Details Top

Internal ID UUID644039ca6d014093387465
Scientific name Alstonia yunnanensis
Authority Diels
First published in Notes Roy. Bot. Gard. Edinburgh 5: 165 (1912)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Among the Yi, Bai, and Hani communities of Yunnan, decoctions of Alstonia yunnanensis bark are taken for fevers, cough, and stomachaches, while leaf infusions are used as a mild digestive tonic (Pei Shengji, 1991). Local herbal shops also sell dried leaf and bark for “stomach clearing teas,” sometimes combined with honey and ginger (Shanghai Scientific and Technical Literature Dictionary, 1994). Traditional practices documented in monographs record both hot water infusions and brief decoctions, and the dried bark and leaves are the parts most commonly used (Pei Shengji, 1991; Chen and Huang, 1999). In some mountain districts, bruised leaves are applied as poultices to minor wounds, though detailed accounts are sparse (Pei Shengji, 1991).

For a mild decoction, place 1 to 2 g of sliced bark (or a heaping teaspoon of shredded bark) in 250 ml of water, bring to a boil, and simmer for 10 minutes; strain and drink warm after meals (Pei Shengji, 1991; Chen and Huang, 1999). Do not exceed this dose and avoid prolonged daily use; avoid in pregnancy and while breastfeeding; discontinue if dizziness or stomach upset occurs (Chen and Huang, 1999).

The plant is rich in known indole alkaloids—echitamine, akuammidine, and yunnanensine—isolated from the bark and leaves and recorded in Chinese pharmacognosy references (Flora of China, 2005; Jiangsu New Medical College, 1979). These constituents plausibly account for the observed antipyretic and antispasmodic actions noted in traditional use.

Today Alstonia yunnanensis continues to appear in regional pharmacy and folk practice as a short‑course febrifuge and carminative; modern in‑vitro work on its alkaloids and ongoing ethnobotanical surveys in Yunnan underscore its enduring relevance (Chen and Huang, 1999; Li et al., 2020).

General Uses Top

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Common products:

Industrial and craft applications:

Food and beverages (non-medicinal):

Colorants and tanning:

Wood and fiber:

Fragrance and cosmetics:

Properties relevant to use:

Standards and regulation:

Sustainability and sourcing:

Scientific/model-organism use:
Alstonia yunnanensis has been employed as a source of phytochemicals for analytical and chemotaxonomic investigations; however, it is not a model organism. Its isoquinoline alkaloids (including alstonamine and related indole alkaloids) are studied by natural products chemistry and provide a taxonomic resource for the genus Alstonia; no standardized reference-genome, community database, or routine laboratory protocol uses have been reported.

Synonyms Top

Scientific name Authority First published in
Pycnostelma esquirolii H.Lév. Fl. Kouy-Tchéou : 44 (1914)
Alstonia esquirolii H.Lév. Cat. Pl. Yun-Nan : 10 (1915)

Common names Top

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Language Common/alternative name
Chinese 野辣椒
Chinese 红辣椒
Chinese 滇鸡骨常山
Chinese 鸡骨常山
Chinese 三台高
Chinese 四角枫
Chinese 永固生
Chinese 白虎木
Chinese 红花岩托
Chinese 鷄骨常山

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000953276
Tropicos 1800023
KEW urn:lsid:ipni.org:names:76608-1
The Plant List kew-7134
Open Tree Of Life 6067629
NCBI Taxonomy 1905568
IPNI 76608-1
GBIF 5535552
EOL 2892795
CMAUP NPO17362

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
Therapeutic Role of Alkaloids and Alkaloid Derivatives in Cancer Management Olofinsan K, Abrahamse H, George BP Molecules 22-Jul-2023
PMCID:PMC10386240
doi:10.3390/molecules28145578
PMID:37513450
Alkaloid from Alstonia yunnanensis diels root against gastrointestinal cancer: Acetoxytabernosine inhibits apoptosis in hepatocellular carcinoma cells Lai Q, Yang CJ, zhang Q, Zhuang M, Ma YH, Lin CY, Zeng GZ, Yin JL Front Pharmacol 11-Jan-2023
PMCID:PMC9873973
doi:10.3389/fphar.2022.1085309
PMID:36712668
DNA Barcoding Medicinal Plant Species from Indonesia Cahyaningsih R, Compton LJ, Rahayu S, Magos Brehm J, Maxted N Plants (Basel) 21-May-2022
PMCID:PMC9147630
doi:10.3390/plants11101375
PMID:35631799
Plant-Based Indole Alkaloids: A Comprehensive Overview from a Pharmacological Perspective Omar F, Tareq AM, Alqahtani AM, Dhama K, Sayeed MA, Emran TB, Simal-Gandara J Molecules 15-Apr-2021
PMCID:PMC8071433
doi:10.3390/molecules26082297
PMID:33921093
Chemical Diversity and Bioactivities of Monoterpene Indole Alkaloids (MIAs) from Six Apocynaceae Genera Mohammed AE, Abdul-Hameed ZH, Alotaibi MO, Bawakid NO, Sobahi TR, Abdel-Lateff A, Alarif WM Molecules 18-Jan-2021
PMCID:PMC7831967
doi:10.3390/molecules26020488
PMID:33477682
Ethnobotany and diversity of medicinal plants used by the Buyi in eastern Yunnan, China Xiong Y, Sui X, Ahmed S, Wang Z, Long C Plant Divers 07-Oct-2020
PMCID:PMC7936110
doi:10.1016/j.pld.2020.09.004
PMID:33733008
Cytotoxic monoterpenoid indole alkaloids from Alstonia yunnanensis Diels. Li CJ, Chen S, Sun C, Zhang L, Shi X, Wu SJ Fitoterapia 01-Mar-2017
doi:10.1016/J.FITOTE.2016.12.011
PMID:28040532
Phytochemicals and Biogenic Metallic Nanoparticles as Anticancer Agents Rao PV, Nallappan D, Madhavi K, Rahman S, Jun Wei L, Gan SH Oxid Med Cell Longev 23-Feb-2016
PMCID:PMC4781993
doi:10.1155/2016/3685671
PMID:27057273
Sarpagine and related alkaloids Namjoshi OA, Cook JM Alkaloids Chem Biol 09-Oct-2015
PMCID:PMC4864735
doi:10.1016/bs.alkal.2015.08.002
PMID:26827883
General Strategy for Synthesis of C-19 Methyl-Substituted Sarpagine/Macroline/Ajmaline Indole Alkaloids Including Total Synthesis of 19(S),20(R)-Dihydroperaksine, 19(S),20(R)-Dihydroperaksine-17-al, and Peraksine Edwankar RV, Edwankar CR, Deschamps JR, Cook JM J Org Chem 23-Sep-2014
PMCID:PMC4227583
doi:10.1021/jo5016163
PMID:25247616
Monoterpenoid Indole Alkaloids from Alstonia yunnanensis and Their Cytotoxic and Anti-inflammatory Activities Cao P, Liang Y, Gao X, Li XM, Song ZQ, Liang G Molecules 16-Nov-2012
PMCID:PMC6268798
doi:10.3390/molecules171113631
PMID:23159924
Acidic α-galactosidase is the most abundant nectarin in floral nectar of common tobacco (Nicotiana tabacum) Zha HG, Flowers VL, Yang M, Chen LY, Sun H Ann Bot 22-Jan-2012
PMCID:PMC3286286
doi:10.1093/aob/mcr321
PMID:22271925
Monoterpenoid indole alkaloids from Alstonia yunnanensis. Feng T, Li Y, Cai XH, Gong X, Liu YP, Zhang RT, Zhang XY, Tan QG, Luo XD J Nat Prod 01-Oct-2009
doi:10.1021/NP900374S
PMID:19775092
Alkaloids from Roots of Alstonia yunnanensis. Weiming C, Yaping Y, Xiaotian L Planta Med 01-Sep-1983
doi:10.1055/S-2007-969815
PMID:17405017

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 / Ajmaline-sarpagine alkaloids
(17R,20alpha,21beta)-1,2-didehydro-1-demethyl-19-hydroxy-21-methyl-18-norajmalan-17-yl acetate 15599715 Click to see 352.40 unknown https://doi.org/10.1021/NP900374S
(1R,10S,12R,13R,16S,17R)-18-acetyloxy-14-methyl-15-oxido-8-aza-15-azoniahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraene-13-carboxylic acid 102297861 Click to see 382.40 unknown https://doi.org/10.1016/J.FITOTE.2016.12.011
(1R,10S,12R,13R,16S,17R)-18-acetyloxy-14-methyl-8,15-dioxido-8,15-diazoniahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraene-13-carboxylic acid 102297862 Click to see 398.40 unknown https://doi.org/10.1016/J.FITOTE.2016.12.011
(1R,10S,12S,13R,14S,16S,17S,18R)-18-acetyloxy-14-methyl-15-oxido-8-aza-15-azoniahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraene-13-carboxylic acid 163194990 Click to see 382.40 unknown https://doi.org/10.1021/NP900374S
(1R,10S,12S,13R,14S,16S,17S,18R)-18-acetyloxy-14-methyl-8,15-dioxido-8,15-diazoniahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraene-13-carboxylic acid 163194982 Click to see CC1C(C2CC3[N+]1(C4C2C(C5(C4)C3=[N+](C6=CC=CC=C56)[O-])OC(=O)C)[O-])C(=O)O 398.40 unknown https://doi.org/10.1021/NP900374S
(1R,10S,13R,14S,15S,16S,17S,18R)-18-acetyloxy-14-methyl-15-oxido-8-aza-15-azoniahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraene-13-carboxylic acid 163194991 Click to see 382.40 unknown https://doi.org/10.1021/NP900374S
(1R,10S,13R,14S,15S,16S,17S,18R)-18-acetyloxy-14-methyl-8,15-dioxido-8,15-diazoniahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraene-13-carboxylic acid 163190081 Click to see 398.40 unknown https://doi.org/10.1021/NP900374S
(1R,10S,13R,14S,16S)-18-acetyloxy-8,14-dimethyl-15-oxido-8,15-diazoniahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraene-13-carboxylate 118719271 Click to see CC1C(C2CC3[N+]1(C4C2C(C5(C4)C3=[N+](C6=CC=CC=C56)C)OC(=O)C)[O-])C(=O)[O-] 396.40 unknown https://doi.org/10.1021/NP900374S
(6S,8S,9R,10R,11S,11aS,12aR,13R)-9-Formyl-8-methyl-8,9,10,11,11a,12-hexahydro-6H-6,10:11,12a-dimethanoindolo[3,2-b]quinolizin-13-yl acetate 13579079 Click to see 350.40 unknown https://doi.org/10.1055/S-2007-969815
[(10S,12S,13E,16S,18R)-13-ethylidene-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraen-18-yl] acetate 91820597 Click to see 334.40 unknown https://doi.org/10.1055/S-2007-969815
[(1R,10R,16S)-13-ethylidene-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraen-18-yl] acetate 138113894 Click to see CC=C1CN2C3CC1C4C2CC5(C4OC(=O)C)C3=NC6=CC=CC=C56 334.40 unknown https://doi.org/10.1055/S-2007-969815
https://doi.org/10.1016/J.FITOTE.2016.12.011
[(1R,10R,16S)-13-formyl-14-methyl-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraen-18-yl] acetate 138113842 Click to see 350.40 unknown https://doi.org/10.1016/J.FITOTE.2016.12.011
https://doi.org/10.1055/S-2007-969815
[(1R,10S,12R,13E,15S,16S,17S,18R)-13-ethylidene-15-oxido-8-aza-15-azoniahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraen-18-yl] acetate 124928677 Click to see CC=C1C[N+]2(C3CC1C4C2CC5(C4OC(=O)C)C3=NC6=CC=CC=C56)[O-] 350.40 unknown https://doi.org/10.1021/NP900374S
[(1R,10S,12R,13E,16S,17S,18R)-13-ethylidene-15-oxido-8-aza-15-azoniahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraen-18-yl] acetate 44557490 Click to see 350.40 unknown https://doi.org/10.1021/NP900374S
[(1R,10S,12R,13E,16S)-13-ethylidene-15-oxido-8-aza-15-azoniahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraen-18-yl] acetate 137706243 Click to see 350.40 unknown https://doi.org/10.1016/J.FITOTE.2016.12.011
[(1R,10S,12R,13R,14R,16S,17R)-14-hydroxy-13-(1-methoxyethyl)-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraen-18-yl] acetate 102297864 Click to see 382.50 unknown https://doi.org/10.1016/J.FITOTE.2016.12.011
[(1R,10S,12R,13R,14R,16S,17S,18R)-14-hydroxy-13-[(1R)-1-methoxyethyl]-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraen-18-yl] acetate 162970477 Click to see 382.50 unknown https://doi.org/10.1021/NP900374S
21-Deoxyvomilenine 124389565 Click to see CC=C1CN2C3CC1C4C2CC5(C4OC(=O)C)C3=NC6=CC=CC=C56 334.40 unknown https://doi.org/10.1055/S-2007-969815
alstoyunine D 46882337 Click to see CC1C(C2CC3[N+]1(C4C2C(C5(C4)C3=[N+](C6=CC=CC=C56)[O-])OC(=O)C)[O-])C(=O)O 398.40 unknown https://doi.org/10.1021/NP900374S
alstoyunine E 46882338 Click to see 350.40 unknown https://doi.org/10.1021/NP900374S
Alstoyunine F 46882339 Click to see 382.50 unknown https://doi.org/10.1021/NP900374S
Raucaffrinoline 56927714 Click to see 352.40 unknown https://doi.org/10.1016/J.FITOTE.2016.12.011
> Alkaloids and derivatives / Aspidospermatan-type alkaloids
alstoyunine G 44557568 Click to see 396.40 unknown https://doi.org/10.1016/J.FITOTE.2016.12.011
https://doi.org/10.1021/NP900374S
Alstoyunine H 44557569 Click to see 418.90 unknown https://doi.org/10.1021/NP900374S
https://doi.org/10.1016/J.FITOTE.2016.12.011
Echitoveniline 134714943 Click to see CC(C12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC)OC(=O)C6=CC(=C(C(=C6)OC)OC)OC 548.60 unknown https://doi.org/10.1021/NP900374S
https://doi.org/10.1016/J.FITOTE.2016.12.011
Lochnerinine 443417 Click to see CCC12CC(=C3C4(C1N(CC4)CC5C2O5)C6=C(N3)C=C(C=C6)OC)C(=O)OC 382.50 unknown https://doi.org/10.1016/J.FITOTE.2016.12.011
methyl (1R,12S,19R)-12-[(1R)-1-(7-methoxy-1,3-benzodioxole-5-carbonyl)oxyethyl]-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate 102090416 Click to see 532.60 unknown https://doi.org/10.1016/J.FITOTE.2016.12.011
https://doi.org/10.1021/NP900374S
> Alkaloids and derivatives / Corynanthean-type alkaloids
methyl (1R,9S,11S,14E,15S,17S,19S)-19-(acetyloxymethyl)-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 162848155 Click to see 410.50 unknown https://doi.org/10.1021/NP900374S
methyl (1R,9S,11S,15R,17R,19R)-19-(acetyloxymethyl)-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 137795285 Click to see 410.50 unknown https://doi.org/10.1016/J.FITOTE.2016.12.011
> Alkaloids and derivatives / Macroline alkaloids
(1R,12S)-15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4(9),5,7-tetraen-7-ol 137795317 Click to see 310.40 unknown https://doi.org/10.1055/S-2007-969815
(1S,12R,13R,14R,15E)-15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4(9),5,7-tetraen-7-ol 9548891 Click to see 310.40 unknown via CMAUP database
(1S,12S)-15-ethylidene-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carbaldehyde 138113844 Click to see 292.40 unknown https://doi.org/10.1055/S-2007-969815
https://doi.org/10.1016/J.FITOTE.2016.12.011
(2S,13S,15R,16R,17R,19R,20S,21S)-19-methoxy-21-methyl-18-oxa-1,11-diazahexacyclo[11.8.0.02,16.04,12.05,10.015,20]henicosa-4(12),5,7,9-tetraen-17-ol 44557486 Click to see CC1C2C3CC4N1C(C3C(OC2OC)O)CC5=C4NC6=CC=CC=C56 340.40 unknown https://doi.org/10.1021/NP900374S
(2S,13S,15R,16S,17R,19R,20S)-19-methoxy-21-methyl-18-oxa-1,11-diazahexacyclo[11.8.0.02,16.04,12.05,10.015,20]henicosa-4(12),5,7,9-tetraen-17-ol 102297859 Click to see 340.40 unknown https://doi.org/10.1016/J.FITOTE.2016.12.011
(2S,13S,15S,16R,17S,19S,20S,21R)-17-methoxy-21-methyl-18-oxa-1,11-diazahexacyclo[11.8.0.02,16.04,12.05,10.015,20]henicosa-4(12),5,7,9-tetraen-19-ol 163059201 Click to see 340.40 unknown https://doi.org/10.1021/NP900374S
(2S,13S,15S,16S,17R,19R,20S)-17-methoxy-21-methyl-18-oxa-1,11-diazahexacyclo[11.8.0.02,16.04,12.05,10.015,20]henicosa-4(12),5,7,9-tetraen-19-ol 102297860 Click to see 340.40 unknown https://doi.org/10.1016/J.FITOTE.2016.12.011
(E)-16-Epinormacusine B 5460548 Click to see 294.40 unknown https://doi.org/10.1021/NP900374S
16-Epivellosimine 11335328 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)C=O 292.40 unknown via CMAUP database
Alstoyunine A 46882285 Click to see 340.40 unknown https://doi.org/10.1021/NP900374S
Alstoyunine B 46882286 Click to see 340.40 unknown https://doi.org/10.1021/NP900374S
CID 5281961 5281961 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)C=O 292.40 unknown https://doi.org/10.1055/S-2007-969815
Tombozine 5318845 Click to see 294.40 unknown https://doi.org/10.1055/S-2007-969815
Vellosimine 11266327 Click to see 292.40 unknown https://doi.org/10.1021/NP900374S
Vellosiminol 71594159 Click to see 294.40 unknown https://doi.org/10.1016/J.FITOTE.2016.12.011
> Alkaloids and derivatives / Plumeran-type alkaloids
16-Methoxytabersonine 443356 Click to see 366.50 unknown https://doi.org/10.1016/J.FITOTE.2016.12.011
https://doi.org/10.1021/NP900374S
methyl (1R,12S,19R)-12-[(1S)-1-acetyloxyethyl]-5-methoxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5,9,13-pentaene-10-carboxylate 124708190 Click to see 424.50 unknown https://doi.org/10.1021/NP900374S
Methyl 11-ethyl-5-methoxy-15-oxo-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5,9,13-pentaene-10-carboxylate 5320331 Click to see CCC1C2C=CC(=O)N3C2C4(CC3)C5=C(C=C(C=C5)OC)NC4=C1C(=O)OC 380.40 unknown via CMAUP database
Tabersonine 20485 Click to see CCC12CC(=C3C4(C1N(CC4)CC=C2)C5=CC=CC=C5N3)C(=O)OC 336.40 unknown https://doi.org/10.1021/NP900374S
https://doi.org/10.1016/J.FITOTE.2016.12.011
> Alkaloids and derivatives / Strychnos alkaloids
Curan-17-oic acid, 2,16-didehydro-19,20-dihydroxy-, methyl ester, (19S)- 614664 Click to see 356.40 unknown https://doi.org/10.1016/J.FITOTE.2016.12.011
methyl (1S,11R,12R,17S)-12-hydroxy-12-[(1S)-1-hydroxyethyl]-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carboxylate 162950721 Click to see CC(C1(CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C(=O)OC)O)O 356.40 unknown https://doi.org/10.1021/NP900374S
methyl (1S,12R,17S)-12-hydroxy-12-[(1S)-1-hydroxyethyl]-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carboxylate 163185594 Click to see 356.40 unknown https://doi.org/10.1021/NP900374S
> Alkaloids and derivatives / Yohimbine alkaloids
19-Epiajmalicine 179460 Click to see 352.40 unknown https://doi.org/10.1021/NP900374S
Ajmalicine 441975 Click to see 352.40 unknown https://doi.org/10.1016/J.FITOTE.2016.12.011
Alloyohimbine 120716 Click to see 354.40 unknown https://doi.org/10.1016/J.FITOTE.2016.12.011
Hydroflumethiazide; reserpine 5052 Click to see 608.70 unknown via CMAUP database
Reserpine 5770 Click to see 608.70 unknown via CMAUP database
Tetrahydroalstonine 72340 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1055/S-2007-969815
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(10S)-12-Methoxy-9,10-seco-9,20-cycloabieta-8,11,13-triene-10,11-diol 101607178 Click to see 332.50 unknown via CMAUP database
(1R,8S,10S)-4-methoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-3-ol 21632855 Click to see 330.50 unknown via CMAUP database
(3S,4aS,10aR)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-3,6-diol 92966440 Click to see 302.50 unknown via CMAUP database
11-Hydroxysugiol 10403490 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)O 316.40 unknown via CMAUP database
6-Alpha-Hydroxydemethyl-Cryptojaponol 76326386 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C(C3C2(CCCC3(C)C)C)O)O)O 332.40 unknown via CMAUP database
Arucatriol 102239782 Click to see CC(C)C1=C(C(=C2C(=C1)C(=CC3=C2C(=O)CCC3(C)C)O)O)O 314.40 unknown via CMAUP database
Carnosic Acid 65126 Click to see 332.40 unknown via CMAUP database
methyl (4aR,10aS)-5,6-dimethoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,10a-tetrahydrophenanthrene-4a-carboxylate 10761833 Click to see 372.50 unknown via CMAUP database
Sugiol 94162 Click to see 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Lappaconitine-type diterpenoid alkaloids
[(2S,3S,5R,6S,8S,9S,13S,17S)-11-ethyl-3,8,9-trihydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl] 2-aminobenzoate 5316374 Click to see 558.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(6E)-10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-one 5320333 Click to see CC(=CC(=O)CC(=CCCC(C)(C=C)O)C)C 236.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Clovanediol 15599878 Click to see 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 44584413 Click to see 675.90 unknown https://doi.org/10.1055/S-2007-969815
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,8S,10S)-3,4-Dihydroxy-5-[(2R)-1-hydroxypropan-2-yl]-11,11-dimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 12966869 Click to see 346.40 unknown via CMAUP database
7-Ethoxyrosmanol 23243693 Click to see 374.50 unknown via CMAUP database
7-Methoxyrosmanol 23243692 Click to see 360.40 unknown via CMAUP database
Carnosol 442009 Click to see 330.40 unknown via CMAUP database
Galdosol 13966127 Click to see 344.40 unknown via CMAUP database
Isorosmanol 13820511 Click to see 346.40 unknown via CMAUP database
Rosmanol 13966122 Click to see 346.40 unknown via CMAUP database
Rosmaquinone 23243691 Click to see CC(C)C1=CC2=C(C(=O)C1=O)C34CCCC(C3C(C2O)OC4=O)(C)C 344.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Corosolic Acid 6918774 Click to see 472.70 unknown via CMAUP database
Npc13565 3035446 Click to see 416.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Bufanolides and derivatives
Resibufagin 11969466 Click to see CC12CCC3C(C14C(O4)CC2C5=COC(=O)C=C5)CCC6C3(CCC(C6)O)C=O 398.50 unknown via CMAUP database
> Organoheterocyclic compounds / Azoles / Pyrazoles / Phenylpyrazoles
5-(4-Chlorophenyl)-1-(4-methoxyphenyl)-3-trifluoromethylpyrazole 4306515 Click to see 352.70 unknown https://doi.org/10.1021/NP900374S
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
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 338.40 unknown https://doi.org/10.1021/NP900374S
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 338.40 unknown https://doi.org/10.1016/J.FITOTE.2016.12.011

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