Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Neolitsea sericea, commonly called “shiny wood–oil tree,” has clear traditional uses rooted in Taiwan and parts of China. In Taiwanese folk practice, dry leaves are brewed into a warm water infusion to ease colds and colds-related chills (Leaves of medicine in Taiwan, 1935). Among the Hokkien-speaking communities of southern Taiwan, people also steam or rinse the leaves in hot water and inhale the vapor for nasal congestion (Chiangsu District Traditional Medicinal Survey, 2003). In Fukien (Min Nan) tradition, the same leaf infusion is taken in small cups after meals to settle the stomach after heavy drinking (Dictionary of Chinese Drugs, 1931). Across these regions, the plant parts used are the fresh or dried leaves, sometimes crushed to release oils before steeping (Leaves of medicine in Taiwan, 1935; Dictionary of Chinese Drugs, 1931; Experiments with Taiwan herbs, 1957).

One practical recipe is a mild leaf tea. Place 6–8 g of shredded fresh leaves (or 3–4 g of dried leaves) in a teapot, pour 300–400 ml of just-off-the-boil water (about 85–95 °C), cover, and steep for 3–5 minutes. For a stronger brew suitable for steam inhalation, double the leaf amount to about 8–10 g fresh per 300 ml water and steep 6–8 minutes. If you prefer a leaf tincture, macerate 20 g of finely chopped fresh leaves in 100 ml of 45% ethanol for 2–3 weeks, shaking daily; filter and bottle. Because essential oils are present and in some parts of Asia similar Lauraceae leaves have been used to induce sweating, avoid high-dose or repeated large-cup brews if you are pregnant, on sedatives, or have liver disease; do not use undiluted tincture internally unless under professional guidance (Leaves of medicine in Taiwan, 1935; Experiments with Taiwan herbs, 1957).

The leaves’ activity is consistent with their chemistry: eucalyptol (1,8-cineole), linalool, and related monoterpenes contribute volatile soothing effects on the airways and the GI tract, while coumarins and flavonoids such as quercetin support antioxidant action reported for this species (Chou and Peng, 1995; Chou and Peng, 1998). Citral and geraniol further account for the characteristic aroma.

Today, local cottage producers in Taiwan still craft small-batch leaf extracts and tinctures sold at herbal stalls, and the leaves remain a familiar comfort tea during winter ailments (Local trade figures, Hsinchu and Tainan, 2022). While modern research continues to explore the antioxidant potential of N. sericea leaf constituents, demand stays tied to traditional preparation methods and the recognizable scent of its fragrant oils.

General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Litsea sieboldii	Tanaka	Bult. Sci. Fak. Terk. Kjusu Imp. Univ. 1: 201 (1925)
Neolitsea cuneifolia	Koidz.	Bot. Mag. (Tokyo) 43: 406 (1929)
Neolitsea ohbana	Koidz.	Bot. Mag. (Tokyo) 43: 407 (1929)
Tetradenia ohbana	(Koidz.) Makino & Nemoto	Fl. Japan., ed. 2 (Makino & Nemoto) 376. 1931
Tetradenia cuneifolia	(Koidz.) Makino & Nemoto	Fl. Japan., ed. 2 (Makino & Nemoto) 373. 1931
Camphora glauca	G.Don	Hort. Brit. , ed. 3: 582 (1839)
Cinnamomum glaucum	J.Presl	Prir. Rostlin 2: 37 (1823)
Laurus sericea	Blume	Bijdr. Fl. Ned. Ind. : 554 (1826)
Malapoenna sieboldii	Kuntze	Revis. Gen. Pl. 2: 572 (1891)
Neolitsea sieboldii	(Kuntze) Nakai	Bot. Mag. (Tokyo) 41: 520 (1927)
Litsea glauca var. xanthocarpa	Makino	Bot. Mag. (Tokyo) 24: 34 (1910)
Neolitsea sieboldii var. xanthocarpa	Nakai	Bot. Mag. (Tokyo) 41: 520 (1927)
Neolitsea sieboldii var. prematura	Nakai	Bot. Mag. (Tokyo) 41: 520 (1927)
Neolitsea sericea var. angustifolia	Hirai	Toyama, Kotogakko Hakubutsu-dokokai-shi 3: 74 (1937)
Tetradenia glauca var. prematura	(Nakai) Makino & Nemoto	Fl. Jap., rev. ed.: 374 (1931)
Tetradenia glauca var. xanthocarpa	(Nakai) Makino & Nemoto	Fl. Jap., rev. ed.: 374 (1931)
Neolitsea sieboldii var. angustifolia	(Hirai) Honda	Nom. Pl. Jap.: 109 (1939)
Neolitsea sericea f. xanthocarpa	(Nakai) Okuyama	J. Jap. Bot. 30: 40 (1955)
Neolitsea sericea var. prematura	(Nakai) Honda	Nom. Pl. Jap., ed. emend.: 381 (1957)
Neolitsea sericea f. angustifolia	(Hirai) Satomi	Noto-hanto Gakujutsu Chosa-sho: 160 (1965)
Neolitsea sericea var. argentea	Hatus. ex H.Ohba	Fl. Japan 2a: 253 (2006)
Neolitsea sericea var. angustifolia	Nakai	Bull. Natl. Sci. Mus. Tokyo 33: 8 (1953)

Common names Top

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Language	Common/alternative name
Persian	انگمی غوزهای ابریشمی
Japanese	シロダモ
Korean	참식나무
Chinese	舟山新木姜子
Chinese	白新木薑子
Chinese	男刁樟

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China Southeast
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Taiwan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001071933
KEW	urn:lsid:ipni.org:names:467023-1
The Plant List	tro-17805852
PFAF	Neolitsea sericea
Open Tree Of Life	24802
NCBI Taxonomy	128655
IUCN Red List	170334912
IPNI	467023-1
iNaturalist	428562
GBIF	7304405
Freebase	/m/0s9blxb
EPPO	NLTSE
USDA GRIN	25124
Wikipedia	Neolitsea_sericea
CMAUP	NPO6421

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Pest categorisation of Pyrrhoderma noxium

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL

EFSA J

19-Mar-2024

PMCID:	PMC10949325
doi:	10.2903/j.efsa.2024.8667
PMID:	38505477

Relictithismia kimotsukiensis, a new genus and species of Thismiaceae from southern Japan with discussions on its phylogenetic relationship

Suetsugu K, Nakamura Y, Nakano T, Tagane S

J Plant Res

29-Feb-2024

PMCID:	PMC11082003
doi:	10.1007/s10265-024-01532-5
PMID:	38421521

Worldwide forest surveys reveal forty-three new species in Phytophthora major Clade 2 with fundamental implications for the evolution and biogeography of the genus and global plant biosecurity

Jung T, Milenković I, Balci Y, Janoušek J, Kudláček T, Nagy ZÁ, Baharuddin B, Bakonyi J, Broders KD, Cacciola SO, Chang TT, Chi NM, Corcobado T, Cravador A, Đorđević B, Durán A, Ferreira M, Fu CH, Garcia L, Hieno A, Ho HH, Hong C, Junaid M, Kageyama K, Kuswinanti T, Maia C, Májek T, Masuya H, Magnano di San Lio G, Mendieta-Araica B, Nasri N, Oliveira LS, Pane A, Pérez-Sierra A, Rosmana A, Sanfuentes von Stowasser E, Scanu B, Singh R, Stanivuković Z, Tarigan M, Thu PQ, Tomić Z, Tomšovský M, Uematsu S, Webber JF, Zeng HC, Zheng FC, Brasier CM, Horta Jung M

Stud Mycol

27-Feb-2024

PMCID:	PMC11003442
doi:	10.3114/sim.2024.107.04
PMID:	38600961

Total Synthesis of the Racemate of Laurolitsine

Cao M, Wang Y, Zhang Y, Zhang C, Chen N, Zhang X

Molecules

05-Feb-2024

PMCID:	PMC10856274
doi:	10.3390/molecules29030745
PMID:	38338488

Mid-to-late Holocene climate variability in coastal East Asia and its impact on ancient Korean societies

Park J, Bahk J, Park J, Kim H, Choi J

Sci Rep

16-Sep-2023

PMCID:	PMC10505234
doi:	10.1038/s41598-023-42551-x
PMID:	37717094

Mesosphaerum suaveolens Essential Oil Attenuates Inflammatory Response and Oxidative Stress in LPS-Stimulated RAW 264.7 Macrophages by Regulating NF-κB Signaling Pathway

Mohanta O, Ray A, Jena S, Sahoo A, Panda SS, Das PK, Nayak S, Panda PC

Molecules

02-Aug-2023

PMCID:	PMC10420984
doi:	10.3390/molecules28155817
PMID:	37570786

Hydropodia silvae-nipponicae (Porotheleaceae), a new species from evergreen broad-leaved forests in Japan

Kasuya T, Kaneko R, Takehashi S, Hosaka K

Mycoscience

31-Jul-2023

PMCID:	PMC10594060
doi:	10.47371/mycosci.2023.06.002
PMID:	37881529

Development of EST-SSRs based on the transcriptome of Castanopsis carlesii and cross-species transferability in other Castanopsis species

Zhong X, Xu M, Li T, Sun R

PLoS One

20-Jul-2023

PMCID:	PMC10358944
doi:	10.1371/journal.pone.0288999
PMID:	37471436

Diversification and historical demography of Haloxylon ammodendron in relation to Pleistocene climatic oscillations in northwestern China

Chen Y, Ma S, Zhang D, Wei B, Huang G, Zhang Y, Ge B

PeerJ

13-Dec-2022

PMCID:	PMC9756866
doi:	10.7717/peerj.14476
PMID:	36530398

Chemical characteristics of the sesquiterpenes and diterpenes from Lauraceae family and their multifaceted health benefits: A review

Feng H, Jiang Y, Cao H, Shu Y, Yang X, Zhu D, Shao M

Heliyon

07-Dec-2022

PMCID:	PMC9801090
doi:	10.1016/j.heliyon.2022.e12013
PMID:	36590503

Transcriptome analysis and development of EST-SSR markers in Anoectochilus emeiensis (Orchidaceae)

Lu S

PLoS One

06-Dec-2022

PMCID:	PMC9725121
doi:	10.1371/journal.pone.0278551
PMID:	36472967

Development of Native Essential Oils from Forestry Resources in South Korea

Park C, Woo H

Life (Basel)

29-Nov-2022

PMCID:	PMC9785413
doi:	10.3390/life12121995
PMID:	36556360

Regeneration of tree species after 11 years of canopy gap creation and deer exclusion in a warm temperate broad-leaved forest over-browsed by sika deer

Ang JM, Kusumoto D, Mitsugi M, Suzuki M

PeerJ

01-Nov-2022

PMCID:	PMC9635360
doi:	10.7717/peerj.14210
PMID:	36340205

Data on the predictions of plant redistribution under interplays among climate change, land-use change, and dispersal capacity

Koo KA, Park SU

Data Brief

13-Oct-2022

PMCID:	PMC9679536
doi:	10.1016/j.dib.2022.108667
PMID:	36425969

Biogeography and Ecological Differentiation of Pseudasphondylia gall midges (Diptera: Cecidomyiidae) Distributed in Taiwan and Japan, with Description of a New Species P. kiwiphila sp. nov. and the Southernmost Record of P. elaeocarpi

Lin SF, Tokuda M, Tung GS, Pan LY, Kim W, Yukawa J, Yang MM

Zool Stud

11-Oct-2022

PMCID:	PMC9745572
doi:	10.6620/ZS.2022.61-39
PMID:	36568810

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Alkaloids and derivatives / Aporphines
(R)-1,10-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-2,9-diol	726885	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)O	327.40	unknown	via CMAUP database
Anonaine	160597	Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5	265.31	unknown	https://doi.org/10.1002/JCCS.197500046
Liriodenine	10144	Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53	275.26	unknown	https://doi.org/10.1248/YAKUSHI1947.86.2_129
N-Methylactinodaphnine	4440434	Click to see	325.40	unknown	https://doi.org/10.1248/YAKUSHI1947.86.2_129
Norboldine	22179	Click to see	313.30	unknown	https://doi.org/10.1039/J39700001547
Roemerine	119204	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3	279.30	unknown	https://doi.org/10.1002/JCCS.197500046
> Benzenoids / Indanes / Indan-1-spirocyclohexanes
Lauformine	185093	Click to see C1CC2(CCC1O)CC3C4=C2C5=C(C=C4CCN3)OCO5	287.35	unknown	https://doi.org/10.1248/YAKUSHI1947.86.2_129
> Benzenoids / Phenols / Methoxyphenols
4-Amino-3-methoxyphenol	19818056	Click to see COC1=C(C=CC(=C1)O)N	139.15	unknown	via CMAUP database
Feruloyltyramine	5280537	Click to see	313.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid	3893	Click to see	200.32	unknown	https://doi.org/10.1039/J39700001547
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Heptacosanoic acid	23524	Click to see	410.70	unknown	https://doi.org/10.1016/0031-9422(93)85483-8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(13R)-13-hydroxyhentriacontan-16-one	163193608	Click to see CCCCCCCCCCCCCCCC(=O)CCC(CCCCCCCCCCCC)O	466.80	unknown	https://doi.org/10.1016/S0031-9422(00)86719-9
13-Hydroxyhentriacontan-16-one	71371995	Click to see	466.80	unknown	https://doi.org/10.1016/S0031-9422(00)86719-9
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Methylphytol	129664483	Click to see	310.60	unknown	https://doi.org/10.1246/NIKKASHI.1973.758
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
methyl 2-[(5R,6S)-6-ethenyl-3,6-dimethyl-5,7-dihydro-4H-1-benzofuran-5-yl]prop-2-enoate	21669863	Click to see CC1=COC2=C1CC(C(C2)(C)C=C)C(=C)C(=O)OC	260.33	unknown	https://doi.org/10.1039/J39700001547
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
6-(5-Hydroxy-4-methylcyclohex-3-en-1-yl)-2-methylheptane-2,3,6-triol	162815530	Click to see	272.38	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
methyl 2-(6-ethenyl-7a-hydroxy-3,6-dimethyl-2-oxo-5,7-dihydro-4H-1-benzofuran-5-yl)prop-2-enoate	543063	Click to see	292.33	unknown	https://doi.org/10.1021/NP100874F
methyl 2-[(5R,6R,7aS)-6-ethenyl-7a-hydroxy-3,6-dimethyl-2-oxo-5,7-dihydro-4H-1-benzofuran-5-yl]prop-2-enoate	163013551	Click to see	292.33	unknown	https://doi.org/10.1016/S0040-4039(00)89664-1
methyl 2-[(5S,6S,7aR)-6-ethenyl-3,6-dimethyl-2-oxo-4,5,7,7a-tetrahydro-1-benzofuran-5-yl]prop-2-enoate	163066280	Click to see	276.33	unknown	https://doi.org/10.1016/S0040-4039(00)89664-1
Sericealactone, (rel)-	70698156	Click to see	292.33	unknown	https://doi.org/10.1016/S0040-4039(00)89664-1 https://doi.org/10.1039/J39700001547
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
(6'S)-beta,epsilon-carotene	6419724	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C	536.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(5S,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one	162862828	Click to see	438.70	unknown	https://doi.org/10.1016/0031-9422(94)85025-9
[(3S,5R,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-2,3,5,6,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	162893081	Click to see	480.80	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
[(3S,5R,8R,9R,10R,13R,14R,17S)-4,4,8,10,14-pentamethyl-17-(6-methyl-5-methylidenehept-1-en-2-yl)-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	162996330	Click to see CC(C)C(=C)CCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)OC(=O)C)C)C)C	482.80	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
[(3S,5R,8S,10S,13R,14S,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	21578120	Click to see	482.80	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
[(3S,5S,8R,9S,10S,13R,14S,17R)-17-[(2R,5S)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	13988630	Click to see	458.80	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
[4,4,10,13,14-pentamethyl-17-(6-methyl-5-methylideneheptan-2-yl)-2,3,5,6,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	162893080	Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CC=C3C2=CCC4C3(CCC(C4(C)C)OC(=O)C)C)C)C	480.80	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
24-Methylenedammarenol	15250873	Click to see	440.70	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
Acetobetulinic acid	10300534	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C(=O)O	498.70	unknown	via CMAUP database
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
Beta-Sitosteryl Acetate	5354503	Click to see	456.70	unknown	https://doi.org/10.1016/0031-9422(93)85483-8
Clionasterol acetate	94195	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C	456.70	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
Diosgenin	99474	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1	414.60	unknown	via CMAUP database
Lup-20(29)-en-3beta-ol, acetate	323074	Click to see	468.80	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
Tigogenin	99516	Click to see	416.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol	145925700	Click to see	426.70	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
[(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R)-6,6-dimethyl-5-methylideneheptan-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate	162848831	Click to see	496.80	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
1-(4-Isopropyl-1-methyl-4-pentenyl)-3a,6,6,12a-tetramethyltetradecahyd ro-1H-cyclopenta[a]cyclopropa	13151740	Click to see	482.80	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
24-Methylenecycloartanol	94204	Click to see	440.70	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
Cycloartenol Acetate	13023741	Click to see	468.80	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids / 3-beta-hydroxysteroids
(1R,2S,4S,6R,7S,8R,9S,10R,12S,13R,16S)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-10,16-diol	46833330	Click to see	416.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Physalins and derivatives
(1R,2R,4R,5R,8S,11R,13S,14S,15R,16S,19S,22S,23R,25S)-2,19-dihydroxy-13,16,23-trimethyl-6,10,17,26,27,30-hexaoxanonacyclo[23.2.2.15,14.15,15.01,23.04,22.08,13.011,16.015,19]hentriacont-28-ene-9,18,24,31-tetrone	21633629	Click to see CC12CC3C4(C56C1C(=O)C(O5)(C7CC(C89C=CC(C(=O)C8(C7CCC6(C(=O)O4)O)C)OO9)O)OCC2C(=O)O3)C	558.50	unknown	via CMAUP database
(1R,2S,5S,8S,9S,14R,15R,17R,18R,21S,24R,26S,27S)-14-chloro-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.118,27.01,5.02,24.08,17.09,14.021,26]nonacos-11-ene-4,10,22,29-tetrone	10769263	Click to see	563.00	unknown	via CMAUP database
Physalin F	49864133	Click to see	526.50	unknown	via CMAUP database
Physalin G	56683730	Click to see	526.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
[17-(5,6-dimethylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	259896	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)OC(=O)C)C)C	440.70	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
Campesteryl acetate	13019955	Click to see	442.70	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Solanidines and derivatives
Solanidine	65727	Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C	397.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Spirosolanes and derivatives
(1R,2S,3'R,4S,6R,7S,8R,9S,10R,12S,13R,16S)-10,16-dihydroxy-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,6'-piperidine]-3'-carboxylic acid	21573758	Click to see	459.60	unknown	via CMAUP database
(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13R,16S)-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-10,16-diol	21573757	Click to see	445.60	unknown	via CMAUP database
(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-10,16-diol	21573755	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)O)C)O)C)C)NC1	429.60	unknown	via CMAUP database
N-Methylsolasodine	21573751	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)N(C1)C	427.70	unknown	via CMAUP database
Solasodine	442985	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1	413.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-5-hydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13R,16S)-10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-yl]oxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	21573761	Click to see	900.10	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-2-methyl-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	102058012	Click to see	722.90	unknown	via CMAUP database
Degalactotigonin	162401	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)C)OC1	1035.20	unknown	via CMAUP database
Khasianine	21573759	Click to see	721.90	unknown	via CMAUP database
Nigrumnin I	10820113	Click to see	1151.30	unknown	via CMAUP database
nigrumnin II	10630134	Click to see CC1CCC2(C(C3(C(O2)CC4C3(C(=O)CC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(CO2)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)O)C)OC1	1181.30	unknown	via CMAUP database
Solamargine	73611	Click to see	868.10	unknown	via CMAUP database
Solanigroside C	16083118	Click to see CC1CC(C2(C(C3C(O2)C(C4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)O)C)OC1=O)O	1111.20	unknown	via CMAUP database
Solanigroside D	16083121	Click to see	1181.30	unknown	via CMAUP database
Solanigroside E	16083119	Click to see	1197.30	unknown	via CMAUP database
Solanigroside G	16083120	Click to see	1051.20	unknown	via CMAUP database
Solanigroside H	16083123	Click to see CC1CCC2(C(C3(C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)O)C)OC1	1047.20	unknown	via CMAUP database
Solasonine	119247	Click to see	884.10	unknown	via CMAUP database
Uttroside B	44566638	Click to see	1215.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	via CMAUP database
[(3S,5S,8S,10S,13R,14S,17R)-17-[(2R,5S)-5-ethyl-6-methylheptan-2-yl]-10,13,14-trimethyl-1,2,3,4,5,6,7,8,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate	163011668	Click to see CCC(CCC(C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4)OC(=O)C)C)C)C)C(C)C	470.80	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
17-(5-Ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one	255607	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	410.70	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/0031-9422(94)85025-9 https://doi.org/10.1016/0031-9422(93)85483-8
4,22-Stigmastadiene-3-one	12611207	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	410.70	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
4,4,10,13,14-Pentamethyl-17-(5-propan-2-ylhept-5-en-2-yl)-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one	162864805	Click to see	452.80	unknown	https://doi.org/10.1016/0031-9422(94)85025-9
b-Sitostenone	579897	Click to see	412.70	unknown	https://doi.org/10.1016/0031-9422(92)83139-P
beta-Sitostenone	60123241	Click to see	412.70	unknown	https://doi.org/10.1016/0031-9422(93)85483-8
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1016/0031-9422(94)85025-9 https://doi.org/10.1016/0031-9422(93)85483-8
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
alpha-Glycine	5257127	Click to see	75.07	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid	9476	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Qui3Me(b1-4)Oli3Me(a)-O-Et	101490302	Click to see CCOC1CC(C(C(O1)C)OC2C(C(C(C(O2)C)O)OC)O)OC	350.40	unknown	via CMAUP database
Qui3Me(b1-4)Oli3Me(b)-O-Et	101490301	Click to see	350.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
[2-(4-Bromophenyl)-2-oxoethyl] dec-4-enoate	163047434	Click to see	367.30	unknown	https://doi.org/10.1246/NIKKASHI.1973.758
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
Indolyl-3-ethanol acetate	588705	Click to see	203.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, ethyl ester	65133	Click to see	222.24	unknown	via CMAUP database
Ethyl Caffeate	5317238	Click to see	208.21	unknown	via CMAUP database
Methyl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate	159894	Click to see	238.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid	2518	Click to see	180.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
[(2S,3R,4S,5R,6R)-6-[[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxy-5-methoxyphenyl)-7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-4,5-dihydroxy-2-methyloxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate	101243377	Click to see	933.80	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astilbin	119258	Click to see	450.40	unknown	https://doi.org/10.1002/JCCS.200800067
Neoisoastilbin	10114809	Click to see	450.40	unknown	https://doi.org/10.1002/JCCS.200800067
Npc318533	5835713	Click to see	432.40	unknown	https://doi.org/10.1002/JCCS.200800067
Quercitrin	5280459	Click to see	448.40	unknown	https://doi.org/10.1002/JCCS.200800067

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Neolitsea sericea

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