Scientific name	Authority	First published in
Taxus canadensis var. floridana	(Chapm.) Silba	Phytologia Mem. 7: 72 (1984)
Taxus baccata subsp. floridana	Pilg.	Pflanzenr. , IV, 5: 113 (1903)
Taxus baccata var. floridana	Elwes in Elwes & A.Henry	Trees Great Britain 1: 100 (1906)
Taxus globosa var. floridana	(Nutt. ex Chapm.) Spjut	J. Bot. Res. Inst. Texas 1: 224 (2007)
Taxus canadensis subsp. floridana	(Nutt. ex Chapm.) Silba	J. Int. Conifer Preserv. Soc. 17: 22 (2010)

Common names Top

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Filter by language:

Language	Common/alternative name
English	florida yew
Arabic	طقسوس فلوريدا
Azerbaijani	florida qaraçöhrəsi
azb	فلوریدا قاراچؤهرهسی
Bulgarian	флоридски тис
German	florida-eibe
Persian	سرخدار فلوریدا
Norwegian Bokmål	floridabarlind
Russian	Тис флоридский

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
- Mexico
  - Mexico Gulf
  - Mexico Northeast
- Southeastern U.S.A.
  - Florida

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000408623
Florida Plant Atlas	1069
USDA Plants	TAFL
Tropicos	31200011
KEW	urn:lsid:ipni.org:names:285874-2
The Plant List	kew-2434140
Missouri Botanical Garden	287302
Open Tree Of Life	1089675
Observations.org	512892
NCBI Taxonomy	156270
Nature Serve	2.155628
IUCN Red List	30965
IPNI	285874-2
iNaturalist	135548
GBIF	5284513
Freebase	/m/0284q62
FEIS	plants/tree/taxflo
EPPO	TAXFL
EOL	128496
Elurikkus	503492
USDA GRIN	415429
Wikipedia	Taxus_floridana

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

Hosts and impacts of elongate hemlock scale (Hemiptera: Diaspididae): A critical review

Venette RC, Ambourn A, Aukema BH, Jetton RM, Petrice TR

Front Insect Sci

12-Feb-2024

PMCID:	PMC10926514
doi:	10.3389/finsc.2024.1356036
PMID:	38469337

Biosynthesis of anticancer phytochemical compounds and their chemistry

Dogra A, Kumar J

Front Pharmacol

09-Mar-2023

PMCID:	PMC10034375
doi:	10.3389/fphar.2023.1136779
PMID:	36969868

Natural Taxanes: From Plant Composition to Human Pharmacology and Toxicity

Nižnanský Ľ, Osinová D, Kuruc R, Hengerics Szabó A, Szórádová A, Masár M, Nižnanská Ž

Int J Mol Sci

09-Dec-2022

PMCID:	PMC9779243
doi:	10.3390/ijms232415619
PMID:	36555256

Gymnosperm Resprouting—A Review

Burrows GE

Plants (Basel)

23-Nov-2021

PMCID:	PMC8705048
doi:	10.3390/plants10122551
PMID:	34961022

Senescence: why and where selection gradients might not decline with age

Roper M, Capdevila P, Salguero-Gómez R

Proc Biol Sci

21-Jul-2021

PMCID:	PMC8292751
doi:	10.1098/rspb.2021.0851
PMID:	34284628

An unexpected noncarpellate epigynous flower from the Jurassic of China

Fu Q, Diez JB, Pole M, García Ávila M, Liu ZJ, Chu H, Hou Y, Yin P, Zhang GQ, Du K, Wang X

eLife

18-Dec-2018

PMCID:	PMC6298773
doi:	10.7554/eLife.38827
PMID:	30558712

Endophytic Fungi—Alternative Sources of Cytotoxic Compounds: A Review

Uzma F, Mohan CD, Hashem A, Konappa NM, Rangappa S, Kamath PV, Singh BP, Mudili V, Gupta VK, Siddaiah CN, Chowdappa S, Alqarawi AA, Abd_Allah EF

Front Pharmacol

26-Apr-2018

PMCID:	PMC5932204
doi:	10.3389/fphar.2018.00309
PMID:	29755344

Gymnosperms on the EDGE

Forest F, Moat J, Baloch E, Brummitt NA, Bachman SP, Ickert-Bond S, Hollingsworth PM, Liston A, Little DP, Mathews S, Rai H, Rydin C, Stevenson DW, Thomas P, Buerki S

Sci Rep

16-Apr-2018

PMCID:	PMC5902588
doi:	10.1038/s41598-018-24365-4
PMID:	29662101

Altered Community Flammability in Florida’s Apalachicola Ravines and Implications for the Persistence of the Endangered Conifer Torreya taxifolia

Mola JM, Varner JM, Jules ES, Spector T

PLoS One

01-Aug-2014

PMCID:	PMC4118970
doi:	10.1371/journal.pone.0103933
PMID:	25084166

A Large Scale Process for Paclitaxel and other Taxanes from the Needles of Taxus x Media Hicksii and Taxus Floridana Using Reverse Phase Column Chromatography

Koppakva V. Rao, Rajendra S. Bhakuni, John Juchum, Richard M. Davies

Informa UK Limited

07-Jul-2007

doi:	10.1080/10826079608001226

Occurrence of 2,6-Dimethoxy cinnamaldehyde in taxus floridana and structural revision of taxiflorine to taxchinin M

Koppaka V Rao, James H Johnson

Elsevier BV

26-Jul-2002

doi:	10.1016/S0031-9422(98)00089-2

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 / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-(3-Hydroxybutyl)phenol	97790	Click to see CC(CCC1=CC=C(C=C1)O)O	166.22	unknown	https://doi.org/10.1016/S0031-9422(98)00089-2
Rhododendrol	919205	Click to see CC(CCC1=CC=C(C=C1)O)O	166.22	unknown	https://doi.org/10.1016/S0031-9422(98)00089-2
> Lignans, neolignans and related compounds / Lignan lactones
(3aR,9aR)-7-hydroxy-9-(4-hydroxy-3-methoxyphenyl)-6-methoxy-3a,4,9,9a-tetrahydro-1H-benzo[f][2]benzofuran-3-one	12303843	Click to see COC1=C(C=C2C(C3COC(=O)C3CC2=C1)C4=CC(=C(C=C4)O)OC)O	356.40	unknown	https://doi.org/10.1016/S0031-9422(98)00089-2
CID 369613	369613	Click to see COC1=C(C=C2C(C3COC(=O)C3CC2=C1)C4=CC(=C(C=C4)O)OC)O	356.40	unknown	https://doi.org/10.1016/S0031-9422(98)00089-2
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Taxanes and derivatives
(2,4,9,15-Tetraacetyloxy-11-hydroxy-10,14,17,17-tetramethyl-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-12-yl) benzoate	163106199	Click to see CC1=C2C(C(C3(C(CC4C(C3C(C(C2(C)C)CC1OC(=O)C)OC(=O)C)(CO4)OC(=O)C)OC(=O)C)C)O)OC(=O)C5=CC=CC=C5	656.70	unknown	https://doi.org/10.1080/10826079608001226
[(1R,2R,3S,4S,7R,9R,10S,11S,12R,15R)-2,4,9,15-tetraacetyloxy-11-hydroxy-10,14,17,17-tetramethyl-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-12-yl] benzoate	163106200	Click to see CC1=C2C(C(C3(C(CC4C(C3C(C(C2(C)C)CC1OC(=O)C)OC(=O)C)(CO4)OC(=O)C)OC(=O)C)C)O)OC(=O)C5=CC=CC=C5	656.70	unknown	https://doi.org/10.1016/S0031-9422(98)00089-2
[(1R,2S,3S,5S,8R,9R,10S,11S,13R,16S)-2,11,16-triacetyloxy-5,8-dihydroxy-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.03,7.013,16]hexadec-6-en-9-yl] benzoate	10794065	Click to see CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1O)C(C)(C)O)OC(=O)C)(CO4)OC(=O)C)OC(=O)C)C)OC(=O)C5=CC=CC=C5)O	630.70	unknown	https://doi.org/10.1016/S0031-9422(98)00089-2
[(1S,2R,3R,4S,7R,9S,10S,11R,12R,15S)-2,4,9,11,12-pentaacetyloxy-10,14,17,17-tetramethyl-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-15-yl] acetate	100926727	Click to see CC1=C2C(C(C3(C(CC4C(C3C(C(C2(C)C)CC1OC(=O)C)OC(=O)C)(CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C	636.70	unknown	https://doi.org/10.1016/S0031-9422(98)00089-2
[(1S,2S,3R,4S,7R,9S,10S,11S,12R,15S)-4,9,11,12,15-pentaacetyloxy-1-hydroxy-10,14,17,17-tetramethyl-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate	5321426	Click to see CC1=C2C(C(C3(C(CC4C(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C5=CC=CC=C5)(CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C	714.80	unknown	https://doi.org/10.1080/10826079608001226
[(1S,2S,3S,5S,8R,9R,10S,11S,13R,16S)-2,11,16-triacetyloxy-5,8-dihydroxy-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.03,7.013,16]hexadec-6-en-9-yl] benzoate	162938348	Click to see CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1O)C(C)(C)O)OC(=O)C)(CO4)OC(=O)C)OC(=O)C)C)OC(=O)C5=CC=CC=C5)O	630.70	unknown	https://doi.org/10.1016/S0031-9422(98)00089-2
[(1S,2S,3S,5S,8R,9R,10S,11S,13R,16S)-2,5,11,16-tetraacetyloxy-8-hydroxy-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.03,7.013,16]hexadec-6-en-9-yl] benzoate	163083402	Click to see CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1OC(=O)C)C(C)(C)O)OC(=O)C)(CO4)OC(=O)C)OC(=O)C)C)OC(=O)C5=CC=CC=C5)O	672.70	unknown	https://doi.org/10.1016/S0031-9422(98)00089-2
[(1S,3S,4S,7S,10S)-4,9,11,12,15-pentaacetyloxy-1-hydroxy-10,14,17,17-tetramethyl-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate	138113828	Click to see CC1=C2C(C(C3(C(CC4C(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C5=CC=CC=C5)(CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C	714.80	unknown	https://doi.org/10.1080/10826079608001226
[2,11,16-Triacetyloxy-5,8-dihydroxy-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.03,7.013,16]hexadec-6-en-9-yl] benzoate	78385520	Click to see CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1O)C(C)(C)O)OC(=O)C)(CO4)OC(=O)C)OC(=O)C)C)OC(=O)C5=CC=CC=C5)O	630.70	unknown	https://doi.org/10.1016/S0031-9422(98)00089-2
[2,5,11,16-Tetraacetyloxy-8-hydroxy-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.03,7.013,16]hexadec-6-en-9-yl] benzoate	78385532	Click to see CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1OC(=O)C)C(C)(C)O)OC(=O)C)(CO4)OC(=O)C)OC(=O)C)C)OC(=O)C5=CC=CC=C5)O	672.70	unknown	https://doi.org/10.1016/S0031-9422(98)00089-2
10-deacetylbaccatin III	154272	Click to see CC1=C2C(C(=O)C3(C(CC4C(C3C(C(C2(C)C)(CC1O)O)OC(=O)C5=CC=CC=C5)(CO4)OC(=O)C)O)C)O	544.60	unknown	https://doi.org/10.1080/10826079608001226 https://doi.org/10.1016/S0031-9422(98)00089-2
Paclitaxel	36314	Click to see CC1=C2C(C(=O)C3(C(CC4C(C3C(C(C2(C)C)(CC1OC(=O)C(C(C5=CC=CC=C5)NC(=O)C6=CC=CC=C6)O)O)OC(=O)C7=CC=CC=C7)(CO4)OC(=O)C)O)C)OC(=O)C	853.90	unknown	https://doi.org/10.1080/10826079608001226
Taxchinin M	10794584	Click to see CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1OC(=O)C)C(C)(C)O)OC(=O)C)(CO4)OC(=O)C)OC(=O)C)C)OC(=O)C5=CC=CC=C5)O	672.70	unknown	https://doi.org/10.1016/S0031-9422(98)00089-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
Ponasterone A	115127	Click to see CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O	464.60	unknown	https://doi.org/10.1016/S0031-9422(98)00089-2
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-(2,6-Dimethoxyphenyl)prop-2-enal	23928193	Click to see COC1=C(C(=CC=C1)OC)C=CC=O	192.21	unknown	https://doi.org/10.1016/S0031-9422(98)00089-2
CID 54191678	54191678	Click to see COC1=C(C(=CC=C1)OC)C=CC=O	192.21	unknown	https://doi.org/10.1016/S0031-9422(98)00089-2

Biological Material Top

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Taxus floridana

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top