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Cymbopogon jwarancusa subsp. olivieri

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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 UUID64402f7f5edff900548432
Scientific name Cymbopogon jwarancusa subsp. olivieri
Authority (Boiss.) Soenarko
First published in Reinwardtia 9: 307 (1977)

Description Top

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Common names 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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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
    • Arabian Peninsula
      • Gulf States
      • Oman
      • Yemen
    • China
      • China South-central
      • Tibet
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq
      • Lebanon-Syria
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000861028
Tropicos 25545241
KEW urn:lsid:ipni.org:names:881774-1
The Plant List kew-406200
Open Tree Of Life 5800629
NCBI Taxonomy 1564040
IPNI 881774-1
GBIF 4138875
USDA GRIN 310139
CMAUP NPO17720

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
Review of phytomedicine, phytochemistry, ethnopharmacology, toxicology, and pharmacological activities of Cymbopogon genus Tibenda JJ, Yi Q, Wang X, Zhao Q Front Pharmacol 29-Aug-2022
PMCID:PMC9465289
doi:10.3389/fphar.2022.997918
PMID:36105217
Basic Principles of Medicinal Herbs Used for Cardiovascular Diseases in Traditional Medicine Bahraini A, Solati M, Dadmehr M, Minaie B, Sadeghpour O Iran J Public Health 01-Feb-2022
PMCID:PMC9273507
doi:10.18502/ijph.v51i2.8702
PMID:35866112
Preparation of a Nanoemulsion of Essential Oil of Acroptilon repens Plant and Evaluation of Its Larvicidal Activity agianst Malaria Vector, Anopheles stephensi Firooziyan S, Osanloo M, Moosa-Kazemi SH, Basseri HR, Hajipirloo HM, Sadaghianifar A, Amani A, Sedaghat MM J Arthropod Borne Dis 30-Sep-2021
PMCID:PMC9759440
doi:10.18502/jad.v15i3.9821
PMID:36579001
Checklist of the grasses of India Kellogg EA, Abbott JR, Bawa KS, Gandhi KN, Kailash BR, Ganeshaiah KN, Shrestha UB, Raven P PhytoKeys 16-Oct-2020
PMCID:PMC10311516
doi:10.3897/phytokeys.163.38393
PMID:37397271
Larvicidal Activity of Elytraria acaulis against Culex quinquefasciatus and Aedes aegypti (Diptera: Culicidae) Sukumaran S, Maheswaran R J Arthropod Borne Dis 30-Sep-2020
PMCID:PMC7903361
doi:10.18502/jad.v14i3.4563
PMID:33644243
Ethnopharmacological study of native medicinal plants and the impact of pastoralism on their loss in arid to semiarid ecosystems of southeastern Iran Sharafatmandrad M, Khosravi Mashizi A Sci Rep 23-Sep-2020
PMCID:PMC7511295
doi:10.1038/s41598-020-72536-z
PMID:32968162
Altitude impact on the chemical profile and biological activities of Satureja thymbra L. essential oil Khalil N, El-Jalel L, Yousif M, Gonaid M BMC Complement Med Ther 12-Jun-2020
PMCID:PMC7290070
doi:10.1186/s12906-020-02982-9
PMID:32532265
Efficacy of Extractions of Iranian Native Plants against Main Malaria Vector, Anopheles stephensi in Iran for Making Appropriate Formulation for Disease Control Vatandoost H, Nikpour F, Hanafi-Bojd AA, Abai MR, Khanavi M, Hajiiakhondi A, Raesi A, Nejati J J Arthropod Borne Dis 31-Dec-2019
PMCID:PMC7188767
PMID:32368551
Antioxidant and Larvicidal Activity of Areal Parts of Scrophularia striata against Malaria Vector Anopheles stephensi Yousefbeyk F, Vatandoost H, Golfakhrabadi F, Mirzaee Z, Abai MR, Amin G, Khanavi M J Arthropod Borne Dis 13-Jun-2018
PMCID:PMC6091803
PMID:30123805
Biological Activities and Composition of Ferulago carduchorum Essential Oil Golfakhrabadi F, Khanavi M, Ostad SN, Saeidnia S, Vatandoost H, Abai MR, Hafizi M, Yousefbeyk F, Rad YR, Baghenegadian A, Ardekani MR J Arthropod Borne Dis 16-Jul-2014
PMCID:PMC4478411
PMID:26114148
Chemical composition and insecticidal activity of plant essential oils from Benin against Anopheles gambiae (Giles) Bossou AD, Mangelinckx S, Yedomonhan H, Boko PM, Akogbeto MC, De Kimpe N, Avlessi F, Sohounhloue DC Parasit Vectors 03-Dec-2013
PMCID:PMC3866997
doi:10.1186/1756-3305-6-337
PMID:24298981
Biochemical Activities of Iranian Cymbopogon olivieri (Boiss) Bor. Essential Oil Mahboubi M, Kazempour N Indian J Pharm Sci 01-Jul-2012
PMCID:PMC3630732
doi:10.4103/0250-474X.107071
PMID:23626392

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(1S,4Z,8R)-5,9,9-trimethyl-2-methylidenebicyclo[6.2.0]dec-4-ene 18502770 Click to see CC1=CCC(=C)C2CC(C2CC1)(C)C 190.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(+)-Isoborneol 6973640 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Borneol 6552009 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Isoborneol 6321405 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(5R,8R,9S,10R,13R,14R,17S)-17-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 40884713 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C 458.70 unknown via CMAUP database
Ocotillol I 101967086 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C 460.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aR,6aS,6bR,8aS,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 51531959 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O 488.70 unknown via CMAUP database
11-Oxoasiatic acid 69624247 Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O 502.70 unknown via CMAUP database
Alphitolic acid 12305768 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C(=O)O 472.70 unknown via CMAUP database
Arjunolic acid 73641 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
Asiatic Acid 119034 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O 488.70 unknown via CMAUP database
Dipterocarpol 441676 Click to see CC(=CCCC(C)(C1CCC2(C1CCC3C2(CCC4C3(CCC(=O)C4(C)C)C)C)C)O)C 442.70 unknown via CMAUP database
Dryobalanone 12309393 Click to see CC(=CCCC(CO)(C1CCC2(C1CCC3C2(CCC4C3(CCC(=O)C4(C)C)C)C)C)O)C 458.70 unknown via CMAUP database
Erythrodiol 101761 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C 442.70 unknown via CMAUP database
Hederagenin 73299 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Methyl oleanonate 10695622 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C(=O)OC)C 468.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Oleanonic acid 12313704 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C(=O)O)C 454.70 unknown via CMAUP database

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