Scientific name	Authority	First published in
Cerasus humilis	Moris	Stirp. Sard. Elench. 1: 17 (1827)
Cerasus prostrata	(Labill.) Ser.	Traité Arbr. Arbust. 5: t. 53, f. 2 (1812)
Microcerasus humilis	M.Roem.	Fam. Nat. Syn. Monogr. 3: 94 (1847)
Hagidryas prostrata	Griseb.	Reise Rumel. 1: 311 (1841)
Prunus humilis	(Moris) Colla	Herb. Pedem. 2: 293 (1834)
Cerasus prostrata var. glabrifolia	(Moris) Browicz	Fl. Turkey 4: 13 (1972)

Common names Top

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Filter by language:

Language	Common/alternative name
English	mountain cherry
English	prostrate cherry
Arabic	خوخ مفترش
German	niederliegende kirsche
diq	bewrınc
Hebrew	דובדבן שרוע
Kabyle	tattefaḥt n yiddawen
Swedish	lingonkörsbär
Turkish	dağ kirazı
Chinese	岩櫻桃
Chinese	平臥櫻桃
Chinese	岩樱桃

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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
- Northern Africa
  - Algeria
  - Morocco
  - Tunisia

Asia-temperate click to expand
- Western Asia
  - East Aegean Islands
  - Lebanon-Syria
  - Turkey

Europe click to expand
- Southeastern Europe
  - Albania
  - Greece
  - Kriti
  - Yugoslavia
- Southwestern Europe
  - Corse
  - France
  - Sardegna
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000985802
Tropicos	27800336
INPN	116117
Flora of Italy	2227
KEW	urn:lsid:ipni.org:names:730142-1
The Plant List	rjp-1309
Open Tree Of Life	307264
Observations.org	139654
NCBI Taxonomy	195662
IUCN Red List	172276
IPNI	730142-1
iNaturalist	322679
GBIF	3021265
Freebase	/m/03byxl5
EPPO	PRNPR
EOL	11164788
USDA GRIN	30077
Wikipedia	Prunus_prostrata
CMAUP	NPO10677

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

Pest categorisation of Didesmococcus unifasciatus

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A

EFSA J

20-Oct-2023

PMCID:	PMC10588555
doi:	10.2903/j.efsa.2023.8319
PMID:	37869254

Nutritional and mineral analysis of the ultimate wild food plants of Lotkuh, Chitral, the Eastern Hindukush Pakistan

Ullah H, Badshah L

Heliyon

11-Mar-2023

PMCID:	PMC10025152
doi:	10.1016/j.heliyon.2023.e14449
PMID:	36950657

Ethnobotanical survey of medicinal wild plants in the Shouf Biosphere Reserve, Lebanon

Hani N, Baydoun S, Nasser H, Ulian T, Arnold-Apostolides N

J Ethnobiol Ethnomed

26-Dec-2022

PMCID:	PMC9791969
doi:	10.1186/s13002-022-00568-y
PMID:	36572929

From Biodiversity to Musketry: Detection of Plant Diversity in Pre-Industrial Peloponnese during the Flora Graeca Expedition

Chimona C, Papadopoulou S, Kolyva F, Mina M, Rhizopoulou S

Life (Basel)

23-Nov-2022

PMCID:	PMC9785030
doi:	10.3390/life12121957
PMID:	36556322

About spirals and pores: Xylariaceae with remarkable germ loci

Voglmayr H, Tello S, Jaklitsch WM, Friebes G, Baral HO, Fournier J

Persoonia

13-Aug-2022

PMCID:	PMC10792227
doi:	10.3767/persoonia.2022.49.02
PMID:	38234381

Exploring the Potential of Chemical Inhibitors for Targeting Post-translational Glycosylation of Coronavirus (SARS-CoV-2)

Tripathi N, Goel B, Bhardwaj N, Vishwakarma RA, Jain SK

ACS Omega

28-Jul-2022

PMCID:	PMC9344791
doi:	10.1021/acsomega.2c02345
PMID:	35937682

Contribution to the Orophilous Cushion-Like Vegetation of Central-Southern and Insular Greece

Musarella CM, Brullo S, del Galdo GG

Plants (Basel)

30-Nov-2020

PMCID:	PMC7760968
doi:	10.3390/plants9121678
PMID:	33266088

Natural Products Database Screening for the Discovery of Naturally Occurring SARS‐Cov‐2 Spike Glycoprotein Blockers

Al‐Sehemi AG, Olotu FA, Dev S, Pannipara M, Soliman ME, Carradori S, Mathew B

ChemistrySelect

16-Nov-2020

PMCID:	PMC7753608
doi:	10.1002/slct.202003349
PMID:	33363254

A new functional JAZ degron sequence in strawberry JAZ1 revealed by structural and interaction studies on the COI1–JA-Ile/COR–JAZs complexes

Garrido-Bigotes A, Valenzuela-Riffo F, Torrejón M, Solano R, Morales-Quintana L, Figueroa CR

Sci Rep

09-Jul-2020

PMCID:	PMC7347570
doi:	10.1038/s41598-020-68213-w
PMID:	32647129

Modified CTAB and TRIzol protocols improve RNA extraction from chemically complex Embryophyta

Jordon-Thaden IE, Chanderbali AS, Gitzendanner MA, Soltis DE

Appl Plant Sci

13-May-2015

PMCID:	PMC4435465
doi:	10.3732/apps.1400105
PMID:	25995975

Two more new species of Aphidura (Hemiptera, Aphididae), and a note on variation in Aphidura bozhkoae Narzikulov

Nieto Nafría JM, Blackman RL, Martin JH

Zookeys

15-Jul-2014

PMCID:	PMC4137310
doi:	10.3897/zookeys.425.7797
PMID:	25147453

The genus Aphidura (Hemiptera, Aphididae) in the collection of the Muséum national d’Histoire naturelle of Paris, with six new species

Nieto Nafría JM, Mier Durante MP, Remaudière G

Zookeys

23-Jul-2013

PMCID:	PMC3744201
doi:	10.3897/zookeys.318.5693
PMID:	23950674

Chemical Constituents of<i>Prunus prostrata</i>

A. Bilia, C. Cecchini, G. Flamini, A. Marsili, I. Morelli

Georg Thieme Verlag KG

07-Nov-2008

doi:	10.1055/S-2006-961751

Coumarins and Other Constituents of Prunus prostrata

A. R. Bilia, C. Cecchini, A. Marsili, I. Morelli, S. Mele

American Chemical Society (ACS)

17-Mar-2005

doi:	10.1021/NP50102A017

Flavans and A-type proanthocyanidins from Prunus prostrata

A.R. Bilia, I. Morelli, M. Hamburger, K. Hostetmann

Elsevier BV

23-Apr-2003

doi:	10.1016/0031-9422(96)00291-9

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
dimethyl (2S,3R,4S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-2-hydroxy-4,6a,6b,11,11,14b-hexamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylate	101630395	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)OC)OC6C(C(C(C(O6)CO)O)O)O)O)C)C)C2C1)C)C(=O)OC)C	692.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,3R,4S,4aS,6aR,6bS,8aS,12aS,14aR,14bR)-2,3-dihydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylic acid	462205	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1)C)C(=O)O)C	502.70	unknown	via CMAUP database
(4aS,6aR,6aS,6bR,8aR,9S,10R,11S,12aR,14bR)-10,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	93492873	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C	488.70	unknown	via CMAUP database
Bayogenin	12305221	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C	488.70	unknown	via CMAUP database
Medicagenic acid	65048	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1)C)C(=O)O)C	502.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1021/NP50102A017
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1S,7abeta)-Hexahydro-2alpha-[(beta-D-glucopyranosyl)oxy]-3beta-(hydroxymethyl)-1H-pyrrolizine-1alpha,7alpha-diol	21576629	Click to see C1CN2C(C(C(C2C1O)O)OC3C(C(C(C(O3)CO)O)O)O)CO	351.35	unknown	via CMAUP database
[(8aalpha)-Octahydro-1beta,6alpha,7beta-trihydroxyindolizin]-8alpha-yl beta-D-glucopyranoside	10089286	Click to see C1CN2CC(C(C(C2C1O)OC3C(C(C(C(O3)CO)O)O)O)O)O	351.35	unknown	via CMAUP database
Benzyl-beta-d-glucopyranoside	13254166	Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O	270.28	unknown	https://doi.org/10.1021/NP50102A017
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3-(3-methylbut-2-enyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoic acid	12312708	Click to see CC(=CCC1=C(C=CC(=C1)C(=O)O)OC2C(C(C(C(O2)CO)O)O)O)C	368.40	unknown	https://doi.org/10.1021/NP50102A017
> Organoheterocyclic compounds / Indolizidines
6-epi-Castanospermine	184806	Click to see C1CN2CC(C(C(C2C1O)O)O)O	189.21	unknown	via CMAUP database
Castanospermine	54445	Click to see C1CN2CC(C(C(C2C1O)O)O)O	189.21	unknown	via CMAUP database
Rel-(1R,6R,7S,8S,8aS)-octahydroindolizine-1,6,7,8-tetraol	13959480	Click to see C1CN2CC(C(C(C2C1O)O)O)O	189.21	unknown	via CMAUP database
> Organoheterocyclic compounds / Piperidines
3-Epi-fagomine	10290867	Click to see C1CNC(C(C1O)O)CO	147.17	unknown	via CMAUP database
Fagomine	72259	Click to see C1CNC(C(C1O)O)CO	147.17	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines
2-Pyrrolidinemethanol, 3-hydroxy-, (2R,3S)-	11073391	Click to see C1CNC(C1O)CO	117.15	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrrolizidines
(1R,2S,3S,7R,8R)-3-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2,7-triol	21576628	Click to see C1CN2C(C(C(C2C1O)O)O)CO	189.21	unknown	via CMAUP database
(1R,2S,3S,7S,8R)-3-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2,7-triol	21576627	Click to see C1CN2C(C(C(C2C1O)O)O)CO	189.21	unknown	via CMAUP database
(1S,2R,3R,7S,7aR)-3-Hydroxymethyl-1,2,7-trihydroxypyrrolizidine	453575	Click to see C1CN2C(C(C(C2C1O)O)O)CO	189.21	unknown	via CMAUP database
(1S,2R,3R,7S,8S)-3-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2,7-triol	14164813	Click to see C1CN2C(C(C(C2C1O)O)O)CO	189.21	unknown	via CMAUP database
3-(Hydroxymethyl)-1,2,7-trihydroxypyrrolizidine	72360	Click to see C1CN2C(C(C(C2C1O)O)O)CO	189.21	unknown	via CMAUP database
3,7a-Diepialexine	189605	Click to see C1CN2C(C(C(C2C1O)O)O)CO	189.21	unknown	via CMAUP database
Australine	442628	Click to see C1CN2C(C(C(C2C1O)O)O)CO	189.21	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-Methoxycoumarin	10748	Click to see COC1=CC2=C(C=C1)C=CC(=O)O2	176.17	unknown	https://doi.org/10.1021/NP50102A017
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
7-hydroxy-5-methoxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one	163106714	Click to see COC1=C(C(=CC2=C1C=CC(=O)O2)O)OC3C(C(C(C(O3)CO)O)O)O	370.31	unknown	https://doi.org/10.1021/NP50102A017
7-hydroxy-6-methoxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one	5281418	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O	370.31	unknown	https://doi.org/10.1055/S-2006-961751
Fraxin	5273568	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O	370.31	unknown	https://doi.org/10.1055/S-2006-961751
Mandshurin	11740722	Click to see COC1=C(C(=C2C=CC(=O)OC2=C1)OC)OC3C(C(C(C(O3)CO)O)O)O	384.30	unknown	https://doi.org/10.1055/S-2006-961751 https://doi.org/10.1021/NP50102A017
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Fraxinol	3047739	Click to see COC1=C(C(=C2C=CC(=O)OC2=C1)OC)O	222.19	unknown	https://doi.org/10.1021/NP50102A017
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	https://doi.org/10.1021/NP50102A017
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1S,13R,21S)-5-(3,4-dihydroxyphenyl)-6,9,17,19,21-pentahydroxy-13-(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),5,9,15,17,19-heptaen-7-one	102062020	Click to see C1=CC(=CC=C1C23C(C(C4=C(C=C(C=C4O2)O)O)C5=C(O3)C=C(C6=C5OC(=C(C6=O)O)C7=CC(=C(C=C7)O)O)O)O)O	572.50	unknown	https://doi.org/10.1016/0031-9422(96)00291-9
(1S,5R,6R,13R,21S)-5-(3,4-dihydroxyphenyl)-13-(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol	101607497	Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC(=C(C=C7)O)O)O	560.50	unknown	https://doi.org/10.1016/0031-9422(96)00291-9
(1S,5S,6R,13R,21S)-5-(3,4-dihydroxyphenyl)-13-(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol	163037221	Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC(=C(C=C7)O)O)O	560.50	unknown	https://doi.org/10.1016/0031-9422(96)00291-9
(1S,5S,6R,13R,21S)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol	73353883	Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O	544.50	unknown	https://doi.org/10.1016/0031-9422(96)00291-9
(2S,2''S,3S,3''R,4S)-3,4',5,7-Tetrahydroxyflavan(2->7,4->8)-3,4',5,7-tetrahydroxyflavan	4023574	Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O	544.50	unknown	https://doi.org/10.1016/0031-9422(96)00291-9
5-(3,4-Dihydroxyphenyl)-6,9,17,19,21-pentahydroxy-13-(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),5,9,15,17,19-heptaen-7-one	162896156	Click to see C1=CC(=CC=C1C23C(C(C4=C(C=C(C=C4O2)O)O)C5=C(O3)C=C(C6=C5OC(=C(C6=O)O)C7=CC(=C(C=C7)O)O)O)O)O	572.50	unknown	https://doi.org/10.1016/0031-9422(96)00291-9
6,9,17,19,21-Pentahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),5,9,15,17,19-heptaen-7-one	73822574	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C4=C(C=C3O)OC5(C(C4C6=C(C=C(C=C6O5)O)O)O)C7=CC=C(C=C7)O)O)O	556.50	unknown	https://doi.org/10.1016/0031-9422(96)00291-9
Ephedrannin A	21676348	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C4=C(C=C3O)OC5(C(C4C6=C(C=C(C=C6O5)O)O)O)C7=CC=C(C=C7)O)O)O	556.50	unknown	https://doi.org/10.1016/0031-9422(96)00291-9
Mahuannin A	5317052	Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O	544.50	unknown	https://doi.org/10.1016/0031-9422(96)00291-9
Prunus inhibitor b	14586216	Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC(=C(C=C7)O)O)O	560.50	unknown	https://doi.org/10.1016/0031-9422(96)00291-9
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol	1203	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1016/0031-9422(96)00291-9
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1016/0031-9422(96)00291-9
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
(2S,3S)-2-(2,5-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol	162892885	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=C(C=CC(=C3)O)O)O	290.27	unknown	https://doi.org/10.1016/0031-9422(96)00291-9
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one	662	Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	288.25	unknown	https://doi.org/10.1021/NP50102A017
Aromadendrin	122850	Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	288.25	unknown	https://doi.org/10.1021/NP50102A017
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	https://doi.org/10.1021/NP50102A017
> 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/10.1021/NP50102A017
> 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	https://doi.org/10.1021/NP50102A017
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R,3R)-2-(2,5-dihydroxyphenyl)-7-methoxy-3,4-dihydro-2H-chromene-3,5-diol	162882069	Click to see COC1=CC(=C2CC(C(OC2=C1)C3=C(C=CC(=C3)O)O)O)O	304.29	unknown	https://doi.org/10.1016/0031-9422(96)00291-9
2-(2,5-dihydroxyphenyl)-7-methoxy-3,4-dihydro-2H-chromene-3,5-diol	162882068	Click to see COC1=CC(=C2CC(C(OC2=C1)C3=C(C=CC(=C3)O)O)O)O	304.29	unknown	https://doi.org/10.1016/0031-9422(96)00291-9
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
2'-Methoxy-3',4',7-trihydroxyisoflavone	101785462	Click to see COC1=C(C=CC(=C1O)O)C2=COC3=C(C2=O)C=CC(=C3)O	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Koparin	5318834	Click to see COC1=C(C(=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O)O	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Afrormosin	5281704	Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)O	298.29	unknown	via CMAUP database

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Prunus prostrata

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