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Ancistrocladus griffithii

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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 UUID64403c95cfc5b198324115
Scientific name Ancistrocladus griffithii
Authority Planch.
First published in Ann. Sci. Nat., Bot. , sér. 3, 13: 318 (1849)

Description Top

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Synonyms Top

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Common names Top

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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
      • Andaman Islands
      • Cambodia
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000970309
Tropicos 50041688
KEW urn:lsid:ipni.org:names:320530-1
The Plant List kew-8762
Open Tree Of Life 389787
NCBI Taxonomy 714099
IPNI 320530-1
iNaturalist 946363
GBIF 3658988
EOL 6874704

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
NMR-Based Chromatography Readouts: Indispensable Tools to “Translate” Analytical Features into Molecular Structures Seger C, Sturm S Cells 07-Nov-2022
PMCID:PMC9658744
doi:10.3390/cells11213526
PMID:36359922
Computational study to discover potent phytochemical inhibitors against drug target, squalene synthase from Leishmania donovani Wadanambi PM, Mannapperuma U Heliyon 31-May-2021
PMCID:PMC8188062
doi:10.1016/j.heliyon.2021.e07178
PMID:34141935
Plant-derived compounds in treatment of leishmaniasis Oryan A Iran J Vet Res 01-Jan-2015
PMCID:PMC4789233
PMID:27175144
Extract screening by HPLC coupled to MS-MS, NMR, and CD: a dimeric and three monomeric naphthylisoquinoline alkaloids from Ancistrocladus griffithii. Bringmann G, Wohlfarth M, Rischer H, Schlauer J, Brun R Phytochemistry 01-Sep-2002
doi:10.1016/S0031-9422(02)00217-0
PMID:12169315
A photometric screening method for dimeric naphthylisoquinoline alkaloids and complete on-line structural elucidation of a dimer in crude plant extracts, by the LC-MS/LC-NMR/LC-CD triad. Bringmann G, Wohlfarth M, Rischer H, Heubes M, Saeb W, Diem S, Herderich M, Schlauer J Anal Chem 01-Jun-2001
doi:10.1021/AC001503Q
PMID:11403302

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
> Organoheterocyclic compounds / Isoquinolines and derivatives / Naphthylisoquinolines
(1R,3R)-7-(4-hydroxy-5-methoxy-7-methylnaphthalen-1-yl)-6-methoxy-1,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-8-ol 163105721 Click to see CC1CC2=CC(=C(C(=C2C(N1C)C)O)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C)OC 407.50 unknown https://doi.org/10.1016/S0031-9422(02)00217-0
(1R,3R)-7-[4-hydroxy-3-[1-hydroxy-5-[(1S,3S)-6-hydroxy-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl]-8-methoxy-6-methylnaphthalen-2-yl]-5-methoxy-7-methylnaphthalen-1-yl]-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-6-ol 163104505 Click to see CC1CC2=CC(=C(C(=C2C(N1)C)OC)C3=C4C=C(C=C(C4=C(C(=C3)C5=C(C6=C(C=C(C(=C6C=C5)C7=C(C=C8CC(NC(C8=C7OC)C)C)O)C)OC)O)O)OC)C)O 784.90 unknown https://doi.org/10.1016/S0031-9422(02)00217-0
(1R,3S)-5-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-6-ol 12306781 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)OC)O)C3=C4C=CC=C(C4=C(C=C3C)OC)OC 407.50 unknown https://doi.org/10.1016/S0031-9422(02)00217-0
(1R,3S)-7-[4-hydroxy-3-[1-hydroxy-4-[(1R,3S)-6-hydroxy-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl]-8-methoxy-6-methylnaphthalen-2-yl]-5-methoxy-7-methylnaphthalen-1-yl]-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-6-ol 11735409 Click to see CC1CC2=CC(=C(C(=C2C(N1)C)OC)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C(C=C8CC(NC(C8=C7OC)C)C)O)O)O 784.90 unknown https://doi.org/10.1016/S0031-9422(02)00217-0
https://doi.org/10.1021/AC001503Q
(1S,3R)-7-(5-hydroxy-4-methoxy-7-methylnaphthalen-1-yl)-8-methoxy-1,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-6-ol 163036661 Click to see CC1CC2=CC(=C(C(=C2C(N1C)C)OC)C3=C4C=C(C=C(C4=C(C=C3)OC)O)C)O 407.50 unknown https://doi.org/10.1016/S0031-9422(02)00217-0
(1S,3S)-7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline-6,8-diol 9977888 Click to see CC1CC2=CC(=C(C(=C2C(N1)C)O)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O 393.50 unknown https://doi.org/10.1016/S0031-9422(02)00217-0
(1S,3S)-7-(5-hydroxy-4-methoxy-7-methylnaphthalen-1-yl)-8-methoxy-1,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-6-ol 636795 Click to see CC1CC2=CC(=C(C(=C2C(N1C)C)OC)C3=C4C=C(C=C(C4=C(C=C3)OC)O)C)O 407.50 unknown https://doi.org/10.1016/S0031-9422(02)00217-0
(1S,3S)-7-(5-hydroxy-4-methoxy-7-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-6-ol 101204923 Click to see CC1CC2=CC(=C(C(=C2C(N1)C)OC)C3=C4C=C(C=C(C4=C(C=C3)OC)O)C)O 393.50 unknown https://doi.org/10.1016/S0031-9422(02)00217-0
Ancistrocladine 161741 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)OC)O)C3=C4C=CC=C(C4=C(C=C3C)OC)OC 407.50 unknown https://doi.org/10.1016/S0031-9422(02)00217-0
Ancistrogriffine C 11003736 Click to see CC1CC2=CC(=C(C(=C2C(N1)C)O)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C)OC 393.50 unknown https://doi.org/10.1016/S0031-9422(02)00217-0

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