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)
Pavetta coffeacea	Wall.	Numer. List : n.° 7290 (1832)
Stylocoryna attenuata	Voigt	Hort. Suburb. Calcutt. : 377 (1845)

Common names Top

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Filter by language:

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
Chinese	假桂烏口樹

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

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan

Asia-tropical click to expand
- Indo-China
  - Cambodia
  - Myanmar
  - Thailand
  - Vietnam

Links to other databases Top

Suggest others/fix!

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

Does local soil factor drive functional leaf trait variation? A test on Neilingding Island, South China

Tong S, Zhang J, Qiao X, Li B, Yang Q, Hu P, Yu S

BMC Ecol Evol

10-Apr-2024

PMCID:	PMC11005248
doi:	10.1186/s12862-024-02227-0
PMID:	38600505

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

Chalcone: A Promising Bioactive Scaffold in Medicinal Chemistry

Rajendran G, Bhanu D, Aruchamy B, Ramani P, Pandurangan N, Bobba KN, Oh EJ, Chung HY, Gangadaran P, Ahn BC

Pharmaceuticals (Basel)

11-Oct-2022

PMCID:	PMC9607481
doi:	10.3390/ph15101250
PMID:	36297362

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!
You can also contribute to this by clicking here.

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	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	242.27	unknown	https://doi.org/10.1021/NP0603931
7-O-Ethylguaiacylglycerol	44421292	Click to see	242.27	unknown	https://doi.org/10.1021/NP0603931
Isoferulaldehyde	9834110	Click to see	178.18	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	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	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	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	840.90	unknown	https://doi.org/10.1021/NP0603931
5'-Methoxyhedyotisol A	44421289	Click to see	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	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	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	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	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	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	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	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	582.60	unknown	https://doi.org/10.1021/NP0603931
Balanophonin	21582569	Click to see	356.40	unknown	https://doi.org/10.1021/NP0603931
Ficusal	10496641	Click to see	330.30	unknown	https://doi.org/10.1021/NP0603931
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
Cinnamic Acid	444539	Click to see	148.16	unknown	https://doi.org/10.1021/NP0603931

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Tarenna attenuata

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top