Corchorus olitorius

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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	UUID6440134ca40e7324830749
Scientific name	Corchorus olitorius
Authority	L.
First published in	Sp. Pl. : 529 (1753)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Corchorus catharticus	Blanco	Fl. Filip. : 442 (1837)
Corchorus decemangularis	Roxb. ex G.Don	Gen. Hist. 1: 544 (1831)
Corchorus lanceolatus	G.Don	Gen. Hist. 1: 543 (1831)
Corchorus longicarpus	G.Don	Gen. Hist. 1: 543 (1831)
Corchorus malchairi	De Wild.	Études Fl. Bangala & Ubangi : 345 (1911)
Corchorus olitorius var. australiensis	Domin	Biblioth. Bot. 22(89): 380 (1927)
Corchorus quinquelocularis	Moench	Methodus : 248 (1794)
Corchorus olitorius var. incisifolius	Asch. & Schweinf.	Mém. Inst. Égypt. 2: 53 1887
Corchorus olitorius f. grandifolius	De Wild.	Ann. Mus. Congo Belge, Bot. V, 2: 45 1908

Common names Top

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Filter by language:

Language	Common/alternative name
English	tossa jute
English	molokhia
English	mulukhiyah
English	mulukhiyyah
English	molokhiyya
English	denje'c'jute
English	molokheyya
English	jute mallow
English	jew's mallow
English	nalta jute
Arabic	ملوخية
Azerbaijani	uzunmeyvəli cut
Azerbaijani	cicuta virosa
bcl	saluyot
Catalan	jute d'aràbia
German	langkapselige jute
German	muskraut
German	molokhia
Fulah	maama laalo
Finnish	intianjuutti
French	corète potagère
Hebrew	מלוכיה נאכלת
Hindi	पटसन
Upper Sorbian	afriski konopjowc
Indonesian	yute
Indonesian	mulukhiyah
Indonesian	molokhia
Indonesian	jute
Japanese	タイワンツナソ
Japanese	シマツナソ
Japanese	モロヘイヤ
Korean	장삭황마
Malay	mulukhiyah
pam	katilpung babai
Polish	juta kolorowa
Polish	juta warzywna
Romanian	iută
Tamil	புண்ணாக்கு கீரை
Tamil	பிண்ணாக்கு கீரை
Ukrainian	Довгоплідний джут
Chinese	长蒴黄麻
Chinese	山麻

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Corchorus olitorius var. malchairi	(De Wild.) R.Wilczek

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 click to expand
- East Tropical Africa
  - Kenya
  - Tanzania
  - Uganda
- Macaronesia
  - Cape Verde
- Northeast Tropical Africa
  - Chad
  - Djibouti
  - Eritrea
  - Ethiopia
  - Somalia
  - Sudan
- Northern Africa
  - Algeria
  - Egypt
  - Libya
  - Morocco
  - Tunisia
- South Tropical Africa
  - Angola
  - Malawi
  - Mozambique
  - Zambia
  - Zimbabwe
- Southern Africa
  - Botswana
  - Kwazulu-Natal
  - Namibia
  - Northern Provinces
- West Tropical Africa
  - Benin
  - Burkina
  - Gambia
  - Ghana
  - Guinea
  - Guinea-Bissau
  - Ivory Coast
  - Liberia
  - Mali
  - Mauritania
  - Niger
  - Nigeria
  - Senegal
  - Sierra Leone
  - Togo
- West-central Tropical Africa
  - Burundi
  - Cameroon
  - Central African Republic
  - Congo
  - Gulf Of Guinea Islands
  - Zaïre
- Western Indian Ocean
  - Mauritius
  - Réunion

Asia-temperate click to expand
- Arabian Peninsula
  - Gulf States
  - Oman
  - Saudi Arabia
  - Yemen
- China
  - China South-central
  - China Southeast
  - Hainan
- Eastern Asia
  - Nansei-shoto
- Middle Asia
  - Turkmenistan
  - Uzbekistan
- Western Asia
  - Afghanistan
  - Cyprus
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Sinai

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - India
  - Nepal
  - Pakistan
  - Sri Lanka
  - West Himalaya
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - South China Sea
  - Thailand
  - Vietnam
- Malesia
  - Lesser Sunda Islands
  - Malaya
  - Philippines

Northern America click to expand
- Mexico
  - Mexico Northwest

Pacific click to expand
- Southwestern Pacific
  - Fiji

Southern America click to expand
- Brazil
  - Brazil Southeast
- Caribbean
  - Bahamas
  - Cuba
  - Haiti
  - Jamaica
  - Leeward Islands
  - Trinidad-Tobago
  - Windward Islands
- Central America
  - Belize
- Western South America
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000620125
UNII	N9OPW9AEQS
USDA Plants	COOL
Tropicos	32200006
INPN	160394
KEW	urn:lsid:ipni.org:names:320796-2
The Plant List	kew-2736427
Open Tree Of Life	578269
Observations.org	136557
NCBI Taxonomy	93759
NBN Atlas	NBNSYS0200003620
Nature Serve	2.158260
IPNI	320796-2
iNaturalist	160868
GBIF	3152084
Freebase	/m/062l6p
EPPO	CRGOL
EOL	584868
USDA GRIN	11458
Wikipedia	Corchorus_olitorius

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_001974825.2	COLO4_1.0	Contig	Basic & Applied Research on Jute Project, Bangladesh Jute Research Institute	2017-01-30	29.0x	319.38 Mb

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

Unveiling the Chemical Composition, Bioactive Profile and Antioxidant Capacity of Dried Egyptian Jew’s Mallow Stems as a Promising Anticancer Agent

Ali MR, Ibrahim HH, Salah-Eldin AA

Molecules

20-Mar-2024

PMCID:	PMC10975874
doi:	10.3390/molecules29061377
PMID:	38543013

Hypoglycemic activity in vivo and in vitro of the Lotus (Nelumbo nucifera Gaertn.) seed skin (testa) phenolic-rich extracts

Xu H, Wang C, Gong L

Food Chem X

16-Mar-2024

PMCID:	PMC10972837
doi:	10.1016/j.fochx.2024.101282
PMID:	38550890

The impact of thermal pretreatment on phytochemical profiles and bioactivity of freeze-dried lily bulbs (Lilium lancifolium)

Cai Y, Quan H, Liu Y, Han X, Lu Y, Lan X, Guo X

Food Chem X

15-Mar-2024

PMCID:	PMC10966175
doi:	10.1016/j.fochx.2024.101284
PMID:	38544934

Anti-diabetic and anti-inflammatory bioactive hits from Coriaria intermedia Matsum. stem and Dracontomelon dao (Blanco) Merr. & Rolfe bark through bioassay-guided fractionation and liquid chromatography-tandem mass spectrometry

Fabian MC, Astorga RM, Atis AA, Pilapil LA, Hernandez CC

Front Pharmacol

08-Mar-2024

PMCID:	PMC10957545
doi:	10.3389/fphar.2024.1349725
PMID:	38523640

Microgreens on the rise: Expanding our horizons from farm to fork

Lone JK, Pandey R, Gayacharan

Heliyon

11-Feb-2024

PMCID:	PMC10881865
doi:	10.1016/j.heliyon.2024.e25870
PMID:	38390124

Properties of mixture of hemp bast and softwood pulp for filter paper manufacture

Yimlamai P, Chitbanyong K, Wanitpinyo K, Puangsin B, Nanta K, Khantayanuwong S, Pisutpiched S, Chaisan T, Fei B, Hiziroglu S

Heliyon

01-Feb-2024

PMCID:	PMC10850592
doi:	10.1016/j.heliyon.2024.e25353
PMID:	38333817

Learning from One-Health approaches to explore links between farming practices, animal, human and ecosystem health in Nigeria

Otu A, Onwusaka O, Meseko C, Effa E, Ebenso B, Isong Abraham I, Ijomanta J, Omileye A, Emelife C, Eziechina S, Suleiman K, Ochu C, Adetimirin V

Front Nutr

26-Jan-2024

PMCID:	PMC10853374
doi:	10.3389/fnut.2024.1216484
PMID:	38344020

Why Are There So Few Basidiomycota and Basal Fungi as Endophytes? A Review

Rungjindamai N, Jones EB

J Fungi (Basel)

15-Jan-2024

PMCID:	PMC10820240
doi:	10.3390/jof10010067
PMID:	38248976

Single molecule real-time sequencing data sets of Hypericum perforatum L. plantlets and cell suspension cultures

Selvakesavan RK, Nuc M, Kolarčik V, Krajewski P, Franklin G

Sci Data

06-Jan-2024

PMCID:	PMC10771467
doi:	10.1038/s41597-023-02878-6
PMID:	38184679

Aspergillus awamori MK788209 cellulase: production, statistical optimization, pea peels saccharification and textile applications

Mostafa FA, Wehaidy HR, Sharaf S, El-Hennawi HM, Mahmoud SA, Saleh SA

Microb Cell Fact

05-Jan-2024

PMCID:	PMC10768301
doi:	10.1186/s12934-023-02286-w
PMID:	38183135

The Evolution of the Intrinsic Flexural Strength of Jute Strands after a Progressive Delignification Process and Their Contribution to the Flexural Strength of PLA-Based Biocomposites

Alonso-Montemayor FJ, Espinach FX, Tarrés Q, Alcalà M, Delgado-Aguilar M, Mutjé P

Polymers (Basel)

21-Dec-2023

PMCID:	PMC10781118
doi:	10.3390/polym16010037
PMID:	38201704

In Planta Detection of Beauveria bassiana (Ascomycota: Hypocreales) Strains as Endophytes in Bean (Phaseolus vulgaris L.)

Cavazos-Vallejo T, Valadez-Lira JA, Orozco-Flores AA, Gomez-Flores R, Ek-Ramos MJ, Quistián-Martínez D, Alcocer-González JM, Tamez-Guerra P

Plants (Basel)

20-Dec-2023

PMCID:	PMC10781017
doi:	10.3390/plants13010022
PMID:	38202330

Comprehensive Analysis of NAC Transcription Factors Reveals Their Evolution in Malvales and Functional Characterization of AsNAC019 and AsNAC098 in Aquilaria sinensis

Yang Z, Mei W, Wang H, Zeng J, Dai H, Ding X

Int J Mol Sci

12-Dec-2023

PMCID:	PMC10744133
doi:	10.3390/ijms242417384
PMID:	38139213

Protocol for imbibed seed piercing for Agrobacterium-mediated transformation of jute

Majumder S, Parida S, Dey N

STAR Protoc

11-Dec-2023

PMCID:	PMC10726289
doi:	10.1016/j.xpro.2023.102767
PMID:	38085641

Genome size variation and evolution during invasive range expansion in an introduced plant

Cang FA, Welles SR, Wong J, Ziaee M, Dlugosch KM

Evol Appl

11-Dec-2023

PMCID:	PMC10810172
doi:	10.1111/eva.13624
PMID:	38283607

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 / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid	72	Click to see C1=CC(=C(C=C1C(=O)O)O)O	154.12	unknown	https://doi.org/10.1002/JSFA.2740420206
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(4R)-4-hydroxy-3,5,5-trimethyl-4-[(E,3R)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one	133561811	Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C	386.40	unknown	https://doi.org/10.1248/CPB.45.464
(4S)-4-hydroxy-3,5,5-trimethyl-4-[(E)-3-oxo-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one	9978316	Click to see CC1=CC(=O)CC(C1(C=CC(=O)COC2C(C(C(C(O2)CO)O)O)O)O)(C)C	400.40	unknown	https://doi.org/10.1248/CPB.45.464
2-(6-Hydroxy-2,6-dimethylocta-2,7-dienoxy)-6-(hydroxymethyl)oxane-3,4,5-triol	72970728	Click to see CC(=CCCC(C)(C=C)O)COC1C(C(C(C(O1)CO)O)O)O	332.39	unknown	https://doi.org/10.1248/CPB.45.464
4-Hydroxy-3,5,5-trimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one	73815023	Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C	386.40	unknown	https://doi.org/10.1248/CPB.45.464
4-Hydroxy-3,5,5-trimethyl-4-[3-oxo-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one	85081135	Click to see CC1=CC(=O)CC(C1(C=CC(=O)COC2C(C(C(C(O2)CO)O)O)O)O)(C)C	400.40	unknown	https://doi.org/10.1248/CPB.45.464
Corchoionoside C	10317980	Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C	386.40	unknown	https://doi.org/10.1248/CPB.45.464
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
(10e,15z)-9,12,13-Trihydroxyoctadeca-10,15-dienoic acid	44559173	Click to see CCC=CCC(C(C=CC(CCCCCCCC(=O)O)O)O)O	328.40	unknown	https://doi.org/10.1248/CPB.46.1008
(10E)-9,12,13-trihydroxyoctadeca-10,15-dienoic acid	164511912	Click to see CCC=CCC(C(C=CC(CCCCCCCC(=O)O)O)O)O	328.40	unknown	https://doi.org/10.1248/CPB.46.1008
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
1-Hexadecanoyl-sn-glycerol	3084463	Click to see CCCCCCCCCCCCCCCC(=O)OCC(CO)O	330.50	unknown	https://doi.org/10.1038/192288B0
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Phytol	5280435	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	https://doi.org/10.3136/FSTR.8.239
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
2-[(1S)-4-methylcyclohex-3-en-1-yl]propan-2-yl acetate	93317	Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C	196.29	unknown	https://doi.org/10.1248/CPB.45.464
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4R,5R,6S)-2-[[(3S,5R,8R,9R,10R,12R,13R,14S,17R)-3,12-dihydroxy-4,4,8,10-tetramethyl-17-[(2S,5S)-2-methyl-5-[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]oxolan-2-yl]-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-14-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162969771	Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC(C4C3(CCC4C5(CCC(O5)C(C)(C)OC6C(C(C(C(O6)CO)O)O)O)C)COC7C(C(C(C(O7)CO)O)O)O)O)C)C	817.00	unknown	https://doi.org/10.1016/J.TETLET.2009.08.014
2-[[3,12-dihydroxy-4,4,8,10-tetramethyl-17-[2-methyl-5-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]oxolan-2-yl]-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-14-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	14683240	Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC(C4C3(CCC4C5(CCC(O5)C(C)(C)OC6C(C(C(C(O6)CO)O)O)O)C)COC7C(C(C(C(O7)CO)O)O)O)O)C)C	817.00	unknown	https://doi.org/10.1016/J.TETLET.2009.08.014
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1038/192288B0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives
3,5,14-trihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carboxaldehyde	5303	Click to see CC12CCC3C(C1(CCC2C4=CC(=O)OC4)O)CCC5(C3(CCC(C5)O)C=O)O	404.50	unknown	https://doi.org/10.1021/JA01638A028
Strophanthidin	6185	Click to see CC12CCC3C(C1(CCC2C4=CC(=O)OC4)O)CCC5(C3(CCC(C5)O)C=O)O	404.50	unknown	https://doi.org/10.1016/S0031-9422(98)00421-X
Strophanthidol	258412	Click to see CC12CCC3C(C1(CCC2C4=CC(=O)OC4)O)CCC5(C3(CCC(C5)O)CO)O	406.50	unknown	https://doi.org/10.1016/S0031-9422(98)00421-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
(3R,5S,10S,13R,14S,17R)-3-[(2R,5S)-4,5-dihydroxy-6-methyloxan-2-yl]oxy-5,14-dihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde	11967805	Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)O	534.60	unknown	https://doi.org/10.1016/S0031-9422(98)00421-X https://doi.org/10.3358/SHOKUEISHI.39.4_256
(3S,5S,10S,13R,14S,17R)-3-[(2R,5S)-6-[[(3R,6S)-4,6-dihydroxy-2-methyloxan-3-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5,14-dihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde	23485	Click to see CC1C(C(CC(O1)O)O)OCC2C(C(C(C(O2)OC3CCC4(C5CCC6(C(CCC6(C5CCC4(C3)O)O)C7=CC(=O)OC7)C)C=O)O)O)O	696.80	unknown	https://doi.org/10.1039/P19890002065 https://doi.org/10.1007/BF00566821 https://doi.org/10.3358/SHOKUEISHI.39.4_256 https://doi.org/10.1248/JHS.47.89 https://doi.org/10.1016/S0031-9422(98)00421-X
(3S,5S,8R,9S,10S,13R,14S,17R)-3-[(2R,4S,5R,6R)-4,5-Dihydroxy-6-methyloxan-2-yl]oxy-5,14-dihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde	12303930	Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)O	534.60	unknown	https://doi.org/10.1016/S0031-9422(98)00421-X https://doi.org/10.1002/HLCA.19570400314
(3S,5S,8R,9S,10S,13R,14S,17R)-5,14-dihydroxy-3-[(2R,4S,5S,6R)-4-hydroxy-6-methyl-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde	162933442	Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)OC7C(C(C(C(O7)CO)O)O)O	696.80	unknown	https://doi.org/10.1016/S0031-9422(98)00421-X
(3S,5S,8R,9S,10S,13R,14S,17R)-5,14-dihydroxy-3-[(2R,4S,5S,6R)-4-hydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxan-2-yl]oxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde	14562773	Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O	858.90	unknown	https://doi.org/10.1039/P19890002065
(3S,5S,8R,9S,13R,14S,17R)-5,14-dihydroxy-3-[(2R,4R,5S,6R)-4-hydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde	6325758	Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)OC7C(C(C(C(O7)CO)O)O)O	696.80	unknown	https://doi.org/10.3358/SHOKUEISHI.39.4_256 https://doi.org/10.1007/BF00566821 https://doi.org/10.1007/BF00565339 https://doi.org/10.1039/P19890002065 https://doi.org/10.3987/COM-98-8146 https://doi.org/10.1016/S0031-9422(98)00421-X https://doi.org/10.1248/JHS.47.89
(8xi,9xi,14xi,17xi)-3-{[(4xi)-2,6-dideoxy-4-O-(D-glucopyranosyl)-beta-D-erythro-hexopyranosyl]oxy}-5,14-dihydroxy-19-oxocard-20(22)-enolide	139291929	Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)OC7C(C(C(C(O7)CO)O)O)O	696.80	unknown	https://doi.org/10.1007/BF00565339 https://doi.org/10.1039/P19890002065 https://doi.org/10.1016/S0031-9422(98)00421-X https://doi.org/10.3987/COM-98-8146 https://doi.org/10.3358/SHOKUEISHI.39.4_256 https://doi.org/10.1248/JHS.47.89 https://doi.org/10.1007/BF00566821
3-[(3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-3-[(2R,4R,5S,6R)-4-hydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one	101286273	Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)O)OC7C(C(C(C(O7)CO)O)O)O	666.80	unknown	https://doi.org/10.1007/BF00566821 https://doi.org/10.3358/SHOKUEISHI.39.4_256 https://doi.org/10.1248/JHS.47.89 https://doi.org/10.1016/S0031-9422(98)00421-X
3-[(3S,5S,8R,9S,10R,13R,14S,17R)-5,14-dihydroxy-3-[(2R,4R,5S,6R)-4-hydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one	44566921	Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C)O)OC7C(C(C(C(O7)CO)O)O)O	682.80	unknown	https://doi.org/10.3987/COM-98-8146
3-[5,11,14-trihydroxy-3-[4-hydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one	78200850	Click to see CC1C(C(CC(O1)OC2CCC3(C4C(CCC3(C2)O)C5(CCC(C5(CC4O)C)C6=CC(=O)OC6)O)C)O)OC7C(C(C(C(O7)CO)O)O)O	698.80	unknown	https://doi.org/10.3987/COM-98-8146
Card-20(22)-enolide, 3-[(2,6-dideoxy-beta-D-xylo-hexopyranosyl)oxy]-14-hydroxy-, (3beta,5beta)-	100953140	Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)O)O	504.70	unknown	https://doi.org/10.1016/S0031-9422(98)00421-X https://doi.org/10.3358/SHOKUEISHI.39.4_256
Corchoroside A	5091219	Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)O	534.60	unknown	https://doi.org/10.1016/S0031-9422(98)00421-X https://doi.org/10.1002/HLCA.19570400314
Corchorozide A	56840797	Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)O	534.60	unknown	https://doi.org/10.1016/S0031-9422(98)00421-X https://doi.org/10.3358/SHOKUEISHI.39.4_256
Corchorusoside B	85091334	Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3C(CC5(C4(CCC5C6=CC(=O)OC6)O)C)O)C)O)OC7C(C(C(C(O7)CO)O)O)O	682.80	unknown	https://doi.org/10.3987/COM-98-8146
Corchorusoside D	85124732	Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3C(CC5(C4(CCC5C6=CC(=O)OC6)O)C)O)CO)O)OC7C(C(C(C(O7)CO)O)O)O	698.80	unknown	https://doi.org/10.3987/COM-98-8146
Desglucocoroloside	15559187	Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)O)O	504.70	unknown	https://doi.org/10.1016/S0031-9422(98)00421-X
Digitoxigenin monodigitoxoside	11961867	Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)O)O	504.70	unknown	https://doi.org/10.1016/S0031-9422(98)00421-X https://doi.org/10.3358/SHOKUEISHI.39.4_256
Erysimoside	12308885	Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)OC7C(C(C(C(O7)CO)O)O)O	696.80	unknown	https://doi.org/10.1039/P19890002065 https://doi.org/10.1016/S0031-9422(98)00421-X https://doi.org/10.1248/JHS.47.89 https://doi.org/10.3358/SHOKUEISHI.39.4_256 https://doi.org/10.1007/BF00566821
Glucoevatromonoside	15137997	Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)O)OC7C(C(C(C(O7)CO)O)O)O	666.80	unknown	https://doi.org/10.3358/SHOKUEISHI.39.4_256 https://doi.org/10.1248/JHS.47.89 https://doi.org/10.1016/S0031-9422(98)00421-X
Helveticoside	441860	Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)O	534.60	unknown	https://doi.org/10.1016/S0031-9422(98)00421-X https://doi.org/10.3358/SHOKUEISHI.39.4_256
Olitoriside	3587049	Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)OC7C(C(C(C(O7)CO)O)O)O	696.80	unknown	https://doi.org/10.1016/S0031-9422(98)00421-X
> 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/10.1038/192288B0
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	https://doi.org/10.1038/192288B0
> 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
Nicotianamine	9882882	Click to see C1CN(C1C(=O)O)CCC(C(=O)O)NCCC(C(=O)O)N	303.31	unknown	https://doi.org/10.3136/FSTI9596T9798.4.223
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid	348159	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1021/JF990347P
3,5-Dicaffeoyl-epi-quinic acid	60150332	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O	516.40	unknown	https://doi.org/10.1021/JF990347P
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1248/CPB.45.464 https://doi.org/10.1021/JF990347P
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-[[6-(3-Hydroxybut-1-enyl)-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	73815034	Click to see CC(C=CC12C(CC(CC1(O2)C)OC3C(C(C(C(O3)CO)O)O)O)(C)C)O	388.50	unknown	https://doi.org/10.1248/CPB.45.464
5a,6a-Epoxy-7E-megastigmene-3a,9e-diol 3-glucoside	131751181	Click to see CC(C=CC12C(CC(CC1(O2)C)OC3C(C(C(C(O3)CO)O)O)O)(C)C)O	388.50	unknown	https://doi.org/10.1248/CPB.45.464
Corchoionoside A	10023166	Click to see CC(C=CC12C(CC(CC1(O2)C)OC3C(C(C(C(O3)CO)O)O)O)(C)C)O	388.50	unknown	https://doi.org/10.1248/CPB.45.464
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
5-Chloro-7-hydroxy-2-(2-hydroxyethyl)-7-methyl-3-(3-methylpent-1-enyl)isoquinoline-6,8-dione	78108622	Click to see CCC(C)C=CC1=CC2=C(C(=O)C(C(=O)C2=CN1CCO)(C)O)Cl	351.80	unknown	https://doi.org/10.1021/JF990347P
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1002/JSFA.2740420206
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Cichoriin	442101	Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)OC3C(C(C(C(O3)CO)O)O)O	340.28	unknown	https://doi.org/10.1248/CPB.45.464
Scopolin	439514	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O	354.31	unknown	https://doi.org/10.1248/CPB.45.464
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
methyl (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-7-yl]oxyoxane-2-carboxylate	44552030	Click to see COC(=O)C1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O	638.50	unknown	https://doi.org/10.1016/J.TETLET.2009.08.014
methyl (2S,3S,4S,5R,6S)-6-[3-[(2R,3S,4R,5R,6S)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate	44552029	Click to see COC(=O)C1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)O)C6=CC=C(C=C6)O)O)O)O)O	800.70	unknown	https://doi.org/10.1016/J.TETLET.2009.08.014
Methyl 3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-7-yl]oxyoxane-2-carboxylate	75067072	Click to see COC(=O)C1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O	638.50	unknown	https://doi.org/10.1016/J.TETLET.2009.08.014
Methyl 6-[3-[3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate	75067071	Click to see COC(=O)C1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)O)C6=CC=C(C=C6)O)O)O)O)O	800.70	unknown	https://doi.org/10.1016/J.TETLET.2009.08.014
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	12304330	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1021/JF990347P
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	51402807	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1248/CPB.45.464
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5378597	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1021/JF990347P
6''-O-Malonylisoquercitrin	10187514	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O)O	550.40	unknown	https://doi.org/10.1021/JF990347P
Astragalin	5282102	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1038/192288B0 https://doi.org/10.1248/CPB.45.464
Isoquercetin	5280804	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1038/192288B0
Isoquercitin	10813969	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1021/JF990347P
Juglanin	5318717	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O	418.30	unknown	https://doi.org/10.1038/192288B0
Quercetin 3-(6''-malonyl-glucoside)	14730813	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O)O	550.40	unknown	https://doi.org/10.1021/JF990347P
Trifolin	5282149	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1038/192288B0

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Corchorus olitorius

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