Corchorus aestuans - Unknown
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Internal ID UUID64401347bf00b357822137
Scientific name Corchorus aestuans
Authority L.
First published in Syst. Nat. ed. 10 , 2: 1079 (1759)

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Synonyms Top

Scientific name Authority First published in
Corchorus acutangulus Lam. Encycl. [J. Lamarck & al.] 2(1): 104. 1786 [16 Oct 1786]
Corchorus acutangulus var. brachycarpus Domin Biblioth. Bot. 22(89): 381 (1927)
Corchorus aesticans Hill Veg. Syst. , ed. 14: 23 (1769)
Corchorus campestris Macfad. Fl. Jamaica 1: 107 (1837)
Corchorus furcatus G.Don Gen. Hist. 1: 544 (1831)
Corchorus fuscus Roxb. Fl. Ind. 2: 582 (1824)
Corchorus oppositiflorus Hassk. Tijdschr. Natuurl. Gesch. Physiol. 12: 126 (1845)

Common names Top

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Language Common/alternative name
English jute
dag salinvogu
Chinese 野黄麻
Chinese 假黄麻
Chinese 甜麻
Chinese 繩黃麻
Chinese 针筒草
Chinese 針筒草

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Corchorus aestuans var. brevicaulis (Hosok.) T.S.Liu & H.C.Lo Fl. Taiwan 3: 695 (1977)

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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Macaronesia
      • Cape Verde
    • Northeast Tropical Africa
      • Chad
      • Ethiopia
      • Socotra
      • Somalia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • West Tropical Africa
      • Benin
      • Burkina
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Mali
      • Mauritania
      • Niger
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre
    • Western Indian Ocean
      • Aldabra
      • Chagos Archipelago
      • Comoros
      • Seychelles
  • Asia-temperate
    • Arabian Peninsula
      • Oman
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Laccadive Islands
      • Maldives
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • South China Sea
      • Thailand
      • Vietnam
    • Malesia
      • Christmas Island
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sulawesi
  • Australasia
    • Australia
      • Northern Territory
      • Queensland
      • Western Australia
  • Northern America
    • Mexico
      • Mexican Pacific Islands
      • Mexico Gulf
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
    • Southeastern U.S.A.
      • Alabama
      • Florida
      • Georgia
      • Louisiana
  • Pacific
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
    • South-central Pacific
      • Society Islands
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
    • Caribbean
      • Bahamas
      • Cayman Islands
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Netherlands Antilles
      • Trinidad-Tobago
      • Turks-caicos Islands
      • Venezuelan Antilles
      • Windward Islands
    • Central America
      • Central American Pacific
      • Costa Rica
      • Guatemala
      • Honduras
      • Nicaragua
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Colombia
      • Ecuador

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000619993
Florida Plant Atlas 2779
Flora of Alabama 3618
USDA Plants COAE
Tropicos 32200001
INPN 447636
KEW urn:lsid:ipni.org:names:320794-2
The Plant List kew-2736302
Open Tree Of Life 615658
NCBI Taxonomy 360610
Nature Serve 2.149911
IPNI 320794-2
iNaturalist 160865
GBIF 3152092
EPPO CRGAE
EOL 584867
USDA GRIN 101655

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
Comparative toxicity, phytochemistry, and use of 53 Philippine medicinal plants Clemen-Pascual LM, Macahig RA, Rojas NR Toxicol Rep 10-Dec-2021
PMCID:PMC8685920
doi:10.1016/j.toxrep.2021.12.002
PMID:34976744
Reference genomes of the two cultivated jute species Zhang L, Ma X, Zhang X, Xu Y, Ibrahim AK, Yao J, Huang H, Chen S, Liao Z, Zhang Q, Niyitanga S, Yu J, Liu Y, Xu X, Wang J, Tao A, Xu J, Chen S, Yang X, He Q, Lin L, Fang P, Zhang L, Ming R, Qi J, Zhang L Plant Biotechnol J 08-Jul-2021
PMCID:PMC8541789
doi:10.1111/pbi.13652
PMID:34170619
Ethnomedicinal Value of Antidiabetic Plants in Bangladesh: A Comprehensive Review Rahman MM, Uddin MJ, Reza AS, Tareq AM, Emran TB, Simal-Gandara J Plants (Basel) 08-Apr-2021
PMCID:PMC8070064
doi:10.3390/plants10040729
PMID:33918026
Pest categorisation of the non‐EU phytoplasmas of tuber‐forming Solanum spp. Bragard C, Dehnen‐Schmutz K, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Bosco D, Chiumenti M, Di Serio F, Galetto L, Marzachì C, Pautasso M, Jacques M EFSA J 23-Dec-2020
PMCID:PMC7757785
doi:10.2903/j.efsa.2020.6356
PMID:33376553
Pest categorisation of the non‐EU phytoplasmas of Cydonia Mill., Fragaria L., Malus Mill., Prunus L., Pyrus L., Ribes L., Rubus L. and Vitis L. Bragard C, Dehnen‐Schmutz K, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Bosco D, Chiumenti M, Di Serio F, Galetto L, Marzachì C, Pautasso M, Jacques M EFSA J 13-Jan-2020
PMCID:PMC7008834
doi:10.2903/j.efsa.2020.5929
PMID:32626484
Antioxidant, Acetylcholinesterase, Butyrylcholinesterase, and α-glucosidase Inhibitory Activities of Corchorus depressus Afzal S, Chaudhry BA, Ahmad A, Uzair M, Afzal K Pharmacogn Mag 13-Nov-2017
PMCID:PMC5701405
doi:10.4103/pm.pm_95_17
PMID:29200727
Challenges with using names to link digital biodiversity information Patterson D, Mozzherin D, Shorthouse DP, Thessen A Biodivers Data J 25-May-2016
PMCID:PMC4910497
doi:10.3897/BDJ.4.e8080
PMID:27346955
Chemical Examination of the Seeds of Cassia spectablis Mithilesh Singh, J. Singh Walter de Gruyter GmbH 21-Feb-2015
doi:10.1515/ZNB-1984-1020
Wild edible plant species utilized by a subsistence farming community in Obalanga sub-county, Amuria district, Uganda Ojelel S, Kakudidi EK J Ethnobiol Ethnomed 10-Feb-2015
PMCID:PMC4429352
doi:10.1186/1746-4269-11-7
PMID:25971428
Corchorusin-D, a saikosaponin-like compound isolated from Corchorus acutangulus Lam., targets mitochondrial apoptotic pathways in leukemic cell lines (HL-60 and U937). Mallick S, Ghosh P, Samanta SK, Kinra S, Pal BC, Gomes A, Vedasiromoni JR Cancer Chemother Pharmacol 01-Sep-2010
doi:10.1007/S00280-009-1214-3
PMID:20033811
Traditional Leafy Vegetables in Senegal: Diversity and Medicinal Uses Mathieu G, Meissa D Afr J Tradit Complement Altern Med 10-Jun-2007
PMCID:PMC2816516
doi:10.4314/ajtcam.v4i4.31239
PMID:20161914
SPECIES COMPOSITION, DISTRIBUTION, LIFE FORMS AND FOLK NOMENCLATURE OF FOREST AND COMMON LAND PLANTS OF WESTERN CHITWAN, NEPAL Dangol DR J Inst Agric Anim Sci 01-Jan-2005
PMCID:PMC3434227
PMID:22962539
Triterpenoid glycosides of Corchorus acutangulus Lam. Shashi B. Mahato, Bikas C. Pal Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19870000629
New triterpenoid saponins from Corchorus acutangulus Shashi B. Mahato, Bikas C. Pal, Sudip K. Sarkar Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80211-5

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 / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown https://doi.org/10.1515/ZNB-1984-1020
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1515/ZNB-1984-1020
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown https://doi.org/10.1515/ZNB-1984-1020
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1515/ZNB-1984-1020
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R,3R,4S,5R,6R)-2-[[(1S,2S,4S,5R,8R,9R,10S,13S,14R,17S,18S)-2-hydroxy-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162957786 Click to see CC1(CCC23COC4(C2C1)C=CC5C6(CCC(C(C6CCC5(C4(CC3O)C)C)(C)CO)OC7C(C(C(C(O7)CO)O)O)O)C)C 634.80 unknown https://doi.org/10.1039/P19870000629
(2R,3R,4S,5R,6R)-2-[[(3S,4aR,6aR,6bS,8S,8aS,14aR,14bS)-8-hydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,14a-dodecahydropicen-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162964068 Click to see CC1(CCC2(C(CC3(C(=C2C1)C=CC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C)C)O)CO)C 618.80 unknown https://doi.org/10.1016/0031-9422(88)80211-5
(2R,3R,4S,5R,6R)-2-[[(3S,4aS,6aR,6bS,8S,8aS,12aR,14aS,14bR)-8-hydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163004735 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)CO)C 620.90 unknown https://doi.org/10.1039/P19870000629
(2R,3R,4S,5R,6R)-2-[[(3S,4R,4aS,6aR,6bS,8S,8aS,12aR,14aR,14bR)-8-hydroxy-4,8a-bis(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162945016 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)CO)OC6C(C(C(C(O6)CO)O)O)O)C)CO)C 636.90 unknown https://doi.org/10.1039/P19870000629
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5R,6R)-2-[[(3S,4aR,6aR,6bS,8S,8aS,12aR,14aR,14bR)-8-hydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 163051559 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)CO)C 783.00 unknown https://doi.org/10.1016/0031-9422(88)80211-5
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5R,6R)-2-[[(3S,4aR,6aR,6bS,8S,8aS,14aR,14bS)-8-hydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,14a-dodecahydropicen-3-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 163062956 Click to see CC1(CCC2(C(CC3(C(=C2C1)C=CC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)O)CO)C 781.00 unknown https://doi.org/10.1016/0031-9422(88)80211-5
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5R,6R)-4,5-dihydroxy-2-[[(1S,2S,4S,5R,8S,10S,13S,14R,17S,18S)-2-hydroxy-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl]oxy]-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 163072935 Click to see CC1(CCC23COC4(C2C1)C=CC5C6(CCC(C(C6CCC5(C4(CC3O)C)C)(C)C)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C 781.00 unknown https://doi.org/10.1039/P19870000629
2-[[2-Hydroxy-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73744945 Click to see CC1(CCC23COC4(C2C1)C=CC5C6(CCC(C(C6CCC5(C4(CC3O)C)C)(C)CO)OC7C(C(C(C(O7)CO)O)O)O)C)C 634.80 unknown https://doi.org/10.1039/P19870000629
2-[[8-Hydroxy-4,8a-bis(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162945015 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)CO)OC6C(C(C(C(O6)CO)O)O)O)C)CO)C 636.90 unknown https://doi.org/10.1039/P19870000629
2-[[8-Hydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,14a-dodecahydropicen-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 14037354 Click to see CC1(CCC2(C(CC3(C(=C2C1)C=CC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C)C)O)CO)C 618.80 unknown https://doi.org/10.1016/0031-9422(88)80211-5
2-[4,5-Dihydroxy-2-[(2-hydroxy-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl)oxy]-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 73744192 Click to see CC1(CCC23COC4(C2C1)C=CC5C6(CCC(C(C6CCC5(C4(CC3O)C)C)(C)C)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C 781.00 unknown https://doi.org/10.1007/S00280-009-1214-3
https://doi.org/10.1039/P19870000629
2-[4,5-Dihydroxy-2-[[8-hydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 14037372 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)CO)C 783.00 unknown https://doi.org/10.1016/0031-9422(88)80211-5
2-[4,5-Dihydroxy-2-[[8-hydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,14a-dodecahydropicen-3-yl]oxy]-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 14037364 Click to see CC1(CCC2(C(CC3(C(=C2C1)C=CC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)O)CO)C 781.00 unknown https://doi.org/10.1016/0031-9422(88)80211-5
Corchorusin D 130973 Click to see CC1(CCC23COC4(C2C1)C=CC5C6(CCC(C(C6CCC5(C4(CC3O)C)C)(C)C)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C 781.00 unknown https://doi.org/10.1007/S00280-009-1214-3
https://doi.org/10.1016/0031-9422(88)80211-5
https://doi.org/10.1039/P19870000629
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5R,6R)-2-[[(3S,4aR,6aS,6bR,8S,8aS,12aR,14bS)-8-hydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 163042518 Click to see CC1(CCC2(C(C1)C3=CC=C4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)CO)C 781.00 unknown https://doi.org/10.1016/0031-9422(88)80211-5
2-[4,5-Dihydroxy-2-[[8-hydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl]oxy]-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 163042517 Click to see CC1(CCC2(C(C1)C3=CC=C4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)CO)C 781.00 unknown https://doi.org/10.1016/0031-9422(88)80211-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1039/P19870000629
2-[[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73072970 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown https://doi.org/10.1039/P19870000629
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1039/P19870000629
Stigmasterol glucoside 6602508 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown https://doi.org/10.1039/P19870000629
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
Lysine 5962 Click to see C(CCN)CC(C(=O)O)N 146.19 unknown https://doi.org/10.1515/ZNB-1984-1020
Threonine 6288 Click to see CC(C(C(=O)O)N)O 119.12 unknown https://doi.org/10.1515/ZNB-1984-1020
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
D-Aspartic acid 83887 Click to see C(C(C(=O)O)N)C(=O)O 133.10 unknown https://doi.org/10.1515/ZNB-1984-1020
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
D-phenylalanine 71567 Click to see C1=CC=C(C=C1)CC(C(=O)O)N 165.19 unknown https://doi.org/10.1515/ZNB-1984-1020
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Serine and derivatives
Serine 5951 Click to see C(C(C(=O)O)N)O 105.09 unknown https://doi.org/10.1515/ZNB-1984-1020
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Valine and derivatives
Valine 6287 Click to see CC(C)C(C(=O)O)N 117.15 unknown https://doi.org/10.1515/ZNB-1984-1020
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
2-amino-3-(6-hydroxy-1H-indol-3-yl)propanoic Acid 9899317 Click to see C1=CC2=C(C=C1O)NC=C2CC(C(=O)O)N 220.22 unknown https://doi.org/10.1039/P19870000629

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