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Plectranthus ornatus

Plectranthus ornatus - 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
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Details Top

Internal ID UUID643fe80fe7f28931288244
Scientific name Plectranthus ornatus
Authority Codd
First published in Bothalia 11: 393 (1975)

Description Top

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Synonyms Top

Scientific name Authority First published in
Coleus comosus Hochst. ex Gürke Bot. Jahrb. Syst. 19: 212 (1894)

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000275711
Tropicos 17602796
KEW urn:lsid:ipni.org:names:454605-1
The Plant List kew-158366
Open Tree Of Life 6084976
NCBI Taxonomy 2171726
IPNI 454605-1
iNaturalist 404996
GBIF 3902679

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
The influence of exotic and native plants on illnesses with physical and spiritual causes in the semiarid region of Piauí, Northeast of Brazil da Silva PH, Ferreira Júnior WS, Zank S, do Nascimento AL, de Abreu MC J Ethnobiol Ethnomed 26-Feb-2024
PMCID:PMC10895823
doi:10.1186/s13002-024-00667-y
PMID:38409039
Back to Nature: Medicinal Plants as Promising Sources for Antibacterial Drugs in the Post-Antibiotic Era Abdallah EM, Alhatlani BY, de Paula Menezes R, Martins CH Plants (Basel) 28-Aug-2023
PMCID:PMC10490416
doi:10.3390/plants12173077
PMID:37687324
Plectranthus Species with Anti-Inflammatory and Analgesic Potential: A Systematic Review on Ethnobotanical and Pharmacological Findings Barbosa MD, Wilairatana P, Leite GM, Delmondes GD, da Silva LY, Júnior SC, Dantas LB, Bezerra DS, de Beltrão IC, Dias DD, Ribeiro-Filho J, Felipe CF, Coutinho HD, de Menezes IR, Kerntopf Mendonça MR Molecules 26-Jul-2023
PMCID:PMC10419981
doi:10.3390/molecules28155653
PMID:37570622
Bovine mastitis, a worldwide impact disease: Prevalence, antimicrobial resistance, and viable alternative approaches Morales-Ubaldo AL, Rivero-Perez N, Valladares-Carranza B, Velázquez-Ordoñez V, Delgadillo-Ruiz L, Zaragoza-Bastida A Vet Anim Sci 24-Jul-2023
PMCID:PMC10400929
doi:10.1016/j.vas.2023.100306
PMID:37547227
Glandular and Non-Glandular Trichomes from Phlomis herba-venti subsp. pungens Leaves: Light, Confocal, and Scanning Electron Microscopy and Histochemistry of the Secretory Products Gostin IN Plants (Basel) 23-Jun-2023
PMCID:PMC10347251
doi:10.3390/plants12132423
PMID:37446984
Mechanisms of Phytochemicals in Anti-Inflammatory and Anti-Cancer Jang JH, Lee TJ Int J Mol Sci 26-Apr-2023
PMCID:PMC10177803
doi:10.3390/ijms24097863
PMID:37175569
Advances in Plants-Derived Bioactives for Cancer Treatment Cruz-Martins N Cells 08-Apr-2023
PMCID:PMC10136607
doi:10.3390/cells12081112
PMID:37190022
Plant Spices as a Source of Antimicrobial Synergic Molecules to Treat Bacterial and Viral Co-Infections Duarte NB, Takahashi JA Molecules 25-Nov-2022
PMCID:PMC9737474
doi:10.3390/molecules27238210
PMID:36500303
Ethnobotany of traditional medicinal plants and associated indigenous knowledge in Dawuro Zone of Southwestern Ethiopia Agize M, Asfaw Z, Nemomissa S, Gebre T J Ethnobiol Ethnomed 21-Jun-2022
PMCID:PMC9210772
doi:10.1186/s13002-022-00546-4
PMID:35729583
Morpho-Anatomical Study And Botanical Identification of Pogostemon auricularius (L.) Hassk. (Lamiaceae) Thi Tran LT, Nguyen TK, Nguyen HT, Nguyen PP, Thi Dang NY, Tran MH, Tran Pham VP, Le AT Sci Prog 19-Apr-2022
PMCID:PMC10358496
doi:10.1177/00368504221094156
PMID:35440237
HPLC/DAD, Antibacterial and Antioxidant Activities of Plectranthus Species (Lamiaceae) Combined with the Chemometric Calculations Rodrigues FF, Boligon AA, Menezes IR, Galvão-Rodrigues FF, Salazas GJ, Nonato CF, Braga NT, Correia FM, Caldas GF, Coutinho HD, Siyadatpanah A, Kim B, Costa JG, Barros AR Molecules 17-Dec-2021
PMCID:PMC8703593
doi:10.3390/molecules26247665
PMID:34946747
Lamiaceae Essential Oils, Phytochemical Profile, Antioxidant, and Biological Activities Ramos da Silva LR, Ferreira OO, Cruz JN, de Jesus Pereira Franco C, Oliveira dos Anjos T, Cascaes MM, Almeida da Costa W, Helena de Aguiar Andrade E, Santana de Oliveira M Evid Based Complement Alternat Med 14-Dec-2021
PMCID:PMC8692021
doi:10.1155/2021/6748052
PMID:34950215
Traditional Medicinal Plants as a Source of Antituberculosis Drugs: A System Review Xu Y, Liang B, Kong C, Sun Z Biomed Res Int 08-Sep-2021
PMCID:PMC8448615
doi:10.1155/2021/9910365
PMID:34541000
The Micromorphology and Histochemistry of Foliar Mixed Indumentum of Leucas lavandulaefolia (Lamiaceae) Naidoo Y, Dladla T, Dewir YH, Gangaram S, Naidoo CM, Rihan HZ Plants (Basel) 25-Aug-2021
PMCID:PMC8465491
doi:10.3390/plants10091767
PMID:34579300
Biofilm Research in Bovine Mastitis Pedersen RR, Krömker V, Bjarnsholt T, Dahl-Pedersen K, Buhl R, Jørgensen E Front Vet Sci 07-May-2021
PMCID:PMC8138050
doi:10.3389/fvets.2021.656810
PMID:34026893

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 / Colensane and clerodane diterpenoids
(E,5R)-5-[(1S,2R,4aR,6S,8aS)-6-hydroxy-1,2,4a-trimethyl-5-methylidene-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl]-5-acetyloxy-3-methylpent-2-enoic acid 11268948 Click to see CC1CCC2(C(C1(C)C(CC(=CC(=O)O)C)OC(=O)C)CCC(C2=C)O)C 378.50 unknown https://doi.org/10.1021/NP049827N
(E,5R)-5-[(1S,2R,4aR,8aS)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-5-acetyloxy-3-methylpent-2-enoic acid 11349010 Click to see CC1CCC2(C(C1(C)C(CC(=CC(=O)O)C)OC(=O)C)CCC=C2C)C 362.50 unknown https://doi.org/10.1021/NP049827N
(E,5R)-5-[(1S,2R,4aR,8aS)-1,2,4a,5-tetramethyl-7-oxo-3,4,8,8a-tetrahydro-2H-naphthalen-1-yl]-5-acetyloxy-3-methylpent-2-enoic acid 11360893 Click to see CC1CCC2(C(C1(C)C(CC(=CC(=O)O)C)OC(=O)C)CC(=O)C=C2C)C 376.50 unknown https://doi.org/10.1021/NP049827N
5-Acetyloxy-5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-enoic acid 72811661 Click to see CC1CCC2(C(C1(C)C(CC(=CC(=O)O)C)OC(=O)C)CCC=C2C)C 362.50 unknown https://doi.org/10.1021/NP049827N
5-acetyloxy-5-(1,2,4a,5-tetramethyl-7-oxo-3,4,8,8a-tetrahydro-2H-naphthalen-1-yl)-3-methylpent-2-enoic acid 72816569 Click to see CC1CCC2(C(C1(C)C(CC(=CC(=O)O)C)OC(=O)C)CC(=O)C=C2C)C 376.50 unknown https://doi.org/10.1021/NP049827N
5-acetyloxy-5-(6-hydroxy-1,2,4a-trimethyl-5-methylidene-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl)-3-methylpent-2-enoic acid 72777084 Click to see CC1CCC2(C(C1(C)C(CC(=CC(=O)O)C)OC(=O)C)CCC(C2=C)O)C 378.50 unknown https://doi.org/10.1021/NP049827N
methyl 5-acetyloxy-5-(1,2,4a,5-tetramethyl-7-oxo-3,4,8,8a-tetrahydro-2H-naphthalen-1-yl)-3-methylpent-2-enoate 73880704 Click to see CC1CCC2(C(C1(C)C(CC(=CC(=O)OC)C)OC(=O)C)CC(=O)C=C2C)C 390.50 unknown https://doi.org/10.1021/NP020203W
Plectrornatin A 637442 Click to see CC1CCC2(C(C1(C)C(CC(=CC(=O)OC)C)OC(=O)C)CC(=O)C=C2C)C 390.50 unknown https://doi.org/10.1021/NP020203W
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(13R)-1alpha,6beta,7beta-Triacetoxy-8,13-epoxylabda-14-ene-11-one 13558108 Click to see CC(=O)OC1CCC(C2C1(C3C(=O)CC(OC3(C(C2OC(=O)C)OC(=O)C)C)(C)C=C)C)(C)C 478.60 unknown https://doi.org/10.1002/MRC.1600
(3-Ethenyl-10-hydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-2,5,6,6a,8,9,10,10b-octahydrobenzo[f]chromen-6-yl) acetate 85109344 Click to see CC(=O)OC1CC2(C(C(=O)CC(O2)(C)C=C)C3(C1C(CCC3O)(C)C)C)C 378.50 unknown https://doi.org/10.1021/NP020203W
(5-acetyloxy-3-ethenyl-10,10b-dihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-5,6,6a,8,9,10-hexahydro-2H-benzo[f]chromen-6-yl) acetate 13561538 Click to see CC(=O)OC1C2C(CCC(C2(C3(C(=O)CC(OC3(C1OC(=O)C)C)(C)C=C)O)C)O)(C)C 452.50 unknown https://doi.org/10.1002/MRC.1600
(5,6-diacetyloxy-3-ethenyl-10b-hydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-5,6,6a,8,9,10-hexahydro-2H-benzo[f]chromen-10-yl) acetate 4093437 Click to see CC(=O)OC1CCC(C2C1(C3(C(=O)CC(OC3(C(C2OC(=O)C)OC(=O)C)C)(C)C=C)O)C)(C)C 494.60 unknown https://doi.org/10.1002/MRC.1600
https://doi.org/10.1021/NP049827N
(5,6-Diacetyloxy-3-ethenyl-3,4a,7,7,10a-pentamethyl-1-oxo-2,5,6,6a,8,9,10,10b-octahydrobenzo[f]chromen-10-yl) acetate 13558106 Click to see CC(=O)OC1CCC(C2C1(C3C(=O)CC(OC3(C(C2OC(=O)C)OC(=O)C)C)(C)C=C)C)(C)C 478.60 unknown https://doi.org/10.1002/MRC.1600
https://doi.org/10.1021/NP049827N
(6-Acetyloxy-3-ethenyl-3,4a,7,7,10a-pentamethyl-1-oxo-2,5,6,6a,8,9,10,10b-octahydrobenzo[f]chromen-10-yl) acetate 163089672 Click to see CC(=O)OC1CCC(C2C1(C3C(=O)CC(OC3(CC2OC(=O)C)C)(C)C=C)C)(C)C 420.50 unknown https://doi.org/10.1021/NP020203W
[(3R,4aR,5S,6S,6aS,10S,10aR,10bS)-5,6-diacetyloxy-3-ethenyl-10b-hydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-5,6,6a,8,9,10-hexahydro-2H-benzo[f]chromen-10-yl] acetate 396204 Click to see CC(=O)OC1CCC(C2C1(C3(C(=O)CC(OC3(C(C2OC(=O)C)OC(=O)C)C)(C)C=C)O)C)(C)C 494.60 unknown https://doi.org/10.1002/MRC.1600
[(3S,4aR,5R,6R,6aR,10R,10aR,10bS)-5,6-diacetyloxy-3-ethenyl-3,4a,7,7,10a-pentamethyl-1-oxo-2,5,6,6a,8,9,10,10b-octahydrobenzo[f]chromen-10-yl] acetate 162978340 Click to see CC(=O)OC1CCC(C2C1(C3C(=O)CC(OC3(C(C2OC(=O)C)OC(=O)C)C)(C)C=C)C)(C)C 478.60 unknown https://doi.org/10.1021/NP049827N
[(3S,4aS,5R,6R,6aR,10R,10aS,10bR)-5,6-diacetyloxy-3-ethenyl-10b-hydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-5,6,6a,8,9,10-hexahydro-2H-benzo[f]chromen-10-yl] acetate 163018682 Click to see CC(=O)OC1CCC(C2C1(C3(C(=O)CC(OC3(C(C2OC(=O)C)OC(=O)C)C)(C)C=C)O)C)(C)C 494.60 unknown https://doi.org/10.1021/NP049827N
3-Hydroxyolean-12-en-28-oic acid 619166 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 https://doi.org/10.1002/MRC.1600
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1002/MRC.1600
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1002/MRC.1600
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1002/MRC.1600
Forskolin J 23254517 Click to see CC(=O)OC1C2C(CCC(C2(C3(C(=O)CC(OC3(C1OC(=O)C)C)(C)C=C)O)C)O)(C)C 452.50 unknown https://doi.org/10.1002/MRC.1600
Olean-12-en-3beta-ol 225689 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1002/MRC.1600
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 https://doi.org/10.1002/MRC.1600
Plectrornatin B 10068236 Click to see CC(=O)OC1CC2(C(C(=O)CC(O2)(C)C=C)C3(C1C(CCC3O)(C)C)C)C 378.50 unknown https://doi.org/10.1021/NP020203W
Plectrornatin C 10319973 Click to see CC(=O)OC1CCC(C2C1(C3C(=O)CC(OC3(CC2OC(=O)C)C)(C)C=C)C)(C)C 420.50 unknown https://doi.org/10.1021/NP020203W
Urs-12-en-3beta-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1002/MRC.1600
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1002/MRC.1600

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