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Internal ID UUID643fdbbb7e47f510536805
Scientific name Ormosia henryi
Authority Prain
First published in J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist.69: 180 (1900)

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Synonyms Top

Scientific name Authority First published in
Ormosia mollis Dunn J. Bot.47: 198 (1909)
Fedorovia henryi (Prain) Yakovlev Bot. Zhurn. (Moscow & Leningrad)56: 656 (1971)
Ormosia dubia Prain J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist.69: 182 (1900)
Ormosia inopinata Prain J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist.69: 181 (1900)
Fedorovia inopinata (Prain) Yakovlev Novosti Sist. Vyssh. Rast.10: 195 (1973)

Common names Top

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Language Common/alternative name
Chinese 花梨木
Chinese 三钱三
Chinese 红豆树
Chinese 花榈木
Chinese 榈木
Chinese 亨氏红豆
Chinese 臭桶柴
Chinese 花櫚木

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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000197170
Tropicos 13044394
KEW urn:lsid:ipni.org:names:510721-1
The Plant List ild-43712
Open Tree Of Life 451709
NCBI Taxonomy 705300
IPNI 510722-1
iNaturalist 706910
GBIF 5355447
EOL 648240
USDA GRIN 25922
Wikipedia Ormosia_henryi

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
Genetic structure of an endangered species Ormosia henryi in southern China, and implications for conservation Zhou C, Xia S, Wen Q, Song Y, Jia Q, Wang T, Liu L, Ouyang T BMC Plant Biol 26-Apr-2023
PMCID:PMC10131447
doi:10.1186/s12870-023-04231-w
PMID:37098472
Changes and transcriptome regulation of endogenous hormones during somatic embryogenesis in Ormosia henryi Prain Wu G, Wei X, Wang X, Wei Y Front Plant Sci 03-Apr-2023
PMCID:PMC10106752
doi:10.3389/fpls.2023.1121259
PMID:37077643
Study on the Difference of Superhydrophobic Characteristics of Different Wood Furniture Substrates Yao X, Kong Z, Yang F, Wu X, Wu Y Polymers (Basel) 25-Mar-2023
PMCID:PMC10096626
doi:10.3390/polym15071644
PMID:37050257
Improving the Physicochemical and Biopharmaceutical Properties of Active Pharmaceutical Ingredients Derived from Traditional Chinese Medicine through Cocrystal Engineering Guan D, Xuan B, Wang C, Long R, Jiang Y, Mao L, Kang J, Wang Z, Chow SF, Zhou Q Pharmaceutics 15-Dec-2021
PMCID:PMC8704577
doi:10.3390/pharmaceutics13122160
PMID:34959440
Local patterns of arbuscular mycorrhizal fungal diversity and community structure in a natural Toona ciliata var. pubescens forest in South Central China Pan J, Wang Q, Guo X, Jiang X, Cheng Q, Fu L, Liu W, Zhang L PeerJ 03-May-2021
PMCID:PMC8101450
doi:10.7717/peerj.11331
PMID:33987014
Plant-derived bioactive compounds produced by Streptomyces variabilis LCP18 associated with Litsea cubeba (Lour.) Pers as potential target to combat human pathogenic bacteria and human cancer cell lines Quach NT, Nguyen QH, Vu TH, Le TT, Ta TT, Nguyen TD, Van Doan T, Van Nguyen T, Dang TT, Nguyen XC, Chu HH, Phi QT Braz J Microbiol 01-May-2021
PMCID:PMC8324668
doi:10.1007/s42770-021-00510-6
PMID:33934292
Predation Pressure in Tea (Camellia sinensis) Plantations in Southeastern China Measured by the Sentinel Prey Method Imboma TS, Gao DP, You MS, You S, Lövei GL Insects 29-Mar-2020
PMCID:PMC7240450
doi:10.3390/insects11040212
PMID:32235345
Genome Comparison Reveals Mutation Hotspots in the Chloroplast Genome and Phylogenetic Relationships of Ormosia Species Liu H, Su Z, Yu S, Liu J, Yin X, Zhang G, Liu W, Li B Biomed Res Int 21-Aug-2019
PMCID:PMC6720362
doi:10.1155/2019/7265030
PMID:31531364
Phytochemical Profile and Antidepressant Effect of Ormosia henryi Prain Leaf Ethanol Extract Lu Y, Zhu S, He Y, Peng C, Wang Z, Tang Q Int J Mol Sci 10-Jul-2019
PMCID:PMC6678957
doi:10.3390/ijms20143396
PMID:31295954
Natural Products from Chinese Medicines with Potential Benefits to Bone Health Che CT, Wong MS, Lam CW Molecules 27-Feb-2016
PMCID:PMC6274145
doi:10.3390/molecules21030239
PMID:26927052
Polyprenylated isoflavanone and isoflavonoids from Ormosia henryi and their cytotoxicity and anti-oxidation activity. Feng S, Hao J, Xu Z, Chen T, Qiu SX Fitoterapia 01-Jan-2012
doi:10.1016/J.FITOTE.2011.10.007
PMID:22037567

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 / Benzophenones
[(3R)-3,7-dihydroxy-5-methoxy-2,2-dimethyl-6-(3-methylbut-2-enyl)-3,4-dihydrochromen-8-yl]-phenylmethanone 163084052 Click to see CC(=CCC1=C(C2=C(C(=C1O)C(=O)C3=CC=CC=C3)OC(C(C2)O)(C)C)OC)C 396.50 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol 11604108 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
Syringaresinol 100067 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
Lup-20(29)-en-3-one 323075 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-, octadecyl ester, (E)-; trans-Caffeic acid stearyl ester 71374400 Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)O 432.60 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
Octadecyl caffeate 5320237 Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)O 432.60 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
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/10.1016/J.FITOTE.2011.10.007
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/10.1016/J.FITOTE.2011.10.007
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 662 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Daidzein 5281708 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)O 254.24 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 8-prenylated isoflavanones
(3S)-3-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 162890242 Click to see CC(=CCC1=CC(=C(C=C1O)O)C2COC3=C(C(=C(C(=C3C2=O)O)CC=C(C)C)O)CC=C(C)C)C 492.60 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(4-hydroxyphenyl)-5-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 189922 Click to see COC1=CC(=CC2=C1C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
4H-1-Benzopyran-4-one, 7-(beta-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)- 4183640 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 416.40 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
5-Hydroxy-3-(4-hydroxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2S,3R,4S,5R)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one 162658878 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC=C(C4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
5-Hydroxy-3-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 162871411 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC=C(C4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
5,7-dihydroxy-3-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxyphenyl]chromen-4-one;Sophoricoside 6078194 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)OC4C(C(C(C(O4)CO)O)O)O 432.40 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
Daidzin 107971 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 416.40 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
Sophoricoside 5321398 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)OC4C(C(C(C(O4)CO)O)O)O 432.40 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
5-hydroxy-3-(4-methoxyphenyl)-7-[(1R,2R,3S,4R,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexyl]oxychromen-4-one 162987876 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4CC(C(C(C4O)O)O)CO 444.40 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
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/10.1016/J.FITOTE.2011.10.007
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
4',7-Dimethoxyisoflavone 136419 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC 282.29 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
7,4'-Dimethoxy-5-hydroxyisoflavone 5386259 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC 298.29 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007
Isoformononetin 3764 Click to see COC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC=C(C=C3)O 268.26 unknown https://doi.org/10.1016/J.FITOTE.2011.10.007

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