We don't have an image yet. Upload an image!

Details Top

Internal ID UUID643fe330d0e34031982939
Scientific name Melodinus tenuicaudatus
Authority Tsiang & P.T.Li
First published in Acta Phytotax. Sin. 11: 353 (1973)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

No known synonyms.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Chinese 山橙叶
Chinese 薄叶山橙

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000240231
Tropicos 1805902
KEW urn:lsid:ipni.org:names:80259-1
Open Tree Of Life 6067876
IPNI 80259-1
GBIF 3621166

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)!
Title Authors Publication Released IDs
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

Add a new one!
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 / Aspidospermatan-type alkaloids
methyl (1R,12S,13S,15R,20R)-12-ethyl-5-methoxy-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2(7),3,5,9-tetraene-10-carboxylate 131876200 Click to see CCC12CC(=C3C4(C1N(CC4)CC5C2O5)C6=C(N3)C=C(C=C6)OC)C(=O)OC 382.50 unknown https://doi.org/10.1055/S-2006-962443
> Alkaloids and derivatives / Eburnan-type alkaloids
methyl (1R,12R,19S)-12-ethyl-4-[(15S,19R)-15-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18),13-pentaen-17-yl]-5-methoxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5,9,13-pentaene-10-carboxylate 102595414 Click to see CCC12CC(N3C4=CC=CC=C4C5=C3C1N(CC5)CC=C2)C6=CC7=C(C=C6OC)NC8=C(CC9(C=CCN1C9C78CC1)CC)C(=O)OC 642.80 unknown https://doi.org/10.1055/S-2006-962443
methyl (1S,12R,19R)-12-ethyl-4-[(15R,17S,19R)-15-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18),13-pentaen-17-yl]-5-methoxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5,9,13-pentaene-10-carboxylate 163043086 Click to see CCC12CC(N3C4=CC=CC=C4C5=C3C1N(CC5)CC=C2)C6=CC7=C(C=C6OC)NC8=C(CC9(C=CCN1C9C78CC1)CC)C(=O)OC 642.80 unknown https://doi.org/10.1055/S-2006-962443
> Alkaloids and derivatives / Macroline alkaloids
Tombozine 5318845 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)CO 294.40 unknown https://doi.org/10.1055/S-2006-962443
> 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/10.1055/S-2006-962443
CID 12082288 12082288 Click to see COC(=O)C12CC3(C=CCN4C3C1(CC4)C5=CC=CC=C5NC2=O)C=C 350.40 unknown https://doi.org/10.1055/S-2006-962443
Scandine 5259866 Click to see COC(=O)C12CC3(C=CCN4C3C1(CC4)C5=CC=CC=C5NC2=O)C=C 350.40 unknown https://doi.org/10.1055/S-2006-962443
> 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/10.1055/S-2006-962443
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/10.1055/S-2006-962443
methyl (1R,9R,10S,11R,12S,19S,20S)-20-methyl-8,16-diazahexacyclo[10.6.1.19,11.01,9.02,7.016,19]icosa-2,4,6,13-tetraene-10-carboxylate 154497671 Click to see CC1C2C3C=CCN4C3C5(C1(C2C(=O)OC)NC6=CC=CC=C65)CC4 336.40 unknown https://doi.org/10.1055/S-2006-962443
methyl (9S,10S,12S,16R,19S,20S)-20-methyl-16-oxido-8-aza-16-azoniahexacyclo[10.6.1.19,11.01,9.02,7.016,19]icosa-2,4,6,13-tetraene-10-carboxylate 163188226 Click to see CC1C2C3C=CC[N+]4(C3C5(C1(C2C(=O)OC)NC6=CC=CC=C65)CC4)[O-] 352.40 unknown https://doi.org/10.1055/S-2006-962443
Vindolinine N-oxide 163184431 Click to see CC1C2C3C=CC[N+]4(C3C5(C1(C2C(=O)OC)NC6=CC=CC=C65)CC4)[O-] 352.40 unknown https://doi.org/10.1055/S-2006-962443
> Benzenoids / Phenol esters
Ibopamine 68555 Click to see CC(C)C(=O)OC1=C(C=C(C=C1)CCNC)OC(=O)C(C)C 307.40 unknown https://doi.org/10.1055/S-2006-962443
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
19-Epivindolinine N-oxide 163184435 Click to see CC1C23CC(C14C5(C2[N+](CC5)(CC=C3)[O-])C6=CC=CC=C6N4)C(=O)OC 352.40 unknown https://doi.org/10.1055/S-2006-962443
methyl (9S,10R,12S,16R,19S,20S)-20-methyl-16-oxido-8-aza-16-azoniahexacyclo[10.6.1.19,12.01,9.02,7.016,19]icosa-2,4,6,13-tetraene-10-carboxylate 163195257 Click to see CC1C23CC(C14C5(C2[N+](CC5)(CC=C3)[O-])C6=CC=CC=C6N4)C(=O)OC 352.40 unknown https://doi.org/10.1055/S-2006-962443
Vindolinine 24148538 Click to see CC1C23CC(C14C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4)C(=O)OC 336.40 unknown https://doi.org/10.1055/S-2006-962443

Biological Material Top ebay Auctions

Please wait .. loading items ..
Loading...

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.