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Tabernaemontana cymosa

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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 UUID643fee7e420fd082231205
Scientific name Tabernaemontana cymosa
Authority Jacq.
First published in Enum. Syst. Pl. : 14 (1760)

Description Top

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Synonyms Top

Scientific name Authority First published in
Merizadenia arcuata Miers Apocyn. S. Amer. : 79 (1878)
Peschiera arcuata (Ruiz & Pav.) Markgr. Notizbl. Bot. Gart. Berlin-Dahlem 14: 171 (1938)
Peschiera buchtienii (H.J.P.Winkl.) Markgr. Notizbl. Bot. Gart. Berlin-Dahlem 14: 171 (1938)
Peschiera concinna Miers Apocyn. S. Amer. : 44 (1878)
Peschiera cymosa (Jacq.) Dugand Caldasia 2: 299 (1943)
Peschiera psychotriifolia Miers Apocyn. S. Amer. : 42 (1878)
Peschiera puberiflora Miers Apocyn. S. Amer. : 43 (1878)
Peschiera umbrosa Miers Apocyn. S. Amer. : 44 (1878)
Taberna cymosa Miers Apocyn. S. Amer. : 62 (1878)
Tabernaemontana arcuata Ruiz & Pav. Fl. Peruv. 2: 22 (1799)
Tabernaemontana buchtienii H.J.P.Winkl. Repert. Spec. Nov. Regni Veg. 7: 244 (1909)
Tabernaemontana concinna (Miers) J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(5): 402 (1959)
Tabernaemontana mapirensis Rusby Bull. New York Bot. Gard. 8: 115 (1912)
Tabernaemontana psychotrifolia Kunth Nov. Gen. Sp. 3: 227 (1819)
Tabernaemontana psychotrioides G.Don Gen. Hist. 4: 90 (1837)
Tabernaemontana umbrosa Kunth Nov. Gen. Sp. 3: 226 (1819)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
    • Caribbean
      • Trinidad-Tobago
    • Northern South America
      • Guyana
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000319820
Tropicos 1801099
KEW urn:lsid:ipni.org:names:82084-1
The Plant List kew-200661
Open Tree Of Life 312295
NCBI Taxonomy 761066
IUCN Red List 180065182
IPNI 82084-1
iNaturalist 549346
GBIF 3617922

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
Medicinal Plants against Viral Infections: A Review of Metabolomics Evidence for the Antiviral Properties and Potentials in Plant Sources Adeosun WB, Loots DT Viruses 31-Jan-2024
PMCID:PMC10892737
doi:10.3390/v16020218
PMID:38399995
Role of phytocompounds as the potential anti-viral agent: an overview Mohanty SS, Sahoo CR, Paidesetty SK, Padhy RN Naunyn Schmiedebergs Arch Pharmacol 09-May-2023
PMCID:PMC10169142
doi:10.1007/s00210-023-02517-2
PMID:37160482
Therapeutic Potential of Medicinal Plants against Dengue Infection: A Mechanistic Viewpoint Altamish M, Khan M, Baig MS, Pathak B, Rani V, Akhtar J, Khan AA, Ahmad S, Krishnan A ACS Omega 06-Jul-2022
PMCID:PMC9301714
doi:10.1021/acsomega.2c00625
PMID:35874231
Production, Transmission, Pathogenesis, and Control of Dengue Virus: A Literature-Based Undivided Perspective Islam MT, Quispe C, Herrera-Bravo J, Sarkar C, Sharma R, Garg N, Fredes LI, Martorell M, Alshehri MM, Sharifi-Rad J, Daştan SD, Calina D, Alsafi R, Alghamdi S, Batiha GE, Cruz-Martins N Biomed Res Int 15-Dec-2021
PMCID:PMC8694986
doi:10.1155/2021/4224816
PMID:34957305
Indole alkaloids inhibit zika and chikungunya virus infection in different cell lines Monsalve-Escudero LM, Loaiza-Cano V, Pájaro-González Y, Oliveros-Díaz AF, Diaz-Castillo F, Quiñones W, Robledo S, Martinez-Gutierrez M BMC Complement Med Ther 28-Aug-2021
PMCID:PMC8397866
doi:10.1186/s12906-021-03386-z
PMID:34454481
The Antiviral and Virucidal Activities of Voacangine and Structural Analogs Extracted from Tabernaemontana cymosa Depend on the Dengue Virus Strain Monsalve-Escudero LM, Loaiza-Cano V, Zapata-Cardona MI, Quintero-Gil DC, Hernández-Mira E, Pájaro-González Y, Oliveros-Díaz AF, Diaz-Castillo F, Quiñones W, Robledo S, Martinez-Gutierrez M Plants (Basel) 23-Jun-2021
PMCID:PMC8309144
doi:10.3390/plants10071280
PMID:34201900
Molecular Human Targets of Bioactive Alkaloid-Type Compounds from Tabernaemontana cymose Jacq. Oliveros-Díaz A, Olivero-Verbel J, Pájaro-González Y, Díaz-Castillo F Molecules 21-Jun-2021
PMCID:PMC8234993
doi:10.3390/molecules26123765
PMID:34205626
Medicinal plants: Treasure for antiviral drug discovery Ali SI, Sheikh WM, Rather MA, Venkatesalu V, Muzamil Bashir S, Nabi SU Phytother Res 16-Feb-2021
PMCID:PMC8013762
doi:10.1002/ptr.7039
PMID:33590931
Major Bioactive Alkaloids and Biological Activities of Tabernaemontana Species (Apocynaceae) Naidoo CM, Naidoo Y, Dewir YH, Murthy HN, El-Hendawy S, Al-Suhaibani N Plants (Basel) 05-Feb-2021
PMCID:PMC7915066
doi:10.3390/plants10020313
PMID:33562893
Phytochemicals as Antiviral Agents: Recent Updates Ghildiyal R, Prakash V, Chaudhary VK, Gupta V, Gabrani R Plant-derived Bioactives 12-May-2020
PMCID:PMC7211506
doi:10.1007/978-981-15-1761-7_12
In vitro and in silico anti-dengue activity of compounds obtained from Psidium guajava through bioprospecting Trujillo-Correa AI, Quintero-Gil DC, Diaz-Castillo F, Quiñones W, Robledo SM, Martinez-Gutierrez M BMC Complement Altern Med 06-Nov-2019
PMCID:PMC6836419
doi:10.1186/s12906-019-2695-1
PMID:31694638
Antiviral effect of compounds derived from the seeds of Mammea americana and Tabernaemontana cymosa on Dengue and Chikungunya virus infections Gómez-Calderón C, Mesa-Castro C, Robledo S, Gómez S, Bolivar-Avila S, Diaz-Castillo F, Martínez-Gutierrez M BMC Complement Altern Med 18-Jan-2017
PMCID:PMC5241984
doi:10.1186/s12906-017-1562-1
PMID:28100218
Monocyclic Phenolic Acids; Hydroxy- and Polyhydroxybenzoic Acids: Occurrence and Recent Bioactivity Studies Khadem S, Marles RJ Molecules 08-Nov-2010
PMCID:PMC6259451
doi:10.3390/molecules15117985
PMID:21060304
Alkaloids and other compounds from seeds of Tabernaemontana cymosa Hans Achenbach, Monika Benirschke, Ruben Torrenegra Elsevier BV 30-Apr-2003
doi:10.1016/S0031-9422(96)00645-0
Alkaloids from stem bark and leaves of Peschiera buchtieni M Azoug Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(95)00050-H

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
Apodine 441984 Click to see COC(=O)C1=C2C3(CCN4C3C5(C1)CC(=O)OC5CC4)C6=CC=CC=C6N2 366.40 unknown https://doi.org/10.1016/0031-9422(95)00050-H
> Alkaloids and derivatives / Corynanthean-type alkaloids
methyl (2R)-2-[(2R,3Z,12bS)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]-3-hydroxypropanoate 6504264 Click to see CC=C1CN2CCC3=C(C2CC1C(CO)C(=O)OC)NC4=CC=CC=C34 354.40 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
> 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/10.1016/0031-9422(95)00050-H
(1S)-1-[(1R,15R,17R,18R)-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraen-17-yl]ethanol 44566758 Click to see CC(C1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45)O 296.40 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
https://doi.org/10.1016/0031-9422(95)00050-H
10-Hydroxycoronaridine 52948159 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)O)C(=O)OC 354.40 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
19-Epi-heyneanine 44566759 Click to see CC(C1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45)O 296.40 unknown https://doi.org/10.1016/0031-9422(95)00050-H
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/10.1016/0031-9422(95)00050-H
Coronaridine 73489 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC 338.40 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
https://doi.org/10.1016/0031-9422(95)00050-H
Ibogamine-18-carboxylic acid, 12-methoxy-, methyl ester 363270 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC 368.50 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
methyl (15S,17S)-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 137628478 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC 338.40 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
https://doi.org/10.1016/0031-9422(95)00050-H
methyl (1R,15S,17R,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 134688048 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC 368.50 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
methyl (1S,11R,13R,15S,16S,18S)-15-ethyl-19-oxa-9,17-diazahexacyclo[15.2.1.02,10.03,8.011,16.013,18]icosa-2(10),3,5,7-tetraene-11-carboxylate 102239678 Click to see CCC1CC2CC3(C1N4C2OC(C4)C5=C3NC6=CC=CC=C65)C(=O)OC 352.40 unknown https://doi.org/10.1016/0031-9422(95)00050-H
methyl (1S,14R,15E,18S)-12-[(1R,15R,17S,18S)-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraen-6-yl]-15-ethylidene-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 102147057 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=C4C=CC(=C5)C6CC7C(C(CC8=C6NC9=CC=CC=C89)NCC7=CC)C(=O)OC 602.80 unknown https://doi.org/10.1016/0031-9422(95)00050-H
methyl (1S,15R,17S,18S)-17-ethyl-11-hydroxy-14-oxo-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 102239681 Click to see CCC1CC2CC3(C1N(C2=O)CC(C4=C3NC5=CC=CC=C54)O)C(=O)OC 368.40 unknown https://doi.org/10.1016/0031-9422(95)00050-H
methyl (1S,15R,17S,18S)-17-ethyl-7-methoxy-14-oxo-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 12110672 Click to see CCC1CC2CC3(C1N(C2=O)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC 382.50 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
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/10.1016/0031-9422(95)00050-H
https://doi.org/10.1016/S0031-9422(96)00645-0
> Alkaloids and derivatives / Macroline alkaloids
(+)-Affinisine 5281346 Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=CC=CC=C45)C)CO 308.40 unknown https://doi.org/10.1016/0031-9422(95)00050-H
[(1S,14R,15Z)-15-ethylidene-3-methyl-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraen-13-yl]methanol 101286222 Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=CC=CC=C45)C)CO 308.40 unknown https://doi.org/10.1016/0031-9422(95)00050-H
18-Hydroxyaffinisine 101927633 Click to see CN1C2=CC=CC=C2C3=C1C4CC5C(C(C3)N4CC5=CCO)CO 324.40 unknown https://doi.org/10.1016/0031-9422(95)00050-H
Demethylaccedinisine 101927634 Click to see CC=C1CNC2CC3=C(C(CC1C2C(=O)OC)C4=CC5=C(C=C4)N(C6=C5CC7C(C8CC6N7CC8=CC)CO)C)NC9=CC=CC=C39 630.80 unknown https://doi.org/10.1016/0031-9422(95)00050-H
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/10.1016/0031-9422(95)00050-H
Tombozine 5318845 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)CO 294.40 unknown https://doi.org/10.1016/0031-9422(95)00050-H
> Alkaloids and derivatives / Plumeran-type alkaloids
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(96)00645-0
methyl (1S,12S,19R)-12-ethyl-16-oxido-8-aza-16-azoniapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9,13-pentaene-10-carboxylate 101702519 Click to see CCC12CC(=C3C4(C1[N+](CC4)(CC=C2)[O-])C5=CC=CC=C5N3)C(=O)OC 352.40 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
Tabersonine 20485 Click to see CCC12CC(=C3C4(C1N(CC4)CC=C2)C5=CC=CC=C5N3)C(=O)OC 336.40 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
> Alkaloids and derivatives / Quebrachamine alkaloids
Voaphylline 10469868 Click to see CCC12CCC3=C(CCN(C1)CC4C2O4)C5=CC=CC=C5N3 296.40 unknown https://doi.org/10.1016/0031-9422(95)00050-H
> Alkaloids and derivatives / Strychnos alkaloids
(+)-Condylocarpine 10914255 Click to see CC=C1C2CCN3C1C4(CC3)C5=CC=CC=C5NC4=C2C(=O)OC 322.40 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
Condylocarpine 5378963 Click to see CC=C1C2CCN3C1C4(CC3)C5=CC=CC=C5NC4=C2C(=O)OC 322.40 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
methyl (1S,2S,16Z)-16-ethylidene-2-(hydroxymethyl)-14-oxido-4-aza-14-azoniatetracyclo[12.2.2.03,11.05,10]octadeca-3(11),5,7,9-tetraene-2-carboxylate 101702518 Click to see CC=C1C[N+]2(CCC1C(C3=C(CC2)C4=CC=CC=C4N3)(CO)C(=O)OC)[O-] 370.40 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
Methyl (1S,2S,16Z)-16-ethylidene-2-(hydroxymethyl)-4,14-diazatetracyclo[12.2.2.03,11.05,10]octadeca-3(11),5,7,9-tetraene-2-carboxylate 20839798 Click to see CC=C1CN2CCC1C(C3=C(CC2)C4=CC=CC=C4N3)(CO)C(=O)OC 354.40 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
Stemmadenin 57506220 Click to see CC=C1CN2CCC1C(C3=C(CC2)C4=CC=CC=C4N3)(CO)C(=O)OC 354.40 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
> Alkaloids and derivatives / Vallesaman alkaloids
methyl (12R,13S,14Z)-14-ethylidene-12-(hydroxymethyl)-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraene-12-carboxylate 101286269 Click to see CC=C1CN2CCC1C(C3=C(C2)C4=CC=CC=C4N3)(CO)C(=O)OC 340.40 unknown https://doi.org/10.1016/0031-9422(95)00050-H
> Alkaloids and derivatives / Vobasan alkaloids
Ceridimine 134716651 Click to see CC=C1CN(C2CC3=C(C(CC1C2C(=O)OC)C4=CC5=C(C=C4)C(=CN5)CCN)NC6=CC=CC=C36)C 496.60 unknown https://doi.org/10.1016/0031-9422(95)00050-H
methyl (1S,12S,14R,15Z,18S)-12-[3-(2-aminoethyl)-1H-indol-6-yl]-15-ethylidene-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 101927635 Click to see CC=C1CNC2CC3=C(C(CC1C2C(=O)OC)C4=CC5=C(C=C4)C(=CN5)CCN)NC6=CC=CC=C36 482.60 unknown https://doi.org/10.1016/0031-9422(95)00050-H
Ochropamine 134716677 Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2C(=O)OC)N(C4=CC=CC=C34)C)C 366.50 unknown https://doi.org/10.1016/0031-9422(95)00050-H
> Alkaloids and derivatives / Yohimbine alkaloids
Tetrahydroalstonine 72340 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(+)-Lyoniresinol 11711453 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO 420.50 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(2E,4E,6E,8E)-12-[[(1S,3R,7R,8R,8aS)-7-hydroxy-8-(3-hydroxypropanoyl)-3,7,8-trimethyl-1,2,3,8a-tetrahydronaphthalen-1-yl]oxy]-10-hydroxy-5,9,11-trimethyl-12-oxo-dodeca-2,4,6,8-tetraenoic acid 6474046 Click to see CC1CC(C2C(=C1)C=CC(C2(C)C(=O)CCO)(C)O)OC(=O)C(C)C(C(=CC=CC(=CC=CC(=O)O)C)C)O 542.70 unknown https://doi.org/10.1016/0031-9422(95)00050-H
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Obtusifoliol 65252 Click to see CC1C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC4C(C)CCC(=C)C(C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
> 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://doi.org/10.1016/0031-9422(95)00050-H
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(3S,4R,4aS)-4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 354447 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 358.34 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
Sweroside 161036 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 358.34 unknown https://doi.org/10.1016/S0031-9422(96)00645-0
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
1,5-dimethyl-6H-pyrido[4,3-b]carbazole 5281407 Click to see CC1=C2C=CN=C(C2=CC3=C1NC4=CC=CC=C43)C 246.31 unknown https://doi.org/10.1016/0031-9422(95)00050-H
Olivacine 96364 Click to see CC1=C2C=CNC(=C2C=C3C1=NC4=CC=CC=C43)C 246.31 unknown https://doi.org/10.1016/0031-9422(95)00050-H
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
(4S,15R,16R,18S)-15-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.04,12.05,10.016,18]icosa-5,7,9,11-tetraen-4-ol 162213031 Click to see CCC12CCC3=NC4=CC=CC=C4C3(CCN(C1)CC5C2O5)O 312.40 unknown https://doi.org/10.1016/0031-9422(95)00050-H

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