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Arnebia speciosa

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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 UUID64400ad02fa67149989788
Scientific name Arnebia speciosa
Authority Aitch. & Hemsl.
First published in J. Linn. Soc., Bot. 18: 81 (1880)

Description Top

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Synonyms Top

Scientific name Authority First published in
Macrotomia nobilis (Rech.f.) Huynh Candollea 26: 170 (1971)
Macrotomia speciosa (Aitch. & Hemsl.) Kitam. Fl. Afgh. : 322 (1960)
Arnebia nobilis Rech.f. Ann. Naturhist. Mus. Wien 58: 58 (1951)
Lithospermum speciosum (Aitch. & Hemsl.) I.M.Johnst. J. Arnold Arbor. 34: 13 (1953)
Lithospermum nobile (Rech.f.) I.M.Johnst. J. Arnold Arbor. 34: 14 (1953)

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

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000549518
Tropicos 50270935
KEW urn:lsid:ipni.org:names:60458842-2
The Plant List kew-2653025
Open Tree Of Life 6062081
IPNI 60458842-2
GBIF 8169708
EOL 2886267

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
Analysis of Commercial ‘Ratanjot’ by TLC Fluorescence Fingerprinting Sayyada Khatoon, Shanta Mehrotra, Usha Shome, B. N. Mehrotra Informa UK Limited 24-Nov-2007
doi:10.3109/13880209309082952
Naphthaquinones of Arnebia nobilis Y.N. Shukla, J.S. Tandon, D.S. Bhakuni, M.M. Dhar Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)86456-0
Constituents of Colocasia formicata, Sagittaria sagittifloria, Arnebia nobilis, Ipomoea paniculata rhododendron niveum, Paspalum scrobiculatum, Mundulea sericea and Duabanga sonneratiodes S.C. Sharma, Y.N. Shukla, J.S. Tandon Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)88557-X
Chemical constituents of the antibiotic fraction of Arnebia nobilis. Shukla YN, Tandon JS, Bhakuni DS, Dhar MM Experientia 01-Jan-1970
doi:10.1007/BF01899915
PMID:4979092

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
> Benzenoids / Naphthalenes / Naphthoquinones
[(1R)-1-(1,4-dihydroxy-5,8-dioxonaphthalen-2-yl)-4-hydroxy-4-methylpentyl] (E)-2-methylbut-2-enoate 163186247 Click to see CC=C(C)C(=O)OC(CCC(C)(C)O)C1=CC(=C2C(=O)C=CC(=O)C2=C1O)O 388.40 unknown https://doi.org/10.1007/BF01899915
[(1S)-1-(5,8-dihydroxy-1,4-dioxonaphthalen-2-yl)-4-hydroxy-4-methylpentyl] 3-methylbut-2-enoate 163190681 Click to see CC(=CC(=O)OC(CCC(C)(C)O)C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)C 388.40 unknown https://doi.org/10.1016/S0031-9422(00)86456-0
[(1S)-1-(5,8-dihydroxy-1,4-dioxonaphthalen-2-yl)-4-hydroxy-4-methylpentyl] acetate 163193227 Click to see CC(=O)OC(CCC(C)(C)O)C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O 348.30 unknown https://doi.org/10.1016/S0031-9422(00)86456-0
[1-(5,8-Dihydroxy-1,4-dioxonaphthalen-2-yl)-4-hydroxy-4-methylpentyl] 3-methylbut-2-enoate 324876 Click to see CC(=CC(=O)OC(CCC(C)(C)O)C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)C 388.40 unknown https://doi.org/10.1016/S0031-9422(00)86456-0
[1-(5,8-Dihydroxy-1,4-dioxonaphthalen-2-yl)-4-hydroxy-4-methylpentyl] acetate 101586704 Click to see CC(=O)OC(CCC(C)(C)O)C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O 348.30 unknown https://doi.org/10.1016/S0031-9422(00)86456-0
1,4-Naphthalenedione,5,8-dihydroxy-2-(1-hydroxy-4-methyl-3-pentenyl)- 149437686 Click to see CC(=CCC(C1=CC(=C2C(=O)C=CC(=O)C2=C1O)O)O)C 288.29 unknown https://doi.org/10.1007/BF01899915
58-dihydroxy-2-[(1S)-1-hydroxy-4-methylpent-3-enyl]naphthalene-14-dione 152743226 Click to see CC(=CCC(C1=CC(=C2C(=O)C=CC(=O)C2=C1O)O)O)C 288.29 unknown https://doi.org/10.1007/BF01899915
Alkannin beta,beta-dimethylacrylate 442720 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)OC(=O)C=C(C)C)C 370.40 unknown https://doi.org/10.1016/S0031-9422(00)86456-0
Arnebin V 85786789 Click to see CC(C)(CCCC1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)O 290.31 unknown https://doi.org/10.1016/S0031-9422(00)86456-0
Dmask 32465 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)OC(=O)C=C(C)C)C 370.40 unknown https://doi.org/10.1016/S0031-9422(00)86456-0
https://doi.org/10.3109/13880209309082952
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Heptacosanoic acid 23524 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 410.70 unknown https://doi.org/10.1016/S0031-9422(00)88557-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol 68171 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCO 382.70 unknown https://doi.org/10.1016/S0031-9422(00)88557-X
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3aS,9aS,9bS)-8-hydroxy-6,9-dimethyl-3-methylidene-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-2,7-dione 102436915 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(=C(C2=O)O)C 260.28 unknown https://doi.org/10.1007/BF01899915

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