Adiantum capillus-veneris - Unknown
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Internal ID UUID64407746009b2179706109
Scientific name Adiantum capillus-veneris
Authority L.
First published in Sp. Pl. 2: 1096. 1753 [1 May 1753] ; & HB. 123. Chr. 138. NPfl. 284

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Synonyms Top

Scientific name Authority First published in
Adiantum visianii Schloss. & Vuk. Fl. Croat. 1319. 1869 (1869)
Adiantum capillaceum Dulac Fl. Hautes-Pyrénées : 36 (1867)
Adiantum cuneifolium Stokes Bot. Mat. Med. 4. 612. 1812 (1812)
Adiantum fumarioides Willd. Sp. Pl., ed. 4 , 5: 452 (1810)
Adiantum maderense Lowe
Adiantum moritzianum Link Fil. Spec. 71. 1841 (1841)
Adiantum repandum Tausch Fil. exs. n. 176.
Adiantum capillus-veneris var. protrusum Fernald Rhodora 52: 203 (1950)
Adiantum modestum Underw. Bull. Torrey Bot. Club 28: 46 (1901)
Adiantum capillus Sw. J. Bot. (Schrader) 1800(2): 83 (1801)
Adiantum capillus-veneris var. modestum (Underw.) Fernald Rhodora 52: 206 (1950)
Adiantum rimicola Sloss. Bull. Torrey Bot. Club 41: 308, tab. 7, fig. 1 (1914)
Adiantum capillus-veneris f. rimicola (Sloss.) Fernald Rhodora 52: 208 (1950)
Adiantum africanum R.Br. Narr. Exped. Zaire : 463 (1818)
Adiantum michelii Christ Bull. Acad. Int. Géogr. Bot. , sér. 3, 20(243): 12 (1910)
Adiantum emarginatum Bory ex Willd. Sp. Pl., ed. 4 , 5: 449 (1810)
Adiantum remyanum Espinosa Bol. Mus. Nac. Hist. Nat., Santiago de Chile 15: 96, pl. 3, pl. 5, g, h. 1936
Adiantum capillus-veneris var. rimicola (Sloss.) Fernald
Adiantum subemarginatum Christ Bull. Herb. Boissier II. 3. 511. 1903 (1903)
Adiantum schaffneri E.Fourn. Bull. Soc. Bot. France 27: 328 (1880)
Adiantum affine Willd. Sp. Pl., ed. 4 , 5: 448 (1810)
Adiantum lingii Ching Acta Phytotax. Sin. 6: 341. 1957. (1957)
Adiantum capillus-veneris var. fissum Christ Monsunia 1: 66 (1900)
Adiantum capillus-veneris f. fissum (Christ) Ching Acta Phytotax. Sin. 6: 343 (1957)
Adiantum capillus-veneris var. trifidum (Willd. ex Bolle) Milde Fil. Eur. : 30 (1867)
Adiantum capillus-veneris var. laciniatum Christ ex Tardieu & C.Chr. Fl. Indo-Chine 7(2): 185–186 1940
Adiantum marginatum Schrad. Gött. Gel. Anz. 1818. 918 (1818)
Adiantum paradiseae Baker Gard. Chron. III. 6. 558. 1889 (1889)
Adiantum pseudocapillus Fée Mém. Foug., 5. Gen. Filic. : 118 (1852)
Adiantum fontanum Salisb. Prodr. Stirp. Chap. Allerton 404. 1796 (1796)
Adiantum trifidum Willd. ex Bolle Bonplandia 3: 121 (1855)
Adiantum coriandrifolium Lam. Fl. Franç. 1: 29 (1779)
Adiantum capillus-veneris f. cristatum Moxley Amer. Fern J. 9: 27. 1919

Common names Top

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Language Common/alternative name
English venus' hair
English venus' hair fern
English black maidenhair
English australian maidenhair fern
English venus's hair fern
English common maidenhair fern
English giant maidenhair fern
English plumed maidenhair fern
English culantrillo
English venushair
English venus' hair-fern
English southern maidenhair
English maidenhair fern
English common maidenhair
English venus'-hair fern
Spanish culantrillo
Afrikaans nooienshaarvaring
Arabic كزبرة البئر
Arabic كزبرة البير
Arabic شعر الخنزير
Arabic شعر الارض
Azerbaijani zöhrətüklü adiant
Belarusian Адыянтум венерын волас
Bulgarian венерин косъм
Catalan falzia
Catalan folguerola
Catalan capil·lera
Czech netík venušin vlas
Czech netík ženský vlas
Welsh briger gwener
German frauenhaarfarn
Greek Αδίαντο
Estonian juusadiantum
Basque garaizka arrunt
Persian پرسیاوشان
Finnish neidonhiussaniainen
Finnish neidonadiantumi
French capillaire de montpellier
French cheveu-de-venus
French capillaire cheveu-de-vénus
Irish dúchosach
Galician capilaria
Hawaiian iwaiwa hawai
Hawaiian iwaiwa
Hawaiian ʻiwaʻiwa kahakaha
Hawaiian ʻiwaʻiwa hāwai
Hawaiian ʻiwaʻiwa
Hawaiian iwaiwa kahakaha
Hebrew שערות שולמית מצויות
Armenian Ադիանտում Վեներայի վարս
Italian capelvenere
Japanese ホウライシダ
Kazakh Шолпаншаш сүмбілі
Korean 봉작고사리
Norwegian Bokmål venushår
Dutch echt venushaar
nv tséłnííʼjí
Polish niekropień właściwy
pms capiler
Punjab ٹھنڈی بوٹی
Portuguese avenca
Portuguese aivenca
Portuguese avenca-das-fontes
Portuguese avenca-de-montpellier
Portuguese cabelo-de-vénus
Portuguese capilária
Portuguese capilária-de-montpellier
Portuguese lágrima-de-sangue
pwn ravutuvutu
Russian Адиантум венерин волос
sd پرسياوشان
Slovak adiant venušin
Albanian majdanozi i egër
Serbian Венерина влас
Swedish venushår
Tonga ʻuluʻitāupoʻou
Turkish venüssaçı
Ukrainian адіант венерин волос
Uzbek boldirqora
Chinese 南方铁线蕨
Chinese 猪鬃草
Chinese 南方鐵線蕨
Chinese 鐵線蕨
Chinese 猪毛针
Chinese 铁线蕨

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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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-0001109469
UNII 6QYR43H87O
Florida Plant Atlas 2591
Flora of Alabama 165
Canadensys 8381
USDA Plants ADCA
Tropicos 26602671
INPN 447951
Flora of Italy 58
KEW urn:lsid:ipni.org:names:325030-2
The Plant List tro-26602671
Missouri Botanical Garden 285802
Open Tree Of Life 164357
NCBI Taxonomy 13818
NBN Atlas NBNSYS0000002034
Nature Serve 2.158611
IUCN Red List 164082
IPNI 17009280-1
iNaturalist 63916
GBIF 2651816
Freebase /m/02kw75
EPPO ADICV
EOL 597687
Calflora (Californian flora) 101
USDA GRIN 401925
Wikipedia Adiantum_capillus-veneris
CMAUP NPO9241
PFAF Adiantum capillus-veneris

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_014529385.2 ASM1452938v2 Chromosome Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences 2022-07-05 115.0x 4.49 Gb

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
A systematic methodology to assess the identity of plants in historical texts: A case study based on the Byzantine pharmacy text John the Physician's Therapeutics Lardos A, Patmore K, Allkin R, Lazarou R, Nesbitt M, Scott AC, Zipser B J Ethnopharmacol 25-Mar-2024
PMCID:PMC7615571
doi:10.1016/j.jep.2023.117622
PMID:38128894
Vegetation–edaphic correlation and importance value index in himalayan ‘ecotone’ temperate conifer forest using the multivariate technique Ali F, Zeb M, Amin M, Rajpar MN, Hidayat S, Khan WR Saudi J Biol Sci 24-Mar-2024
PMCID:PMC11000104
doi:10.1016/j.sjbs.2024.103983
PMID:38590389
In Silico Analysis of Glutamate Receptors in Capsicum chinense: Structure, Evolution, and Molecular Interactions León-García F, García-Laynes F, Estrada-Tapia G, Monforte-González M, Martínez-Estevez M, Echevarría-Machado I Plants (Basel) 12-Mar-2024
PMCID:PMC10975470
doi:10.3390/plants13060812
PMID:38592787
The Molecular Mechanism of the Response of Rice to Arsenic Stress and Effective Strategies to Reduce the Accumulation of Arsenic in Grain Geng A, Lian W, Wang Y, Liu M, Zhang Y, Wang X, Chen G Int J Mol Sci 01-Mar-2024
PMCID:PMC10932103
doi:10.3390/ijms25052861
PMID:38474107
Exploring the benefits of wild plants in dietary nutrition: investigating perspectives, choices, health impacts and sustainable practices Anwar T, Qureshi H, Shahzadi S, Siddiqi EH, Ali HM, Abdelhamid MM, Nazim M BMC Complement Med Ther 14-Feb-2024
PMCID:PMC10865668
doi:10.1186/s12906-024-04379-4
PMID:38355544
The Oldest Bryophyte Herbarium Specimens from Central Europe, Collected by M. E. Boretius in 1717: Taxonomy, Nomenclature, Datation and Ethnopharmacology Drobnik J, Stebel A, Graniszewska M Plants (Basel) 24-Jan-2024
PMCID:PMC10857619
doi:10.3390/plants13030349
PMID:38337882
An update about beneficial effects of medicinal plants in aquaculture: A review Dadras F, Velisek J, Zuskova E Vet Med (Praha) 26-Dec-2023
PMCID:PMC10828785
doi:10.17221/96/2023-VETMED
PMID:38303995
Assembly and comparative analysis of the complete mitochondrial genome of Trigonella foenum-graecum L. He Y, Liu W, Wang J BMC Genomics 08-Dec-2023
PMCID:PMC10704837
doi:10.1186/s12864-023-09865-6
PMID:38066419
Genome-wide identification and evolutionary view of ALOG gene family in Solanaceae Turchetto C, Silvério AD, Waschburger EL, Lacerda ME, Quintana IV, Turchetto-Zolet AC Genet Mol Biol 01-Dec-2023
PMCID:PMC10695626
doi:10.1590/1415-4757-GMB-2023-0142
PMID:38048778
Antimicrobial Potential of Different Isolates of Chaetomium globosum Combined with Liquid Chromatography Tandem Mass Spectrometry Chemical Profiling Goda MS, El-Kattan N, Abdel-Azeem MA, Allam KA, Badr JM, Nassar NA, Almalki AJ, Alharbi M, Elhady SS, Eltamany EE Biomolecules 21-Nov-2023
PMCID:PMC10742071
doi:10.3390/biom13121683
PMID:38136556
Recent updates on nano-phyto-formulations based therapeutic intervention for cancer treatment WAHI A, BISHNOI M, RAINA N, SINGH MA, VERMA P, GUPTA PK, KAUR G, TULI HS, GUPTA M Oncol Res 15-Nov-2023
PMCID:PMC10767243
doi:10.32604/or.2023.042228
PMID:38188681
Ethno-Dentistry of Medicinal Plants Used in North Waziristan, Pakistan Rehman S, Iqbal Z, Qureshi R, AlOmar TS, Almasoud N, Younas M, Rauf A, Irfan M Int Dent J 11-Nov-2023
PMCID:PMC10988256
doi:10.1016/j.identj.2023.10.001
PMID:37953188
Bioinformatics Analysis of MSH1 Genes of Green Plants: Multiple Parallel Length Expansions, Intron Gains and Losses, Partial Gene Duplications, and Alternative Splicing Bai MZ, Guo YY Int J Mol Sci 03-Sep-2023
PMCID:PMC10487979
doi:10.3390/ijms241713620
PMID:37686425
Targeting SARS-CoV-2 Non-Structural Proteins Tam D, Lorenzo-Leal AC, Hernández LR, Bach H Int J Mol Sci 20-Aug-2023
PMCID:PMC10455537
doi:10.3390/ijms241613002
PMID:37629182
Bioactive Steroids Bearing Oxirane Ring Dembitsky VM Biomedicines 09-Aug-2023
PMCID:PMC10452232
doi:10.3390/biomedicines11082237
PMID:37626733

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Octanoic acid 379 Click to see CCCCCCCC(=O)O 144.21 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
4alpha-Hydroxyfilicane-3-one 10928366 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CCC5(C4CCC(=O)C5(C)O)C)C)C)C)C 442.70 unknown https://doi.org/10.1248/CPB.50.1273
8-Hydroxy-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]chrysen-9-one 85319101 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CCC5(C4CCC(=O)C5(C)O)C)C)C)C)C 442.70 unknown https://doi.org/10.1248/CPB.50.1273
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/10.1248/CPB.50.1273
https://doi.org/10.1248/CPB.47.543
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
Diploptene 92155 Click to see CC(=C)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1248/CPB.50.1273
https://doi.org/10.1002/CHIN.200307128
https://doi.org/10.1248/CPB.47.543
Diplopterol 164874 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC5C(C)(C)O)C)C)C)C)C 428.70 unknown https://doi.org/10.1248/CPB.50.1273
https://doi.org/10.1002/CHIN.200307128
https://doi.org/10.1248/CPB.47.543
Hopene b 605866 Click to see CC(=C)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1248/CPB.50.1273
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Camphene 440966 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
Camphor (synthetic) 159055 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Curcumene 442360 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown via CMAUP database
(1S,3R,6R,8S,9S)-3,9-dimethyl-6-prop-1-en-2-yl-2-oxatricyclo[6.3.0.01,3]undecane 11117572 Click to see CC1CCC23C1CC(CCC2(O3)C)C(=C)C 220.35 unknown via CMAUP database
(6S)-6-methyl-5-(3-oxobutyl)-2-propan-2-ylidenecyclohept-4-en-1-one 21769417 Click to see CC1CC(=O)C(=C(C)C)CC=C1CCC(=O)C 234.33 unknown via CMAUP database
(S)-Turmerone 14367555 Click to see CC1=CCC(=CC1)C(C)CC(=O)C=C(C)C 218.33 unknown via CMAUP database
9-Oxoneoprocurcumenol 101720148 Click to see CC1=C2CCC(C2CC(=C(C)C)C(=O)C1=O)(C)O 248.32 unknown via CMAUP database
Bicyclo(4.1.0)heptan-3-one, 1-methyl-4-(1-methylethylidene)-7-(3-oxobutyl)-, (1S,6R,7R)- 153845 Click to see CC(=C1CC2C(C2(CC1=O)C)CCC(=O)C)C 234.33 unknown via CMAUP database
Neoprocurcumenol 14543200 Click to see CC1=C2CCC(C2CC(=C(C)C)C(=O)C1)(C)O 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1S,4E,10S)-8-[(E)-1-(Acetoxymethyl)ethylidene]-1,5-dimethyl-11-oxabicyclo[8.1.0]undec-4-en-7-one 101528955 Click to see CC1=CCCC2(C(O2)CC(=C(C)COC(=O)C)C(=O)C1)C 292.40 unknown via CMAUP database
(6E,10S)-6,10-dimethyl-3-propan-2-ylidenecyclodec-6-ene-1,4-dione 10421549 Click to see CC1CCC=C(CC(=O)C(=C(C)C)CC1=O)C 234.33 unknown via CMAUP database
(6E)-3-[(E)-1-(Acetoxymethyl)ethylidene]-6,10alpha-dimethyl-6-cyclodecene-1,4-dione 21769412 Click to see CC1CCC=C(CC(=O)C(=C(C)COC(=O)C)CC1=O)C 292.40 unknown via CMAUP database
(6E)-3-[(E)-1-(Hydroxymethyl)ethylidene]-6,10alpha-dimethyl-6-cyclodecene-1,4-dione 21769413 Click to see CC1CCC=C(CC(=O)C(=C(C)CO)CC1=O)C 250.33 unknown via CMAUP database
Germacr-1(10)-ene-5,8-dione 6441391 Click to see CC1CCC=C(CC(=O)C(CC1=O)C(C)C)C 236.35 unknown via CMAUP database
Germacrone 6436348 Click to see CC1=CCC(=C(C)C)C(=O)CC(=CCC1)C 218.33 unknown via CMAUP database
Germacrone 4,5-epoxide 11637239 Click to see CC1=CCCC2(C(O2)CC(=C(C)C)C(=O)C1)C 234.33 unknown via CMAUP database
Neocurdione 10466651 Click to see CC1CCC=C(CC(=O)C(CC1=O)C(C)C)C 236.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(1S,3abeta,8abeta)-Octahydro-1beta,4beta-dihydroxy-7-isopropylidene-1,4-dimethylazulen-6(5H)-one 14632999 Click to see CC(=C1CC2C(CCC2(C)O)C(CC1=O)(C)O)C 252.35 unknown via CMAUP database
(3S,3aS,8aR)-3-hydroxy-3-methyl-8-methylidene-5-propan-2-ylidene-2,3a,4,8a-tetrahydro-1H-azulen-6-one 14543198 Click to see CC(=C1CC2C(CCC2(C)O)C(=C)CC1=O)C 234.33 unknown via CMAUP database
4,10-Epizedoarondiol 24834047 Click to see CC(=C1CC2C(CCC2(C)O)C(CC1=O)(C)O)C 252.35 unknown via CMAUP database
Aerugidiol 11776892 Click to see CC1=CC(=O)C(=C(C)C)CC2C1(CCC2(C)O)O 250.33 unknown via CMAUP database
Epiprocurcumenol 10263440 Click to see CC1=CC(=O)C(=C(C)C)CC2C1CCC2(C)O 234.33 unknown via CMAUP database
Isozedoarondiol 14632998 Click to see CC(=C1CC2C(CCC2(C)O)C(CC1=O)(C)O)C 252.35 unknown via CMAUP database
Methylzedoarondiol 21626407 Click to see CC(=C1CC2C(CCC2(C)O)C(CC1=O)(C)OC)C 266.38 unknown via CMAUP database
Phaeocaulisin E 14633000 Click to see CC(=C1CC2C(CCC2(C)O)C(CC1=O)(C)O)C 252.35 unknown via CMAUP database
Procurcumenol 189061 Click to see CC1=CC(=O)C(=C(C)C)CC2C1CCC2(C)O 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(3R,3aR,5bR,6R,7aS,11aS,11bR,13aS,13bR)-3a,5b,8,8,11a,13a-hexamethyl-3-propan-2-yl-1,2,3,4,6,7,7a,9,10,11,11b,12,13,13b-tetradecahydrocyclopenta[a]chrysen-6-ol 10670137 Click to see CC(C)C1CCC2C1(CC=C3C2(CCC4C3(C(CC5C4(CCCC5(C)C)C)O)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.47.543
3a,5b,8,8,11a,13a-Hexamethyl-3-propan-2-yl-1,2,3,4,6,7,7a,9,10,11,11b,12,13,13b-tetradecahydrocyclopenta[a]chrysen-6-ol 14544104 Click to see CC(C)C1CCC2C1(CC=C3C2(CCC4C3(C(CC5C4(CCCC5(C)C)C)O)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.47.543
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,4aR,6aS,6bR,10S,12aR,14bS)-10-hydroxy-2-(hydroxymethyl)-2,6a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 23641088 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)CO)C(=O)O)C)C)C 472.70 unknown via CMAUP database
(3R,3aR,5aR,5bR,7aR,9R,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-9-ol 11796715 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.47.543
(3R,3aR,5aR,5bR,7aS,11aS,13aS,13bR)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-2,3,4,5,5b,6,7,7a,9,10,11,13b-dodecahydro-1H-cyclopenta[a]chrysen-13-one 101528974 Click to see CC(C)C1CCC2C1(CCC3(C2(C(=O)C=C4C3CCC5C4(CCCC5(C)C)C)C)C)C 424.70 unknown https://doi.org/10.1248/CPB.50.1273
https://doi.org/10.1248/CPB.47.543
(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/10.1248/CPB.50.1273
https://doi.org/10.1248/CPB.47.543
(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/10.1248/CPB.50.1273
https://doi.org/10.1248/CPB.47.543
(5a,8,8,11a,13a-Pentamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,7a,9,10,11,13,13b-tetradecahydrocyclopenta[a]chrysen-3a-yl)methanol 85199981 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCCC5(C)C)C)C)C)CO 426.70 unknown https://doi.org/10.1248/CPB.50.1273
https://doi.org/10.1248/CPB.47.543
(6aR,6aR,6bR,8aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-tetradecahydro-1H-picen-3-one 162861354 Click to see CC1(CCC2(CCC3(C(C2C1)CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.50.1273
[(3R,3aS,5aR,5bR,7aS,11aS,13aS,13bS)-5a,8,8,11a,13a-pentamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,7a,9,10,11,13,13b-tetradecahydrocyclopenta[a]chrysen-3a-yl]methanol 10598553 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCCC5(C)C)C)C)C)CO 426.70 unknown https://doi.org/10.1248/CPB.50.1273
https://doi.org/10.1248/CPB.47.543
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-13-ol 85387697 Click to see CC(C)C1CCC2C1(CCC3(C2(C(C=C4C3CCC5C4(CCCC5(C)C)C)O)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.50.1273
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/10.1248/CPB.50.1273
https://doi.org/10.1248/CPB.47.543
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]chrysen-9-ol 74819513 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4C3=CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.47.543
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/10.1248/CPB.50.1273
https://doi.org/10.1248/CPB.47.543
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/10.1248/CPB.50.1273
https://doi.org/10.1248/CPB.47.543
3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-2,3,4,5,5b,6,7,7a,9,10,11,13b-dodecahydro-1H-cyclopenta[a]chrysen-13-one 13857713 Click to see CC(C)C1CCC2C1(CCC3(C2(C(=O)C=C4C3CCC5C4(CCCC5(C)C)C)C)C)C 424.70 unknown https://doi.org/10.1248/CPB.50.1273
https://doi.org/10.1248/CPB.47.543
4,4,6a,6b,8a,11,11,14b-Octamethyl-1,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-octadecahydro-2H-picen-3-one 612782 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown https://doi.org/10.1248/CPB.50.1273
4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,6a,7,8,9,10,13,14,14a-dodecahydro-1H-picen-3-one 15559505 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C)C 424.70 unknown https://doi.org/10.1248/CPB.50.1273
beta-Amyrone 12306160 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown https://doi.org/10.1248/CPB.50.1273
Fern-7en-3a-ol 10646117 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4C3=CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.47.543
Ferna-9(11)-ene-12beta-ol 11069955 Click to see CC(C)C1CCC2C1(CCC3(C2(C(C=C4C3CCC5C4(CCCC5(C)C)C)O)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.50.1273
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/10.1248/CPB.50.1273
https://doi.org/10.1248/CPB.47.543
Germanicone 21594102 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C)C 424.70 unknown https://doi.org/10.1248/CPB.50.1273
Neohop-12-ene 13857697 Click to see CC(C)C1CCC2C1(CCC3(C2=CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1248/CPB.50.1273
https://doi.org/10.1248/CPB.47.543
Olean-12-en-3-one 6454747 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown https://doi.org/10.1248/CPB.50.1273
https://doi.org/10.1002/CHIN.200307128
Sorghumol 621134 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.47.543
> Lipids and lipid-like molecules / Steroids and steroid derivatives
(3R,3aR,5aR,5bR,9R,11bR,13aS,13bR)-3a,5a,8,8,11b,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,9,10,11,12,13,13b-tetradecahydrocyclopenta[a]chrysen-9-ol 10812378 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CCC5=C4CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.47.543
(3R,3aR,5aR,5bS,9R,11aS,11bR,13aS,13bR)-3a,5a,8,8,11b,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,9,10,11,11a,12,13,13b-tetradecahydrocyclopenta[a]chrysen-9-ol 10598552 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CC=C5C4CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.47.543
2,5,10,13,19,20-Hexamethyl-6-propan-2-yl-18-oxahexacyclo[11.9.0.02,10.05,9.014,20.017,19]docosane 78384886 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CCC5(C4CCC6C5(O6)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.47.543
3a,5a,8,8,11b,13a-Hexamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,9,10,11,12,13,13b-tetradecahydrocyclopenta[a]chrysen-9-ol 85276167 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CCC5=C4CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.47.543
3a,5a,8,8,11b,13a-Hexamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,9,10,11,11a,12,13,13b-tetradecahydrocyclopenta[a]chrysene 15558359 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CC=C5C4CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1248/CPB.47.543
Adian-5-ene 15558361 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CC=C5C4CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1248/CPB.47.543
Adiantoxide 101297696 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CCC5(C4CCC6C5(O6)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.50.1273
https://doi.org/10.1248/CPB.47.543
beta-Simiarenol 623604 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CC=C5C4CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.47.543
D:B-Friedo-B/':A/'-neogammacer-5-ene 21582920 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CC=C5C4CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1248/CPB.47.543
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
1-[(3R,3aS,5aR,5bR,7aS,11aS,11bR,13aS,13bR)-3a,5a,5b,8,8,11a,13b-heptamethyl-2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a-tetradecahydro-1H-cyclopenta[a]chrysen-3-yl]ethanol 162817119 Click to see CC(C1CCC2(C1(CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1248/CPB.50.1273
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
5a,5b,8,8,11a,13b-hexamethyl-2,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-tetradecahydro-1H-cyclopenta[a]chrysen-3-one 14605584 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC5=O)C)C)C)C)C 384.60 unknown https://doi.org/10.1248/CPB.50.1273
https://doi.org/10.1248/CPB.47.543
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
1-[(3R,3aR,5aR,5bR,7aS,11aS,11bR,13aR,13bR)-3-hydroxy-5a,5b,8,8,11a,13b-hexamethyl-2,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-tetradecahydro-1H-cyclopenta[a]chrysen-3-yl]ethanone 21159071 Click to see CC(=O)C1(CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1248/CPB.50.1273
https://doi.org/10.1248/CPB.47.543
1-[(3R,3aR,5bR,11aS,13aR)-3-hydroxy-5a,5b,8,8,11a,13b-hexamethyl-2,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-tetradecahydro-1H-cyclopenta[a]chrysen-3-yl]ethanone 5318299 Click to see CC(=O)C1(CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C)O 428.70 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/S0040-4020(01)82826-X
https://doi.org/10.1248/CPB.50.1273
https://doi.org/10.1248/CPB.47.543
Isoadiantone 3041569 Click to see CC(=O)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 412.70 unknown https://doi.org/10.1248/CPB.50.1273
https://doi.org/10.1248/CPB.47.543
> 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
> Organoheterocyclic compounds / Diazines / Pyrazines
2,3,5,6-Tetramethylpyrazine 14296 Click to see CC1=C(N=C(C(=N1)C)C)C 136.19 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
(6S,14R,18S)-6,10,10,14,15,20-hexamethyl-21-oxahexacyclo[17.3.2.01,18.02,15.05,14.06,11]tetracosan-20-ol 5316485 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C46CCC5C(OC6)(C)O)C)C)C)C 428.70 unknown https://doi.org/10.1002/CHIN.200430172
Adipedatol 12127456 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C46CCC5C(OC6)(C)O)C)C)C)C 428.70 unknown https://doi.org/10.1002/CHIN.200430172
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
trans-4-Methoxycinnamic acid 699414 Click to see COC1=CC=C(C=C1)C=CC(=O)O 178.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Depsides and depsidones
Psoromic acid 23725 Click to see CC1=CC(=C(C2=C1C(=O)OC3=C(O2)C(=CC(=C3C)OC)C(=O)O)C=O)O 358.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1E,6E)-1-(3-hydroxyphenyl)-7-(4-hydroxyphenyl)hepta-1,6-diene-3,5-dione 24808577 Click to see C1=CC(=CC(=C1)O)C=CC(=O)CC(=O)C=CC2=CC=C(C=C2)O 308.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
(1,7-Bis(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione) 2889 Click to see COC1=C(C=CC(=C1)C=CC(=O)CC(=O)C=CC2=CC(=C(C=C2)O)OC)O 368.40 unknown via CMAUP database
(1E,4Z,6E)-5-hydroxy-1,7-bis(4-hydroxy-3-methoxyphenyl)hepta-1,4,6-trien-3-one 5281767 Click to see COC1=C(C=CC(=C1)C=CC(=CC(=O)C=CC2=CC(=C(C=C2)O)OC)O)O 368.40 unknown via CMAUP database
Bisdemethoxycurcumin 5315472 Click to see C1=CC(=CC=C1C=CC(=O)CC(=O)C=CC2=CC=C(C=C2)O)O 308.30 unknown via CMAUP database
Curcumin 969516 Click to see COC1=C(C=CC(=C1)C=CC(=O)CC(=O)C=CC2=CC(=C(C=C2)O)OC)O 368.40 unknown via CMAUP database
Demethoxycurcumin 5469424 Click to see COC1=C(C=CC(=C1)C=CC(=O)CC(=O)C=CC2=CC=C(C=C2)O)O 338.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Kaempferol 3-O-sulfate 44259052 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OS(=O)(=O)O)O 366.30 unknown https://doi.org/10.1016/0031-9422(82)83080-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
Miquelianin (Quercetin 3-O-glucuronide) 13258914 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
CID 44258797 44258797 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database

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