Scientific name	Authority	First published in
Globularia adolphi	Sennen	Bol. Soc. Ibér. Ci. Nat. 35: 25 (1936)
Globularia bolosii	Sennen	Bol. Soc. Aragonesa Ci. Nat. 11: 238 (1912)
Globularia caespitosa	Ortega ex A.DC.	Prodr. 12: 612 (1848)
Globularia cambessedesii subsp. hispanica	Willk.	Suppl. Prodr. Fl. Hispan. : 141 (1893)
Globularia castellana	Sennen	Bull. Acad. Int. Géogr. Bot. 21: 123 (1911)
Globularia multicaulis	Ten. ex Nyman	Consp. Fl. Eur. : 608 (1881)
Globularia pungens	Pourr. ex Willk. & Lange	Prodr. Fl. Hispan. 2: 384 (1865)
Globularia linifolia subsp. hispanica	(Willk.) M.B.Crespo & Mateo	Fl. Montiberica 45: 92 (2010)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Arabic	تاسلغي
Czech	koulenka prodloužená
Chinese	斑点地团花

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

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

Asia-temperate click to expand
- Caucasus
  - North Caucasus
- Middle Asia
  - Kazakhstan

Europe click to expand
- Eastern Europe
  - Central European Russia
  - East European Russia
  - South European Russia
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Switzerland
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Corse
  - France
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000703801
Tropicos	14200006
INPN	100338
Flora of Italy	5075
KEW	urn:lsid:ipni.org:names:813058-1
Missouri Botanical Garden	299836
Open Tree Of Life	7053916
Observations.org	70097
NCBI Taxonomy	2078961
IPNI	813058-1
iNaturalist	355374
GBIF	5578472
Wikipedia	Globularia_bisnagarica

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

Recent evolution of flowering time across multiple European plant species correlates with changes in aridity

Rauschkolb R, Durka W, Godefroid S, Dixon L, Bossdorf O, Ensslin A, Scheepens JF

Oecologia

18-Jul-2023

PMCID:	PMC10386928
doi:	10.1007/s00442-023-05414-w
PMID:	37462737

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

Breaking the silence of the 500-year-old smiling garden of everlasting flowers: The En Tibi book herbarium

Stefanaki A, Porck H, Grimaldi IM, Thurn N, Pugliano V, Kardinaal A, Salemink J, Thijsse G, Chavannes-Mazel C, Kwakkel E, van Andel T

PLoS One

26-Jun-2019

PMCID:	PMC6594601
doi:	10.1371/journal.pone.0217779
PMID:	31242215

Dormancy and endosperm presence influence the ex situ conservation potential in central European calcareous grassland plants

Tausch S, Leipold M, Reisch C, Poschlod P

AoB Plants

25-Jun-2019

PMCID:	PMC6735842
doi:	10.1093/aobpla/plz035
PMID:	31528324

Long-term survival and successful conservation? Low genetic diversity but no evidence for reduced reproductive success at the north-westernmost range edge of Poa badensis (Poaceae) in Central Europe

Plenk K, Bardy K, Höhn M, Kropf M

Biodivers Conserv

27-Feb-2019

PMCID:	PMC6399750
doi:	10.1007/s10531-019-01722-x
PMID:	30906115

A higher‐level classification of the Pannonian and western Pontic steppe grasslands (Central and Eastern Europe)

Willner W, Kuzemko A, Dengler J, Chytrý M, Bauer N, Becker T, Biţă‐Nicolae C, Botta‐Dukát Z, Čarni A, Csiky J, Igić R, Kącki Z, Korotchenko I, Kropf M, Krstivojević‐Ćuk M, Krstonošić D, Rédei T, Ruprecht E, Schratt‐Ehrendorfer L, Semenishchenkov Y, Stančić Z, Vashenyak Y, Vynokurov D, Janišová M

Appl Veg Sci

16-Sep-2016

PMCID:	PMC5348766
doi:	10.1111/avsc.12265
PMID:	28356815

Genetic diversity of natural orchardgrass (Dactylis glomerata L.) populations in three regions in Europe

Last L, Widmer F, Fjellstad W, Stoyanova S, Kölliker R

BMC Genet

29-Oct-2013

PMCID:	PMC4231346
doi:	10.1186/1471-2156-14-102
PMID:	24165514

ChemInform Abstract: Flavonoid, Phenylethanoid and Iridoid Glycosides from Globularia aphyllanthes

Hasan Kirmizibekmez, Carla Bassarello, Sonia Piacente, Galip Akaydin, Ihsan Calis

Wiley

15-Jun-2009

doi:	10.1002/CHIN.200927180

Random Distribution Pattern and Non-adaptivity of Genome Size in a Highly Variable Population of Festuca pallens

Šmarda P, Bureš P, Horová L

Ann Bot

12-Jun-2007

PMCID:	PMC2735304
doi:	10.1093/aob/mcm095
PMID:	17565968

Acylated 6-hydroxyluteolin diglucosides from Globularia elongata

Barbara Klimek

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(88)80626-5

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 / Monoterpenoids / Bicyclic monoterpenoids
(2S)-2-[(3E)-4,8-dimethylnona-3,7-dienyl]-2,8-dimethyl-3,4-dihydrochromen-6-ol	163194297	Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)C)O	328.50	unknown	https://doi.org/10.1002/CHIN.200927180
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
2-[[5-Hydroxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	348157	Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O	346.33	unknown	https://doi.org/10.1002/CHIN.200927180
7-(Acetyloxymethyl)-5-hydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid	13935238	Click to see CC(=O)OCC1=CC(C2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O	432.40	unknown	https://doi.org/10.1002/CHIN.200927180
Asperulosidic acid	11968867	Click to see CC(=O)OCC1=CC(C2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O	432.40	unknown	https://doi.org/10.1002/CHIN.200927180
Aucubin	91458	Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O	346.33	unknown	https://doi.org/10.1002/CHIN.200927180
Daphylloside	21602024	Click to see CC(=O)OCC1=CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O	446.40	unknown	https://doi.org/10.1002/CHIN.200927180
Desacetyl asperulosidic acid	12315348	Click to see C1=C(C2C(C1O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO	390.34	unknown	https://doi.org/10.1002/CHIN.200927180
Methyl 7-(acetyloxymethyl)-5-hydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate	12309039	Click to see CC(=O)OCC1=CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O	446.40	unknown	https://doi.org/10.1002/CHIN.200927180
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1S,4aS)-7-(acetyloxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6-tetrahydrocyclopenta[c]pyran-4-carboxylic acid	21592389	Click to see CC(=O)OCC1=C2C(CC1)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O	416.40	unknown	https://doi.org/10.1002/CHIN.200927180
[(1aS)-1abeta-[(Benzoyloxy)methyl]-6alpha-hydroxy-1a,1balpha,2,5aalpha,6,6abeta-hexahydrooxireno[4,5]cyclopenta[1,2-c]pyran-2alpha-yl]beta-D-glucopyranoside	23846544	Click to see C1=CC=C(C=C1)C(=O)OCC23C4C(C=COC4OC5C(C(C(C(O5)CO)O)O)O)C(C2O3)O	466.40	unknown	https://doi.org/10.1002/CHIN.200927180
[2-Oxo-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[5.3.1.04,11]undeca-1(10),5-dien-6-yl]methyl benzoate	162987652	Click to see C1=CC=C(C=C1)C(=O)OCC2=CC3C4C2C(OC=C4C(=O)O3)OC5C(C(C(C(O5)CO)O)O)O	476.40	unknown	https://doi.org/10.1002/CHIN.200927180
[5-(hexopyranosyloxy)-1-oxo-2a,4a,5,7b-tetrahydro-1H-2,6-dioxacyclopenta[cd]inden-4-yl]methyl acetate	233330	Click to see CC(=O)OCC1=CC2C3C1C(OC=C3C(=O)O2)OC4C(C(C(C(O4)CO)O)O)O	414.40	unknown	https://doi.org/10.1002/CHIN.200927180
[5-Hydroxy-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-2-yl]methyl 3-phenylprop-2-enoate	151789	Click to see C1=CC=C(C=C1)C=CC(=O)OCC23C4C(C=COC4OC5C(C(C(C(O5)CO)O)O)O)C(C2O3)O	492.50	unknown	https://doi.org/10.1002/CHIN.200927180
[5-Hydroxy-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-2-yl]methyl benzoate	74192690	Click to see C1=CC=C(C=C1)C(=O)OCC23C4C(C=COC4OC5C(C(C(C(O5)CO)O)O)O)C(C2O3)O	466.40	unknown	https://doi.org/10.1002/CHIN.200927180
2-[[5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	3917786	Click to see C1=COC(C2C1C(C3C2(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O	362.33	unknown	https://doi.org/10.1002/CHIN.200927180
7-(Acetyloxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6-tetrahydrocyclopenta[c]pyran-4-carboxylic acid	73809347	Click to see CC(=O)OCC1=C2C(CC1)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O	416.40	unknown	https://doi.org/10.1002/CHIN.200927180
Asperuloside	84298	Click to see CC(=O)OCC1=CC2C3C1C(OC=C3C(=O)O2)OC4C(C(C(C(O4)CO)O)O)O	414.40	unknown	https://doi.org/10.1002/CHIN.200927180
Besperuloside	101390414	Click to see C1=CC=C(C=C1)C(=O)OCC2=CC3C4C2C(OC=C4C(=O)O3)OC5C(C(C(C(O5)CO)O)O)O	476.40	unknown	https://doi.org/10.1002/CHIN.200927180
Catalpol	91520	Click to see C1=COC(C2C1C(C3C2(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O	362.33	unknown	https://doi.org/10.1002/CHIN.200927180
Globularin	21603201	Click to see C1=CC=C(C=C1)C=CC(=O)OCC23C4C(C=COC4OC5C(C(C(C(O5)CO)O)O)O)C(C2O3)O	492.50	unknown	https://doi.org/10.1002/CHIN.200927180
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[4-[3,4-Dihydroxy-6-methyl-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate	85220730	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)OC5C(C(C(CO5)O)O)O	756.70	unknown	https://doi.org/10.1002/CHIN.200927180
[4-[3,4-Dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate	162956870	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O	786.70	unknown	https://doi.org/10.1002/CHIN.200927180
Rossicaside	13916145	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O	786.70	unknown	https://doi.org/10.1002/CHIN.200927180
Trichosanthoside A	10652682	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)OC5C(C(C(CO5)O)O)O	756.70	unknown	https://doi.org/10.1002/CHIN.200927180
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Acteoside;Kusaginin;TJC160	354009	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1002/CHIN.200927180
Verbascoside	5281800	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1002/CHIN.200927180
> Phenylpropanoids and polyketides / Flavonoids / Flavones
6-Hydroxyluteolin	5281642	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O)O)O	302.23	unknown	https://doi.org/10.1016/0031-9422(88)80626-5
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1016/0031-9422(88)80626-5
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	https://doi.org/10.1016/0031-9422(88)80626-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[5-(1,2-Dihydroxyethyl)-3,4-dihydroxyoxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	13179952	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)C(CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1002/CHIN.200927180
Isoquercitrin	5484006	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)C(CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1002/CHIN.200927180
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	13942686	Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)OC3C(C(C(OC3OC4=C(C(=C5C(=C4)OC(=CC5=O)C6=CC(=C(C=C6)O)O)O)O)CO)O)O)O)O)O)O)O	788.70	unknown	https://doi.org/10.1016/0031-9422(88)80626-5 https://doi.org/10.1002/CHIN.200927180
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate	13942688	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3C(C(C(OC3OC4=C(C(=C5C(=C4)OC(=CC5=O)C6=CC(=C(C=C6)O)O)O)O)CO)O)O)O)O)O)O	772.70	unknown	https://doi.org/10.1016/0031-9422(88)80626-5
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl benzoate	102285489	Click to see C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC3C(C(C(OC3OC4=C(C(=C5C(=C4)OC(=CC5=O)C6=CC(=C(C=C6)O)O)O)O)CO)O)O)O)O)O	730.60	unknown	https://doi.org/10.1002/CHIN.200927180
[6-[2-[2-(3,4-Dihydroxyphenyl)-5,6-dihydroxy-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate	74977874	Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)OC3C(C(C(OC3OC4=C(C(=C5C(=C4)OC(=CC5=O)C6=CC(=C(C=C6)O)O)O)O)CO)O)O)O)O)O)O)O	788.70	unknown	https://doi.org/10.1016/0031-9422(88)80626-5 https://doi.org/10.1002/CHIN.200927180
[6-[2-[2-(3,4-Dihydroxyphenyl)-5,6-dihydroxy-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate	74977873	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3C(C(C(OC3OC4=C(C(=C5C(=C4)OC(=CC5=O)C6=CC(=C(C=C6)O)O)O)O)CO)O)O)O)O)O)O	772.70	unknown	https://doi.org/10.1016/0031-9422(88)80626-5
[6-[2-[2-(3,4-Dihydroxyphenyl)-5,6-dihydroxy-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl benzoate	162970632	Click to see C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC3C(C(C(OC3OC4=C(C(=C5C(=C4)OC(=CC5=O)C6=CC(=C(C=C6)O)O)O)O)CO)O)O)O)O)O	730.60	unknown	https://doi.org/10.1002/CHIN.200927180
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-2-(3,4-dihydroxyphenyl)-5,6-dihydroxychromen-4-one	13942682	Click to see C1=CC(=C(C=C1C2=CC(=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)O	626.50	unknown	https://doi.org/10.1016/0031-9422(88)80626-5
7-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,6-dihydroxychromen-4-one	11657403	Click to see C1=CC(=C(C=C1C2=CC(=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)O	626.50	unknown	https://doi.org/10.1016/0031-9422(88)80626-5

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.

Globularia bisnagarica

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