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Morus notabilis

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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 UUID6440554f520db747186988
Scientific name Morus notabilis
Authority C.K.Schneid.
First published in Pl. Wilson. 3: 293 (1916)

Description Top

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Synonyms Top

Scientific name Authority First published in
Morus yunnanensis Koidz. Fl. Symb. Orient.-Asiat. : 89 (1930)
Morus mongolica var. yunnanensis (Koidz.) C.Y.Wu & Z.Y.Cao Acta Bot. Yunnan. 17: 154 (1995)

Common names Top

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Language Common/alternative name
Arabic توت بارز
Chinese 川桑

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001240250
Tropicos 50106636
KEW urn:lsid:ipni.org:names:584374-1
The Plant List tro-50106636
Open Tree Of Life 695389
NCBI Taxonomy 981085
IUCN Red List 152821729
IPNI 584374-1
GBIF 5569682
Wikipedia Morus_notabilis
CMAUP NPO5877

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCF_000414095.1 ASM41409v2 Scaffold BGI 2013-08-07 236.0x 305.54 Mb

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
BnAP2-12 overexpression delays ramie flowering: evidence from AP2/ERF gene expression Zhang X, Peng W, Chen H, Xing H Front Plant Sci 25-Mar-2024
PMCID:PMC10999622
doi:10.3389/fpls.2024.1367837
PMID:38590749
The evolutionary origin of naturally occurring intermolecular Diels-Alderases from Morus alba Ding Q, Guo N, Gao L, McKee M, Wu D, Yang J, Fan J, Weng JK, Lei X Nat Commun 20-Mar-2024
PMCID:PMC10954736
doi:10.1038/s41467-024-46845-0
PMID:38509059
Integrating transcriptomics and metabolomics to analyze the defense response of Morus notabilis to mulberry ring rot disease Qian Q, Deng X, Mureed S, Gan Y, Xu D, Wang X, Ali H Front Microbiol 12-Mar-2024
PMCID:PMC10963518
doi:10.3389/fmicb.2024.1373827
PMID:38533335
Mining and functional characterization of NADPH-cytochrome P450 reductases of the DNJ biosynthetic pathway in mulberry leaves Liao Y, Du W, Wan J, Fan J, Pi J, Wu M, Wei Y, Ouyang Z BMC Plant Biol 23-Feb-2024
PMCID:PMC10885410
doi:10.1186/s12870-024-04815-0
PMID:38395770
Integrated transcriptomic and metabolomic analyses elucidate the mechanism of flavonoid biosynthesis in the regulation of mulberry seed germination under salt stress Wang Y, Jiang W, Li C, Wang Z, Lu C, Cheng J, Wei S, Yang J, Yang Q BMC Plant Biol 21-Feb-2024
PMCID:PMC10880279
doi:10.1186/s12870-024-04804-3
PMID:38383312
Transcriptomic Insights and Cytochrome P450 Gene Analysis in Kadsura coccinea for Lignan Biosynthesis Fu H, Guo C, Peng J, Shao F, Sheng S, Wang S Genes (Basel) 21-Feb-2024
PMCID:PMC10969973
doi:10.3390/genes15030270
PMID:38540329
Chromosome-level genome assembly of Hippophae gyantsensis Chen M, Yang D, Yang S, Yang X, Chen Z, Yang T, Yang Y, Yang Y Sci Data 25-Jan-2024
PMCID:PMC10810969
doi:10.1038/s41597-024-02909-w
PMID:38272931
Functional Characterization of CsF3Ha and Its Promoter in Response to Visible Light and Plant Growth Regulators in the Tea Plant Bai Y, Zou R, Zhang H, Li J, Wu T Plants (Basel) 11-Jan-2024
PMCID:PMC10820056
doi:10.3390/plants13020196
PMID:38256750
Advancing understanding of Ficus carica: a comprehensive genomic analysis reveals evolutionary patterns and metabolic pathway insights Bao Y, He M, Zhang C, Jiang S, Zhao L, Ye Z, Sun Q, Xia Z, Zou M Front Plant Sci 07-Dec-2023
PMCID:PMC10754049
doi:10.3389/fpls.2023.1298417
PMID:38155853
The Stilbene Synthase Family in Arachis: A Genome-Wide Study and Functional Characterization in Response to Stress Brasileiro AC, Gimenes MA, Pereira BM, Mota AP, Aguiar MN, Martins AC, Passos MA, Guimaraes PM Genes (Basel) 05-Dec-2023
PMCID:PMC10742623
doi:10.3390/genes14122181
PMID:38137003
PbHsfC1a‐coordinates ABA biosynthesis and H2O2 signalling pathways to improve drought tolerance in Pyrus betulaefolia Zhang F, Wang C, Yao J, Xing C, Xu K, Zhang Z, Chen Q, Qiao Q, Dong H, Han C, Lin L, Zhang S, Huang X Plant Biotechnol J 02-Dec-2023
PMCID:PMC11022796
doi:10.1111/pbi.14255
PMID:38041554
Biosynthetic pathways and related genes regulation of bioactive ingredients in mulberry leaves Lu N, Zhang L, Tian Y, Yang J, Zheng S, Wang L, Guo W Plant Signal Behav 28-Nov-2023
PMCID:PMC10761104
doi:10.1080/15592324.2023.2287881
PMID:38014901
Antioxidants of Non-Enzymatic Nature: Their Function in Higher Plant Cells and the Ways of Boosting Their Biosynthesis Rudenko NN, Vetoshkina DV, Marenkova TV, Borisova-Mubarakshina MM Antioxidants (Basel) 17-Nov-2023
PMCID:PMC10669185
doi:10.3390/antiox12112014
PMID:38001867
Gene Cloning and Characterization of Transcription Factor FtNAC10 in Tartary Buckwheat (Fagopyrum tataricum (L.) Gaertn.) Li J, Li X, Jia C, Liu D Int J Mol Sci 14-Nov-2023
PMCID:PMC10671190
doi:10.3390/ijms242216317
PMID:38003506
Plant salinity stress, sensing, and its mitigation through WRKY Rai GK, Mishra S, Chouhan R, Mushtaq M, Chowdhary AA, Rai PK, Kumar RR, Kumar P, Perez-Alfocea F, Colla G, Cardarelli M, Srivastava V, Gandhi SG Front Plant Sci 04-Oct-2023
PMCID:PMC10582725
doi:10.3389/fpls.2023.1238507
PMID:37860245

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
2-[(1S,2R,4R,4aR,6R,8R,8aS)-4-acetyloxy-8-benzoyloxy-1-(cyanomethyl)-6-ethenyl-4a-hydroxy-1,6-dimethyl-5-oxo-2,3,4,7,8,8a-hexahydronaphthalen-2-yl]-2-methylpropanoic acid 15548729 Click to see CC(=O)OC1CC(C(C2C1(C(=O)C(CC2OC(=O)C3=CC=CC=C3)(C)C=C)O)(C)CC#N)C(C)(C)C(=O)O 525.60 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
[(2S,3S,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-3-ethenyl-2,6,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 10032594 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 692.70 unknown via CMAUP database
Neoorthosiphol A 10055454 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C 692.70 unknown via CMAUP database
Staminol B 11802781 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(C(C(C3=O)(C)O)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)OC(=O)C 692.70 unknown via CMAUP database
staminol C 11490943 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C)O)OC(=O)C5=CC=CC=C5)(C)C 692.70 unknown via CMAUP database
staminol D 11455867 Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C)(C)C 568.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(13R)-1alpha-(Benzoyloxy)-2alpha-acetoxy-3alpha,7alpha,8-trihydroxypimara-15-ene-11,14-dione 101228589 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(=O)CC(C3=O)(C)C=C)O)O)(C)C)O 528.60 unknown via CMAUP database
(13R)-1alpha-(Benzoyloxy)-2alpha,8-dihydroxy-3alpha,7alpha-diacetoxypimara-15-ene-11,14-dione 101228590 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)O)OC(=O)C)(C)C 570.60 unknown via CMAUP database
(13R)-1alpha,11alpha-Bis(benzoyloxy)-2alpha,6beta,8-trihydroxy-3alpha,7alpha-diacetoxypimara-15-ene-14-one 10930480 Click to see CC(=O)OC1C(C2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C)O 692.70 unknown via CMAUP database
(13R)-1alpha,11alpha-Bis(benzoyloxy)-2alpha,7alpha,8-trihydroxy-3alpha-acetoxypimara-15-ene-14-one 10919284 Click to see CC(=O)OC1C(C(C2(C(C1(C)C)CC(C3(C2C(CC(C3=O)(C)C=C)OC(=O)C4=CC=CC=C4)O)O)C)OC(=O)C5=CC=CC=C5)O 634.70 unknown via CMAUP database
(13S)-1alpha,11alpha-Bis(benzoyloxy)-3alpha,7alpha-diacetoxy-2alpha,8beta,12alpha-trihydroxypimara-15-ene-14-one 10032595 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 692.70 unknown via CMAUP database
(2S,3R)-2-(2,3-dihydroxyphenyl)-3,5,7-trihydroxy-2-[(6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]-3H-chromen-4-one 162984551 Click to see CC(=CCCC(=CCCC(=CCC1(C(C(=O)C2=C(C=C(C=C2O1)O)O)O)C3=C(C(=CC=C3)O)O)C)C)C 508.60 unknown https://doi.org/10.1016/J.BMCL.2011.06.020
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7-diacetyloxy-5-benzoyloxy-2-ethenyl-10,10a-dihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 10327179 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(CC(C3=O)(C)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)OC(=O)C 676.70 unknown via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7,10-triacetyloxy-5-benzoyloxy-2-ethenyl-10a-hydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 9987409 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C 718.80 unknown via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,9S,10R,10aR)-6,10-diacetyloxy-5-benzoyloxy-2-ethenyl-7,9,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 10101175 Click to see CC(=O)OC1C(C(C2C(C(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(CC(C3=O)(C)C=C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)O)(C)C)O 692.70 unknown via CMAUP database
[(2S,3S,4R,4aS,4bR,7R,8aR,9R,10aS)-9-acetyloxy-4-benzoyloxy-7-ethenyl-3,8a-dihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-2-yl] benzoate 10258500 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)O)OC(=O)C5=CC=CC=C5)(C)C 632.70 unknown via CMAUP database
[(2S,3S,4R,4aS,4bS,5R,7R,8aR,9R,10aS)-2,3-diacetyloxy-7-ethenyl-5,8a,9-trihydroxy-1,1,4a,7-tetramethyl-8-oxo-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-4-yl] benzoate 10076785 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(CC(C3=O)(C)C=C)O)O)O)(C)C)OC(=O)C 572.60 unknown via CMAUP database
[(2S,3S,4S,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-2-ethenyl-3,6,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 44583688 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 692.70 unknown via CMAUP database
[(4aR,4bR,7R,8aR,9R,10aR)-3-acetyloxy-7-ethenyl-8a-hydroxy-1,1,4a,7-tetramethyl-2,5,8-trioxo-6,9,10,10a-tetrahydro-4bH-phenanthren-9-yl] acetate 10072248 Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C)(C)C 446.50 unknown via CMAUP database
Notabilisin B 56663045 Click to see CC(=CCCC(=CCCC(=CCC1(C(C(=O)C2=C(C=C(C=C2O1)O)O)O)C3=C(C(=CC=C3)O)O)C)C)C 508.60 unknown https://doi.org/10.1016/J.BMCL.2011.06.020
orthosiphol A 15385858 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C 676.70 unknown via CMAUP database
orthosiphol B 15385859 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 676.70 unknown via CMAUP database
orthosiphol D 44583689 Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C)(C)C 552.60 unknown via CMAUP database
orthosiphol I 10674582 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(=O)CC(C3=O)(C)C=C)O)O)(C)C)OC(=O)C 570.60 unknown via CMAUP database
orthosiphol J 10438744 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C)(C)C 612.70 unknown via CMAUP database
Orthosiphol K 10054824 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)O)(C)C 634.70 unknown via CMAUP database
Orthosiphol L 10101176 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C 692.70 unknown via CMAUP database
Orthosiphol M 10030927 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)O)(C)C 570.60 unknown via CMAUP database
Orthosiphol N 10258499 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(=O)CC(C3=O)(C)C=C)O)O)(C)C)OC(=O)C5=CC=CC=C5 632.70 unknown via CMAUP database
orthosiphol O 10032464 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C5=CC=CC=C5)(C)C 676.70 unknown via CMAUP database
Orthosiphol S 10099906 Click to see CC1(C2CC(C3(C(C2(C(C(=O)C1OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)C)C(=O)CC(C3=O)(C)C=C)O)O)C 588.60 unknown via CMAUP database
orthosiphol T 11082749 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(CC(C3=O)(C)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)O 634.70 unknown via CMAUP database
Orthosiphol U 637182 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C)(C)C 614.70 unknown via CMAUP database
Orthosiphol V 10951947 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)O)OC(=O)C)(C)C 572.60 unknown via CMAUP database
Orthosiphol W 11071897 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)O)(C)C 572.60 unknown via CMAUP database
Orthosiphol X 10054823 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(CC(C3=O)(C)C=C)O)O)O)(C)C)OC(=O)C5=CC=CC=C5 634.70 unknown via CMAUP database
Orthosiphol Y 11144807 Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C)(C)C 448.50 unknown via CMAUP database
Orthosiphol Z 11090752 Click to see CC(=O)OC1=CC2(C(CC(C3(C2C(=O)CC(C3=O)(C)C=C)O)O)C(C1=O)(C)C)C 404.50 unknown via CMAUP database
orthosiphonone A 10439492 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C5=CC=CC=C5)(C)C 674.70 unknown via CMAUP database
orthosiphonone C 11226314 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)O)OC(=O)C4=CC=CC=C4)O)(C)C 528.60 unknown via CMAUP database
Siphonol A 10952715 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)CO)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C 734.80 unknown via CMAUP database
Siphonol B 11017910 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)CO)C(CC(C3=O)(C)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)OC(=O)C 692.70 unknown via CMAUP database
Siphonol C 11115145 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)CO)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 692.70 unknown via CMAUP database
SiphonolD 11828707 Click to see CC(=O)OCC12C(CC(C3(C1C(CC(C3=O)(C)C=C)OC(=O)C4=CC=CC=C4)O)O)C(C(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C 734.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Norstaminone A 10414921 Click to see CC(=O)C(=CC1C(=O)C(CC2C1(C(C(C(C2(C)C)O)OC(=O)C)OC(=O)C3=CC=CC=C3)C)OC(=O)C)C=C 540.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Vomifoliol 5280462 Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C 224.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,4S,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-4,9-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 21604188 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C(=O)O 472.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
Siphonol E 10963687 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=O)O)CO)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C 736.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
14-deoxo-14-O-acetylorthosiphol Y 21578028 Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(C(CC3O)(C)C=C)OC(=O)C)O)C)OC(=O)C)(C)C 492.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
Asperglaucide 10026486 Click to see CC(=O)OCC(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3 444.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
Norstaminolactone A 11146922 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C14OC(=O)C(O4)(C(C3OC(=O)C5=CC=CC=C5)CNC)C)C)OC(=O)C6=CC=CC=C6)OC(=O)C)O)(C)C 707.80 unknown via CMAUP database
Staminol A 10628761 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C 734.80 unknown via CMAUP database
Staminolactone A 10770905 Click to see CC(=O)OC1C(C(C2CC(C34C(C2(C1OC(=O)C5=CC=CC=C5)C)C(C(C(O3)(C(=O)O4)C)C=C)OC(=O)C6=CC=CC=C6)O)(C)C)OC(=O)C 690.70 unknown via CMAUP database
Staminolactone B 10676125 Click to see CC(=O)OC1C(C(C2CC(C34C(C2(C1OC(=O)C5=CC=CC=C5)C)C(C(C(O3)(OC4=O)C)C=C)OC(=O)C6=CC=CC=C6)O)(C)C)OC(=O)C 690.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
2-[(1S,2R,4R,4aR,6R,8R,8aS)-4-acetyloxy-8-benzoyloxy-1-(carboxymethyl)-6-ethenyl-4a-hydroxy-1,6-dimethyl-5-oxo-2,3,4,7,8,8a-hexahydronaphthalen-2-yl]-2-methylpropanoic acid 15548710 Click to see CC(=O)OC1CC(C(C2C1(C(=O)C(CC2OC(=O)C3=CC=CC=C3)(C)C=C)O)(C)CC(=O)O)C(C)(C)C(=O)O 544.60 unknown via CMAUP database
secoorthosiphol B 15548728 Click to see CC(=O)OC1CC(C(C2C1(C(=O)C(CC2OC(=O)C3=CC=CC=C3)(C)C=C)O)(C)CC(=O)O)C(C)(C)C(=O)OC 558.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
L-Tartaric acid 444305 Click to see C(C(C(=O)O)O)(C(=O)O)O 150.09 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
[(1S,2S,3R,4S,5S,7S,9R,10R,12R,15S,16S,17S)-4,9-diacetyloxy-3-benzoyloxy-5,10,15-trihydroxy-2,6,6,12-tetramethyl-11,13-dioxatetracyclo[8.7.0.02,7.012,16]heptadecan-17-yl] benzoate 10963538 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(OC4(C(C3OC(=O)C5=CC=CC=C5)C(CO4)O)C)O)C)OC(=O)C6=CC=CC=C6)OC(=O)C)O)(C)C 696.70 unknown via CMAUP database
Norstaminol A 11765116 Click to see CC(=O)OC1C(C(C2CC3C4(O3)C(C2(C1OC(=O)C5=CC=CC=C5)C)C(C6C(COC6(O4)C)O)OC(=O)C7=CC=CC=C7)(C)C)OC(=O)C 678.70 unknown via CMAUP database
Norstaminol C 10951829 Click to see CC(=O)C1=CC2C3(C(CC(C24OCC1O4)OC(=O)C)C(C(C(C3OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C)C 556.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
[(1R,2S,5S)-5-[2,6-dihydroxy-4-(6-hydroxy-1-benzofuran-2-yl)phenyl]-2-(2,4-dihydroxyphenyl)-3-methylcyclohex-3-en-1-yl]-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]methanone 5458824 Click to see CC1=CC(CC(C1C2=C(C=C(C=C2)O)O)C(=O)C3=C(C(=C(C=C3)O)CC=C(C)C)O)C4=C(C=C(C=C4O)C5=CC6=C(O5)C=C(C=C6)O)O 648.70 unknown https://doi.org/10.1016/J.BMCL.2011.06.020
[(1R,2S,6S)-2-[2,6-dihydroxy-4-(6-hydroxy-1-benzofuran-2-yl)phenyl]-6-(2,4-dihydroxyphenyl)-4-methylcyclohex-3-en-1-yl]-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]methanone 14334313 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C(=C(C=C3)O)CC=C(C)C)O)C4=C(C=C(C=C4O)C5=CC6=C(O5)C=C(C=C6)O)O 648.70 unknown https://doi.org/10.1016/J.BMCL.2011.06.020
Chalcomoracin 434768 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C(=C(C=C3)O)CC=C(C)C)O)C4=C(C=C(C=C4O)C5=CC6=C(O5)C=C(C=C6)O)O 648.70 unknown https://doi.org/10.1016/J.BMCL.2011.06.020
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-rosmarinic acid 639655 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown via CMAUP database
2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-, ethyl ester 66883 Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O 208.21 unknown via CMAUP database
Methyl 3,4-dihydroxycinnamate 92202 Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O 194.18 unknown via CMAUP database
Methyl rosmarinate 6479915 Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 374.30 unknown via CMAUP database
p-Hydroxyphenethyl trans-ferulate 637308 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCCC2=CC=C(C=C2)O)O 314.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(2E)-1-[3-[(1S,5S,6R)-6-[2,4-Dihydroxy-3-(3-methyl-2-buten-1-yl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methyl-2-cyclohexen-1-yl]-2,4-dihydroxyphenyl]-3-(2,4-dihydroxyphenyl)-2-propen-1-one 13194890 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C(=C(C=C3)O)CC=C(C)C)O)C4=C(C=CC(=C4O)C(=O)C=CC5=C(C=C(C=C5)O)O)O 678.70 unknown https://doi.org/10.1016/J.BMCL.2011.06.020
(E)-1-[3-[(1S,5S,6R)-6-[3,5-dihydroxy-4-(3-methylbut-2-enyl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one 45485201 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=CC(=C(C(=C3)O)CC=C(C)C)O)C4=C(C=CC(=C4O)C(=O)C=CC5=C(C=C(C=C5)O)O)O 678.70 unknown https://doi.org/10.1016/J.BMCL.2011.06.020
1-[3-[6-[2,4-Dihydroxy-3-(3-methylbut-2-enyl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one 73167443 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C(=C(C=C3)O)CC=C(C)C)O)C4=C(C=CC(=C4O)C(=O)C=CC5=C(C=C(C=C5)O)O)O 678.70 unknown https://doi.org/10.1016/J.BMCL.2011.06.020
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans
(2S)-2alpha-(2-Hydroxy-4-methoxyphenyl)-7-hydroxy-8-prenyl-3,4-dihydro-2H-1-benzopyran 57393562 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2)C3=C(C=C(C=C3)OC)O)O)C 340.40 unknown via CMAUP database
(2S)-2alpha-(4-Hydroxyphenyl)-7-hydroxy-8-prenyl-3,4-dihydro-2H-1-benzopyran 57402293 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2)C3=CC=C(C=C3)O)O)C 310.40 unknown via CMAUP database
4-[(2S)-5-hydroxy-7-methoxy-8-(3-methylbut-2-enyl)-3,4-dihydro-2H-chromen-2-yl]benzene-1,3-diol 44567161 Click to see CC(=CCC1=C(C=C(C2=C1OC(CC2)C3=C(C=C(C=C3)O)O)O)OC)C 356.40 unknown via CMAUP database
Morusyunnansin F 57333040 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2)C3=C(C=C(C=C3)O)O)O)C 326.40 unknown via CMAUP database
Morusyunnansins E 57333039 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2)C3=C(C=C(C=C3)O)O)OC)CO 356.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 2-prenylated flavones
2-[2-(3,7-Dimethylocta-2,6-dienyl)-3,4-dihydroxyphenyl]-3,5,7-trihydroxy-8-(3-methylbut-2-enyl)chromen-4-one 76024748 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)O)C2=C(C(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)C)C 506.60 unknown https://doi.org/10.1016/J.BMCL.2011.06.020
2-[2-(3,7-Dimethylocta-2,6-dienyl)-3,4-dihydroxyphenyl]-5,7-dihydroxy-3-methoxychromen-4-one 76024747 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)C)C 452.50 unknown https://doi.org/10.1016/J.BMCL.2011.06.020
Notabilisin A 53363478 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)C)C 452.50 unknown https://doi.org/10.1016/J.BMCL.2011.06.020
Notabilisin C 53363479 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)O)C2=C(C(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)C)C 506.60 unknown https://doi.org/10.1016/J.BMCL.2011.06.020
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4-[(2R)-8-(2-hydroxyethyl)-7-methoxy-3,4-dihydro-2H-chromen-2-yl]benzene-1,3-diol 53468592 Click to see COC1=C(C2=C(CCC(O2)C3=C(C=C(C=C3)O)O)C=C1)CCO 316.30 unknown via CMAUP database
5-Hydroxy-3',4',6,7-tetramethoxyflavone 152430 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC 358.30 unknown via CMAUP database
5-Hydroxy-3',4',7-trimethoxyflavone 5272653 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown via CMAUP database
6-Hydroxy-5,7-dimethoxy-2-(4-methoxyphenyl)-4H-chromen-4-one 243760 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)OC 328.30 unknown via CMAUP database
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown via CMAUP database
Ladanein 3084066 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O 314.29 unknown via CMAUP database
Salvigenin 161271 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 328.30 unknown via CMAUP database
Sinensetin 145659 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC 372.40 unknown via CMAUP database
Tetramethylscutellarein 96118 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC 342.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
2-(3,4-Dimethoxyphenyl)-6,7,8-trimethoxy-4H-1-benzopyran-4-one 44584772 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=CC(=C(C(=C3O2)OC)OC)OC)OC 372.40 unknown via CMAUP database

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