Anigozanthos preissii, also known as the Albany cat's paw, is a perennial herb found only in Western Australia. It has long leaves that grow from a rhizome underground, and tall stalks that produce large red, orange, and yellow flowers in October and November. This plant can reach a height of 0.8 metres and has grey-green leaves arranged in a rosette at ground level. It is commonly found in the Warren region and along the southern coast of Southwest Australia. The species was first described by Stephan Endlicher and named after botanist Ludwig Preiss.

Synonyms Top

Scientific name	Authority	First published in
Anigozanthos preissii var. plumosus	Endl.	Pl. Preiss. 2: 26 (1848)

Common names Top

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Language	Common/alternative name
Vietnamese	chân mèo albany

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

Australasia click to expand
- Australia
  - Western Australia

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000340106
Tropicos	50223430
KEW	urn:lsid:ipni.org:names:429584-1
The Plant List	kew-220323
Open Tree Of Life	446438
NCBI Taxonomy	95948
IPNI	429584-1
iNaturalist	123217
GBIF	2765869
Freebase	/m/04n0p3n
EOL	1126309
USDA GRIN	454837
Wikipedia	Anigozanthos_preissii

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

Diarylheptanoid Derivatives (Musellins A–F) and Dimeric Phenylphenalenones from Seed Coats of Musella lasiocarpa, the Chinese Dwarf Banana

Lyu H, Chen Y, Gershenzon J, Paetz C

J Nat Prod

31-May-2023

PMCID:	PMC10294256
doi:	10.1021/acs.jnatprod.3c00273
PMID:	37256742

Mitochondria-Mediated Apoptosis of HCC Cells Triggered by Knockdown of Glutamate Dehydrogenase 1: Perspective for Its Inhibition through Quercetin and Permethylated Anigopreissin A

Marsico M, Santarsiero A, Pappalardo I, Convertini P, Chiummiento L, Sardone A, Di Noia MA, Infantino V, Todisco S

Biomedicines

11-Nov-2021

PMCID:	PMC8615521
doi:	10.3390/biomedicines9111664
PMID:	34829892

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

The Intramolecular Diels-Alder Reaction of Diarylheptanoids — Quantum Chemical Calculation of Structural Features Favoring the Formation of Phenylphenalenones

Monakhova Y, Schneider B

Molecules

23-Apr-2014

PMCID:	PMC6271999
doi:	10.3390/molecules19045231
PMID:	24762963

Organogenic nodule development in hop (Humulus lupulus L.): Transcript and metabolic responses

Fortes AM, Santos F, Choi YH, Silva MS, Figueiredo A, Sousa L, Pessoa F, Santos BA, Sebastiana M, Palme K, Malhó R, Verpoorte R, Pais MS

BMC Genomics

29-Sep-2008

PMCID:	PMC2573896
doi:	10.1186/1471-2164-9-445
PMID:	18823540

The Biosynthetic Origin of the Central One-Carbon Unit of Phenylphenalenones in<i>Anigozanthos preissii</i>

Dirk Hölscher, Bernd Schneider

Informa UK Limited

07-Jul-2007

doi:	10.1080/10575639508043208

Differentiation-dependent levels of benzofuran-type resveratrol dimers in root cultures of Anigozanthos preissii.

Schneider B

Phytochemistry

01-Sep-2003

doi:	10.1016/S0031-9422(03)00193-6
PMID:	12943763

A resveratrol dimer from Anigozanthos preissii and Musa cavendish

D. Hölscher, B. Schneider

Elsevier BV

13-May-2003

doi:	10.1016/0031-9422(96)00317-2

Phenylphenalenones from root cultures of Anigozanthos preissii

Dirk Hölscher, Bernd Schneider

Elsevier BV

05-Apr-2003

doi:	10.1016/S0031-9422(96)00679-6

Dihydrocinnamic acids are involved in the biosynthesis of phenylphenalenones in Anigozanthos preissii

Bettina Schmitt, Bernd Schneider

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(99)00116-8

Phenylpropanoid interconversion in Anigozanthos preissii observed by high-performance liquid chromatography-nuclear magnetic resonance spectroscopy.

Schmitt B, Schneider B

Phytochem Anal

01-Jan-2001

doi:	10.1002/1099-1565(200101/02)12:1<43::AID-PCA546>3.0.CO;2-Z
PMID:	11704960

Variability of phenylpropanoid precursors in the biosynthesis of phenylphenalenones in Anigozanthos preissii.

Schmitt B, Hölscher D, Schneider B

Phytochemistry

01-Feb-2000

doi:	10.1016/S0031-9422(99)00544-0
PMID:	10703053

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.1016/S0031-9422(99)00116-8
> 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	https://doi.org/10.1016/S0031-9422(99)00116-8
> Benzenoids / Naphthalenes / Phenylnaphthalenes
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/S0031-9422(96)00679-6 https://doi.org/10.1016/S0031-9422(99)00544-0
2,3-Dimethoxy-4-phenylphenalen-1-one	85730244	Click to see COC1=C(C(=O)C2=CC=CC3=C2C1=C(C=C3)C4=CC=CC=C4)OC	316.30	unknown	https://doi.org/10.1016/S0031-9422(96)00679-6
5-Hydroxy-2,6-dimethoxy-7-phenylphenalen-1-one	85730242	Click to see COC1=CC2=CC(=C(C3=C(C=CC(=C23)C1=O)C4=CC=CC=C4)OC)O	332.30	unknown	https://doi.org/10.1016/S0031-9422(96)00679-6
5-Hydroxy-6-methoxy-7-phenylphenalen-1-one	85730238	Click to see COC1=C(C=C2C=CC(=O)C3=C2C1=C(C=C3)C4=CC=CC=C4)O	302.30	unknown	https://doi.org/10.1016/S0031-9422(96)00679-6
7,8-Dimethoxy-6-phenylphenalen-1-one	85730248	Click to see COC1=C(C2=C(C=CC3=C2C(=C1)C(=O)C=C3)C4=CC=CC=C4)OC	316.30	unknown	https://doi.org/10.1016/S0031-9422(96)00679-6
9-(3,4-Dihydroxyphenyl)-2-hydroxy-1H-phenalen-1-one	85846875	Click to see C1=CC2=C3C(=C1)C=C(C(=O)C3=C(C=C2)C4=CC(=C(C=C4)O)O)O	304.30	unknown	https://doi.org/10.1016/S0031-9422(96)00679-6 https://doi.org/10.1016/S0031-9422(99)00544-0
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/S0031-9422(96)00679-6 https://doi.org/10.1016/S0031-9422(99)00544-0
Hydroxyanigorufone	11471752	Click to see C1=CC2=C3C(=C1)C=C(C(=O)C3=C(C=C2)C4=CC=C(C=C4)O)O	288.30	unknown	https://doi.org/10.1016/S0031-9422(96)00679-6 https://doi.org/10.1016/S0031-9422(99)00116-8 https://doi.org/10.1016/S0031-9422(99)00544-0 https://doi.org/10.1080/10575639508043208
Musanolone F	10734307	Click to see COC1=C(C=CC(=C1)C2=C3C4=C(C=CC=C4C=C(C3=O)O)C=C2)O	318.30	unknown	https://doi.org/10.1016/S0031-9422(99)00544-0
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Amphilectane, neoamphilectane, cycloamphilectane, and adociane diterpenoids
3,3'-Bis(4''-hydroxyanigorufone)	136703905	Click to see C1=CC2=C3C(=C1)C(=C(C(=O)C3=C(C=C2)C4=CC=C(C=C4)O)O)C5=C(C(=O)C6=C(C=CC7=C6C5=CC=C7)C8=CC=C(C=C8)O)O	574.60	unknown	https://doi.org/10.1016/S0031-9422(96)00679-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
(E)-3-(4-hydroxycyclohexa-2,4-dien-1-yl)prop-2-enoic acid	17928043	Click to see C1C=C(C=CC1C=CC(=O)O)O	166.17	unknown	https://doi.org/10.1002/1099-1565(200101/02)12:1<43::AID-PCA546>3.0.CO;2-Z
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde	126	Click to see C1=CC(=CC=C1C=O)O	122.12	unknown	https://doi.org/10.1016/S0031-9422(99)00116-8
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,3R,4S,5S,6R)-2-[[3-(3,5-dihydroxyphenyl)-2-(4-hydroxyphenyl)-6-[(E)-2-(4-hydroxyphenyl)ethenyl]-1-benzofuran-4-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163037034	Click to see C1=CC(=CC=C1C=CC2=CC3=C(C(=C2)OC4C(C(C(C(O4)CO)O)O)O)C(=C(O3)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)O	614.60	unknown	https://doi.org/10.1016/S0031-9422(03)00193-6
(2S,3R,4S,5S,6R)-2-[4-[3-(3,5-dihydroxyphenyl)-4-hydroxy-6-[(E)-2-(4-hydroxyphenyl)ethenyl]-1-benzofuran-2-yl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	21575645	Click to see C1=CC(=CC=C1C=CC2=CC(=C3C(=C2)OC(=C3C4=CC(=CC(=C4)O)O)C5=CC=C(C=C5)OC6C(C(C(C(O6)CO)O)O)O)O)O	614.60	unknown	https://doi.org/10.1016/S0031-9422(03)00193-6
(2S,3R,4S,5S,6R)-2-[4-[3-(3,5-dihydroxyphenyl)-6-[(E)-2-(4-hydroxyphenyl)ethenyl]-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1-benzofuran-2-yl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162906048	Click to see C1=CC(=CC=C1C=CC2=CC3=C(C(=C2)OC4C(C(C(C(O4)CO)O)O)O)C(=C(O3)C5=CC=C(C=C5)OC6C(C(C(C(O6)CO)O)O)O)C7=CC(=CC(=C7)O)O)O	776.70	unknown	https://doi.org/10.1016/S0031-9422(03)00193-6
2-[[3-(3,5-Dihydroxyphenyl)-2-(4-hydroxyphenyl)-6-[2-(4-hydroxyphenyl)ethenyl]-1-benzofuran-4-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163037033	Click to see C1=CC(=CC=C1C=CC2=CC3=C(C(=C2)OC4C(C(C(C(O4)CO)O)O)O)C(=C(O3)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)O	614.60	unknown	https://doi.org/10.1016/S0031-9422(03)00193-6
2-[4-[3-(3,5-Dihydroxyphenyl)-4-hydroxy-6-[2-(4-hydroxyphenyl)ethenyl]-1-benzofuran-2-yl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	73802319	Click to see C1=CC(=CC=C1C=CC2=CC(=C3C(=C2)OC(=C3C4=CC(=CC(=C4)O)O)C5=CC=C(C=C5)OC6C(C(C(C(O6)CO)O)O)O)O)O	614.60	unknown	https://doi.org/10.1016/S0031-9422(03)00193-6
2-[4-[3-(3,5-Dihydroxyphenyl)-6-[2-(4-hydroxyphenyl)ethenyl]-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1-benzofuran-2-yl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162906047	Click to see C1=CC(=CC=C1C=CC2=CC3=C(C(=C2)OC4C(C(C(C(O4)CO)O)O)O)C(=C(O3)C5=CC=C(C=C5)OC6C(C(C(C(O6)CO)O)O)O)C7=CC(=CC(=C7)O)O)O	776.70	unknown	https://doi.org/10.1016/S0031-9422(03)00193-6
5-[4-Hydroxy-2-(4-hydroxyphenyl)-6-[2-(4-hydroxyphenyl)ethenyl]-1-benzofuran-3-yl]benzene-1,3-diol	78200664	Click to see C1=CC(=CC=C1C=CC2=CC(=C3C(=C2)OC(=C3C4=CC(=CC(=C4)O)O)C5=CC=C(C=C5)O)O)O	452.50	unknown	https://doi.org/10.1016/0031-9422(96)00317-2 https://doi.org/10.1016/S0031-9422(03)00193-6
Anigopreissin A	636473	Click to see C1=CC(=CC=C1C=CC2=CC(=C3C(=C2)OC(=C3C4=CC(=CC(=C4)O)O)C5=CC=C(C=C5)O)O)O	452.50	unknown	https://doi.org/10.1016/S0031-9422(03)00193-6 https://doi.org/10.1016/0031-9422(96)00317-2
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl-	8784	Click to see C1=CC=C(C=C1)C=CC(=O)O	148.16	unknown	https://doi.org/10.1002/1099-1565(200101/02)12:1<43::AID-PCA546>3.0.CO;2-Z
Cinnamic acid	444539	Click to see C1=CC=C(C=C1)C=CC(=O)O	148.16	unknown	https://doi.org/10.1002/1099-1565(200101/02)12:1<43::AID-PCA546>3.0.CO;2-Z
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid	709	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1016/S0031-9422(99)00116-8
4-Hydroxycinnamic acid	322	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1016/S0031-9422(99)00116-8
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1016/S0031-9422(99)00116-8 https://doi.org/10.1002/1099-1565(200101/02)12:1<43::AID-PCA546>3.0.CO;2-Z
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1002/1099-1565(200101/02)12:1<43::AID-PCA546>3.0.CO;2-Z https://doi.org/10.1016/S0031-9422(99)00116-8
> 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/S0031-9422(99)00116-8
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/S0031-9422(99)00116-8
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(4-Hydroxyphenyl)propionic acid	10394	Click to see C1=CC(=CC=C1CCC(=O)O)O	166.17	unknown	https://doi.org/10.1002/1099-1565(200101/02)12:1<43::AID-PCA546>3.0.CO;2-Z https://doi.org/10.1016/S0031-9422(99)00116-8

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Anigozanthos preissii

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