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Gynochthodes officinalis

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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 UUID6440432375a7d196816762
Scientific name Gynochthodes officinalis
Authority (F.C.How) Razafim. & B.Bremer
First published in Adansonia , sér. 3, 33: 293 (2011)

Description Top

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Synonyms Top

Scientific name Authority First published in
Morinda officinalis F.C.How Acta Phytotax. Sin. 7: 326 (1958)
Morinda officinalis var. hirsuta F.C.How Acta Phytotax. Sin. 7: 328. 1958

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001043032
Tropicos 100376367
KEW urn:lsid:ipni.org:names:77117592-1
The Plant List tro-100376367
Open Tree Of Life 69470
NCBI Taxonomy 266091
IPNI 77117592-1
GBIF 7356096
USDA GRIN 466783
CMAUP NPO27363
CMAUP NPO30972

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
GCA_046128155.1 ASM4612815v1 Chromosome South China Agricultural University 2024-12-18 10.0x 411.75 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
Ceria nanoparticles: biomedical applications and toxicity N/A J Zhejiang Univ Sci B 10-May-2024
PMCID:PMC11087188
doi:10.1631/jzus.B2300854
PMID:38725338
Microbiota-Gut-Brain Axis Dysregulation in Alzheimer's Disease: Multi-Pathway Effects and Therapeutic Potential Qu L, Li Y, Liu F, Fang Y, He J, Ma J, Xu T, Wang L, Lei P, Dong H, Jin L, Yang Q, Wu W, Sun D Aging Dis 07-May-2024
PMCID:PMC11081173
doi:10.14336/AD.2023.0823-2
PMID:37728579
The Preparation and Characterization of Quinoa Protein Gels and Application in Eggless Bread Xu Q, Zhang X, Zuo Z, Zhang M, Li T, Wang L Foods 21-Apr-2024
PMCID:PMC11049172
doi:10.3390/foods13081271
PMID:38672943
Gut microbiota-host lipid crosstalk in Alzheimer’s disease: implications for disease progression and therapeutics Luo YX, Yang LL, Yao XQ Mol Neurodegener 16-Apr-2024
PMCID:PMC11020986
doi:10.1186/s13024-024-00720-0
PMID:38627829
Deciphering the intricate linkage between the gut microbiota and Alzheimer's disease: Elucidating mechanistic pathways promising therapeutic strategies Liang J, Wang Y, Liu B, Dong X, Cai W, Zhang N, Zhang H CNS Neurosci Ther 07-Apr-2024
PMCID:PMC10999574
doi:10.1111/cns.14704
PMID:38584341
Exploring the antioxidant potential of endophytic fungi: a review on methods for extraction and quantification of total antioxidant capacity (TAC) Asomadu RO, Ezeorba TP, Ezike TC, Uzoechina JO 3 Biotech 05-Apr-2024
PMCID:PMC10997672
doi:10.1007/s13205-024-03970-3
PMID:38585410
Traditional Chinese medicine in osteoporosis: from pathogenesis to potential activity Cao G, Hu S, Ning Y, Dou X, Ding C, Wang L, Wang Z, Sang X, Yang Q, Shi J, Hao M, Han X Front Pharmacol 02-Apr-2024
PMCID:PMC11019011
doi:10.3389/fphar.2024.1370900
PMID:38628648
The Potential of Exosomes for Osteoporosis Treatment: A Review He Y, Chen Y Drug Des Devel Ther 28-Mar-2024
PMCID:PMC10984200
doi:10.2147/DDDT.S437596
PMID:38562519
Identification and Expression Analysis of R2R3-MYB Transcription Factors Associated with Flavonoid Biosynthesis in Panax quinquefolius Song G, Yan Y, Guo C, Chen J, Wang Y, Wang Y, Zhang J, Gao C, Lian J, Piao X, Di P Int J Mol Sci 26-Mar-2024
PMCID:PMC11011825
doi:10.3390/ijms25073709
PMID:38612520
Wenyang-Tianjing-Jieyu Decoction Improves Depression Rats of Kidney Yang Deficiency Pattern by Regulating T Cell Homeostasis and Inflammation Level Zhang T, Wang J, Wang Y, He L, Lv S, Wang Y, Li W Neuropsychiatr Dis Treat 22-Mar-2024
PMCID:PMC10966763
doi:10.2147/NDT.S445636
PMID:38545129
The impact of dietary supplementation of polysaccharide derived from Polygonatum sibiricum on growth, antioxidant capacity, meat quality, digestive physiology, and gut microbiota in broiler chickens Yang B, Li X, Mesalam NM, Elsadek MF, Abdel-Moneim AM Poult Sci 21-Mar-2024
PMCID:PMC11016799
doi:10.1016/j.psj.2024.103675
PMID:38593546
Analysis of global gene expression using RNA-sequencing reveals novel mechanism of Yanghe Pingchuan decoction in the treatment of asthma Pan L, He B, Gong C, Sun Y, Duan X, Han Y, Chu J, Wang Y BMC Pulm Med 18-Mar-2024
PMCID:PMC10949728
doi:10.1186/s12890-024-02952-8
PMID:38500104
Preparation, structural characterization, biological activity, and nutritional applications of oligosaccharides Chen YJ, Sui X, Wang Y, Zhao ZH, Han TH, Liu YJ, Zhang JN, Zhou P, Yang K, Ye ZH Food Chem X 15-Mar-2024
PMCID:PMC10966145
doi:10.1016/j.fochx.2024.101289
PMID:38544933
Gut microbiota and its metabolites in Alzheimer’s disease: from pathogenesis to treatment Zou X, Zou G, Zou X, Wang K, Chen Z PeerJ 13-Mar-2024
PMCID:PMC10944166
doi:10.7717/peerj.17061
PMID:38495755
Microbiota–gut–brain axis and its therapeutic applications in neurodegenerative diseases Loh JS, Mak WQ, Tan LK, Ng CX, Chan HH, Yeow SH, Foo JB, Ong YS, How CW, Khaw KY Signal Transduct Target Ther 16-Feb-2024
PMCID:PMC10869798
doi:10.1038/s41392-024-01743-1
PMID:38360862

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
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
Anthraquinone-2-carboxylic acid 67030 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C=C(C=C3)C(=O)O 252.22 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
1-Hydroxy-2-methoxyanthraquinone 80103 Click to see COC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown via CMAUP database
1-Hydroxy-2-methylanthraquinone 160817 Click to see CC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)O 238.24 unknown via CMAUP database
1-Hydroxy-2,3-dimethylanthracene-9,10-dione 1382 Click to see CC1=CC2=C(C(=C1C)O)C(=O)C3=CC=CC=C3C2=O 252.26 unknown https://doi.org/10.1248/CPB.43.1462
1-Hydroxyanthraquinone 8512 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=CC=C3)O 224.21 unknown via CMAUP database
1-Methylanthraquinone 70379 Click to see CC1=C2C(=CC=C1)C(=O)C3=CC=CC=C3C2=O 222.24 unknown https://doi.org/10.1055/S-0028-1097264
1,2-Dimethoxyanthracene-9,10-Dione 4217712 Click to see COC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)OC 268.26 unknown via CMAUP database
2-Methoxyanthraquinone 18646 Click to see COC1=CC2=C(C=C1)C(=O)C3=CC=CC=C3C2=O 238.24 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254270/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253840/
2-Methylanthraquinone 6773 Click to see CC1=CC2=C(C=C1)C(=O)C3=CC=CC=C3C2=O 222.24 unknown https://doi.org/10.1248/CPB.43.1462
9,10-Anthracenedione, 1-hydroxy-3-(hydroxmethyl)- 171106 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=CC(=C3)CO)O 254.24 unknown https://doi.org/10.1248/CPB.43.1462
Danthron 2950 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O 240.21 unknown via CMAUP database
Digiferruginol 32209 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3)CO)O 254.24 unknown via CMAUP database
Morindin 151621 Click to see CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC(=C3O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 564.50 unknown via CMAUP database
Physcione 10639 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC 284.26 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254270/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253840/
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,2-Dihydroxy-3-methylanthraquinone 429241 Click to see CC1=CC2=C(C(=C1O)O)C(=O)C3=CC=CC=C3C2=O 254.24 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254270/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253840/
1,3-Dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione 102138994 Click to see COCOC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 300.26 unknown https://doi.org/10.1248/CPB.43.1462
1,3-Dihydroxy-2-methoxyanthracene-9,10-dione 146101 Click to see COC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 270.24 unknown via CMAUP database
1,3,8-Trihydroxy-2-methoxyanthraquinone 25202463 Click to see COC1=C(C=C2C(=C1O)C(=O)C3=C(C2=O)C=CC=C3O)O 286.24 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254270/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253840/
1,6-Dihydroxy-2-methoxyanthraquinone 132521 Click to see COC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC(=C3)O)O 270.24 unknown via CMAUP database
2-(Methoxymethyl)-1,3-dihydroxyanthraquinone 149782 Click to see COCC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 284.26 unknown https://doi.org/10.1248/CPB.43.1462
2-Hydroxy-3-(hydroxymethyl)anthraquinone 44445519 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C=C(C(=C3)CO)O 254.24 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254270/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253840/
2-Hydroxyanthraquinone 11796 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C=C(C=C3)O 224.21 unknown via CMAUP database
Alizarin 1-methyl ether 80309 Click to see COC1=C(C=CC2=C1C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254270/
https://doi.org/10.1248/CPB.43.1462
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253840/
Rubiadin 124062 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown https://doi.org/10.1248/CPB.43.1462
https://doi.org/10.1055/S-0028-1097264
Rubiadin 1-methyl ether 96191 Click to see CC1=C(C=C2C(=C1OC)C(=O)C3=CC=CC=C3C2=O)O 268.26 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254270/
https://doi.org/10.1080/14786419.2011.608676
https://doi.org/10.1055/S-0028-1097264
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253840/
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Taxanes and derivatives
[(2R,3R,5S,7S,8S,9R,10R)-7,9,10-triacetyloxy-5-hydroxy-8,12,15,15-tetramethyl-4-methylidene-2-tricyclo[9.3.1.03,8]pentadec-11-enyl] 2-methylbutanoate 5318282 Click to see CCC(C)C(=O)OC1C2CCC(=C(C2(C)C)C(C(C3(C1C(=C)C(CC3OC(=O)C)O)C)OC(=O)C)OC(=O)C)C 562.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3S,4S,5R,6R)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[[(1R,2S,4R)-1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl]oxy]oxane-3,4,5-triol 14526909 Click to see CC1(C2CCC1(C(C2)OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O)C)C 448.50 unknown https://doi.org/10.1248/CPB.43.1462
Borneol7-O-[beta-D-apiofuranosyl-(1-->6)]-beta-D-glucopyranoside 14526908 Click to see CC1(C2CCC1(C(C2)OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O)C)C 448.50 unknown https://doi.org/10.1248/CPB.43.1462
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,7R,7aS)-7-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylic acid 3488508 Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O 390.34 unknown https://doi.org/10.1248/CPB.43.1462
https://doi.org/10.1248/BPB.28.1915
7-(Acetyloxymethyl)-5-hydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid 13935238 Click to see CC(=O)OCC1=CC(C2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 432.40 unknown https://doi.org/10.1248/CPB.43.1462
7-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylic acid 11574644 Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O 390.34 unknown via CMAUP database
Asperulosidic acid 11968867 Click to see CC(=O)OCC1=CC(C2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 432.40 unknown https://doi.org/10.1248/CPB.43.1462
Deacetylasperulosidic acid 12315350 Click to see C1=C(C2C(C1O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO 390.34 unknown https://doi.org/10.1248/CPB.43.1462
https://doi.org/10.1248/BPB.28.1915
Desacetyl asperulosidic acid 12315348 Click to see C1=C(C2C(C1O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO 390.34 unknown https://doi.org/10.1248/CPB.43.1462
https://doi.org/10.1248/BPB.28.1915
Methyl 6-hydroxy-7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 4490437 Click to see COC(=O)C1=COC(C2C1CC(C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 406.40 unknown https://doi.org/10.1248/CPB.43.1462
Monotropein 73466 Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O 390.34 unknown https://doi.org/10.1248/CPB.43.1462
https://doi.org/10.1248/BPB.28.1915
Morofficinaloside 10453987 Click to see COC(=O)C1=COC(C2C1CC(C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 406.40 unknown https://doi.org/10.1248/CPB.43.1462
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
7-(hydroxymethyl)-4,4a,5,7a-tetrahydro-3H-cyclopenta[c]pyran-1-one 15768074 Click to see C1COC(=O)C2C1CC=C2CO 168.19 unknown https://doi.org/10.1248/CPB.43.1462
Morindolide 10397184 Click to see C1COC(=O)C2C1CC=C2CO 168.19 unknown https://doi.org/10.1248/CPB.43.1462
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
1,10-Dihydroxy-9-(hydroxymethyl)-1,2,6A,6B,9,12A-hexamethyl-2,3,4,5,6,7,8,8A,10,11,12,12B,13,14B-tetradecahydropicene-4A-carboxylic acid 12315074 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1248/CPB.43.1462
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
Canophyllol 7330581 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)CO)C)C)C)C 442.70 unknown via CMAUP database
Epifriedelanol 119242 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown via CMAUP database
Friedelane 15559345 Click to see CC1CCCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 412.70 unknown via CMAUP database
Rotungenic Acid 12315077 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1248/CPB.43.1462
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(8R,9S,10R,13R,14R)-17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 137706654 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-0028-1097264
(8S,9S,10R,13R,14S,17R)-17-(5-ethyl-6-methylheptan-2-yl)-3-hydroxy-10,13-dimethyl-1,2,3,4,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-7-one 138113837 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown https://doi.org/10.1248/CPB.43.1462
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/CPB.43.1462
https://doi.org/10.1055/S-0028-1097264
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/CPB.43.1462
3-Hydroxystigmast-5-en-7-one 160608 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown https://doi.org/10.1248/CPB.43.1462
3beta-Hydroxyporiferast-5-en-7-one 14779505 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown https://doi.org/10.1248/CPB.43.1462
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/CPB.43.1462
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
Asperuloside tetraacetate 443336 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C3C4C(C=C3COC(=O)C)OC(=O)C4=CO2)OC(=O)C)OC(=O)C)OC(=O)C 582.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
[5-(hexopyranosyloxy)-1-oxo-2a,4a,5,7b-tetrahydro-1H-2,6-dioxacyclopenta[cd]inden-4-yl]methyl acetate 233330 Click to see CC(=O)OCC1=CC2C3C1C(OC=C3C(=O)O2)OC4C(C(C(C(O4)CO)O)O)O 414.40 unknown https://doi.org/10.1248/CPB.43.1462
Asperuloside 84298 Click to see CC(=O)OCC1=CC2C3C1C(OC=C3C(=O)O2)OC4C(C(C(C(O4)CO)O)O)O 414.40 unknown https://doi.org/10.1248/CPB.43.1462
beta-D-Fructofuranosyl alpha-D-glucopyranoside 91692850 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
Sucrose NF 46782954 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1055/S-0028-1097264
D-Mannose 18950 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1055/S-0028-1097264
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Inulopentaose 101110146 Click to see C(C1C(C(C(O1)(CO)OCC2(C(C(C(O2)CO)O)O)OCC3(C(C(C(O3)CO)O)O)OCC4(C(C(C(O4)CO)O)O)OCC(=O)C(C(C(CO)O)O)O)O)O)O 828.70 unknown via CMAUP database
Inulotetraose 101110145 Click to see C(C1C(C(C(O1)(CO)OCC2(C(C(C(O2)CO)O)O)OCC3(C(C(C(O3)CO)O)O)OCC(=O)C(C(C(CO)O)O)O)O)O)O 666.60 unknown via CMAUP database
Inulotriose 101708615 Click to see C(C1C(C(C(O1)(CO)OCC2(C(C(C(O2)CO)O)O)OCC(=O)C(C(C(CO)O)O)O)O)O)O 504.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,5-Dihydroxyxanthone 5480299 Click to see C1=CC2=C(C(=C1)O)OC3=CC=CC(=C3C2=O)O 228.20 unknown via CMAUP database
Buchanaxanthone 5481840 Click to see COC1=C(C=CC2=C1OC3=CC=CC(=C3C2=O)O)O 258.23 unknown via CMAUP database
Euxanthone 5281631 Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O 228.20 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
1,3,5-Trihydroxy-2-prenyl-9H-xanthene-9-one 9995643 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC=C3O)O)C 312.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
Calabaxanthone 341188 Click to see CC(=CCC1=C(C=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)OC)C 392.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
6-Deoxyjacareubin 5281629 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=CC=C4)O)C 310.30 unknown via CMAUP database
Jacareubin 5281644 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)C 326.30 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
D-ascorbic acid 54690394 Click to see C(C(C1C(=C(C(=O)O1)O)O)O)O 176.12 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(4r,5s)-5-Hydroxyhexan-4-olide 10887941 Click to see CC(C1CCC(=O)O1)O 130.14 unknown https://doi.org/10.1248/CPB.43.1462
5-(1-Hydroxyethyl)oxolan-2-one 100900 Click to see CC(C1CCC(=O)O1)O 130.14 unknown https://doi.org/10.1248/CPB.43.1462
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253840/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254270/
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
(10S,11S)-10,11,16,16-tetramethyl-6-propyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1,5,7,13,17-pentaene-4,12-dione 12444385 Click to see CCCC1=CC(=O)OC2=C3C=CC(OC3=C4C(=O)C(C(OC4=C12)C)C)(C)C 368.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans
Ohioensin-A 442531 Click to see C1C2C3C(C4=C(C=CC(=C4)O)C5=C3C(=C(C=C5O)O)C1=O)OC6=CC=CC=C26 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
(10R,11R)-10,11,16,16-tetramethyl-6-phenyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1,5,7,13,17-pentaene-4,12-dione 11014914 Click to see CC1C(OC2=C3C(=CC(=O)OC3=C4C=CC(OC4=C2C1=O)(C)C)C5=CC=CC=C5)C 402.40 unknown via CMAUP database

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