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Tabernaemontana coffeoides

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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 UUID643fee7d2a917744439012
Scientific name Tabernaemontana coffeoides
Authority Bojer ex A.DC.
First published in Prodr. 8: 370 (1844)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tabernaemontana coffeifolia Bojer ex Baker Fl. Mauritius : 224 (1877)
Tabernaemontana membranacea A.DC. Prodr. 8: 370 (1844)
Tabernaemontana modesta Baker J. Bot. 20: 219 (1882)
Hazunta modesta var. divaricata Pichon Notul. Syst. (Paris) 13: 208. 1948
Hazunta modesta var. methuenii (Stapf & M.L.Green) Pichon Notul. Syst. (Paris) 13: 208. 1948
Conopharyngia coffeoides Summerh. Bull. Misc. Inform. Kew 1928: 392 (1928)
Ervatamia membranacea (DC.) Markgr. Mitt. Bot. Staatssamml. München 1: 29 (1950)
Ervatamia methuenii Stapf & M.L.Green Bull. Misc. Inform. Kew 1913: 78 (1913)
Ervatamia modesta (Baker) Stapf Bull. Misc. Inform. Kew 1913: 78. (1913)
Hazunta angustifolia Pichon Notul. Syst. (Paris) 13: 208 (1948)
Hazunta coffeoides (Bojer ex A.DC.) Pichon Notul. Syst. (Paris) 13: 208 (1948)
Hazunta costata Markgr. Adansonia , n.s., 10: 27 (1970)
Hazunta graciliflora Pichon Notul. Syst. (Paris) 13: 209 (1948)
Hazunta membranacea (A.DC.) Pichon Notul. Syst. (Paris) 13: 208 (1948)
Hazunta membranacea f. pilifera Markgr. Adansonia , n.s., 12: 222 (1972)
Hazunta modesta (Baker) Pichon Notul. Syst. (Paris) 13: 207 (1948)
Hazunta silicicola Pichon Notul. Syst. (Paris) 13: 208 (1948)
Hazunta velutina Pichon Notul. Syst. (Paris) 13: 208 (1948)

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-0000319790
Tropicos 1802002
INPN 807543
KEW urn:lsid:ipni.org:names:82059-1
The Plant List kew-200634
Open Tree Of Life 886976
NCBI Taxonomy 761058
IUCN Red List 64563628
IPNI 82059-1
iNaturalist 487328
GBIF 3618255
Freebase /m/0wkrgtt
Wikipedia Tabernaemontana_coffeoides

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
A Sample-Centric and Knowledge-Driven Computational Framework for Natural Products Drug Discovery Gaudry A, Pagni M, Mehl F, Moretti S, Quiros-Guerrero LM, Cappelletti L, Rutz A, Kaiser M, Marcourt L, Queiroz EF, Ioset JR, Grondin A, David B, Wolfender JL, Allard PM ACS Cent Sci 20-Feb-2024
PMCID:PMC10979503
doi:10.1021/acscentsci.3c00800
PMID:38559298
Open and reusable annotated mass spectrometry dataset of a chemodiverse collection of 1,600 plant extracts Allard PM, Gaudry A, Quirós-Guerrero LM, Rutz A, Dounoue-Kubo M, Walker TW, Defossez E, Long C, Grondin A, David B, Wolfender JL Gigascience 18-Jan-2023
PMCID:PMC9845059
doi:10.1093/gigascience/giac124
PMID:36649739
Novel Approach to Classify Plants Based on Metabolite-Content Similarity Liu K, Abdullah AA, Huang M, Nishioka T, Altaf-Ul-Amin M, Kanaya S Biomed Res Int 09-Jan-2017
PMCID:PMC5253511
doi:10.1155/2017/5296729
PMID:28164123
Structure and Stereochemistry of Hazuntamine, a New Bisindole Alkaloid from Hazunta modesta var. Methuenii Subvar. Methuenii Bhupesh C. Das, Anne-Marie Bui, Eric Guittet, V屍onique Stoven The Japan Institute of Heterocyclic Chemistry 31-Mar-2009
doi:10.3987/COM-93-6644
Hazuntiphyllidine and Anhydrohazuntiphyllidine, Two New Bisindole Alkaloids from Hazunta modesta var. modesta subvar, divaricata Anne-Marie Bui, Bhupesh C. Das, Eric Guittet, Pierre Potier American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50074A025
Structure of Hazuntiphylline, a Novel Symmetrical Bisindole Alkloid from Hazunta modesta var. modesta subvar. divaricata Anne-Marie Bui, Bhupesh C. Das, Eric Guittet, Jean-Yves Lallemand, Pierre Potier American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50044A022
Étude chimiotaxonomique de deux espéces nouvelles de Hazunta (Apocynaceae) Anne-Marie But, Pierre Potier auMiguel Urrea, Alain Clastres, Dominique Laurent, Maurice-Marie Debray Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(79)83016-2
Étude chimiotaxonomique de Hazunta modesta A Bui Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82103-2
Étude chimiotaxonomique de quelques espéces de Hazunta Anne-Marie Bui, Maurice-Marie Debray, Pierre Boiteau, Pierre Potier Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)89235-3

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
12,14'-Diethylspiro[14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2,4,6,8-tetraene-10,10'-16-oxa-8,19-diazaheptacyclo[10.9.1.11,14.02,7.08,22.015,17.019,23]tricosa-2,4,6-triene]-22'-ol 162997737 Click to see CCC12CC3CC4(CC5(C6C(O6)CN7C5C8(C4=NC9=CC=CC=C98)CC7)CC)CN4C3(C3(C1N(CC3)CC1C2O1)C1=CC=CC=C14)O 630.80 unknown https://doi.org/10.1021/NP50074A025
Hazuntiphylline 190556 Click to see CCC12CC3CN4C5=CC=CC=C5C67C48C(CC9(C6N(CC7)CC4C9O4)CC)CN4C3(O8)C3(C1N(CC3)CC1C2O1)C1=CC=CC=C14 630.80 unknown https://doi.org/10.1021/NP50044A022
https://doi.org/10.1021/NP50074A025
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/S0031-9422(00)82103-2
methyl (1R,12R,16S,22R)-15-oxa-8,19-diazahexacyclo[10.9.1.01,9.02,7.012,16.019,22]docosa-2,4,6,9-tetraene-10-carboxylate 134963058 Click to see COC(=O)C1=C2C3(CCN4C3C5(C1)CCOC5CC4)C6=CC=CC=C6N2 352.40 unknown https://doi.org/10.1016/S0031-9422(00)82103-2
methyl (1R,12S,13S,14R,19R)-12-ethyl-13,14-dihydroxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate 162929030 Click to see CCC12CC(=C3C4(C1N(CC4)CC(C2O)O)C5=CC=CC=C5N3)C(=O)OC 370.40 unknown https://doi.org/10.1016/S0031-9422(00)82103-2
> Alkaloids and derivatives / Ibogan-type alkaloids
(1R,15S,17S)-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene 51055165 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45 280.40 unknown https://doi.org/10.3987/COM-93-6644
6,9-Methano-5H-pyrido[1',2':1,2]azepino[4,5-b]indole, 7-ethyl-6,6a,7,8,9,10,12,13-octahydro-, [6R-(6alpha,6abeta,7beta,9alpha)]- 500053 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45 280.40 unknown https://doi.org/10.3987/COM-93-6644
> Alkaloids and derivatives / Plumeran-type alkaloids
Jerantinine A 25112179 Click to see CCC12CC(=C3C4(C1N(CC4)CC=C2)C5=CC(=C(C=C5N3)OC)O)C(=O)OC 382.50 unknown https://doi.org/10.1016/0031-9422(79)83016-2
methyl (1R,12R,19S)-12-ethyl-15-oxo-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9,13-pentaene-10-carboxylate 10915101 Click to see CCC12CC(=C3C4(C1N(CC4)C(=O)C=C2)C5=CC=CC=C5N3)C(=O)OC 350.40 unknown https://doi.org/10.1016/S0031-9422(00)82103-2
> Alkaloids and derivatives / Vobasan alkaloids
(1S,12S,14S,15S,18S)-10-[(1S,12S,14S,15S,18S)-18-carboxy-15-ethyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-15-ethyl-12-hydroxy-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylic acid 102076557 Click to see CCC1CN(C2CC3=C(C(CC1C2C(=O)O)N4C5=CC=CC=C5C6=C4C(CC7C(CN(C(C6)C7C(=O)O)C)CC)O)NC8=CC=CC=C38)C 666.80 unknown https://doi.org/10.3987/COM-93-6644
Dregamine 99108 Click to see CCC1CN(C2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34)C 354.40 unknown https://doi.org/10.3987/COM-93-6644
methyl (1S,14S,15S,18R)-15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 45268651 Click to see CCC1CN(C2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34)C 354.40 unknown https://doi.org/10.3987/COM-93-6644
methyl (1S,14S,15S)-15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 20056338 Click to see CCC1CN(C2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34)C 354.40 unknown https://doi.org/10.3987/COM-93-6644
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
Ellipticine 3213 Click to see CC1=C2C=CN=CC2=C(C3=C1NC4=CC=CC=C43)C 246.31 unknown https://doi.org/10.3987/COM-93-6644
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
(3S,7R)-7-ethyl-5-methyl-5,12-diazatetracyclo[9.7.0.03,8.013,18]octadeca-1(11),13,15,17-tetraene-2,10-dione 102242490 Click to see CCC1CN(CC2C1CC(=O)C3=C(C2=O)C4=CC=CC=C4N3)C 310.40 unknown https://doi.org/10.3987/COM-93-6644
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
Methuenine 6441095 Click to see CC=C1CN(CC2C1CC(=O)C3=C(C2)C4=CC=CC=C4N3)C 294.40 unknown https://doi.org/10.1016/S0031-9422(00)89235-3
https://doi.org/10.3987/COM-93-6644
Pyrido(3',4':4,5)cyclohept(1,2-b)indol-6(2H)-one, 4-ethylidene-1,3,4,4a,5,7,12,12a-octahydro-2-methyl-, (4E,4aR,12aR)- 6440473 Click to see CC=C1CN(CC2C1CC(=O)C3=C(C2)C4=CC=CC=C4N3)C 294.40 unknown https://doi.org/10.3987/COM-93-6644
Silicine 21586678 Click to see CCC1CN(CC2C1CC(=O)C3=C(C2)C4=CC=CC=C4N3)C 296.40 unknown https://doi.org/10.3987/COM-93-6644

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