The Natural Products and Pharmacological Biodiversity of Brown Algae from the Genus Dictyopteris

Authors

  • Mohammed I. Rushdi South Valley University https://orcid.org/0000-0001-9488-4019
  • Dr. iman Abdelraheem South Valley University
  • Prof. Dr. Hani Saber South Valley University
  • Prof. Dr. Eman Zekry Attia Minia University
  • Prof. Dr. Usama Ramadan Abdelmohsen Deraya University

DOI:

https://doi.org/10.29356/jmcs.v66i1.1639

Keywords:

Marine, natural products, brown algae, Dictyopteris, Phaeophyceae

Abstract

Abstract. Genus Dictyopteris is an important genus among marine seaweeds and is excessively distributed and known by its ocean smell due to its secondary metabolites including C11-hydrocarbons and sulfur compounds. This chemical feature is responsible for its interesting biological properties. This review detected the literature from 1959 to 2021 on the genus Dictyopteris and revealed the secondary metabolites, together with biological activities of the genus Dictyopteris to create the base for additional studies on its clinical and pharmaceutical applications.

 

Resumen. El género Dictyopteris es un género importante entre las algas marinas y está excesivamente distribuido y conocido por su olor a océano debido a sus metabolitos secundarios que incluyen hidrocarburos C11 y compuestos de azufre. Esta característica química es responsable de sus interesantes propiedades biológicas. Esta revisión detectó la literatura de 1959 a 2021 sobre el género Dictyopteris y reveló los metabolitos secundarios, junto con las actividades biológicas del género Dictyopteris, para crear la base para estudios adicionales sobre sus aplicaciones clínicas y farmacéuticas.

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Author Biographies

Mohammed I. Rushdi, South Valley University

Department of Pharmacognosy, Faculty of Pharmacy.

Dr. iman Abdelraheem, South Valley University

Department of Pharmacognosy, Faculty of Pharmacy.

Prof. Dr. Hani Saber, South Valley University

Department of Botany and Microbiology, Faculty of Science.

Prof. Dr. Eman Zekry Attia, Minia University

Department of Pharmacognosy, Faculty of Pharmacy.

Prof. Dr. Usama Ramadan Abdelmohsen, Deraya University

Department of Pharmacognosy, Faculty of Pharmacy.

References

Rushdi, M. I., et al. Nat. Prod. Res. 2020, 1-19. DOI: 10.1080/14786419.2020.1731741

Nishibayashi, T.; Inoh, S. Bot. Mag. (Tokyo). 1959, 72, 261-268.

Guiry, M.; Guiry, G. AlgaeBase, NUI, Galway. 2021. https://www.algaebase.org/

Moore, R. E. Acc. Chem. Res. 1977, 10, 40-47. DOI: https://doi.org/10.1021/ar50110a002

Boland, W. Proc. Natl. Acad. Sci. U.S.A. 1995, 92, 37-43. DOI: https://doi.org/10.1073/pnas.92.1.37

Wirth, D., et al. Helv. Chim. Acta. 1992, 75, 734-744. DOI: https://doi.org/10.1002/hlca.19920750309

Lever, J., et al. Mar. Drugs. 2020, 18, 142. DOI:10.3390/md18030142

Isroni, W.; Bahri, A. S. IOP Conf. Ser. Earth Environ. Sci. 2020, 493, 012014. DOI: 10.1088/1755-1315/493/1/012014

Moore, R. E.; Pettus, J. A. Tetrahedron Lett. 1968, 4787-4790. DOI: 10.1016/S0040-4039(00)75957-0

Moore, R. E.; Yost, G. J. Chem. Soc. Chem. Commun. 1973, 937-938. DOI: 10.1039/C39730000937

Moore, R. E.; Pettus, J. A.; Mistysyn, J. J. Org. Chem. 1974, 39, 2201-2207. DOI:: 10.1021/jo00929a013

Pickenhagen, W., et al. Helv. Chim. Acta. 1973, 56, 1868-1874. DOI: https://doi.org/10.1002/hlca.19730560607

Moore, R. E. J. Chem. Soc., Chem. Commun. 1971, 1168-1169. DOI: 10.1039/c2971001168b

Schotten, T.; Boland, W.; Jaenicke, L. Tetrahedron Lett. 1986, 27, 2349-2352. DOI: https://doi.org/10.1016/S0040-4039(00)84526-8

Morio, A.; Katsuhiro, K.; Hisashi, T. Bull. Chem. Soc. Jpn. 1994, 67, 1141-1146.

Gosch, B. J., et al. J. Appl. Phycol. 2015, 27, 1607-1622. DOI: 10.1007/s10811-014-0474-4

Vinayak, R. C.; Sabu, A.; Chatterji, A. J. Evid.-Based Integr. Med. 2011, 2011, 673083. DOI: 10.1093/ecam/neq024

Costa, L. S., et al. Biomed. Pharmacother. 2010, 64, 21-28. DOI: https://doi.org/10.1016/j.biopha.2009.03.005

Magalhaes, K. D., et al. Int. J. Mol. Sci. 2011, 12, 3352-3365. DOI: https://doi.org/10.3390/ijms12053352

Rodrigues, S., et al. Biotechnol. Appl. Biochem. 2020, 192, 665–679. DOI: https://doi.org/10.1007/s12010-020-03344-4

König, G. M.; Wright, A. D. Magn. Reson. Chem. 1995, 33, 178-183. DOI: https://doi.org/10.1016/0031-9422(89)80070-6

Hutson, K. S., et al. Int. J. Parasitol. Parasites. 2012, 42, 1135-1141. DOI: https://doi.org/10.1016/j.ijpara.2012.09.007

Sousa, M. B. d., et al. Food Sci. Biotechnol. 2008, 28, 953-958. DOI: https://doi.org/10.1590/S0101-20612008000400030

Khotimchenko, S. V. Phytochemistry. 1995, 38, 1411-1415. DOI: https://doi.org/10.1016/0031-9422(94)00819-F

Cui, Y., et al. Int. J. Biol. Macromol. 2018, 117, 256-263. DOI: 10.1016/j.ijbiomac.2018.05.134

Yang, E.-J., et al. Asian Pac. J. Trop. Biomed. 2014, 4, 529-537. DOI: https://doi.org/10.12980/APJTB.4.2014C1099

Xu, N., et al. J. Appl. Phycol. 2004, 16, 451-456. DOI: 10.1007/s10811-004-5508-x

Xiancui, L., et al. J. Oceanol. Limnol. 2005, 23, 354-356. DOI: 10.1007/BF02847160

Jeon, H., et al. Molecules. 2019, 24, 1420-3049. DOI: 10.3390/molecules24020276

Qiao, Y.-Y., et al. Mar. Drugs. 2009, 7, 600-604. DOI: https://doi.org/10.3390/md7040600

Suzuki, M.; Kowata, N.; Kurosawa, E. Bull. Chem. Soc. Jpn. 1981, 54, 2366-2368, DOI: 10.1246/bcsj.54.2366

Hodgson, D. M.; Salik, S.; Fox, D. J. J. Org. Chem. 2010, 75, 2157-2168. DOI: https://doi.org/10.1021/jo9022974

Kajiwara, T., et al. Phytochemistry. 1989, 28, 636-639. DOI: https://doi.org/10.1016/0031-9422(89)80070-6

McMurry, J. E.; Ko?ovský, P. Tetrahedron Lett. 1985, 26, 2171-2172. DOI: https://doi.org/10.1016/S0040-4039(00)98953-6

Yao, Y.-Q., et al. Cancer Lett. 2008, 264, 127-134. DOI: https://doi.org/10.1016/j.canlet.2008.01.049

Yang, D., et al. Am. J. Cancer Res. 2021, 11, 370-388.

Song, F. H., et al. J. Asian Nat. Prod. Res. 2005, 7, 777-781. DOI: 10.1080/1028602032000169532

Xu, X.-l., et al. Mar. Sci. 2012, 36, 81-84.

Park, S. H., et al. Int. J. Mol. Sci. 2019, 20, 651. DOI: https://doi.org/10.3390/ijms20030651

Yang, H. H., et al. Arch. Pharm. Res. 2015, 38, 876-884. DOI: 10.1007/s12272-014-0435-0

Vizetto-Duarte, C., et al. Phytomedicine. 2016, 23, 550-557. DOI: https://doi.org/10.1016/j.phymed.2016.02.008

Song, F. H., et al. Zhongguo Zhong Yao Za Zhi. 2006, 31, 125-8. DOI: http://www.ncbi.nlm.nih.gov/pubmed/16570798

Lee, J. M., et al. J. Fish. Aquat. Sci. 2020, 23, 1-6.

Hwang, E., et al. Mar. Biotechnol. 2014, 16, 361-370. DOI: 10.1007/s10126-013-9554-8

Rushdi, M. I., et al. RSC Adv. 2020, 10, 24951-24972. DOI: 10.1039/D0RA03576A

Jiang, H., et al. Oncol. Lett. 2018, 15, 3458-3463. DOI: https://doi.org/10.3892/ol.2018.7769

Song, Y., et al. Food Sci. Biotechnol. 2017, 26, 489-494. DOI: 10.1007/s10068-017-0067-5

Kim, K., et al. Int. J. Pharmacol. 2009, 5, 298-306

Rushdi, M. I., et al. S. Afr. J. Bot. 2021, 141, 37-48. DOI: https://doi.org/10.1016/j.sajb.2021.04.018

Cho, J.-Y., et al. Biosci. Biotechnol. Biochem. 1998, 62, 2273-2276. DOI: 10.1271/bbb.62.2273

Peungvicha, P., et al. J. Ethnopharmacol. 1998, 62, 79-84. DOI: https://doi.org/10.1016/S0378-8741(98)00061-0

Wen, W., et al. Molecules. 2009, 14, 2273-7. DOI: http://www.ncbi.nlm.nih.gov/pubmed/19553898

Ji, N. Y., et al. Mar. Drugs. 2009, 7, 355-60. DOI: 10.3390/md7030355

Etsuro, K., et al. Bull. Chem. Soc. Jpn. 1966, 39, 2509-2512. DOI: 10.1246/bcsj.39.2509

Song, F., et al. J. Nat. Prod. 2006, 69, 1261-1266. DOI: 10.1021/np060076u

Song, F., et al. J. Nat. Prod. 2004, 67, 1644-1649. DOI: 10.1021/np040099d

Song, F., et al. J. Nat. Prod. 2005, 68, 1309-1313. DOI: 10.1021/np040227y

Minoru, S., et al. Chem. Lett. 1990, 19, 2187-2190.

Segawa, M.; Yamano, K.; Shirahama, H. Phytochemistry. 1990, 29, 973-974. DOI: https://doi.org/10.1016/0031-9422(90)80058-O

Toshi, I.; Koji, Y.; Tadashi, M. Bull. Chem. Soc. Jpn. 1964, 37, 1053-1055. DOI: 10.1246/bcsj.37.1053

Hay, M. E., et al. Mar. Ecol. . 1988, 48, 185-192.

Schnitzler, I., et al. Oecologia. 2001, 126, 515-521. DOI: https://doi.org/10.1007/s004420000546

Ur Rehman, N., et al. Mar. Drugs. 2019, 17, 666. DOI: https://doi.org/10.3390/md17120666

León-Deniz, L. V., et al. Pharm. Biol. 2009, 47, 864-871.

Ballantine, D. L., et al. Hydrobiologia. 1987, 151, 463-469.

Bianco, É., et al. Molecules. 2013, 18, 5761-5778, DOI: https://doi.org/10.3390/molecules18055761

Syracuse, S. M. Repositório Institucional da UFSC. 2018, https://repositorio.ufsc.br/handle/123456789/191938

Melo, K. R., et al. Molecules. 2013, 18, 14543-63. DOI: 10.3390/molecules181214543

Melo, K. R. T., et al. Holos. 2012, 1, 29-40.

Teixeira, V., et al. Nat. Prod. Commun. 2006, 1, 293- 297.

Rushdi, M. I., et al. S. Afr. J. Bot. 2020, 132, 226-241. DOI: https://doi.org/10.1016/j.sajb.2020.04.031

Yamamoto, Y., et al. Z. Naturforsch. C. 2001, 56, 6-12. DOI: https://doi.org/10.1515/znc-2001-1-202

Kajiwara, T., et al. Z. Naturforsch. C. 2003, 58, 109. DOI: 10.1515/znc-2003-1-219

Yamada, K.; Tan, H.; Hirota, K. Tetrahedron Lett. 1980, 21, 4873-4874. DOI: https://doi.org/10.1016/0040-4039(80)80163-8

Vlachos, V.; Critchley, A.; Von Holy, A. Bot. Mar. 1999, 42, 165-173. DOI: https://doi.org/10.1515/BOT.1999.019

Khallil, A.; Daghman, I.; FadyAA. J. Microbiol. Mod. Tech. 2015, 1, 1- 9

Aoun, Z. B.; Said, R. B.; Farhat, F. Bot. Mar. 2010, 53, 259-264. DOI: https://doi.org/10.1515/BOT.2010.027

Ammar, H. H., et al. Food Chem. 2018, 239, 165-171. DOI: https://doi.org/10.1016/j.foodchem.2017.06.108

Akremi, N., et al. S. Afr. J. Bot. 2017, 108, 308-314. DOI: https://doi.org/10.1016/j.sajb.2016.08.009

Ozdemir, G., et al. Pharm. Biol. 2006, 44, 183-188. DOI: 10.1080/13880200600685949

Dimou, M., et al. J. Nat. Prod. 2016, 79, 584-589. DOI: https://doi.org/10.1021/acs.jnatprod.5b01031

Daskalaki, M. G., et al. Mar. Drugs. 2020, 18, 527. DOI: https://doi.org/10.3390/md18110527

AliAboutabl, E., et al. Med. Aromat. Plant. Sci. Biotechnol. 2010, 4, 41-48

Hofmann, M.; Eichenberger, W. Plant. Cell. .Physiol. 1998, 39, 508-515

Schmid, M., et al. Food Chem. 2018, 265, 70-77. DOI: https://doi.org/10.1016/j.foodchem.2018.05.060

Roller, P.; Au, K.; Moore, R. E. Chem. Commun. 1971, 503-504. DOI: 10.1039/c29710000503

Percival, E.; Anisur Rahman, M.; Weigel, H. Phytochemistry. 1981, 20, 1579-1582. DOI: https://doi.org/10.1016/S0031-9422(00)98535-2

Sokolova, R. V., et al. Chem. Nat. Compd. 2011, 47, 329-334. DOI: 10.1007/s10600-011-9925-1

Kolsi, R. B. A., et al. J. Pharmacogn. Phytochem. 2017, 6, 109-113

Riad, N., et al. Microchem. J. 2020, 152, 104415. DOI: https://doi.org/10.1016/j.microc.2019.104415

Yamada, K., et al. Tetrahedron. 1986, 42, 3775-3780. DOI:10.1016/S0040-4020(01)87531-1

Yamada, K.; Tan, H.; Tatematsu, H. J. Chem. Soc., Chem. Commun. 1979, 13, 572-573. DOI: 10.1039/C39790000572

Jeong, S.-Y., et al. Nat. Prod. Sci. 2012, 18, 130-136.

Kang, K. A., et al. J. Cancer Prev. 2014, 19, 118-124. DOI: 10.15430/JCP.2014.19.2.118

Feng, M.-T., et al. Phytochemistry. 2018, 146, 25-35. DOI: https://doi.org/10.1016/j.phytochem.2017.11.013

Chen, Z., et al. J. Agric. Food Chem. 2014, 62, 6130-6137.

Yang, F., et al. Fitoterapia. 2018, 130, 241-246.

Breuer, O., et al. Eur. J. Biochem. 1993, 215, 705-710. DOI: 10.1111/j.1432-1033.1993.tb18082.x

Millanvoye-Van Brussel, E., et al. Biochem. J. 2004, 380, 533-539. DOI: https://doi.org/10.1042/bj20040069

Ishibashi, F., et al. Biosci. Biotechnol. Biochem. 2013, 77, 1120-1122. DOI: https://doi.org/10.1271/bbb.130018

Shimizu, H., et al. Biochem. Biophys. Res. Commun. 2015, 457, 718-722. DOI: https://doi.org/10.1016/j.bbrc.2015.01.059

Kumagai, M., et al. Molecules. 2018, 23, 1214. DOI: https://doi.org/10.3390/molecules23051214

Kurata, K.; Taniguchi, K.; Suzuki, M. Phytochemistry. 1996, 41, 749-752. DOI: 10.1016/0031-9422(95)00651-6

Dave, M.-N., et al. Heterocycles. 1984, 22, 2301-2307

Wang, H.-S., et al. Eur. J. Org. Chem. 2018, 2018, 915-925. DOI: 10.1002/ejoc.201800026

Laube, T., et al. Tetrahedron. 2002, 58, 4299-4309. DOI: https://doi.org/10.1016/S0040-4020(02)00346-0

Shaikh, H. S. N.a. J. Adv. Res. Rev. 2020, 3, 169-181.

Fenical, W., et al. Phytochemistry. 1972, 11, 1161-1163. DOI: https://doi.org/10.1016/S0031-9422(00)88472-1

Fenical, W., et al. J. Org. Chem. 1973, 38, 2383-2386. DOI: 10.1021/jo00953a022

Yamada, S., et al. PloS one. 2014, 9, e113509. DOI: https://doi.org/10.1371/journal.pone.0113509

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Published

2021-12-27

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Vol. 66 No. 1 (2022): Regular Issue

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