Pseudodictamnus aucheri

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Internal ID UUID64406a55306ad230199848
Scientific name Pseudodictamnus aucheri
Authority (Boiss.) Salmaki & Siadati
First published in Taxon 67(4): 779. 2018

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Synonyms Top

Scientific name Authority First published in
Ballota aucheri Boiss. Diagn. Pl. Orient. 5: 39 (1844)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

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Database ID/link to page
World Flora Online wfo-0001428533
Tropicos 100489008
KEW urn:lsid:ipni.org:names:77191003-1
NCBI Taxonomy 694340
IPNI 77191003-1
iNaturalist 1062308
GBIF 10680781

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Determination of the Absolute Configuration of Ballonigrin Lactone A Using Density Functional Theory Calculations Naseem M, Asghar S, Farooq U, Lakhani A, Altaf Y, Hashmi MA ACS Omega 04-Jan-2023
PMCID:PMC9850775
doi:10.1021/acsomega.2c03858
PMID:36687041
Exploration of Lamiaceae in Cardio Vascular Diseases and Functional Foods: Medicine as Food and Food as Medicine Chakrabartty I, Mohanta YK, Nongbet A, Mohanta TK, Mahanta S, Das N, Saravanan M, Sharma N Front Pharmacol 14-Jun-2022
PMCID:PMC9237463
doi:10.3389/fphar.2022.894814
PMID:35774598
Persianone, a dimeric diterpene from Ballota aucheri A. Rustaiyan, M.H. Mosslemin-Kupaii, F. Papastergiou, J. Jakupovic Elsevier BV 01-May-2003
doi:10.1016/0031-9422(95)00344-7
Furolabdanes and related compounds fromBallota aucheri A. Rustaiyan, M.H. Mosslemin-Kupaii, C. Zdero Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)83073-T

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
13-epi-Preleoheterin 102187096 Click to see 334.40 unknown https://doi.org/10.1016/0031-9422(91)83073-T
CID 162923730 162923730 Click to see CCOC1CC2(CCC3(O2)C(C(=O)C(C4C3(CCCC4(C)C)C)C)C)CO1 378.50 unknown https://doi.org/10.1016/0031-9422(91)83073-T
CID 162923731 162923731 Click to see CCOC1CC2(CCC3(O2)C(C(=O)C(C4C3(CCCC4(C)C)C)C)C)CO1 378.50 unknown https://doi.org/10.1016/0031-9422(91)83073-T
CID 163076815 163076815 Click to see CC1C2C(CCCC2(C3(CCC4(O3)CC(OC4)OC)C(C1=O)C)C)(C)C 364.50 unknown https://doi.org/10.1016/0031-9422(91)83073-T
CID 163076816 163076816 Click to see 364.50 unknown https://doi.org/10.1016/0031-9422(91)83073-T
CID 163076817 163076817 Click to see CC1C2C(CCCC2(C3(CCC4(O3)CC(OC4)OC)C(C1=O)C)C)(C)C 364.50 unknown https://doi.org/10.1016/0031-9422(91)83073-T
CID 163102243 163102243 Click to see CC1C(C(=O)C2C(CCCC2(C13CCC4(O3)COC=C4)C)(C)C)O 334.40 unknown https://doi.org/10.1016/0031-9422(91)83073-T
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(1S,4As,8aS)-4-[2-(furan-3-yl)ethyl]-1-hydroxy-3,4a,8,8-tetramethyl-5,6,7,8a-tetrahydro-1H-naphthalen-2-one 15765314 Click to see 316.40 unknown https://doi.org/10.1016/0031-9422(95)00344-7
(2R,3R,4R,4aS,8aS)-4-[2-(furan-3-yl)ethyl]-2,4-dihydroxy-3,4a,8,8-tetramethyl-2,3,5,6,7,8a-hexahydronaphthalen-1-one 15726751 Click to see CC1C(C(=O)C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)O 334.40 unknown https://doi.org/10.1016/0031-9422(95)00344-7
https://doi.org/10.1016/0031-9422(91)83073-T
(2R,4aS)-2-[[(2R,4aS)-4-[2-(furan-3-yl)ethyl]-4-hydroxy-3,4a,8,8-tetramethyl-1-oxo-2,3,5,6,7,8a-hexahydronaphthalen-2-yl]oxy]-4-[2-(furan-3-yl)ethyl]-3,4a,8,8-tetramethyl-5,6,7,8a-tetrahydro-2H-naphthalen-1-one 5459214 Click to see 632.90 unknown https://doi.org/10.1016/0031-9422(95)00344-7
4-[2-(Furan-3-yl)ethyl]-2,4-dihydroxy-3,4a,8,8-tetramethyl-2,3,5,6,7,8a-hexahydronaphthalen-1-one 162953770 Click to see 334.40 unknown https://doi.org/10.1016/0031-9422(91)83073-T
https://doi.org/10.1016/0031-9422(95)00344-7
6beta-Hydroxyhispanone 22297677 Click to see CC1=C(C2(CCCC(C2C(C1=O)O)(C)C)C)CCC3=COC=C3 316.40 unknown https://doi.org/10.1016/0031-9422(95)00344-7
Persianinone 495301 Click to see 632.90 unknown https://doi.org/10.1016/0031-9422(95)00344-7
Persianone 15765316 Click to see 632.90 unknown https://doi.org/10.1016/0031-9422(95)00344-7
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha-acyloxy carbonyl compounds / Alpha-acyloxy ketones
Ballotinone 21596426 Click to see 346.40 unknown https://doi.org/10.1016/0031-9422(91)83073-T
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
9-[2-(Furan-3-yl)ethyl]-4,8,10-trimethyl-2-oxatricyclo[6.3.1.04,12]dodec-9-ene-3,11-dione 73811267 Click to see 328.40 unknown https://doi.org/10.1016/0031-9422(95)00344-7
Ballonigrin 21596483 Click to see CC1=C(C2(CCCC3(C2C(C1=O)OC3=O)C)C)CCC4=COC=C4 328.40 unknown https://doi.org/10.1016/0031-9422(95)00344-7
> Organoheterocyclic compounds / Heteroaromatic compounds
(5aR)-5-[2-(furan-3-yl)ethyl]-4,5a,9,9-tetramethyl-7,8-dihydro-6H-2-benzoxepin-3-one 163020858 Click to see CC1=C(C2(CCCC(C2=COC1=O)(C)C)C)CCC3=COC=C3 314.40 unknown https://doi.org/10.1016/0031-9422(91)83073-T
5-[2-(furan-3-yl)ethyl]-4,5a,9,9-tetramethyl-7,8-dihydro-6H-2-benzoxepin-3-one 163020857 Click to see CC1=C(C2(CCCC(C2=COC1=O)(C)C)C)CCC3=COC=C3 314.40 unknown https://doi.org/10.1016/0031-9422(91)83073-T
> Organoheterocyclic compounds / Isobenzofurans
1-[(1S,3R,3aS,7aS)-3-[2-(furan-3-yl)ethyl]-3-hydroxy-3a,7,7-trimethyl-4,5,6,7a-tetrahydro-1H-2-benzofuran-1-yl]propan-1-one 15765315 Click to see 334.40 unknown https://doi.org/10.1016/0031-9422(95)00344-7
1-[3-[2-(furan-3-yl)ethyl]-3-hydroxy-3a,7,7-trimethyl-4,5,6,7a-tetrahydro-1H-2-benzofuran-1-yl]propan-1-one 163060591 Click to see 334.40 unknown https://doi.org/10.1016/0031-9422(95)00344-7

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