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Leitneria floridana is a deciduous dioecious shrub or small tree found in the southern United States. It has light wood with a density less than that of cork and typically reaches 2-4 m tall, occasionally up to 8 m. The leaves are alternate, simple lanceolate, 5-20 cm long and 3-6 cm broad. It was previously treated as the only species in the family Leitneriaceae, but is now in the family Simaroubaceae in the Sapindales. Fossil record shows that †Leitneria venosa persisted in Italy until the Early Pleistocene and Leitneria sp. is also among the species listed in the Early Pliocene San Gimigniano flora. It is named after the German natural scientist E. F. Leitner.

Synonyms Top

Scientific name	Authority	First published in
Myrica floridana	(Chapm.) Alph.Wood	Amer. Bot. Fl. : 309 (1870)

Common names Top

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Filter by language:

Language	Common/alternative name
English	corkwood
Persian	درخت چوبپنبهای آمریکا
Japanese	レイトネリア属
Korean	레이트네리아과
Korean	레이트네리아목
Korean	레이트네리아속
Korean	레이트네리아 플로리다나
Russian	Лейтнериевые
Russian	Лейтнериецветные
Russian	Лейтнерия флоридская
Russian	Лейтнерия

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Northern America click to expand
- North-central U.S.A.
  - Missouri
- South-central U.S.A.
  - Texas
- Southeastern U.S.A.
  - Arkansas
  - Florida
  - Georgia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001072347
Florida Plant Atlas	2374
USDA Plants	LEFL
Tropicos	18000001
KEW	urn:lsid:ipni.org:names:526149-1
The Plant List	tro-18000001
Missouri Botanical Garden	281693
Open Tree Of Life	594985
NCBI Taxonomy	83908
Nature Serve	2.1052216
IUCN Red List	30937
IPNI	526149-1
iNaturalist	157706
GBIF	5361951
Freebase	/m/06hm0r
EPPO	LTNFL
EOL	594782
USDA GRIN	314436
Wikipedia	Leitneria
CMAUP	NPO809

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

Plastome evolution and phylogeny of the tribe Ruteae (Rutaceae)

Liu Q, Gao Y, Dong W, Zhao L

Ecol Evol

09-Feb-2023

PMCID:	PMC9911629
doi:	10.1002/ece3.9821
PMID:	36789335

Complete chloroplast genome of the desert date (Balanites aegyptiaca (L.) Del. comparative analysis, and phylogenetic relationships among the members of Zygophyllaceae

AL-Juhani WS, Alharbi SA, Al Aboud NM, Aljohani AY

BMC Genomics

31-Aug-2022

PMCID:	PMC9434970
doi:	10.1186/s12864-022-08850-9
PMID:	36045328

The complete chloroplast genome sequence of Picrasma quassioides (D. Don) Benn. 1844 (Simaroubaceae)

Qin L, Xiaoshan G, Guo Y, Huaxi H, Huiye Z, Zhu Y, Chen R

Mitochondrial DNA B Resour

23-Jun-2022

PMCID:	PMC9245974
doi:	10.1080/23802359.2022.2087545
PMID:	35783065

Complete chloroplast genome of Toona ciliata Roem. var. pubescens (Franch.) Hand.-Mazz (Meliaceae), ‘Chinese mahogany’

Lu Z, Dong X, Fan Y, Liu W, Dai J, Han X, Liu J

Mitochondrial DNA B Resour

16-Mar-2022

PMCID:	PMC8933019
doi:	10.1080/23802359.2022.2049987
PMID:	35311208

Comparative genomics and phylogenetic relationships of two endemic and endangered species (Handeliodendron bodinieri and Eurycorymbus cavaleriei) of two monotypic genera within Sapindales

Yang J, Hu G, Hu G

BMC Genomics

06-Jan-2022

PMCID:	PMC8734052
doi:	10.1186/s12864-021-08259-w
PMID:	34991482

Biological Activity of Naturally Derived Naphthyridines

Chabowska G, Barg E, Wójcicka A

Molecules

16-Jul-2021

PMCID:	PMC8306249
doi:	10.3390/molecules26144324
PMID:	34299599

Complete Chloroplast Genomes of 14 Mangroves: Phylogenetic and Comparative Genomic Analyses

Shi C, Han K, Li L, Seim I, Lee SM, Xu X, Yang H, Fan G, Liu X

Biomed Res Int

05-May-2020

PMCID:	PMC7225854
doi:	10.1155/2020/8731857
PMID:	32462024

Structure-Activity-Relationship and Mechanistic Insights for Anti-HIV Natural Products

Kaur R, Sharma P, Gupta GK, Ntie-Kang F, Kumar D

Molecules

29-Apr-2020

PMCID:	PMC7249135
doi:	10.3390/molecules25092070
PMID:	32365518

First Phylogeny of Bitterbush Family, Picramniaceae (Picramniales)

Shipunov A, Carr S, Furniss S, Pay K, Pirani JR

Plants (Basel)

21-Feb-2020

PMCID:	PMC7076446
doi:	10.3390/plants9020284
PMID:	32098193

Complete chloroplast genome sequence of Peganum harmala, an important medicinal plant

Zha X, Zhao P, Gao F, Zhou Y

Mitochondrial DNA B Resour

16-Jan-2020

PMCID:	PMC7748625
doi:	10.1080/23802359.2019.1711230
PMID:	33366688

The complete chloroplast genome of the multipurpose and traditional herb, Ruta graveolens L.

Ling LZ, Zhang SD

Mitochondrial DNA B Resour

18-Oct-2019

PMCID:	PMC7707451
doi:	10.1080/23802359.2019.1678426
PMID:	33366131

Complete chloroplast genome of an endangered endemic tree, handeliodendron bodinieri (levl.) rehder (sapindaceae) from karst forests of southwest China

Tian X, Li X, Miao H, Xue C, Wang B, Guo Y, Zhang G

Mitochondrial DNA B Resour

27-Sep-2019

PMCID:	PMC7707296
doi:	10.1080/23802359.2019.1671251
PMID:	33365952

Complete plastome sequence of Atalantia kwangtungensis (Rutaceae): an endemic “near threatened” shrub in South China

Zhu ZX, Wang JH, Sun XZ, Zhao KK, Wang HF

Mitochondrial DNA B Resour

03-Jul-2018

PMCID:	PMC7800406
doi:	10.1080/23802359.2018.1483764
PMID:	33474301

Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus

Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J

Int J Mol Sci

14-May-2018

PMCID:	PMC5983620
doi:	10.3390/ijms19051459
PMID:	29757986

Complete plastome sequencing from Toona (Meliaceae) and phylogenomic analyses within Sapindales

Lin N, Moore MJ, Deng T, Sun H, Yang L, Sun Y, Wang H

Appl Plant Sci

27-Apr-2018

PMCID:	PMC5947613
doi:	10.1002/aps3.1040
PMID:	30131882

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
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
1-Methoxycanthinone	483522	Click to see COC1=CN=C2C=CC(=O)N3C2=C1C4=CC=CC=C43	250.25	unknown	https://doi.org/10.1021/NP000260U
5-Methoxycanthin-6-one	259218	Click to see COC1=CC2=NC=CC3=C2N(C1=O)C4=CC=CC=C34	250.25	unknown	https://doi.org/10.1016/S0305-1978(02)00074-1 https://doi.org/10.1021/NP000260U
> Benzenoids
Bauhinoxepin J	16680047	Click to see COC1=CC(=O)C2=C(C1=O)CCC3=CC=CC=C3O2	256.25	unknown	via CMAUP database
> 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	via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
Bauhinoxepin I	16679966	Click to see CC1=C(C(=O)C2=C(C1=O)OC3=C(CC2)C=C(C=C3)O)OC	286.28	unknown	via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Bauhinoxepin H	16680046	Click to see CC1=C(C(=O)C2=C(C1=O)OC3=CC=CC(=C3CC2)O)OC	286.28	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol	11604108	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1021/NP000260U
Syringaresinol	100067	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1021/NP000260U
Syringaresinol, (+)-	443023	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1021/NP000260U
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
Lariciresinol	332427	Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	https://doi.org/10.1021/NP000260U
Lariciresinol, (+)-	134203	Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	https://doi.org/10.1021/NP000260U
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
[(2R)-2,3-dihydroxypropyl] (9E,12E)-octadeca-9,12-dienoate	40565473	Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC(CO)O	354.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
2,3-dihydroxypropyl (9Z)-octadec-9-enoate	25021708	Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC(CO)O	356.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Trilinolein	5322095	Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCC=CCCCCC)OC(=O)CCCCCCCC=CCC=CCCCCC	879.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
8a-methyl-4-methylidene-6-prop-1-en-2-yl-2,3,5,6,7,8-hexahydro-1H-naphthalene-1,3,4a-triol	72815158	Click to see CC(=C)C1CCC2(C(CC(C(=C)C2(C1)O)O)O)C	252.35	unknown	https://doi.org/10.1021/NP000260U
Leitneridanin A	10243937	Click to see CC(=C)C1CCC2(C(CC(C(=C)C2(C1)O)O)O)C	252.35	unknown	https://doi.org/10.1021/NP000260U
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1E,6S,8S)-6-hydroxy-5-methylidene-8-prop-1-en-2-ylcyclodecene-1-carbaldehyde	162928803	Click to see CC(=C)C1CCC(=CCCC(=C)C(C1)O)C=O	234.33	unknown	https://doi.org/10.1021/NP000260U
6-Hydroxy-5-methylidene-8-prop-1-en-2-ylcyclodecene-1-carbaldehyde	85107150	Click to see CC(=C)C1CCC(=CCCC(=C)C(C1)O)C=O	234.33	unknown	https://doi.org/10.1021/NP000260U
Leitneridanin B	10059936	Click to see CC(=C)C1CCC(=CCCC(=C)C(C1)O)C=O	234.33	unknown	https://doi.org/10.1021/NP000260U
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(+)-Simalikalactone	15161842	Click to see CCC(C)C(=O)OC1C2C3(C(C(C4C2(CO3)C(CC5C4(C(C(=O)C=C5C)O)C)OC1=O)O)O)C	478.50	unknown	https://doi.org/10.1021/NP000260U
[(1R,2S,3R,6R,8S,12S,13S,14R,15R,16S,17S)-12,15,16-trihydroxy-9,13,17-trimethyl-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-en-3-yl] (2S)-2-acetyloxy-2-methylbutanoate	44566234	Click to see CCC(C)(C(=O)OC1C2C3(C(C(C4C2(CO3)C(CC5C4(C(C(=O)C=C5C)O)C)OC1=O)O)O)C)OC(=O)C	536.60	unknown	https://doi.org/10.1021/NP000260U
[(1R,2S,3R,6R,8S,12S,13S,14R,15R,16S)-12,15,16-trihydroxy-9,13,17-trimethyl-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-en-3-yl] 2-methylbutanoate	320171	Click to see CCC(C)C(=O)OC1C2C3(C(C(C4C2(CO3)C(CC5C4(C(C(=O)C=C5C)O)C)OC1=O)O)O)C	478.50	unknown	https://doi.org/10.1021/NP000260U
CID 429906	429906	Click to see CCC(C)(C(=O)OC1C2C3(C(C(C4C2(CO3)C(CC5C4(C(C(=O)C=C5C)O)C)OC1=O)O)O)C)OC(=O)C	536.60	unknown	https://doi.org/10.1021/NP000260U
CID 44576302	44576302	Click to see CCC(C)(C(=O)OC1C2C3(C(C(C4C2(CO3)C(CC5C4(C(C(=O)C=C5C)O)C)OC1=O)O)O)C)OC(=O)C	536.60	unknown	https://doi.org/10.1021/NP000260U
Simalikalactone D	441808	Click to see CCC(C)C(=O)OC1C2C3(C(C(C4C2(CO3)C(CC5C4(C(C(=O)C=C5C)O)C)OC1=O)O)O)C	478.50	unknown	https://doi.org/10.1021/NP000260U
Simalikilactone D	118701222	Click to see CCC(C)C(=O)OC1C2C3(C(C(C4C2(CO3)C(CC5C4(C(C(=O)C=C5C)O)C)OC1=O)O)O)C	478.50	unknown	https://doi.org/10.1021/NP000260U
Similikalactone D	500023	Click to see CCC(C)C(=O)OC1C2C3(C(C(C4C2(CO3)C(CC5C4(C(C(=O)C=C5C)O)C)OC1=O)O)O)C	478.50	unknown	https://doi.org/10.1021/NP000260U
Unii-3T62wcm8EK	441804	Click to see CCC(C(=O)OC1C2C3(C(C(C4C2(CO3)C(CC5C4(C(C(=O)C=C5C)O)C)OC1=O)O)O)C)OC(=O)C	522.50	unknown	https://doi.org/10.1021/NP000260U
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-O-p-Coumaroyloleanolic acid	10579517	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)C)C)C2C1)C)C(=O)O)C	602.80	unknown	via CMAUP database
Betulinic Acid	64971	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	via CMAUP database
Lupenone	92158	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C	424.70	unknown	via CMAUP database
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
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	via CMAUP database
Squalene	638072	Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C	410.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(6S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-6-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one	86333780	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C	426.70	unknown	via CMAUP database
3-Hydroxystigmast-5-en-7-one	160608	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C	428.70	unknown	via CMAUP database
3beta-(6-O-Palmitoyl-beta-D-glucopyranosyloxy)-5alpha-stigmast-5-en-7-one	102317884	Click to see CCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4C(=O)C=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O	829.20	unknown	via CMAUP database
6alpha-Hydroxystigmast-4-en-3-one	9867274	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)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
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
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	via CMAUP database
Sitoindoside I	9832350	Click to see CCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O	815.30	unknown	via CMAUP database
Stigmast-5-ene-3,7-dione	10717344	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(=O)C4)C)C)C(C)C	426.70	unknown	via CMAUP database
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
> Organic acids and derivatives / Keto acids and derivatives / Alpha-keto acids and derivatives
Pyruvic Acid	1060	Click to see CC(=O)C(=O)O	88.06	unknown	via CMAUP database
> Organic acids and derivatives / Organic phosphoric acids and derivatives / Phosphate esters
1-Carboxyethenoxy(oxonio)phosphinate	58114173	Click to see C=C(C(=O)O)OP(=O)([OH2+])[O-]	168.04	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Glycerin	753	Click to see C(C(CO)O)O	92.09	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5,7-Dihydroxychromone	5281343	Click to see C1=COC2=CC(=CC(=C2C1=O)O)O	178.14	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzoxepines / Dibenzoxepines
Bauhiniastatin 1	11687814	Click to see CC1=C(C(=O)C2=C(C1=O)OC3=CC=CC(=C3C=C2)O)OC	284.26	unknown	via CMAUP database
Bauhiniastatin 2	11609116	Click to see CC1=C(C2=C(C=CC3=C(C=CC=C3O2)O)C(=C1OC)OC)O	300.30	unknown	via CMAUP database
Bauhiniastatin 3	11623581	Click to see CC1=C(C=C2C=CC3=C(C=CC(=C3OC2=C1O)O)OC)OC	300.30	unknown	via CMAUP database
Bauhiniastatin 4	11666202	Click to see CC1=C(C=C2C=CC3=C(C=CC=C3OC2=C1OC)O)O	270.28	unknown	via CMAUP database
Bauhinoxepin C	16679963	Click to see CC1=C(C=C2CCC3=C(C=CC=C3OC2=C1O)O)OC	272.29	unknown	via CMAUP database
Bauhinoxepin D	16680044	Click to see CC1=C(C=C2CCC3=C(C=CC=C3OC2=C1OC)O)O	272.29	unknown	via CMAUP database
Bauhinoxepin E	16679964	Click to see CC1=C(C(=C2CCC3=C(C=CC=C3OC2=C1OC)O)O)OC	302.32	unknown	via CMAUP database
Bauhinoxepin F	16680045	Click to see CC1=C(C(=C2CCC3=C(C=CC=C3OC2=C1OC)O)OC)O	302.32	unknown	via CMAUP database
Pacharin	11851219	Click to see CC1=C(C=C2C=CC3=C(C=CC=C3OC2=C1O)O)OC	270.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Bauhibenzofurin A	44423123	Click to see COC1=CC(=C(C(=C1)OC)O)C2CC3=CC=CC=C3O2	272.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Demethoxymatteucinol	180550	Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)C)O	284.31	unknown	via CMAUP database
Eriodyctiol (flavanone)	373261	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	288.25	unknown	via CMAUP database
Strobopinin	442520	Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O	270.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(-)-Taxifolin	712316	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	via CMAUP database
(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-6-(3-oxobutyl)-2,3-dihydrochromen-4-one	100956085	Click to see CC(=O)CCC1=C(C2=C(C=C1O)OC(C(C2=O)O)C3=CC(=C(C=C3)O)O)O	374.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin	5281607	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	254.24	unknown	via CMAUP database
Matteuorien	10401497	Click to see CC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=CC=C3)C)O	282.29	unknown	via CMAUP database
Strobochrysin	11536318	Click to see CC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=CC=C3)O	268.26	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	via CMAUP database
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	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin	5280681	Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	316.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
2-(3,5-Dimethoxyphenethyl)phenol	19423974	Click to see COC1=CC(=CC(=C1)CCC2=CC=CC=C2O)OC	258.31	unknown	via CMAUP database
2-[2-(2-Hydroxyphenyl)ethyl]-4,6-dimethoxyphenol	22753775	Click to see COC1=CC(=C(C(=C1)OC)O)CCC2=CC=CC=C2O	274.31	unknown	via CMAUP database
Batatasin IV	181271	Click to see COC1=CC(=CC(=C1)O)CCC2=CC=CC=C2O	244.28	unknown	via CMAUP database
Bauhinol E	16680048	Click to see CC1=C(C=C(C=C1OC)CCC2=CC=CC=C2O)O	258.31	unknown	via CMAUP database
Dihydropinosylvin	442700	Click to see C1=CC=C(C=C1)CCC2=CC(=CC(=C2)O)O	214.26	unknown	via CMAUP database
Phenol, 3-methoxy-5-(2-phenylethyl)-	636980	Click to see COC1=CC(=CC(=C1)O)CCC2=CC=CC=C2	228.29	unknown	via CMAUP database

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Leitneria floridana

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