Dorstenia mannii is a type of plant belonging to the genus Dorstenia. It contains three compounds, 6,8-Diprenyleriodictyol, dorsmanin C, and dorsmanin F, which are unique to this species. These compounds have been identified and studied for their potential medicinal properties. D. mannii is a unique and valuable plant species with potential benefits for human health.

Synonyms Top

Scientific name	Authority	First published in
Dorstenia intermedia	Engl.	Monogr. Afrik. Pflanzen-Fam. 1: 17 (1898)
Dorstenia ophiocoma	K.Schum. ex Engl.	Bot. Jahrb. Syst. 20: 145 (1894)
Dorstenia vermoesenii	De Wild.	Pl. Bequaert. 6: 70 (1932)
Dorstenia ophiocoma var. longipes	Engl.	Monogr. Afrik. Pflanzen-Fam. 1: 18 1898
Dorstenia ophiocoma var. minor	Rendle	Fl. Trop. Afr. 6: 32 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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Name	Authority	First published in
Dorstenia mannii var. alternans	(Engl.) Hijman	Bull. Mus. Natl. Hist. Nat., B, Adansonia 3: 314 (1981 publ. 1982)
Dorstenia mannii var. humilis	(Hijman & C.C.Berg) Hijman	Bull. Mus. Natl. Hist. Nat., B, Adansonia 3: 315 (1981 publ. 1982)
Dorstenia mannii var. mougasii	Hijman	Bull. Mus. Natl. Hist. Nat., B, Adansonia 3: 313 (1981 publ. 1982)
Dorstenia mannii var. mungensis	(Engl.) Hijman	Bull. Mus. Natl. Hist. Nat., B, Adansonia 3: 314 (1981 publ. 1982)
Dorstenia mannii var. stipulata	(Rendle) Hijman	Bull. Mus. Natl. Hist. Nat., B, Adansonia 3: 315 (1981 publ. 1982)

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

Africa click to expand
- West Tropical Africa
  - Nigeria
- West-central Tropical Africa
  - Cameroon
  - Congo
  - Equatorial Guinea
  - Gabon
  - Zaïre

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000654502
Tropicos	21301886
KEW	urn:lsid:ipni.org:names:851587-1
The Plant List	kew-2775748
Open Tree Of Life	923990
NCBI Taxonomy	194258
IPNI	851587-1
iNaturalist	934937
GBIF	7262540
Freebase	/m/0pmdtmw
EPPO	DOJMM
USDA GRIN	415444
Wikipedia	Dorstenia_mannii
CMAUP	NPO19487

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

In vitro activities and mechanisms of action of anti-cancer molecules from African medicinal plants: a systematic review

Adico MD, Bayala B, Zoure AA, Lagarde A, Bazie JT, Traore L, Buñay J, Yonli AT, Djigma F, Bambara HA, Baron S, Simporé J, Lobaccaro JM

Am J Cancer Res

15-Mar-2024

PMCID:	PMC10998760
doi:	10.62347/AUHB5811
PMID:	38590420

Biochanin A Inhibits the Growth and Biofilm of Candida Species

Janeczko M, Kochanowicz E

Pharmaceuticals (Basel)

09-Jan-2024

PMCID:	PMC10818846
doi:	10.3390/ph17010089
PMID:	38256922

Chemistry and Biological Activities of Cannflavins of the Cannabis Plant

Abdel-Kader MS, Radwan MM, Metwaly AM, Eissa IH, Hazekamp A, Sohly MA

Cannabis Cannabinoid Res

04-Dec-2023

PMCID:	PMC10714118
doi:	10.1089/can.2023.0128
PMID:	37756221

Prenylated Flavonoids in Topical Infections and Wound Healing

Sychrová A, Škovranová G, Čulenová M, Bittner Fialová S

Molecules

13-Jul-2022

PMCID:	PMC9323352
doi:	10.3390/molecules27144491
PMID:	35889363

Determination of Anti-Alzheimer’s Disease Activity of Selected Plant Ingredients

Tuzimski T, Petruczynik A

Molecules

18-May-2022

PMCID:	PMC9147832
doi:	10.3390/molecules27103222
PMID:	35630702

Search for Antimicrobial Activity Among Fifty-Two Natural and Synthetic Compounds Identifies Anthraquinone and Polyacetylene Classes That Inhibit Mycobacterium tuberculosis

Pollo LA, Martin EF, Machado VR, Cantillon D, Wildner LM, Bazzo ML, Waddell SJ, Biavatti MW, Sandjo LP

Front Microbiol

18-Jan-2021

PMCID:	PMC7847937
doi:	10.3389/fmicb.2020.622629
PMID:	33537021

Ethnobotany and the Role of Plant Natural Products in Antibiotic Drug Discovery

Porras G, Chassagne F, Lyles JT, Marquez L, Dettweiler M, Salam AM, Samarakoon T, Shabih S, Farrokhi DR, Quave CL

Chem Rev

09-Nov-2020

PMCID:	PMC8183567
doi:	10.1021/acs.chemrev.0c00922
PMID:	33164487

Prevalence and Therapeutic Challenges of Fungal Drug Resistance: Role for Plants in Drug Discovery

Marquez L, Quave CL

Antibiotics (Basel)

31-Mar-2020

PMCID:	PMC7235788
doi:	10.3390/antibiotics9040150
PMID:	32244276

The Antioxidant Activity of Prenylflavonoids

Santos CM, Silva AM

Molecules

06-Feb-2020

PMCID:	PMC7037609
doi:	10.3390/molecules25030696
PMID:	32041233

Current trends in the pharmacological management of Chagas disease

Ribeiro V, Dias N, Paiva T, Hagström-Bex L, Nitz N, Pratesi R, Hecht M

Int J Parasitol Drugs Drug Resist

10-Dec-2019

PMCID:	PMC6928327
doi:	10.1016/j.ijpddr.2019.11.004
PMID:	31862616

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

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

Early State Research on Antifungal Natural Products

Negri M, Salci TP, Shinobu-Mesquita CS, Capoci IR, Svidzinski TI, Seki Kioshima E

Molecules

07-Mar-2014

PMCID:	PMC6271505
doi:	10.3390/molecules19032925
PMID:	24609016

Traditional Medicines in Africa: An Appraisal of Ten Potent African Medicinal Plants

Mahomoodally MF

Evid Based Complement Alternat Med

03-Dec-2013

PMCID:	PMC3866779
doi:	10.1155/2013/617459
PMID:	24367388

Antimicrobial activities of the methanol extract and compounds from the twigs of Dorstenia mannii (Moraceae)

Mbaveng AT, Kuete V, Ngameni B, Beng VP, Ngadjui BT, Meyer JJ, Lall N

BMC Complement Altern Med

29-Jun-2012

PMCID:	PMC3403998
doi:	10.1186/1472-6882-12-83
PMID:	22747736

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 / Benzenesulfonic acids and derivatives
Sulfanilic acid	8479	Click to see C1=CC(=CC=C1N)S(=O)(=O)O	173.19	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Tyramine	5610	Click to see C1=CC(=CC=C1CCN)O	137.18	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Nonacosane	12409	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC	408.80	unknown	via CMAUP database
> Lignans, neolignans and related compounds
Cannabisin E	71448966	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)OC(C(C3=CC(=C(C=C3)O)OC)O)C(=O)NCCC4=CC=C(C=C4)O	642.70	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(98)00324-0
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(3R)-5-[(1S,4aS,6R,8aS)-6-bromo-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-1-en-3-ol	162959704	Click to see CC1(C2CCC(=C)C(C2(CCC1Br)C)CCC(C)(C=C)O)C	369.40	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(97)01120-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
[3,4,5-triacetyloxy-6-[[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-yl]oxy]oxan-2-yl]methyl acetate	12895762	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)C)C)C(C)C	745.00	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
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/10.1016/S0031-9422(00)00215-6
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/10.1016/S0031-9422(00)00215-6
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(00)00215-6
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(00)00215-6
Tetraacetyldaucosterol	12895763	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)C)C)C(C)C	745.00	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron	21883788	Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-]	116.07	unknown	via CMAUP database
> Organic acids and derivatives / Keto acids and derivatives / Alpha-keto acids and derivatives
Pyruvic Acid	1060	Click to see CC(=O)C(=O)O	88.06	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline	305	Click to see C[N+](C)(C)CCO	104.17	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines / Acyl cholines
Acetylcholine	187	Click to see CC(=O)OCC[N+](C)(C)C	146.21	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucosinolates / Alkylglucosinolates
Sinigrin	6911854	Click to see C=CCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O	359.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol	11850	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(8R)-8-(2,2-dimethyl-3,4-dihydrochromen-6-yl)-2,2-dimethyl-3,4,7,8-tetrahydropyrano[3,2-g]chromen-6-one	163016279	Click to see CC1(CCC2=CC3=C(C=C2O1)OC(CC3=O)C4=CC5=C(C=C4)OC(CC5)(C)C)C	392.50	unknown	https://doi.org/10.1016/S0031-9422(97)01120-5
(8S)-8-(2,2-dimethyl-3,4-dihydrochromen-6-yl)-2,2-dimethyl-3,4,7,8-tetrahydropyrano[3,2-g]chromen-6-one	163016280	Click to see CC1(CCC2=CC3=C(C=C2O1)OC(CC3=O)C4=CC5=C(C=C4)OC(CC5)(C)C)C	392.50	unknown	https://doi.org/10.1016/S0031-9422(97)01120-5
(8S)-8-(2,2-dimethyl-3,4-dihydrochromen-6-yl)-5-hydroxy-2,2-dimethyl-3,4,7,8-tetrahydropyrano[3,2-g]chromen-6-one	163005157	Click to see CC1(CCC2=C(O1)C=CC(=C2)C3CC(=O)C4=C(O3)C=C5C(=C4O)CCC(O5)(C)C)C	408.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
Dorsmanin B	10524567	Click to see CC1(CCC2=CC3=C(C=C2O1)OC(CC3=O)C4=CC5=C(C=C4)OC(CC5)(C)C)C	392.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(97)01120-5
Paratocarpin J	15200532	Click to see CC1(CCC2=C(O1)C=CC(=C2)C3CC(=O)C4=C(O3)C=C5C(=C4O)CCC(O5)(C)C)C	408.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(-)-6,7-[2''-(1-Hydroxy-1-methylethyl)dihydrofurano]-8-prenyl-5,3',4'-trihydroxyflavanone	42607993	Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC(=C(C=C4)O)O)O)CC(O2)C(C)(C)O)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(98)00324-0
(2R,7R)-7-(3,4-dihydroxyphenyl)-4-hydroxy-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	163005188	Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC(=C(C=C4)O)O)O)CC(O2)C(C)(C)O)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(98)00324-0
(2R,8R)-2-(3,4-dihydroxyphenyl)-5-hydroxy-8-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-enyl)-2,3,8,9-tetrahydrofuro[2,3-h]chromen-4-one	162908641	Click to see CC(=CCC1=C(C2=C(C3=C1OC(C3)C(C)(C)O)OC(CC2=O)C4=CC(=C(C=C4)O)O)O)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
(2S,7R)-7-(3,4-dihydroxyphenyl)-4-hydroxy-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	163005186	Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC(=C(C=C4)O)O)O)CC(O2)C(C)(C)O)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
(2S,7S)-7-(3,4-dihydroxyphenyl)-4-hydroxy-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	163005187	Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC(=C(C=C4)O)O)O)CC(O2)C(C)(C)O)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(98)00324-0
(2S,8S)-2-(3,4-dihydroxyphenyl)-5-hydroxy-8-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-enyl)-2,3,8,9-tetrahydrofuro[2,3-h]chromen-4-one	162908642	Click to see CC(=CCC1=C(C2=C(C3=C1OC(C3)C(C)(C)O)OC(CC2=O)C4=CC(=C(C=C4)O)O)O)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(98)00324-0
(2S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2R)-2-hydroxy-3-methylbut-3-enyl]-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	163041148	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC(=C(C=C3)O)O)CC(C(=C)C)O)O)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(98)00324-0
(4R)-4-(3,4-dihydroxyphenyl)-10,10,16,16-tetramethyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1(14),2(7),8(13)-trien-6-one	163071345	Click to see CC1(CCC2=C(O1)C3=C(C4=C2OC(CC4=O)C5=CC(=C(C=C5)O)O)OC(CC3)(C)C)C	424.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(98)00324-0
(8R)-8-(3,4-dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-3,4,7,8-tetrahydropyrano[3,2-g]chromen-6-one	162998118	Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC(=C(C=C4)O)O)O)CCC(O2)(C)C)C	424.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
2-(3,4-Dihydroxyphenyl)-5-hydroxy-8-(1-hydroxy-1-methyl-ethyl)-6-(3-methylbut-2-enyl)-2,3,8,9-tetrahydrofuro[2,3-h]chromen-4-one	10527064	Click to see CC(=CCC1=C(C2=C(C3=C1OC(C3)C(C)(C)O)OC(CC2=O)C4=CC(=C(C=C4)O)O)O)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(98)00324-0
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-8-(2-hydroxy-3-methylbut-3-enyl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	10670764	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC(=C(C=C3)O)O)CC(C(=C)C)O)O)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(98)00324-0
2',3'-h]Chromen-4-one	10812253	Click to see CC1(CCC2=C(O1)C3=C(C4=C2OC(CC4=O)C5=CC(=C(C=C5)O)O)OC(CC3)(C)C)C	424.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(98)00324-0
4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-8-(2-hydroxy-3-methyl-3-butenyl)-6-(3-methyl-2-butenyl)-, (2S)-	134693652	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC(=C(C=C3)O)O)CC(C(=C)C)O)O)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(98)00324-0
5,7,3',4'-Tetrahydroxy-6,8-di-C-prenylflavanone	4063836	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC(=C(C=C3)O)O)CC=C(C)C)O)C	424.50	unknown	https://doi.org/10.1016/S0031-9422(97)01120-5 https://doi.org/10.1016/S0031-9422(98)00324-0
6,8-Diprenyleriodictyol	101705716	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC(=C(C=C3)O)O)CC=C(C)C)O)C	424.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(97)01120-5 https://doi.org/10.1016/S0031-9422(98)00324-0
7-(3,4-Dihydroxyphenyl)-4-hydroxy-2-(1-hydroxy-1-methyl-ethyl)-9-(3-methylbut-2-enyl)-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	4301534	Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC(=C(C=C4)O)O)O)CC(O2)C(C)(C)O)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(98)00324-0
8-(3,4-Dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-3,4,7,8-tetrahydropyrano[3,2-g]chromen-6-one	12049757	Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC(=C(C=C4)O)O)O)CCC(O2)(C)C)C	424.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
8-(3,4-Dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one	12049756	Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC(=C(C=C4)O)O)O)C=CC(O2)(C)C)C	422.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
Dorsmanin E	42608003	Click to see CC1(CCC2=C(O1)C3=C(C4=C2OC(CC4=O)C5=CC(=C(C=C5)O)O)OC(CC3)(C)C)C	424.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(98)00324-0
Dorsmanin F	42607992	Click to see CC(=CCC1=C(C2=C(C3=C1OC(C3)C(C)(C)O)OC(CC2=O)C4=CC(=C(C=C4)O)O)O)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(98)00324-0
Dorsmanin H	42607995	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC(=C(C=C3)O)O)CC(C(=C)C)O)O)C	440.50	unknown	via CMAUP database
Dorsmanin I	637828	Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC(=C(C=C4)O)O)O)C=CC(O2)(C)C)C	422.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
Dorsmanin J	42608002	Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC(=C(C=C4)O)O)O)CCC(O2)(C)C)C	424.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(4aR,8S,10aS)-8-(3,4-dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-3,4,4a,7,8,10a-hexahydropyrano[3,2-g]chromen-6-one	162921430	Click to see CC(=CCC1=C2C(=C(C3C1OC(CC3)(C)C)O)C(=O)CC(O2)C4=CC(=C(C=C4)O)O)C	426.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
(4aR,8S,10aS)-8-(3,4-dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-4a,7,8,10a-tetrahydropyrano[3,2-g]chromen-6-one	163102739	Click to see CC(=CCC1=C2C(=C(C3C1OC(C=C3)(C)C)O)C(=O)CC(O2)C4=CC(=C(C=C4)O)O)C	424.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
8-(3,4-Dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-3,4,4a,7,8,10a-hexahydropyrano[3,2-g]chromen-6-one	162921429	Click to see CC(=CCC1=C2C(=C(C3C1OC(CC3)(C)C)O)C(=O)CC(O2)C4=CC(=C(C=C4)O)O)C	426.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
8-(3,4-Dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-4a,7,8,10a-tetrahydropyrano[3,2-g]chromen-6-one	163102738	Click to see CC(=CCC1=C2C(=C(C3C1OC(C=C3)(C)C)O)C(=O)CC(O2)C4=CC(=C(C=C4)O)O)C	424.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(-)-Fustin	12310641	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O	288.25	unknown	via CMAUP database
Fustin	5317435	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O	288.25	unknown	via CMAUP database
Garbanzol	442410	Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O	272.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
2-(3,4-Dihydroxyphenyl)-6-(3,7-dimethylocta-2,6-dienyl)-3,5-dihydroxy-8,8-dimethylpyrano[2,3-h]chromen-4-one	403814	Click to see CC(=CCCC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=C(O3)C4=CC(=C(C=C4)O)O)O)C=CC(O2)(C)C)C)C	504.60	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(97)01120-5
2-(3,4-dihydroxyphenyl)-6-[(2Z)-3,7-dimethylocta-2,6-dienyl]-3,5-dihydroxy-8,8-dimethyl-pyrano[2,3-h]chromen-4-one	71594567	Click to see CC(=CCCC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=C(O3)C4=CC(=C(C=C4)O)O)O)C=CC(O2)(C)C)C)C	504.60	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
dorsmanin C	5472481	Click to see CC(=CCCC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=C(O3)C4=CC(=C(C=C4)O)O)O)C=CC(O2)(C)C)C)C	504.60	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(98)00017-X https://doi.org/10.1016/S0031-9422(97)01120-5
Gancaonin P	5481966	Click to see CC(=CCC1=C(C2=C(C=C1O)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O)C	370.40	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6,8-bis(3-methylbut-2-enyl)chromen-4-one	10669924	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)CC=C(C)C)O)C	422.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
Dorsmanin D	10599726	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)OC)O)CC=C(C)C)O)C	452.50	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(98)00017-X https://doi.org/10.1016/S0031-9422(97)01120-5
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferide	5281666	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	via CMAUP database
Robinetin	5281692	Click to see C1=CC2=C(C=C1O)OC(=C(C2=O)O)C3=CC(=C(C(=C3)O)O)O	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	44559826	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	via CMAUP database
Diosmin	5281613	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O	608.50	unknown	via CMAUP database
Hesperidin	10621	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O	610.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Gossypetin hexamethyl ether	146093	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3OC)OC)OC)OC)OC	402.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-1-[(4S)-4,5-dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl]-3-phenylprop-2-en-1-one	163194581	Click to see CC1(CC(C2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=CC=C3)O)C	324.40	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
(E)-1-[(4S)-5-hydroxy-4-methoxy-2,2-dimethyl-3,4-dihydrochromen-6-yl]-3-phenylprop-2-en-1-one	163193871	Click to see CC1(CC(C2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=CC=C3)OC)C	338.40	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
1-(4,5-Dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-3-phenylprop-2-en-1-one	162900704	Click to see CC1(CC(C2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=CC=C3)O)C	324.40	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
1-(5-Hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-3-(4-hydroxyphenyl)prop-2-en-1-one	403813	Click to see CC1(CCC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C	324.40	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(97)01120-5
1-(5-Hydroxy-4-methoxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-3-phenylprop-2-en-1-one	163045977	Click to see CC1(CC(C2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=CC=C3)OC)C	338.40	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
4-Methoxylonchocarpin	10472189	Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)OC)C	336.40	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6
5-Hydroxy-6-(4-hydroxycinnamoyl)-2,2-dimethylchromene	3662729	Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C	322.40	unknown	https://doi.org/10.1016/S0031-9422(97)01120-5
dorsmanin A	5472480	Click to see CC1(CCC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C	324.40	unknown	https://doi.org/10.1016/S0031-9422(00)00215-6 https://doi.org/10.1016/S0031-9422(97)01120-5
Isobavachromene	5889042	Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C	322.40	unknown	https://doi.org/10.1016/S0031-9422(97)01120-5 https://doi.org/10.1016/S0031-9422(00)00215-6

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Dorstenia mannii

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