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Illigera luzonensis

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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 UUID6440469dc6ed2737310952
Scientific name Illigera luzonensis
Authority Merr.
First published in Publ. Bur. Sci. Gov. Lab. 17: 18 (1904)

Description Top

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Synonyms Top

Scientific name Authority First published in
Gronovia ternata Blanco Fl. Filip. [F.M. Blanco] 187 (1837).
Illigera appendiculata S.Vidal Sin. Gen. Pl. Leños. Filip. , Atlas: t. 48, f. F (1883)
Illigera cardiophylla Merr. Philipp. J. Sci., C 9: 292 (1914)
Illigera reticulata Merr. Philipp. J. Sci., C 9: 291 (1914)
Henschelia luzonensis C.Presl Reliq. Haenk. ii. 81. t. 63 (1831).
Illigera meyeniana Kunth ex Walp. Nov. Actorum Acad. Caes. Leop.-Carol. Nat. Cur. 19(Suppl. 1): 410 (1843)
Illigera ternata Dunn J. Linn. Soc., Bot. 38: 294 (1908)
Illigera pubescens Merr. Philipp. J. Sci., C 9: 446 (1914 publ. 1915)

Common names Top

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Language Common/alternative name
Arabic إليجيرية لوزونية
Japanese テングノハナ
Chinese 台湾青藤
Chinese 呂宋青藤

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001065358
Tropicos 15300080
KEW urn:lsid:ipni.org:names:170656-1
The Plant List tro-15300080
Open Tree Of Life 730771
NCBI Taxonomy 74946
IPNI 170656-1
iNaturalist 736902
GBIF 5549991
EOL 5393059

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
Climbing strategies of Taiwan climbers Chen PH, Chung AC, Lin HC, Yang SZ Bot Stud 22-Sep-2023
PMCID:PMC10516820
doi:10.1186/s40529-023-00399-4
PMID:37736799
Stem cambial variants of Taiwan lianas Yang SZ, Chen PH, Chen JJ Bot Stud 24-Sep-2022
PMCID:PMC9509506
doi:10.1186/s40529-022-00358-5
PMID:36153445
Current update on herbal sources of antithrombotic activity—a comprehensive review Subramani B, Sathiyarajeswaran P Egypt J Intern Med 07-Mar-2022
PMCID:PMC8899788
doi:10.1186/s43162-021-00090-9
PMID:35283622
Plant Alkaloids as Antiplatelet Agent: Drugs of the Future in the Light of Recent Developments Ain QU, Khan H, Mubarak MS, Pervaiz A Front Pharmacol 22-Sep-2016
PMCID:PMC5032615
doi:10.3389/fphar.2016.00292
PMID:27713699
Ethnomedicinal, Phytochemical and Pharmacological Profile of Anthriscus sylvestris as an Alternative Source for Anticancer Lignans Olaru OT, Niţulescu GM, Orțan A, Dinu-Pîrvu CE Molecules 17-Aug-2015
PMCID:PMC6331990
doi:10.3390/molecules200815003
PMID:26287153
Studies on the Alkaloids of <i>Illigera Luzonensis</i> (Presl.) Merr Sian‐Ling Liu Wiley 04-Jun-2015
doi:10.1002/JCCS.197700035
The Constituents of Roots and Stems of Illigera luzonensis and Their Anti-Platelet Aggregation Effects Huang CH, Chan YY, Kuo PC, Chen YF, Chang RJ, Chen IS, Wu SJ, Wu TS Int J Mol Sci 31-Jul-2014
PMCID:PMC4159803
doi:10.3390/ijms150813424
PMID:25089876
Aporphine alkaloids and cytotoxic lignans from the roots of Illigera luzonensis. Chen JJ, Hung HC, Sung PJ, Chen IS, Kuo WL Phytochemistry 01-Apr-2011
doi:10.1016/J.PHYTOCHEM.2010.12.015
PMID:21315382
Endangered vascular plants in Japan: —Present status and a proposal for conservation— Iwatsuki K Proc Jpn Acad Ser B Phys Biol Sci 01-Oct-2008
PMCID:PMC3722017
doi:10.2183/pjab/84.275
PMID:18941303
Bioactive alkaloids from Illigera luzonensis. Chen KS, Wu YC, Teng CM, Ko FN, Wu TS J Nat Prod 01-Jun-1997
doi:10.1021/NP9700735
PMID:9214740
[Alkaloids of Illigera luzonensis (Presl) Merr]. Wang SJ, Cheng SH Yakugaku Zasshi 01-Jan-1970
doi:10.1248/YAKUSHI1947.88.9_1148
PMID:5751283

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 / Aporphines
(+)-(S)-N-Acetylcaaverine 52937890 Click to see CC(=O)N1CCC2=CC(=C(C3=C2C1CC4=CC=CC=C43)O)OC 309.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
(+)-(S)-N-Butyrylcaaverine 52937790 Click to see CCCC(=O)N1CCC2=CC(=C(C3=C2C1CC4=CC=CC=C43)O)OC 337.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
(+)-(S)-N-Propionylcaaverine 52937889 Click to see CCC(=O)N1CCC2=CC(=C(C3=C2C1CC4=CC=CC=C43)O)OC 323.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
(+)-Launobine 5318956 Click to see COC1=C(C2=C(CC3C4=C2C5=C(C=C4CCN3)OCO5)C=C1)O 311.30 unknown https://doi.org/10.1021/NP9700735
https://doi.org/10.1002/JCCS.197700035
(+/-)-Dicentrine 630859 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)OC)OC)OCO3 339.40 unknown https://doi.org/10.1021/NP9700735
(12R)-17-methoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-18-ol 163023985 Click to see COC1=C(C2=C(CC3C4=C2C5=C(C=C4CCN3)OCO5)C=C1)O 311.30 unknown https://doi.org/10.1002/JCCS.197700035
(12S)-4,6,19,21-tetraoxa-13-azahexacyclo[10.10.1.02,10.03,7.016,23.018,22]tricosa-1(23),2(10),3(7),8,16,18(22)-hexaene 821351 Click to see C1CNC2CC3=C(C4=C2C1=CC5=C4OCO5)C6=C(C=C3)OCO6 309.30 unknown https://doi.org/10.1021/NP9700735
1,11-dimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-2,10-diol 12310425 Click to see COC1=C(C=CC2=C1C3=C4C(C2)NCCC4=CC(=C3OC)O)O 313.30 unknown https://doi.org/10.1021/NP9700735
1,2-Methylenedioxy-9-hydroxy-10-methoxynoraporphine 5089476 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C5=C(C=C4CCN3)OCO5)O 311.30 unknown https://doi.org/10.1021/NP9700735
https://doi.org/10.1248/YAKUSHI1947.88.9_1148
11,12-Dimethoxy-7-methyl-6,7,7a,8-tetrahydro-5h-[1,3]benzodioxolo[6,5,4-de]benzo[g]quinoline 273033 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)OC)OC)OCO3 339.40 unknown https://doi.org/10.1021/NP9700735
Actinodaphnine 160502 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C5=C(C=C4CCN3)OCO5)O 311.30 unknown https://doi.org/10.1248/YAKUSHI1947.88.9_1148
https://doi.org/10.1021/NP9700735
Bulbocapnine 12441 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)OC)O)OCO3 325.40 unknown https://doi.org/10.1021/NP9700735
Cassythicine 4440434 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)OC)O)OCO3 325.40 unknown https://doi.org/10.1021/NP9700735
Cassythicine 442194 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)OC)O)OCO3 325.40 unknown https://doi.org/10.1021/NP9700735
d-Bulbocapnine 9276 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)OC)O)OCO3 325.40 unknown https://doi.org/10.1021/NP9700735
Dicentrine 101300 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)OC)OC)OCO3 339.40 unknown https://doi.org/10.1021/NP9700735
Dicentrinone 177744 Click to see COC1=C(C=C2C(=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O)OC 335.30 unknown https://doi.org/10.1021/NP9700735
Hernovine 10425723 Click to see COC1=C(C=CC2=C1C3=C4C(C2)NCCC4=CC(=C3OC)O)O 313.30 unknown https://doi.org/10.1021/NP9700735
Launobine 177134 Click to see COC1=C(C2=C(CC3C4=C2C5=C(C=C4CCN3)OCO5)C=C1)O 311.30 unknown https://doi.org/10.1021/NP9700735
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown https://doi.org/10.1021/NP9700735
N-Hormyldehydrocaaverine 52937893 Click to see COC1=C(C2=C3C(=C1)CCN(C3=CC4=CC=CC=C42)C=O)O 293.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
O-Methylbulbocapnine 10246564 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)OC)OC)OCO3 339.40 unknown https://doi.org/10.1021/NP9700735
> Alkaloids and derivatives / Aporphines / Hydroxy-7-aporphines
(+)-(6aR,7R,E)-N-(2-Butenoyl)norushinsunine 52937892 Click to see CC=CC(=O)N1CCC2=CC3=C(C4=C2C1C(C5=CC=CC=C54)O)OCO3 349.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
(+)-(6aR,7R)-N-Butyrylnorushinsunine 52937891 Click to see CCCC(=O)N1CCC2=CC3=C(C4=C2C1C(C5=CC=CC=C54)O)OCO3 351.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
1-[(12R,13R)-13-hydroxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaen-11-yl]but-2-en-1-one 162910420 Click to see CC=CC(=O)N1CCC2=CC3=C(C4=C2C1C(C5=CC=CC=C54)O)OCO3 349.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see COC(=O)C1=CC=C(C=C1)O 152.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
> Benzenoids / Phenols / Methoxyphenols
N-Trans-feruloyltramine 5280537 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
2(3H)-Furanone, 4-(1,3-benzodioxol-5-ylmethyl)dihydro-3-((3,4,5-trimethoxyphenyl)methyl)- 2988 Click to see COC1=CC(=CC(=C1OC)OC)CC2C(COC2=O)CC3=CC4=C(C=C3)OCO4 400.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
Yatein 442835 Click to see COC1=CC(=CC(=C1OC)OC)CC2C(COC2=O)CC3=CC4=C(C=C3)OCO4 400.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
> Lignans, neolignans and related compounds / Lignan lactones
(-)-Deoxypodophyllotoxin 2203 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O 398.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
Deoxypodophyllotoxin 345501 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O 398.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(6beta,24R)-6-Hydroxystigmast-4-en-3-one 14769504 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C 428.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
6beta-Hydroxystigmast-4-en-3-one 9823926 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C 428.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
3-Methyl-4,8-dihydroxy-3,4-dihydroisocoumarin 169539 Click to see CC1C(C2=C(C(=CC=C2)O)C(=O)O1)O 194.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
trans-4-Hydroxymellein 10262028 Click to see CC1C(C2=C(C(=CC=C2)O)C(=O)O1)O 194.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
N-Phenethyl-3-phenyl-acrylamide 795855 Click to see C1=CC=C(C=C1)CCNC(=O)C=CC2=CC=CC=C2 251.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
N-phenethyl-3-phenylprop-2-enamide 583000 Click to see C1=CC=C(C=C1)CCNC(=O)C=CC2=CC=CC=C2 251.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
(Z)-3-(4-hydroxy-3,5-dimethoxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]prop-2-enamide 52937894 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)NCCC2=CC=C(C=C2)O 343.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
3-(4-hydroxy-3,5-dimethoxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]prop-2-enamide 25202112 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)NCCC2=CC=C(C=C2)O 343.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
n-cis-Feruloyltyramine 6440659 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
N-feruloyltyramine; Moupinamide 125213 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015
N-Trans-Sinapoyltyramine 25245053 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)NCCC2=CC=C(C=C2)O 343.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.015

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