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Calophyllum polyanthum

Calophyllum polyanthum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID64400eef3d977868512805
Scientific name Calophyllum polyanthum
Authority Wall. ex Planch. & Triana
First published in Mém. Soc. Phys. Genève 12(2): 423. 1849

Description Top

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Synonyms Top

Scientific name Authority First published in
Calophyllum elatum Bedd. Rep. Conservator Forests 1863-1864: 31 (1864)
Calophyllum smilesianum Craib Bull. Misc. Inform. Kew 1924: 85 (1924)
Calophyllum smilesianum var. luteum Craib Bull. Misc. Inform. Kew 1924: 86 1924
Calophyllum williamsianum Craib Bull. Misc. Inform. Kew 1924: 86 (1924)

Common names Top

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Language Common/alternative name
Bengali কামদেব (উদ্ভিদ)
Bengali কামদেব
Kannada ಕೂವೆ ಮರ
Malayalam പുന്നപ്പൈൻ
Chinese 滇南红厚壳
Chinese 云南胡桐
Chinese 滇南紅厚殻

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
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000581286
KEW urn:lsid:ipni.org:names:427265-1
The Plant List kew-2693442
Open Tree Of Life 3915311
NCBI Taxonomy 1679397
IPNI 427265-1
iNaturalist 569103
GBIF 5556276
USDA GRIN 411480
Wikipedia Calophyllum_polyanthum

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
Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India? Kumar BM Agrofor Syst 07-Apr-2023
PMCID:PMC10081327
doi:10.1007/s10457-023-00821-7
PMID:37193256
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
Assessing the effectiveness of community managed forests for plant diversity conservation in Meghalaya, Northeast India Mir AH, Sarma K, Upadhaya K Plant Divers 15-Dec-2021
PMCID:PMC9209898
doi:10.1016/j.pld.2021.11.010
PMID:35769587
Naturally Occurring Calanolides: Occurrence, Biosynthesis, and Pharmacological Properties Including Therapeutic Potential Nahar L, Talukdar AD, Nath D, Nath S, Mehan A, Ismail FM, Sarker SD Molecules 28-Oct-2020
PMCID:PMC7663239
doi:10.3390/molecules25214983
PMID:33126458
The Arbuscular Mycorrhizal Fungus Funneliformis mosseae Alters Bacterial Communities in Subtropical Forest Soils during Litter Decomposition Gui H, Purahong W, Hyde KD, Xu J, Mortimer PE Front Microbiol 20-Jun-2017
PMCID:PMC5476864
doi:10.3389/fmicb.2017.01120
PMID:28676797
Arbuscular mycorrhiza enhance the rate of litter decomposition while inhibiting soil microbial community development Gui H, Hyde K, Xu J, Mortimer P Sci Rep 08-Feb-2017
PMCID:PMC5296878
doi:10.1038/srep42184
PMID:28176855
Photosynthesis and Photosynthetic Electron Flow in the Alpine Evergreen Species Quercus guyavifolia in Winter Huang W, Hu H, Zhang SB Front Plant Sci 20-Oct-2016
PMCID:PMC5071824
doi:10.3389/fpls.2016.01511
PMID:27812359
Molecular Mechanisms of Phosphorus Metabolism and Transport during Leaf Senescence Stigter KA, Plaxton WC Plants (Basel) 16-Dec-2015
PMCID:PMC4844268
doi:10.3390/plants4040773
PMID:27135351
Isolation, Bioactivity, and Production of ortho-Hydroxydaidzein and ortho-Hydroxygenistein Chang TS Int J Mol Sci 03-Apr-2014
PMCID:PMC4013590
doi:10.3390/ijms15045699
PMID:24705463
Medicinal plants from swidden fallows and sacred forest of the Karen and the Lawa in Thailand Junsongduang A, Balslev H, Inta A, Jampeetong A, Wangpakapattanawong P J Ethnobiol Ethnomed 24-Jun-2013
PMCID:PMC3702467
doi:10.1186/1746-4269-9-44
PMID:23800255
Chromanone Derivatives from the Pericarps of <i>Calophyllum polyanthum</i> Huan Wang, Qian‐Yun Sun, Fu‐Mei Yang, Chun‐Lin Long, Yue‐Hu Wang, Gui‐Hua Tang, Fu‐Wei Zhao, Hong‐Mei Niu, Qiao‐Qin Huang, Jin‐Jin Xu, Yusuke Wataya, Li‐Juan Ma Wiley 11-Nov-2010
doi:10.1002/HLCA.201000066
Monocyclic Phenolic Acids; Hydroxy- and Polyhydroxybenzoic Acids: Occurrence and Recent Bioactivity Studies Khadem S, Marles RJ Molecules 08-Nov-2010
PMCID:PMC6259451
doi:10.3390/molecules15117985
PMID:21060304
Two new 4-arylcoumarins from the seeds of Calophyllum polyanthum. Zhong H, Ruan JL, Yao QQ J Asian Nat Prod Res 01-Jul-2010
doi:10.1080/10286020.2010.484806
PMID:20628934
Two pyranocoumarins from the seeds of Calophyllum polyanthum. Ma CH, Chen B, Qi HY, Li BG, Zhang GL J Nat Prod 01-Sep-2004
doi:10.1021/NP0499158
PMID:15387670

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1080/10286020.2010.484806
https://doi.org/10.1021/NP0499158
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
3,5-Dihydroxy-4-methoxybenzoic acid 78016 Click to see COC1=C(C=C(C=C1O)C(=O)O)O 184.15 unknown https://doi.org/10.1021/NP0499158
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1021/NP0499158
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
3,5-Dimethoxybenzoic Acid 14332 Click to see COC1=CC(=CC(=C1)C(=O)O)OC 182.17 unknown https://doi.org/10.1021/NP0499158
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3-Hydroxy-4-methoxybenzoic acid 12575 Click to see COC1=C(C=C(C=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1080/10286020.2010.484806
4-Methoxysalicylic acid 75231 Click to see COC1=CC(=C(C=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1021/NP0499158
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1021/NP0499158
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1021/NP0499158
> 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/10.1021/NP0499158
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/10.1021/NP0499158
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP0499158
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP0499158
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
(3R)-3-[(2S,3R)-5-hydroxy-7-methoxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-3,4-dihydro-2H-chromen-6-yl]hexanoic acid 163002112 Click to see CCCC(CC(=O)O)C1=C(C(=C2C(=C1O)CC(C(O2)C)C)CC=C(C)C)OC 390.50 unknown https://doi.org/10.1002/HLCA.201000066
3-[5-hydroxy-7-methoxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-3,4-dihydro-2H-chromen-6-yl]hexanoic acid 163002111 Click to see CCCC(CC(=O)O)C1=C(C(=C2C(=C1O)CC(C(O2)C)C)CC=C(C)C)OC 390.50 unknown https://doi.org/10.1002/HLCA.201000066
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
(3R)-3-[(2R,3S)-5-hydroxy-7-methoxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-4-oxo-2,3-dihydrochromen-6-yl]hexanoic acid 163188275 Click to see CCCC(CC(=O)O)C1=C(C(=C2C(=C1O)C(=O)C(C(O2)C)C)CC=C(C)C)OC 404.50 unknown https://doi.org/10.1002/HLCA.201000066
3-[5-Hydroxy-7-methoxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-4-oxo-2,3-dihydrochromen-6-yl]hexanoic acid 75576402 Click to see CCCC(CC(=O)O)C1=C(C(=C2C(=C1O)C(=O)C(C(O2)C)C)CC=C(C)C)OC 404.50 unknown https://doi.org/10.1002/HLCA.201000066
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
(3R)-3-[(2R,3R)-5-hydroxy-2,3,8,8-tetramethyl-4-oxo-2,3-dihydropyrano[2,3-h]chromen-6-yl]octanoic acid 162889244 Click to see CCCCCC(CC(=O)O)C1=C2C(=C3C(=C1O)C(=O)C(C(O3)C)C)C=CC(O2)(C)C 416.50 unknown https://doi.org/10.1002/HLCA.201000066
(3R)-3-[(2R,3S)-5-hydroxy-2,3,8,8-tetramethyl-4-oxo-2,3-dihydropyrano[2,3-h]chromen-6-yl]octanoic acid 162889243 Click to see CCCCCC(CC(=O)O)C1=C2C(=C3C(=C1O)C(=O)C(C(O3)C)C)C=CC(O2)(C)C 416.50 unknown https://doi.org/10.1002/HLCA.201000066
(3R)-3-[(7R,8R)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]-3-phenylpropanoic acid 162850349 Click to see CC1C(OC2=C(C1=O)C(=C3C=CC(OC3=C2C(CC(=O)O)C4=CC=CC=C4)(C)C)O)C 422.50 unknown https://doi.org/10.1002/HLCA.201000066
(3R)-3-[(7R,8S)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]hexanoic acid 23250748 Click to see CCCC(CC(=O)O)C1=C2C(=C(C3=C1OC(C(C3=O)C)C)O)C=CC(O2)(C)C 388.50 unknown https://doi.org/10.1002/HLCA.201000066
(3R)-3-[(7R,8S)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]octanoic acid 163030896 Click to see CCCCCC(CC(=O)O)C1=C2C(=C(C3=C1OC(C(C3=O)C)C)O)C=CC(O2)(C)C 416.50 unknown https://doi.org/10.1002/HLCA.201000066
(3S)-3-[(2S,3R)-5-hydroxy-2,3,8,8-tetramethyl-4-oxo-2,3-dihydropyrano[2,3-h]chromen-10-yl]hexanoic acid 162881125 Click to see CCCC(CC(=O)O)C1=CC(OC2=C1C3=C(C(=C2)O)C(=O)C(C(O3)C)C)(C)C 388.50 unknown https://doi.org/10.1002/HLCA.201000066
(3S)-3-[(7S,8S)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]hexanoic acid 51414569 Click to see CCCC(CC(=O)O)C1=C2C(=C(C3=C1OC(C(C3=O)C)C)O)C=CC(O2)(C)C 388.50 unknown https://doi.org/10.1002/HLCA.201000066
3-(5-Hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl)-3-phenylpropanoic acid 12302861 Click to see CC1C(OC2=C(C1=O)C(=C3C=CC(OC3=C2C(CC(=O)O)C4=CC=CC=C4)(C)C)O)C 422.50 unknown https://doi.org/10.1002/HLCA.201000066
3-(5-Hydroxy-2,3,8,8-tetramethyl-4-oxo-2,3-dihydropyrano[2,3-h]chromen-10-yl)hexanoic acid 162881124 Click to see CCCC(CC(=O)O)C1=CC(OC2=C1C3=C(C(=C2)O)C(=O)C(C(O3)C)C)(C)C 388.50 unknown https://doi.org/10.1002/HLCA.201000066
3-(5-Hydroxy-2,3,8,8-tetramethyl-4-oxo-2,3-dihydropyrano[2,3-h]chromen-6-yl)octanoic acid 75576401 Click to see CCCCCC(CC(=O)O)C1=C2C(=C3C(=C1O)C(=O)C(C(O3)C)C)C=CC(O2)(C)C 416.50 unknown https://doi.org/10.1002/HLCA.201000066
CID 12300170 12300170 Click to see CCCCCC(CC(=O)O)C1=C2C(=C(C3=C1OC(C(C3=O)C)C)O)C=CC(O2)(C)C 416.50 unknown https://doi.org/10.1002/HLCA.201000066
Isoapetalic acid 341189 Click to see CCCC(CC(=O)O)C1=C2C(=C(C3=C1OC(C(C3=O)C)C)O)C=CC(O2)(C)C 388.50 unknown https://doi.org/10.1002/HLCA.201000066
methyl (3S)-3-[(7S,8S)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]hexanoate 162921532 Click to see CCCC(CC(=O)OC)C1=C2C(=C(C3=C1OC(C(C3=O)C)C)O)C=CC(O2)(C)C 402.50 unknown https://doi.org/10.1002/HLCA.201000066
Methyl 3-(5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl)hexanoate 73802883 Click to see CCCC(CC(=O)OC)C1=C2C(=C(C3=C1OC(C(C3=O)C)C)O)C=CC(O2)(C)C 402.50 unknown https://doi.org/10.1002/HLCA.201000066
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Orobol 5281801 Click to see C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O)O 286.24 unknown https://doi.org/10.1021/NP0499158
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavones
6,7-Dihydroxy-4-(4-methoxyphenyl)-2H-chromen-2-one 162920871 Click to see COC1=CC=C(C=C1)C2=CC(=O)OC3=CC(=C(C=C23)O)O 284.26 unknown https://doi.org/10.1080/10286020.2010.484806
7-Hydroxy-4-(4-hydroxyphenyl)-6,8-dimethoxychromen-2-one 46856032 Click to see COC1=C(C(=C2C(=C1)C(=CC(=O)O2)C3=CC=C(C=C3)O)OC)O 314.29 unknown https://doi.org/10.1080/10286020.2010.484806
7-Hydroxy-4-(4-methoxyphenyl)chromen-2-one 5350173 Click to see COC1=CC=C(C=C1)C2=CC(=O)OC3=C2C=CC(=C3)O 268.26 unknown https://doi.org/10.1080/10286020.2010.484806
7-Hydroxy-6,8-dimethoxy-4-(4-methoxyphenyl)chromen-2-one 46856033 Click to see COC1=CC=C(C=C1)C2=CC(=O)OC3=C(C(=C(C=C23)OC)O)OC 328.30 unknown https://doi.org/10.1080/10286020.2010.484806
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
(2R,3R,10R)-5-hydroxy-2,3-dimethyl-6-(3-methylbut-2-enyl)-10-phenyl-2,3,9,10-tetrahydropyrano[2,3-h]chromene-4,8-dione 162978900 Click to see CC1C(OC2=C(C1=O)C(=C(C3=C2C(CC(=O)O3)C4=CC=CC=C4)CC=C(C)C)O)C 406.50 unknown https://doi.org/10.1021/NP0499158
(2R,3S,10R)-5-hydroxy-2,3-dimethyl-6-(3-methylbut-2-enyl)-10-phenyl-2,3,9,10-tetrahydropyrano[2,3-h]chromene-4,8-dione 162978901 Click to see CC1C(OC2=C(C1=O)C(=C(C3=C2C(CC(=O)O3)C4=CC=CC=C4)CC=C(C)C)O)C 406.50 unknown https://doi.org/10.1021/NP0499158
5-Hydroxy-2,3-dimethyl-6-(3-methylbut-2-enyl)-10-phenyl-2,3,9,10-tetrahydropyrano[2,3-h]chromene-4,8-dione 72747944 Click to see CC1C(OC2=C(C1=O)C(=C(C3=C2C(CC(=O)O3)C4=CC=CC=C4)CC=C(C)C)O)C 406.50 unknown https://doi.org/10.1021/NP0499158

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