic potential of phenolics from functional foods and their
mechanisms. Food Sci. Hum. Wellness. 2023, 12(4), 986–1007. doi: 10.1016/j.fshw.2022.10.020
Gonzales, A. M.; Orlando, R. A. Curcumin and resveratrol inhibit nuclear factor-kappaB-mediated cytokine
expression in adipocytes. Nutr. Metab. (Lond.) 2008, 5, 17. https://doi.org/10.1186/1743-7075-5-17
González-Flores, D. Ingestion of Japanese plums (Prunus salicina Lindl. cv. Crimson Globe) increases the urinary
6-sulfatoxymelatonin and total antioxidant capacity levels in young. middle-aged and elderly humans: Nutritional and functional characterization of their content. J. Food & Nutr . Res. 2011, 50(January 2011), 229–236. http://search.
ebscohost.com/login.aspx?direct=true&profile=ehost&scope=site&authtype=crawler&jrnl=13368672&AN=6 9859318&h=zPCKRcfGYf0CFqNn7gao70rHyIxNi/nICiToAOC5xTyf5vwnWzeZjr0hGzro5j3KsoNwT5B7g/ GxajZV/rALmw==&crl=c
Grace, M. H.; Ribnicky, D. M.; Kuhn, P.; Poulev, A.; Logendra, S.; Yousef, G. G.; Raskin, I.; Lila, M. A.
Hypoglycemic activity of a novel anthocyanin-rich formulation from lowbush blueberry, vaccinium angustifolium aiton. Phytomedicine. 2009, 16(5), 406–415. doi: 10.1016/j.phymed.2009.02.018
Guo, J.; Li, L.; Pan, J.; Qiu, G.-Q.; Li, A.; Huang, G.; Xu, L. [Pharmacological mechanism of Semen Litchi on
antagonizing insulin resistance in rats with type 2 diabetes]. Zhong Yao Cai. 2004, 27(6), 435–438. https://
api.semanticscholar.org/CorpusID:28063784
Gupta, R. C.; Chang, D.; Nammi, S.; Bensoussan, A.; Bilinski, K.; Roufogalis, B. D. Interactions between
antidiabetic drugs and herbs: An overview of mechanisms of action and clinical implications. Diabetol. Metab. Syndr. 2017, 9(1), 1–12. doi: 10.1186/s13098-017-0254-9
Haghani, F.; Arabnezhad, M. R.; Mohammadi, S.; Ghaffarian-Bahraman, A. Aloe vera and streptozotocin-
induced diabetes mellitus. Rev. Bras. Farmacogn. 2022, 32(2), 174–187. doi: 10.1007/s43450-022-00231-3 Grover, J. K.; Y adav , S.; V ats, V. Medicinal_plants_of_India_with_anti_diab. J. Ethnopharmacol. 2002, 81, 81–100. Jiao, P.; Feng, B.; Li, Y.; He, Q.; Xu, H. Hepatic ERK activity plays a role in energy metabolism. Mol. Cell.
Endocrinol. 2013, 375(1–2), 157–166. doi: 10.1016/j.mce.2013.05.021 Jn, S.; Ps, C.; Vd, M.; Sk, J. Role of fenugreek (Trigonella foenum graecum) on in management of diabetes
disease. ~ 184 ~ J Pharmacogn. Phytochem. 2019, 8(4), 184–187. http://dx.doi.org/10.1100/2012/859892. Kadam, R. A.; Dhumal, N. D.; Khyade, V. B. The mulberry, morus alba (L.): The medicinal herbal source for
human health. Int. J. Curr . Micr obiol. Appl. Sci. 2019, 8(04), 2941–2964. doi: 10.20546/ijcmas.2019.804.341 Kamble, H.; Kandhare, A. D.; Bodhankar, S.; Mohan, V.; Thakurdesai, P. Effect of low molecular weight
galactomannans from fenugreek seeds on animal models of diabetes mellitus. Biomed. Aging Pathol. 2013,
3(3), 145–151. doi: 10.1016/j.biomag.2013.06.002 Kanetkar, P.; Singhal, R.; Kamat, M. Gymnema sylvestre: A memoir. J. Clin. Biochem. Nutr. 2007, 41(2),
77–81. doi: 10.3164/jcbn.2007010
Kassaian, N.; Azad, L.; Kassaian, N. Effect of fenugreek seeds on blood glucose and lipid profiles in type 2
diabetic patients. Int. J. Vitam. Nutr. Res., 2009, 79(1), 34–39. Khalil, O. A. Antidiabetic activity of Rosmarinus officinalis and its relationship with the antioxidant property.
Afr. J. Pharm. Pharmacol. 2012, 6(14). doi: 10.5897/ajpp12.162 Khan, A. R.; Mushtaq, N.; Fiaz, H.; Islam, Z. U. Antioxidative properties of spices and their impact on
postprandial blood glucose in humans. Adv. Life Sci. 2019, 7(1), 5–9. Klajnert, B.; Przygodzki, T. Therapeutic applications of dendrimers. Postepy Biochem. 2003, 49(4), 290–297. Klein, R.; Klein, B. E. K.; Moss, S. E.; Cruickshanks, K. J. The medical management of hyperglycemia over a
10-year period in people with diabetes. Diabetes Care. 1996, 19(7), 744–750. doi: 10.2337/diacare.19.7.744
278 
Krishnasamy, G.; Muthusamy, K.; Chellappan, D. R.; Subbiah, N. Antidiabetic, antihyperlipidaemic, and
antioxidant activity of syzygium densiflorum fruits in streptozotocin and nicotinamide-induced diabetic rats.
Pharm. Biol. 2016, 54(9), 1716–1726. doi: 10.3109/13880209.2015.1125932 Kumar, A.; Goel, M. K.; Jain, R. B.; Khanna, P.; Chaudhary, V. India towards diabetes control: Key issues.
Australas. Med. J. 2013, 6(10), 524–531. doi: 10.4066/AMJ.2013.1791 Kumar, R.; Saha, P.; Lokare, P.; Datta, K.; Selvakumar, P.; Chourasia, A. Systemic review of ocimum sanctum
(Tulsi): Morphological characteristics, phytoconstituents and therapeutic applications. Int. J. Res. Appl. Sci.
Biotechnol. 2022, 9(2), 221–226. doi: 10.31033/ijrasb.9.2.15 Laha, S.; Paul, S. Gymnema sylvestre (Gurmar): A potent herb with anti-diabetic and antioxidant potential.
Phcog. J. 2019, 11(2), 201–206. doi: 10.5530/pj.2019.11.33 Lee, B. H.; Chen, C. H.; Hsu, Y. Y.; Chuang, P. T.; Shih, M. K.; Hsu, W. H. Polysaccharides obtained from
cordyceps militaris alleviate hyperglycemia by regulating gut microbiota in mice fed a high-fat/sucrose diet.
Foods. 2021, 10(8), 1870. doi: 10.3390/foods10081870 Lee, J.; Noh, S.; Lim, S.; Kim, B. Plant extracts for type 2 diabetes: From traditional medicine to modern drug
discovery. Antioxidants. 2021, 10(1), 1–42. doi: 10.3390/antiox10010081 Les, F.; Cásedas, G.; Gómez, C.; Moliner, C.; Valero, M. S.; López, V. The role of anthocyanins as antidiabetic
agents: From molecular mechanisms to in vivo and human studies. J. Physiol. Biochem. 2021, 77(1), 109–131.
doi: 10.1007/s13105-020-00739-z
Leung, L.; Birtwhistle, R.; Kotecha, J.; Hannah, S.; Cuthbertson, S. Anti-diabetic and hypoglycaemic effects
of Momordica charantia (bitter melon): A mini review. Br. J. Nutr. 2009, 102(12), 1703–1708. doi: 10.1017/
S0007114509992054 Li, J.; Liu, T.; Wang, L.; Guo, X.; Xu, T.; Wu, L.; Qin, L.; Sun, W. Antihyperglycemic and antihyperlipidemic
action of cinnamaldehyde in C57blks/j Db/db mice. J. Tradit. Chin. Med. 2012, 32(3), 446–452. doi: 10.1016/
s0254-6272(13)60053-9 Liu, C. M.; Ma, J. Q.; Sun, J. M.; Feng, Z. J.; Cheng, C.; Yang, W.; Jiang, H. Association of changes in
ER stress-mediated signaling pathway with lead-induced insulin resistance and apoptosis in rats and their
prevention by A-type dimeric epigallocatechin-3-gallate. Food Chem. Toxicol. 2017, 110(September),
325–332. doi: 10.1016/j.fct.2017.10.040
Liu, Y.; Zhang, H.; Dai, X.; Zhu, R.; Chen, B.; Xia, B.; Ye, Z.; Zhao, D.; Gao, S.; Orekhov, A. N.; Zhang, D.;
W ang, L.; Guo, S. A comprehensive review on the phytochemistry , pharmacokinetics, and antidiabetic effect
of Ginseng. Phytomedicine. 2021, 92, 153717. doi: 10.1016/j.phymed.2021.153717 Lopes, G.; Silva, M.; Vasconcelos, V. The pharmacological potential of cyanobacteria. The Pharmacological
Potential of Cyanobacteria. 2022, 57(October), 1–340. doi: 10.1016/B978-0-12-821491-6.00011-9 Ma, J.; Meng, X.; Liu, Y.; Yin, C.; Zhang, T.; Wang, P.; Park, Y. K.; Jung, H. W. Effects of a rhizome aqueous
extract of Dioscorea batatas and its bioactive compound, allantoin in high fat diet and streptozotocin-induced
diabetic mice and the regulation of liver, pancreas and skeletal muscle dysfunction. J. Ethnopharmacol.
2020, 259(February), 112926. doi: 10.1016/j.jep.2020.112926 Madiwalar, V. S.; Dwivedi, P. S. R.; Patil, A.; Gaonkar, S. M. N.; Kumbhar, V. J.; Khanal, P.; Patil, B. M. Ficus
benghalensis promotes the glucose uptake- Evidence with in silico and in vitro. J. Diabetes Metab. Disord.
2022, 21(1), 429–438. doi: 10.1007/s40200-022-00989-2 Magnuson, B.; Ekim, B.; Fingar, D. C. Regulation and function of ribosomal protein S6 kinase (S6K) within
mTOR signalling networks. Biochem. J. 2012, 441(1), 1–21. doi: 10.1042/BJ20110892 Manikandan, R.; Anand, A. V.; Kumar, S.; Pushpa. Phytochemical and in vitro antidiabetic activity of psidium
guajava leaves. Phcog. J. 2016, 8(4), 392–394. doi: 10.5530/pj.2016.4.13 Material, E. S.; Society, T. R.; Figure, S. Electronic Supplementary Material (ESI) for Food & Function. 2019,
361, 0–6. Mohammadi, E.; Behnam, B.; Mohammadinejad, R.; Guest, P. C.; Simental-Mendía, L. E.; Sahebkar, A.
Antidiabetic properties of curcumin: Insights on new mechanisms. Adv . Exp. Med. Biol. 2021, 1291(August),
151–164. doi: 10.1007/978-3-030-56153-6_9
Muley, A.; Muley, P.; Shah, M. Coffee to reduce risk of type 2 diabetes? : A systematic review. Curr. Diabetes
Rev. 2012, 8(3), 162–168. doi: 10.2174/157339912800564016
Naimi, M.; Vlavcheski, F.; Shamshoum, H.; Tsiani, E. Rosemary extract as a potential anti-hyperglycemic
agent: Current evidence and future perspectives. Nutrients. 2017, 9(9), 1–19. doi: 10.3390/nu9090968
 279
Nasser Singab, A.; Youssef, F. S. Medicinal plants with potential antidiabetic activity and their assessment.
Med. Aromat. Plants. 2014, 03(01), 1–12. doi: 10.4172/2167-0412.1000151 Noh, J. S.; Park, C. H.; Yokozawa, T. Treatment with oligonol, a low-molecular polyphenol derived from
lychee fruit, attenuates diabetes-induced hepatic damage through regulation of oxidative stress and lipid
metabolism. Br. J. Nutr. 2011, 106(7), 1013–1022. doi: 10.1017/S0007114511001322 Olatunde, A.; Mohammed, A.; Ibrahim, M. A.; Shuaibu, M. N. Influence of methoxylation on the anti-diabetic
activity of ρ-hydroxybenzaldehyde in type 2 diabetic rat model. In: Phytomedicine Plus (Vol. 1, Issue 1).
Elsevier B.V. 2021, doi: 10.1016/j.phyplu.2020.100003 Pathak, R.; Sharma, H. A review on medicinal uses of cinnamomum verum (Cinnamon). J. Drug Deliv. Ther.
2021, 11(6-S), 161–166. doi: 10.22270/jddt.v11i6-s.5145 Patole, V. C.; Awari, D.; Chaudhari, S. Resveratrol-loaded microsponge gel for wound healing: In vitro and in
vivo characterization. Turk. J. Pharm. Sci. 2023, 20(1), 23–34. doi: 10.4274/tjps.galenos.2022.93275 Paul, S. A review on ethno medicinal plants of southern parts of West Bengal with anti-diabetic potential. ~ 98
~ J. Med. Plants Stud. 2022, 10(4), 98–101. www.plantsjournal.com Poli, V.; Aparna, Y.; Reddy Motireddy, S. 6-Gingerol, new insights into its anti-diabetic potential with special
reference to AMPK pathway: A review. J. Food Nutr Res. 2022, 10(10), 681–695. doi: 10.12691/jfnr-10-10-6 Poolsup, N.; Suksomboon, N.; Kurnianta, P. D. M.; Deawjaroen, K. Effects of curcumin on glycemic control
and lipid profile in prediabetes and type 2 diabetes mellitus: A systematic review and meta-analysis. PLoS
One. 2019, 14(4), 1–18. doi: 10.1371/journal.pone.0215840 Puri, D.; Prabhu, K.; Murthy, P. Mechanism of action of a hypoglycemic principle isolated from fenugreek
seeds. J. Physiol. Pharmacol. 2002, 46, 457–462. Qin, B.; Panickar, K. S.; Anderson, R. A. Cinnamon: Potential role in the prevention of insulin resistance,
metabolic syndrome, and type 2 diabetes. J. Diabetes Sci. T echnol. 2010, 4(3), 685–693. doi: 10.1177/19322968
1000400324 Rajagopal, K.; Sasikala, K. Antihyperglycaemic and antihyperlipidaemic effects of nymphaea stellata in
alloxan-induced diabetic rats. Singapore Med. J. 2008, 49(2), 137–141. Sabet, F.; Asgary, S.; Rahimi, P.; Mahzouni, P.; Madani, H. Antidiabetic effect of hydroalcoholic extract of
Carthamus tinctorius L. in alloxan-induced diabetic rats. J. Res. Med. Sci. 2012, 17(6), 386–392. Said, A.; Ross, M.; Trout, K.; Zhang, J. Simulation of surface water for un-gauged areas with storage-attenuation
wetlands. J. Am. Water Resour. Assoc. 2007, 43(2), 546–556. doi: 10.1111/j.1752-1688.2007.00043.x Sarah, W .; Gojka, R.; Sicree, R.; Hilary King, A. G. Estimates for the year 2000 and projections for 2030. World
Health. 2004, 27(5), 1047–1053. Sayago, C.; Camargo, V.; Barbosa, F.; Gularte, C.; Pereira, G.; Miotto, S.; Cechinel Filho, V.; Luiz Puntel, R.;
Folmer, V.; Mendez, A. Chemical composition and in vitro antioxidant activity of hydro-ethanolic extracts
from Bauhinia forficata subsp. pruinosa and B. variegata. Acta Biol. Hung. 2013, 64(1), 21–33. doi: 10.1556/
ABiol.64.2013.1.3 Semwal, D. K.; Kumar, A.; Aswal, S.; Chauhan, A.; Semwal, R. B. Protective and therapeutic effects of
natural products against diabetes mellitus via regenerating pancreatic β-cells and restoring their dysfunction.
Phytother. Res. 2021, 35(3), 1218–1229. doi: 10.1002/ptr.6885 Sharma, N.; Soni, R.; Sharma, M.; Chatterjee, S.; Parihar, N.; Mukarram, M.; kale, R.; Sayyed, A. A.; Behera,
S. K.; Khairnar, A. Chlorogenic acid: A polyphenol from coffee rendered neuroprotection against rotenone-
induced Parkinson’s disease by GLP-1 secretion. Mol. Neurobiol
s12035-022-03005-z Sivakumar, T.; Deepa, B. A critical review on antidiabetic potential of herbal plants and its their bioactive
components. J. Univ. Shanghai Sci. Technol. 2023, 25(1), 303–314. doi: 10.51201/JUSST/23/0141 Soares, J. C. M.; Costa, S. T. da; Cecim, M. Níveis glicêmicos e de colesterol em ratos com Diabetes Mellitus
aloxano induzido, tratados com infusão de Bauhinia candicans ou syzygium jambolanum. Cienc. Rural.
2000, 30(1), 113–118. doi: 10.1590/s0103-84782000000100018 Sridhar, S N C; Sengupta, P.; Palawat, S.; P. S, D.; George, G.; Paul, A. T. Synthesis, molecular modelling, in
vitro and in vivo evaluation of conophylline inspired novel benzyloxy substituted indole glyoxylamides as
potent pancreatic lipase inhibitors. J. Biomol. Struct. Dyn. 2022, 40(19), 9530–9542. doi: 10.1080/07391102.
2021.1930168
. 2022, 59(11), 6834–6856. doi: 10.1007/
280 
Stote, K. S.; Wilson, M. M.; Hallenbeck, D.; Thomas, K.; Rourke, J. M.; Sweeney , M. I.; Gottschall-Pass, K. T.;
Gosmanov, A. R. Effect of blueberry consumption on cardiometabolic health parameters in men with type 2
diabetes: An 8-week, double-blind, randomized, placebo-controlled trial. Curr. Dev. Nutr. 2020, 4(4), 1–10.
doi: 10.1093/CDN/NZAA030 Takahashi, T.; Miyazawa, M. Potent α-glucosidase inhibitors from safflower (Carthamus tinctorius L.) seed.
Phytother. Res. 2012, 26(5), 722–726. doi: 10.1002/ptr.3622 Upendra Rao, M.; Sreenivasulu, M.; Chengaiah, B.; Jaganmohan Reddy, K.; Madhusudhana Chetty, C. Herbal
medicines for diabetes mellitus: A review. Int. J. Pharmtech Res. 2010, 2(3), 1883–1892. van Dam, R. M.; Willett, W. C.; Manson, J. E.; Hu, F . B. Cof fee, caf feine, and risk of type 2 diabetes. Diabetes
Care. 2006, 29(2), 398–403. doi: 10.2337/diacare.29.02.06.dc05-1512 Vo, T. S.; Vo, T. T. B. C.; Vo, T. T. T. N. Coffee: Health effects and various disease treatments. Food Health.
2022, 8(4), 344–358. doi: 10.3153/fh22032 Wankhede, S.; Mohan, V.; Thakurdesai, P. Beneficial effects of fenugreek glycoside supplementation in male
subjects during resistance training: A randomized controlled pilot study. J. Sport Health Sci. 2016, 5(2),
176–182. doi: 10.1016/j.jshs.2014.09.005
Wojcik, M.; Krawczyk, M.; Wozniak, L. A. Antidiabetic activity of curcumin. In: Nutritional and Therapeutic
Interventions for Diabetes and Metabolic Syndrome. 2nd edn. Elsevier Inc. 2018, doi: 10.1016/
B978-0-12-812019-4.00031-3 Wojcik, M.; Krawczyk, M.; Wojcik, P.; Cypryk, K.; Wozniak, L. A. Molecular mechanisms underlying
curcumin-mediated therapeutic effects in type 2 diabetes and cancer. Oxid. Med. Cell. Longev. 2018, 2018,
9698258. doi: 10.1155/2018/9698258
Wu, F.; Chen, X. [A review of pharmacological study on Astragalus membranaceus (Fisch.) Bge]. Zhong Yao
Cai. 2004, 27(3), 232–234.
Yang, H. J.; Kim, M. J.; Kwon, D. Y.; Kim, D. S.; Lee, Y. H.; Kim, J. E.; Park, S. Anti-diabetic activities of
gastrodia elata blume water extracts are mediated mainly by potentiating glucose-stimulated insulin secretion and
increasing β-cell mass in non-obese type 2 diabetic animals. Nutrients. 2016, 8(3), 161. doi: 10.3390/nu8030161 Yaribeygi, H.; Katsiki, N.; Behnam, B.; Iranpanah, H.; Sahebkar, A. MicroRNAs and type 2 diabetes mellitus:
Molecular mechanisms and the effect of antidiabetic drug treatment. Metab. Clin. Exp. 2018, 87, 48–55. doi:
10.1016/j.metabol.2018.07.001
Y oung, S. N. How to increase serotonin in the human brain without drugs. J. Psych. Neurosci. 2007, 32(6), 394–399. Yuan, C.-S.; Bieber, E. J. Textbook of Complementary and Alternative Medicine. CRC Press. 2003. Zhao, M.; Zhang, Z. F.; Ding, Y.; Wang, J. B.; Li, Y. Astragalus polysaccharide improves palmitate-induced
insulin resistance by inhibiting PTP1B and NF-κB in C2C12 myotubes. Mol. 2012, 17(6), 7083–7092. doi:
10.3390/molecules17067083
Zheng, J.; Cheng, J.; Zheng, S.; Feng, Q.; Xiao, X. Curcumin, a polyphenolic curcuminoid with its protective
effects and molecular mechanisms in diabetes and diabetic cardiomyopathy. Front. Pharmacol. 2018,
9(MAY), 1–10. doi: 10.3389/fphar.2018.00472
Zheng, Y.; Ren, W.; Zhang, L.; Zhang, Y.; Liu, D.; Liu, Y. A review of the pharmacological action of astragalus
polysaccharide. Front. Pharmacol. 2020, 11(March), 1–15. doi: 10.3389/fphar.2020.00349
CHAPTER 13

Marine-Derived Natural Products with Anticancer Properties

POPAT MOHITE
1

2

3

1,*
, RAMDAS PANDHARE2, and DESHRAJ CHUMBHALE
3
*Corresponding author
ABSTRACT
In recent years, marine environments have emerged as promising sources of bioactive compounds with potent anticancer properties. Marine organisms, such as sponges, corals, mollusks, algae, and bacteria, have been found to produce a plethora of natural products exhibiting remarkable cytotoxicity against various cancer cell lines. This chapter high­lights the diversity and sources of marine-derived natural products with proven anticancer potential. It also emphasizes the various strategies employed in the isolation, identification, and characterization of bioactive compounds from marine sources. The chemical struc­tures, mechanisms of action, and preclinical and clinical studies of marine-derived natural products including alkaloids, terpenoids, peptides, polyketides, and steroids are described in detail. Furthermore, the limitations associated with the development of marine-derived natural products as anticancer drugs, including the need for sustainable collection methods, synthetic analogs for structure–activity relationship studies, and overcoming issues related to bioavailability and toxicity, are addressed. Strategies to enhance the production and supply of these compounds through biotechnology and synthetic biology approaches are also discussed. In conclusion, marine-derived natural products represent a valuable source of anticancer agents with diverse chemical structures and mechanisms of action. Continued research in this field, holds promise for the future discovery and development of marine­derived anticancer drugs.

13.1 INTRODUCTION

In recent years, most of the lead compounds that have been shown to be useful in a wide range of pharmacological applications come from marine sources. It is noteworthy that
282 
marine microorganisms are still the source of a significant number of essential bioactive compounds, although not many people are aware of this fact. There are microorganisms living in a broad variety of environments, ranging from the fine sand on a beach to the enormous ocean, which accounts for the majority of the earth’s biosphere. Microbes, especially those that reside in water, are able to survive in environments with high temperatures, high pressures, and incredible quantities of food. The therapeutic efficacy of biological materials derived from natural sources is evaluated with the use of high­throughput screening methods to facilitate the development of a method or product that is economically more viable. One of the greatest environments for bio-prospecting is marine habitat because it has a high number of microorganisms that have not yet been investigated. Microbes are very excellent at recognizing, responding, and adapting to their surroundings. To survive and thrive in their environment, they produce various secondary metabolites. Both biotechnology and medicine have made use of compounds that are produced under stress by organisms (Karthikeyan et al., 2022). There are still many bioactive molecules in the marine environment which are a promising source of nutraceuticals and functional foods. Many studies have used biotechnology to find and synthesize novel substances with the goal of expanding the variety of important chemicals already found in the ocean and making them more accessible. When compared to other biological reserves, ocean has received surprisingly less attention. It is the home to a diverse array of species, each of which has its own set of unique biological characteristics. It has been reported that algae and microalgae are an affluent source of bioactive chemicals that may be used in the preparation of nutritionally beneficial meals. Compounds derived from marine animals are particularly intriguing because of the fluctuations in salt, temperature, and light which occur as a natural aspect of marine atmosphere. Quantity and variety of marine functional components might increase by increasing the number of studies into locating and creating marine chemicals employing biotechnology. Marine bio-resources are responsible for the production of bioactive substances such as enzymes, peptides, proteins, phenolic compounds, polysaccharides, and fatty acids. These compounds have a relatively narrow use and a high level of potency. Proteins derived from marine sources include beneficial components of diets due to the myriad of fascinating and one-of-a-kind features that they possess. These properties include the capacity to produce gels and foams, as well as the ability to operate as an antibacterial agent. Phenolic compounds are an appealing candidate for usage in a variety of biotechnological contexts. One of the most promising sites to look for naturally occurring bioactive metabolites that are safe for the environment is in microalgae. Microalgae are living creatures that produce food by using light as an energy source. These are aquatic organisms that produce fatty acids, carotenoid pigments, and phenolic compounds (Avila and Angulo-Preckler, 2020).

13.2 MARINE BIOACTIVE COMPOUNDS

The development of antibiotic resistance in microorganisms is an issue that threatens the health of people all over the world. There is an urgent need for the development of