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Melodinus fusiformis

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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 UUID643fe32fe062a208655140
Scientific name Melodinus fusiformis
Authority Champ. ex Benth.
First published in Hooker's J. Bot. Kew Gard. Misc. 4: 332 (1852)

Description Top

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Synonyms Top

Scientific name Authority First published in
Melodinus brachyphyllus Merr. J. Arnold Arbor. 23: 191 (1942)
Melodinus edulis H.Lév. Repert. Spec. Nov. Regni Veg. 11: 549 (1913)
Melodinus esquirolii H.Lév. Repert. Spec. Nov. Regni Veg. 11: 549 (1913)
Melodinus flavus H.Lév. Repert. Spec. Nov. Regni Veg. 11: 548 (1913)
Melodinus fulvus H.Lév. Repert. Spec. Nov. Regni Veg. 11: 548. 1913 (1913)
Melodinus hemsleyanus Diels Bot. Jahrb. Syst. 29: 539 (1900)
Melodinus lanceolatus Merr. Philipp. J. Sci. 27: 52 (1925)
Melodinus magnificus Tsiang Sunyatsenia 3: 128 (1936)
Melodinus morsei Tsiang Sunyatsenia 6: 110 (1941)
Melodinus seguinii H.Lév. Repert. Spec. Nov. Regni Veg. 2: 114 (1906)
Melodinus wrightioides Hand.-Mazz. Beih. Bot. Centralbl. 56B: 460 (1937)
Melodinus yunnanensis Tsiang & P.T.Li Acta Phytotax. Sin. 11: 355 (1973)
Trachelospermum esquirolii H.Lév. Fl. Kouy-Tchéou : 32 (1914)

Common names Top

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Language Common/alternative name
Chinese 龙州山橙
Chinese 尖山橙
Chinese 川山橙
Chinese 石芽枫
Chinese 竹藤
Chinese 茶藤
Chinese 薄叶山橙
Chinese 藤皮黄
Chinese 雷打果
Chinese 鸡腿果

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
    • Indo-China
      • Cambodia
      • Laos
      • Thailand
      • Vietnam
    • Malesia
      • Philippines

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000240166
Tropicos 1803112
KEW urn:lsid:ipni.org:names:80201-1
The Plant List kew-124209
Open Tree Of Life 194019
NCBI Taxonomy 582713
IPNI 80201-1
iNaturalist 705608
GBIF 3621774
Freebase /m/02xblbq
Wikipedia Melodinus_fusiformis

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
Ethnobotanical study on herbal tea drinks in Guangxi, China Long T, Hu R, Cheng Z, Xu C, Hu Q, Liu Q, Gu R, Huang Y, Long C J Ethnobiol Ethnomed 31-Mar-2023
PMCID:PMC10064729
doi:10.1186/s13002-023-00579-3
PMID:37004116
Plant-Based Indole Alkaloids: A Comprehensive Overview from a Pharmacological Perspective Omar F, Tareq AM, Alqahtani AM, Dhama K, Sayeed MA, Emran TB, Simal-Gandara J Molecules 15-Apr-2021
PMCID:PMC8071433
doi:10.3390/molecules26082297
PMID:33921093
Ligand Fishing: A Remarkable Strategy for Discovering Bioactive Compounds from Complex Mixture of Natural Products Zhuo R, Liu H, Liu N, Wang Y Molecules 11-Nov-2016
PMCID:PMC6274472
doi:10.3390/molecules21111516
PMID:27845727
Comparison of analytical techniques for the identification of bioactive compounds from natural products Cies¸la Ł, Moaddel R Nat Prod Rep 01-Jul-2016
PMCID:PMC5042860
doi:10.1039/c6np00016a
PMID:27367973
The identification of a novel SIRT6 modulator from Trigonella foenum-graecum using ligand fishing with protein coated magnetic beads Singh N, Ravichandran S, Spelman K, Fugmann SD, Moaddel R J Chromatogr B Analyt Technol Biomed Life Sci 15-Mar-2014
PMCID:PMC4127357
doi:10.1016/j.jchromb.2014.03.016
PMID:24704183
Acetylcholinesterase immobilized capillary reactors coupled to protein coated magnetic beads: A new tool for plant extract ligand screening Vanzolini KL, Jiang Z, Zhang X, Vieira LC, Corrêa AG, Cardoso CL, Cass QB, Moaddel R Talanta 31-Jul-2013
PMCID:PMC3826612
doi:10.1016/j.talanta.2013.07.046
PMID:24148457
Melomorsine, a New Dimeric Indoline Alkaloid from Melodinus morsei Ya-Li He, Wei-Ming Chen, Xiao-Zhang Feng American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50105A016
The alkaloids of Melodinus morsei He Ya-Li, Chen Wei-Ming, Feng Xiao-Zhang Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)89527-8
Study on the Alkaloids of Melodinus tenuicaudatus. Zhou YL, Ye JH, Li ZM, Huang ZH Planta Med 01-Aug-1988
doi:10.1055/S-2006-962443
PMID:17265274

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 / Aspidofractine alkaloids
(-)-Venalstonine 821468 Click to see COC(=O)C1CC23CCC14C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4 336.40 unknown https://doi.org/10.1016/S0031-9422(00)89527-8
methyl (1R,9R,16S,18R,21R)-15-hydroxy-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7-triene-18-carboxylate 101675236 Click to see COC(=O)C1CC23CCC14C5(C2N(CCC3O)CC5)C6=CC=CC=C6N4 354.40 unknown https://doi.org/10.1016/S0031-9422(00)89527-8
Methyl (9R,18R,21S)-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7-triene-18-carboxylate 21123851 Click to see COC(=O)C1CC23CCCN4C2C5(C1(CC3)NC6=CC=CC=C65)CC4 338.40 unknown https://doi.org/10.1016/S0031-9422(00)89527-8
> Alkaloids and derivatives / Aspidospermatan-type alkaloids
(1R,9R,12R,19R)-12-Ethyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6-triene 6857472 Click to see CCC12CCCN3C1C4(CC3)C(CC2)NC5=CC=CC=C45 282.40 unknown https://doi.org/10.1021/NP50105A016
Aspidospermidine 580281 Click to see CCC12CCCN3C1C4(CC3)C(CC2)NC5=CC=CC=C45 282.40 unknown https://doi.org/10.1021/NP50105A016
methyl (10R,28R,29R)-10,28-diethyl-2-oxa-6,14,24,37-tetrazaundecacyclo[26.9.2.110,14.01,30.03,20.05,18.07,17.022,30.024,29.031,36.017,40]tetraconta-3,5(18),7,11,19,31,33,35-octaene-38-carboxylate 102469734 Click to see CCC12CCCN3C1C45C(C3)CC6=CC7=C(C=C6OC4(C(C2)C(=O)OC)NC8=CC=CC=C58)NC9=CCC1(C=CCN2C1C97CC2)CC 644.80 unknown https://doi.org/10.1021/NP50105A016
Vincadifformine 94255 Click to see CCC12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC 338.40 unknown https://doi.org/10.1016/S0031-9422(00)89527-8
> Alkaloids and derivatives / Melodinus alkaloids
10-Hydroxyscandine 12082289 Click to see COC(=O)C12CC3(C=CCN4C3C1(CC4)C5=C(C=CC(=C5)O)NC2=O)C=C 366.40 unknown https://doi.org/10.1016/S0031-9422(00)89527-8
Meloscandonine 12082290 Click to see CC1C(=O)C23CC14C=CCN5C4C2(CC5)C6=CC=CC=C6NC3=O 320.40 unknown https://doi.org/10.1016/S0031-9422(00)89527-8
Scandine 5259866 Click to see COC(=O)C12CC3(C=CCN4C3C1(CC4)C5=CC=CC=C5NC2=O)C=C 350.40 unknown https://doi.org/10.1016/S0031-9422(00)89527-8
> Alkaloids and derivatives / Plumeran-type alkaloids
16-Hydroxytabersonine 443326 Click to see CCC12CC(=C3C4(C1N(CC4)CC=C2)C5=C(N3)C=C(C=C5)O)C(=O)OC 352.40 unknown https://doi.org/10.1016/S0031-9422(00)89527-8
https://doi.org/10.1021/NP50105A016
16-Methoxytabersonine 443356 Click to see CCC12CC(=C3C4(C1N(CC4)CC=C2)C5=C(N3)C=C(C=C5)OC)C(=O)OC 366.50 unknown https://doi.org/10.1016/S0031-9422(00)89527-8
Tabersonine 20485 Click to see CCC12CC(=C3C4(C1N(CC4)CC=C2)C5=CC=CC=C5N3)C(=O)OC 336.40 unknown https://doi.org/10.1016/S0031-9422(00)89527-8
> Alkaloids and derivatives / Quebrachamine alkaloids
Quebrachamine 92990 Click to see CCC12CCCN(C1)CCC3=C(CC2)NC4=CC=CC=C34 282.40 unknown https://doi.org/10.1016/S0031-9422(00)89527-8
> Alkaloids and derivatives / Strychnos alkaloids
methyl (1S,17R,18S)-18-ethyl-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carboxylate 134716702 Click to see CCC1C2CCN3C1C4(CC3)C5=CC=CC=C5NC4=C2C(=O)OC 324.40 unknown https://doi.org/10.1016/S0031-9422(00)89527-8
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
methyl (1R,9S,10S,12S,13R,20S)-9-hydroxy-12-methyl-11-oxa-8,17-diazahexacyclo[11.6.1.110,13.01,9.02,7.017,20]henicosa-2,4,6,14-tetraene-10-carboxylate 154497669 Click to see CC1C23CC(O1)(C4(C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4)O)C(=O)OC 368.40 unknown https://doi.org/10.1021/NP50105A016
methyl (1R,9S,12S,13R,20S)-9-hydroxy-12-methyl-11-oxa-8,17-diazahexacyclo[11.6.1.110,13.01,9.02,7.017,20]henicosa-2,4,6,14-tetraene-10-carboxylate 163185982 Click to see CC1C23CC(O1)(C4(C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4)O)C(=O)OC 368.40 unknown https://doi.org/10.1021/NP50105A016
Methyl 6,7-didehydro-2,20-cycloaspidospermidine-3-carboxylate 120879 Click to see CC1C23CC(C14C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4)C(=O)OC 336.40 unknown https://doi.org/10.1016/S0031-9422(00)89527-8
https://doi.org/10.1055/S-2006-962443
Vincoline 3032566 Click to see CC1C23CC(O1)(C4(C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4)O)C(=O)OC 368.40 unknown https://doi.org/10.1021/NP50105A016
Vindolinine 24148538 Click to see CC1C23CC(C14C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4)C(=O)OC 336.40 unknown https://doi.org/10.1016/S0031-9422(00)89527-8
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
2-[(2R,3Z,12bS)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]ethanol 21595545 Click to see CC=C1CN2CCC3=C(C2CC1CCO)NC4=CC=CC=C34 296.40 unknown https://doi.org/10.1021/NP50105A016
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
(1S,4R,12R,15R)-15-ethyl-11-aza-1-azoniapentacyclo[13.3.1.01,12.04,12.05,10]nonadeca-5,7,9-trien-4-ol 163188936 Click to see CCC12CCC[N+]3(C1)CCC4(C3(CC2)NC5=CC=CC=C54)O 299.40 unknown https://doi.org/10.1021/NP50105A016
Rhazidine 3084227 Click to see CCC12CCC[N+]3(C1)CCC4(C3(CC2)NC5=CC=CC=C54)O 299.40 unknown https://doi.org/10.1021/NP50105A016

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