Scientific name	Authority	First published in
Dorstenia bicornis	Schweinf.	Bot. Zeitung (Berlin) 29: 332 (1871)
Dorstenia gilletii	De Wild.	Bull. Herb. Boissier , sér. 2, 1: 838 (1901)
Dorstenia klaineana	Pierre ex Heckel & Schlagd.	Compt. Rend. Hebd. Séances Acad. Sci. 133: 940 (1901)
Dorstenia klainei	Heckel	Bull. Soc. Bot. France 47: 260 (1901)
Dorstenia lukafuensis	De Wild.	Ann. Mus. Congo Belge, Bot. , sér. 4, 1: 28 (1902)
Dorstenia massonii	Bureau	Bull. Soc. Bot. France 33: 70 (1886)
Dorstenia psiluroides	Engl.	Wiss. Erg. Deut. Zentr.-Afr. Exped., Bot. 2: 181 (1911)
Dorstenia psilurus var. scabra	Bureau	Prodr. 17: 273 1873
Dorstenia scabra	Engl.	Bot. Jahrb. Syst. 20: 142 (1894)
Dorstenia stolzii	Engl.	Bot. Jahrb. Syst. 51: 432 (1914)
Dorstenia tenuifolia	Engl.	Bot. Jahrb. Syst. 33: 116 (1902)
Dorstenia psiluroides f. subintegra	Engl.	Wiss. Erg. Deut. Zentr.-Afr. Exped., Bot. 2: 1911
Dorstenia psilurus var. subintegrifolia	De Wild.	Bull. Herb. Boissier, sér. 2, 1: 838 1901
Dorstenia psilurus var. brevicaudata	Rendle	J. Bot. 53: 301 1915
Dorstenia psilurus var. compacta	De Wild.	Pl. Nov. Horti Then. 1(7): 1907
Dorstenia scabra var. denticulata	Engl.	Monogr. Afrik. Pflanzen-Fam. 1898
Dorstenia scabra var. longicaudata	Engl.	Bot. Jahrb. Syst. 51: 431 1914
Dorstenia scabra var. subintegrifolia	(De Wild.) Rendle	Fl. Trop. Afr. 6(2): 52 1916

Common names Top

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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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Name	Authority	First published in
Dorstenia psilurus f. subintegrifolia	De Wild.

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

Africa click to expand
- East Tropical Africa
  - Tanzania
  - Uganda
- Northeast Tropical Africa
  - Sudan
- South Tropical Africa
  - Angola
  - Malawi
  - Mozambique
  - Zambia
  - Zimbabwe
- West Tropical Africa
  - Nigeria
- West-central Tropical Africa
  - Cameroon
  - Central African Republic
  - Congo
  - Gabon
  - Rwanda
  - Zaïre

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000654605
Tropicos	21300961
INPN	629584
KEW	urn:lsid:ipni.org:names:851624-1
The Plant List	kew-2775845
Open Tree Of Life	564311
Observations.org	341319
NCBI Taxonomy	106723
IPNI	851624-1
iNaturalist	430967
iNaturalist	430966
iNaturalist	430963
iNaturalist	430965
GBIF	3763387
EPPO	DOJPS
EOL	11901441
Elurikkus	409682

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

Chronic Gastric Ulcer Healing Actions of the Aqueous Extracts of Staple Plant Foods of the North-West, Adamawa, and West Regions of Cameroon

Mikwangock HD, Tamfu AN, Amang AP, Siwe GT, Mezui C, Kucukaydin S, Enow-Orock EG, Tan PV

Biomed Res Int

09-Jan-2023

PMCID:	PMC9842419
doi:	10.1155/2023/2657278
PMID:	36654868

How Should the Worldwide Knowledge of Traditional Cancer Healing Be Integrated with Herbs and Mushrooms into Modern Molecular Pharmacology?

Kirdeeva Y, Fedorova O, Daks A, Barlev N, Shuvalov O

Pharmaceuticals (Basel)

14-Jul-2022

PMCID:	PMC9320176
doi:	10.3390/ph15070868
PMID:	35890166

A review of alpha-glucosidase inhibitors from plants as potential candidates for the treatment of type-2 diabetes

Dirir AM, Daou M, Yousef AF, Yousef LF

Phytochem Rev

16-Aug-2021

PMCID:	PMC8364835
doi:	10.1007/s11101-021-09773-1
PMID:	34421444

Potent Cytotoxicity of Four Cameroonian Plant Extracts on Different Cancer Cell Lines

Somaida A, Tariq I, Ambreen G, Abdelsalam AM, Ayoub AM, Wojcik M, Dzoyem JP, Bakowsky U

Pharmaceuticals (Basel)

31-Oct-2020

PMCID:	PMC7693157
doi:	10.3390/ph13110357
PMID:	33142782

Antibacterial and Antibiotic Modifying Potential of Crude Extracts, Fractions, and Compounds from Acacia polyacantha Willd. against MDR Gram-Negative Bacteria

Mambe FT, Na-Iya J, Fotso GW, Ashu F, Ngameni B, Ngadjui BT, Beng VP, Kuete V

Evid Based Complement Alternat Med

07-Mar-2019

PMCID:	PMC6431460
doi:	10.1155/2019/7507549
PMID:	30956683

African Herbal Remedies with Antioxidant Activity: A Potential Resource Base for Wound Treatment

Gulumian M, Yahaya ES, Steenkamp V

Evid Based Complement Alternat Med

22-Nov-2018

PMCID:	PMC6282146
doi:	10.1155/2018/4089541
PMID:	30595712

First large-scale ethnobotanical survey in the province of Uíge, northern Angola

Lautenschläger T, Monizi M, Pedro M, Mandombe JL, Bránquima MF, Heinze C, Neinhuis C

J Ethnobiol Ethnomed

25-Jul-2018

PMCID:	PMC6060550
doi:	10.1186/s13002-018-0238-3
PMID:	30045744

Multidrug resistant bacteria are sensitive to Euphorbia prostrata and six others Cameroonian medicinal plants extracts

Voukeng IK, Beng VP, Kuete V

BMC Res Notes

25-Jul-2017

PMCID:	PMC5526298
doi:	10.1186/s13104-017-2665-y
PMID:	28743314

Potential of Central, Eastern and Western Africa Medicinal Plants for Cancer Therapy: Spotlight on Resistant Cells and Molecular Targets

Mbaveng AT, Kuete V, Efferth T

Front Pharmacol

02-Jun-2017

PMCID:	PMC5454075
doi:	10.3389/fphar.2017.00343
PMID:	28626426

Antibacterial and antibiotic-resistance modifying activity of the extracts and compounds from Nauclea pobeguinii against Gram-negative multi-drug resistant phenotypes

Seukep JA, Sandjo LP, Ngadjui BT, Kuete V

BMC Complement Altern Med

07-Jul-2016

PMCID:	PMC4937598
doi:	10.1186/s12906-016-1173-2
PMID:	27386848

In vitro antibacterial and antibiotic-potentiation activities of the methanol extracts from Beilschmiedia acuta, Clausena anisata, Newbouldia laevis and Polyscias fulva against multidrug-resistant Gram-negative bacteria

Tankeo SB, Tane P, Kuete V

BMC Complement Altern Med

22-Nov-2015

PMCID:	PMC4655084
doi:	10.1186/s12906-015-0944-5
PMID:	26590804

African Flora Has the Potential to Fight Multidrug Resistance of Cancer

Kuete V, Efferth T

Biomed Res Int

15-Apr-2015

PMCID:	PMC4413252
doi:	10.1155/2015/914813
PMID:	25961047

Induction of mitochondrial dependent apoptosis and cell cycle arrest in human promyelocytic leukemia HL-60 cells by an extract from Dorstenia psilurus: a spice from Cameroon

Pieme CA, Guru SK, Ambassa P, Kumar S, Ngameni B, Ngogang JY, Bhushan S, Saxena AK

BMC Complement Altern Med

10-Sep-2013

PMCID:	PMC3847675
doi:	10.1186/1472-6882-13-223
PMID:	24016040

Antibacterial and antibiotic-potentiation activities of the methanol extract of some cameroonian spices against Gram-negative multi-drug resistant phenotypes

Voukeng IK, Kuete V, Dzoyem JP, Fankam AG, Noumedem JA, Kuiate JR, Pages JM

BMC Res Notes

15-Jun-2012

PMCID:	PMC3438083
doi:	10.1186/1756-0500-5-299
PMID:	22709668

Triprenylated flavonoids from Dorstenia psilurus and their alpha-glucosidase inhibition properties.

Tabopda TK, Ngoupayo J, Awoussong PK, Mitaine-Offer AC, Ali MS, Ngadjui BT, Lacaille-Dubois MA

J Nat Prod

01-Dec-2008

doi:	10.1021/NP800509U
PMID:	19061390

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
Octadecane-1,4-diol	18949695	Click to see CCCCCCCCCCCCCCC(CCCO)O	286.50	unknown	https://doi.org/10.1016/S0031-9422(98)00017-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
8-(2-hydroxypropan-2-yl)-2,5-dimethyl-2,3,4,4a,6,7,8,8a-octahydro-1H-naphthalene-1,5-diol	85196090	Click to see CC1CCC2C(C1O)C(CCC2(C)O)C(C)(C)O	256.38	unknown	https://doi.org/10.1016/S0031-9422(99)00211-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1021/NP800509U https://doi.org/10.1016/S0031-9422(98)00017-X
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/S0031-9422(98)00017-X https://doi.org/10.1021/NP800509U
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1021/NP800509U https://doi.org/10.1016/S0031-9422(98)00017-X
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	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	https://doi.org/10.1016/S0031-9422(98)00017-X
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	https://doi.org/10.1016/S0031-9422(98)00017-X
> Organoheterocyclic compounds / Benzofurans
Methyl 3-(6-hydroxy-1-benzofuran-5-yl)propanoate	15391031	Click to see COC(=O)CCC1=C(C=C2C(=C1)C=CO2)O	220.22	unknown	https://doi.org/10.1016/S0031-9422(98)00017-X
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
Dorsilurin E	15478906	Click to see CC1(CCC2=C(O1)C3=C(C4=C2OC(=C5C=CC(=O)C=C5O)C6=C4OC(CC6)(C)C)OC(CC3)(C)C)C	490.60	unknown	https://doi.org/10.1016/S0031-9422(99)00211-3
> Organoheterocyclic compounds / Piperidines
1-Deoxynojirimycin	29435	Click to see C1C(C(C(C(N1)CO)O)O)O	163.17	unknown	https://doi.org/10.1021/NP800509U
2-(Hydroxymethyl)piperidine-3,4,5-triol	1374	Click to see C1C(C(C(C(N1)CO)O)O)O	163.17	unknown	https://doi.org/10.1021/NP800509U
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, octadecyl ester	149044	Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC	446.70	unknown	https://doi.org/10.1016/S0031-9422(98)00017-X
Isostearyl ferulate	23124075	Click to see CC(C)CCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC	446.70	unknown	https://doi.org/10.1016/S0031-9422(98)00017-X
Octadecyl ferulate	5320256	Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC	446.70	unknown	https://doi.org/10.1016/S0031-9422(98)00017-X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Octadecyl 3-(4-hydroxyphenyl)prop-2-enoate	54330376	Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(C=C1)O	416.60	unknown	https://doi.org/10.1016/S0031-9422(98)00017-X
Octadecyl p-coumarate	12018904	Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(C=C1)O	416.60	unknown	https://doi.org/10.1016/S0031-9422(98)00017-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Psoralen	6199	Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C=C21	186.16	unknown	https://doi.org/10.1016/S0031-9422(98)00017-X https://doi.org/10.1021/NP800509U
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
(9R)-2-(2,4-dihydroxyphenyl)-5,9-dihydroxy-8,8-dimethyl-3,6-bis(3-methylbut-2-enyl)-9,10-dihydropyrano[2,3-h]chromen-4-one	162894155	Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=C(O3)C4=C(C=C(C=C4)O)O)CC=C(C)C)CC(C(O2)(C)C)O)C	506.60	unknown	https://doi.org/10.1016/S0031-9422(98)00017-X
(9S)-2-(2,4-dihydroxyphenyl)-5,9-dihydroxy-8,8-dimethyl-3,6-bis(3-methylbut-2-enyl)-9,10-dihydropyrano[2,3-h]chromen-4-one	162894156	Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=C(O3)C4=C(C=C(C=C4)O)O)CC=C(C)C)CC(C(O2)(C)C)O)C	506.60	unknown	https://doi.org/10.1016/S0031-9422(98)00017-X
2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3,6-bis(3-methylbut-2-enyl)chromen-4-one	163021147	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)CC=C(C)C)CC(C(=C)C)O)O)C	506.60	unknown	https://doi.org/10.1016/S0031-9422(99)00211-3
3,5-Dihydroxy-2-[3-hydroxy-4-(2-hydroxy-3-methylbut-3-enyl)phenyl]-8,8-dimethyl-6-(3-methylbut-2-enyl)-9,10-dihydropyrano[2,3-h]chromen-4-one	74399253	Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=C(O3)C4=CC(=C(C=C4)CC(C(=C)C)O)O)O)CCC(O2)(C)C)C	506.60	unknown	https://doi.org/10.1021/NP800509U
3,5,7-Trihydroxy-2-[3-hydroxy-4-(2-hydroxy-3-methylbut-3-enyl)phenyl]-6,8-bis(3-methylbut-2-enyl)chromen-4-one	74400534	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)CC(C(=C)C)O)O)O)CC=C(C)C)O)C	506.60	unknown	https://doi.org/10.1021/NP800509U
5,9-Dihydroxy-8-[3-hydroxy-4-(2-hydroxy-3-methylbut-3-enyl)phenyl]-2,2-dimethyl-6-(3-methylbut-2-enyl)-3,4-dihydropyrano[2,3-f]chromen-10-one	74400455	Click to see CC(=CCC1=C2C(=C3C(=C1O)CCC(O3)(C)C)C(=O)C(=C(O2)C4=CC(=C(C=C4)CC(C(=C)C)O)O)O)C	506.60	unknown	https://doi.org/10.1021/NP800509U
Dorsilurin A	15391029	Click to see CC(=CCC1=C(C=CC(=C1O)C2=CC(=O)C3=C(C(=C(C(=C3O2)CC=C(C)C)O)CC=C(C)C)O)O)C	490.60	unknown	https://doi.org/10.1016/S0031-9422(98)00017-X
Dorsilurin B	15391030	Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=C(O3)C4=C(C=C(C=C4)O)O)CC=C(C)C)CC(C(O2)(C)C)O)C	506.60	unknown	https://doi.org/10.1016/S0031-9422(98)00017-X
dorsilurin C	15478904	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC4=C(C=C3)C=CC(O4)(C)C)O)CC=C(C)C)O)C	488.60	unknown	https://doi.org/10.1021/NP800509U https://doi.org/10.1016/S0031-9422(99)00211-3
Dorsilurin D	15478905	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)CC=C(C)C)CC(C(=C)C)O)O)C	506.60	unknown	https://doi.org/10.1016/S0031-9422(99)00211-3
Dorsilurin F	25147638	Click to see CC(=CCC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)CC=C(C)C)O)CC=C(C)C)O)O)O)C	490.60	unknown	https://doi.org/10.1021/NP800509U
Dorsilurin G	25181116	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)CC(C(=C)C)O)O)O)CC=C(C)C)O)C	506.60	unknown	https://doi.org/10.1021/NP800509U
Dorsilurin H	25180897	Click to see CC(=CCC1=C2C(=C3C(=C1O)CCC(O3)(C)C)C(=O)C(=C(O2)C4=CC(=C(C=C4)CC(C(=C)C)O)O)O)C	506.60	unknown	https://doi.org/10.1021/NP800509U
Dorsilurin I	25178184	Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=C(O3)C4=CC(=C(C=C4)CC(C(=C)C)O)O)O)CCC(O2)(C)C)C	506.60	unknown	https://doi.org/10.1021/NP800509U
Dorsilurin J	25180898	Click to see CC(=CCC1=C(C=C(C=C1)C2=C(C(=O)C3=C4C(=C(C(=C3O2)CC=C(C)C)O)CCC(O4)(C)C)O)O)C	490.60	unknown	https://doi.org/10.1021/NP800509U
Dorsilurin K	25178185	Click to see CC(=CCC1=C(C=C(C=C1)C2=C(C(=O)C3=C4C(=C5C(=C3O2)CCC(O5)(C)C)CCC(O4)(C)C)O)O)C	490.60	unknown	https://doi.org/10.1021/NP800509U

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Dorstenia psilurus

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