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Isodon rugosus

Isodon rugosus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Isodon rugosus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fdf82b265f443450349
Scientific name Isodon rugosus
Authority (Wall.) Codd
First published in Taxon 17: 239 (1968)

Description Top

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Synonyms Top

Scientific name Authority First published in
Isodon plectranthoides Schrad. ex Benth. Labiat. Gen. Spec. : 43 (1832)
Lumnitzera densiflora (Roth) Spreng. Syst. Veg., ed. 16 [Sprengel] 2: 687. 1825 [Jan-May 1825]
Ocimum densiflorum Roth Nov. Pl. Sp. : 275 (1821)
Plectranthus rugosus Wall. ex Benth. Pl. Asiat. Rar. 2: 17 (1830)
Rabdosia rugosa (Wall. ex Benth.) H.Hara J. Jap. Bot. 47: 199 (1972)

Common names Top

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Language Common/alternative name
Chinese 皱叶香茶菜

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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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
  • Asia-temperate
    • Arabian Peninsula
      • Oman
    • China
      • Tibet
    • Western Asia
      • Afghanistan
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • East Himalaya
      • Nepal
      • Pakistan
      • West Himalaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000217958
Tropicos 17607203
KEW urn:lsid:ipni.org:names:448611-1
The Plant List kew-103022
Open Tree Of Life 23547
NCBI Taxonomy 204135
IPNI 448611-1
iNaturalist 126049
GBIF 5608857
EOL 2898985
USDA GRIN 407617

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
Vegetation–edaphic correlation and importance value index in himalayan ‘ecotone’ temperate conifer forest using the multivariate technique Ali F, Zeb M, Amin M, Rajpar MN, Hidayat S, Khan WR Saudi J Biol Sci 24-Mar-2024
PMCID:PMC11000104
doi:10.1016/j.sjbs.2024.103983
PMID:38590389
Habitat suitability modelling of Koklass pheasant (Pucrasia macrolopha) in moist temperate forest Badrulislam, Khan KA, Khalil S, Hussain M, Saqib Z, Altaf J, Hadi R, Habiba U PLoS One 15-Feb-2024
PMCID:PMC10868740
doi:10.1371/journal.pone.0296921
PMID:38359051
Investigation of anti-nociceptive, anti-inflammatory potential and ADMET studies of pure compounds isolated from Isodon rugosus Wall. ex Benth Alshehri OM, Zeb A, Mukarram Shah SM, Mahnashi MH, Asiri SA, Alqahtani O, Sadiq A, Ibrar M, Alshamrani S, Jan MS Front Pharmacol 13-Feb-2024
PMCID:PMC10897015
doi:10.3389/fphar.2024.1328128
PMID:38414736
Ethno-Dentistry of Medicinal Plants Used in North Waziristan, Pakistan Rehman S, Iqbal Z, Qureshi R, AlOmar TS, Almasoud N, Younas M, Rauf A, Irfan M Int Dent J 11-Nov-2023
PMCID:PMC10988256
doi:10.1016/j.identj.2023.10.001
PMID:37953188
Ethnobotanical Insights into Medicinal and Culinary Plant Use: The Dwindling Traditional Heritage of the Dard Ethnic Group in the Gurez Region of the Kashmir Valley, India Ahad L, Hassan M, Amjad MS, Mir RA, Vitasović-Kosić I, Bussmann RW, Binish Z Plants (Basel) 17-Oct-2023
PMCID:PMC10610420
doi:10.3390/plants12203599
PMID:37896062
The Optimization of Medium Conditions and Auxins in the Induction of Adventitious Roots of Pokeweed (Phytolacca americana L.) and Their Phytochemical Constituents Trunjaruen A, Luecha P, Taratima W Scientifica (Cairo) 21-Aug-2023
PMCID:PMC10462441
doi:10.1155/2023/2983812
PMID:37645570
Application of Rosmarinic Acid with Its Derivatives in the Treatment of Microbial Pathogens Kernou ON, Azzouz Z, Madani K, Rijo P Molecules 22-May-2023
PMCID:PMC10220798
doi:10.3390/molecules28104243
PMID:37241981
Traditional foraging for ecological transition? Wild food ethnobotany among three ethnic groups in the highlands of the eastern Hindukush, North Pakistan Khan AH, Adil M, Aziz MA, Sõukand R, Pieroni A J Ethnobiol Ethnomed 31-Mar-2023
PMCID:PMC10064566
doi:10.1186/s13002-023-00581-9
PMID:37004043
Natural product-driven dual COX-LOX inhibitors: Overview of recent studies on the development of novel anti-inflammatory agents Mukhopadhyay N, Shukla A, Makhal PN, Kaki VR Heliyon 14-Mar-2023
PMCID:PMC10068128
doi:10.1016/j.heliyon.2023.e14569
PMID:37020932
Exploring soil bacterial diversity in different micro-vegetational habitats of Dachigam National Park in North-western Himalaya Mushtaq H, Ganai BA, Jehangir A Sci Rep 22-Feb-2023
PMCID:PMC9947166
doi:10.1038/s41598-023-30187-w
PMID:36813837
Evaluation of Senna tora (L.) Roxb. leaves as source of bioactive molecules with antioxidant, anti-inflammatory and antibacterial potential Rahman MM, Al Noman MA, Khatun S, Alam R, Shetu MM, Talukder EK, Imon RR, Biswas MY, Anis-Ul-Haque KM, Uddin MJ, Akhter S Heliyon 19-Jan-2023
PMCID:PMC9898628
doi:10.1016/j.heliyon.2023.e12855
PMID:36747926
Antibacterial and Photodegradation of Organic Dyes Using Lamiaceae-Mediated ZnO Nanoparticles: A Review Mutukwa D, Taziwa RT, Khotseng L Nanomaterials (Basel) 16-Dec-2022
PMCID:PMC9785588
doi:10.3390/nano12244469
PMID:36558321
A Cross-Cultural Analysis of Medicinal Plant Utilization among the Four Ethnic Communities in Northern Regions of Jammu and Kashmir, India Mir TA, Jan M, Jan HA, Bussmann RW, Sisto F, Fadlalla IM Biology (Basel) 27-Oct-2022
PMCID:PMC9687545
doi:10.3390/biology11111578
PMID:36358279
Herbal Arsenal against Skin Ailments: A Review Supported by In Silico Molecular Docking Studies Singab AN, Mostafa NM, Fawzy IM, Bhatia D, Suryawanshi PT, Kabra A Molecules 21-Sep-2022
PMCID:PMC9572213
doi:10.3390/molecules27196207
PMID:36234737
A Comprehensive Review of Rosmarinic Acid: From Phytochemistry to Pharmacology and Its New Insight Guan H, Luo W, Bao B, Cao Y, Cheng F, Yu S, Fan Q, Zhang L, Wu Q, Shan M Molecules 20-May-2022
PMCID:PMC9143754
doi:10.3390/molecules27103292
PMID:35630768

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 / Diterpenoids / Kaurane diterpenoids
(1S,2S,8R,9S,11R)-9,10,15,18-tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 138107787 Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4O)C(=C)C5=O)(OC3)O)O)O)C 364.40 unknown https://doi.org/10.1055/S-2003-38889
(9,10-Dihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl) acetate 10475500 Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3CCC(C4)C(=C)C5=O)O)(C)C 390.50 unknown https://doi.org/10.1055/S-2003-38889
(9,10,18-Trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl) acetate 429192 Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3CCC(C4O)C(=C)C5=O)O)(C)C 406.50 unknown https://doi.org/10.1021/NP200140J
https://doi.org/10.1055/S-2003-38889
[(1R,2R,5S,8R,9R,10R,11S,15R)-9,10-dihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate 125463139 Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3CCC(C4)C(=C)C5=O)O)(C)C 390.50 unknown https://doi.org/10.1055/S-2003-38889
[(1S,2S,5R,10S,11R,15S,18R)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate 6325508 Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3CCC(C4O)C(=C)C5=O)O)(C)C 406.50 unknown https://doi.org/10.1055/S-2003-37031-2
https://doi.org/10.1021/NP200140J
[(2S,5S,9S,10R,11R,15R,18R)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate 101306857 Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3CCC(C4O)C(=C)C5=O)O)(C)C 406.50 unknown https://doi.org/10.1055/S-2003-38889
9,10,15-Trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 9997896 Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4)C(=C)C5=O)(OC3)O)O)O)C 348.40 unknown https://doi.org/10.1055/S-2003-38889
CID 34174831 34174831 Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3CCC(C4)C(=C)C5=O)O)(C)C 390.50 unknown https://doi.org/10.1055/S-2003-38889
Effusanin A 34174827 Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4)C(=C)C5=O)(OC3)O)O)O)C 348.40 unknown https://doi.org/10.1055/S-2003-38889
Effusanin E 24721137 Click to see CC1(CCC(C23C1C(C(C45C2C(CC(C4)C(=C)C5=O)O)(OC3)O)O)O)C 364.40 unknown https://doi.org/10.1055/S-2003-38889
Kaur-16-en-15-one, 1-(acetyloxy)-7,20-epoxy-6,7,14-trihydroxy-, (1alpha,6beta,7alpha,14R)- 12305580 Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3CCC(C4O)C(=C)C5=O)O)(C)C 406.50 unknown https://doi.org/10.1055/S-2003-38889
Lasiodonin 12305578 Click to see CC1(CCC(C23C1C(C(C45C2C(CC(C4)C(=C)C5=O)O)(OC3)O)O)O)C 364.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
https://doi.org/10.1055/S-2003-38889
Oridonin 5321010 Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4O)C(=C)C5=O)(OC3)O)O)O)C 364.40 unknown https://doi.org/10.1055/S-2003-38889
Rubescensin A 3576890 Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4O)C(=C)C5=O)(OC3)O)O)O)C 364.40 unknown https://doi.org/10.1055/S-2003-38889
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2S,4aR,6aR,6aS,6bR,8aR,10R,12aR,14bS)-10-hydroxy-1,4a,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-2-carboxylic acid 101643020 Click to see CC1C(CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0040-4020(82)85077-1
(1S,2R,4aR,6aR,6aS,6bR,8aR,10R,12aR,14bS)-10-acetyloxy-2,4a,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-1-carboxylic acid 162883244 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C(=O)O)C)C 498.70 unknown https://doi.org/10.1016/S0031-9422(00)95277-4
(1S,2R,4aR,6aR,6aS,6bR,8aR,10R,12aR,14bS)-10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-1-carboxylic acid 154731119 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C(=O)O)C)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)95277-4
(1S,2S,4aR,6aR,6aR,6bR,8aR,10R,12aR,14bS)-10-hydroxy-1,2,4a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 163026022 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/0040-4020(82)85077-1
(3R,4aR,6aR,6bS,8aR,11R,12S,12aS,14aR,14bR)-12-(hydroxymethyl)-4,4,6a,6b,8a,11,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 163079620 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1CO)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(00)95277-4
10-acetyloxy-2,4a,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-1-carboxylic acid 162883243 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C(=O)O)C)C 498.70 unknown https://doi.org/10.1016/S0031-9422(00)95277-4
10-hydroxy-1,2,4a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 12314030 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/0040-4020(82)85077-1
10-hydroxy-1,4a,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-2-carboxylic acid 124222330 Click to see CC1C(CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0040-4020(82)85077-1
10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-1-carboxylic acid 3515456 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C(=O)O)C)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)95277-4
12-(hydroxymethyl)-4,4,6a,6b,8a,11,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 163079618 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1CO)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(00)95277-4
> 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/S0031-9422(00)95277-4
Beta-Sitosterol 222284 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/S0031-9422(00)95277-4

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