Scientific name	Authority	First published in
Leucosedum album	Fourr.	Ann. Soc. Linn. Lyon sér. 2, 16: 384. 1868
Oreosedum serpentini	(Janch.) Grulich	Preslia 56: 44 (1984)
Oreosedum album	(L.) Grulich	Preslia 56: 44 (1984)
Sedum clusianum	Guss.	Fl. Sicul. Syn. 1: 516 (1843)
Sedum chrisianum	Hort Flor. ex Mast.	Gard. Chron. , n.s., 10: 717 (1878)
Sedum athoum	DC.	Prodr. 3: 407 (1828)
Sedum balticum	C.Hartm.	Handb. Skand. Fl. , ed. 9: 128 (1864)
Sedum micranthum	Bast. ex DC.	Fl. Franç. , ed. 3, 5: 523 (1815)
Sedum muleyanum	Sennen & Mauricio	Cat. Fl. Rif Orient. : 147 (1933)
Sedum gombertii	Sennen	Diagn. Nouv. : 281 (1936)
Sedum serpentini	Janch.	Oesterr. Bot. Z. 69: 173 (1920)
Sedum angulatum	hort. ex Mast.	Gard. Chron. , n.s., 10: 717 (1878)
Sedum albellum	Willk.	Prodr. Fl. Hispan. 3: 141 (1874)
Sedum teretifolium	Lam.	Fl. Franç. (Lamarck) 3: 84. 1779 [1778 publ. after 21 Mar 1779]
Sedum turgidum	Ramond ex DC.	Fl. Franç. , ed. 3, 4: 390 (1805)
Sedum vermiculifolium	P.Fourn.	Monde Pl. 36: 11 (1935)
Sedum vermiculare	Gaterau	Desc. Pl. Montauban : 84 (1789)
Sedum album subsp. micranthum	(Bastard ex DC.) Syme	Engl. Bot. ed. 3B, 4: 53 1865
Oreosedum album subsp. micranthum	(DC.) Velayos	Anales Jard. Bot. Madrid 45: 584 (1988 publ. 1989)
Oreosedum album var. micranthum	(de Candolle) P.Heath	Sussex Cact. Succ. Soc. Yearb. 1987: 55 (1987)

Common names Top

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Filter by language:

Language	Common/alternative name
English	white stonecrop
Arabic	سدم أبيض
Bulgarian	бяла тлъстига
Catalan	crespinell blanc
Czech	rozchodník bílý
Welsh	briweg wen
Danish	hvid stenurt
German	weiße fetthenne
German	weisser mauerpfeffer
Estonian	valge kukehari
Basque	teilatu-belar zuri
Persian	ناز سفید
Finnish	valkomaksaruoho
French	orpin blanc
Hungarian	fehér varjúháj
Icelandic	ljósahnoðri
Cornish	bewles gwynn
Norwegian Bokmål	hvitbergknapp
Dutch	wit vetkruid
Polish	rozchodnik biały
Slovak	rozchodník biely
Serbian	beli žednjak
Swedish	vit fetknopp
Ukrainian	Очиток білий
Chinese	白弁庆草
Chinese	玉米石
Chinese	白景天

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Sedum album subsp. rupimelitense	Mifsud, R.Stephenson & Thiede	Phytotaxa 227: 138 (2015)
Sedum album subsp. serpentini	(Janch.) Barina	Distrib. Atlas Vasc. Pl. Albania : 466 (2017)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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

Africa click to expand
- Northern Africa
  - Algeria
  - Libya
  - Morocco
  - Tunisia

Asia-temperate click to expand
- Caucasus
  - Transcaucasus
- Western Asia
  - Iran
  - Lebanon-Syria
  - Turkey

Australasia click to expand
- Australia
  - Tasmania

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Krym
  - Northwest European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Great Britain
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Eastern Canada
  - New Brunswick
  - Ontario
  - Québec
- North-central U.S.A.
  - Illinois
- Northeastern U.S.A.
  - Indiana
  - Maine
  - Michigan
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Vermont
  - West Virginia
- Northwestern U.S.A.
  - Oregon
  - Washington
- Southwestern U.S.A.
  - California
  - Utah
- Western Canada
  - British Columbia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000438148
Canadensys	4663
USDA Plants	SEAL
Tropicos	8900024
INPN	122106
Flora of Italy	1754
KEW	urn:lsid:ipni.org:names:275022-1
The Plant List	kew-2484837
Missouri Botanical Garden	279379
PFAF	Sedum album
Open Tree Of Life	387654
Observations.org	7437
NCBI Taxonomy	23029
NBN Atlas	NBNSYS0000003473
Nature Serve	2.151813
IPNI	275022-1
iNaturalist	79025
GBIF	5362008
Freebase	/m/043r3zv
EPPO	SEDAL
EOL	585419
Elurikkus	7199
Calflora (Californian flora)	8531
USDA GRIN	33472
Wikipedia	Sedum_album

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_006409495.1	Sedum_album_v3	Contig	Michigan State University	2019-06-24	55.0x	288.25 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

The Cissus quadrangularis genome reveals its adaptive features in an arid habitat

Li Q, Wang Y, Zhou H, Liu Y, Gichuki DK, Hou Y, Zhang J, Aryal R, Hu G, Wan T, Amenu SG, Gituru RW, Xin H, Wang Q

Hortic Res

02-Feb-2024

PMCID:	PMC11001597
doi:	10.1093/hr/uhae038
PMID:	38595910

The Orophilous Shrubby Vegetation of the Juniperetalia hemisphaericae Order in Sicily: A Refuge Habitat for Many Endemic Vascular Species

Sciandrello S, Giusso del Galdo G

Plants (Basel)

31-Jan-2024

PMCID:	PMC10857485
doi:	10.3390/plants13030423
PMID:	38337957

Insights into the Superrosids phylogeny and flavonoid synthesis from the telomere-to-telomere gap-free genome assembly of Penthorum chinense Pursh

Wang Z, Zhou J, Pan J, Cheng W, Fang J, Lv Q, Lin X, Cheng W, Zhang L, Cheng K

Hortic Res

19-Dec-2023

PMCID:	PMC10857932
doi:	10.1093/hr/uhad274
PMID:	38344651

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

Defining Mechanisms of C3 to CAM Photosynthesis Transition toward Enhancing Crop Stress Resilience

Tan B, Chen S

Int J Mol Sci

22-Aug-2023

PMCID:	PMC10487458
doi:	10.3390/ijms241713072
PMID:	37685878

Breathing Fresh Air in the City: Implementing Avenue Trees as a Sustainable Solution to Reduce Particulate Pollution in Urban Agglomerations

Mandal M, Popek R, Przybysz A, Roy A, Das S, Sarkar A

Plants (Basel)

03-Apr-2023

PMCID:	PMC10097214
doi:	10.3390/plants12071545
PMID:	37050171

Diel dynamics of multi-omics in elkhorn fern provide new insights into weak CAM photosynthesis

Li C, Huang W, Han X, Zhao G, Zhang W, He W, Nie B, Chen X, Zhang T, Bai W, Zhang X, He J, Zhao C, Fernie AR, Tschaplinski TJ, Yang X, Yan S, Wang L

Plant Commun

23-Mar-2023

PMCID:	PMC10504562
doi:	10.1016/j.xplc.2023.100594
PMID:	36960529

Characterization of Volatile Organic Compound Emissions and CO2 Uptake from Eco-roof Plants

Laguerre A, Brennan DL, Starry O, Rosenstiel TN, Gall ET

Build Environ

05-Mar-2023

PMCID:	PMC10104446
doi:	10.1016/j.buildenv.2023.110158
PMID:	37065504

High-quality Cymbidium mannii genome and multifaceted regulation of crassulacean acid metabolism in epiphytes

Fan W, He ZS, Zhe M, Feng JQ, Zhang L, Huang Y, Liu F, Huang JL, Ya JD, Zhang SB, Yang JB, Zhu A, Li DZ

Plant Commun

21-Feb-2023

PMCID:	PMC10504564
doi:	10.1016/j.xplc.2023.100564
PMID:	36809882

Widely targeted metabolomics analysis reveals the mechanism of quality improvement of flue-cured tobacco

Meng L, Song W, Chen S, Hu F, Pang B, Cheng J, He B, Sun F

Front Plant Sci

29-Nov-2022

PMCID:	PMC9746875
doi:	10.3389/fpls.2022.1074029
PMID:	36523627

Effects of Prickly Burnet (Sarcopoterium spinosum (L.) Spach.) Control and Sheep Grazing on Hay Yield and Quality on Gökçeada Island, Turkey

Alatürk F, Gökkuş A, Özaslan Parlak A, Baytekin H, Tölü C

Animals (Basel)

08-Nov-2022

PMCID:	PMC9686760
doi:	10.3390/ani12223073
PMID:	36428300

Sustainable green roofs: a comprehensive review of influential factors

Shahmohammad M, Hosseinzadeh M, Dvorak B, Bordbar F, Shahmohammadmirab H, Aghamohammadi N

Environ Sci Pollut Res Int

03-Oct-2022

PMCID:	PMC9528882
doi:	10.1007/s11356-022-23405-x
PMID:	36190639

A genome for Cissus illustrates features underlying its evolutionary success in dry savannas

Xin H, Wang Y, Li Q, Wan T, Hou Y, Liu Y, Gichuki DK, Zhou H, Zhu Z, Xu C, Zhou Y, Liu Z, Li R, Liu B, Lu L, Jiang H, Zhang J, Wan J, Aryal R, Hu G, Chen Z, Gituru RW, Liang Z, Wen J, Wang Q

Hortic Res

13-Sep-2022

PMCID:	PMC9715578
doi:	10.1093/hr/uhac208
PMID:	36467268

Effect of CO2 Content in Air on the Activity of Carbonic Anhydrases in Cytoplasm, Chloroplasts, and Mitochondria and the Expression Level of Carbonic Anhydrase Genes of the α- and β-Families in Arabidopsis thaliana Leaves

Rudenko NN, Ignatova LK, Naydov IA, Novichkova NS, Ivanov BN

Plants (Basel)

14-Aug-2022

PMCID:	PMC9414674
doi:	10.3390/plants11162113
PMID:	36015416

Physiological Adaptation and Plant Distribution along a Steep Hydrological Gradient

Sand-Jensen K, Borum J, Møller CL, Baastrup-Spohr L

Plants (Basel)

24-Jun-2022

PMCID:	PMC9269611
doi:	10.3390/plants11131683
PMID:	35807635

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 / Phenethylamines
Phenethylamine	1001	Click to see C1=CC=C(C=C1)CCN	121.18	unknown	https://doi.org/10.1016/S0031-9422(00)97554-X
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Gossypetin	5280647	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)O)O)O	318.23	unknown	https://doi.org/10.1016/0031-9422(95)00573-0
Hibiscetin	15559735	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)O	334.23	unknown	https://doi.org/10.1016/0031-9422(95)00573-0
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	https://doi.org/10.1016/S0031-9422(00)97941-X
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	https://doi.org/10.1016/S0031-9422(00)97941-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-8-O-glucuronides
(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[3,5,7-trihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-8-yl]oxyoxane-2-carboxylic acid	163029622	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	478.40	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[3,5,7-trihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-8-yl]oxyoxane-2-carboxylic acid	15926904	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	478.40	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X
3,4,5-Trihydroxy-6-[3,5,7-trihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-8-yl]oxyoxane-2-carboxylic acid	15926903	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	478.40	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X
Gossypetin 8-O-beta-D-glucuronide;Gossypetin-8-O-(c)micro-D-glucuronide	15926905	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O	494.40	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X
Hibifolin	5490334	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O	494.40	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Quercetin-4'-o-glucoside	12442954	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	464.40	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X
Spiraeoside	5320844	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	464.40	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one	5353915	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/10.1016/S0031-9422(00)97941-X
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one	13988312	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)OC)O)O)O	462.40	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X
isorhamnetin 3-O-rhamnoside	23634491	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)OC)O)O)O	462.40	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X
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/10.1016/S0031-9422(00)97941-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3,5-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	12302035	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	478.40	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	102153728	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O	624.50	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	139031077	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O	624.50	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X
5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one	14353471	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O	624.50	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X
7-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	162942828	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)OC)O)O)O	786.70	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X
7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one	14353476	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O	640.50	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X
7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	162942830	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)OC)O)O)O	786.70	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X
7-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one	14353475	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O	640.50	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X
7-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one	14353473	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)OC)O)O)O	786.70	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X
Isorhamnetin 7-glucoside	6455477	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	478.40	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin	5280681	Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	316.26	unknown	https://doi.org/10.1016/S0031-9422(00)97941-X

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Sedum album

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