Trifolium subterraneum, also known as subterranean clover, is a species of clover that is native to Europe, Southwest Asia, Northwest Africa, and Macaronesia. It is unique in that it develops its seeds underground, a characteristic not found in other clovers. This allows it to thrive in poor-quality soil, making it a popular choice for animal fodder. There are three subspecies of subterranean clover, each with its own ideal climate and soil type, making it adaptable to a wide range of environments. It is self-fertilizing and less attractive to certain pests, making it a low-maintenance crop. Subterranean clover was first discovered and promoted by Amos William Howard in South Australia, and its value as a fodder crop spread across Australia and to other countries. In 1936, Yvonne Aitken and Jim Harrison conducted extensive research on the species, determining that its flowering time is controlled by daylight and temperature changes.

Synonyms Top

Scientific name	Authority	First published in
Calycomorphum subterraneum	(L.) C.Presl	Symb. Bot.1: 50 (1831)
Trifolium subterraneum var. subterraneum	L.	Israel Journal of Botany 14 1965
Trifolium yanninicum	(Katzn. & Morley) Katzn.	Israel J. Bot. 23: 69 1974
Trifolium subterraneum subsp. longipes	(H.Gay) Cout.	Fl. Portugal2: 409 (1939)

Common names Top

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Filter by language:

Language	Common/alternative name
English	subterranean clover
English	sub clover
Arabic	نفل مطمور
Bulgarian	подземна детелина
Catalan	trèvol subterrani
Catalan	trèfle semeur
Czech	jetel podzemní
Welsh	meillionen ymguddiol
German	trèfle semeur
German	bodenfrüchtiger klee
Persian	شبدر زیرزمینی
Finnish	maa-apila
French	trèfle semeur
French	trèfle souterrain
French	trèfle enterreur
Hungarian	földbentermő here
Icelandic	jarðsmári
Lithuanian	trèfle semeur
Macedonian	Подземна детелина
Dutch	ondergrondse klaver
Dutch	onderaardse klaver
Swedish	grävklöver
Swedish	trèfle semeur
Chinese	地车轴草
Chinese	地三叶

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Trifolium subterraneum subsp. oxaloides	Bunge ex Nyman	Consp. Fl. Eur.: 177 (1878)
Trifolium subterraneum subsp. subterraneum		Unknown

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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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

Africa click to expand
- Macaronesia
  - Azores
  - Canary Islands
  - Madeira
- Northern Africa
  - Algeria
  - Libya
  - Morocco
  - Tunisia
- Southern Africa
  - Cape Provinces

Antarctica click to expand
- Subantarctic Islands
  - Tristan Da Cunha

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Eastern Asia
  - Japan
- Western Asia
  - East Aegean Islands
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - India

Australasia click to expand
- Australia
  - New South Wales
  - Norfolk Island
  - Queensland
  - South Australia
  - Tasmania
  - Victoria
  - Western Australia
- New Zealand
  - Chatham Islands
  - Kermadec Islands
  - New Zealand North
  - New Zealand South

Europe click to expand
- Eastern Europe
  - Belarus
  - Krym
  - Ukraine
- Middle Europe
  - Belgium
  - Czechoslovakia
  - Hungary
  - Netherlands
- Northern Europe
  - Great Britain
  - Ireland
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Northwestern U.S.A.
  - Oregon
- Southwestern U.S.A.
  - California

Pacific click to expand
- North-central Pacific
  - Hawaii

Southern America click to expand
- Brazil
  - Brazil South
- Southern South America
  - Argentina Northeast
  - Chile Central
  - Uruguay

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000213094
Canadensys	5934
USDA Plants	TRSU3
Tropicos	13034267
INPN	127498
Flora of Italy	2688
KEW	urn:lsid:ipni.org:names:523761-1
The Plant List	ild-8165
Open Tree Of Life	539553
Observations.org	2788
NCBI Taxonomy	3900
NBN Atlas	NBNSYS0000003242
Nature Serve	2.160617
IUCN Red List	176372
IPNI	523761-1
iNaturalist	60201
GBIF	5359330
Freebase	/m/07f7nj
EPPO	TRFSU
EOL	703458
Elurikkus	8011
Calflora (Californian flora)	8106
USDA GRIN	300628
Wikipedia	Trifolium_subterraneum
CMAUP	NPO19488

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
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_951799995.1	drTriSubt1.1	Chromosome	WELLCOME SANGER INSTITUTE	2023-05-27	40.0x	461.37 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

Genome assembly of Melilotus officinalis provides a new reference genome for functional genomics

Meng A, Li X, Li Z, Miao F, Ma L, Li S, Sun W, Huang J, Yang G

BMC Genom Data

18-Apr-2024

PMCID:	PMC11025269
doi:	10.1186/s12863-024-01224-y
PMID:	38637749

Novel SNP markers for flowering and seed quality traits in faba bean (Vicia faba L.): characterization and GWAS of a diversity panel

Ohm H, Åstrand J, Ceplitis A, Bengtsson D, Hammenhag C, Chawade A, Grimberg Å

Front Plant Sci

06-Mar-2024

PMCID:	PMC10950902
doi:	10.3389/fpls.2024.1348014
PMID:	38510437

A genomic toolkit for winged bean Psophocarpus tetragonolobus

Ho WK, Tanzi AS, Sang F, Tsoutsoura N, Shah N, Moore C, Bhosale R, Wright V, Massawe F, Mayes S

Nat Commun

01-Mar-2024

PMCID:	PMC10907731
doi:	10.1038/s41467-024-45048-x
PMID:	38429275

Holistic Approaches to Plant Stress Alleviation: A Comprehensive Review of the Role of Organic Compounds and Beneficial Bacteria in Promoting Growth and Health

Hathurusinghe SH, Azizoglu U, Shin JH

Plants (Basel)

29-Feb-2024

PMCID:	PMC10934532
doi:	10.3390/plants13050695
PMID:	38475541

Long-term liming changes pasture mineral profile

Li GD, Conyers MK, Refshauge G, Ataollahi F, Hayes RC

Sci Rep

12-Feb-2024

PMCID:	PMC10861585
doi:	10.1038/s41598-024-53908-1
PMID:	38347031

Comparative Analysis of Chloroplast Pan-Genomes and Transcriptomics Reveals Cold Adaptation in Medicago sativa

Zhang T, Chen X, Yan W, Li M, Huang W, Liu Q, Li Y, Guo C, Shu Y

Int J Mol Sci

01-Feb-2024

PMCID:	PMC10855486
doi:	10.3390/ijms25031776
PMID:	38339052

Australian Cool-Season Pulse Seed-Borne Virus Research: 1. Alfalfa and Cucumber Mosaic Viruses and Less Important Viruses

Jones RA, Congdon BS

Viruses

18-Jan-2024

PMCID:	PMC10819373
doi:	10.3390/v16010144
PMID:	38257844

Complete Chloroplast Genomes of Pterodon emarginatus Vogel and Pterodon pubescens Benth: Comparative and Phylogenetic Analyses

Brito JB, Antunes AM, Ferreira RD, de Campos Telles MP, Targueta CP, Soares TN

Curr Genomics

12-Dec-2023

PMCID:	PMC10758126
doi:	10.2174/0113892029244147231016050434
PMID:	38169762

Signaling in Legume–Rhizobia Symbiosis

Shumilina J, Soboleva A, Abakumov E, Shtark OY, Zhukov VA, Frolov A

Int J Mol Sci

12-Dec-2023

PMCID:	PMC10743482
doi:	10.3390/ijms242417397
PMID:	38139226

Effects of Elevated Temperature on Pisum sativum Nodule Development: I—Detailed Characteristic of Unusual Apical Senescence

Serova TA, Kusakin PG, Kitaeva AB, Seliverstova EV, Gorshkov AP, Romanyuk DA, Zhukov VA, Tsyganova AV, Tsyganov VE

Int J Mol Sci

05-Dec-2023

PMCID:	PMC10742560
doi:	10.3390/ijms242417144
PMID:	38138973

Aphanomyces macrosporus sp. nov. Causing Root Rot in Barley and Some Other Plants

Wikström M, Persson L, Fatehi J

J Fungi (Basel)

27-Nov-2023

PMCID:	PMC10744466
doi:	10.3390/jof9121144
PMID:	38132745

Effects of elevated carbon dioxide on plant growth and leaf photosynthesis of annual ryegrass along a phosphorus deficiency gradient

Li F, He C, Chang Z, Ma C, Yu J, Liu L, Zhang Y, Hao L

Front Plant Sci

27-Nov-2023

PMCID:	PMC10711278
doi:	10.3389/fpls.2023.1271262
PMID:	38089800

Reviewing ecological implications of mycorrhizal fungal interactions in the Brassicaceae

Trautwig AN, Jackson MR, Kivlin SN, Stinson KA

Front Plant Sci

22-Nov-2023

PMCID:	PMC10698685
doi:	10.3389/fpls.2023.1269815
PMID:	38078074

The Role of Genistein in Mammalian Reproduction

Guelfi G, Pasquariello R, Anipchenko P, Capaccia C, Pennarossa G, Brevini TA, Gandolfi F, Zerani M, Maranesi M

Molecules

05-Nov-2023

PMCID:	PMC10647478
doi:	10.3390/molecules28217436
PMID:	37959856

Calcium in the Life Cycle of Legume Root Nodules

Zartdinova R, Nikitin A

Indian J Microbiol

27-Oct-2023

PMCID:	PMC10682328
doi:	10.1007/s12088-023-01107-3
PMID:	38031601

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 / Corynanthean-type alkaloids
methyl 2-{3-ethenyl-1H,2H,3H,4H,6H,7H,12H,12bH-indolo[2,3-a]quinolizin-2-yl}-3-hydroxypropanoate	5321352	Click to see COC(=O)C(CO)C1CC2C3=C(CCN2CC1C=C)C4=CC=CC=C4N3	354.40	unknown	https://doi.org/10.1021/NP970503R
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Himeic Acid A	11774903	Click to see CC(CC(=O)NC(=O)C1=COC(=CC1=O)C=CCCCCCCCCC(=O)O)C(=O)O	435.50	unknown	via CMAUP database
Himeic acid B	21579676	Click to see C1=C(OC=C(C1=O)C(=O)N)C=CCCCCCCCCC(=O)O	321.40	unknown	via CMAUP database
himeic acid C	21777983	Click to see CC(CC(=O)NC(=O)C1=CNC(=CC1=O)C=CCCCCCCCCC(=O)O)C(=O)O	434.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-oct-1-en-3-yloxy-6-[[(3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol	163194749	Click to see CCCCCC(C=C)OC1C(C(C(C(O1)COC2C(C(C(CO2)O)O)O)O)O)O	422.50	unknown	https://doi.org/10.1021/NP970503R
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
Hexadecanoic acid propylamide	10379895	Click to see CCCCCCCCCCCCCCCC(=O)NCCC	297.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Alloxanthin	6443740	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C#CC2=C(CC(CC2(C)C)O)C)C)C	564.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral	638011	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3S,4aS)-3,8-dimethyl-5-prop-1-en-2-yl-1,2,3,4,4a,5,6,8a-octahydronaphthalene	5315586	Click to see CC1CCC2C(C1)C(CC=C2C)C(=C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene	5280489	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C	536.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R)-3,5,5-trimethyl-4-[(3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-[(1R)-2,6,6-trimethylcyclohex-2-en-1-yl]octadeca-3,5,7,9,11,13,15,17-octaen-1-ynyl]cyclohex-3-en-1-ol	101289802	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C	550.90	unknown	via CMAUP database
(4R,5R)-4-hydroxy-4-[(3E,5E,7E,9E,11E,13E,15E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyl-2-oxooctadeca-3,5,7,9,11,13,15-heptaen-17-ynyl]-3,3,5-trimethylcyclohexan-1-one	23428074	Click to see CC1CC(=O)CC(C1(CC(=O)C(=CC=CC(=CC=CC=C(C)C=CC=C(C)C#CC2=C(CC(CC2(C)C)O)C)C)C)O)(C)C	598.90	unknown	via CMAUP database
19'-Hexanoyloxyisomytiloxanthin	16061209	Click to see CCCCCC(=O)OCC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)CC1(C(CC(=O)CC1(C)C)C)O)C)C#CC2=C(CC(CC2(C)C)O)C	713.00	unknown	via CMAUP database
Amarouciaxanthin B/Sidnyaxanthin	16061221	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)CC2(C(=CC(=O)CC2(C)C)C)O)C)C	596.80	unknown	via CMAUP database
CID 23428237	23428237	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)C=C2C(=CC(=O)CC2(C)C)C)C)C	578.80	unknown	via CMAUP database
Halocynthiaxanthin	11966451	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)CC23C(CC(CC2(O3)C)O)(C)C)C)C	598.90	unknown	via CMAUP database
Mytiloxanthin	11365423	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=CC(=O)C2(CC(CC2(C)C)O)C)O)C)C	598.90	unknown	via CMAUP database
NV766Twa77	102146782	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2(C(CC(CC2(C)O)O)(C)C)O)C)C	600.90	unknown	via CMAUP database
Pectenol A/(Pectenol)	16061215	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(C(C(CC2(C)C)O)O)C)C)C	582.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
7-Dehydrocholesterol	439423	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C	384.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Brassicasterol	5281327	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	398.70	unknown	via CMAUP database
Ergosterol	444679	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C	396.60	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
Notoamide J	25180709	Click to see CC(C)(C=C)C1(C2=C(C=C(C=C2)O)NC1=O)CC3C(=O)N4CCCC4C(=O)N3	383.40	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Betaine	247	Click to see C[N+](C)(C)CC(=O)[O-]	117.15	unknown	via CMAUP database
N,N,N-trimethylglycinium	248	Click to see C[N+](C)(C)CC(=O)O	118.15	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
Arginine	6322	Click to see C(CC(C(=O)O)N)CN=C(N)N	174.20	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
3,3'-Methylenebis(tyrosine)	3082144	Click to see C1=CC(=C(C=C1CC(C(=O)O)N)CC2=C(C=CC(=C2)CC(C(=O)O)N)O)O	374.40	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Kainoids
CID 17753955	17753955	Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O	311.33	unknown	via CMAUP database
Domoic acid C5'-diastereomer	5311075	Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O	311.33	unknown	via CMAUP database
Isodomoic acid F	101790920	Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O	311.33	unknown	via CMAUP database
> Organic acids and derivatives / Organic sulfonic acids and derivatives / Organosulfonic acids and derivatives / Organosulfonic acids
Taurine	1123	Click to see C(CS(=O)(=O)O)N	125.15	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Alkanolamines / 1,2-aminoalcohols / N-acylethanolamines
Anandamide	5281969	Click to see CCCCCC=CCC=CCC=CCC=CCCCC(=O)NCCO	347.50	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Primary amines / Monoalkylamines
Cadaverine	273	Click to see C(CCN)CCN	102.18	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Beta-hydroxy ketones
Aspermytin A	9993091	Click to see CC1CCC2C(C1)C=CC(C2(C)C(=O)CCO)(C)O	266.38	unknown	via CMAUP database
> Organoheterocyclic compounds / Azaspirodecane derivatives
CID 101396440	101396440	Click to see CC1CC2C3C(CC4(O3)C(CC(CN4)C)C)OC(C1)(O2)CC(=C)C5C(CC(C(O5)(C(C6CC7C(O6)CC(C8(O7)CCC9(O8)C=CCC(O9)C=CCCC(=O)O)C)O)O)C)C	842.10	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodiazepines / 1,4-benzodiazepines
(3R,3'R)-3'-(3-hydroxyphenyl)-4-methylspiro[1H-1,4-benzodiazepine-3,2'-oxirane]-2,5-dione	92278353	Click to see CN1C(=O)C2=CC=CC=C2NC(=O)C13C(O3)C4=CC(=CC=C4)O	310.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(3S,8aS)-3-[[(3R)-7,7-dimethyl-3-(2-methylbut-3-en-2-yl)-2-oxo-1H-pyrano[2,3-g]indol-3-yl]methyl]-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione	16127840	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C3(CC4C(=O)N5CCCC5C(=O)N4)C(C)(C)C=C)C	449.50	unknown	via CMAUP database
Notoamide A	16128040	Click to see CC1(C=CC2=C(O1)C=CC3=C2N(C(=O)C34CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)C	463.50	unknown	via CMAUP database
Notoamide B	16127923	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C34CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)C	447.50	unknown	via CMAUP database
Notoamide H	25180895	Click to see CC1(C=CC2=C(O1)C=CC3=C2N(C(=O)C34C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)O)C	479.50	unknown	via CMAUP database
Notoamide O	102043608	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4(C3=O)C(C5CC67CCCN6C(=O)C5(C(O4)O)NC7=O)(C)C)C	479.50	unknown	via CMAUP database
Notoamide Q	46919487	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C3(CC4C(=O)N5CCCC5(C(=O)N4)OC)C(C)(C)C=C)C	479.60	unknown	via CMAUP database
Sclerotiamide	10647785	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C34C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)C	463.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
Notoamide D	16127841	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4(C3(CC5N4C(=O)C6CCCN6C5=O)O)C(C)(C)C=C)C	449.50	unknown	via CMAUP database
Notoamide K	25180896	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4(C3(CC5(N4C(=O)C6CCCN6C5=O)O)O)C(C)(C)C=C)C	465.50	unknown	via CMAUP database
Notoamide P	46919486	Click to see CC1(C=CC2=C3C(=CC(=C2O1)Br)C4(CC5(C(=O)N6CCCC6C(=O)N5C4(N3)C(C)(C)C=C)O)O)C	544.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
Viridicatol	115033	Click to see C1=CC=C2C(=C1)C(=C(C(=O)N2)O)C3=CC(=CC=C3)O	253.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Pyrroloquinolines
(+)-Stephacidin A	16127922	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)C	431.50	unknown	via CMAUP database
Notoamide F	25180710	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)OC)C	461.60	unknown	via CMAUP database
Notoamide G	25180707	Click to see CC1(C=CC2=C(O1)C=CC3=C2N(C4=C3C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)OC)O)C	477.60	unknown	via CMAUP database
Notoamide I	25180708	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3C(=O)C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)C	445.50	unknown	via CMAUP database
notoamide R	46919488	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)C	447.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(-)-Phaselic acid	4484594	Click to see C1=CC(=C(C=C1C=CC(=O)OC(CC(=O)O)C(=O)O)O)O	296.23	unknown	https://doi.org/10.1021/NP970503R
Phaselic acid, (-)-	92299542	Click to see C1=CC(=C(C=C1C=CC(=O)OC(CC(=O)O)C(=O)O)O)O	296.23	unknown	https://doi.org/10.1021/NP970503R
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Liquiritigenin	114829	Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O	256.25	unknown	https://doi.org/10.1016/S0031-9422(00)85667-8
> Phenylpropanoids and polyketides / Flavonoids / Flavones
4',7-Dihydroxyflavone	5282073	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)O	254.24	unknown	https://doi.org/10.1016/S0031-9422(00)85667-8
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1016/S0031-9422(00)85667-8
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Fisetin	5281614	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O	286.24	unknown	https://doi.org/10.1016/S0031-9422(00)85667-8
Geraldol	5482101	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3)O)O)O	300.26	unknown	https://doi.org/10.1016/S0031-9422(00)85667-8
Isorhamnetin	5281654	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	316.26	unknown	https://doi.org/10.1016/S0031-9422(00)85667-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(E)-1-(2,4-dihydroxyphenyl)-3-[3-methoxy-4-[(2S,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-en-1-one	162992677	Click to see COC1=C(C=CC(=C1)C=CC(=O)C2=C(C=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(00)85667-8
3,7-dihydroxy-2-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one	162916309	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O	462.40	unknown	https://doi.org/10.1016/S0031-9422(00)85667-8
3,7-dihydroxy-2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one	162897577	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O	432.40	unknown	https://doi.org/10.1016/S0031-9422(00)85667-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Geraldone	5281618	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C=C3)O)O	284.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Daidzein	5281708	Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)O	254.24	unknown	https://doi.org/10.1071/AR9670047 https://doi.org/10.1016/S0021-9150(99)00029-5
Genistein	5280961	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O	270.24	unknown	https://doi.org/10.1016/S0021-9150(99)00029-5 https://doi.org/10.1021/JF00049A020 https://doi.org/10.1016/0160-9327(76)90004-1 https://doi.org/10.1071/AR9670047
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanols
(2S,3R)-2,5,7-trihydroxy-3-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one	162900254	Click to see C1=CC(=CC=C1C2C(OC3=CC(=CC(=C3C2=O)O)O)O)O	288.25	unknown	https://doi.org/10.1021/NP970503R
2-Hydroxy-2,3-dihydrogenistein	443902	Click to see C1=CC(=CC=C1C2C(OC3=CC(=CC(=C3C2=O)O)O)O)O	288.25	unknown	https://doi.org/10.1021/NP970503R
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(4-Methoxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	3733033	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O	430.40	unknown	https://doi.org/10.1021/NP970503R
6''-O-Malonylgenistin	131750882	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O	518.40	unknown	https://doi.org/10.1021/NP970503R
Biochanin A 7-(6-malonylglucoside)	131751062	Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O	532.40	unknown	https://doi.org/10.1021/NP970503R
Biochanin A 7-O-(6-O-malonyl-beta-D-glucoside)	5282148	Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O	532.40	unknown	https://doi.org/10.1021/NP970503R
Genistin	5281377	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	https://doi.org/10.1021/NP970503R
Genistoside	5284639	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	https://doi.org/10.1021/NP970503R
Malonylgenistin	15934091	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O	518.40	unknown	https://doi.org/10.1021/NP970503R
Ononin	442813	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O	430.40	unknown	https://doi.org/10.1021/NP970503R
Sissotrin	5280781	Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O	446.40	unknown	https://doi.org/10.1021/NP970503R
Sissotrine	5358913	Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O	446.40	unknown	https://doi.org/10.1021/NP970503R
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
2,5,7-Trihydroxy-3-(4-methoxyphenyl)-2,3-dihydrochromen-4-one	9904478	Click to see COC1=CC=C(C=C1)C2C(OC3=CC(=CC(=C3C2=O)O)O)O	302.28	unknown	https://doi.org/10.1021/NP970503R
2,5,7-Trihydroxy-4'-methoxyisoflavanone	25203449	Click to see COC1=CC=C(C=C1)C2C(OC3=CC(=CC(=C3C2=O)O)O)O	302.28	unknown	https://doi.org/10.1021/NP970503R
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Biochanin A	5280373	Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O	284.26	unknown	https://doi.org/10.1021/JF00049A020 https://doi.org/10.1016/S0021-9150(99)00029-5 https://doi.org/10.1021/NP970503R
biochanin A(1-)	25203224	Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)[O-])O	283.25	unknown	via CMAUP database
CID 10378473	10378473	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O	271.24	unknown	via CMAUP database
Formononetin	5280378	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O	268.26	unknown	https://doi.org/10.1021/JF00049A020 https://doi.org/10.1071/AR9670047 https://doi.org/10.1016/S0021-9150(99)00029-5 https://doi.org/10.1021/NP970503R https://doi.org/10.1016/0160-9327(76)90004-1
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Homobutein	6438092	Click to see COC1=C(C=CC(=C1)C=CC(=O)C2=C(C=C(C=C2)O)O)O	286.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Saxitoxins, gonyautoxins, and derivatives
[(3aS,4R,10aS)-2,6-diamino-9,9,10,10-tetrahydroxy-3,3a,4,8-tetrahydropyrrolo[1,2-c]purin-4-yl]methoxycarbonylsulfamic acid	102411283	Click to see C1C(C(C23N1C(=NC(C2NC(=N3)N)COC(=O)NS(=O)(=O)O)N)(O)O)(O)O	411.35	unknown	via CMAUP database
[(3aS,4R,9S,10aS)-2,6-diamino-9,10,10-trihydroxy-3a,4,8,9-tetrahydro-3H-pyrrolo[1,2-c]purin-4-yl]methoxycarbonylsulfamic acid	44587284	Click to see C1C(C(C23N1C(=NC(C2NC(=N3)N)COC(=O)NS(=O)(=O)O)N)(O)O)O	395.35	unknown	via CMAUP database
11,11-Dihydroxysaxitoxin	102411284	Click to see C1C(C(C23N1C(=NC(C2N=C(N3)N)COC(=O)N)N)(O)O)(O)O	331.29	unknown	via CMAUP database
11beta-Hydroxysaxitoxin	60135304	Click to see C1C(C(C23N1C(=NC(C2N=C(N3)N)COC(=O)N)N)(O)O)O	315.29	unknown	via CMAUP database

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Trifolium subterraneum

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