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Uncaria perrottetii

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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 UUID643ff009667df047177577
Scientific name Uncaria perrottetii
Authority Merr.
First published in Philipp. J. Sci., C 8: 60 (1913)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ourouparia perrottetii Baill. Bull. Mens. Soc. Linn. Paris 1: 227 (1879)
Sabicea perrottetii A.Rich. Mém. Rubiac. : 148 (1830)
Uncaria hookeri S.Vidal Phan. Cuming. Philipp. : 177 (1885)

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000329300
Tropicos 100271395
KEW urn:lsid:ipni.org:names:768290-1
The Plant List kew-209852
Open Tree Of Life 3881138
IPNI 768290-1
GBIF 5338116
EOL 1108578
Wikipedia Uncaria_perrottetii
CMAUP NPO14773

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

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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 / Benzoic acids
4-(3-Methylbut-2-enoxy)benzoic acid 267137 Click to see CC(=CCOC1=CC=C(C=C1)C(=O)O)C 206.24 unknown via CMAUP database
> Lignans, neolignans and related compounds / Cyclobutane lignans
Bisosthenone 14409177 Click to see CC(=O)C1C(C(C1C(=O)C)C2=C(C=CC3=C2OC(=O)C=C3)OC)C4=C(C=CC5=C4OC(=O)C=C5)OC 488.50 unknown via CMAUP database
> Organoheterocyclic compounds / Indolizidines
(3R,20S)-19alpha-Methyl-2-oxoformosanan-16-carboxylic acid methyl ester 98363 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown via CMAUP database
methyl (1R,4aS,5aR,6R,10aS)-1-methyl-2'-oxospiro[1,4a,5,5a,7,8,10,10a-octahydropyrano[3,4-f]indolizine-6,3'-1H-indole]-4-carboxylate 11943653 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown via CMAUP database
Speciophylline 168985 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown via CMAUP database
Uncarine F 12304288 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
1,3-dihydroxy-N-methylacridone 5282066 Click to see CN1C2=CC=CC=C2C(=O)C3=C1C=C(C=C3O)O 241.24 unknown via CMAUP database
Citramine 85583910 Click to see CN1C2=CC(=C(C(=C2C(=O)C3=C1C(=C(C=C3)O)OC)O)OC)O 317.29 unknown via CMAUP database
Citrusamine 14038956 Click to see CN1C2=C(C(=CC(=C2)OC)O)C(=O)C3=C1C(=CC=C3)O 271.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
7-Methoxy-8-[(E)-3-oxo-1-butenyl]-2H-1-benzopyran-2-one 13917410 Click to see CC(=O)C=CC1=C(C=CC2=C1OC(=O)C=C2)OC 244.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
6-[[(2R)-3,3-Dimethyloxiran-2-yl]methyl]-7-methoxychromen-2-one 11184527 Click to see CC1(C(O1)CC2=C(C=C3C(=C2)C=CC(=O)O3)OC)C 260.28 unknown via CMAUP database
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Osthenol 5320318 Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)O)C 230.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
(9R,10R)-9,10-Dihydroxy-9,10-dihydro-5-methoxy-8,8-dimethyl-2H,8H-benzo[1,2-b:3,4-b']dipyran-2-one 14213971 Click to see CC1(C(C(C2=C3C(=C(C=C2O1)OC)C=CC(=O)O3)O)O)C 292.28 unknown via CMAUP database
5-Hydroxyseselin 11334023 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC(=O)C=C3)O)C 244.24 unknown via CMAUP database
5-Methoxyseselin 290897 Click to see CC1(C=CC2=C3C(=C(C=C2O1)OC)C=CC(=O)O3)C 258.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Clausarin 5315945 Click to see CC1(C=CC2=C(O1)C(=C3C(=C2O)C=C(C(=O)O3)C(C)(C)C=C)C(C)(C)C=C)C 380.50 unknown via CMAUP database
nor-Dentatin 5495613 Click to see CC1(C=CC2=C(O1)C(=C3C(=C2O)C=CC(=O)O3)C(C)(C)C=C)C 312.40 unknown via CMAUP database
Ponfolin 174673 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C(C)(C)C=C)OC(=O)C=C3)OC(C)(C)C=C)C 380.50 unknown via CMAUP database
Trachyphyllin 71436449 Click to see CC(=CCC1=C2C(=C(C3=C1OC(C=C3)(C)C)O)C=CC(=O)O2)C 312.40 unknown via CMAUP database
Xanthoxyletin 66548 Click to see CC1(C=CC2=C(O1)C=C3C(=C2OC)C=CC(=O)O3)C 258.27 unknown via CMAUP database
Xanthyletin 65188 Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 51535943 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC(=C(C=C3)O)OC)CC=C(C)C)O)C 438.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(2S)-5-hydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-2,3-dihydropyrano[2,3-h]chromen-4-one 14187086 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC(CC3=O)C4=CC=C(C=C4)O)O)C 338.40 unknown via CMAUP database

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