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Millettia brandisiana

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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 UUID643fd981d5d62805170294
Scientific name Millettia brandisiana
Authority Kurz
First published in J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist.42: 69 (1873)

Description Top

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Synonyms Top

Scientific name Authority First published in
Millettia laotica Gagnep. Notul. Syst. (Paris)2: 358 (1913)
Millettia venusta Craib Bull. Misc. Inform. Kew1927: 59 (1927)
Millettia multiflora Collett & Hemsl. J. Linn. Soc., Bot.28: 41 (1890)
Phaseoloides brandisiana (Kurz) Kuntze Revis. Gen. Pl.1: 201 (1891)

Common names Top

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Language Common/alternative name
Thai กระพี้จั่น
Thai จั่น
Chinese 镇康岩豆藤

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
    • Indian Subcontinent
      • Bangladesh
    • Indo-China
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000185916
Tropicos 13035900
KEW urn:lsid:ipni.org:names:507295-1
The Plant List ild-32251
Open Tree Of Life 3920568
NCBI Taxonomy 1993599
IPNI 507295-1
GBIF 5355870
EOL 643646
CMAUP NPO24609

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
Study on the absolute configuration and biological activity of rotenoids from the leaves and twigs of Millettia pyrrhocarpa Mattapha, Forest & Hawkins, sp. Nov Sananboonudom S, Kaewnoi A, Pompimon W, Narakaew S, Jiajaroen S, Chainok K, nuntasaen N, Suksen K, Chairoungdua A, Limthongkul J, Naparswad C, Pikulthong S, Meepowpan P, Wingwon B, Charoenphakinrattana N, Udomputtimekakul P BMC Complement Med Ther 04-May-2023
PMCID:PMC10161675
doi:10.1186/s12906-023-03963-4
PMID:37143007
Impact of Drying Processes on Phenolics and In Vitro Health-Related Activities of Indigenous Plants in Thailand Sirichai P, Kittibunchakul S, Thangsiri S, On-Nom N, Chupeerach C, Temviriyanukul P, Inthachat W, Nuchuchua O, Aursalung A, Sahasakul Y, Charoenkiatkul S, Suttisansanee U Plants (Basel) 22-Jan-2022
PMCID:PMC8838347
doi:10.3390/plants11030294
PMID:35161275
Above-ground carbon stock and REDD+ opportunities of community-managed forests in northern Thailand Thammanu S, Han H, Marod D, Srichaichana J, Chung J PLoS One 18-Aug-2021
PMCID:PMC8372953
doi:10.1371/journal.pone.0256005
PMID:34407113
Wild food plants and fungi sold in the markets of Luang Prabang, Lao PDR Łuczaj Ł, Lamxay V, Tongchan K, Xayphakatsa K, Phimmakong K, Radavanh S, Kanyasone V, Pietras M, Karbarz M J Ethnobiol Ethnomed 26-Jan-2021
PMCID:PMC7835671
doi:10.1186/s13002-020-00423-y
PMID:33499871
Monitoring of forage and nutrition before and after reintroduction of banteng (Bos javanicus d’ Alton, 1823) to Salakphra Wildlife Sanctuary, Thailand Chaiyarat R, Sakchan P, Panprayun G, Thongthip N, Nakbun S Sci Rep 07-Jul-2020
PMCID:PMC7341747
doi:10.1038/s41598-020-67942-2
PMID:32636423
Traditional Uses of Leguminosae among the Karen in Thailand Sutjaritjai N, Wangpakapattanawong P, Balslev H, Inta A Plants (Basel) 13-Dec-2019
PMCID:PMC6963713
doi:10.3390/plants8120600
PMID:31847100
Death receptor 5 targeting activity-guided isolation of isoflavones from Millettia brandisiana and Ardisia colorata and evaluation of ability to induce TRAIL-mediated apoptosis. Kikuchi H, Ohtsuki T, Koyano T, Kowithayakorn T, Sakai T, Ishibashi M Bioorg Med Chem 01-Feb-2009
doi:10.1016/J.BMC.2008.12.033
PMID:19124248
Isoflavones and rotenoids from the leaves of Millettia brandisiana. Pancharoen O, Athipornchai A, Panthong A, Taylor WC Chem Pharm Bull (Tokyo) 01-Jun-2008
doi:10.1248/CPB.56.835
PMID:18520090
Brandisianins A-F, isoflavonoids isolated from Millettia brandisiana in a screening program for death-receptor expression enhancement activity. Kikuchi H, Ohtsuki T, Koyano T, Kowithayakorn T, Sakai T, Ishibashi M J Nat Prod 01-Dec-2007
doi:10.1021/NP0703904
PMID:18039011

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
16Z-pentacosenoic acid 5312567 Click to see CCCCCCCCC=CCCCCCCCCCCCCCCC(=O)O 380.60 unknown via CMAUP database
16Z-tricosenoic acid 5312563 Click to see CCCCCCC=CCCCCCCCCCCCCCCC(=O)O 352.60 unknown via CMAUP database
18Z-pentacosenoic acid 5312569 Click to see CCCCCCC=CCCCCCCCCCCCCCCCCC(=O)O 380.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/CPB.56.835
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/CPB.56.835
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1021/NP0703904
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1021/NP0703904
> 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/10.1021/NP0703904
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/10.1021/NP0703904
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
3,8,9-trimethoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-2,10-diol 162886374 Click to see COC1=C(C(=C2C(=C1)C3COC4=CC(=C(C=C4C3O2)O)OC)O)OC 346.30 unknown https://doi.org/10.1021/NP0703904
brandisianin F 24763561 Click to see COC1=C(C(=C2C(=C1)C3COC4=CC(=C(C=C4C3O2)O)OC)O)OC 346.30 unknown https://doi.org/10.1021/NP0703904
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
5-Hydroxy-7-(3-methylbut-2-enoxy)-3-[4-(3-methylbut-2-enoxy)phenyl]chromen-4-one 101855821 Click to see CC(=CCOC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OCC=C(C)C)C 406.50 unknown https://doi.org/10.1248/CPB.56.835
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
Viridiflorin 44257314 Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC(=C(C=C3OC)O)OC)O)C 398.40 unknown https://doi.org/10.1248/CPB.56.835
https://doi.org/10.1021/NP0703904
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3-[2,5-Dimethoxy-3-(3-methylbut-2-enoxy)phenyl]-5,7-dihydroxychromen-4-one 163068256 Click to see CC(=CCOC1=CC(=CC(=C1OC)C2=COC3=CC(=CC(=C3C2=O)O)O)OC)C 398.40 unknown https://doi.org/10.1021/NP0703904
5-Hydroxy-3-(4-hydroxy-2,5-dimethoxyphenyl)-8-prop-1-en-2-yl-8,9-dihydrofuro[2,3-h]chromen-4-one 24990948 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC=C(C3=O)C4=CC(=C(C=C4OC)O)OC)O 396.40 unknown https://doi.org/10.1021/NP0703904
5,7-Dihydroxy-3-(4-hydroxy-2,5-dimethoxyphenyl)-8-(4-hydroxy-3-methylbut-2-enyl)chromen-4-one 163009138 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=CO2)C3=CC(=C(C=C3OC)O)OC)CO 414.40 unknown https://doi.org/10.1021/NP0703904
5,7-dihydroxy-3-(4-hydroxy-2,5-dimethoxyphenyl)-8-[(E)-4-hydroxy-3-methylbut-2-enyl]chromen-4-one 24763560 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=CO2)C3=CC(=C(C=C3OC)O)OC)CO 414.40 unknown https://doi.org/10.1021/NP0703904
brandisianin A 24763480 Click to see CC(=CCOC1=C(C=C(C(=C1)OC)C2=COC3=CC(=CC(=C3C2=O)O)O)OC)C 398.40 unknown https://doi.org/10.1021/NP0703904
brandisianin B 24763481 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC=C(C3=O)C4=CC(=C(C=C4OC)O)OC)O 396.40 unknown https://doi.org/10.1021/NP0703904
brandisianin C 24763482 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=CO2)C3=CC(=C(C=C3OC)O)OC)C 398.40 unknown https://doi.org/10.1021/NP0703904
Olibergin A 5324507 Click to see COC1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)OC)O 330.29 unknown https://doi.org/10.1021/NP0703904
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
2'-Hydroxyformononetin 5280551 Click to see COC1=CC(=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown https://doi.org/10.1016/J.BMC.2008.12.033
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
3-[2,5-Dimethoxy-4-(3-methylbut-2-enoxy)phenyl]-5,7-dimethoxychromen-4-one 25058575 Click to see CC(=CCOC1=C(C=C(C(=C1)OC)C2=COC3=C(C2=O)C(=CC(=C3)OC)OC)OC)C 426.50 unknown https://doi.org/10.1248/CPB.56.835
5-Hydroxy-7-methoxy-3-(2,4,5-trimethoxyphenyl)chromen-4-one 7330527 Click to see COC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC(=C(C=C3OC)OC)OC)O 358.30 unknown https://doi.org/10.1248/CPB.56.835
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
(8R)-5-hydroxy-3-(4-hydroxy-2,5-dimethoxyphenyl)-8-(hydroxymethyl)-8-methylpyrano[2,3-h]chromen-4-one 24180632 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC=C(C3=O)C4=CC(=C(C=C4OC)O)OC)O)CO 412.40 unknown https://doi.org/10.1021/NP0703904
4'-Demethyltoxicarol isoflavone 14057034 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC=C(C3=O)C4=CC(=C(C=C4OC)O)OC)O)C 396.40 unknown https://doi.org/10.1021/NP0703904
https://doi.org/10.1016/J.BMC.2008.12.033
5-Hydroxy-3-(4-hydroxy-2,5-dimethoxyphenyl)-8-(hydroxymethyl)-8-methylpyrano[2,3-h]chromen-4-one 101447475 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC=C(C3=O)C4=CC(=C(C=C4OC)O)OC)O)CO 412.40 unknown https://doi.org/10.1021/NP0703904
Toxicarolisoflavone 14057036 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC=C(C3=O)C4=CC(=C(C=C4OC)OC)OC)O)C 410.40 unknown https://doi.org/10.1248/CPB.56.835
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(1R,14R)-11,14-dihydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.0^{3,12.0^{4,9.0^{15,20]docosa-3(12),4(9),5,10,15,17,19-heptaen-13-one 13846202 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)C 426.40 unknown https://doi.org/10.1248/CPB.56.835
(22S)-11,22-dihydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-1(14),3(12),4(9),5,10,15,17,19-octaen-13-one 162871967 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4O)OC)OC)O)C 424.40 unknown https://doi.org/10.1248/CPB.56.835
(6aR,12aR)-11-hydroxy-2,3,9-trimethoxy-6a,12a-dihydro-6H-chromeno[3,4-b]chromen-12-one 162898477 Click to see COC1=CC(=C2C(=C1)OC3COC4=CC(=C(C=C4C3C2=O)OC)OC)O 358.30 unknown https://doi.org/10.1248/CPB.56.835
(6aS,12aS)-11-hydroxy-2,3,9-trimethoxy-6a,12a-dihydro-6H-chromeno[3,4-b]chromen-12-one 137646096 Click to see COC1=CC(=C2C(=C1)OC3COC4=CC(=C(C=C4C3C2=O)OC)OC)O 358.30 unknown https://doi.org/10.1248/CPB.56.835
(6S)-6,11-dihydroxy-2,3,9-trimethoxy-6H-chromeno[3,4-b]chromen-12-one 163031144 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C4=CC(=C(C=C4OC3O)OC)OC)O 372.30 unknown https://doi.org/10.1248/CPB.56.835
11-Hydroxy-2,3,9-trimethoxy-6h-chromeno[3,4-b]chromen-12-one 101368147 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C4=CC(=C(C=C4OC3)OC)OC)O 356.30 unknown https://doi.org/10.1248/CPB.56.835
11-Hydroxytephrosin 155725 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)C 426.40 unknown https://doi.org/10.1248/CPB.56.835
11,12a-Dihydroxy-2,3,9-trimethoxy-6,6a-dihydrochromeno[3,4-b]chromen-12-one 45359766 Click to see COC1=CC(=C2C(=C1)OC3COC4=CC(=C(C=C4C3(C2=O)O)OC)OC)O 374.30 unknown https://doi.org/10.1248/CPB.56.835
6-Deoxyclitoracetal 11740108 Click to see COC1=CC(=C2C(=C1)OC3COC4=CC(=C(C=C4C3(C2=O)O)OC)OC)O 374.30 unknown https://doi.org/10.1248/CPB.56.835
6-Hydroxy-6a,12a-dehydro-alpha-toxicarol 44257423 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4O)OC)OC)O)C 424.40 unknown https://doi.org/10.1248/CPB.56.835
6-Hydroxy-9,10-dimethoxy-3,3-dimethyl-13,13a-dihydro-3H,7aH-pyrano[2,3-c:6,5-f']dichromen-7-one 243723 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O)C 410.40 unknown https://doi.org/10.1248/CPB.56.835
alpha-Toxicarol 442826 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O)C 410.40 unknown https://doi.org/10.1248/CPB.56.835
Dehydrotoxicarol 5491616 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC)O)C 408.40 unknown https://doi.org/10.1248/CPB.56.835
Sermundone 44257403 Click to see COC1=CC(=C2C(=C1)OC3COC4=CC(=C(C=C4C3C2=O)OC)OC)O 358.30 unknown https://doi.org/10.1248/CPB.56.835
Stemonal 44257425 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C4=CC(=C(C=C4OC3O)OC)OC)O 372.30 unknown https://doi.org/10.1248/CPB.56.835
Villosol 5490819 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC)O 408.40 unknown https://doi.org/10.1248/CPB.56.835

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