Scientific name	Authority	First published in
Vitex alata	Willd.	Neue Schriften Ges. Naturf. Freunde Berlin 4: 203 (1803)
Vitex altissima f. alata	(Willd.) Moldenke	Phytologia 22(2): 126. 1971
Vitex appendiculata	Rottler ex C.B.Clarke	Fl. Brit. India [J. D. Hooker] 4(12): 584. 1885 [Aug 1885]
Vitex latifolia	Wight ex Steud.	Nomencl. Bot. , ed. 2, 2: 777 (1841)
Vitex zeylanica	Turcz.	Bull. Soc. Imp. Naturalistes Moscou 36(II): 223 (1863)

Common names Top

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Filter by language:

Language	Common/alternative name
Malayalam	മൈല
Tamil	காட்டு நொச்சி

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - India
  - Sri Lanka
- Indo-China
  - Laos
- Malesia
  - Jawa
  - Sumatera
- Papuasia
  - New Guinea

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000332933
Tropicos	33700020
INPN	706925
KEW	urn:lsid:ipni.org:names:865578-1
The Plant List	kew-213311
Open Tree Of Life	697227
NCBI Taxonomy	549680
IPNI	865578-1
iNaturalist	751719
GBIF	3882022
USDA GRIN	41815
Wikipedia	Vitex_altissima

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

A comprehensive review of ethnomedicinal approaches, phytochemical analysis, and pharmacological potential of Vitex trifolia L.

Mottaghipisheh J, Kamali M, Doustimotlagh AH, Nowroozzadeh MH, Rasekh F, Hashempur MH, Iraji A

Front Pharmacol

21-Mar-2024

PMCID:	PMC10991721
doi:	10.3389/fphar.2024.1322083
PMID:	38576489

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

Hippophae rhamnoides L. (sea buckthorn) mediated green synthesis of copper nanoparticles and their application in anticancer activity

Dadhwal P, Dhingra HK, Dwivedi V, Alarifi S, Kalasariya H, Yadav VK, Patel A

Front Mol Biosci

24-Aug-2023

PMCID:	PMC10484619
doi:	10.3389/fmolb.2023.1246728
PMID:	37692067

Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India?

Kumar BM

Agrofor Syst

07-Apr-2023

PMCID:	PMC10081327
doi:	10.1007/s10457-023-00821-7
PMID:	37193256

Traditional Medicinal Uses, Phytochemistry, Biological Properties, and Health Applications of Vitex sp.

Kamal N, Mio Asni NS, Rozlan IN, Mohd Azmi MA, Mazlan NW, Mediani A, Baharum SN, Latip J, Assaw S, Edrada-Ebel RA

Plants (Basel)

26-Jul-2022

PMCID:	PMC9370779
doi:	10.3390/plants11151944
PMID:	35893648

Flower-like SnO2 Nanoparticle Biofabrication Using Pometia pinnata Leaf Extract and Study on Its Photocatalytic and Antibacterial Activities

Fatimah I, Purwiandono G, Hidayat H, Sagadevan S, Ghazali SA, Oh WC, Doong RA

Nanomaterials (Basel)

10-Nov-2021

PMCID:	PMC8623890
doi:	10.3390/nano11113012
PMID:	34835776

A Brief Overview of Potential Treatments for Viral Diseases Using Natural Plant Compounds: The Case of SARS-Cov

Abiri R, Abdul-Hamid H, Sytar O, Abiri R, Bezerra de Almeida E Jr, Sharma SK, Bulgakov VP, Arroo RR, Malik S

Molecules

24-Jun-2021

PMCID:	PMC8270261
doi:	10.3390/molecules26133868
PMID:	34202844

Evidence-based traditional Siddha formulations for prophylaxis and management of respiratory symptoms in COVID-19 pandemic-a review

Prakash P, Meena R, Stanley Abraham L, Sunkar S, Govindaraju K, Pully D, Samrot AV

Biocatal Agric Biotechnol

07-Jun-2021

PMCID:	PMC8180453
doi:	10.1016/j.bcab.2021.102056
PMID:	34122672

Ecosystem-level carbon storage and its links to diversity, structural and environmental drivers in tropical forests of Western Ghats, India

Kothandaraman S, Dar JA, Sundarapandian S, Dayanandan S, Khan ML

Sci Rep

10-Aug-2020

PMCID:	PMC7417561
doi:	10.1038/s41598-020-70313-6
PMID:	32778785

Antimicrobial Lipids from Plants and Marine Organisms: An Overview of the Current State-of-the-Art and Future Prospects

Alves E, Dias M, Lopes D, Almeida A, Domingues MD, Rey F

Antibiotics (Basel)

24-Jul-2020

PMCID:	PMC7459900
doi:	10.3390/antibiotics9080441
PMID:	32722192

COVID-19: Environment concern and impact of Indian medicinal system

Kumar V, Singh SB, Singh S

J Environ Chem Eng

06-Jun-2020

PMCID:	PMC7836929
doi:	10.1016/j.jece.2020.104144
PMID:	33520648

On the hunt for the alternate host of Hemileia vastatrix

Koutouleas A, Jørgen Lyngs Jørgensen H, Jensen B, Lillesø JB, Junge A, Ræbild A

Ecol Evol

23-Nov-2019

PMCID:	PMC6912922
doi:	10.1002/ece3.5755
PMID:	31871671

The potential protective effect of Commelina nudiflora L. against carbon tetrachloride (CCl4)-induced hepatotoxicity in rats, mediated by suppression of oxidative stress and inflammation

Shah MD, D’Souza UJ, Iqbal M

Environ Health Prev Med

11-Sep-2017

PMCID:	PMC5664843
doi:	10.1186/s12199-017-0673-0
PMID:	29165163

Inhibition of New Delhi Metallo-β-Lactamase 1 (NDM-1) Producing Escherichia coli IR-6 by Selected Plant Extracts and Their Synergistic Actions with Antibiotics

Chandar B, Poovitha S, Ilango K, MohanKumar R, Parani M

Front Microbiol

22-Aug-2017

PMCID:	PMC5572277
doi:	10.3389/fmicb.2017.01580
PMID:	28878746

Wound Healing Property Review of Siam Weed, Chromolaena odorata

Sirinthipaporn A, Jiraungkoorskul W

Pharmacogn Rev

01-Jan-2017

PMCID:	PMC5414454
doi:	10.4103/phrev.phrev_53_16
PMID:	28503052

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
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
[(3S,4R,5S)-5-(1,3-benzodioxol-5-yl)-4-(hydroxymethyl)oxolan-3-yl]-(4-methoxy-1,3-benzodioxol-5-yl)methanone	11632717	Click to see COC1=C(C=CC2=C1OCO2)C(=O)C3COC(C3CO)C4=CC5=C(C=C4)OCO5	400.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.008
[5-(1,3-Benzodioxol-5-yl)-4-(hydroxymethyl)oxolan-3-yl]-(4-methoxy-1,3-benzodioxol-5-yl)methanone	73036171	Click to see COC1=C(C=CC2=C1OCO2)C(=O)C3COC(C3CO)C4=CC5=C(C=C4)OCO5	400.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.008
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,6S,7S,7aS)-1-[(2S,3R,4S,5S,6R)-6-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-4,5-dihydroxy-3-(4-hydroxybenzoyl)oxyoxan-2-yl]oxy-6-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid	11365823	Click to see CC1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)OC(=O)C5=CC=C(C=C5)O)O	658.60	unknown	https://doi.org/10.1021/NP040117R
(1S,4aS,7S,7aS)-1-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-3-(4-hydroxybenzoyl)oxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid	16655052	Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC=C(C=C4)O)O	496.50	unknown	https://doi.org/10.1021/NP040117R
(1S,4aS,7S,7aS)-1-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-3-(4-hydroxybenzoyl)oxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid	154497074	Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC=C(C=C4)O)O	496.50	unknown	https://doi.org/10.1021/NP040117R
(1S,4aS,7S,7aS)-1-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-3-(4-hydroxybenzoyl)oxy-6-[[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxy-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid	11181450	Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O)O)OC(=O)C5=CC=C(C=C5)O)O	672.60	unknown	https://doi.org/10.1021/NP040117R
(1S,4aS,7S,7aS)-1-[(2S,3R,4S,5S,6R)-6-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-4,5-dihydroxy-3-(4-hydroxybenzoyl)oxyoxan-2-yl]oxy-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid	11181364	Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)OC(=O)C5=CC=C(C=C5)O)O	658.60	unknown	https://doi.org/10.1021/NP040117R
[(1S,4aS,5R,7aR)-5-hydroxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-7-yl]methyl 4-hydroxybenzoate	162876019	Click to see C1=COC(C2C1C(C=C2COC(=O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O	466.40	unknown	https://doi.org/10.1021/NP040117R
[(1S,4aS,5R,7aS)-5-hydroxy-1-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-7-yl]methyl 4-hydroxybenzoate	154496122	Click to see C1=COC(C2C1C(C=C2COC(=O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O	466.40	unknown	https://doi.org/10.1021/NP040117R
2'-p-Hydroxybenzoyl mussaenosidic acid	73298898	Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC=C(C=C4)O)O	496.50	unknown	https://doi.org/10.1021/NP040117R
Negundoside	9935561	Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC=C(C=C4)O)O	496.50	unknown	https://doi.org/10.1021/NP040117R
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	14019173	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	650.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.008
kaji-ichigoside F1	14019178	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	650.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.008
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,4aS,6aR,6aS,6bR,8aR,9S,10S,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,6a,6b,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	102250836	Click to see CC1C2C3=CCC4C(C3(CCC2(CCC1=C)C(=O)O)C)(CCC5C4(CC(C(C5(C)CO)O)O)C)C	486.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.008
10,11-Dihydroxy-9-(hydroxymethyl)-1,6a,6b,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	23132228	Click to see CC1C2C3=CCC4C(C3(CCC2(CCC1=C)C(=O)O)C)(CCC5C4(CC(C(C5(C)CO)O)O)C)C	486.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.008
2,3-Dihydroxyolean-12-en-28-oic acid	3694932	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/10.1016/J.PHYTOCHEM.2005.05.008
2,3,24-Trihydroxy-12-ursen-28-oic acid	296191	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O	488.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.008
2alpha,3alpha,24-Trihydroxyurs-12-en-28-oic acid	12308659	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O	488.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.008
3-Epicorosolic acid	15917998	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.PHYTOCHEM.2005.05.008
beta-Ursolic acid	220774	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/10.1016/J.PHYTOCHEM.2005.05.008
Colosolic 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/10.1016/J.PHYTOCHEM.2005.05.008
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/10.1016/J.PHYTOCHEM.2005.05.008
epi-Maslinic acid	25564831	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/10.1016/J.PHYTOCHEM.2005.05.008
Euscaphic Acid	471426	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O	488.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.008
Jacarandic acid	13653335	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O	488.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.008
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/10.1016/J.PHYTOCHEM.2005.05.008
Tormentic acid	73193	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O	488.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.008
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/10.1016/J.PHYTOCHEM.2005.05.008
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(1S,4aS,6S,7aS)-1-[(2S,3R,4S,5S,6R)-6-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-4,5-dihydroxy-3-(4-hydroxybenzoyl)oxyoxan-2-yl]oxy-6-hydroxy-7-methylidene-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid	11787128	Click to see C=C1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)OC(=O)C5=CC=C(C=C5)O)O	656.60	unknown	https://doi.org/10.1021/NP040117R
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-8-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 4-hydroxybenzoate	11671370	Click to see C1=CC(=CC=C1C(=O)OC2C(C(C(OC2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)CO)O)O)O	568.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.008
[(2S,3R,4S,5S,6S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-8-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 4-hydroxybenzoate	154495966	Click to see C1=CC(=CC=C1C(=O)OC2C(C(C(OC2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)CO)O)O)O	568.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.008
[2-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-8-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 4-hydroxybenzoate	73049063	Click to see C1=CC(=CC=C1C(=O)OC2C(C(C(OC2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)CO)O)O)O	568.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.008
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	5378180	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.008
Vitexin	5280441	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.008
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-(alpha-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one	12304095	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.008
Apigenin 7-O-glucoside	5385553	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.008
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.008

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Vitex altissima

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