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Mallotus macrostachyus

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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 UUID643fe26525b28126164896
Scientific name Mallotus macrostachyus
Authority Müll.Arg.
First published in Prodr. 15(2): 963 (1866)

Description Top

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Synonyms Top

Scientific name Authority First published in
Mallotus insignis Müll.Arg. Linnaea 34: 193 (1865)
Rottlera macrostachya Miq. Fl. Ned. Ind., Eerste Bijv. : 454 (1861)

Common names Top

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Language Common/alternative name
Indonesian balik angin
Indonesian kayu kapit
Chinese 大穗野桐

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-tropical
    • Indo-China
      • Thailand
    • Malesia
      • Borneo
      • Malaya
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000234615
Tropicos 12807624
KEW urn:lsid:ipni.org:names:351610-1
The Plant List kew-118963
Open Tree Of Life 762461
NCBI Taxonomy 396487
IPNI 351610-1
iNaturalist 427120
GBIF 5378613
EOL 1154819

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
Insight into the effect of low temperature treatment on trichome density and related differentially expressed genes in Chinese cabbage Sun P, Huang C, Zhang L, Wu D, Zhang W, Yu S, Fu G, Cheng S, Wang Z, Deng Q, Zhu G, Liu P PLoS One 15-Sep-2022
PMCID:PMC9477275
doi:10.1371/journal.pone.0274530
PMID:36107960
Legumes from the Paleocene sediments of India and their ecological significance Bhatia H, Srivastava G, Mehrotra RC Plant Divers 14-Aug-2022
PMCID:PMC10105134
doi:10.1016/j.pld.2022.08.001
PMID:37069925
Species richness of riparian vegetation after three decades of Kenyir dam establishment Shahimi S, Salam R, Salim JM, Ahmad A Data Brief 23-May-2019
PMCID:PMC6554223
doi:10.1016/j.dib.2019.104045
PMID:31194175
Chemical constituents of Mallotus macrostachyus growing in Vietnam and cytotoxic activity of some cycloartane derivatives Nguyen Hoai Nam, Phan Van Kiem, Ninh Khac Ban, Nguyen Phuong Thao, Nguyen Xuan Nhiem, Nguyen Xuan Cuong, Christophe Tistaert, Bieke Dejaegher, Yvan Vander Heyden, Joëlle Quetin-Leclercq, Do Thi Thao, Chau Van Minh Elsevier BV 25-Jul-2011
doi:10.1016/J.PHYTOL.2011.07.007
New Insights into the Properties of Pubescent Surfaces: Peach Fruit as a Model Fernández V, Khayet M, Montero-Prado P, Heredia-Guerrero JA, Liakopoulos G, Karabourniotis G, del Río V, Domínguez E, Tacchini I, Nerín C, Val J, Heredia A Plant Physiol 17-Jun-2011
PMCID:PMC3149954
doi:10.1104/pp.111.176305
PMID:21685175

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
2-(Hydroxymethyl)-6-[2-methoxy-4-[6-[3-methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]phenoxy]oxane-3,4,5-triol 13991179 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)OC6C(C(C(C(O6)CO)O)O)O 682.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
Liriodendrin 226371 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC 742.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
Pinoresinol diglucoside 174003 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)OC6C(C(C(C(O6)CO)O)O)O 682.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-[4-Hydroxy-7-(3-methylbut-2-enyl)-1,3-dihydro-2-benzofuran-1-yl]octane-2,3-diol 162851137 Click to see CCCCCC(C(CC1C2=C(C=CC(=C2CO1)O)CC=C(C)C)O)O 348.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(4S)-4-hydroxy-3,5,5-trimethyl-4-[(3R)-3-[(1R,2R,3S,4R,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexyl]oxybutyl]cyclohex-2-en-1-one 162948377 Click to see CC1=CC(=O)CC(C1(CCC(C)OC2CC(C(C(C2O)O)O)CO)O)(C)C 386.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
CID 12443227 12443227 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
Epitaraxerol 344467 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,3R,6R,8R,11S,12S,15R,16R)-15-[(2R)-5-hydroxypentan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 163088389 Click to see CC(CCCO)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 402.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
(1S,3R,8R,11S,12S,15R,16R)-15-[(2R)-4-hydroxybutan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 162923920 Click to see CC(CCO)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 386.60 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
(1S,3R,8R,11S,12S,15R,16R)-15-[(2R)-5-hydroxypentan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 21599949 Click to see CC(CCCO)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 400.60 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
(4R)-4-[(1S,3R,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-6-oxo-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]pentanoic acid 162946784 Click to see CC(CCC(=O)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 414.60 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
Friedelanol 101341 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
Friedelinol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives
(4R)-4-[(1S,2R,5R,6R,9R,10R,13S,15S)-13-hydroxy-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadec-18-en-5-yl]pentanoic acid 162866611 Click to see CC(CCC(=O)O)C1CCC2C1(CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C 404.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(Hydroxymethyl)-6-phenylmethoxyoxane-3,4,5-triol 4984739 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
Benzyl alcohol xylopyranosyl-(1-6)-glucopyranoside 14730864 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O 402.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
Benzyl beta-d-glucopyranoside 188977 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
Benzyl beta-primeveroside 131248 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O 402.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxamides / Nicotinamides
1-Methyl-6-oxo-1,6-dihydropyridine-3-carboxamide 69698 Click to see CN1C=C(C=CC1=O)C(=O)N 152.15 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Calendoflavobioside 14034827 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
Kaempferol 3-neohesperidoside 5318761 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
Kaempferol-3-O-glucorhamnoside 13915496 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007
Quercetin 3-neohesperidoside 5491657 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.07.007

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