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Millettia extensa

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fd981b72c9220115076
Scientific name Millettia extensa
Authority (Benth.) Baker

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Millettia auriculata Brandis

Common names Top

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Language Common/alternative name
Chinese 扩展崖豆藤
Chinese 擴展崖豆藤

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
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • West Himalaya
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000185910
Tropicos 13035913
KEW urn:lsid:ipni.org:names:507364-1
The Plant List ild-32243
Open Tree Of Life 3920579
NCBI Taxonomy 1712208
IPNI 507364-1
GBIF 5355773
EOL 643640
USDA GRIN 311899
Wikipedia Millettia_extensa
CMAUP NPO19429

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
Siwalik plant megafossil diversity in the Eastern Himalayas: A review Khan MA, Mahato S, Spicer RA, Spicer TE, Ali A, Hazra T, Bera S Plant Divers 17-Dec-2022
PMCID:PMC10311196
doi:10.1016/j.pld.2022.12.003
PMID:37397603
Rare prenylated isoflavonoids from the young twigs of Millettia extensa and their cytotoxic activities Cheenpracha S, Chokchaisiri R, Laphookhieo S, Limtharakul T, Thepmalee C RSC Adv 24-Oct-2022
PMCID:PMC9590589
doi:10.1039/d2ra05950a
PMID:36337981
Ethnoveterinary use of plants and its implication for sustainable livestock management in Nepal Uprety Y, Karki S, Poudel RC, Kunwar RM Front Vet Sci 09-Sep-2022
PMCID:PMC9500146
doi:10.3389/fvets.2022.930533
PMID:36157185
Prenylated Flavonoids in Topical Infections and Wound Healing Sychrová A, Škovranová G, Čulenová M, Bittner Fialová S Molecules 13-Jul-2022
PMCID:PMC9323352
doi:10.3390/molecules27144491
PMID:35889363
A review on genus Millettia: Traditional uses, phytochemicals and pharmacological activities Jena R, Rath D, Rout SS, Kar DM Saudi Pharm J 05-Nov-2020
PMCID:PMC7783215
doi:10.1016/j.jsps.2020.10.015
PMID:33424261
Antimicrobial, Anthelmintic, and Antiviral Activity of Plants Traditionally Used for Treating Infectious Disease in the Similipal Biosphere Reserve, Odisha, India Panda SK, Padhi L, Leyssen P, Liu M, Neyts J, Luyten W Front Pharmacol 23-Oct-2017
PMCID:PMC5660100
doi:10.3389/fphar.2017.00658
PMID:29109684
Large Scale Screening of Ethnomedicinal Plants for Identification of Potential Antibacterial Compounds Panda SK, Mohanta YK, Padhi L, Park YH, Mohanta TK, Bae H Molecules 14-Mar-2016
PMCID:PMC6274442
doi:10.3390/molecules21030293
PMID:26985889
SPECIES COMPOSITION, DISTRIBUTION, LIFE FORMS AND FOLK NOMENCLATURE OF FOREST AND COMMON LAND PLANTS OF WESTERN CHITWAN, NEPAL Dangol DR J Inst Agric Anim Sci 01-Jan-2005
PMCID:PMC3434227
PMID:22962539
Three prenylated isoflavones from Milletia auriculata E Rao Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)80206-T
Isoaurmillone, an isoflavone from the pods of Milletia auriculata Bodhendu B. Gupta, Anjan Bhattacharyya, Santi R. Mitra, Narayan Adityachaudhury Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(83)80256-8
PLANT DIVERSITY OF WESTERN CHITWAN FLORISTIC APPROACH Dangol DR, Shivakoti GP J Nat Hist Mus 01-Jan-2001
PMCID:PMC3418710
PMID:22899874

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 / Prenol lipids / Triterpenoids
2alpha-Hydroxy-3beta-acetyloxy-betulic acid 67993145 Click to see 514.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(1S,2S,13S,15R)-15-[(Z)-4,4-dimethoxy-3-methylbut-2-enyl]-7-[(2E)-3,7-dimethylocta-2,6-dienyl]-6,8-dihydroxy-17,17-dimethyl-5-(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraene-10,14-dione 10532388 Click to see 660.80 unknown via CMAUP database
(1S,2S,13S,15R)-6-[(2E)-3,7-dimethylocta-2,6-dienoxy]-8-hydroxy-17,17-dimethyl-5,15-bis(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4(9),5,7,11-tetraene-10,14-dione 25208760 Click to see 600.80 unknown via CMAUP database
(1S,2S,13S,15R)-6,8-dihydroxy-17,17-dimethyl-5,13,15-tris(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraene-10,14-dione 10554272 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=CC4(CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C)CC=C(C)C)C 532.70 unknown via CMAUP database
(1S,2S,13S,15R)-6,8-dihydroxy-17,17-dimethyl-5,15-bis(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraene-10,14-dione 57393978 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C)C 464.50 unknown via CMAUP database
(1S,2S,13S,15R)-6,8-dihydroxy-17,17-dimethyl-5,7,15-tris(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraene-10,14-dione 101389904 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C)CC=C(C)C)O)C 532.70 unknown via CMAUP database
(E)-4-[(1S,2S,13S,15R)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-enyl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enoic acid 46867195 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C(=O)O)CC=C(C)C)O)C 562.60 unknown via CMAUP database
(E)-4-[(1S,2S,13S,15R)-7-[(2E)-3,7-dimethylocta-2,6-dienyl]-6,8-dihydroxy-17,17-dimethyl-5-(3-methylbut-2-enyl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal 10603834 Click to see CC(=CCCC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C=O)CC=C(C)C)O)C)C 614.80 unknown via CMAUP database
(Z)-4-[(1S,2S,13S,15R)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-enyl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enoic acid 101389902 Click to see 562.60 unknown via CMAUP database
(Z)-4-[(1S,2S,13S,15R)-7-[(2E)-3,7-dimethylocta-2,6-dienyl]-6,8-dihydroxy-17,17-dimethyl-5-(3-methylbut-2-enyl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal 10841474 Click to see 614.80 unknown via CMAUP database
Deoxygambogenin 10817397 Click to see 600.80 unknown via CMAUP database
Gambogenic Acid 10794070 Click to see CC(=CCCC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C(=O)O)CC=C(C)C)O)C)C 630.80 unknown via CMAUP database
Isogambogenic acid 101389903 Click to see 630.80 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(-)-Morellic Acid 54580250 Click to see 560.60 unknown via CMAUP database
(1S,2S,17R,19R)-12-hydroxy-19-[(E)-4-hydroxy-3-methylbut-2-enyl]-17-methoxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaene-14,18-dione 25208912 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)(C(=O)C5(OC6(C)C)CC=C(C)CO)OC)O)C=CC(O2)(C)C)C 576.70 unknown via CMAUP database
(1S,2S,17S,19R)-12-hydroxy-19-[(E)-4-hydroxy-3-methylbut-2-enyl]-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaene-14,18-dione 101389908 Click to see 546.60 unknown via CMAUP database
(1S,2S,17S,19R)-12-hydroxy-8,8,21,21-tetramethyl-5,19-bis(3-methylbut-2-enyl)-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaene-14,18-dione 11432549 Click to see 530.60 unknown via CMAUP database
(1S,2S,17S,19R)-19-[(Z)-4,4-dimethoxy-3-methylbut-2-enyl]-12-hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaene-14,18-dione 10769730 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(OC)OC)O)C=CC(O2)(C)C)C 590.70 unknown via CMAUP database
(1S,2S,8R,17S,19R)-12-hydroxy-8,21,21-trimethyl-5,19-bis(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaene-14,18-dione 101690778 Click to see 598.80 unknown via CMAUP database
(E)-4-[(1S,2S,15R,16S,17S,19R)-12-hydroxy-16-methoxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11-tetraen-19-yl]-2-methylbut-2-enal 11801290 Click to see 576.70 unknown via CMAUP database
(E)-4-[(1S,2S,17S,19R)-12-hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid 101389907 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)C 560.60 unknown via CMAUP database
(Z)-2-(hydroxymethyl)-4-[(1S,2S,8R,17S,19R)-12-hydroxy-8,21,21-trimethyl-5-(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]but-2-enoic acid 102402040 Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)CC=C(C)C)OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(CO)C(=O)O)O)C)C 644.70 unknown via CMAUP database
(Z)-2-(hydroxymethyl)-4-[(1S,2S,8S,17S,19R)-12-hydroxy-8,21,21-trimethyl-5-(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]but-2-enoic acid 102402042 Click to see 644.70 unknown via CMAUP database
(Z)-4-[(1R,2R,17R,19S)-12-hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid 102533562 Click to see 560.60 unknown via CMAUP database
(Z)-4-[(1S,2S,15R,16S,17S,19R)-12-hydroxy-16-methoxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11-tetraen-19-yl]-2-methylbut-2-enoic acid 10507667 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C(C4C3=O)OC)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)C 592.70 unknown via CMAUP database
(Z)-4-[(1S,2S,8R,17R,19R)-12-hydroxy-17-methoxy-8,21,21-trimethyl-5-(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid 25208439 Click to see 658.80 unknown via CMAUP database
(Z)-4-[(1S,2S,8S,17R,19R)-12-hydroxy-17-methoxy-8,21,21-trimethyl-5-(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid 25208762 Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)CC=C(C)C)OC45C6CC(C=C4C3=O)(C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)OC)O)C)C 658.80 unknown via CMAUP database
7-Methoxydeoxymorellin 70697915 Click to see 560.70 unknown via CMAUP database
CID 12313004 12313004 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C=O)O)C=CC(O2)(C)C)C 544.60 unknown via CMAUP database
Epigambogic acid 101406629 Click to see 628.70 unknown via CMAUP database
Gambogic Acid 9852185 Click to see 628.70 unknown via CMAUP database
Gambogic acid B 101377135 Click to see 674.80 unknown via CMAUP database
Gambogoic acid A 101377134 Click to see 660.80 unknown via CMAUP database
Isogambogic acid 70697925 Click to see 628.70 unknown via CMAUP database
S-Isogambogic acid 102402041 Click to see 628.70 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
Auricularine 441990 Click to see CC1=CC2C(C(C34C2(NC5=CC=CC=C53)N(CC4)C)C6=C(C7=CC=CC=C7N6)CCN(C)C)C(C1)(C)C 494.70 unknown https://doi.org/10.1016/0031-9422(92)80206-T
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Isoaurmillone 44257351 Click to see CC(=CCOC1=CC=C(C=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)OC)O)C 368.40 unknown https://doi.org/10.1016/0031-9422(83)80256-8
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
Auriculatin 5358847 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=C(C=C(C=C4)O)O)O)C=CC(O2)(C)C)C 420.50 unknown https://doi.org/10.1016/0031-9422(92)80206-T
Auriculin 5491651 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=C(C=C(C=C4)OC)O)O)C=CC(O2)(C)C)C 434.50 unknown https://doi.org/10.1016/0031-9422(92)80206-T
Isoauriculatin 5491650 Click to see 420.50 unknown https://doi.org/10.1016/0031-9422(92)80206-T
Millettin 157189 Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C5=C(O4)C=C(C=C5)O)O)C=CC(O2)(C)C)C 418.40 unknown https://doi.org/10.1016/0031-9422(92)80206-T
Warangalone 5379679 Click to see 404.50 unknown https://doi.org/10.1016/0031-9422(92)80206-T
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
Sumatrol 442824 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O 410.40 unknown https://doi.org/10.1016/0031-9422(92)80206-T

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