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Adiantum caudatum

Adiantum caudatum - 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 UUID64407715a8003706439676
Scientific name Adiantum caudatum
Authority L.
First published in Mant. Pl. : 308 (1771)

Description Top

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It is also found in the tropical regions of Africa, Central and South America, and the Caribbean.

Description
Adiantum caudatum is a small, delicate fern with long, slender fronds that grow up to 30 cm long. The fronds are divided into small leaflets that are arranged in a fan-like pattern. The leaflets are bright green in color and have a glossy sheen. The sori, or reproductive structures, are located on the underside of the leaflets.

Adiantum caudatum, commonly known as walking maidenhair, tailed maidenhair, or trailing maidenhair, is a small, delicate fern found in shaded areas in south-east countries such as Bangladesh, Burma, India, Nepal, Philippines, Thailand, China, Vietnam, as well as in the tropical regions of Africa, Central and South America, and the Caribbean. It has long, slender fronds up to 30 cm long, divided into small leaflets arranged in a fan-like pattern. The leaflets are bright green in color and have a glossy sheen, with sori, or reproductive structures, located on the underside.

Synonyms Top

Scientific name Authority First published in
Adiantum assamicum B.K.Nayar Bull. Nation. Bot. Gard. (Lucknow) 94: 1, f.1-4. 1964
Adiantum borneense Gand. Bull. Soc. Bot. France 66: 305 (1920)
Adiantum flagelliferum Wall. Numer. List : n.° 76 (1829)
Adiantum lomesam B.K.Nayar & Geev. Fern Fl. Malabar 140 (1993)
Adiantum lyratum Blanco Fl. Filip. 832. 1837 (1837)
Adiantum caudatum var. angustilobatum Bonap. Notes Pteridol. 7: 173–174 1918

Common names Top

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Language Common/alternative name
English tailed maidenhair
Arabic برشاوشان مذيل
Chinese 猪鬃草
Chinese 鞭叶铁线蕨
Chinese 鞭葉鐵線蕨

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Adiantum caudatum var. hirsutum (Bory) Bonap. Notes Pteridol. 13: 176 1921

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Sri Lanka
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sulawesi
    • Papuasia
      • New Guinea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001107188
Florida Plant Atlas 1997
USDA Plants ADCA3
Tropicos 26600008
INPN 447952
KEW urn:lsid:ipni.org:names:325033-2
The Plant List tro-26600008
Open Tree Of Life 498759
Observations.org 410243
NCBI Taxonomy 1073774
Nature Serve 2.142601
IPNI 325033-2
iNaturalist 158019
GBIF 2651833
Freebase /m/0wyzcpz
EOL 596889
Elurikkus 268893
Wikipedia Adiantum_caudatum
CMAUP NPO4789

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
Bioactive Steroids Bearing Oxirane Ring Dembitsky VM Biomedicines 09-Aug-2023
PMCID:PMC10452232
doi:10.3390/biomedicines11082237
PMID:37626733
Comprehensive evolutionary analysis of the TCP gene family: Further insights for its origin, expansion, and diversification Wang JL, Wang HW, Cao YN, Kan SL, Liu YY Front Plant Sci 02-Sep-2022
PMCID:PMC9480096
doi:10.3389/fpls.2022.994567
PMID:36119616
Full-length transcriptome analysis of Adiantum flabellulatum gametophyte Cai Z, Xie Z, Huang L, Wang Z, Pan M, Yu X, Xu S, Luo J PeerJ 09-Mar-2022
PMCID:PMC8917799
doi:10.7717/peerj.13079
PMID:35287343
Phytochemical profile and in vitro antioxidant activity of Emelia M (EMB), Mshikazi and Delosma H herbal medicines as demonstrated in THP-1 and Jurkat leukaemia cell lines Adeniyi JN, Nlooto M, Ngcobo M, Moodley R, Gomo E Afr Health Sci 01-Dec-2021
PMCID:PMC8889806
doi:10.4314/ahs.v21i4.51
PMID:35283952
Application of Polypodiopsida Class in Nanotechnology–Potential towards Development of More Effective Bioactive Solutions Fierascu I, Fierascu RC, Ungureanu C, Draghiceanu OA, Soare LC Antioxidants (Basel) 08-May-2021
PMCID:PMC8151343
doi:10.3390/antiox10050748
PMID:34066800
Nanotechnologies: An Innovative Tool to Release Natural Extracts with Antimicrobial Properties Spizzirri UG, Aiello F, Carullo G, Facente A, Restuccia D Pharmaceutics 06-Feb-2021
PMCID:PMC7915176
doi:10.3390/pharmaceutics13020230
PMID:33562128
Optimization of Total Phenolic and Flavonoid Contents of Defatted Pitaya (Hylocereus polyrhizus) Seed Extract and Its Antioxidant Properties Zulkifli SA, Abd Gani SS, Zaidan UH, Halmi MI Molecules 12-Feb-2020
PMCID:PMC7070736
doi:10.3390/molecules25040787
PMID:32059460
Vascular Epiphytic Medicinal Plants as Sources of Therapeutic Agents: Their Ethnopharmacological Uses, Chemical Composition, and Biological Activities Nugraha AS, Triatmoko B, Wangchuk P, Keller PA Biomolecules 24-Jan-2020
PMCID:PMC7072150
doi:10.3390/biom10020181
PMID:31991657
Identification and evolutionary analysis of chalcone isomerase-fold proteins in ferns Ni R, Zhu TT, Zhang XS, Wang PY, Sun CJ, Qiao YN, Lou HX, Cheng AX J Exp Bot 26-Sep-2019
PMCID:PMC6913697
doi:10.1093/jxb/erz425
PMID:31557291
Ethnomedicinal knowledge of the rural communities of Dhirkot, Azad Jammu and Kashmir, Pakistan Farooq A, Amjad MS, Ahmad K, Altaf M, Umair M, Abbasi AM J Ethnobiol Ethnomed 30-Aug-2019
PMCID:PMC6716831
doi:10.1186/s13002-019-0323-2
PMID:31470868
10KP: A phylodiverse genome sequencing plan Cheng S, Melkonian M, Smith SA, Brockington S, Archibald JM, Delaux PM, Li FW, Melkonian B, Mavrodiev EV, Sun W, Fu Y, Yang H, Soltis DE, Graham SW, Soltis PS, Liu X, Xu X, Wong GK Gigascience 20-Feb-2018
PMCID:PMC5869286
doi:10.1093/gigascience/giy013
PMID:29618049
A review of the use of pteridophytes for treating human ailments Baskaran XR, Geo Vigila AV, Zhang SZ, Feng SX, Liao WB J Zhejiang Univ Sci B 01-Feb-2018
PMCID:PMC5833325
doi:10.1631/jzus.B1600344
PMID:29405039
Large-scale phylogenomic analysis resolves a backbone phylogeny in ferns Shen H, Jin D, Shu JP, Zhou XL, Lei M, Wei R, Shang H, Wei HJ, Zhang R, Liu L, Gu YF, Zhang XC, Yan YH Gigascience 24-Nov-2017
PMCID:PMC5795342
doi:10.1093/gigascience/gix116
PMID:29186447
Analysis on bioaccumulation of metals in aquatic environment of Beas River Basin: A case study from Kanjli wetland Singh N, Kaur M, Katnoria JK Geohealth 30-May-2017
PMCID:PMC7007077
doi:10.1002/2017GH000062
PMID:32158984
Eco-Floristic studies of native plants of the Beer Hills along the Indus River in the districts Haripur and Abbottabad, Pakistan Bano S, Khan SM, Alam J, Alqarawi AA, Abd_Allah EF, Ahmad Z, Rahman IU, Ahmad H, Aldubise A, Hashem A Saudi J Biol Sci 27-Feb-2017
PMCID:PMC5936874
doi:10.1016/j.sjbs.2017.02.009
PMID:29740247

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown via CMAUP database
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Tetracosanol 10472 Click to see CCCCCCCCCCCCCCCCCCCCCCCCO 354.70 unknown via CMAUP database
Docosanol 12620 Click to see CCCCCCCCCCCCCCCCCCCCCCO 326.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(R)-nonacosan-10-ol 342803 Click to see CCCCCCCCCCCCCCCCCCCC(CCCCCCCCC)O 424.80 unknown via CMAUP database
1-Eicosanol 12404 Click to see CCCCCCCCCCCCCCCCCCCCO 298.50 unknown via CMAUP database
8-Acetoxy-3-hydroxy-1,9,14-pentadecatriene-4,6-diyne 90860448 Click to see CC(=O)OC(C=CCCCC=C)C#CC#CC(C=C)O 272.34 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(3R,3aR,5aR,5bS,7aS,8S,9R,11aS,11bR,13aS,13bR)-8-methoxy-3a,5a,7a,8,11b,13a-hexamethyl-3-propan-2-yl-2,3,4,5,5b,6,7,9,10,11,11a,12,13,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-ol 163049038 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CCC5(C4CCC(C5(C)OC)O)C)C)C)C)C 458.80 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
3a,5a,7a,8,11b,13a-Hexamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,10,11,11a,12,13,13b-tetradecahydrocyclopenta[a]chrysene 5260101 Click to see CC1=CCCC2C1(CCC3C2(CCC4(C3(CCC5(C4CCC5C(C)C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
8-methoxy-3a,5a,7a,8,11b,13a-hexamethyl-3-propan-2-yl-2,3,4,5,5b,6,7,9,10,11,11a,12,13,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-ol 163049036 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CCC5(C4CCC(C5(C)OC)O)C)C)C)C)C 458.80 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
Filic-3-ene 12309889 Click to see CC1=CCCC2C1(CCC3C2(CCC4(C3(CCC5(C4CCC5C(C)C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(1R,2R,5S,7S,10R,11S,14R,15S,20S)-1,2,10,15,19,19-hexamethyl-7-propan-2-yl-6-oxahexacyclo[12.8.0.02,11.05,7.05,10.015,20]docosane 101289688 Click to see CC(C)C12CCC3(C1(O2)CCC4(C3CCC5C4(CCC6C5(CCCC6(C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
1,2,10,15,19,19-Hexamethyl-7-propan-2-yl-6-oxahexacyclo[12.8.0.02,11.05,7.05,10.015,20]docosane 13873999 Click to see CC(C)C12CCC3(C1(O2)CCC4(C3CCC5C4(CCC6C5(CCCC6(C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2S,5S,6S,9R,10R,13S,14R,15S,17S)-14-hydroxy-5,10,13,18,18-pentamethyl-9-propan-2-yl-23-oxahexacyclo[13.6.2.01,17.02,14.05,13.06,10]tricosan-22-one 162989208 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4C3(C5CC6C4(CCCC6(C)C)C(=O)O5)O)C)C)C 456.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
(1R,3R,3aR,5aR,5bR,7aS,11aS,13aS,13bR)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,7a,9,10,11,13,13b-tetradecahydrocyclopenta[a]chrysen-1-ol 100934190 Click to see CC(C)C1CC(C2C1(CCC3(C2(CC=C4C3CCC5C4(CCCC5(C)C)C)C)C)C)O 426.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
(1R,3R,3aR,5aS,7aS,11aS,13aS,13bR)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,7,7a,9,10,11,13,13b-dodecahydrocyclopenta[a]chrysen-1-ol 102023953 Click to see CC(C)C1CC(C2C1(CCC3(C2(CC=C4C3=CCC5C4(CCCC5(C)C)C)C)C)C)O 424.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
(3R,3aR,5aR,5bS,7aS,11aS,13aS,13bR)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,7a,9,10,11,13,13b-tetradecahydrocyclopenta[a]chrysene 12309129 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
(3R,3aR,5aS,7aS,11aS,11bR,13aS,13bR)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,7,7a,9,10,11,11b,12,13,13b-tetradecahydrocyclopenta[a]chrysene 13857703 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4C3=CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
(3R,3aR,5aS,7aS,11aS,13aS,13bR)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,7,7a,9,10,11,13,13b-dodecahydrocyclopenta[a]chrysene 13857712 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3=CCC5C4(CCCC5(C)C)C)C)C)C 408.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
(3R,3aS,5aS,5bR,7aS,11aS,11bR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-3-propan-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13b-tetradecahydrocyclopenta[a]chrysene 162985264 Click to see CC(C)C1CCC2C1(CCC3(C2=CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
19alpha-Hydroxyfern-7-ene 100934191 Click to see CC(C)C1CC(C2C1(CCC3(C2(CCC4C3=CCC5C4(CCCC5(C)C)C)C)C)C)O 426.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
3a,5a,8,8,11a,13a-Hexamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,7a,9,10,11,13,13b-tetradecahydrocyclopenta[a]chrysen-1-ol 162871009 Click to see CC(C)C1CC(C2C1(CCC3(C2(CC=C4C3CCC5C4(CCCC5(C)C)C)C)C)C)O 426.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
3a,5a,8,8,11a,13a-Hexamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,7a,9,10,11,13,13b-tetradecahydrocyclopenta[a]chrysene 4481463 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
3a,5a,8,8,11a,13a-Hexamethyl-3-propan-2-yl-1,2,3,4,5,6,7,7a,9,10,11,12,13,13b-tetradecahydrocyclopenta[a]chrysene 12311004 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4=C3CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
3a,5a,8,8,11a,13a-Hexamethyl-3-propan-2-yl-1,2,3,4,5,7,7a,9,10,11,11b,12,13,13b-tetradecahydrocyclopenta[a]chrysene 13857699 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4C3=CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
3a,5a,8,8,11a,13a-Hexamethyl-3-propan-2-yl-1,2,3,4,5,7,7a,9,10,11,13,13b-dodecahydrocyclopenta[a]chrysen-1-ol 162982011 Click to see CC(C)C1CC(C2C1(CCC3(C2(CC=C4C3=CCC5C4(CCCC5(C)C)C)C)C)C)O 424.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
3a,5a,8,8,11a,13a-Hexamethyl-3-propan-2-yl-1,2,3,4,5,7,7a,9,10,11,13,13b-dodecahydrocyclopenta[a]chrysene 13857710 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3=CCC5C4(CCCC5(C)C)C)C)C)C 408.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
8-Fernene 12311007 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4=C3CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
8alpha-Hydroxyfernan-25,7beta-olide 636899 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4C3(C5CC6C4(CCCC6(C)C)C(=O)O5)O)C)C)C 456.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
Bauerenol 111220 Click to see CC1CCC2(CCC3(C4=CCC5C(C(CCC5(C4CCC3(C2C1C)C)C)O)(C)C)C)C 426.70 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
CID 137796495 137796495 Click to see CC(C)C1CC(C2C1(CCC3(C2(CCC4C3=CCC5C4(CCCC5(C)C)C)C)C)C)O 426.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
Eburicol 9803310 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 440.70 unknown via CMAUP database
Fern-8-ene 12311006 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4=C3CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
Fernene 441679 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
Filicene 12309888 Click to see CC1=CCCC2C1(CCC3C2(CCC4(C3(CCC5(C4CCC5C(C)C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
Lanosta-7,24-dienol 12302189 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown via CMAUP database
Lanosterol 246983 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Neochlorogenin 12303066 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)O)C)O)C)C)OC1 432.60 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
Hopene II 12310619 Click to see CC(C)C1CCC2=C3CCC4C5(CCCC(C5CCC4(C3(CCC12C)C)C)(C)C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
31-Norlanostenol 14845298 Click to see CC1C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC4C(C)CCCC(C)C)C)C 414.70 unknown via CMAUP database
4alpha,14alpha-Dimethyl-5alpha-cholesta-8,24-dien-3beta-ol 15101557 Click to see CC1C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC4C(C)CCC=C(C)C)C)C 412.70 unknown via CMAUP database
Cholesterol 5997 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown via CMAUP database
Lophenol 160482 Click to see CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCCC(C)C)C)C)O 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
31-Norcycloartenol 14524546 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC=C(C)C)C 412.70 unknown via CMAUP database
Cycloartenol 92110 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
24-Methylenecholesterol 92113 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 398.70 unknown via CMAUP database
Campesterol 173183 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 / Oxosteroids / 20-oxosteroids
1-(1-Hydroxy-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl)ethanone 162943984 Click to see CC(=O)C1CC(C2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
1-(5a,5b,8,8,11a,13b-Hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl)ethanone 15558362 Click to see CC(=O)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
1-[(1R,3S,3aS,5aR,5bR,7aS,11aS,11bR,13aS,13bS)-1-hydroxy-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl]ethanone 163185393 Click to see CC(=O)C1CC(C2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
1-[(3aS,5bR,11aS)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl]ethanone 5318494 Click to see CC(=O)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 412.70 unknown via CMAUP database
Adiantone 15558363 Click to see CC(=O)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
Isoadiantone 3041569 Click to see CC(=O)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
24-Ethylcholesta-5,24-dien-3beta-ol 5283643 Click to see CCC(=C(C)C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 412.70 unknown via CMAUP database
alpha1-Sitosterol 9548595 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4C)O)C)C)C(C)C 426.70 unknown via CMAUP database
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
Fucosterol 5281326 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 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 via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
14-Hydroxy-5,10,13,18,18-pentamethyl-9-propan-2-yl-23-oxahexacyclo[13.6.2.01,17.02,14.05,13.06,10]tricosan-22-one 78200701 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4C3(C5CC6C4(CCCC6(C)C)C(=O)O5)O)C)C)C 456.70 unknown https://doi.org/10.1016/S0031-9422(01)00198-4
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
(5R,6R,8R)-5,6,7,8-tetrahydroxy-2-(2-phenylethyl)-5,6,7,8-tetrahydrochromen-4-one 5320522 Click to see C1=CC=C(C=C1)CCC2=CC(=O)C3=C(O2)C(C(C(C3O)O)O)O 318.32 unknown via CMAUP database

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