Terminalia arjuna

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Subtypes (subspecies, varieties, subvarieties, forms)

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Scientific Literature

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Details Top

Internal ID	UUID643ff90b91b81416556852
Scientific name	Terminalia arjuna
Authority	(Roxb. ex DC.) Wight & Arn.
First published in	Prodr. Fl. Ind. Orient. : 314 (1834)

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Synonyms Top

Scientific name	Authority	First published in
Myrobalanus cuneata	Kuntze	Revis. Gen. Pl. 1: 236 (1891)
Pentaptera obovata	DC.	Prodr. 3: 14 (1828)
Pentaptera glabra	Roxb.	Fl. Ind. (Roxburgh) 2: 440. 1832
Pentaptera angustifolia	Roxb.	Fl. Ind. ed. 1832 , 2: 437 (1832)
Terminalia cuneata	Roth	Nov. Pl. Sp. : 380 (1821)
Terminalia berryi	Wight & Arn.	Prodr. Fl. Ind. Orient. : 314 (1834)
Terminalia psidiifolia	Delile	Voy. Méroé 4(prepr.): 92 (1826)
Terminalia urjan	Royle	Ill. Bot. Himal. Mts. [Royle] 209. 1835 [Apr 1835]
Terminalia glabra	Wight & Arn.	Prodr. Fl. Ind. Orient. : 314 (1834)
Terminalia ovalifolia	Rottler ex C.B.Clarke	Fl. Brit. India 2: 447 (1878)
Pentaptera arjuna	Roxb. ex DC.	Prodr. 3: 15 (1828)

Common names Top

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Language	Common/alternative name
English	arjuna
English	arjun tree
Arabic	إهليلج أرجوانا
Assamese	অৰ্জুন গছ
Bengali	অর্জুন
Persian	درخت ارجون
French	arjunier
Hebrew	טרמינליה הודית
Hindi	अर्जुन वृक्ष
Japanese	アジュンナ
Japanese	アルジュナ (植物)
Kannada	ಮತ್ತಿ
Malayalam	ആറ്റുമരുത്
Malayalam	നീർമരുത്
Malayalam	പുലമാറ്റി
Marathi	अर्जुनसादडा
Marathi	अर्जुन वृक्ष
Oriya	ଅର୍ଜୁନ ଗଛ
Oriya	ଅର୍ଜ୍ଜୁନ
Punjabi	ਅਰਜੁਨ
Polish	migdałecznik arjuna
Russian	арджуна
Russian	Кукубха
Russian	Терминалия арджуна
sa	अर्जुनवृक्षः
sa	अश्वत्थः
sd	ارجن
Sinhala	කුඹුක්
Tamil	மருதம்
Telugu	తెల్ల మద్ది
Urdu	ارجن (درخت)
Chinese	阿江榄仁
Chinese	阿江欖仁
Chinese	阿周陀那

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) 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

Africa click to expand
- Western Indian Ocean
  - Mauritius
  - Rodrigues

Asia-temperate click to expand
- China
  - China Southeast

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - India
  - Pakistan
  - Sri Lanka

Southern America click to expand
- Caribbean
  - Trinidad-Tobago
  - Venezuelan Antilles
- Northern South America
  - Venezuela

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000407013
UNII	5T6S1T25EB
Florida Plant Atlas	4423
Tropicos	8200009
INPN	630783
KEW	urn:lsid:ipni.org:names:170962-1
The Plant List	kew-2431544
Open Tree Of Life	369280
NCBI Taxonomy	172200
IPNI	170962-1
iNaturalist	464765
GBIF	3699548
Freebase	/m/026c3fm
EPPO	TEMAJ
EOL	2876252
USDA GRIN	80199
Wikipedia	Terminalia_arjuna

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

Slow pyrolysis of Terminalia catappa L. municipal solid waste and the use of the aqueous fraction produced for bovine mastitis control

Vinturelle R, Cabral TD, Oliveira PC, Salles JP, Faria JV, Teixeira GP, Faria RX, Veloso MC, Romeiro GA, Chagas ED

Biochem Biophys Rep

09-Apr-2024

PMCID:	PMC11016915
doi:	10.1016/j.bbrep.2024.101704
PMID:	38623537

Isolation and characterization of a newly discovered plant growth-promoting endophytic fungal strain from the genus Talaromyces

Kharkwal AC, Joshi H, Shandilya C, Dabral S, Kumar N, Varma A

Sci Rep

12-Mar-2024

PMCID:	PMC10933278
doi:	10.1038/s41598-024-54687-5
PMID:	38472228

Characterization of carbon fluxes, stock and nutrients in the sacred forest groves and invasive vegetation stands within the human dominated landscapes of a tropical semi-arid region

Akil Prasath RV, Mohanraj R, Balaramdas KR, Jhony Kumar Tagore A, Raja P, Rajasekaran A

Sci Rep

24-Feb-2024

PMCID:	PMC10894248
doi:	10.1038/s41598-024-55294-0
PMID:	38402350

Enhancing the lipid stability of foods of animal origin using edible packaging systems

Bhat ZF, Bhat HF, Manzoor M, Abdi G, Aadil RM, Hassoun A, Aït-Kaddour A

Food Chem X

14-Feb-2024

PMCID:	PMC10879673
doi:	10.1016/j.fochx.2024.101185
PMID:	38384687

Structural and electrochemical evaluation of renewable carbons and their composites on different carbonization temperatures for supercapacitor applications

Shrestha D

Heliyon

08-Feb-2024

PMCID:	PMC10869866
doi:	10.1016/j.heliyon.2024.e25628
PMID:	38370182

Biochemical characterization of bioinspired nanosuspensions from Swertia chirayita extract and their therapeutic effects through nanotechnology approach

Raza A, Ali T, Naeem M, Asim M, Hussain F, Li Z, Nasir A

PLoS One

08-Feb-2024

PMCID:	PMC10852254
doi:	10.1371/journal.pone.0293116
PMID:	38330034

Medicinal herbs and their metabolites with biological potential to protect and combat liver toxicity and its disorders: A review

Islam Shawon S, Nargis Reyda R, Qais N

Heliyon

01-Feb-2024

PMCID:	PMC10864916
doi:	10.1016/j.heliyon.2024.e25340
PMID:	38356556

A Comparative In Vitro Analysis of Antimicrobial Effectiveness and Compressive Resilience in Chirata and Terminalia arjuna Modified Glass Ionomer Cement

Devi K, Paulraj J, George RS, Shanmugam R, Maiti S

Cureus

13-Jan-2024

PMCID:	PMC10859781
doi:	10.7759/cureus.52198
PMID:	38347981

Investigating the phenology and interactions of competitive plant species co-occurring with invasive Lantana camara in Indian Himalayan Region

Kumar A, Singh S, Kumar D, Singh RK, Gupta AK, Premkumar K, Chand HB, Kewat AK

Sci Rep

03-Jan-2024

PMCID:	PMC10764828
doi:	10.1038/s41598-023-50287-x
PMID:	38172161

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

Silvicultural Practices for Diversity Conservation and Invasive Species Suppression in Forest Ecosystems of the Bundala National Park, Sri Lanka

Suraweera C, Gallo J, Vacek Z, Cukor J, Vacek S, Baláš M

Plants (Basel)

31-Dec-2023

PMCID:	PMC10780521
doi:	10.3390/plants13010121
PMID:	38202429

Cytocompatibility, Antimicrobial and Antioxidant Activity of a Mucoadhesive Biopolymeric Hydrogel Embedding Selenium Nanoparticles Phytosynthesized by Sea Buckthorn Leaf Extract

Tritean N, Dimitriu L, Dima ȘO, Stoica R, Trică B, Ghiurea M, Moraru I, Cimpean A, Oancea F, Constantinescu-Aruxandei D

Pharmaceuticals (Basel)

22-Dec-2023

PMCID:	PMC10819796
doi:	10.3390/ph17010023
PMID:	38256857

Insights into Zika Virus Pathogenesis and Potential Therapeutic Strategies

Camacho-Concha N, Santana-Román ME, Sánchez NC, Velasco I, Pando-Robles V, Pedraza-Alva G, Pérez-Martínez L

Biomedicines

15-Dec-2023

PMCID:	PMC10741857
doi:	10.3390/biomedicines11123316
PMID:	38137537

Masson pine pollen aqueous extract ameliorates cadmium-induced kidney damage in rats

Hu Z, Chen S, Shi T, Dong Z, Cheng M, Li N, Zhao H, Zhu H, Han C, Xu L

Front Mol Biosci

06-Dec-2023

PMCID:	PMC10748820
doi:	10.3389/fmolb.2023.1249744
PMID:	38143799

Review green synthesis of silver nanoparticles by using plant extracts and their antimicrobial activity

Abada E, Mashraqi A, Modafer Y, Al Abboud MA, El-Shabasy A

Saudi J Biol Sci

26-Nov-2023

PMCID:	PMC10749906
doi:	10.1016/j.sjbs.2023.103877
PMID:	38148949

Phytochemical Profile Top

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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 / 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/10.1016/S0378-8741(96)01421-3 https://doi.org/10.1016/S0031-9422(97)01078-9 https://doi.org/10.1016/0031-9422(82)83042-2
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Ethyl gallate	13250	Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O	198.17	unknown	https://doi.org/10.1016/S0378-8741(96)01421-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
8-Hydroxyhexadecanoic acid	15569773	Click to see CCCCCCCCC(CCCCCCC(=O)O)O	272.42	unknown	https://doi.org/10.1016/0031-9422(82)83042-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,10S,11S,12aS,14bR)-10,11-dihydroxy-12a-(hydroxymethyl)-2,2,6a,6b,9,9-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	3052779	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)CO)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	650.80	unknown	https://doi.org/10.1016/S0731-7085(01)00590-8 https://doi.org/10.1016/0031-9422(82)83042-2 https://doi.org/10.1002/PCA.643
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aS,6aS,6bR,10R,11R,12aS,14bR)-10,11-dihydroxy-12a-(hydroxymethyl)-2,2,6a,6b,9,9-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	182035	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)CO)C)C2C1)C)C(=O)O)C	488.70	unknown	https://doi.org/10.1055/S-2006-959380 https://doi.org/10.1016/0031-9422(91)83075-V https://doi.org/10.1016/S0731-7085(01)00590-8 https://doi.org/10.1002/PCA.643
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 1,10,11-trihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	58880815	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	650.80	unknown	https://doi.org/10.1002/PCA.643 https://doi.org/10.1016/S0731-7085(01)00590-8
Arjugenin	12444386	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1O)C)C(=O)O)C	504.70	unknown	https://doi.org/10.1002/PCA.643 https://doi.org/10.1016/S0731-7085(01)00590-8
arjunglucoside I	14658050	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	666.80	unknown	https://doi.org/10.1002/PCA.643
Arjunic acid	15385516	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1O)C)C(=O)O)C	488.70	unknown	https://doi.org/10.1002/PCA.643 https://doi.org/10.1016/0031-9422(91)83075-V https://doi.org/10.1055/S-2006-959380 https://doi.org/10.1016/S0731-7085(01)00590-8
Arjunolic acid	73641	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C	488.70	unknown	https://doi.org/10.1016/S0731-7085(01)00590-8 https://doi.org/10.1002/PCA.643 https://doi.org/10.1016/0031-9422(91)83075-V
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1055/S-2006-959380 https://doi.org/10.1016/0031-9422(91)83075-V
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1055/S-2006-959380 https://doi.org/10.1016/S0040-4020(01)93250-8 https://doi.org/10.1016/0031-9422(82)83042-2 https://doi.org/10.1016/0031-9422(83)85039-0
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/10.1055/S-2006-959380
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(2R,3R,4R,5S,6S)-6-[2-oxo-2-(3,4,5-trihydroxyphenyl)ethyl]-3,4,5-tris[(3,4,5-trihydroxybenzoyl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	162817372	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)CC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O	938.70	unknown	https://doi.org/10.1016/S0031-9422(97)01078-9
[(2R,3R,4R,5S)-3,4,5-tris[(3,4,5-trihydroxybenzoyl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	11520609	Click to see C1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O	772.60	unknown	https://doi.org/10.1016/S0031-9422(97)01078-9
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(+)-Leucocyanidin	155206	Click to see C1=CC(=C(C=C1C2C(C(C3=C(C=C(C=C3O2)O)O)O)O)O)O	306.27	unknown	https://doi.org/10.1002/CHIN.197048417
Leucocianidol	440833	Click to see C1=CC(=C(C=C1C2C(C(C3=C(C=C(C=C3O2)O)O)O)O)O)O	306.27	unknown	https://doi.org/10.1016/0031-9422(82)83042-2
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1016/S0378-8741(96)01421-3
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R)-2-(2,4-dimethoxyphenyl)-5,7-dimethoxy-2,3-dihydrochromen-4-one	154496183	Click to see COC1=CC(=C(C=C1)C2CC(=O)C3=C(O2)C=C(C=C3OC)OC)OC	344.40	unknown	https://doi.org/10.1055/S-0028-1097325
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
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/10.1055/S-2006-959380
> Phenylpropanoids and polyketides / Tannins / Complex tannins
Psidinin C	131752695	Click to see C1C(C(OC2=C1C(=CC3=C2C4C5C(OC(=O)C6=CC(=C(C(=C6C7=C(C(=O)C4(C7C(=O)O5)O3)O)O)O)O)C8C(COC(=O)C9=CC(=C(C(=C9C1=C(C(=C(C=C1C(=O)O8)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)C1=CC(=C(C(=C1)O)O)O)O	1194.90	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.006
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(15R)-3,4,5,11,12,13,21,22,23,26,27,38,39-tridecahydroxy-9,14,17,29,36-pentaoxaoctacyclo[29.8.0.02,7.010,15.019,24.025,34.028,33.032,37]nonatriaconta-1(39),2,4,6,19,21,23,25,27,31,33,37-dodecaene-8,18,30,35-tetrone	134694222	Click to see C1C2C(C(C(C(O2)O)O)O)OC(=O)C3=CC(=C(C(=C3C4=C(C(=C5C6=C4C(=O)OC7=C(C(=C(C8=C(C(=C(C=C8C(=O)O1)O)O)O)C(=C67)C(=O)O5)O)O)O)O)O)O)O	782.50	unknown	https://doi.org/10.1016/S0031-9422(97)01078-9 https://doi.org/10.1016/J.FITOTE.2010.01.006
(1R,2R,19S,20S,22R)-7,8,9,12,13,14,28,29,30,33,34,35-dodecahydroxy-20-[2-oxo-2-(3,4,5-trihydroxyphenyl)ethyl]-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-dodecaene-4,17,25,38-tetrone	162817370	Click to see C1C2C(C3C(C(O2)CC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O	934.70	unknown	https://doi.org/10.1016/S0031-9422(97)01078-9
[(10R,11R,13R,14R,15S)-3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-14-yl] 3,4,5-trihydroxy-2-(6,7,13,14-tetrahydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4(16),5,7,11,13-hexaen-5-yl)benzoate	101589227	Click to see C1=C2C(=C(C(=C1O)O)O)C3=C(C(=C(C=C3C(=O)OC4C(C(C(OC4O)CO)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C7C8=C6C(=O)OC9=C8C(=CC(=C9O)O)C(=O)O7)O)O)O)O)O)OC2=O)O)O)O	934.60	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.006
[(10R,11R)-10-[(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	101601178	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/10.1016/J.FITOTE.2010.01.006
Arjunin	102316370	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(=C6C7=C5C(=O)OC8=C(C(=C(C9=C(C(=C(C=C9C(=O)O1)O)O)O)C(=C78)C(=O)O6)O)O)O)O)O)O)O	934.60	unknown	https://doi.org/10.1016/S0031-9422(97)01078-9
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/10.1016/J.FITOTE.2010.01.006
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/10.1016/J.FITOTE.2010.01.006
CID 16175790	16175790	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(=C8C9=C7C(=O)OC2=C9C(=CC(=C2O)OC2=C(C(=C(C=C2C(=O)O1)O)O)O)C(=O)O8)O)O)O)O)O	1084.70	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.006
CID 5464368	5464368	Click to see C1C2C(C(C(C(O2)O)O)O)OC(=O)C3=CC(=C(C(=C3C4=C(C(=C5C6=C4C(=O)OC7=C(C(=C(C8=C(C(=C(C=C8C(=O)O1)O)O)O)C(=C67)C(=O)O5)O)O)O)O)O)O)O	782.50	unknown	https://doi.org/10.1016/S0031-9422(97)01078-9
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/10.1615/JENVIRONPATHOLTOXICOLONCOL.V20.I1.20 https://doi.org/10.1016/S0031-9422(97)01078-9
Punicalagin	44584733	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(=C8C9=C7C(=O)OC2=C(C(=C(C3=C(C(=C(C=C3C(=O)O1)O)O)O)C(=C92)C(=O)O8)O)O)O)O)O)O)O	1084.70	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.006
Punicalin	5388496	Click to see C1C2C(C(C(C(O2)O)O)O)OC(=O)C3=CC(=C(C(=C3C4=C(C(=C5C6=C4C(=O)OC7=C(C(=C(C8=C(C(=C(C=C8C(=O)O1)O)O)O)C(=C67)C(=O)O5)O)O)O)O)O)O)O	782.50	unknown	https://doi.org/10.1016/S0031-9422(97)01078-9

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Terminalia arjuna

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