Hesperis matronalis, also known as dame's rocket, is a flowering plant in the Brassicaceae family. It is native to Eurasia but has been cultivated in many other parts of the world for its attractive spring blooms. It has multiple common names and is often confused with native Phlox species. It is a biennial or short-lived perennial and can become a weed in some areas. The plant has showy flowers in various shades of lavender and purple, and some double-flowered varieties exist. It is easy to grow and self-seeds quickly, making it a popular choice for gardens. However, it has been found to be ecologically invasive in North America. The plant is also edible, with young leaves and seeds being used in salads. It is native to southern Europe but has been introduced to many other temperate regions. In some areas, it is considered a noxious weed and is banned or restricted.

Synonyms Top

Scientific name	Authority	First published in
Viola matronalis	Garsault	Fig. Pl. Med. 4: t. 623. 1764, nom. inval., opus utique oppressum; Descr. Pl. Anim. 361. 1767; Thell. in Bull. Herb. Boiss. Ser. II. viii. 908.
Antoniana sylvestris	Bubani	Fl. Pyren. 3: 170 (1901)
Crucifera matronalis	E.H.L.Krause	Deutschl. Fl. Abbild. , ed. 2, 6: 119 (1902)
Deilosma inodora	Fuss	Fl. Transsilv. : 57 (1866)
Deilosma matronalis	Andrz. ex DC.	Syst. Nat. [Candolle] 2: 450. 1821 [late May 1821]
Deilosma nivea	Fuss	Fl. Transsilv. : 57 (1866)
Deilosma runcinata	Fuss	Fl. Transsilv. : 56 (1866)
Deilosma sibirica	Andrz. ex DC.	Syst. Nat. 1: 451 (1817)
Hesperis albiflora	Schur	Verh. Mitth. Siebenbürg. Vereins Naturwiss. Hermannstadt 4: 66 (1853)
Hesperis bituminosa	Willd.	Enum. Pl. Hort. Berol. , Suppl.: 45 (1814)
Hesperis euganea	Marsili ex Ten.	Fl. Napol. 1(Prodr.): XXXVIII (1812)
Hesperis heterophylla	Ten.	Fl. Napol. 1(Prodr.): XXXIX (1812)
Hesperis hortensis	Pers. ex Steud.	Nomencl. Bot. : 402 (1821)
Hesperis oblongipetala	Borbás	Magyar Bot. Lapok 1: 379 (1902)
Hesperis pontica	Zapał.	Bull. Int. Acad. Sci. Cracovie, Cl. Sci. Math., Sér. B, Sci. Nat. 12: 1158 (1912)
Hesperis pycnotricha	Borbás & Degen	Magyar Bot. Lapok 1: 17 (1902)
Hesperis sabauda	Rouy & Foucaud	Fl. France 2: 3 (1895)
Hesperis theophrasti subsp. graeca	Dvořák	Phyton (Horn) 15: 119 (1973)
Hesperis umbrosa	Herbich	Stirp. Rar. Bucov. : 48 (1853)
Hesperis unguinosa	Schrank	Pl. Rar. Hort. Monac. : t. 77 (1821)
Hesperis voronovii	N.Busch	Trudy Bot. Inst. Akad. Nauk S.S.S.R., Ser. 1, Fl. Sist. Vyssh. Rast. 3: 358 (1937)
Hesperis meyeriana	(Trautv.) N.Busch	Fl. URSS 8: 246 (1939)
Hesperis matronalis var. matronalis	L.
Hesperis adenosepala	Borbás	Magyar Bot. Lapok 1: 379 (1902).
Hesperis adzharica	Tzvelev	Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 19: 144 (1959)
Hesperis caucasica	Rupr.	Fl. Caucasi : 91 (1869)
Hesperis transcaucasica	Tzvelev	Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 19: 130 (1959)
Hesperis oreophila	Kitag.	Rep. Exped. Manchoukuo Sect. IV 4: 84 (1936)
Hesperis matronalis var. elata	(Hornem.) Schmalh.
Hesperis matronalis subsp. sibirica	(L.) G.V.Krylov
Hesperis matronalis var. sibirica	(L.) DC.
Hesperis sibirica var. alba	Georgi

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	rogue's gillyflower
English	dame's-violet
Spanish	mother of the-evening
Spanish	winter gilliflower
Spanish	sweet rocket
Spanish	summer lilac
Spanish	night scented gilliflower
Spanish	mother-of-the-evening
Spanish	mother of-the-evening
Spanish	mother of the evening
Spanish	dames-wort
Spanish	dames wort
Spanish	damask violet
Arabic	لورانس زهرة الصباح
Arabic	زهرة المساء الجميلة
Arabic	جوليانا نسائية
Arabic	بنفسج السيدات
Arabic	زهرة الماء
Arabic	بنفسج السيدة
Arabic	البنفسج الدمشقي
Azerbaijani	gecə bənövşəsi gecəgülü
Bulgarian	вечерница
Bulgarian	Вечерник
Czech	večernice vonná
Welsh	croes yr hwyr
German	gewöhnliche nachtviole
German	gemeine nachtviole
German	matronenblume
Estonian	harilik öölill
Persian	هسپریس بانوان
Finnish	tarhaillakko
French	julienne des dames
French	julienne
Hungarian	hölgyestike
Japanese	ハナダイコン
Japanese	はなだいこん
Lithuanian	vakarutė
Norwegian Bokmål	dagfiol
Dutch	damastbloem
Norwegian Nynorsk	dagfiol
Polish	wieczornik damski
Russian	вечерник
Russian	Вечерница обыкновенная
Russian	ночная фиалка
Russian	вечерница ночная фиалка
Slovak	večernica voňavá
Swedish	trädgårdsnattviol
Chinese	紫花南芥
Chinese	欧亚香花芥

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Hesperis matronalis subsp. adzharica	Cullen
Hesperis matronalis subsp. candida	(Kit.) Hegi & Em.Schmid	Ill. Fl. Mitt.-Eur. 4(1): 467. 1919 (1919)
Hesperis matronalis subsp. cladotricha	(Borbás) Hayek	Repert. Spec. Nov. Regni Veg. Beih. 30(1): 416. 1925 (1925)
Hesperis matronalis subsp. nivea	Kulcz.
Hesperis matronalis subsp. sintenisii	(F.Dvořák) A.Duran	Türk. Bitkileri List. : 279 (2012)
Hesperis matronalis subsp. voronovii	(N.Busch) P.W.Ball	Feddes Repert. Spec. Nov. Regni Veg. 68: 194 1963
Hesperis matronalis subsp. vrabelyiana	Soó	Magyar Fl. 3: 371. 1968

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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

Antarctica click to expand
- Subantarctic Islands
  - Falkland Islands

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - Xinjiang
- Eastern Asia
  - Japan
- Middle Asia
  - Kazakhstan
  - Kirgizstan
- Russian Far East
  - Kuril Islands
  - Primorye
- Siberia
  - Altay
  - West Siberia
- Western Asia
  - Lebanon-Syria
  - Turkey

Australasia click to expand
- New Zealand
  - New Zealand North
  - New Zealand South

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - East European Russia
  - Krym
  - North European Russia
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Great Britain
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - France
  - Spain

Northern America click to expand
- Eastern Canada
  - Newfoundland
  - Nova Scotia
  - Ontario
  - Prince Edward Island
  - Québec
- North-central U.S.A.
  - Illinois
  - Iowa
  - Kansas
  - Minnesota
  - Missouri
  - Nebraska
  - North Dakota
  - South Dakota
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Maine
  - Massachusetts
  - Michigan
  - New Hampshire
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - Vermont
  - West Virginia
- Northwestern U.S.A.
  - Colorado
  - Idaho
  - Montana
  - Oregon
  - Washington
  - Wyoming
- South-central U.S.A.
  - New Mexico
- Southeastern U.S.A.
  - Alabama
  - Arkansas
  - Delaware
  - District Of Columbia
  - Kentucky
  - Maryland
  - North Carolina
  - Tennessee
  - Virginia
- Southwestern U.S.A.
  - California
  - Nevada
  - Utah
- Western Canada
  - Alberta
  - British Columbia
  - Manitoba
  - Saskatchewan

Southern America click to expand
- Southern South America
  - Argentina South
  - Chile South

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000721077
Flora of Alabama	1256
Canadensys	4054
USDA Plants	HEMA3
Tropicos	4100184
INPN	101460
Flora of Italy	1362
KEW	urn:lsid:ipni.org:names:285087-1
The Plant List	kew-2847567
Plantarium	18656
Missouri Botanical Garden	278038
PaleoBotany	41140
Open Tree Of Life	281533
NCBI Taxonomy	264418
NBN Atlas	NBNSYS0000002902
Nature Serve	2.157721
IPNI	285087-1
iNaturalist	47697
GBIF	3042291
Freebase	/m/034qz5
WisFlora	3837
EPPO	HEVMA
EOL	583891
Elurikkus	5067
Calflora (Californian flora)	4114
USDA GRIN	18933
Wikipedia	Hesperis_matronalis
CMAUP	NPO17222

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

Plant Invasion Ecology

Sukhorukov AP

Plants (Basel)

17-Nov-2023

PMCID:	PMC10674497
doi:	10.3390/plants12223887
PMID:	38005783

The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.)

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

PMCID:	PMC10602594
doi:	10.1371/journal.pone.0291734
PMID:	37792900

The influence of climate warming on flowering phenology in relation to historical annual and seasonal temperatures and plant functional traits

Geissler C, Davidson A, Niesenbaum RA

PeerJ

21-Apr-2023

PMCID:	PMC10124540
doi:	10.7717/peerj.15188
PMID:	37101791

Wild and weedy Hesperis matronalis hosts turnip mosaic virus across heterogeneous landscapes in upstate New York

Lombardi EM, Peters J, Jacob L, Power AG

Virus Res

28-Nov-2022

PMCID:	PMC10194180
doi:	10.1016/j.virusres.2022.199011
PMID:	36511291

Initial assemblage characteristics determine the functional dynamics of flower‐strip plant communities

Gardarin A, Valantin‐Morison M

Ecol Evol

18-Oct-2022

PMCID:	PMC9579737
doi:	10.1002/ece3.9435
PMID:	36267684

Reinventory of the vascular plants of Mormon Island Crane Meadows after forty years of restoration, invasion, and climate change

Caven AJ, Wiese JD

Heliyon

03-Jun-2022

PMCID:	PMC9192816
doi:	10.1016/j.heliyon.2022.e09640
PMID:	35711997

Where Is Garlic Mustard? Understanding the Ecological Context for Invasions of Alliaria petiolata

Rodgers VL, Scanga SE, Kolozsvary MB, Garneau DE, Kilgore JS, Anderson LJ, Hopfensperger KN, Aguilera AG, Urban RA, Juneau KJ

Bioscience

30-Mar-2022

PMCID:	PMC9169898
doi:	10.1093/biosci/biac012
PMID:	35677290

Tracing the Evolution of the Angiosperm Genome from the Cytogenetic Point of View

Borowska-Zuchowska N, Senderowicz M, Trunova D, Kolano B

Plants (Basel)

16-Mar-2022

PMCID:	PMC8953110
doi:	10.3390/plants11060784
PMID:	35336666

Competitive Interactions between Two Non-Native Species (Alliaria petiolata [M. Bieb.] Cavara & Grande and Hesperis matronalis L.) and a Native Species (Ageratina altissima [L.] R.M. King & H. Rob.)

Paulus KR, Marshall JM

Plants (Basel)

29-Jan-2022

PMCID:	PMC8839745
doi:	10.3390/plants11030374
PMID:	35161355

Lepidium graminifolium L.: Glucosinolate Profile and Antiproliferative Potential of Volatile Isolates

Đulović A, Burčul F, Čulić VČ, Ruščić M, Brzović P, Montaut S, Rollin P, Blažević I

Molecules

27-Aug-2021

PMCID:	PMC8434519
doi:	10.3390/molecules26175183
PMID:	34500622

Biodiversity in a Cool-Climate Vineyard: A Case Study from Quebec

Vincent C, Lasnier J, de Coussergues CH, Baril A

Insects

19-Aug-2021

PMCID:	PMC8396841
doi:	10.3390/insects12080750
PMID:	34442316

An unknown hotspot of plant diversity in the heart of the Central Apennine: flora and vegetation outline of Mt. Pozzoni-St. Rufo valley (Cittareale, Rieti)

Lattanzi E, Del Vico E, Tranquilli R, Farris E, Marignani M, Rosati L

PhytoKeys

31-May-2021

PMCID:	PMC8390790
doi:	10.3897/phytokeys.178.62947
PMID:	34475797

Comparative phylogenetics of repetitive elements in a diverse order of flowering plants (Brassicales)

Beric A, Mabry ME, Harkess AE, Brose J, Schranz ME, Conant GC, Edger PP, Meyers BC, Pires JC

G3 (Bethesda)

16-May-2021

PMCID:	PMC8495927
doi:	10.1093/g3journal/jkab140
PMID:	33993297

The effects of climate change on floral anthocyanin polymorphisms

Sullivan CN, Koski MH

Proc Biol Sci

03-Mar-2021

PMCID:	PMC7935138
doi:	10.1098/rspb.2020.2693
PMID:	33653138

Understanding Alstroemeria pallida Flower Colour: Links between Phenotype, Anthocyanins and Gene Expression

Donoso A, Rivas C, Zamorano A, Peña Á, Handford M, Aros D

Plants (Basel)

29-Dec-2020

PMCID:	PMC7824551
doi:	10.3390/plants10010055
PMID:	33383740

Phytochemical Profile Top

Add a new one!

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
Phenethyl acetate	7654	Click to see CC(=O)OCCC1=CC=CC=C1	164.20	unknown	https://doi.org/10.1016/0031-9422(94)00332-N
Phenylethyl Alcohol	6054	Click to see C1=CC=C(C=C1)CCO	122.16	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009 https://doi.org/10.1016/0031-9422(94)00332-N
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Benzyl Benzoate	2345	Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2	212.24	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
Methyl Anthranilate	8635	Click to see COC(=O)C1=CC=CC=C1N	151.16	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
Methyl Salicylate	4133	Click to see COC(=O)C1=CC=CC=C1O	152.15	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
> 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	via CMAUP database
> 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	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde	240	Click to see C1=CC=C(C=C1)C=O	106.12	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol	244	Click to see C1=CC=C(C=C1)CO	108.14	unknown	https://doi.org/10.1016/0031-9422(94)00332-N https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
> Benzenoids / Benzene and substituted derivatives / Benzyl cyanides
Phenylacetonitrile	8794	Click to see C1=CC=C(C=C1)CC#N	117.15	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
Benzyl acetate	8785	Click to see CC(=O)OCC1=CC=CC=C1	150.17	unknown	https://doi.org/10.1016/0031-9422(94)00332-N
Benzyl propionate	31219	Click to see CCC(=O)OCC1=CC=CC=C1	164.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
Phenylacetaldehyde	998	Click to see C1=CC=C(C=C1)CC=O	120.15	unknown	https://doi.org/10.1016/0031-9422(94)00332-N
> Benzenoids / Benzene and substituted derivatives / Phenylacetic acids / 2(hydroxyphenyl)acetic acids
2-Hydroxy-5-butoxyphenylacetic acid	15108711	Click to see CCCCOC1=CC(=C(C=C1)O)CC(=O)O	224.25	unknown	via CMAUP database
> Benzenoids / Phenols / Benzenediols / Hydroquinones
Butyl 2-(2,5-dihydroxyphenyl)acetate	44217017	Click to see CCCCOC(=O)CC1=C(C=CC(=C1)O)O	224.25	unknown	via CMAUP database
Ethyl 2,5-dihydroxyphenylacetate	297396	Click to see CCOC(=O)CC1=C(C=CC(=C1)O)O	196.20	unknown	via CMAUP database
Methyl 2-(2,5-dihydroxyphenyl)acetate	13790504	Click to see COC(=O)CC1=C(C=CC(=C1)O)O	182.17	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol	3314	Click to see COC1=C(C=CC(=C1)CC=C)O	164.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
Maesol	128958	Click to see CC1=C(C=C(C=C1OC)CCCCCCCCCCCCC2=CC(=C(C(=C2)OC)C)O)O	442.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Entadamide-A-beta-D-glucopyranoside	101616680	Click to see CSC=CC(=O)NCCOC1C(C(C(C(O1)CO)O)O)O	323.36	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)-	5281553	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1016/0031-9422(94)00332-N https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
beta-Ocimene, (3Z)-	5320250	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1016/0031-9422(94)00332-N https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
Linalool, (-)-	443158	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1016/0031-9422(94)00332-N
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009 https://doi.org/10.1016/0031-9422(94)00332-N
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene	440968	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
(-)-beta-Pinene	440967	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1016/0031-9422(94)00332-N https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1016/0031-9422(94)00332-N https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1016/0031-9422(94)00332-N
Sabinene	10887971	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol	443162	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009 https://doi.org/10.1016/0031-9422(94)00332-N
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1016/0031-9422(94)00332-N
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3E,7E)-4,8,12-trimethyltrideca-1,3,7,11-tetraene	6443227	Click to see CC(=CCCC(=CCCC(=CC=C)C)C)C	218.38	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3-[(2S,3R,4R)-4-[[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aR,5S,6R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,6-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	72737016	Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(C(C(C6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(CO8)(COC9C(C(CO9)(CO)O)O)O)O)O)O)C)C)C)COC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O	1544.60	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-3-[(2S,3R,4R)-4-[[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	72736851	Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CCC6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(CO8)(COC9C(C(CO9)(CO)O)O)O)O)C)C)C)COC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O	1512.60	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl] (4aR,5S,6R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,6-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	72736852	Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(C(C(C6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(CO8)O)O)O)O)O)C)C)C)COC9C(C(C(CO9)O)OC1C(C(C(CO1)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O	1412.50	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-6-(acetyloxymethyl)-3-[(2S,3R,4R)-4-[[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]oxy-4,5-dihydroxyoxan-2-yl] (4aR,5S,6R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,6-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	72737187	Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(C(C(C6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)COC(=O)C)O)O)OC8C(C(CO8)(COC9C(C(CO9)(CO)O)O)O)O)O)O)C)C)C)COC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O	1586.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Entagenic acid	21594206	Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(C(C2O)O)C)C)(C)C)O)C)C(=O)O)C	488.70	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Alkanolamines / 1,2-aminoalcohols / N-acylethanolamines
Entadamide B	3035981	Click to see CSC(CC(=O)NCCO)SC	209.30	unknown	via CMAUP database
N-(2-Hydroxyethyl)-3-methylthiopropenamide	6439215	Click to see CSC=CC(=O)NCCO	161.22	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-beta-d-Glucopyranosyloxy-5-butoxyphenylacetic acid	15108713	Click to see CCCCOC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)CC(=O)O	386.40	unknown	via CMAUP database
butyl 2-[5-hydroxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]acetate	102143698	Click to see CCCCOC(=O)CC1=C(C=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O	386.40	unknown	via CMAUP database
Phaseoloidin	14104237	Click to see C1=CC(=C(C=C1O)CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O	330.29	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
6-Methyl-5-hepten-2-one	9862	Click to see CC(=CCCC(=O)C)C	126.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
> Organoheterocyclic compounds / Epoxides
(3S)-2,2-dimethyl-3-[(2E)-3-methylpenta-2,4-dienyl]oxirane	10898884	Click to see CC(=CCC1C(O1)(C)C)C=C	152.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
> Organoheterocyclic compounds / Oxanes
(3S,6S)-6-ethenyl-2,2,6-trimethyloxan-3-ol	6427787	Click to see CC1(C(CCC(O1)(C)C=C)O)C	170.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
> Organoheterocyclic compounds / Tetrahydrofurans
2-[(2R,5S)-5-ethenyl-5-methyloxolan-2-yl]propan-2-ol	6428573	Click to see CC1(CCC(O1)C(C)(C)O)C=C	170.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
trans-Linalool oxide	6432254	Click to see CC1(CCC(O1)C(C)(C)O)C=C	170.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.12.009
> Organosulfur compounds / Sulfoxides
1-Isothiocyanato-6-(methylsulfinyl)hexane	9815648	Click to see CS(=O)CCCCCCN=C=S	205.30	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.17-0846
1-isothiocyanato-6-[(S)-methylsulfinyl]hexane	94046233	Click to see CS(=O)CCCCCCN=C=S	205.30	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.17-0846
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(1R,8S,9R,16R,18S,27S)-9-(3,4-dihydroxyphenyl)-5,8,16,21,23-pentahydroxy-2,10,17,26-tetraoxaheptacyclo[14.11.1.01,13.03,12.06,11.018,27.020,25]octacosa-3(12),4,6(11),13,20,22,24-heptaen-15-one	101925531	Click to see C1C(C(OC2=C1C(=CC3=C2C4=CC(=O)C5(CC4(O3)C6C(O5)CC7=C(C=C(C=C7O6)O)O)O)O)C8=CC(=C(C=C8)O)O)O	576.50	unknown	via CMAUP database
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
Epicatechin	72276	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin	72277	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Naringenin	439246	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Aromadendrin	122850	Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	288.25	unknown	via CMAUP database
Taxifolin	439533	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
4',7-Dihydroxyflavone	5282073	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)O	254.24	unknown	via CMAUP database
4H-1-Benzopyran-4-one, 2-(3,5-dihydroxyphenyl)-5,7-dihydroxy-	5487757	Click to see C1=C(C=C(C=C1O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	286.24	unknown	via CMAUP database
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Galangin	5281616	Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
Isorhamnetin	5281654	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	316.26	unknown	via CMAUP database
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	via CMAUP database
Rhamnocitrin	5320946	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=C(C=C3)O)O	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Ayanin	5280682	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)O	344.30	unknown	via CMAUP database
Kaempferol 3,7,4'-trimethyl ether	5468749	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC	328.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
2'-O-Methylisoliquiritigenin	5319688	Click to see COC1=C(C=CC(=C1)O)C(=O)C=CC2=CC=C(C=C2)O	270.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-Phenylpropionic acid	107	Click to see C1=CC=C(C=C1)CCC(=O)O	150.17	unknown	https://doi.org/10.1016/0031-9422(94)00332-N

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Hesperis matronalis

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top