Scientific name	Authority	First published in
Teucrium leucosceptrum	Voigt	Hort. Suburb. Calcutt. : 463 (1845)
Teucrium macrostachyum	Wall. ex Benth.	Labiat. Gen. Spec. : 664 (1835)
Clerodendrum leucosceptrum	D.Don	Prodr. Fl. Nepal. : 103 (1825)
Comanthosphace nepalensis	Kitam. & Murata	Acta Phytotax. Geobot. 15: 109 (1954)

Common names Top

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Filter by language:

Language	Common/alternative name
Chinese	米团花
Chinese	蜂蜜树
Chinese	山蜂蜜
Chinese	明堂花
Chinese	渍糖树
Chinese	渍糖花
Chinese	白杖木
Chinese	羊巴巴
Chinese	蜜蜂树花

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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 South-central
  - Tibet

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - Nepal
  - West Himalaya
- Indo-China
  - Laos
  - Myanmar
  - Thailand
  - Vietnam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000227354
Tropicos	17606951
KEW	urn:lsid:ipni.org:names:449566-1
The Plant List	kew-112074
Open Tree Of Life	333118
NCBI Taxonomy	694369
IPNI	449566-1
iNaturalist	498527
GBIF	3885429
EOL	2893922
USDA GRIN	21988
CMAUP	NPO98

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

DNA Barcoding and Fertilization Strategies in Sideritis syriaca subsp. syriaca, a Local Endemic Plant of Crete with High Medicinal Value

Paschalidis K, Fanourakis D, Tsaniklidis G, Tsichlas I, Tzanakakis VA, Bilias F, Samara E, Ipsilantis I, Grigoriadou K, Samartza I, Matsi T, Tsoktouridis G, Krigas N

Int J Mol Sci

04-Feb-2024

PMCID:	PMC10856587
doi:	10.3390/ijms25031891
PMID:	38339166

The functional evolution of architecturally different plant geranyl diphosphate synthases from geranylgeranyl diphosphate synthase

Song S, Jin R, Chen Y, He S, Li K, Tang Q, Wang Q, Wang L, Kong M, Dudareva N, Smith BJ, Zhou F, Lu S

Plant Cell

17-Mar-2023

PMCID:	PMC10226565
doi:	10.1093/plcell/koad083
PMID:	36929908

The complete chloroplast genome of Elsholtzia fruticosa (D. Don) Rehd. (Labiatae), an ornamental plant with high medicinal value

Yu X, Song YR, Zhao ZN

Mitochondrial DNA B Resour

28-Feb-2023

PMCID:	PMC9980026
doi:	10.1080/23802359.2023.2183069
PMID:	36876144

Secondary Metabolites in Nectar-Mediated Plant-Pollinator Relationships

Barberis M, Calabrese D, Galloni M, Nepi M

Plants (Basel)

25-Jan-2023

PMCID:	PMC9920422
doi:	10.3390/plants12030550
PMID:	36771634

Diversity, distribution, and sustainability of traditional medicinal plants in Kaski district, western Nepal

Khakurel D, Uprety Y, Ahn G, Cha JY, Kim WY, Lee SH, Rajbhandary S

Front Pharmacol

20-Dec-2022

PMCID:	PMC9807671
doi:	10.3389/fphar.2022.1076351
PMID:	36605393

Total Synthesis of Terpenes and Their Biological Significance: A Critical Review

Kanwal A, Bilal M, Rasool N, Zubair M, Shah SA, Zakaria ZA

Pharmaceuticals (Basel)

11-Nov-2022

PMCID:	PMC9699253
doi:	10.3390/ph15111392
PMID:	36422521

Functional analysis of Pogostemon cablin farnesyl pyrophosphate synthase gene and its binding transcription factor PcWRKY44 in regulating biosynthesis of patchouli alcohol

Wang X, Tang Y, Huang H, Wu D, Chen X, Li J, Zheng H, Zhan R, Chen L

Front Plant Sci

26-Aug-2022

PMCID:	PMC9458891
doi:	10.3389/fpls.2022.946629
PMID:	36092423

Functional Prediction of trans-Prenyltransferases Reveals the Distribution of GFPPSs in Species beyond the Brassicaceae Clade

Zhang J, Ma Y, Chen Q, Yang M, Feng D, Zhou F, Wang G, Wang C

Int J Mol Sci

22-Aug-2022

PMCID:	PMC9409350
doi:	10.3390/ijms23169471
PMID:	36012736

Fungal Endophytes: A Potential Source of Antibacterial Compounds

Deshmukh SK, Dufossé L, Chhipa H, Saxena S, Mahajan GB, Gupta MK

J Fungi (Basel)

08-Feb-2022

PMCID:	PMC8877021
doi:	10.3390/jof8020164
PMID:	35205918

The Biosynthesis and Transport of Ophiobolins in Aspergillus ustus 094102

Yan J, Pang J, Liang J, Yu W, Liao X, Aobulikasimu A, Yi X, Yin Y, Deng Z, Hong K

Int J Mol Sci

08-Feb-2022

PMCID:	PMC8836403
doi:	10.3390/ijms23031903
PMID:	35163826

Convergent evolution of a blood-red nectar pigment in vertebrate-pollinated flowers

Roy R, Moreno N, Brockman SA, Kostanecki A, Zambre A, Holl C, Solhaug EM, Minami A, Snell-Rood EC, Hampton M, Bee MA, Chiari Y, Hegeman AD, Carter CJ

Proc Natl Acad Sci U S A

24-Jan-2022

PMCID:	PMC8812537
doi:	10.1073/pnas.2114420119
PMID:	35074876

An extremely promiscuous terpenoid synthase from the Lamiaceae plant Colquhounia coccinea var. mollis catalyzes the formation of sester-/di-/sesqui-/mono-terpenoids

Li DS, Hua J, Luo SH, Liu YC, Chen YG, Ling Y, Guo K, Liu Y, Li SH

Plant Commun

12-Aug-2021

PMCID:	PMC8554039
doi:	10.1016/j.xplc.2021.100233
PMID:	34746763

Systematic Placement of the Enigmatic Southeast Asian Genus Paralamium and an Updated Phylogeny of Tribe Pogostemoneae (Lamiaceae Subfamily Lamioideae)

Zhao F, Wu YW, Drew BT, Yao G, Chen YP, Cai J, Liu ED, Li B, Xiang CL

Front Plant Sci

16-Apr-2021

PMCID:	PMC8085563
doi:	10.3389/fpls.2021.646133
PMID:	33936133

Occurrence and biosynthesis of plant sesterterpenes (C25), a new addition to terpene diversity

Chen Q, Li J, Ma Y, Yuan W, Zhang P, Wang G

Plant Commun

30-Mar-2021

PMCID:	PMC8553974
doi:	10.1016/j.xplc.2021.100184
PMID:	34746758

Pattern of forest recovery and carbon stock following shifting cultivation in Manipur, North-East India

Thong P, Sahoo UK, Thangjam U, Pebam R

PLoS One

08-Oct-2020

PMCID:	PMC7544089
doi:	10.1371/journal.pone.0239906
PMID:	33031401

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 / Anthracenes / Anthraquinones
Physcione	10639	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC	284.26	unknown	https://doi.org/10.1016/J.PHYTOL.2009.10.007
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
[(E)-3-methyloctadec-2-enyl] (5R,9S)-5,9,12-trimethyltridecanoate	163191161	Click to see CCCCCCCCCCCCCCCC(=CCOC(=O)CCCC(C)CCCC(C)CCC(C)C)C	520.90	unknown	https://doi.org/10.1016/J.PHYTOL.2009.10.007
3-methyloctadec-2-enyl (5R,9S)-5,9,12-trimethyltridecanoate	162981354	Click to see CCCCCCCCCCCCCCCC(=CCOC(=O)CCCC(C)CCCC(C)CCC(C)C)C	520.90	unknown	https://doi.org/10.1016/J.PHYTOL.2009.10.007
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	https://doi.org/10.1016/J.PHYTOL.2009.10.007
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
(4S,27R)-4,27-dipropyltriacont-15-enedioic acid	162875369	Click to see CCCC(CCCCCCCCCCC=CCCCCCCCCCCC(CCC)CCC(=O)O)CCC(=O)O	564.90	unknown	https://doi.org/10.1016/J.PHYTOL.2009.10.007
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
10,12-Octadecadienoic acid	5282801	Click to see CCCCCC=CC=CCCCCCCCCC(=O)O	280.40	unknown	https://doi.org/10.1016/J.PHYTOL.2009.10.007
Octadeca-10,12-dienoic acid	49823191	Click to see CCCCCC=CC=CCCCCCCCCC(=O)O	280.40	unknown	https://doi.org/10.1016/J.PHYTOL.2009.10.007
Octadeca-5,13-dienoic acid	162953161	Click to see CCCCC=CCCCCCCC=CCCCC(=O)O	280.40	unknown	https://doi.org/10.1016/J.PHYTOL.2009.10.007
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(E)-(7R,11R)-3,7,11,15-tetramethylhexadec-2-ene-1-ol	145386	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	https://doi.org/10.1021/OL040040Y
[(7S,11S)-3,7,11,15-tetramethylhexadec-2-enyl] ethaneperoxoate	162869817	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCOOC(=O)C)C	354.60	unknown	https://doi.org/10.1016/J.PHYTOL.2009.10.007
[(E,7S,11S)-3,7,11,15-tetramethylhexadec-2-enyl] ethaneperoxoate	163195030	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCOOC(=O)C)C	354.60	unknown	https://doi.org/10.1016/J.PHYTOL.2009.10.007
Phytol	5280435	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	https://doi.org/10.1021/OL040040Y
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,3S,3aS,4R,4aR,7R,7aS,8aS)-3a-hydroxy-1,4,7-trimethyl-1-[2-(3-methylfuran-2-yl)ethyl]-3-(2-methylprop-1-enyl)-3,4,4a,5,6,7,7a,8a-octahydrocyclopenta[f][2]benzofuran-8-one	163002981	Click to see CC1CCC2C1C(=O)C3C(OC(C3(C2C)O)C=C(C)C)(C)CCC4=C(C=CO4)C	400.50	unknown	https://doi.org/10.1002/ANGE.201000449
(1R,3S,3aS,4R,4aR,7R,7aS,8aS)-3a,7a-dihydroxy-1,4,7-trimethyl-1-[2-(3-methylfuran-2-yl)ethyl]-3-(2-methylprop-1-enyl)-4,4a,5,6,7,8a-hexahydro-3H-cyclopenta[f][2]benzofuran-8-one	138978679	Click to see CC1CCC2C1(C(=O)C3C(OC(C3(C2C)O)C=C(C)C)(C)CCC4=C(C=CO4)C)O	416.50	unknown	https://doi.org/10.1002/ANGE.201000449
(1S,3R,3aR,4S,4aS,7S,7aR,8aR)-3a-hydroxy-1-[[(1R,5S)-5-hydroxy-3-methyl-2-oxocyclopent-3-en-1-yl]methyl]-1,4,7-trimethyl-3-(2-methylprop-1-enyl)-3,4,4a,5,6,7,7a,8a-octahydrocyclopenta[f][2]benzofuran-8-one	52937183	Click to see CC1CCC2C1C(=O)C3C(OC(C3(C2C)O)C=C(C)C)(C)CC4C(C=C(C4=O)C)O	416.50	unknown	https://doi.org/10.1021/OL200380V
(1S,3R,3aR,4S,4aS,7S,7aR,8aR)-3a,7a-dihydroxy-1-[[(1S,5R)-5-hydroxy-3-methyl-2-oxocyclopent-3-en-1-yl]methyl]-1,4,7-trimethyl-3-(2-methylprop-1-enyl)-4,4a,5,6,7,8a-hexahydro-3H-cyclopenta[f][2]benzofuran-8-one	52937182	Click to see CC1CCC2C1(C(=O)C3C(OC(C3(C2C)O)C=C(C)C)(C)CC4C(C=C(C4=O)C)O)O	432.50	unknown	https://doi.org/10.1021/OL200380V
(4R,5S)-5-[(2R)-3-[(4aR,5S,5aS,6R,8aS,9R,9aR)-4a,5,9a-trihydroxy-3,6,9-trimethyl-5a,6,7,8,8a,9-hexahydro-2H-cyclopenta[g]chromen-5-yl]-2-methyl-3-oxopropyl]-4-hydroxy-2-methylcyclopent-2-en-1-one	162937423	Click to see CC1CCC2C1C(C3(C=C(COC3(C2C)O)C)O)(C(=O)C(C)CC4C(C=C(C4=O)C)O)O	448.50	unknown	https://doi.org/10.1515/ZNB-2007-0418
3a-Hydroxy-1,4,7-trimethyl-1-[2-(3-methylfuran-2-yl)ethyl]-3-(2-methylprop-1-enyl)-3,4,4a,5,6,7,7a,8a-octahydrocyclopenta[f][2]benzofuran-8-one	75235409	Click to see CC1CCC2C1C(=O)C3C(OC(C3(C2C)O)C=C(C)C)(C)CCC4=C(C=CO4)C	400.50	unknown	https://doi.org/10.1002/ANGE.201000449
3a,7a-dihydroxy-1,4,7-trimethyl-1-[2-(3-methylfuran-2-yl)ethyl]-3-(2-methylprop-1-enyl)-4,4a,5,6,7,8a-hexahydro-3H-cyclopenta[f][2]benzofuran-8-one	75235408	Click to see CC1CCC2C1(C(=O)C3C(OC(C3(C2C)O)C=C(C)C)(C)CCC4=C(C=CO4)C)O	416.50	unknown	https://doi.org/10.1002/ANGE.201000449
5-[3-(4a,5,9a-trihydroxy-3,6,9-trimethyl-5a,6,7,8,8a,9-hexahydro-2H-cyclopenta[g]chromen-5-yl)-2-methyl-3-oxopropyl]-4-hydroxy-2-methylcyclopent-2-en-1-one	85425766	Click to see CC1CCC2C1C(C3(C=C(COC3(C2C)O)C)O)(C(=O)C(C)CC4C(C=C(C4=O)C)O)O	448.50	unknown	https://doi.org/10.1515/ZNB-2007-0418 https://doi.org/10.1021/OL040040Y
Leucosesterterpenone	11178395	Click to see CC1CCC2C1C(C3(C=C(COC3(C2C)O)C)O)(C(=O)C(C)CC4C(C=C(C4=O)C)O)O	448.50	unknown	https://doi.org/10.1515/ZNB-2007-0418 https://doi.org/10.1021/OL040040Y
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(5S)-5-[(3S)-4-[(4aR,5S,5aS,6R,8aS,9R,9aR)-4a,5,9a-trihydroxy-3,6,9-trimethyl-5a,6,7,8,8a,9-hexahydro-2H-cyclopenta[g]chromen-5-yl]-3-methyl-4-oxobutyl]-5-hydroxy-4-methylfuran-2-one	163185103	Click to see CC1CCC2C1C(C3(C=C(COC3(C2C)O)C)O)(C(=O)C(C)CCC4(C(=CC(=O)O4)C)O)O	464.50	unknown	https://doi.org/10.1515/ZNB-2007-0418
2-[4-(4,8a-dihydroxy-2,2,5,8-tetramethyl-4a,5,6,7,7a,8-hexahydrocyclopenta[f][1]benzofuran-4-yl)-3-methyl-4-oxobutyl]-3-methyl-2H-furan-5-one	72748201	Click to see CC1CCC2C1C(C3=CC(OC3(C2C)O)(C)C)(C(=O)C(C)CCC4C(=CC(=O)O4)C)O	432.50	unknown	https://doi.org/10.1021/OL040040Y
2-[4-(4a,5,9a-trihydroxy-3,6,9-trimethyl-5a,6,7,8,8a,9-hexahydro-2H-cyclopenta[g]chromen-5-yl)-3-methyl-4-oxobutyl]-3-methyl-2H-furan-5-one	85141729	Click to see CC1CCC2C1C(C3(C=C(COC3(C2C)O)C)O)(C(=O)C(C)CCC4C(=CC(=O)O4)C)O	448.50	unknown	https://doi.org/10.1021/JO030337U
5-[4-(4a,5,9a-trihydroxy-3,6,9-trimethyl-5a,6,7,8,8a,9-hexahydro-2H-cyclopenta[g]chromen-5-yl)-3-methyl-4-oxobutyl]-5-hydroxy-4-methylfuran-2-one	162863489	Click to see CC1CCC2C1C(C3(C=C(COC3(C2C)O)C)O)(C(=O)C(C)CCC4(C(=CC(=O)O4)C)O)O	464.50	unknown	https://doi.org/10.1515/ZNB-2007-0418
Leucosceptrine	10433808	Click to see CC1CCC2C1C(C3(C=C(COC3(C2C)O)C)O)(C(=O)C(C)CCC4C(=CC(=O)O4)C)O	448.50	unknown	https://doi.org/10.1021/JO030337U
Leucosesterlactone	11201309	Click to see CC1CCC2C1C(C3=CC(OC3(C2C)O)(C)C)(C(=O)C(C)CCC4C(=CC(=O)O4)C)O	432.50	unknown	https://doi.org/10.1021/OL040040Y
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,6aR,6aR,6bR,8aR,12aS,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,6,6a,7,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol	162970806	Click to see CC1(CCC2(CCC3(C(C2C1)CCC4C3(CC=C5C4(CCC(C5(C)C)O)C)C)C)C)C	426.70	unknown	https://doi.org/10.1016/J.PHYTOL.2009.10.007
(4aR,6aS,6aS,6bR,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,10,11,12,13,14b-dodecahydropicene-4a-carboxylic acid	162946312	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC=C5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	454.70	unknown	https://doi.org/10.1515/ZNB-2007-0418
10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,10,11,12,13,14b-dodecahydropicene-4a-carboxylic acid	75303863	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC=C5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	454.70	unknown	https://doi.org/10.1515/ZNB-2007-0418
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/J.PHYTOL.2009.10.007
Olean-12-en-3beta-ol	225689	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/J.PHYTOL.2009.10.007
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
1-[(3S,8S,9S,10R,13R,14S,17R)-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-yl]ethanone	162896259	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)C(=O)C)C)C)C(C)C	440.70	unknown	https://doi.org/10.1016/J.PHYTOL.2009.10.007
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/J.PHYTOL.2009.10.007
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
Methyl 2-[14-acetyloxy-6-(furan-3-yl)-13-hydroxy-1,5,15,15-tetramethyl-8,17-dioxo-7,18-dioxatetracyclo[11.3.2.02,11.05,10]octadec-10-en-16-yl]-2-hydroxyacetate	162983214	Click to see CC(=O)OC1C(C(C2(C3CCC4(C(OC(=O)CC4=C3CC1(OC2=O)O)C5=COC=C5)C)C)C(C(=O)OC)O)(C)C	560.60	unknown	https://doi.org/10.1016/J.PHYTOL.2009.10.007
> Organoheterocyclic compounds / Oxepanes
5-Ethenyl-2,5,11,11-tetramethyl-9-methylidene-15-oxatetracyclo[8.4.1.01,10.02,7]pentadec-7-ene-3,8-diol	163073313	Click to see CC1(CCCC23C1(O2)C(=C)C(=C4C3(C(CC(C4)(C)C=C)O)C)O)C	330.50	unknown	https://doi.org/10.1016/J.PHYTOL.2009.10.007
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(1R,5R,6R,6aS,7S,9aR)-1,6,7-Tris(4-hydroxyphenyl)-5-(3,5-dihydroxyphenyl)-8,9-(1,3-dihydroxy-2-butene-1,4-diylidene)-6,6a,7,8,9,9a-hexahydro-5H-2-oxa-1H-cyclohepta[jkl]-as-indacene-4-ol	101103994	Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC(=CC(=C7)O)O)C(=C6)O)C8=CC=C(C=C8)O)C9=CC=C(C=C9)O)O	680.70	unknown	via CMAUP database
(1S,4R,5R,11R,12R,15R,16R,22S)-4,15-bis(3,5-dihydroxyphenyl)-5,11,16,22-tetrakis(4-hydroxyphenyl)-6,17-dioxahexacyclo[10.9.1.02,10.03,7.013,21.014,18]docosa-2(10),3(7),8,13(21),14(18),19-hexaene-9,20-diol	101053432	Click to see C1=CC(=CC=C1C2C3C(C4=C(C2C5=C3C6=C(C=C5O)OC(C6C7=CC(=CC(=C7)O)O)C8=CC=C(C=C8)O)C9=C(C=C4O)OC(C9C1=CC(=CC(=C1)O)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O	906.90	unknown	via CMAUP database
(1S,4R,5R,11R,12R,15R,16S,22S)-4,15-bis(3,5-dihydroxyphenyl)-5,11,16,22-tetrakis(4-hydroxyphenyl)-6,17-dioxahexacyclo[10.9.1.02,10.03,7.013,21.014,18]docosa-2(10),3(7),8,13(21),14(18),19-hexaene-9,20-diol	101103995	Click to see C1=CC(=CC=C1C2C3C(C4=C(C2C5=C3C6=C(C=C5O)OC(C6C7=CC(=CC(=C7)O)O)C8=CC=C(C=C8)O)C9=C(C=C4O)OC(C9C1=CC(=CC(=C1)O)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O	906.90	unknown	via CMAUP database
(2R,9S,10S,11S,12S)-12-(3,5-dihydroxyphenyl)-2-[(R)-[(1S,2R,3R,9S,10S,17S)-3-(3,5-dihydroxyphenyl)-5,13,15-trihydroxy-2,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaen-6-yl]-(4-hydroxyphenyl)methyl]-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.03,8.013,17]heptadeca-1(16),3(8),4,6,13(17),14-hexaene-5,7,14,16-tetrol	16149368	Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC(=CC(=C7)O)O)C(=C6C(C8C9=C(C(C1C(C(C2=C1C8=C(C=C2O)O)C1=CC(=CC(=C1)O)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)C(=CC(=C9)O)O)C1=CC=C(C=C1)O)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O	1361.40	unknown	via CMAUP database
(2R,9S,10S,11S,12S)-12-(3,5-dihydroxyphenyl)-2-[(R)-[(1S,2R,3R,9S,10S,17S)-3-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-5,13,15-trihydroxy-2,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaen-6-yl]-(4-hydroxyphenyl)methyl]-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.03,8.013,17]heptadeca-1(16),3(8),4,6,13(17),14-hexaene-5,7,14,16-tetrol	16151489	Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C(C5=C(C=C(C(=C35)C2C6=CC(=CC(=C6)O)O)O)O)C(C7=CC=C(C=C7)O)C8=C(C9=C1C(C(C9C2=C3C(C(OC3=CC(=C2)O)C2=CC=C(C=C2)O)C2=CC(=CC(=C2)O)O)C2=CC=C(C=C2)O)C(C2=C(C=C(C=C2O)O)C2C1=C8OC2C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O)C1=CC=C(C=C1)O)O	1587.60	unknown	via CMAUP database
1beta,11alpha-Bis(4-hydroxyphenyl)-2alpha-[2alpha-(4-hydroxyphenyl)-3beta-(3,5-dihydroxyphenyl)-6-(beta-D-glucopyranosyloxy)-2,3-dihydrobenzofuran-4-yl]-3-hydroxy-5,6beta-[(S)-2-(4-hydroxyphenyl)-1-oxaethane-1,2-diyl]-1,2,11,11abeta-tetrahydro-6H-dibenzo[cd,g]azulene-8,10-diol	21606280	Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=C8C(C(OC8=CC(=C7)OC9C(C(C(C(O9)CO)O)O)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)C(=C6)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O	1069.10	unknown	via CMAUP database
1beta,11alpha-Bis(4-hydroxyphenyl)-2alpha-[2alpha-(4-hydroxyphenyl)-3beta-[3-(beta-D-glucopyranosyloxy)-5-hydroxyphenyl]-6-hydroxy-2,3-dihydrobenzofuran-4-yl]-3-hydroxy-5,6beta-[(S)-2-(4-hydroxyphenyl)-1-oxaethane-1,2-diyl]-1,2,11,11abeta-tetrahydro-6H-dibenzo[cd,g]azulene-8,10-diol	21606279	Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=C8C(C(OC8=CC(=C7)O)C9=CC=C(C=C9)O)C1=CC(=CC(=C1)OC1C(C(C(C(O1)CO)O)O)O)O)C(=C6)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O	1069.10	unknown	via CMAUP database
5-[(2R,3S)-6-hydroxy-2-(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol	5315234	Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O	454.50	unknown	via CMAUP database
Epsilon-viniferin	5281728	Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O	454.50	unknown	via CMAUP database
vaticanol A	44566412	Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC(=CC(=C7)O)O)C(=C6)O)C8=CC=C(C=C8)O)C9=CC=C(C=C9)O)O	680.70	unknown	via CMAUP database
Vaticanol B	10010985	Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=C8C(C(OC8=CC(=C7)O)C9=CC=C(C=C9)O)C1=CC(=CC(=C1)O)O)C(=C6)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O	906.90	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Scutellarein 4'-methyl ether	11174076	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O	300.26	unknown	https://doi.org/10.1016/J.PHYTOL.2009.10.007
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin	5281628	Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O	300.26	unknown	https://doi.org/10.1016/J.PHYTOL.2009.10.007
Pectolinarigenin	5320438	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O	314.29	unknown	https://doi.org/10.1016/J.PHYTOL.2009.10.007
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
6-Hydroxy-7,8-dimethoxy-2-(4-methoxyphenyl)chromen-4-one	162869818	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=CC(=C(C(=C3O2)OC)OC)O	328.30	unknown	https://doi.org/10.1016/J.PHYTOL.2009.10.007
> Phenylpropanoids and polyketides / Stilbenes
1,3-Benzenediol, 5-[(1Z)-2-(4-hydroxyphenyl)ethenyl]-	5056	Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O	228.24	unknown	via CMAUP database
Resveratrol	445154	Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O	228.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
(2S,3R,4S,5S,6R)-2-[3-hydroxy-5-[2-(4-hydroxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	73642	Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O	390.40	unknown	via CMAUP database
Piceid	5281718	Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O	390.40	unknown	via CMAUP database

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Leucosceptrum canum

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