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Hypericum brasiliense

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64405b8531548213666602
Scientific name Hypericum brasiliense
Authority Choisy
First published in Prodr. 1: 547 (1824)

Description Top

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Synonyms Top

Scientific name Authority First published in
Hypericum bolivianum R.Keller Bull. Herb. Boissier , sér. 2, 8: 189 (1908)
Hypericum stylosum Rusby Bull. New York Bot. Gard. 4: 326 (1907)
Hypericum laxiusculum A.St.-Hil., A.Juss. & Cambess. Pl. Usuel. Bras. : t. 62 (1828)
Receveura graveolens Vell. Fl. Flumin. : 237 (1829)
Hypericum punctulatum A.St.-Hil. Fl. Bras. Merid. 1: 334 (1828)
Hypericum brasiliense var. angustifolium Reichardt Fl. Bras. 12(1): 193 (1878)
Hypericum brasiliense var. punctulatum (A.St.-Hil.) R.Keller Bull. Herb. Boissier , sér. 2, 3: 1126 (1903)
Sarothra brasiliensis (Choisy) Y.Kimura Nov. Fl. Jap. 10: 233 (1951)
Hypericum anceps Larrañaga Escritos D. A. Larrañaga 2: 239 (1923)
Hypericum brasiliense var. latifolium Reichardt Fl. Bras. (Martius) 12(1): 193. 1878 [1 Dec 1878]

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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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
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001296104
Tropicos 7801378
KEW urn:lsid:ipni.org:names:278573-2
The Plant List tro-7801378
Open Tree Of Life 5264504
NCBI Taxonomy 1341022
IPNI 278573-2
GBIF 7330346
EPPO HYPBR
EOL 5707266
USDA GRIN 459892

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
In vitro antimicrobial and antibiofilm screening of eighteen Iranian medicinal plants Hamidi M, Toosi AM, Javadi B, Asili J, Soheili V, Shakeri A BMC Complement Med Ther 28-Mar-2024
PMCID:PMC10976835
doi:10.1186/s12906-024-04437-x
PMID:38549139
The combined application of rutin and silicon alleviates osmotic stress in maize seedlings by triggering accumulation of osmolytes and antioxidants’ defense mechanisms Altansambar N, Sezgin Muslu A, Kadıoglu A Physiol Mol Biol Plants 09-Mar-2024
PMCID:PMC11018582
doi:10.1007/s12298-024-01430-z
PMID:38633275
The Multiple Promoting Effects of Suaeda glauca Root Exudates on the Growth of Alfalfa under NaCl Stress Dong L, Hua Y, Gao Z, Wu H, Hou Y, Chu Y, Zhang J, Cui G Plants (Basel) 07-Mar-2024
PMCID:PMC10974879
doi:10.3390/plants13060752
PMID:38592745
Ethylene and Jasmonates Signaling Network Mediating Secondary Metabolites under Abiotic Stress Pérez-Llorca M, Pollmann S, Müller M Int J Mol Sci 22-Mar-2023
PMCID:PMC10051637
doi:10.3390/ijms24065990
PMID:36983071
Plant Metabolomics: An Overview of the Role of Primary and Secondary Metabolites against Different Environmental Stress Factors Salam U, Ullah S, Tang ZH, Elateeq AA, Khan Y, Khan J, Khan A, Ali S Life (Basel) 06-Mar-2023
PMCID:PMC10051737
doi:10.3390/life13030706
PMID:36983860
Ethyl acetate fractions of Myrciaria floribunda, Ocotea pulchella, and Ocotea notata exhibit promising in vitro activity against Sporothrix brasiliensis isolates with low susceptibility to itraconazole de Souza LC, Reis NF, Alcântara LM, da Silveira Souto SR, de Araújo Penna B, Santos RC, Robbs BK, Machado FP, Castro HC, Machado RL, Rocha L, de Souza Baptista AR Braz J Microbiol 26-Jan-2023
PMCID:PMC9944169
doi:10.1007/s42770-023-00904-8
PMID:36701111
Kaempferol: Antimicrobial Properties, Sources, Clinical, and Traditional Applications Periferakis A, Periferakis K, Badarau IA, Petran EM, Popa DC, Caruntu A, Costache RS, Scheau C, Caruntu C, Costache DO Int J Mol Sci 30-Nov-2022
PMCID:PMC9740324
doi:10.3390/ijms232315054
PMID:36499380
Does phenotyping of Hypericum secondary metabolism reveal a tolerance to biotic/abiotic stressors? Bruňáková K, Bálintová M, Petijová L, Čellárová E Front Plant Sci 30-Nov-2022
PMCID:PMC9748567
doi:10.3389/fpls.2022.1042375
PMID:36531362
The bacterial consortia promote plant growth and secondary metabolite accumulation in Astragalus mongholicus under drought stress Lin Y, Zhang H, Li P, Jin J, Li Z BMC Plant Biol 07-Oct-2022
PMCID:PMC9541091
doi:10.1186/s12870-022-03859-4
PMID:36203134
Natural Products Inhibitors of Monoamine Oxidases—Potential New Drug Leads for Neuroprotection, Neurological Disorders, and Neuroblastoma Chaurasiya ND, Leon F, Muhammad I, Tekwani BL Molecules 04-Jul-2022
PMCID:PMC9268457
doi:10.3390/molecules27134297
PMID:35807542
Profiling of Essential Oils from the Leaves of Pistacia lentiscus Collected in the Algerian Region of Tizi-Ouzou: Evidence of Chemical Variations Associated with Climatic Contrasts between Littoral and Mountain Samples Sehaki C, Jullian N, Choque E, Dauwe R, Fontaine JX, Molinie R, Ayati F, Fernane F, Gontier E Molecules 28-Jun-2022
PMCID:PMC9268259
doi:10.3390/molecules27134148
PMID:35807395
A Global Overview of Diversity and Phylogeny of the Rust Genus Uromyces Gautam AK, Avasthi S, Verma RK, Sushma, Niranjan M, Devadatha B, Jayawardena RS, Suwannarach N, Karunarathna SC J Fungi (Basel) 14-Jun-2022
PMCID:PMC9224716
doi:10.3390/jof8060633
PMID:35736116
Metabolite profiling and protein quantification to a large library of 96 horsegram (Macrotyloma uniflorum) germplasm Gautam M, Chahota RK Sci Rep 12-May-2022
PMCID:PMC9098527
doi:10.1038/s41598-022-11962-7
PMID:35552498
Plant Secondary Metabolites Produced in Response to Abiotic Stresses Has Potential Application in Pharmaceutical Product Development Yeshi K, Crayn D, Ritmejerytė E, Wangchuk P Molecules 05-Jan-2022
PMCID:PMC8746929
doi:10.3390/molecules27010313
PMID:35011546
The Effect of Foliar Application of Melatonin on Changes in Secondary Metabolite Contents in Two Citrus Species Under Drought Stress Conditions Jafari M, Shahsavar A Front Plant Sci 08-Sep-2021
PMCID:PMC8455919
doi:10.3389/fpls.2021.692735
PMID:34567024

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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Chamigranes
[(3S,4S,6R)-4-Bromo-5,5,9-trimethyl-1-methylidenespiro[5.5]undec-9-en-3-yl] acetate 5326339 Click to see CC1=CCC2(CC1)C(=C)CC(C(C2(C)C)Br)OC(=O)C 341.30 unknown https://doi.org/10.1016/0031-9422(95)00848-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
[(1S,8R,11S,13R,18S,19S)-13,17-dihydroxy-14,14,18-trimethyl-9-oxo-4,10-dioxapentacyclo[9.7.1.03,7.08,19.013,18]nonadeca-3(7),5-dien-12-yl] acetate 138113978 Click to see CC(=O)OC1C2C3C(CC4=C(C3C(=O)O2)C=CO4)C5(C1(C(CCC5O)(C)C)O)C 404.50 unknown https://doi.org/10.1016/0031-9422(95)00848-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
2-(hydroxymethyl)-6-[6-hydroxy-6-methyl-2-(3,6,12-trihydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl)hept-4-en-2-yl]oxyoxane-3,4,5-triol 162993531 Click to see CC1(C(CCC2(C1C(CC3(C2CC(C4C3(CCC4C(C)(CC=CC(C)(C)O)OC5C(C(C(C(O5)CO)O)O)O)C)O)C)O)C)O)C 654.90 unknown https://doi.org/10.1016/0031-9422(95)00848-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
2-(1,4',6',12',17',17'-Hexamethylspiro[3,6-dioxabicyclo[3.1.0]hexane-4,8'-9-oxahexacyclo[11.9.0.01,21.04,12.05,10.016,21]docosane]-18'-yl)oxyoxane-3,4,5-triol 72992688 Click to see CC1CC2(C3C(O3)(CO2)C)OC4C1C5(CCC67CC68CCC(C(C8CCC7C5(C4)C)(C)C)OC9C(C(C(CO9)O)O)O)C 602.80 unknown https://doi.org/10.1016/0031-9422(95)00848-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1016/0031-9422(95)00507-4
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(95)00507-4
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(95)00507-4
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,13,14-tetradecahydropicen-3-yl) acetate 3580556 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3=C2CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(95)00507-4
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
methyl (1R,2S,5E)-2-[(2Z,4E)-1-acetyloxy-6-hydroxy-6-methylhepta-2,4-dien-2-yl]-5-methyl-9-methylidenecyclonon-5-ene-1-carboxylate 23655344 Click to see CC1=CCCC(=C)C(C(CC1)C(=CC=CC(C)(C)O)COC(=O)C)C(=O)OC 390.50 unknown https://doi.org/10.1016/0031-9422(95)00848-9
> Organic acids and derivatives / Vinylogous acids
Japonicin A 356268 Click to see CC(C)C(=O)C1=C(C(=C(C(C1=O)(C)C)O)CC2=C(C(C(=O)C(=C2O)C(=O)C(C)C)(C)C)O)O 460.50 unknown https://doi.org/10.1016/0031-9422(95)00507-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / Aminoglycosides
Mathemycin A 73208367 Click to see CC1CCC(=O)OC(C(C(CC(CC(C(C(CC(CC(C(C(CC(CC(C(C(C(C=C(C(C(C=C(C(C(C=CCCC1O)C)O)C)C)O)C)OC2C(C(C(C(O2)CO)O)O)O)O)C)O)O)O)C)O)O)O)C)O)O)OC3C(C(C(C(O3)C)O)N)O)C)C(C)CC(C)CCCCCCN 1397.80 unknown https://doi.org/10.1016/0031-9422(95)00507-4
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
hyperbrasilol C 391023 Click to see CC1=C(C(C(=O)C(=C1O)CC2=C(C(=C(C(=C2O)CC=C(C)C)O)C(=O)C(C)C)O)(CC=C(C)C)C(=O)C(C)C)O 554.70 unknown https://doi.org/10.1016/0031-9422(95)00848-9
Uliginosin A 5315117 Click to see CC(C)C(=O)C1=C(C(=C(C(=C1O)CC2=C(C(C(=O)C(=C2O)C(=O)C(C)C)(C)C)O)O)CC=C(C)C)O 500.60 unknown https://doi.org/10.1016/0031-9422(95)00507-4
> Organic oxygen compounds / Organooxygen compounds / Ethers / Dialkyl ethers
N-[(2E,4Z,6E,8S,10S,12S,14S)-8,10,12,14-tetramethoxy-5,7-dimethylheptadeca-2,4,6,16-tetraen-2-yl]methanimine 162987183 Click to see CC(=CC=C(C)N=C)C=C(C)C(CC(CC(CC(CC=C)OC)OC)OC)OC 407.60 unknown https://doi.org/10.1016/0031-9422(95)00848-9
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
4-[[5,7-Dihydroxy-2,2-dimethyl-6-(2-methylpropanoyl)chromen-8-yl]methyl]-3,5-dihydroxy-6-methyl-6-(3-methylbut-2-enyl)-2-(2-methylpropanoyl)cyclohexa-2,4-dien-1-one 10370372 Click to see CC(C)C(=O)C1=C(C(=C2C(=C1O)C=CC(O2)(C)C)CC3=C(C(C(=O)C(=C3O)C(=O)C(C)C)(C)CC=C(C)C)O)O 552.70 unknown https://doi.org/10.1016/0031-9422(95)00848-9
4-[[5,7-Dihydroxy-2,2-dimethyl-8-(2-methylpropanoyl)chromen-6-yl]methyl]-3,5-dihydroxy-6-methyl-6-(3-methylbut-2-enyl)-2-(2-methylpropanoyl)cyclohexa-2,4-dien-1-one 10030509 Click to see CC(C)C(=O)C1=C(C(=C(C(C1=O)(C)CC=C(C)C)O)CC2=C(C(=C3C(=C2O)C=CC(O3)(C)C)C(=O)C(C)C)O)O 552.70 unknown https://doi.org/10.1016/0031-9422(95)00848-9
4-[[7,9-Dihydroxy-2,2,4,4-tetramethyl-8-(2-methylpropanoyl)-1,3,3a,9b-tetrahydrocyclopenta[c]chromen-6-yl]methyl]-3,5-dihydroxy-6,6-dimethyl-2-(2-methylpropanoyl)cyclohexa-2,4-dien-1-one 10370755 Click to see CC(C)C(=O)C1=C(C2=C(C(=C1O)CC3=C(C(C(=O)C(=C3O)C(=O)C(C)C)(C)C)O)OC(C4C2CC(C4)(C)C)(C)C)O 568.70 unknown https://doi.org/10.1016/0031-9422(95)00507-4
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
5-Hydroxy-1-methoxyxanthone 479656 Click to see COC1=CC=CC2=C1C(=O)C3=C(O2)C(=CC=C3)O 242.23 unknown https://doi.org/10.1016/S0031-9422(00)89727-7
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
6-Deoxyjacareubin 5281629 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=CC=C4)O)C 310.30 unknown https://doi.org/10.1016/S0031-9422(00)89727-7
> Organoheterocyclic compounds / Furopyrans
Hyperbrasilone 197685 Click to see CC1C(C2=C(O1)OC(=CC2=O)C3=CC=C(C=C3)O)(C)C 272.29 unknown https://doi.org/10.1016/S0031-9422(00)89727-7
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Isopropylfuran 12200728 Click to see CC(C)C1=CC=CO1 110.15 unknown https://doi.org/10.1016/0031-9422(95)00507-4
> Organoheterocyclic compounds / Pyrrolidines / Pyrrolidones / Pyrrolidine-3-ones
(3E,5S)-3-[[(1S,4aS,6R,8aR)-1,6-dimethyl-2-[(E)-prop-1-enyl]-4a,5,6,7,8,8a-hexahydro-2H-naphthalen-1-yl]-hydroxymethylidene]-5-(hydroxymethyl)pyrrolidine-2,4-dione 102245587 Click to see CC=CC1C=CC2CC(CCC2C1(C)C(=C3C(=O)C(NC3=O)CO)O)C 359.50 unknown https://doi.org/10.1016/0031-9422(95)00507-4
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Botryllamide A 10254699 Click to see COC1=C(C=C(C=C1Br)C=CNC(=O)C(=CC2=CC=C(C=C2)O)OC)Br 483.10 unknown https://doi.org/10.1016/0031-9422(95)00507-4
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/0031-9422(95)00507-4
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/0031-9422(95)00507-4
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1016/0031-9422(95)00507-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/0031-9422(95)00507-4
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/0031-9422(95)00507-4
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/10.1016/0031-9422(95)00507-4
3-[5-(1,2-Dihydroxyethyl)-3,4-dihydroxyoxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 13179952 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)C(CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/0031-9422(95)00507-4
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/10.1016/0031-9422(95)00507-4
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/0031-9422(95)00507-4
Isoquercitrin 5484006 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)C(CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/0031-9422(95)00507-4
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/10.1016/0031-9422(95)00507-4
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/10.1016/0031-9422(95)00507-4

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