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Brucea antidysenterica

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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 UUID64400de2f02d0135169813
Scientific name Brucea antidysenterica
Authority J.F.Mill.
First published in Icon. Anim. Pl. t. 25. [1779-1789] ; Cimelia Botanica, t. 25 (1796)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lussa antidysenterica Kuntze Revis. Gen. Pl. 1: 104 (1891)
Trichilia siderotricha Chiov. Atti Reale Accad. Italia, Mem. Cl. Sci. Fis. 11: 24 (1940)
Brucea abyssinica Spreng. Pl. Min. Cogn. Pug. 2: 90 (1815)
Brucea erythraeae Chiov. Ann. Bot. (Rome) 10: 384 (1912)
Brucea ferruginea L'Hér. Stirp. Nov. : 19 (1785)
Brucea salutaris A.Chev. Mém. Soc. Bot. France 8: 145 (1912)

Common names Top

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Language Common/alternative name
Amharic የደጋ ኣባሎ

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000572696
Tropicos 29400172
KEW urn:lsid:ipni.org:names:813601-1
The Plant List kew-2683962
Open Tree Of Life 908291
NCBI Taxonomy 459111
IUCN Red List 153944265
IPNI 813603-1
iNaturalist 133550
GBIF 5555223
EOL 5632071
CMAUP NPO21014

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
Ethnobotanical study of traditional medicinal plants used by the local Gamo people in Boreda Abaya District, Gamo Zone, southern Ethiopia Zemede J, Mekuria T, Ochieng CO, Onjalalaina GE, Hu GW J Ethnobiol Ethnomed 28-Feb-2024
PMCID:PMC10900619
doi:10.1186/s13002-024-00666-z
PMID:38419092
The mechanistic role of natural antimicrobials in preventing Staphylococcus aureus invasion of MAC-T cells using an in vitro mastitis model Balta I, McCleery D, David SR, Pet E, Stef D, Iancu T, Pet I, Stef L, Corcionivoschi N Ir Vet J 27-Feb-2024
PMCID:PMC10898119
doi:10.1186/s13620-024-00265-0
PMID:38414081
Ethnoveterinary medicinal plants and their utilization by the people of Soro District, Hadiya Zone, southern Ethiopia Hankiso M, Asfaw Z, Warkineh B, Abebe A, Sisay B, Debella A J Ethnobiol Ethnomed 22-Feb-2024
PMCID:PMC10885532
doi:10.1186/s13002-024-00651-6
PMID:38389077
Medicinal Plants in Treating Hepatitis B Among Communities of Central Region of Ethiopia Beykaso G, Teklehaymanot T, Mulu A, Berhe N, Alemayehu DH, Giday M Hepat Med 29-Dec-2023
PMCID:PMC10759923
doi:10.2147/HMER.S440351
PMID:38170153
Ethnobotanical and ethnopharmacological survey of medicinal tree species used in the treatment of diseases by forest-fringe communities of Southwestern Ghana Asigbaase M, Adusu D, Musah AA, Anaba L, Nsor CA, Abugre S, Derkyi M Heliyon 14-Dec-2023
PMCID:PMC10788458
doi:10.1016/j.heliyon.2023.e23645
PMID:38226220
Ethnobotanical Study of Medicinal Plants Used against Human Diseases in Zuway Dugda District, Ethiopia Megersa M, Nedi T, Belachew S Evid Based Complement Alternat Med 18-Oct-2023
PMCID:PMC10599937
doi:10.1155/2023/5545294
PMID:37886427
Floristic composition and plant community distribution along environmental gradients in Guard dry Afromontane forest of Northwestern Ethiopia Dagne Y, Birhanu L BMC Ecol Evol 28-Aug-2023
PMCID:PMC10463663
doi:10.1186/s12862-023-02154-6
PMID:37635212
Plant species diversity, plant use, and classification of agroforestry homegardens in southern and southwestern Ethiopia Kassa G, Bekele T, Demissew S, Abebe T Heliyon 25-May-2023
PMCID:PMC10241864
doi:10.1016/j.heliyon.2023.e16341
PMID:37287606
Evaluation of the Biological Properties of an Optimized Extract of Polygonum cuspidatum Using Ultrasonic-Assisted Extraction Fletes-Vargas G, Rodríguez-Rodríguez R, Pacheco N, Pérez-Larios A, Espinosa-Andrews H Molecules 13-May-2023
PMCID:PMC10222076
doi:10.3390/molecules28104079
PMID:37241822
Population Structure and Regeneration Status of Woody Plant Species in Tulu Korma Dry Afromontane Forest, West Shewa Zone, Oromia, Ethiopia Deressa D, Egigu MC, Sasikumar JM Scientifica (Cairo) 20-Apr-2023
PMCID:PMC10139819
doi:10.1155/2023/9964663
PMID:37122810
In vitro Anti-Leishmanial Activities of Methanol Extract of Brucea antidysenterica J.F. Mill Seeds and Its Solvent Fractions Ketema T, Tadele M, Gebrie Z, Makonnen E, Hailu A, Abay SM J Exp Pharmacol 13-Mar-2023
PMCID:PMC10022440
doi:10.2147/JEP.S397352
PMID:36937078
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Cytotoxicity of the methanol extracts and compounds of Brucea antidysenterica (Simaroubaceae) towards multifactorial drug-resistant human cancer cell lines Youmbi LM, Makong YS, Mbaveng AT, Tankeo SB, Fotso GW, Ndjakou BL, Wansi JD, Beng VP, Sewald N, Ngadjui BT, Efferth T, Kuete V BMC Complement Med Ther 15-Feb-2023
PMCID:PMC9930359
doi:10.1186/s12906-023-03877-1
PMID:36793009
Land use/land cover dynamics driven changes in woody species diversity and ecosystem services value in tropical rainforest frontier: A 20-year history Berhanu Y, Dalle G, Sintayehu DW, Kelboro G, Nigussie A Heliyon 14-Feb-2023
PMCID:PMC9971171
doi:10.1016/j.heliyon.2023.e13711
PMID:36865457
Traditional Herbal Remedies in the Management of Metabolic Disorders in Ethiopia: A Systematic Review of Ethnobotanical Studies and Pharmacological Activities Tola MA, Ibrahim F, Melak H, Tafesse T, Alemayehu M, Nigussie G Evid Based Complement Alternat Med 12-Jan-2023
PMCID:PMC9851791
doi:10.1155/2023/1413038
PMID:36686979

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 / Indolonaphthyridine alkaloids
1-Methoxycanthinone 483522 Click to see COC1=CN=C2C=CC(=O)N3C2=C1C4=CC=CC=C43 250.25 unknown https://doi.org/10.1055/S-2006-962656
11-Hydroxycanthin-6-one 337601 Click to see C1=CC(=O)C2=C3C=CNC4=C3N(C2=C1)C(=O)C=C4 236.22 unknown https://doi.org/10.1021/NP50045A007
5-Methoxycanthin-6-one 259218 Click to see COC1=CC2=NC=CC3=C2N(C1=O)C4=CC=CC=C34 250.25 unknown https://doi.org/10.1055/S-2007-969432
Canthin-6-one 97176 Click to see C1=CC=C2C(=C1)C3=C4N2C(=O)C=CC4=NC=C3 220.23 unknown https://doi.org/10.1055/S-2007-969432
https://doi.org/10.1021/NP50045A007
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
13-Oxopodocarp-8(14)-en-18-oic acid 26183540 Click to see CC12CCCC(C1CCC3=CC(=O)CCC23)(C)C(=O)O 276.40 unknown via CMAUP database
7,15-Dihydroxypodocarp-8(14)-en-13-one 10731307 Click to see CC1(CCCC2(C1CC(C3=CC(=O)CCC32)O)C)CO 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aR,4bR,10S,10aR)-10-hydroxy-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-6-oxo-3,4,4b,5,10,10a-hexahydro-2H-phenanthrene-1-carboxylic acid 46895239 Click to see CC12CCCC(C1C(C=C3C2CC(=O)C(=C3)C(C)(C)O)O)(C)C(=O)O 348.40 unknown via CMAUP database
12-Hydroxyabietic acid 52325853 Click to see CC(C)C1=CC2=CCC3C(C2CC1O)(CCCC3(C)C(=O)O)C 318.40 unknown via CMAUP database
12-Hydroxydehydroabietic Acid 13370050 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)O 316.40 unknown via CMAUP database
12alpha-Methoxyabieta-7,13-diene-18-oic acid 49871253 Click to see CC(C)C1=CC2=CCC3C(C2CC1OC)(CCCC3(C)C(=O)O)C 332.50 unknown via CMAUP database
13-Hydroxy-8,11,13-podocarpatriene-18-oic acid 11558144 Click to see CC12CCCC(C1CCC3=C2C=CC(=C3)O)(C)C(=O)O 274.35 unknown via CMAUP database
15-Hydroxy-7-oxodehydroabietic acid 14017925 Click to see CC12CCCC(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)(C)C(=O)O 330.40 unknown via CMAUP database
15-Hydroxydehydroabietic acid 14487943 Click to see CC12CCCC(C1CCC3=C2C=CC(=C3)C(C)(C)O)(C)C(=O)O 316.40 unknown via CMAUP database
15,18-Dihydroxyabieta-8,11,13-trien-7-one 3009631 Click to see CC1(CCCC2(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)C)CO 316.40 unknown via CMAUP database
18-Nor-4,15-dihydroxyabieta-8,11,13-trien-7-one 3009629 Click to see CC12CCCC(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)(C)O 302.40 unknown via CMAUP database
18-Norabieta-8,11,13-trien-4-ol 15605917 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)O)C 272.40 unknown via CMAUP database
18-Norabieta-8,11,13-triene-4,15-diol 11709045 Click to see CC12CCCC(C1CCC3=C2C=CC(=C3)C(C)(C)O)(C)O 288.40 unknown via CMAUP database
19-Nor-4-hydroxyabieta-8,11,13-trien-7-one 91884799 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)O)C 286.40 unknown via CMAUP database
2-[(2R)-5-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]-3,6-dihydro-2H-pyran-2-yl]prop-2-enoic acid 9976572 Click to see CC(=CCCC(=CCCC(=CCCC1=CCC(OC1)C(=C)C(=O)O)C)C)C 372.50 unknown https://doi.org/10.1021/NP50054A010
7-Oxo-12alpha,13beta-dihydroxyabietane-8(14)-ene-18-oic acid 101521440 Click to see CC(C)C1(C=C2C(CC1O)C3(CCCC(C3CC2=O)(C)C(=O)O)C)O 350.40 unknown via CMAUP database
7-Oxodehydroabietinol 15715176 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)CO)C 300.40 unknown via CMAUP database
Abieta-8,11,13-triene-7,15,18-triol 91895315 Click to see CC1(CCCC2(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)C)CO 318.40 unknown via CMAUP database
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Dehydroabietic acid 94391 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown via CMAUP database
Dehydroabietinol 15586718 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)CO)C 286.50 unknown via CMAUP database
Junicedric acid 38347252 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)CC(=O)O 336.50 unknown via CMAUP database
Methyl 7,15-dihydroxydehydroabietate 91895316 Click to see CC12CCCC(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)(C)C(=O)OC 346.50 unknown via CMAUP database
Pimaric acid 220338 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(9S,13S,17S,1R,3R,15R)-11,15,16-trihydroxy-17-(Methoxycarbonyl)-9,13-dimethyl-5,18-dioxa-4,12-dioxopentacyclo[12.5.0.0<1,6>.0<2,17>.0<8,13>]nonadec-10-en-3-yl (2E)-3,4-dimethylpent-2-enoate 15953936 Click to see CC1C=C(C(=O)C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)O 548.60 unknown https://doi.org/10.1021/NP50102A010
Bruceanol A 127805 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C6=CC=CC=C6)(OC5)C(=O)OC)O)O)C)O 542.50 unknown https://doi.org/10.1021/NP50042A017
Bruceanol B 127804 Click to see CCCCCC(=O)OC1C2C34COC2(C(C(C3C5(C(CC4OC1=O)C(=CC(=O)C5O)C)C)O)O)C(=O)OC 536.60 unknown https://doi.org/10.1021/NP50042A017
Bruceanol C 6440833 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)C(=O)C(=O)C=C(C)C(C)(C)OC(=O)C)(OC5)C(=O)OC)O)O)C)O 618.60 unknown https://doi.org/10.1021/NP50056A031
Bruceanol F 6438914 Click to see CC1C=C(C(=O)C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)O 548.60 unknown https://doi.org/10.1021/NP50102A010
Bruceanol G 6440620 Click to see CC1CC(=O)C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(OC5)C(=O)OC)O)O)C)O 608.60 unknown https://doi.org/10.1021/NP50126A019
Bruceanol H 10745249 Click to see CC1CC(C(=O)C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)O 550.60 unknown https://doi.org/10.1021/NP50126A019
Bruceanol-A 21120899 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C6=CC=CC=C6)(OC5)C(=O)OC)O)O)C)O 542.50 unknown https://doi.org/10.1021/NP50042A017
Bruceantin 5281304 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)O 548.60 unknown https://doi.org/10.1271/BBB.59.974
https://doi.org/10.1021/NP50102A010
Bruceantinoside B 44559340 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O 710.70 unknown https://doi.org/10.1021/NP50016A013
Bruceantinoside C 73355974 Click to see CC1C=C(C(=O)C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O 768.80 unknown https://doi.org/10.1021/NP50054A010
CID 16727447 16727447 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)O 548.60 unknown via CMAUP database
CID 6438433 6438433 Click to see CC1CC(C(=O)C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)O 550.60 unknown https://doi.org/10.1021/NP50126A019
Dehydrobruceantarin 315123 Click to see CC1=C2CC3C45COC(C4C(C(=O)O3)OC(=O)C6=CC=CC=C6)(C(C(C5C2(C=C(C1=O)O)C)O)O)C(=O)OC 540.50 unknown https://doi.org/10.1021/NP50082A011
Dehydrobruceantin 15330899 Click to see CC1=C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(C(C(C5C2(C=C(C1=O)O)C)O)O)C(=O)OC 546.60 unknown https://doi.org/10.1021/NP50082A011
https://doi.org/10.1246/BCSJ.65.2684
Dehydrobruceantinol 54604632 Click to see CC1=C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(C(C(C5C2(C=C(C1=O)O)C)O)O)C(=O)OC 604.60 unknown https://doi.org/10.1021/NP50082A011
https://doi.org/10.1246/BCSJ.65.2684
Isobrucein B 99530 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C)(OC5)C(=O)OC)O)O)C)O 480.50 unknown https://doi.org/10.1021/NP50042A017
https://doi.org/10.1021/NP50102A010
methyl (1beta,11beta,12alpha,15beta)-15-{[(2E)-3,4-dimethylpent-2-enoyl]oxy}-1,11,12-trihydroxy-2,16-dioxo-13,20-epoxypicrasan-21-oate 91666325 Click to see CC1CC(=O)C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)O 550.60 unknown https://doi.org/10.1021/NP50102A010
methyl (1R,2S,3R,6R,13S,14R,15R,16S,17S)-3-benzoyloxy-11,15,16-trihydroxy-9,13-dimethyl-4,10-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadeca-8,11-diene-17-carboxylate 101967073 Click to see CC1=C2CC3C45COC(C4C(C(=O)O3)OC(=O)C6=CC=CC=C6)(C(C(C5C2(C=C(C1=O)O)C)O)O)C(=O)OC 540.50 unknown https://doi.org/10.1021/NP50082A011
https://doi.org/10.1246/BCSJ.65.2684
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17R)-3-[(E)-4-acetyloxy-3,4-dimethylpent-2-enoyl]oxy-10,15,16-trihydroxy-9,13-dimethyl-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 44584511 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(OC5)C(=O)OC)O)O)C)O 606.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-3-[(E)-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 54604526 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC 710.70 unknown https://doi.org/10.1021/NP50016A013
methyl (1R,2S,3R,6R,8S,9S,13S,14S,15R,16S,17S)-3-[(E)-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,12-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-10-ene-17-carboxylate 101659164 Click to see CC1C=C(C(=O)C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O 710.70 unknown https://doi.org/10.1021/NP50102A010
https://doi.org/10.1021/NP50054A010
methyl (2S,3R,6R,13S,17S)-3-[(E)-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 24884096 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O 710.70 unknown via CMAUP database
Methyl 3-(3,4-dimethylpent-2-enoyloxy)-11,15,16-trihydroxy-9,13-dimethyl-4,10-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadeca-8,11-diene-17-carboxylate 315122 Click to see CC1=C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(C(C(C5C2(C=C(C1=O)O)C)O)O)C(=O)OC 546.60 unknown https://doi.org/10.1021/NP50082A011
Methyl 3-(4-acetyloxy-3,4-dimethylpent-2-enoyl)oxy-11,15,16-trihydroxy-9,13-dimethyl-4,10-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadeca-8,11-diene-17-carboxylate 3954719 Click to see CC1=C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(C(C(C5C2(C=C(C1=O)O)C)O)O)C(=O)OC 604.60 unknown https://doi.org/10.1021/NP50082A011
Methyl 3-[(E)-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,12-dioxo-11-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-10-ene-17-carboxylate 6436230 Click to see CC1C=C(C(=O)C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O 710.70 unknown https://doi.org/10.1021/NP50016A013
https://doi.org/10.1021/NP50062A033
Picras-3-en-21-oic acid, 15-((3,4-dimethyl-1-oxo-2-pentenyl)oxy)-13,20-epoxy-1,11,12-trihydroxy-2,16-dioxo-, methyl ester, (1beta,11beta,12alpha,15beta(E))- 6444292 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(CO5)C(=O)OC)O)O)C)O 548.60 unknown https://doi.org/10.1021/NP50102A010
Picras-3-en-21-oic acid, 15-((3,4-dimethyl-1-oxo-2-pentenyl)oxy)-13,20-epoxy-1,11,12-trihydroxy-2,16-dioxo-,methyl ester, (1beta,11beta,12alpha,15beta(E))- 70697724 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)O 548.60 unknown https://doi.org/10.1021/NP50102A010
Picrasan-21-oic acid, 15-((3,4-dimethyl-1-oxo-2-pentenyl)oxy)-13,20-epoxy-1,11,12-trihydroxy-2,16-dioxo-, methyl ester, (1beta,11beta,12alpha,15beta(E))- 6444293 Click to see CC1CC(=O)C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(CO5)C(=O)OC)O)O)C)O 550.60 unknown https://doi.org/10.1021/NP50102A010
Yadanzioside N 6451089 Click to see CC1C=C(C(=O)C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O 710.70 unknown https://doi.org/10.1021/NP50102A010
https://doi.org/10.1021/NP50054A010
Yadanzioside P 73345262 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O 710.70 unknown https://doi.org/10.1021/NP50062A033
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
Bruceanic acid C 6439338 Click to see CC(=CC(=O)OC1C2C34COC2(C(C(C3C(C(CC4OC1=O)C(=O)C)CC(=O)OC)O)O)C(=O)OC)C(C)(C)OC(=O)C 610.60 unknown https://doi.org/10.1021/NP50072A020
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
Bruceanic acid D 6439339 Click to see CC(=CC(=O)OC1C2C34COC2(C(C(C3C(C(CC4OC1=O)C(=O)C)CC(=O)OC)O)O)C(=O)OC)C(C)(C)O 568.60 unknown https://doi.org/10.1021/NP50072A020
CID 125553 125553 Click to see CC(=O)C1CC2C34COC(C3C(C(=O)O2)OC(=O)C5=CC=CC=C5)(C(C(C4C1(C)CC(=O)O)O)O)C(=O)OC 546.50 unknown https://doi.org/10.1021/NP50072A020
Methyl bruceanic acid A 5960381 Click to see CC(C)C(=CC(=O)OC1C2C34COC2(C(C(C3C(C(CC4OC1=O)C(=O)C)(C)CC(=O)OC)O)O)C(=O)OC)C 566.60 unknown https://doi.org/10.1021/NP50072A020
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Bruceanic acid A 44567023 Click to see CC(C)C(=CC(=O)OC1C2C34COC2(C(C(C3C(C(CC4CC1=O)C(=O)C)(C)CC(=O)O)O)O)C(=O)OC)C 550.60 unknown https://doi.org/10.1021/NP50072A020
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Pinyunin A 46895238 Click to see CC1(C2C(O1)C3CCC4C(C3=CC2=O)(CCCC4(C)C(=O)O)C)C 332.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
Planchol E 53350155 Click to see CC12C(CC(=O)O1)C3C(O2)C(=O)C4=C(C=C(C=C4O3)O)O 292.24 unknown via CMAUP database
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
Angustanoic acid D 10760330 Click to see CC1(CCCC2(C1CCC3=CC4(CCC32OO4)C(C)(C)O)C)C(=O)O 350.40 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones / Naphthopyranone glycosides
Bruceantinoside A 6436226 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC 710.70 unknown https://doi.org/10.1021/NP50016A013
methyl (1R,2S,3R,6R,13S,15R,17S)-3-[(E)-4-acetyloxy-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 6324812 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC 768.80 unknown https://doi.org/10.1021/NP50054A010
methyl (1R,2S,3R,6R,8S,13S,14R,15R,16S)-3-[(E)-4-acetyloxy-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 134715119 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC 768.80 unknown https://doi.org/10.1021/NP50054A010
methyl (1R,2S,3R,6R,8S,13S,14R,15R,16S)-3-benzoyloxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 134715122 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C6=CC=CC=C6)(C(C(C5C2(C=C(C1=O)OC7C(C(C(C(O7)CO)O)O)O)C)O)O)C(=O)OC 704.70 unknown https://doi.org/10.1021/NP50062A033
Yadanzioside M 72961 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C6=CC=CC=C6)(C(C(C5C2(C=C(C1=O)OC7C(C(C(C(O7)CO)O)O)O)C)O)O)C(=O)OC 704.70 unknown https://doi.org/10.1021/NP50062A033

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