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Solanum aethiopicum

Solanum aethiopicum - Unknown
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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 UUID64404180018a7919289036
Scientific name Solanum aethiopicum
Authority L.
First published in Cent. Pl. 2: 10. 1756.

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Lycopersicon aethiopicum (L.) Mill. Gard. Dict. ed. 8, no. 3. 1768.
Solanum aethiopicum Jacq. Hort. Bot. Vindob. 1: 4, tab. 12. 1770.
Solanum aethiopicum var. aculeatum Dunal Hist. Nat. Solanum 148. 1813.
Solanum aethiopicum var. armatum Bitter Repert. Spec. Nov. Regni Veg. Beih. 16: 46. 1923.
Solanum aethiopicum var. giorgii (De Wild.) Bitter Repert. Spec. Nov. Regni Veg. Beih. 16: 46. 1923.
Solanum aethiopicum var. inerme Dunal Hist. Nat. Solanum 148. 1813.
Solanum aethiopicum var. integrifolium (Poir.) O.E.Schulz Symb. Antill. (Urban) 6: 211. 1909.
Solanum aethiopicum var. modicelobatum Bitter Repert. Spec. Nov. Regni Veg. Beih. 16: 46. 1923.
Solanum aethiopicum var. paaschenianum (H.J.P.Winkl.) Bitter Repert. Spec. Nov. Regni Veg. Beih. 16: 47. 1923.
Solanum aurantiacum Sendtn. Fl. Bras. (Martius) 10: 55. 1846.
Solanum aurantium Larrañaga Escritos Damaso Antonio Larranaga 2: 88. 1923.
Solanum brieyi De Wild. Bull. Jard. Bot. État Bruxelles 4: 404. 1914.
Solanum elaeagnifolium Herb. Willdenow ex Steud. Nomencl. Bot. ed. 2, 2: 602. 1841.
Solanum elskensii De Wild. Bull. Jard. Bot. État Bruxelles 4: 403. 1914.
Solanum geminifolium Thonn. Beskr. Guin. Pl. 121 [141]. 1827.
Solanum gilo Req. ex Dunal Prodr. [A. P. de Candolle] 13(1): 360. 1852.
Solanum gilo subsp. megalacanthum Bitter Repert. Spec. Nov. Regni Veg. Beih. 16: 59. 1923.
Solanum gilo subsp. monteiroi (C.H.Wright) Bitter Repert. Spec. Nov. Regni Veg. Beih. 16: 56. 1923.
Solanum gilo var. ellipsoideum Bitter Repert. Spec. Nov. Regni Veg. Beih. 16: 53. 1923.
Solanum gilo var. erectifructum Bitter Repert. Spec. Nov. Regni Veg. Beih. 16: 54. 1923.
Solanum gilo var. pierreanum (Pailleux & Bois) Bitter Repert. Spec. Nov. Regni Veg. Beih. 16: 54. 1923.
Solanum gilo var. sparseaculeatum Bitter Repert. Spec. Nov. Regni Veg. Beih. 16: 59. 1923
Solanum giorgii De Wild. Bull. Jard. Bot. État Bruxelles 4: 401. 1914.
Solanum hybridum Jacq. Hort. Bot. Vindob. 2: 51, tab. 113. 1772-1773.
Solanum indicum subsp. ambifarium Bitter Repert. Spec. Nov. Regni Veg. Beih. 16: 37. 1923.
Solanum integrifolium Poir. Encycl. (Lamarck) 4: 301. 1797.
Solanum kupperi Markgr. Mitt. Bot. Staatssamml. München 1: 30. 1950.
Solanum lobelii Ten. Ann. Sci. Nat., Bot. ser. 3, 14: 344. 1850.
Solanum lusitanicum Dunal Hist. Nat. Solanum 238. 1813.
Solanum melongena var. inerme C.H.Wright Fl. Trop. Afr. (Oliver et al.) 4: 243. 1906.
Solanum monteiroi C.H.Wright Bull. Misc. Inform. Kew 1894: 127. 1894.
Solanum naumannii Engl. Bot. Jahrb. Syst. 8: 64. 1886.
Solanum obtusifolium Willd. Enum. Pl. Suppl. [Willdenow] 11. 1813.
Solanum obtusifolium Schltdl. & Cham. Linnaea 5: 113. 1830.
Solanum olivare Pailleux & Bois Potag. Cur., ed. 2, 386. 1892.
Solanum ovatifolium De Wild. Pl. Bequaert. 1: 432. 1922.
Solanum paaschenianum H.J.P.Winkl. Bot. Jahrb. Syst. 41: 285. 1908.
Solanum pierreanum Pailleux & Bois Rev. Sci. Nat. Appl. 37: 483. 1890.
Solanum poggei Dammer Bot. Jahrb. Syst. 48: 242. 1912.
Solanum pseudomelongena Ten. Ann. Sci. Nat., Bot. ser. 3, 14: 345. 1850.
Solanum racemiflorum Dunal Hist. Nat. Solanum 147. 1813.
Solanum scabrum Zuccagni Cent. Observ. Bot., no. 50: [21]. 1806.
Solanum sparsespinosum De Wild. Bull. Jard. Bot. État Bruxelles 4: 399. 1914.
Solanum subsessile De Wild. Bull. Jard. Bot. État Bruxelles 4: 407. 1914.
Solanum sudanense Hammerstein Beih. Tropenpflanzer 19: 95. 1919.
Solanum texanum hort. ex Ten. Atti Real Ist. Incoragg. Sci. Nat. Napoli 8: 328. 1855.
Solanum texanum Dunal Prodr. [A. P. de Candolle] 13(1): 359. 1852.
Solanum worsleyi W.Watson Gard. Chron. 27: 18. 1900.
Solanum zuccagnianum Dunal Hist. Nat. Solanum 149, tab. 11. 1813.
Solanum zuccagnianum var. allogonum Dunal Prodr. [A. P. de Candolle] 13(1): 351. 1852.
Solanum melongena var. scarlatineum Alef.

Common names Top

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Language Common/alternative name
English ethiopian nightshade
Arabic قوطه
Arabic باذنجان قوطه
Arabic حدق أثيوبي
Catalan fals tomàquet
German Äthiopische eierfrucht
Fulah yaaloore
Indonesian tomat pahit
ln mosangó
Portuguese jiloeiro
Swahili nyanya chungu
Thai มะเขือขม
Thai มะเขือเอธิโอเปีย
Chinese 金银茄
Chinese 红茄
Chinese 玩茄

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Eritrea
      • Ethiopia
      • Somalia
      • Sudan
    • Northern Africa
      • Egypt
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
    • West Tropical Africa
      • Benin
      • Burkina
      • Ghana
      • Guinea
      • Ivory Coast
      • Liberia
      • Mali
      • Niger
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Equatorial Guinea
      • Gabon
      • Gulf Of Guinea Islands
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Madagascar
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Taiwan
  • Northern America
    • North-central U.S.A.
      • Illinois
    • Northwestern U.S.A.
      • Colorado
    • Southeastern U.S.A.
      • Kentucky
  • Southern America
    • Brazil
      • Brazil West-central
    • Caribbean
      • Windward Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001025760
UNII JT03U9K3Y3
USDA Plants SOAE2
Tropicos 29600093
INPN 630691
KEW urn:lsid:ipni.org:names:818158-1
The Plant List tro-29600093
PFAF Solanum aethiopicum
Open Tree Of Life 886496
Observations.org 87865
NCBI Taxonomy 205524
IPNI 818158-1
iNaturalist 431630
GBIF 2929847
Freebase /m/06mf3b
EPPO SOLAE
EOL 484230
USDA GRIN 100448
Wikipedia Solanum_aethiopicum
CMAUP NPO3628

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
De novo assembly of the complete mitochondrial genome of pepino (Solanum muricatum) using PacBio HiFi sequencing: insights into structure, phylogenetic implications, and RNA editing Li Z, Liu J, Liang M, Guo Y, Chen X, Wu H, Jin S BMC Plant Biol 04-May-2024
PMCID:PMC11069145
doi:10.1186/s12870-024-04978-w
PMID:38702620
Unravelling taboos and cultural beliefs associated with hidden hunger among pregnant and breast-feeding women in Buyende district Eastern Uganda Tugume P, Mustafa AS, Walusansa A, Ojelel S, Nyachwo EB, Muhumuza E, Nampeera M, Kabbale F, Ssenku JE J Ethnobiol Ethnomed 02-May-2024
PMCID:PMC11064283
doi:10.1186/s13002-024-00682-z
PMID:38693532
Pest risk assessment of African Leucinodes species for the European Union Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Civera AV, Yuen J, Zappalà L, Mally R, Czwienczek E, Gobbi A, López Mercadal J, Maiorano A, Mosbach‐Schulz O, Pautasso M, Rossi E, Stancanelli G, Tramontini S, Van der Werf W EFSA J 29-Apr-2024
PMCID:PMC11056852
doi:10.2903/j.efsa.2024.8739
PMID:38686343
Risk assessment of Retithrips syriacus for the EU Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, van der Werf W, Yuen J, Zappalà L, Bezerra Lima ÉF, Makowski D, Crotta M, Gobbi A, Golic D, Maiorano A, Mosbach‐Schulz O, Rossi E, Terzidou A, Vicent Civera A EFSA J 29-Apr-2024
PMCID:PMC11056851
doi:10.2903/j.efsa.2024.8741
PMID:38686341
Solanum aculeatissimum and Solanum torvum chloroplast genome sequences: a comparative analysis with other Solanum chloroplast genomes Zhang L, Yi C, Xia X, Jiang Z, Du L, Yang S, Yang X BMC Genomics 26-Apr-2024
PMCID:PMC11046870
doi:10.1186/s12864-024-10190-9
PMID:38671394
Traditional lore on the healing effects of therapeutic plants used by the local communities around Simien Mountains National Park, northwestern Ethiopia Seraw E, Melkamu Y, Masresha G J Ethnobiol Ethnomed 17-Apr-2024
PMCID:PMC11025143
doi:10.1186/s13002-024-00678-9
PMID:38632559
Ripening process in exocarps of scarlet eggplant (Solanum aethiopicum) and banana (Musa spp.) investigated by Raman spectroscopy Campos MT, Maia LF, Popović-Djordjević J, Edwards HG, de Oliveira LF Food Chem (Oxf) 16-Apr-2024
PMCID:PMC11039347
doi:10.1016/j.fochms.2024.100204
PMID:38659653
Pest risk assessment of Leucinodes orbonalis for the European Union Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Vicent Civera A, Yuen J, Zappalà L, Mally R, Czwienczek E, Gobbi A, López Mercadal J, Maiorano A, Mosbach‐Schulz O, Pautasso M, Rossi E, Stancanelli G, Tramontini S, Van der Werf W EFSA J 12-Mar-2024
PMCID:PMC10928798
doi:10.2903/j.efsa.2024.8498
PMID:38476322
Heat and salinity stress on the African eggplant F1 Djamba, a Kumba cultivar David-Rogeat N, Broadley MR, Stavridou E Front Plant Sci 14-Feb-2024
PMCID:PMC10926531
doi:10.3389/fpls.2024.1323665
PMID:38469326
Bacillus-based biocontrol beyond chemical control in central Africa: the challenge of turning myth into reality Nihorimbere G, Korangi Alleluya V, Nimbeshaho F, Nihorimbere V, Legrève A, Ongena M Front Plant Sci 06-Feb-2024
PMCID:PMC10877027
doi:10.3389/fpls.2024.1349357
PMID:38379944
Rapid and low-cost screening for single and combined effects of drought and heat stress on the morpho-physiological traits of African eggplant (Solanum aethiopicum) germplasm Opoku VA, Adu MO, Asare PA, Asante J, Hygienus G, Andersen MN PLoS One 30-Jan-2024
PMCID:PMC10826938
doi:10.1371/journal.pone.0295512
PMID:38289974
Exploring biodiversity and ethnobotanical significance of Solanum species in Uzbekistan: unveiling the cultural wealth and ethnopharmacological uses Gafforov Y, Rašeta M, Zafar M, Makhkamov T, Yarasheva M, Chen JJ, Zhumagul M, Wang M, Ghosh S, Abbasi AM, Yuldashev A, Mamarakhimov O, Alosaimi AA, Berdieva D, Rapior S Front Pharmacol 24-Jan-2024
PMCID:PMC10851437
doi:10.3389/fphar.2023.1287793
PMID:38333226
Study on medicinal food plants in the Gaoligongshan Biosphere Reserve, the richest biocultural diversity center in China Cheng Z, Lin S, Wu Z, Lin C, Zhang Q, Xu C, Li J, Long C J Ethnobiol Ethnomed 15-Jan-2024
PMCID:PMC10790445
doi:10.1186/s13002-023-00638-9
PMID:38225656
Plant diversity and ethnobotanical importance of home gardens in Ghana’s middle belt: a cross-sectional survey of the Sunyani municipality Ofosu-Bamfo B, Yawson D, Asare KB, Dadeboe VO, Buabeng IK, Aggrey J, Dapillah DA, Boateng DK, Offe E, Alhassan TA J Ethnobiol Ethnomed 13-Dec-2023
PMCID:PMC10717692
doi:10.1186/s13002-023-00632-1
PMID:38093362
Solanum aethiopicum L. from the Basilicata region as a source of specialized metabolites with promising anti-obesity effects: phytochemical characterization and in vivo investigation in high fat diet-fed mice Ponticelli M, Hidalgo-García L, Diez-Echave P, Vezza T, Romero M, Robles-Vera I, Duarte J, De Biasio F, Gorgoglione D, Lela L, Galvez J, Milella L Front Pharmacol 22-Nov-2023
PMCID:PMC10702577
doi:10.3389/fphar.2023.1306135
PMID:38074123

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 / Benzoyl derivatives
15-Oxolaurene 23426957 Click to see CC1C(=C)CCC1(C)C2=CC=C(C=C2)C=O 214.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
15-Hydroxylaurene 23426955 Click to see CC1C(=C)CCC1(C)C2=CC=C(C=C2)CO 216.32 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
[4-[(1R,2S)-1,2-dimethyl-3-methylidenecyclopentyl]phenyl]methyl acetate 23426956 Click to see CC1C(=C)CCC1(C)C2=CC=C(C=C2)COC(=O)C 258.35 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
2,6-Dimethoxy-4-(2-methoxyphenyl)phenol 44720381 Click to see COC1=CC=CC=C1C2=CC(=C(C(=C2)OC)O)OC 260.28 unknown via CMAUP database
Aucuparin 442508 Click to see COC1=CC(=CC(=C1O)OC)C2=CC=CC=C2 230.26 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Toluenes
1-[(1R,2S)-1,2-dimethyl-3-methylidenecyclopentyl]-4-methylbenzene 11790230 Click to see CC1C(=C)CCC1(C)C2=CC=C(C=C2)C 200.32 unknown via CMAUP database
> Benzenoids / Phenols / Cresols / Meta cresols
2-[(1R,2R,3E)-3-(bromomethylidene)-1,2-dimethylcyclopentyl]-5-methylphenol 12305606 Click to see CC1C(=CBr)CCC1(C)C2=C(C=C(C=C2)C)O 295.21 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
1-[(1R,2S)-1,2-dimethyl-3-methylidenecyclopentyl]-4-methylcyclohexa-1,4-diene 14865952 Click to see CC1C(=C)CCC1(C)C2=CCC(=CC2)C 202.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2S,4aR,4bS,6aS,11aS,11bR)-2-[(2R,3R,4S,5S,6R)-4-hydroxy-6-(hydroxymethyl)-3,5-bis[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]peroxy]oxan-2-yl]oxy-4a,6a,7-trimethyl-8-[3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-2,3,4,4b,5,6,11,11a,11b,12-decahydro-1H-indeno[2,1-a]phenanthrene-10-carboxylic acid 101244082 Click to see CC1C(C(C(C(O1)OOC2C(OC(C(C2O)OOC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC8=C(C=C(C(=C87)C)CCC(C)COC9C(C(C(C(O9)CO)O)O)O)C(=O)O)C)C)CO)O)O)O 1115.20 unknown https://doi.org/10.1016/S0040-4039(03)01147-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3Z,6R,7S,9Z,12E)-pentadeca-3,9,12-trien-1-yne-6,7-diol 23424689 Click to see CCC=CCC=CCC(C(CC=CC#C)O)O 234.33 unknown via CMAUP database
(6R,7R,9Z,12E)-3,9,12-Pentadecatriene-1-yne-6,7-diol 11264813 Click to see CCC=CCC=CCC(C(CC=CC#C)O)O 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
[(E,7S,11S)-3,7,11,15-tetramethylhexadec-2-enyl] acetate 92973629 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCOC(=O)C)C 338.60 unknown via CMAUP database
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
Rel-(7S,11S,E)-3,7,11,15-tetramethylhexadec-2-en-1-ol 40467768 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids
1-[(3R,5S,9S,10R)-10-hydroxy-6,9,10-trimethylspiro[4.5]dec-6-en-3-yl]ethanone 23427059 Click to see CC1CC=C(C2(C1(C)O)CCC(C2)C(=O)C)C 236.35 unknown via CMAUP database
15-Norlubiminol 76330546 Click to see CC1CC(CC(C12CCC(C2)C(=C)C)O)O 224.34 unknown https://doi.org/10.1515/ZNC-2001-3-403
https://doi.org/10.1271/BBB.65.1805
Aethione 10036509 Click to see CC1CC(CC(=O)C12CCC(C2)C(=C)C)O 222.32 unknown https://doi.org/10.1515/ZNC-2001-9-1007
https://doi.org/10.1515/ZNC-2001-3-403
Laurenon A 23427058 Click to see CC1CC=C(C2(C1(C)O)CCC(C2)C(=O)C)C 236.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3R,5S,6R,8S,10S)-8-hydroxy-6-methyl-3-prop-1-en-2-ylspiro[4.5]decane-10-carboxylic acid 10399980 Click to see CC1CC(CC(C12CCC(C2)C(=C)C)C(=O)O)O 252.35 unknown https://doi.org/10.1515/ZNC-2001-9-1007
https://doi.org/10.1515/ZNC-2001-3-403
Anhydro-beta-rotunol 11195296 Click to see CC1=CC(=O)C=C(C12CCC(C2)C(=C)C)C 216.32 unknown https://doi.org/10.1515/ZNC-2001-3-403
https://doi.org/10.1515/ZNC-2001-9-1007
Epilubimin 21594965 Click to see CC1CC(CC(C12CCC(C2)C(=C)C)C=O)O 236.35 unknown https://doi.org/10.1515/ZNC-2001-3-403
https://doi.org/10.1515/ZNC-2001-9-1007
Epilubiminoic acid 101121340 Click to see CC1CC(CC(C12CCC(C2)C(=C)C)C(=O)O)O 252.35 unknown https://doi.org/10.1515/ZNC-2001-9-1007
https://doi.org/10.1515/ZNC-2001-3-403
gamma-BISABOLENE, (E)- 5352437 Click to see CC1=CCC(=C(C)CCC=C(C)C)CC1 204.35 unknown via CMAUP database
Lubimin 442383 Click to see CC1CC(CC(C12CCC(C2)C(=C)C)C=O)O 236.35 unknown https://doi.org/10.1515/ZNC-2001-9-1007
https://doi.org/10.1515/ZNC-2001-3-403
Lubiminol 10376937 Click to see CC1CC(CC(C12CCC(C2)C(=C)C)CO)O 238.37 unknown https://doi.org/10.1515/ZNC-2001-9-1007
Selin-4,7(11)-diene 23425324 Click to see CC1=C2CC(=C(C)C)CCC2(CCC1)C 204.35 unknown via CMAUP database
Solavetivone 442399 Click to see CC1CC(=O)C=C(C12CCC(C2)C(=C)C)C 218.33 unknown https://doi.org/10.1515/ZNC-2001-3-403
https://doi.org/10.1515/ZNC-2001-9-1007
Spiro(4.5)dec-6-en-8-one, 2-(1-(hydroxymethyl)ethenyl)-6,10-dimethyl-, (2R,5S,10R)- 92006712 Click to see CC1CC(=O)C=C(C12CCC(C2)C(=C)CO)C 234.33 unknown https://doi.org/10.1515/ZNC-2001-3-403
https://doi.org/10.1515/ZNC-2001-9-1007
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Chamigranes
(1R,1'S,2'S,5R,6S)-2',3-dibromo-1'-chloro-1',4,4,6-tetramethylspiro[7-oxabicyclo[4.1.0]hept-2-ene-5,4'-cyclohexane] 14371607 Click to see CC1(C(=CC2C(C13CCC(C(C3)Br)(C)Cl)(O2)C)Br)C 412.59 unknown via CMAUP database
(1R,1'S,4'S,5R,5'S,6S)-3,4'-dibromo-5'-chloro-4,4,5',6-tetramethylspiro[7-oxabicyclo[4.1.0]hept-2-ene-5,2'-cyclohexane]-1'-ol 15385746 Click to see CC1(C(=CC2C(C13CC(C(CC3O)(C)Cl)Br)(O2)C)Br)C 428.58 unknown via CMAUP database
(1R,3R,6S,8R,11R)-8-bromo-4,11,12,12-tetramethyl-7-oxatricyclo[6.3.1.01,6]dodeca-4,9-diene-3,11-diol 21637490 Click to see CC1=CC2C3(CC1O)C(C(O2)(C=CC3(C)O)Br)(C)C 329.23 unknown via CMAUP database
(1R,6S,8R,11R)-3,8-dibromo-4,11,12,12-tetramethyl-7-oxatricyclo[6.3.1.01,6]dodeca-3,9-dien-11-ol 21773247 Click to see CC1=C(CC23C(C1)OC(C2(C)C)(C=CC3(C)O)Br)Br 392.13 unknown via CMAUP database
(1S,1'S,2R,2'S,4R,6R)-2',4-dibromo-1'-chloro-1,1',3,3-tetramethylspiro[7-oxabicyclo[4.1.0]heptane-2,4'-cyclohexane] 21634305 Click to see CC1(C(CC2C(C13CCC(C(C3)Br)(C)Cl)(O2)C)Br)C 414.60 unknown via CMAUP database
(2R,4R,6S,9S,10S)-4,10-dibromo-9-chloro-5,5,9-trimethyl-1-methylidenespiro[5.5]undecan-2-ol 23424644 Click to see CC1(C(CC(C(=C)C12CCC(C(C2)Br)(C)Cl)O)Br)C 414.60 unknown via CMAUP database
(2R,6S,9S,10S)-4,10-dibromo-9-chloro-5,5,9-trimethyl-1-methylidenespiro[5.5]undec-3-en-2-ol 23426577 Click to see CC1(C(=CC(C(=C)C12CCC(C(C2)Br)(C)Cl)O)Br)C 412.59 unknown via CMAUP database
(4R,6S,9S,10S)-4,10-dibromo-1,5,5,9-tetramethylspiro[5.5]undec-1-en-9-ol 23424645 Click to see CC1=CCC(C(C12CCC(C(C2)Br)(C)O)(C)C)Br 380.16 unknown via CMAUP database
(4R,6S,9S,10S)-4,10-dibromo-9-chloro-5,5,9-trimethyl-1-methylidenespiro[5.5]undecane 23424643 Click to see CC1(C(CCC(=C)C12CCC(C(C2)Br)(C)Cl)Br)C 398.60 unknown via CMAUP database
(4S,6R,9R,10R)-4,9-dibromo-10-chloro-5,5,9-trimethyl-1-methylidenespiro[5.5]undecane 21675022 Click to see CC1(C(CCC(=C)C12CCC(C(C2)Cl)(C)Br)Br)C 398.60 unknown via CMAUP database
(6S,9S,10S)-4,10-dibromo-9-chloro-5,5,9-trimethyl-1-methylidenespiro[5.5]undec-3-en-2-one 23426578 Click to see CC1(C(=CC(=O)C(=C)C12CCC(C(C2)Br)(C)Cl)Br)C 410.57 unknown via CMAUP database
(6S)-1,5,5,9-Tetramethyl-4beta,8alpha-dibromo-9beta-chlorospiro[5.5]undeca-1-ene 14108781 Click to see CC1=CCC(C(C12CCC(C(C2)Br)(C)Cl)(C)C)Br 398.60 unknown via CMAUP database
10-Bromo-beta-chamigrene 21675030 Click to see CC1=CCC2(CC1)C(=C)CCC(C2(C)C)Br 283.25 unknown via CMAUP database
2,10-Dibromo-3-hydroxy-alpha-chamigrene 101356858 Click to see CC1=CCC(C(C12CCC(C(C2)Br)(C)O)(C)C)Br 380.16 unknown via CMAUP database
CID 636451 636451 Click to see CC1(C23CC(C(CC2OC1(C=CC3(C)O)Br)(C)Cl)Br)C 428.58 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(3R,4aR,8aR)-8a-methyl-5-methylidene-3-propan-2-yl-2,3,4,6,7,8-hexahydro-1H-naphthalen-4a-ol 23426660 Click to see CC(C)C1CCC2(CCCC(=C)C2(C1)O)C 222.37 unknown via CMAUP database
Cycloeudesmol 442362 Click to see CC1CCCC2(C13CC3(CC2)C(C)(C)O)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1055/S-0028-1097933
Lup-20(29)-ene-3beta,28-diol 221023 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1055/S-0028-1097933
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Spirosolanes and derivatives
(1R,2R,4S,5'R,6R,7S,8S,9S,12S,13R,16R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol 162857922 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1 413.60 unknown https://doi.org/10.1055/S-0028-1097933
Solancarpidine 5250 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1 413.60 unknown https://doi.org/10.1055/S-0028-1097933
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-2-[[(2S,4aR,4bS,6aS,7R,11aS,11bR)-4a,6a,7-trimethyl-8-[3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-2,3,4,4b,5,6,7,8,11,11a,11b,12-dodecahydro-1H-indeno[2,1-a]phenanthren-2-yl]oxy]-4-hydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 101248367 Click to see CC1C(C=CC2=C1C3(CCC4C(C3C2)CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(CO7)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)CCC(C)COC9C(C(C(C(O9)CO)O)O)O 1027.20 unknown https://doi.org/10.1016/S0040-4039(03)01147-X
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-6-[[(2S,4aR,4bS,6aS,7R,11aS,11bR)-4a,6a,7-trimethyl-8-[3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-2,3,4,4b,5,6,7,8,11,11a,11b,12-dodecahydro-1H-indeno[2,1-a]phenanthren-2-yl]oxy]-4-hydroxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 101248366 Click to see CC1C(C=CC2=C1C3(CCC4C(C3C2)CC=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)CCC(C)COC9C(C(C(C(O9)CO)O)O)O 1041.20 unknown https://doi.org/10.1016/S0040-4039(03)01147-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
[4-[(1R,2S)-1,2-dimethyl-3-methylidenecyclopentyl]cyclohexa-1,4-dien-1-yl]methyl acetate 23426954 Click to see CC1C(=C)CCC1(C)C2=CCC(=CC2)COC(=O)C 260.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
[4-[(1R,2S)-1,2-dimethyl-3-methylidenecyclopentyl]cyclohexa-1,4-dien-1-yl]methanol 23426953 Click to see CC1C(=C)CCC1(C)C2=CCC(=CC2)CO 218.33 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
(2R,3R,5R)-5-[(E,1R)-1-bromohex-3-enyl]-2-[(E)-pent-2-en-4-ynyl]oxolan-3-ol 11758790 Click to see CCC=CCC(C1CC(C(O1)CC=CC#C)O)Br 313.23 unknown via CMAUP database
[(2R,3R,5R)-5-[(E,1S)-1-bromohex-3-enyl]-2-[(E)-pent-2-en-4-ynyl]oxolan-3-yl] acetate 11772642 Click to see CCC=CCC(C1CC(C(O1)CC=CC#C)OC(=O)C)Br 355.30 unknown via CMAUP database
trans-Kumausyne 10882777 Click to see CCC=CCC(C1CC(C(O1)CC=CC#C)OC(=O)C)Br 355.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-2-[[(2S,4aR,4bS,6aS,11aS,11bR)-4a,6a,7-trimethyl-8-[(3R)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-2,3,4,4b,5,6,11,11a,11b,12-decahydro-1H-indeno[2,1-a]phenanthren-2-yl]oxy]-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 163032910 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC6(C(C5CC=C4C3)CC7=C6C(=C(C=C7)CCC(C)COC8C(C(C(C(O8)CO)O)O)O)C)C)C)CO)O)OC9C(C(C(CO9)O)O)O)O)O)O 1025.20 unknown https://doi.org/10.1016/S0040-4039(03)01147-X
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-6-[[(2S,4aR,4bS,6aS,11aS,11bR)-4a,6a,7-trimethyl-8-[(3R)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-2,3,4,4b,5,6,11,11a,11b,12-decahydro-1H-indeno[2,1-a]phenanthren-2-yl]oxy]-4-hydroxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162941791 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)CC8=C7C(=C(C=C8)CCC(C)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)CO)O)O)O 1039.20 unknown https://doi.org/10.1016/S0040-4039(03)01147-X
(2S,4aR,4bS,6aS,11aS,11bR)-2-[(2R,3R,4S,5S,6R)-4-hydroxy-6-(hydroxymethyl)-3,5-bis[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy]oxan-2-yl]oxy-4a,6a,7-trimethyl-8-[(3R)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-2,3,4,4b,5,6,11,11a,11b,12-decahydro-1H-indeno[2,1-a]phenanthrene-10-carboxylic acid 163032747 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)CC8=C(C=C(C(=C87)C)CCC(C)COC9C(C(C(C(O9)CO)O)O)O)C(=O)O)C)C)CO)O)O)O 1083.20 unknown https://doi.org/10.1016/S0040-4039(03)01147-X
2-[2-[[4a,6a,7-trimethyl-8-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-2,3,4,4b,5,6,11,11a,11b,12-decahydro-1H-indeno[2,1-a]phenanthren-2-yl]oxy]-5-hydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 73821788 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC6(C(C5CC=C4C3)CC7=C6C(=C(C=C7)CCC(C)COC8C(C(C(C(O8)CO)O)O)O)C)C)C)CO)O)OC9C(C(C(CO9)O)O)O)O)O)O 1025.20 unknown https://doi.org/10.1016/S0040-4039(03)01147-X
2-[4-hydroxy-6-(hydroxymethyl)-3,5-bis[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy-4a,6a,7-trimethyl-8-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-2,3,4,4b,5,6,11,11a,11b,12-decahydro-1H-indeno[2,1-a]phenanthrene-10-carboxylic acid 73821789 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)CC8=C(C=C(C(=C87)C)CCC(C)COC9C(C(C(C(O9)CO)O)O)O)C(=O)O)C)C)CO)O)O)O 1083.20 unknown https://doi.org/10.1016/S0040-4039(03)01147-X
2-[6-[[4a,6a,7-trimethyl-8-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-2,3,4,4b,5,6,11,11a,11b,12-decahydro-1H-indeno[2,1-a]phenanthren-2-yl]oxy]-4-hydroxy-2-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 73821786 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)CC8=C7C(=C(C=C8)CCC(C)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)CO)O)O)O 1039.20 unknown https://doi.org/10.1016/S0040-4039(03)01147-X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,5-Dibromo-4-Hydroxybenzaldehyde 18100 Click to see C1=C(C=C(C(=C1Br)O)Br)C=O 279.91 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4'-Hydroxyacetophenone 7469 Click to see CC(=O)C1=CC=C(C=C1)O 136.15 unknown via CMAUP database
> Organoheterocyclic compounds / Coumarans
Isoaplysin 11822545 Click to see CC1CCC2(C1(OC3=C2C=CC(=C3)C)CBr)C 295.21 unknown via CMAUP database
> Organoheterocyclic compounds / Dioxepanes / 1,3-dioxepanes
(1S,3R,5S,7R)-7,11,11-trimethyl-3-prop-1-en-2-yl-4,6-dioxatricyclo[5.4.0.01,5]undec-8-en-10-one 23426796 Click to see CC(=C)C1CC23C(O1)OC2(C=CC(=O)C3(C)C)C 248.32 unknown via CMAUP database
(1S,3R,5S,7S,8S)-10-bromo-7,11,11-trimethyl-3-prop-1-en-2-yl-4,6-dioxatricyclo[5.4.0.01,5]undec-9-en-8-ol 23425344 Click to see CC(=C)C1CC23C(O1)OC2(C(C=C(C3(C)C)Br)O)C 329.23 unknown via CMAUP database
(1S,3R,5S,7S,8S)-10-bromo-8-chloro-7,11,11-trimethyl-3-prop-1-en-2-yl-4,6-dioxatricyclo[5.4.0.01,5]undec-9-ene 23426795 Click to see CC(=C)C1CC23C(O1)OC2(C(C=C(C3(C)C)Br)Cl)C 347.67 unknown via CMAUP database
(1S,3R,5S,7S,8S)-8,10-dibromo-7,11,11-trimethyl-3-prop-1-en-2-yl-4,6-dioxatricyclo[5.4.0.01,5]undec-9-ene 23426794 Click to see CC(=C)C1CC23C(O1)OC2(C(C=C(C3(C)C)Br)Br)C 392.13 unknown via CMAUP database
> Organoheterocyclic compounds / Dioxepanes / 1,4-dioxepanes
(+)-Z-Isolaureatin 16062462 Click to see CCC(C1CC2C(CC(O2)C(O1)CC=CC#C)Br)Br 392.13 unknown via CMAUP database
(1S,2S,4R,6S,7S)-7-bromo-4-[(1S)-1-bromopropyl]-2-[(E)-pent-2-en-4-ynyl]-3,9-dioxabicyclo[4.2.1]nonane 11101244 Click to see CCC(C1CC2C(CC(O2)C(O1)CC=CC#C)Br)Br 392.13 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
(1R,3R,4S,6S,8R,10S)-4,10-dibromo-3-ethyl-8-[(E)-pent-2-en-4-ynyl]-2,7-dioxabicyclo[4.2.2]decane 14731401 Click to see CCC1C(CC2C(CC(O1)C(O2)CC=CC#C)Br)Br 392.13 unknown via CMAUP database
(1S,5S,6R,8R,9R)-2,5,6,8-tetramethyl-7-oxatricyclo[6.2.2.01,6]dodec-2-en-9-ol 23424606 Click to see CC1CC=C(C23C1(OC(CC2)(C(C3)O)C)C)C 236.35 unknown via CMAUP database
> Organoheterocyclic compounds / Oxepanes
(1R,3R,5R,6R,8R)-5-bromo-3-[(1S)-1-bromopropyl]-8-[(Z)-pent-2-en-4-ynyl]-2,7-dioxabicyclo[4.2.1]nonane 101599860 Click to see CCC(C1CC(C2CC(O1)C(O2)CC=CC#C)Br)Br 392.13 unknown via CMAUP database
(1S,3R,5S,6S,8S)-5-bromo-3-[(1S)-1-bromopropyl]-8-[(Z)-pent-2-en-4-ynyl]-2,7-dioxabicyclo[4.2.1]nonane 11326787 Click to see CCC(C1CC(C2CC(O1)C(O2)CC=CC#C)Br)Br 392.13 unknown via CMAUP database
Laurencial 11086786 Click to see CC1(C(=CC2(C13CCC(C(C3)O2)(C)Cl)C)C=O)C 268.78 unknown via CMAUP database
> Organoheterocyclic compounds / Oxetanes
(1S,2S,4R,6R,7R)-6-bromo-4-[(1S)-1-bromopropyl]-2-[(Z)-pent-2-en-4-ynyl]-3,8-dioxabicyclo[5.1.1]nonane 11101243 Click to see CCC(C1CC(C2CC(O2)C(O1)CC=CC#C)Br)Br 392.13 unknown via CMAUP database
(3E)-Laureatin 102095592 Click to see CCC(C1CC(C2CC(O2)C(O1)CC=CC#C)Br)Br 392.13 unknown via CMAUP database
> Organoheterocyclic compounds / Oxocins
2H-Oxocin-2-methanol, 7-bromo-8-ethyl-3,6,7,8-tetrahydro-alpha-2-penten-4-ynyl-, acetate, (E)-(alphaR,2R,7S,8R)- 6436276 Click to see CCC1C(CC=CCC(O1)C(CC=CC#C)OC(=O)C)Br 355.30 unknown via CMAUP database
Prelaureatin 10870702 Click to see CCC(C1CC=CCC(C(O1)CC=CC#C)O)Br 313.23 unknown via CMAUP database
> Organoheterocyclic compounds / Oxolanes
Notoryne 23427873 Click to see CCC1C(CC(O1)C2CC(C(O2)CC=CC#C)Cl)Br 347.67 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Phlorizin 6072 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)O)O)O 436.40 unknown via CMAUP database

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