Database	ID/link to page
World Flora Online	wfo-0000606352
KEW	urn:lsid:ipni.org:names:429938-1
The Plant List	kew-272248
Open Tree Of Life	234109
NCBI Taxonomy	95970
IUCN Red List	185226
IPNI	429938-1
iNaturalist	320601
GBIF	2765891
EPPO	WACTH
EOL	865748
Elurikkus	209682
USDA GRIN	41942
Wikipedia	Wachendorfia_thyrsiflora

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

Precursor‐Directed Synthesis of Apoptosis‐Initiating N‐Hydroxyalkyl Phenylbenzoisoquinolindione Alkaloids

Chen Y, Dahse H, Paetz C, Schneider B

ChemistryOpen

07-Dec-2022

PMCID:	PMC9728486
doi:	10.1002/open.202200157
PMID:	36478420

Engineered biosynthesis of plant polyketides by type III polyketide synthases in microorganisms

Liu C, Li S

Front Bioeng Biotechnol

14-Oct-2022

PMCID:	PMC9614166
doi:	10.3389/fbioe.2022.1017190
PMID:	36312548

Recent Developments in Therapeutic and Nutraceutical Applications of p-Methoxycinnamic Acid from Plant Origin

Płowuszyńska A, Gliszczyńska A

Molecules

23-Jun-2021

PMCID:	PMC8270276
doi:	10.3390/molecules26133827
PMID:	34201697

Octaketide Synthase from Polygonum cuspidatum Implements Emodin Biosynthesis in Arabidopsis thaliana

Guo Y, Nassar S, Ma L, Feng G, Li X, Chen M, Chai T, Abdel-Rahman IA, Beuerle T, Beerhues L, Wang H, Liu B

Plant Cell Physiol

04-Feb-2021

PMCID:	PMC8286135
doi:	10.1093/pcp/pcaa135
PMID:	33537755

Floating treatment wetlands integrated with microbial fuel cell for the treatment of urban wastewaters and bioenergy generation

Colares GS, Dell’Osbel N, Barbosa CV, Lutterbeck C, Oliveira GA, Rodrigues LR, Bergmann CP, Lopez DR, Rodriguez AL, Vymazal J, Machado EL

Sci Total Environ

24-Sep-2020

PMCID:	PMC7513814
doi:	10.1016/j.scitotenv.2020.142474
PMID:	33071144

Plant functional trait data and reflectance spectra for 22 palmiet wetland species

Rebelo AJ, Somers B, Esler KJ, Meire P

Data Brief

30-Aug-2018

PMCID:	PMC6143752
doi:	10.1016/j.dib.2018.08.113
PMID:	30238029

All that glitters is not Ramularia

Videira SI, Groenewald JZ, Braun U, Shin HD, Crous PW

Stud Mycol

29-Jun-2016

PMCID:	PMC4986539
doi:	10.1016/j.simyco.2016.06.001
PMID:	27570325

Heterologous Production of Curcuminoids

Rodrigues JL, Prather KL, Kluskens LD, Rodrigues LR

Microbiol Mol Biol Rev

28-Jan-2015

PMCID:	PMC4402967
doi:	10.1128/MMBR.00031-14
PMID:	25631288

Elucidating the Ramularia eucalypti species complex

Videira SI, Groenewald JZ, Kolecka A, van Haren L, Boekhout T, Crous PW

Persoonia

20-Nov-2014

PMCID:	PMC4510271
doi:	10.3767/003158515X685670
PMID:	26240445

Ginger and turmeric expressed sequence tags identify signature genes for rhizome identity and development and the biosynthesis of curcuminoids, gingerols and terpenoids

Koo HJ, McDowell ET, Ma X, Greer KA, Kapteyn J, Xie Z, Descour A, Kim H, Yu Y, Kudrna D, Wing RA, Soderlund CA, Gang DR

BMC Plant Biol

15-Feb-2013

PMCID:	PMC3608961
doi:	10.1186/1471-2229-13-27
PMID:	23410187

Benzalacetone Synthase

Shimokawa Y, Morita H, Abe I

Front Plant Sci

21-Mar-2012

PMCID:	PMC3355727
doi:	10.3389/fpls.2012.00057
PMID:	22645592

Phenylphenalenones and related natural products from Wachendorfia thyrsiflora L.

Jingjing Fang, Christian Paetz, Dirk Hölscher, Tobias Munde, Bernd Schneider

Elsevier BV

21-Apr-2011

doi:	10.1016/J.PHYTOL.2011.03.006

Structural and Biochemical Elucidation of Mechanism for Decarboxylative Condensation of β-Keto Acid by Curcumin Synthase

Katsuyama Y, Miyazono KI, Tanokura M, Ohnishi Y, Horinouchi S

J Biol Chem

09-Dec-2010

PMCID:	PMC3057783
doi:	10.1074/jbc.M110.196279
PMID:	21148316

Unusual intron in the second exon of a Type III polyketide synthase gene of Alpinia calcarata Rosc.

Radhakrishnan EK, Varghese RT, Vasudevan SE

Genet Mol Biol

01-Mar-2010

PMCID:	PMC3036070
doi:	10.1590/S1415-47572010000100024
PMID:	21637618

O-Methylation of phenylphenalenone phytoalexins in Musaacuminata and Wachendorfia thyrsiflora.

Otálvaro F, Jitsaeng K, Munde T, Echeverri F, Quiñones W, Schneider B

Phytochemistry

01-Feb-2010

doi:	10.1016/J.PHYTOCHEM.2009.10.019
PMID:	19939423

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 / Terphenyls / P-terphenyls
[4-Acetyloxy-2,5-dihydroxy-3,6-bis(4-hydroxyphenyl)phenyl] 3-hydroxybutanoate	56663851	Click to see CC(CC(=O)OC1=C(C(=C(C(=C1O)C2=CC=C(C=C2)O)OC(=O)C)O)C3=CC=C(C=C3)O)O	454.40	unknown	https://doi.org/10.1016/J.PHYTOL.2011.03.006
> Benzenoids / Naphthalenes / Naphthols and derivatives
(4R)-7-hydroxy-4,8-dimethoxy-10-phenyl-3-oxatricyclo[7.3.1.05,13]trideca-1(13),5,7,9,11-pentaen-2-one	638191	Click to see COC1C2=CC(=C(C3=C(C=CC(=C23)C(=O)O1)C4=CC=CC=C4)OC)O	336.30	unknown	https://doi.org/10.1016/J.PHYTOL.2011.03.006
7-Hydroxy-4,8-dimethoxy-10-phenyl-3-oxatricyclo[7.3.1.05,13]trideca-1(13),5,7,9,11-pentaen-2-one	12093863	Click to see COC1C2=CC(=C(C3=C(C=CC(=C23)C(=O)O1)C4=CC=CC=C4)OC)O	336.30	unknown	https://doi.org/10.1016/J.PHYTOL.2011.03.006
> Benzenoids / Naphthalenes / Phenylnaphthalenes
[(2R,3S,4S,5R,6S)-6-(2,5-dihydroxy-6-oxo-9-phenylphenalen-1-yl)oxy-3,4,5-trihydroxyoxan-2-yl]methyl N-carbamoylcarbamate	11103619	Click to see C1=CC=C(C=C1)C2=C3C4=C(C=C2)C(=O)C(=CC4=CC(=C3OC5C(C(C(C(O5)COC(=O)NC(=O)N)O)O)O)O)O	552.50	unknown	https://doi.org/10.1016/J.PHYTOL.2011.03.006
2-methoxy-9-phenyl-1H-phenalen-1-one	10085389	Click to see COC1=CC2=CC=CC3=C2C(=C(C=C3)C4=CC=CC=C4)C1=O	286.30	unknown	https://doi.org/10.1016/J.PHYTOL.2011.03.006
2-methoxy-9-phenyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenalen-1-one	162866649	Click to see COC1=CC2=C(C=CC3=C2C(=C(C=C3)C4=CC=CC=C4)C1=O)OC5C(C(C(C(O5)CO)O)O)O	464.50	unknown	https://doi.org/10.1016/J.PHYTOL.2011.03.006
2,5,6-Trihydroxy-9-phenyl-1H-phenalen-1-one	71365818	Click to see C1=CC=C(C=C1)C2=C3C4=C(C=C2)C(=C(C=C4C=C(C3=O)O)O)O	304.30	unknown	https://doi.org/10.1016/J.PHYTOL.2011.03.006
2,6-Dihydroxy-5-methoxy-7-phenylphenalen-1-one	162936181	Click to see COC1=C(C2=C(C=CC3=C2C(=C1)C=C(C3=O)O)C4=CC=CC=C4)O	318.30	unknown	https://doi.org/10.1016/J.PHYTOL.2011.03.006
2,6-Dihydroxy-5-methoxy-9-phenylphenalen-1-one	71436128	Click to see COC1=C(C2=C3C(=C1)C=C(C(=O)C3=C(C=C2)C4=CC=CC=C4)O)O	318.30	unknown	https://doi.org/10.1016/S0031-9422(00)91320-7 https://doi.org/10.1016/J.PHYTOL.2011.03.006
4-Phenyl-1H,3H-naphtho[1,8-cd]pyran-1,3-dione	11818168	Click to see C1=CC=C(C=C1)C2=C3C4=C(C=CC=C4C(=O)OC3=O)C=C2	274.30	unknown	https://doi.org/10.1016/J.PHYTOL.2011.03.006
Anigorufone	636472	Click to see C1=CC=C(C=C1)C2=C3C4=C(C=CC=C4C=C(C3=O)O)C=C2	272.30	unknown	https://doi.org/10.1016/J.PHYTOL.2011.03.006
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(7-methoxy-2-oxo-10-phenyl-3-oxatricyclo[7.3.1.05,13]trideca-1(13),5,7,9,11-pentaen-8-yl)oxy]oxan-2-yl]methyl N-carbamoylcarbamate	10886176	Click to see COC1=C(C2=C(C=CC3=C2C(=C1)COC3=O)C4=CC=CC=C4)OC5C(C(C(C(O5)COC(=O)NC(=O)N)O)O)O	554.50	unknown	https://doi.org/10.1016/J.PHYTOL.2011.03.006
[3,4,5-trihydroxy-6-[(7-methoxy-2-oxo-10-phenyl-3-oxatricyclo[7.3.1.05,13]trideca-1(13),5,7,9,11-pentaen-8-yl)oxy]oxan-2-yl]methyl N-carbamoylcarbamate	85302618	Click to see COC1=C(C2=C(C=CC3=C2C(=C1)COC3=O)C4=CC=CC=C4)OC5C(C(C(C(O5)COC(=O)NC(=O)N)O)O)O	554.50	unknown	https://doi.org/10.1016/J.PHYTOL.2011.03.006
7-hydroxy-10-(4-hydroxyphenyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-oxatricyclo[7.3.1.05,13]trideca-1(13),5,7,9,11-pentaen-2-one	162923690	Click to see C1C2=CC(=C(C3=C(C=CC(=C23)C(=O)O1)C4=CC=C(C=C4)O)OC5C(C(C(C(O5)CO)O)O)O)O	470.40	unknown	https://doi.org/10.1016/J.PHYTOL.2011.03.006
7-hydroxy-10-phenyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-oxatricyclo[7.3.1.05,13]trideca-1(13),5,7,9,11-pentaen-2-one	162980607	Click to see C1C2=CC(=C(C3=C(C=CC(=C23)C(=O)O1)C4=CC=CC=C4)OC5C(C(C(C(O5)CO)O)O)O)O	454.40	unknown	https://doi.org/10.1016/J.PHYTOL.2011.03.006
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes / Benzoxanthenes
5-Hydroxy-2-methoxy-6-oxa-benzo[def]chrysen-1-one	21592294	Click to see COC1=CC2=CC(=C3C4=C(C=CC(=C24)C1=O)C5=CC=CC=C5O3)O	316.30	unknown	https://doi.org/10.1016/J.PHYTOL.2011.03.006
5-Methoxy-6-oxa-benzo[def]chrysen-1-one	636791	Click to see COC1=C2C3=C(C=CC4=C3C(=C1)C=CC4=O)C5=CC=CC=C5O2	300.30	unknown	https://doi.org/10.1016/J.PHYTOL.2011.03.006
5-Methoxy-6-oxa-benzo[def]chrysen-3-one	636441	Click to see COC1=C2C3=C(C=CC4=C3C(=C1)C(=O)C=C4)C5=CC=CC=C5O2	300.30	unknown	https://doi.org/10.1080/10575630290033079
Lachnanthofluorene	21592295	Click to see C1=CC=C2C(=C1)C3=C4C5=C(C=C3)C(=O)C(=CC5=CC(=C4O2)O)O	302.30	unknown	https://doi.org/10.1016/J.PHYTOL.2011.03.006
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
7-Methoxy-10-phenyl-3-oxatricyclo[7.3.1.05,13]trideca-1(13),4,6,9,11-pentaene-2,8-dione	10859663	Click to see COC1=CC2=COC(=O)C3=C2C(=C(C=C3)C4=CC=CC=C4)C1=O	304.30	unknown	https://doi.org/10.1016/J.PHYTOL.2011.03.006
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans
(1S,13S,14R,26R)-1,14-dihydroxy-9,22-diphenyl-2,15-dioxaoctacyclo[21.3.1.110,14.03,12.06,11.013,26.016,25.019,24]octacosa-3(12),4,6(11),7,9,16(25),17,19(24),20,22-decaene-27,28-dione	162978124	Click to see C1=CC=C(C=C1)C2=C3C4=C(C=C2)C=CC5=C4C6C7C8=C(C=CC9=C8C(=C(C=C9)C1=CC=CC=C1)C(=O)C7(O5)O)OC6(C3=O)O	574.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.10.019
1,14-Dihydroxy-9,22-diphenyl-2,15-dioxaoctacyclo[21.3.1.110,14.03,12.06,11.013,26.016,25.019,24]octacosa-3(12),4,6(11),7,9,16(25),17,19(24),20,22-decaene-27,28-dione	78200663	Click to see C1=CC=C(C=C1)C2=C3C4=C(C=C2)C=CC5=C4C6C7C8=C(C=CC9=C8C(=C(C=C9)C1=CC=CC=C1)C(=O)C7(O5)O)OC6(C3=O)O	574.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.10.019 https://doi.org/10.1016/J.PHYTOL.2011.03.006
rel-(6aR,13aR,14dR,14eR)-6a,13a-dihydroxy-1,8-diphenyl-6a,13a,14d,14e-tetrahydronaphtho[8,1,2-hij]naphtho[2',1',8':1,8,7]isochromeno[5,4,3-cde]isochromene-7,14-dione	636470	Click to see C1=CC=C(C=C1)C2=C3C4=C(C=C2)C=CC5=C4C6C7C8=C(C=CC9=C8C(=C(C=C9)C1=CC=CC=C1)C(=O)C7(O5)O)OC6(C3=O)O	574.60	unknown	https://doi.org/10.1016/J.PHYTOL.2011.03.006

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Wachendorfia thyrsiflora

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