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7. Barrutia, R.R. R., Barreto, I.B., & Velásquez, T.D. M. (2020). Germination of Cinchona
ofcinalis L. seeds in three soils types of Cajamarca, Peru. Revista Cubana de Ciencias
Forestales, 8(1), 75–87.
8. Chatterjee, S. (1992). In domestication studies of some medicinally important exotic plants
growing in India. In WOCMAP I-medicinal and aromatic plants conference: Part 3 of 4 331
(pp.151–158).
9. Fischer, C.A. F. (1944). Growing Cinchona under American Control. Torreya, 44(1), 1–5.
10. Nandi, R. (1993). Cultivation of cinchona and production of its alkaloids in India (pp.1–67).
S.Nandi.
11. Jäger, H., & Kowarik, I. (2010). Resilience of native plant community following manual
control of invasive Cinchona pubescens in Galápagos. Restoration Ecology, 18, 103–112.
12. Boyce, J.S. (1938). Forest pathology. Forest Pathology.
13. Hartley, C.P. (1919). Damping-off in forest nurseries. US Government Printing Ofce.
14. Heim, R. (1940). Un Agaric rhizomorphique parasite des semis de Quinquina en HauteGuinée. Journal d’agriculture traditionnelle et de botanique appliquée, 20(222), 77–87.
15. Hunger, F.W. T. (1907). Proeve omtrent schaduw-cultuur met Deli-tabak op Sumatra’s oost-
kust. G.Kolff & Company.
16. Aerts, R.J., Stoker, A., Beishuizen, M., Jaarsma, I., Van De Heuvel, M., Van Der Meijden,
E., etal. (1992). Detrimental effects ofCinchona leaf alkaloids on larvae of the polyphagous
insectSpodoptera exigua. Journal of Chemical Ecology, 18(11), 1955–1964.
17. Dayrit, F.M., Guidote, A.M., Jr., Generalao, M.L., & Serna, C. (1994). Determination of the
quinine content in the bark of the cinchona tree grown in Mt. Kitanglad.
18. Nair, K.P. (2021). Tree crops. Springer.
19. Tracy, J.W. (1996). Drugs used in the chemotherapy of protozoal infections. In Goodman
and Gilman’s the pharmacological basis of therapeutics (pp.965–985).
20. Genne, P., Duchamp, O., Solary, E., Pinard, D., Belon, J., Dimanche-Boitrel, M., etal. (1994).
Comparative effects of quinine and cinchonine in reversing multidrug resistance on human
leukemic cell line K562/ADM. Leukemia, 8(1), 160–164.
21. Munther, K., & Homoud, M. (2008). Tufts-new England medical center. In Introduction to
Antiarrhythmic agents. Spring.
22. McCalley, D.V. (1990). Quantitative analysis of alkaloids from cinchona bark by highperformance liquid chromatography. Analyst, 115(10), 1355–1358.
23. Cheng, G.G., Cai, X.H., Zhang, B. H., Li, Y., Gu, J., Bao, M. F., etal. (2014). Cinchona
alkaloids from Cinchona succirubra and Cinchona ledgeriana. Planta Medica, 80(02/03),
223–230.
24. Hariyanti, H., Mauludin, R., Sumirtapura, Y. C., & Kurniati, N. F. (2022). A review:
Pharmacological activities of quinoline alkaloid of Cinchona sp.
25. Martins, D., & Nunez, C. V. (2015). Secondary metabolites from Rubiaceae species.
Molecules, 20(7), 13422–13495.
26. Sundowo, A., Artanti, N., Hana, M., Minarti, M. & Primahana, G. (2017, November).
Phytochemical screening, total phenolic, total avonoids contents and antioxidant activity of
Cinchona ledgeriana leaves ethanol extract. In AIP conference proceedings (Vol. 1904, no. 1,
p.020067). AIP Publishing LLC.
27. Canales, N. A., Hansen, T.N. G., Cornett, C., Walker, K., Driver, F., Antonelli, A., etal.
(2020). Historical chemical annotations of cinchona bark collections are comparable to
results from current day high-pressure liquid chromatography technologies. Journal of
Ethnopharmacology, 249, 112375.
28. Maldonado, C., Barnes, C.J., Cornett, C., Holmfred, E., Hansen, S.H., Persson, C., etal.
(2017). Phylogeny predicts the quantity of antimalarial alkaloids within the iconic yellow
cinchona bark (Rubiaceae: Cinchona calisaya). Frontiers in Plant Science, 8, 391.
29. Kacprzak, K.M. (2013). Chemistry and biology of cinchona alkaloids. Natural Products, 1,
605–641.
S. Aslam etal.

10 Cinchona
https://t.me/medicina_free
30. Júnior, W.S. F., Cruz, M.P., dos Santos, L.L., & Medeiros, M.F. T. (2012). Use and importance of quina (Cinchona spp.) and ipeca (Carapichea ipecacuanha (Brot.) L.Andersson):
Plants for medicinal use from the 16th century to the present. Journal of Herbal Medicine,
2(4), 103–112.
31. Pratiwi, D.R., Sulistyaningsih, Y.C., & Ratnadewi, D. (2020). Localization of alkaloid and
other secondary metabolites in Cinchona ledgeriana Moens: Anatomical and histochemical
studies on fresh tissues and cultured cells. HAYATI Journal of Biosciences, 27(1), 1–1.
32. MN, R., & Padh, H. (2003). Antioxidant activity of Cinchona ofcinalis stem bark extracts.
Advances in Traditional Medicine, 3(4), 205–211.
33. Noriega, P., Sola, M., Barukcic, A., Garcia, K., & Osorio, E. (2015). Cosmetic antioxidant
potential of extracts from species of the Cinchona pubescens (Vahl). International Journal of
Phytocosmetics and Natural Ingredients, 2(1), 14–14.
34. Ezekwesili, C. N., Ogbunugafor, H. A., & Ezekwesili-Oli, J. O. (2012). Anti-diabetic
activity of aqueous extracts of Vitex doniana leaves and Cinchona calisaya bark in alloxan–
induced diabetic rats. International Journal of Tropical Disease & Health, 2(4), 290–300.
35. Somavilla, N.S., Cosenza, G.P., Fagg, C.W., & Brandão, M.G. (2017). Morpho-anatomy
and chemical prole of native species used as substitute of quina (Cinchona spp.) in Brazilian
traditional medicine. Part II: Remijia ferruginea. Revista Brasileira de Farmacognosia, 27,
153–157.
36. Ortiz Crespo, F. (1994). La Cinchona antes y después del Virreinato del Conde de Chinchón.
Interciencia, 19(3), 130–136.
37. de Boer, H.J., & Thulin, M. (2005). Lectotypication of Callicocca ipecacuanha Brot. and
neotypication of Cephaelis acuminata H.Karst., with reference to the drug ipecac. Taxon,
54(4), 1080–1082.
38. Möller, M., Herzer, K., Wenger, T., Herr, I., & Wink, M. (2007). The alkaloid emetine as a
promising agent for the induction and enhancement of drug-induced apoptosis in leukemia
cells. Oncology Reports, 18(3), 737–744.
39. Christensen, S.B. (2015). Drugs and drug leads based on natural products for treatment and
prophylaxis of malaria. In Evidence-Based Validation of Herbal Medicine (pp. 307–319).
Elsevier.
40. Dobson, C. M. (2001). The structural basis of protein folding and its links with human
disease. Philosophical Transactions of the Royal Society of London. Series B: Biological
Sciences, 356(1406), 133–145.
41. Achan, J., Talisuna, A.O., Erhart, A., Yeka, A., Tibenderana, J.K., Baliraine, F.N., et al.
(2011). Quinine, an old anti-malarial drug in a modern world: Role in the treatment of
malaria. Malaria Journal, 10(1), 1–12.
42. Cosenza, G. P., Somavilla, N. S., Fagg, C. W., & Brandão, M. G. (2013). Bitter plants
used as substitute of Cinchona spp.(quina) in Brazilian traditional medicine. Journal of
Ethnopharmacology, 149(3), 790–796.
43. Shanks, G.D. (2016). Historical review: Problematic malaria prophylaxis with quinine. The
American Journal of Tropical Medicine and Hygiene, 95(2), 269.
44. Sanders, N.G., Meyers, D.J., & Sullivan, D.J. (2014). Antimalarial efcacy of hydroxyethylapoquinine (SN-119) and its derivatives. Antimicrobial Agents and Chemotherapy, 58(2),
820–827.
45. Mohammadi, S., Jafari, B., Asgharian, P., Martorell, M., & Shari-Rad, J. (2020). Medicinal
plants used in the treatment of malaria: A key emphasis to Artemisia, cinchona, Cryptolepis,
and Tabebuia genera. Phytotherapy Research, 34(7), 1556–1569.
46. Leung, A.Y. (1980). Encyclopedia of common natural ingredients used in food, drugs, and
cosmetics. Wiley.
47. Mangou, F., Platel, D.F., & Haumont, G. (1998). Plasmodium falciparum: Modulation by
phenobarbital of sensitivity to quinine, chloroquine and meoquine invitro. Transactions of
the Royal Society of Tropical Medicine and Hygiene, 92(5), 561–562.
245

246
https://t.me/medicina_free
48. Watt, G., Na-Nakorn, A., Bateman, D., Plubha, N., Mothanaprakoon, P., Edstein, M., &
Webster, H.K. (1993). Amplication of quinine cardiac effects by the resistance-reversing
agent prochlorperazine in falciparum malaria (p. 96346). Armed Forces Research Inst of
Medical Sciences APO San Francisco.
49. de Vries, P.J., Bich, N.N., Van Thien, H., Hung, L.N., Anh, T.K., Kager, P.A., etal. (2000).
Combinations of artemisinin and quinine for uncomplicated falciparum malaria: Efcacy and
pharmacodynamics. Antimicrobial Agents and Chemotherapy, 44(5), 1302–1308.
50. Kremsner, P.G., Radloff, P., Metzger, W., Wildling, E., Mordmüller, B., Philipps, J., etal.
(1995). Quinine plus clindamycin improves chemotherapy of severe malaria in children.
Antimicrobial Agents and Chemotherapy, 39(7), 1603–1605.
51. Olin, B.R., & Hebel, S. (1994). Drug facts and comparisons. Facts and Comparisons St.
52. Jacoby, D.B., & Youngson, R.M. (2004). Encyclopedia of family health. Marshall Cavendish.
53. Semedo, M.G., Dias-Silva, N., Miguéis, J., & Pita, J.R. (2021). Quinine in otology and neurotology: Ototoxicity and historic role in therapy. Otology & Neurotology, 42(1), 145–152.
54. McGready, R., Cho, T., Villegas, L., Brockman, A., van Vugt, M., Looareesuwan, S., etal.
(2001). Randomized comparison of quinine-clindamycin versus artesunate in the treatment
of falciparum malaria in pregnancy. Transactions of the Royal Society of Tropical Medicine
and Hygiene, 95(6), 651–656.
55. Adam, I., Ibrahim, M., Aelbasit, I., & El Bashir, M. (2004). Low-dose quinine for treatment
of chloroquine-resistant falciparum malaria in Sudanese pregnant women. EMHJ-Eastern
Mediterranean Health Journal, 10(4–5), 554–559.
56. Vinetz, J.M., Clain, J., Bounkeua, V., Eastman, R.T., & Fidock, D. (2011). Chemotherapy of
malaria. The pharmacological basis of therapeutics, 12, 1383–1418.
57. Lell, B., & Kremsner, P.G. (2002). Clindamycin as an antimalarial drug: Review of clinical
trials. Antimicrobial Agents and Chemotherapy, 46(8), 2315–2320.
58. Philipson, A., Sabath, L., & Charles, D. (1976). Erythromycin and clindamycin absorption
and elimination in pregnant women. Clinical Pharmacology & Therapeutics, 19(1), 68–77.
59. Jansen, P., Veenhuizen, K., Wesseling, A., de Boo, T., & Verbeek, A. (1997). Randomised
controlled trial of hydroquinine in muscle cramps. The Lancet, 349(9051), 528–532.
60. Younis, N. K., Zareef, R. O., Al Hassan, S. N., Bitar, F., Eid, A. H., & Arabi,
M.Hydroxychloroquine in COVID-19 patients: Pros and cons. Frontiers in Pharmacology,
2020, 11, 597985.
61. Sinha, N., & Balayla, G. (2020). Hydroxychloroquine and covid-19. Postgraduate Medical
Journal, 96(1139), 550–555.
62. Garcia-Cremades, M., Solans, B. P., Hughes, E., Ernest, J.P., Wallender, E., Aweeka, F.,
Luetkemeyer, A. F., & Savic, R. M. (2020). Optimizing hydroxychloroquine dosing for
patients with COVID-19: An integrative modeling approach for effective drug repurposing.
Clinical Pharmacology & Therapeutics, 108(2), 253–263.
63. Große, M., Ruetalo, N., Businger, R., Rheber, S., Setz, C., & Rauch, P., etal. (2020). Evidence
that quinine exhibits antiviral activity against SARS-CoV-2 infection invitro.
64. Taylor, W.R. J., & White, N.J. (2004). Antimalarial drug toxicity. Drug Safety, 27(1), 25–61.
65. Bozic, B., Uzelac, T.V., Kezic, A., & Bajcetic, M. (2018). The role of quinidine in the pharmacological therapy of ventricular arrhythmias ‘quinidine’. Mini Reviews in Medicinal
Chemistry, 18(6), 468–475.
66. Shaftel, N., & Halpern, A. (1958). The quinidine problem. Angiology, 9(1), 34–46.
67. Linenthal, A. (1955). The use of quinidine in the treatment of cardiac arrhythmias. Modern
Concepts of Cardiovascular Disease, 24(11), 299–301.
68. Halpern, A., Shaftel, N., & Bovi, A.M. (1958). The synthesis and study of quinidine polygalacturonate. American Journal of Pharmacy and the Sciences Supporting Public Health,
130(6), 190–201.
69. Schwartz, G. (1959). A clinical evaluation of quinidine polygalacturonate. Angiology, 10(2),
115–119.
S. Aslam etal.

10 Cinchona
https://t.me/medicina_free
70. Sokolow, M., & Perloff, D.B. (1961). The clinical pharmacology and use of quinidine in
heart disease. Progress in Cardiovascular Diseases, 3(4), 316–330.
71. Kumar, S., & Egbuna, C. (2019). Phytochemistry: An in-silico and in-vitro update. Springer.
72. Zhang, B.M., Zhi-Bin, W.A. N. G., Ping, X.I. N., Qiu-Hong, W.A. N.G., He, B. U., &
Kuang, H.X. (2018). Phytochemistry and pharmacology of genus Ephedra. Chinese Journal
of Natural Medicines, 16(11), 811–828.
73. Wink, M. (2012). Medicinal plants: A source of anti-parasitic secondary metabolites.
Molecules, 17(11), 12771–12791.
74. Ramawat, K. G., & Mérillon, J. M. (2013). Phytochemistry, Botany and Metabolism of
Alkaloids, Phenolics and Terpenes, Natural products. Springer.
75. Jo, Y.J., Lee, H.I., Kim, N., Hwang, D., Lee, J., Lee, G.R., etal. (2021). Cinchonine inhibits
osteoclast differentiation by regulating TAK1 and AKT, and promotes osteogenesis. Journal
of Cellular Physiology, 236(3), 1854–1865.
76. Jung, S.A., Choi, M., Kim, S., Yu, R., & Park, T. (2012). Cinchonine prevents high-fat-diet-
induced obesity through downregulation of adipogenesis and adipose inammation. PPAR
Research.
77. Eyal, S. (2018). The fever tree: From malaria to neurological diseases. Toxins, 10(12), 491.
78. Tyagi, R., Sharma, G., Jasuja, N.D., & Menghani, E. (2016). Indian medicinal plants as an
effective antimicrobial agent. Journal of Critical Reviews, 3(2), 69–71.
79. Rojas, J.J., Ochoa, V.J., Ocampo, S.A., & Muñoz, J.F. (2006). Screening for antimicrobial
activity of ten medicinal plants used in Colombian folkloric medicine: A possible alternative in the treatment of non-nosocomial infections. BMC Complementary and Alternative
Medicine, 6(1), 1–6.
80. Pap, T., Van Der Laan, W.H., Aupperle, K.R., Gay, R.E., Verheijen, J.H., Firestein, G.S.,
et al. (2000). Modulation of broblast-mediated cartilage degradation by articular chondrocytes in rheumatoid arthritis. Arthritis & Rheumatism: Ofcial Journal of the American
College of Rheumatology, 43(11), 2531–2536.
81. Sae-Tan, S., Grove, K.A., Kennett, M.J., & Lambert, J.D. (2011). (−)-Epigallocatechin-3-
gallate increases the expression of genes related to fat oxidation in the skeletal muscle of high
fat-fed mice. Food & Function, 2(2), 111–116.
82. Kampa, M., Alexaki, V.I., Notas, G., Nii, A.P., Nistikaki, A., Hatzoglou, A., etal. (2004).
Antiproliferative and apoptotic effects of selective phenolic acids on T47D human breast
cancer cells: Potential mechanisms of action. Breast Cancer Research, 6(2), 1–12.
83. Sohail, M. I., Siddiqui, A., Erum, N., & Kamran, M. (2021). Phytomedicine and the
COVID-19 pandemic. In Phytomedicine (pp.693–708). Academic.
84. Große, M., Ruetalo, N., Layer, M., Hu, D., Businger, R., Rheber, S., etal. (2021). Quinine
inhibits infection of human cell lines with SARS-CoV-2. Viruses, 13(4), 647.
85. Zribi, B., Roy, E., Pallandre, A., Chebil, S., Koubaa, M., Mejri, N., etal. (2016). A microuidic electrochemical biosensor based on multiwall carbon nanotube/ferrocene for genomic
DNA detection of Mycobacterium tuberculosis in clinical isolates. Biomicrouidics,
10(1), 014115.
86. Yang, G.Z., Zhu, J.K., Yin, X.D., Yan, Y.F., Wang, Y.L., Shang, X.F., etal. (2019). Design,
synthesis, and antifungal evaluation of novel quinoline derivatives inspired from natural quinine alkaloids. Journal of Agricultural and Food Chemistry, 67(41), 11340–11353.
87. Ou, H.C., Keating, S., Wu, P., Simon, J.A., Raible, D.W., & Rubel, E.W. (2012). Quinoline
ring derivatives protect against aminoglycoside-induced hair cell death in the zebrash lateral
line. Journal of the Association for Research in Otolaryngology, 13(6), 759–770.
88. Rabbitt, L., Mulkerrin, E.C., & O’Keeffe, S.T. (2016). A review of nocturnal leg cramps in
older people. Age and Ageing, 45(6), 776–782.
89. El-Tawil, S., Al Musa, T., Valli, H., Lunn, M. P., Brassington, R., El-Tawil, T., & Weber,
M. (2015). Quinine for muscle cramps. Cochrane Database of Systematic Reviews, 4,
CD005044.
247

248
https://t.me/medicina_free
90. Gisselmann, G., Alisch, D., Welbers-Joop, B., & Hatt, H. (2018). Effects of quinine, quinidine and chloroquine on human muscle nicotinic acetylcholine receptors. Frontiers in
Pharmacology, 9, 1339.
91. Li, Y., & Tian, J. (2016). Evaluation of local anesthetic and antipyretic activities of cinchona
alkaloids in some animal models. Tropical Journal of Pharmaceutical Research, 15(8),
1663–1666.
92. Che, Z.P., Yang, J.M., Zhang, S., Sun, D., Tian, Y.E., Liu, S.M., et al. (2021). Synthesis
of novel 9 R/S-acyloxy derivatives of cinchonidine and cinchonine as insecticidal agents.
Journal of Asian Natural Products Research, 23(2), 163–175.
93. Raheem, I.T., Goodman, S.N., & Jacobsen, E.N. (2004). Catalytic asymmetric total syntheses of quinine and quinidine. Journal of the American Chemical Society, 126(3), 706–707.
94. Zhao, M.X., Chen, M.X., Tang, W.H., Wei, D.K., Dai, T.L., & Shi, M. (2012). Cinchona
alkaloid catalyzed Regio-and enantioselective allylic amination of Morita–Baylis–Hillman
carbonates with Isatins. European Journal of Organic Chemistry, 2012(19), 3598–3606.
95. Quigley, C., Rodríguez-Docampo, Z., & Connon, S.J. (2012). Highly tunable arylated cinchona alkaloids as bifunctional catalysts. Chemical Communications, 48(10), 1443–1445.
96. Dijkstra, G. D., Kellogg, R. M., Wynberg, H., Svendsen, J. S., Marko, I., & Sharpless,
K. B. (1989). Conformational study of cinchona alkaloids. A combined NMR, molecular mechanics and x-ray approach. Journal of the American Chemical Society, 111(21),
8069–8076.
97. Lai, J., Ma, Z., Mink, L., Mueller, L.J., & Zaera, F. (2009). Inuence of peripheral groups on
the physical and chemical behavior of cinchona alkaloids. The Journal of Physical Chemistry
B, 113(34), 11696–11701.
98. Yeboah, E.M., Yeboah, S.O., & Singh, G.S. (2011). Recent applications of cinchona alkaloids and their derivatives as catalysts in metal-free asymmetric synthesis. Tetrahedron, 67, 10.
99. Lajkó, G., Orosz, T., Grecsó, N., Fekete, B., Palkó, M., Fülöp, F., et al. (2016). Highperformance liquid chromatographic enantioseparation of cyclic β-aminohydroxamic acids
on zwitterionic chiral stationary phases based on cinchona alkaloids. Analytica Chimica
Acta, 921, 84–94.
100. Leete, E. (1969). Biosynthesis of quinine and related alkaloids. Accounts of Chemical
Research, 2(2), 59–64.
101. O’Connor, S.E., & Maresh, J.J. (2006). Chemistry and biology of monoterpene indole alkaloid biosynthesis. Natural Product Reports, 23(4), 532–547.
102. Dewick, P.M. (2002). Medicinal natural products: A biosynthetic approach. Wiley.
103. Keeble, T. (1997). A cure for the ague: The contribution of Robert Talbor (1642–81). Journal
of the Royal Society of Medicine, 90(5), 285–290.
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Chapter 11
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Patchouli
MuhammadUmarIjaz, AliAkbar, HaseebAnwar, SanaInam,
AsmaAshraf, andMuhammadRiaz
11.1 Introduction
Pelletier-Sautelet was the person who discovered the plant (P. cablin) for the rst
time and named it Pogostemon patchouli in 1845. This plant was generally known
as “cabalam” in the certain regions of Philippines. A scientist named Holmes characterized this plant as Pogostemon cablin in 1896 [1]. P. cablin is exclusively indig-
enous to the Philippines as well as it can also grow naturally in various South Asian
regions. In South East Asia, patchouli is a signicantly regarded as perennial herb
that blooms efciently in warm, humid environmental conditions [2].
P. cablin grows in soil which is considerably enriched with nutrients, shaded
with other trees or certain other objects, having well-drainage system and receives
frequent irrigation supply as well as moderate rainy seasons. In general, patchouli
plant grows and reproduces at its best in areas having similar environmental conditions to those in the Philippines such as Southern India, Andaman and Nicobar
Islands [1]. This plant can grow approximately up to 500m above the sea level &
can survive in moderate temperature of about 22–28 °C.Furthermore, humidity
M. U. Ijaz · A. Akbar
Department of Zoology, Wildlife and Fisheries, University of Agriculture,
Faisalabad, Pakistan
H. Anwar
Department of Physiology, Government College University, Faisalabad, Pakistan
S. Inam
Department of pharmacy, Government College University, Faisalabad, Pakistan
A. Ashraf (
Department of Zoology, Government College University, Faisalabad, Pakistan
e-mail: asmaashraf@gcuf.edu.pk
M. Riaz
Department of Pharmacy, Shaheed Benazir Bhutto University, Sheringal, Pakistan
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2023
M. Zia-Ul-Haq et al. (eds.), Essentials of Medicinal and Aromatic Crops,
https://doi.org/10.1007/978-3-031-35403-8_11
*)
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level of over 75% following PH level of 5.5–6.2 is considered as favorable for optimum growth and high-quality essential oils of P. cablin [3].
P. cablin is also regarded as an efcient and protable crop which is widely distributed in several regions of Malaysia, Singapore Indonesia and China [3, 4].
P. cablin plant is well known for its potent therapeutic abilities such as antioxidant,
antimutagenic, antimicrobial, antiplatelet, antidepressant, antithrombotic, aphrodisiac, analgesic, antiemetic, cytotoxic and brinolytic properties [5, 6].
Furthermore, essential oil of P. cablin is also used to treat sadness, involves in
relaxing mind, regulation of appetite, reduces stress and stimulate sex attraction.
Additionally, patchouli plant has antibacterial, antifungal, as well as insecticidal
properties [5]. All the aforementioned characteristics enable this plant to be universally recognized as a commercial crop with signicant industrial importance as well
as certain biological properties [7, 8].
M. U. Ijaz et al.
11.1.1 Taxonomic Position
P. cablin is a member of mint family, Lamiaceae. The taxonomic classication of
this plant is given as:
Kingdom: Plantae
Division: Magnoliophyta
Class: Magnoliopsida
Order: Lamiales
Family: Lamiaceae (Labiatae)
Genus: Pogostemon
Species: P. cablin
11.1.2 Morphological Features
P. cablin is a quadrangular plant which can grow up to 1–1.2m in length having
extensive branching with upright stature. Leaves of this plant are simple, decussate,
opposite. When grown in the open environment leaves of this plant are visible as
purplish-green in coloure, but they can turn bright green when grown in the shady
environmental conditions [9].
Using electron microscopy, the epidermal and mesophyll kinds of secretory
glands are discovered in immature P. cablin plant leaves. Both the adaxial and abax-
ial epidermis of this plant give rise to glandular trichomes [10]. The micromorphological traits of patchouli owers and its pollens collected from various populations
revealed the existence of variations in morphology with alterations in environmental
conditions [11].

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251
11.2 Nutritive andBioactive Compounds
P. cablin contains approximately 14.19% crude protein, 3.85% fat and 17.09% of
crude bers. P. cablin waste also contains bioactive compounds such as tannins,
steroids, glycosides, anthraquinones, steroids, terpenoids, tannins, saponins, phenol, alkaloids as well as avonoids [12].
11.2.1 Aerial Parts
Alpha-guaiene (6.4–17.9%), pogostol (0.3–5.0%), alpha-bulnesene (9.0–15.2%),
and (E)-caryophyllene (2.1–3.6%), Patchouli alcohol (42.2–57.7%), seychellene
(3.4–6.9%), are the main components of the essential oils of aerial parts (inorescence, leaves & entire aerial parts) of p. cablin [13].
11.2.2 Roots
The larger concentrations of norpatchoulenol (5.3%), Beta-pinene (4.5%) and
pogostone (70.2%) are the characteristic compounds of oils extracted from roots of
P. cablin (Table11.1) [13].
11.3 Chemical Composition ofP.Cablin
Zhang etal. investigated Twenty-four molecules from P. cablin plant, the majority
of those include volatile compounds. P. cablin contains 7-patchoulene, Geranium
ketone, alpha-patchoulene, 5-cedrol, alpha-bulnesene, and eucalyptus oil ketene
which accounts for 96% of aforementioned volatile compounds [14]. In addition,
four potential patchoulene derivatives such as 2b, 12-dihydroxypatchoulol, 3a,
8a-dihydroxypatchoulol, 6 hydroxy patchoulol and 8a, 9a-dihydroxypatchoulol
were isolated from aerial region of P. cablin [15].
Table 11.1 Nutritive and bioactive compounds in P. cablin
Plant part Compound Percentage Reference
Aerial parts Pogostol 0.3–5.0%
Patchouli alcohol 42.2–57.7%
Alpha-bulnesene 3.4–6.9%
Roots Beta-pinene 4.5%
Pogostone 70.2%
[13]

252
isorhamnetin-3-O-b-Dgalactoside
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M. U. Ijaz et al.
Pachypodol and Retusine are the two signicant avones that Guan etal. isolated
from patchouli plant [16]. Furthermore, multiple other avones of non-volatile
nature are also isolated by Zhang et al. and Itokawa et al. which includes
5-hydroxy-3,3-,4-,5,7-pentahydroxyavone (4), 5-hydroxy-3,4-,7trimethoxyavone (3), and 5-hydroxy-4-,7-dimethoxyavone (3) [14, 17].
Similar to this, Ding etal. investigated ethanol-based extraction from aerial parts
of P. cablin, obtaining a number of glycosides from it such as apigenin 7-(O-methyl
glucuronide), apigenin 7-galacturonide and quercetin-7-b-D [18]. Moreover, numerous other nonvolatile chemical types have also been isolated from P. cablin in recent
years for example 5-hydroxy 3, 4-, 7- trimethoxy avone and 5-hydroxy-4-,7- dimethoxyavone [19].
Additionally, Huang etal. isolated four avonoid glycosides from the ethanol
extract of the stem and leaf of P. cablin. This extraction resulted in the isolation of
isorhamnetin-3-O-b-Dgalactoside (12) and isisolidone- 7-O-a-L-rhamn from
P. cablin [20]. Meanwhile, Li etal. revealed the following information on several
avonoids that are isolated from P. cablin: 4-, 5-dihydroxy-3, 7-dimethoxyava-
none (I), 5-hydroxy-7, 3-, 4-trimethoxyavanone (II) [11]. [Fig. 11.1 and Table 11.2]
5 - cedrol
H
H
H
O
H
O
O
O
H
O
OO
H
O
H
O
H
O
-
]
H
O
O
O
O
H
Alpha-Patchoulene
H
OO
O
4-, 5dihydrody-3, 7dimethoxyflavan
-one
O
H
O
O
Fig. 11.1 Structure of 5-cedrole, alpha patchoulene, isorhamnetin-3-O-b-Dgalactoside
(Glycoside) and 4-, 5-dihydroxy-3, 7-dimethoxyavanone (Flavonoid)

11 P atch ouli
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253
Table 11.2
Plant Isolated compound References
Patchouli
Therapeutic compounds derived from P. cablin
5- cedrol [14]
Alpha-patchoulene
Geranium ketone
Derivatives of
patchoulene
Glycosides Isorhamnetin-3-O-b-Dgalactoside [20]
Flavonoids 4-, 5-dihydroxy-3,
2b, 12-dihydroxypatchoulol [15]
3a, 8a-dihydroxypatchoulol
8a, 9a Dihydroxypatchoulol
6-Hydroxy Patchoulol
Isisolidone- 7-O-a-L-rhamn
7-dimethoxyavanone
5-hydroxy-7, 3-,
4-trimethoxyavanone
[11]
11.4 Cultivation ofP.Cablin
11.4.1 Why Vegetative Propagation is Preferred inP.Cablin?
P. cablin is an asexually reproducing plant and it is generally cultivated by utilizing
10- to 12-centimeter-long stem parts with three to four nodes in each. The lack of
seeds has led to the adoption of this strategy for better cultivation of p. cablin. For
vegetative propagation, stem parts containing minimum 2 or more leaves are preferred due to their greater capacity for roots and shooting [21].
11.4.2 How toGet Better Stem andRoots withBest Herbage
ofP.Cablin?
In order to promote better root & stem growth in patchouli Garbuio etal. suggested
that utilizing stem parts from the apical and medium regions that contains minimum
2 leaves and nodes are favorable. Because it prefers the shady environment, P. cab-
lin can be grown as an intercrop. It needs deep, loamy, fertile soil that is somewhat
acidic and well-drained along with an annual rainfall between 300 and
400- centimeters with reliable frequent system of irrigation [22]. For high quality
essential oil along with better crop yield, certain conditions with a soil pH between
5.5 and 6.2, humidity of 75% & a temperature between 22 and 28 °C are optimal [23].
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