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Details Top

Internal ID UUID644009153296a900692009
Scientific name Anaxagorea luzonensis
Authority A.Gray
First published in U.S. Expl. Exped., Phan. 1: 27 (1854)

Description Top

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Synonyms Top

Scientific name Authority First published in
Rhopalocarpus fruticosus Teijsm. & Binn. ex Miq. Ann. Mus. Bot. Lugduno-Batavi 2: 22. 1865
Anaxagorea fruticosa Scheff. Flora 52: 302 (1869)
Anaxagorea zeylanica Hook.f. & Thomson Fl. Ind. 1: 144 (1855)

Common names Top

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Language Common/alternative name
Chinese 蒙蒿子
Chinese 长柄灯台树
Chinese 吕宋蒙蒿子

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000533464
Tropicos 1602297
KEW urn:lsid:ipni.org:names:72039-1
The Plant List kew-2636375
Open Tree Of Life 842464
NCBI Taxonomy 235716
IUCN Red List 146907737
IPNI 72039-1
GBIF 3156868
EOL 1054122
CMAUP NPO1179

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
The Inhibitory Effect of KerraTM, KSTM, and MinozaTM on Human Papillomavirus Infection and Cervical Cancer Choowongkomon K, Choengpanya K, Pientong C, Ekalaksananan T, Talawat S, Srathong P, Chuerduangphui J Medicina (Kaunas) 14-Dec-2023
PMCID:PMC10745032
doi:10.3390/medicina59122169
PMID:38138272
Phosphodiesterase 5 and Arginase Inhibitory Activities of the Extracts from Some Members of Nelumbonaceae and Nymphaeaceae Families Panklai T, Suphrom N, Temkitthawon P, Totoson P, Chootip K, Yang XL, Ge HM, Yao ZJ, Chaichamnong N, Ingkaninan K, Girard C Molecules 02-Aug-2023
PMCID:PMC10420992
doi:10.3390/molecules28155821
PMID:37570790
Analytical determination, antioxidant and anti-inflammatory activities of Bhamrung-Lohit a traditional Thai medicine Panchakul C, Thongdeeying P, Itharat A, Pipatrattanaseree W, Kongkwamcharoen C, Davies NM Res Pharm Sci 01-Jun-2023
PMCID:PMC10443669
doi:10.4103/1735-5362.378091
PMID:37614616
Xanthones: Biosynthesis and Trafficking in Plants, Fungi and Lichens Badiali C, Petruccelli V, Brasili E, Pasqua G Plants (Basel) 04-Feb-2023
PMCID:PMC9967055
doi:10.3390/plants12040694
PMID:36840041
Model yeast as a versatile tool to examine the antioxidant and anti-ageing potential of flavonoids, extracted from medicinal plants Zahoor H, Watchaputi K, Hata J, Pabuprapap W, Suksamrarn A, Chua LS, Soontorngun N Front Pharmacol 02-Sep-2022
PMCID:PMC9479101
doi:10.3389/fphar.2022.980066
PMID:36120300
DNA Barcoding Medicinal Plant Species from Indonesia Cahyaningsih R, Compton LJ, Rahayu S, Magos Brehm J, Maxted N Plants (Basel) 21-May-2022
PMCID:PMC9147630
doi:10.3390/plants11101375
PMID:35631799
Phytochemical Screening by LC-ESI-MS/MS and Effect of the Ethyl Acetate Fraction from Leaves and Stems of Jatropha macrantha Müll Arg. on Ketamine-Induced Erectile Dysfunction in Rats Tinco-Jayo JA, Aguilar-Felices EJ, Enciso-Roca EC, Arroyo-Acevedo JL, Herrera-Calderon O Molecules 25-Dec-2021
PMCID:PMC8746923
doi:10.3390/molecules27010115
PMID:35011347
Serial Section-Based Three-Dimensional Reconstruction of Anaxagorea (Annonaceae) Carpel Vasculature and Implications for the Morphological Relationship between the Carpel and the Ovule Li Y, Du W, Chen Y, Wang S, Wang XF Plants (Basel) 19-Oct-2021
PMCID:PMC8540277
doi:10.3390/plants10102221
PMID:34686030
Trienone analogs of curcuminoids induce fetal hemoglobin synthesis via demethylation at Gγ-globin gene promoter Nuamsee K, Chuprajob T, Pabuprapap W, Jintaridth P, Munkongdee T, Phannasil P, Vadolas J, Chaichompoo P, Suksamrarn A, Svasti S Sci Rep 20-Apr-2021
PMCID:PMC8058333
doi:10.1038/s41598-021-87738-2
PMID:33879818
Evaluation of estrogenic potency of a standardized hops extract on mammary gland biology and on MNU-induced mammary tumor growth in rats Keiler AM, Macejova D, Dietz BM, Bolton JL, Pauli GF, Chen SN, van Breemen RB, Nikolic D, Goerl F, Muders MH, Zierau O, Vollmer G J Steroid Biochem Mol Biol 28-Sep-2017
PMCID:PMC5760272
doi:10.1016/j.jsbmb.2017.09.020
PMID:28964928
A mega-phylogeny of the Annonaceae: taxonomic placement of five enigmatic genera and support for a new tribe, Phoenicantheae Guo X, Tang CC, Thomas DC, Couvreur TL, Saunders RM Sci Rep 04-Aug-2017
PMCID:PMC5544705
doi:10.1038/s41598-017-07252-2
PMID:28779135
ChemInform Abstract: Studies on the Constituents of Anaxagorea luzonensis A. Gray. Ryoko Gonda, Tadahiro Takeda, Toshiyuki Akiyama Wiley 31-May-2010
doi:10.1002/CHIN.200052210
The pharmacognosy of Humulus lupulus L. (hops) with an emphasis on estrogenic properties Chadwick LR, Pauli GF, Farnsworth NR Phytomedicine 01-Jul-2005
PMCID:PMC1852439
doi:10.1016/j.phymed.2004.07.006
PMID:16360942
Studies on the constituents of Anaxagorea luzonensis A. GRAY. Gonda R, Takeda T, Akiyama T Chem Pharm Bull (Tokyo) 01-Aug-2000
doi:10.1248/CPB.48.1219
PMID:10959592

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
> Alkaloids and derivatives / 6,6a-secoaporphines
Phenanthro(3,4-d)-1,3-dioxole-5-ethanamine, N,N-dimethyl- 161379 Click to see CN(C)CCC1=CC2=C(C3=C1C=CC4=CC=CC=C43)OCO2 293.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
beta-Cyclanoline 5316230 Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=C(C2)C(=C(C=C4)OC)O)O)OC 342.40 unknown via CMAUP database
Cyclanoline 3082134 Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=C(C2)C(=C(C=C4)OC)O)O)OC 342.40 unknown via CMAUP database
Jatrorrhizine 72323 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)O)OC)OC 338.40 unknown via CMAUP database
> Lignans, neolignans and related compounds
(1S,14S)-9,20,25-trimethoxy-15-methyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaen-21-ol 10531530 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=CC(=C(C=C7CCN6)OC)O3)C=C5)O)OC 594.70 unknown via CMAUP database
Fangchinoline 73481 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC 608.70 unknown via CMAUP database
Fenfangjine C 102121829 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=CC(=C(C=C7CC[N+]6(C)[O-])OC)O3)C=C5)O)OC 624.70 unknown via CMAUP database
N2-Methylfangchinoline 14753650 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CC[N+]6(C)C)OC)O)OC)OC 623.80 unknown via CMAUP database
N2-Methyltetrandrine 14753654 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CC[N+]6(C)C)OC)OC)OC)OC 637.80 unknown via CMAUP database
O-Methylberbamine 5351212 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown via CMAUP database
Tetrandrine 73078 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown via CMAUP database
Thalrugosine 100257 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC 608.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3,5-Trihydroxyxanthone 5281663 Click to see C1=CC2=C(C(=C1)O)OC3=CC(=CC(=C3C2=O)O)O 244.20 unknown https://doi.org/10.1248/CPB.48.1219
https://doi.org/10.1002/CHIN.200052210
1,3,5,6-Tetrahydroxyxanthone 5479774 Click to see C1=CC(=C(C2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)O 260.20 unknown https://doi.org/10.1002/CHIN.200052210
1,3,6-Trihydroxy-5-methoxyxanthone 5493675 Click to see COC1=C(C=CC2=C1OC3=CC(=CC(=C3C2=O)O)O)O 274.22 unknown https://doi.org/10.1002/CHIN.200052210
3,6-Dihydroxy-1,5-dimethoxyxanthen-9-one 54423682 Click to see COC1=CC(=CC2=C1C(=O)C3=C(O2)C(=C(C=C3)O)OC)O 288.25 unknown https://doi.org/10.1002/CHIN.200052210
9H-Xanthen-9-one, 3,5-dihydroxy-1-methoxy- 5479771 Click to see COC1=CC(=CC2=C1C(=O)C3=C(O2)C(=CC=C3)O)O 258.23 unknown https://doi.org/10.1002/CHIN.200052210
Gentisein 5281635 Click to see C1=CC2=C(C=C1O)C(=O)C3=C(C=C(C=C3O2)O)O 244.20 unknown https://doi.org/10.1248/CPB.48.1219
https://doi.org/10.1002/CHIN.200052210
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
1,3,5-Trihydroxy-2-prenyl-9H-xanthene-9-one 9995643 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC=C3O)O)C 312.30 unknown https://doi.org/10.1002/CHIN.200052210
1,3,5-Trihydroxy-6-methoxy-2-(3-methylbut-2-enyl)xanthen-9-one 10617258 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC(=C3O)OC)O)C 342.30 unknown https://doi.org/10.1002/CHIN.200052210
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
1,3,5-Trihydroxy-4-(3-hydroxy-3-methylbutyl)xanthone 10806296 Click to see CC(C)(CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C(=CC=C3)O)O 330.30 unknown https://doi.org/10.1002/CHIN.200052210
1,3,5-Trihydroxy-4-(3-methylbut-2-en-1-yl)-9H-xanthen-9-one 10335672 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C(=CC=C3)O)C 312.30 unknown https://doi.org/10.1002/CHIN.200052210
1,3,6-Trihydroxy-4-(3-methylbut-2-enyl)xanthen-9-one 10591176 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C=C(C=C3)O)C 312.30 unknown https://doi.org/10.1002/CHIN.200052210
1,3,6-Trihydroxy-5-methoxy-4-(3-methylbut-2-enyl)xanthen-9-one 10854769 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C(=C(C=C3)O)OC)C 342.30 unknown https://doi.org/10.1002/CHIN.200052210
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
3-[4-[[(1S)-7-(7-hydroxy-6-methoxy-2-methylisoquinolin-2-ium-8-yl)oxy-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenoxy]-4-methoxybenzaldehyde 10675588 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)C=O)OC)OC5=C6C=[N+](C=CC6=CC(=C5O)OC)C)OC 621.70 unknown via CMAUP database
8-[[(1S)-1-[[4-[5-(hydroxymethyl)-2-methoxyphenoxy]phenyl]methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-7-yl]oxy]-6-methoxy-2-methylisoquinolin-2-ium-7-ol 639560 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CO)OC)OC5=C6C=[N+](C=CC6=CC(=C5O)OC)C)OC 623.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+/-)-Taxifolin 471 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1002/CHIN.200052210
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1002/CHIN.200052210
https://doi.org/10.1248/CPB.48.1219
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown https://doi.org/10.1002/CHIN.200052210
https://doi.org/10.1248/CPB.48.1219
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
Gancaonin P 5481966 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O)C 370.40 unknown https://doi.org/10.1248/CPB.48.1219
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,7-Trihydroxy-2-(4-hydroxy-2-methoxyphenyl)chromen-4-one 10018620 Click to see COC1=C(C=CC(=C1)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 316.26 unknown https://doi.org/10.1002/CHIN.200052210
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/10.1002/CHIN.200052210
https://doi.org/10.1248/CPB.48.1219
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1248/CPB.48.1219
https://doi.org/10.1002/CHIN.200052210
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1248/CPB.48.1219
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44259225 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1248/CPB.48.1219
Quercetin 7-O-glucoside 5381351 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1248/CPB.48.1219
> 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/10.1248/CPB.48.1219
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-O-Methylorobol 5319744 Click to see COC1=C(C=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O 300.26 unknown https://doi.org/10.1248/CPB.48.1219
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
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/10.1002/CHIN.200052210
https://doi.org/10.1248/CPB.48.1219
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
Stephaflavone A 12087758 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)C4=C(OC5=CC(=CC(=C5C4=O)O)OC)C6=CC=C(C=C6)OC)O 594.60 unknown via CMAUP database
Stephaflavone B 5324248 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)C4=C(OC5=CC(=CC(=C5C4=O)O)OC)C6=CC=C(C=C6)O)O 580.50 unknown via CMAUP database

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