Boesenbergia rotunda

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Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID643ff1d83beb2891861172
Scientific name	Boesenbergia rotunda
Authority	(L.) Mansf.
First published in	Kulturpflanze 6:239. (1958); Lectotypified in: Notes Roy. Bot. Gard. Edinburgh 31. (1972) by Burtt B.L. & Smith R.M.

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Boesenbergia baimaii	Saensouk & K.Larsen	Nordic J. Bot. 21:595. (2002)
Boesenbergia cochinchinensis	(Gagnep.) Loes.	Nat. Pflanzenfam. Ed. 2 (A):571
Boesenbergia pandurata	(Roxb.) Schltr.	Repert. Spec. Nov. Regni Veg. 12:316. (1913)
Curcuma rotunda	L.	Sp. pl. 2
Gastrochilus panduratus	(Roxb.) Ridl.	J. Straits Branch Roy. Asiat. Soc. 32:114. (1899)
Gastrochilus rotundus	(L.) Alston	in Trimen, H., Handb. fl. Ceylon 281
Kaempferia cochinchinensis	Gagnep.	Bull. Soc. Bot. France 54:165. (1907); Lectotypified in: Gard. Bull. Singapore 68 (2). (2016) by Mood, J.D., Tanaka, N., Aung, M.M. & Murata, J.
Kaempferia ovata	Roscoe	Trans. Linn. Soc. London 8:351. (1807)
Kaempferia pandurata	Roxb.	Asiat. Res. 11:328. (1810); Lectotypified in: Philipp. J. Sci. 142. (2014) by Veldkamp, J.F.
Zingiber xanthorhizum	Moon	Cat. Pl. Ceylon 1

Common names Top

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Language	Common/alternative name
English	fingerroot
English	rotund boesenbergia
English	chinese ginger
ban	temu kunci
German	fingerwurz
German	chinesischer ingwer
Esperanto	Ĉina zingibro
Persian	زنجبیل چینی
Hungarian	kínai gyömbér
Hungarian	kracsaj
Hungarian	ujjgyökér
Indonesian	temu kunci
Japanese	クラチャーイ
Japanese	オオバンガジュツ
jv	temu kunci
mad	koncè
Malay	pokok temu kunci
Dutch	chinese gember
Dutch	vingerwortel
Dutch	temu kunci
Dutch	temoe koentjie
su	kunci
Thai	กระชาย
Chinese	凹唇薑
Chinese	凹唇姜

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China South-central

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - India
  - Sri Lanka
- Indo-China
  - Andaman Islands
  - Cambodia
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Sumatera

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000341663
UNII	YJH4Q18M8V
USDA Plants	BORO4
Tropicos	34500543
INPN	853561
KEW	urn:lsid:ipni.org:names:872224-1
The Plant List	kew-221874
Open Tree Of Life	55241
NCBI Taxonomy	97729
IUCN Red List	44392164
IPNI	872224-1
iNaturalist	139956
GBIF	2758480
Freebase	/m/0160dh
EOL	1125981
USDA GRIN	100983
Wikipedia	Boesenbergia_rotunda
CMAUP	NPO24946
CMAUP	NPO27600

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_024364735.1	CEBAR_Bro_1.0	Scaffold	Centre for research in biotechnology for agriculture (CEBAR), University of Malaya	2022-07-21	100.0x	2.19 Gb

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 Nephroprotective Activity of Boesenbergia Rotunda Rhizome by Reducing Creatinine, Urea Nitrogen, Glutamic Pyruvic Transaminase, and Malondialdehyde Levels in the Blood and Attenuating the Expression of Havcr1 (KIM-1), Lcn2 (NGAL), Casp3, and Casp7 Genes in the Kidney Cortex of Cisplatin-Induced Sprague-Dawley Rats

Sujana D, Sumiwi SA, Saptarini NM, Levita J

J Exp Pharmacol

06-May-2024

PMCID:	PMC11086399
doi:	10.2147/JEP.S459483
PMID:	38736464

Enhancing effect of natural adjuvant, panduratin A, on antibacterial activity of colistin against multidrug-resistant Acinetobacter baumannii

Thadtapong N, Chaturongakul S, Napaswad C, Dubbs P, Soodvilai S

Sci Rep

29-Apr-2024

PMCID:	PMC11059350
doi:	10.1038/s41598-024-60627-0
PMID:	38684853

Separation Methods of Phenolic Compounds from Plant Extract as Antioxidant Agents Candidate

Susanti I, Pratiwi R, Rosandi Y, Hasanah AN

Plants (Basel)

27-Mar-2024

PMCID:	PMC11013868
doi:	10.3390/plants13070965
PMID:	38611494

Physicochemical and biological properties of encapsulated Boesenbergia rotunda extract with different wall materials in enhancing antioxidant, mineralogenic and osteogenic activities of MC3T3-E1 cells

Saah S, Siriwan D, Trisonthi P, Dueramae S

Saudi Pharm J

20-Feb-2024

PMCID:	PMC10897896
doi:	10.1016/j.jsps.2024.101998
PMID:	38414781

Oral sub-chronic toxicity of fingerroot (Boesenbergia rotunda) rhizome extract formulation in Wistar rats

Techapichetvanich P, Tangpanithandee S, Supannapan K, Wongwiwatthananukit S, Chang LC, Khemawoot P

Toxicol Rep

30-Jan-2024

PMCID:	PMC10847838
doi:	10.1016/j.toxrep.2024.01.013
PMID:	38328737

Unveiling the Antiviral Properties of Panduratin A through SARS-CoV-2 Infection Modeling in Cardiomyocytes

Linn AK, Manopwisedjaroen S, Kanjanasirirat P, Borwornpinyo S, Hongeng S, Phanthong P, Thitithanyanont A

Int J Mol Sci

24-Jan-2024

PMCID:	PMC10855687
doi:	10.3390/ijms25031427
PMID:	38338708

Revealing Propolis Potential Activity on Inhibiting Estrogen Receptor and Heat Shock Protein 90 Overexpressed in Breast Cancer by Bioinformatics Approaches

Simanjuntak MV, Jauhar MM, Syaifie PH, Arda AG, Mardliyati E, Shalannanda W, Hermanto BR, Anshori I

Bioinform Biol Insights

24-Jan-2024

PMCID:	PMC10809879
doi:	10.1177/11779322231224187
PMID:	38274992

Boesenbergia rotunda and Its Pinostrobin for Atopic Dermatitis: Dual 5-Lipoxygenase and Cyclooxygenase-2 Inhibitor and Its Mechanistic Study through Steady-State Kinetics and Molecular Modeling

Liana D, Eurtivong C, Phanumartwiwath A

Antioxidants (Basel)

05-Jan-2024

PMCID:	PMC10812521
doi:	10.3390/antiox13010074
PMID:	38247498

Targeting Signalling Pathways in Chronic Wound Healing

Bonnici L, Suleiman S, Schembri-Wismayer P, Cassar A

Int J Mol Sci

19-Dec-2023

PMCID:	PMC10779022
doi:	10.3390/ijms25010050
PMID:	38203220

The Inhibitory Effect of KerraTM, KSTM, and MinozaTM on Human Papillomavirus Infection and Cervical Cancer

Choowongkomon K, Choengpanya K, Pientong C, Ekalaksananan T, Talawat S, Srathong P, Chuerduangphui J

Medicina (Kaunas)

14-Dec-2023

PMCID:	PMC10745032
doi:	10.3390/medicina59122169
PMID:	38138272

Pinostrobin attenuates azoxymethane-induced colorectal cytotoxicity in rats through augmentation of apoptotic Bax/Bcl-2 proteins and antioxidants

Ali Abed Wahab B, Ain Salehen N, Abdulla MA, A.j. Jabbar A, Abdel Aziz Ibrahim I, Almaimani G, AbdulMonam Zainel M, Bamagous GA, Almaimani RA, Almasmoum HA, Ghaith MM, Farrash WF, Almutawif YA

SAGE Open Med

08-Dec-2023

PMCID:	PMC10710114
doi:	10.1177/20503121231216585
PMID:	38078205

Discovering Potential Compounds for Venous Disease Treatment through Virtual Screening and Network Pharmacology Approach

Barrera-Vázquez OS, Escobar-Ramírez JL, Santiago-Mejía J, Carrasco-Ortega OF, Magos-Guerrero GA

Molecules

05-Dec-2023

PMCID:	PMC10745828
doi:	10.3390/molecules28247937
PMID:	38138427

Litsea glaucescens Kuth possesses bactericidal activity against Listeria monocytogenes

Gress-Antonio CD, Rivero-Perez N, Marquina-Bahena S, Alvarez L, Zaragoza-Bastida A, Martínez-Juárez VM, Sosa-Gutierrez CG, Ocampo-López J, Zepeda-Bastida A, Ojeda-Ramírez D

PeerJ

01-Dec-2023

PMCID:	PMC10695109
doi:	10.7717/peerj.16522
PMID:	38054017

Evaluation of Physical Properties of Denture Base Resins Containing Silver Nanoparticles of Aloe barbadensis Miller, Morinda citrifolia, and Boesenbergia rotunda and Its Anti-microbial Effect: An In Vitro Study

Kaul S, Ahmed S, Nandini VV, Lathief J, Boruah S

Cureus

04-Nov-2023

PMCID:	PMC10695085
doi:	10.7759/cureus.48260
PMID:	38054116

Pinostrobin mitigates neurodegeneration through an up-regulation of antioxidants and GDNF in a rat model of Parkinson’s disease

Kongsui R, Promsrisuk T, Klimaschewski L, Sriraksa N, Jittiwat J, Thongrong S

F1000Res

27-Oct-2023

PMCID:	PMC10904945
doi:	10.12688/f1000research.134891.1
PMID:	38434672

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
[(1S,2R,4R,5R,6S,7R)-5-acetyloxy-6-benzoyloxy-3,8-dioxatricyclo[5.1.0.02,4]octan-4-yl]methyl benzoate	163067720	Click to see CC(=O)OC1C(C2C(O2)C3C1(O3)COC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5	424.40	unknown	https://doi.org/10.1016/S0031-9422(01)00451-4
5-Cyclohexene-1,2,3,4-tetrol, 2-[(benzoyloxy)methyl]-, 4-benzoate, (1R,2S,3R,4S)-	14283261	Click to see C1=CC=C(C=C1)C(=O)OCC2(C(C=CC(C2O)OC(=O)C3=CC=CC=C3)O)O	384.40	unknown	https://doi.org/10.1016/S0031-9422(01)00451-4
Crotepoxide	161314	Click to see CC(=O)OC1C2C(O2)C3C(C1OC(=O)C)(O3)COC(=O)C4=CC=CC=C4	362.30	unknown	https://doi.org/10.1016/S0031-9422(01)00451-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Isopimaric Acid	442048	Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)O)C)C1)C=C	302.50	unknown	https://doi.org/10.1016/S0031-9422(01)00451-4
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
3,7-Dimethyl-2,6-octadien-1-ol	4458	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1248/CPB.56.956
Citral	638011	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	https://doi.org/10.1016/0031-9422(93)80020-S
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1248/CPB.56.956
Neral	643779	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	https://doi.org/10.1016/0031-9422(93)80020-S
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
methyl (1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-ene-1-carboxylate	24864449	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)OC)C2=CC=CC=C2	298.40	unknown	https://doi.org/10.1248/CPB.56.491
methyl (1S,5R,6S)-4-methyl-5-(3-methylbut-2-enyl)-6-phenylcyclohex-3-ene-1-carboxylate	163040699	Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)OC	298.40	unknown	https://doi.org/10.1248/CPB.56.491
Methyl 3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-ene-1-carboxylate	74337645	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)OC)C2=CC=CC=C2	298.40	unknown	https://doi.org/10.1248/CPB.56.491
Methyl 4-methyl-5-(3-methylbut-2-enyl)-6-phenylcyclohex-3-ene-1-carboxylate	74337646	Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)OC	298.40	unknown	https://doi.org/10.1248/CPB.56.491
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(6-Hydroxy-4-methoxy-1-benzofuran-7-yl)-[3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone	74337544	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CO3)C4=CC=CC=C4	430.50	unknown	https://doi.org/10.1248/CPB.56.491
[(2R)-5-hydroxy-7-methoxy-2-methyl-2-(4-methylpent-3-enyl)chromen-6-yl]-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone	162949724	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C3C(=C2O)C=CC(O3)(C)CCC=C(C)C)OC)C4=CC=CC=C4	540.70	unknown	https://doi.org/10.1248/CPB.56.491
[(2R)-7-hydroxy-5-methoxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-[(1R,2R,6S)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone	163083698	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)CCC=C(C)C)C4=CC=CC=C4	540.70	unknown	https://doi.org/10.1071/CH9870455
[(2R)-7-hydroxy-5-methoxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone	101855692	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)CCC=C(C)C)C4=CC=CC=C4	540.70	unknown	https://doi.org/10.1248/CPB.56.491
[(2S)-7-Hydroxy-5-methoxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-8-yl][(1R,2S,6R)-3-methyl-2-(3-methyl-2-butenyl)-6-phenyl-3-cyclohexenyl]methanone	101855694	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)CCC=C(C)C)C4=CC=CC=C4	540.70	unknown	https://doi.org/10.1248/CPB.56.491
[(2S)-7-hydroxy-5-methoxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-[(1R,2R,6S)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone	163083697	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)CCC=C(C)C)C4=CC=CC=C4	540.70	unknown	https://doi.org/10.1071/CH9870455
[5-Hydroxy-7-methoxy-2-methyl-2-(4-methylpent-3-enyl)chromen-6-yl]-[3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone	74337546	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C3C(=C2O)C=CC(O3)(C)CCC=C(C)C)OC)C4=CC=CC=C4	540.70	unknown	https://doi.org/10.1248/CPB.56.491
[7-Hydroxy-5-methoxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-[3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone	163083696	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)CCC=C(C)C)C4=CC=CC=C4	540.70	unknown	https://doi.org/10.1248/CPB.56.491 https://doi.org/10.1071/CH9870455
Panduratin D	24864268	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CO3)C4=CC=CC=C4	430.50	unknown	https://doi.org/10.1248/CPB.56.491
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
2-[2-[4,5-Dihydroxy-2-(hydroxymethyl)-6-(14-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxyoxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	162971644	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(C(CC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)C)C)OC1	919.10	unknown	https://doi.org/10.1248/CPB.56.956
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1S,2S,3R,7R,8S,9R,11R,13S)-1,9-dihydroxy-9,13-dimethyl-4-methylidene-8-(2-methylpropanoyloxy)-5-oxo-6,14-dioxatricyclo[9.2.1.03,7]tetradecan-2-yl] 2-methylbut-2-enoate	123441477	Click to see CC=C(C)C(=O)OC1C2C(C(C(CC3CC(C1(O3)O)C)(C)O)OC(=O)C(C)C)OC(=O)C2=C	466.50	unknown	via CMAUP database
[(1S,2S,3R,7R,8S,9R,11R,13S)-1,9-dihydroxy-9,13-dimethyl-8-(3-methylbutanoyloxy)-4-methylidene-5-oxo-6,14-dioxatricyclo[9.2.1.03,7]tetradecan-2-yl] 2-methylbut-2-enoate	123772000	Click to see CC=C(C)C(=O)OC1C2C(C(C(CC3CC(C1(O3)O)C)(C)O)OC(=O)CC(C)C)OC(=O)C2=C	480.50	unknown	via CMAUP database
[(1S,2S,3R,7R,8S,9R,11R,13S)-8-but-2-enoyloxy-1,9-dihydroxy-9,13-dimethyl-4-methylidene-5-oxo-6,14-dioxatricyclo[9.2.1.03,7]tetradecan-2-yl] 2-methylbut-2-enoate	123438394	Click to see CC=CC(=O)OC1C2C(C(C3(C(CC(O3)CC1(C)O)C)O)OC(=O)C(=CC)C)C(=C)C(=O)O2	464.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(2,4-dihydroxy-6-methoxyphenyl)-[(1R,2R,5R)-3-methyl-2-(3-methylbut-2-enyl)-5-phenylcyclohex-3-en-1-yl]methanone	163106945	Click to see CC1=CC(CC(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=CC=C3	406.50	unknown	https://doi.org/10.1248/CPB.56.956
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(7-Hydroxy-5-methoxy-2,2-dimethylchromen-8-yl)-[3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone	74337545	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)C)C4=CC=CC=C4	472.60	unknown	https://doi.org/10.1248/CPB.56.491
Panduratin E	24864269	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)C)C4=CC=CC=C4	472.60	unknown	https://doi.org/10.1248/CPB.56.491
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(-)-Nicolaioidesin B	637029	Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)OC)O	406.50	unknown	https://doi.org/10.1021/NP070286M
(+/-)-nicolaioidesin A	10894788	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)OC)O)C3=CC=CC=C3	406.50	unknown	via CMAUP database
(+/-)-nicolaioidesin C	11729201	Click to see CC(=CCCC1=CCC(C(C1)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)OC)O)C	406.50	unknown	https://doi.org/10.1248/CPB.56.956
(1'R,2'S,6'R)-2-Hydroxyisopanduratin A	23656472	Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)O)O	392.50	unknown	https://doi.org/10.1021/NP070286M
(2-hydroxy-4,6-dimethoxyphenyl)-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone	44444916	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)OC)O)C3=CC=CC=C3	420.50	unknown	via CMAUP database
(2,4-dihydroxy-6-methoxyphenyl)-[(1R,6R)-4-(4-methylpent-3-enyl)-6-phenylcyclohex-3-en-1-yl]methanone	10692728	Click to see CC(=CCCC1=CCC(C(C1)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3OC)O)O)C	406.50	unknown	https://doi.org/10.1248/CPB.56.956
(2,4-dihydroxy-6-methoxyphenyl)-[(1S,2R,6S)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone	54597285	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=CC=C3	406.50	unknown	https://doi.org/10.1248/CPB.56.956
(2,4-dihydroxy-6-methoxyphenyl)-[(1S,6S)-4-(4-methylpent-3-enyl)-6-phenylcyclohex-3-en-1-yl]methanone	24950680	Click to see CC(=CCCC1=CCC(C(C1)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3OC)O)O)C	406.50	unknown	https://doi.org/10.1248/CPB.56.956
(2,4-Dihydroxy-6-methoxyphenyl)-[3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone	66976619	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=CC=C3	406.50	unknown	https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1021/NP070286M
(2,4-Dihydroxy-6-methoxyphenyl)-[4-(4-methylpent-3-enyl)-6-phenylcyclohex-3-en-1-yl]methanone	74371309	Click to see CC(=CCCC1=CCC(C(C1)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3OC)O)O)C	406.50	unknown	https://doi.org/10.1248/CPB.56.956
(2,4-Dihydroxy-6-methoxyphenyl)-[4-methyl-5-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone	162942005	Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3OC)O)O	406.50	unknown	https://doi.org/10.1021/NP070286M
(2,4-Dihydroxy-6-methoxyphenyl)-[6-(4-hydroxyphenyl)-3-methyl-2-(3-methylbut-2-enyl)cyclohex-3-en-1-yl]methanone	78413420	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=C(C=C3)O	422.50	unknown	https://doi.org/10.1016/J.BMC.2005.10.019 https://doi.org/10.1021/NP070286M
(2,6-dihydroxy-4-methoxyphenyl)-[(1S,2R,6S)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone	25023021	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)OC)O)C3=CC=CC=C3	406.50	unknown	https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1055/S-2005-864149 https://doi.org/10.1021/NP070286M
(2,6-dihydroxy-4-methoxyphenyl)-[(1S,6S)-4-(4-methylpent-3-enyl)-6-phenylcyclohex-3-en-1-yl]methanone	24950679	Click to see CC(=CCCC1=CCC(C(C1)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)OC)O)C	406.50	unknown	https://doi.org/10.1248/CPB.56.956
[(1R,2S,6R)-6-(4-hydroxyphenyl)-3-methyl-2-(3-methylbut-2-enyl)cyclohex-3-en-1-yl]-(2,4,6-trihydroxyphenyl)methanone	163049404	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)O)O)C3=CC=C(C=C3)O	408.50	unknown	https://doi.org/10.1016/J.BMC.2005.10.019
[(1S,2R,6S)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]-(2,4,6-trihydroxyphenyl)methanone	25023022	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)O)O)C3=CC=CC=C3	392.50	unknown	https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1021/NP070286M
[3-Methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]-(2,4,6-trihydroxyphenyl)methanone	22297208	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)O)O)C3=CC=CC=C3	392.50	unknown	https://doi.org/10.1016/J.BMCL.2005.12.075 https://doi.org/10.1016/S0031-9422(01)00451-4 https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1248/BPB.30.2141 https://doi.org/10.1021/NP070286M
[6-(4-Hydroxyphenyl)-3-methyl-2-(3-methylbut-2-enyl)cyclohex-3-en-1-yl]-(2,4,6-trihydroxyphenyl)methanone	163049403	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)O)O)C3=CC=C(C=C3)O	408.50	unknown	https://doi.org/10.1016/J.BMC.2005.10.019
4-hydroxypanduratin A	636530	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)O)O)C3=CC=CC=C3	392.50	unknown	https://doi.org/10.1016/J.BMCL.2005.12.075 https://doi.org/10.1016/S0031-9422(01)00451-4 https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1248/BPB.30.2141 https://doi.org/10.1021/NP070286M https://doi.org/10.1021/JF010016O
Isopanduratin A	10069916	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=CC=C3	406.50	unknown	https://doi.org/10.1248/CPB.56.956
Isopanduratin A1	44444913	Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3OC)O)O	406.50	unknown	https://doi.org/10.1021/NP070286M
Methanone, (2,6-dihydroxy-4-methoxyphenyl)[(1R,5S,6R)-4-methyl-5-(3-methyl-2-butenyl)-6-phenyl-3-cyclohexen-1-yl]-, rel-	22297525	Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)OC)O	406.50	unknown	https://doi.org/10.1021/NP070286M
Methanone, (2,6-dihydroxy-4-methoxyphenyl)[(1R,6R)-4-(4-methyl-3-pentenyl)-6-phenyl-3-cyclohexen-1-yl]-, rel-	73076249	Click to see CC(=CCCC1=CCC(C(C1)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)OC)O)C	406.50	unknown	https://doi.org/10.1248/CPB.56.956
Panduratin	91192388	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)OC)O)C3=CC=CC=C3	406.50	unknown	https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1055/S-2005-864149 https://doi.org/10.1021/NP070286M
Panduratin A	6483648	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)OC)O)C3=CC=CC=C3	406.50	unknown	https://doi.org/10.1071/CH9840449 https://doi.org/10.1055/S-2008-1081352 https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1016/0031-9422(93)80020-S https://doi.org/10.1055/S-2003-45190 https://doi.org/10.1007/S11418-006-0100-0 https://doi.org/10.1071/CH9841739 https://doi.org/10.1021/NP070286M https://doi.org/10.1016/S0031-9422(01)00451-4 https://doi.org/10.1055/S-2008-1034297 https://doi.org/10.1021/JF010016O
Panduratin C	6483647	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=C(C=C3)O	422.50	unknown	https://doi.org/10.1016/J.BMC.2005.10.019 https://doi.org/10.1021/NP070286M
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-6-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,7-dihydroxy-2-phenyl-2,3-dihydrochromen-4-one	44444915	Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O)C)C	392.50	unknown	https://doi.org/10.1021/NP070286M
(2S)-6-Geranylpinostrobin	44444914	Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)OC)C)C	406.50	unknown	https://doi.org/10.1021/NP070286M
6-(3,7-Dimethylocta-2,6-dienyl)-5-hydroxy-7-methoxy-2-phenyl-2,3-dihydrochromen-4-one	163015187	Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)OC)C)C	406.50	unknown	https://doi.org/10.1021/NP070286M
6-(3,7-Dimethylocta-2,6-dienyl)-5,7-dihydroxy-2-phenyl-2,3-dihydrochromen-4-one	68976171	Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O)C)C	392.50	unknown	https://doi.org/10.1021/NP070286M
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-8-geranylpinostrobin	23656470	Click to see CC(=CCCC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC)C)C	406.50	unknown	https://doi.org/10.1021/NP070286M
(2S)-8-[(2E)-3,7-dimethylocta-2,6-dienyl]-5-hydroxy-7-methoxy-2-phenyl-2,3-dihydrochromen-4-one	101863273	Click to see CC(=CCCC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC)C)C	406.50	unknown	https://doi.org/10.1248/CPB.56.956
(2S)-8-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,7-dihydroxy-2-phenyl-2,3-dihydrochromen-4-one	38363541	Click to see CC(=CCCC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3)C)C	392.50	unknown	https://doi.org/10.1248/CPB.56.956
8-(3,7-Dimethylocta-2,6-dienyl)-5-hydroxy-7-methoxy-2-phenyl-2,3-dihydrochromen-4-one	74080980	Click to see CC(=CCCC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC)C)C	406.50	unknown	https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1021/NP070286M
8-(3,7-Dimethylocta-2,6-dienyl)-5,7-dihydroxy-2-phenyl-2,3-dihydrochromen-4-one	85414149	Click to see CC(=CCCC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3)C)C	392.50	unknown	https://doi.org/10.1248/CPB.56.956
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-8-[(2E,4S)-3,7-dimethylocta-2,6-dien-4-yl]-5,7-dihydroxy-2-phenyl-2,3-dihydrochromen-4-one	163194766	Click to see CC=C(C)C(CC=C(C)C)C1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)O	392.50	unknown	https://doi.org/10.1248/CPB.56.956
4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-phenyl-, (2R)-	667544	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	https://doi.org/10.1021/NP070286M
5,7-Dihydroxyflavanone	238782	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	https://doi.org/10.1016/J.BMCL.2005.12.075 https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1016/S0031-9422(01)00451-4 https://doi.org/10.1021/NP070286M
8-(3,7-Dimethylocta-2,6-dien-4-yl)-5,7-dihydroxy-2-phenyl-2,3-dihydrochromen-4-one	162887821	Click to see CC=C(C)C(CC=C(C)C)C1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)O	392.50	unknown	https://doi.org/10.1248/CPB.56.956
Pinocembrin	68071	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	https://doi.org/10.1080/13880200500385194 https://doi.org/10.1021/NP070286M https://doi.org/10.1021/JF010016O https://doi.org/10.1016/S0031-9422(01)00451-4 https://doi.org/10.1016/0031-9422(93)80020-S https://doi.org/10.1016/J.BMCL.2005.12.075 https://doi.org/10.1248/CPB.56.956
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
(2R)-7-hydroxy-2-(4-hydroxyphenyl)-5-methoxy-2,3-dihydrochromen-4-one	40577064	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)O)O	286.28	unknown	https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1021/NP070286M
5-O-Methylnaringenin	182315	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)O)O	286.28	unknown	https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1021/NP070286M
7-Hydroxy-5-methoxy-2-phenylchroman-4-one	4053302	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1016/J.BMCL.2005.12.075 https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1021/NP070286M https://doi.org/10.1080/13880200500385194 https://doi.org/10.1016/0031-9422(93)80020-S https://doi.org/10.1271/BBB.90114
Alpinetin	154279	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1016/J.BMCL.2005.12.075 https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1021/NP070286M https://doi.org/10.1271/BBB.90114
Naringenin 5-methyl ether	188424	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)O)O	286.28	unknown	https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1021/NP070286M
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R)-5,7-Dimethoxyflavanone	689012	Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC	284.31	unknown	via CMAUP database
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one	689011	Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC	284.31	unknown	https://doi.org/10.1016/0031-9422(83)83075-1
(2S)-8-[(2E,4S)-3,7-dimethylocta-2,6-dien-4-yl]-5-hydroxy-7-methoxy-2-phenyl-2,3-dihydrochromen-4-one	163186408	Click to see CC=C(C)C(CC=C(C)C)C1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC	406.50	unknown	https://doi.org/10.1248/CPB.56.956
3,5,7-Trimethoxyflavone	117900	Click to see COC1=CC2=C(C(=C1)OC)C(=O)C(=C(O2)C3=CC=CC=C3)OC	312.30	unknown	https://doi.org/10.1016/0031-9422(83)83075-1
3',4',5,7-Tetramethoxyflavone	631170	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC)OC	342.30	unknown	https://doi.org/10.1016/0031-9422(83)83075-1
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	https://doi.org/10.1016/0031-9422(83)83075-1
5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxychroman-4-one	348130	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O	286.28	unknown	https://doi.org/10.1016/S0031-9422(01)00451-4
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	https://doi.org/10.1016/J.BMCL.2005.12.075 https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1271/BBB.90114 https://doi.org/10.1016/S0031-9422(01)00451-4 https://doi.org/10.1071/CH9840449 https://doi.org/10.1080/13880200500385194 https://doi.org/10.1021/JF010016O https://doi.org/10.1016/0031-9422(93)80020-S https://doi.org/10.1021/NP070286M https://doi.org/10.1016/0031-9422(83)83075-1
5-Hydroxy-7-methoxyflavanone	4101463	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1016/0031-9422(83)83075-1 https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1016/S0031-9422(01)00451-4 https://doi.org/10.1021/NP070286M https://doi.org/10.1016/J.BMCL.2005.12.075 https://doi.org/10.1271/BBB.90114 https://doi.org/10.1071/CH9840449
5,7-Dimethoxyflavanone	378567	Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC	284.31	unknown	https://doi.org/10.1016/0031-9422(83)83075-1
5,7-Dimethoxyflavone	88881	Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3	282.29	unknown	https://doi.org/10.1016/0031-9422(83)83075-1 https://doi.org/10.1055/S-2006-961905
8-(3,7-Dimethylocta-2,6-dien-4-yl)-5-hydroxy-7-methoxy-2-phenyl-2,3-dihydrochromen-4-one	162901006	Click to see CC=C(C)C(CC=C(C)C)C1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC	406.50	unknown	https://doi.org/10.1248/CPB.56.956
Apigenin 7,4'-dimethyl ether	5281601	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O	298.29	unknown	https://doi.org/10.1016/0031-9422(83)83075-1
Apigenin trimethyl ether	79730	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC	312.30	unknown	https://doi.org/10.1016/0031-9422(83)83075-1
Kaempferol 3,7,4'-trimethyl ether	5468749	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC	328.30	unknown	https://doi.org/10.1016/0031-9422(83)83075-1
Pinostrobin	6950539	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1016/0031-9422(93)80020-S https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1016/S0031-9422(01)00451-4 https://doi.org/10.1021/NP070286M https://doi.org/10.1080/13880200500385194 https://doi.org/10.1071/CH9840449 https://doi.org/10.1021/JF010016O
Quercetin pentamethyl ether	97332	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)OC)OC	372.40	unknown	via CMAUP database
Retusin	5352005	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC	358.30	unknown	https://doi.org/10.1016/0031-9422(83)83075-1
Sakuranetin	73571	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O	286.28	unknown	https://doi.org/10.1016/S0031-9422(01)00451-4
Tectochrysin	5281954	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O	268.26	unknown	https://doi.org/10.1016/0031-9422(83)83075-1 https://doi.org/10.1021/NP070286M
Tetramethylkaempferol	631095	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)OC	342.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(2S,8S)-5-hydroxy-2-methyl-2-(4-methylpent-3-enyl)-8-phenyl-7,8-dihydropyrano[3,2-g]chromen-6-one	162981219	Click to see CC(=CCCC1(C=CC2=C(C3=C(C=C2O1)OC(CC3=O)C4=CC=CC=C4)O)C)C	390.50	unknown	https://doi.org/10.1021/NP070286M
5-Hydroxy-2-methyl-2-(4-methylpent-3-enyl)-8-phenyl-7,8-dihydropyrano[3,2-g]chromen-6-one	162981218	Click to see CC(=CCCC1(C=CC2=C(C3=C(C=C2O1)OC(CC3=O)C4=CC=CC=C4)O)C)C	390.50	unknown	https://doi.org/10.1021/NP070286M
> Phenylpropanoids and polyketides / Kavalactones
2H-Pyran-2-one, 4-methoxy-6-(2-phenylethyl)-	160673	Click to see COC1=CC(=O)OC(=C1)CCC2=CC=CC=C2	230.26	unknown	https://doi.org/10.1016/S0031-9422(01)00451-4
4-Methoxy-6-(2-phenylethenyl)-2h-pyran-2-one	164901	Click to see COC1=CC(=O)OC(=C1)C=CC2=CC=CC=C2	228.24	unknown	https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1021/NP070286M
Demethoxyyangonin	5273621	Click to see COC1=CC(=O)OC(=C1)C=CC2=CC=CC=C2	228.24	unknown	https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1021/NP070286M
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
2',6'-Dihydroxy-4'-methoxydihydrochalcone	169676	Click to see COC1=CC(=C(C(=C1)O)C(=O)CCC2=CC=CC=C2)O	272.29	unknown	https://doi.org/10.1248/CPB.56.956
4,2',4'-Trihydroxy-6'-methoxydihydrochalcone	42607705	Click to see COC1=CC(=CC(=C1C(=O)CCC2=CC=C(C=C2)O)O)O	288.29	unknown	https://doi.org/10.1016/J.BMC.2005.10.019
Phloretin	4788	Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2O)O)O)O	274.27	unknown	https://doi.org/10.1016/J.BMC.2005.10.019
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-1-[(1R,4S,13R)-9-hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7,9,11-trien-8-yl]-3-phenylprop-2-en-1-one	101306880	Click to see CC1(C2CCC3(CC2C4=C(O3)C=C(C(=C4O1)C(=O)C=CC5=CC=CC=C5)O)C)C	390.50	unknown	https://doi.org/10.1071/CH9840449
(E)-1-[(2R)-7-hydroxy-5-methoxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-3-phenylprop-2-en-1-one	163004499	Click to see CC(=CCCC1(C=CC2=C(C=C(C(=C2O1)C(=O)C=CC3=CC=CC=C3)O)OC)C)C	404.50	unknown	https://doi.org/10.1071/CH9840449 https://doi.org/10.1021/NP070286M
(E)-1-[(2S)-5-hydroxy-7-methoxy-2-methyl-2-(4-methylpent-3-enyl)chromen-6-yl]-3-phenylprop-2-en-1-one	154496269	Click to see CC(=CCCC1(C=CC2=C(C(=C(C=C2O1)OC)C(=O)C=CC3=CC=CC=C3)O)C)C	404.50	unknown	https://doi.org/10.1021/NP070286M https://doi.org/10.1071/CH9841739
(E)-1-[(2S)-7-hydroxy-5-methoxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-3-phenylprop-2-en-1-one	154496268	Click to see CC(=CCCC1(C=CC2=C(C=C(C(=C2O1)C(=O)C=CC3=CC=CC=C3)O)OC)C)C	404.50	unknown	https://doi.org/10.1016/S0031-9422(01)00451-4
1-(2,4-Dihydroxy-6-methoxyphenyl)-3-phenylprop-2-en-1-one	154102	Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O	270.28	unknown	https://doi.org/10.1016/J.BMCL.2005.12.075 https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1021/NP070286M https://doi.org/10.1016/J.BMC.2005.10.019
1-(9-Hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7,9,11-trien-8-yl)-3-phenylprop-2-en-1-one	74074113	Click to see CC1(C2CCC3(CC2C4=C(O3)C=C(C(=C4O1)C(=O)C=CC5=CC=CC=C5)O)C)C	390.50	unknown	https://doi.org/10.1071/CH9840449
1-[5-Hydroxy-7-methoxy-2-methyl-2-(4-methylpent-3-enyl)chromen-6-yl]-3-phenylprop-2-en-1-one	74076149	Click to see CC(=CCCC1(C=CC2=C(C(=C(C=C2O1)OC)C(=O)C=CC3=CC=CC=C3)O)C)C	404.50	unknown	https://doi.org/10.1021/NP070286M
1-[7-Hydroxy-5-methoxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-3-phenylprop-2-en-1-one	5256732	Click to see CC(=CCCC1(C=CC2=C(C=C(C(=C2O1)C(=O)C=CC3=CC=CC=C3)O)OC)C)C	404.50	unknown	https://doi.org/10.1071/CH9840449 https://doi.org/10.1021/NP070286M
2',4-Dihydroxy-4',6'-dimethoxychalcone	6293081	Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=C(C=C2)O)O	300.30	unknown	https://doi.org/10.1021/NP070286M
2',4',4-Trihydroxy-6'-methoxychalcone	162957	Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=C(C=C2)O)O)O	286.28	unknown	https://doi.org/10.1016/J.BMC.2005.10.019
3-Phenyl-1-(2,4,6-trihydroxyphenyl)prop-2-en-1-one	460718	Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2O)O)O	256.25	unknown	https://doi.org/10.1271/BBB.90114
boesenbergin A	6313827	Click to see CC(=CCCC1(C=CC2=C(C=C(C(=C2O1)C(=O)C=CC3=CC=CC=C3)O)OC)C)C	404.50	unknown	https://doi.org/10.1071/CH9840449
Cardamonin	641785	Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O	270.28	unknown	https://doi.org/10.1016/0031-9422(93)80020-S https://doi.org/10.1271/BBB.57.1971 https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1021/NP070286M https://doi.org/10.1016/J.BMCL.2005.12.075 https://doi.org/10.1016/J.BMC.2005.10.019 https://doi.org/10.1021/JF010016O
CID 5179897	5179897	Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=C(C=C2)O)O	300.30	unknown	https://doi.org/10.1021/NP070286M
Flavokawain A	5355469	Click to see COC1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2OC)OC)O	314.30	unknown	https://doi.org/10.1016/S0031-9422(01)00451-4
Helichrysetin	6253344	Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=C(C=C2)O)O)O	286.28	unknown	https://doi.org/10.1016/J.BMC.2005.10.019
Pinocembrin chalcone	6474295	Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2O)O)O	256.25	unknown	https://doi.org/10.1271/BBB.90114 https://doi.org/10.1021/JF010016O
Pinostrobin chalcone	5316793	Click to see COC1=CC(=C(C(=C1)O)C(=O)C=CC2=CC=CC=C2)O	270.28	unknown	https://doi.org/10.1016/S0031-9422(01)00451-4
Rubranine	42607681	Click to see CC1(C2CCC3(CC2C4=C(O3)C=C(C(=C4O1)C(=O)C=CC5=CC=CC=C5)O)C)C	390.50	unknown	https://doi.org/10.1016/S0031-9422(01)00451-4 https://doi.org/10.1071/CH9840449
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
(E)-1-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4-dihydroxy-6-methoxyphenyl]-3-phenylprop-2-en-1-one	23656471	Click to see CC(=CCCC(=CCC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=CC=C2)O)C)C	406.50	unknown	https://doi.org/10.1021/NP070286M
1-[3-(3,7-Dimethylocta-2,6-dienyl)-2,4-dihydroxy-6-methoxyphenyl]-3-phenylprop-2-en-1-one	74080981	Click to see CC(=CCCC(=CCC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=CC=C2)O)C)C	406.50	unknown	https://doi.org/10.1021/NP070286M
> Phenylpropanoids and polyketides / Stilbenes
2,4-Dihydroxy-6-phenethyl-benzoic acid methyl ester	14195786	Click to see COC(=O)C1=C(C=C(C=C1O)O)CCC2=CC=CC=C2	272.29	unknown	https://doi.org/10.1248/CPB.56.956
3,7-Dimethylocta-2,6-dienyl 2,4-dihydroxy-6-(2-phenylethyl)benzoate	74080979	Click to see CC(=CCCC(=CCOC(=O)C1=C(C=C(C=C1O)O)CCC2=CC=CC=C2)C)C	394.50	unknown	https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1021/NP070286M
Geranyl-2,4-dihydroxy-6-phenethylbenzoate	23656469	Click to see CC(=CCCC(=CCOC(=O)C1=C(C=C(C=C1O)O)CCC2=CC=CC=C2)C)C	394.50	unknown	https://doi.org/10.1248/CPB.56.956 https://doi.org/10.1021/NP070286M

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Boesenbergia rotunda

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