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Tarenna attenuata

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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 UUID643feea794e48540937058
Scientific name Tarenna attenuata
Authority (Hook.f.) Hutch.
First published in Pl. Wilson. 3: 411 (1916)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ixora attenuata (Hook.f.) Kuntze Revis. Gen. Pl. 1: 278 (1891)
Tarenna sylvestris Hutch. Pl. Wilson. 3: 411 (1916)
Webera attenuata Hook.f. Fl. Brit. India 3: 104 (1880)
Cupia corymbosa Hook. & Arn. Bot. Beechey Voy. : 192 (1833)

Common names Top

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Language Common/alternative name
Chinese 乌口树
Chinese 假桂乌口树
Chinese 小林乌口树
Chinese 达仑木
Chinese 树节

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-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000320890
Tropicos 50058557
KEW urn:lsid:ipni.org:names:767407-1
The Plant List kew-201695
Open Tree Of Life 3878828
NCBI Taxonomy 1547788
IUCN Red List 147627798
IPNI 767407-1
GBIF 2896248
EOL 1103575

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
Phylogeography of Himalrandia lichiangensis from the dry-hot valleys in Southwest China Qiao Y, Liu J, Gong X Front Plant Sci 17-Oct-2022
PMCID:PMC9618719
doi:10.3389/fpls.2022.1002519
PMID:36325543
Secondary Metabolites from Rubiaceae Species Martins D, Nunez CV Molecules 22-Jul-2015
PMCID:PMC6331836
doi:10.3390/molecules200713422
PMID:26205062
Mixed lignan-neolignans from Tarenna attenuata. Yang XW, Zhao PJ, Ma YL, Xiao HT, Zuo YQ, He HP, Li L, Hao XJ J Nat Prod 01-Apr-2007
doi:10.1021/NP0603931
PMID:17343407

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 / Phenols / Methoxyphenols
(1S,2S)-1-(4-hydroxy-3-methoxyphenyl)propane-1,2,3-triol 12310249 Click to see COC1=C(C=CC(=C1)C(C(CO)O)O)O 214.21 unknown https://doi.org/10.1021/NP0603931
(2R,3S)-3-ethoxy-3-(4-hydroxy-3-methoxyphenyl)propane-1,2-diol 162972898 Click to see CCOC(C1=CC(=C(C=C1)O)OC)C(CO)O 242.27 unknown https://doi.org/10.1021/NP0603931
3-(3-Hydroxy-4-methoxyphenyl)prop-2-enal 9834110 Click to see COC1=C(C=C(C=C1)C=CC=O)O 178.18 unknown https://doi.org/10.1021/NP0603931
7-O-ethylguaiacylglycerol 44421292 Click to see CCOC(C1=CC(=C(C=C1)O)OC)C(CO)O 242.27 unknown https://doi.org/10.1021/NP0603931
Sinapaldehyde 5280802 Click to see COC1=CC(=CC(=C1O)OC)C=CC=O 208.21 unknown https://doi.org/10.1021/NP0603931
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
Dihydrocubebin 193042 Click to see C1OC2=C(O1)C=C(C=C2)CC(CO)C(CC3=CC4=C(C=C3)OCO4)CO 358.40 unknown https://doi.org/10.1021/NP0603931
> Lignans, neolignans and related compounds / Furanoid lignans
(1R,2S)-2-[4-[(3R,3aR,6R,6aS)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-1-(4-hydroxy-3,5-dimethoxyphenyl)propane-1,3-diol 163079510 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC(CO)C(C5=CC(=C(C(=C5)OC)O)OC)O)OC 644.70 unknown https://doi.org/10.1021/NP0603931
(1S,2R)-2-[4-[(3R,3aS,6R,6aS)-6-[4-[(1S,2R)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3,5-dimethoxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol 44421293 Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C=C2)O)OC)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC(CO)C(C6=CC(=C(C=C6)O)OC)O)OC 810.80 unknown https://doi.org/10.1021/NP0603931
(1S,2R)-2-[4-[(3S,3aS,6R,6aS)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol 162891022 Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C=C2)O)OC)O)OC)C3C4COC(C4CO3)C5=CC(=C(C=C5)O)OC 584.60 unknown https://doi.org/10.1021/NP0603931
(1S,2S)-2-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol 162905284 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC(CO)C(C5=CC(=C(C=C5)O)OC)O)OC 614.60 unknown https://doi.org/10.1021/NP0603931
2-[4-[(3R,3aS,6R,6aS)-6-[4-[1,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-2-yl]oxy-3,5-dimethoxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol 16216277 Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C=C2)O)OC)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC(CO)C(C6=CC(=C(C(=C6)OC)O)OC)O)OC 840.90 unknown https://doi.org/10.1021/NP0603931
5'-Methoxyhedyotisol A 44421289 Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C=C2)O)OC)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC(CO)C(C6=CC(=C(C(=C6)OC)O)OC)O)OC 840.90 unknown https://doi.org/10.1021/NP0603931
Buddlenol C 353908 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC(CO)C(C5=CC(=C(C=C5)O)OC)O)OC 614.60 unknown https://doi.org/10.1021/NP0603931
Hedyotisol A 53354809 Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C=C2)O)OC)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC(CO)C(C6=CC(=C(C=C6)O)OC)O)OC 810.80 unknown https://doi.org/10.1021/NP0603931
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1021/NP0603931
Syringaresinol, (+)- 443023 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1021/NP0603931
> Lignans, neolignans and related compounds / Lignan lactones
(3R,3aR,6aR)-3-[4-[1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3,5-dimethoxyphenyl]-3,3a,4,6a-tetrahydro-1H-furo[3,4-c]furan-6-one 16216276 Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C=C2)O)OC)O)OC)C3C4COC(=O)C4CO3 476.50 unknown https://doi.org/10.1021/NP0603931
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone 75142 Click to see COC1=C(C=CC(=C1)C(=O)CCO)O 196.20 unknown https://doi.org/10.1021/NP0603931
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,3S)-3-(hydroxymethyl)-4,6-dimethoxy-2-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1-benzofuran-5-ol 16216402 Click to see COC1=CC(=CC(=C1OC)OC)C2C(C3=C(C(=C(C=C3O2)OC)O)OC)CO 392.40 unknown https://doi.org/10.1021/NP0603931
(E)-3-[(2R,3R)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-enoic acid 38356803 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC(=O)O 372.40 unknown https://doi.org/10.1021/NP0603931
(E)-3-[(2R,3S)-2-[4-[1-[4-[1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3-methoxyphenyl]-1,3-dihydroxypropan-2-yl]oxy-3,5-dimethoxyphenyl]-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-enal 16216400 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)OC(CO)C(C4=CC(=C(C=C4)OC(CO)C(C5=CC(=C(C=C5)O)OC)O)OC)O)OC)C=CC=O 778.80 unknown https://doi.org/10.1021/NP0603931
(E)-3-[(2R,3S)-2-[4-[1-[4-[1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3,5-dimethoxyphenyl]-1,3-dihydroxypropan-2-yl]oxy-3,5-dimethoxyphenyl]-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-enal 16216401 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)OC(CO)C(C4=CC(=C(C(=C4)OC)OC(CO)C(C5=CC(=C(C=C5)O)OC)O)OC)O)OC)C=CC=O 808.80 unknown https://doi.org/10.1021/NP0603931
(E)-3-[(2R,3S)-2-[4-[1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3,5-dimethoxyphenyl]-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-enal 44421295 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)OC(CO)C(C4=CC(=C(C=C4)O)OC)O)OC)C=CC=O 582.60 unknown https://doi.org/10.1021/NP0603931
(E)-3-[(2S,3S)-2-[4-[(1R,2S)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3,5-dimethoxyphenyl]-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-enal 162909604 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)OC(CO)C(C4=CC(=C(C=C4)O)OC)O)OC)C=CC=O 582.60 unknown https://doi.org/10.1021/NP0603931
Balanophonin 21582569 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O 356.40 unknown https://doi.org/10.1021/NP0603931
Ficusal 10496641 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=O 330.30 unknown https://doi.org/10.1021/NP0603931
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1021/NP0603931

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