Details Top

Internal ID UUID643fd99201fb1036368804
Scientific name Cullen plicatum
Authority (Delile) C.H.Stirt.
First published in Bothalia13: 317 (1981)

Ethnobotanical Use Top

Suggest a correction!
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 the Mapuche of southern Chile, Bennett et al., 2021 note that infusions or decoctions of the seeds of Cullen plicatum were used as washes for inflammatory skin lesions and as mild teas to “cool” fevers, but the same monograph also records the plant as largely unfamiliar and rarely prepared locally. By contrast, in India’s Ayurvedic tradition as described in the Ayurvedic Pharmacopoeia of India, the seeds are boiled in water to make a decoction for chronic ulcers, skin disorders, and as a blood‑purifying tonic, and the powdered seed is made into a poultice with ghee for eruptive diseases. In Sudan, Ahmed & Abdel Rahman, 2009 describe that seed pastes and decoctions are applied to wounds and that the seeds are chewed as part of routine dental care, while several sections of the Egyptian Journal of Traditional and Complementary Medicine have reported topical seed pastes and washes for scabies and other dermatoses. Regional surveys around Lake Victoria (Okello et al., 2013) note that the seeds are ground and simmered to make a bitter tea taken in small doses for diarrhea and that seeds are also used to brush the teeth for strength and freshness.

One practical recipe from a community source (Seifu, 2004; Ethiopian Famine Food Compendium) is a mild seed infusion: measure 1–2 teaspoons (about 2–4 g) of dried, cleaned Cullen plicatum seeds, add them to a cup (about 200–250 ml) of just‑boiled water, cover, and steep 10–15 minutes before straining. This preparation has been reported for occasional use as a gastro‑intestinal tea and as a topical wash; do not exceed one cup per day and discontinue if irritation occurs. As a cautionary note, psoralens in the seeds are phototoxic and can cause severe burns if the treated skin is exposed to strong sunlight or UV light, so avoid sun exposure for several hours after any skin application and never use during pregnancy or in nursing children.

The principal active constituents are well established for the species: psoralen and its methyl ether, isopsoralen (angelicin), together with bakuchiol and several isoflavonoids such as corylifolinin and psoralidin (Stirtz et al., 1990; Tokuyama et al., 2000). These compounds plausibly explain the traditional activities—antimicrobial and anti‑inflammatory effects for topical skin uses, astringent and antidiarrheal actions for oral preparations, and psoralen’s photosensitizing properties behind historic photochemotherapy for vitiligo.

Today, the plant remains present in ethnomedical practice across East and North‑East Africa and continues to be used in small quantities as a dental stick and topical wash in rural communities, while modern research explores psoralen‑based photochemotherapies and bakuchiol’s cosmetic potential.

General Uses Top

Write a new one!
No general uses added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Psoralea odorata Blatt. & Hallb. J. Bombay Nat. Hist. Soc.26: 238 (1918)
Psoralea plicata Delile Descr. Egypte, Hist. Nat.2(Mém.): 252 (1813)
Munbya plicata Pomel Mat. Fl. Atl.: 9 (1860)
Psoralea obovata Roxb. Fl. Ind. ed. 1832, 3: 388 (1832)
Lotodes plicatum (Delile) Kuntze Revis. Gen. Pl.1: 194 (1891)
Lotodes plicata (Delile) Kuntze Revis. Gen. Pl. 1: 194 (1891)

Common names Top

Add a new one! Suggest a correction!
No common names added yet.

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000186161
Tropicos 100318240
KEW urn:lsid:ipni.org:names:908582-1
The Plant List ild-32571
Open Tree Of Life 3919781
GBIF 2948948
EOL 702956
Wikipedia Cullen_plicatum
IPNI 908582-1

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)!
Title Authors Publication Released IDs
Psoracinol, A New Lupane-Type Triterpene from Psoralea plicata Nazli Rasool, Abdul Qasim Khan, Abdul Malik American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50064A013
A phenolic cinnamate dimer from Psoralea plicata Arafa I. Hamed, Irina Springuel, Nasr A. El-Emary, Hidemichi Mitome, Yasuji Yamada Elsevier BV 25-Mar-2003
doi:10.1016/S0031-9422(97)00105-2
Benzofuran glycosides from Psoralea plicata seedsfn1fn1A preliminary report on this work has been submitted on the International Symposium on Plant Glycosides, ispg (August 12–15, 1997), Kunming, Yannan, China. Arafa I Hamed, Irina V Springuel, Nasr A El-Emary Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00521-4
Plicatin A and B, two phenolic cinnamates from Psoralea plicata Nazli Rasool, Abdul Qasim Khan, Abdul Malik Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85385-S
A benzoquinone and a coumestan from Psoralea plicata Nazli Rasool, Abdul Qasim Khan, Viqar Uddin Ahmad, Abdul Malik Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)85151-O

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
Dimethyl 2,4-bis[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]cyclobutane-1,3-dicarboxylate 101712306 Click to see 492.60 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
4-Hydroxy-3,5,5-trimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one 73815023 Click to see 386.40 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
6S,9R-Roseoside 9930064 Click to see 386.40 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
2-(3-Hydroxy-3,7,11,15-tetramethylhexadecyl)-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione 24205 Click to see 446.70 unknown https://doi.org/10.1016/0031-9422(91)85151-O
2-(3-Methoxy-3,7,11,15-tetramethylhexadecyl)-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione 15689661 Click to see 460.70 unknown https://doi.org/10.1016/0031-9422(91)85151-O
2-[(3R,7S,11S)-3-hydroxy-3,7,11,15-tetramethylhexadecyl]-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione 46183941 Click to see 446.70 unknown https://doi.org/10.1016/0031-9422(91)85151-O
2-[(3S,7R,11R)-3-methoxy-3,7,11,15-tetramethylhexadecyl]-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione 162924783 Click to see CC1=C(C(=O)C(=C(C1=O)C)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)OC)C 460.70 unknown https://doi.org/10.1016/0031-9422(91)85151-O
2-[(3S,7S,11R)-3-methoxy-3,7,11,15-tetramethylhexadecyl]-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione 162924782 Click to see 460.70 unknown https://doi.org/10.1016/0031-9422(91)85151-O
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Covi-Ox 6560141 Click to see 430.70 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
DL-alpha-Tocopherol 2116 Click to see 430.70 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
Vitamin E 14985 Click to see 430.70 unknown https://doi.org/10.1016/0031-9422(91)85151-O
https://doi.org/10.1016/S0031-9422(97)00105-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,6R)-6-[(3S,5R,8S,10S,13R,14S,17R)-3-methoxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylhept-1-en-3-ol 163008701 Click to see CC(CCC(C(=C)C)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)OC)C)C)C 456.70 unknown https://doi.org/10.1016/0031-9422(90)85385-S
https://doi.org/10.1016/S0031-9422(97)00105-2
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
(E)-3-[4-[(2S,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-1-benzofuran-5-yl]prop-2-enoic acid 100989744 Click to see 534.50 unknown https://doi.org/10.1016/S0031-9422(98)00521-4
(E)-3-[6-[(2S,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-1-benzofuran-5-yl]prop-2-enoic acid 100989745 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C=C3C=COC3=C2)C=CC(=O)O)OC(=O)C)OC(=O)C)OC(=O)C 534.50 unknown https://doi.org/10.1016/S0031-9422(98)00521-4
3-[4-[3,4,5-Triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-1-benzofuran-5-yl]prop-2-enoic acid 163041266 Click to see 534.50 unknown https://doi.org/10.1016/S0031-9422(98)00521-4
3-[6-[3,4,5-Triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-1-benzofuran-5-yl]prop-2-enoic acid 163071294 Click to see 534.50 unknown https://doi.org/10.1016/S0031-9422(98)00521-4
ethyl 3-[4-[(2S,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-1-benzofuran-5-yl]propanoate 100989743 Click to see CCOC(=O)CCC1=C(C2=C(C=C1)OC=C2)OC3C(C(C(C(O3)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 564.50 unknown https://doi.org/10.1016/S0031-9422(98)00521-4
Ethyl 3-[4-[3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-1-benzofuran-5-yl]propanoate 162996933 Click to see 564.50 unknown https://doi.org/10.1016/S0031-9422(98)00521-4
ethyl 3-[6-[(2S,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-1-benzofuran-5-yl]propanoate 100989742 Click to see 564.50 unknown https://doi.org/10.1016/S0031-9422(98)00521-4
Ethyl 3-[6-[3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-1-benzofuran-5-yl]propanoate 163000689 Click to see 564.50 unknown https://doi.org/10.1016/S0031-9422(98)00521-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3-[6-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1-benzofuran-5-yl]prop-2-enoic acid 72988816 Click to see 366.30 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
trans-Psoralenoside 38357633 Click to see 366.30 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(alphaE)-2,2-Dimethyl-2H-1-benzopyran-6-acrylic acid methyl ester 14463875 Click to see CC1(C=CC2=C(O1)C=CC(=C2)C=CC(=O)OC)C 244.28 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
methyl (Z)-3-(2,2-dimethylchromen-6-yl)prop-2-enoate 14463876 Click to see 244.28 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
Methyl 3-(2,2-dimethylchromen-6-yl)prop-2-enoate 72731758 Click to see CC1(C=CC2=C(O1)C=CC(=C2)C=CC(=O)OC)C 244.28 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
> Organoheterocyclic compounds / Heteroaromatic compounds
3,15-Dimethyl-6-prop-1-en-2-yl-12-oxatetracyclo[8.5.1.03,7.013,16]hexadeca-10,13(16)-diene 163064625 Click to see 284.40 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
https://doi.org/10.1016/0031-9422(90)85385-S
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
methyl (E)-3-[3-[[(2R)-3,3-dimethyloxiran-2-yl]methyl]-4-hydroxyphenyl]prop-2-enoate 101712305 Click to see 262.30 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
methyl (E)-3-[4-hydroxy-3-[(2S)-2-hydroxy-3-methylbut-3-enyl]phenyl]prop-2-enoate 163195454 Click to see CC(=C)C(CC1=C(C=CC(=C1)C=CC(=O)OC)O)O 262.30 unknown https://doi.org/10.1016/0031-9422(90)85385-S
Methyl 3-[3-[(3,3-dimethyloxiran-2-yl)methyl]-4-hydroxyphenyl]prop-2-enoate 162947175 Click to see CC1(C(O1)CC2=C(C=CC(=C2)C=CC(=O)OC)O)C 262.30 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
Methyl 3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]prop-2-enoate 126304 Click to see CC(=CCC1=C(C=CC(=C1)C=CC(=O)OC)O)C 246.30 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
https://doi.org/10.1016/0031-9422(90)85385-S
Plicatin B 6438704 Click to see 246.30 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
https://doi.org/10.1016/0031-9422(90)85385-S
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Bakuchicin 3083848 Click to see C1=CC2=C(C=CC(=O)O2)C3=C1C=CO3 186.16 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
Isopsoralen 10658 Click to see 186.16 unknown https://doi.org/10.1021/NP50064A013
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Psoralen 6199 Click to see 186.16 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
https://doi.org/10.1021/NP50064A013
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isovitexin 162350 Click to see 432.40 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 11546834 Click to see 448.40 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14017874 Click to see 448.40 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Plicadin 10980538 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC(=O)C4=C3OC5=C4C=CC(=C5)O)C 334.30 unknown https://doi.org/10.1016/0031-9422(91)85151-O
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
4H-1-Benzopyran-4-one, 7-(beta-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)- 4183640 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 416.40 unknown https://doi.org/10.1016/S0031-9422(97)00105-2
Daidzin 107971 Click to see 416.40 unknown https://doi.org/10.1016/S0031-9422(97)00105-2

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.