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Delphinium potaninii

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Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
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Details Top

Internal ID UUID6440162d4ec73497896998
Scientific name Delphinium potaninii
Authority Huth
First published in Bull. Herb. Boissier 1: 332 (1893)

Description Top

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Synonyms Top

Scientific name Authority First published in
Delphinium fargesii Franch. Bull. Annuel Soc. Philom. Paris , sér. 8, 5: 164 (1893)
Delphinium potaninii var. jiufengshanense W.J.Zhang & G.H.Chen Acta Phytotax. Sin. 39: 88 (2001)
Delphinium grandiflorum var. potaninii (Huth) Brühl Ann. Roy. Bot. Gard. (Calcutta) 5: 98 1896
Delphinium potaninii var. latibracteolatum W.T.Wang Acta Bot. Sin. 10: 147 1962

Common names Top

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Language Common/alternative name
Chinese 紫桔梗
Chinese 峨山草乌
Chinese 黑水翠雀花

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Delphinium potaninii var. bonvalotii (Franch.) W.T.Wang Bull. Bot. Res., Harbin 16: 156 (1996)

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

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-0000640588
Tropicos 27104759
KEW urn:lsid:ipni.org:names:710919-1
The Plant List kew-2760256
Open Tree Of Life 699542
NCBI Taxonomy 1045306
IPNI 710919-1
GBIF 7277801
EOL 2873742

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)!
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Title Authors Publication Released IDs
Norditerpenoid alkaloids from Delphinium nordhagenii. Shaheen F, Zeeshan M, Ahmad M, Anjum S, Ali S, Fun HK, Choudhary MI, Atta-ur-Rahman J Nat Prod 01-May-2006
doi:10.1021/NP050478M
PMID:16724850
Norditerpenoid alkaloids from the roots of Delphinium potaninii Hai-Yan Pu, Feng-Peng Wang, Chun-Tao Che Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(96)00256-7
New C(19)-diterpenoid alkaloids from the roots of Delphinium potaninii var. jiufengshanense. Shen XL, Zhou XL, Chen QH, Chen DL, Wang FP Chem Pharm Bull (Tokyo) 01-Sep-2002
doi:10.1248/CPB.50.1265
PMID:12237549
Two new norditerpenoid alkaloids from Delphinium potaninii. Pu H, Xu Q, Wang F, Che CT Planta Med 01-Oct-1996
doi:10.1055/S-2006-957940
PMID:17252482

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 / Aconitane-type diterpenoid alkaloids
(11-Formyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl)methyl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate 163061423 Click to see CC1CC(=O)N(C1=O)C2=CC=CC=C2C(=O)OCC34CCC(C56C3C(C(C5N(C4)C=O)(C7(CC(C8CC6C7C8OC)OC)O)O)OC)OC 682.80 unknown https://doi.org/10.1055/S-2006-957940
(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-8,9-dihydroxy-13-(hydroxymethyl)-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-11-carbaldehyde 162990294 Click to see COC1CCC2(CN(C3C14C2C(C3(C5(CC(C6CC4C5C6OC)OC)O)O)OC)C=O)CO 467.60 unknown https://doi.org/10.1055/S-2006-957940
(1S,2R,3R,4S,5S,6R,7R,8S,9S,10S,13S,16S,17R,18S)-7,9-dihydroxy-13-(hydroxymethyl)-4,6,8,16,18-pentamethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-11-carbaldehyde 101998850 Click to see COC1CCC2(CN(C3C14C2C(C3(C5(C6C4CC(C6OC)C(C5O)OC)OC)O)OC)C=O)CO 497.60 unknown https://doi.org/10.1016/0031-9422(96)00256-7
(1S,2R,3R,4S,5S,6S,8R,10S,13S,16S,17R,18S)-11-ethyl-6,8,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,9,16-triol 134715261 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)OC)O)OC)O)COC 467.60 unknown https://doi.org/10.1021/NP050478M
(1S,2R,3S,4R,5R,6R,8R,9S,13S,16R,17R,18R)-11-ethyl-4,6,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9,16-triol 137705073 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)O)COC 467.60 unknown https://doi.org/10.1021/NP050478M
(1S,5R,6S,8R,9S,13S,16S)-11-ethyl-13-(hydroxymethyl)-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 145994515 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)CO 467.60 unknown https://doi.org/10.1021/NP050478M
(8,9-Dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl)methyl 2-aminobenzoate 85400144 Click to see COC1CCC2(CNC3C14C2C(C3(C5(CC(C6CC4C5C6OC)OC)O)O)OC)COC(=O)C7=CC=CC=C7N 558.70 unknown https://doi.org/10.1248/CPB.50.1265
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18R)-11-ethyl-8,9-dihydroxy-6,16,18-trimethoxy-4-[(2S)-2-methylbutanoyl]oxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-aminobenzoate 162967472 Click to see CCC(C)C(=O)OC1C2CC3C1C(CC2OC)(C4(C(C5C36C4N(CC5(CCC6OC)COC(=O)C7=CC=CC=C7N)CC)OC)O)O 656.80 unknown https://doi.org/10.1248/CPB.50.1265
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18R)-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-aminobenzoate 162993535 Click to see COC1CCC2(CNC3C14C2C(C3(C5(CC(C6CC4C5C6OC)OC)O)O)OC)COC(=O)C7=CC=CC=C7N 558.70 unknown https://doi.org/10.1248/CPB.50.1265
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-[[(3R)-4-amino-3-methyl-4-oxobutanoyl]amino]benzoate 101341025 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7NC(=O)CC(C)C(=O)N 699.80 unknown https://doi.org/10.1021/NP050478M
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-8,9-dihydroxy-6,16,18-trimethoxy-4-[(2S)-2-methylbutanoyl]oxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-aminobenzoate 101190666 Click to see CCC(C)C(=O)OC1C2CC3C1C(CC2OC)(C4(C(C5C36C4N(CC5(CCC6OC)COC(=O)C7=CC=CC=C7N)CC)OC)O)O 656.80 unknown https://doi.org/10.1248/CPB.50.1265
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-formyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-[(3S)-3-methyl-2,5-dioxopyrrolidin-1-yl]benzoate 163061424 Click to see CC1CC(=O)N(C1=O)C2=CC=CC=C2C(=O)OCC34CCC(C56C3C(C(C5N(C4)C=O)(C7(CC(C8CC6C7C8OC)OC)O)O)OC)OC 682.80 unknown https://doi.org/10.1055/S-2006-957940
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-aminobenzoate 101190668 Click to see COC1CCC2(CNC3C14C2C(C3(C5(CC(C6CC4C5C6OC)OC)O)O)OC)COC(=O)C7=CC=CC=C7N 558.70 unknown https://doi.org/10.1248/CPB.50.1265
[(1S,2R,3R,4S,5S,6R,7R,8S,9S,10S,13S,16S,17R,18S)-11-formyl-7,9-dihydroxy-4,6,8,16,18-pentamethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate 101998852 Click to see CC1CC(=O)N(C1=O)C2=CC=CC=C2C(=O)OCC34CCC(C56C3C(C(C5N(C4)C=O)(C7(C8C6CC(C8OC)C(C7O)OC)OC)O)OC)OC 712.80 unknown https://doi.org/10.1016/0031-9422(96)00256-7
[(1S,2R,3R,4S,5S,6R,7R,8S,9S,10S,13S,16S,17R,18S)-11-formyl-7,9-dihydroxy-4,6,8,16,18-pentamethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-aminobenzoate 101998851 Click to see COC1CCC2(CN(C3C14C2C(C3(C5(C6C4CC(C6OC)C(C5O)OC)OC)O)OC)C=O)COC(=O)C7=CC=CC=C7N 616.70 unknown https://doi.org/10.1016/0031-9422(96)00256-7
[(1S,4S,5R,6S,8R,9S,13S,16S)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate 139292146 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7N8C(=O)CC(C8=O)C 682.80 unknown https://doi.org/10.1021/NP050478M
[(5R,8R)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-[(4-amino-2-methyl-4-oxobutanoyl)amino]benzoate 145994478 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7NC(=O)C(C)CC(=O)N 699.80 unknown https://doi.org/10.1021/NP050478M
[11-Ethyl-8,9-dihydroxy-6,16,18-trimethoxy-4-(2-methylbutanoyloxy)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-aminobenzoate 73079456 Click to see CCC(C)C(=O)OC1C2CC3C1C(CC2OC)(C4(C(C5C36C4N(CC5(CCC6OC)COC(=O)C7=CC=CC=C7N)CC)OC)O)O 656.80 unknown https://doi.org/10.1248/CPB.50.1265
8,9-Dihydroxy-13-(hydroxymethyl)-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-11-carbaldehyde 162990293 Click to see COC1CCC2(CN(C3C14C2C(C3(C5(CC(C6CC4C5C6OC)OC)O)O)OC)C=O)CO 467.60 unknown https://doi.org/10.1055/S-2006-957940
Anthranoyllycoctonine 441708 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7N 586.70 unknown https://doi.org/10.1021/NP050478M
Delavaine A 441723 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7NC(=O)C(C)CC(=O)OC 714.80 unknown https://doi.org/10.1021/NP050478M
Delavaine B 133065623 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7NC(=O)CC(C)C(=O)OC 714.80 unknown https://doi.org/10.1021/NP050478M

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