Scientific name	Authority	First published in
Geranium aconitifolium var. album	B.Ghosh & U.C.Bhattach.	J. Econ. Taxon. Bot. 10: 312 (1987 publ. 1988)
Geranium acutilobum	Coincy	J. Bot. (Morot) 12: 56 (1898)
Geranium collinum var. londesii	(Fisch. ex Link) Tzvelev	Fl. Vostochnoi Evropy 9: 378 (1996)
Geranium collinum var. wakhanicum	Paulsen	Bot. Tidsskr. 27: 133 1906
Geranium exul	Rech.f. & Riedl	Ann. Naturhist. Mus. Wien 65: 32 (1962)
Geranium humifusum	R.Knuth & R.Knuth	Jahresber. Schles. Ges. Vaterl. Cult. 81(2): 16 (1904)
Geranium londesii	Fisch. ex Link	Enum. Hort. Berol. Alt. 2: 196 (1822)
Geranium longipedatum	St.-Lag.	Ann. Soc. Bot. Lyon 7: 126 (1880)
Geranium longipes	DC.	Mém. Soc. Phys. Genève 1: 442 (1822)
Geranium minutum	Ikonn.	Opred. Vyssh. Rast. Badakhshana : 243 (1979)
Geranium pseudoaconitifolium	Blatt.	J. Bombay Nat. Hist. Soc. 36: 956 (1933)
Geranium pseudoaconitifolium var. album	(B.Ghosh & U.C.Bhattach.) Aswal & Mehrotra	Indian J. Forest. 13: 66 (1990)
Geranium wakhanicum	(Pauls.) Ikonn.	Novosti Sist. Vyssh. Rast. 8: 275 (1971)
Geranium collinum var. eglandulosum	Ledeb.	Fl. Ross. 1: 467 1842

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	hill geranium
Belarusian	герань узгоркавая
Armenian	Խորդենի բլրային
Russian	Герань ваханская
Russian	Герань холмовая
tg	Анҷибари тал
Uzbek	anjabor
Chinese	丘陵老鹳草

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 directly at 4°C.

Requires Darkness: These seeds need to be covered with soil or otherwise kept in the dark to germinate properly. Light inhibits their germination process.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - Xinjiang
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Mongolia
  - Mongolia
- Siberia
  - Altay
  - West Siberia
- Western Asia
  - Afghanistan
  - Iran
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Nepal
  - Pakistan
  - West Himalaya

Europe click to expand
- Eastern Europe
  - Belarus
  - Central European Russia
  - East European Russia
  - Krym
  - South European Russia
  - Ukraine
- Southeastern Europe
  - Romania
- Southwestern Europe
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000700259
Tropicos	13900731
KEW	urn:lsid:ipni.org:names:372909-1
The Plant List	kew-2823065
Plantarium	17465
Open Tree Of Life	3942131
Observations.org	118267
NCBI Taxonomy	1368250
NBN Atlas	NBNSYS0200002232
IPNI	372909-1
iNaturalist	486931
GBIF	2891237
EPPO	GERCL
EOL	130339
Elurikkus	325728
USDA GRIN	419399
CMAUP	NPO3521

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

Nutrient addition alters plant community productivity but not the species diversity of a mountain meadow in Tajikistan

Mekhrovar O, Li YM, Abdullo M, Sino Y, Fan L

Front Plant Sci

15-Jan-2024

PMCID:	PMC10822985
doi:	10.3389/fpls.2023.1235388
PMID:	38288411

Children in All Policies (CAP) 2030 Citizen Science for Climate Change Resilience: a cross-sectional pilot study engaging adolescents to study climate hazards, biodiversity and nutrition in rural Nepal

Hoernke K, Shrestha A, Pokhrel B, Timberlake T, Giri S, Sapkota S, Dalglish S, Costello A, Saville N

Wellcome Open Res

11-Dec-2023

PMCID:	PMC10904941
doi:	10.12688/wellcomeopenres.18591.1
PMID:	38434744

The transfer of 137Cs and heavy metals to tissues within the organs of snails

Baigazinov Z, Lukashenko S, Silybayeva B, Zharykbasova K, Bukabayeva Z, Muhamediarov N, Kantbayeva B, Kozhakhmetova B, Ganbaatar T, Toth-Bodrogi E, Hegedus M, Kovacs T

Sci Rep

21-Sep-2023

PMCID:	PMC10514058
doi:	10.1038/s41598-023-42580-6
PMID:	37735228

Approaches to Decrease Hyperglycemia by Targeting Impaired Hepatic Glucose Homeostasis Using Medicinal Plants

Mata-Torres G, Andrade-Cetto A, Espinoza-Hernández F

Front Pharmacol

23-Dec-2021

PMCID:	PMC8733686
doi:	10.3389/fphar.2021.809994
PMID:	35002743

In Silico Approaches to Identify Polyphenol Compounds as α-Glucosidase and α-Amylase Inhibitors against Type-II Diabetes

Riyaphan J, Pham DC, Leong MK, Weng CF

Biomolecules

14-Dec-2021

PMCID:	PMC8699780
doi:	10.3390/biom11121877
PMID:	34944521

Kursi Wufarikun Ziyabit Improves the Physiological Changes by Regulating Endoplasmic Reticulum Stress in the Type 2 Diabetes db/db Mice

Edirs S, Jiang L, Xin X, Aisa HA

Evid Based Complement Alternat Med

16-Aug-2021

PMCID:	PMC8384507
doi:	10.1155/2021/2100128
PMID:	34447452

The transfer of 241Am and 137Cs to the tissues of broilers’ organs

Mamyrbayeva AS, Baigazinov ZA, Lukashenko SN, Panitskiy AV, Karatayev SS, Shatrov AN, Baigazy SA, Bazarbayeva AB, Hegedűs M, Tóth-Bodrogi E, Kovács T

PLoS One

01-Jul-2020

PMCID:	PMC7329069
doi:	10.1371/journal.pone.0235109
PMID:	32609724

In silico analysis of antidiabetic potential of phenolic compounds from blue corn (Zea mays L.) and black bean (Phaseolus vulgaris L.)

Damián-Medina K, Salinas-Moreno Y, Milenkovic D, Figueroa-Yáñez L, Marino-Marmolejo E, Higuera-Ciapara I, Vallejo-Cardona A, Lugo-Cervantes E

Heliyon

27-Mar-2020

PMCID:	PMC7110303
doi:	10.1016/j.heliyon.2020.e03632
PMID:	32258479

Exploring the inhibitory mechanism of piceatannol on α-glucosidase relevant to diabetes mellitus

Jiang L, Wang Z, Wang X, Wang S, Cao J, Liu Y

RSC Adv

29-Jan-2020

PMCID:	PMC9049079
doi:	10.1039/c9ra09028b
PMID:	35495253

Crop wild relatives of Kazakhstani Tien Shan: Flora, vegetation, resources

Sitpayeva GT, Kudabayevа GM, Dimeyeva LA, Gemejiyeva NG, Vesselova PV

Plant Divers

31-Oct-2019

PMCID:	PMC7046504
doi:	10.1016/j.pld.2019.10.003
PMID:	32140634

Plant diversity of the Kangchenjunga Landscape, Eastern Himalayas

Kandel P, Chettri N, Chaudhary RP, Badola HK, Gaira KS, Wangchuk S, Bidha N, Uprety Y, Sharma E

Plant Divers

26-Apr-2019

PMCID:	PMC6702437
doi:	10.1016/j.pld.2019.04.006
PMID:	31453415

Phylogenetic study of the endemic species Oxytropis almaatensis (Fabaceae) based on nuclear ribosomal DNA ITS sequences

Almerekova S, Mukhitdinov N, Abugalieva S

BMC Plant Biol

14-Nov-2017

PMCID:	PMC5688500
doi:	10.1186/s12870-017-1128-x
PMID:	29143653

An NMR-Based Metabolomic Approach to Unravel the Preventive Effect of Water-Soluble Extract from Dendrobium officinale Kimura & Migo on Streptozotocin-Induced Diabetes in Mice

Zheng H, Pan L, Xu P, Zhu J, Wang R, Zhu W, Hu Y, Gao H

Molecules

15-Sep-2017

PMCID:	PMC6151757
doi:	10.3390/molecules22091543
PMID:	28914810

Evaluation of the Antidiabetic Activity and Chemical Composition of Geranium collinum Root Extracts—Computational and Experimental Investigations

Numonov S, Edirs S, Bobakulov K, Qureshi MN, Bozorov K, Sharopov F, Setzer WN, Zhao H, Habasi M, Sharofova M, Aisa HA

Molecules

13-Jun-2017

PMCID:	PMC6152703
doi:	10.3390/molecules22060983
PMID:	28608836

Optimization of Extraction Process for Antidiabetic and Antioxidant Activities of Kursi Wufarikun Ziyabit Using Response Surface Methodology and Quantitative Analysis of Main Components

Edirs S, Turak A, Numonov S, Xin X, Aisa HA

Evid Based Complement Alternat Med

17-May-2017

PMCID:	PMC5450171
doi:	10.1155/2017/6761719
PMID:	28596795

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
> Alkaloids and derivatives / Aporphines
(-)-Isoboldine	6971182	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC	327.40	unknown	via CMAUP database
Isoboldine	133323	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC	327.40	unknown	via CMAUP database
> Alkaloids and derivatives / Pavine alkaloids
(-)-Argemonine	442168	Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)OC)OC)OC)OC	355.40	unknown	via CMAUP database
(+)-Caryachine	12305286	Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O	325.40	unknown	via CMAUP database
(1R,12R)-16-Methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-15-ol	3082467	Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4	325.40	unknown	via CMAUP database
(1R,12S)-15,16-dimethoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-1-ol	10948236	Click to see CN1C2CC3=CC4=C(C=C3C1(CC5=CC(=C(C=C25)OC)OC)O)OCO4	355.40	unknown	via CMAUP database
(1R,12S)-23-methyl-5,7,16,18-tetraoxa-23-azahexacyclo[10.10.1.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaen-1-ol	11110561	Click to see CN1C2CC3=CC4=C(C=C3C1(CC5=CC6=C(C=C25)OCO6)O)OCO4	339.30	unknown	via CMAUP database
(1R,9R)-5,12-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10,12,14-hexaene-4,13-diol	11869664	Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)O	327.40	unknown	via CMAUP database
(1S,12S,20R)-15-methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol	102304441	Click to see C[N+]1(C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O)[O-]	341.40	unknown	via CMAUP database
(1S,12S,20R)-16-methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-15-ol	102304443	Click to see C[N+]1(C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4)[O-]	341.40	unknown	via CMAUP database
(1S,12S)-15-methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol	11823545	Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O	325.40	unknown	via CMAUP database
(1S,12S)-5,7,16,18-tetraoxa-23-azahexacyclo[10.10.1.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaene	11012304	Click to see C1C2C3=CC4=C(C=C3CC(N2)C5=CC6=C(C=C51)OCO6)OCO4	309.30	unknown	via CMAUP database
(1S,9S)-4,13-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2(7),3,5,10,12,14-hexaene-3,12-diol	92856799	Click to see CN1C2CC3=C(C1CC4=CC(=C(C=C24)O)OC)C(=C(C=C3)OC)O	327.40	unknown	via CMAUP database
(1S,9S)-5,12-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10,12,14-hexaene-4,13-diol	12300156	Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)O	327.40	unknown	via CMAUP database
Caryachine	44575219	Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4	325.40	unknown	via CMAUP database
Crychine	193382	Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC6=C(C=C25)OCO6)OCO4	323.30	unknown	via CMAUP database
Escholtzine	12304178	Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC6=C(C=C25)OCO6)OCO4	323.30	unknown	via CMAUP database
> Alkaloids and derivatives / Proaporphines
(+)-8,9-Dihydrostepharine	13819281	Click to see COC1=C(C2=C3C(CC24CCC(=O)C=C4)NCCC3=C1)OC	299.40	unknown	via CMAUP database
(1'S,2S,4R)-10-methoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1',11-diol	10870351	Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(C=C4)O)O)OC	301.40	unknown	via CMAUP database
Isoamuronine	12306127	Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(=O)C=C4)OC)OC	313.40	unknown	via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Berberine	2353	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC	336.40	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
3,4-Dihydroxy-5-methoxybenzoic acid	19829	Click to see COC1=CC(=CC(=C1O)O)C(=O)O	184.15	unknown	https://doi.org/10.1007/BF00567786
> 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/10.1007/BF00567786
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
alpha-Tocopherolquinone	2734086	Click to see CC1=C(C(=O)C(=C(C1=O)C)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O)C	446.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene	638072	Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C	410.70	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Cryptocaryone	10379026	Click to see C1C2C(C=CC(=O)C2=C(C=CC3=CC=CC=C3)O)OC1=O	282.29	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives
6-Methyl-[1,3]dioxolo[4,5-g]isoquinolin-6-ium	2753983	Click to see C[N+]1=CC2=CC3=C(C=C2C=C1)OCO3	188.20	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
4-(6,7-Dimethoxyisoquinoline-1-ylmethyl)phenol	21814573	Click to see COC1=C(C=C2C(=C1)C=CN=C2CC3=CC=C(C=C3)O)OC	295.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
Doryanin	12998814	Click to see CN1C=CC2=CC3=C(C=C2C1=O)OCO3	203.19	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
7-O-Methylcryptochinone A	46939685	Click to see COC1CC2=C(C3C1OC(=O)C3)C(=O)CC(O2)C4=CC=CC=C4	314.30	unknown	via CMAUP database
Cryptocaryanone A	10356404	Click to see C1C2C(C=CC3=C2C(=O)CC(O3)C4=CC=CC=C4)OC1=O	282.29	unknown	via CMAUP database
Cryptochinone A	46939683	Click to see C1C2C(C(CC3=C2C(=O)CC(O3)C4=CC=CC=C4)O)OC1=O	300.30	unknown	via CMAUP database
Cryptochinone B	46939684	Click to see C1C2C(C(CC3=C2C(=O)CC(O3)C4=CC=CC=C4)O)OC1=O	300.30	unknown	via CMAUP database
Cryptochinone D	46939686	Click to see COC1CC2=C(C3C1OC(=O)C3)C(=O)CC(O2)C4=CC=CC=C4	314.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(1'S,2R,4R)-10,11-dimethoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,6'-cyclohex-2-ene]-1'-ol	10914050	Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC=CC4O)OC)OC	315.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Hexacosyl (E)-ferulate	5318033	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC	558.90	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-7-hydroxyflavanone	688857	Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3	240.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(-)-Epitaxifolin	712318	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 / Flavonols
3,7,8,4'-Tetrahydroxyflavone	22239065	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3)O)O)O)O	286.24	unknown	https://doi.org/10.1007/BF00567786
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/10.1007/BF00567786
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	54579866	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/10.1007/BF00569822
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5378597	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1007/BF00569822
3-(beta-D-Arabinopyranosyloxy)-5,7-dihydroxy-2-(3,4-dihydroxyphenyl)-4H-1-benzopyran-4-one	21722017	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)O	434.30	unknown	https://doi.org/10.1007/BF00569822
Isoquercitin	10813969	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1007/BF00569822
Reynoutrin	5878729	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)O	434.30	unknown	https://doi.org/10.1007/BF00569822
Vitamin P	5293655	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/10.1007/BF00569822
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4H-1-Benzopyran-4-one, 5-hydroxy-3,7-dimethoxy-2-phenyl-	5748697	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=CC=C3)O	298.29	unknown	via CMAUP database
5-Hydroxy-7-methoxy-2-phenylchroman-4-one	73201	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O	270.28	unknown	via CMAUP database
Mosloflavone	471722	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O)OC	298.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Hydroxy-3,7,8-trimethoxyflavone	21632881	Click to see COC1=C(C2=C(C(=C1)O)C(=O)C(=C(O2)C3=CC=CC=C3)OC)OC	328.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Larrein	9993268	Click to see COC1=C(C=CC(=C1O)C(=O)C=CC2=CC=CC=C2)O	270.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-12-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate	5153915	Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O	786.60	unknown	https://doi.org/10.1007/BF00564295
1-Desgalloyleugeniin	9918701	Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O	786.60	unknown	https://doi.org/10.1007/BF00564295
Ellagic Acid	5281855	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O	302.19	unknown	https://doi.org/10.1007/BF00567786

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.

Geranium collinum

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