Language	Common/alternative name
Czech	lindera tupolaločná
Persian	برگبوی خاور دور
Japanese	ダンコウバイ
Korean	생강나무
Chinese	三桠乌药
Chinese	三钻七
Chinese	三钻风
Chinese	三键风
Chinese	山姜
Chinese	红叶甘檀
Chinese	三椏烏藥

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name	Authority	First published in
Lindera obtusiloba var. heterophylla	(Meisn.) H.P.Tsui	Fl. Reipubl. Popularis Sin. 31: 416 (1982)
Lindera obtusiloba var. obtusiloba		Unknown

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
  - Manchuria
  - Tibet
- Eastern Asia
  - Japan
  - Korea

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - East Himalaya
  - Nepal
- Indo-China
  - Myanmar

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001070367
Tropicos	17800797
KEW	urn:lsid:ipni.org:names:465417-1
The Plant List	tro-17800797
Open Tree Of Life	356836
NCBI Taxonomy	155295
IUCN Red List	136775422
IPNI	465417-1
iNaturalist	448339
GBIF	7304491
Freebase	/m/0285mtf
EPPO	LIEOB
EOL	5394457
USDA GRIN	22300
Wikipedia	Lindera_obtusiloba
CMAUP	NPO10654

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

Three-tiered authentication of herbal traditional Chinese medicine ingredients used in women’s health provides progressive qualitative and quantitative insight

Mück F, Scotti F, Mauvisseau Q, Thorbek BL, Wangensteen H, de Boer HJ

Front Pharmacol

05-Feb-2024

PMCID:	PMC10875096
doi:	10.3389/fphar.2024.1353434
PMID:	38375033

Uncovering floral composition of paper wasp nests (Hymenoptera: Vespidae: Polistes) through DNA metabarcoding

Mohamadzade Namin S, Son M, Jung C

Sci Rep

03-Feb-2024

PMCID:	PMC10838270
doi:	10.1038/s41598-024-52834-6
PMID:	38310136

Radical oxygen species: an important breakthrough point for botanical drugs to regulate oxidative stress and treat the disorder of glycolipid metabolism

Luo M, Zheng Y, Tang S, Gu L, Zhu Y, Ying R, Liu Y, Ma J, Guo R, Gao P, Zhang C

Front Pharmacol

12-May-2023

PMCID:	PMC10213330
doi:	10.3389/fphar.2023.1166178
PMID:	37251336

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

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

New evidence of the emergence of the East Asian monsoon in the early Palaeogene

Su LF, Zhang QQ, Sun YK, Zhang SL, Smith T, Li CS

Sci Rep

28-Nov-2022

PMCID:	PMC9705385
doi:	10.1038/s41598-022-24298-z
PMID:	36443349

Genetic structure and trait variation within a maple hybrid zone underscore North China as an overlooked diversity hotspot

Yang R, Deng YW, Liu Y, Zhao J, Bao L, Ge JP, Wang HF

Sci Rep

17-Aug-2022

PMCID:	PMC9385851
doi:	10.1038/s41598-022-17538-9
PMID:	35977961

Floral morphology and phenology of Sassafras tzumu (Lauraceae)

Yang Z, Tan C, Wei YM, Rohwer JG, Liu B, Yang Y

BMC Plant Biol

08-Jul-2022

PMCID:	PMC9264512
doi:	10.1186/s12870-022-03714-6
PMID:	35799123

The Modulation of Melanogenesis in B16 Cells Upon Treatment with Plant Extracts and Isolated Plant Compounds

Merecz-Sadowska A, Sitarek P, Kowalczyk T, Zajdel K, Kucharska E, Zajdel R

Molecules

07-Jul-2022

PMCID:	PMC9324663
doi:	10.3390/molecules27144360
PMID:	35889231

Stepped Geomorphology Shaped the Phylogeographic Structure of a Widespread Tree Species (Toxicodendron vernicifluum, Anacardiaceae) in East Asia

Wang L, Li Y, Noshiro S, Suzuki M, Arai T, Kobayashi K, Xie L, Zhang M, He N, Fang Y, Zhang F

Front Plant Sci

02-Jun-2022

PMCID:	PMC9201781
doi:	10.3389/fpls.2022.920054
PMID:	35720535

Vegetation Classification and Distribution Patterns in the South Slope of Yarlung Zangbo Grand Canyon National Nature Reserve, Eastern Himalayas

Wu PP, Wang Z, Jia NX, Dong SQ, Qu XY, Qiao XG, Liu CC, Guo K

Plants (Basel)

28-Apr-2022

PMCID:	PMC9105001
doi:	10.3390/plants11091194
PMID:	35567195

Recent Advances in the Antiproliferative and Proapoptotic Activity of Various Plant Extracts and Constituents against Murine Malignant Melanoma

Dumitraș DA, Andrei S

Molecules

17-Apr-2022

PMCID:	PMC9028509
doi:	10.3390/molecules27082585
PMID:	35458783

Effects of Forest Healing Anti-Aging Program on Psychological, Physiological, and Physical Health of Older People with Mild Cognitive Impairment

Baek JE, Jung JH, Shin HJ, Kim SH, Sung SY, Park SJ, Hahm SC, Cho HY, Lee MG

Int J Environ Res Public Health

16-Apr-2022

PMCID:	PMC9027266
doi:	10.3390/ijerph19084863
PMID:	35457728

Current update on herbal sources of antithrombotic activity—a comprehensive review

Subramani B, Sathiyarajeswaran P

Egypt J Intern Med

07-Mar-2022

PMCID:	PMC8899788
doi:	10.1186/s43162-021-00090-9
PMID:	35283622

Potential clinical applications of phytopharmaceuticals for the in‐patient management of coagulopathies in COVID‐19

Mukherjee AK, Chattopadhyay DJ

Phytother Res

11-Feb-2022

PMCID:	PMC9111032
doi:	10.1002/ptr.7408
PMID:	35147268

Phytochemical Profile Top

Add a new one!

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	via CMAUP database
> Benzenoids / Naphthalenes / Phenylnaphthalenes
2-methoxy-9-phenyl-1H-phenalen-1-one	10085389	Click to see COC1=CC2=CC=CC3=C2C(=C(C=C3)C4=CC=CC=C4)C1=O	286.30	unknown	via CMAUP database
2,3-Dimethoxy-4-phenyl-1H-phenalen-1-one	85730244	Click to see COC1=C(C(=O)C2=CC=CC3=C2C1=C(C=C3)C4=CC=CC=C4)OC	316.30	unknown	via CMAUP database
2,6-Dimethoxy-5-hydroxy-7-phenyl-1H-phenalen-1-one	85730242	Click to see COC1=CC2=CC(=C(C3=C(C=CC(=C23)C1=O)C4=CC=CC=C4)OC)O	332.30	unknown	via CMAUP database
5-Hydroxy-6-methoxy-7-phenyl-1H-phenalen-1-one	85730238	Click to see COC1=C(C=C2C=CC(=O)C3=C2C1=C(C=C3)C4=CC=CC=C4)O	302.30	unknown	via CMAUP database
6-Phenyl-7,8-dimethoxy-1H-phenalen-1-one	85730248	Click to see COC1=C(C2=C(C=CC3=C2C(=C1)C(=O)C=C3)C4=CC=CC=C4)OC	316.30	unknown	via CMAUP database
Anigorufone	636472	Click to see C1=CC=C(C=C1)C2=C3C4=C(C=CC=C4C=C(C3=O)O)C=C2	272.30	unknown	via CMAUP database
Dihydroxyanigorufone	85846875	Click to see C1=CC2=C3C(=C1)C=C(C(=O)C3=C(C=C2)C4=CC(=C(C=C4)O)O)O	304.30	unknown	via CMAUP database
Hydroxyanigorufone	11471752	Click to see C1=CC2=C3C(=C1)C=C(C(=O)C3=C(C=C2)C4=CC=C(C=C4)O)O	288.30	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Asarinin	101612	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	via CMAUP database
Pluviatilol	70695727	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O	356.40	unknown	https://doi.org/10.1007/BF02979069
Sesamin	72307	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	via CMAUP database
Syringaresinol, (+)-	443023	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1007/BF02979069
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
trans-10-Octadecenoic acid	5282760	Click to see CCCCCCCC=CCCCCCCCCC(=O)O	282.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
(Z)-4-Decenoic acid	5312351	Click to see CCCCCC=CCCC(=O)O	170.25	unknown	via CMAUP database
4-Decenoic acid, (4E)-	5282726	Click to see CCCCCC=CCCC(=O)O	170.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Haperforin F	11114000	Click to see CC1(C23CC(=O)OC2(C4CCC(C(C(=O)C4(C3CC(=O)O1)C)(C(=O)OC)O)(C)C(=O)C5=COC=C5)C)C	516.50	unknown	https://doi.org/10.1248/CPB.48.614
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(8R,9S,10S,13R,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	51051617	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CCC4C3(CC=C(C4)O)C)C	400.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
Campesteryl ferulate	15056832	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C=CC5=CC(=C(C=C5)O)OC)C)C	576.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8R,9R,10S,13R,14R,17R)-17-[(E,2R,5R)-5-ethyl-6-methylhept-3-en-2-yl]-3,10,13-trimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene	50930798	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)C)C)C)C(C)C	410.70	unknown	via CMAUP database
(3R,8R,9R,10S,13R,14R,17S)-17-[(2R,5R)-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	162965363	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/S0031-9422(00)88485-X
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/S0031-9422(00)88485-X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde	126	Click to see C1=CC(=CC=C1C=O)O	122.12	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(2e,3r,4r)-2-(11-Dodecenylidene)-3-hydroxy-4-methoxy-4-methylbutanolide	10662755	Click to see CC1(C(C(=CCCCCCCCCCC=C)C(=O)O1)O)OC	310.40	unknown	https://doi.org/10.1248/CPB.48.614
3-Dodec-11-enylidene-4-hydroxy-5-methoxy-5-methyloxolan-2-one	75214750	Click to see CC1(C(C(=CCCCCCCCCCC=C)C(=O)O1)O)OC	310.40	unknown	https://doi.org/10.1248/CPB.48.614
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
3-(1-Methoxy-11-dodecenyl)-5-methylene-2,5-dihydrofuran-2-one	9994490	Click to see COC(CCCCCCCCCC=C)C1=CC(=C)OC1=O	292.40	unknown	https://doi.org/10.1248/CPB.48.614
3-[(1S)-1-methoxydodec-11-enyl]-5-methylidenefuran-2-one	162989275	Click to see COC(CCCCCCCCCC=C)C1=CC(=C)OC1=O	292.40	unknown	https://doi.org/10.1248/CPB.48.614
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(2z,3s,4s)-2-(11-Dodecenylidene)-3-hydroxy-4-methylbutanolide	10401436	Click to see CC1C(C(=CCCCCCCCCCC=C)C(=O)O1)O	280.40	unknown	https://doi.org/10.1248/CPB.48.614
> Organoheterocyclic compounds / Oxolanes
Isooblusilactonc A	6442493	Click to see CCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O	308.50	unknown	via CMAUP database
Isoobtusilactone	5318618	Click to see C=CCCCCCCCCCC=C1C(C(=C)OC1=O)O	278.40	unknown	via CMAUP database
Isoobtusilactone B	101286261	Click to see CCCCCCCCC=CCCCCCC=C1C(C(=C)OC1=O)O	334.50	unknown	via CMAUP database
Obtusilactone	6442495	Click to see C=CCCCCCCCCCC=C1C(C(=C)OC1=O)O	278.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
(3Z)-4-hydroxy-5-methylidene-3-tetradecylideneoxolan-2-one	10448019	Click to see CCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O	308.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Anigopreissin A	636473	Click to see C1=CC(=CC=C1C=CC2=CC(=C3C(=C2)OC(=C3C4=CC(=CC(=C4)O)O)C5=CC=C(C=C5)O)O)O	452.50	unknown	via CMAUP database
Anigopreissin A-4a-O-beta-D-glucopyranoside	21575645	Click to see C1=CC(=CC=C1C=CC2=CC(=C3C(=C2)OC(=C3C4=CC(=CC(=C4)O)O)C5=CC=C(C=C5)OC6C(C(C(C(O6)CO)O)O)O)O)O	614.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	via CMAUP database
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(4-Hydroxyphenyl)propionic acid	10394	Click to see C1=CC(=CC=C1CCC(=O)O)O	166.17	unknown	via CMAUP database

Biological Material Top

Contributors Top

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Collections Top

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Lindera obtusiloba

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top