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Internal ID UUID64402169c5236308111279
Scientific name Hypericum pseudopetiolatum
Authority R.Keller
First published in Bull. Herb. Boissier 5: 638 (1897)

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Synonyms Top

Scientific name Authority First published in
Hypericum fukudae H.Koidz. J. Pl. Iwateken 2(2): 88 (1937)
Hypericum koshiense Koidz. Acta Phytotax. Geobot. 6: 210 (1937)
Hypericum lygophyllum H.Koidz. J. Pl. Iwateken 2(2): 85 (1937)
Hypericum oliganthum f. montanum Y.Kimura Bot. Mag. (Tokyo) 52: 190 1938
Hypericum oliganthum f. suberectum Y.Kimura Bot. Mag. (Tokyo) 52: 190 1938
Hypericum oliganthum f. elatum Y.Kimura Bot. Mag. (Tokyo) 52: 190 1938
Hypericum pseudopetiolatum f. elatum (Y.Kimura) Y.Kimura J. Jap. Bot. 15: 296 1939
Hypericum pseudopetiolatum f. montanum (Y.Kimura) Y.Kimura J. Jap. Bot. 15: 296 1939
Hypericum pseudopetiolatum f. koshiense (Koidz.) Y.Kimura J. Jap. Bot. 15: 297 1939
Hypericum pseudopetiolatum f. suberectum (Y.Kimura) Y.Kimura J. Jap. Bot. 15: 297 1939
Hypericum penthorodes f. lucidum Y.Kimura J. Jap. Bot. 15: 300 1939

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Language Common/alternative name
Chinese 短柄金丝桃

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

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Database ID/link to page
World Flora Online wfo-0000728161
Tropicos 7800891
KEW urn:lsid:ipni.org:names:433757-1
The Plant List kew-2858760
Open Tree Of Life 1023853
NCBI Taxonomy 282551
IPNI 433757-1
GBIF 3712795
EOL 5708073
Elurikkus 400683

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)!
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Title Authors Publication Released IDs
Antiproliferative Effects of St. John’s Wort, Its Derivatives, and Other Hypericum Species in Hematologic Malignancies Allegra A, Tonacci A, Spagnolo EV, Musolino C, Gangemi S Int J Mol Sci 25-Dec-2020
PMCID:PMC7795730
doi:10.3390/ijms22010146
PMID:33375664
Petiolins J-M, prenylated acylphloroglucinols from Hypericum pseudopetiolatum var. kiusianum. Tanaka N, Otani M, Kashiwada Y, Takaishi Y, Shibazaki A, Gonoi T, Shiro M, Kobayashi J Bioorg Med Chem Lett 01-Aug-2010
doi:10.1016/J.BMCL.2010.06.047
PMID:20598881
Petiolins F-I, benzophenone rhamnosides from Hypericum pseudopetiolatum var. kiusianum. Tanaka N, Kubota T, Kashiwada Y, Takaishi Y, Kobayashi J Chem Pharm Bull (Tokyo) 01-Oct-2009
doi:10.1248/CPB.57.1171
PMID:19801884
Petiolins D and E, Phloroglucinol Derivatives from Hypericum pseudopetiolatum var. kiusianum Jun'ichi Kobayashi, Naonobu Tanaka, Takaaki Kubota, Haruaki Ishiyama, Yoshiki Kashiwada, Yoshihisa Takaishi, Junji Ito, Yuzuru Mikami, Motoo Shiro The Japan Institute of Heterocyclic Chemistry 27-Mar-2009
doi:10.3987/COM-08-S(D)64
Petiolins A-C, phloroglucinol derivatives from Hypericum pseudopetiolatum var. kiusianum. Tanaka N, Kubota T, Ishiyama H, Araki A, Kashiwada Y, Takaishi Y, Mikami Y, Kobayashi J Bioorg Med Chem 15-May-2008
doi:10.1016/J.BMC.2008.03.076
PMID:18430575

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 / Aristolane sesquiterpenoids
[(1R,1aS,7S,7aS,7bS)-1,7,7a-trimethyl-2,4,5,6,7,7b-hexahydro-1aH-cyclopropa[a]naphthalen-1-yl]methanol 162955814 Click to see CC1CCCC2=CCC3C(C12C)C3(C)CO 220.35 unknown https://doi.org/10.1016/J.BMC.2008.03.076
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
(2,8-Diacetyloxy-7-hydroxy-5,9-dimethyl-4-propanoyloxy-11-prop-1-en-2-yl-16-oxatetracyclo[7.5.2.01,10.03,7]hexadec-12-en-14-yl) benzoate 162977277 Click to see CCC(=O)OC1C(CC2(C1C(C34COC(C3C(C=CC4OC(=O)C5=CC=CC=C5)C(=C)C)(C2OC(=O)C)C)OC(=O)C)O)C 610.70 unknown https://doi.org/10.1016/J.BMC.2008.03.076
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(3,5-Dihydroxyphenyl)-[2,4-dihydroxy-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyphenyl]methanone 154791040 Click to see CC1C(C(C(C(O1)OC2=CC(=CC(=C2C(=O)C3=CC(=CC(=C3)O)O)O)O)O)O)O 408.40 unknown https://doi.org/10.1248/CPB.57.1171
[(2S,3R,4R,5R,6S)-5-acetyloxy-2-[2-(3,5-dihydroxybenzoyl)-3,5-dihydroxyphenoxy]-4-hydroxy-6-methyloxan-3-yl] benzoate 44473624 Click to see CC1C(C(C(C(O1)OC2=CC(=CC(=C2C(=O)C3=CC(=CC(=C3)O)O)O)O)OC(=O)C4=CC=CC=C4)O)OC(=O)C 554.50 unknown https://doi.org/10.1248/CPB.57.1171
[(2S,3R,4S,5S,6S)-5-acetyloxy-2-[2-(3,5-dihydroxybenzoyl)-3,5-dihydroxyphenoxy]-3-hydroxy-6-methyloxan-4-yl] benzoate 44473469 Click to see CC1C(C(C(C(O1)OC2=CC(=CC(=C2C(=O)C3=CC(=CC(=C3)O)O)O)O)O)OC(=O)C4=CC=CC=C4)OC(=O)C 554.50 unknown https://doi.org/10.1248/CPB.57.1171
[5-Acetyloxy-2-[2-(3,5-dihydroxybenzoyl)-3,5-dihydroxyphenoxy]-3-hydroxy-6-methyloxan-4-yl] benzoate 163078057 Click to see CC1C(C(C(C(O1)OC2=CC(=CC(=C2C(=O)C3=CC(=CC(=C3)O)O)O)O)O)OC(=O)C4=CC=CC=C4)OC(=O)C 554.50 unknown https://doi.org/10.1248/CPB.57.1171
[5-Acetyloxy-2-[2-(3,5-dihydroxybenzoyl)-3,5-dihydroxyphenoxy]-4-hydroxy-6-methyloxan-3-yl] benzoate 162956119 Click to see CC1C(C(C(C(O1)OC2=CC(=CC(=C2C(=O)C3=CC(=CC(=C3)O)O)O)O)OC(=O)C4=CC=CC=C4)O)OC(=O)C 554.50 unknown https://doi.org/10.1248/CPB.57.1171
[6-[2-(3,5-Dihydroxybenzoyl)-3,5-dihydroxyphenoxy]-4,5-dihydroxy-2-methyloxan-3-yl] acetate 162847144 Click to see CC1C(C(C(C(O1)OC2=CC(=CC(=C2C(=O)C3=CC(=CC(=C3)O)O)O)O)O)O)OC(=O)C 450.40 unknown https://doi.org/10.1248/CPB.57.1171
2-[(2R)-butan-2-yl]-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162960570 Click to see CCC(C)C1=CC(=O)C2=C(C=C(C=C2O1)OC3C(C(C(C(O3)CO)O)O)O)O 396.40 unknown https://doi.org/10.3987/COM-08-S(D)64
2-Butan-2-yl-5-hydroxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 74932499 Click to see CCC(C)C1=CC(=O)C2=C(C=C(C=C2O1)OC3C(C(C(C(O3)CO)O)O)O)O 396.40 unknown https://doi.org/10.3987/COM-08-S(D)64
Petiolin F 44473468 Click to see CC1C(C(C(C(O1)OC2=CC(=CC(=C2C(=O)C3=CC(=CC(=C3)O)O)O)O)O)O)O 408.40 unknown https://doi.org/10.1248/CPB.57.1171
Petiolin G 44473623 Click to see CC1C(C(C(C(O1)OC2=CC(=CC(=C2C(=O)C3=CC(=CC(=C3)O)O)O)O)O)O)OC(=O)C 450.40 unknown https://doi.org/10.1248/CPB.57.1171
> Organoheterocyclic compounds / Benzofurans
(2R,3aS)-2-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-5,5-dimethyl-7-[(2R)-2-methylbutanoyl]-3a-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-4,6-dione 163028355 Click to see CCC(C)C(=O)C1=C2C(CC(O2)C(C)(CCC=C(C)C)O)(C(=O)C(C1=O)(C)C)CC=C(C)C 458.60 unknown https://doi.org/10.1016/J.BMCL.2010.06.047
2-(2-Hydroxy-6-methylhept-5-en-2-yl)-5,5-dimethyl-3a-(3-methylbut-2-enyl)-7-(2-methylpropanoyl)-2,3-dihydro-1-benzofuran-4,6-dione 75308892 Click to see CC(C)C(=O)C1=C2C(CC(O2)C(C)(CCC=C(C)C)O)(C(=O)C(C1=O)(C)C)CC=C(C)C 444.60 unknown https://doi.org/10.1016/J.BMCL.2010.06.047
2-(2-Hydroxy-6-methylhept-5-en-2-yl)-5,5-dimethyl-7-(2-methylbutanoyl)-3a-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-4,6-dione 75308891 Click to see CCC(C)C(=O)C1=C2C(CC(O2)C(C)(CCC=C(C)C)O)(C(=O)C(C1=O)(C)C)CC=C(C)C 458.60 unknown https://doi.org/10.1016/J.BMCL.2010.06.047
Petiolin L 49862717 Click to see CCC(C)C(=O)C1=C2C(CC(O2)C(C)(CCC=C(C)C)O)(C(=O)C(C1=O)(C)C)CC=C(C)C 458.60 unknown https://doi.org/10.1016/J.BMCL.2010.06.047
Petiolin M 49862718 Click to see CC(C)C(=O)C1=C2C(CC(O2)C(C)(CCC=C(C)C)O)(C(=O)C(C1=O)(C)C)CC=C(C)C 444.60 unknown https://doi.org/10.1016/J.BMCL.2010.06.047
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
2-Methyl-1-[3,5,7-trihydroxy-2,6-dimethyl-2-(4-methylpent-3-enyl)-3,4-dihydrochromen-8-yl]propan-1-one 75251606 Click to see CC1=C(C2=C(C(=C1O)C(=O)C(C)C)OC(C(C2)O)(C)CCC=C(C)C)O 362.50 unknown https://doi.org/10.1016/J.BMCL.2010.06.047
Petiolin J 46911680 Click to see CC1=C(C2=C(C(=C1O)C(=O)C(C)C)OC(C(C2)O)(C)CCC=C(C)C)O 362.50 unknown https://doi.org/10.1016/J.BMCL.2010.06.047
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
1-[(1R,4S,13R)-8-[(2E)-3,7-dimethylocta-2,6-dienyl]-9-hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7(12),8,10-trien-10-yl]-2-methylpropan-1-one 163194364 Click to see CC(C)C(=O)C1=C2C3=C(C(=C1O)CC=C(C)CCC=C(C)C)OC(C4C3CC(O2)(CC4)C)(C)C 466.70 unknown https://doi.org/10.3987/COM-08-S(D)64
1-[8-(3,7-Dimethylocta-2,6-dienyl)-9-hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7(12),8,10-trien-10-yl]-2-methylpropan-1-one 74932498 Click to see CC(C)C(=O)C1=C2C3=C(C(=C1O)CC=C(C)CCC=C(C)C)OC(C4C3CC(O2)(CC4)C)(C)C 466.70 unknown https://doi.org/10.3987/COM-08-S(D)64
Petiolin K 49862649 Click to see CC1=C(C(=C2C3=C1OC(C4C3CC(O2)(CC4)C)(C)C)C(=O)C(C)C)O 344.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.047
> Organoheterocyclic compounds / Pyrans
(2R)-5-hydroxy-2,8,8-trimethyl-2-(4-methylpent-3-enyl)-6-(2-methylpropanoyl)chromen-7-one 163193582 Click to see CC(C)C(=O)C1=C(C2=C(C(C1=O)(C)C)OC(C=C2)(C)CCC=C(C)C)O 358.50 unknown https://doi.org/10.1016/J.BMC.2008.03.076
(2R)-5-hydroxy-2,8,8-trimethyl-6-[(2R)-2-methylbutanoyl]-2-(4-methylpent-3-enyl)chromen-7-one 163034221 Click to see CCC(C)C(=O)C1=C(C2=C(C(C1=O)(C)C)OC(C=C2)(C)CCC=C(C)C)O 372.50 unknown https://doi.org/10.1016/J.BMC.2008.03.076
Petiolin A 44576700 Click to see CC(C)C(=O)C1=C(C2=C(C(C1=O)(C)C)OC(C=C2)(C)CCC=C(C)C)O 358.50 unknown https://doi.org/10.1016/J.BMC.2008.03.076
Petiolin B 44576741 Click to see CCC(C)C(=O)C1=C(C2=C(C(C1=O)(C)C)OC(C=C2)(C)CCC=C(C)C)O 372.50 unknown https://doi.org/10.1016/J.BMC.2008.03.076

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