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Swartzia polyphylla

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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
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Details Top

Internal ID UUID643fd595e8b1e510361845
Scientific name Swartzia polyphylla
Authority DC.
First published in Mém. Légum.: 411 (1826)

Description Top

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Synonyms Top

Scientific name Authority First published in
Swartzia urubuensis Ducke Bol. Técn. Inst. Agron. N.2: 21 (1944)
Tunatea acuminata (Vogel) Kuntze
Swartzia opacifolia J.F.Macbr. Publ. Field Mus. Nat. Hist., Bot. Ser.13(3): 226 (1943)
Swartzia platygyne Ducke Arch. Jard. Bot. Rio de Janeiro3: 127 (1922)
Tounatea polyphylla (DC.) Taub. Bot. Centralbl.47: 390 (1891)

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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Germination/Propagation Top

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No germination or propagation data was added yet.

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-0000164157
Tropicos 13001786
INPN 733787
KEW urn:lsid:ipni.org:names:519994-1
The Plant List ild-10569
Open Tree Of Life 643757
NCBI Taxonomy 450104
IUCN Red List 170269522
IPNI 246753-2
GBIF 5351880
EOL 418123
USDA GRIN 437185

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
Iridoids and Amino Acid Derivatives from the Paraguayan Crude Drug Adenocalymma marginatum (ysypó hû) Schmeda-Hirschmann G, Burgos-Edwards A, Jiménez-Aspee F, Mieres-Castro D, Theoduloz C, Pormetter L, Fogel R, Céspedes C, Soria N, Valdez S Molecules 01-Jan-2020
PMCID:PMC6983124
doi:10.3390/molecules25010180
PMID:31906356
Hyperdominance in Amazonian forest carbon cycling Fauset S, Johnson MO, Gloor M, Baker TR, Monteagudo M. A, Brienen RJ, Feldpausch TR, Lopez-Gonzalez G, Malhi Y, ter Steege H, Pitman NC, Baraloto C, Engel J, Pétronelli P, Andrade A, Camargo JL, Laurance SG, Laurance WF, Chave J, Allie E, Vargas PN, Terborgh JW, Ruokolainen K, Silveira M, Aymard C. GA, Arroyo L, Bonal D, Ramirez-Angulo H, Araujo-Murakami A, Neill D, Hérault B, Dourdain A, Torres-Lezama A, Marimon BS, Salomão RP, Comiskey JA, Réjou-Méchain M, Toledo M, Licona JC, Alarcón A, Prieto A, Rudas A, van der Meer PJ, Killeen TJ, Marimon Junior BH, Poorter L, Boot RG, Stergios B, Torre EV, Costa FR, Levis C, Schietti J, Souza P, Groot N, Arets E, Moscoso VC, Castro W, Coronado EN, Peña-Claros M, Stahl C, Barroso J, Talbot J, Vieira IC, van der Heijden G, Thomas R, Vos VA, Almeida EC, Davila EÁ, Aragão LE, Erwin TL, Morandi PS, de Oliveira EA, Valadão MB, Zagt RJ, van der Hout P, Loayza PA, Pipoly JJ, Wang O, Alexiades M, Cerón CE, Huamantupa-Chuquimaco I, Di Fiore A, Peacock J, Camacho NC, Umetsu RK, de Camargo PB, Burnham RJ, Herrera R, Quesada CA, Stropp J, Vieira SA, Steininger M, Rodríguez CR, Restrepo Z, Muelbert AE, Lewis SL, Pickavance GC, Phillips OL Nat Commun 28-Apr-2015
PMCID:PMC4423203
doi:10.1038/ncomms7857
PMID:25919449
Plant Polyphenols and Their Anti-Cariogenic Properties:A Review Ferrazzano GF, Amato I, Ingenito A, Zarrelli A, Pinto G, Pollio A Molecules 11-Feb-2011
PMCID:PMC6259836
doi:10.3390/molecules16021486
PMID:21317840
Submerged in darkness: adaptations to prolonged submergence by woody species of the Amazonian floodplains Parolin P Ann Bot 10-Nov-2008
PMCID:PMC2707320
doi:10.1093/aob/mcn216
PMID:19001429
The Chemical and Biological Profile of a Red Clover (Trifolium pratense) Phase II Clinical Extract Booth NL, Overk CR, Yao P, Burdette JE, Nikolic D, Chen SN, Bolton JL, van Breemen RB, Pauli GF, Farnsworth NR J Altern Complement Med 01-Mar-2006
PMCID:PMC1780253
doi:10.1089/acm.2006.12.133
PMID:16566672
Larvicidal, antimycobacterial and antifungal compounds from the bark of the Peruvian plant Swartzia polyphylla DC. Rojas R, Bustamante B, Ventosilla P, Fernádez I, Caviedes L, Gilman RH, Lock O, Hammond GB Chem Pharm Bull (Tokyo) 01-Feb-2006
doi:10.1248/CPB.54.278
PMID:16462085
Ferreirinol, a New 3-Hydroxyisoflavanone from <i>Swartzia polyphylla</i> Jennifer L. DuBois, Albert T. Sneden American Chemical Society (ACS) 26-Jul-2002
doi:10.1021/NP960122Y
Dihydrolicoisoflavone, a new isoflavanone from Swartzia polyphylla. DuBois JL, Sneden AT J Nat Prod 01-Apr-1995
doi:10.1021/NP50118A028
PMID:7623042
Isoflavanones from the heartwood of Swartzia polyphylla and their antibacterial activity against cariogenic bacteria. Osawa K, Yasuda H, Maruyama T, Morita H, Takeya K, Itokawa H Chem Pharm Bull (Tokyo) 01-Nov-1992
doi:10.1248/CPB.40.2970
PMID:1477911

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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,4R,4aS,8aR)-1,6-dimethyl-4-prop-1-en-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 163063171 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(=C)C 220.35 unknown https://doi.org/10.1248/CPB.54.278
(1S,4S,4aS,8aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 12302227 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1248/CPB.54.278
1,6-dimethyl-4-prop-1-en-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 163063170 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(=C)C 220.35 unknown https://doi.org/10.1248/CPB.54.278
Cedrelanol 160799 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1248/CPB.54.278
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1248/CPB.40.2970
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1248/CPB.40.2970
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1248/CPB.40.2970
https://doi.org/10.1021/NP50118A028
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
(3S)-3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one 124300749 Click to see C1C(C(=O)C2=C(C=C(C=C2O1)O)O)C3=C(C=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/NP50118A028
https://doi.org/10.1248/CPB.40.2970
Dalbergioidin 181994 Click to see C1C(C(=O)C2=C(C=C(C=C2O1)O)O)C3=C(C=C(C=C3)O)O 288.25 unknown https://doi.org/10.1248/CPB.40.2970
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 3-prenylated isoflavanones
(S)-Licoisoflavone A 134715142 Click to see CC(=CCC1=C(C=CC(=C1O)C2COC3=CC(=CC(=C3C2=O)O)O)O)C 356.40 unknown https://doi.org/10.1021/NP50118A028
Dihydrolicoisoflavone 10405960 Click to see CC(=CCC1=C(C=CC(=C1O)C2COC3=CC(=CC(=C3C2=O)O)O)O)C 356.40 unknown https://doi.org/10.1021/NP50118A028
https://doi.org/10.1021/NP960122Y
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(3R)-5,7-dihydroxy-3-(2-hydroxy-4-methoxyphenyl)-2,3-dihydrochromen-4-one 162928043 Click to see COC1=CC(=C(C=C1)C2COC3=CC(=CC(=C3C2=O)O)O)O 302.28 unknown https://doi.org/10.1021/NP50118A028
https://doi.org/10.1248/CPB.40.2970
(3R)-5,7-dihydroxy-3-(4-methoxyphenyl)-2,3-dihydrochromen-4-one 124302738 Click to see COC1=CC=C(C=C1)C2COC3=CC(=CC(=C3C2=O)O)O 286.28 unknown https://doi.org/10.1021/NP50118A028
(3S)-3,5,7-trihydroxy-3-(2-hydroxy-4-methoxyphenyl)-2H-chromen-4-one 44446903 Click to see COC1=CC(=C(C=C1)C2(COC3=CC(=CC(=C3C2=O)O)O)O)O 318.28 unknown https://doi.org/10.1021/NP960122Y
(3S)-3alpha-(4-Methoxyphenyl)-5,7-dihydroxy-2H-1-benzopyran-4(3H)-one 102437294 Click to see COC1=CC=C(C=C1)C2COC3=CC(=CC(=C3C2=O)O)O 286.28 unknown https://doi.org/10.1248/CPB.40.2970
https://doi.org/10.1248/CPB.54.278
3,5,7-trihydroxy-3-(2-hydroxy-4-methoxyphenyl)-2H-chromen-4-one 10567534 Click to see COC1=CC(=C(C=C1)C2(COC3=CC(=CC(=C3C2=O)O)O)O)O 318.28 unknown https://doi.org/10.1021/NP960122Y
Dihydrobiochanin A 439784 Click to see COC1=CC=C(C=C1)C2COC3=CC(=CC(=C3C2=O)O)O 286.28 unknown https://doi.org/10.1021/NP50118A028
https://doi.org/10.1248/CPB.40.2970
https://doi.org/10.1248/CPB.54.278
Ferreirin 442771 Click to see COC1=CC(=C(C=C1)C2COC3=CC(=CC(=C3C2=O)O)O)O 302.28 unknown https://doi.org/10.1248/CPB.40.2970
https://doi.org/10.1021/NP50118A028
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Biochanin A 5280373 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O 284.26 unknown https://doi.org/10.1021/NP50118A028
https://doi.org/10.1248/CPB.54.278
https://doi.org/10.1021/NP960122Y
https://doi.org/10.1248/CPB.40.2970
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown https://doi.org/10.1248/CPB.40.2970
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids
(3S)-3-(2,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-2,3-dihydrochromen-4-one 9995069 Click to see COC1=CC(=C2C(=C1)OCC(C2=O)C3=C(C=C(C=C3)O)O)O 302.28 unknown https://doi.org/10.1248/CPB.40.2970
3-(2,4-Dihydroxyphenyl)-5-hydroxy-7-methoxy-2,3-dihydrochromen-4-one 9882842 Click to see COC1=CC(=C2C(=C1)OCC(C2=O)C3=C(C=C(C=C3)O)O)O 302.28 unknown https://doi.org/10.1248/CPB.40.2970

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