Botanical species · safety record

Magnolia salicifolia

The EFSA Compendium of Botanicals holds 55 constituent measurements for Magnolia salicifolia. This page reports what those source records contain and how to reach them. It carries no effect estimate, no dose and no recommendation.

Accepted name in source: Magnolia salicifolia (Siebold & Zucc.) Maxim.

55Constituent measurements

0Safety records

12Cited sources

0Licensed products (Canada)

Regulatory presence

No Health Canada licensed natural health product in the snapshot names this species as a medicinal ingredient under this exact binomial. Absence here means absence from this one register under this one name, not absence from trade, and not a safety verdict.

What the records describe

Constituents measured

Plant parts

Preparations

Recorded constituents

What analytical work has found in this species, at which plant part and preparation. A measured constituent is a fact about material, not about effect.

Substance	Plant part	Preparation	Concentration	Analytical method	Source
Asarone	Bud	Solvent extraction	—	GC-MS	Resolve DOI
Benzaldehyde	Bud	Solvent extraction	—	GC-MS	Resolve DOI
Benzene-1,2-diol	Bud	Solvent extraction	—	Standard Chromatographic tests (paper- thin layer- and column chromatography)	Resolve DOI
Camphor	Bud	Solvent extraction	—	GC-MS	Resolve DOI
Cinnamyl alcohol	Bud	Solvent extraction	—	Standard Chromatographic tests (paper- thin layer- and column chromatography)	Resolve DOI
Coclaurine	Bud	—	—	Unspecified	Resolve DOI
Coclaurine	Bud	Solvent extraction	—	Unspecified	Resolve DOI
Coniferin	Bud	Solvent extraction	—	Standard Chromatographic tests (paper- thin layer- and column chromatography)	Resolve DOI
Fenchone	Bud	Solvent extraction	—	GC-MS	Resolve DOI
Isosafrole	Bud	Solvent extraction	—	Standard Chromatographic tests (paper- thin layer- and column chromatography)	Resolve DOI
Methyleugenol	Bud	Solvent extraction	—	GC-MS	Resolve DOI
Methyleugenol	Bud	Solvent extraction	—	Standard Chromatographic tests (paper- thin layer- and column chromatography)	Resolve DOI
Myristicin	Bud	Solvent extraction	—	GC-MS	Resolve DOI
Myristicin	Bud	Solvent extraction	—	Standard Chromatographic tests (paper- thin layer- and column chromatography)	Resolve DOI
N-methylcoclaurine	Bud	Solvent extraction	—	Unspecified	Resolve DOI
Neolignans	Bud	Solvent extraction	—	GC-MS	Resolve DOI
Pinoresinol	Bud	Solvent extraction	—	Standard Chromatographic tests (paper- thin layer- and column chromatography)	Resolve DOI
Reticuline	Bud	—	—	Unspecified	Resolve DOI
Reticuline	Bud	Solvent extraction	—	Unspecified	Resolve DOI
Safrole	Bud	Solvent extraction	—	GC-MS	Resolve DOI
Safrole	Bud	Solvent extraction	—	Standard Chromatographic tests (paper- thin layer- and column chromatography)	Resolve DOI
(+)-diasyringaresinol	Bud	Solvent extraction	0.003 Percent	HPLC-UV	No resolvable identifier
(+)-epiaschantin	Bud	Solvent extraction	1.5479 Percent	HPLC-UV	No resolvable identifier
(+)-epieudesmine	Bud	Solvent extraction	0.7711 Percent	HPLC-UV	No resolvable identifier
1,8-cineole	Aerial part of plants	Essential oil	≥ 1.2 Percent	Gaschromatography (GC)	No resolvable identifier
1,8-cineole	Aerial part of plants	Essential oil	≤ 34 Percent	Gaschromatography (GC)	No resolvable identifier
4-hydroxybenzaldehyde	Flower	Solvent extraction	≥ 14.7 Percent	GC-MS	No resolvable identifier
4-hydroxybenzaldehyde	Flower	Solvent extraction	≤ 18.6 Percent	GC-MS	No resolvable identifier
Asarone	Flower	Solvent extraction	≤ 19.7 Percent	GC-MS	No resolvable identifier
Asarone	Flower	Solvent extraction	≥ 6.3 Percent	GC-MS	No resolvable identifier
Benzaldehyde	Flower	Solvent extraction	—	Chromatographic tests	No resolvable identifier
Camphor	Aerial part of plants	Essential oil	≥ 0.2 Percent	Gaschromatography (GC)	No resolvable identifier
Camphor	Aerial part of plants	Essential oil	≤ 2 Percent	Gaschromatography (GC)	No resolvable identifier
Costunolide	Fruit unspecified	Solvent extraction	—	High Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)	No resolvable identifier
Epi-magnolin a	Bud	Solvent extraction	0.0022 Percent	HPLC-UV	No resolvable identifier
Estragole	Aerial part of plants	Essential oil	≥ 0.5 Percent	Gaschromatography (GC)	No resolvable identifier
Estragole	Aerial part of plants	Essential oil	≤ 4.8 Percent	Gaschromatography (GC)	No resolvable identifier
Eugenol	Leaves	Solvent extraction	0.2 Percent	GC-MS	No resolvable identifier
Kobusin	Bud	Solvent extraction	0.0029 Percent	HPLC-UV	No resolvable identifier
Liriodenine	Leaves	Solvent extraction	—	Chromatographic tests	No resolvable identifier

40 of 55 records are shown, ordered so that records carrying a resolvable reference come first.

Cited sources

The literature the compendium cites for this species. Metatron Health has no relationship with these authors or journals and earns nothing from citing them.

KIKUCHI, T., KADOTA, S., YANADA, K., TANAKA, K., WATANABE, K., YOSHIZAKI, M., YOKOI, T., SHINGU, T. ISOLATION AND STRUCTURE OF MAGNOSALIN AND MAGNOSHININ, NEW NEOLIGNANS FROM MAGNOLIA-SALICIFORIA MAXIM . Chemical & pharmaceutical bulletin, 1983, vol. 31, no. 3, p. 1112-1114.
TSURUGA, T., EBIZUKA, Y., NAKAJIMA, J., CHUN, YT., NOGUCHI, H., IITAKA, Y., SANKAWA, U. BIOLOGICALLY-ACTIVE CONSTITUENTS OF MAGNOLIA-SALICIFOLIA - INHIBITORS OF INDUCED HISTAMINE-RELEASE FROM RAT MAST-CELLS . Chemical & pharmaceutical bulletin, 1991, vol. 39, no. 12, p. 3265-3271.
FURMANOWA, M., JOZEFOWICZ, J. ALKALOIDS AS TAXONOMIC MARKERS IN SOME SPECIES OF MAGNOLIA L AND LIRIODENDRON L . Acta societatis botanicorum poloniae, 1980, vol. 49, no. 4, p. 527-535.
TSURUGA, T., EBIZUKA, Y., NAKAJIMA, J., CHUN, YT., NOGUCHI, H., IITAKA, Y., SANKAWA, U. ISOLATION OF A NEW NEOLIGNAN, MAGNOSALICIN, FROM MAGNOLIA-SALICIFOLIA. Tetrahedron letters, 1984, vol. 25, no. 37, p. 4129-4132. DOI
Zuma, Hiroshi., Toyota, Masao., Asakawa, Yoshinori., Kawano, Shoichi. Naphthalene- a constituent of Magnolia flowers. Phytochemistry (oxford), 1996, vol. 42, no. 4, p. 999-1004.
FUJITA, S., FUJITA, Y. COMPARATIVE BIOCHEMICAL AND CHEMO-TAXONOMICAL STUDIES OF ESSENTIAL OILS OF MAGNOLIA-SALICIFOLIA MAXIM .2. . Chemical & pharmaceutical bulletin, 1974, vol. 22, no. 3, p. 707-709.
Fang, Zhe., Shen, Chang Min., Moon, Dong Cheul., Son, Kun Ho., Son, Jong Keun., Woo, Mi Hee. Quantitative and pattern recognition analyses for the quality evaluation of Magnoliae Flos by HPLC. Bulletin of the korean chemical society, 2010, vol. 31, no. 11, p. 3371-3381.
Kelm, MA., Nair, MG., Schutzki, RA. Mosquitocidal compounds from Magnolia salicifolia. International journal of pharmacognosy, 1997, vol. 35, no. 2, p. 84-90.
Li, Jun., Tanaka, Makoto., Kurasawa, Katsuki., Ikeda, Tsuyoshi., Nohara, Toshihiro. Studies of the chemical constituents of the flower buds of Magnolia kobus and M-salicifolia . Journal of natural medicines, 2007, vol. 61, no. 2, p. 222-223. DOI
Tomita, Masao., Nakano, Tatsuhiko. Alkaloids of magnoliaceous plants. III. Alkaloids of Magnolia salicifolia. Yakugaku zasshi, 1952, vol. 72, p. 197-203.
KIMURA, I., CHUI, LH., FUJITANI, K., KIKUCHI, T., KIMURA, M. INOTROPIC EFFECTS OF (+/-)-HIGENAMINE AND ITS CHEMICALLY RELATED COMPONENTS, (+)-R-COCLAURINE AND (+)-S-RETICULINE, CONTAINED IN THE TRADITIONAL SINO-JAPANESE MEDICINES BUSHI AND SHIN-I IN ISOLATED GUINEA-PIG PAPILLARY-MUSCLE . Japanese journal of pharmacology, 1989, vol. 50, no. 1, p. 75-78. DOI
KIMURA, I., KIMURA, M., YOSHIZAKI, M., YANADA, K., KADOTA, S., KIKUCHI, T. NEUROMUSCULAR BLOCKING ACTION OF ALKALOIDS FROM A JAPANESE CRUDE DRUG SHIN-I (FLOS MAGNOLIAE) IN FROG SKELETAL-MUSCLE . Planta medica, 1983, vol. 48, no. 1, p. 43-47. DOI

Boundary

A constituent measurement is a fact about material at a stated preparation, not a statement about what that material does in a person. An adverse-effect or genotoxicity record is an observation reported in a source, most often in an animal or laboratory model. Neither is a Metatron Health conclusion about causality, human risk or benefit, and the absence of a record is not proof that a preparation is safe. Nothing here is diagnosis, prescribing or individual medical care.

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