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Saururus cernuus

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644003a1251af858076760
Scientific name Saururus cernuus
Authority L.
First published in Sp. Pl. 1: 341. 1753 [1 May 1753]

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Ornamental horticulture: cultivated as a water garden and pond plant for its decorative foliage and flower spikes; sold by aquatic plant nurseries.
- Riparian and wetland restoration plantings: used in ecological restoration projects to stabilize soils, provide habitat, and enhance biodiversity; supplied by specialist nurseries.

Properties relevant to use:
- Emergent aquatic growth habit; tolerates saturated soils and periodic flooding; spreads via rhizomes; produces heart-shaped leaves and erect spikes of small white flowers; suitable for both submerged and emergent cultivation; rapid vegetative spread facilitates establishment in restoration settings.

Standards and regulation:
- Subject to general horticultural trade regulations, such as labeling and phytosanitary requirements for aquatic plants in the United States (e.g., under the Federal Plant Protection Act); may also be subject to state-level noxious weed regulations if wild populations are considered invasive.

Sustainability and sourcing:
- Commercially propagated through division and seed; production is largely cultivated rather than wild harvest; sourcing from specialist nurseries minimizes impact on natural populations; responsible propagation practices support sustainable supply for ornamental and restoration markets.

Synonyms Top

Scientific name Authority First published in
Neobiondia silvestrii Pamp. Nuovo Giorn. Bot. Ital. , n.s., 17: 263 (1910)
Mattuschkia aquatica J.F.Gmel. Syst. Nat., ed. 13[bis]. 2(1): 589. 1791 [late Sep-Nov 1791]
Saururus cernuus f. submersus Glück Biol. Morphol. Untersuch. Wasser- Sumpfgewächse 3: 69 (1911)

Common names Top

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Language Common/alternative name
English lizard's tail
English lizard's-tail
English dragon's tail
English swamp root
English water-dragon
Arabic صروة منحنية
Czech ještěrkovec nicí
German eidechsenschwanz
German amerikanischer molchschwanz
Persian دممارمولکی
Upper Sorbian wšědny saururus
Swedish Ödlesvans
Chinese 蜥尾草

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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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-0000493601
Florida Plant Atlas 3598
Flora of Alabama 3378
Canadensys 9224
USDA Plants SACE
Tropicos 29000003
INPN 611351
Flora of Italy 241
KEW urn:lsid:ipni.org:names:284624-2
The Plant List kew-2582994
Missouri Botanical Garden 286856
Open Tree Of Life 1009423
NCBI Taxonomy 13260
Nature Serve 2.129260
IUCN Red List 64324394
IPNI 328555-2
iNaturalist 60742
GBIF 5384932
Freebase /m/02p8tzn
EPPO SUACE
EOL 597359
USDA GRIN 33191
Wikipedia Saururus_cernuus
CMAUP NPO12012

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
Marine-Derived Leads as Anticancer Candidates by Disrupting Hypoxic Signaling through Hypoxia-Inducible Factors Inhibition Garcia MR, Andrade PB, Lefranc F, Gomes NG Mar Drugs 23-Mar-2024
PMCID:PMC11051506
doi:10.3390/md22040143
PMID:38667760
Plant Resource Use and Pattern of Usage by the Naturalized Orchid Bee (Euglossa dilemma: Hymenoptera: Apidae) in Florida Pemberton RW Insects 27-Nov-2023
PMCID:PMC10743517
doi:10.3390/insects14120909
PMID:38132583
Exploring the known chemical space of the plant kingdom: insights into taxonomic patterns, knowledge gaps, and bioactive regions Domingo-Fernández D, Gadiya Y, Mubeen S, Healey D, Norman BH, Colluru V J Cheminform 10-Nov-2023
PMCID:PMC10636812
doi:10.1186/s13321-023-00778-w
PMID:37950325
Evaluating the Antischistosomal Activity of Dehydrodieugenol B and Its Methyl Ether Isolated from Nectandra leucantha—A Preclinical Study against Schistosoma mansoni Infection Rocha VC, Cajas RA, Andrade-de-Siqueira AI, Almeida RB, Godoy-Silva J, Gonçalves MM, Lago JH, de Moraes J ACS Omega 18-Oct-2023
PMCID:PMC10620922
doi:10.1021/acsomega.3c06111
PMID:37929107
Manassantin A inhibits tumour growth under hypoxia through the activation of chaperone-mediated autophagy by modulating Hsp90 activity Byun JK, Lee SH, Moon EJ, Park MH, Jang H, Weitzel DH, Kim HH, Basnet N, Kwon DY, Lee CT, Stephenson TN, Jeong JH, Patel BA, Park SJ, Chi JT, Dewhirst MW, Hong J, Lee YM Br J Cancer 09-Feb-2023
PMCID:PMC10070431
doi:10.1038/s41416-023-02148-7
PMID:36759727
Neolignans isolated from Saururus cernuus L. (Saururaceae) exhibit efficacy against Schistosoma mansoni Brito JR, Wilairatana P, Roquini DB, Parra BC, Gonçalves MM, Souza DC, Ferreira EA, Salvadori MC, Teixeira FS, Lago JH, de Moraes J Sci Rep 11-Nov-2022
PMCID:PMC9652300
doi:10.1038/s41598-022-23110-2
PMID:36369516
Discordant Phylogenomic Placement of Hydnoraceae and Lactoridaceae Within Piperales Using Data From All Three Genomes Jost M, Samain MS, Marques I, Graham SW, Wanke S Front Plant Sci 12-Apr-2021
PMCID:PMC8072514
doi:10.3389/fpls.2021.642598
PMID:33912209
Role of glioblastoma stem cells in cancer therapeutic resistance: a perspective on antineoplastic agents from natural sources and chemical derivatives Alves AL, Gomes IN, Carloni AC, Rosa MN, da Silva LS, Evangelista AF, Reis RM, Silva VA Stem Cell Res Ther 24-Mar-2021
PMCID:PMC7992331
doi:10.1186/s13287-021-02231-x
PMID:33762015
Phytodepuration of Nitrate Contaminated Water Using Four Different Tree Species Regni L, Bartucca ML, Pannacci E, Tei F, Del Buono D, Proietti P Plants (Basel) 10-Mar-2021
PMCID:PMC8001374
doi:10.3390/plants10030515
PMID:33801882
Hypoxia- and dexamethasone-dependent HIF1α-glucocorticoid receptor interaction leads to degradation of glucocorticoid receptor in pituitary adenomas Zhang C, Dong X, Mao W, Wang C, Ma B, Hu L, Chen R Am J Transl Res 15-Feb-2021
PMCID:PMC7868828
PMID:33594318
Use of Natural Products in Leishmaniasis Chemotherapy: An Overview Gervazoni LF, Barcellos GB, Ferreira-Paes T, Almeida-Amaral EE Front Chem 23-Nov-2020
PMCID:PMC7732490
doi:10.3389/fchem.2020.579891
PMID:33330368
Data of soil, vegetation and bird species found on double-crested cormorant colonies in the southeastern United States Moran Veum L, Dorr BS, Hanson-Dorr K, Moore RJ, Rush SA Data Brief 29-Oct-2019
PMCID:PMC6859226
doi:10.1016/j.dib.2019.104726
PMID:31763391
Early Miocene flora of central Kazakhstan (Turgai Plateau) and its paleoenvironmental implications Svetlana P, Torsten U, Anna A, Valentina T, Polina T, Yaowu X Plant Divers 16-Apr-2019
PMCID:PMC6702428
doi:10.1016/j.pld.2019.04.002
PMID:31453418
The Phytochemistry of Cherokee Aromatic Medicinal Plants Setzer WN Medicines (Basel) 12-Nov-2018
PMCID:PMC6313439
doi:10.3390/medicines5040121
PMID:30424560
The Emergence of Earliest Angiosperms may be Earlier than Fossil Evidence Indicates Salomo K, Smith JF, Feild TS, Samain MS, Bond L, Davidson C, Zimmers J, Neinhuis C, Wanke S Syst Bot 18-Dec-2017
PMCID:PMC5792071
doi:10.1600/036364417X696438
PMID:29398773

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
> Alkaloids and derivatives / Aristolactams
Cepharanone B 162739 Click to see 279.29 unknown https://doi.org/10.1021/NP50068A006
Sauristolactam 131002 Click to see 279.29 unknown https://doi.org/10.1021/NP50068A006
> Alkaloids and derivatives / Morphinans
Morphine 5288826 Click to see CN1CCC23C4C1CC5=C2C(=C(C=C5)O)OC3C(C=C4)O 285.34 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Catechols
Epinephrine 5816 Click to see CNCC(C1=CC(=C(C=C1)O)O)O 183.20 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans
Guaiacin 11724027 Click to see 328.40 unknown https://doi.org/10.1021/NP50022A005
https://doi.org/10.1080/10826079708000478
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
(-)-Dihydroguaiaretic acid 11602375 Click to see 330.40 unknown https://doi.org/10.1016/S0031-9422(00)00076-5
(2S,3R)-1,4-bis(1,3-benzodioxol-5-yl)-2,3-dimethylbutan-1-one 14583728 Click to see 340.40 unknown https://doi.org/10.1021/NP50067A036
5-[4-(3,4-Dihydroxy-5-methoxyphenyl)-2,3-dimethylbutyl]-3-methoxybenzene-1,2-diol 73207442 Click to see 362.40 unknown https://doi.org/10.1016/S0031-9422(00)00076-5
5-[4-(4-Hydroxy-3,5-dimethoxyphenyl)-2,3-dimethylbutyl]-3-methoxybenzene-1,2-diol 73207443 Click to see 376.40 unknown https://doi.org/10.1016/S0031-9422(00)00076-5
Austrobailignan 5 185825 Click to see CC(CC1=CC2=C(C=C1)OCO2)C(C)CC3=CC4=C(C=C3)OCO4 326.40 unknown https://doi.org/10.1080/10826079708000478
https://doi.org/10.1021/NP50067A036
https://doi.org/10.1021/NP50022A005
Dihydroguaiaretic Acid 161924 Click to see 330.40 unknown https://doi.org/10.1016/S0031-9422(00)00076-5
Macelignan 10404245 Click to see CC(CC1=CC2=C(C=C1)OCO2)C(C)CC3=CC(=C(C=C3)O)OC 328.40 unknown https://doi.org/10.1021/NP50067A036
Sauriol A 15965507 Click to see 362.40 unknown https://doi.org/10.1016/S0031-9422(00)00076-5
Sauriol B 15965508 Click to see 376.40 unknown https://doi.org/10.1016/S0031-9422(00)00076-5
Saururenin 145709712 Click to see 340.50 unknown https://doi.org/10.1021/NP50067A036
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(+)-Galbacin 442873 Click to see 340.40 unknown https://doi.org/10.1021/NP50067A036
(1R,2R)-1-(1,3-benzodioxol-5-yl)-2-[4-[(2R,3R,4R,5R)-5-[4-[(1R,2R)-1-(3,4-dimethoxyphenyl)-1-hydroxypropan-2-yl]oxy-3-methoxyphenyl]-3,4-dimethyloxolan-2-yl]-2-methoxyphenoxy]propan-1-ol 163008538 Click to see 716.80 unknown https://doi.org/10.1021/NP030514M
(1R,2R)-1-(1,3-benzodioxol-5-yl)-2-[4-[(2R,3S,4R,5S)-5-[4-[(1R,2R)-1-(3,4-dimethoxyphenyl)-1-hydroxypropan-2-yl]oxy-3-methoxyphenyl]-3,4-dimethyloxolan-2-yl]-2-methoxyphenoxy]propan-1-ol 158356097 Click to see 716.80 unknown https://doi.org/10.1021/NP030514M
(1R,2S)-1-(3,4-dimethoxyphenyl)-2-[4-[(2S,3R,4R,5S)-5-(3,4-dimethoxyphenyl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenoxy]propan-1-ol 163011444 Click to see 552.70 unknown https://doi.org/10.1016/S0031-9422(00)00076-5
(2R,3R,4R,5S)-2,5-Bis-(3,4-dimethoxy-phenyl)-3,4-dimethyl-tetrahydro-furan 44340797 Click to see 372.50 unknown via CMAUP database
1-(3,4-dimethoxyphenyl)-2-[4-[(2S,3R,4R,5S)-5-[4-[2-(3,4-dimethoxyphenyl)-2-hydroxy-1-methyl-ethoxy]-3-methoxy-phenyl]-3,4-dimethyl-tetrahydrofuran-2-yl]-2-methoxy-phenoxy]propan-1-ol 44336126 Click to see 732.90 unknown https://doi.org/10.1016/0031-6989(87)90117-2
https://doi.org/10.1080/10826079708000478
https://doi.org/10.1016/S0040-4039(01)99818-1
1-(3,4-Dimethoxyphenyl)-2-[4-[5-(3,4-dimethoxyphenyl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenoxy]propan-1-ol 11410271 Click to see 552.70 unknown https://doi.org/10.1016/S0031-9422(00)00076-5
1-(3,4-Dimethoxyphenyl)-2-[4-[5-[4-[1-(3,4-dimethoxyphenyl)-1-hydroxypropan-2-yl]oxy-3-methoxyphenyl]-3,4-dimethyloxolan-2-yl]-2-methoxyphenoxy]propan-1-ol 10190528 Click to see 732.90 unknown https://doi.org/10.1007/BF02975136
https://doi.org/10.1055/S-2003-818007
1-(3,4-Dimethoxyphenyl)-3-[4-[5-[4-[3-(3,4-dimethoxyphenyl)-3-hydroxypropoxy]-3-methoxyphenyl]-3,4-dimethyloxolan-2-yl]-2-methoxyphenoxy]propan-1-ol 145892 Click to see CC1C(C(OC1C2=CC(=C(C=C2)OCCC(C3=CC(=C(C=C3)OC)OC)O)OC)C4=CC(=C(C=C4)OCCC(C5=CC(=C(C=C5)OC)OC)O)OC)C 732.90 unknown https://doi.org/10.1016/0031-6989(87)90117-2
https://doi.org/10.1080/10826079708000478
https://doi.org/10.1007/BF02975136
https://doi.org/10.1055/S-2003-818007
4-[(1R,2R)-2-[4-[(2S,3S,4R,5R)-5-[4-[(1R,2R)-1-(1,3-benzodioxol-5-yl)-1-hydroxypropan-2-yl]oxy-3-methoxyphenyl]-3,4-dimethyloxolan-2-yl]-2-methoxyphenoxy]-1-hydroxypropyl]-2-methoxyphenol 162947077 Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC(C)C(C3=CC4=C(C=C3)OCO4)O)OC)C5=CC(=C(C=C5)OC(C)C(C6=CC(=C(C=C6)O)OC)O)OC)C 702.80 unknown https://doi.org/10.1021/NP030514M
4-[(2S,3R,4R,5S)-5-[4-[(1R,2S)-1-(3,4-dimethoxyphenyl)-1-hydroxypropan-2-yl]oxy-3-methoxyphenyl]-3,4-dimethyloxolan-2-yl]-2-methoxyphenol 163193653 Click to see 538.60 unknown https://doi.org/10.1016/S0031-9422(00)00076-5
4-[2-[4-[5-[4-[1-(1,3-Benzodioxol-5-yl)-1-hydroxypropan-2-yl]oxy-3-methoxyphenyl]-3,4-dimethyloxolan-2-yl]-2-methoxyphenoxy]-1-hydroxypropyl]-2-methoxyphenol 11297006 Click to see 702.80 unknown https://doi.org/10.1021/NP030514M
4-O-Demethylmanassantin B 10055535 Click to see 702.80 unknown https://doi.org/10.1021/NP030514M
Calopiptin 12302265 Click to see 356.40 unknown https://doi.org/10.1021/NP50067A036
CID 11399874 11399874 Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC(C)C(C3=CC4=C(C=C3)OCO4)O)OC)C5=CC(=C(C=C5)OC(C)C(C6=CC(=C(C=C6)OC)OC)O)OC)C 716.80 unknown https://doi.org/10.1016/J.ANTIVIRAL.2009.11.002
https://doi.org/10.1021/NP030514M
https://doi.org/10.1055/S-2003-818007
https://doi.org/10.1007/S12272-009-2010-7
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3284739/
Furan, 2,5-bis(3,4-dimethoxyphenyl)tetrahydro-3,4-dimethyl-, (2R,3S,4S,5R)-rel-(+)- 158504 Click to see 372.50 unknown https://doi.org/10.1016/S0031-9422(00)00076-5
Galbelgin 609882 Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC)OC)C3=CC(=C(C=C3)OC)OC)C 372.50 unknown https://doi.org/10.1016/S0031-9422(03)00391-1
https://doi.org/10.1016/S0031-9422(00)00076-5
Manassantin B 10439828 Click to see 716.80 unknown https://doi.org/10.1021/NP030514M
https://doi.org/10.1080/10826079708000478
https://doi.org/10.1016/S0040-4039(01)99818-1
Saucerneol 73199957 Click to see 538.60 unknown https://doi.org/10.1016/S0031-9422(00)00076-5
https://doi.org/10.1080/10826079708000478
https://doi.org/10.1016/S0040-4039(01)99818-1
Saucerneol methyl ether 101263260 Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC)OC)C3=C(C=C(C=C3)OC(C)C(C4=CC(=C(C=C4)OC)OC)O)OC)C 552.70 unknown https://doi.org/10.1016/S0031-9422(00)00076-5
https://doi.org/10.1080/10826079708000478
Saucernetin 443018 Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC)OC)C3=CC(=C(C=C3)OC)OC)C 372.50 unknown https://doi.org/10.1016/S0031-9422(00)00076-5
https://doi.org/10.1080/10826079708000478
https://doi.org/10.1016/S0031-9422(03)00391-1
https://doi.org/10.1021/NP50022A005
Veraguensin 443026 Click to see 372.50 unknown https://doi.org/10.1021/NP50022A005
https://doi.org/10.1080/10826079708000478
Zuihonin A 338287 Click to see 340.40 unknown https://doi.org/10.1021/NP50067A036
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
CID 22494956 22494956 Click to see 174.19 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
12,13-Dehydrogeranylgeraniol 10469408 Click to see CC(=CC=CC(=CCCC(=CCCC(=CCO)C)C)C)C 288.50 unknown https://doi.org/10.1021/NP0101346
3,7,11,15-Tetramethylhexadeca-2,6,10,12,14-pentaen-1-ol 85151945 Click to see CC(=CC=CC(=CCCC(=CCCC(=CCO)C)C)C)C 288.50 unknown https://doi.org/10.1021/NP0101346
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Farnesene, (6Z)- 5317319 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,2R,5R,6R,7S,8R,11R)-5,7,11-trihydroxy-7-(methoxymethyl)-2-methylspiro[9-oxatricyclo[6.3.1.01,5]dodecane-6,3'-oxetane]-2',10-dione 9997459 Click to see 342.34 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
Saupirin 181128 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)OC(=O)C(=C)CO 346.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives
(1S,2R,3'S,5S,6S,9S,11R,14R,15S,17R,19R,21R)-2,3',6-trimethylspiro[16,18-dioxahexacyclo[15.3.1.02,15.05,14.06,11.015,19]henicosane-21,2'-oxirane]-9-ol 72701755 Click to see CC1C2(O1)C3CC4C5(C3(CCC6C5CCC7C6(CCC(C7)O)C)C)OC2O4 374.50 unknown via CMAUP database
5-[(1R,2S,4R,5R,6R,7R,10S,11S,14S,16S)-5,11,14,16-tetrahydroxy-7-methyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-6-yl]pyran-2-one 46939053 Click to see CC12CCC3C(C14C(O4)C(C2C5=COC(=O)C=C5)O)CCC6(C3(CCC(C6)O)O)O 418.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Monohydroxy bile acids, alcohols and derivatives
(3ss,5ss)-3-Hydroxycholan-24-oic acid 92849605 Click to see 376.60 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
5beta-Dermophol 5284186 Click to see CC(CCCC(CO)(CO)O)C1CCC2C1(C(CC3C2C(CC4C3(CCC(C4)O)C)O)O)C 468.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
(3S,7S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2S)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,7-diol 15571096 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C 402.70 unknown via CMAUP database
Cholesterol 5997 Click to see 386.70 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 / Oxosteroids
Bufotricosaroide B 46939055 Click to see CC1C(C2CCC3(C2(C(=O)C(C4C3CCC5C4(CCC(C5)O)C)O)C)O1)C=O 390.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
[(1R,2S,4R,5R,6S,7R,10S,11S,14S,16R)-14-hydroxy-7,11-dimethyl-6-[(Z)-1-oxobut-2-en-2-yl]-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-5-yl] acetate 72702443 Click to see CC=C(C=O)C1C(C2C3(C1(CCC4C3CCC5C4(CCC(C5)O)C)C)O2)OC(=O)C 416.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
methyl 4-[(3S,5R,8R,9S,10S,13S)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-4-oxobutanoate 72701756 Click to see CC12CCC(CC1CCC3C2CCC4(C3=CC=C4C(=O)CCC(=O)OC)C)O 386.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
[(1R,2S,4R,5R,6R,7R,10S,11S,14S,16S)-11,14,16-trihydroxy-7-methyl-6-(6-oxopyran-3-yl)-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-5-yl] acetate 49818154 Click to see 460.50 unknown via CMAUP database
[(1S,2R,5R,7S,10S,11S,14R,15R,20S)-16-ethenyl-7-hydroxy-10,14-dimethyl-18-oxapentacyclo[13.3.2.01,14.02,11.05,10]icos-16-en-20-yl] acetate 72702444 Click to see 400.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
14,16-dihydroxybufa-5,20,22-trienolide, (14beta,16beta)-form, 16-Ac 46938953 Click to see 426.50 unknown via CMAUP database
3beta,16beta-Dihydroxybufa-8(14),20,22-trienolide 46938954 Click to see 384.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Bufanolides and derivatives
(1R,6R)-6-[(1R,2S,4R,6S,7R,10S,11S,14S,16R)-14-hydroxy-7,11-dimethyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-6-yl]-2,7-dioxabicyclo[4.1.0]hept-4-en-3-one 10092398 Click to see 400.50 unknown via CMAUP database
(2S)-2-[[7-[[(3S,5R,8R,9S,10S,13R,14S,16S,17R)-16-acetyloxy-14-hydroxy-10,13-dimethyl-17-(6-oxopyran-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl]oxy]-7-oxoheptanoyl]amino]-5-(diaminomethylideneamino)pentanoic acid 46930230 Click to see 742.90 unknown via CMAUP database
(2S)-2-[[8-[[(1R,2S,4R,5R,6R,7R,10S,11S,14S,16R)-5-acetyloxy-7,11-dimethyl-6-(6-oxopyran-3-yl)-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-14-yl]oxy]-8-oxooctanoyl]amino]-5-(diaminomethylideneamino)pentanoic acid 102003563 Click to see CC(=O)OC1C(C2(CCC3C(C24C1O4)CCC5C3(CCC(C5)OC(=O)CCCCCCC(=O)NC(CCCN=C(N)N)C(=O)O)C)C)C6=COC(=O)C=C6 754.90 unknown via CMAUP database
(2S)-2-[[9-[[(1R,2S,4R,5R,6R,7R,10S,11R,14S,16S)-5-acetyloxy-16-hydroxy-7,11-dimethyl-6-(6-oxopyran-3-yl)-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-14-yl]oxy]-9-oxononanoyl]amino]-5-(diaminomethylideneamino)pentanoic acid 46930229 Click to see 784.90 unknown via CMAUP database
(2S)-5-(diaminomethylideneamino)-2-[[4-[[(1R,2S,4R,6R,7R,10S,11S,14S,16R)-7,11-dimethyl-6-(6-oxopyran-3-yl)-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-14-yl]oxy]-4-oxobutanoyl]amino]pentanoic acid 102574724 Click to see CC12CCC(CC1CCC3C2CCC4(C35C(O5)CC4C6=COC(=O)C=C6)C)OC(=O)CCC(=O)NC(CCCN=C(N)N)C(=O)O 640.80 unknown via CMAUP database
12beta-Hydroxyresibufogenin 15513541 Click to see CC12CCC(CC1CCC3C2CC(C4(C35C(O5)CC4C6=COC(=O)C=C6)C)O)O 400.50 unknown via CMAUP database
19-Hydroxyresibufogenin 12314891 Click to see CC12CCC3C(C14C(O4)CC2C5=COC(=O)C=C5)CCC6C3(CCC(C6)O)CO 400.50 unknown via CMAUP database
19-oxo-cinobufotalin-3-O-adipate-arginine 53253803 Click to see 756.80 unknown via CMAUP database
19-Oxo-desacetylcinobufagin 11144140 Click to see 414.50 unknown via CMAUP database
19-Oxobufalin 10883889 Click to see 400.50 unknown via CMAUP database
1Beta-Hydroxybufalin 10993111 Click to see 402.50 unknown via CMAUP database
20S,21-epoxy-resibufogenin formate 11026341 Click to see CC12CCC(CC1CCC3C2CCC4(C35C(O5)CC4C67C=CC(=O)OC6O7)C)OC=O 428.50 unknown via CMAUP database
20S,21-Epoxyresibufogenin 10453620 Click to see 400.50 unknown via CMAUP database
3-epi-Resibufogenin 70684536 Click to see 384.50 unknown via CMAUP database
5-[(1R,2S,4R,5R,6R,7R,10S,11R,14S,16R)-5,14-dihydroxy-11-(hydroxymethyl)-7-methyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-6-yl]pyran-2-one 15513543 Click to see 416.50 unknown via CMAUP database
5-[(1R,2S,4R,5S,6R,7R,10S,11S,14S,16R)-5,14-dihydroxy-7,11-dimethyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-6-yl]pyran-2-one 12186697 Click to see 400.50 unknown via CMAUP database
5-[(1R,2S,4R,6R,7R,10R,11S,14S,16R)-14-hydroxy-7,11-dimethyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-6-yl]pyran-2-one 122173140 Click to see 384.50 unknown via CMAUP database
5-[(1R,3R,5R,8R,9S,10S,11S,13R,14S,17R)-1,3,11,14-tetrahydroxy-10,13-dimethyl-12-oxo-2,3,4,5,6,7,8,9,11,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one 46938951 Click to see CC12C(CCC3C1C(C(=O)C4(C3(CCC4C5=COC(=O)C=C5)O)C)O)CC(CC2O)O 432.50 unknown via CMAUP database
5-[(3S,5R,8R,9S,10S,12R,13S,14S,16S,17R)-3,12,14,16-tetrahydroxy-10,13-dimethyl-11-oxo-2,3,4,5,6,7,8,9,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one 46938952 Click to see 432.50 unknown via CMAUP database
5-[(3S,5R,8R,9S,10S,13R,14S,17S)-3-hydroxy-10,13-dimethyl-15-oxo-1,2,3,4,5,6,7,8,9,11,12,14,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]pyran-2-one 12308599 Click to see 384.50 unknown via CMAUP database
5-[(3S,5S,8R,9S,10R,13R,14S,17S)-3,5-dihydroxy-10,13-dimethyl-15-oxo-2,3,4,6,7,8,9,11,12,14,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one 46938950 Click to see 400.50 unknown via CMAUP database
8-[[(1R,2S,4R,5R,6R,7R,10S,11S,14S,16R)-5-acetyloxy-7,11-dimethyl-6-(6-oxopyran-3-yl)-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-14-yl]oxy]-8-oxooctanoic acid 70697081 Click to see 598.70 unknown via CMAUP database
Arenobufagin 12305198 Click to see 416.50 unknown via CMAUP database
Bufa-20,22-dienolide, 3-((8-((4-((aminoiminomethyl)amino)-1-carboxybutyl)amino)-1,8-dioxooctyl)oxy)-14-hydroxy-, (3beta(S),5beta)- 99882 Click to see CC12CCC(CC1CCC3C2CCC4(C3(CCC4C5=COC(=O)C=C5)O)C)OC(=O)CCCCCCC(=O)NC(CCCN=C(N)N)C(=O)O 698.90 unknown via CMAUP database
Bufalin 9547215 Click to see 386.50 unknown via CMAUP database
bufalin-3-O-suberoyl ester 67050194 Click to see 542.70 unknown via CMAUP database
bufalin-3-O-succinate-arginine 102595428 Click to see 642.80 unknown via CMAUP database
Bufarenogin 167607 Click to see CC12CCC(CC1CCC3C2C(=O)C(C4(C3(CCC4C5=COC(=O)C=C5)O)C)O)O 416.50 unknown via CMAUP database
Bufogenin 6917974 Click to see CC12CCC(CC1CCC3C2CCC4(C35C(O5)CC4C6=COC(=O)C=C6)C)O 384.50 unknown via CMAUP database
Bufogenin B 12358889 Click to see CC12CCC(CC1CCC3C2CCC4(C3(CC(C4C5=COC(=O)C=C5)O)O)C)O 402.50 unknown via CMAUP database
Bufotalin 12302120 Click to see 444.60 unknown via CMAUP database
Bufotalinin 101286213 Click to see 414.50 unknown via CMAUP database
Bufotoxin 20054854 Click to see 756.90 unknown via CMAUP database
Cinobufagin 11969542 Click to see 442.50 unknown via CMAUP database
Cinobufagin-3-hemisuccinate 11969464 Click to see CC(=O)OC1C(C2(CCC3C(C24C1O4)CCC5C3(CCC(C5)OC(=O)CCC(=O)O)C)C)C6=COC(=O)C=C6 542.60 unknown via CMAUP database
Cinobufaginol 12303266 Click to see CC(=O)OC1C(C2(CCC3C(C24C1O4)CCC5C3(CCC(C5)O)CO)C)C6=COC(=O)C=C6 458.50 unknown via CMAUP database
Cinobufotalin 259776 Click to see 458.50 unknown via CMAUP database
Desacetylcinobufagin 11877495 Click to see 400.50 unknown via CMAUP database
Desacetylcinobufotalin 15513544 Click to see CC12CCC(CC1(CCC3C2CCC4(C35C(O5)C(C4C6=COC(=O)C=C6)O)C)O)O 416.50 unknown via CMAUP database
Gamabufotalin 259803 Click to see 402.50 unknown via CMAUP database
Hellebrigenin 259577 Click to see CC12CCC3C(C1(CCC2C4=COC(=O)C=C4)O)CCC5(C3(CCC(C5)O)C=O)O 416.50 unknown via CMAUP database
Hellebrigenin 3-acetate 267436 Click to see 458.50 unknown via CMAUP database
Marinobufagenin 11969465 Click to see 400.50 unknown via CMAUP database
Npc97210 102093790 Click to see 472.50 unknown via CMAUP database
Pseudobufarenogin 204810 Click to see 416.50 unknown via CMAUP database
Telocinobufagin 259991 Click to see 402.50 unknown via CMAUP database
Telocinobufatoxin 156077 Click to see CC12CCC(CC1(CCC3C2CCC4(C3(CCC4C5=COC(=O)C=C5)O)C)O)OC(=O)CCCCCCC(=O)NC(CCCN=C(N)N)C(=O)O 714.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Gamma amino acids and derivatives
4-Ammoniobutanoate 6992099 Click to see 103.12 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Hydroxyindoles
2-(5-hydroxy-1H-indol-3-yl)ethylurea 70959828 Click to see 219.24 unknown via CMAUP database
Bufoserotonin C 101460862 Click to see CC(=O)C1=CC(=CN1CCC2=CNC3=C2C=C(C=C3)O)NC(=O)C 325.40 unknown via CMAUP database
Bufotenin oxide 3083669 Click to see 220.27 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives
Bufotenidine 3083591 Click to see 218.29 unknown via CMAUP database
Tryptamine 1150 Click to see C1=CC=C2C(=C1)C(=CN2)CCN 160.22 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives / Serotonins
Bufotenine 10257 Click to see 204.27 unknown via CMAUP database
N-Methylserotonin 150885 Click to see CNCCC1=CNC2=C1C=C(C=C2)O 190.24 unknown via CMAUP database
Serotonin 5202 Click to see C1=CC2=C(C=C1O)C(=CN2)CCN 176.21 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives / Serotonins / N-acylserotonins
8-[2-(5-hydroxy-1H-indol-3-yl)ethylamino]-8-oxooctanoic acid 101460861 Click to see 332.40 unknown via CMAUP database
Bufobutanoic Acid 10612485 Click to see 276.29 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
(1S,2R,5S,7S,10R,11S,14R,15R,16S,17R)-5,7-dihydroxy-10,14,17-trimethyl-18-oxapentacyclo[13.3.2.01,14.02,11.05,10]icosane-16-carbaldehyde 46939054 Click to see CC1C(C2CCC3(C2(CCC4C3CCC5(C4(CCC(C5)O)C)O)C)O1)C=O 376.50 unknown via CMAUP database
(1S,2R,5S,7S,10R,11S,14R,15R)-16-ethenyl-10,14-dimethyl-18-oxapentacyclo[13.3.2.01,14.02,11.05,10]icos-16-ene-5,7-diol 72702445 Click to see CC12CCC(CC1(CCC3C2CCC4(C35CCC4C(=CO5)C=C)C)O)O 358.50 unknown via CMAUP database
> Organoheterocyclic compounds / Pteridines and derivatives / Pterins and derivatives / Biopterins and derivatives
2-amino-6-[(1R,2R)-1,2,3-trihydroxypropyl]-1H-pteridin-4-one 444632 Click to see 253.22 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Bufogargarizin A 49818075 Click to see 458.50 unknown via CMAUP database
Bufogargarizin B 49818153 Click to see 458.50 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Pyrroloquinolines / Pyrrolo[4,3,2-de]quinolines
7,7-Dimethyl-2-aza-7-azoniatricyclo[6.3.1.04,12]dodeca-1(12),3,8,10-tetraen-9-olate 5316436 Click to see 202.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(-)-Licarin A 6442393 Click to see 326.40 unknown https://doi.org/10.1080/10826079708000478
https://doi.org/10.1016/S0031-9422(00)00076-5
(+/-)-trans-Dehydrodiisoeugenol 73548 Click to see 326.40 unknown https://doi.org/10.1016/S0031-9422(00)00076-5
Licarin A 5281836 Click to see 326.40 unknown https://doi.org/10.1080/10826079708000478
https://doi.org/10.1016/S0031-9422(00)00076-5

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