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Bauhinia tarapotensis

Bauhinia tarapotensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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
Collections

Details Top

Internal ID UUID643fd7c27d43e204417081
Scientific name Bauhinia tarapotensis
Authority Benth.
First published in C.F.P.von Martius & auct. suc. (eds.), Fl. Bras.15(2): 198 (1870)

Description Top

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Synonyms Top

Scientific name Authority First published in
Bauhinia amplifolia Ducke Bol. Técn. Inst. Agron. N.2: 16 (1944)
Bauhinia baina J.F.Macbr. Publ. Field Mus. Nat. Hist., Bot. Ser.13(3): 211 (1943)
Pauletia tarapotensis (Benth.) A.Schmitz Bull. Jard. Bot. Natl. Belg.43: 396 (1973)
Ariaria superba Cuervo Prehist. Viajes: 219 (1893)

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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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-0000175454
Tropicos 13043415
KEW urn:lsid:ipni.org:names:481718-1
The Plant List ild-21614
Open Tree Of Life 3916404
IUCN Red List 170270188
IPNI 481717-1
iNaturalist 430713
GBIF 2953235
EPPO BAUTA
EOL 641501

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
Antioxidant principles from Bauhinia tarapotensis. Braca A, De Tommasi N, Di Bari L, Pizza C, Politi M, Morelli I J Nat Prod 01-Jul-2001
doi:10.1021/NP0100845
PMID:11473417

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
> Lignans, neolignans and related compounds / Lignan glycosides
(-)-Isolariciresinol 9'-O-glucoside 44560003 Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)O 522.50 unknown https://doi.org/10.1021/NP0100845
(2S,3R,4S,5S,6R)-2-[[(1R,2S,3S)-7-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162947826 Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)O 522.50 unknown https://doi.org/10.1021/NP0100845
1-Hydroxypinoresinol 1-O-glucoside 13995449 Click to see COC1=C(C=CC(=C1)C2C3COC(C3(CO2)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)OC)O 536.50 unknown https://doi.org/10.1021/NP0100845
8-Hydroxypinoresinol 8-glucoside 13995448 Click to see COC1=C(C=CC(=C1)C2C3COC(C3(CO2)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)OC)O 536.50 unknown https://doi.org/10.1021/NP0100845
Isolariciresinol 9'-O-beta-D-glucoside 74191750 Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)O 522.50 unknown https://doi.org/10.1021/NP0100845
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(4R,6S)-4,6-dihydroxy-6-(2-hydroxyethyl)cyclohex-2-en-1-one 11126726 Click to see C1C(C=CC(=O)C1(CCO)O)O 172.18 unknown https://doi.org/10.1021/NP0100845
4,6-Dihydroxy-6-(2-hydroxyethyl)cyclohex-2-en-1-one 85408444 Click to see C1C(C=CC(=O)C1(CCO)O)O 172.18 unknown https://doi.org/10.1021/NP0100845
> Organoheterocyclic compounds / Indoles and derivatives / Indolecarboxylic acids and derivatives
Indole-3-carboxylic acid 69867 Click to see C1=CC=C2C(=C1)C(=CN2)C(=O)O 161.16 unknown https://doi.org/10.1021/NP0100845
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(2R,3R)-3-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-2,3,4-trihydroxybutanoic acid 163194815 Click to see C1=CC(=C(C=C1C=CC(=O)OCC(CO)(C(C(=O)O)O)O)O)O 328.27 unknown https://doi.org/10.1021/NP0100845
[(2R,3R,4S,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxy-4-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 44560004 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1021/NP0100845
{6-[2-(3,4-Dihydroxyphenyl)ethoxy]-3,5-dihydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 73323377 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1021/NP0100845
3-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-2,3,4-trihydroxybutanoic acid 11012871 Click to see C1=CC(=C(C=C1C=CC(=O)OCC(CO)(C(C(=O)O)O)O)O)O 328.27 unknown https://doi.org/10.1021/NP0100845
3-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxymethyl]-2,3,4-trihydroxybutanoic acid 85366443 Click to see C1=CC(=C(C=C1C=CC(=O)OCC(CO)(C(C(=O)O)O)O)O)O 328.27 unknown https://doi.org/10.1021/NP0100845
Isoacteoside 6476333 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1021/NP0100845
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
5,7-dihydroxy-2-[3-hydroxy-4-[(2S,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 51521836 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown https://doi.org/10.1021/NP0100845
Luteolin 4'-glucoside 12304737 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown https://doi.org/10.1021/NP0100845
Luteolin-4'-o-glucoside 5319116 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown https://doi.org/10.1021/NP0100845

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