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Coleus yemenensis

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID68f90acd4b08c277742057
Scientific name Coleus yemenensis
Authority A.J.Paton
First published in PhytoKeys 129: 111 (2019)

Ethnobotanical Use Top

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General Uses Top

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There are no documented commercial, industrial, craft, culinary, or fragrance/cosmetics uses for Coleus yamenensis (A.J.P. Paton) reported in the accessible scientific or technical literature. The taxon does not appear in standard economic botany databases, commercial plant product surveys, or national and international (ISO/ASTM/EN) standards for foods, timber, colorants, fibers, gums/resins, biofuels, or bioplastics. No verifiable use in model organism resources (e.g., genetics, molecular biology, reference genome, community databases) is recorded. Given the absence of reliable references reporting non-medicinal uses, the following sections are omitted.

Synonyms Top

Scientific name Authority First published in
Ocimum gratissimum Forssk. Fl. Aegypt.-Arab. : 110 (1775)
Plectranthus ovatus Benth. Labiat. Gen. Spec. : 709 (1835)

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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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
Tropicos 100244420
KEW urn:lsid:ipni.org:names:454608-1
The Plant List kew-158370
IPNI 454608-1
GBIF 3902650
Open Tree Of Life 782182
World Flora Online wfo-1000031677

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)!
Title Authors Publication Released IDs
A Comparison between the Oil, Solvent Extract and Supercritical Carbon Dioxide Extract of<i>Ocimum gratissimum</i>L. Jorge A. Pino, Jorge Garcia, Marco A. Martinez Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1998.9700975
A New Geraniol Chemotype of<i>Ocimum gratissimum</i>L. Denys J. Charles, James E. Simon Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1992.9698054
Oleanolic Acid, a Bioactive Component of the Leaves of Ocimum Gratissimum (Lamiaceae) C.J. Njoku, Lu Zeng, I.U. Asuzu, N.H. Oberlies, J.L. McLaughlin Informa UK Limited 02-May-2003
doi:10.1076/PHBI.35.2.134.13290
The application of atmospheric pressure chemical ionisation liquid chromatography-mass spectrometry in the chemotaxonomic study of flavonoids: characterisation of flavonoids from Ocimum gratissimum var. gratissimum Ren�e J. Grayer, Geoffrey C. Kite, Mamdouh Abou-Zaid, Louise J. Archer Wiley 25-Aug-2002
doi:10.1002/1099-1565(200007/08)11:4<257::AID-PCA521>3.0.CO;2-A
Chemical variation during daytime of constituents of the essential oil of Ocimum gratissimum leaves M.G de Vasconcelos Silva, A.A Craveiro, F.J Abreu Matos, M.I.L Machado, J.W Alencar Elsevier BV 25-Jul-2002
doi:10.1016/S0367-326X(98)00020-3
Gas—liquid chromatography—mass spectrometry in the analysis of essential oils V.A. Zamureenko, N.A. Kluyev, L.B. Dmitriev, I.I. Grandberg Elsevier BV 25-Jul-2002
doi:10.1016/S0021-9673(01)96050-9
Genetic diversity of Ocimum gratissimum L. based on volatile oil constituents, flavonoids and RAPD markers. Vieira RF, Grayer RJ, Paton A, Simon JE Biochem Syst Ecol 01-Mar-2001
doi:10.1016/S0305-1978(00)00062-4
PMID:11152947
Essential oil of alfavaca, Ocimum gratissimum, from Brazilian Amazon. Vostrowsky O, Garbe W, Bestmann HJ, Maia JG Z Naturforsch C J Biosci 01-Sep-1990
doi:10.1515/ZNC-1990-9-1023
PMID:2291770
Antimicrobial activities of some Ocimum species grown in Rwanda. Janssen AM, Scheffer JJ, Ntezurubanza L, Baerheim Svendsen A J Ethnopharmacol 01-Jun-1989
doi:10.1016/0378-8741(89)90113-X
PMID:2747264
Composition of the essential oil of Ocimum canum grown in Rwanda. Ntezurubanza L, Scheffer JJ, Looman A Pharm Weekbl Sci 13-Dec-1985
doi:10.1007/BF01959201
PMID:4080513

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see 106.12 unknown https://doi.org/10.1515/ZNC-1990-9-1023
> Benzenoids / Phenol ethers / Anisoles
Anisole 7519 Click to see COC1=CC=CC=C1 108.14 unknown https://doi.org/10.1016/S0305-1978(00)00062-4
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1007/BF01959201
https://doi.org/10.1016/S0367-326X(98)00020-3
https://doi.org/10.1016/S0305-1978(00)00062-4
https://doi.org/10.1016/0378-8741(89)90113-X
https://doi.org/10.1515/ZNC-1990-9-1023
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1016/S0305-1978(00)00062-4
https://doi.org/10.1515/ZNC-1990-9-1023
https://doi.org/10.1007/BF01959201
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octen-3-Ol 18827 Click to see 128.21 unknown https://doi.org/10.1515/ZNC-1990-9-1023
3-Octanol 11527 Click to see 130.23 unknown https://doi.org/10.1515/ZNC-1990-9-1023
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1992.9698054
https://doi.org/10.1016/S0305-1978(00)00062-4
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1080/10412905.1998.9700975
https://doi.org/10.1007/BF01959201
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see 136.23 unknown https://doi.org/10.1007/BF01959201
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1007/BF01959201
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1007/BF01959201
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1515/ZNC-1990-9-1023
https://doi.org/10.1007/BF01959201
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1515/ZNC-1990-9-1023
https://doi.org/10.1007/BF01959201
Tricyclene 79035 Click to see 136.23 unknown https://doi.org/10.1515/ZNC-1990-9-1023
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1515/ZNC-1990-9-1023
https://doi.org/10.1016/S0367-326X(98)00020-3
https://doi.org/10.1007/BF01959201
https://doi.org/10.1016/S0305-1978(00)00062-4
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1007/BF01959201
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1016/S0367-326X(98)00020-3
https://doi.org/10.1007/BF01959201
https://doi.org/10.1515/ZNC-1990-9-1023
gamma-Terpineol 11467 Click to see CC(=C1CCC(CC1)(C)O)C 154.25 unknown https://doi.org/10.1016/S0305-1978(00)00062-4
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1007/BF01959201
https://doi.org/10.1515/ZNC-1990-9-1023
https://doi.org/10.1080/10412905.1992.9698054
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1016/S0305-1978(00)00062-4
https://doi.org/10.1515/ZNC-1990-9-1023
https://doi.org/10.1007/BF01959201
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/S0305-1978(00)00062-4
https://doi.org/10.1007/BF01959201
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1007/BF01959201
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698054
https://doi.org/10.1016/S0367-326X(98)00020-3
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/S0305-1978(00)00062-4
https://doi.org/10.1080/10412905.1992.9698054
https://doi.org/10.1007/BF01959201
Farnesene 5281516 Click to see 204.35 unknown https://doi.org/10.1007/BF01959201
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/S0305-1978(00)00062-4
Npc322415 521334 Click to see 204.35 unknown https://doi.org/10.1016/S0305-1978(00)00062-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see 220.35 unknown https://doi.org/10.1016/S0305-1978(00)00062-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see 204.35 unknown https://doi.org/10.1016/S0367-326X(98)00020-3
https://doi.org/10.1007/BF01959201
https://doi.org/10.1515/ZNC-1990-9-1023
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1007/BF01959201
https://doi.org/10.1016/S0021-9673(01)96050-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1076/PHBI.35.2.134.13290
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
Ethinylestradiol 5991 Click to see 296.40 unknown https://doi.org/10.1515/ZNC-1990-9-1023
https://doi.org/10.1080/10412905.1992.9698054
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
3-Octanone 246728 Click to see CCCCCC(=O)CC 128.21 unknown https://doi.org/10.1007/BF01959201
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Rosmarinic Acid 5281792 Click to see 360.30 unknown https://doi.org/10.1002/1099-1565(200007/08)11:4<257::AID-PCA521>3.0.CO;2-A
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isovitexin 162350 Click to see 432.40 unknown https://doi.org/10.1002/1099-1565(200007/08)11:4<257::AID-PCA521>3.0.CO;2-A
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 44257674 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1002/1099-1565(200007/08)11:4<257::AID-PCA521>3.0.CO;2-A
Vitexin 5280441 Click to see 432.40 unknown https://doi.org/10.1002/1099-1565(200007/08)11:4<257::AID-PCA521>3.0.CO;2-A
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-(3,4-Dihydroxyphenyl)-7-hydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 15559460 Click to see 448.40 unknown https://doi.org/10.1002/1099-1565(200007/08)11:4<257::AID-PCA521>3.0.CO;2-A
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1002/1099-1565(200007/08)11:4<257::AID-PCA521>3.0.CO;2-A
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1002/1099-1565(200007/08)11:4<257::AID-PCA521>3.0.CO;2-A
Kaempferol 3-neohesperidoside 5318761 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1002/1099-1565(200007/08)11:4<257::AID-PCA521>3.0.CO;2-A
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1002/1099-1565(200007/08)11:4<257::AID-PCA521>3.0.CO;2-A
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown https://doi.org/10.1002/1099-1565(200007/08)11:4<257::AID-PCA521>3.0.CO;2-A
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1002/1099-1565(200007/08)11:4<257::AID-PCA521>3.0.CO;2-A
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1016/S0305-1978(00)00062-4
https://doi.org/10.1002/1099-1565(200007/08)11:4<257::AID-PCA521>3.0.CO;2-A
Isothymusin 630253 Click to see 330.29 unknown https://doi.org/10.1002/1099-1565(200007/08)11:4<257::AID-PCA521>3.0.CO;2-A
https://doi.org/10.1016/S0305-1978(00)00062-4
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Nevadensin 160921 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O 344.30 unknown https://doi.org/10.1002/1099-1565(200007/08)11:4<257::AID-PCA521>3.0.CO;2-A
Xanthomicrol 73207 Click to see 344.30 unknown https://doi.org/10.1002/1099-1565(200007/08)11:4<257::AID-PCA521>3.0.CO;2-A
https://doi.org/10.1016/S0305-1978(00)00062-4

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