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Tabernaemontana bovina

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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 UUID643fee7ba5c68824578441
Scientific name Tabernaemontana bovina
Authority Lour.
First published in Fl. Cochinch. : 118 (1790)

Description Top

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It is a shrub or small tree that grows up to 4 meters tall. The leaves are opposite, oblong-lanceolate, and up to 8 cm long. The flowers are white, fragrant, and arranged in umbels. The fruit is a drupe, up to 2 cm in diameter, with a single seed.

Tabernaemontana bovina is a species of plant in the Apocynaceae family, native to southern China and northern Indochina. It is a shrub or small tree that can reach up to 4 meters in height. Its leaves are opposite, oblong-lanceolate, and up to 8 cm long. The flowers are white, fragrant, and arranged in umbels, while the fruit is a drupe, up to 2 cm in diameter, with a single seed.

Synonyms Top

Scientific name Authority First published in
Tabernaemontana balansae Pit. Fl. Indo-Chine 3: 1148 (1933)
Tabernaemontana bonii Pit. Fl. Indo-Chine 3: 1151 (1933)
Tabernaemontana nemoralis Pit. Fl. Indo-Chine 3: 1155 (1933)
Tabernaemontana officinalis (Tsiang) P.T.Li Guihaia 6: 172 (1986)
Tabernaemontana pallida Hu J. Arnold Arbor. 6: 143 (1925)
Tabernaemontana daktoensis (Lý) Lý Fl. Vietnam 5: 152 (2007)
Tabernaemontana dakgleiensis (Lý) Lý Fl. Vietnam 5: 134 (2007)
Tabernaemontana hoabinhensis (Lý) Lý Fl. Vietnam 5: 139 (2007)
Tabernaemontana longocuspidata (Lý) Lý Fl. Vietnam 5: 148 (2007)
Tabernaemontana balansae var. macrophylla (Lý) Lý Fl. Vietnam 5: 138 (2007)
Ervatamia balansae (Pit.) Pichon Mém. Mus. Natl. Hist. Nat. 27: 219 (1948)
Ervatamia balansae var. macrophylla Lý Feddes Repert. 97: 451 (1986)
Ervatamia bonii (Pit.) Pichon Mém. Mus. Natl. Hist. Nat. 27: 219 (1948)
Ervatamia bovina (Lour.) Markgr. Notizbl. Bot. Gart. Berlin-Dahlem 12: 547 (1935)
Ervatamia dakgleiensis Lý Feddes Repert. 92: 621 (1981)
Ervatamia daktoensis Lý Feddes Repert. 92: 624 (1981)
Ervatamia hoabinhensis Lý J. Biol. (Vietnam) 3(3): 21 (1981)
Ervatamia lamdongensis Lý Feddes Repert. 96: 179 (1985)
Ervatamia longocuspidata Lý Feddes Repert. 96: 29 (1985)
Ervatamia nemoralis (Pit.) Markgr. Notizbl. Bot. Gart. Berlin-Dahlem 12: 547 (1935)
Ervatamia officinalis Tsiang Acta Phytotax. Sin. 8: 239 (1963)
Ervatamia pallida Pierre in Spire, Caoutch. Indo-Chine 141 (1906).
Ervatamia petelotii Lý Feddes Repert. 96: 25 (1985)
Ervatamia tonkinensis (Pierre ex Pit.) Markgr. Notizbl. Bot. Gart. Berlin-Dahlem 12: 547 (1935)

Common names Top

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Language Common/alternative name
Chinese 药用狗牙花

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
  • Asia-tropical
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000319746
Tropicos 1801988
KEW urn:lsid:ipni.org:names:82026-1
The Plant List kew-200594
Open Tree Of Life 5794157
Observations.org 278340
IUCN Red List 147624535
IPNI 82026-1
iNaturalist 503364
GBIF 3618689
Freebase /m/012cdxz5
Elurikkus 385062
Wikipedia Tabernaemontana_bovina

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
Iboga-Type Alkaloids from Ervatamia officinalis. Tang BQ, Wang WJ, Huang XJ, Li GQ, Wang L, Jiang RW, Yang TT, Shi L, Zhang XQ, Ye WC J Nat Prod 22-Aug-2014
doi:10.1021/NP500240B
PMID:25093992
Chemical constituents antioxidant and anticholinesterasic activity of Tabernaemontana catharinensis. Nicola C, Salvador M, Gower AE, Moura S, Echeverrigaray S ScientificWorldJournal 28-Jul-2013
PMCID:PMC3745974
doi:10.1155/2013/519858
PMID:23983637
Indole alkaloids from three species of the Ervatamia genus: E. officinalis, E. divaricata, and E. divaricata Gouyahua. Zhang H, Wang XN, Lin LP, Ding J, Yue JM J Nat Prod 01-Jan-2007
doi:10.1021/NP060344O
PMID:17253850
Two Further bis-indole alkaloids fromTabernaemontana bovina Helmut Ripperger, Christine Kamperdick, Günter Adam, Trinh Phuong Lien, Tran Van Sung Wiley 03-Dec-2005
doi:10.1002/(SICI)1521-3897(199907)341:5<506::AID-PRAC506>3.0.CO;2-E
Indole alkaloids from Tabernaemontana australis (Muell. Arg) Miers that inhibit acetylcholinesterase enzyme. Andrade MT, Lima JA, Pinto AC, Rezende CM, Carvalho MP, Epifanio RA Bioorg Med Chem 02-Jun-2005
doi:10.1016/J.BMC.2005.03.045
PMID:15911323
Indole alkaloids from tabernaemontana bovina Trinh Phuong Lien, Helmut Ripperger, Andrea Porzel, Kurt Merzweiler, Tran Van Sung, Günter Adam Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00127-7
Bis-indole alkaloids from Tabernaemontana bovina. Lien TP, Kamperdick C, Van Sung T, Adam G, Ripperger H Phytochemistry 20-Nov-1998
doi:10.1016/S0031-9422(98)00227-1
PMID:11711104

Phytochemical Profile Top

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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 / Akuammilan and related alkaloids
methyl (1R,10S,12R,13E,18S)-13-ethylidene-8,15-diazapentacyclo[10.5.1.01,9.02,7.010,15]octadeca-2,4,6,8-tetraene-18-carboxylate 95224807 Click to see CC=C1CN2CCC34C(C1CC2C3=NC5=CC=CC=C45)C(=O)OC 322.40 unknown https://doi.org/10.1021/NP060344O
Strictamin 5324377 Click to see CC=C1CN2CCC34C(C1CC2C3=NC5=CC=CC=C45)C(=O)OC 322.40 unknown https://doi.org/10.1021/NP060344O
Strictamine 21159178 Click to see CC=C1CN2CCC34C(C1CC2C3=NC5=CC=CC=C45)C(=O)OC 322.40 unknown https://doi.org/10.1021/NP060344O
> Alkaloids and derivatives / Aspidospermatan-type alkaloids
(1S,9R,12R,13S,15S,20R)-12-ethyl-8-methyl-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2,4,6-trien-16-one 100927176 Click to see CCC12CCC3C4(C1N(CC4)C(=O)C5C2O5)C6=CC=CC=C6N3C 324.40 unknown https://doi.org/10.1016/S0031-9422(98)00127-7
(1S,9S,12S,13S,15R,20R)-12-ethyl-4-[(1R,9R,12S,13S,15R,20R)-12-ethyl-8-methyl-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2,4,6-trien-9-yl]-8-methyl-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2(7),3,5-triene 162874695 Click to see CCC12CCC3C4(C1N(CC4)CC5C2O5)C6=C(N3C)C=CC(=C6)C78CCC9(C1C(O1)CN1C9C7(CC1)C1=CC=CC=C1N8C)CC 618.80 unknown https://doi.org/10.1016/S0031-9422(98)00227-1
(1S,9S,12S,13S,15R,20R)-12-ethyl-4-[(1S,9R,12S,13S,15R,20R)-12-ethyl-8-methyl-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2,4,6-trien-9-yl]-8-methyl-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2(7),3,5-triene 100927794 Click to see CCC12CCC3C4(C1N(CC4)CC5C2O5)C6=C(N3C)C=CC(=C6)C78CCC9(C1C(O1)CN1C9C7(CC1)C1=CC=CC=C1N8C)CC 618.80 unknown https://doi.org/10.1016/S0031-9422(98)00227-1
(1S,9S,12S,13S,15R,20R)-12-ethyl-8-methyl-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2,4,6-triene 11415660 Click to see CCC12CCC3C4(C1N(CC4)CC5C2O5)C6=CC=CC=C6N3C 310.40 unknown https://doi.org/10.1016/S0031-9422(98)00127-7
(1S,9S,12S,13S,15S,20R)-12-ethyl-8-methyl-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2,4,6-trien-16-one 163052203 Click to see CCC12CCC3C4(C1N(CC4)C(=O)C5C2O5)C6=CC=CC=C6N3C 324.40 unknown https://doi.org/10.1016/S0031-9422(98)00127-7
12-Ethyl-8-methyl-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2,4,6-triene 72952784 Click to see CCC12CCC3C4(C1N(CC4)CC5C2O5)C6=CC=CC=C6N3C 310.40 unknown https://doi.org/10.1016/S0031-9422(98)00127-7
Conophyllidine 44566831 Click to see CCC12CC(=C3C4(C1N(CC4)CC=C2)C5=C(N3)C=C6C(=C5)C7C(O6)C(C8(CC(=C9C1(C8N7CC1)C1=CC(=C(C(=C1N9)OC)OC)O)C(=O)OC)CC)O)C(=O)OC 778.90 unknown https://doi.org/10.1021/NP060344O
dimethyl (2R,6S,13R,22R,23R,24R,35S,38S,39R)-13,24-diethyl-23,32-dihydroxy-30,31-dimethoxy-21-oxa-1,9,17,28-tetrazaundecacyclo[22.13.1.16,9.02,22.03,20.05,18.06,16.027,35.029,34.035,38.013,39]nonatriaconta-3,5(18),11,15,19,26,29,31,33-nonaene-15,26-dicarboxylate 162818904 Click to see CCC12CC(=C3C4(C1N(CC4)CC=C2)C5=C(N3)C=C6C(=C5)C7C(O6)C(C8(CC(=C9C1(C8N7CC1)C1=CC(=C(C(=C1N9)OC)OC)O)C(=O)OC)CC)O)C(=O)OC 778.90 unknown https://doi.org/10.1021/NP060344O
methyl (1R,12S,13S,15R,16R,20R)-12-ethyl-16-[(1S,9S,12S,13S,15R,20R)-12-ethyl-8-methyl-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2,4,6-trien-3-yl]-4-hydroxy-5,6-dimethoxy-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2,4,6,9-tetraene-10-carboxylate 163103564 Click to see CCC12CCC3C4(C1N(CC4)CC5C2O5)C6=C(C=CC=C6N3C)C7C8C(O8)C9(CC(=C1C2(C9N7CC2)C2=CC(=C(C(=C2N1)OC)OC)O)C(=O)OC)CC 736.90 unknown https://doi.org/10.1016/S0031-9422(98)00127-7
Methyl 12-ethyl-16-(12-ethyl-8-methyl-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2,4,6-trien-3-yl)-4-hydroxy-5,6-dimethoxy-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2,4,6,9-tetraene-10-carboxylate 163103563 Click to see CCC12CCC3C4(C1N(CC4)CC5C2O5)C6=C(C=CC=C6N3C)C7C8C(O8)C9(CC(=C1C2(C9N7CC2)C2=CC(=C(C(=C2N1)OC)OC)O)C(=O)OC)CC 736.90 unknown https://doi.org/10.1016/S0031-9422(98)00127-7
> Alkaloids and derivatives / Corynanthean-type alkaloids
methyl (13Z)-13-ethylidene-18-formyl-8,15-diazapentacyclo[10.5.1.01,9.02,7.010,15]octadeca-2,4,6,8-tetraene-18-carboxylate 5324378 Click to see CC=C1CN2CCC34C5=CC=CC=C5N=C3C2CC1C4(C=O)C(=O)OC 350.40 unknown https://doi.org/10.1021/NP060344O
methyl (1R,10R,12R,13Z,18R)-13-ethylidene-18-formyl-8,15-diazapentacyclo[10.5.1.01,9.02,7.010,15]octadeca-2,4,6,8-tetraene-18-carboxylate 163186541 Click to see CC=C1CN2CCC34C5=CC=CC=C5N=C3C2CC1C4(C=O)C(=O)OC 350.40 unknown https://doi.org/10.1021/NP060344O
> Alkaloids and derivatives / Eburnan-type alkaloids
Dehydroepivincamine 182094 Click to see CCC12CC(N3C4=CC=CC=C4C5=C3C1N(CC5)CC=C2)(C(=O)OC)O 352.40 unknown https://doi.org/10.1021/NP060344O
> Alkaloids and derivatives / Ibogan-type alkaloids
(1R,10R,15R,17S,18S)-17-ethyl-6,7-dimethoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2,4,6,8-tetraene 163106244 Click to see CCC1CC2CC3C1N(C2)CCC4C3=NC5=CC(=C(C=C45)OC)OC 340.50 unknown https://doi.org/10.1016/S0031-9422(98)00127-7
(1R,10S,15R,17S,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2,4(9),5,7-tetraen-10-ol 11110205 Click to see CCC1CC2CC3C1N(C2)CCC4(C3=NC5=C4C=C(C=C5)OC)O 326.40 unknown https://doi.org/10.1021/NP500240B
(1R,15S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene 89578867 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC 310.40 unknown https://doi.org/10.1021/NP060344O
https://doi.org/10.1016/S0031-9422(98)00127-7
10-Methoxyibogamine 442108 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC 310.40 unknown https://doi.org/10.1021/NP060344O
https://doi.org/10.1016/S0031-9422(98)00127-7
12,13-Dimethoxyibogamine 193302 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)OC 340.50 unknown https://doi.org/10.1016/S0031-9422(98)00127-7
16'-Demethoxycarbonylvoacamine 44418785 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC 646.90 unknown https://doi.org/10.1021/NP060344O
19(S)-Hydroxyconopharyngine 102004638 Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)OC)C(=O)OC)O 414.50 unknown https://doi.org/10.1016/S0031-9422(98)00127-7
3-Oxoibogaine hydroxyindolenine 163184296 Click to see CCC1CC2CC3C1N(C2=O)CCC4(C3=NC5=C4C=C(C=C5)OC)O 340.40 unknown https://doi.org/10.1021/NP500240B
Ibogaine 197060 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC 310.40 unknown https://doi.org/10.1016/S0031-9422(98)00127-7
https://doi.org/10.1021/NP060344O
methyl (1R,12S,14R,15S)-15-ethyl-12-[(1R,15R,17S,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraen-6-yl]-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 44418784 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)C6CC7C(CN(C(C7C(=O)OC)CC8=C6NC9=CC=CC=C89)C)CC 648.90 unknown https://doi.org/10.1021/NP060344O
methyl (1R,12S,14S)-15-ethylidene-12-[(1R,15R,17S,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraen-6-yl]-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 162999249 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC 646.90 unknown https://doi.org/10.1021/NP060344O
methyl (1S,14R,15R,17S,18S)-17-ethyl-14-hydroxy-6,7-dimethoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 163106545 Click to see CCC1CC2CC3(C1N(C2O)CCC4=C3NC5=CC(=C(C=C45)OC)OC)C(=O)OC 414.50 unknown https://doi.org/10.1021/NP060344O
methyl (1S,15R,17S,18S)-17-[(1S)-1-hydroxyethyl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 101243095 Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)OC)C(=O)OC)O 384.50 unknown https://doi.org/10.1016/S0031-9422(98)00227-1
methyl (1S,15R,17S,18S)-17-[(1S)-1-hydroxyethyl]-6,7-dimethoxy-3,13-diazapentacyclo[13.3.1.0^{2,10.0^{4,9.0^{13,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 138376516 Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)OC)C(=O)OC)O 414.50 unknown https://doi.org/10.1016/S0031-9422(98)00127-7
methyl (1S,17S,18S)-17-[(1S)-1-hydroxyethyl]-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 163187265 Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC)O 384.50 unknown https://doi.org/10.1021/NP060344O
Voacristine 196982 Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC)O 384.50 unknown https://doi.org/10.1021/NP060344O
> Alkaloids and derivatives / Macroline alkaloids
Methyl (12S,14S,15E)-15-ethylidene-13-(hydroxymethyl)-3-methyl-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate 134716706 Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=CC=CC=C45)C)(CO)C(=O)OC 366.50 unknown https://doi.org/10.1021/NP060344O
Methyl 15-ethylidene-13-(hydroxymethyl)-3-methyl-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate 99116 Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=CC=CC=C45)C)(CO)C(=O)OC 366.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745974/
https://doi.org/10.1016/J.BMC.2005.03.045
https://doi.org/10.1021/NP060344O
Sarpagan-16-carboxylic acid, 17-hydroxy-1-methyl-, methyl ester, (16R)- 12444908 Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=CC=CC=C45)C)(CO)C(=O)OC 366.50 unknown https://doi.org/10.1021/NP060344O
> Alkaloids and derivatives / Plumeran-type alkaloids
(1S,12S,14S,19R)-14-ethyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,8-tetraen-14-ol 163090373 Click to see CCC1(CC2CCC3=NC4=CC=CC=C4C35C2N(C1)CC5)O 296.40 unknown https://doi.org/10.1021/NP060344O
> Alkaloids and derivatives / Quebrachamine alkaloids
(15S,16S,18R)-15-ethyl-9-methoxy-17-oxa-1,11-diazapentacyclo[13.4.1.04,12.05,10.016,18]icosa-4(12),5(10),6,8-tetraene 163024810 Click to see CCC12CCC3=C(CCN(C1)CC4C2O4)C5=C(N3)C(=CC=C5)OC 326.40 unknown https://doi.org/10.1021/NP060344O
12-Methoxyvoaphylline 13342867 Click to see CCC12CN(CCC3=C(CC1OC)NC4=CC=CC=C34)CC5C2O5 326.40 unknown https://doi.org/10.1021/NP060344O
Hecubine 11438319 Click to see CCC12CCC3=C(CCN(C1)CC4C2O4)C5=CC=CC=C5N3C 310.40 unknown https://doi.org/10.1016/S0031-9422(98)00127-7
> Alkaloids and derivatives / Vobasan alkaloids
(1S,14R,15E,18R)-15-ethylidene-18-(hydroxymethyl)-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-one 163015309 Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2CO)NC4=CC=CC=C34)C 324.40 unknown https://doi.org/10.1021/NP060344O
(1S,14R,15Z,18R)-15-ethylidene-18-(hydroxymethyl)-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-one 101926661 Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2CO)NC4=CC=CC=C34)C 324.40 unknown https://doi.org/10.1021/NP060344O
methyl (1R,14S,15E,18S)-15-ethylidene-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 36688305 Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34)C 352.40 unknown https://doi.org/10.1021/NP060344O
methyl (1S,12S,14R,15E,18S)-15-ethylidene-12-[(1S,9S,12S,13S,15R,20R)-12-ethyl-8-methyl-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2(7),3,5-trien-4-yl]-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 102469677 Click to see CCC12CCC3C4(C1N(CC4)CC5C2O5)C6=C(N3C)C=CC(=C6)C7CC8C(C(CC9=C7NC1=CC=CC=C91)N(CC8=CC)C)C(=O)OC 646.90 unknown https://doi.org/10.1002/(SICI)1521-3897(199907)341:5<506::AID-PRAC506>3.0.CO;2-E
methyl (1S,14R,15Z,18S)-15-ethylidene-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 101281359 Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34)C 352.40 unknown https://doi.org/10.1021/NP060344O
Tabernaemontavine 102276358 Click to see CCC12CCC3C4(C1N(CC4)CC5C2O5)C6=C(N3C)C=CC(=C6)C7CC8C(=CC)CN(C(C8(CO)C(=O)OC)CC9=C7NC1=CC=CC=C91)C 676.90 unknown https://doi.org/10.1002/(SICI)1521-3897(199907)341:5<506::AID-PRAC506>3.0.CO;2-E
> Alkaloids and derivatives / Yohimbine alkaloids
Cathenamine 443361 Click to see CC1C2=CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 350.40 unknown https://doi.org/10.1021/NP500240B
> Benzenoids / Phenol ethers / Anisoles
Ervaoffines D 163184308 Click to see CCC1CC2CC3C1N(C2=O)CCC(=O)C4=C(C=CC(=C4)OC)NC3=O 356.40 unknown https://doi.org/10.1021/NP500240B
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
methyl (2S,3R,4R)-3-ethenyl-4-[[(1S)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl]methyl]-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 154497529 Click to see COC(=O)C1=COC(C(C1CC2C3=C(CCN2)C4=CC=CC=C4N3)C=C)OC5C(C(C(C(O5)CO)O)O)O 530.60 unknown https://doi.org/10.1021/NP500240B
Strictosidine 161336 Click to see COC(=O)C1=COC(C(C1CC2C3=C(CCN2)C4=CC=CC=C4N3)C=C)OC5C(C(C(C(O5)CO)O)O)O 530.60 unknown https://doi.org/10.1021/NP500240B
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
[(1R,2S,5R,6R,10R,13R,14S,16S)-6-(furan-3-yl)-13-hydroxy-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadec-11-en-14-yl] (E)-2-methylbut-2-enoate 162917517 Click to see CC=C(C)C(=O)OC1C(C(C2(C3CCC4(C(C3=CC1(C2=O)O)CC(=O)OC4C5=COC=C5)C)C)CC(=O)OC)(C)C 568.70 unknown https://doi.org/10.1016/S0031-9422(98)00227-1
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
(5Z)-2-(5-bromo-1H-indole-3-carbonyl)-5-[(6-hydroxy-1H-indol-3-yl)methylidene]-1H-imidazol-4-one 10456352 Click to see C1=CC2=C(C=C1O)NC=C2C=C3C(=O)N=C(N3)C(=O)C4=CNC5=C4C=C(C=C5)Br 449.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745974/
https://doi.org/10.1016/J.BMC.2005.03.045
https://doi.org/10.1021/NP060344O
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
(3R,7S,8S)-7-ethyl-5-methyl-5,12-diazatetracyclo[9.7.0.03,8.013,18]octadeca-1(11),13,15,17-tetraene-2,10-dione 101774113 Click to see CCC1CN(CC2C1CC(=O)C3=C(C2=O)C4=CC=CC=C4N3)C 310.40 unknown https://doi.org/10.1021/NP060344O
(7S,8S)-7-ethyl-5-methyl-5,12-diazatetracyclo[9.7.0.03,8.013,18]octadeca-1(11),2,13,15,17-pentaen-10-one 101774115 Click to see CCC1CN(CC2=CC3=C(C(=O)CC12)NC4=CC=CC=C43)C 294.40 unknown https://doi.org/10.1021/NP060344O
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
(3R,7S,8S)-7-ethyl-5-methyl-5,12-diazatetracyclo[9.7.0.03,8.013,18]octadeca-1(11),13,15,17-tetraen-10-one 101774112 Click to see CCC1CN(CC2C1CC(=O)C3=C(C2)C4=CC=CC=C4N3)C 296.40 unknown https://doi.org/10.1021/NP060344O
(3S,7S,8S)-7-ethyl-5-methyl-5,12-diazatetracyclo[9.7.0.03,8.013,18]octadeca-1(11),13,15,17-tetraen-10-one 101774114 Click to see CCC1CN(CC2C1CC(=O)C3=C(C2)C4=CC=CC=C4N3)C 296.40 unknown https://doi.org/10.1021/NP060344O
7-Ethyl-5-methyl-5,12-diazatetracyclo[9.7.0.03,8.013,18]octadeca-1(11),13,15,17-tetraen-10-one 73806781 Click to see CCC1CN(CC2C1CC(=O)C3=C(C2)C4=CC=CC=C4N3)C 296.40 unknown https://doi.org/10.1021/NP060344O
Methuenine 6441095 Click to see CC=C1CN(CC2C1CC(=O)C3=C(C2)C4=CC=CC=C4N3)C 294.40 unknown https://doi.org/10.1021/NP060344O
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
1-[(1R,15R)-3,13-diazapentacyclo[13.3.1.01,13.02,10.04,9]nonadeca-2(10),4,6,8,17-pentaen-17-yl]ethanone 102103442 Click to see CC(=O)C1=CC23CC(C1)CN2CCC4=C3NC5=CC=CC=C45 292.40 unknown https://doi.org/10.1021/NP500240B
4,21-Dehydrogeissoschizine 5280619 Click to see CC=C1C=[N+]2CCC3=C(C2CC1C(=CO)C(=O)OC)NC4=CC=CC=C34 351.40 unknown https://doi.org/10.1021/NP500240B
methyl (1R,9R,11S,14E,15R,17S,19S)-14-ethylidene-18-oxa-2,12-diazahexacyclo[9.6.1.19,15.01,9.03,8.012,17]nonadeca-3,5,7-triene-19-carboxylate 85473463 Click to see CC=C1CN2C3CC1C(C45C3(NC6=CC=CC=C64)OC2C5)C(=O)OC 338.40 unknown https://doi.org/10.1021/NP060344O
methyl (1R,9R,11S,14E,17S)-14-ethylidene-18-oxa-2,12-diazahexacyclo[9.6.1.19,15.01,9.03,8.012,17]nonadeca-3,5,7-triene-19-carboxylate 102004475 Click to see CC=C1CN2C3CC1C(C45C3(NC6=CC=CC=C64)OC2C5)C(=O)OC 338.40 unknown https://doi.org/10.1021/NP060344O
> Organoheterocyclic compounds / Quinolizidines
Iboluteine 21589055 Click to see CCC1CC2CC3C1N(C2)CCC34C(=O)C5=C(N4)C=CC(=C5)OC 326.40 unknown https://doi.org/10.1021/NP500240B

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