Lagerstroemia speciosa, also known as giant crepe-myrtle, Queen's crepe-myrtle, banabá plant, or pride of India, is a deciduous tree native to tropical southern Asia. Its name "Queen's Flower" comes from the specific epithet 'reginae', meaning "imperial or flower of the queen". The tree produces beautiful pink, purple, and lilac flowers that last for several months. It is also known for its strong timber, second only to teak. The tree is cultivated for its ornamental value and is used in traditional medicine for its medicinal properties. In Hindu mythology, it is believed that worshipping Lord Brahma will result in the blossoming of these flowers, bringing prosperity to the house. In Buddhism, it is said to have been used as the tree for achieving enlightenment by two Buddhas. It is recognized as the state flower of Maharashtra in India.

Synonyms Top

Scientific name	Authority	First published in
Lagerstroemia punctata	Blume	Mus. Bot. 2: 126 (1856)
Lagerstroemia plicifolia	Stokes	Bot. Mat. Med. 3: 105 (1812)
Lagerstroemia munchausia	Willd.	Sp. Pl., ed. 4 , 2: 1178 (1799)
Lagerstroemia reginae	Roxb.	Pl. Coromandel 1: 46 (1796)
Lagerstroemia major	Retz.	Observ. Bot. 1: 20 (1779)
Lagerstroemia flos-reginae	Retz.	Observ. Bot. 5: 25 (1788)
Lagerstroemia hirsuta	Willd.	Sp. Pl., ed. 4 , 2: 1178 (1799)
Lagerstroemia augusta	Wall.	Numer. List [Wallich] n. 2113. 1829
Munchausia speciosa	Münchh.	Hausvater 5: 357 (1770).
Munchausia ovata	J.St.-Hil.	Expos. Fam. Nat. 2: 176 (1805)
Murtughas hirsuta	Kuntze	Revis. Gen. Pl. 1: 249 (1891)
Murtughas punctata	Kuntze	Revis. Gen. Pl. 1: 250 (1891)
Murtughas speciosa	Kuntze	Revis. Gen. Pl. 1: 249 (1891)
Sotularia malabarica	Raf.	Sylva Tellur. : 98 (1838)
Adambea glabra	Lam.	Encycl. 1: 39 (1783)
Adambea hirsuta	Lam.	Encycl. 1: 39 (1783)

Common names Top

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Filter by language:

Language	Common/alternative name
English	giant crape-myrtle
English	pride of india
Assamese	এজাৰ
bcl	banaba
bjn	bungur
Bengali	জারুল
German	königinblume
Greek	Λαγερστροιμία η μεγαλοπρεπής
Persian	درختچه توری ملکه
French	lagerstrœmia speciosa
Gujarati	જરૂલ
Hindi	जरुल
Japanese	バナバ
Japanese	大花百日紅
Japanese	オオバナサルスベリ
Malayalam	പുൽവായ്
Malayalam	പൂമരുത്
Malayalam	വെടമരുത്
Malayalam	മരുതി
Malayalam	മണിമരുത്
Malayalam	പേമരുത്
Malayalam	പൂമരിത
Malayalam	പുലമരു
Malayalam	പീമരുത്
Malayalam	പീകടുക്കൈ
Malayalam	പിള്ളൈമരുത്
Malayalam	പിളളമരുത്
Malayalam	പിളമരുത്
Malayalam	ജാറൂൾ
Malayalam	അടമരുത്
Malayalam	queen's crape-myrtle
Malayalam	lagerstroemia reginae
Malayalam	giant crape-myrtle
Malayalam	വെൺമരുത്
Marathi	ताम्हण
Burmese	ပျဉ်းမ
pam	mitla
Polish	lagerstremia wspaniała
Portuguese	resedá-gigante
Portuguese	resedá gigante
Tamil	கதலி
Telugu	సొగసులచెట్టు
Thai	อินทนิล
Thai	อินทนิลน้ำ
Thai	ตะแบกอินเดีย
Vietnamese	bằng lăng
Vietnamese	hoa bằng lăng
Chinese	大葉紫薇
Chinese	大叶紫薇
Chinese	大花紫薇
Chinese	百日红

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Lagerstroemia speciosa subsp. intermedia	(Koehne) Deepu & Pandur.	Phytotaxa 296(3): 297 (2017)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Western Indian Ocean
  - Comoros

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

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Sri Lanka
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - New Guinea

Pacific click to expand
- Northwestern Pacific
  - Marianas
- Southwestern Pacific
  - Fiji
  - Vanuatu

Southern America click to expand
- Caribbean
  - Cuba
  - Dominican Republic
  - Haiti
  - Jamaica
  - Leeward Islands
  - Puerto Rico
  - Trinidad-Tobago
  - Venezuelan Antilles

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000366693
UNII	UOV610JOOF
USDA Plants	LASP
Tropicos	19200243
INPN	445739
KEW	urn:lsid:ipni.org:names:553618-1
The Plant List	kew-2353907
Open Tree Of Life	838580
NCBI Taxonomy	122810
IPNI	553618-1
iNaturalist	133607
GBIF	3188724
Freebase	/m/0d2s9s
EPPO	LAESP
EOL	582108
USDA GRIN	21399
Wikipedia	Lagerstroemia_speciosa
CMAUP	NPO5032

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Pest categorisation of Pyrrhoderma noxium

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

EFSA J

19-Mar-2024

PMCID:	PMC10949325
doi:	10.2903/j.efsa.2024.8667
PMID:	38505477

Oxidative Stress: The Role of Antioxidant Phytochemicals in the Prevention and Treatment of Diseases

Muscolo A, Mariateresa O, Giulio T, Mariateresa R

Int J Mol Sci

13-Mar-2024

PMCID:	PMC10970659
doi:	10.3390/ijms25063264
PMID:	38542238

Genomic evidence for rediploidization and adaptive evolution following the whole-genome triplication

Feng X, Chen Q, Wu W, Wang J, Li G, Xu S, Shao S, Liu M, Zhong C, Wu CI, Shi S, He Z

Nat Commun

22-Feb-2024

PMCID:	PMC10884412
doi:	10.1038/s41467-024-46080-7
PMID:	38388712

Exploring synthesis and applications of green nanoparticles and the role of nanotechnology in wastewater treatment

Rathod S, Preetam S, Pandey C, Bera SP

Biotechnol Rep (Amst)

26-Jan-2024

PMCID:	PMC10850744
doi:	10.1016/j.btre.2024.e00830
PMID:	38332899

Dietary Supplementation with 23-Hydroxy Ursolic Acid Reduces the Severity and Incidence of Acute Experimental Autoimmune Encephalomyelitis (EAE) in a Murine Model of Multiple Sclerosis

Asmis R, Medrano MT, Chase Huizar C, Griffith WP, Forsthuber TG

Nutrients

25-Jan-2024

PMCID:	PMC10856865
doi:	10.3390/nu16030348
PMID:	38337633

Phenolic Compounds and Antioxidant Capacity Comparison of Wild-Type and Yellow-Leaf gl1 Mutant of Lagerstroemia indica

Li S, Yin M, Wang P, Gao L, Lv F, Yang R, Li Y, Wang Q, Li L, Liu Y, Wang S

Plants (Basel)

20-Jan-2024

PMCID:	PMC10818265
doi:	10.3390/plants13020315
PMID:	38276772

Silver nanoparticles improve the fungicidal properties of Rhazya stricta decne aqueous extract against plant pathogens

Al-Sahli SA, Al-Otibi F, Alharbi RI, Amina M, Al Musayeib NM

Sci Rep

14-Jan-2024

PMCID:	PMC10788342
doi:	10.1038/s41598-024-51855-5
PMID:	38221517

Cuticular wax biosynthesis in blueberries (Vaccinium corymbosum L.): Transcript and metabolite changes during ripening and storage affect key fruit quality traits

Yan Y, Gagalova KK, Gerbrandt EM, Castellarin SD

Hortic Res

09-Jan-2024

PMCID:	PMC10923646
doi:	10.1093/hr/uhae004
PMID:	38464479

Retracted: Lagerstroemia speciosa Ameliorated Blood Pressure in LNAME Induced Hypertension in Experimental Rats through NO/cGMP and Oxidative Stress Modulation

International BR

Biomed Res Int

09-Jan-2024

PMCID:	PMC10791357
doi:	10.1155/2024/9792123
PMID:	38230062

Lagerstroemia speciosa Pers. (Lythraceae) Ethanolic Extract Attenuates Isoniazid-Induced Oxidative Stress and Hepatic Inflammation in Rats

Rohit Singh T, Ezhilarasan D, Karthick M, Shree Harini K

Cureus

03-Jan-2024

PMCID:	PMC10837052
doi:	10.7759/cureus.51609
PMID:	38313882

Geometric entropy of plant leaves: A measure of morphological complexity

Muraleedharan V, Rajan SC, R J

PLoS One

02-Jan-2024

PMCID:	PMC10760904
doi:	10.1371/journal.pone.0293596
PMID:	38166118

Seasonal variation of two floral patterns in Clematis ‘Vyvyan Pennell’ and its underlying mechanism

Wang Y, Pan Y, Peng L, Wang J

BMC Plant Biol

02-Jan-2024

PMCID:	PMC10759560
doi:	10.1186/s12870-023-04696-9
PMID:	38166716

Genome-Wide Analysis of the MADS-Box Gene Family in Hibiscus syriacus and Their Role in Floral Organ Development

Wang J, Ye H, Li X, Lv X, Lou J, Chen Y, Yu S, Zhang L

Int J Mol Sci

28-Dec-2023

PMCID:	PMC10779063
doi:	10.3390/ijms25010406
PMID:	38203576

Unveiling the Potent Antiviral and Antioxidant Activities of an Aqueous Extract from Caesalpinia mimosoides Lamk: Cheminformatics and Molecular Docking Approaches

Klamrak A, Nabnueangsap J, Narkpuk J, Saengkun Y, Janpan P, Nopkuesuk N, Chaveerach A, Teeravechyan S, Rahman SS, Dobutr T, Sitthiwong P, Maraming P, Nualkaew N, Jangpromma N, Patramanon R, Daduang S, Daduang J

Foods

25-Dec-2023

PMCID:	PMC10778375
doi:	10.3390/foods13010081
PMID:	38201109

Molecular Docking Study of Phytosterols in Lygodium microphyllum Towards SIRT1 and AMPK, the in vitro Brine Shrimp Toxicity Test, and the Phenols and Sterols Levels in the Extract

Anggreini P, Kuncoro H, Sumiwi SA, Levita J

J Exp Pharmacol

22-Dec-2023

PMCID:	PMC10751218
doi:	10.2147/JEP.S438435
PMID:	38148923

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
1,2-Benzenedi(carboxylic-14C)acid, dibutyl ester	171810	Click to see CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC	282.33	unknown	via CMAUP database
2-Ethylhexyl trimethylsilyl phthalate	91735738	Click to see CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)O[Si](C)(C)C	350.50	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.1021/JF802152Z
> 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/10.1021/JF802152Z
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	https://doi.org/10.1021/JF802152Z
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl palmitate	12366	Click to see CCCCCCCCCCCCCCCC(=O)OCC	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid	445639	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	https://doi.org/10.1016/0031-9422(90)83061-5
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	https://doi.org/10.1016/0031-9422(90)83061-5
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	https://doi.org/10.1016/0031-9422(90)83061-5
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Nonanedioate	3801344	Click to see C(CCCC(=O)[O-])CCCC(=O)[O-]	186.20	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
2-Ethylhexan-1-ol	7720	Click to see CCCCC(CC)CO	130.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
10,13-Octadecadienoic acid	54284936	Click to see CCCCC=CCC=CCCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
9-keto-11Z-octadecenoic acid	131839815	Click to see CCCCCCC=CCC(=O)CCCCCCCC(=O)O	296.40	unknown	https://doi.org/10.1016/0031-9422(90)83061-5
9-Oxooctadec-11-enoic acid	163041763	Click to see CCCCCCC=CCC(=O)CCCCCCCC(=O)O	296.40	unknown	https://doi.org/10.1016/0031-9422(90)83061-5
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	https://doi.org/10.1016/0031-9422(90)83061-5
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2-hexadecen-1-OL	5366244	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	https://doi.org/10.1080/10286020310001596024
Phytol	5280435	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	https://doi.org/10.1080/10286020310001596024
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral	638011	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Lutein	5281243	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C	568.90	unknown	https://doi.org/10.1080/10286020310001596024
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-10,11-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	15917996	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	https://doi.org/10.1021/JF802152Z
(1S,2R,4aS,6aS,6aS,6bR,8aS,9S,11R,12aR,14bS)-8a,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-1,2,3,4,5,6,6a,7,8,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	51340198	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5(C4(CC(CC5(C)CO)O)C)O)C)C2C1C)C)C(=O)O	488.70	unknown	via CMAUP database
(1S,2R,4aS,6aS,6bR,10R,11R,12aR,14bS)-10,11-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	5316084	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	https://doi.org/10.1016/J.DIABRES.2006.01.010
(4aS,6aS,6aS,6bR,8aR,10R,11R,12aR,14bS)-10,11-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	11887403	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C	472.70	unknown	via CMAUP database
23-Hydroxyursolic Acid	14136881	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	via CMAUP database
Corosolic acid	6918774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	https://doi.org/10.1021/JF802152Z https://doi.org/10.1002/CHIN.200337151 https://doi.org/10.1016/J.DIABRES.2006.01.010 https://doi.org/10.1248/CPB.41.2129
Maslinic Acid	73659	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C	472.70	unknown	https://doi.org/10.1248/CPB.41.2129
Oleanolic Acid (Caryophyllin)	49867939	Click to see CC1(CC2C(CCC3(C2=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(C1)C(=O)O)C	456.70	unknown	via CMAUP database
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1002/CHIN.200337151
Ursolic acid (Malol)	49867942	Click to see CC1CC(C2CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
Virgatic acid	14489125	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	470.70	unknown	https://doi.org/10.1002/CHIN.200337151
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
24-Methylene-cycloartanol	9547213	Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	440.70	unknown	https://doi.org/10.1080/10286020310001596024
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1080/10286020310001596024
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1080/10286020310001596024
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1002/CHIN.200337151
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1002/CHIN.200337151
> Organoheterocyclic compounds / Indolizidines
Isopteropodine	9885603	Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O	368.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
9-[2-(Furan-3-yl)ethyl]-4-hydroxy-9,10,12-trimethyl-2-oxatricyclo[6.3.1.04,12]dodec-5-en-3-one	162988601	Click to see CC1CC2C3(C(C1(C)CCC4=COC=C4)CC=CC3(C(=O)O2)O)C	330.40	unknown	https://doi.org/10.1080/10286020310001596024
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid	2518	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1021/JF802152Z
4-Hydroxycinnamic acid	322	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1021/JF802152Z
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1021/JF802152Z
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1021/JF802152Z
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Kaempferol oxoanion	25202062	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)[O-])O	285.23	unknown	via CMAUP database
Quercetin-7-olate	46906036	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)[O-])O)O	301.23	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	https://doi.org/10.1021/JF802152Z
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/10.1021/JF802152Z
> 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/10.1021/JF802152Z
4-[5,7-dihydroxy-4-oxo-3-[(3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-yl]-2-hydroxyphenolate	54758589	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-]	463.40	unknown	via CMAUP database
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/10.1021/JF802152Z
> Phenylpropanoids and polyketides / Macrolides and analogues
Lagerstroemine	78385190	Click to see COC1=C(C2=C(C=C1)C3CC(CC4N3CCCC4)OC(=O)CCC5=CC2=C(C=C5)O)OC	437.50	unknown	https://doi.org/10.1055/S-2002-20251
> Phenylpropanoids and polyketides / Tannins
1,3,6-tri-O-galloyl-beta-D-glucose	452707	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O	636.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(10R,11S,13R,14R,15S)-3,4,5,11,14,20,21,22-octahydroxy-13-(hydroxymethyl)-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaene-8,17-dione	14035454	Click to see C1=C2C(=C(C(=C1O)O)O)C3=C(C(=C(C=C3C(=O)OC4C(C(C(OC4O)CO)O)OC2=O)O)O)O	482.30	unknown	https://doi.org/10.1021/JF802152Z
(10S,11S)-11-[(10R,11R)-3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.02,7]octadeca-1(18),2,4,6,14,16-hexaene-10-carboxylic acid	162947329	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C(OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O4)O)O)O)O)O)O)C(=O)O)O	800.50	unknown	https://doi.org/10.1248/CPB.40.2975
(10S,11S)-11-[(10R,11S)-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.02,7]octadeca-1(18),2,4,6,14,16-hexaene-10-carboxylic acid	163083929	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C(OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O4)O)O)O)O)O)O)C(=O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O	952.60	unknown	https://doi.org/10.1248/CPB.40.2975
(1R,2R,20S,42S,46S)-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-pentadecahydroxy-46-[(2R,3R,4R,5S)-2,3,4,5-tetrahydroxyoxan-2-yl]-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone	163186112	Click to see C1C(C(C(C(O1)(C2C3C4C5C(COC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O5)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C(=C9O)O)O)C1=C(C2=C(C(=C1O)O)O)C(=O)O3)C(=O)O4)O)O)O)O)O)O)O	1066.70	unknown	https://doi.org/10.1248/CPB.40.2975
(1S,2R,20R,42R)-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-pentadecahydroxy-4,17,22,40,44-pentaoxo-3,18,21,41,43-pentaoxaoctacyclo[27.13.3.02,20.05,10.011,16.023,28.033,45.034,39]pentatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34,36,38-pentadecaene-42-carboxylic acid	16142456	Click to see C1C2C(C3C(OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C(=C5C(=O)O3)C6=C(C(=C(C=C6C(=O)O2)O)O)O)O)O)O)O)O)O)C(=O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O	950.60	unknown	via CMAUP database
(2R,3R)-3-[(10S,11S)-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-2,3-dihydroxypropanoic acid	163193104	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C(C(C(=O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	650.50	unknown	https://doi.org/10.1248/CPB.40.2975
(3,4,5,12,13,21,22,23-Octahydroxy-8,18-dioxo-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	13932611	Click to see C1C2C(C(C(C(O2)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O	634.50	unknown	https://doi.org/10.1248/CPB.40.2975
(7,13-Dihydroxy-14-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl) hydrogen sulfate	11545697	Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)O)OS(=O)(=O)O)O	396.30	unknown	https://doi.org/10.1021/JF802152Z
[(10R,11S)-10-[(14R,15S,19R)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate	162948033	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O	936.60	unknown	https://doi.org/10.1021/JF802152Z
[(10R,11S)-10-[(14R,15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate	17999934	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O	936.60	unknown	https://doi.org/10.1021/JF802152Z
[1-(2,3,4,7,8,9,19-Heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl)-1,3-dihydroxypropan-2-yl] 3,4,5-trihydroxybenzoate	14035445	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC(CO)C(C2C3C(C4=C(C(=C(C(=C4C(=O)O3)C5=C(C(=C(C=C5C(=O)O2)O)O)O)O)O)O)O)O	634.50	unknown	https://doi.org/10.1021/JF802152Z
[10-(2,3,4,7,8,9,19-Heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl)-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 2-[(7,8,9,12,13,14,20,28,29,30,33,34-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-35-yl)oxy]-3,4,5-trihydroxybenzoate	162971283	Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)OC8=C(C(=C(C=C8C(=O)OC9COC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)OC9C1C2C(C3=C(C(=C(C(=C3C(=O)O2)C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)O)O)O)O)O)O)O)O)O	1719.20	unknown	https://doi.org/10.1055/S-2002-20251
1-Epi-castalagin	12302512	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	934.60	unknown	https://doi.org/10.1248/CPB.40.2975
11-(3,4,5,11,17,18,19-Heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl)-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.02,7]octadeca-1(18),2,4,6,14,16-hexaene-10-carboxylic acid	85137751	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C(OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O4)O)O)O)O)O)O)C(=O)O)O	800.50	unknown	https://doi.org/10.1248/CPB.40.2975
14-(3,4,5,11,17,18,19-Heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl)-2,3,4,7,8,9,19-heptahydroxy-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaene-12,17-dione	14035439	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O	784.50	unknown	https://doi.org/10.1021/JF802152Z
2-O,3-O-[4,4',5,5',6,6'-Hexahydroxy-1,1'-biphenyl-2,2'-diylbis(carbonyl)]-beta-D-glucopyranose	11754973	Click to see C1=C2C(=C(C(=C1O)O)O)C3=C(C(=C(C=C3C(=O)OC4C(C(C(OC4O)CO)O)OC2=O)O)O)O	482.30	unknown	https://doi.org/10.1021/JF802152Z
2,3-(S)-hexahydroxydiphenoyl-D-glucose	492390	Click to see C1=C2C(=C(C(=C1O)O)O)C3=C(C(=C(C=C3C(=O)OC4C(C(C(OC4O)CO)O)OC2=O)O)O)O	482.30	unknown	https://doi.org/10.1021/JF802152Z
2,3,4-Trihydroxy-5-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]benzoic acid	101156920	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)OC5=C(C(=C(C(=C5)C(=O)O)O)O)O	470.30	unknown	via CMAUP database
2,3,8-Tri-O-methylellagic acid	5281860	Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)O)C(=O)O2)OC	344.30	unknown	https://doi.org/10.1021/JF802152Z
3-[3,4,5,17,18,19-Hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-2,3-dihydroxypropanoic acid	85130969	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C(C(C(=O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	650.50	unknown	https://doi.org/10.1248/CPB.40.2975
3-O-methylellagic acid	13915428	Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O)O	316.22	unknown	https://doi.org/10.1021/JF802152Z
3,3'-Di-O-methylellagic acid	5488919	Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)OC)O)O	330.24	unknown	https://doi.org/10.1021/JF802152Z
3,3',4-tri-O-methylflavellagic acid	14412544	Click to see COC1=C(C=C2C3=C1OC(=O)C4=C3C(=C(C(=C4O)OC)OC)OC2=O)O	360.30	unknown	via CMAUP database
3,4,8,9,10-Pentahydroxybenzo[c]chromen-6-one	18504424	Click to see C1=CC(=C(C2=C1C3=C(C(=C(C=C3C(=O)O2)O)O)O)O)O	276.20	unknown	https://doi.org/10.1021/JF802152Z
4-O,6-O-(2,2',3,3',4,4'-Hexahydroxybiphenyl-6,6'-diylbiscarbonyl)-3-O-(3,4,5-trihydroxybenzoyl)-alpha-D-glucopyranose	10461723	Click to see C1C2C(C(C(C(O2)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O	634.50	unknown	https://doi.org/10.1248/CPB.40.2975
4,4'-Di-O-methylellagic acid	11580745	Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4O)OC)C(=O)O2)O	330.24	unknown	via CMAUP database
7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-Pentadecahydroxy-46-(2,3,4,5-tetrahydroxyoxan-2-yl)-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone	14428075	Click to see C1C(C(C(C(O1)(C2C3C4C5C(COC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O5)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C(=C9O)O)O)C1=C(C2=C(C(=C1O)O)O)C(=O)O3)C(=O)O4)O)O)O)O)O)O)O	1066.70	unknown	https://doi.org/10.1248/CPB.40.2975
Casuariin	14035442	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O	784.50	unknown	https://doi.org/10.1021/JF802152Z
CID 12302513	12302513	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	934.60	unknown	https://doi.org/10.1248/CPB.40.2975
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/10.1016/J.JEP.2004.04.012 https://doi.org/10.1021/JF802152Z
Hippophaenin A	16130427	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C(OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O4)O)O)O)O)O)O)C(=O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O	952.60	unknown	https://doi.org/10.1248/CPB.40.2975
Kzeyiyxacmutrm-uhfffaoysa-	44631480	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C(C(C(=O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O	802.60	unknown	via CMAUP database
Punicacortein A	14035447	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC(CO)C(C2C3C(C4=C(C(=C(C(=C4C(=O)O3)C5=C(C(=C(C=C5C(=O)O2)O)O)O)O)O)O)O)O	634.50	unknown	https://doi.org/10.1021/JF802152Z
Stachyurin	157395	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O	936.60	unknown	https://doi.org/10.1021/JF802152Z
Vescalagin	168165	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	934.60	unknown	https://doi.org/10.1248/CPB.40.2975

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Lagerstroemia speciosa

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