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Suregada glomerulata

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
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Details Top

Internal ID UUID643fedebf3224002683164
Scientific name Suregada glomerulata
Authority Baill.
First published in Étude Euphorb. : 396 (1858)

Description Top

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Synonyms Top

Scientific name Authority First published in
Suregada borneensis (Pax & K.Hoffm.) Croizat Bull. Jard. Bot. Buitenzorg , sér. 3, 17: 217 (1942)
Suregada meliocarpa (Elmer) Croizat Bull. Jard. Bot. Buitenzorg , sér. 3, 17: 216 (1942)
Suregada microcarpa (Pax & K.Hoffm.) Croizat Bull. Jard. Bot. Buitenzorg , sér. 3, 17: 216 (1942)
Suregada mindanaensis (Elmer) Croizat Bull. Jard. Bot. Buitenzorg , sér. 3, 17: 216 (1942)
Suregada papuana (Pax & K.Hoffm.) Croizat Bull. Jard. Bot. Buitenzorg , sér. 3, 17: 216 (1942)
Suregada philippinensis (Pax & K.Hoffm.) Croizat Bull. Jard. Bot. Buitenzorg , sér. 3, 17: 216 (1942)
Suregada pulgarensis (Elmer) Croizat Bull. Jard. Bot. Buitenzorg , sér. 3, 17: 216 (1942)
Suregada rubra (Ridl.) Croizat Bull. Jard. Bot. Buitenzorg , sér. 3, 17: 217 (1942)
Suregada spicata Baill. Étude Euphorb. : 396 (1858)
Suregada subglomerata (Elmer) Croizat Bull. Jard. Bot. Buitenzorg , sér. 3, 17: 216 (1942)
Gelonium glomerulatum Hassk. Cat. Hort. Bot. Bogor. Alt. : 237 (1844)
Gelonium spicatum Hassk. Cat. Hort. Bot. Bogor. Alt. : 237 (1844)
Erythrocarpus glomerulatus Blume Bijdr. Fl. Ned. Ind. : 605 (1826)
Erythrocarpus spicatus Blume Bijdr. Fl. Ned. Ind. : 605 (1826)
Gelonium borneense Pax & K.Hoffm. Mitt. Inst. Allg. Bot. Hamburg 7: 230 (1931)
Gelonium meliocarpum Elmer Leafl. Philipp. Bot. 3: 919 (1910)
Gelonium microcarpum Pax & K.Hoffm. Pflanzenr. , IV, 147, IV: 19 (1912)
Gelonium mindanaense Elmer Leafl. Philipp. Bot. 7: 2640 (1915)
Gelonium papuanum Pax Pflanzenr. , IV, 147, IV: 20 (1912)
Gelonium philippinense Pax & K.Hoffm. Pflanzenr. , IV, 147, IV: 20 (1912)
Gelonium pulgarense Elmer Leafl. Philipp. Bot. 4: 1293 (1911)
Gelonium rubrum Ridl. Bull. Misc. Inform. Kew 1926: 81 (1926)
Gelonium subglomerulatum Elmer Leafl. Philipp. Bot. 4: 1292 (1911)

Common names Top

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Language Common/alternative name
Chinese 白树

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
  • Asia-tropical
    • Indo-China
      • Cambodia
      • Laos
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000317650
Tropicos 50064926
KEW urn:lsid:ipni.org:names:356667-1
The Plant List kew-198602
Open Tree Of Life 1082259
NCBI Taxonomy 316821
IUCN Red List 147631595
IPNI 356667-1
GBIF 3054917
EOL 1150013

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
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
Antimicrobial Secondary Metabolites from the Mangrove Plants of Asia and the Pacific Sulaiman M, Nissapatorn V, Rahmatullah M, Paul AK, Rajagopal M, Rusdi NA, Seelan JS, Suleiman M, Zakaria ZA, Wiart C Mar Drugs 15-Oct-2022
PMCID:PMC9605323
doi:10.3390/md20100643
PMID:36286466
Tropical forest soils serve as substantial and persistent methane sinks Zhao JF, Peng SS, Chen MP, Wang GZ, Cui YB, Liao LG, Feng JG, Zhu B, Liu WJ, Yang LY, Tan ZH Sci Rep 14-Nov-2019
PMCID:PMC6856371
doi:10.1038/s41598-019-51515-z
PMID:31728015
EARE-1, a Transcriptionally Active Ty1/Copia-Like Retrotransposon Has Colonized the Genome of Excoecaria agallocha through Horizontal Transfer Huang J, Wang Y, Liu W, Shen X, Fan Q, Jian S, Tang T Front Plant Sci 24-Jan-2017
PMCID:PMC5258746
doi:10.3389/fpls.2017.00045
PMID:28174588
α-Glucosidase-inhibitory iminosugars from the leaves of Suregada glomerulata. Yan RY, Wang HQ, Liu C, Kang J, Chen RY Bioorg Med Chem 01-Nov-2013
doi:10.1016/J.BMC.2013.07.048
PMID:23993676
Screening of α-Glucosidase Inhibitory Activity from Some Plants of Apocynaceae, Clusiaceae, Euphorbiaceae, and Rubiaceae Elya B, Basah K, Mun'im A, Yuliastuti W, Bangun A, Septiana EK J Biomed Biotechnol 07-Dec-2011
PMCID:PMC3236488
doi:10.1155/2012/281078
PMID:22187534
Two new diterpenoids from Suregada glomerulata (Blume) Baill Ren Yi Yan, Ruo Yun Chen, De Quan Yu Elsevier BV 07-Mar-2011
doi:10.1016/J.CCLET.2010.12.015
Hamiguitan Range: A sanctuary for native flora Amoroso VB, Aspiras RA Saudi J Biol Sci 21-Jul-2010
PMCID:PMC3730927
doi:10.1016/j.sjbs.2010.07.003
PMID:23961098
Diterpenoids from the roots of Suregada glomerulata. Yan RY, Tan YX, Cui XQ, Chen RY, Yu DQ J Nat Prod 01-Feb-2008
doi:10.1021/NP0705211
PMID:18205316
The complete nucleotide sequence of the cassava (Manihot esculenta) chloroplast genome and the evolution of atpF in Malpighiales: RNA editing and multiple losses of a group II intron Daniell H, Wurdack KJ, Kanagaraj A, Lee SB, Saski C, Jansen RK Theor Appl Genet 24-Jan-2008
PMCID:PMC2587239
doi:10.1007/s00122-007-0706-y
PMID:18214421

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives
(2R,3R,4R,5S,6R)-2-(hydroxymethyl)-6-(8-hydroxyoctyl)piperidine-3,4,5-triol 72204016 Click to see C(CCCCO)CCCC1C(C(C(C(N1)CO)O)O)O 291.38 unknown https://doi.org/10.1016/J.BMC.2013.07.048
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Annonaceous acetogenins
Annojahnin 10507637 Click to see CCCCCCCCCCCCC=CCCC(C(CCCCCCC(=O)CCCCCCCC1=CC(OC1=O)C)O)O 590.90 unknown https://doi.org/10.1016/J.BMC.2013.07.048
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4aS,4bR,7S,10aS)-7-ethenyl-7-(hydroxymethyl)-1,1,4a-trimethyl-3,4,4b,5,6,9,10,10a-octahydrophenanthren-2-one 24799513 Click to see CC1(C2CCC3=CC(CCC3C2(CCC1=O)C)(CO)C=C)C 302.50 unknown https://doi.org/10.1021/NP0705211
7-Ethenyl-7-(hydroxymethyl)-1,1,4a-trimethyl-3,4,4b,5,6,9,10,10a-octahydrophenanthren-2-one 74318585 Click to see CC1(C2CCC3=CC(CCC3C2(CCC1=O)C)(CO)C=C)C 302.50 unknown https://doi.org/10.1021/NP0705211
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1S,3R,4S,6R,9S,10R,13R)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-3,6-diol 24799514 Click to see CC1(C(CCC2(C1C(CC34C2CCC(C3)C(=C)C4)O)C)O)C 304.50 unknown https://doi.org/10.1021/NP0705211
5,5,9-Trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-3,6-diol 74318586 Click to see CC1(C(CCC2(C1C(CC34C2CCC(C3)C(=C)C4)O)C)O)C 304.50 unknown https://doi.org/10.1021/NP0705211
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
5-Chloro-2,10-dioxatricyclo[5.3.1.04,11]undecane-4,6-diol 14413753 Click to see C1COC2C3C1C(C(C3(CO2)O)Cl)O 220.65 unknown https://doi.org/10.1016/J.BMC.2013.07.048
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-(1R,3R,6S,7S,8R,11S)-3,8,12-trihydroxy-alpha-muurolene 139588432 Click to see CC1=CC(C(C2C1CC(C(=C2)C)O)C(C)CO)O 252.35 unknown https://doi.org/10.1016/J.BMC.2013.07.048
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,4S,7S,8R,10S,11S,12S)-7-hydroxy-10-methoxy-7,13,13-trimethyl-4-propan-2-yl-18-oxapentacyclo[9.5.2.01,12.02,9.04,8]octadec-2(9)-ene-3,5,17-trione 10788052 Click to see CC(C)C12C(C3=C(C1=O)C45CCCC(C4C(C3OC)OC5=O)(C)C)C(CC2=O)(C)O 416.50 unknown https://doi.org/10.1016/J.BMC.2013.07.048
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(3R,4aS,6S,10aR,11aS,11bR)-3,6-dihydroxy-4,4,8,11b-tetramethyl-2,3,4a,5,6,10a,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-9-one 24799512 Click to see CC1=C2C=C3C(CC2OC1=O)C4(CCC(C(C4CC3O)(C)C)O)C 332.40 unknown https://doi.org/10.1021/NP0705211
(4aR,6S,10aR,11aS,11bR)-6-hydroxy-4,4,8,11b-tetramethyl-2,3,4a,5,6,10a,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-9-one 15275763 Click to see CC1=C2C=C3C(CC2OC1=O)C4(CCCC(C4CC3O)(C)C)C 316.40 unknown https://doi.org/10.1021/NP0705211
3,6-dihydroxy-4,4,8,11b-tetramethyl-2,3,4a,5,6,10a,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-9-one 74318584 Click to see CC1=C2C=C3C(CC2OC1=O)C4(CCC(C(C4CC3O)(C)C)O)C 332.40 unknown https://doi.org/10.1021/NP0705211
6-hydroxy-4,4,8,11b-tetramethyl-2,3,4a,5,6,10a,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-9-one 162944436 Click to see CC1=C2C=C3C(CC2OC1=O)C4(CCCC(C4CC3O)(C)C)C 316.40 unknown https://doi.org/10.1021/NP0705211
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
(1S,3aS,3bS,4S,5aR,9aR,9bS,11aS)-3b,4-dihydroxy-1,6,6,9a-tetramethyl-3a,4,5,5a,7,8,9,9b,10,11a-decahydro-1H-naphtho[1,2-g][1]benzofuran-2,11-dione 24799330 Click to see CC1C2C(C3(C(CC4C(CCCC4(C3CC2=O)C)(C)C)O)O)OC1=O 350.40 unknown https://doi.org/10.1021/NP0705211
3b,4-dihydroxy-1,6,6,9a-tetramethyl-3a,4,5,5a,7,8,9,9b,10,11a-decahydro-1H-naphtho[1,2-g][1]benzofuran-2,11-dione 74318533 Click to see CC1C2C(C3(C(CC4C(CCCC4(C3CC2=O)C)(C)C)O)O)OC1=O 350.40 unknown https://doi.org/10.1021/NP0705211
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4S,5S,6R)-1-butyl-2-(hydroxymethyl)-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]piperidine-3,4,5-triol 72204018 Click to see CCCCN1C(C(C(C(C1COC2C(C(C(C(O2)CO)O)O)O)O)O)O)CO 411.40 unknown https://doi.org/10.1016/J.BMC.2013.07.048
(2R,3R,4S,5S,6R)-2-(hydroxymethyl)-1-methyl-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]piperidine-3,4,5-triol 72203844 Click to see CN1C(C(C(C(C1COC2C(C(C(C(O2)CO)O)O)O)O)O)O)CO 369.36 unknown https://doi.org/10.1016/J.BMC.2013.07.048
(2R,3R,4S,5S,6R)-2-(hydroxymethyl)-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]piperidine-3,4,5-triol 457676 Click to see C(C1C(C(C(C(N1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)O 355.34 unknown https://doi.org/10.1016/J.BMC.2013.07.048
(2R,3R,4S,5S,6R)-2-(hydroxymethyl)-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]piperidine-3,4,5-triol 70461665 Click to see C(C1C(C(C(C(N1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)O 355.34 unknown https://doi.org/10.1016/J.BMC.2013.07.048
> Organoheterocyclic compounds / Naphthofurans
(1R,2S,5R,7S,8R,17R)-2,7,14-trimethyl-16-oxapentacyclo[9.7.0.02,8.05,7.013,17]octadeca-11,13-dien-15-one 162966422 Click to see CC1=C2C=C3CCC4C(C3CC2OC1=O)(CCC5C4(C5)C)C 298.40 unknown https://doi.org/10.1016/J.CCLET.2010.12.015
(1S,2R,5R,7S,8R,10S,17R)-10-hydroxy-14-(hydroxymethyl)-2,7-dimethyl-16-oxapentacyclo[9.7.0.02,8.05,7.013,17]octadeca-11,13-dien-15-one 24799332 Click to see CC12CCC3CC3(C1CC(C4=CC5=C(C(=O)OC5CC24)CO)O)C 330.40 unknown https://doi.org/10.1021/NP0705211
10-Hydroxy-14-(hydroxymethyl)-2,7-dimethyl-16-oxapentacyclo[9.7.0.02,8.05,7.013,17]octadeca-11,13-dien-15-one 74318535 Click to see CC12CCC3CC3(C1CC(C4=CC5=C(C(=O)OC5CC24)CO)O)C 330.40 unknown https://doi.org/10.1021/NP0705211
Jolkinolide B 161954 Click to see CC1=C2C3C4(O3)CCC5C(CCCC5(C4C6C2(O6)OC1=O)C)(C)C 330.40 unknown https://doi.org/10.1021/NP0705211
> Organoheterocyclic compounds / Piperidines
(2R,3R,4R,5S,6R)-2-(hydroxymethyl)-1,6-dimethylpiperidine-3,4,5-triol 72204017 Click to see CC1C(C(C(C(N1C)CO)O)O)O 191.22 unknown https://doi.org/10.1016/J.BMC.2013.07.048
(2R,3R,5S,6R)-2,6-bis(hydroxymethyl)-1-methylpiperidine-3,5-diol 72204019 Click to see CN1C(C(CC(C1CO)O)O)CO 191.22 unknown https://doi.org/10.1016/J.BMC.2013.07.048
(2R,3S,5R,6S)-2,6-bis(hydroxymethyl)-1-methylpiperidine-3,5-diol 72204015 Click to see CN1C(C(CC(C1CO)O)O)CO 191.22 unknown https://doi.org/10.1016/J.BMC.2013.07.048
alpha-7-Deoxyhomonojirimycin 10921056 Click to see CC1C(C(C(C(N1)CO)O)O)O 177.20 unknown https://doi.org/10.1016/J.BMC.2013.07.048
> Organoheterocyclic compounds / Pyrrolidines
2,5-Dideoxy-2,5-imino-glycero-D-manno-heptitol 10198040 Click to see C(C1C(C(C(N1)C(CO)O)O)O)O 193.20 unknown https://doi.org/10.1016/J.BMC.2013.07.048
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
4,4,9-Trimethyl-3,12,14-trioxa-9-azatetracyclo[8.7.0.02,7.011,15]heptadeca-1(10),2(7),5,11(15),16-pentaen-8-one 163104545 Click to see CC1(C=CC2=C(O1)C3=C(C4=C(C=C3)OCO4)N(C2=O)C)C 285.29 unknown https://doi.org/10.1016/J.BMC.2013.07.048

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