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Petchia ceylanica

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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 UUID643fe6bc1736c629441681
Scientific name Petchia ceylanica
Authority Livera
First published in Ann. Roy. Bot. Gard. (Peradeniya) 10: 140 (1926)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pulassarium ceylanicum Kuntze Revis. Gen. Pl. 2: 417 (1891)
Alyxia ceylanica Wight Icon. Pl. Ind. Orient. 4: t. 1293 (1848)
Alyxia zeylanica Walp. Ann. Bot. Syst. 3: 33 (1852)
Gynopogon ceylanicus (Wight) K.Schum. Nat. Pflanzenfam. 4(2): 151. 1895 (1895)

Common names Top

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Language Common/alternative name
Russian Петхия цейлонская

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-0000267784
Tropicos 50113102
KEW urn:lsid:ipni.org:names:81104-1
The Plant List kew-150789
Open Tree Of Life 618440
NCBI Taxonomy 396312
IPNI 81104-1
GBIF 3617286
EOL 5327540

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
New Bisindole Alkaloids from Petchia Ceylanica _ Atta-ur-Rahman, Azra Pervin, Anjun Muzaffar, Kuruneruge Tuley Dayanada de Silva, Wellage Susil Jayalath Silva The Japan Institute of Heterocyclic Chemistry 24-Feb-2009
doi:10.3987/COM-88-4572
Alcaloëdes du Petchia ceylanica André Cavé, Nicole Kunesch, Jean Bruneton, Robert Goutarel, Gladwin Percy Wannigama American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50054A034
Isolation and structural studies on the alkaloids of Petchia ceylanica Atta-ur-Rahman, W.S.J. Silva, K.A. Alvi, K.T. de Silva Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81450-8
Alkaloids of Petchia ceylanica Atta-Ur-Rahman, Azra Pervin, Anjum Muzaffar, K.T.D. De Silva, W.S.J. Silva Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80311-5

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 / Aspidospermatan-type alkaloids
Lochnericine 11382599 Click to see CCC12CC(=C3C4(C1N(CC4)CC5C2O5)C6=CC=CC=C6N3)C(=O)OC 352.40 unknown https://doi.org/10.1016/0031-9422(89)80311-5
https://doi.org/10.1021/NP50054A034
methyl (1R,12S,13S,15R,20R)-12-[(1R)-1-hydroxyethyl]-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2,4,6,9-tetraene-10-carboxylate 154585485 Click to see CC(C12CC(=C3C4(C1N(CC4)CC5C2O5)C6=CC=CC=C6N3)C(=O)OC)O 368.40 unknown https://doi.org/10.1016/S0031-9422(00)81450-8
methyl (1S,3R,13R,17R,18R)-18-[(1S)-1-hydroxyethyl]-2-oxa-6,16-diazahexacyclo[14.3.1.03,18.05,13.07,12.013,17]icosa-4,7,9,11-tetraene-4-carboxylate 163023928 Click to see CC(C12CC3CN4C1C5(CC4)C6=CC=CC=C6NC5=C(C2O3)C(=O)OC)O 368.40 unknown https://doi.org/10.1016/0031-9422(89)80311-5
Methyl 18-(1-hydroxyethyl)-2-oxa-6,16-diazahexacyclo[14.3.1.03,18.05,13.07,12.013,17]icosa-4,7,9,11-tetraene-4-carboxylate 163023926 Click to see CC(C12CC3CN4C1C5(CC4)C6=CC=CC=C6NC5=C(C2O3)C(=O)OC)O 368.40 unknown https://doi.org/10.1016/0031-9422(89)80311-5
> Alkaloids and derivatives / Yohimbine alkaloids
Ajmalicine 441975 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1016/0031-9422(89)80311-5
Cabucine 443030 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=C4C=C(C=C5)OC 382.50 unknown https://doi.org/10.1016/0031-9422(89)80311-5
methyl (1S,15R,16S,18R,19R,20S)-18-hydroxy-16-methyl-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8-tetraene-19-carboxylate 14413744 Click to see CC1C2CN3CCC4=C(C3CC2C(C(O1)O)C(=O)OC)NC5=CC=CC=C45 370.40 unknown https://doi.org/10.1016/0031-9422(89)80311-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acid esters
methyl (1S,10S,11S,12Z,17S)-12-ethylidene-2-oxo-9,14-diazapentacyclo[9.5.2.01,9.03,8.014,17]octadeca-3,5,7-triene-10-carboxylate 14191532 Click to see CC=C1CN2CCC34C2CC1C(N3C5=CC=CC=C5C4=O)C(=O)OC 338.40 unknown https://doi.org/10.1016/0031-9422(89)80311-5
> Organoheterocyclic compounds / Benzofurans / Dibenzofurans
dimethyl (1S,12R,13E,30R,36R,37R)-13-ethylidene-3',8,26-trimethylspiro[22-oxa-8,15,26,33-tetrazaundecacyclo[28.5.1.112,18.01,27.02,25.04,23.05,21.07,19.09,15.09,18.027,33]heptatriaconta-2(25),3,5,7(19),20,23-hexaene-31,2'-oxirane]-36,37-dicarboxylate 102079731 Click to see CC=C1CN2CCC34C2(CCC1C3C(=O)OC)N(C5=C4C=C6C(=C5)C7=CC8=C(C=C7O6)N(C91C82CCN9CC3(C(O3)C)C(C2C(=O)OC)CC1)C)C 704.90 unknown https://doi.org/10.1016/0031-9422(89)80311-5
methyl (1R,13R,14R,17S,22R,30S,33R,34E,39R)-34-ethylidene-17-[(1R)-1-hydroxyethyl]-9,29-dimethyl-15-oxo-5,16-dioxa-9,19,29,36-tetrazaundecacyclo[31.5.1.01,30.02,28.04,26.06,25.08,23.010,22.013,17.014,22.030,36]nonatriaconta-2(28),3,6,8(23),24,26-hexaene-39-carboxylate 102075875 Click to see CC=C1CN2CCC34C2(CCC1C3C(=O)OC)N(C5=C4C=C6C(=C5)C7=CC8=C(C=C7O6)N(C9C81CCNCC2(C(C1C(=O)O2)CC9)C(C)O)C)C 692.80 unknown https://doi.org/10.3987/COM-88-4572
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
methyl (1R,12R,13Z,18R)-13-ethylidene-4-methoxy-8-methyl-8,15-diazapentacyclo[10.5.1.01,9.02,7.09,15]octadeca-2(7),3,5-triene-18-carboxylate 101967169 Click to see CC=C1CN2CCC34C2(CCC1C3C(=O)OC)N(C5=C4C=C(C=C5)OC)C 368.50 unknown https://doi.org/10.1016/0031-9422(89)80311-5
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
dimethyl (13Z)-13-ethylidene-3',8,26-trimethylspiro[22-oxa-8,15,26,33-tetrazaundecacyclo[28.5.1.112,18.01,27.02,25.04,23.05,21.07,19.09,15.09,18.028,33]heptatriaconta-2(25),3,5,7(19),20,23-hexaene-31,2'-oxirane]-36,37-dicarboxylate 102079780 Click to see CC=C1CN2CCC34C2(CCC1C3C(=O)OC)N(C5=C4C=C6C(=C5)C7=CC8=C(C=C7O6)N(C9C81CCN2C9CC(C1C(=O)OC)C1(C2)C(O1)C)C)C 704.90 unknown https://doi.org/10.1016/0031-9422(89)80311-5
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Fraxetin 5273569 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)O 208.17 unknown https://doi.org/10.1016/0031-9422(89)80311-5
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(8R,9S,10R,11R)-11-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl] benzoate 53388465 Click to see CC1C(C(C2=CC(=C(C(=C2C3=C(C4=C(C=C3C1O)OCO4)OC)OC)OC)OC)OC(=O)C5=CC=CC=C5)C 536.60 unknown https://doi.org/10.3987/COM-88-4572

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