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Himatanthus sucuuba

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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
Collections

Details Top

Internal ID UUID64403e42530ab449978680
Scientific name Himatanthus sucuuba
Authority (Spruce ex Müll.Arg.) Woodson
First published in Ann. Missouri Bot. Gard. 1938, xxv. 193, in obs. 198 (1937).

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Portuguese sucuuba

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

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000982467
Tropicos 1801500
INPN 732599
KEW urn:lsid:ipni.org:names:122696-2
The Plant List kew-99313
PFAF Himatanthus sucuuba
Open Tree Of Life 6067905
IPNI 79283-1
GBIF 3621365

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
Contribution to the study of Himatanthus sucuuba: latex macromolecule, microelements and carbohydrates Jefferson Rocha de A. SILVA, Ana Claudia F. AMARAL, Antonio C. SIANI, Claudia M. REZENDE, Judith FELCMAN, Angelo C. PINTO FapUNIFESP (SciELO) 16-May-2015
doi:10.1590/1809-4392200331110
Ésteres triterpênicos de Himatanthus sucuuba (Spruce) Woodson Jefferson Rocha de A. Silva, Claudia M. Rezende, Ângelo C. Pinto, Maria L. B. Pinheiro, Milade C. Cordeiro, Everaldo Tamborini, Cláudia M. Young, Vanderlan da S. Bolzani FapUNIFESP (SciELO) 26-Apr-2005
doi:10.1590/S0100-40421998000600005
A bioactive spirolactone iridoid and triterpenoids from Himatanthus sucuuba. Wood CA, Lee K, Vaisberg AJ, Kingston DG, Neto CC, Hammond GB Chem Pharm Bull (Tokyo) 01-Nov-2001
doi:10.1248/CPB.49.1477
PMID:11724243
Anti-inflammatory and analgesic activities of the latex containing triterpenes from Himatanthus sucuuba. de Miranda AL, Silva JR, Rezende CM, Neves JS, Parrini SC, Pinheiro ML, Cordeiro MC, Tamborini E, Pinto AC Planta Med 01-Apr-2000
doi:10.1055/S-2000-8572
PMID:10821061
Confluentic acid and 2'-O-methylperlatolic acid, monoamine oxidase B inhibitors in a Brazilian plant, Himatanthus sucuuba. Endo Y, Hayashi H, Sato T, Maruno M, Ohta T, Nozoe S Chem Pharm Bull (Tokyo) 01-Jun-1994
doi:10.1248/CPB.42.1198
PMID:8069971

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1248/CPB.42.1198
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1248/CPB.42.1198
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Isoplumericin 5281543 Click to see CC=C1C2C3(C=CC4C3C(O2)OC=C4C(=O)OC)OC1=O 290.27 unknown https://doi.org/10.1248/CPB.42.1198
https://doi.org/10.1590/S0100-40421998000600005
methyl (1R,4R,8S,10S,11E,14S)-11-ethylidene-12-oxo-7,9,13-trioxatetracyclo[6.5.1.01,10.04,14]tetradeca-2,5-diene-5-carboxylate 161287690 Click to see CC=C1C2C3(C=CC4C3C(O2)OC=C4C(=O)OC)OC1=O 290.27 unknown https://doi.org/10.1248/CPB.49.1477
Methyl 3-ethylidene-2-oxo-3,3a,7a,9b-tetrahydro-2H,4aH-1,4,5-trioxadicyclopenta[a,hi]indene-7-carboxylate 533578 Click to see CC=C1C2C3(C=CC4C3C(O2)OC=C4C(=O)OC)OC1=O 290.27 unknown https://doi.org/10.1590/S0100-40421998000600005
Plumericin 5281545 Click to see CC=C1C2C3(C=CC4C3C(O2)OC=C4C(=O)OC)OC1=O 290.27 unknown https://doi.org/10.1248/CPB.42.1198
https://doi.org/10.1248/CPB.49.1477
https://doi.org/10.1590/S0100-40421998000600005
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl) 3-phenylprop-2-enoate 612773 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C=CC6=CC=CC=C6)C)C)C2C1C)C)C 556.90 unknown https://doi.org/10.1590/S0100-40421998000600005
[(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-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] (E)-3-phenylprop-2-enoate 162949773 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C=CC6=CC=CC=C6)C)C 556.90 unknown https://doi.org/10.1590/S0100-40421998000600005
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-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] (E)-3-phenylprop-2-enoate 162949778 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C=CC6=CC=CC=C6)C)C 556.90 unknown https://doi.org/10.1248/CPB.49.1477
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-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] 3-phenylpropanoate 162871363 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)CCC6=CC=CC=C6)C)C 558.90 unknown https://doi.org/10.1248/CPB.49.1477
[(1R,3aR,5aR,7aR,9S,11aR,11bR,13aR,13bR)-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] acetate 163187380 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1248/CPB.49.1477
[(4aR,6aR,6bS,8aR,11R,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] (E)-3-phenylprop-2-enoate 162942750 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C=CC6=CC=CC=C6)C)C)C2C1C)C)C 556.90 unknown https://doi.org/10.1590/S0100-40421998000600005
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1248/CPB.49.1477
alpha-Amyrin cinnamate 5471661 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C=CC6=CC=CC=C6)C)C)C2C1C)C)C 556.90 unknown https://doi.org/10.1248/CPB.49.1477
Lupeol acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1055/S-2000-8572
https://doi.org/10.1248/CPB.49.1477
Lupeol trans-cinnamate 5471662 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C=CC6=CC=CC=C6)C)C 556.90 unknown https://doi.org/10.1248/CPB.49.1477
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
(25S)-11alpha,20,26-trihydroxyecdysone 16755647 Click to see CC12CC(C3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(CO)O)O)O)O)O 512.60 unknown https://doi.org/10.1248/CPB.49.1477
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal 19233 Click to see CC(C(C(C(C=O)O)O)O)O 164.16 unknown https://doi.org/10.1590/1809-4392200331110
(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1590/1809-4392200331110
(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal 3037556 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1590/1809-4392200331110
D-Galactose 6036 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1590/1809-4392200331110
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1590/1809-4392200331110
L-Rhamnose 25310 Click to see CC1C(C(C(C(O1)O)O)O)O 164.16 unknown https://doi.org/10.1590/1809-4392200331110
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
(2S,3R,4R)-2,3,4,5-tetrahydroxypentanal 66308 Click to see C(C(C(C(C=O)O)O)O)O 150.13 unknown https://doi.org/10.1590/1809-4392200331110
D-Xylose 135191 Click to see C1C(C(C(C(O1)O)O)O)O 150.13 unknown https://doi.org/10.1590/1809-4392200331110
DL-Xylose 644160 Click to see C(C(C(C(C=O)O)O)O)O 150.13 unknown https://doi.org/10.1590/1809-4392200331110
L-Arabinose 439195 Click to see C1C(C(C(C(O1)O)O)O)O 150.13 unknown https://doi.org/10.1590/1809-4392200331110
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1248/CPB.42.1198
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
[8,8-Dimethyl-10-(3-methylbutanoyloxy)-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl] 2-methylbut-2-enoate 75596126 Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)CC(C)C 428.50 unknown https://doi.org/10.1590/S0100-40421998000600005
> Phenylpropanoids and polyketides / Depsides and depsidones
2'-O-Methylperlatolic acid 3084728 Click to see CCCCCC1=C(C(=CC(=C1)OC)O)C(=O)OC2=CC(=C(C(=C2)OC)C(=O)O)CCCCC 458.50 unknown https://doi.org/10.1248/CPB.42.1198
Confluentic acid 99614 Click to see CCCCCC1=C(C(=CC(=C1)OC(=O)C2=C(C=C(C=C2O)OC)CC(=O)CCCCC)OC)C(=O)O 500.60 unknown https://doi.org/10.1248/CPB.42.1198

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