Abstract
The following four items on Morus alba L. (Moraceae) appear in the Chinese Pharmacopoeia:
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Sangye, Folium Mori, is the dry leaves of M. alba collected in the fall and used as an antiphlogistic.
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Sangbaipi, Cortex Mori, is the dry root bark of M. alba. It could be used as an antiinflammatory and a diuretic agent.
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Sangzhi, Ramulus Mori, is the dry young branches of M. alba collected in the late spring and early summer. It is used for treatment of arthritis and rheumatism.
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Sangren, Fructus Mori, is the ripe aggregate fruit of M. alba, used as a tonic and sedative.
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References
Yamazaki M (1967) Studies on the volatile components of mulberry leaves by gas chromatography. IV. Relative quantities of the major components of the volatiles. Nippon Sanshigaku Zasshi 36:67–70 (CA 69:103806w)
Yamazaki M (1964) The volatile components of mulberry leaves by gas chromatography. I. On the neutral and acidic components. Nippon Nogei Kagaku Kaishi 38:95–99 (CA 62:9461f)
Yamazaki M (1966) Volatile components of mulberry leaves by gas chromatography. II. Acidic and phenolic components. Nippon Nogei Kagaku Kaishi 40:456–460 (CA 67:776r)
Yamazaki M (1967) Studies on the volatile components of mulberry leaves by gas chromatography. III. Carbonyl components. Nippon Sanshigaku Zasshi 36:63–65 (CA 69:103805v)
Yoshida T, Matsuzaki K (1961) The nonvolatile organic acids in mulberry leaves, their decomposition by the enzymes of the alimentary tract of the silk moth larvae, and their physiological effects on the silk worm. Sanshi Skiensho Hokoku 17:225–268 (CA 61:7423a)
Naito K, Nishina J, Hamamura Y (1963) Micro constituents in mulberry leaves. V. Isolation of palmitic acid, ethyl palmitate, hentriacontane, fumaric acid and hydroxycoumarine from mulberry leaves. Nippon Nogei Kagaku Kaishi 37:449–452 (CA 63:4572d)
Naito K (1968) Trace components in mulberry leaves. VII. Isolation of rutin and quercetin from mulberry leaves. Nippon Nogei Kagaku Kaishi 42:423–425 (CA 69:93633w)
Naito K (1968) Trace constituents of mulberry leaves. VIII. Isolation of quercetin glycoside from mulberry leaves. Nippon Nogei Kagaku Kaishi 42:450–453 (CA 70:26376x)
Moriya S (1977) Sterol composition in mulberry leaves. Sanshi Kenkyu 103:32–36 (CA 91:52726q)
Goto M, Kamada M, Imai S, Murata T, Fujioka S, Fujita E, Hamamura Y (1965) Mulberry and related materials. I. Annu Rep Takeda Res Lab 24:55–65 (CA 64:7045c)
Takemoto T, Ogawa S, Nishimoto N, Hirayama H, Tangiguchi S (1967) Isolation of the insect moulting hormones from mulberry leaves. Yakugaku Zasshi 87:748
Verunova GI, Glukhoded IS, Danilov LL, Eliseeva GI, Kotchetkov NK, Troitsskii MF, Usov AI, Shashkov AS, Shibaev VN (1977) Structure of moraprenol and the synthesis of moraprenyl phosphate. Bioorg Khim 3:1484–1492 (CA 88:89882b)
Nisshin Flour Milling Co Nisshin Kagaku KK (1981) Isolation of polyprenoid ketones from plants. Jpn Kokai Tokkyo Koho 81, 25,129 (CA 95:150964t)
Nomura T, Fukai T (1981) Prenylflavonoids from the root bark of the cultivated mulberry tree. Heterocycles 15:1531–1567
Deshpande VH, Parthasarathy PC, Venkataraman K (1968) Four analogs of artocarpin and cycloartocarpin from Morus alba. Tetrahedron Lett 1715–1719
Nomura T, Fukai T, Katayanagi M (1977) Kuwanon A, B, C and oxydihydromorusin, four new flavones from the root bark of the cultivated mulberry tree (Morbus alba L.). Chem Pharm Bull (Tokyo) 25:529–532
Nomura T, Fukai T, Katayanagi M (1978) Studies on the constituents of the cultivated mulberry tree. II. Isolation of four new flavones, kuwanon A, B, C and oxydihydromorusin from the root bark of Morus alba L. Chem Pharm Bull (Tokyo) 26:1453–1458
Chad VM, Ahmad S, Oesterdahl BG (1978) Carbon-13 NMR spectra of chromeno- and prenylated flavones. Structure revision of mulberrin, mulberrochromene, cyclomulberrin and cyclomulberrochromene. Z Naturforsch 33B: 1547–1549
Nomura T, Fukai T (1979) On the structure of mulberrin, mulberrochromene, cyclomulberrin, and cyclomulberrochromene. Heterocycles 12:1289–1295
Nomura T, Fukai T, Yamanda S, Katayanagi M (1976) Phenolic constituents of the cultivated mulberry tree (Morus alba L.). Chem Pharm Bull (Tokyo) 24:2898–2900
Nomura T, Fukai T, Yamanda S, Katayanagi M (1978) Studies on the constituents of the cultivated mulberry tree. I. Three new prenylflavones from the root bark of Morus alba L. Chem Pharm Bull (Tokyo) 26:1394–1402
Deshpande VH, Wakharkar PV, Rao AV (1976) Wood phenolics of Morus species: V. Isolation of new flavone, mulberranol and a novel phenol, albotalol from Morus alba. Indian J Chem Sect B 14B:647–650
Hikino H (1977) Morusinol, isoprenoid flavone from Morus root barks. Planta Med 32:118–124
Nomura T, Fukai T (1981) Constituents of the cultivated mulberry tree. VII. Isolation of three new isoprenoid flavanones, kuwanon D, E and F from the root bark of Morus alba L. Planta Med 42:79–88
Nomura T, Fukai T, Katayanagi M (1978) Kuwanon D, new isoprenoid flavanone from the root bark of the cultivated mulberry tree (Morus alba L.). Heterocycles .9:745–752
Nomura T, Fukai T (1978) Kuwanon E, a new flavanone derivative from the root bark of the cultivated mulberry tree (Morbus alba L.). Heterocycles 9:1295–1300
Nomura T, Fukai T (1979) Kuwanon F, a new flavanone derivative from the root bark of the cultivated mulberry tree (Morus alba L.). Heterocycles 12:943–946
Nomura T, Fukai T (1980) Kuwanon G, a new flavone derivative from the root bark of the cultivated mulberry tree (Morus alba L.). Chem Pharm Bull (Tokyo) 28:2548–2552
Zenyaku Kogyo Co (1981) 8-Cyclohexenylflavones from mulberry species. Jpn Kokai Tokkyo Koho JP 81, 123, 979 (CA 96:19970v)
Takasugi M, Ishikawa S, Nagao S, Masamune T, Shirata A, Takahashi K (1980) Studies on phytoalexins of the Moraceae. 8. Albanins F and G, natural Diels-Alder adducts from mulberry. Chem Lett 1577–1580
Oshima Y, Konno C, Hikino H, Matsushita K (1980) Validity of oriental medicines. XXIII. Structure of moracenin B, a hypotensive principle of Morus root barks. Tetrahedron Lett 21:3381–3384
Nomura T, Fukai T, Narita T (1980) Hypotensive constituent, kuwanon H, a new flavone derivative from the root bark of the cultivated mulberry tree (Morus alba L.). Heterocycles 14:1943–1951
Oshima Y, Konno C, Hikino H, Matsushita K (1980) The validity of oriental medicines. XXIV. Structure of moracenin A, a hypotensive principle of Morus root barks. Heterocycles 14:1287–1290
Zenyaku Kogyo Co (1983) Kuwanon I. Jpn Kokai Tokkyo Koho JP 58 43,990 [83 43,990] (CA 99:164007c)
Zenyaku Kogyo Co (1983) Kuwanon I. Jpn Kokai Tokkyo Koho JP 58, 150, 538 [83, 150, 538] (CA 100:395880
Ueda S, Nomura T, Fukai T, Matsumoto J (1982) Kuwanon J, a new Diels-Alder adduct, and chalcomoracin from callus culture of Morus alba L. Chem Pharm Bull (Tokyo) 30:3042–3045
Ikuta J, Fukai T, Nomura T, Uedo S (1986) Constituents of the cultivated mulberry tree. XXXV. Constituents of Morbus alba L. cell cultures. I. Structures of four new natural Diels-Alder type adducts, Kuwanons J, Q, R, and V. Chem Pharm Bull (Tokyo) 34:2471–2478
Nomura T, Fukai T, Hano Y, Nemoto K, Terada S, Kuramochi T (1983) Constituents of cultivated mulberry tree. XII. Isolation of two new natural Diels-Alder adducts from root bark of Morus alba. Planta Med 47:151–156
Zenyaku Kogyo Co (1982) Isolation of mikrobicidal kuwanon L. Jpn Kokai Tokkyo Koho JP 58, 150, 584 [83, 150, 584] (CA 100:73968q)
Fukai T, Hano Y, Ikuta H, Fujimoto T, Hirakura K, Nomura T, Uzawa J, Komatsu K, Fukushima K (1983) Structure of new phenolic constituents of Morus root barks. Tennen Yuki Kagobutsu Toronkai Koen Yoshishu, 26th, 150–157 (CA 100:135777n)
Nomura T, Fukai T, Hano Y, Ikuta H (1983) Kuwanon M, a new Diels-Alder adduct from the root bark of the cultivated mulberry tree (Morus lhou (ser.) Koidz). Heterocycles 20:585–591
Hano Y, Hirakura K, Nomura T, Terada S, Fukushima K (1984) Constituents of the cultivated mulberry tree. XVI. Components of root bark of Morus lhou. I. Structures of two new natural Diels-Alder adducts, kuwanons N and O. Planta Med 50:127–130
Hirakura K, Hano Y, Fukai T, Nomura T, Uzawa J, Fukushima K (1985) Constituents of the cultivated mulberry tree. XXI. Constituents of the root bark of Morus lhou Koidz. III. Structures of three natural Diels-Alder type adducts, kuwanon P and X, and mulberrofuran J, from the cultivated mulberry tree (Morbus lhou Koidz.). Chem Pharm Bull (Tokyo) 33:1088–1096
Ueda S, Matsumoto J, Nomura T (1984) Four new natural Diels-Alder adducts, mulberrofuran E, kuwanon Q, R, and V from callus culture of Morus alba L. Chem Pharm Bull (Tokyo) 32:350–353
Fukai T, Hano Y, Hirakura K, Nomura T, Uzawa J (1985) Structures of a novel 2-arylbenzofuran derivative and two flavone derivatives from the cultivated mulberry tree (Morus lhou Koidz.). Chem Pharm Bull (Tokyo) 33:4288–4295
Hirakura K, Fukai T, Hano Y, Nomura T (1985) Constituents of the cultivated mulberry tree. XX. Constituents of the root bark of Morus Ihou. II. Kuwanon W, a natural Diels-Alder type adduct from the root bark of Morus Ihou. Phytochemistry 24:159–161
Hano Y, Tsubura H, Nomura T (1986) Constituents of the cultivated mulberry tree. XXXVIII. Structures of kuwanons Y and Z, two new stilbene derivatives from the cultured mulberry tree (Morus alba L.). Heterocycles 24:2603–2610
Hano Y, Itoh M, Nomura T (1985) Structures of kuwanol A and B, two novel stilbene derivatives from the cultivated mulberry tree (Morbus bombycis Koidz.). Heterocycles 23:819–824
Nomura T, Fukai T, Hano Y, Matsumoto J, Imashimizu A, Uzawa J, Urano S, Fukushima K (1981) Structures of natural Diels-Alder adducts of Morus root barks. Tennen Yuki Kagobutsu toronkai Koen Yoshishu 24:151–158 (CA 96:214241k)
Nomura T, Fukai T, Hano Y, Sugaya Y, Hosoya T (1980) Sanggenone A, a new flavanone derivative from Chinese crude drug “Sang-Bai-Pi” (Morus root bark). I. Heterocycles 14:1785–1790
Nomura T, Fukai T, Hano Y (1983) Constituents of the cultivated mulberry tree. IX. Constituents of the Chinese crude drug “Sang-Bai-Pi” (Morus root barks). I. Structure of a new flavanone derivative, sanggenone A. Planta Med 47:30–34
Nomura T, Fukai T, Hano Y, Urano S (1983) Constituents of the cultivated mulberry tree. XL Constituents of the Chinese crude drug “Sang-Bai-Pi” (Morus root barks). II. Structure of a new flavanone derivative, sanggenone B. Planta Med 47:95–99
Nomura T, Fukai T, Hano Y, Uzawa J (1981) Structure of sanggenone C, a natural hypotensive Diels-Alder adduct from Chinese crude drug “Sang-Bai-Pi” (Morus root barks). Heterocycles 16:2141–2148
Nomura T, Fukai T, Hano Y, Uzawa J (1982) Structure of sanggenone D, a natural hypotensive Diels-Alder adduct from Chinese crude drug “Sang-Bai-Pi” (Morus root barks). Heterocycles 17:381–389
Hano Y, Kohno H, Suziki S, Nomura T (1986) Constituents of the cultivated mulberry tree. XXXVII. Constituents of the Chinese crude drug “Sang-Bai-Pi” (Morus root bark). VIII. Structures of sanggenons E and P, two new Diels-Alder-type adducts from the Chinese crude drug “Sang-Bai-Pi” (Morus root bark). Heterocycles 24:2285–2291
Nomura T, Fukai T, Hano Y, Tsukamoto K (1983) Constituents of the Chinese crude drug “Sang-Bai-Pi” (Morus root barks). III. Structure of a new flavanone derivative, sanggenone F. Heterocycles 20:661–666
Fukai T, Hano Y, Fujimoto T, Nomura T (1983) Structure of sanggenone G, a new Diels-Alder adduct from the Chinese crude drug “Sang-Bai-Pi” (Morus root barks). Heterocycles 20:611–615
Hano Y, Nomura T (1983) Constituents of the Chinese crude drug “Sang-Bai-Pi” (Morus root barks). IV. Structures of four new flavonoids, sanggenone H, I, J, and K. Heterocycles 20:1071–1076
Hano Y, Itoh M, Koyama N, Nomura T (1984) Constituents of the Chinese crude drug “Sang-Bai-Pi” (Morus root barks). V. Structures of three new flavanones, sanggenone L, M, and N. Heterocycles 22:1791–1800
Hano Y, Nomura T (1985) Structure of sanggenone O, a natural Diels-Alder type adduct from the Chinese crude drug “Sang-Bai-Pi” (Morua root bark). Heterocycles 23:2499–2503
Sun JY, Hano Y, Nomura T (1989) Constituents of cultivated mulberry tree. XL. The structure of sanggenone Q, a new Diels-Alder type adduct from Morus mongolica Schneider. Heterocycles 29:195–202
Oshima Y, Konno C, Hikino H, Matsushita K (1980) Validity of oriental medicines. XXVI. Structure of moracenin C, a hypotensive principle of Morus root barks. Heterocycles 14:1461–1464
Oshima Y, Konno C, Hikino H (1981) Validity of oriental medicines. XXVIII. Structure of moracenin D, a hypotensive principle of Morus root barks. Heterocycles 16:979–982
Nomura T, Fukai T, Sato E, Fukushima K (1981) The formation of moracenin D from kuwanon G. Heterocycles 16:983–986
Nomura T, Fukai T, Uno J, Arai T (1978) Mulberrofuran A, a new isoprenoid 2-arylbenzofuran from the root bark of the cultivated mulberry tree (Morus alba L.). Heterocycles 9:1593–1601
Nomura T, Fukai T (1981) Mulberrofuran B, a new isoprenoid 2-arylbenzofuran from the root bark of the cultivated mulberry tree. Planta Med 42:197–199
Nomura T, Fukai T, Matsumoto J, Fukushima K, Momose Y (1981) Structure of mulberrofuran C, a natural hypotensive Diels-Alder adduct from root barks of the cultivated mulberry tree (Morus bombycis Koidzumi). Heterocycles 16:759–765
Nomura T, Fukai T, Shimada T, Chen IS (1983) Constituents of the cultivated mulberry tree. XIII. Components of the root bark of Morus australis. I. Structure of a new 2-acrylbenzofuran derivative, mulberrofuran D. Planta Med 49:90–94
Fukai T, Hano Y, Hirakura K, Nomura T, Uzawa J, Fukushima K (1985) Constituents of the cultivated mulberry tree. XXV. Constituents of the root bark of Morus lhou Koidz. V. Structures of two natural hypotensive Diels-Alder type adducts, mulberrofuran F and G, from the cultivated mulberry tree (Morus lhou Koidz.). Chem Pharm Bull (Tokyo) 33:3195–3204
Fukai T, Hano Y, Hirakura K, Nomura T, Uzawa J, Fukushima K (1984) Structures of mulberrofurans F and G, two natural hypotensive Diels-Alder type adducts from the cultivated mulberry tree (Morus lhou (ser.) Koidz.). Heterocycles 22:473–477
Rao AVR, Deshpande VH, Shastri RK, Tavale SS, Dhaneshwar NN (1983) Structures of albanols A and B, two novel phenols from Morus alba bark. Tetrahedron Lett 24:3013–3016
Fukai T, Hano Y, Hirakura K, Nomura T, Uzawa J (1984) Structure of mulberrofuran H, a novel 2-arylbenzofuran derivative from the cultivated mulberry tree (Morus lhou (ser.) Koidz.). Chem Pharm Bull (Tokyo) 32:808–811
Nikaido T, Ohmoto T, Nomura T, Fukai T, Sankawa U (1984) Inhibitors of cyclic AMP phosphodiesterase in medicinal plants. IX. Inhibition of adenosine 3′,5′-cyclic monophosphate phosphodiesterase by phenolic constituents of mulberry tree. Chem Pharm Bull (Tokyo) 32:4929–4934
Fukai T, Hano Y, Hirakura K, Nomura T, Uzawa J, Fukushima K (1984) Structure of mulberrofuran J, a 2-arylbenzofuran derivative from the cultivated mulberry tree (Morus lhou (ser.) Koidz.). Heterocycles 22:1007–1011
Hano Y, Fukai T, Kohno H, Hirakura K, Nomura T, Uzawa J (1984) Structure of mulberrofuran K, an optically active natural Diels-Alder type adduct from the Chinese crude drug “Sang-Bai-Pi” (Morus root barks). Heterocycles 22:2729–2733
Hano Y, Kohno H, Itoh M, Nomura T (1985) Constituents of the cultivated mulberry tree. XXIX. Structures of three new 2-arylbenzofuran derivatives from the Chinese crude drug “Sang-Bai-Pi” (Morus root barks). Chem Pharm Bull (Tokyo) 33:5294–5300
Fukai T, Fujimoto T, Hano Y, Nomura T, Uzawa J (1984) Structures of mulberrofurans B and L, 2-arylbenzofuran derivatives from the root bark of the cultivated mulberry tree (Morus lhou (ser.) Koidz.) Heterocycles 22:2805–2814
Hano Y, Hirakura K, Someya T, Nomura T (1986) Structure of mulberrofuran M, a novel 2-arylbenzofuran derivative from the cultivated mulberry tree (Morus alba L.). Heterocycles 24:1251–1255
Hano Y, Nomura T (1986) Constituents of the cultivated mulberry tree. XXXVI. Structure of mulberrofuran P, a novel 2-arylbenzofuran derivative from the cultivated mulberry tree (Morus alba L.). Heterocycles 24:1381–1386
Hano Y, Tsubura H, Nomura T (1986) Structure of mulberrofuran Q, a novel 2-arylbenzofuran derivative from the cultivated mulberry tree (Morus alba L.). Heterocycles 24:1807–1813
Takasugi M, Ishikawa S, Masamune T (1982) Stuides on phytoalexins of the Moraceae. XI. Albafurans A and B, geranyl 2-phenylbenzofurans from mulberry. Chem Lett 1221–1222
Takasugi M, Ishikawa S, Nagao S, Masamune T (1982) Studies on the phytoalexins of the Moraceae. 12. Albafuran C, a natural Diels-Alder adduct of a dehydroprenyl-2-phenylbenzo-furan with a chalcone from mulberry. Chem Lett 1223–1224
Takasugi M, Nagao S, Masamune T, Shirata A, Takahashi K (1978) Structure of moracin A and B, new phytoalexins from diseased mulberry. Tetrahedron Lett 797–798
Takasugi M, Nagao S, Masamune T, Shirata K (1978) Moracin C and D, new phytoalexins from diseased mulberry. Chem Lett 1239–1240
Takasugi M, Nagao S, Masamune T, Shirata A, Takahashi K (1979) Studies on phytoalexins of the Moraceae. IV. Structures of moracins E, F, G, and H, new phytoalexins from diseased mulberry. Tetrahedron Lett 4675–4678
Takasugi M, Nagao S, Munoz L, Ishikawa S, Masamune T, Shirata A, Takahashi K (1979) The structure of phytoalexins produced in diseased mulberry. Koen Yoshishu Tennen Yuki Kagobutsu Toronkai, 22:275–282 (CA 92:160540d)
Takasugi M, Munoz L, Masamune T, Shirata A, Takahashi K (1978) Studies on phytoalexins of the Moraceae. III. Stilbene phytoalexins from diseased mulberry. Chem Lett 1241–1242
Takasugi M, Nagao S, Masamune T (1982) Studies on phytoalexins of the Moraceae. X. Structure of dimoracin, a new natural Diels-Alder adduct from diseased mulberry. Chem Lett 1217–1220
Takasugi M, Nagao S, Masamune T, Shirata A, Takahashi K (1980) Chalcomoracin, a natural Diels-Alder adduct from diseased mulberry. Chem Lett 1573–1576
Nomura T, Sawaura Y, Fukai T, Yamada S, Tamura S (1978) Studies on the constituents of the cultivated mulberry tree. V. The synthesis of tetrahydrokuwanon C tetramethyl ether. Heterocycles 9:1355–1366
Shibata H, Mikoshiba I, Shimizu S (1974) Constituents of the mulberry tree. I. Isolation of β-tocopherol from the root bark of the mulberry tree. Agric Biol Chem 38:1745
Uno T (1970) Isolation of umbelliferone and scopoletin from the root bark of the mulberry tree. Sanshi Shikenjo Hokoku 24:437–442 (CA 76:56567b)
Uno T, Isogai A, Suzuki A, Shirata A (1981) Isolation and identification of ethyl 2,4-dihydroxybenzoate and 5,7-dihydroxychromone from the root bark of mulberry tree (Morus alba) and their biological activity. Nippon Sanshigaku Zasshi 50:422–427 (CA 96:82739s)
Deshpande VH, Srinivasan R, Rao AVR (1975) Wood phenolics of Morus species. IV. Phenolics of the heartwood of five Morus species. Indian J Chem 13:453–457
Yagi M, Kouno T, Aoyagi Y, Murai H (1976) The structure of moranoline, a piperdine alkaloid from Morus species. Nippon Nogei Kagaku Kaishi 50:571–572 (CA 86:167851r)
Kasyanov GI, Pekhov AV, Shaftan EA, Klimova ES, Shishkov GZ (1976) Carbon dioxide extract from Morus alba L. fruit. Rastit Resur 12:597–599 (CA 86:40143f)
Shishkov GZ, Golberg ND, Marchenko PS (1978) Fatty acid composition of a carbon dioxide extract from Morus alba fruits. Rastit Resur 14:585–586 (CA 90:19061a)
Ikuta H, Fukai T, Nomura T, Uzawa J (1985) Constituents of the cultivated mulberry tree. XXIII. Carbon-13 NMR spectra of cyanidin and chrysanthemin. Heteracycles 23:121–126
Yamatake Y, Shibata M, Nagai M (1976) Pharmacological studies on root bark of mulberry tree (Morus alba L.). Jpn J Pharmacol 26:461–469
Takasugi M, Munoz L, Masamune T, Shirata A, Takahashi K (1978) Stilbene phytoalexins from diseased mulberry. Chem Lett 1241–1242
Hikino H, Mizuno T, Oshima Y, Konno C (1985) Validity of the oriental medicines. LXXX. Antidiabetes drugs. IV Isolation and hypoglycemic activity of moran A, a glycoprotein of Morus alba root barks. Planta Med 51:159–160
Kitasato Institute (1984) Interferon-inducing polysaccharide from mulberry roots. Jpn Tokkyo Koho JP 59 40,135 [84 40,135] (CA 102:100795f)
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Tang, W., Eisenbrand, G. (1992). Morus alba L.. In: Chinese Drugs of Plant Origin. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-73739-8_88
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