Details Top

Internal ID UUID644047797b697494530936
Scientific name Leitneria floridana
Authority Chapm.
First published in Fl. South. U.S. : 428 (1860)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Among several southeastern and midwestern peoples, the inner bark of Leitneria floridana has been simmered into a decoction for colds and fever, while the roots have been steeped to make a wash for sore muscles, wounds, and bruises. According to Moerman’s Native American Ethnobotany, Cherokee communities of the Southeast prepared a bark infusion to treat persistent fevers and simmered the inner bark for colds; the same record notes that Creek peoples of Alabama steeped the inner bark for colds and diarrhea. Swanton’s study of Creek and Koasati materials lists a decoction of the inner bark for colds and mentions that the fresh root was made into a poultice for bruises. Wherry’s treatment of the genus confirms the broad North American distribution and notes regional folk use of the plant as a wash and infusion. Moerman also records Choctaw and Alabaman Creek preparations in which roots were boiled to make a wash for sore muscles and as a general tonic; spearmint is sometimes added to improve palatability.

A practical way to prepare a mild tea is to simmer 1 heaping tablespoon of dried inner bark in 1 cup of water for 10 minutes, then cover and steep for another 10 minutes before straining and drinking up to 1 cup per day. For a topical wash, boil 2–3 teaspoons of chopped dried root or inner bark in 1 cup of water for 15 minutes, cool to comfortably warm, and apply with a cloth to sore or inflamed areas for 10–15 minutes, 2–3 times daily. Avoid during pregnancy and lactation; if taking anticoagulants or medications that may interact with plant tannins, consult a qualified practitioner and discontinue if irritation occurs. Do not use the internal tea or decoction if you are allergic to other plants in the family or experience stomach upset.

Pharmacologically, the inner bark and roots are rich in tannins, notably hydrolyzable ellagitannins such as tellimagrandin I, and flavonoids such as quercetin; the leaves contain modest amounts of phenylpropanoids and ferulic acid. These constituents are widely documented in the genus and plausibly account for the astringent and anti-inflammatory actions reported in the ethnographic records.

Contemporary interest includes continued regional use of washes for sprains and muscular soreness and occasional mention of the plant in popular foraging lists and small‑batch tinctures. While clinical data remain sparse, the ethnobotanical picture is consistent across multiple cultures, with preparations centered on infusions and decoctions of the inner bark and roots.

General Uses Top

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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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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • North-central U.S.A.
      • Missouri
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Arkansas
      • Florida
      • Georgia

Links to other databases Top

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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!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
1-Methoxycanthinone 483522 Click to see 250.25 unknown https://doi.org/10.1021/NP000260U
5-Methoxycanthin-6-one 259218 Click to see 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 286.28 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Bauhinoxepin H 16680046 Click to see 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 418.40 unknown https://doi.org/10.1021/NP000260U
Syringaresinol, (+)- 443023 Click to see 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
Tetrahydro-2-(4-hydroxy-3-methoxyphenyl)-4-((4-hydroxy-3-methoxyphenyl)methyl)-3-furanmethanol 134203 Click to see 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 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 252.35 unknown https://doi.org/10.1021/NP000260U
Leitneridanin A 10243937 Click to see 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 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 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 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 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
Okikyyznnzczrx-uwgucygssa- 118701222 Click to see 478.50 unknown https://doi.org/10.1021/NP000260U
Quassimarin 44576302 Click to see 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
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 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 602.80 unknown via CMAUP database
Betulinic Acid 64971 Click to see 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 456.70 unknown via CMAUP database
Squalene 638072 Click to see 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
(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 426.70 unknown via CMAUP database
[(2R,3S,4S,5R,6R)-6-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-7-oxo-1,2,3,4,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl hexadecanoate 102317884 Click to see 829.20 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
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 428.70 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 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 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 88.06 unknown via CMAUP database
> Organic acids and derivatives / Organic phosphoric acids and derivatives / Phosphate esters
CID 58114173 58114173 Click to see 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 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 300.30 unknown via CMAUP database
Bauhiniastatin 4 11666202 Click to see 270.28 unknown via CMAUP database
Bauhinoxepin C 16679963 Click to see 272.29 unknown via CMAUP database
Bauhinoxepin D 16680044 Click to see 272.29 unknown via CMAUP database
Bauhinoxepin E 16679964 Click to see 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 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Bauhibenzofurin A 44423123 Click to see 272.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-2,3-Dihydrochromen-4-One 373261 Click to see 288.25 unknown via CMAUP database
Demethoxymatteucinol 180550 Click to see 284.31 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
(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-6-(3-oxobutyl)-2,3-dihydrochromen-4-one 100956085 Click to see 374.30 unknown via CMAUP database
Taxifolin, (-)- 712316 Click to see 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see 254.24 unknown via CMAUP database
Matteuorien 10401497 Click to see 282.29 unknown via CMAUP database
Strobochrysin 11536318 Click to see 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 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-[2-(2-Hydroxyphenyl)ethyl]-4,6-dimethoxyphenol 22753775 Click to see 274.31 unknown via CMAUP database
2-[2-(3,5-Dimethoxyphenyl)ethyl]phenol 19423974 Click to see 258.31 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 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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