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Trichocolea tomentella

Trichocolea tomentella - Unknown
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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 UUID6440502a09811311582505
Scientific name Trichocolea tomentella
Authority (Ehrh.) Dumort.
First published in Syll. Jungerm. Europ. 67 1831

Description Top

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Trichocolea tomentella is a type of liverwort that is part of the Trichocoleaceae family. It can be found all over the world.

Synonyms Top

Scientific name Authority First published in
Jungermannia tomentella Ehrh. Beitr. Naturk. 2: 150 1785
Jungermannia pluma Reinw., Blume & Nees Nova Acta Phys.-Med. Acad. Caes. Leop.-Carol. Nat. Cur. 12: 209 [Hepat. Jav.] 209 [Hepat 1825

Common names Top

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Language Common/alternative name
Czech pěknice plstnatá
Welsh gwlanlys hardd
German filziges haarkelchmoos
Estonian viltjas udesammal
Finnish harsosammal
Japanese ムクムクゴケ
Lithuanian pūkuotoji apuokė
Dutch wolmos
Swedish dunmossa
Chinese 绒苔

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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No subvariety added yet.

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001196781
USDA Plants TRTO5
Tropicos 35185995
INPN 6650
The Plant List tro-35185995
Open Tree Of Life 683248
Observations.org 17807
NCBI Taxonomy 53022
NBN Atlas NHMSYS0000310803
Nature Serve 2.127632
iNaturalist 155773
GBIF 2689242
EPPO TOATO
EOL 604101
Elurikkus 7984
Wikipedia Trichocolea_tomentella
CMAUP NPO7049

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
The Genetic Diversity of Pleurozium schreberi: A Preliminary Study Based on the atpB-rbcL Świsłowski P, Domagała PJ, Rajfur M Plants (Basel) 05-Oct-2023
PMCID:PMC10574878
doi:10.3390/plants12193487
PMID:37836227
The Bryophyte Flora of Vienna Zechmeister HG, Kropik M Plants (Basel) 20-Aug-2023
PMCID:PMC10458201
doi:10.3390/plants12163002
PMID:37631214
The Liverwort and Hornwort Flora of Jeju Island, Republic of Korea: A Volcanic Island with a Unique Mixture of Subtropical, Temperate, Boreal, and Arctomontane Taxa Choi SS, Bakalin VA, Bum HM, Park SJ, Kim DS, Ahn US, Moon MO Plants (Basel) 20-Jun-2023
PMCID:PMC10301385
doi:10.3390/plants12122384
PMID:37376013
Liverwort and Hornwort Flora of Hoàng Liên National Park and the Adjacent Areas (North Vietnam, Indochina) Bakalin VA, Klimova KG, Nguyen VS, Nguyen HM, Bakalin DA, Choi SS Plants (Basel) 29-Apr-2023
PMCID:PMC10181137
doi:10.3390/plants12091841
PMID:37176900
Bioactive Compounds Produced by Endophytic Microorganisms Associated with Bryophytes—The “Bryendophytes” Stelmasiewicz M, Świątek Ł, Gibbons S, Ludwiczuk A Molecules 05-Apr-2023
PMCID:PMC10096483
doi:10.3390/molecules28073246
PMID:37050009
Nuclear DNA Amounts in Chinese Bryophytes Estimated by Flow Cytometry: Variation Patterns and Biological Significances Li D, Luo G, Guo S, Huang R, Yang J, Cao T, Yu J Plants (Basel) 05-Apr-2023
PMCID:PMC10096954
doi:10.3390/plants12071564
PMID:37050190
Non-Protein Thiol Compounds and Antioxidant Responses Involved in Bryophyte Heavy-Metal Tolerance Salbitani G, Maresca V, Cianciullo P, Bossa R, Carfagna S, Basile A Int J Mol Sci 10-Mar-2023
PMCID:PMC10049163
doi:10.3390/ijms24065302
PMID:36982378
In Vitro Efficacy of Extracts and Isolated Bioactive Compounds from Ascomycota Fungi in the Treatment of Colorectal Cancer: A Systematic Review Luque C, Cepero A, Perazzoli G, Mesas C, Quiñonero F, Cabeza L, Prados J, Melguizo C Pharmaceuticals (Basel) 23-Dec-2022
PMCID:PMC9864996
doi:10.3390/ph16010022
PMID:36678519
Phylotranscriptomics of liverworts: revisiting the backbone phylogeny and ancestral gene duplications Dong S, Yu J, Zhang L, Goffinet B, Liu Y Ann Bot 08-Sep-2022
PMCID:PMC9851303
doi:10.1093/aob/mcac113
PMID:36075207
The Taxonomically Richest Liverwort Hemiboreal Flora in Eurasia Is in the South Kurils Bakalin VA, Klimova KG, Bakalin DA, Choi SS Plants (Basel) 25-Aug-2022
PMCID:PMC9460601
doi:10.3390/plants11172200
PMID:36079582
Phytochemical Profile and Anticancer Potential of Endophytic Microorganisms from Liverwort Species, Marchantia polymorpha L. Stelmasiewicz M, Świątek Ł, Ludwiczuk A Molecules 28-Dec-2021
PMCID:PMC8746834
doi:10.3390/molecules27010153
PMID:35011384
Potential of Anti-Cancer Activity of Secondary Metabolic Products from Marine Fungi Noman E, Al-Shaibani MM, Bakhrebah MA, Almoheer R, Al-Sahari M, Al-Gheethi A, Radin Mohamed RM, Almulaiky YQ, Abdulaal WH J Fungi (Basel) 30-May-2021
PMCID:PMC8229146
doi:10.3390/jof7060436
PMID:34070936
Bryo-Activities: A Review on How Bryophytes Are Contributing to the Arsenal of Natural Bioactive Compounds against Fungi Commisso M, Guarino F, Marchi L, Muto A, Piro A, Degola F Plants (Basel) 21-Jan-2021
PMCID:PMC7911284
doi:10.3390/plants10020203
PMID:33494524
Blepharostoma trichophyllum S.L. (Marchantiophyta): The Complex of Sibling Species and Hybrids Bakalin VA, Vilnet AA, Choi SS, Nguyen VS Plants (Basel) 23-Oct-2020
PMCID:PMC7716226
doi:10.3390/plants9111423
PMID:33114166
Metabolomic-guided discovery of cyclic nonribosomal peptides from Xylaria ellisii sp. nov., a leaf and stem endophyte of Vaccinium angustifolium Ibrahim A, Tanney JB, Fei F, Seifert KA, Cutler GC, Capretta A, Miller JD, Sumarah MW Sci Rep 12-Mar-2020
PMCID:PMC7067778
doi:10.1038/s41598-020-61088-x
PMID:32165688

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 / m-Hydroxybenzoic acid esters
Methyl 4-(3,7-dimethyl-5-oxoocta-2,6-dienoxy)-3-hydroxybenzoate 85120624 Click to see CC(=CC(=O)CC(=CCOC1=C(C=C(C=C1)C(=O)OC)O)C)C 318.40 unknown https://doi.org/10.1021/NP9603378
methyl 4-[(2E)-3,7-dimethyl-5-oxoocta-2,6-dienoxy]-3-hydroxybenzoate 10358497 Click to see CC(=CC(=O)CC(=CCOC1=C(C=C(C=C1)C(=O)OC)O)C)C 318.40 unknown https://doi.org/10.1021/NP9603378
> 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 https://doi.org/10.1016/0031-9422(81)85270-3
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
(3,7-Dimethyl-5-oxoocta-2,6-dienyl) 4-hydroxy-3-methoxybenzoate 71439450 Click to see CC(=CC(=O)CC(=CCOC(=O)C1=CC(=C(C=C1)O)OC)C)C 318.40 unknown https://doi.org/10.1016/0031-9422(81)85270-3
https://doi.org/10.1007/BF01944646
[(2E)-3,7-dimethyl-5-oxoocta-2,6-dienyl] 4-hydroxy-3-methoxybenzoate 101324746 Click to see CC(=CC(=O)CC(=CCOC(=O)C1=CC(=C(C=C1)O)OC)C)C 318.40 unknown https://doi.org/10.1016/0031-9422(81)85270-3
https://doi.org/10.1007/BF01944646
Methyl 3-methoxy-4-(3-methylbut-2-enoxy)benzoate 10682111 Click to see CC(=CCOC1=C(C=C(C=C1)C(=O)OC)OC)C 250.29 unknown https://doi.org/10.1016/S0031-9422(01)00002-4
Methyl 4-(2-hydroperoxy-7-methyl-3-methylidene-5-oxooct-6-enoxy)-3-methoxybenzoate 101141716 Click to see CC(=CC(=O)CC(=C)C(COC1=C(C=C(C=C1)C(=O)OC)OC)OO)C 364.40 unknown https://doi.org/10.1016/S0031-9422(01)00002-4
Methyl 4-(3,7-dimethyl-5-oxoocta-2,6-dienoxy)-3-methoxybenzoate 54378673 Click to see CC(=CC(=O)CC(=CCOC1=C(C=C(C=C1)C(=O)OC)OC)C)C 332.40 unknown https://doi.org/10.1021/NP9603378
Methyl 4-(3,7-dimethyl-5-oxoocta-3,6-dienoxy)-3-methoxybenzoate 85179390 Click to see CC(=CC(=O)C=C(C)CCOC1=C(C=C(C=C1)C(=O)OC)OC)C 332.40 unknown https://doi.org/10.1021/NP9603378
Methyl 4-(3,7-dimethylocta-2,6-dienoxy)-3-methoxybenzoate 85197517 Click to see CC(=CCCC(=CCOC1=C(C=C(C=C1)C(=O)OC)OC)C)C 318.40 unknown https://doi.org/10.1021/NP9603378
https://doi.org/10.1016/S0031-9422(01)00002-4
methyl 4-[(2S)-2-hydroperoxy-7-methyl-3-methylidene-5-oxooct-6-enoxy]-3-methoxybenzoate 163053722 Click to see CC(=CC(=O)CC(=C)C(COC1=C(C=C(C=C1)C(=O)OC)OC)OO)C 364.40 unknown https://doi.org/10.1016/S0031-9422(01)00002-4
methyl 4-[(3Z)-3,7-dimethyl-5-oxoocta-3,6-dienoxy]-3-methoxybenzoate 10544554 Click to see CC(=CC(=O)C=C(C)CCOC1=C(C=C(C=C1)C(=O)OC)OC)C 332.40 unknown https://doi.org/10.1021/NP9603378
Methyl 4[(2e)-3,7-dimethyl-2,6-octadienyl]oxy-3-methoxybenzoate 10591651 Click to see CC(=CCCC(=CCOC1=C(C=C(C=C1)C(=O)OC)OC)C)C 318.40 unknown https://doi.org/10.1021/NP9603378
https://doi.org/10.1016/S0031-9422(01)00002-4
Methyl 4[(2e)-3,7-dimethyl-5-oxo-2,6-octadienyl]oxy-3-methoxybenzoate 10246179 Click to see CC(=CC(=O)CC(=CCOC1=C(C=C(C=C1)C(=O)OC)OC)C)C 332.40 unknown https://doi.org/10.1021/NP9603378
Methyl vanillate 19844 Click to see COC1=C(C=CC(=C1)C(=O)OC)O 182.17 unknown https://doi.org/10.1016/0031-9422(81)85270-3
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
(3,3-Dimethyloxiran-2-yl)methyl 3,4-dimethoxybenzoate 163060853 Click to see CC1(C(O1)COC(=O)C2=CC(=C(C=C2)OC)OC)C 266.29 unknown https://doi.org/10.1016/0031-9422(81)85270-3
(3,7-Dimethyl-5-oxoocta-1,3,6-trienyl) 3,4-dimethoxybenzoate 162959889 Click to see CC(=CC(=O)C=C(C)C=COC(=O)C1=CC(=C(C=C1)OC)OC)C 330.40 unknown https://doi.org/10.1016/0031-9422(81)85270-3
(3,7-Dimethyl-5-oxoocta-3,6-dienyl) 3,4-dimethoxybenzoate 85937540 Click to see CC(=CC(=O)C=C(C)CCOC(=O)C1=CC(=C(C=C1)OC)OC)C 332.40 unknown https://doi.org/10.1007/BF01944646
https://doi.org/10.1016/0031-9422(81)85270-3
(5-Hydroxy-3,7-dimethylocta-2,6-dienyl) 3,4-dimethoxybenzoate 162950186 Click to see CC(=CC(CC(=CCOC(=O)C1=CC(=C(C=C1)OC)OC)C)O)C 334.40 unknown https://doi.org/10.1016/0031-9422(81)85270-3
[(2E,5R)-5-hydroxy-3,7-dimethylocta-2,6-dienyl] 3,4-dimethoxybenzoate 163186342 Click to see CC(=CC(CC(=CCOC(=O)C1=CC(=C(C=C1)OC)OC)C)O)C 334.40 unknown https://doi.org/10.1016/0031-9422(81)85270-3
[(2E)-3,7-dimethyl-5-oxoocta-2,6-dienyl] 3,4-dimethoxybenzoate 15127824 Click to see CC(=CC(=O)CC(=CCOC(=O)C1=CC(=C(C=C1)OC)OC)C)C 332.40 unknown https://doi.org/10.1016/0031-9422(81)85270-3
https://doi.org/10.1007/BF01944646
[(2R)-3,3-dimethyloxiran-2-yl]methyl 3,4-dimethoxybenzoate 163060854 Click to see CC1(C(O1)COC(=O)C2=CC(=C(C=C2)OC)OC)C 266.29 unknown https://doi.org/10.1016/0031-9422(81)85270-3
[(3E)-3,7-dimethyl-5-oxoocta-3,6-dienyl] 3,4-dimethoxybenzoate 15127825 Click to see CC(=CC(=O)C=C(C)CCOC(=O)C1=CC(=C(C=C1)OC)OC)C 332.40 unknown https://doi.org/10.1007/BF01944646
https://doi.org/10.1016/0031-9422(81)85270-3
3-Methylbut-2-en-1-yl 3,4-dimethoxybenzoate 15127823 Click to see CC(=CCOC(=O)C1=CC(=C(C=C1)OC)OC)C 250.29 unknown https://doi.org/10.1016/0031-9422(81)85270-3
https://doi.org/10.1007/BF01944646
3,7-Dimethyl-5-oxoocta-2,6-dien-1-yl 3,4-dimethoxybenzoate 53439722 Click to see CC(=CC(=O)CC(=CCOC(=O)C1=CC(=C(C=C1)OC)OC)C)C 332.40 unknown https://doi.org/10.1007/BF01944646
https://doi.org/10.1016/0031-9422(81)85270-3
3,7-Dimethylocta-2,4,6-trienyl 3,4-dimethoxybenzoate 162951115 Click to see CC(=CC=CC(=CCOC(=O)C1=CC(=C(C=C1)OC)OC)C)C 316.40 unknown https://doi.org/10.1016/0031-9422(81)85270-3
3,7-Dimethylocta-2,6-dienyl 3,4-dimethoxybenzoate 162960301 Click to see CC(=CCCC(=CCOC(=O)C1=CC(=C(C=C1)OC)OC)C)C 318.40 unknown https://doi.org/10.1016/0031-9422(81)85270-3
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Protocatechuic acid, methyl ester 287064 Click to see COC(=O)C1=CC(=C(C=C1)O)O 168.15 unknown https://doi.org/10.1016/0031-9422(81)85270-3
> Hydrocarbon derivatives / Tropones
7-(dimethylamino)-1,2,3,10-tetramethoxy-6,7-dihydro-5H-benzo[a]heptalen-9-one 3885665 Click to see CN(C)C1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC 385.50 unknown https://doi.org/10.1021/NP9603378
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
4,8-Methanoazulene, decahydro-3a,4,8a-trimethyl-7-methylene-, (3aR,4R,8R,8aS)-rel- 524194 Click to see CC12CCC(=C)C(C1)C3(C2(CCC3)C)C 204.35 unknown https://doi.org/10.1016/0031-9422(81)85270-3
beta-Barbatene 14109421 Click to see CC12CCC(=C)C(C1)C3(C2(CCC3)C)C 204.35 unknown https://doi.org/10.1016/0031-9422(81)85270-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4aS,5S,6S,8aR)-6-hydroxy-2,5-dimethyl-5-(4-methylpent-3-enyl)-3,4,4a,6,7,8-hexahydronaphthalene-1,8a-dicarbaldehyde 102117177 Click to see CC1=C(C2(CCC(C(C2CC1)(C)CCC=C(C)C)O)C=O)C=O 318.40 unknown https://doi.org/10.1016/0031-9422(81)85270-3
(4aS,5S,8aR)-2,5-dimethyl-5-(4-methylpent-3-enyl)-3,4,4a,6,7,8-hexahydronaphthalene-1,8a-dicarbaldehyde 13874392 Click to see CC1=C(C2(CCCC(C2CC1)(C)CCC=C(C)C)C=O)C=O 302.50 unknown https://doi.org/10.1016/0031-9422(81)85270-3
2,5-Dimethyl-5-(4-methylpent-3-enyl)-3,4,4a,6,7,8-hexahydronaphthalene-1,8a-dicarbaldehyde 13874391 Click to see CC1=C(C2(CCCC(C2CC1)(C)CCC=C(C)C)C=O)C=O 302.50 unknown https://doi.org/10.1016/0031-9422(81)85270-3
6-Hydroxy-2,5-dimethyl-5-(4-methylpent-3-enyl)-3,4,4a,6,7,8-hexahydronaphthalene-1,8a-dicarbaldehyde 162892212 Click to see CC1=C(C2(CCC(C(C2CC1)(C)CCC=C(C)C)O)C=O)C=O 318.40 unknown https://doi.org/10.1016/0031-9422(81)85270-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(E)-(7R,11R)-3,7,11,15-tetramethylhexadec-2-ene-1-ol 145386 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/S0031-9422(01)00002-4
Rel-(7S,11S,E)-3,7,11,15-tetramethylhexadec-2-en-1-ol 40467768 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/S0031-9422(01)00002-4
> 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 https://doi.org/10.1016/0031-9422(81)85270-3
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1016/0031-9422(81)85270-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/0031-9422(81)85270-3
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/0031-9422(81)85270-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(95)00184-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
[8a-Hydroxy-3,4a,5-trimethyl-9-(2-methylbut-2-enoyloxy)-4,5,6,7,8,9-hexahydrobenzo[f][1]benzofuran-4-yl] 3-methylpent-2-enoate 163032956 Click to see CCC(=CC(=O)OC1C2=C(C(C3(C1(C(CCC3)C)C)O)OC(=O)C(=CC)C)OC=C2C)C 444.60 unknown https://doi.org/10.1016/0031-9422(81)85270-3
1-(5-bromo-3,7-dihydroxy-8,8a-dimethyl-7,8-dihydro-1H-naphthalen-2-yl)ethanone 162912617 Click to see CC1C(C=C(C2=CC(=C(CC12C)C(=O)C)O)Br)O 313.19 unknown https://doi.org/10.1016/0031-9422(81)85270-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
methyl (4S,5E,6S)-5-ethylidene-4-[2-[(2R)-2-[(1S,2R,3R,4S)-4-[2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-2-(hydroxymethyl)-3-methylcyclopentyl]propoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163186982 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC(C)C3CC(C(C3CO)C)OC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC 961.00 unknown https://doi.org/10.1016/0031-9422(81)85270-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
20-Hydroxyecdysone 5459840 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown via CMAUP database
24-epi-Pterosterone 11027254 Click to see CC(C)C(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)O 480.60 unknown via CMAUP database
25S-Inokosterone 12358616 Click to see CC(CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)CO 480.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
Ponasterone A 115127 Click to see CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O 464.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
22,23-Dihydrobrassicasterol 5283637 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
[(2R,3S,4S,5R,6R)-6-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5S)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl hexadecanoate 13051627 Click to see CCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(C)C(C)C)C)C)O)O)O 801.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(01)00002-4
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
Sitoindoside I 9832350 Click to see CCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O 815.30 unknown via CMAUP database
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(01)00002-4
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
1-Naphthalenemethanol, 1,4,4a,5,6,7,8,8a-octahydro-2,5,5,8a-tetramethyl- 298071 Click to see CC1=CCC2C(CCCC2(C1CO)C)(C)C 222.37 unknown https://doi.org/10.1016/0031-9422(81)85270-3
Drimenol 3080551 Click to see CC1=CCC2C(CCCC2(C1CO)C)(C)C 222.37 unknown https://doi.org/10.1016/0031-9422(81)85270-3
> Organoheterocyclic compounds / Benzodioxoles
(3,3-Dimethyloxiran-2-yl)methyl 1,3-benzodioxole-5-carboxylate 163049394 Click to see CC1(C(O1)COC(=O)C2=CC3=C(C=C2)OCO3)C 250.25 unknown https://doi.org/10.1016/0031-9422(81)85270-3
[(2S)-3,3-dimethyloxiran-2-yl]methyl 1,3-benzodioxole-5-carboxylate 163049395 Click to see CC1(C(O1)COC(=O)C2=CC3=C(C=C2)OCO3)C 250.25 unknown https://doi.org/10.1016/0031-9422(81)85270-3
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,3R)-4-[(E)-2-carboxyethenyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carboxylic acid 10316325 Click to see C1=CC(=C(C=C1C2C(C3=C(C=CC(=C3O2)O)C=CC(=O)O)C(=O)O)O)O 358.30 unknown via CMAUP database
(3R,4R,5R)-5-[(2S,3R)-4-[(E)-2-carboxyethenyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carbonyl]oxy-3,4-dihydroxycyclohexene-1-carboxylic acid 10436502 Click to see C1C(C(C(C=C1C(=O)O)O)O)OC(=O)C2C(OC3=C(C=CC(=C23)C=CC(=O)O)O)C4=CC(=C(C=C4)O)O 514.40 unknown via CMAUP database
Przewalskinic acid A 9975641 Click to see C1=CC(=C(C=C1C2C(C3=C(C=CC(=C3O2)O)C=CC(=O)O)C(=O)O)O)O 358.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Woodorien 192694 Click to see COC(=O)C1=CC(=C(C=C1)O)OC2C(C(C(C(O2)CO)O)O)O 330.29 unknown via CMAUP database

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