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Details Top

Internal ID UUID64401cbbdc16d067516428
Scientific name Fissistigma glaucescens
Authority Merr.
First published in Philipp. J. Sci. 15: 132 (1919)

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Synonyms Top

Scientific name Authority First published in
Fissistigma obtusifolium Merr. Philipp. J. Sci. 21: 242 (1922)
Melodorum glaucescens Hance J. Bot. 19: 112 (1881)

Common names Top

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Language Common/alternative name
Vietnamese cách thư lá trắng
Chinese 乌骨藤
Chinese 白叶瓜馥木
Chinese 裏白瓜馥木
Chinese 大样酒饼藤
Chinese 大棕古猩峡
Chinese 火索藤

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China Southeast
      • Hainan
    • Eastern Asia
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000691145
Tropicos 1602636
KEW urn:lsid:ipni.org:names:73020-1
The Plant List kew-2813095
Open Tree Of Life 656189
NCBI Taxonomy 296847
IPNI 73020-1
iNaturalist 708916
GBIF 3157333
EOL 1054054

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
Fissistigma oldhamii (Hemsl.) Merr.: Ethnomedicinal, Phytochemistry, and Pharmacological Aspects Bailly C Plants (Basel) 07-Dec-2023
PMCID:PMC10748316
doi:10.3390/plants12244094
PMID:38140421
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
Xiaoaiping improves the general state of rats with malignant ascites secondary to gastric cancer by blocking the TGF-β1 signaling pathway Xu W, Liu Y Am J Transl Res 15-Jan-2023
PMCID:PMC9908485
PMID:36777819
Mechanism-based targeting of cardiac arrhythmias by phytochemicals and medicinal herbs: A comprehensive review of preclinical and clinical evidence Soltani D, Azizi B, Rahimi R, Talasaz AH, Rezaeizadeh H, Vasheghani-Farahani A Front Cardiovasc Med 29-Sep-2022
PMCID:PMC9559844
doi:10.3389/fcvm.2022.990063
PMID:36247473
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
Screening an In-House Isoquinoline Alkaloids Library for New Blockers of Voltage-Gated Na+ Channels Using Voltage Sensor Fluorescent Probes: Hits and Biases Coquerel Q, Legendre C, Frangieh J, Waard SD, Montnach J, Cmarko L, Khoury J, Hassane CS, Bréard D, Siegler B, Fajloun Z, De Pomyers H, Mabrouk K, Weiss N, Henrion D, Richomme P, Mattei C, Waard MD, Le Ray AM, Legros C Molecules 28-Jun-2022
PMCID:PMC9268414
doi:10.3390/molecules27134133
PMID:35807390
Potent Inhibition of Human Cytochrome P450 3A4 by Biflavone Components from Ginkgo Biloba and Selaginella Tamariscina Wang B, Shi C, Feng L, Pan W, Tian XG, Sun CP, Wang C, Ning J, Lv X, Wang Y, Yuan QH, Guan RX, Zhang HL, Ma XC, Ma TH Front Pharmacol 28-Feb-2022
PMCID:PMC8920304
doi:10.3389/fphar.2022.856784
PMID:35295338
A review on plants and herbal components with antiarrhythmic activities and their interaction with current cardiac drugs Beik A, Joukar S, Najafipour H J Tradit Complement Med 06-Apr-2020
PMCID:PMC7340875
doi:10.1016/j.jtcme.2020.03.002
PMID:32670823
Seasonal variations in group leaf characteristics in species with red young leaves Zhang TJ, Tian XS, Liu XT, Huang XD, Peng CL Sci Rep 11-Nov-2019
PMCID:PMC6848096
doi:10.1038/s41598-019-52753-x
PMID:31712569
Natural Antispasmodics: Source, Stereochemical Configuration, and Biological Activity Martínez-Pérez EF, Juárez ZN, Hernández LR, Bach H Biomed Res Int 08-Oct-2018
PMCID:PMC6196993
doi:10.1155/2018/3819714
PMID:30402474
Liriodenine enhances radiosensitivity in esophageal cancer ECA-109 cells by inducing apoptosis and G2/M arrest Wu G, Chen G, Zhou J, Zhu H, Chu J, Zhang F Oncol Lett 02-Aug-2018
PMCID:PMC6144705
doi:10.3892/ol.2018.9253
PMID:30250568
Alkaloids from the Leaves of <i>Fissistigma Glaucescens</i> Wen‐Li Lo, Fang‐Rong Chang, Yang‐Chang Wu Wiley 01-May-2015
doi:10.1002/JCCS.200000172
Liriodenine induces the apoptosis of human laryngocarcinoma cells via the upregulation of p53 expression LI L, XU Y, WANG B Oncol Lett 29-Dec-2014
PMCID:PMC4314988
doi:10.3892/ol.2014.2834
PMID:25663867
The Environment, Not Space, Dominantly Structures the Landscape Patterns of the Richness and Composition of the Tropical Understory Vegetation Hu YH, Sheng DY, Xiang YZ, Yang ZJ, Xu DP, Zhang NN, Shi LL PLoS One 22-Nov-2013
PMCID:PMC3838366
doi:10.1371/journal.pone.0081308
PMID:24278417
Kuafumine, a Novel Cytotoxic Oxoaporphine Alkaloid from Fissistigma glausescens Tian-Shung Wu, Yang-Chang Wu, Sheng-Teh Lu, Kuo-Hsiung Lee The Japan Institute of Heterocyclic Chemistry 16-Feb-2009
doi:10.3987/R-1987-01-0009

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
> Alkaloids and derivatives / 6,6a-secoaporphines
Atherosperminine 96918 Click to see CN(C)CCC1=CC(=C(C2=C1C=CC3=CC=CC=C32)OC)OC 309.40 unknown https://doi.org/10.1016/S0031-9422(00)82561-3
https://doi.org/10.1016/0014-2999(93)90099-4
Fissicesine N-oxide 14635658 Click to see C[N+](C)(CCC1=CC(=C(C2=C1C=CC3=C2C=CC=C3OC)OC)OC)[O-] 355.40 unknown https://doi.org/10.1016/0031-9422(90)83088-I
N-noratherosperminine 10957406 Click to see CNCCC1=CC(=C(C2=C1C=CC3=CC=CC=C32)OC)OC 295.40 unknown https://doi.org/10.1016/S0031-9422(00)82561-3
N,N-dimethyl-2-(3,4,8-trimethoxyphenanthren-1-yl)ethanamine 14635657 Click to see CN(C)CCC1=CC(=C(C2=C1C=CC3=C2C=CC=C3OC)OC)OC 339.40 unknown https://doi.org/10.1016/0031-9422(90)83088-I
> Alkaloids and derivatives / Aporphines
(-)-Crebanine 139080500 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5OC)OC)OCO3.CN1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5OC)OC)OCO3 678.80 unknown https://doi.org/10.1016/S0031-9422(00)82561-3
(12R)-15,16-dimethoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaene 13996837 Click to see COC1=C(C2=C(C=C1)C3=C4C(C2)NCCC4=CC5=C3OCO5)OC 325.40 unknown https://doi.org/10.1016/S0031-9422(00)82561-3
1-(16-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-11-yl)ethanone 162895328 Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5)OC)OCO3 337.40 unknown https://doi.org/10.1002/JCCS.200000172
1-(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-11-yl)ethanone 163041376 Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=C4C=C(C=C5)OC)OCO3 337.40 unknown https://doi.org/10.1002/JCCS.200000172
1-[(12R)-16-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-11-yl]ethanone 10246449 Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5)OC)OCO3 337.40 unknown https://doi.org/10.1002/JCCS.200000172
1-Methoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-2-ol 12308663 Click to see COC1=C(C=C2CCNC3C2=C1C4=CC=CC=C4C3)O 267.32 unknown https://doi.org/10.1016/S0031-9422(00)82561-3
1,2-Methylenedioxy-9-methoxynoraporphine 431059 Click to see COC1=CC2=C(C=C1)C3=C4C(C2)NCCC4=CC5=C3OCO5 295.30 unknown https://doi.org/10.1002/JCCS.200000172
15-Hydroxy-16-methoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,9,11,14(19),15,17-octaen-13-one 163035870 Click to see COC1=C(C2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O)O 321.30 unknown https://doi.org/10.1002/JCCS.200000172
15,16-Dihydroxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,9,11,14(19),15,17-octaen-13-one 162954576 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=C3C=CC(=C5O)O 307.26 unknown https://doi.org/10.1016/S0031-9422(00)82561-3
15,16-Dimethoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaene 13996836 Click to see COC1=C(C2=C(C=C1)C3=C4C(C2)NCCC4=CC5=C3OCO5)OC 325.40 unknown https://doi.org/10.1016/S0031-9422(00)82561-3
7,15,16-Trimethoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1,6,8(20),9,11,14(19),15,17-octaen-13-one 162894764 Click to see COC1=C(C2=C(C=C1)C3=C4C(=C(C5=C3C(=NC=C5)C2=O)OC)OCO4)OC 365.30 unknown https://doi.org/10.1002/JCCS.200000172
https://doi.org/10.3987/R-1987-01-0009
8H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinolin-8-one, 9,10-dimethoxy- 3084713 Click to see COC1=C(C2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O)OC 335.30 unknown https://doi.org/10.1002/JCCS.200000172
https://doi.org/10.1016/S0031-9422(00)82561-3
Asimilobine 160875 Click to see COC1=C(C=C2CCNC3C2=C1C4=CC=CC=C4C3)O 267.32 unknown https://doi.org/10.1016/S0031-9422(00)82561-3
Atherospermidine 77514 Click to see COC1=C2C(=C3C4=CC=CC=C4C(=O)C5=NC=CC1=C35)OCO2 305.30 unknown https://doi.org/10.1002/JCCS.200000172
Lanuginosine 97622 Click to see COC1=CC2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O 305.30 unknown https://doi.org/10.1002/JCCS.200000172
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/10.1002/JCCS.200000172
Xylopine 160503 Click to see COC1=CC2=C(C=C1)C3=C4C(C2)NCCC4=CC5=C3OCO5 295.30 unknown https://doi.org/10.1002/JCCS.200000172
> Alkaloids and derivatives / Aporphines / 4,5-dioxoaporphines
4,5-Dioxodehydroasimilobine 10108434 Click to see COC1=C(C=C2C3=C1C4=CC=CC=C4C=C3NC(=O)C2=O)O 293.27 unknown https://doi.org/10.1002/JCCS.200000172
Norcepharadione B 189168 Click to see COC1=C(C2=C3C(=C1)C(=O)C(=O)NC3=CC4=CC=CC=C42)OC 307.30 unknown https://doi.org/10.1002/JCCS.200000172
> Alkaloids and derivatives / Aristolactams
Aristolactam AII 148657 Click to see COC1=C(C=C2C3=C1C4=CC=CC=C4C=C3NC2=O)O 265.26 unknown https://doi.org/10.1002/JCCS.200000172
Aristolactam BII 162739 Click to see COC1=C(C2=C3C(=C1)C(=O)NC3=CC4=CC=CC=C42)OC 279.29 unknown https://doi.org/10.1002/JCCS.200000172
Aristolactam BIII 14526428 Click to see COC1=CC2=C3C4=C(C=C2C=C1)NC(=O)C4=CC(=C3OC)OC 309.30 unknown https://doi.org/10.1002/JCCS.200000172
Goniothalactam 10447198 Click to see COC1=C(C2=C3C=C(C=CC3=CC4=C2C(=C1)C(=O)N4)O)OC 295.29 unknown https://doi.org/10.1002/JCCS.200000172
Piperolactam A 3081016 Click to see COC1=C(C2=C3C(=C1)C(=O)NC3=CC4=CC=CC=C42)O 265.26 unknown https://doi.org/10.1002/JCCS.200000172
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(S)-Scoulerine 439654 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O 327.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1910235/
https://doi.org/10.1016/S0031-9422(00)82561-3
2,10-dimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-3,9-diol 53463364 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)O)OC)C=C1)O 327.40 unknown https://doi.org/10.1016/S0031-9422(00)82561-3
2,9-Dimethoxy-5,8,13,13a-tetrahydro-6H-isoquino[3,2-a]isoquinoline-3,10-diol 14378574 Click to see COC1=C(C=C2CCN3CC4=C(CC3C2=C1)C=CC(=C4OC)O)O 327.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1910235/
Isoscoulerine 188442 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)O)OC)C=C1)O 327.40 unknown https://doi.org/10.1016/S0031-9422(00)82561-3
> 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/10.1002/JCCS.200000172
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
2-(2,6,6-Trimethyl-4-oxocyclohex-2-en-1-yl)acetamide 129995904 Click to see CC1=CC(=O)CC(C1CC(=O)N)(C)C 195.26 unknown https://doi.org/10.1002/JCCS.200000172
2-[(1S)-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl]acetamide 131168921 Click to see CC1=CC(=O)CC(C1CC(=O)N)(C)C 195.26 unknown https://doi.org/10.1002/JCCS.200000172
Glaucenamide 101413759 Click to see CC1=CCC(=O)C(C1CC(=O)N)(C)C 195.26 unknown https://doi.org/10.1002/JCCS.200000172
> Organoheterocyclic compounds / Furopyrans
Tricycloalterfurene A 139589793 Click to see CC(=CCCC(=CC1CC2(C(O1)CC3=C(O2)C(CCC3=O)O)C)C)C 346.50 unknown https://doi.org/10.1002/JCCS.200000172
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
4-(4-Hydroxy-3-methoxyphenyl)-1-[(4-hydroxyphenyl)methylamino]but-3-en-2-one 162850211 Click to see COC1=C(C=CC(=C1)C=CC(=O)CNCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1002/JCCS.200000172

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