Scientific name	Authority	First published in
Vitex arborea	Roxb.	Fl. Ind. ed. 1832 , 3: 73 (1832)
Vitex articulata	Steud.	Nomencl. Bot. , ed. 2, 2: 777 (1841)
Vitex bracteata	Herb.Horsf. ex Miq.	Fl. Ned. Ind. 2: 862 (1858)
Vitex buddingii	Moldenke	Phytologia 4: 59 (1952)
Vitex digitata	Wight ex Steud.	Nomencl. Bot. , ed. 2, 2: 777 (1841)
Vitex heterophylla	Blume ex Miq.	Fl. Ned. Ind. ii. 862.
Vitex heterophylla var. puberula	H.J.Lam	Verben. Malay. Archip. : 189 (1919)
Vitex heterophylla var. velutina	Koord. & Valeton	Bijdr. Boomsoort. Java 7: 107. 1900
Vitex inaequifolia	Turcz.	Bull. Soc. Imp. Naturalistes Moscou 36(II): 223 (1863)
Vitex latifolia	Lam.	Encycl. 2: 613 (1788)
Vitex pinnata f. glabrescens	Moldenke	Phytologia 33: 375 (1976)
Vitex pinnata f. ptilota	(Dop.) Moldenke	Phytologia 49: 432 (1981)
Vitex pubescens	Vahl	Symb. Bot. 3: 85 (1794)
Vitex pubescens var. ptilota	Dop	Bull. Soc. Hist. Nat. Toulouse 57: 198 1928
Vitex quinata var. puberula	(H.J.Lam) Moldenke	Phytologia 3: 489 1951
Vitex sebesiae	H.J.Lam ex van Leeuwen	Bull. Jard. Bot. Buitenzorg , sér. 3, 5: 176 (1922)
Vitex turczaninowii f. puberula	(H.J.Lam) Moldenke	Phytologia 51: 163 (1982)
Vitex velutina	Koord.	Exkurs.-Fl. Java 3: 137 (1912)
Wallrothia articulata	Roth	Nov. Pl. Sp. : 317 (1821)
Pistaciovitex pinnata	(L.) Kuntze	Lex. Gen. Phan. : 442 (1903)
Vitex puberula	Miq.	Fl. Ned. Ind., Eerste Bijv. 242. 1860 (1860)
Vitex pubescens var. lilacina	Kuntze	Revis. Gen. Pl. 511. 1891
Vitex pubescens var. bicolor	Kuntze	Revis. Gen. Pl. 511. 1891
Vitex pubescens var. pantjarensis	Hochr.	Candollea 5: 191. 1934

Common names Top

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Filter by language:

Language	Common/alternative name
ace	manè
bjn	halaban
Malayalam	ആറ്റുമയില
Thai	ตีนนก

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

Africa click to expand
- Western Indian Ocean
  - Madagascar

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

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000333365
Tropicos	33700715
KEW	urn:lsid:ipni.org:names:865935-1
The Plant List	kew-213709
Open Tree Of Life	563754
NCBI Taxonomy	548852
IUCN Red List	62019896
IPNI	865935-1
iNaturalist	426356
GBIF	7309306
Freebase	/m/05h42d8
USDA GRIN	41834
Wikipedia	Vitex_pinnata
CMAUP	NPO305

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

Vitex Genus as a Source of Antimicrobial Agents

Islam Z, Caldeira GI, Caniça M, Islam N, Silva O

Plants (Basel)

29-Jan-2024

PMCID:	PMC10857077
doi:	10.3390/plants13030401
PMID:	38337934

Wood decay fungi show enhanced biodeterioration of low-density polyethylene in the absence of wood in culture media

Perera P, Herath H, Paranagama PA, Wijesinghe P, Attanayake RN

PLoS One

26-Jul-2023

PMCID:	PMC10370761
doi:	10.1371/journal.pone.0288133
PMID:	37494333

Screening and Elucidation of Chemical Structures of Novel Mammalian α-Glucosidase Inhibitors Targeting Anti-Diabetes Drug from Herbals Used by E De Ethnic Tribe in Vietnam

Nguyen VB, Wang SL, Phan TQ, Pham TH, Huang HT, Liaw CC, Nguyen AD

Pharmaceuticals (Basel)

17-May-2023

PMCID:	PMC10223997
doi:	10.3390/ph16050756
PMID:	37242539

Pest categorisation of Milviscutulus mangiferae

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

EFSA J

24-Feb-2023

PMCID:	PMC9951084
doi:	10.2903/j.efsa.2023.7846
PMID:	36846380

Current and future outlook of loaded components in hydrogel composites for the treatment of chronic diabetic ulcers

Cui J, Zhang S, Cheng S, Shen H

Front Bioeng Biotechnol

13-Feb-2023

PMCID:	PMC9968980
doi:	10.3389/fbioe.2023.1077490
PMID:	36860881

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

The Angiosperm Stem Hemiparasitic Genus Cassytha (Lauraceae) and Its Host Interactions: A Review

Zhang H, Florentine S, Tennakoon KU

Front Plant Sci

06-Jun-2022

PMCID:	PMC9208266
doi:	10.3389/fpls.2022.864110
PMID:	35734256

Recent Developments in Metabolomics Studies of Endophytic Fungi

Nagarajan K, Ibrahim B, Ahmad Bawadikji A, Lim JW, Tong WY, Leong CR, Khaw KY, Tan WN

J Fungi (Basel)

29-Dec-2021

PMCID:	PMC8781825
doi:	10.3390/jof8010028
PMID:	35049968

Phytoremediation and Microorganisms-Assisted Phytoremediation of Mercury-Contaminated Soils: Challenges and Perspectives

Tiodar ED, Văcar CL, Podar D

Int J Environ Res Public Health

02-Mar-2021

PMCID:	PMC7967564
doi:	10.3390/ijerph18052435
PMID:	33801363

Factors influencing riverine utilization patterns in two sympatric macaques

Otani Y, Bernard H, Wong A, Tangah J, Tuuga A, Hanya G, Matsuda I

Sci Rep

25-Sep-2020

PMCID:	PMC7519036
doi:	10.1038/s41598-020-72606-2
PMID:	32978415

Evaluation of antioxidant, antibacterial and wound healing activities of Vitex pinnata

Shafie NA, Suhaili NA, Taha H, Ahmad N

F1000Res

07-Aug-2020

PMCID:	PMC7445684
doi:	10.12688/f1000research.21310.1
PMID:	32874549

Secondary Metabolites of Lasiodiplodia theobromae: Distribution, Chemical Diversity, Bioactivity, and Implications of Their Occurrence

Salvatore MM, Alves A, Andolfi A

Toxins (Basel)

17-Jul-2020

PMCID:	PMC7405015
doi:	10.3390/toxins12070457
PMID:	32709023

Assessment of the applicability of wood anatomy and DNA barcoding to detect the timber adulterations in Sri Lanka

Kannangara S, Karunarathne S, Ranaweera L, Ananda K, Ranathunga D, Jayarathne H, Weebadde C, Sooriyapathirana S

Sci Rep

09-Mar-2020

PMCID:	PMC7062781
doi:	10.1038/s41598-020-61415-2
PMID:	32152386

Conspectus of flora, fauna and micro-climate data in Tasik Kenyir from Mac 2015–February 2016

Afiq Ramlee MN, Hussin MF, Roslan A, Rosmidi FH, Pesiu E, Aisyah A Rahim N, Izzati Ahmad NI, David G, Zakaria AA, Adanan NA, Basri HH, Aznan Ariffin MS, Bartholomew CV, Zahidin MA, Lola MS, Abdullah MT

Data Brief

27-Feb-2020

PMCID:	PMC7066060
doi:	10.1016/j.dib.2020.105328
PMID:	32181296

Growth evaluation of several types of energy crops from tropical shrubs species

Susanto D, Auliana A, Amirta R

F1000Res

25-Mar-2019

PMCID:	PMC8994084
doi:	10.12688/f1000research.18063.1
PMID:	35444798

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 / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
galloyl(-3)[galloyl(-6)]b-Glc	44421782	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O	484.40	unknown	via CMAUP database
Methyl gallate	7428	Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O	184.15	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
(1S,3aR,4S,6aR)-Tetrahydro-1-(4-hydroxy-3-methoxyphenyl)-4-[4-(6-O-galloyl-beta-D-glucopyranosyloxy)-3-methoxyphenyl]-1H,3H-furo[3,4-c]furan	44470458	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)COC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)O)OC)O	672.60	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	486614	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O	520.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(1S,5R,8R)-8-[(3R)-3-(6-O-Galloyl-beta-D-glucopyranosyloxy)butyl]-1,5-dimethyl-6-oxabicyclo[3.2.1]octane-3-one	101503539	Click to see CC(CCC1C2(CC(=O)CC1(OC2)C)C)OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O	540.60	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[(Z)-hex-3-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	5318045	Click to see CCC=CCCOC1C(C(C(C(O1)CO)O)O)O	262.30	unknown	via CMAUP database
(4R)-4-[(3R)-3-(6-O-Galloyl-beta-D-glucopyranosyloxy)-1-butenyl]3,5,5-trimethyl-2-cyclohexene-1-one	44184344	Click to see CC1=CC(=O)CC(C1C=CC(C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)(C)C	522.50	unknown	via CMAUP database
(6R,9R)-3-Oxo-alpha-ionol glucoside	9820702	Click to see CC1=CC(=O)CC(C1C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C	370.40	unknown	via CMAUP database
2-Hexenyl-beta-glucopyranoside	6450053	Click to see CCCC=CCOC1C(C(C(C(O1)CO)O)O)O	262.30	unknown	via CMAUP database
3Eec4Q65S4	21630888	Click to see CC1=CC(=O)CC(C1C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C	370.40	unknown	via CMAUP database
icariside B5	14135399	Click to see CC1=CC(=O)CC(C1(CCC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C	388.50	unknown	via CMAUP database
Lauroside E	101367898	Click to see CC(CCC1C(=CC(=O)CC1(C)C)CO)OC2C(C(C(C(O2)CO)O)O)O	388.50	unknown	via CMAUP database
Macarangioside A	16062725	Click to see CC1=CC(=O)CC(C1(CCC(C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)(C)C	540.60	unknown	via CMAUP database
Macarangioside D	101412231	Click to see CC(C=CC1C(=CC(=O)CC1(C)C)CO)OC2C(C(C(C(O2)CO)O)O)O	386.40	unknown	via CMAUP database
Macarangioside F	44470459	Click to see CC(CCC1C2(CC(=O)CC1(OC2)C)C)OC3C(C(C(C(O3)CO)O)O)O	388.50	unknown	via CMAUP database
Mallophenol B	11156928	Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)(C)C	538.50	unknown	via CMAUP database
Roseoside	9930064	Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C	386.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Euphorbiasteroid	15940183	Click to see CC1CC2(C(C1OC(=O)CC3=CC=CC=C3)C(C4(CCC5C(C5(C)C)C=C(C2=O)C)CO4)OC(=O)C)OC(=O)C	552.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
5-[(1S,2R,4aR,8aS)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-ol	71446681	Click to see CC1CCC2(C(C1(C)CCC(=CCO)C)CCC=C2C)C	290.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
blumenol B	14135402	Click to see CC1=CC(=O)CC(C1(CCC(C)O)O)(C)C	226.31	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	via CMAUP database
beta-Amyrone	12306160	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C	424.70	unknown	via CMAUP database
Epifriedelanol	119242	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O	428.70	unknown	via CMAUP database
Friedelanol	101341	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O	428.70	unknown	via CMAUP database
Friedelin	91472	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3R,6S)-2,3,6,7-tetrahydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	13470433	Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(CO)O)O)O)O	496.60	unknown	https://doi.org/10.1016/S0031-9422(97)00102-7
(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R)-2,5,6-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	101218682	Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(CCC(C(C)(C)O)O)O)O	480.60	unknown	https://doi.org/10.1016/S0031-9422(00)94985-9
(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2S,5R)-2,5,6-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	12020130	Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(CCC(C(C)(C)O)O)O)O	480.60	unknown	https://doi.org/10.1016/S0031-9422(00)94985-9
2,3,11,14-tetrahydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	4254739	Click to see CC12CC(C3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O)O	496.60	unknown	https://doi.org/10.1016/S0031-9422(00)94985-9
2,3,14-trihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	271605	Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O	480.60	unknown	https://doi.org/10.1016/S0031-9422(00)94985-9
2,3,14-trihydroxy-10,13-dimethyl-17-(2,3,6,7-tetrahydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	13470434	Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(CO)O)O)O)O	496.60	unknown	https://doi.org/10.1016/S0031-9422(97)00102-7
2,3,14-trihydroxy-10,13-dimethyl-17-(2,5,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	72747540	Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(CCC(C(C)(C)O)O)O)O	480.60	unknown	https://doi.org/10.1016/S0031-9422(00)94985-9
20-Hydroxyecdysone	5459840	Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O	480.60	unknown	https://doi.org/10.1016/S0031-9422(00)94985-9
Turkesterone	14376672	Click to see CC12CC(C3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O)O	496.60	unknown	https://doi.org/10.1016/S0031-9422(00)94985-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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	11870456	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
5alpha-Stigmastane-3,6-dione	13992092	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CCC(=O)C4)C)C)C(C)C	428.70	unknown	via CMAUP database
6beta-Hydroxystigmast-4-en-3-one	9823926	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C	428.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(1R,6R)-1-[(S)-3-Hydroxybutyl]-2,2-dimethyl-7-oxaspiro[5.2]octane-4-one	5319213	Click to see CC(CCC1C(CC(=O)CC12CO2)(C)C)O	226.31	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxepanes
4-[(1R,3R,5S,8R)-3-hydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]butan-2-one	11424667	Click to see CC(=O)CCC1C2(CC(CC1(OC2)C)O)C	226.31	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / 3-pyridinecarbonitriles
Malloapeltine	45079694	Click to see COC1=C(C=[N+](C=C1)[O-])C#N	150.13	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R)-2beta-[3-Methoxy-4-(beta-D-glucopyranosyloxy)phenyl]-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydrobenzofuran-3alpha-methanol	10625848	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)CCCO	522.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Scopolin	439514	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O	354.31	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 2-prenylated flavans / 2-prenylated flavanones
(2S)-2-[2-(3,7-dimethylocta-2,6-dienyl)-3,4-dihydroxyphenyl]-5,7-dihydroxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	91152580	Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)O)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)C)C	492.60	unknown	via CMAUP database
(2S)-2-[2-[(2E)-3,7-dimethylocta-2,6-dienyl]-3-hydroxy-4-methoxyphenyl]-5-hydroxy-7-methoxy-2,3-dihydrochromen-4-one	11351463	Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)OC)C2CC(=O)C3=C(C=C(C=C3O2)OC)O)C)C	452.50	unknown	via CMAUP database
(2S)-2-[2-[(2E)-3,7-dimethylocta-2,6-dienyl]-3-hydroxy-4-methoxyphenyl]-5-hydroxy-7-methoxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	11375844	Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)OC)C2CC(=O)C3=C(C(=C(C=C3O2)OC)CC=C(C)C)O)C)C	520.70	unknown	via CMAUP database
(2S)-2-[2-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,4-dimethoxyphenyl]-5-hydroxy-7-methoxy-2,3-dihydrochromen-4-one	11476850	Click to see CC(=CCCC(=CCC1=C(C=CC(=C1OC)OC)C2CC(=O)C3=C(C=C(C=C3O2)OC)O)C)C	466.60	unknown	via CMAUP database
(2S)-2-[2-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,4-dimethoxyphenyl]-5-hydroxy-7-methoxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	11466771	Click to see CC(=CCCC(=CCC1=C(C=CC(=C1OC)OC)C2CC(=O)C3=C(C(=C(C=C3O2)OC)CC=C(C)C)O)C)C	534.70	unknown	via CMAUP database
3',4'-Dihydro-5,7,8'-trihydroxy-2'alpha-methyl-6-(3-methyl-2-butenyl)-2'-(4-methyl-1,3-pentadienyl)-2alpha,5'-bi[2H-1-benzopyran]-4(3H)-one	25155065	Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=C4CCC(OC4=C(C=C3)O)(C)C=CC=C(C)C)O)C	490.60	unknown	via CMAUP database
3',4'-Dihydro-5,7,8'-trihydroxy-2'beta-methyl-6-(3-methyl-2-butenyl)-2'-(4-methyl-1,3-pentadienyl)-2alpha,5'-bi[2H-1-benzopyran]-4(3H)-one	25155334	Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=C4CCC(OC4=C(C=C3)O)(C)C=CC=C(C)C)O)C	490.60	unknown	via CMAUP database
Macaflavanone F	25155066	Click to see CC(=CCCC1(CCC2=C(C=CC(=C2O1)O)C3CC(=O)C4=C(O3)C=C(C(=C4O)CC=C(C)C)O)C)C	492.60	unknown	via CMAUP database
Macaflavanone G	25155335	Click to see CC(=CCCC1(CCC2=C(C=CC(=C2O1)O)C3CC(=O)C4=C(O3)C=C(C(=C4O)CC=C(C)C)O)C)C	492.60	unknown	via CMAUP database
nymphaeol B	10387631	Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)O)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C)C	424.50	unknown	via CMAUP database
nymphaeol C	10323393	Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)O)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)C)C	492.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-2-(3,4-dimethoxyphenyl)-6-[(2E)-3,7-dimethylocta-2,6-dienyl]-5-hydroxy-7-methoxy-2,3-dihydrochromen-4-one	11294269	Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1O)C(=O)CC(O2)C3=CC(=C(C=C3)OC)OC)OC)C)C	466.60	unknown	via CMAUP database
(2S)-5,7-dihydroxy-2-[(2R)-8-hydroxy-2-methyl-2-(4-methylpent-3-enyl)chromen-5-yl]-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	25155068	Click to see CC(=CCCC1(C=CC2=C(C=CC(=C2O1)O)C3CC(=O)C4=C(O3)C=C(C(=C4O)CC=C(C)C)O)C)C	490.60	unknown	via CMAUP database
Macaflavanone C	25155069	Click to see CC(=CCCC1(C=CC2=C(C=CC(=C2O1)O)C3CC(=O)C4=C(O3)C=C(C(=C4O)CC=C(C)C)O)C)C	490.60	unknown	via CMAUP database
Nymphaeol A	639465	Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3)O)O)O)C)C	424.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-(beta-D-Arabinopyranosyloxy)-5,7-dihydroxy-2-(3,4-dihydroxyphenyl)-4H-1-benzopyran-4-one	21722017	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	434.30	unknown	via CMAUP database
Hyperoside	5281643	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	464.40	unknown	via CMAUP database
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,4-di-O-galloyl-alpha-d-glucopyranose	14605152	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(OC(C(C2O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)CO	484.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
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	via CMAUP database
Geraniin	3001497	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	952.60	unknown	via CMAUP database
Punicafolin	5320800	Click to see C1C2C(C(C(C(O2)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(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O	938.70	unknown	via CMAUP database

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Vitex pinnata

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