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Homalomena occulta

Homalomena occulta - Unknown
Part: Unknown
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 UUID643fdf3d18149341330633
Scientific name Homalomena occulta
Authority Schott
First published in Melet. Bot. : 20 (1832)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Spirospatha occulta Raf. Fl. Tellur. 4: 8 (1838)
Zantedeschia occulta Spreng. Syst. Veg. 3: 765 (1826)
Calla occulta Lour. Fl. Cochinch. : 532 (1790)

Common names Top

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Language Common/alternative name
Vietnamese thiên niên kiện
za go'ngaeucah
Chinese 千年健
Chinese 香芋
Chinese 一包针
Chinese 假苏芋
Chinese 团芋
Chinese 湾洪

Subspecies (abbr. subsp./ssp.) Top

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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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No forms added yet.

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000214861
UNII B9CX8785YJ
Tropicos 2102838
KEW urn:lsid:ipni.org:names:87255-1
The Plant List kew-100023
Open Tree Of Life 77535
Observations.org 280583
NCBI Taxonomy 714477
IPNI 87255-1
iNaturalist 362908
GBIF 2868708
EOL 1142910
Elurikkus 320728
USDA GRIN 423435
CMAUP NPO4044

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
Chonggu Granules Improve Cartilage Matrix Metabolism in Knee Osteoarthritis via the miR-148a-3p/Wnt/β-Catenin Pathway Cheng L, Huang C, Li M, Shang S, Chen J, Tang Z J Inflamm Res 20-Oct-2023
PMCID:PMC10596237
doi:10.2147/JIR.S428582
PMID:37881649
Network pharmacology analysis and clinical verification of Jishe Qushi capsules in rheumatoid arthritis treatment Li Y, Zhang N, Peng X, Ma W, Qin Y, Yao X, Huang C, Zhang X Medicine (Baltimore) 25-Aug-2023
PMCID:PMC10470707
doi:10.1097/MD.0000000000034883
PMID:37653836
The effects of acupuncture combined with western medicine in the treatment of neck, shoulder, lumbar and leg pain Shan Y, Zhang J, Ma Y, Zhang Y Am J Transl Res 15-Jun-2023
PMCID:PMC10331671
PMID:37434859
Gastrodia elata BI.:A Comprehensive Review of Its Traditional Use, Botany, Phytochemistry, Pharmacology, and Pharmacokinetics Wu YN, Wen SH, Zhang W, Yu SS, Yang K, Liu D, Zhao CB, Sun J Evid Based Complement Alternat Med 18-Apr-2023
PMCID:PMC10129437
doi:10.1155/2023/5606021
PMID:37114145
Inhibitory Effect of Jinwujiangu Prescription on Peripheral Blood Osteoclasts in Patients with Rheumatoid Arthritis and the Relevant Molecular Mechanism Huang Y, Gao X, An Y, Zeng P, Chen C, Ma W, Yao X Mediators Inflamm 08-Feb-2023
PMCID:PMC9931489
doi:10.1155/2023/4814412
PMID:36816744
Pest categorisation of Colletotrichum aenigma , C. alienum , C. perseae , C. siamense and C. theobromicola Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Migheli Q, Vloutoglou I, Czwienczek E, Maiorano A, Streissl F, Reignault PL EFSA J 25-Aug-2022
PMCID:PMC9405523
doi:10.2903/j.efsa.2022.7529
PMID:36034322
Metabonomics Study of the Hematopoietic Effect of Medicinal Wine Maoji Jiu on a Blood Deficiency Rat Model by Ultra-High-Performance Liquid Chromatography Coupled to Quadrupole Time-of-Flight Mass Spectrometry and a Pattern Recognition Approach Zeng F, Xu Y, Li Y, Yan Z, Li L Molecules 13-Jun-2022
PMCID:PMC9227738
doi:10.3390/molecules27123791
PMID:35744917
Yaobishu Regulates Inflammatory, Metabolic, Autophagic, and Apoptosis Pathways to Attenuate Lumbar Disc Herniation Li X, Li S, Zang Z, He Y Oxid Med Cell Longev 14-May-2022
PMCID:PMC9125431
doi:10.1155/2022/3861380
PMID:35615578
Magnetic Molecularly Imprinted Polymers: An Update on Their Use in the Separation of Active Compounds from Natural Products Ariani MD, Zuhrotun A, Manesiotis P, Hasanah AN Polymers (Basel) 29-Mar-2022
PMCID:PMC9003505
doi:10.3390/polym14071389
PMID:35406265
Structures, Occurrences and Biosynthesis of 11,12,13-Tri-nor-Sesquiterpenes, an Intriguing Class of Bioactive Metabolites Coca-Ruíz V, Suárez I, Aleu J, Collado IG Plants (Basel) 14-Mar-2022
PMCID:PMC8949605
doi:10.3390/plants11060769
PMID:35336651
Jinwujiangu Capsule Treats Fibroblast-Like Synoviocytes of Rheumatoid Arthritis by Inhibiting Pyroptosis via the NLRP3/CAPSES/GSDMD Pathway Ling Y, Xiao M, Huang ZW, Xu H, Huang FQ, Ren NN, Chen CM, Lu DM, Yao XM, Xiao LN, Ma WK Evid Based Complement Alternat Med 22-Nov-2021
PMCID:PMC8629621
doi:10.1155/2021/4836992
PMID:34853599
The Effect of Chinese Medicine Compound in the Treatment of Rheumatoid Arthritis on the Level of Rheumatoid Factor and Anti-Cyclic Citrullinated Peptide Antibodies: A Systematic Review and Meta-Analysis Tang X, Liu Z, Yang Z, Xu S, Wang M, Chen X, Wen Z, Huang R Front Pharmacol 30-Jun-2021
PMCID:PMC8278104
doi:10.3389/fphar.2021.686360
PMID:34276376
Stemodane Diterpenes and Diterpenoids: Isolation, Structure Elucidation, Biogenesis, Biosynthesis, Biological Activity, Biotransformations, Metabolites and Derivatives Biological Activity, Rearrangements Leonelli F, Migneco LM, Valletta A, Marini Bettolo R Molecules 07-May-2021
PMCID:PMC8124710
doi:10.3390/molecules26092761
PMID:34067136
Characterization of the complete chloroplast genome of Homalomena occulta (Lour.) Schott Zhang K, Wu K, Lu S, Zhang J, Ma X, Wang Y, Huang L, Wang X, Xia X Mitochondrial DNA B Resour 18-Mar-2021
PMCID:PMC7995840
doi:10.1080/23802359.2021.1895690
PMID:33796723
Molecularly Imprinted Polymer (MIP) Applications in Natural Product Studies Based on Medicinal Plant and Secondary Metabolite Analysis Karimi Baker Z, Sardari S Iran Biomed J 10-Jan-2021
PMCID:PMC7921521
doi:10.29252/ibj.25.2.68
PMID:33461288

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 / 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
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2-(11Z)-11-Heptadecen-1-yl-6-hydroxybenzoic acid 44133540 Click to see CCCCCC=CCCCCCCCCCCC1=C(C(=CC=C1)O)C(=O)O 374.60 unknown via CMAUP database
2-[(6Z,9Z,12Z)-heptadeca-6,9,12-trienyl]-6-hydroxybenzoic acid 44133541 Click to see CCCCC=CCC=CCC=CCCCCCC1=C(C(=CC=C1)O)C(=O)O 370.50 unknown via CMAUP database
2-[(9E,12E)-heptadeca-9,12-dienyl]-6-hydroxybenzoic acid 101688430 Click to see CCCCC=CCC=CCCCCCCCCC1=C(C(=CC=C1)O)C(=O)O 372.50 unknown via CMAUP database
2-Hydroxy-6-(12-Phenyldodecyl)Benzoic Acid 14655079 Click to see C1=CC=C(C=C1)CCCCCCCCCCCCC2=C(C(=CC=C2)O)C(=O)O 382.50 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Cumenes
m-Cymene 10812 Click to see CC1=CC(=CC=C1)C(C)C 134.22 unknown via CMAUP database
> Benzenoids / Phenol ethers
2-Methoxyethyl phenyl ether 96375 Click to see COCCOC1=CC=CC=C1 152.19 unknown https://doi.org/10.1055/S-2006-960126
> Benzenoids / Phenol ethers / Anisoles
Anethole 637563 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown https://doi.org/10.1055/S-2006-960126
Methoxy-4-propenylbenzene 7703 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown https://doi.org/10.1055/S-2006-960126
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1055/S-2006-960126
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(3R,6R,7R,7aS)-6-ethenyl-3,6-dimethyl-7-prop-1-en-2-yl-3,3a,4,5,7,7a-hexahydro-1-benzofuran-2-one 6325974 Click to see CC1C2CCC(C(C2OC1=O)C(=C)C)(C)C=C 234.33 unknown https://doi.org/10.1055/S-2006-960126
Saussurea lactone 556963 Click to see CC1C2CCC(C(C2OC1=O)C(=C)C)(C)C=C 234.33 unknown https://doi.org/10.1055/S-2006-960126
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
2,6-Octadiene, 1-methoxy-3,7-dimethyl- 5365849 Click to see CC(=CCCC(=CCOC)C)C 168.28 unknown https://doi.org/10.1055/S-2006-960126
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown via CMAUP database
Citral 638011 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown via CMAUP database
Citronellal 7794 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown https://doi.org/10.1055/S-2006-960126
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1055/S-2006-960126
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1055/S-2006-960126
Methyl nerate 5365912 Click to see CC(=CCCC(=CC(=O)OC)C)C 182.26 unknown https://doi.org/10.1055/S-2006-960126
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown via CMAUP database
Neral 643779 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown via CMAUP database
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene 440968 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(-)-beta-Pinene 440967 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown via CMAUP database
(-)-Sabinene 11051711 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown via CMAUP database
(+)-2-Carene 78249 Click to see CC1=CC2C(C2(C)C)CC1 136.23 unknown via CMAUP database
(+)-3-Carene 443156 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown via CMAUP database
(+)-Camphene 92221 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1055/S-2006-960126
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1055/S-2006-960126
Isoborneol 6321405 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol 443162 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1055/S-2006-960126
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1055/S-2006-960126
alpha-PHELLANDRENE, (-)- 442482 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown via CMAUP database
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1055/S-2006-960126
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1055/S-2006-960126
Limonene, (-)- 439250 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Piperitone 6987 Click to see CC1=CC(=O)C(CC1)C(C)C 152.23 unknown https://doi.org/10.1055/S-2006-960126
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
Eucarvone 136330 Click to see CC1=CC=CC(CC1=O)(C)C 150.22 unknown https://doi.org/10.1055/S-2006-960126
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Gamma-cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960126
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-960126
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315594 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1055/S-2006-960126
1,2,4a,5,6,8a-Hexahydro-1-isopropyl-4,7-dimethylnaphthalene 101708 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-960126
3-(2-Hydroxy-2-methylpropyl)-4,7a-dimethyl-2,3,3a,5,6,7-hexahydro-1H-indene-4,7-diol 78069537 Click to see CC12CCC(C1C(CCC2O)(C)O)CC(C)(C)O 256.38 unknown https://doi.org/10.1002/CBDV.200790081
https://doi.org/10.1016/J.PHYTOCHEM.2008.05.023
7,10-Dihydroxy-1,7-dimethyl-4-isopropylbicyclo[4.4.0]dec-3-ene 12313755 Click to see CC(C)C1=CCC2(C(CCC(C2C1)(C)O)O)C 238.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.05.023
https://doi.org/10.1080/14786419.2014.934238
https://doi.org/10.1080/14786410802187817
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-960126
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-960126
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1055/S-2006-960126
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960126
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960126
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960126
Oplodiol 12313756 Click to see CC(C)C1=CCC2(C(CCC(C2C1)(C)O)O)C 238.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.05.023
https://doi.org/10.1080/14786410802187817
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
1,7-di-epi-alpha-Cedrene 10878276 Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-960126
alpha-Cederene 442348 Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-960126
CID 21119906 21119906 Click to see CC1CCC2C13CC(C2(C)C)C(=C)C(C3)O 220.35 unknown https://doi.org/10.1055/S-2006-960126
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(3R,5S)-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7-hexahydro-1H-naphthalene 5317160 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-960126
Eremophilene 12309744 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-960126
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
4,8a-dimethyl-6-propan-2-yl-2,3,4a,5,7,8-hexahydro-1H-naphthalene-1,4,6-triol 73323499 Click to see CC(C)C1(CCC2(C(CCC(C2C1)(C)O)O)C)O 256.38 unknown https://doi.org/10.1002/CBDV.200790081
https://doi.org/10.1016/J.PHYTOCHEM.2008.05.023
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(3S,3aS,4R,5S,8R,8aS)-5,8a-dimethyl-3-propan-2-yl-1,2,3,3a,4,6,7,8-octahydroazulene-4,5,8-triol 162971510 Click to see CC(C)C1CCC2(C1C(C(CCC2O)(C)O)O)C 256.38 unknown https://doi.org/10.1080/14786410802187817
5,8a-Dimethyl-3-propan-2-yl-1,2,3,3a,4,6,7,8-octahydroazulene-4,5,8-triol 85158312 Click to see CC(C)C1CCC2(C1C(C(CCC2O)(C)O)O)C 256.38 unknown https://doi.org/10.1080/14786410802187817
> 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
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 via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Trimethyl 1,2,3-propanetricarboxylate 581486 Click to see COC(=O)CC(CC(=O)OC)C(=O)OC 218.20 unknown via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(2S)-2-Hydroxybutanedioic acid 222656 Click to see C(C(C(=O)O)O)C(=O)O 134.09 unknown via CMAUP database
(R)-Dimethyl 2-hydroxysuccinate 11062697 Click to see COC(=O)CC(C(=O)OC)O 162.14 unknown via CMAUP database
(S)-Dimethyl 2-hydroxysuccinate 10285815 Click to see COC(=O)CC(C(=O)OC)O 162.14 unknown via CMAUP database
D-malate 92824 Click to see C(C(C(=O)O)O)C(=O)O 134.09 unknown via CMAUP database
Dimethyl malate 12674 Click to see COC(=O)CC(C(=O)OC)O 162.14 unknown via CMAUP database
Hydron;2-hydroxybutanedioate 20130941 Click to see [H+].[H+].C(C(C(=O)[O-])O)C(=O)[O-] 134.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Patchouli alcohol 10955174 Click to see CC1CCC2(C(C3CCC2(C1C3)C)(C)C)O 222.37 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Erythritol 222285 Click to see C(C(C(CO)O)O)O 122.12 unknown via CMAUP database
Galactitol 11850 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Hydroxymethylfurfural 237332 Click to see C1=C(OC(=C1)C=O)CO 126.11 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
(S)-alpha-Citronellal 72941617 Click to see CC(CCCC(=C)C)CC=O 154.25 unknown https://doi.org/10.1055/S-2006-960126
> Organoheterocyclic compounds / Furans / Furoic acid and derivatives / Furoic acids
2-Furoic acid 6919 Click to see C1=COC(=C1)C(=O)O 112.08 unknown via CMAUP database
5-Hydroxymethyl-2-furancarboxylic acid 80642 Click to see C1=C(OC(=C1)C(=O)O)CO 142.11 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(S)-3-Hydroxy-gamma-butyrolactone 7269389 Click to see C1C(COC1=O)O 102.09 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
Kushenol V 10572194 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3O)O)OC)O)C 386.40 unknown https://doi.org/10.1055/S-2006-960126

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