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Pycnarrhena ozantha

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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 UUID6440011821414710256444
Scientific name Pycnarrhena ozantha
Authority Diels
First published in Bot. Jahrb. Syst. 52: 187 (1915)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pycnarrhena papuana Kaneh. & Hatus. Bot. Mag. (Tokyo) 56: 473 (1942)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000474063
Tropicos 100451194
KEW urn:lsid:ipni.org:names:581315-1
Open Tree Of Life 6130017
NCBI Taxonomy 2812727
IPNI 581315-1
GBIF 3830708
CMAUP NPO3092

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)!
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Title Authors Publication Released IDs
Tumour Inhibitory Plants. Two New Bisbenzylisoquinoline Alkaloids From Pycnarrhena ozantha (Menispermaceae) J Loder, R Nearn CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9722193
The Bisbenzylisoquinoline Alkaloids of Pycnarrhena ozantha Marie-Line Abouchacra, Michael Leboeuf, Hélène Guinaudeau, André Cavé, Pierre Cabalion American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50051A006

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Aminobenzoic acids and derivatives / Aminobenzoic acids
Anthranilic acid 227 Click to see C1=CC=C(C(=C1)C(=O)O)N 137.14 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown via CMAUP database
> Lignans, neolignans and related compounds
(+)-2-Norberbamine 9873326 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6)OC)OC)O)OC 594.70 unknown https://doi.org/10.1021/NP50051A006
(10S,23R)-28,29,36-trimethoxy-9-methyl-2,16-dioxa-9,24-diazaheptacyclo[21.6.2.23,6.212,15.117,21.05,10.027,31]hexatriaconta-1(29),3(36),4,6(35),12(34),13,15(33),17,19,21(32),27,30-dodecaen-18-ol 162700763 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C(=C7CCN6)OC)OC)O3)O)OC 594.70 unknown https://doi.org/10.1021/NP50051A006
(1R,14S)-20,25-dimethoxy-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.29,12.13,7.114,18.027,31.022,33]hexatriaconta-3(36),4,6,9(35),10,12(34),18,20,22(33),24,26,31-dodecaene-6,21-diol 21144589 Click to see COC1=C2C=C3C(CC4=CC(=C(C=C4)O)OC5=CC=C(CC6C7=C(O2)C(=C(C=C7CCN6)OC)O)C=C5)NCCC3=C1 566.60 unknown https://doi.org/10.1071/CH9722193
(1S,14R)-20,25-dimethoxy-30-methyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaene-9,21-diol 12299860 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6)OC)O)O)OC 580.70 unknown https://doi.org/10.1071/CH9722193
https://doi.org/10.1021/NP50051A006
(1S,14R)-20,25-dimethoxy-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaene-9,21-diol 13890735 Click to see COC1=C2C=C3C(CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O2)C(=C(C=C7CCN6)OC)O)O)NCCC3=C1 566.60 unknown https://doi.org/10.1021/NP50051A006
(1S,14R)-20,25-dimethoxy-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.29,12.13,7.114,18.027,31.022,33]hexatriaconta-3(36),4,6,9(35),10,12(34),18,20,22(33),24,26,31-dodecaene-6,21-diol 162965868 Click to see COC1=C2C=C3C(CC4=CC(=C(C=C4)O)OC5=CC=C(CC6C7=C(O2)C(=C(C=C7CCN6)OC)O)C=C5)NCCC3=C1 566.60 unknown https://doi.org/10.1071/CH9722193
(1S,14R)-9,20,25-trimethoxy-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaen-21-ol 13890737 Click to see COC1=C2C=C(CC3C4=C(C(=C(C=C4CCN3)OC)O)OC5=C(C=C6CCNC(C6=C5)CC7=CC=C(O2)C=C7)OC)C=C1 580.70 unknown https://doi.org/10.1021/NP50051A006
20,25-Dimethoxy-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.29,12.13,7.114,18.027,31.022,33]hexatriaconta-3(36),4,6,9(35),10,12(34),18,20,22(33),24,26,31-dodecaene-6,21-diol 425997 Click to see COC1=C2C=C3C(CC4=CC(=C(C=C4)O)OC5=CC=C(CC6C7=C(O2)C(=C(C=C7CCN6)OC)O)C=C5)NCCC3=C1 566.60 unknown https://doi.org/10.1071/CH9722193
Daphnoline 261477 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6)OC)O3)O)O)OC 580.70 unknown https://doi.org/10.1021/NP50051A006
N2-Demethylthalrugosine 13890733 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6)OC)O)OC)OC 594.70 unknown https://doi.org/10.1021/NP50051A006
> Organoheterocyclic compounds / Indoles and derivatives / Indolecarboxylic acids and derivatives
Indole-3-carboxylic acid 69867 Click to see C1=CC=C2C(=C1)C(=CN2)C(=O)O 161.16 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Indole 798 Click to see C1=CC=C2C(=C1)C=CN2 117.15 unknown via CMAUP database
Indole-3-carboxaldehyde 10256 Click to see C1=CC=C2C(=C1)C(=CN2)C=O 145.16 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
Indole-3-acetamide 397 Click to see C1=CC=C2C(=C1)C(=CN2)CC(=O)N 174.20 unknown via CMAUP database
Tryptophol 10685 Click to see C1=CC=C2C(=C1)C(=CN2)CCO 161.20 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
(2S)-2-Hydroxy-3-(1H-indol-3-YL)propanoic acid 676157 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)O 205.21 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives / Indole-3-acetic acid derivatives
Indole-3-acetic acid 802 Click to see C1=CC=C2C(=C1)C(=CN2)CC(=O)O 175.18 unknown via CMAUP database

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