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Aconitum forrestii

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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 UUID644006fb6145c800188153
Scientific name Aconitum forrestii
Authority Stapf
First published in Bull. Misc. Inform. Kew 1910: 19 (1910)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aconitum likiangense F.H.Chen & Liu Bull. Fan Mem. Inst. Biol. , Bot. 11: 46 (1941)

Common names Top

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Language Common/alternative name
Chinese 黄草乌
Chinese 丽江乌头

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000517274
Tropicos 27102952
KEW urn:lsid:ipni.org:names:707368-1
The Plant List kew-2618726
Open Tree Of Life 556432
NCBI Taxonomy 219065
IPNI 707368-1
GBIF 3925306
EOL 2873287
USDA GRIN 1339
CMAUP NPO12113

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
Sequencing and characterization of the chloroplast genome of Aconitum forrestii Stapf provide insights into phylogenetics in Aconitum Yang MH, Xia CL, Guan YH, Zhang HZ, Chen XB, Wang Y Mitochondrial DNA B Resour 24-Jun-2022
PMCID:PMC9246018
doi:10.1080/23802359.2022.2088307
PMID:35783038
A new diterpenoid alkaloid from Aconitum hemsleyanum. Luo ZH, Chen Y, Sun XY, Fan H, Li W, Deng L, Yin TP Nat Prod Res 01-May-2020
doi:10.1080/14786419.2018.1560292
PMID:30663368
Important Poisonous Plants in Tibetan Ethnomedicine Ma L, Gu R, Tang L, Chen ZE, Di R, Long C Toxins (Basel) 14-Jan-2015
PMCID:PMC4303819
doi:10.3390/toxins7010138
PMID:25594733
Chemical constituents of Aconitum tanguticum LUO Ming China Journal of Chinese Materia Medica 19-Jun-2012
doi:10.4268/CJCMM20120916
The Structures of Four New C19-Diterpenoid Alkaloids from Aconitum forrestii Stapf S. William Pelletier, Balawant S. Joshi, Jan A. Glinski, Hitesh P. Chokshi, Szu-ying Chen, Krishna Bhandary, Kuantee Go The Japan Institute of Heterocyclic Chemistry 16-Feb-2009
doi:10.3987/S-1987-01-0365
Simultaneous determination of three aconitum alkaloids in urine by LC-MS-MS. ZhaohongWang, Wang Z, Wen J, He Y J Pharm Biomed Anal 21-Sep-2007
doi:10.1016/J.JPBA.2007.04.016
PMID:17555909
The Structures of Forestine and Foresticine, Two New C<sub>19</sub>-Diterpenoid Alkaloids from Aconitum forrestii Stapf S. W. Pelletier, Chen Szu Ying, B. S. Joshi, Haridutt K. Desai American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50033A013
Norditerpenoid alkaloids from the processed tubers of Aconitum carmichaeli. Shim SH, Kim JS, Kang SS Chem Pharm Bull (Tokyo) 01-Aug-2003
doi:10.1248/CPB.51.999
PMID:12913245
Liwaconitine, a New Diterpenoid Alkaloid from Aconitum forrestii. Chongheng W, Dihua C, Weiliang S Planta Med 01-May-1983
doi:10.1055/S-2007-969879
PMID:17404943

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 / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
p-Anisic acid 7478 Click to see COC1=CC=C(C=C1)C(=O)O 152.15 unknown https://doi.org/10.4268/CJCMM20120916
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2S,4S)-4-(hydroxymethyl)-5-methylhexane-1,2,4,5-tetrol 162925146 Click to see CC(C)(C(CC(CO)O)(CO)O)O 194.23 unknown https://doi.org/10.3987/S-1987-01-0365
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(2R,3R,4S,5S,6S,8R,13S,16S,17R,18R)-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 139035022 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)OC)COC 451.60 unknown https://doi.org/10.1021/NP50033A013
(2R,3R,4S,5S,6S,8S,13S,16S,17R)-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 146014457 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown https://doi.org/10.1021/NP50033A013
(2R,3R,6S,8R,13S,17R)-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 5315807 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)OC)COC 451.60 unknown https://doi.org/10.1021/NP50033A013
(6S,8S,13S)-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 5321607 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown https://doi.org/10.1021/NP50033A013
[(1S,2R,3R,4R,5R,6S,8R,9R,10R,13R,14R,16S,17S,18R)-8-acetyloxy-11-ethyl-5,14-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 134715408 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC(=O)C)OC)OC)O)COC 659.80 unknown https://doi.org/10.4268/CJCMM20120916
https://doi.org/10.1055/S-2007-969879
https://doi.org/10.1021/NP50033A013
[(1S,2R,3R,4R,5S,6S,8R,9R,10R,13S,16S,17R,18R)-11-ethyl-5,8-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 101939160 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)O)OC)OC)COC 601.70 unknown https://doi.org/10.1021/NP50033A013
[(1S,2R,3R,4S,5R,6S,8R,9R,10R,13S,16S,17R,18R)-11-ethyl-8-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 163083346 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC(=O)C7=CC=C(C=C7)OC)OC)O)OC)OC)COC 585.70 unknown https://doi.org/10.3987/S-1987-01-0365
[(1S,2R,3R,4S,5R,6S,8S,9S,10R,13S,16S,17R)-8-ethoxy-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate 162937319 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)OCC)OC)COC 491.70 unknown https://doi.org/10.3987/S-1987-01-0365
[(1S,4R,5S,6S,8R,13R,14R,16S,18R)-8-acetyloxy-11-ethyl-5,14-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 11422434 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC(=O)C)OC)OC)O)COC 659.80 unknown via CMAUP database
[(1S,5S,8R,10R,13S)-8-acetyloxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 145994473 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC(=O)C)OC)OC)COC 643.80 unknown https://doi.org/10.1055/S-2007-969879
[(2R,3R,5S,6S,8R,13R,17S)-8-acetyloxy-11-ethyl-5,14-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 5315414 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC(=O)C)OC)OC)O)COC 659.80 unknown https://doi.org/10.1055/S-2007-969879
https://doi.org/10.1021/NP50033A013
[(2R,3R,5S,6S,8R,13S,17R)-8-acetyloxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 5316126 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC(=O)C)OC)OC)COC 643.80 unknown https://doi.org/10.1055/S-2007-969879
[(2R,3R,6S,8R,13S,17R)-8-acetyloxy-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 5315214 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC(=O)C7=CC=C(C=C7)OC)OC)OC(=O)C)OC)OC)COC 627.80 unknown via CMAUP database
[(2S,3S,5R,8R,13S,17S)-8-acetyloxy-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 138114719 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC(=O)C7=CC=C(C=C7)OC)OC)OC(=O)C)OC)OC)COC 627.80 unknown https://doi.org/10.1055/S-2007-969879
[11-Ethyl-8-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 13817025 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC(=O)C7=CC=C(C=C7)OC)OC)O)OC)OC)COC 585.70 unknown https://doi.org/10.3987/S-1987-01-0365
[8-Ethoxy-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate 13817023 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)OCC)OC)COC 491.70 unknown https://doi.org/10.3987/S-1987-01-0365
11-Ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,18-triol 14707731 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)O)OC)COC 437.60 unknown https://doi.org/10.1021/NP50033A013
8-O-Ethylyunaconitine 102469270 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OCC)OC)OC)O)COC 645.80 unknown https://doi.org/10.3987/S-1987-01-0365
Cammaconine 441715 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)CO 407.50 unknown https://doi.org/10.4268/CJCMM20120916
https://doi.org/10.1055/S-2007-969879
Chasmaconitine 101600179 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=CC=C7)O)OC)OC(=O)C)OC)OC)COC 613.70 unknown https://doi.org/10.1055/S-2007-969879
https://doi.org/10.4268/CJCMM20120916
CID 11250863 11250863 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC(=O)C)OC)OC)O)COC 659.80 unknown https://doi.org/10.3987/S-1987-01-0365
Foresaconitine 13817036 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC(=O)C7=CC=C(C=C7)OC)OC)OC(=O)C)OC)OC)COC 627.80 unknown https://doi.org/10.1248/CPB.51.999
Foresticine 185130 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6O)O)OC)O)O)OC)COC 453.60 unknown https://doi.org/10.1021/NP50033A013
Toroko base II 165283 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)OC)COC 451.60 unknown via CMAUP database
Vilmorrianine C 20055981 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC(=O)C7=CC=C(C=C7)OC)OC)OC(=O)C)OC)OC)COC 627.80 unknown https://doi.org/10.4268/CJCMM20120916
Yunaconitine 155569 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC(=O)C)OC)OC)O)COC 659.80 unknown https://doi.org/10.1016/J.JPBA.2007.04.016
https://doi.org/10.3987/S-1987-01-0365
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Lappaconitine-type diterpenoid alkaloids
(5S,6S,8S,10R,13R)-11-ethyl-6,16-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 145994510 Click to see CCN1CC2CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC 377.50 unknown https://doi.org/10.1055/S-2007-969879
https://doi.org/10.4268/CJCMM20120916
https://doi.org/10.1080/14786419.2018.1560292
Aconosine 170126 Click to see CCN1CC2CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC 377.50 unknown https://doi.org/10.1055/S-2007-969879
https://doi.org/10.1080/14786419.2018.1560292
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(17alpha,23E)-5alpha-Dammara-20,23-diene-3beta,25-diol 9955042 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC4C(=C)CC=CC(C)(C)O)C)C)C 442.70 unknown via CMAUP database
Diosgenin 99474 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown via CMAUP database
Yamogenin 441900 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(25R)-3beta-[4-O-[4-O-(alpha-L-Rhamnopyranosyl)-alpha-L-rhamnopyranosyl]-beta-D-glucopyranosyloxy]spirosta-5-ene 21603983 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol 21603986 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)C)OC1 1015.20 unknown via CMAUP database
Borassoside A 16204068 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
Borassoside B 102155844 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC19C(CC(CO9)CO)O 901.00 unknown via CMAUP database
Borassoside C 102155845 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC19C(CC(CO9)CO)O 901.00 unknown via CMAUP database
Borassoside D 16204180 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)OC1 722.90 unknown via CMAUP database
Borassoside E 16204181 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
Borassoside F 16204183 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)C)OC1 1015.20 unknown via CMAUP database
Collettinside III 10653210 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
Dioscin 119245 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
Disogluside 11827970 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)OC1 576.80 unknown via CMAUP database
Methylprotodioscin 11263254 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC 1063.20 unknown via CMAUP database
Progenin II 44429638 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)OC1 722.90 unknown via CMAUP database
Prosapogenin A 11061578 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1 722.90 unknown via CMAUP database
Protodioscin 441891 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1049.20 unknown via CMAUP database
Pseudoprotodioscin 21637110 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC8C7C(=C(O8)CCC(C)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)CO)O)O)O 1031.20 unknown via CMAUP database
Trigonelloside C 441899 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1049.20 unknown via CMAUP database
Yamogenin 3-O-neohesperidoside 441901 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1 722.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4-O-beta-D-mannopyranosyl-alpha-D-mannopyranose 5288769 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
Gal(a1-6)a-Man 11724912 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)O)O)O)O)O)O)O)O 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
beta-D-Manp-(1->4)-beta-D-Manp-(1->4)-beta-D-Manp 5287808 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)O)CO)CO)O)O)O)O 504.40 unknown via CMAUP database

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