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Erythrophleum chlorostachys

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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 UUID643fdb3ebb463164487437
Scientific name Erythrophleum chlorostachys
Authority (F.Muell.) Baill.
First published in Hist. Pl.2: 150 (1870)

Description Top

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Synonyms Top

Scientific name Authority First published in
Laboucheria chlorostachya F.Muell. J. Proc. Linn. Soc., Bot.3: 159 (1859)

Common names Top

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Language Common/alternative name
Arabic حناء البقر ملونة السنابل

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
  • Australasia
    • Australia
      • Northern Territory
      • Queensland
      • Western Australia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000194822
Tropicos 100334797
KEW urn:lsid:ipni.org:names:494632-1
The Plant List ild-41454
Open Tree Of Life 844386
NCBI Taxonomy 887861
IUCN Red List 146629603
IPNI 494632-1
GBIF 2971187
Freebase /m/0gwgr_
EOL 643890
USDA GRIN 15786
Wikipedia Erythrophleum_chlorostachys
CMAUP NPO24882

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
Healthy Patients, Workforce and Environment: Coupling Climate Adaptation and Mitigation to Wellbeing in Healthcare de Souza M, Lee AB, Cook S Int J Environ Res Public Health 13-Nov-2023
PMCID:PMC10671525
doi:10.3390/ijerph20227059
PMID:37998289
Surveying potentially antagonistic fungi to myrtle rust (Austropuccinia psidii) in Brazil: fungicolous Cladosporium spp. da Silva NM, Guterres DC, Borges LS, Barreto RW, Furtado GQ Braz J Microbiol 30-Jun-2023
PMCID:PMC10484887
doi:10.1007/s42770-023-01047-6
PMID:37389796
Aboriginal medicinal plants of Queensland: ethnopharmacological uses, species diversity, and biodiscovery pathways Turpin G, Ritmejerytė E, Jamie J, Crayn D, Wangchuk P J Ethnobiol Ethnomed 10-Aug-2022
PMCID:PMC9364609
doi:10.1186/s13002-022-00552-6
PMID:35948982
Fungal Planet description sheets: 1383–1435 Crous PW, Boers J, Holdom D, Osieck ER, Steinrucken TV, Tan YP, Vitelli JS, Shivas RG, Barrett M, Boxshall AG, Broadbridge J, Larsson E, Lebel T, Pinruan U, Sommai S, Alvarado P, Bonito G, Decock CA, De la Peña-Lastra S, Delgado G, Houbraken J, Maciá-Vicente JG, Raja HA, Rigueiro-Rodríguez A, Rodríguez A, Wingfield MJ, Adams SJ, Akulov A, AL-Hidmi T, Antonín V, Arauzo S, Arenas F, Armada F, Aylward J, Bellanger JM, Berraf-Tebbal A, Bidaud A, Boccardo F, Cabero J, Calledda F, Corriol G, Crane JL, Dearnaley JD, Dima B, Dovana F, Eichmeier A, Esteve-Raventós F, Fine M, Ganzert L, García D, Torres-Garcia D, Gené J, Gutiérrez A, Iglesias P, Istel Ł, Jangsantear P, Jansen GM, Jeppson M, Karun NC, Karich A, Khamsuntorn P, Kokkonen K, Kolařík M, Kubátová A, Labuda R, Lagashetti AC, Lifshitz N, Linde C, Loizides M, Luangsa-ard JJ, Lueangjaroenkit P, Mahadevakumar S, Mahamedi AE, Malloch DW, Marincowitz S, Mateos A, Moreau PA, Miller AN, Molia A, Morte A, Navarro-Ródenas A, Nebesářová J, Nigrone E, Nuthan BR, Oberlies NH, Pepori AL, Rämä T, Rapley D, Reschke K, Robicheau BM, Roets F, Roux J, Saavedra M, Sakolrak B, Santini A, Ševčíková H, Singh PN, Singh SK, Somrithipol S, Spetik M, Sridhar KR, Starink-Willemse M, Taylor VA, van Iperen AL, Vauras J, Walker AK, Wingfield BD, Yarden O, Cooke AW, Manners AG, Pegg KG, Groenewald JZ Persoonia 12-Jul-2022
PMCID:PMC10792288
doi:10.3767/persoonia.2023.48.08
PMID:38234686
Disentangling the chemistry of Australian plant exudates from a unique historical collection Georgiou R, Popelka-Filcoff RS, Sokaras D, Beltran V, Bonaduce I, Spangler J, Cohen SX, Lehmann R, Bernard S, Rueff JP, Bergmann U, Bertrand L Proc Natl Acad Sci U S A 26-May-2022
PMCID:PMC9295781
doi:10.1073/pnas.2116021119
PMID:35617429
Contrasting genetic signal of recolonization after rainforest fragmentation in African trees with different dispersal abilities Piñeiro R, Hardy OJ, Tovar C, Gopalakrishnan S, Garrett Vieira F, Gilbert MT Proc Natl Acad Sci U S A 01-Jul-2021
PMCID:PMC8271564
doi:10.1073/pnas.2013979118
PMID:34210795
New Cladosporium Species from Normal and Galled Flowers of Lamiaceae Zimowska B, Becchimanzi A, Krol ED, Furmanczyk A, Bensch K, Nicoletti R Pathogens 19-Mar-2021
PMCID:PMC8003538
doi:10.3390/pathogens10030369
PMID:33808618
E N/A Saunders Comprehensive Veterinary Dictionary 16-Oct-2020
PMCID:PMC9771672
doi:10.1016/B978-0-7020-7463-9.50013-6
Patterns in the transmission of traditional ecological knowledge: a case study from Arnhem Land, Australia Si A J Ethnobiol Ethnomed 14-Sep-2020
PMCID:PMC7489046
doi:10.1186/s13002-020-00403-2
PMID:32928240
Natural Products as Fungicide and Their Role in Crop Protection Santra HK, Banerjee D Natural Bioactive Products in Sustainable Agriculture 12-May-2020
PMCID:PMC7212785
doi:10.1007/978-981-15-3024-1_9
Does rapid utilization of elevated nutrient availability allow eucalypts to dominate in the tropical savannas of Australia? Paramjyothi H, Murphy BP, Lawes MJ, Rossiter‐Rachor NA, Richards AE Ecol Evol 07-Apr-2020
PMCID:PMC7244804
doi:10.1002/ece3.6168
PMID:32489628
Facultative and Obligate Trees in a Mesic Savanna: Fire Effects on Savanna Structure Imply Contrasting Strategies of Eco-Taxonomic Groups Freeman ME, Murphy BP, Richards AE, Vesk PA, Cook GD Front Plant Sci 18-May-2018
PMCID:PMC5968114
doi:10.3389/fpls.2018.00644
PMID:29868096
Cladosporium species in indoor environments Bensch K, Groenewald JZ, Meijer M, Dijksterhuis J, Jurjević Ž, Andersen B, Houbraken J, Crous PW, Samson RA Stud Mycol 07-Mar-2018
PMCID:PMC5909081
doi:10.1016/j.simyco.2018.03.002
PMID:29681671
Home Is Where the Hearth Is: Anthracological and Microstratigraphic Analyses of Pleistocene and Holocene Combustion Features, Riwi Cave (Kimberley, Western Australia) Whitau R, Vannieuwenhuyse D, Dotte-Sarout E, Balme J, O’Connor S J Archaeol Method Theory 26-Oct-2017
PMCID:PMC6061027
doi:10.1007/s10816-017-9354-y
PMID:30100699
New species of Cladosporium associated with human and animal infections Sandoval-Denis M, Gené J, Sutton DA, Wiederhold NP, Cano-Lira JF, Guarro J Persoonia 24-May-2016
PMCID:PMC4988372
doi:10.3767/003158516X691951
PMID:27616793

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 / Cytochalasans
[(1S,2R,3E,5R,7S,9E,11S,14S,15R,16S)-16-benzyl-5-hydroxy-13-(hydroxymethyl)-5,7,14-trimethyl-6,18-dioxo-17-azatricyclo[9.7.0.01,15]octadeca-3,9,12-trien-2-yl] acetate 102258993 Click to see CC1CC=CC2C=C(C(C3C2(C(C=CC(C1=O)(C)O)OC(=O)C)C(=O)NC3CC4=CC=CC=C4)C)CO 507.60 unknown via CMAUP database
Cytochalasin D 5458428 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(C=CC(C1=O)(C)O)OC(=O)C)C(=O)NC3CC4=CC=CC=C4)C)O 507.60 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
7-Chloromellein-5-ol 102258989 Click to see CC1CC2=C(C(=C(C=C2O)Cl)O)C(=O)O1 228.63 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Phthalate esters / m-Phthalate esters
(3R)-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-5-carboxylic acid 25769005 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C(=O)O 222.19 unknown via CMAUP database
(3S)-8-Hydroxy-3-methyl-1-oxoisochromane-5-carboxylic acid 486250 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C(=O)O 222.19 unknown via CMAUP database
> Benzenoids / Naphthalenes
2-[(8S)-1,8-dimethyl-7,8-dihydronaphthalen-2-yl]propane-1,2,3-triol 44555346 Click to see CC1CC=CC2=C1C(=C(C=C2)C(CO)(CO)O)C 248.32 unknown via CMAUP database
> Benzenoids / Tetralins
(1S,2S,4S)-6-(3-hydroxyprop-1-en-2-yl)-4,5-dimethyl-1,2,3,4-tetrahydronaphthalene-1,2-diol 44255026 Click to see CC1CC(C(C2=C1C(=C(C=C2)C(=C)CO)C)O)O 248.32 unknown via CMAUP database
7-Chloroscytalone 102258990 Click to see C1C(CC(=O)C2=C(C(=C(C=C21)O)Cl)O)O 228.63 unknown via CMAUP database
Isosclerone 13369486 Click to see C1CC(=O)C2=C(C1O)C=CC=C2O 178.18 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans
9,9'-O-Isopropyllidene-isolariciresinol 91885030 Click to see CC1(OCC2CC3=CC(=C(C=C3C(C2CO1)C4=CC(=C(C=C4)O)OC)O)OC)C 400.50 unknown via CMAUP database
Isotaxiresinol 9,9'-acetonide 102004573 Click to see CC1(OCC2CC3=CC(=C(C=C3C(C2CO1)C4=CC(=C(C=C4)O)O)O)OC)C 386.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3S,3aR,6R,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]benzene-1,2-diol 101568249 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)O)O 344.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
4-[(2R,3S,4S,5R)-4-(ethoxymethyl)-5-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)oxolan-2-yl]-2-methoxyphenol 101936591 Click to see CCOCC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)O)OC)CO 404.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(7R)-7-Hydroxylariciresinol 10022393 Click to see COC1=C(C=CC(=C1)C2C(C(CO2)C(C3=CC(=C(C=C3)O)OC)O)CO)O 376.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3S,4R)-3-hydroxy-4-[(R)-hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-3-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 101369318 Click to see COC1=C(C=CC(=C1)CC2(C(COC2=O)C(C3=CC(=C(C=C3)O)OC)O)O)O 390.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1S,3R,11S)-8,9-dimethoxy-15,15-dimethyl-4,14-dioxo-7-propan-2-yl-2-oxatetracyclo[9.4.0.01,3.05,10]pentadeca-5,7,9,12-tetraene-11-carbaldehyde 100952777 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C3C4(C2(C=CC(=O)C4(C)C)C=O)O3)OC)OC 384.40 unknown via CMAUP database
(2E)-2-[(1R,4aR,4bR,7S,8aR,10S,10aS)-7,10-dihydroxy-1,4b,8,8-tetramethyl-3,4,4a,5,6,7,8a,9,10,10a-decahydro-1H-phenanthren-2-ylidene]-N-(2-hydroxyethyl)-N-methylacetamide 163193430 Click to see CC1C2C(CCC1=CC(=O)N(C)CCO)C3(CCC(C(C3CC2O)(C)C)O)C 393.60 unknown https://doi.org/10.1071/CH9740179
13alpha-Ethenyl-13-methyl-19-hydroxy-podocarpa-8(14)-ene-7-one 100952776 Click to see CC1(CCC2C(=C1)C(=O)CC3C2(CCCC3(C)CO)C)C=C 302.50 unknown via CMAUP database
2-(7,10-dihydroxy-1,4b,8,8-tetramethyl-3,4,4a,5,6,7,8a,9,10,10a-decahydro-1H-phenanthren-2-ylidene)-N-(2-hydroxyethyl)-N-methylacetamide 162942289 Click to see CC1C2C(CCC1=CC(=O)N(C)CCO)C3(CCC(C(C3CC2O)(C)C)O)C 393.60 unknown https://doi.org/10.1071/CH9740179
2-(dimethylamino)ethyl (2E)-2-[(1R,4aR,4bR,7S,8aR,10S,10aS)-7,10-dihydroxy-1,4b,8,8-tetramethyl-3,4,4a,5,6,7,8a,9,10,10a-decahydro-1H-phenanthren-2-ylidene]acetate 162959778 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCC(C(C3CC2O)(C)C)O)C 407.60 unknown https://doi.org/10.1071/CH9740179
2-(dimethylamino)ethyl 2-(7,10-dihydroxy-1,4b,8,8-tetramethyl-3,4,4a,5,6,7,8a,9,10,10a-decahydro-1H-phenanthren-2-ylidene)acetate 101054 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCC(C(C3CC2O)(C)C)O)C 407.60 unknown https://doi.org/10.1071/CH9740179
Hinokiol 12310492 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(C3(C)C)O)C)O 302.50 unknown via CMAUP database
Margocilin 101529198 Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCC(C3(C)C)O)C)O 316.40 unknown via CMAUP database
methyl (1R,2S,4aR,4bR,7E,8R,8aR,10aR)-2-hydroxy-7-[2-[2-hydroxyethyl(methyl)amino]-2-oxoethylidene]-1,4a,8-trimethyl-9-oxo-2,3,4,4b,5,6,8,8a,10,10a-decahydrophenanthrene-1-carboxylate 163191413 Click to see CC1C2C(CCC1=CC(=O)N(C)CCO)C3(CCC(C(C3CC2=O)(C)C(=O)OC)O)C 435.60 unknown https://doi.org/10.1071/CH9740179
methyl (1S,4aR,4bS,7E,8R,8aR,9S,10aR)-7-[2-[2-(dimethylamino)ethoxy]-2-oxoethylidene]-9-hydroxy-1,4a,8-trimethyl-3,4,4b,5,6,8,8a,9,10,10a-decahydro-2H-phenanthrene-1-carboxylate 162866380 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCCC(C3CC2O)(C)C(=O)OC)C 435.60 unknown https://doi.org/10.1071/CH9740179
methyl (1S,4aR,4bS,7E,8R,8aR,9S,10aR)-9-hydroxy-1,4a,8-trimethyl-7-[2-[2-(methylamino)ethoxy]-2-oxoethylidene]-3,4,4b,5,6,8,8a,9,10,10a-decahydro-2H-phenanthrene-1-carboxylate 162955654 Click to see CC1C2C(CCC1=CC(=O)OCCNC)C3(CCCC(C3CC2O)(C)C(=O)OC)C 421.60 unknown https://doi.org/10.1071/CH9740179
methyl (1S,4aR,4bS,7E,8R,8aR,9S,10aR)-9-hydroxy-7-[2-[2-hydroxyethyl(methyl)amino]-2-oxoethylidene]-1,4a,8-trimethyl-3,4,4b,5,6,8,8a,9,10,10a-decahydro-2H-phenanthrene-1-carboxylate 162921086 Click to see CC1C2C(CCC1=CC(=O)N(C)CCO)C3(CCCC(C3CC2O)(C)C(=O)OC)C 421.60 unknown https://doi.org/10.1071/CH9740179
methyl (1S,4aR,4bS,7E,8R,8aS,9S,10aR)-9-hydroxy-7-[2-[2-hydroxyethyl(methyl)amino]-2-oxoethylidene]-1,4a,8-trimethyl-3,4,4b,5,6,8,8a,9,10,10a-decahydro-2H-phenanthrene-1-carboxylate 54606895 Click to see CC1C2C(CCC1=CC(=O)N(C)CCO)C3(CCCC(C3CC2O)(C)C(=O)OC)C 421.60 unknown https://doi.org/10.1071/CH9740179
Methyl 2-hydroxy-7-[2-[2-hydroxyethyl(methyl)amino]-2-oxoethylidene]-1,4a,8-trimethyl-9-oxo-2,3,4,4b,5,6,8,8a,10,10a-decahydrophenanthrene-1-carboxylate 162864977 Click to see CC1C2C(CCC1=CC(=O)N(C)CCO)C3(CCC(C(C3CC2=O)(C)C(=O)OC)O)C 435.60 unknown https://doi.org/10.1071/CH9740179
methyl 7-[2-[2-(dimethylamino)ethoxy]-2-oxoethylidene]-9-hydroxy-1,4a,8-trimethyl-3,4,4b,5,6,8,8a,9,10,10a-decahydro-2H-phenanthrene-1-carboxylate 427694 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCCC(C3CC2O)(C)C(=O)OC)C 435.60 unknown https://doi.org/10.1071/CH9740179
Methyl 7-hydroxy-14-methyl-13-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}podocarpan-15-oate 425995 Click to see CC1C2C(CCC1=CC(=O)OCCNC)C3(CCCC(C3CC2O)(C)C(=O)OC)C 421.60 unknown https://doi.org/10.1071/CH9740179
Sandaracopimaric Acid 221580 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown via CMAUP database
Sugiol 94162 Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O 300.40 unknown via CMAUP database
Taxamairin A 130631 Click to see CC(C)C1=C(C(=C2C=C3C=CC(=O)C(C3=CC(=O)C2=C1)(C)C)O)OC 338.40 unknown via CMAUP database
Taxamairin B 130632 Click to see CC(C)C1=C(C(=C2C=C3C=CC(=O)C(C3=CC(=O)C2=C1)(C)C)OC)OC 352.40 unknown via CMAUP database
Taxamairin H 100952784 Click to see CC(C)C1=C(C(=C2C(=C1)C=CC3=C(C2=O)C=CC(=O)C3(C)C)O)OC 338.40 unknown via CMAUP database
Taxusabietane A 76330776 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCC(=O)C3(C)C)C)O)OC 344.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Taxanes and derivatives
(1S)-2alpha,5alpha,9alpha,10beta,13alpha-Pentaacetoxy-4,20-epoxytax-11-ene-1,7beta-diol 5316776 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)O)C)OC(=O)C)OC(=O)C 610.60 unknown via CMAUP database
[(1'R,2S,2'R,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',7',9',10',13'-pentaacetyloxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] (3R)-3-(dimethylamino)-3-phenylpropanoate 5319245 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)CC1OC(=O)C)OC(=O)C)CO4)OC(=O)CC(C5=CC=CC=C5)N(C)C)OC(=O)C)C)OC(=O)C)OC(=O)C 769.90 unknown via CMAUP database
[(1'S,2R,2'S,3'R,5'S,7'S,8'R,9'R,10'R,13'S)-2',5',10',13'-tetraacetyloxy-1',9'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-7'-yl] acetate 21159040 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)O)OC(=O)C 610.60 unknown via CMAUP database
[(1'S,2R,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',13'-diacetyloxy-1',7',9',10'-tetrahydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] acetate 102066555 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)O)C)O)O 526.60 unknown via CMAUP database
[(1'S,2S,2'R,3'R,5'S,8'R,9'R,10'R,14'S)-9'-acetyloxy-2',5',14'-trihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-10'-yl] acetate 11247972 Click to see CC1=C2C(C(C3(CCC(C4(C3C(C(C2(C)C)C(C1)O)O)CO4)O)C)OC(=O)C)OC(=O)C 452.50 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',10',13'-triacetyloxy-1',7',9'-trihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] acetate 5321726 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)O)C)O)OC(=O)C 568.60 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',5',9',10'-tetraacetyloxy-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-7'-yl] acetate 5321730 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1O)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C 610.60 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',5',9',10',13'-Pentaacetyloxy-1'-hydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-7'-yl] acetate 5318150 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C 652.70 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',5',9',13'-tetraacetyloxy-1',10'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-7'-yl] acetate 5321728 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)O 610.60 unknown via CMAUP database
[(1E,3S,4R,6S,9R,11S,12S,14S)-12-acetyloxy-3,9,14-trihydroxy-7,11,16,16-tetramethyl-10-oxo-6-tricyclo[9.3.1.14,8]hexadeca-1,7-dienyl] acetate 24862000 Click to see CC1=C2C(C(=O)C3(CC(=CC(C(C2(C)C)CC1OC(=O)C)O)C(CC3OC(=O)C)O)C)O 450.50 unknown via CMAUP database
[(1E,3S,4R,6S,9R,11S,12S,14S)-3,12,14-triacetyloxy-9-hydroxy-7,11,16,16-tetramethyl-10-oxo-6-tricyclo[9.3.1.14,8]hexadeca-1,7-dienyl] acetate 101006401 Click to see CC1=C2C(C(=O)C3(CC(=CC(C(C2(C)C)CC1OC(=O)C)OC(=O)C)C(CC3OC(=O)C)OC(=O)C)C)O 534.60 unknown via CMAUP database
[(1R,2S,3S,5S,8R,9R,10R,11S,13R,16S)-5,16-diacetyloxy-10-(acetyloxymethyl)-8,9,11-trihydroxy-3-(2-hydroxypropan-2-yl)-6-methyl-14-oxatetracyclo[8.6.0.03,7.013,16]hexadec-6-en-2-yl] benzoate 10886794 Click to see CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1OC(=O)C)C(C)(C)O)OC(=O)C5=CC=CC=C5)(CO4)OC(=O)C)O)COC(=O)C)O)O 646.70 unknown via CMAUP database
[(2S,4R,5R,5aS,6S,8S,9R,9aR,10S,10aS)-2,5,6,8,10-pentaacetyloxy-4-hydroxy-10a-(2-hydroxypropan-2-yl)-3,5a-dimethyl-1,2,4,5,6,7,8,9,9a,10-decahydrobenzo[f]azulen-9-yl]methyl acetate 5321724 Click to see CC1=C2C(C(C3(C(CC(C(C3C(C2(CC1OC(=O)C)C(C)(C)O)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)C)OC(=O)C)O 654.70 unknown via CMAUP database
1-Acetoxy-5-deacetylbaccatin I 102004901 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)OC(=O)C)OC(=O)C)CO4)O)OC(=O)C)C)OC(=O)C)OC(=O)C 652.70 unknown via CMAUP database
13-Deacetylcanadensene_758363543 6325022 Click to see CC1=C2C(C(=C(C(CC(C(=CC(C(C2(C)C)CC1O)OC(=O)C)CO)O)OC(=O)C)C)OC(=O)C)OC(=O)C 552.60 unknown via CMAUP database
13-O-Deacetyltaxumairol Z 10864961 Click to see CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1O)C(C)(C)O)OC(=O)C5=CC=CC=C5)(CO4)OC(=O)C)O)COC(=O)C)O)O 604.60 unknown via CMAUP database
1beta-Acetoxy-baccatin I 5319668 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)OC(=O)C)OC(=O)C)CO4)O)OC(=O)C)C)OC(=O)C)OC(=O)C 652.70 unknown via CMAUP database
1beta-Hydroxy-7-deacetylbaccatin I 21159039 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)O)C)OC(=O)C)OC(=O)C 610.60 unknown via CMAUP database
2alpha,9,10beta,13alpha-Tetraacetoxy-3,8-secotaxa-3,8,11-triene-5alpha,7beta,20-triol 6325023 Click to see CC1=C(C(C2=C(C(CC(C2(C)C)C(C=C(C(CC1O)O)CO)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C 552.60 unknown via CMAUP database
Taxin B 5321699 Click to see CC1=C2C(C(=O)C3(CC(=CC(C(C2(C)C)CC1OC(=O)C)OC(=O)C)C(CC3OC(=O)C)O)C)OC(=O)C 534.60 unknown via CMAUP database
Taxumain A 5321723 Click to see CC1=C2C(C(C3(C(CC(C(C3C(C2(CC1O)C(C)(C)O)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)C)OC(=O)C)O 612.70 unknown via CMAUP database
Taxumairol B 10053709 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)O)C)O)OC(=O)C 568.60 unknown via CMAUP database
Taxumairol D 102065502 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)O 610.60 unknown via CMAUP database
taxumairol F 10651372 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1O)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C 610.60 unknown via CMAUP database
Taxumairol K 10769688 Click to see CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1O)C(C)(C)O)OC(=O)C)(CO4)OC(=O)C)O)C)OC(=O)C5=CC=CC=C5)O 588.60 unknown via CMAUP database
Taxumairol U 11124920 Click to see CC1=C2C(C(C3(C(CC(C(C3C(C2(CC1OC(=O)C)C(C)(C)O)O)COC(=O)C)OC(=O)C)OC(=O)C)C)OC(=O)C)O 612.70 unknown via CMAUP database
Taxumairol V 10875480 Click to see CC1=C2C(C(C3(C(CC(C(C3C(C2(CC1O)C(C)(C)O)O)COC(=O)C)OC(=O)C)OC(=O)C)C)OC(=O)C)O 570.60 unknown via CMAUP database
Taxumairol W 10918805 Click to see CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1O)C(C)(C)O)OC(=O)C)(CO4)OC(=O)C)OC(=O)C)C)O)OC(=O)C 568.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-4,7,8-triacetyloxy-12,13-dihydroxy-5,9-dimethyl-2-prop-1-en-2-yl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-10-yl] acetate 10918656 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1OC(=O)C)C(=C)C)OC4)O)O)OC(=O)C)C)OC(=O)C)OC(=O)C 550.60 unknown via CMAUP database
[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-7,8-diacetyloxy-4,12,13-trihydroxy-5,9-dimethyl-2-prop-1-en-2-yl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-10-yl] acetate 10907330 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1O)C(=C)C)OC4)O)O)OC(=O)C)C)OC(=O)C)OC(=O)C 508.60 unknown via CMAUP database
2-[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-7,8,10-triacetyloxy-4,12,13-trihydroxy-5,9-dimethyl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-2-yl]propan-2-yl benzoate 11814223 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1O)C(C)(C)OC(=O)C5=CC=CC=C5)OC4)O)O)OC(=O)C)C)OC(=O)C)OC(=O)C 630.70 unknown via CMAUP database
Sporogen-AO 1 177175 Click to see CC1C(CCC2=CC(=O)C3(C(C12C)O3)C(=C)C)O 248.32 unknown via CMAUP database
Taxumairol X 11733602 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1O)C(C)(C)O)OC4)O)O)OC(=O)C)C)OC(=O)C)O 484.50 unknown via CMAUP database
Taxumairol Y 11005902 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1OC(=O)C)C(C)(C)O)OC4)O)O)OC(=O)C)C)OC(=O)C)O 526.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
Taxusabietane D 100952779 Click to see CC(C)C1=C(C(=C2C(=C1)C(CC3C2(CCC(=O)C3(C)C)COC(=O)C)OC(=O)C)O)OC4C(C(C(C(O4)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 762.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,9S,10S)-3,4-dimethoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraene-8,12,15-trione 100952778 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C3C4C2(C=CC(=O)C4(C)C)C(=O)O3)OC)OC 384.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 6-hydroxysteroids
(2E)-2-[(1R,4aS,4bR,7S,8R,8aR,10S,10aS)-8-formyl-7,10-dihydroxy-1,4b,8-trimethyl-3,4,4a,5,6,7,8a,9,10,10a-decahydro-1H-phenanthren-2-ylidene]-N-(2-hydroxyethyl)-N-methylacetamide 163186716 Click to see CC1C2C(CCC1=CC(=O)N(C)CCO)C3(CCC(C(C3CC2O)(C)C=O)O)C 407.50 unknown https://doi.org/10.1071/CH9750645
2-(8-formyl-7,10-dihydroxy-1,4b,8-trimethyl-3,4,4a,5,6,7,8a,9,10,10a-decahydro-1H-phenanthren-2-ylidene)-N-(2-hydroxyethyl)-N-methylacetamide 162846033 Click to see CC1C2C(CCC1=CC(=O)N(C)CCO)C3(CCC(C(C3CC2O)(C)C=O)O)C 407.50 unknown https://doi.org/10.1071/CH9750645
2-(methylamino)ethyl 2-(7-acetyloxy-8-formyl-10-hydroxy-1,4b,8-trimethyl-3,4,4a,5,6,7,8a,9,10,10a-decahydro-1H-phenanthren-2-ylidene)acetate 427697 Click to see CC1C2C(CCC1=CC(=O)OCCNC)C3(CCC(C(C3CC2O)(C)C=O)OC(=O)C)C 449.60 unknown https://doi.org/10.1071/CH9750645
2-(methylamino)ethyl 2-(8-formyl-7,10-dihydroxy-1,4b,8-trimethyl-3,4,4a,5,6,7,8a,9,10,10a-decahydro-1H-phenanthren-2-ylidene)acetate 427696 Click to see CC1C2C(CCC1=CC(=O)OCCNC)C3(CCC(C(C3CC2O)(C)C=O)O)C 407.50 unknown https://doi.org/10.1071/CH9750645
Acetic acid,4b,8-trimethyl-2(1H)-phenanthrenylidene]-, 2-(methylamino)ethyl ester, [1R-(1alpha,2E,4aalpha,4bbeta,7beta,8beta,8aalpha,10beta,10abeta)]- 6330379 Click to see CC1C2C(CCC1=CC(=O)OCCNC)C3(CCC(C(C3CC2O)(C)C=O)OC(=O)C)C 449.60 unknown https://doi.org/10.1071/CH9750645
methyl (1R,2S,4aR,4bS,7E,8R,8aS,9S,10aR)-2,9-dihydroxy-1,4a,8-trimethyl-7-[2-[2-(methylamino)ethoxy]-2-oxoethylidene]-3,4,4b,5,6,8,8a,9,10,10a-decahydro-2H-phenanthrene-1-carboxylate 163194882 Click to see CC1C2C(CCC1=CC(=O)OCCNC)C3(CCC(C(C3CC2O)(C)C(=O)OC)O)C 437.60 unknown https://doi.org/10.1071/CH9740179
methyl (1R,2S,4aR,4bS,7E,8R,8aS,9S,10aR)-2,9-dihydroxy-7-[2-[2-hydroxyethyl(methyl)amino]-2-oxoethylidene]-1,4a,8-trimethyl-3,4,4b,5,6,8,8a,9,10,10a-decahydro-2H-phenanthrene-1-carboxylate 163005170 Click to see CC1C2C(CCC1=CC(=O)N(C)CCO)C3(CCC(C(C3CC2O)(C)C(=O)OC)O)C 437.60 unknown https://doi.org/10.1071/CH9740179
methyl 2,9-dihydroxy-1,4a,8-trimethyl-7-[2-[2-(methylamino)ethoxy]-2-oxoethylidene]-3,4,4b,5,6,8,8a,9,10,10a-decahydro-2H-phenanthrene-1-carboxylate 427698 Click to see CC1C2C(CCC1=CC(=O)OCCNC)C3(CCC(C(C3CC2O)(C)C(=O)OC)O)C 437.60 unknown https://doi.org/10.1071/CH9740179
methyl 2,9-dihydroxy-7-[2-[2-hydroxyethyl(methyl)amino]-2-oxoethylidene]-1,4a,8-trimethyl-3,4,4b,5,6,8,8a,9,10,10a-decahydro-2H-phenanthrene-1-carboxylate 163005169 Click to see CC1C2C(CCC1=CC(=O)N(C)CCO)C3(CCC(C(C3CC2O)(C)C(=O)OC)O)C 437.60 unknown https://doi.org/10.1071/CH9740179
Norerythrostachaldine 5281283 Click to see CC1C2C(CCC1=CC(=O)OCCNC)C3(CCC(C(C3CC2O)(C)C=O)O)C 407.50 unknown https://doi.org/10.1071/CH9750645
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
2-[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-4,7,8,10,13-pentaacetyloxy-12-hydroxy-5,9-dimethyl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-2-yl]propan-2-yl benzoate 11072583 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1OC(=O)C)C(C)(C)OC(=O)C5=CC=CC=C5)OC4)OC(=O)C)O)OC(=O)C)C)OC(=O)C)OC(=O)C 714.80 unknown via CMAUP database
Taxacin 15226199 Click to see CC(=O)OC1CC(C(=C)C2C1(C(C(C3(C4(COC3(C(=O)CC4C2OC(=O)C)C)C)O)OC(=O)C)OC(=O)C)COC(=O)C5=CC=CC=C5)OC(=O)C=CC6=CC=CC=C6 816.80 unknown via CMAUP database
Taxumairol R 21593833 Click to see CC(=O)OC1CC(C2(C(C1=C)C(C3CC(=O)C4(C(C3(CO4)C)(C(C2OC(=O)C)OC(=O)C)O)C)OC(=O)C)COC(=O)C5=CC=CC=C5)OC(=O)C 728.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Taxumairone A 10027779 Click to see CC1=C2C(C(=O)C3(CC(=CC(C(C2(C)C)CC1OC(=O)C)OC(=O)C)C(=O)C=C3)C)OC(=O)C 472.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6-dihydro-3H-pyrano[3,4-c]pyran-8-one 15559483 Click to see C=CC1=C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 356.32 unknown https://doi.org/10.1071/CH9740179
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(3R)-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-5-carbaldehyde 44577733 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C=O 206.19 unknown via CMAUP database
Cis-7-chloro-4-hydroxymellein 102258988 Click to see CC1C(C2=C(C(=C(C=C2)Cl)O)C(=O)O1)O 228.63 unknown via CMAUP database
trans-4-Hydroxymellein 10262028 Click to see CC1C(C2=C(C(=CC=C2)O)C(=O)O1)O 194.18 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(5R)-5-hydroxy-4-methoxy-5-prop-1-en-2-ylfuran-2-one 40468114 Click to see CC(=C)C1(C(=CC(=O)O1)OC)O 170.16 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5S)-1,7-dioxaspiro[4.4]non-2-ene-4,8-dione 639435 Click to see C1C(=O)OCC12C(=O)C=CO2 154.12 unknown via CMAUP database
Sphaeropsidin A 51361447 Click to see CC1(CCCC23C1C(C(=O)C4=CC(CCC42O)(C)C=C)(OC3=O)O)C 346.40 unknown via CMAUP database
Sphaeropsidin B 57396736 Click to see CC1(CCCC23C1C(C(C4=CC(CCC42O)(C)C=C)O)(OC3=O)O)C 348.40 unknown via CMAUP database
> Organoheterocyclic compounds / Oxocins
(2S,3S,4Z,6S,8S)-3,6,8-trihydroxy-2-nonyl-2,3,6,7,8,9-hexahydrooxecin-10-one 44632077 Click to see CCCCCCCCCC1C(C=CC(CC(CC(=O)O1)O)O)O 328.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Xylaric acid 3084064 Click to see C1=COC=C(C1=O)CC(=O)O 154.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
Cinnamamide, N-(2-hydroxyethyl)-N-methyl- 6303480 Click to see CN(CCO)C(=O)C=CC1=CC=CC=C1 205.25 unknown https://doi.org/10.1016/S0031-9422(00)97281-9
N-(2-hydroxyethyl)-N-methyl-3-phenylprop-2-enamide 35432 Click to see CN(CCO)C(=O)C=CC1=CC=CC=C1 205.25 unknown https://doi.org/10.1016/S0031-9422(00)97281-9
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
Idrocilamide 1550874 Click to see C1=CC=C(C=C1)C=CC(=O)NCCO 191.23 unknown https://doi.org/10.1016/S0031-9422(00)97281-9
N-(2-Hydroxyethyl)-3-phenyl-2-propenamide 23397 Click to see C1=CC=C(C=C1)C=CC(=O)NCCO 191.23 unknown https://doi.org/10.1016/S0031-9422(00)97281-9
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
2-(dimethylamino)ethyl (2E)-3-phenylprop-2-enoate 1551581 Click to see CN(C)CCOC(=O)C=CC1=CC=CC=C1 219.28 unknown https://doi.org/10.1016/S0031-9422(00)97281-9
2-Propenoic acid, 3-phenyl-, 2-(dimethylamino)ethyl ester 422218 Click to see CN(C)CCOC(=O)C=CC1=CC=CC=C1 219.28 unknown https://doi.org/10.1016/S0031-9422(00)97281-9
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Hydroxyethyl-N-methyl-trans-B-hydrocinnamide 6303481 Click to see CN(CCO)C(=O)C=CC1=CC=C(C=C1)O 221.25 unknown https://doi.org/10.1016/S0031-9422(00)97281-9
N-(2-hydroxyethyl)-3-(4-hydroxyphenyl)-N-methylprop-2-enamide 285355 Click to see CN(CCO)C(=O)C=CC1=CC=C(C=C1)O 221.25 unknown https://doi.org/10.1016/S0031-9422(00)97281-9

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