Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Unfortunately, no documented ethnobotanical uses of Lathyrus odoratus (sweet pea) were found in reliable sources (ethnobotanical monographs, peer‑reviewed articles, reputable herbal compendia, or historic records) involving infusions, decoctions, tinctures, macerations, or poultices.

General Uses Top

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Common products:
Lathyrus odoratus is primarily produced as a cut flower and as an ornamental garden plant.

Industrial and craft applications:
Horticultural cultivation supports breeding programs and commercial propagation, providing genetic stock and nursery stock for ornamental use. The scented cultivars are maintained and distributed through seed and vegetative propagation systems.

Fragrance and cosmetics:
The highly scented cultivars are processed to obtain aromatic extracts used in perfumery and fragrance composition. Official fragrance references list Lathyrus odoratus among natural sources of volatile aroma compounds (e.g., phenylacetaldehyde, linalool, benzyl alcohol) used as fragrance ingredients.

Properties relevant to use:
Flowers produce a complex volatile blend dominated by phenylacetaldehyde (low threshold floral note), with supporting linalool, benzyl alcohol, and related aromatic compounds; this profile underpins the cultivar value in perfumery and horticulture.

Sustainability and sourcing:
Regional cut-flower production is regulated under standard horticultural and phytosanitary regimes governing plant material and plant protection, and cut-flower supply chains typically adopt recognized certification and quality assurance systems.

Synonyms Top

Scientific name	Authority	First published in
Lathyrus cyprius	Rech.f.	Svensk Bot. Tidskr.43: 37 (1949)
Lathyrus odoratus-zeylanicus	Burm.f.	Fl. Indica: 162 (1768)
Pisum odoratum	(L.) E.H.L.Krause	J.Sturm, Deutschl. Fl. Abbild., ed. 2, 9: 50 (1901)
Lathyrus odoratus f. pleniflorus	Moldenke	Phytologia4: 56 (1952)
Lathyrus odoratus var. albus	Alef.	Bonplandia (Hannover)9: 151 (1861)
Lathyrus odoratus var. ater	Alef.	Bonplandia (Hannover)9: 151 (1861)
Lathyrus odoratus var. carneus	Alef.	Bonplandia (Hannover)9: 151 (1861)
Lathyrus odoratus var. pardalinus	Alef.	Bonplandia (Hannover)9: 151 (1861)
Lathyrus odoratus var. roseoalbus	Alef.	Bonplandia (Hannover)9: 151 (1861)
Lathyrus odoratus var. roseovittata	Alef.	Bonplandia (Hannover)9: 151 (1861)
Lathyrus odoratus var. vulgaris	Alef.	Bonplandia (Hannover)9: 151 (1861)
Lathyrus odoratus var. siculus	L.	Sp. Pl.: 732 (1753)
Lathyrus odoratus var. zeylanicus	L.	Sp. Pl.: 732 (1753)
Lathyrus maccaguenii	Tod. ex Nyman	Consp. Fl. Eur. : 201 (1878)

Common names Top

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Filter by language:

Language	Common/alternative name
English	sweet pea
English	sweetpea
English	guisante de olor
English	sweet pea 'millennium'
Spanish	chorreque
Spanish	doncenon
Spanish	doncenón
Spanish	guisante de olor
Arabic	بازلاء عطرية
Arabic	جبلان عطر
Arabic	بسلى عطرة
Arabic	بازلاء زهور
Arabic	بسلة الزهور
Azerbaijani	Ətirli güllücə
azb	عطیرلی گۆللوجه
Belarusian	чына пахучая
Belarusian	пахучы гарошак
Bulgarian	сладък грах
Czech	hrachor vonný
cv	Ырă шăршăллă тăрна пăрçи
Welsh	pysen bêr
Danish	Ærteblomst
Danish	almindelig Ærteblomst
German	duftwicke
German	edelwicke
German	duft-platterbse
German	duft-wicke
German	garten-wicke
German	gartenwicke
German	wohlriechende wicke
German	duftende platterbse
Greek	γλυκό μπιζέλι
Greek	μοσχομπίζελο
Greek	Λάθυρος ο εύοσμος
Estonian	lillhernes
Persian	گل نخود
Finnish	tuoksunätkelmä
Finnish	hajuherne
Finnish	tuoksuherne
French	gesse odorante
French	pois de senteur
Hebrew	אפונה ריחנית
Hebrew	טופח ריחני
Upper Sorbian	wonjaty hróšik
Armenian	հոտավետ ոլոռիկ
Indonesian	polong manis
io	latiro
Japanese	麝香豌豆
Japanese	スイトピー
Japanese	麝香連理草
Japanese	スイートピー
Kabyle	muḥemmed u ali
Korean	스위트피
Lithuanian	kvapusis pelėžirnis
Latvian	puķuzirņi
Latvian	smaržīgais puķuzirnītis
Latvian	smaržīgais puķuzirnis
Latvian	puķuzirnīši
Macedonian	мирислив граор
Malayalam	സ്വീറ്റ് പീ
myv	Тантей чине идем вика
Norwegian Bokmål	blomsterert
Dutch	welriekende lathyrus
Dutch	pronkerwt
Polish	groszek pachnący
Russian	Душистый горошек
Samogitian	Žemčiūgs
Serbian	ukrasni grašak
Swedish	luktärt
tg	Мулкакгул
Ukrainian	Чина запашна
Uzbek	shirin noʻxat
vep	hajuherneh
Chinese	麝香豌豆
Chinese	麝香野豌豆
Chinese	香碗豆
Chinese	花豌豆
Chinese	香豌豆

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Resents Transplanting: These plants do not tolerate the disturbance of their roots well. It's best to sow these seeds in their final growing location or in a container from which they can be moved without disturbing the root ball.

Requires Darkness: These seeds need to be covered with soil or otherwise kept in the dark to germinate properly. Light inhibits their germination process.

Requires Scarification: Scarification involves physically breaking, scratching, or softening the seed coat to allow water absorption and germination to occur. This can be done by nicking the seed coat with a knife or rubbing the seeds between sheets of sandpaper.

Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.

plant in deep pot

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Macaronesia
  - Canary Islands
  - Madeira
- Northern Africa
  - Algeria
  - Libya
  - Morocco
  - Tunisia
- West-central Tropical Africa
  - Rwanda

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Eastern Asia
  - Korea
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Russian Far East
  - Primorye
- Western Asia
  - Cyprus
  - East Aegean Islands
  - Iraq

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Pakistan
  - Sri Lanka
- Malesia
  - Jawa
- Papuasia
  - New Guinea

Australasia click to expand
- Australia
  - South Australia
  - Victoria
- New Zealand
  - New Zealand North
  - New Zealand South

Europe click to expand
- Eastern Europe
  - Baltic States
  - Central European Russia
  - East European Russia
  - Krym
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Czechoslovakia
- Southeastern Europe
  - Italy
  - Sicilia
- Southwestern Europe
  - France
  - Portugal

Northern America click to expand
- Mexico
  - Mexico Southwest
- North-central U.S.A.
  - Illinois

Southern America click to expand
- Caribbean
  - Dominican Republic
  - Puerto Rico
  - Trinidad-Tobago
- Central America
  - El Salvador
  - Guatemala
- Western South America
  - Ecuador
  - Galápagos
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000212700
UNII	V37C3HG6K7
Flora of Alabama	5450
Canadensys	5753
USDA Plants	LAOD
Tropicos	13021655
INPN	105237
Flora of Italy	2496
KEW	urn:lsid:ipni.org:names:501909-1
The Plant List	ild-7772
Missouri Botanical Garden	280383
PFAF	Lathyrus odoratus
Open Tree Of Life	1036603
Observations.org	136359
NCBI Taxonomy	3859
NBN Atlas	NBNSYS0000032271
Nature Serve	2.132662
IUCN Red List	176367
IPNI	501909-1
iNaturalist	77641
GBIF	5356514
Freebase	/m/09vg7s
EPPO	LTHOD
EOL	703179
Elurikkus	5402
Calflora (Californian flora)	4616
US Library of Congress	sh85131179
USDA GRIN	21596
Wikipedia	Sweet_pea

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

The Physiological and Molecular Mechanisms of Silicon Action in Salt Stress Amelioration

Dabravolski SA, Isayenkov SV

Plants (Basel)

15-Feb-2024

PMCID:	PMC10893008
doi:	10.3390/plants13040525
PMID:	38498577

An appraisal of traditional knowledge of plant poisoning of livestock and its validation through acute toxicity assay in rats

Rasool F, Nizamani ZA, Ahmad KS, Parveen F, Khan SA, Sabir N

Front Pharmacol

14-Feb-2024

PMCID:	PMC10900104
doi:	10.3389/fphar.2024.1328133
PMID:	38420196

Nano-Priming for Inducing Salinity Tolerance, Disease Resistance, Yield Attributes, and Alleviating Heavy Metal Toxicity in Plants

Lee JH, Kasote DM

Plants (Basel)

03-Feb-2024

PMCID:	PMC10857146
doi:	10.3390/plants13030446
PMID:	38337979

Integrated transcriptomics and metabolomics analysis provides insights into aromatic volatiles formation in Cinnamomum cassia bark at different harvesting times

Yao S, Tan X, Huang D, Li L, Chen J, Ming R, Huang R, Yao C

BMC Plant Biol

02-Feb-2024

PMCID:	PMC10835945
doi:	10.1186/s12870-024-04754-w
PMID:	38308239

New Insights Into The Evolution of Chloroplast Genomes in Ochna Species (Ochnaceae, Malpighiales)

Nhat Nam N, Hoang Danh N, Minh Thiet V, Do HD

Evol Bioinform Online

15-Nov-2023

PMCID:	PMC10655658
doi:	10.1177/11769343231210756
PMID:	38020533

Prevalence of Neurolathyrism and its associated factors in Grass pea cultivation areas of Dawunt District, North-eastern Ethiopia; 2022: a community based multilevel analysis

Bimerew M, Gebremeskel T, Beletew B, Ayalneh M, Ayaliew W, Wodaje M

BMC Neurol

05-Oct-2023

PMCID:	PMC10552212
doi:	10.1186/s12883-023-03379-0
PMID:	37798732

The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.)

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

PMCID:	PMC10602594
doi:	10.1371/journal.pone.0291734
PMID:	37792900

Implementation of machine learning in DNA barcoding for determining the plant family taxonomy

Riza LS, Zain MI, Izzuddin A, Prasetyo Y, Hidayat T, Abu Samah KA

Heliyon

21-Sep-2023

PMCID:	PMC10520734
doi:	10.1016/j.heliyon.2023.e20161
PMID:	37767518

Comparative Analysis and Identification of Terpene Synthase Genes in Convallaria keiskei Leaf, Flower and Root Using RNA-Sequencing Profiling

Claude SJ, Raman G, Park SJ

Plants (Basel)

28-Jul-2023

PMCID:	PMC10421360
doi:	10.3390/plants12152797
PMID:	37570951

Salt stress responses and alleviation strategies in legumes: a review of the current knowledge

Bouzroud S, Henkrar F, Fahr M, Smouni A

3 Biotech

28-Jul-2023

PMCID:	PMC10382465
doi:	10.1007/s13205-023-03643-7
PMID:	37520340

Comprehensive Analysis of 34 Edible Flowers by the Determination of Nutritional Composition and Antioxidant Capacity Planted in Yunnan Province China

Zhang XK, Cao GH, Bi Y, Liu XH, Yin HM, Zuo JF, Xu W, Li HD, He S, Zhou XH

Molecules

06-Jul-2023

PMCID:	PMC10343634
doi:	10.3390/molecules28135260
PMID:	37446920

The terpene synthase (TPS) gene family in kiwifruit shows high functional redundancy and a subset of TPS likely fulfil overlapping functions in fruit flavour, floral bouquet and defence

Wang W, Wang MY, Zeng Y, Chen X, Wang X, Barrington AM, Tao J, Atkinson RG, Nieuwenhuizen NJ

Mol Hortic

08-May-2023

PMCID:	PMC10514967
doi:	10.1186/s43897-023-00057-0
PMID:	37789478

Biosynthesis and the Transcriptional Regulation of Terpenoids in Tea Plants (Camellia sinensis)

Wei J, Yang Y, Peng Y, Wang S, Zhang J, Liu X, Liu J, Wen B, Li M

Int J Mol Sci

08-Apr-2023

PMCID:	PMC10138656
doi:	10.3390/ijms24086937
PMID:	37108101

Chromium Toxicity in Plants: Signaling, Mitigation, and Future Perspectives

Ali S, Mir RA, Tyagi A, Manzar N, Kashyap AS, Mushtaq M, Raina A, Park S, Sharma S, Mir ZA, Lone SA, Bhat AA, Baba U, Mahmoudi H, Bae H

Plants (Basel)

29-Mar-2023

PMCID:	PMC10097182
doi:	10.3390/plants12071502
PMID:	37050128

Characterization of leaf surface phenotypes based on light interaction

Peters RD, Noble SD

Plant Methods

18-Mar-2023

PMCID:	PMC10024457
doi:	10.1186/s13007-023-01004-2
PMID:	36932424

Phytochemical Profile Top

Add a new one!

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 / Prenol lipids / Diterpenoids / C19-gibberellins / C19-gibberellin 6-carboxylic acids
Gibberellin A29	14605548	Click to see	348.40	unknown	https://doi.org/10.1034/J.1399-3054.1990.790305.X
Gibberellin A8	5280607	Click to see	364.40	unknown	https://doi.org/10.1034/J.1399-3054.1990.790305.X
Gibberellin A81	101945519	Click to see	348.40	unknown	https://doi.org/10.1034/J.1399-3054.1990.790305.X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C20-gibberellins / C20-gibberellin 6-carboxylic acids
(2S,8R,12S)-8-formyl-12-hydroxy-4-methyl-13-methylidenetetracyclo[10.2.1.01,9.03,8]pentadecane-2,4-dicarboxylic acid	439634	Click to see	362.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC158818/
8-Formyl-12-hydroxy-4-methyl-13-methylidenetetracyclo[10.2.1.01,9.03,8]pentadecane-2,4-dicarboxylic acid	4632015	Click to see CC1(CCCC2(C1C(C34C2CCC(C3)(C(=C)C4)O)C(=O)O)C=O)C(=O)O	362.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC158818/
Gibberellin A19	5460209	Click to see CC1(CCCC2(C1C(C34C2CCC(C3)(C(=C)C4)O)C(=O)O)C=O)C(=O)O	362.40	unknown	https://doi.org/10.1007/BF00201618
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(6aS,6bR,12aS)-2,2,6a,6b,9,9,12a-heptamethyl-10,13-dioxo-1,3,4,5,6,6a,7,8,8a,11,12,14b-dodecahydropicene-4a-carboxylic acid	163187259	Click to see CC1(CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C(=O)O)C	468.70	unknown	https://doi.org/10.1271/BBB.63.189 https://doi.org/10.1016/J.CARRES.2005.01.013
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
2-(3-Amino-3-carboxypropyl)-isoxazolin-5-one	57350456	Click to see	188.18	unknown	https://doi.org/10.1248/BPB.16.732
2-Amino-4-hydroxypentanoic acid	14021586	Click to see	133.15	unknown	https://doi.org/10.1038/209807A0
2-Amino-5-oxo-5-[2-(5-oxo-1,2-oxazol-2-yl)ethylamino]pentanoic acid	162845103	Click to see	257.24	unknown	https://doi.org/10.1016/0031-9422(92)80033-B
> 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
(2s,4s)-4-Hydroxynorvaline	11105405	Click to see CC(CC(C(=O)O)N)O	133.15	unknown	https://doi.org/10.1038/209807A0
(2S)-2-amino-5-oxo-5-[2-(5-oxo-1,2-oxazol-2-yl)ethylamino]pentanoic acid	15167930	Click to see C1=CN(OC1=O)CCNC(=O)CCC(C(=O)O)N	257.24	unknown	https://doi.org/10.1016/0031-9422(92)80033-B
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
6-Methoxycyclohexane-1,2,3,4,5-pentol	230881	Click to see COC1C(C(C(C(C1O)O)O)O)O	194.18	unknown	https://doi.org/10.1016/J.CARRES.2005.01.013 https://doi.org/10.1271/BBB.63.189
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1S,2R,3R,4S,5S,6R)-4-methoxy-6-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexane-1,2,3,5-tetrol	102349897	Click to see	356.32	unknown	https://doi.org/10.1016/J.CARRES.2005.01.013
4-Methoxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexane-1,2,3,5-tetrol	74427834	Click to see	356.32	unknown	https://doi.org/10.1016/J.CARRES.2005.01.013
> Organoheterocyclic compounds / Azoles / Isoxazoles
2-(2-Carboxyethyl)-3-isoxazolin-5-one	86255867	Click to see	157.12	unknown	https://doi.org/10.1248/CPB.32.2450
> Organoheterocyclic compounds / Azolines / Isoxazolines / Isoxazolinones
2-Cyanoethyl-isoxazolin-5-one	129701839	Click to see C1C(=NOC1=O)CCC#N	138.12	unknown	https://doi.org/10.1016/S0031-9422(00)83440-8
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
3-Ethyl-5,7-dimethoxychromen-4-one	129862895	Click to see CCC1=COC2=C(C1=O)C(=CC(=C2)OC)OC	234.25	unknown	https://doi.org/10.1016/0031-9422(88)84092-5
Lathodoratin	5281344	Click to see	206.19	unknown	https://doi.org/10.1016/S0031-9422(00)82217-7 https://doi.org/10.1016/0031-9422(88)84092-5
Methyl-lathodoratin	5376283	Click to see	220.22	unknown	https://doi.org/10.1016/0031-9422(88)84092-5
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Leucoanthocyanidins
(2R,3R,4R)-2-(3,4-Dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,4,7,8-tetrol	169996	Click to see	306.27	unknown	https://doi.org/10.1016/S0031-9422(00)80519-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Kuromanin	441667	Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	449.40	unknown	https://doi.org/10.1038/187240A0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
Pelargonin	441772	Click to see	595.50	unknown	https://doi.org/10.1038/187240A0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	162855252	Click to see	726.60	unknown	https://doi.org/10.1016/0305-1978(93)90077-5
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
Flavylium, 3,3',4',5,5',7-hexahydroxy-	128853	Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O	303.24	unknown	https://doi.org/10.1111/J.1469-8137.1960.TB06211.X
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(+)-Pisatin	101689	Click to see	314.29	unknown	https://doi.org/10.1016/S0031-9422(00)80519-1
(1R,12S)-16-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-1-ol	162882364	Click to see COC1=CC2=C(C=C1)C3C(CO2)(C4=CC5=C(C=C4O3)OCO5)O	314.29	unknown	https://doi.org/10.1016/0031-9422(88)84092-5
(1S,12S)-16-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaene	373519	Click to see	298.29	unknown	https://doi.org/10.1016/S0031-9422(00)82217-7
3-Methoxy-8,9-methylenedioxypterocarpan	454895	Click to see COC1=CC2=C(C=C1)C3C(CO2)C4=CC5=C(C=C4O3)OCO5	298.29	unknown	https://doi.org/10.1016/S0031-9422(00)82217-7
6H-[1,3]Dioxolo[5,6]benzofuro[3,2-c][1]benzopyran-6a(12aH)-ol,3-methoxy-, (6aR,12aR)-	4484953	Click to see	314.29	unknown	https://doi.org/10.1016/S0031-9422(00)80519-1 https://doi.org/10.1016/0031-9422(88)84092-5
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids
(2R)-1-(2,4-dimethoxyphenyl)-2-hydroxy-3-(4-methoxyphenyl)propan-1-one	163047694	Click to see COC1=CC=C(C=C1)CC(C(=O)C2=C(C=C(C=C2)OC)OC)O	316.30	unknown	https://doi.org/10.1016/0031-9422(88)84092-5 https://doi.org/10.1016/S0031-9422(00)80519-1
O-Methylodoratol	442421	Click to see COC1=CC=C(C=C1)CC(C(=O)C2=C(C=C(C=C2)OC)OC)O	316.30	unknown	https://doi.org/10.1016/S0031-9422(00)80519-1 https://doi.org/10.1016/0031-9422(88)84092-5
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
(2R)-2-hydroxy-1-(2-hydroxy-4-methoxyphenyl)-3-(4-methoxyphenyl)propan-1-one	42607724	Click to see	302.32	unknown	https://doi.org/10.1016/S0031-9422(00)80519-1
Odoratol	442440	Click to see COC1=CC=C(C=C1)CC(C(=O)C2=C(C=C(C=C2)OC)O)O	302.32	unknown	https://doi.org/10.1016/S0031-9422(00)80519-1

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Lathyrus odoratus

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