Davallia divaricata

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID64404cfd4e7bb345912020
Scientific name	Davallia divaricata
Authority	Blume
First published in	Enum. Pl. Javae 2: 237. 1828 ; & HB. 96. Chr. 300. NPfl. 214

Description Top

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It is a small, evergreen fern with a creeping rhizome and fronds that are divided into two parts. The fronds are up to 30 cm long and have a triangular shape. The sori are found on the underside of the fronds and are covered by a kidney-shaped indusium.

Davallia divaricata is a small, evergreen fern native to tropical Southeast Asia. It has a creeping rhizome and fronds that are divided into two parts and can reach up to 30 cm long. The underside of the fronds have sori which are covered by a kidney-shaped indusium. It is part of the genus Davallia and family Davalliaceae.

Synonyms Top

Scientific name	Authority	First published in
Araiostegia decurrens	(Hook.) Kato	Acta Phytotax. Geobot. 26: 158 (1975)
Davallia decurrens	Hook.	Sp. Fil. 1: 167 (1846)
Davallia lobbiana	T.Moore	Index Fil. : 296 (1861)
Davallia mucronata	Blume	Enum. Pl. Javae 2: 235 (1828)
Davallia mucronata	Kunze	Bot. Zeitung (Berlin) 6: 216 (1848)
Davallia polyantha	Hook.	Sp. Fil. 1: 168 (1846)
Davallia sumatrana	Copel.	Philipp. J. Sci., C 9: 230 (1914)
Wibelia decurrens	(Hook.) M.Kato & Tsutsumi	Acta Phytotax. Geobot. 59: 13 (2008)
Wibelia divaricata	(Blume) M.Kato & Tsutsumi	Acta Phytotax. Geobot. 59: 13 (2008)
Microlepia decurrens	(Hook.) Fée	Mém. Foug., 5. Gen. Filic. : 326 (1852)
Microlepia polyantha	(Hook.) Fée	Mém. Foug., 5. Gen. Filic. : 327 (1852)
Davallia amabilis	Ching	Fl. Reipubl. Popularis Sin. 2: 376. 1959. (1959)
Davallia austro-sinica	Ching	Fl. Reipubl. Popularis Sin. 2: 367 (1959)
Davallia orientalis	C.Chr.	Bull. Dept. Biol. Sun Yatsen Univ. 3: 104, t.43. 1932 ; & no. 6. 9. 1933.
Araiostegia divaricata	(Blume) Kato	Acta Phytotax. Geobot. 26: 158 (1975)

Common names Top

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Filter by language:

Language	Common/alternative name
Chinese	大叶骨碎补
Chinese	大葉骨碎補
Chinese	马劳爪

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
Araiostegia divaricata var. formosana	(Hayata) M.Kato	Acta Phytotax. Geobot. 26(5–6): 158 1975

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
  - Hainan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - East Himalaya
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - New Guinea

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001124802
Tropicos	26621020
KEW	urn:lsid:ipni.org:names:17078690-1
Open Tree Of Life	217455
NCBI Taxonomy	328196
IPNI	17078690-1
iNaturalist	982839
GBIF	7310464
Freebase	/m/0wym53n
Wikipedia	Davallia_divaricata
CMAUP	NPO6756
CMAUP	NPO9717
KEW	urn:lsid:ipni.org:names:17428130-1
IPNI	17428130-1
World Flora Online	wfo-0000140419

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

Indoor metabolites and chemicals outperform microbiome in classifying childhood asthma and allergic rhinitis

Sun Y, Tang H, Du S, Chen Y, Ou Z, Zhang M, Chen Z, Tang Z, Zhang D, Chen T, Xu Y, Li J, Norback D, Hashim JH, Hashim Z, Shao J, Fu X, Zhao Z

Eco Environ Health

22-Aug-2023

PMCID:	PMC10902507
doi:	10.1016/j.eehl.2023.08.001
PMID:	38435359

An Ethnopharmaceutical Study on the Hypolipidemic Formulae in Taiwan Issued by Traditional Chinese Medicine Pharmacies

Chi MH, Chao J, Ko CY, Huang SS

Front Pharmacol

15-Sep-2022

PMCID:	PMC9520573
doi:	10.3389/fphar.2022.900693
PMID:	36188612

Ethnobotanical Survey of Natural Galactagogues Prescribed in Traditional Chinese Medicine Pharmacies in Taiwan

Chao J, Ko CY, Lin CY, Tomoji M, Huang CH, Chiang HC, Yang JJ, Huang SS, Su SY

Front Pharmacol

12-Feb-2021

PMCID:	PMC7928277
doi:	10.3389/fphar.2020.625869
PMID:	33679390

Ethnobotanical study on medicinal plants used by Mulam people in Guangxi, China

Hu R, Lin C, Xu W, Liu Y, Long C

J Ethnobiol Ethnomed

02-Jul-2020

PMCID:	PMC7333293
doi:	10.1186/s13002-020-00387-z
PMID:	32616044

An ethnobotanical survey of wild edible plants used by the Yi people of Liangshan Prefecture, Sichuan Province, China

Wang J, Seyler BC, Ticktin T, Zeng Y, Ayu K

J Ethnobiol Ethnomed

26-Feb-2020

PMCID:	PMC7045740
doi:	10.1186/s13002-019-0349-5
PMID:	32102675

Vascular Epiphytic Medicinal Plants as Sources of Therapeutic Agents: Their Ethnopharmacological Uses, Chemical Composition, and Biological Activities

Nugraha AS, Triatmoko B, Wangchuk P, Keller PA

Biomolecules

24-Jan-2020

PMCID:	PMC7072150
doi:	10.3390/biom10020181
PMID:	31991657

A review of the use of pteridophytes for treating human ailments

Baskaran XR, Geo Vigila AV, Zhang SZ, Feng SX, Liao WB

J Zhejiang Univ Sci B

01-Feb-2018

PMCID:	PMC5833325
doi:	10.1631/jzus.B1600344
PMID:	29405039

Chemical and Chemotaxonomical Studies on Filices. LVI. Studies on the Constituents of the Davalliaceous Ferns (1)

TAKAO MURAKAMI, HIROSHI WADA, NOBUTOSHI TANAKA, TADAYUKI KURAISHI, YASUHISA SAIKI, CHIUMING CHEN

Pharmaceutical Society of Japan

20-Apr-2017

doi:	10.1248/YAKUSHI1947.105.7_649

Phytochemicals from fern species: potential for medicine applications

Cao H, Chai TT, Wang X, Morais-Braga MF, Yang JH, Wong FC, Wang R, Yao H, Cao J, Cornara L, Burlando B, Wang Y, Xiao J, Coutinho HD

Phytochem Rev

28-Jan-2017

PMCID:	PMC7089528
doi:	10.1007/s11101-016-9488-7
PMID:	32214919

Kaempferol – A dietary anticancer molecule with multiple mechanisms of action: Recent trends and advancements

Kashyap D, Sharma A, Tuli HS, Sak K, Punia S, Mukherjee TK

J Funct Foods

18-Jan-2017

PMCID:	PMC7104980
doi:	10.1016/j.jff.2017.01.022
PMID:	32288791

Contribution to the Pteridophyte Flora of Langkawi Archipelago, Peninsular Malaysia

Maideen H, Damanhuri A

Trop Life Sci Res

01-Dec-2015

PMCID:	PMC4729403
PMID:	26868714

(−)-Epicatechin-3-O-β-d-allopyranoside from Davallia formosana, Prevents Diabetes and Hyperlipidemia by Regulation of Glucose Transporter 4 and AMP-Activated Protein Kinase Phosphorylation in High-Fat-Fed Mice

Shih CC, Wu JB, Jian JY, Lin CH, Ho HY

Int J Mol Sci

20-Oct-2015

PMCID:	PMC4632785
doi:	10.3390/ijms161024983
PMID:	26492243

Medicinal Plants and Other Living Organisms with Antitumor Potential against Lung Cancer

Monteiro LD, Bastos KX, Barbosa-Filho JM, de Athayde-Filho PF, Diniz MD, Sobral MV

Evid Based Complement Alternat Med

24-Jul-2014

PMCID:	PMC4131470
doi:	10.1155/2014/604152
PMID:	25147575

The Suppressive Activities of Six Sources of Medicinal Ferns Known as Gusuibu on Heat-Labile Enterotoxin-Induced Diarrhea

Chang HC, Chen JC, Yang JL, Tsay HS, Hsiang CY, Ho TY

Molecules

18-Feb-2014

PMCID:	PMC6271568
doi:	10.3390/molecules19022114
PMID:	24552982

The Effects of Davallic Acid from Davallia divaricata Blume on Apoptosis Induction in A549 Lung Cancer Cells

Cheng AS, Chang WC, Cheng YH, Chen KY, Chen KH, Chang TL

Molecules

01-Nov-2012

PMCID:	PMC6268845
doi:	10.3390/molecules171112938
PMID:	23117433

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
(3R)-5,8-dihydroxy-3-methyl-3,4-dihydroisochromen-1-one	10442609	Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)O	194.18	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
6-Methylsalicylic Acid	11279	Click to see CC1=C(C(=CC=C1)O)C(=O)O	152.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzophenones
2,4,6,3',5'-Pentahydroxybenzophenone	19910294	Click to see C1=C(C=C(C=C1O)O)C(=O)C2=C(C=C(C=C2O)O)O	262.21	unknown	via CMAUP database
3,4,5,3'-Tetrahydroxybenzophenone	52948815	Click to see C1=CC(=CC(=C1)O)C(=O)C2=CC(=C(C(=C2)O)O)O	246.21	unknown	via CMAUP database
3',6-Dihydroxy-2,4,4'-trimethoxybenzophenone	101763992	Click to see COC1=C(C=C(C=C1)C(=O)C2=C(C=C(C=C2OC)OC)O)O	304.29	unknown	via CMAUP database
Maclurin	68213	Click to see C1=CC(=C(C=C1C(=O)C2=C(C=C(C=C2O)O)O)O)O	262.21	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Lignoceric Acid	11197	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O	368.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides
1-(beta-D-Glucopyranosyl)-3-ethyl-4-methyl-1H-pyrrole-2,5-dione	100933901	Click to see CCC1=C(C(=O)N(C1=O)C2C(C(C(C(O2)CO)O)O)O)C	301.29	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
3beta-Hydroxy-27-norcycloarta-23-ene-25-one	21626061	Click to see CC(CC=CC(=O)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	426.70	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Guanidines / Biguanides
Metformin	4091	Click to see CN(C)C(=N)N=C(N)N	129.16	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Garcimangosone D	11003703	Click to see C1=CC=C(C=C1)C(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)O)O	392.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Botryosphaerinone	102161310	Click to see CCC=CCC1CC(=O)CC1CC(=O)O	210.27	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Botryosphaeridione	44605081	Click to see CC1C(=O)C=CC2=CC(=O)C(=CC12C)O	204.22	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3,7-Trihydroxy-2-methoxyxanthone	12133315	Click to see COC1=C(C2=C(C=C1O)OC3=C(C2=O)C=C(C=C3)O)O	274.22	unknown	via CMAUP database
1,4,5,6-Tetrahydroxy-2-(2-methylbut-3-en-2-yl)xanthen-9-one	10426622	Click to see CC(C)(C=C)C1=CC(=C2C(=C1O)C(=O)C3=C(O2)C(=C(C=C3)O)O)O	328.30	unknown	via CMAUP database
2-(1,1-Dimethyl-2-propenyl)-1,4,5-trihydroxy-9H-xanthen-9-one	364825	Click to see CC(C)(C=C)C1=CC(=C2C(=C1O)C(=O)C3=C(O2)C(=CC=C3)O)O	312.30	unknown	via CMAUP database
BR-Xanthone B	14034125	Click to see COC1=C(C=C(C2=C1C(=O)C3=C(O2)C(=CC=C3)O)O)O	274.22	unknown	via CMAUP database
Euxanthone	5281631	Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O	228.20	unknown	via CMAUP database
Gentisein	5281635	Click to see C1=CC2=C(C=C1O)C(=O)C3=C(C=C(C=C3O2)O)O	244.20	unknown	via CMAUP database
Norathyriol	5281656	Click to see C1=C(C=C2C(=C1O)C(=O)C3=CC(=C(C=C3O2)O)O)O	260.20	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
1-Hydroxy-3,6,7-trimethoxy-2-(3-methyl-2-butenyl)-8-(3-hydroxy-3-methyl-1E-butenyl)-xanthone	5319715	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(C(=C(C=C3O2)OC)OC)C=CC(C)(C)O)OC)C	454.50	unknown	via CMAUP database
1,3,7-Trihydroxy-2-prenylxanthone	5495920	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=C(C=C3)O)O)C	312.30	unknown	via CMAUP database
1,5-Dihydroxy-3-methoxy-2-prenylxanthone	10449043	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C(=CC=C3)O)OC)C	326.30	unknown	via CMAUP database
1,5,8-Trihydroxy-3-methoxy-2-(3-methylbut-2-en-1-yl)-9H-xanthen-9-one	14162674	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(C=CC(=C3O2)O)O)OC)C	342.30	unknown	via CMAUP database
1,6-Dihydroxy-3-methoxy-2-prenylxanthone	14162675	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=C(C=C3)O)OC)C	326.30	unknown	via CMAUP database
1,6-Dihydroxy-3,7-dimethoxy-2-(3-methyl-2-butenyl)-8-(3-hydroxy-3-methyl-1E-butenyl)-xanthone	5319262	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=C(C(=C3C=CC(C)(C)O)OC)O)OC)C	440.50	unknown	via CMAUP database
1,7-Dihydroxy-3-methoxy-2-prenylxanthone	509269	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=CC(=C3)O)OC)C	326.30	unknown	via CMAUP database
2-(3,7-Dimethylocta-2,6-dienyl)-1,3,5,8-tetrahydroxyxanthen-9-one	72988981	Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C=CC(=C3C2=O)O)O)O)C)C	396.40	unknown	via CMAUP database
Cowagarcinone B	5316764	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=CC(=C(C=C3O2)O)OC)OC)C	356.40	unknown	via CMAUP database
garcinone B	5495928	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(C(=C3)O)OC(C=C4)(C)C)O)C	394.40	unknown	via CMAUP database
Mangostenone D	11696901	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(C(=C3)O)OC(CC4)(C)C)O)C	396.40	unknown	via CMAUP database
Mangostinone	6478778	Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC=C3O)O)C)C	380.40	unknown	via CMAUP database
Smeathxanthone A	11509473	Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C=CC(=C3C2=O)O)O)O)C)C	396.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
1,3,8-trihydroxy-4-(3-hydroxy-3-methylbutanoyl)-2-(3-methylbut-2-enyl)xanthen-9-one	102234394	Click to see CC(=CCC1=C(C2=C(C(=C1O)C(=O)CC(C)(C)O)OC3=CC=CC(=C3C2=O)O)O)C	412.40	unknown	via CMAUP database
1,5,8-Trihydroxy-3-methoxy-2,4-bis(3-methylbut-2-enyl)xanthen-9-one	11711264	Click to see CC(=CCC1=C(C2=C(C(=C1OC)CC=C(C)C)OC3=C(C=CC(=C3C2=O)O)O)O)C	410.50	unknown	via CMAUP database
10,16-Dihydroxy-6,6,19,19-tetramethyl-15-(3-methylbut-2-enyl)-5,13,18-trioxapentacyclo[12.8.0.03,12.04,9.017,22]docosa-1(22),3(12),4(9),7,10,14,16,20-octaen-2-one	71437595	Click to see CC(=CCC1=C2C(=C3C=CC(OC3=C1O)(C)C)C(=O)C4=C(O2)C=C(C5=C4OC(C=C5)(C)C)O)C	460.50	unknown	via CMAUP database
5,8,9-Trihydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one	10046140	Click to see CC(=CCC1=C2C(=CC(=C1O)O)C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)C	394.40	unknown	via CMAUP database
8-Deoxygartanin	392450	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)C(=CC=C3)O)CC=C(C)C)O)C	380.40	unknown	via CMAUP database
Cudraxanthone G	42645953	Click to see CC(=CCC1=C(C2=C(C(=C1OC)CC=C(C)C)OC3=C(C2=O)C=CC=C3O)O)C	394.50	unknown	via CMAUP database
Garcinone A	70689919	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)C=C(C=C3)O)CC=C(C)C)O)C	380.40	unknown	via CMAUP database
Gartanin	5281633	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(C=CC(=C3O2)O)O)CC=C(C)C)O)C	396.40	unknown	via CMAUP database
Mangostenone B	21672078	Click to see CC(=CCC1=C2C(=C3CCC(OC3=C1O)(C)C)C(=O)C4=C(C5=C(C=C4O2)OC(C=C5)(C)C)O)C	462.50	unknown	via CMAUP database
Tovophyllin A	42645954	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C(=C4C(=C3C2=O)C=CC(O4)(C)C)O)CC=C(C)C)O)C	462.50	unknown	via CMAUP database
Tovophyllin B	509268	Click to see CC(=CCC1=C2C(=C3C=CC(OC3=C1O)(C)C)C(=O)C4=C(C5=C(C=C4O2)OC(C=C5)(C)C)O)C	460.50	unknown	via CMAUP database
Trapezifolixanthone	188341	Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=CC=C4O)O)C=CC(O2)(C)C)C	378.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
(2S,3R)-3,4,8-trihydroxy-2-(2-hydroxypropan-2-yl)-7-methoxy-6-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-b]xanthen-5-one	11546716	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C4O)C(C)(C)O)O)O)OC)C	442.50	unknown	via CMAUP database
(3S)-3,5,9-trihydroxy-8-methoxy-2,2-dimethyl-7-(3-methylbut-2-enyl)-3,4-dihydropyrano[3,2-b]xanthen-6-one	92448128	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C(C4)O)(C)C)O)O)OC)C	426.50	unknown	via CMAUP database
1-(3,3-Dimethylbutyl)-3,6,8-trihydroxy-2-methoxy-7-(3-methylbut-2-enyl)xanthen-9-one	89172625	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CCC(C)(C)C)O)C	426.50	unknown	via CMAUP database
1-Isomangostin	5281641	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C=C(C4=C3OC(CC4)(C)C)O)O)OC)C	410.50	unknown	via CMAUP database
1,3,6,7-Tetrahydroxy-8-prenylxanthone	15307924	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)O)C	328.30	unknown	via CMAUP database
1,3,7-Trihydroxy-2-(3-methyl-2-butenyl)-8-(3-methyl-3-hydroxybutyl)-9H-xanthene-9-one	102234393	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C=C3)O)CCC(C)(C)O)O)C	398.40	unknown	via CMAUP database
11Alpha-Mangostanin	46880204	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C4)C(C)(C)O)O)O)OC)C	426.50	unknown	via CMAUP database
3-Isomangostin	13873655	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(CC4)(C)C)O)O)OC)C	410.50	unknown	via CMAUP database
3,5,9-Trihydroxy-8-methoxy-2,2-dimethyl-7-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one	68229267	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C(=C4)O)(C)C)O)O)OC)C	424.40	unknown	via CMAUP database
3,6-Dimethylmangostin	231412	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(C(=C(C=C3O2)OC)OC)CC=C(C)C)OC)C	438.50	unknown	via CMAUP database
4-Hydroxy-7,8-dimethoxy-6-(3-methylbut-2-enyl)furo[3,2-b]xanthen-5-one	101193830	Click to see CC(=CCC1=C2C(=CC(=C1OC)OC)OC3=C(C2=O)C(=C4C=COC4=C3)O)C	380.40	unknown	via CMAUP database
6-Deoxy-gamma-mangostin	13873657	Click to see CC(=CCC1=C(C=CC2=C1C(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)C	380.40	unknown	via CMAUP database
7-Methoxy-2-(3-methyl-2-butenyl)-8-(3-methyl-2-oxo-3-butenyl)-1,3,6-trihydroxyxanthone	69074110	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CC(=O)C(=C)C)O)C	424.40	unknown	via CMAUP database
9-Hydroxycalabaxanthone	5495929	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)O)OC)C	408.40	unknown	via CMAUP database
9-Hydroxycalabaxanthone hydrate	56840489	Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C=C(C(=C4CCC(C)(C)O)OC)O)C	426.50	unknown	via CMAUP database
Beta-Mangostin	5495925	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=C(C(=C3CC=C(C)C)OC)O)OC)C	424.50	unknown	via CMAUP database
Cratoxyxanthone	46879489	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C4C5=C(C(=C(C6=C5OC7=C(C6=O)C(=C(C(=C7)O)OC)CC=C(C)C)O)CC=C(C)C)O)C(C)(C)O)O)O)OC)C	834.90	unknown	via CMAUP database
Demethylcalabaxanthone	509270	Click to see CC(=CCC1=C(C=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)O)C	378.40	unknown	via CMAUP database
Dulxanthone D	10405091	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)C	342.30	unknown	via CMAUP database
gamma-Mangostin	5464078	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)O)CC=C(C)C)O)C	396.40	unknown	via CMAUP database
Garcimangosone A	10874207	Click to see CC(=CCC1=C2C(=C(C3=C1C(=O)C4=C(C5=C(C=C4O3)OC(C=C5)(C)C)O)O)C=CC(O2)(C)C)C	460.50	unknown	via CMAUP database
Garcinone C	44159808	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)O)CCC(C)(C)O)O)C	414.40	unknown	via CMAUP database
Garcinone D	5495926	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CCC(C)(C)O)O)C	428.50	unknown	via CMAUP database
Garcinone E	10298511	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C(=C(C(=C3C2=O)CC=C(C)C)O)O)CC=C(C)C)O)C	464.50	unknown	via CMAUP database
Mangostenone A	509267	Click to see CC(=CCC1=C2C(=C3C=CC(OC3=C1O)(C)C)OC4=CC5=C(C=CC(O5)(C)C)C(=C4C2=O)O)C	460.50	unknown	via CMAUP database
Mangostin	5281650	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CC=C(C)C)O)C	410.50	unknown	via CMAUP database
Rubraxanthone	9953366	Click to see CC(=CCCC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)C)C	410.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
10,22-Dihydroxy-7,7,18,18-tetramethyl-8,13,17-trioxapentacyclo[12.8.0.03,12.04,9.016,21]docosa-1(22),3(12),4(9),10,14,16(21),19-heptaen-2-one	56840488	Click to see CC1(CCC2=C(O1)C(=CC3=C2C(=O)C4=C(C5=C(C=C4O3)OC(C=C5)(C)C)O)O)C	394.40	unknown	via CMAUP database
Br-Xanthone A	13964005	Click to see CC1(CCC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C=C(C5=C4CCC(O5)(C)C)O)C	396.40	unknown	via CMAUP database
Brasilixanthone B	5324261	Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C=C(C5=C4C=CC(O5)(C)C)O)C	392.40	unknown	via CMAUP database
Garcimangosone B	11143989	Click to see CC1(CCC2=C3C(=CC(=C2O1)OC)OC4=CC5=C(C=CC(O5)(C)C)C(=C4C3=O)O)C	408.40	unknown	via CMAUP database
Macluraxanthone	5281646	Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C(C)(C)C=C)OC4=C(C3=O)C=CC(=C4O)O)O)C	394.40	unknown	via CMAUP database
O-Demethylforbexanthone	45269778	Click to see CC1(C=CC2=CC3=C(C(=C2O1)O)OC4=CC(=CC(=C4C3=O)O)O)C	326.30	unknown	via CMAUP database
Thwaitesixanthone	392169	Click to see CC1(C=CC2=C(O1)C=CC3=C2C(=O)C4=C(C5=C(C=C4O3)OC(C=C5)(C)C)O)C	376.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(3R)-8-Hydroxy-3-methyl-3,4-dihydro-1H-2-benzopyran-1-one	114679	Click to see CC1CC2=C(C(=CC=C2)O)C(=O)O1	178.18	unknown	via CMAUP database
cis-4-Hydroxymellein	10420140	Click to see CC1C(C2=C(C(=CC=C2)O)C(=O)O1)O	194.18	unknown	via CMAUP database
trans-4-Hydroxymellein	10262028	Click to see CC1C(C2=C(C(=CC=C2)O)C(=O)O1)O	194.18	unknown	via CMAUP database
> Organoheterocyclic compounds / Dioxanes / 1,3-dioxanes
Botryosphaerihydrofuran	44605288	Click to see CC1COC23C1(O2)CC4(C(C=CC4=C3)C)C	218.29	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3S,4S)-4-acetyl-3-methyloxolan-2-one	118708002	Click to see CC1C(COC1=O)C(=O)C	142.15	unknown	via CMAUP database
Botryosphaerilactone A	102161309	Click to see CC1C(C(OC1OCC2C(C(=O)OC2C)C)C)CO	272.34	unknown	via CMAUP database
Botryosphaerilactone B	44605080	Click to see CC1C(COC1OCC2C(C(=O)OC2C)C)C(=O)C	270.32	unknown	via CMAUP database
Botryosphaerilactone C	102161308	Click to see CC1C(C(OC1OCC2C(C(=O)OC2C)C)C)CO	272.34	unknown	via CMAUP database
Dihydro-4-(hydroxymethyl)-3,5-dimethyl-2	102125217	Click to see CC1C(C(OC1=O)C)CO	144.17	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
Lasiolactone	89352705	Click to see CCCC1CC=CC(=O)O1	140.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Egonol	485186	Click to see COC1=CC(=CC2=C1OC(=C2)C3=CC4=C(C=C3)OCO4)CCCO	326.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,2'R,3R,3'R)-2,2'-Bis(3,4-dihydroxyphenyl)-3,3',4,4'-tetrahydro-2H,2'H-4,8'-bichromene-3,3',5,5',7,7'-hexol	5320711	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1016/0031-9422(89)80138-4
(2R,3R,4S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-6-[(2R,3R,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-4-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-6-yl]-3,4-dihydro-2H-chromene-3,5,7-triol	101872119	Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C5C(=C(C(=C6)O)C7C(C(OC8=CC(=CC(=C78)O)O)C9=CC(=C(C=C9)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O	1155.00	unknown	https://doi.org/10.1016/0031-9422(90)89050-J
2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-6-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-6-yl]-3,4-dihydro-2H-chromene-3,5,7-triol	16170671	Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C5C(=C(C(=C6)O)C7C(C(OC8=CC(=CC(=C78)O)O)C9=CC(=C(C=C9)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O	1155.00	unknown	https://doi.org/10.1016/0031-9422(90)89050-J
2-[(2R,3R,4S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]acetic acid	101872122	Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C(=C(C=C3O)O)C4C(C(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)CC(=O)O)O)O)O	636.60	unknown	https://doi.org/10.1016/0031-9422(90)89050-J
2-[2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]acetic acid	14463086	Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C(=C(C=C3O)O)C4C(C(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)CC(=O)O)O)O)O	636.60	unknown	https://doi.org/10.1016/0031-9422(90)89050-J
5-Hydroxy-8-[5-hydroxy-7-methoxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]-7-methoxy-2-(4-methoxyphenyl)chromen-4-one	11103936	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)OC)O)OC	594.60	unknown	via CMAUP database
Proanthocyanidin A1	9872976	Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O	576.50	unknown	via CMAUP database
Procyanidin A2	124025	Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O	576.50	unknown	via CMAUP database
Procyanidin B2, (+)-	122738	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1016/0031-9422(89)80138-4
Procyanidin B5	124017	Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]acetic acid	14463077	Click to see C1=CC(=C(C=C1C2C(C(C3=C(C=C(C=C3O2)O)O)CC(=O)O)O)O)O	348.30	unknown	https://doi.org/10.1016/0031-9422(90)89050-J
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
Dryopteric acid	11393902	Click to see C1=CC(=C(C=C1C2C(C(C3=C(C=C(C=C3O2)O)O)CC(=O)O)O)O)O	348.30	unknown	https://doi.org/10.1016/0031-9422(90)89050-J
Epicatechin	72276	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1016/0031-9422(90)89050-J https://doi.org/10.1016/0031-9422(89)80138-4
methyl 2-[(2R,3R,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]acetate	14463085	Click to see COC(=O)CC1C(C(OC2=CC(=CC(=C12)O)O)C3=CC(=C(C=C3)O)O)O	362.30	unknown	https://doi.org/10.1016/0031-9422(90)89050-J
methyl 2-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]acetate	14463083	Click to see COC(=O)CC1C(C(OC2=CC(=CC(=C12)O)O)C3=CC(=C(C=C3)O)O)O	362.30	unknown	https://doi.org/10.1016/0031-9422(90)89050-J
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astilbin	119258	Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	450.40	unknown	via CMAUP database
Astragalin	5282102	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1248/YAKUSHI1947.105.7_649
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Galangin 3-methyl ether	5281946	Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	284.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
(5R) 5-hydroxylasiodiplodin	10638525	Click to see CC1CC(CCCCCC2=C(C(=CC(=C2)O)OC)C(=O)O1)O	308.40	unknown	via CMAUP database
(5S) 5-hydroxylasiodiplodin	10733600	Click to see CC1CC(CCCCCC2=C(C(=CC(=C2)O)OC)C(=O)O1)O	308.40	unknown	via CMAUP database
Lasiodiplodin	14562696	Click to see CC1CCCCCCCC2=C(C(=CC(=C2)O)OC)C(=O)O1	292.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(2R,3R,4S,5R,6S)-6-hydroxy-4,5-bis[(3,4,5-trihydroxybenzoyl)oxy]-2-[(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	16157969	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(OC(C(C9OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)COC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O	1725.20	unknown	via CMAUP database
alpha-Pedunculagin	13834142	Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O	784.50	unknown	via CMAUP database
beta-Pedunculagin	5320441	Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O	784.50	unknown	via CMAUP database
Casuarictin	73644	Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O	936.60	unknown	via CMAUP database
CID 12302513	12302513	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	934.60	unknown	via CMAUP database
Ellagic Acid	5281855	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O	302.19	unknown	via CMAUP database
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	via CMAUP database
Phyllyraeoidin	16170028	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(OC(C(C9OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=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	1877.30	unknown	via CMAUP database

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Davallia divaricata

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