Glycyrrhiza pallidiflora

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Internal ID	UUID643fd98a0677c960651929
Scientific name	Glycyrrhiza pallidiflora
Authority	Maxim.
First published in	Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans9: 97 (1859)

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The article discusses the plant Glycyrrhiza pallidiflora, a member of the bean family Fabaceae and closely related to liquorice. It is a perennial herb found in East Asia, specifically in Mongolia, Manchuria, and parts of China. The taxonomy of the plant was described by Maxim in 1859. The article also includes information about the plant's distribution and its classification within the Fabaceae family. The code for the plant's appearance on the website is also provided, including a specific theme for night mode.

Synonyms Top

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Common names Top

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Language	Common/alternative name
Arabic	عرقسوس شاحب الأزهار
Chinese	刺果甘草
Chinese	狗甘草
Chinese	狗甘草根
Chinese	胡苍耳
Chinese	马狼柴
Chinese	马狼秆

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
  - Inner Mongolia
  - Manchuria
- Eastern Asia
  - Korea
- Mongolia
  - Mongolia
- Russian Far East
  - Khabarovsk
  - Primorye

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000186030
Tropicos	13019872
KEW	urn:lsid:ipni.org:names:496965-1
The Plant List	ild-32409
Open Tree Of Life	629594
Observations.org	137285
NCBI Taxonomy	74859
IPNI	496965-1
GBIF	2965741
EOL	643699
Elurikkus	342973
USDA GRIN	413348
CMAUP	NPO15413
Wikipedia	Glycyrrhiza_pallidiflora

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

Comparative genomics and phylogenomics of the genus Glycyrrhiza (Fabaceae) based on chloroplast genomes

Wu L, Fan P, Cai J, Zang C, Lin Y, Xu Z, Wu Z, Gao W, Song J, Yao H

Front Pharmacol

07-Mar-2024

PMCID:	PMC10955637
doi:	10.3389/fphar.2024.1371390
PMID:	38515836

Dirigent isoflavene-forming PsPTS2: 3D structure, stereochemical, and kinetic characterization comparison with pterocarpan-forming PsPTS1 homolog in pea

Meng Q, Moinuddin SG, Celoy RM, Smith CA, Young RP, Costa MA, Freeman RA, Fukaya M, Kim DN, Cort JR, Hawes MC, van Etten HD, Pandey P, Chittiboyina AG, Ferreira D, Davin LB, Lewis NG

J Biol Chem

14-Jan-2024

PMCID:	PMC10882141
doi:	10.1016/j.jbc.2024.105647
PMID:	38219818

Implementation of machine learning in DNA barcoding for determining the plant family taxonomy

Riza LS, Zain MI, Izzuddin A, Prasetyo Y, Hidayat T, Abu Samah KA

Heliyon

21-Sep-2023

PMCID:	PMC10520734
doi:	10.1016/j.heliyon.2023.e20161
PMID:	37767518

Liquorice Toxicity: A Comprehensive Narrative Review

Ceccuzzi G, Rapino A, Perna B, Costanzini A, Farinelli A, Fiorica I, Marziani B, Cianci A, Rossin F, Cesaro AE, Spampinato MD, De Giorgio R, Guarino M

Nutrients

05-Sep-2023

PMCID:	PMC10537237
doi:	10.3390/nu15183866
PMID:	37764649

Sustainable Applications of Endophytic Bacteria and Their Physiological/Biochemical Roles on Medicinal and Herbal Plants: Review

Tshikhudo PP, Ntushelo K, Mudau FN

Microorganisms

10-Feb-2023

PMCID:	PMC9967847
doi:	10.3390/microorganisms11020453
PMID:	36838418

Novel Mango Ginger Bioactive (2,4,6-Trihydroxy-3,5-diprenyldihydrochalcone) Inhibits Mitochondrial Metabolism in Combination with Avocatin B

Jayasankar V, Vrdoljak N, Roma A, Ahmed N, Tcheng M, Minden MD, Spagnuolo PA

ACS Omega

07-Jan-2022

PMCID:	PMC8771686
doi:	10.1021/acsomega.1c04053
PMID:	35071863

Glycyrrhiza Genus: Enlightening Phytochemical Components for Pharmacological and Health-Promoting Abilities

Sharifi-Rad J, Quispe C, Herrera-Bravo J, Belén LH, Kaur R, Kregiel D, Uprety Y, Beyatli A, Yeskaliyeva B, Kırkın C, Özçelik B, Sen S, Acharya K, Sharopov F, Cruz-Martins N, Kumar M, Razis AF, Sunusi U, Kamal RM, Shaheen S, Suleria HA

Oxid Med Cell Longev

24-Jul-2021

PMCID:	PMC8328722
doi:	10.1155/2021/7571132
PMID:	34349875

Molecular Basis of C-30 Product Regioselectivity of Legume Oxidases Involved in High-Value Triterpenoid Biosynthesis

Fanani MZ, Fukushima EO, Sawai S, Tang J, Ishimori M, Sudo H, Ohyama K, Seki H, Saito K, Muranaka T

Front Plant Sci

26-Nov-2019

PMCID:	PMC6901910
doi:	10.3389/fpls.2019.01520
PMID:	31850023

Formononetin: A Review of Its Anticancer Potentials and Mechanisms

Tay KC, Tan LT, Chan CK, Hong SL, Chan KG, Yap WH, Pusparajah P, Lee LH, Goh BH

Front Pharmacol

26-Jul-2019

PMCID:	PMC6676344
doi:	10.3389/fphar.2019.00820
PMID:	31402861

Using SSR-HRM to Identify Closely Related Species in Herbal Medicine Products: A Case Study on Licorice

Li J, Xiong C, He X, Lu Z, Zhang X, Chen X, Sun W

Front Pharmacol

24-Apr-2018

PMCID:	PMC5928318
doi:	10.3389/fphar.2018.00407
PMID:	29740326

Pharmacological Activities and Phytochemical Constituents

Öztürk M, Altay V, Hakeem KR, Akçiçek E

Liquorice

20-Mar-2018

PMCID:	PMC7120246
doi:	10.1007/978-3-319-74240-3_7

Selected hepatoprotective herbal medicines: Evidence from ethnomedicinal applications, animal models, and possible mechanism of actions

Ali M, Khan T, Fatima K, Ali QU, Ovais M, Khalil AT, Ullah I, Raza A, Shinwari ZK, Idrees M

Phytother Res

19-Oct-2017

PMCID:	PMC7167792
doi:	10.1002/ptr.5957
PMID:	29047177

Diversity and plant growth promoting properties of rhizobia isolated from root nodules of Ononis arvensis

Wdowiak-Wróbel S, Marek-Kozaczuk M, Kalita M, Karaś M, Wójcik M, Małek W

Antonie Van Leeuwenhoek

12-May-2017

PMCID:	PMC5511607
doi:	10.1007/s10482-017-0883-x
PMID:	28500544

Specificity in Legume-Rhizobia Symbioses

Andrews M, Andrews ME

Int J Mol Sci

26-Mar-2017

PMCID:	PMC5412291
doi:	10.3390/ijms18040705
PMID:	28346361

Novel Approach to Classify Plants Based on Metabolite-Content Similarity

Liu K, Abdullah AA, Huang M, Nishioka T, Altaf-Ul-Amin M, Kanaya S

Biomed Res Int

09-Jan-2017

PMCID:	PMC5253511
doi:	10.1155/2017/5296729
PMID:	28164123

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Alkaloids and derivatives / Erythrina alkaloids / Erythrinanes
Erythrinine	3084503	Click to see COC1CC23C(=CCN2CC(C4=CC5=C(C=C34)OCO5)O)C=C1	313.30	unknown	https://doi.org/10.1016/S0031-9422(01)00268-0
> Alkaloids and derivatives / Harmala alkaloids
1-Methoxyethyl-4,8-dimethoxy-9H-pyrido[3,4-b]indole	5316865	Click to see COCCC1=NC=C(C2=C1NC3=C2C=CC=C3OC)OC	286.33	unknown	via CMAUP database
> 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	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
Dehydrodigallic acid	14057208	Click to see C1=C(C=C(C(=C1O)O)OC2=C(C(=C(C=C2C(=O)O)O)O)O)C(=O)O	338.22	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
5-Hydroxy-4,13-dimethoxy-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2,4,6,10,13-pentaen-12-one	5320383	Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=CC(=C(C=C34)OC)O)OC	327.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Methyl 11-hydroxy-2,6,10,10,14,21-hexamethyl-16,22-dioxo-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-ene-5-carboxylate	5317769	Click to see CC1(C2CCC3(C(C2(CCC1O)C)C(=O)C=C4C3(CCC5(C4CC6(CC5OC6=O)C)C)C(=O)OC)C)C	512.70	unknown	via CMAUP database
Olean-12-en-28-oic acid, 3,21-dihydroxy-, gamma-lactone, (3beta,21beta)-	21594250	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC26CC1OC6=O)C)C)(C)C)O)C)C	454.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
(2R)-2-phenyl-2-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyacetonitrile	154497290	Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O	295.29	unknown	https://doi.org/10.3987/COM-89-5304
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin	69894	Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O	192.17	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S)-7-hydroxy-8-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydrochromen-4-one	163011623	Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=CC=C3)O)C	308.40	unknown	https://doi.org/10.3987/COM-89-5304
(S)-2,3-Dihydro-5,7-dihydroxy-2-phenyl-6,8-diprenyl-4H-1-benzopyran-4-one	25775471	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)CC=C(C)C)O)C	392.50	unknown	https://doi.org/10.3987/COM-89-5304
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	3951	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)CC=C(C)C)O)C	408.50	unknown	https://doi.org/10.3987/COM-89-5304
5,7-Dihydroxy-6,8-di-C-prenylflavanone	11143677	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)CC=C(C)C)O)C	392.50	unknown	https://doi.org/10.3987/COM-89-5304
7-Hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	11609510	Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)C	324.40	unknown	https://doi.org/10.3987/COM-89-5304
Isobavachin	193679	Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)C	324.40	unknown	https://doi.org/10.3987/COM-89-5304
Ovaliflavanone B	480762	Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=CC=C3)O)C	308.40	unknown	https://doi.org/10.3987/COM-89-5304
Senegalensin	124035	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)CC=C(C)C)O)C	408.50	unknown	https://doi.org/10.3987/COM-89-5304
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)-	1889	Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O	256.25	unknown	https://doi.org/10.3987/COM-89-5304
Liquiritigenin	114829	Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O	256.25	unknown	https://doi.org/10.1016/0305-1978(93)90090-E https://doi.org/10.3987/COM-89-5304
> 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	https://doi.org/10.1016/0305-1978(93)90090-E
Kaempferol 3,7-di-O-sulfate	12988285	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OS(=O)(=O)O)O)OS(=O)(=O)O)O	446.40	unknown	via CMAUP database
> 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	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
Tamarixetin	5281699	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	316.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Cacticin	5318644	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	478.40	unknown	https://doi.org/10.1248/BPB.23.602
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	71541772	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O	430.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
[5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxo-3-sulfonatooxychromen-7-yl] sulfate	21676171	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OS(=O)(=O)[O-])O)OS(=O)(=O)[O-])O	474.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3S)-7-hydroxy-3-(4-hydroxybenzoyl)-2,3-dihydrochromen-4-one	162850984	Click to see C1C(C(=O)C2=C(O1)C=C(C=C2)O)C(=O)C3=CC=C(C=C3)O	284.26	unknown	https://doi.org/10.3987/COM-89-5304
7-Hydroxy-3-(4-hydroxybenzoyl)-2,3-dihydrochromen-4-one	21591151	Click to see C1C(C(=O)C2=C(O1)C=C(C=C2)O)C(=O)C3=CC=C(C=C3)O	284.26	unknown	https://doi.org/10.3987/COM-89-5304
> Phenylpropanoids and polyketides / Isoflavonoids
(11aS)-9-methoxy-11aH-[1]benzofuro[3,2-c]chromen-3-ol	162964924	Click to see COC1=CC2=C(C=C1)C3=COC4=C(C3O2)C=CC(=C4)O	268.26	unknown	https://doi.org/10.3987/COM-89-5304
9-methoxy-11aH-[1]benzofuro[3,2-c]chromen-3-ol	14833388	Click to see COC1=CC2=C(C=C1)C3=COC4=C(C3O2)C=CC(=C4)O	268.26	unknown	https://doi.org/10.3987/COM-89-5304
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
9-methoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-[1]benzofuro[3,2-c]chromen-6-one	101158846	Click to see COC1=CC2=C(C=C1)C3=C(O2)C4=C(C=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC3=O	444.40	unknown	https://doi.org/10.1016/S0031-9422(01)00268-0
9-Methoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-[1]benzofuro[3,2-c]chromen-6-one	163043848	Click to see COC1=CC2=C(C=C1)C3=C(O2)C4=C(C=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC3=O	444.40	unknown	https://doi.org/10.1016/S0031-9422(01)00268-0
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Maackiain 3-O-glucoside	4485132	Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6	446.40	unknown	https://doi.org/10.1016/S0031-9422(01)00268-0
(2S,3R,4S,5R,6R)-2-[[(6aR,11aR)-10-hydroxy-9-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163043026	Click to see COC1=C(C2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(02)00093-6
(2S,3R,4S,5R,6R)-2-[[(6aS,11aS)-6a-hydroxy-9-methoxy-6,11a-dihydro-[1]benzofuro[3,2-c]chromen-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163074977	Click to see COC1=CC2=C(C=C1)C3(COC4=C(C3O2)C=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(02)00093-6
(2S,3R,4S,5R,6S)-2-[[(6aR,11aR)-9-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	154496990	Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O	432.40	unknown	https://doi.org/10.1016/S0031-9422(02)00093-6
(2S,3R,4S,5S,6R)-2-[(10-hydroxy-9-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	11972396	Click to see COC1=C(C2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(01)00268-0
(2S,3R,4S,5S,6R)-2-[(6a-hydroxy-9-methoxy-6,11a-dihydro-[1]benzofuro[3,2-c]chromen-3-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	11972397	Click to see COC1=CC2=C(C=C1)C3(COC4=C(C3O2)C=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(01)00268-0
(2S,3R,4S,5S,6R)-2-[[(6aR,11aR)-10-hydroxy-9-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	101192599	Click to see COC1=C(C2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(02)00093-6
(2S,3R,4S,5S,6R)-2-[[(6aS,11aS)-6a-hydroxy-9-methoxy-6,11a-dihydro-[1]benzofuro[3,2-c]chromen-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	101192600	Click to see COC1=CC2=C(C=C1)C3(COC4=C(C3O2)C=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(02)00093-6
2-[(10-hydroxy-9-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	73157777	Click to see COC1=C(C2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(02)00093-6
2-[(6a-Hydroxy-9-methoxy-6,11a-dihydro-[1]benzofuro[3,2-c]chromen-3-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	22297386	Click to see COC1=CC2=C(C=C1)C3(COC4=C(C3O2)C=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(02)00093-6
3-Hydroxy-8,9-methylenedioxypterocarpane	363863	Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5	284.26	unknown	https://doi.org/10.1016/S0031-9422(01)00268-0
Maackiain	91510	Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5	284.26	unknown	https://doi.org/10.1016/S0031-9422(01)00268-0
Medicarpin	336327	Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O	270.28	unknown	https://doi.org/10.1016/0305-1978(93)90090-E https://doi.org/10.3987/COM-89-5304
Medicarpin 3-O-glucoside	23724664	Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O	432.40	unknown	https://doi.org/10.1016/S0031-9422(02)00093-6
Medicocarpin	44257429	Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O	432.40	unknown	https://doi.org/10.1016/S0031-9422(02)00093-6
Trifolirhizin	442827	Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6	446.40	unknown	https://doi.org/10.1016/S0031-9422(01)00268-0
> Phenylpropanoids and polyketides / Isoflavonoids / Hydroxyisoflavonoids
7,2'-Dihydroxy-4'-methoxy-3-phenylcoumarin	12539028	Click to see COC1=CC(=C(C=C1)C2=CC3=C(C=C(C=C3)O)OC2=O)O	284.26	unknown	https://doi.org/10.1016/0305-1978(93)90090-E
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(2R)-4-hydroxy-6-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-5-one	94856057	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)O	354.40	unknown	https://doi.org/10.1016/S0031-9422(01)00268-0
(2S)-4-hydroxy-6-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-5-one	94856056	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)O	354.40	unknown	https://doi.org/10.1016/S0031-9422(01)00268-0
4-Hydroxy-6-(4-hydroxyphenyl)-2-prop-1-en-2-yl-2,3-dihydrofuro[3,2-g]chromen-5-one	12108704	Click to see CC(=C)C1CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O	336.30	unknown	https://doi.org/10.1016/S0031-9422(01)00268-0
Erythrinin C	44257283	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)O	354.40	unknown	https://doi.org/10.1016/S0031-9422(01)00268-0
Licoagroisoflavone	636883	Click to see CC(=C)C1CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O	336.30	unknown	https://doi.org/10.1016/S0031-9422(01)00268-0
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(2-hydroxy-4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	163052947	Click to see COC1=CC(=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O	446.40	unknown	https://doi.org/10.1016/S0031-9422(02)00093-6
3-(2-Hydroxy-4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	163052946	Click to see COC1=CC(=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O	446.40	unknown	https://doi.org/10.1016/S0031-9422(02)00093-6
3-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	154496292	Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O	446.40	unknown	https://doi.org/10.1016/S0031-9422(02)00093-6
3-(4-methoxyphenyl)-7-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	154497130	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O	430.40	unknown	https://doi.org/10.1016/S0031-9422(01)00268-0
3-(4-methoxyphenyl)-7-[(2S,4S,5R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	44257215	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O	430.40	unknown	https://doi.org/10.1016/0305-1978(93)90090-E https://doi.org/10.1016/S0031-9422(02)00093-6 https://doi.org/10.1016/S0031-9422(01)00268-0
3-(4-Methoxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	3733033	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O	430.40	unknown	https://doi.org/10.1016/S0031-9422(01)00268-0
6-methoxy-3-(4-methoxyphenyl)-7-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	154496114	Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)OC4C(C(C(C(O4)CO)O)O)O	460.40	unknown	https://doi.org/10.1016/0305-1978(93)90090-E
Calycosin 7-galactoside	91973796	Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O	446.40	unknown	https://doi.org/10.1016/S0031-9422(02)00093-6
CALYCOSIN 7-O-beta-D-GLUCOSIDE	5318267	Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O	446.40	unknown	https://doi.org/10.1016/S0031-9422(02)00093-6
Formononetin 7-(6''-malonylglucoside)	131750877	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O	516.40	unknown	https://doi.org/10.1016/S0031-9422(02)00093-6
Formononetin 7-O-glucoside-6''-O-malonate	23724663	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O	516.40	unknown	https://doi.org/10.1016/S0031-9422(02)00093-6
Ononin	442813	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O	430.40	unknown	https://doi.org/10.1016/0305-1978(93)90090-E https://doi.org/10.1016/S0031-9422(01)00268-0
Wistin	10095770	Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)OC4C(C(C(C(O4)CO)O)O)O	460.40	unknown	https://doi.org/10.1016/0305-1978(93)90090-E
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
Vestitol	92503	Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O	272.29	unknown	https://doi.org/10.1021/NP2004775 https://doi.org/10.1016/0305-1978(93)90090-E
Vestitol, (-)-	182259	Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O	272.29	unknown	https://doi.org/10.1016/0305-1978(93)90090-E
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Calycosin	5280448	Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O	284.26	unknown	https://doi.org/10.3987/COM-89-5304 https://doi.org/10.1016/S0031-9422(01)00268-0
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
2'-Hydroxyformononetin	5280551	Click to see COC1=CC(=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O	284.26	unknown	https://doi.org/10.1016/0305-1978(93)90090-E
7,2'-Dihydroxy-6,4'-dimethoxyisoflavone	44257255	Click to see COC1=CC(=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)O)O	314.29	unknown	https://doi.org/10.3987/COM-89-5260 https://doi.org/10.3987/COM-89-5304
Afrormosin	5281704	Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)O	298.29	unknown	https://doi.org/10.3987/COM-89-5304 https://doi.org/10.1016/0305-1978(93)90090-E
CID 10378473	10378473	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O	271.24	unknown	via CMAUP database
Formononetin	5280378	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O	268.26	unknown	https://doi.org/10.1016/0305-1978(93)90090-E https://doi.org/10.3987/COM-89-5304
Pallidiflorin	5320382	Click to see COC1=CC=C(C=C1)C2=COC3=CC=CC(=C3C2=O)O	268.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
4',7-Dimethoxyisoflavone	136419	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC	282.29	unknown	https://doi.org/10.3987/COM-89-5304
Prunetin	5281804	Click to see COC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)O)O	284.26	unknown	https://doi.org/10.3987/COM-89-5304
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
(2S)-1-(2,4-dihydroxyphenyl)-3-(4-hydroxyphenyl)-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-1-one	162843435	Click to see C1=CC(=CC=C1CC(C(=O)C2=C(C=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O	436.40	unknown	https://doi.org/10.1016/S0031-9422(02)00093-6
1-(2,4-dihydroxyphenyl)-3-(4-hydroxyphenyl)-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-1-one	11968696	Click to see C1=CC(=CC=C1CC(C(=O)C2=C(C=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O	436.40	unknown	https://doi.org/10.1016/S0031-9422(01)00268-0
1-(2,4-Dihydroxyphenyl)-3-(4-hydroxyphenyl)-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-1-one	73157179	Click to see C1=CC(=CC=C1CC(C(=O)C2=C(C=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O	436.40	unknown	https://doi.org/10.1016/S0031-9422(02)00093-6
Gancaonin J	21591150	Click to see CC(=CCC1=CC(=C(C(=C1O)CC=C(C)C)O)C(=O)CCC2=CC=C(C=C2)O)C	394.50	unknown	https://doi.org/10.3987/COM-89-5260 https://doi.org/10.3987/COM-89-5304
Licoagroside F	42607722	Click to see C1=CC(=CC=C1CC(C(=O)C2=C(C=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O	436.40	unknown	https://doi.org/10.1016/S0031-9422(02)00093-6
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
GU17;ISL;Isoliquiritigen	425	Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O	256.25	unknown	https://doi.org/10.3987/COM-89-5304 https://doi.org/10.1016/S0031-9422(01)00268-0
Trihydroxychalcone	638278	Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O	256.25	unknown	https://doi.org/10.1016/0305-1978(93)90090-E https://doi.org/10.1016/S0031-9422(01)00268-0 https://doi.org/10.3987/COM-89-5304
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retro-dihydrochalcones
2'-O-Methyllicodione	439850	Click to see COC1=C(C=CC(=C1)O)C(=O)CC(=O)C2=CC=C(C=C2)O	286.28	unknown	https://doi.org/10.3987/COM-89-5260 https://doi.org/10.3987/COM-89-5304 https://doi.org/10.1016/0305-1978(93)90090-E
Licodione	439528	Click to see C1=CC(=CC=C1C(=O)CC(=O)C2=C(C=C(C=C2)O)O)O	272.25	unknown	https://doi.org/10.1016/0305-1978(93)90090-E https://doi.org/10.1271/BBB.63.1618
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retrochalcones
4-Hydroxy-2,4'-dimethoxychalcone	5317768	Click to see COC1=CC=C(C=C1)C(=O)C=CC2=C(C=C(C=C2)O)OC	284.31	unknown	via CMAUP database
CID 182171	182171	Click to see COC1=C(C=CC(=C1)O)C=CC(=O)C2=CC=C(C=C2)O	270.28	unknown	https://doi.org/10.1016/S0031-9422(01)00268-0 https://doi.org/10.3987/COM-89-5304
Echinatin	6442675	Click to see COC1=C(C=CC(=C1)O)C=CC(=O)C2=CC=C(C=C2)O	270.28	unknown	https://doi.org/10.1016/S0031-9422(01)00268-0 https://doi.org/10.3987/COM-89-5304 https://doi.org/10.1016/0305-1978(93)90090-E

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Glycyrrhiza pallidiflora

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