Sarracenia flava - Unknown
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Details Top

Internal ID UUID6440039f3e649475020980
Scientific name Sarracenia flava
Authority L.
First published in Sp. Pl. : 510 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Sarracenia rugelii Shuttlew. ex A.DC. Prodr. 17: 6 (1873)
Sarracenia atrosanguinea Hort.Bull ex André Ill. Hort. 27: 87, t. 386 (1880)
Sarracenia fildesii G.Nicholson Ill. Dict. Gard. 3: 262 (1886)
Sarracenia acuta Raf. Autik. Bot. : 34 (1840)
Sarracenia gronovii var. flava (L.) Alph.Wood Class-book Bot. (ed. 1861). 222. 1861

Common names Top

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Language Common/alternative name
English yellow pitcher plant
English yellow pitcherplant
English trumpet-leaved pitcher plant
Arabic عشبة الأباريق البوقية الصفراء
German gelbe schlauchpflanze
Hungarian sárga kürtvirág
Japanese キバナヘイシソウ
Dutch gele trompetbekerplant
Chinese 黄瓶子草

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Middle Europe
      • Austria
    • Northern Europe
      • Great Britain
    • Southwestern Europe
      • France
  • Northern America
    • Northwestern U.S.A.
      • Washington
    • Southeastern U.S.A.
      • Alabama
      • Florida
      • Georgia
      • Maryland
      • North Carolina
      • South Carolina
      • Virginia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000493567
Florida Plant Atlas 3265
Flora of Alabama 3350
USDA Plants SAFL4
Tropicos 28900009
INPN 717531
KEW urn:lsid:ipni.org:names:30118747-2
The Plant List kew-2582938
Missouri Botanical Garden 286843
Open Tree Of Life 639946
NCBI Taxonomy 4359
NBN Atlas NBNSYS0000033278
Nature Serve 2.160353
IUCN Red List 39715
IPNI 30118747-2
iNaturalist 81900
GBIF 5421391
Freebase /m/066hxx
EPPO SRNFL
EOL 584636
USDA GRIN 410910
Wikipedia Sarracenia_flava
CMAUP NPO27837

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_035668175.1 ASM3566817v1 Scaffold Iridian Genomes 2024-01-16 50.0x 878.76 Mb

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 Genome Sequences of 17 Species of Carnivorous Plants Procko C, Chory J, Pirro S Biodivers Genomes 14-Nov-2023
PMCID:PMC10662931
doi:10.56179/001c.90164
PMID:37990687
Naming the menagerie: creativity, culture and consequences in the formation of scientific names Heard SB, Mlynarek JJ Proc Biol Sci 01-Nov-2023
PMCID:PMC10618856
doi:10.1098/rspb.2023.1970
PMID:37909078
Rampant chloroplast capture in Sarracenia revealed by plastome phylogeny Baldwin E, McNair M, Leebens-Mack J Front Plant Sci 14-Aug-2023
PMCID:PMC10497973
doi:10.3389/fpls.2023.1237749
PMID:37711293
Diversification of ranunculaceous petals in shape supports a generalized model for plant lateral organ morphogenesis and evolution Cheng J, Yao X, Li X, Yue L, Duan X, Li B, Fu X, Li S, Shan H, Yin X, Whitewoods C, Coen E, Kong H Sci Adv 21-Apr-2023
PMCID:PMC10121167
doi:10.1126/sciadv.adf8049
PMID:37083529
Volatile organic compounds influence prey composition in Sarracenia carnivorous plants Dupont C, Buatois B, Bessiere JM, Villemant C, Hattermann T, Gomez D, Gaume L PLoS One 19-Apr-2023
PMCID:PMC10115284
doi:10.1371/journal.pone.0277603
PMID:37074981
Omics Approaches in Uncovering Molecular Evolution and Physiology of Botanical Carnivory Baharin A, Ting TY, Goh HH Plants (Basel) 15-Jan-2023
PMCID:PMC9867145
doi:10.3390/plants12020408
PMID:36679121
Selective Bacterial Community Enrichment between the Pitcher Plants Sarracenia minor and Sarracenia flava Yourstone SM, Weinstein I, Ademski E, Shank EA, Stasulli NM Microbiol Spectr 24-Nov-2021
PMCID:PMC8612160
doi:10.1128/Spectrum.00696-21
PMID:34817222
Recent ecophysiological, biochemical and evolutional insights into plant carnivory Adamec L, Matušíková I, Pavlovič A Ann Bot 10-Jun-2021
PMCID:PMC8389183
doi:10.1093/aob/mcab071
PMID:34111238
Metabolomic analysis reveals reliance on secondary plant metabolites to facilitate carnivory in the Cape sundew, Drosera capensis Hatcher CR, Sommer U, Heaney LM, Millett J Ann Bot 02-Jun-2021
PMCID:PMC8389465
doi:10.1093/aob/mcab065
PMID:34077503
Role of phosphoglucomutase in regulating trehalose metabolism in Nilaparvata lugens Pan BY, Liu YK, Wu HK, Pang XQ, Wang SG, Tang B, Xu CD 3 Biotech 23-Jan-2020
PMCID:PMC6977789
doi:10.1007/s13205-020-2053-5
PMID:32030330
The function of secondary metabolites in plant carnivory Hatcher CR, Ryves DB, Millett J Ann Bot 11-Dec-2019
PMCID:PMC7061172
doi:10.1093/aob/mcz191
PMID:31760424
Endocytosis and Digestion in Carnivorous Pitcher Plants of the Family Sarraceniaceae Koller-Peroutka M, Krammer S, Pavlik A, Edlinger M, Lang I, Adlassnig W Plants (Basel) 24-Sep-2019
PMCID:PMC6843295
doi:10.3390/plants8100367
PMID:31554185
A carnivorous plant genetic map: pitcher/insect-capture QTL on a genetic linkage map of Sarracenia Malmberg RL, Rogers WL, Alabady MS Life Sci Alliance 29-Nov-2018
PMCID:PMC6265660
doi:10.26508/lsa.201800146
PMID:30519677
Evaluating the adaptive evolutionary convergence of carnivorous plant taxa through functional genomics Wheeler GL, Carstens BC PeerJ 31-Jan-2018
PMCID:PMC5797450
doi:10.7717/peerj.4322
PMID:29404217
Plant Secondary Metabolites as Anticancer Agents: Successes in Clinical Trials and Therapeutic Application Seca AM, Pinto DC Int J Mol Sci 16-Jan-2018
PMCID:PMC5796209
doi:10.3390/ijms19010263
PMID:29337925

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
> Alkaloids and derivatives
(S)-2-Propylpiperidine 441072 Click to see CCCC1CCCCN1 127.23 unknown via CMAUP database
d-Conicine 21583848 Click to see CCCC1CCCC[NH2+]1 128.24 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
5-Oxooctanoic acid 280190 Click to see CCCC(=O)CCCC(=O)O 158.19 unknown https://doi.org/10.1007/BF02003710
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aS,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 124304322 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1002/JPS.2600650226
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carbaldehyde 124407318 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C=O 440.70 unknown https://doi.org/10.1016/S0031-9422(00)86845-4
(3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-propan-2-ylidene-3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-tetradecahydro-2H-cyclopenta[a]chrysene-3a-carboxylic acid 162970214 Click to see CC(=C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O)C 456.70 unknown https://doi.org/10.1002/JPS.2600630427
3-O-Acetyloleanolic acid 151202 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown via CMAUP database
3beta-Acetoxy-11alpha,12alpha-epoxyoleanan-28,13beta-olide 21626351 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2C4C(O4)C56C3(CCC7(C5CC(CC7)(C)C)C(=O)O6)C)C)C 512.70 unknown via CMAUP database
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carbaldehyde 317607 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C=O 440.70 unknown https://doi.org/10.1016/S0031-9422(00)86845-4
9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-propan-2-ylidene-3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-tetradecahydro-2H-cyclopenta[a]chrysene-3a-carboxylic acid 162970213 Click to see CC(=C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O)C 456.70 unknown https://doi.org/10.1002/JPS.2600630427
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1002/JPS.2600650226
beta-Sitosteryl palmitate 9852570 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 653.10 unknown via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/S0031-9422(00)86845-4
Betulinaldehyde 99615 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C=O 440.70 unknown https://doi.org/10.1016/S0031-9422(00)86845-4
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)86845-4
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1002/JPS.2600650226
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
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
Urs-12-en-3beta-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1002/JPS.2600650226
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(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 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1002/JPS.2600650226
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1002/JPS.2600650226
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
5-Oxooctanal 12538121 Click to see CCCC(=O)CCCC=O 142.20 unknown https://doi.org/10.1007/BF02003710
> Organoheterocyclic compounds / Azaspirodecane derivatives
(5S,9R,13R,16S)-N,6,13-trimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-16-amine 5316046 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)NC)C)CN1 328.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
(1S,5R,6R,7R,8R)-7-(1,3-benzodioxol-5-yl)-8-hydroxy-5-methoxy-6-methyl-3-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one 162937219 Click to see CC1C(C2C(C1(C=C(C2=O)CC=C)OC)O)C3=CC4=C(C=C3)OCO4 342.40 unknown https://doi.org/10.1021/JA00422A048
> Organoheterocyclic compounds / Dioxanes / 1,3-dioxanes
CID 10998704 10998704 Click to see CC1C2C3CC(O1)OC2OC=C3C(=O)OC 226.23 unknown via CMAUP database
methyl (1R,3R,7R,8S,9S)-9-methyl-2,4,10-trioxatricyclo[5.3.1.03,8]undec-5-ene-6-carboxylate 162850435 Click to see CC1C2C3CC(O1)OC2OC=C3C(=O)OC 226.23 unknown https://doi.org/10.1021/JA00422A048
methyl (3R,8S)-9-methyl-2,4,10-trioxatricyclo[5.3.1.03,8]undec-5-ene-6-carboxylate 5321136 Click to see CC1C2C3CC(O1)OC2OC=C3C(=O)OC 226.23 unknown https://doi.org/10.1016/S0031-9422(00)86845-4
https://doi.org/10.1021/JA00422A048
methyl (7S,8S,9S)-9-methyl-2,4,10-trioxatricyclo[5.3.1.03,8]undec-5-ene-6-carboxylate 134715197 Click to see CC1C2C3CC(O1)OC2OC=C3C(=O)OC 226.23 unknown https://doi.org/10.1016/S0031-9422(00)86845-4
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
gamma-Coniceine 442632 Click to see CCCC1=NCCCC1 125.21 unknown https://doi.org/10.1007/BF02003710
> Organoheterocyclic compounds / Pyrrolizidines
Sarranicine 6440939 Click to see CC=C(C)C(=O)OC1CCN2C1C(CC2)COC(=O)C(=CC)CO 337.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-8-methyl-6-(3-methyl-2-butenyl)-2-phenyl-, (S)- 179806 Click to see CC1=C(C(=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)CC=C(C)C)O 338.40 unknown via CMAUP database
6-Prenylpinocembrin 6546086 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O)C 324.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S)-5,7-Dihydroxy-6-methyl-8-prenylflavanone 102154219 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)CC=C(C)C)O 338.40 unknown via CMAUP database
(S)-5,7-dihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)chroman-4-one 45272659 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)OC)C 354.40 unknown via CMAUP database
4'-O-Methyl-6-methyl-8-prenylnaringenin 16099396 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)OC)CC=C(C)C)O 368.40 unknown via CMAUP database
8-Prenylpinostrobin 14721597 Click to see CC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC)C 338.40 unknown via CMAUP database
Glabranin 124049 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3)C 324.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
5,4',1''-Trihydroxy-6,7-(3'',3''-dimethylchroman)flavone 102154220 Click to see CC1(CC(C2=C(O1)C=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)O)C 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3-dihydrochromen-4-one 5317364 Click to see C1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 436.40 unknown https://doi.org/10.1016/0305-1978(77)90039-4

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