Hypericum oblongifolium - Unknown
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Internal ID UUID6440216427f70901661336
Scientific name Hypericum oblongifolium
Authority Choisy
First published in Prodr. Monogr. Hypéric. : 42 (1821)

Description Top

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Synonyms Top

Scientific name Authority First published in
Norysca cernua (Roxb. ex D.Don) Voigt Hort. Suburb. Calcutt. : 90 (1845)
Norysca oblongifolia (Choisy) Blume Mus. Bot. 2: 22 (1856)
Hypericum cernuum Roxb. ex D.Don Prodr. Fl. Nepal. 218 1825
Hypericum speciosum Wall. Numer. List : n.º 4803 (1831)
Hypericum patulum var. oblongifolium (Choisy) Koehne Deutsch. Dendrol. 415. 1893
Hypericum cernuum Roxb. ex D.Don Prodr. Fl. Nepal. : 218 (1825)

Common names Top

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Language Common/alternative name
English pendant st. john's wort
Bengali চিত্রই

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Nepal
      • Pakistan
      • West Himalaya

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000728037
Tropicos 7800038
KEW urn:lsid:ipni.org:names:433668-1
The Plant List kew-2858607
Open Tree Of Life 870726
NCBI Taxonomy 673930
IPNI 433668-1
GBIF 3713869
EOL 2878480
USDA GRIN 19597
Wikipedia Hypericum_oblongifolium
CMAUP NPO26529

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
Natural antioxidants that act against Alzheimer’s disease through modulation of the NRF2 pathway: a focus on their molecular mechanisms of action Sidiropoulou GA, Metaxas A, Kourti M Front Endocrinol (Lausanne) 03-Jul-2023
PMCID:PMC10351420
doi:10.3389/fendo.2023.1217730
PMID:37465125
Folicitin abrogates scopolamine induced oxidative stress, hyperlipidemia mediated neuronal synapse and memory dysfunction in mice Gul S, Attaullah S, Alsugoor MH, Bawazeer S, Shah SA, Khan S, Salahuddin HS, Ullah M Heliyon 15-Jun-2023
PMCID:PMC10320035
doi:10.1016/j.heliyon.2023.e16930
PMID:37416682
Effect of in vitro simulated digestion on the anti-Helicobacter Pylori activity of different Propolis extracts Governa P, Romagnoli G, Albanese P, Rossi F, Manetti F, Biagi M J Enzyme Inhib Med Chem 14-Mar-2023
PMCID:PMC10026752
doi:10.1080/14756366.2023.2183810
PMID:36916299
Folecitin Isolated from Hypericum oblongifolium Exerts Neuroprotection against Lipopolysaccharide-Induced Neuronal Synapse and Memory Dysfunction via p-AKT/Nrf-2/HO-1 Signalling Pathway Farooq U, Sahibzada MU, Khan T, Ullah R, Shahid M, Khusro A, Seidel V, Abdellattif MH, Emran TB Evid Based Complement Alternat Med 28-Mar-2022
PMCID:PMC8979689
doi:10.1155/2022/9419918
PMID:35388307
Ethnomedicinal Plants Used in the Health Care System: Survey of the Mid Hills of Solan District, Himachal Pradesh, India Kumar M, Radha, Devi H, Prakash S, Rathore S, Thakur M, Puri S, Pundir A, Bangar SP, Changan S, Ilakiya T, Samota MK, Damale RD, Singh S, Berwal MK, Dhumal S, Bhoite AG, Sharma A, Senapathy M, Bhushan B, Maurya VK, Asha, Natta S, Amarowicz R, Mekhemar M Plants (Basel) 05-Sep-2021
PMCID:PMC8467016
doi:10.3390/plants10091842
PMID:34579373
Isolation, Characterization and Neuroprotective Activity of Folecitin: An In Vivo Study Farooq U, Khan T, Shah SA, Hossain MS, Ali Y, Ullah R, Raziq N, Shahid M, Capasso R Life (Basel) 12-Aug-2021
PMCID:PMC8400650
doi:10.3390/life11080825
PMID:34440569
Natural Xanthones and Skin Inflammatory Diseases: Multitargeting Mechanisms of Action and Potential Application Gunter NV, Teh SS, Lim YM, Mah SH Front Pharmacol 03-Dec-2020
PMCID:PMC7793909
doi:10.3389/fphar.2020.594202
PMID:33424605
Xanthones, A Promising Anti-Inflammatory Scaffold: Structure, Activity, and Drug Likeness Analysis Feng Z, Lu X, Gan L, Zhang Q, Lin L Molecules 30-Jan-2020
PMCID:PMC7037265
doi:10.3390/molecules25030598
PMID:32019180
Pharmacological basis for the use of Hypericum oblongifolium as a medicinal plant in the management of pain, inflammation and pyrexia Raziq N, Saeed M, Shahid M, Muhammad N, Khan H, Gul F BMC Complement Altern Med 01-Feb-2016
PMCID:PMC4736148
doi:10.1186/s12906-016-1018-z
PMID:26832937
Anti-Helicobacter pylori and Urease Inhibition Activities of Some Traditional Medicinal Plants Amin M, Anwar F, Naz F, Mehmood T, Saari N Molecules 07-Feb-2013
PMCID:PMC6270356
doi:10.3390/molecules18022135
PMID:23434867
Hyperinols A and B, chymotrypsin inhibiting triterpenes from Hypericum oblongifolium. Ferheen S, Ahmed E, Malik A, Afza N, Lodhi MA, Choudhary MI Chem Pharm Bull (Tokyo) 01-Aug-2006
doi:10.1248/CPB.54.1088
PMID:16880649

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 / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
Hexacosyl tetracosanoate 5315798 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCCCCCCCC 733.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octatriacontanol 13847926 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 551.00 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
Shikimic acid 8742 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
Kielcorin 13834128 Click to see COC1=C(C=CC(=C1)C2C(OC3=C4C(=CC(=C3O2)OC)C(=O)C5=CC=CC=C5O4)CO)O 436.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3-dihydroxy-5-methoxy-9H-xanthen-9-one 12026489 Click to see COC1=CC=CC2=C1OC3=CC(=CC(=C3C2=O)O)O 258.23 unknown via CMAUP database
3,4,5-Trihydroxy-9H-xanthen-9-one 46209537 Click to see C1=CC2=C(C(=C1)O)OC3=C(C2=O)C=CC(=C3O)O 244.20 unknown via CMAUP database
4-Hydroxy-2,3-dimethoxyxanthone 378690 Click to see COC1=C(C(=C2C(=C1)C(=O)C3=CC=CC=C3O2)O)OC 272.25 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
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1R,4S,5R,8S,10S,13R,14S,17R,18R,19R)-10-hydroxy-4,5,9,9,13,19-hexamethyl-20-methylidene-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-23-one 162999236 Click to see CC1C2C3(CCC1=C)CCC4(C2(CCC5C4(CCC6C5(CCC(C6(C)C)O)C)C)OC3=O)C 454.70 unknown https://doi.org/10.1248/CPB.54.1088
(1R,4S,5S,8S,10S,13S,14S,17R,18R,19S,22S)-10,22-dihydroxy-4,5,9,9,13,19-hexamethyl-20-methylidene-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-23-one 162853364 Click to see CC1C2C3(CCC4(C2(CCC5C4(CCC6C5(CCC(C6(C)C)O)C)C)OC3=O)C)C(CC1=C)O 470.70 unknown https://doi.org/10.1248/CPB.54.1088
10-Hydroxy-4,5,9,9,13,19-hexamethyl-20-methylidene-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-23-one 73236223 Click to see CC1C2C3(CCC1=C)CCC4(C2(CCC5C4(CCC6C5(CCC(C6(C)C)O)C)C)OC3=O)C 454.70 unknown https://doi.org/10.1248/CPB.54.1088
10,22-Dihydroxy-4,5,9,9,13,19-hexamethyl-20-methylidene-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-23-one 73236224 Click to see CC1C2C3(CCC4(C2(CCC5C4(CCC6C5(CCC(C6(C)C)O)C)C)OC3=O)C)C(CC1=C)O 470.70 unknown https://doi.org/10.1248/CPB.54.1088
hyperinol A 16081994 Click to see CC1C2C3(CCC1=C)CCC4(C2(CCC5C4(CCC6C5(CCC(C6(C)C)O)C)C)OC3=O)C 454.70 unknown https://doi.org/10.1248/CPB.54.1088
Hyperinol B 16081995 Click to see CC1C2C3(CCC4(C2(CCC5C4(CCC6C5(CCC(C6(C)C)O)C)C)OC3=O)C)C(CC1=C)O 470.70 unknown https://doi.org/10.1248/CPB.54.1088
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3,4-Dihydroxy-trans-cinnamic acid tetracosyl ester 5320239 Click to see CCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)O 516.80 unknown via CMAUP database
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown via CMAUP database
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 via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
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 via CMAUP database
Rhamnetin 5281691 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O 316.26 unknown via CMAUP database

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