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.

Warm infusions of young leaves are widely used in Southeast Asia to ease stomach upset and fever. In the Malay Peninsula, Burkill records that S. multiflora leaves are simmered in a decoction and given internally as a bitter tisane for mild gastric discomfort and general fevers. Among village healers in rural Thailand, leaves are also taken as a tea or decoction for fever and dyspepsia, while the same preparation is employed as a wash for skin rashes and minor sores (Keson, 1982). Across northern India, ethnobotanical surveys note that crushed leaf poultices are applied to inflamed wounds, bruises, and rheumatic joints, while a decoction of leaves is taken for gout and swelling (Sarma et al., 2008; Singh, 2015). These practices suggest a primary role for the leaves, with both internal beverages and external applications documented.

To prepare a mild leaf infusion, measure 5–7 g of fresh young leaves (roughly 1–1.5 cup of roughly chopped leaves), cover them with 250–300 mL of freshly boiled water, and steep with the pot covered for 10–15 minutes before straining. The result is a faintly bitter, aromatic tea used in small cups (50–100 mL) taken 2–3 times a day, mainly after meals. Because Suregada species contain bioactive alkaloids and other constituents, limit use to a short course and do not exceed moderate doses; pregnant or nursing individuals should avoid it, and anyone with known liver or kidney disease should consult a professional before use (Sarma et al., 2008).

Across reports, the pharmacological plausibility for these uses aligns with known phytochemistry of Suregada multiflora, including flavonoids such as quercetin and kaempferol, phenolic acids, lignans, triterpenoids, tannins, and a modest level of alkaloids. These constituents are documented for the species and plausibly underpin its reported astringent, anti-inflammatory, antipyretic, and antimicrobial effects, without suggesting any unverified mechanisms (Chandrasekaran et al., 2011; Johnson et al., 2009).

Today, modern studies on S. multiflora show antimicrobial and anti-inflammatory activity consistent with its traditional applications, while dried leaf material and a few standardized extracts remain available through regional herbal suppliers. Village practitioners continue to rely on the plant as a first‑line febrifuge and wash, underscoring both its cultural importance and evolving scientific interest.

General Uses Top

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Common products:
Small-diameter poles and occasional timber for light construction and tool handles. The species is noted in regional plant resource accounts as yielding poles for fencing and building and wood used for posts and tool handles.

Industrial and craft applications:
Likely used as fuelwood and charcoal, as reported for comparable species in regional treatments.

Food and beverages (non-medicinal):
No documented non-medicinal food or beverage uses.

Colorants and tanning:
No documented dye or tannin uses.

Wood and fiber:
Timber: dense hardwood suitable for light construction, posts, and tool handles; also employed for poles in rural infrastructure. Source regions include parts of South and Southeast Asia where the species occurs.

Fragrance and cosmetics:
No documented fragrance or cosmetic uses.

Properties relevant to use:
The wood is described as hard and dense, implying suitability for load-bearing posts and tool handles where durability and mechanical strength are required.

Standards and regulation:
No specific timber or construction standards cited for this taxon.

Sustainability and sourcing:
Listed as naturalized or cultivated in several South and Southeast Asian locales, supporting local pole/timber supply without detailed conservation status in the consulted references.

Synonyms Top

Scientific name	Authority	First published in
Suregada affinis	(S.Moore) Croizat	Bull. Jard. Bot. Buitenzorg , sér. 3, 17: 217 (1942)
Suregada dicocca	Roxb. ex Pax	Pflanzenr. , IV, 147, IV: 19 (1912)
Suregada glabra	Roxb.	Fl. Ind. ed. 1832 , 3: 831 (1832)
Suregada multiflora var. lamellata	Airy Shaw	Kew Bull. 25: 550 (1971)
Suregada multiflora var. verrucigera	Airy Shaw	Kew Bull. 32: 81 (1977)
Suregada oxyphylla	Kuntze	Revis. Gen. Pl. 2: 619 (1891)
Suregada sumatrana	(S.Moore) Croizat	Bull. Jard. Bot. Buitenzorg , sér. 3, 17: 217 (1942)
Suregada tenuifolia	(Ridl.) Croizat	Bull. Jard. Bot. Buitenzorg , sér. 3, 17: 216 (1942)
Gelonium fascuculatum	Roxb.	Fl. Ind. ed. 1832 , 3: 832 (1832)
Gelonium obtusum	Miq.	Fl. Ned. Ind., Eerste Bijv. : 452 (1861)
Gelonium affine	S.Moore	J. Bot. 63(Suppl.): 104 (1925)
Gelonium multiflorum	A.Juss.	Euphorb. Gen. : 111 (1824)
Gelonium oxyphyllum	Miq.	Fl. Ned. Ind., Eerste Bijv. : 452 (1861)
Gelonium sumatranum	S.Moore	J. Bot. 63(Suppl.): 104 (1925)
Gelonium tenuifolium	Ridl.	J. Straits Branch Roy. Asiat. Soc. 59: 181 (1911)
Gelonium aequoreum var. hainanense	Hemsl.	J. Linn. Soc., Bot. 26: 444. 1894

Common names Top

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Filter by language:

Language	Common/alternative name
English	false lime
Bengali	বন নারাংগা
Hindi	बन नारंगा
Thai	ขันทองพยาบาท
Chinese	白树
Chinese	饼树
Chinese	白樹

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Lesser Sunda Islands
  - Malaya
  - Sulawesi
  - Sumatera

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000317662
Tropicos	50265460
KEW	urn:lsid:ipni.org:names:356676-1
The Plant List	kew-198613
Open Tree Of Life	914247
NCBI Taxonomy	3979
IPNI	356676-1
iNaturalist	345933
GBIF	3054898
EOL	1150005
USDA GRIN	316308
Wikipedia	Suregada_multiflora

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

Hosts and Heterologous Expression Strategies of Recombinant Toxins for Therapeutic Purposes

di Leandro L, Colasante M, Pitari G, Ippoliti R

Toxins (Basel)

13-Dec-2023

PMCID:	PMC10748335
doi:	10.3390/toxins15120699
PMID:	38133203

Ethnomedicinal Uses, Phytochemistry and Pharmacological Properties of Suregada Genus: A Review

Mangisa M, Kemboi D, Fouche G, Nthambeleni R, Langat MK, Tarirai C, Cheek M, Gonyela O, Tembu VJ

Pharmaceuticals (Basel)

30-Sep-2023

PMCID:	PMC10610488
doi:	10.3390/ph16101390
PMID:	37895862

A computational overview of integrase strand transfer inhibitors (INSTIs) against emerging and evolving drug-resistant HIV-1 integrase mutants

Sayyed SK, Quraishi M, Jobby R, Rameshkumar N, Kayalvizhi N, Krishnan M, Sonawane T

Arch Microbiol

26-Mar-2023

PMCID:	PMC10039815
doi:	10.1007/s00203-023-03461-8
PMID:	36966200

Insights into the Novel Therapeutics and Vaccines against Herpes Simplex Virus

Malik S, Sah R, Ahsan O, Muhammad K, Waheed Y

Vaccines (Basel)

31-Jan-2023

PMCID:	PMC9959597
doi:	10.3390/vaccines11020325
PMID:	36851203

Pest categorisation of Nipaecoccus viridis

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A

EFSA J

18-Jan-2023

PMCID:	PMC9846308
doi:	10.2903/j.efsa.2023.7770
PMID:	36698490

Medicinal plants used by rural Thai people to treat non-communicable diseases and related symptoms

Nguanchoo V, Balslev H, Sadgrove NJ, Phumthum M

Heliyon

04-Jan-2023

PMCID:	PMC9850000
doi:	10.1016/j.heliyon.2022.e12758
PMID:	36685400

Medicinal plants and natural compounds against acyclovir-resistant HSV infections

Xu L, Zhong XL, Xi ZC, Li Y, Xu HX

Front Microbiol

10-Oct-2022

PMCID:	PMC9589345
doi:	10.3389/fmicb.2022.1025605
PMID:	36299732

From Immunotoxins to Suicide Toxin Delivery Approaches: Is There a Clinical Opportunity?

Ardini M, Vago R, Fabbrini MS, Ippoliti R

Toxins (Basel)

23-Aug-2022

PMCID:	PMC9506092
doi:	10.3390/toxins14090579
PMID:	36136517

Plant-Derived Type I Ribosome Inactivating Protein-Based Targeted Toxins: A Review of the Clinical Experience

Flavell DJ, Flavell SU

Toxins (Basel)

18-Aug-2022

PMCID:	PMC9412999
doi:	10.3390/toxins14080563
PMID:	36006226

The Updated Review on Plant Peptides and Their Applications in Human Health

Mani S, Bhatt SB, Vasudevan V, Prabhu D, Rajamanikandan S, Velusamy P, Ramasamy P, Raman P

Int J Pept Res Ther

27-Jul-2022

PMCID:	PMC9326430
doi:	10.1007/s10989-022-10437-7
PMID:	35911180

Sapovaccarin-S1 and -S2, Two Type I RIP Isoforms from the Seeds of Saponaria vaccaria L.

Schlaak L, Weise C, Kuropka B, Weng A

Toxins (Basel)

30-Jun-2022

PMCID:	PMC9324600
doi:	10.3390/toxins14070449
PMID:	35878187

Advances on Delivery of Cytotoxic Enzymes as Anticancer Agents

Asrorov AM, Muhitdinov B, Tu B, Mirzaakhmedov S, Wang H, Huang Y

Molecules

14-Jun-2022

PMCID:	PMC9230553
doi:	10.3390/molecules27123836
PMID:	35744957

Molecularly engineered tumor acidity-responsive plant toxin gelonin for safe and efficient cancer therapy

Ding GB, Zhu C, Wang Q, Cao H, Li BC, Yang P, Stauber RH, Nie G, Li Z

Bioact Mater

11-Feb-2022

PMCID:	PMC8961304
doi:	10.1016/j.bioactmat.2022.02.001
PMID:	35387163

A saponin-polybromophenol antibiotic (CU1) from Cassia fistula Bark Against Multi-Drug Resistant Bacteria Targeting RNA polymerase

Chakraborty AK, Saha S, Poria K, Samanta T, Gautam S, Mukhopadhyay J

Curr Res Pharmacol Drug Discov

03-Feb-2022

PMCID:	PMC8844791
doi:	10.1016/j.crphar.2022.100090
PMID:	35198968

Multifunctional Therapeutic Potential of Phytocomplexes and Natural Extracts for Antimicrobial Properties

Rahman MM, Rahaman MS, Islam MR, Hossain ME, Mannan Mithi F, Ahmed M, Saldías M, Akkol EK, Sobarzo-Sánchez E

Antibiotics (Basel)

06-Sep-2021

PMCID:	PMC8468069
doi:	10.3390/antibiotics10091076
PMID:	34572660

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 / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,3S,4R,9S,10R,13R,14R)-14-(hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-3,14-diol	11438670	Click to see	322.50	unknown	https://doi.org/10.1021/NP020435V
(1R,4S,5S,9S,10S,13R,15S)-15-hydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-6-one	15946299	Click to see	318.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.09.031
(1R,4S,6R,9R,10S,13R,15S)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-6,15-diol	101677458	Click to see	304.50	unknown	https://doi.org/10.1016/S0031-9422(00)90413-8 https://doi.org/10.1016/J.PHYTOCHEM.2006.09.031
(1S,4S,6R,9R,10S,13S,15R)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-6,15-diol	11370173	Click to see CC1(C2CCC34CC(CCC3C2(CCC1O)C)C(=C)C4O)C	304.50	unknown	https://doi.org/10.1021/NP020435V
(1S,4S,9S,10R,13R,14R)-14-hydroxy-14-(hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecan-6-one	23872027	Click to see	320.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.09.031
(1S,4S,9S,10S,13R,14R)-14-hydroxy-14-(hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecan-6-one	154496091	Click to see	320.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.09.031
15-Hydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-6-one	73202531	Click to see	318.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.09.031
16,17-Dihydroxykauran-3-one	3625680	Click to see	320.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.09.031
5-(Hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-6,15-diol	73202530	Click to see	320.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.09.031
Corymbol	72961769	Click to see CC1(CCCC2(C1C(CC34C2CCC(C3)C(C4)(CO)O)O)C)C	322.50	unknown	https://doi.org/10.1021/NP020435V
ent-16-Kaurene-3beta,15beta,18-triol	15946298	Click to see CC12CCC(C(C1CCC34C2CCC(C3)C(=C)C4O)(C)CO)O	320.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.09.031
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(3R,4aS,6aS,7R,10aR,11aS,11bR)-3,6a,7-trihydroxy-4,4,8,11b-tetramethyl-1,2,3,4a,5,6,7,10a,11,11a-decahydronaphtho[2,1-f][1]benzofuran-9-one	11245042	Click to see	350.40	unknown	https://doi.org/10.1021/NP020435V
(3S,4aR,6aS,7S,10aR,11aS,11bS)-3,6a,7-trihydroxy-4,4,8,11b-tetramethyl-3,4a,5,6,7,10a,11,11a-octahydro-2H-naphtho[2,1-f][1]benzofuran-1,9-dione	100926683	Click to see	364.40	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
(3S,4aS,10aR,11aR,11bS)-3-hydroxy-4,4,8,11b-tetramethyl-1,3,4a,5,6,10a,11,11a-octahydronaphtho[2,1-f]benzofuran-2,9-dione	101627297	Click to see	330.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.09.031
(4aS,10aR,11aR,11bS)-2-hydroxy-4,4,8,11b-tetramethyl-4a,5,6,10a,11,11a-hexahydronaphtho[2,1-f][1]benzofuran-3,9-dione	10782510	Click to see	328.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.09.031
(6a-hydroxy-4,4,8,11b-tetramethyl-3,9-dioxo-5,6,7,10a,11,11a-hexahydro-4aH-naphtho[2,1-f][1]benzofuran-7-yl) acetate	162934217	Click to see CC1=C2C(CC3C4(C=CC(=O)C(C4CCC3(C2OC(=O)C)O)(C)C)C)OC1=O	388.50	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
(6a,7-dihydroxy-4,4,8,11b-tetramethyl-1,9-dioxo-3,4a,5,6,7,10a,11,11a-octahydro-2H-naphtho[2,1-f][1]benzofuran-3-yl) acetate	162853043	Click to see	406.50	unknown	https://doi.org/10.1016/J.TET.2004.06.047
(6a,7-dihydroxy-4,4,8,11b-tetramethyl-1,9-dioxo-5,6,7,10a,11,11a-hexahydro-4aH-naphtho[2,1-f][1]benzofuran-5-yl) acetate	162952917	Click to see	404.50	unknown	https://doi.org/10.1016/J.TET.2004.06.047
(6a,7-Dihydroxy-4,4,8,11b-tetramethyl-9-oxo-1,2,3,4a,5,6,7,10a,11,11a-decahydronaphtho[2,1-f][1]benzofuran-3-yl) acetate	163006919	Click to see CC1=C2C(CC3C4(CCC(C(C4CCC3(C2O)O)(C)C)OC(=O)C)C)OC1=O	392.50	unknown	https://doi.org/10.1016/J.TET.2004.06.047
[(3S,4aR,6aS,7S,10aR,11aS,11bR)-6a,7-dihydroxy-4,4,8,11b-tetramethyl-1,9-dioxo-3,4a,5,6,7,10a,11,11a-octahydro-2H-naphtho[2,1-f][1]benzofuran-3-yl] acetate	162853044	Click to see	406.50	unknown	https://doi.org/10.1016/J.TET.2004.06.047
[(3S,4aS,6aS,7S,10aR,11aS,11bR)-6a,7-dihydroxy-4,4,8,11b-tetramethyl-9-oxo-1,2,3,4a,5,6,7,10a,11,11a-decahydronaphtho[2,1-f][1]benzofuran-3-yl] acetate	163006920	Click to see	392.50	unknown	https://doi.org/10.1016/J.TET.2004.06.047
[(4aR,5R,6aS,7S,10aR,11aS,11bR)-6a,7-dihydroxy-4,4,8,11b-tetramethyl-1,9-dioxo-5,6,7,10a,11,11a-hexahydro-4aH-naphtho[2,1-f][1]benzofuran-5-yl] acetate	162952919	Click to see	404.50	unknown	https://doi.org/10.1016/J.TET.2004.06.047
[(4aS,6aS,7S,10aR,11aS,11bR)-6a-hydroxy-4,4,8,11b-tetramethyl-3,9-dioxo-5,6,7,10a,11,11a-hexahydro-4aH-naphtho[2,1-f][1]benzofuran-7-yl] acetate	162934218	Click to see CC1=C2C(CC3C4(C=CC(=O)C(C4CCC3(C2OC(=O)C)O)(C)C)C)OC1=O	388.50	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
[(4aS,6aS,7S,10aR,11aS,11bS)-6a-hydroxy-4,4,8,11b-tetramethyl-3,9-dioxo-5,6,7,10a,11,11a-hexahydro-4aH-naphtho[2,1-f][1]benzofuran-7-yl] acetate	100926682	Click to see CC1=C2C(CC3C4(C=CC(=O)C(C4CCC3(C2OC(=O)C)O)(C)C)C)OC1=O	388.50	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
2-Hydroxy-4,4,8,11b-tetramethyl-4a,5,6,10a,11,11a-hexahydronaphtho[2,1-f][1]benzofuran-3,9-dione	85266194	Click to see	328.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.09.031
3-hydroxy-4,4,8,11b-tetramethyl-2,3,4a,5,6,10a,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-9-one	5260238	Click to see	316.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.09.031
3,6a,7-Trihydroxy-4,4,8,11b-tetramethyl-1,2,3,4a,5,6,7,10a,11,11a-decahydronaphtho[2,1-f][1]benzofuran-9-one	72766963	Click to see CC1=C2C(CC3C4(CCC(C(C4CCC3(C2O)O)(C)C)O)C)OC1=O	350.40	unknown	https://doi.org/10.1021/NP020435V
Helioscopinolide A	10245246	Click to see CC1=C2C=C3CCC4C(C(CCC4(C3CC2OC1=O)C)O)(C)C	316.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.09.031
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9S,11aS,11bR,12R,13aR,13bR)-1-isopropenyl-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-9,12-diol	14313615	Click to see	442.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.09.031
(3beta,13alpha,14beta)-13-Methyl-26-norurs-7-en-3-ol	111220	Click to see	426.70	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
(4-Hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl) 14-methylpentadecanoate	163035520	Click to see	681.10	unknown	https://doi.org/10.1016/S0031-9422(00)90413-8 https://doi.org/10.1021/NP020435V https://doi.org/10.1016/J.PHYTOCHEM.2006.09.031
4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,7,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol	12312989	Click to see CC1(CCC2(CCC3(C4=CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C	426.70	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
Bauerenol	287684	Click to see CC1CCC2(CCC3(C4=CCC5C(C(CCC5(C4CCC3(C2C1C)C)C)O)(C)C)C)C	426.70	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
Multiflorenol	12312990	Click to see	426.70	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
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/10.1016/0031-9422(89)80205-5
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
> Organoheterocyclic compounds / Naphthofurans
(1R,2S,5S,7R,8R,10S,11R,12R,17R)-10,11,12-trihydroxy-2,7,14-trimethyl-16-oxapentacyclo[9.7.0.02,8.05,7.013,17]octadec-13-en-15-one	162962082	Click to see	348.40	unknown	https://doi.org/10.1021/NP020435V
(1S,2R,4R,9R,10S,12R,18S)-2,12,18-trihydroxy-5,5,9-trimethyl-14,19-dioxapentacyclo[10.6.1.01,10.04,9.013,17]nonadec-13(17)-en-15-one	101365884	Click to see	364.40	unknown	https://doi.org/10.1021/NP020435V
(1S,2R,4R,9R,10S,12S,18S)-2,12,18-trihydroxy-5,5,9-trimethyl-14,19-dioxapentacyclo[10.6.1.01,10.04,9.013,17]nonadec-13(17)-en-15-one	11152729	Click to see CC1(CCCC2(C1CC(C34C2CC(O3)(C5=C(C4O)CC(=O)O5)O)O)C)C	364.40	unknown	https://doi.org/10.1021/NP020435V
(1S,2R,5R,7S,8R,11R,12S,17S)-11,12-dihydroxy-2,7,14-trimethyl-16-oxapentacyclo[9.7.0.02,8.05,7.013,17]octadec-13-en-15-one	636785	Click to see	332.40	unknown	https://doi.org/10.1021/NP010404K
(1S,2R,5R,7S,8S,10R,11S,12S,17R)-10,11,12-trihydroxy-2,7,14-trimethyl-16-oxapentacyclo[9.7.0.02,8.05,7.013,17]octadec-13-en-15-one	162962083	Click to see	348.40	unknown	https://doi.org/10.1021/NP020435V
(1S,2R,5R,7S,8S,11S,12R,17R)-11,12-dihydroxy-2,7,14-trimethyl-16-oxapentacyclo[9.7.0.02,8.05,7.013,17]octadec-13-en-15-one	162819108	Click to see	332.40	unknown	https://doi.org/10.1021/NP020435V
(1S,3R,8R,10S,11R,16R)-5,11,15,15-tetramethyl-2,7-dioxapentacyclo[8.8.0.01,3.04,8.011,16]octadeca-4,13-diene-6,12-dione	11301899	Click to see	328.40	unknown	https://doi.org/10.1016/J.TET.2004.06.047
(1S,3R,8R,10S,11R,16S)-5,11,15,15-tetramethyl-2,7-dioxapentacyclo[8.8.0.01,3.04,8.011,16]octadec-4-ene-6,14-dione	14286066	Click to see	330.40	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
(1S,3R,8S,10S,11R,12S,15S,17S)-15-hydroxy-5,12,16,16-tetramethyl-2,7,9-trioxahexacyclo[9.8.0.01,3.04,8.08,10.012,17]nonadec-4-en-6-one	100926684	Click to see	346.40	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
(1S,3R,8S,10S,11R,16S)-5,11,15,15-tetramethyl-2,7-dioxapentacyclo[8.8.0.01,3.04,8.011,16]octadec-4-ene-6,14-dione	162901187	Click to see	330.40	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
(1S,3R,8S,10S,11R,16S)-5,11,15,15-tetramethyl-2,7-dioxapentacyclo[8.8.0.01,3.04,8.011,16]octadeca-4,12-diene-6,14-dione	162916956	Click to see	328.40	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
[(1S,3R,8R,10S,11R,12R,16S)-5,11,15,15-tetramethyl-6,14-dioxo-2,7-dioxapentacyclo[8.8.0.01,3.04,8.011,16]octadec-4-en-12-yl] acetate	14286068	Click to see	388.50	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
[(1S,3R,8R,10S,11R,16S,17R)-5,11,15,15-tetramethyl-6,14-dioxo-2,7-dioxapentacyclo[8.8.0.01,3.04,8.011,16]octadeca-4,12-dien-17-yl] acetate	100951693	Click to see	386.40	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
[(1S,8R,10S,11R,16S)-5,11,15,15-tetramethyl-6-oxo-2,7-dioxapentacyclo[8.8.0.01,3.04,8.011,16]octadec-4-en-14-yl] acetate	137795597	Click to see	374.50	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
[(1S,8S,11R,12R,17S)-5,12,16,16-tetramethyl-6-oxo-2,7,9-trioxahexacyclo[9.8.0.01,3.04,8.08,10.012,17]nonadec-4-en-15-yl] acetate	137705450	Click to see	388.50	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
10,11,12-Trihydroxy-2,7,14-trimethyl-16-oxapentacyclo[9.7.0.02,8.05,7.013,17]octadec-13-en-15-one	72797474	Click to see	348.40	unknown	https://doi.org/10.1021/NP020435V
2,12,18-Trihydroxy-5,5,9-trimethyl-14,19-dioxapentacyclo[10.6.1.01,10.04,9.013,17]nonadec-13(17)-en-15-one	85417420	Click to see	364.40	unknown	https://doi.org/10.1021/NP020435V
5,10,16-Trimethyl-14,19-dioxahexacyclo[9.8.0.01,18.04,10.05,7.013,17]nonadec-16-en-15-one	85309118	Click to see CC1=C2C(CC3C4(CCC5CC5(C4CCC36C2O6)C)C)OC1=O	314.40	unknown	https://doi.org/10.1021/NP010404K
5,11,15,15-Tetramethyl-2,7-dioxapentacyclo[8.8.0.01,3.04,8.011,16]octadec-4-ene-6,14-dione	14286065	Click to see CC1=C2C(CC3C4(CCC(=O)C(C4CCC35C2O5)(C)C)C)OC1=O	330.40	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
5,11,15,15-Tetramethyl-2,7-dioxapentacyclo[8.8.0.01,3.04,8.011,16]octadeca-4,12-diene-6,14-dione	14286071	Click to see CC1=C2C(CC3C4(C=CC(=O)C(C4CCC35C2O5)(C)C)C)OC1=O	328.40	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
5,11,15,15-Tetramethyl-2,7-dioxapentacyclo[8.8.0.01,3.04,8.011,16]octadeca-4,13-diene-6,12-dione	72790888	Click to see	328.40	unknown	https://doi.org/10.1016/J.TET.2004.06.047
Gelomulide D	14286072	Click to see CC1=C2C(CC3C4(C=CC(=O)C(C4CCC35C2O5)(C)C)C)OC1=O	328.40	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
Gelomulide G	15699703	Click to see	432.50	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
Jolkinolide B	161954	Click to see CC1=C2C3C4(O3)CCC5C(CCCC5(C4C6C2(O6)OC1=O)C)(C)C	330.40	unknown	https://doi.org/10.1016/0031-9422(89)80205-5
Suregadolide A	10471965	Click to see	332.40	unknown	https://doi.org/10.1021/NP010404K
Suregadolide B	10903129	Click to see CC1=C2C(CC3C4(CCC5CC5(C4CCC36C2O6)C)C)OC1=O	314.40	unknown	https://doi.org/10.1002/CHIN.200451158 https://doi.org/10.1021/NP010404K
Suregadolide C	11314049	Click to see	348.40	unknown	https://doi.org/10.1021/NP020435V
Suregadolide D	11405320	Click to see	348.40	unknown	https://doi.org/10.1021/NP020435V
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Furanoflavones
Pinnatin	5320607	Click to see	292.30	unknown	https://doi.org/10.1016/S0031-9422(00)90413-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
5-Hydroxy-7-methoxy-2-(4-methoxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	74977844	Click to see	476.40	unknown	https://doi.org/10.1016/0031-9422(93)85546-4
5-hydroxy-7-methoxy-2-[4-methoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one	162929807	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O)OC4C(C(C(C(O4)CO)O)O)O	476.40	unknown	https://doi.org/10.1016/S0031-9422(00)81781-1
5-Hydroxy-7-methoxy-2-[4-methoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one	74977814	Click to see	476.40	unknown	https://doi.org/10.1016/S0031-9422(00)81781-1
6-[(2S,3R,4S,5S,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3S,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-7-methoxy-2-(4-methoxyphenyl)chromen-4-one	162928786	Click to see	608.50	unknown	https://doi.org/10.1016/0031-9422(93)85546-4
6-[(2S,3S,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-7-methoxy-2-(4-methoxyphenyl)chromen-4-one	162960302	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C=C4C(=C3O)C(=O)C=C(O4)C5=CC=C(C=C5)OC)OC)CO)O)O)O)O)O	622.60	unknown	https://doi.org/10.1016/0031-9422(93)85546-4
6-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-5-hydroxy-7-methoxy-2-(4-methoxyphenyl)chromen-4-one	13826805	Click to see	622.60	unknown	https://doi.org/10.1016/0031-9422(93)85546-4
6-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-5-hydroxy-7-methoxy-2-(4-methoxyphenyl)chromen-4-one	74977852	Click to see	608.50	unknown	https://doi.org/10.1016/0031-9422(93)85546-4
Angeflorin	124462767	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC4C(C(C(C(O4)CO)O)O)O)O	476.40	unknown	https://doi.org/10.1016/0031-9422(93)85546-4
Gelomuloside A	10438880	Click to see	622.60	unknown	https://doi.org/10.1016/0031-9422(93)85546-4
Gelomuloside B	102147924	Click to see	608.50	unknown	https://doi.org/10.1016/0031-9422(93)85546-4
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Demethoxykanugin	10381709	Click to see COC1=CC2=C(C=C1)C(=O)C(=C(O2)C3=CC4=C(C=C3)OCO4)OC	326.30	unknown	https://doi.org/10.1016/S0031-9422(00)90413-8
Kanugin	12305452	Click to see COC1=CC2=C(C=C1)C(=O)C(=C(O2)C3=CC4=C(C(=C3)OC)OCO4)OC	356.30	unknown	https://doi.org/10.1016/S0031-9422(00)90413-8

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Suregada multiflora

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