Rorippa indica

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Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

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Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID643ff853c2409908351521
Scientific name	Rorippa indica
Authority	(L.) Hiern
First published in	Cat. Afr. Pl. (Hiern) 1(1): xxvi, Addit. & Corr.. 1896

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Nasturtium indicum	DC.	Syst. Nat. 2: 199 (1821)
Nasturtium apetalum	A.Chev.	Cat. Pl. Jard. Bot. Saigon : 14 (1919)
Nasturtium apetalum	DC.	Syst. Nat. 2: 200 (1821)
Nasturtium obtusulum	(Miq.) Koidz.	Acta Phytotax. Geobot. 3: 149 (1934)
Sisymbrium sinapifolium	St.-Lag.	Ann. Soc. Bot. Lyon 7: 135 (1880)
Sisymbrium indicum	L.	Mant. Pl. : 93 (1767)
Sisymbrium apetalum	Lour.	Fl. Cochinch. : 400 (1790)
Sinapis benghalensis	Roxb. ex DC.	Syst. Nat. 2: 198 (1821)
Sinapis divaricata	Roxb.	Fl. Ind. ed. 1832 , 3: 123 (1832)
Sinapis pusilla	Roxb.	Fl. Ind. ed. 1832 , 3: 125 (1832)
Cardamine glandulosa	Blanco	Fl. Filip. : 521 (1837)
Cardamine lamontii	Hance	J. Bot. 14: 363 (1876)
Clandestinaria indica	Spach	Hist. Nat. Vég. 6: 429 (1838)
Radicula indica	Standl.	Smithsonian Misc. Collect. 68(5): 2 (1917)
Nasturtium heterophyllum	D.Don	Prodr. Fl. Nepal. : 202 (1825)
Cardamine atrovirens	(Hornem.) Kuntze	Revis. Gen. Pl. 1: 24. 1891
Nasturtium montanum	Wall. ex Hook.f. & Thomson	J. Proc. Linn. Soc., Bot. 5: 139 (1861)
Sisymbrium sinapis	Burm.f.	Fl. Indica : 140 (1768)
Nasturtium sinapis	(Burm.f.) O.E.Schulz	Repert. Spec. Nov. Regni Veg. 33: 278 (1934)
Rorippa montana	(Wall. ex Hook.f. & Thomson) Small	Fl. S.E. U.S. , ed. 2: 1336 (1913)
Rorippa sinapis	(Burm.f.) Ohwi & Hara	J. Jap. Bot. 12: 899 (1936)
Nasturtium atrovirens	DC.	Syst. Nat. 2: 201 (1821)
Sisymbrium atrovirens	Hornem.	Hort. Bot. Hafn. , Suppl.: 72 (1819)
Nasturtium diffusum	DC.	Prodr. 1: 139 (1824)
Rorippa atrovirens	(Hornem.) Ohwi & Hara	J. Jap. Bot. 12: 900 (1936)
Nasturtium montanum	(Nutt.) Kuntze	Revis. Gen. Pl. 2: 937. 1891 [5 Nov 1891]
Radicula indica	J.M.Macoun	Ottawa Naturalist 26: 162. 1913

Common names Top

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Language	Common/alternative name
English	variable-leaf yellowcress
English	variableleaf yellowcress
Japanese	イヌガラシ
Korean	개갓냉이
Chinese	田葛菜
Chinese	香薺菜
Chinese	雞肉菜
Chinese	幹油菜
Chinese	香荠菜
Chinese	辣米菜
Chinese	葛菜
Chinese	石豇豆
Chinese	葶苈
Chinese	天菜子
Chinese	印度蔊菜
Chinese	旱菜
Chinese	江剪刀草
Chinese	干油菜
Chinese	野油菜
Chinese	塘葛菜
Chinese	薄菜
Chinese	蔊菜
Chinese	野菜子
Chinese	葶藶

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northern Africa
  - Egypt
- West-central Tropical Africa
  - Cameroon
  - Congo
  - Gulf Of Guinea Islands
  - Zaïre

Asia-temperate click to expand
- Caucasus
  - Transcaucasus
- China
  - China North-central
  - China South-central
  - China Southeast
  - Hainan
  - Manchuria
  - Qinghai
  - Tibet
  - Xinjiang
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Taiwan

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

Northern America click to expand
- North-central U.S.A.
  - Illinois
- Northeastern U.S.A.
  - New York
- Northwestern U.S.A.
  - Oregon
- Southeastern U.S.A.
  - Louisiana
  - Mississippi
- Western Canada
  - British Columbia

Southern America click to expand
- Brazil
  - Brazil South
  - Brazil Southeast
- Caribbean
  - Trinidad-Tobago
- Central America
  - El Salvador
  - Honduras
- Northern South America
  - Venezuela
- Western South America
  - Colombia
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000399604
Canadensys	9659
USDA Plants	ROIN
Tropicos	4104624
KEW	urn:lsid:ipni.org:names:222144-2
The Plant List	kew-2417289
Open Tree Of Life	341724
NCBI Taxonomy	50499
Nature Serve	2.133655
IPNI	222144-2
iNaturalist	167965
GBIF	3053472
EPPO	RORIN
EOL	583932
USDA GRIN	105509

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

Reviewing ecological implications of mycorrhizal fungal interactions in the Brassicaceae

Trautwig AN, Jackson MR, Kivlin SN, Stinson KA

Front Plant Sci

22-Nov-2023

PMCID:	PMC10698685
doi:	10.3389/fpls.2023.1269815
PMID:	38078074

Wild edible plants and their cultural significance among the Zhuang ethnic group in Fangchenggang, Guangxi, China

Liu S, Huang X, Bin Z, Yu B, Lu Z, Hu R, Long C

J Ethnobiol Ethnomed

08-Nov-2023

PMCID:	PMC10631048
doi:	10.1186/s13002-023-00623-2
PMID:	37940945

Analysis of gaps in rapeseed (Brassica napus L.) collections in European genebanks

Weise S, Hoekstra R, Kutschan KJ, Oppermann M, van Treuren R, Lohwasser U

Front Plant Sci

09-Oct-2023

PMCID:	PMC10591083
doi:	10.3389/fpls.2023.1244467
PMID:	37877086

Antagonistic RALF peptides control an intergeneric hybridization barrier on Brassicaceae stigmas

Lan Z, Song Z, Wang Z, Li L, Liu Y, Zhi S, Wang R, Wang J, Li Q, Bleckmann A, Zhang L, Dresselhaus T, Dong J, Gu H, Zhong S, Qu LJ

Cell

07-Oct-2023

PMCID:	PMC10615786
doi:	10.1016/j.cell.2023.09.003
PMID:	37806310

Extremely high relative growth rate makes the cabbage white, Pieris rapae, a global pest with highly abundant and migratory nature

Konno K

Sci Rep

15-Jun-2023

PMCID:	PMC10272114
doi:	10.1038/s41598-023-36735-8
PMID:	37322167

Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China

Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C

J Ethnobiol Ethnomed

30-May-2023

PMCID:	PMC10230803
doi:	10.1186/s13002-023-00594-4
PMID:	37254191

Phenology and Diversity of Weeds in the Agriculture and Horticulture Cropping Systems of Indian Western Himalayas: Understanding Implications for Agro-Ecosystems

Haq SM, Lone FA, Kumar M, Calixto ES, Waheed M, Casini R, Mahmoud EA, Elansary HO

Plants (Basel)

08-Mar-2023

PMCID:	PMC10051328
doi:	10.3390/plants12061222
PMID:	36986911

Testing hypotheses of a coevolutionary key innovation reveals a complex suite of traits involved in defusing the mustard oil bomb

Okamura Y, Dort H, Reichelt M, Tunström K, Wheat CW, Vogel H

Proc Natl Acad Sci U S A

12-Dec-2022

PMCID:	PMC9907077
doi:	10.1073/pnas.2208447119
PMID:	36508662

Influence of organic rice production mode on weed composition in the soil seed bank of paddy fields

Gao P, Wang H, Deng S, Dong E, Dai Q

Front Plant Sci

21-Nov-2022

PMCID:	PMC9720393
doi:	10.3389/fpls.2022.1056975
PMID:	36479513

Potential cellular endocrinology mechanisms underlying the effects of Chinese herbal medicine therapy on asthma

Meng Z, Chen H, Deng C, Meng S

Front Endocrinol (Lausanne)

16-Aug-2022

PMCID:	PMC9424672
doi:	10.3389/fendo.2022.916328
PMID:	36051395

A multi‐year dormancy strategy in a cabbage beetle population in southeastern China

Tang J, Liu X, He H, Huang L, Wu S, Xue F

Ecol Evol

07-May-2022

PMCID:	PMC9077826
doi:	10.1002/ece3.8900
PMID:	35571750

The Resistance of Seven Host Plants to Tetranychus merganser Boudreaux (Acari: Tetranychidae)

Treviño-Barbosa G, Ordaz-Silva S, Gaona-García G, Hernández-Juárez A, Mora-Ravelo SG, Chacón Hernández JC

Insects

04-Feb-2022

PMCID:	PMC8878337
doi:	10.3390/insects13020167
PMID:	35206740

Map-based cloning and promoter variation analysis of the lobed leaf gene BoLMI1a in ornamental kale (Brassica oleracea L. var. acephala)

Zhang B, Chen W, Li X, Ren W, Chen L, Han F, Fang Z, Yang L, Zhuang M, Lv H, Wang Y, Zhang Y

BMC Plant Biol

06-Oct-2021

PMCID:	PMC8496080
doi:	10.1186/s12870-021-03223-y
PMID:	34615469

Setup of an Ultrasonic-Assisted Extraction to Obtain High Phenolic Recovery in Crataegus monogyna Leaves

Martín-García B, Razola-Díaz MD, Gómez-Caravaca AM, Benítez G, Verardo V

Molecules

27-Jul-2021

PMCID:	PMC8347228
doi:	10.3390/molecules26154536
PMID:	34361687

Composition and distribution of vegetation in the water level fluctuating zone of the Lantsang cascade reservoir system using UAV multispectral imagery

Jiang W, Liu L, Xiao H, Zhu S, Li W, Liu Y

PLoS One

29-Mar-2021

PMCID:	PMC8007002
doi:	10.1371/journal.pone.0247682
PMID:	33780473

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
> Alkaloids and derivatives / Corynanthean-type alkaloids
Hirsutine	3037884	Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=CC=CC=C34	368.50	unknown	https://doi.org/10.1016/0031-9422(95)00005-R
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid	243	Click to see C1=CC=C(C=C1)C(=O)O	122.12	unknown	https://doi.org/10.1002/JCCS.199500136
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.1016/0031-9422(95)00005-R
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid	10742	Click to see COC1=CC(=CC(=C1O)OC)C(=O)O	198.17	unknown	https://doi.org/10.1016/0031-9422(95)00005-R
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	https://doi.org/10.1002/JCCS.199500136
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	https://doi.org/10.1002/JCCS.199500136 https://doi.org/10.1016/0031-9422(95)00005-R
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid	338	Click to see C1=CC=C(C(=C1)C(=O)O)O	138.12	unknown	https://doi.org/10.1016/0031-9422(95)00005-R
> Benzenoids / Phenols / Benzenediols / Catechols
Catechol	289	Click to see C1=CC=C(C(=C1)O)O	110.11	unknown	https://doi.org/10.1016/0031-9422(95)00005-R
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	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/10.1002/JCCS.199500136
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/10.1002/JCCS.199500136
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucosinolates / Alkylglucosinolates
Glucobrassicin	9601691	Click to see C1=CC=C2C(=C1)C(=CN2)CC(=NOS(=O)(=O)O)SC3C(C(C(C(O3)CO)O)O)O	448.50	unknown	https://doi.org/10.1016/S0367-326X(02)00061-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Salireposide	117440	Click to see C1=CC=C(C=C1)C(=O)OCC2=C(C=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O	406.40	unknown	https://doi.org/10.1002/JCCS.199500136
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
3-Indoleacetonitrile	351795	Click to see C1=CC=C2C(=C1)C(=CN2)CC#N	156.18	unknown	https://doi.org/10.1016/S0367-326X(02)00061-8
> Organosulfur compounds / Sulfonyls / Sulfones
9-(Methylsulfonyl)nonylamine	101417644	Click to see CS(=O)(=O)CCCCCCCCCN	221.36	unknown	https://doi.org/10.1016/0031-9422(95)00005-R
> Organosulfur compounds / Sulfoxides
1-Isothiocyanato-9-(methylsulfinyl)nonane	9921221	Click to see CS(=O)CCCCCCCCCN=C=S	247.40	unknown	https://doi.org/10.1007/BF00981918 https://doi.org/10.1016/0031-9422(95)00005-R
Camelinin	9856525	Click to see CS(=O)CCCCCCCCCCN=C=S	261.50	unknown	https://doi.org/10.1007/BF00981918 https://doi.org/10.1016/0031-9422(95)00005-R
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate	4628123	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O	386.30	unknown	https://doi.org/10.1002/JCCS.199500136
1-O-Sinapoyl-beta-D-glucose	5280406	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O	386.30	unknown	https://doi.org/10.1002/JCCS.199500136
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid	709	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1002/JCCS.199500136
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1002/JCCS.199500136
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1002/JCCS.199500136
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5S,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	163067830	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)OC5C(C(C(C(O5)COC(=O)C=CC6=CC(=C(C=C6)O)O)O)O)O	756.70	unknown	https://doi.org/10.1002/JCCS.199500136
4',5,7-Trihydroxy-3-(alpha-D-arabinopyranosyloxy)flavone	11625890	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O	418.30	unknown	https://doi.org/10.1002/JCCS.199500136
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxychromen-4-one	14749097	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O	418.30	unknown	https://doi.org/10.1002/JCCS.199500136
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5462193	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/10.1002/JCCS.199500136
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/10.1002/JCCS.199500136
Quercitrin	5280459	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1002/JCCS.199500136
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R,6S)-6-[3,5-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	101685309	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)OC5C(C(C(C(O5)COC(=O)C=CC6=CC(=C(C=C6)O)O)O)O)O	756.70	unknown	https://doi.org/10.1002/JCCS.199500136
[6-[6-[3,5-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate	162914995	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)OC5C(C(C(C(O5)COC(=O)C=CC6=CC(=C(C=C6)O)O)O)O)O	756.70	unknown	https://doi.org/10.1002/JCCS.199500136
3,5-Dihydroxy-2-(4-hydroxyphenyl)-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one	13940823	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O	432.40	unknown	https://doi.org/10.1002/JCCS.199500136
3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	25203835	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1002/JCCS.199500136
kaempferol 3-O-beta-D-glucopyranosyl-7-O-beta-L-rhamnopyranoside	25202803	Click to see CC1C(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	594.50	unknown	https://doi.org/10.1002/JCCS.199500136
Kaempferol-3-O-glucoside-7-O-rhamnoside	14035324	Click to see CC1C(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	594.50	unknown	https://doi.org/10.1002/JCCS.199500136
Kaempferol-7-o-glucoside	5480982	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1002/JCCS.199500136
Kaempferol-7-rhamnoside	25079965	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O	432.40	unknown	https://doi.org/10.1002/JCCS.199500136
Quercetin 7-rhamnoside	14130919	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C=C4)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1002/JCCS.199500136
Vincetoxicoside B	5748601	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C=C4)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1002/JCCS.199500136

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Rorippa indica

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