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Ajuga iva

Ajuga iva - 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 UUID64403728ee260899582058
Scientific name Ajuga iva
Authority (L.) Schreb.
First published in Plantarum Verticillatarum Unilabiatarum Genera et Species 1774

Description Top

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Synonyms Top

Scientific name Authority First published in
Abiga cistifolia St.-Lag. Ann. Soc. Bot. Lyon 7: 85 (1880)
Moscharia arabica Vitman Summa Pl. v. 278. 1791
Moscharia asperidifolia Forssk. Fl. Aegypt.-Arab. p. lxxiv. 1775 [1 Oct 1775]
Moscharia forskahlii J.F.Gmel. Syst. Nat., ed. 13[bis]. 2(1): 275. 1791 [late Sep-Nov 1791]
Teucrium iva L. Sp. Pl. : 563 (1753)
Teucrium moschatum Mill. Gard. Dict. ed. 8 : n.º 15 (1768)
Bugula moschata Bubani Fl. Pyren. 1: 472 (1897)
Bulga iva Kuntze Revis. Gen. Pl. 2: 512 (1891)
Chamaepitys iva Fourr. Ann. Soc. Linn. Lyon , n.s., 17: 138 (1869)
Chamaepithys moschata Garsault Fig. Pl. Med. 2: t. 218. 1764, nom. inval., opus utique oppressum; Descr. Pl. Anim. 143. 1767; Thell. in Bull. Herb. Boiss. Ser. II. viii. 788.
Chamaepitys pseudoiva Fourr. Ann. Soc. Linn. Lyon , n.s., 17: 138 (1869)
Ajuga humilis Porta Atti Imp. Regia Accad. Rovereto , ser. 2, 9: 56 (1891)
Ajuga iva subsp. pseudoiva (Robill. & Castagne ex DC.) Briq. Lab. Alp. Mar. : 112 (1891)
Ajuga iva var. pseudoiva (Robill. & Castagne ex DC.) Steud. Nomencl. Bot. , ed. 2, 1: 46 (1840)
Ajuga iva f. punctata Radic Acta Bot. Croat. 33: 225 (1974)
Ajuga iva var. spathulifolia Mutel Fl. Franç. Herbor. 3: 55. 1836
Ajuga moschata Mill. ex Schreb. Pl. Verticill. Unilab. Gen. Sp. : xxvi (1773)
Ajuga pseudoiva Robill. & Castagne ex DC. Fl. Franç. , ed. 3, 5: 395 (1815)
Moscharia asperifolia Forssk. Fl. Aegypt.-Arab. p. lxxiv. 1775 [1 Oct 1775]

Common names Top

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Language Common/alternative name
Spanish hierba de vaca
Spanish antilide segunda
Spanish bugula almizclada
Spanish iva comun
Spanish iva común
Spanish pinillo amizclado
Arabic عجوقة عطرية
Arabic أجوجا
Arabic سندقورة
Catalan iva
Catalan fulla de creu
German moschus-günsel
German mittelmeer-günsel
Croatian cjelolisna ivica
Kabyle lmesk iẓekwan

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

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000934146
Tropicos 50288814
INPN 80983
Flora of Italy 4416
KEW urn:lsid:ipni.org:names:444598-1
The Plant List kew-5293
Open Tree Of Life 5793033
Observations.org 129555
NCBI Taxonomy 2026104
NBN Atlas NHMSYS0000455715
IPNI 98446-3
iNaturalist 71174
GBIF 7307171
EPPO AIUIV
EOL 5372930
Elurikkus 586173
USDA GRIN 401501
Wikipedia Ajuga_iva
PFAF Ajuga iva

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
Ethnobotanical survey on herbal remedies for the management of type 2 diabetes in the Casablanca-Settat region, Morocco Arraji M, Al Wachami N, Boumendil K, Chebabe M, Mochhoury L, Laamiri FZ, Barkaoui M, Chahboune M BMC Complement Med Ther 15-Apr-2024
PMCID:PMC11017650
doi:10.1186/s12906-024-04468-4
PMID:38622669
A systematic methodology to assess the identity of plants in historical texts: A case study based on the Byzantine pharmacy text John the Physician's Therapeutics Lardos A, Patmore K, Allkin R, Lazarou R, Nesbitt M, Scott AC, Zipser B J Ethnopharmacol 25-Mar-2024
PMCID:PMC7615571
doi:10.1016/j.jep.2023.117622
PMID:38128894
Therapeutics to Treat Psychiatric and Neurological Disorders: A Promising Perspective from Algerian Traditional Medicine Larit F, León F Plants (Basel) 15-Nov-2023
PMCID:PMC10674704
doi:10.3390/plants12223860
PMID:38005756
Antidiarrheal and antioxidant activities of Ajuga iva (L.) leave extract Ladjimi MH, Ben Barka Z, Lahbib K, Ben Miled H, Ben Rhouma K, Sakly M, Tebourbi O Heliyon 21-Oct-2023
PMCID:PMC10628661
doi:10.1016/j.heliyon.2023.e21139
PMID:37942157
Natural Antimicrobials: A Reservoir to Contrast Listeria monocytogenes Ricci A, Lazzi C, Bernini V Microorganisms 15-Oct-2023
PMCID:PMC10609241
doi:10.3390/microorganisms11102568
PMID:37894226
Road Impact on Plant Colonization in the Arid Timanfaya National Park Bernardos M, Cornejo NS, Torres Hassan AD, Cabrera R, Arévalo JR Plants (Basel) 13-Oct-2023
PMCID:PMC10610428
doi:10.3390/plants12203568
PMID:37896031
Hypoglycemic and Hypotensive Effects of Calycotome villosa Subsp. intermedia Seeds in Meriones shawi Rats: In Vivo, Ex Vivo, and In Vitro Investigations Lyoussi B, Laaroussi H, Cherkaoui-Tangi K, Hano C, Morel N Evid Based Complement Alternat Med 11-May-2023
PMCID:PMC10195170
doi:10.1155/2023/3081102
PMID:37215635
Phytochemical Profile, Antioxidant, Antimicrobial, and Antidiabetic Activities of Ajuga iva (L.) Saidi S, Remok F, Handaq N, Drioiche A, Gourich AA, Menyiy NE, Amalich S, Elouardi M, Touijer H, Bouhrim M, Bouissane L, Nafidi HA, Bin Jardan YA, Bourhia M, Zair T Life (Basel) 11-May-2023
PMCID:PMC10222250
doi:10.3390/life13051165
PMID:37240812
Exploring Iberian Peninsula Lamiaceae as Potential Therapeutic Approaches in Wound Healing Marques MP, Mendonça L, Neves BG, Varela C, Oliveira P, Cabral C Pharmaceuticals (Basel) 24-Feb-2023
PMCID:PMC10056130
doi:10.3390/ph16030347
PMID:36986446
A New Lavender (Lavandula multifida L.) Ecotype from Arid Tunisia, with Differential Essential Oil Composition and Higher Antimicrobial Potential Tofah ML, Mseddi K, Al-Abbasi OK, Ben Yazid A, Khechine A, Gdoura R, Khannous L Life (Basel) 30-Dec-2022
PMCID:PMC9866874
doi:10.3390/life13010103
PMID:36676052
A Quantitative Study on the Ethnobotanical Knowledge about Wild Edible Plants among the Population of Messiwa Ghanimi R, Ouhammou A, Babahmad RA, Cherkaoui M Ethiop J Health Sci 01-Nov-2022
PMCID:PMC9692160
doi:10.4314/ejhs.v32i6.22
PMID:36475263
Chemical Composition, Antioxidant, and Antimicrobial Activities of Leaves of Ajuga Iva Ammar H, Touihri I, Kholif AE, M’Rabet Y, Jaouadi R, Chahine M, Marti ME, Vargas-Bello-Pérez E, Hosni K Molecules 20-Oct-2022
PMCID:PMC9607272
doi:10.3390/molecules27207102
PMID:36296695
In Vitro Antimitotic and Hypoglycemic Effect Study and Acute Toxicity Assessment of the Aqueous and Organic Extracts of Chamaerops humilis L. var. argentea Andre Lachkar N, Lamchouri F, Toufik H Biomed Res Int 14-Oct-2022
PMCID:PMC9586795
doi:10.1155/2022/4303506
PMID:36277886
Antidiabetic effects of Brugmansia aurea leaf extract by modulating the glucose levels, insulin resistance, and oxidative stress mechanism Fatima N, Anwar F, Saleem U, Khan A, Ahmad B, Shahzadi I, Ahmad H, Ismail T Front Nutr 11-Oct-2022
PMCID:PMC9592987
doi:10.3389/fnut.2022.1005341
PMID:36304231
Ethnopharmacological Survey, Mineral and Chemical Content, In Vitro Antioxidant, and Antibacterial Activities of Aqueous and Organic Extracts of Chamaerops humilis L. var. argentea Andre Leaves Lachkar N, Lamchouri F, Toufik H Biomed Res Int 05-Aug-2022
PMCID:PMC9410792
doi:10.1155/2022/1091247
PMID:36033551

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 / Triterpenoids
(3S,4S,5R)-4-[(2R,3R)-2,3-dihydroxy-3-[(5R,9R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]butyl]-3,5-dimethyloxolan-2-one 122130059 Click to see CC1C(C(OC1=O)C)CC(C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)O 520.70 unknown https://doi.org/10.1016/S0031-9422(00)97527-7
(3S,4S,5R)-4-[(3R)-3-hydroxy-2-oxo-3-[(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]butyl]-3,5-dimethyloxolan-2-one 44566366 Click to see CC1C(C(OC1=O)C)CC(=O)C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O 518.60 unknown https://doi.org/10.1016/S0031-9422(00)97527-7
(3S,4S,5R)-4-[(3S)-3-hydroxy-3-[(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]butyl]-3,5-dimethyloxolan-2-one 162983657 Click to see CC1C(C(OC1=O)C)CCC(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O 504.70 unknown https://doi.org/10.1016/S0031-9422(00)97527-7
4-[3-hydroxy-2-oxo-3-(2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)butyl]-3,5-dimethyloxolan-2-one 75072014 Click to see CC1C(C(OC1=O)C)CC(=O)C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O 518.60 unknown https://doi.org/10.1016/S0031-9422(00)97527-7
4-[3-hydroxy-3-(2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)butyl]-3,5-dimethyloxolan-2-one 162983656 Click to see CC1C(C(OC1=O)C)CCC(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O 504.70 unknown https://doi.org/10.1016/S0031-9422(00)97527-7
Cyasterone 119444 Click to see CC1C(C(OC1=O)C)CC(C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)O 520.70 unknown https://doi.org/10.1016/S0031-9422(00)97527-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
(2R,3S,5S,10S,13S,14R,17R)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2S,3S,5S)-2,3,6-trihydroxy-5,6-dimethylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 133562183 Click to see CC(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)C(C)(C)O 494.70 unknown https://doi.org/10.1016/S0031-9422(00)97527-7
(2S,3R,5R,10R,13R,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-5,6-dimethylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 5319224 Click to see CC(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)C(C)(C)O 494.70 unknown https://doi.org/10.1016/S0031-9422(00)97527-7
(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3R)-2,3,6-trihydroxy-6-methyl-5-methylideneheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 13889301 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CC(=C)C(C)(C)O)O)O)O 492.60 unknown https://doi.org/10.1016/S0031-9422(00)97527-7
Makisterone A 12312690 Click to see CC(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)C(C)(C)O 494.70 unknown https://doi.org/10.1016/S0031-9422(00)97527-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
(2R)-4-[(1R)-1-hydroxyethyl]-2-[(1R)-1-hydroxy-1-[(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]ethyl]-5-methyl-2,3-dihydropyran-6-one 152754669 Click to see CC1=C(CC(OC1=O)C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)C(C)O 518.60 unknown https://doi.org/10.1016/S0031-9422(00)97527-7
4-(1-hydroxyethyl)-2-[1-hydroxy-1-(2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)ethyl]-5-methyl-2,3-dihydropyran-6-one 162998998 Click to see CC1=C(CC(OC1=O)C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)C(C)O 518.60 unknown https://doi.org/10.1016/S0031-9422(00)97527-7
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1R,2S,3S,4aR,5S,6R,8S,8aR)-5-[(2S,3aS,5S,6aR)-5-ethoxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl]-8-acetyloxy-8a-(acetyloxymethyl)-3-hydroxy-5,6-dimethylspiro[3,4,4a,6,7,8-hexahydro-2H-naphthalene-1,2'-oxirane]-2-yl] 2-methylpropanoate 163188355 Click to see CCOC1CC2CC(OC2O1)C3(C(CC(C4(C3CC(C(C45CO5)OC(=O)C(C)C)O)COC(=O)C)OC(=O)C)C)C 582.70 unknown https://doi.org/10.1246/CL.1982.1053
[(1R,2S,3S,4aR,5S,6R,8S,8aR)-5-[(3aR,5R,6aS)-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-5-yl]-8-acetyloxy-8a-(acetyloxymethyl)-3-hydroxy-5,6-dimethylspiro[3,4,4a,6,7,8-hexahydro-2H-naphthalene-1,2'-oxirane]-2-yl] (2R)-2-methylbutanoate 162937625 Click to see CCC(C)C(=O)OC1C(CC2C(C(CC(C2(C13CO3)COC(=O)C)OC(=O)C)C)(C)C4CC5CCOC5O4)O 552.70 unknown https://doi.org/10.1246/CL.1982.1053
[(1R,2S,3S,4aR,5S,6R,8S,8aR)-5-[(3aR,5R,6aS)-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-5-yl]-8-acetyloxy-8a-(acetyloxymethyl)-3-hydroxy-5,6-dimethylspiro[3,4,4a,6,7,8-hexahydro-2H-naphthalene-1,2'-oxirane]-2-yl] 2-methylpropanoate 162907388 Click to see CC1CC(C2(C(C1(C)C3CC4CCOC4O3)CC(C(C25CO5)OC(=O)C(C)C)O)COC(=O)C)OC(=O)C 538.60 unknown https://doi.org/10.1246/CL.1982.1053
[(1R,2S,3S,4aR,5S,6R,8S,8aR)-5-[(3aR,5S,6aS)-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-5-yl]-8-acetyloxy-8a-(acetyloxymethyl)-3-hydroxy-5,6-dimethylspiro[3,4,4a,6,7,8-hexahydro-2H-naphthalene-1,2'-oxirane]-2-yl] (2S)-2-methylbutanoate 76308713 Click to see CCC(C)C(=O)OC1C(CC2C(C(CC(C2(C13CO3)COC(=O)C)OC(=O)C)C)(C)C4CC5CCOC5O4)O 552.70 unknown https://doi.org/10.1016/S0305-1978(00)00012-0
[5-(2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-5-yl)-8-acetyloxy-8a-(acetyloxymethyl)-3-hydroxy-5,6-dimethylspiro[3,4,4a,6,7,8-hexahydro-2H-naphthalene-1,2'-oxirane]-2-yl] 2-methylpropanoate 53462657 Click to see CC1CC(C2(C(C1(C)C3CC4CCOC4O3)CC(C(C25CO5)OC(=O)C(C)C)O)COC(=O)C)OC(=O)C 538.60 unknown https://doi.org/10.1246/CL.1982.1053
[5-(2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-5-yl)-8-acetyloxy-8a-(acetyloxymethyl)-5,6-dimethylspiro[3,4,4a,6,7,8-hexahydro-2H-naphthalene-1,2'-oxirane]-2-yl] 2-methylpropanoate 53462656 Click to see CC1CC(C2(C(C1(C)C3CC4CCOC4O3)CCC(C25CO5)OC(=O)C(C)C)COC(=O)C)OC(=O)C 522.60 unknown https://doi.org/10.1246/CL.1982.1053
[8-acetyloxy-8a-(acetyloxymethyl)-5-(5-ethoxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl)-3-hydroxy-5,6-dimethylspiro[3,4,4a,6,7,8-hexahydro-2H-naphthalene-1,2'-oxirane]-2-yl] 2-methylpropanoate 73744540 Click to see CCOC1CC2CC(OC2O1)C3(C(CC(C4(C3CC(C(C45CO5)OC(=O)C(C)C)O)COC(=O)C)OC(=O)C)C)C 582.70 unknown https://doi.org/10.1246/CL.1982.1053
CID 14757825 14757825 Click to see CCC(C)C(=O)OC1C(CC2C(C(CC(C2(C13CO3)COC(=O)C)OC(=O)C)C)(C)C4CC5CCOC5O4)O 552.70 unknown https://doi.org/10.1246/CL.1982.1053
Hativene A 10721736 Click to see CC1CC(C2(C(C1(C)C3CC4CC(OC4O3)OC)CC(C(C25CO5)OC(=O)C(C)C)O)COC(=O)C)OC(=O)C 568.70 unknown https://doi.org/10.1016/S0367-326X(99)00146-X
Hativene B 10793121 Click to see CC1CC(C2(C(C1(C)C3CC4CC(OC4O3)OC)CC(C(C25CO5)OC(=O)C(C)C)O)COC(=O)C)OC(=O)C 568.70 unknown https://doi.org/10.1016/S0367-326X(99)00146-X
Hativene C 10745609 Click to see CC1CC(C2(C(C1(C)C3CC4CC(OC4O3)OC)CC(C(C25CO5)OC(=O)C(C)C)O)COC(=O)C)OC(=O)C 568.70 unknown https://doi.org/10.1016/S0367-326X(99)00146-X
Ivain Ii 21123570 Click to see CC1CC(C2(C(C1(C)C3CC4CCOC4O3)CCC(C25CO5)OC(=O)C(C)C)COC(=O)C)OC(=O)C 522.60 unknown https://doi.org/10.1246/CL.1982.1053
Ivain IV 157527 Click to see CCC(C)C(=O)OC1C(CC2C(C(CC(C2(C13CO3)COC(=O)C)OC(=O)C)C)(C)C4CC5CCOC5O4)O 552.70 unknown https://doi.org/10.1016/S0305-1978(00)00012-0
Lupulin A 10841022 Click to see CCC(C)C(=O)OC1C(CC2C(C(CC(C2(C13CO3)COC(=O)C)OC(=O)C)C)(C)C4CC5CC(OC5O4)OC)O 582.70 unknown https://doi.org/10.1016/S0367-326X(99)00146-X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10236079/

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