Loropetalum chinense

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Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

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Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID6440469a14fdf962841976
Scientific name	Loropetalum chinense
Authority	(R.Br.) Oliv.
First published in	Trans. Linn. Soc. London 23: 459 (1862)

Description Top

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Loropetalum chinense, commonly known as loropetalum, Chinese fringe flower and strap flower, is an evergreen shrub with two forms; a white- (to pale-yellow-) flowering green-leafed variety and a pink-flowering variety with leaves varying from bronze-red when new to olive-green or burgundy when mature. It grows best in fertile, slightly acidic soil in full sun and is hardy down to -15 degrees Celsius (5 degrees Fahrenheit). It is a popular ornamental plant, grown for its prolific clusters of flowers and (in the case of the pink flowering variety) deeply coloured foliage. The leaves, flowers and roots of L. chinense are all used in traditional Chinese medicine. There are many cultivars of Loropetalum chinense, including 'Pizazz', 'Rubrum', 'Ruby', 'Blush', 'Burgundy', 'Fire Dance', 'Hines Purpleleaf', 'Purple Majesty', 'Raspberry Fringe', 'Razzle-Dazzle', 'Zhuzhou Fuchsia', 'Black Pearl', 'Chang Nian Hong', 'China Pink', 'Emerald Snow', 'Ever Red', 'Gr

Synonyms Top

Scientific name	Authority	First published in
Hamamelis chinensis	R.Br.	Narr. Journey China : 375 (1818)
Loropetalum subcapitatum	Chun ex H.T.Chang	Acta Sci. Nat. Univ. Sunyatseni 1959(2): 35 (1959)
Tetrathyrium simaoense	Y.Y.Qian	Acta Bot. Yunnan. 16: 235 (1994)
Loropetalum indicum	K.Y.Tong	Bull. Dept. Biol. Coll. Sci. Sun Yatsen Univ. 2: 36 (1930)

Common names Top

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Filter by language:

Language	Common/alternative name
English	chinese fringe flower
English	loropetalum
English	strap flower
Azerbaijani	Çin loropetalumu
Japanese	トキワマンサク
Chinese	木继木
Chinese	槛木叶
Chinese	槛木根
Chinese	槛花
Chinese	檵木
Chinese	檵花叶
Chinese	繼木

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Loropetalum chinense var. coloratum	C.Q.Huang	Bull. Bot. Res., Harbin 16: 508 (2001)
Loropetalum chinense var. rubrum	Yieh	J. Chin. Soc. Hort. Sci. 1942(2): 33. (1942)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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 South-central
  - China Southeast
- Eastern Asia
  - Japan
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
- Indo-China
  - Thailand

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0001065276
Florida Plant Atlas	4846
Flora of Alabama	5453
Tropicos	15100094
KEW	urn:lsid:ipni.org:names:430722-1
The Plant List	tro-15100094
Missouri Botanical Garden	281039
Open Tree Of Life	1009297
NCBI Taxonomy	64118
IPNI	430722-1
iNaturalist	186063
GBIF	7329104
Freebase	/m/02x7m4h
EPPO	LORCH
EOL	2887422
USDA GRIN	22674
Wikipedia	Loropetalum_chinense
CMAUP	NPO18881

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

Conserved DNA sequence analysis reveals the phylogeography and evolutionary events of Akebia trifoliata in the region across the eastern edge of the Tibetan Plateau and subtropical China

Dong Q, Zhang Y, Zhong S, Zhang Q, Yang H, Yang H, Yi X, Tan F, Chen C, Luo P

BMC Ecol Evol

23-Apr-2024

PMCID:	PMC11040917
doi:	10.1186/s12862-024-02243-0
PMID:	38654171

Quadrat soil pollen signal reflects plant important values in forests and shrublands from subtropical China

Li K, Tan B, Liao M, Ni J

Front Plant Sci

20-Mar-2024

PMCID:	PMC10987713
doi:	10.3389/fpls.2024.1348182
PMID:	38571712

First Record of Comparative Plastid Genome Analysis and Phylogenetic Relationships among Corylopsis Siebold & Zucc. (Hamamelidaceae)

Kim TH, Ha YH, Setoguchi H, Choi K, Kim SC, Kim HJ

Genes (Basel)

20-Mar-2024

PMCID:	PMC10970243
doi:	10.3390/genes15030380
PMID:	38540439

Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China

Luo J, Li Q, He J, Yan J, Zhang S, Chang X, Wu T

J Ethnobiol Ethnomed

18-Mar-2024

PMCID:	PMC10946099
doi:	10.1186/s13002-024-00676-x
PMID:	38500123

Soil bacterial community in a photovoltaic system adopted different survival strategies to cope with small-scale light stress under different vegetation restoration modes

Luo Z, Luo J, Wu S, Luo X, Sui X

Front Microbiol

14-Mar-2024

PMCID:	PMC10972850
doi:	10.3389/fmicb.2024.1365234
PMID:	38550859

Commodity risk assessment of Cornus alba and Cornus sanguinea plants from the UK

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, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Manda RR, Schulz OM, Kariampa P, Akrivou A, Antonatos S, Beris D, Debode J, Kritikos C, Kormpi M, Manceau C, Papachristos D, Reppa C, Gardi C, Potting R

EFSA J

12-Mar-2024

PMCID:	PMC10928767
doi:	10.2903/j.efsa.2024.8657
PMID:	38476319

Monitor the freshness of shrimp by smart halochromic films based on gelatin/pectin loaded with pistachio peel anthocyanin nanoemulsion

Taheri-Yeganeh A, Ahari H, Mashak Z, Jafari SM

Food Chem X

20-Feb-2024

PMCID:	PMC10901912
doi:	10.1016/j.fochx.2024.101217
PMID:	38426072

The Complete Mitochondrial Genome of Paeonia lactiflora Pall. (Saxifragales: Paeoniaceae): Evidence of Gene Transfer from Chloroplast to Mitochondrial Genome

Tang P, Ni Y, Li J, Lu Q, Liu C, Guo J

Genes (Basel)

14-Feb-2024

PMCID:	PMC10888214
doi:	10.3390/genes15020239
PMID:	38397228

Differential distribution shifts in two subregions of East Asian subtropical evergreen broadleaved forests—a case of Magnoliaceae

Wu HY, Liu YH, He QX, Ye JW, Tian B

Front Plant Sci

23-Jan-2024

PMCID:	PMC10844446
doi:	10.3389/fpls.2023.1326207
PMID:	38322424

Commodity risk assessment of Corylus avellana plants from the UK

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P

EFSA J

12-Jan-2024

PMCID:	PMC10784871
doi:	10.2903/j.efsa.2024.8495
PMID:	38222930

Plant life history strategies vary in subtropical forests with different disturbance histories: an assessment of biodiversity, biomass, and functional traits

Liu J, Xia H, Zheng Z, Wang Y, Chen J, Ni J, Yu M, Zheng W, Liu L

Front Plant Sci

10-Jan-2024

PMCID:	PMC10806164
doi:	10.3389/fpls.2023.1230149
PMID:	38269140

Understory vegetation diversity patterns of Platycladus orientalis and Pinus elliottii communities in Central and Southern China

Deng N, Caixia L, Ma F, Song Q, Tian Y

Open Life Sci

22-Dec-2023

PMCID:	PMC10752000
doi:	10.1515/biol-2022-0791
PMID:	38152580

Sugar feeding by invasive mosquito species on ornamental and wild plants

Upshur IF, Fehlman M, Parikh V, Vinauger C, Lahondère C

Sci Rep

13-Dec-2023

PMCID:	PMC10719288
doi:	10.1038/s41598-023-48089-2
PMID:	38092771

First Report of Colletotrichum fructicola, C. rhizophorae sp. nov. and C. thailandica sp. nov. on Mangrove in Thailand

Norphanphoun C, Hyde KD

Pathogens

10-Dec-2023

PMCID:	PMC10747506
doi:	10.3390/pathogens12121436
PMID:	38133319

Diaporthe Species on Palms: Molecular Re-Assessment and Species Boundaries Delimitation in the D. arecae Species Complex

Pereira DS, Hilário S, Gonçalves MF, Phillips AJ

Microorganisms

06-Nov-2023

PMCID:	PMC10673533
doi:	10.3390/microorganisms11112717
PMID:	38004729

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Pentacosanol	92247	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCO	368.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1S,4aR,4bS,7R,10aR)-7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid	12309236	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C	302.50	unknown	via CMAUP database
(2S,4aR,5S,8aR)-5-[(3R)-3-hydroxy-3-methyl-pent-4-enyl]-1,1,4a-trimethyl-6-methylene-decalin-2-ol	479909	Click to see CC1(C2CCC(=C)C(C2(CCC1O)C)CCC(C)(C=C)O)C	306.50	unknown	via CMAUP database
(4aS,4bR,7S,10aS)-7-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-9-one	11460910	Click to see CC(C)C1(CCC2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O	304.50	unknown	via CMAUP database
[(1R,4aS,4bR,7S,9R,10aR)-9-acetyloxy-7-hydroxy-1,4a-dimethyl-7-propan-2-yl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-1-yl]methyl acetate	11165677	Click to see CC(C)C1(CCC2C(=C1)C(CC3C2(CCCC3(C)COC(=O)C)C)OC(=O)C)O	406.60	unknown	via CMAUP database
[(1R,4aS,4bR,7S,9R,10aR)-9-acetyloxy-7-methoxy-1,4a-dimethyl-7-propan-2-yl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-1-yl]methyl acetate	23251064	Click to see CC(C)C1(CCC2C(=C1)C(CC3C2(CCCC3(C)COC(=O)C)C)OC(=O)C)OC	420.60	unknown	via CMAUP database
7-Dehydroabietanone	11289118	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)C)C	284.40	unknown	via CMAUP database
7-Oxodehydroabietinol	15715176	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)CO)C	300.40	unknown	via CMAUP database
7alpha-Hydroxydehydroabietinol	21626425	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)CO)C	302.50	unknown	via CMAUP database
7Beta,18-Dihydroxydehydroabietanol	21632835	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)CO)C	302.50	unknown	via CMAUP database
Abietal	443479	Click to see CC(C)C1=CC2=CCC3C(CCCC3(C2CC1)C)(C)C=O	286.50	unknown	via CMAUP database
Abietic acid	10569	Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C	302.50	unknown	via CMAUP database
Abietyl alcohol	443474	Click to see CC(C)C1=CC2=CCC3C(CCCC3(C2CC1)C)(C)CO	288.50	unknown	via CMAUP database
Dehydroabietal	11694869	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C=O)C	284.40	unknown	via CMAUP database
Dehydroabietinol	15586718	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)CO)C	286.50	unknown	via CMAUP database
Manool	3034394	Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)C	290.50	unknown	via CMAUP database
Neoabietic acid	221118	Click to see CC(=C1CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C	302.50	unknown	via CMAUP database
Palustradienol	13652174	Click to see CC(C)C1=CC2=C(CC1)C3(CCCC(C3CC2)(C)CO)C	288.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(5Z)-2-methyl-6-[(1R)-4-methylcyclohex-3-en-1-yl]hepta-2,5-dien-4-one	12299867	Click to see CC1=CCC(CC1)C(=CC(=O)C=C(C)C)C	218.33	unknown	via CMAUP database
alpha-Atlantone	12299868	Click to see CC1=CCC(CC1)C(=CC(=O)C=C(C)C)C	218.33	unknown	via CMAUP database
Epicubenol	12046149	Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Himachalane and lippifoliane sesquiterpenoids
(-)-alpha-Himachalene	11830551	Click to see CC1=CC2C(CC1)C(=C)CCCC2(C)C	204.35	unknown	via CMAUP database
beta-Himachalene	11586487	Click to see CC1=CC2C(=C(CCCC2(C)C)C)CC1	204.35	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
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
1,3,4-Trihydroxy-5-[3-(4-hydroxyphenyl)prop-2-enoyloxy]cyclohexane-1-carboxylic acid	53420248	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O	338.31	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid	348159	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	https://doi.org/10.1016/S0031-9422(00)95107-0
5-p-Coumaroylquinic acid, (Z)-	90478782	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O	338.31	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
Chlorogenic Acid	1794427	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	https://doi.org/10.1016/S0031-9422(00)95107-0
Chlorogensaure	12310830	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
trans-5-O-(4-coumaroyl)-D-quinic acid	6441280	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O	338.31	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
Shikimic acid	8742	Click to see C1C(C(C(C=C1C(=O)O)O)O)O	174.15	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
Z7Myl7H1AA	10909635	Click to see CC1=CCC(CC1)C(=O)C	138.21	unknown	via CMAUP database
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
[(1R,2S,6R,7S,12R)-2,6-dimethyl-12-propan-2-yl-13,14-dioxatetracyclo[10.2.2.01,10.02,7]hexadec-10-en-6-yl]methanol	11267184	Click to see CC(C)C12CCC3(C(=C1)CCC4C3(CCCC4(C)CO)C)OO2	320.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
1-(1H-indol-1-ium-3-yl)-N,N-dimethylmethanamine	101928958	Click to see CN(C)CC1=C[NH2+]C2=CC=CC=C21	175.25	unknown	via CMAUP database
Gramine	6890	Click to see CN(C)CC1=CNC2=CC=CC=C21	174.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Syringetin	5281953	Click to see COC1=CC(=CC(=C1O)OC)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	346.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Loropetalin D	44259006	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O	752.60	unknown	https://doi.org/10.1016/S0031-9422(97)00295-1
Myricetin 3-beta-D-glucopyranoside	12311099	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O	480.40	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
myricetin 3-O-alpha-D-glucopyranoside	10299455	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O	480.40	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
myricetin 3-O-beta-D-glucopyranoside	5318606	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O	480.40	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
Myricitrin	5281673	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O	464.40	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
> Phenylpropanoids and polyketides / Tannins
.beta-Penta-O-galloyl-D-glucose	374874	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O	940.70	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
[5-Hydroxy-3,4,6-tris[(3,4,5-trihydroxybenzoyl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	14188629	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O	788.60	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
1,2,3,6-Tetragalloyl-beta-D-glucopyranose	5153644	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O	788.60	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
1,2,6-Trigalloyl-beta-D-glucopyranose	3357644	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O	636.50	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
1,2,6-Trigalloylglucose	440308	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O	636.50	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
1,3,4,6-Tetragalloylglucose	471531	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O	788.60	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
NP-003686	73178	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O	788.60	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
Pentagalloylglucose	65238	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O	940.70	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(3,4,5,12,13,21,22,23-Octahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl) 3,4,5-trihydroxybenzoate	13932611	Click to see C1C2C(C(C(C(O2)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O	634.50	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
[(10R,11R,12R,13S,15R)-3,4,5,12,13,21,22,23-octahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate	10461723	Click to see C1C2C(C(C(C(O2)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O	634.50	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
[(2R,3R,4S,5R,6R)-2,5-dihydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxybenzoyl)oxyoxan-3-yl] 3,4,5-trihydroxy-2-[[(10R,11S,12R,13S,15R)-4,21,22,23-tetrahydroxy-8,18-dioxo-3,11,12-tris[(3,4,5-trihydroxybenzoyl)oxy]-13-[3,4,5-trihydroxy-2-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]benzoyl]oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-5-yl]oxy]benzoate	163192010	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C5=C6C(=C4)C(=O)OC7=C6C(=CC(=C7O)O)C(=O)O5)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)OC1=C(C(=C(C=C1C(=O)OC1C(C(C(OC1O)CO)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O	1873.30	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-(3,4,5-trihydroxybenzoyl)oxy-6-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxan-3-yl] 3,4,5-trihydroxy-2-[[(10R,11S,12R,13S,15R)-3,4,5,22,23-pentahydroxy-8,18-dioxo-11,12,13-tris[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-21-yl]oxy]benzoate	16142555	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)OC8=C(C(=C(C=C8C(=O)OC9C(C(C(OC9OC(=O)C1=CC(=C(C(=C1)O)O)O)COC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O)O)O	1573.10	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
[2,5-Dihydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxybenzoyl)oxyoxan-3-yl] 3,4,5-trihydroxy-2-[[4,21,22,23-tetrahydroxy-8,18-dioxo-3,11,12-tris[(3,4,5-trihydroxybenzoyl)oxy]-13-[3,4,5-trihydroxy-2-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]benzoyl]oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-5-yl]oxy]benzoate	163030367	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C5=C6C(=C4)C(=O)OC7=C6C(=CC(=C7O)O)C(=O)O5)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)OC1=C(C(=C(C=C1C(=O)OC1C(C(C(OC1O)CO)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O	1873.30	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 2-[[4,5,6,22,23,26,27,31,32,33,39,47,48,49,52,53-hexadecahydroxy-9,18,36,44,56,62-hexaoxo-12,13,59-tris[(3,4,5-trihydroxybenzoyl)oxy]-2,10,17,29,37,40,43,57,63,64-decaoxaundecacyclo[39.12.5.414,28.111,15.138,42.03,8.019,24.030,35.045,50.051,55.025,61]tetrahexaconta-1(53),3,5,7,19,21,23,25,27,30,32,34,45,47,49,51,54,60-octadecaen-21-yl]oxy]-3,4,5-trihydroxybenzoate	162808035	Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C7C(C(C(O6)OC(=O)C8=CC(=C(C(=C8OC9=C(C(=C2C(=C9)C(=O)OCC3C(C(C(C(O3)O)OC(=O)C3=CC(=C(C(=C3OC3=C(C(=C5C(=C3)C(=O)O7)O)O)O)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C3=CC(=C(C(=C32)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	2505.70	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-12-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate	5153915	Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O	786.60	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
[4,5-Dihydroxy-2-(3,4,5-trihydroxybenzoyl)oxy-6-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxan-3-yl] 3,4,5-trihydroxy-2-[[3,4,5,22,23-pentahydroxy-8,18-dioxo-11,12,13-tris[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-21-yl]oxy]benzoate	162869424	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)OC8=C(C(=C(C=C8C(=O)OC9C(C(C(OC9OC(=O)C1=CC(=C(C(=C1)O)O)O)COC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O)O)O	1573.10	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
[4,5,6,21,22,23,26,27,31,32,33,39,47,48,49,52,53-Heptadecahydroxy-9,18,36,44,56,62-hexaoxo-12,13-bis[(3,4,5-trihydroxybenzoyl)oxy]-2,10,17,29,37,40,43,57,63,64-decaoxaundecacyclo[39.12.5.414,28.111,15.138,42.03,8.019,24.030,35.045,50.051,55.025,61]tetrahexaconta-1(53),3,5,7,19,21,23,25,27,30,32,34,45,47,49,51,54,60-octadecaen-59-yl] 3,4,5-trihydroxybenzoate	16174386	Click to see C1C2C3C(C(C(O2)O)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OC7C(COC(=O)C8=CC(=C(C(=C86)O)O)O)OC(C(C7OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2OC2=C(C(=C(C(=C2)C(=O)O1)C1=C(C(=C(C=C1C(=O)O3)O)O)O)O)O)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O	1721.20	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
1-Desgalloyleugeniin	9918701	Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O	786.60	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
Camelliin B	16130317	Click to see C1C(C2C(C(OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OC6C(COC(=O)C7=CC(=C(C(=C75)O)O)O)OC(C(C6OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C3=CC(=C(C(=C3OC3=C(C(=C(C(=C3)C(=O)O1)C1=C(C(=C(C=C1C(=O)O2)O)O)O)O)O)O)O)O)O)O)O)O)O)C=O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O	1721.20	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
CID 11766372	11766372	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O	938.70	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
CID 16165063	16165063	Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)OC7=C(C(=C(C=C7C(=O)OC8C(C(C9C(O8)COC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)O9)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O	1723.20	unknown	https://doi.org/10.1248/CPB.38.3296
CID 16170073	16170073	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)OC8=C(C(=C(C=C8C(=O)O)O)O)O)O)O)O)O)O	1106.80	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
CID 16174857	16174857	Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)OC7=C(C(=C(C=C7C(=O)OC8C(C(C9C(O8)COC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)O9)O)O)O)O)O)OC1=C(C(=C(C=C1C(=O)OC1C(C(C2C(O1)COC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)O2)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O	2659.80	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
CID 442690	442690	Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O	786.60	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
Eugeniin	442679	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O	938.70	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
Gemin D	471119	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C(C(C=O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O	634.50	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
Rugosin A	16132354	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)OC8=C(C(=C(C=C8C(=O)O)O)O)O)O)O)O)O)O	1106.80	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
Rugosin D	16129626	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C(C(C(O6)OC(=O)C7=CC(=C(C(=C7)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C25)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1875.30	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
Rugosin E	16129738	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)OC4=C(C(=C(C=C4C(=O)OC5C(C(C6C(O5)COC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O6)O)O)O)O)O)O)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O)C(C(C=O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O	1723.20	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0
Tellimagrandin II	151590	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O	938.70	unknown	https://doi.org/10.1016/S0031-9422(00)95107-0

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Loropetalum chinense

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