Scientific name	Authority	First published in
Myrcia caerulescens	Kiaersk.	Enum. Myrt. Bras. : 79 (1893)
Myrcia camaraeana	DC.	Prodr. 3: 251 (1828)
Myrcia ellipticifolia	Cambess.	Fl. Bras. Merid. 2: 312 (1832)
Myrcia glaberrima	Barb.Rodr. ex Chodat & Hassl.	Bull. Herb. Boissier Ser. II. vii. 803 (1907), nomen.
Myrcia glaucescens	Kiaersk.	Enum. Myrt. Bras. : 83 (1893)
Myrcia multiflora f. glaucescens	(O.Berg) D.Legrand	in Fl. Ilustr. Catar. 1(Mirt.): 305 1969
Myrcia multiflora var. glaucescens	(O.Berg) D.Legrand	in Fl. Ilustr. Catar. 1(Mirt.): 305 1969
Myrcia multiflora f. ovalifolia	(O.Berg) D.Legrand	in Fl. Ilustr. Catar. 1(Mirt.): 308 1969
Myrcia multiflora var. ramulosa	D.Legrand	Fl. Ilustr. Catarin. 1(Mirt.): 309. 1969
Myrcia ovalifolia	Kiaersk.	Enum. Myrt. Bras. : 84 (1893)
Myrcia pallida	(O.Berg) N.Silveira	Loefgrenia 88: 2 (1985)
Myrcia sphaerocarpa	DC.	Prodr. 3: 251 (1828)
Myrcia taubatensis	Kiaersk.	Enum. Myrt. Bras. : 79 (1893)
Myrtus multiflora	Spreng.	Syst. Veg. 2: 485 (1825)
Aulomyrcia buxifolia	O.Berg	Fl. Bras. 14(1): 80 (1857)
Aulomyrcia caerulescens	O.Berg	Fl. Bras. 14(1): 80 (1857)
Aulomyrcia caesia	O.Berg	Fl. Bras. 14(1): 83 (1857)
Aulomyrcia camaraeana	O.Berg	Linnaea 27: 50 (1855)
Aulomyrcia glaucescens	O.Berg	Fl. Bras. 14(1): 81 (1857)
Aulomyrcia goyazensis	O.Berg	Fl. Bras. 14(1): 85 (1857)
Aulomyrcia multiflora	O.Berg	Linnaea 27: 47 (1855)
Aulomyrcia ovalifolia	O.Berg	Fl. Bras. 14(1): 81 (1857)
Aulomyrcia pallida	O.Berg	Fl. Bras. 14(1): 87 (1857)
Aulomyrcia perforata	O.Berg	Fl. Bras. 14(1): 83 (1857)
Aulomyrcia sphaerocarpa	O.Berg	Linnaea 27: 51 (1855)
Aulomyrcia vinacea	Steyerm.	Fieldiana, Bot. 28: 1008 (1957)
Aulomyrcia glaucescens var. grandifolia	O.Berg	Fl. Bras. 14(1): 81 (1857)
Aulomyrcia glaucescens var. parvifolia	O.Berg	Fl. Bras. 14(1): 82 (1857)
Aulomyrcia laruotteana var. peruviana	O.Berg	Fl. Bras. 14(1): 91 (1857)
Aulomyrcia multiflora var. grandifolia	O.Berg	Linnaea 30: 660 (1861)
Aulomyrcia sphaerocarpa var. arborescens	O.Berg	Fl. Bras. 14(1): 85 (1857)
Aulomyrcia sphaerocarpa var. complicata	O.Berg	Fl. Bras. 14(1): 86 (1857)
Aulomyrcia sphaerocarpa var. gracilis	O.Berg	Fl. Bras. 14(1): 85 (1857)
Aulomyrcia sphaerocarpa var. intermedia	O.Berg	Fl. Bras. 14(1): 85 (1857)
Aulomyrcia sphaerocarpa var. obtusata	O.Berg	Fl. Bras. 14(1): 86 (1857)
Aulomyrcia sphaerocarpa var. ovata	O.Berg	Fl. Bras. 14(1): 86 (1857)
Aulomyrcia sphaerocarpa var. pauciflora	O.Berg	Fl. Bras. 14(1): 86 (1857)
Myrcia heringeriana	Mattos	Loefgrenia 126: 2 (2008)
Cumetea multiflora	Raf.	Sylva Tellur. : 106 (1838)
Eugenia multiflora	Lam.	Encycl. 3: 202 (1789)

Common names Top

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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

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Caribbean
  - Trinidad-Tobago
- Northern South America
  - French Guiana
  - Guyana
  - Suriname
  - Venezuela
- Southern South America
  - Argentina Northeast
  - Paraguay
  - Uruguay
- Western South America
  - Bolivia
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000247667
UNII	HJN9902K3U
Tropicos	22101878
INPN	734434
KEW	urn:lsid:ipni.org:names:598990-1
The Plant List	kew-131421
Open Tree Of Life	87267
NCBI Taxonomy	375255
IUCN Red List	113042991
IPNI	598990-1
iNaturalist	560899
GBIF	3175074
USDA GRIN	402642

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

Ethnobotanical contributions to global fishing communities: a review

Mendoza JN, Hanazaki N, Prūse B, Martini A, Bittner MV, Kochalski S, Macusi E, Ciriaco A, Mattalia G, Sõukand R

J Ethnobiol Ethnomed

02-Dec-2023

PMCID:	PMC10693712
doi:	10.1186/s13002-023-00630-3
PMID:	38042774

Exploring the chemical composition, in vitro and in silico study of the anticandidal properties of annonaceae species essential oils from the Amazon

Cascaes MM, Marques da Silva SH, de Oliveira MS, Cruz JN, de Moraes ÂA, do Nascimento LD, Ferreira OO, Guilhon GM, Andrade EH

PLoS One

24-Aug-2023

PMCID:	PMC10449155
doi:	10.1371/journal.pone.0289991
PMID:	37616214

Bark production of generalist and specialist species across savannas and forests in the Cerrado

Chiminazzo MA, Bombo AB, Charles-Dominique T, Fidelis A

Ann Bot

18-Jan-2023

PMCID:	PMC10147323
doi:	10.1093/aob/mcad014
PMID:	36651635

The anatomy of the seed-coat includes diagnostic characters in the subtribe Eugeniinae (Myrteae, Myrtaceae)

Sbais PG, Machado NC, Valdemarin KS, Thadeo M, Mazine FF, Mourão KS

Front Plant Sci

05-Oct-2022

PMCID:	PMC9580042
doi:	10.3389/fpls.2022.981884
PMID:	36275536

Essential Oils in Respiratory Mycosis: A Review

Zuzarte M, Salgueiro L

Molecules

28-Jun-2022

PMCID:	PMC9268412
doi:	10.3390/molecules27134140
PMID:	35807386

The Multifunctional Role of Herbal Products in the Management of Diabetes and Obesity: A Comprehensive Review

Rahman MM, Islam MR, Shohag S, Hossain ME, Rahaman MS, Islam F, Ahmed M, Mitra S, Khandaker MU, Idris AM, Chidambaram K, Emran TB, Cavalu S

Molecules

06-Mar-2022

PMCID:	PMC8911649
doi:	10.3390/molecules27051713
PMID:	35268815

Chemical Composition and Antifungal Activity of Myrcia multiflora and Eugenia florida Essential Oils

Ferreira OO, da Silva SH, de Oliveira MS, Andrade EH

Molecules

30-Nov-2021

PMCID:	PMC8658826
doi:	10.3390/molecules26237259
PMID:	34885839

Research Progress of NMR in Natural Product Quantification

Wang ZF, You YL, Li FF, Kong WR, Wang SQ

Molecules

19-Oct-2021

PMCID:	PMC8541192
doi:	10.3390/molecules26206308
PMID:	34684890

Habitat filtering drives the local distribution of congeneric species in a Brazilian white‐sand flooded tropical forest

Ribeiro KF, Martins VF, Wiegand T, Santos FA

Ecol Evol

17-Jan-2021

PMCID:	PMC7882942
doi:	10.1002/ece3.7169
PMID:	33614004

1, 5-dicaffeoylquinic acid, an α-glucosidase inhibitor from the root of Dorema ammoniacum D. Don

Etemadi-Tajbakhsh N, Faramarzi MA, Delnavazi MR

Res Pharm Sci

19-Oct-2020

PMCID:	PMC7879791
doi:	10.4103/1735-5362.297845
PMID:	33628284

Development and Validation of an LC-MS/MS Assay to Quantitate 2′,4′,6′-Trihydroxyacetophenone in Rat and Dog Plasma and its Application to a Pharmacokinetic Study

Yoo HJ, Hwang SJ, Lee JH, Shim WS, Choi YW, Cho SM, Chung EK, Park JB, Lee KT

Molecules

23-Sep-2020

PMCID:	PMC7583961
doi:	10.3390/molecules25194373
PMID:	32977631

Use of visible spectrophotometric fingerprint and chemometric approaches for the differentiation of Mimosa scabrella Bentham honeydew honey

Bergamo G, Seraglio SK, Gonzaga LV, Fett R, Costa AC

J Food Sci Technol

13-Apr-2020

PMCID:	PMC7520470
doi:	10.1007/s13197-020-04425-2
PMID:	33071318

Opposite latitudinal patterns for bird and arthropod predation revealed in experiments with differently colored artificial prey

Zvereva EL, Castagneyrol B, Cornelissen T, Forsman A, Hernández‐Agüero JA, Klemola T, Paolucci L, Polo V, Salinas N, Theron KJ, Xu G, Zverev V, Kozlov MV

Ecol Evol

25-Nov-2019

PMCID:	PMC6953658
doi:	10.1002/ece3.5862
PMID:	31938518

Optimization of Ultrasound-Assisted Extraction of Polyphenols from Myrtus communis L. Pericarp

Bouaoudia-Madi N, Boulekbache-Makhlouf L, Madani K, Silva AM, Dairi S, Oukhmanou–Bensidhoum S, Cardoso SM

Antioxidants (Basel)

02-Jul-2019

PMCID:	PMC6680771
doi:	10.3390/antiox8070205
PMID:	31269759

Biotechnology, In Vitro Production of Natural Bioactive Compounds, Herbal Preparation, and Disease Management (Treatment and Prevention)

Alamgir AN

Therapeutic Use of Medicinal Plants and their Extracts: Volume 2

24-Jun-2018

PMCID:	PMC7123938
doi:	10.1007/978-3-319-92387-1_7

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 / 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/10.1248/CPB.46.113
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Benzoic acid, 2-hydroxy-6-(8-pentadecenyl)-	368156	Click to see CCCCCCC=CCCCCCCCC1=C(C(=CC=C1)O)C(=O)O	346.50	unknown	https://doi.org/10.1248/CPB.46.113
Ginkgolic acid	5281858	Click to see CCCCCCC=CCCCCCCCC1=C(C(=CC=C1)O)C(=O)O	346.50	unknown	https://doi.org/10.1248/CPB.46.113
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
5-Hydroxy-4,8,12-trimethyl-1-(2,6,6-trimethyl-1-cyclohexen-1-yl)-1-pentadecen-7-one	85225982	Click to see CCCC(C)CCCC(C)C(=O)CC(C(C)CC=CC1=C(CCCC1(C)C)C)O	404.70	unknown	https://doi.org/10.1248/CPB.46.113
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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/10.1248/CPB.46.113
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/10.1248/CPB.46.113
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[6-(2-Acetyl-3,5-dihydroxyphenoxy)-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	78173111	Click to see CC(=O)C1=C(C=C(C=C1OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)O	482.40	unknown	https://doi.org/10.1248/CPB.46.113
1-[2,4-Dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethanone	14655247	Click to see CC(=O)C1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)O)O	330.29	unknown	https://doi.org/10.1248/CPB.46.113
Myrciaphenone A	179470	Click to see CC(=O)C1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)O)O	330.29	unknown	https://doi.org/10.1248/CPB.46.113
Myrciaphenone B	183139	Click to see CC(=O)C1=C(C=C(C=C1OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)O	482.40	unknown	https://doi.org/10.1248/CPB.46.113
> Organoheterocyclic compounds / Indolizidines
(-)-uniflorine A	9794258	Click to see C1C(C(C2N1CC(C(C2O)O)O)O)O	205.21	unknown	https://doi.org/10.1021/NP900435D
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol	1203	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/10.1248/CPB.46.113
Cianidanol	9064	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/10.1248/CPB.46.113
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
5,7-Dihydroxy-2-[5-hydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-6,8-dimethyl-2,3-dihydrochromen-4-one	162846805	Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=CC(=C3)O)OC4C(C(C(C(O4)CO)O)O)O)C)O	478.40	unknown	https://doi.org/10.1248/CPB.50.429
Myrciacitrin III	10073779	Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=CC(=C3)O)OC4C(C(C(C(O4)CO)O)O)O)C)O	478.40	unknown	https://doi.org/10.1248/CPB.50.429
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4R,5R,6S)-2-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] 3,4,5-trihydroxybenzoate	5316590	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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O	616.50	unknown	https://doi.org/10.1248/CPB.46.113
[2-[5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] 3,4,5-trihydroxybenzoate	59386481	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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O	616.50	unknown	https://doi.org/10.1248/CPB.46.113
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one	44259215	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	434.30	unknown	https://doi.org/10.1248/CPB.46.113
2-(3,5-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-3-[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	44259504	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)OC)O)O)O)O	478.40	unknown	https://doi.org/10.1248/CPB.46.113
Desmanthin 1	44259450	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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O	616.50	unknown	https://doi.org/10.1248/CPB.46.113
Guaijaverin	5481224	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	434.30	unknown	https://doi.org/10.1248/CPB.46.113
Mearnsetin 3-rhamnoside; Myricetin 4'-methyl ether-3-O-rhamnoside	15560174	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)OC)O)O)O)O	478.40	unknown	https://doi.org/10.1248/CPB.46.113
Mearnsitrin	6918652	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)OC)O)O)O)O	478.40	unknown	https://doi.org/10.1248/CPB.46.113
Myricetin 3-rhamnoside	5352000	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/10.1248/CPB.46.113
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/10.1248/CPB.46.113
Quercetin 3-O-rhamnoside	5353915	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	448.40	unknown	https://doi.org/10.1248/CPB.46.113
Quercitrin	5280459	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	448.40	unknown	https://doi.org/10.1248/CPB.46.113
Reynoutrin	5878729	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	434.30	unknown	https://doi.org/10.1248/CPB.46.113
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[6-[[2-(2,5-Dihydroxyphenyl)-5-hydroxy-6,8-dimethyl-4-oxo-2,3-dihydrochromen-7-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate	85105161	Click to see CC1=C(C2=C(C(=C1OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O)C)OC(CC2=O)C5=C(C=CC(=C5)O)O)O	624.60	unknown	https://doi.org/10.1248/CPB.50.429
[6-[[2-(2,5-Dihydroxyphenyl)-5-hydroxy-6,8-dimethyl-4-oxo-2,3-dihydrochromen-7-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 4-hydroxybenzoate	85124222	Click to see CC1=C(C2=C(C(=C1OC3C(C(C(C(O3)COC(=O)C4=CC=C(C=C4)O)O)O)O)C)OC(CC2=O)C5=C(C=CC(=C5)O)O)O	598.50	unknown	https://doi.org/10.1248/CPB.50.429
5-Hydroxy-2-(2-hydroxy-5-methoxyphenyl)-6,8-dimethyl-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one	53463197	Click to see CC1=C(C2=C(C(=C1OC3C(C(C(C(O3)CO)O)O)O)C)OC(CC2=O)C4=C(C=CC(=C4)OC)O)O	492.50	unknown	https://doi.org/10.1248/CPB.46.113
Myrciacitrin I	183137	Click to see CC1=C(C2=C(C(=C1OC3C(C(C(C(O3)CO)O)O)O)C)OC(CC2=O)C4=C(C=CC(=C4)O)O)O	478.40	unknown	https://doi.org/10.1248/CPB.46.113
myrciacitrin II	183138	Click to see CC1=C(C2=C(C(=C1OC3C(C(C(C(O3)CO)O)O)O)C)OC(CC2=O)C4=C(C=CC(=C4)OC)O)O	492.50	unknown	https://doi.org/10.1248/CPB.46.113
Myrciacitrin IV	10054688	Click to see CC1=C(C2=C(C(=C1OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O)C)OC(CC2=O)C5=C(C=CC(=C5)O)O)O	624.60	unknown	https://doi.org/10.1248/CPB.50.429
Myrciacitrin V	10371340	Click to see CC1=C(C2=C(C(=C1OC3C(C(C(C(O3)COC(=O)C4=CC=C(C=C4)O)O)O)O)C)OC(CC2=O)C5=C(C=CC(=C5)O)O)O	598.50	unknown	https://doi.org/10.1248/CPB.50.429

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Myrcia multiflora

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