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Glochidion zeylanicum

Glochidion zeylanicum - Unknown
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Author: Public Domain - WikiMedia
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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 UUID64403d07ccb0a872598105
Scientific name Glochidion zeylanicum
Authority (Gaertn.) A.Juss.
First published in Euphorb. Gen. : 107 (1824)

Description Top

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Synonyms Top

Scientific name Authority First published in
Phyllanthus anabaptizatus Müll.Arg. Prodr. 15(2): 421 (1866)
Phyllanthus ferdinandii var. supra-axillaris Benth. Fl. Austral. 6: 96 1873
Bradleia zeylanica Gaertn. Fruct. Sem. Pl. 2: 128 (1791)
Agyneia flexuosa B.Heyne ex Wall. Numer. List [Wallich] n. 7863. 1847
Diasperus zeylanicus (Gaertn.) Kuntze Revis. Gen. Pl. 2: 601 (1891)
Epistylium zeylanicum Baill. Étude Euphorb. : 648 (1858)
Glochidion canaranum (Müll.Arg.) Bedd. Fl. Sylv. S. India cxcii. 1873 (1873)
Glochidion ferdinandi var. supra-axillaris (Benth.) F.M.Bailey The Queensland Flora 5 1902
Glochidion lanceolatum var. liukiuense (Hayata) Hurus. J. Fac. Sci. Univ. Tokyo, Sect. 3, Bot. 6: 332. 1954
Glochidion zeylanicum var. malayanum J.J.Sm. Bijdr. Boomsoort. Java 12: 118. 1910
Glochidion zeylanicum var. nitidum (Roxb.) Haines Bot. Bihar Orissa 2: 132. 1921
Bradleja zeylanica Gaertn. Fruct. Sem. Pl. 2: 128 1791

Common names Top

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Language Common/alternative name
Japanese カキバカンコノキ
Japanese glochidion zeylanicum (gaertn.)
Chinese 山柑算盘子
Chinese 金龟树
Chinese 大叶面豆果
Chinese 錫蘭饅頭果
Chinese 香港算盘子
Chinese 锡兰馒头果
Chinese 香港算盤子

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Glochidion zeylanicum var. arborescens (Blume) Chakrab. & M.Gangop. J. Econ. Taxon. Bot. 19: 228 (1995)
Glochidion zeylanicum var. arunachalense Chakrab. & M.Gangop. J. Econ. Taxon. Bot. 19(1): 229 (1995).
Glochidion zeylanicum var. paucicarpum Chakrab. & N.P.Balakr. J. Econ. Taxon. Bot. 28(1): 123 (-125; figs.). 2004
Glochidion zeylanicum var. tomentosum (Dalzell) Trimen Syst. Cat. Fl. Pl. Ceylon : 79 (1885)
Glochidion zeylanicum var. zeylanicum Unknown

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
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
      • Tibet
    • Eastern Asia
      • Japan
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Sulawesi
      • Sumatera
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
      • Solomon Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000973663
Tropicos 12800194
KEW urn:lsid:ipni.org:names:349711-1
The Plant List kew-90844
Open Tree Of Life 1051538
NCBI Taxonomy 271535
IUCN Red List 147646560
IPNI 349711-1
iNaturalist 340543
GBIF 3080562
EOL 1143086
CMAUP NPO15526

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
Insights into the Neuroprotective Potential of Epicatechin: Effects against Aβ-Induced Toxicity in Caenorhabditis elegans Ayuda-Durán B, Garzón-García L, González-Manzano S, Santos-Buelga C, González-Paramás AM Antioxidants (Basel) 08-Jan-2024
PMCID:PMC10812808
doi:10.3390/antiox13010079
PMID:38247503
Polysaccharides from Brasenia schreberi with Great Antioxidant Ability and the Potential Application in Yogurt Wang Y, Zou Y, Fang Q, Feng R, Zhang J, Zhou W, Wei Q Molecules 26-Dec-2023
PMCID:PMC10780003
doi:10.3390/molecules29010150
PMID:38202733
Plant Extracts as Skin Care and Therapeutic Agents Michalak M Int J Mol Sci 22-Oct-2023
PMCID:PMC10607442
doi:10.3390/ijms242015444
PMID:37895122
Effects of Vegetal Extracts and Metabolites against Oxidative Stress and Associated Diseases: Studies in Caenorhabditis elegans Hernández-Cruz EY, Eugenio-Pérez D, Ramírez-Magaña KJ, Pedraza-Chaverri J ACS Omega 27-Feb-2023
PMCID:PMC10018526
doi:10.1021/acsomega.2c07025
PMID:36936291
Antioxidant and Anti-Skin Aging Potential of Selected Thai Plants: In Vitro Evaluation and In Silico Target Prediction Chaikhong K, Chumpolphant S, Rangsinth P, Sillapachaiyaporn C, Chuchawankul S, Tencomnao T, Prasansuklab A Plants (Basel) 22-Dec-2022
PMCID:PMC9823845
doi:10.3390/plants12010065
PMID:36616194
Siwalik plant megafossil diversity in the Eastern Himalayas: A review Khan MA, Mahato S, Spicer RA, Spicer TE, Ali A, Hazra T, Bera S Plant Divers 17-Dec-2022
PMCID:PMC10311196
doi:10.1016/j.pld.2022.12.003
PMID:37397603
Genera of phytopathogenic fungi: GOPHY 4 Chen Q, Bakhshi M, Balci Y, Broders KD, Cheewangkoon R, Chen SF, Fan XL, Gramaje D, Halleen F, Jung MH, Jiang N, Jung T, Májek T, Marincowitz S, Milenković I, Mostert L, Nakashima C, Nurul Faziha I, Pan M, Raza M, Scanu B, Spies CF, Suhaizan L, Suzuki H, Tian CM, Tomšovský M, Úrbez-Torres JR, Wang W, Wingfield BD, Wingfield MJ, Yang Q, Yang X, Zare R, Zhao P, Groenewald JZ, Cai L, Crous PW Stud Mycol 02-Jun-2022
PMCID:PMC9365048
doi:10.3114/sim.2022.101.06
PMID:36059898
Natural Bioactive Products and Alzheimer’s Disease Pathology: Lessons from Caenorhabditis elegans Transgenic Models Navarro-Hortal MD, Romero-Márquez JM, Osta S, Jiménez-Trigo V, Muñoz-Ollero P, Varela-López A Diseases 13-May-2022
PMCID:PMC9149938
doi:10.3390/diseases10020028
PMID:35645249
Caenorhabditis elegans as an in vivo model for food bioactives: A review Mudd N, Liceaga AM Curr Res Food Sci 13-May-2022
PMCID:PMC9126841
doi:10.1016/j.crfs.2022.05.001
PMID:35619588
Oxidation and Antioxidation of Natural Products in the Model Organism Caenorhabditis elegans Zhu A, Zheng F, Zhang W, Li L, Li Y, Hu H, Wu Y, Bao W, Li G, Wang Q, Li H Antioxidants (Basel) 02-Apr-2022
PMCID:PMC9029379
doi:10.3390/antiox11040705
PMID:35453390
Lasia spinosa Chemical Composition and Therapeutic Potential: A Literature-Based Review Hossain R, Quispe C, Herrera-Bravo J, Islam MS, Sarkar C, Islam MT, Martorell M, Cruz-Martins N, Al-Harrasi A, Al-Rawahi A, Sharifi-Rad J, Ibrayeva M, Daştan SD, Alshehri MM, Calina D, Cho WC Oxid Med Cell Longev 28-Dec-2021
PMCID:PMC8727140
doi:10.1155/2021/1602437
PMID:34992714
Bioactive Phytochemicals with Anti-Aging and Lifespan Extending Potentials in Caenorhabditis elegans Okoro NO, Odiba AS, Osadebe PO, Omeje EO, Liao G, Fang W, Jin C, Wang B Molecules 02-Dec-2021
PMCID:PMC8658929
doi:10.3390/molecules26237323
PMID:34885907
Oleuropein Enhances Stress Resistance and Extends Lifespan via Insulin/IGF-1 and SKN-1/Nrf2 Signaling Pathway in Caenorhabditis elegans Feng S, Zhang C, Chen T, Zhou L, Huang Y, Yuan M, Li T, Ding C Antioxidants (Basel) 27-Oct-2021
PMCID:PMC8614835
doi:10.3390/antiox10111697
PMID:34829568
Neuroprotective Effects against Glutamate-Induced HT-22 Hippocampal Cell Damage and Caenorhabditis elegans Lifespan/Healthspan Enhancing Activity of Auricularia polytricha Mushroom Extracts Sillapachaiyaporn C, Rangsinth P, Nilkhet S, Ung AT, Chuchawankul S, Tencomnao T Pharmaceuticals (Basel) 29-Sep-2021
PMCID:PMC8539790
doi:10.3390/ph14101001
PMID:34681226
Role of Phytochemicals in Cancer Chemoprevention: Insights George BP, Chandran R, Abrahamse H Antioxidants (Basel) 14-Sep-2021
PMCID:PMC8466984
doi:10.3390/antiox10091455
PMID:34573087

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 / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[(2R,3R,4S,5R,6R)-6-[[(6S,7aS)-2-oxo-5,6,7,7a-tetrahydro-4H-1-benzofuran-6-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 162978862 Click to see C1CC2=CC(=O)OC2CC1OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O 468.40 unknown https://doi.org/10.1248/CPB.48.1084
[(2R,3S,4S,5R,6R)-6-[[(3aS,6R,7aR)-2-oxo-3a,6,7,7a-tetrahydro-3H-1-benzofuran-6-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 11798488 Click to see C1C(C=CC2C1OC(=O)C2)OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O 468.40 unknown https://doi.org/10.1248/CPB.48.547
https://doi.org/10.1248/CPB.48.1084
[(2R,3S,4S,5R,6R)-6-[[(6S,7aS)-2-oxo-5,6,7,7a-tetrahydro-4H-1-benzofuran-6-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 10552227 Click to see C1CC2=CC(=O)OC2CC1OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O 468.40 unknown https://doi.org/10.1248/CPB.48.547
[3,4,5-trihydroxy-6-[(2-oxo-3a,6,7,7a-tetrahydro-3H-1-benzofuran-6-yl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 73106204 Click to see C1C(C=CC2C1OC(=O)C2)OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O 468.40 unknown https://doi.org/10.1248/CPB.48.547
[3,4,5-trihydroxy-6-[(2-oxo-5,6,7,7a-tetrahydro-4H-1-benzofuran-6-yl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 85182254 Click to see C1CC2=CC(=O)OC2CC1OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O 468.40 unknown https://doi.org/10.1248/CPB.48.547
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-Isolariciresinol 9'-O-glucoside 93473218 Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)O 522.50 unknown https://doi.org/10.1248/CPB.48.1084
(+)-Isolariciresinol-3alpha-O-beta-D-glucopyranoside 10625849 Click to see COC1=C(C=C2C(C(C(CC2=C1)COC3C(C(C(C(O3)CO)O)O)O)CO)C4=CC(=C(C=C4)O)OC)O 522.50 unknown https://doi.org/10.1248/CPB.48.1084
Isolariciresinol 9-O-beta-D-glucoside 85210374 Click to see COC1=C(C=C2C(C(C(CC2=C1)COC3C(C(C(C(O3)CO)O)O)O)CO)C4=CC(=C(C=C4)O)OC)O 522.50 unknown https://doi.org/10.1248/CPB.48.1084
Isolariciresinol 9'-O-beta-D-glucoside 74191750 Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)O 522.50 unknown https://doi.org/10.1248/CPB.48.1084
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E,2S)-4-[(1R,2R,4S)-1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl]but-3-en-2-yl]oxyoxane-3,4,5-triol 6325609 Click to see CC(C=CC1(C(CC(CC1(C)O)O)(C)C)O)OC2C(C(C(C(O2)CO)O)O)O 406.50 unknown https://doi.org/10.1016/S0031-9422(02)00614-3
2-(Hydroxymethyl)-6-[4-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)but-3-en-2-yloxy]oxane-3,4,5-triol 74029756 Click to see CC(C=CC1(C(CC(CC1(C)O)O)(C)C)O)OC2C(C(C(C(O2)CO)O)O)O 406.50 unknown https://doi.org/10.1016/S0031-9422(02)00614-3
Blumenol B 9-O-glucoside 14135398 Click to see CC1=CC(=O)CC(C1(CCC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 388.50 unknown https://doi.org/10.1248/CPB.51.286
icariside B5 14135399 Click to see CC1=CC(=O)CC(C1(CCC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 388.50 unknown https://doi.org/10.1248/CPB.51.286
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Annonaceous acetogenins
(2R)-4-[(2S,8R,13S,14S,17S,18R)-2,8,13,14,17,18-hexahydroxytriacontyl]-2-methyl-2H-furan-5-one 162899402 Click to see CCCCCCCCCCCCC(C(CCC(C(CCCCC(CCCCCC(CC1=CC(OC1=O)C)O)O)O)O)O)O 614.90 unknown https://doi.org/10.1248/CPB.48.547
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3R,4S,5S,6R)-2-[(1S,3R,4R)-3,4-dihydroxy-4-[(E,3S)-3-hydroxybut-1-enyl]-3,5,5-trimethylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 23638287 Click to see CC(C=CC1(C(CC(CC1(C)O)OC2C(C(C(C(O2)CO)O)O)O)(C)C)O)O 406.50 unknown https://doi.org/10.1016/S0031-9422(02)00614-3
(4R)-4-[(3S)-3-hydroxybutyl]-5,5-dimethyl-3-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohex-2-en-1-one 162891466 Click to see CC(CCC1C(=CC(=O)CC1(C)C)COC2C(C(C(C(O2)CO)O)O)O)O 388.50 unknown https://doi.org/10.1248/CPB.51.286
(4R)-4-[(E,3S)-3-hydroxybut-1-enyl]-5,5-dimethyl-3-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohex-2-en-1-one 163020010 Click to see CC(C=CC1C(=CC(=O)CC1(C)C)COC2C(C(C(C(O2)CO)O)O)O)O 386.40 unknown https://doi.org/10.1248/CPB.51.286
2-[3,4-Dihydroxy-4-(3-hydroxybut-1-enyl)-3,5,5-trimethylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 74029755 Click to see CC(C=CC1(C(CC(CC1(C)O)OC2C(C(C(C(O2)CO)O)O)O)(C)C)O)O 406.50 unknown https://doi.org/10.1016/S0031-9422(02)00614-3
4-(3-Hydroxybut-1-enyl)-5,5-dimethyl-3-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohex-2-en-1-one 85354749 Click to see CC(C=CC1C(=CC(=O)CC1(C)C)COC2C(C(C(C(O2)CO)O)O)O)O 386.40 unknown https://doi.org/10.1248/CPB.51.286
4-(3-Hydroxybutyl)-5,5-dimethyl-3-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohex-2-en-1-one 85318568 Click to see CC(CCC1C(=CC(=O)CC1(C)C)COC2C(C(C(C(O2)CO)O)O)O)O 388.50 unknown https://doi.org/10.1248/CPB.51.286
4-Hydroxy-4-(3-hydroxybut-1-enyl)-5,5-dimethyl-3-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohex-2-en-1-one 73118663 Click to see CC(C=CC1(C(=CC(=O)CC1(C)C)COC2C(C(C(C(O2)CO)O)O)O)O)O 402.40 unknown https://doi.org/10.1248/CPB.51.286
CID 15628135 15628135 Click to see CC(=O)C=C=C1C(CC(CC1(C)O)OC2C(C(C(C(O2)CO)O)O)O)(C)C 386.40 unknown https://doi.org/10.1248/CPB.51.286
Glochidionionoside A 11825585 Click to see CC(C=CC1(C(=CC(=O)CC1(C)C)COC2C(C(C(C(O2)CO)O)O)O)O)O 402.40 unknown https://doi.org/10.1248/CPB.51.286
GlochidionionosideB 10927206 Click to see CC(CCC1C(=CC(=O)CC1(C)C)COC2C(C(C(C(O2)CO)O)O)O)O 388.50 unknown https://doi.org/10.1248/CPB.51.286
GlochidionionosideC 11025480 Click to see CC(C=CC1C(=CC(=O)CC1(C)C)COC2C(C(C(C(O2)CO)O)O)O)O 386.40 unknown https://doi.org/10.1248/CPB.51.286
GlochidionionosideD 11101100 Click to see CC(=O)C=C=C1C(CC(CC1(C)O)OC2C(C(C(C(O2)CO)O)O)O)(C)C 386.40 unknown https://doi.org/10.1248/CPB.51.286
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aS,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,11b,12,13,13a,13b-dodecahydro-1H-cyclopenta[a]chrysen-9-one 44559199 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C=CC(=O)C5(C)C)C)C)C 422.70 unknown via CMAUP database
(1R,3aR,5aR,5bR,7aR,11R,11aR,11bS,13aS,13bR)-11-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 44559215 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(=O)C5(C)C)O)C)C)C 440.70 unknown via CMAUP database
(1R,3aR,5aR,5bR,7aS,9S,11S,11aR,11bS,13aS,13bR)-3a,5a,5b,8,8,11a-hexamethyl-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-9,11-diol 44559213 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C 442.70 unknown via CMAUP database
1beta-Hydroxylup-20(29)-en-3-one 14167334 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(=O)C5(C)C)O)C)C)C 440.70 unknown https://doi.org/10.1055/S-2004-835858
20(29)-Lupene-1beta,3beta-diol 488250 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C 442.70 unknown https://doi.org/10.1055/S-2004-835858
3-Epiglochidiol 13969552 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C 442.70 unknown https://doi.org/10.1055/S-2004-835858
3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,11b,12,13,13a,13b-dodecahydro-1H-cyclopenta[a]chrysen-9-one 4106989 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C=CC(=O)C5(C)C)C)C)C 422.70 unknown https://doi.org/10.1055/S-2004-835858
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1055/S-2004-835858
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1055/S-2004-835858
Glochidiol 13969554 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C 442.70 unknown https://doi.org/10.1055/S-2004-835858
Glochidone 13942832 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C=CC(=O)C5(C)C)C)C)C 422.70 unknown https://doi.org/10.1055/S-2004-835858
Glochidonol 14167335 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(=O)C5(C)C)O)C)C)C 440.70 unknown https://doi.org/10.1055/S-2004-835858
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1055/S-2004-835858
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1055/S-2004-835858
> Nucleosides, nucleotides, and analogues / Ribonucleoside 3-phosphates
Adenosine 2',3'-bisphosphoric acid 54162515 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)OP(=O)(O)O)OP(=O)(O)O)N 427.20 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron 21883788 Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-] 116.07 unknown via CMAUP database
Butanedioate;hydron 21952380 Click to see [H+].[H+].C(CC(=O)[O-])C(=O)[O-] 118.09 unknown via CMAUP database
Maleic Acid 444266 Click to see C(=CC(=O)O)C(=O)O 116.07 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Aconitic acid 309 Click to see C(C(=CC(=O)O)C(=O)O)C(=O)O 174.11 unknown via CMAUP database
> Organic acids and derivatives / Keto acids and derivatives / Gamma-keto acids and derivatives
2-Oxoglutaric acid 51 Click to see C(CC(=O)O)C(=O)C(=O)O 146.10 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(3aS,6R,7aR)-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,6,7,7a-tetrahydro-3H-1-benzofuran-2-one 10829178 Click to see C1C(C=CC2C1OC(=O)C2)OC3C(C(C(C(O3)CO)O)O)O 316.30 unknown https://doi.org/10.1248/CPB.48.547
https://doi.org/10.1248/CPB.48.1084
(6R,7aR)-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-4H-1-benzofuran-2-one 101017358 Click to see C1CC2=CC(=O)OC2CC1OC3C(C(C(C(O3)CO)O)O)O 316.30 unknown https://doi.org/10.1248/CPB.48.547
(6R,7aS)-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,7a-dihydro-6H-1-benzofuran-2-one 11723136 Click to see C1C(C=CC2=CC(=O)OC21)OC3C(C(C(C(O3)CO)O)O)O 314.29 unknown https://doi.org/10.1248/CPB.48.547
https://doi.org/10.1248/CPB.48.1084
(6S,7aR)-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-4H-1-benzofuran-2-one 162881957 Click to see C1CC2=CC(=O)OC2CC1OC3C(C(C(C(O3)CO)O)O)O 316.30 unknown https://doi.org/10.1248/CPB.48.1084
(6S,7aS)-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-4H-1-benzofuran-2-one 101017359 Click to see C1CC2=CC(=O)OC2CC1OC3C(C(C(C(O3)CO)O)O)O 316.30 unknown https://doi.org/10.1248/CPB.48.1084
https://doi.org/10.1248/CPB.48.547
6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,6,7,7a-tetrahydro-3H-1-benzofuran-2-one 85281895 Click to see C1C(C=CC2C1OC(=O)C2)OC3C(C(C(C(O3)CO)O)O)O 316.30 unknown https://doi.org/10.1248/CPB.48.547
6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-4H-1-benzofuran-2-one 162881956 Click to see C1CC2=CC(=O)OC2CC1OC3C(C(C(C(O3)CO)O)O)O 316.30 unknown https://doi.org/10.1248/CPB.48.547
Phyllanthurinolactone 10957981 Click to see C1C(C=CC2=CC(=O)OC21)OC3C(C(C(C(O3)CO)O)O)O 314.29 unknown https://doi.org/10.1248/CPB.48.1084
https://doi.org/10.1248/CPB.48.547
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[2-[(2S,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-6-hydroxy-4-methoxyphenyl]-(3,5-dihydroxyphenyl)methanone 163032925 Click to see COC1=CC(=C(C(=C1)OC2C(C(C(O2)CO)O)O)C(=O)C3=CC(=CC(=C3)O)O)O 408.40 unknown https://doi.org/10.1248/CPB.48.1084
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(7'R,8'R)-4,7'-Epoxy-3',5-dimethoxy-4',9,9'-lignanetriol 9'-glucoside 14558383 Click to see COC1=CC(=CC2=C1OC(C2COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)CCCO 522.50 unknown https://doi.org/10.1248/CPB.48.1084
(7R,8S)-dihydrodehydrodiconiferyl alcohol 9-O-beta-D-glucopyranoside 44577121 Click to see COC1=CC(=CC2=C1OC(C2COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)CCCO 522.50 unknown https://doi.org/10.1248/CPB.48.1084
3-[(2S,3R)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl hydrogen sulfate 10575104 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCOS(=O)(=O)O 440.50 unknown https://doi.org/10.1248/CPB.48.1084
3-[2-(4-Hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl hydrogen sulfate 85191060 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCOS(=O)(=O)O 440.50 unknown https://doi.org/10.1248/CPB.48.1084
Dihydrodehydroconiferyl alcohol 4-O-glucoside 14681438 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)CCCO 522.50 unknown https://doi.org/10.1248/CPB.48.1084
Glochidioboside 24982202 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCOC4C(C(C(C(O4)CO)O)O)O 522.50 unknown https://doi.org/10.1248/CPB.48.1084
Urolignoside 10602086 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)CCCO 522.50 unknown https://doi.org/10.1248/CPB.48.1084
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin 114776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1248/CPB.49.921
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 5378180 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1248/CPB.49.921
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1248/CPB.49.921
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-[4-(3,7-dihydroxy-5-methoxy-3,4-dihydro-2H-chromen-2-yl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73090565 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C(CC4=C(O3)C=C(C=C4OC)O)O 510.50 unknown https://doi.org/10.1248/CPB.49.921
Glochiflavanoside C 11762951 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C(CC4=C(O3)C=C(C=C4OC)O)O 510.50 unknown https://doi.org/10.1248/CPB.49.921
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-[[7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-methoxy-3,4-dihydro-2H-chromen-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 85314951 Click to see COC1=CC(=CC2=C1CC(C(O2)C3=CC(=C(C=C3)O)OC)OC4C(C(C(C(O4)CO)O)O)O)O 480.50 unknown https://doi.org/10.1248/CPB.49.921
Glochiflavanoside D 10917811 Click to see COC1=CC(=CC2=C1CC(C(O2)C3=CC(=C(C=C3)O)OC)OC4C(C(C(C(O4)CO)O)O)O)O 480.50 unknown https://doi.org/10.1248/CPB.49.921
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-[[3-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-methoxy-3,4-dihydro-2H-chromen-7-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73113397 Click to see COC1=CC(=CC2=C1CC(C(O2)C3=CC(=C(C=C3)O)OC)O)OC4C(C(C(C(O4)CO)O)O)O 480.50 unknown https://doi.org/10.1248/CPB.49.921
2-[[3-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-5-methoxy-3,4-dihydro-2H-chromen-7-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 85399915 Click to see COC1=CC(=CC(=C1O)OC)C2C(CC3=C(O2)C=C(C=C3OC)OC4C(C(C(C(O4)CO)O)O)O)O 510.50 unknown https://doi.org/10.1248/CPB.49.921
Glochiflavanoside A 11812840 Click to see COC1=CC(=CC2=C1CC(C(O2)C3=CC(=C(C=C3)O)OC)O)OC4C(C(C(C(O4)CO)O)O)O 480.50 unknown https://doi.org/10.1248/CPB.49.921
Glochiflavanoside B 11103219 Click to see COC1=CC(=CC(=C1O)OC)C2C(CC3=C(O2)C=C(C=C3OC)OC4C(C(C(C(O4)CO)O)O)O)O 510.50 unknown https://doi.org/10.1248/CPB.49.921

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