Lepidium meyenii

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID643ff3e3a8ded128760977
Scientific name	Lepidium meyenii
Authority	Walp.
First published in	Nov. Actorum Acad. Caes. Leop.-Carol. Nat. Cur. 19(Suppl. 1): 249 (1843)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Lepidium gelidum	Wedd.	Ann. Sci. Nat., Bot. , sér. 5, 1: 283 (1864)
Lepidium weddellii	O.E.Schulz	Notizbl. Bot. Gart. Berlin-Dahlem 11: 391 (1932)
Lepidium meyenii var. gelidum	Hosseus	Bol. Acad. Nac. Ci. Republ. Argent. 26: 101 (1921)
Lepidium meyenii subsp. gelidum	Thell.	Neue Denkschr. Schweiz. Naturf. Ges. 41(Abh. 1): 203 (1906)
Lepidium meyenii var. affine	Thell.	Neue Denkschr. Schweiz. Naturf. Ges. 41(Abh. 1): 204 (1906)
Lepidium peruvianum	G.Chacón	Revista Peru. Biol. 3: 202 (1990)
Lepidium affine	Wedd.	Ann. Sci. Nat., Bot. , sér. 5, 1: 284 (1864)
Lepidium orbignyanum	Wedd.

Common names Top

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Filter by language:

Language	Common/alternative name
English	maca
Spanish	maca
Spanish	maca - lepidium meyenii
Arabic	عشبة الماكا
Azerbaijani	lepidium peruvianum
ba	Ҡандалагөл
Czech	řeřicha peruánská
German	maca
German	peruanischer ginseng
German	maca-pflanze
German	maca (pflanze)
German	lepidium peruvianum chacón
German	lepidium peruvianum
Greek	Μάκα
Persian	جینسینگ پرویی
Finnish	andienkrassi
Finnish	maca-juuri
French	maca
Hungarian	maca
Hungarian	perui ginzeng
Italian	maca
Japanese	maca
Japanese	マカ
Korean	마카
la	lepidium peruvianum chacon
Lithuanian	maca
Lithuanian	peruvinė pipirnė
Macedonian	Мака
Portuguese	maca peruana
Quechua	ayaq chichira
Quechua	maca
Quechua	maka
Quechua	lepidium peruvianum
Quechua	hayaq willk'u
Quechua	anu kara
Romanian	maca
Russian	Мака перуанская
Russian	Клоповник Мейена
Slovak	Žerucha peruánska
Slovenian	maca
Serbian	peruanska maka
Swedish	maca
Turkish	maca
Chinese	瑪卡
Chinese	玛咖
Chinese	印加萝卜

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

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Southern America click to expand
- Southern South America
  - Argentina Northwest
  - Chile North
- Western South America
  - Bolivia
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000358330
UNII	94866V8426
USDA Plants	LEME19
Tropicos	4100898
KEW	urn:lsid:ipni.org:names:286286-1
The Plant List	kew-2337886
Open Tree Of Life	681784
Observations.org	420170
NCBI Taxonomy	153348
IPNI	286286-1
iNaturalist	372676
GBIF	5377042
Freebase	/m/04_n9y
EPPO	LEPME
EOL	483599
Elurikkus	530591
US Library of Congress	sh98005069
USDA GRIN	21767
Wikipedia	Lepidium_meyenii

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

UPLC-TQD-MS/MS Method Validation for Quality Control of Alkaloid Content in Lepidium meyenii (Maca)-Containing Food and Dietary Supplements

Le NT, Foubert K, Theunis M, Naessens T, Bozdag M, Van Der Veken P, Pieters L, Tuenter E

ACS Omega

26-Mar-2024

PMCID:	PMC11007719
doi:	10.1021/acsomega.3c09356
PMID:	38617670

Adulteration of Brain Health (Cognitive, Mood, and Sleep Enhancement) Food Supplements by the Addition of Pharmaceutical Drugs: A Comprehensive Review of Analytical Approaches and Trends

Paiva R, Correia M, Delerue-Matos C, Amaral JS

Foods

16-Mar-2024

PMCID:	PMC10969376
doi:	10.3390/foods13060908
PMID:	38540898

Nutraceuticals known to promote hair growth do not interfere with the inhibitory action of tamoxifen in MCF7, T47D and BT483 breast cancer cell lines

Baker R, Dell’Acqua G, Richards A, Thornton MJ

PLoS One

26-Feb-2024

PMCID:	PMC10896530
doi:	10.1371/journal.pone.0297080
PMID:	38408073

Effect of MCH1, a fatty-acid amide hydrolase inhibitor, on the depressive-like behavior and gene expression of endocannabinoid and dopaminergic-signaling system in the mouse nucleus accumbens

Medina-Saldivar C, Pardo GV, Pacheco-Otalora LF

Braz J Med Biol Res

19-Feb-2024

PMCID:	PMC10880885
doi:	10.1590/1414-431X2024e12857
PMID:	38381881

Not All Maca Is Created Equal: A Review of Colors, Nutrition, Phytochemicals, and Clinical Uses

Minich DM, Ross K, Frame J, Fahoum M, Warner W, Meissner HO

Nutrients

14-Feb-2024

PMCID:	PMC10892513
doi:	10.3390/nu16040530
PMID:	38398854

The effects of herbal plant extract on the growth performance, blood parameters, nutrient digestibility and carcase quality of rabbits: A meta-analysis

Adli DN, Sugiharto S, Irawan A, Tribudi YA, Wibowo S, Azmi AF, Sjofjan O, Jayanegara A, Tistiana H, Wahyono T, Aditya S, Sholikin MM, Sadarman S

Heliyon

10-Feb-2024

PMCID:	PMC10877253
doi:	10.1016/j.heliyon.2024.e25724
PMID:	38380018

Influence of β-Ionone in the Phytotoxicity of the Rhizome of Iris pallida Lam

Sothearith Y, Appiah KS, Sophea C, Smith J, Samal S, Motobayashi T, Fujii Y

Plants (Basel)

22-Jan-2024

PMCID:	PMC10819377
doi:	10.3390/plants13020326
PMID:	38276783

Effects of Black Maca supplement on isokinetics muscular performance of elite women’s handball players: placebo-controlled, crossover study

Kang S, Ahn BO, Park MH, Lim ST, Lee E

Food Nutr Res

15-Dec-2023

PMCID:	PMC10770698
doi:	10.29219/fnr.v67.10250
PMID:	38187794

The Protective Effect of Auricularia cornea var. Li. Polysaccharide on Alcoholic Liver Disease and Its Effect on Intestinal Microbiota

Wang T, Jia Z, An C, Ren P, Yang Y, Wang W, Su L

Molecules

08-Dec-2023

PMCID:	PMC10745760
doi:	10.3390/molecules28248003
PMID:	38138493

Antifatigue effects and antioxidant activity in polysaccharide fractions from Chinese yam bulbils

Zhou H, Zhang X, Huang R, Su T

Food Sci Nutr

21-Nov-2023

PMCID:	PMC10867482
doi:	10.1002/fsn3.3836
PMID:	38370048

Jatonik polyherbal mixture induced rat liver MMPT pore opening in normal Wistar rat: In vitro and in vivo studies

Folashade OP, Boyenle ID, Oyedeji TA, Ojeniyi FD, Damilare AA, Ehigie LO, Ehigie AF

Chin Herb Med

16-Oct-2023

PMCID:	PMC10874763
doi:	10.1016/j.chmed.2023.06.002
PMID:	38375053

Role of the pharmacist in the management of postmenopausal breast cancer treatment with vasomotor symptoms: A case report

Undeberg MR, Barash A, McKeirnan KC

Explor Res Clin Soc Pharm

24-Aug-2023

PMCID:	PMC10485165
doi:	10.1016/j.rcsop.2023.100324
PMID:	37694166

Dietary Supplements for Erectile Dysfunction: Analysis of Marketed Products, Systematic Review, Meta-Analysis and Rational Use

Petre GC, Francini-Pesenti F, Vitagliano A, Grande G, Ferlin A, Garolla A

Nutrients

22-Aug-2023

PMCID:	PMC10490034
doi:	10.3390/nu15173677
PMID:	37686709

Dietary Polysaccharides Exert Anti-Fatigue Functions via the Gut-Muscle Axis: Advances and Prospectives

Zhou Y, Chu Z, Luo Y, Yang F, Cao F, Luo F, Lin Q

Foods

17-Aug-2023

PMCID:	PMC10453516
doi:	10.3390/foods12163083
PMID:	37628082

Botanical drugs for treating erectile dysfunction: clinical evidence

Xu D, Zhang Y, Bai J, Yuan H, Wang T, Liu J, Song W, Ma D

Front Pharmacol

16-Aug-2023

PMCID:	PMC10467024
doi:	10.3389/fphar.2023.1232774
PMID:	37654605

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 / Harmala alkaloids
2,3,4,9-Tetrahydro-1-methyl-1H-pyrido(3,4-B)indole-3-carboxylic acid, trans-(-)-	148447	Click to see CC1C2=C(CC(N1)C(=O)O)C3=CC=CC=C3N2	230.26	unknown	https://doi.org/10.1021/JF020280X
Tetrahydroharman-3-carboxylic acid	73530	Click to see CC1C2=C(CC(N1)C(=O)O)C3=CC=CC=C3N2	230.26	unknown	https://doi.org/10.1021/JF020280X
> Benzenoids / Benzene and substituted derivatives
Benzyl Isothiocyanate	2346	Click to see C1=CC=C(C=C1)CN=C=S	149.21	unknown	https://doi.org/10.1248/CPB.50.988 https://doi.org/10.1021/JF020280X
Mesitylene	7947	Click to see CC1=CC(=CC(=C1)C)C	120.19	unknown	https://doi.org/10.1016/S0031-9422(02)00208-X
Methyl mandelate	78066	Click to see COC(=O)C(C1=CC=CC=C1)O	166.17	unknown	https://doi.org/10.1007/S10565-006-0033-0
N-benzyl-5-oxooctadeca-6,8-dienamide	85815809	Click to see CCCCCCCCCC=CC=CC(=O)CCCC(=O)NCC1=CC=CC=C1	383.60	unknown	https://doi.org/10.1016/S0031-9422(01)00395-8
N-Benzylheptadecanamide	86237120	Click to see CCCCCCCCCCCCCCCCC(=O)NCC1=CC=CC=C1	359.60	unknown	https://doi.org/10.1002/PCA.871
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
(2R)-2-benzoyloxybutanedioic acid	71011646	Click to see C1=CC=C(C=C1)C(=O)OC(CC(=O)O)C(=O)O	238.19	unknown	https://doi.org/10.1021/JF020280X
Benzoylmalic acid	13953341	Click to see C1=CC=C(C=C1)C(=O)OC(CC(=O)O)C(=O)O	238.19	unknown	https://doi.org/10.1021/JF020280X
Methyl benzoate	7150	Click to see COC(=O)C1=CC=CC=C1	136.15	unknown	https://doi.org/10.1016/S0031-9422(02)00208-X
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde	240	Click to see C1=CC=C(C=C1)C=O	106.12	unknown	https://doi.org/10.1016/S0031-9422(02)00208-X
> Benzenoids / Benzene and substituted derivatives / Benzyl cyanides
(3-Methoxyphenyl)acetonitrile	88310	Click to see COC1=CC=CC(=C1)CC#N	147.17	unknown	https://doi.org/10.1016/S0031-9422(02)00208-X
Phenylacetonitrile	8794	Click to see C1=CC=C(C=C1)CC#N	117.15	unknown	https://doi.org/10.1016/S0031-9422(02)00208-X
> Benzenoids / Benzene and substituted derivatives / Benzyl thiocyanates
Benzyl thiocyanate	18170	Click to see C1=CC=C(C=C1)CSC#N	149.21	unknown	https://doi.org/10.1016/S0031-9422(02)00208-X
> Benzenoids / Benzene and substituted derivatives / Xylenes / p-Xylenes
P-Xylene	7809	Click to see CC1=CC=C(C=C1)C	106.16	unknown	https://doi.org/10.1016/S0031-9422(02)00208-X
> Benzenoids / Phenol ethers / Anisoles
(9Z,12Z)-N-(3-Methoxybenzyl)octadeca-9,12-dienamide	73346043	Click to see CCCCCC=CCC=CCCCCCCCC(=O)NCC1=CC(=CC=C1)OC	399.60	unknown	https://doi.org/10.1002/PCA.871
(9Z)-N-[(3-Methoxyphenyl)methyl]-9-octadecenamide	73346080	Click to see CCCCCCCCC=CCCCCCCCC(=O)NCC1=CC(=CC=C1)OC	401.60	unknown	https://doi.org/10.1002/PCA.871
m-Methoxybenzylisothiocyanate	126512	Click to see COC1=CC=CC(=C1)CN=C=S	179.24	unknown	https://doi.org/10.1021/JF020280X
N-((3-Methoxyphenyl)methyl)octadeca-9,12,15-trienamide, (9Z,12Z,15Z)-	73353637	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)NCC1=CC(=CC=C1)OC	397.60	unknown	https://doi.org/10.1002/PCA.871
N-(3-Methoxybenzyl)palmitamide	71765531	Click to see CCCCCCCCCCCCCCCC(=O)NCC1=CC(=CC=C1)OC	375.60	unknown	https://doi.org/10.1021/JF048529T https://doi.org/10.1002/PCA.871
> Benzenoids / Phenols / Methoxyphenols
2-Methoxy-4-vinylphenol	332	Click to see COC1=C(C=CC(=C1)C=C)O	150.17	unknown	https://doi.org/10.1016/S0031-9422(02)00208-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl arachidate	14259	Click to see CCCCCCCCCCCCCCCCCCCC(=O)OC	326.60	unknown	https://doi.org/10.1007/S10565-006-0033-0
Methyl oleate	5364509	Click to see CCCCCCCCC=CCCCCCCCC(=O)OC	296.50	unknown	https://doi.org/10.1007/S10565-006-0033-0
Methyl palmitate	8181	Click to see CCCCCCCCCCCCCCCC(=O)OC	270.50	unknown	https://doi.org/10.1007/S10565-006-0033-0
Methyl Stearate	8201	Click to see CCCCCCCCCCCCCCCCCC(=O)OC	298.50	unknown	https://doi.org/10.1007/S10565-006-0033-0
Methyl tetracosanoate	75546	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)OC	382.70	unknown	https://doi.org/10.1007/S10565-006-0033-0
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
2-Oxo-nonadecanoic acid	5312918	Click to see CCCCCCCCCCCCCCCCCC(=O)C(=O)O	312.50	unknown	https://doi.org/10.1007/S10565-006-0033-0
Myristic Acid	11005	Click to see CCCCCCCCCCCCCC(=O)O	228.37	unknown	https://doi.org/10.1016/S0090-4295(99)00549-X
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	https://doi.org/10.1016/S0031-9422(01)00395-8 https://doi.org/10.1016/S0090-4295(99)00549-X
Palmitoleic Acid	445638	Click to see CCCCCCC=CCCCCCCCC(=O)O	254.41	unknown	https://doi.org/10.1016/S0090-4295(99)00549-X
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	https://doi.org/10.1016/S0090-4295(99)00549-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid	2969	Click to see CCCCCCCCCC(=O)O	172.26	unknown	https://doi.org/10.1016/S0090-4295(99)00549-X
Lauric Acid	3893	Click to see CCCCCCCCCCCC(=O)O	200.32	unknown	https://doi.org/10.1016/S0090-4295(99)00549-X
Octanoic acid	379	Click to see CCCCCCCC(=O)O	144.21	unknown	https://doi.org/10.1016/S0090-4295(99)00549-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(12Z,15Z)-N-benzyl-9-oxooctadeca-12,15-dienamide	21579711	Click to see CCC=CCC=CCCC(=O)CCCCCCCC(=O)NCC1=CC=CC=C1	383.60	unknown	https://doi.org/10.1021/JF048529T
(9E,11E)-N-benzyl-13-oxooctadeca-9,11-dienamide	21579712	Click to see CCCCCC(=O)C=CC=CCCCCCCCC(=O)NCC1=CC=CC=C1	383.60	unknown	https://doi.org/10.1021/JF048529T
(Z)-N-benzyl-9-oxooctadec-12-enamide	21579710	Click to see CCCCCC=CCCC(=O)CCCCCCCC(=O)NCC1=CC=CC=C1	385.60	unknown	https://doi.org/10.1021/JF048529T
(Z)-N-benzyltetracos-15-enamide	73347575	Click to see CCCCCCCCC=CCCCCCCCCCCCCCC(=O)NCC1=CC=CC=C1	455.80	unknown	https://doi.org/10.1021/JF048529T
Macamide 1	11198769	Click to see CCCCCCCCCCCCCCCC(=O)NCC1=CC=CC=C1	345.60	unknown	https://doi.org/10.1248/CPB.50.988 https://doi.org/10.1002/PCA.871 https://doi.org/10.1016/S0031-9422(01)00395-8
Macamide 2	71770342	Click to see CCCCCCCCCC=CC=CC(=O)CCCC(=O)NCC1=CC=CC=C1	383.60	unknown	https://doi.org/10.1016/S0031-9422(01)00395-8
N-Benzyl-(9Z,12Z,15Z)-octadecatrienamide	68741582	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)NCC1=CC=CC=C1	367.60	unknown	https://doi.org/10.1002/PCA.871
N-benzyl-13-oxooctadeca-9,11-dienamide	73804200	Click to see CCCCCC(=O)C=CC=CCCCCCCCC(=O)NCC1=CC=CC=C1	383.60	unknown	https://doi.org/10.1021/JF048529T
N-Benzyl-9-oxooctadec-12-enamide	71406899	Click to see CCCCCC=CCCC(=O)CCCCCCCC(=O)NCC1=CC=CC=C1	385.60	unknown	https://doi.org/10.1021/JF048529T
N-benzyl-9-oxooctadeca-12,15-dienamide	73804199	Click to see CCC=CCC=CCCC(=O)CCCCCCCC(=O)NCC1=CC=CC=C1	383.60	unknown	https://doi.org/10.1021/JF048529T
N-Benzyl-linoleamide	68742556	Click to see CCCCCC=CCC=CCCCCCCCC(=O)NCC1=CC=CC=C1	369.60	unknown	https://doi.org/10.1002/PCA.871
N-benzyloctanamide	245677	Click to see CCCCCCCC(=O)NCC1=CC=CC=C1	233.35	unknown	https://doi.org/10.1016/S0090-4295(99)00549-X
N-benzyloleamide	49865534	Click to see CCCCCCCCC=CCCCCCCCC(=O)NCC1=CC=CC=C1	371.60	unknown	https://doi.org/10.1002/PCA.871
N-Benzylpentadecanamide	102326455	Click to see CCCCCCCCCCCCCCC(=O)NCC1=CC=CC=C1	331.50	unknown	https://doi.org/10.1002/PCA.871
N-benzylstearamide	220495	Click to see CCCCCCCCCCCCCCCCCC(=O)NCC1=CC=CC=C1	373.60	unknown	https://doi.org/10.1002/PCA.871
N-benzyltetracos-15-enamide	86035032	Click to see CCCCCCCCC=CCCCCCCCCCCCCCC(=O)NCC1=CC=CC=C1	455.80	unknown	https://doi.org/10.1021/JF048529T
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
5-Oxooctadeca-6,8-dienoic acid	85815814	Click to see CCCCCCCCCC=CC=CC(=O)CCCC(=O)O	294.40	unknown	https://doi.org/10.1016/S0031-9422(01)00395-8
9,12-Octadecadienoic acid, (E,Z)-	5282798	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	https://doi.org/10.1248/CPB.50.988
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	https://doi.org/10.1248/CPB.50.988
Linolenic Acid	5280934	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O	278.40	unknown	https://doi.org/10.1016/S0090-4295(99)00549-X https://doi.org/10.1248/CPB.50.988
Macaene	90478988	Click to see CCCCCCCCCC=CC=CC(=O)CCCC(=O)O	294.40	unknown	https://doi.org/10.1016/S0031-9422(01)00395-8 https://doi.org/10.1016/S0090-4295(99)00549-X
Methyl elaidolinolenate	5367462	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OC	292.50	unknown	https://doi.org/10.1007/S10565-006-0033-0
Methyl linoleate	5284421	Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC	294.50	unknown	https://doi.org/10.1007/S10565-006-0033-0
Methyl linolenate	5319706	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OC	292.50	unknown	https://doi.org/10.1007/S10565-006-0033-0
Octadeca-9,12,15-trienoic acid	5282822	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O	278.40	unknown	https://doi.org/10.1016/S0090-4295(99)00549-X https://doi.org/10.1248/CPB.50.988
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2-hexadecen-1-OL	5366244	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	https://doi.org/10.1016/S0031-9422(02)00208-X
Phytol	5280435	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	https://doi.org/10.1016/S0031-9422(02)00208-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Myrtenal	61130	Click to see CC1(C2CC=C(C1C2)C=O)C	150.22	unknown	https://doi.org/10.1016/S0031-9422(02)00208-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,2S,3S,6R,7R,8R)-1,3-dimethyl-8-prop-1-en-2-yltricyclo[4.4.0.02,7]decan-3-ol	162901363	Click to see CC(=C)C1CCC2(C3C1C2C(CC3)(C)O)C	220.35	unknown	https://doi.org/10.1021/NP030031I
Alpha-Panasinsen	91748736	Click to see CC1=CCCC2(C13CC(C3CC2)(C)C)C	204.35	unknown	https://doi.org/10.1021/NP030031I
beta-Ionone	638014	Click to see CC1=C(C(CCC1)(C)C)C=CC(=O)C	192.30	unknown	https://doi.org/10.1016/S0031-9422(02)00208-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	134766514	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/S0090-4295(99)00549-X
5-Cholestene-3-ol, 24-methyl-	312822	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/S0090-4295(99)00549-X
Brassicasterol	5281327	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	398.70	unknown	https://doi.org/10.1007/S10565-006-0033-0
Ergost-5-en-3-ol	18660356	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1007/S10565-006-0033-0
> 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/10.1007/S10565-006-0033-0 https://doi.org/10.1016/S0090-4295(99)00549-X https://doi.org/10.1016/S0031-9422(01)00395-8
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1007/S10565-006-0033-0 https://doi.org/10.1016/S0031-9422(01)00395-8 https://doi.org/10.1016/S0090-4295(99)00549-X
Fucosterol	5281326	Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1007/S10565-006-0033-0
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0090-4295(99)00549-X
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Uridine	6029	Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O	244.20	unknown	https://doi.org/10.1021/JF020280X
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(2S,3S,4R)-4-methoxy-6-oxo-2-[(E,3S,5R,6S)-3,5,6-triacetyloxyhept-1-enyl]oxan-3-yl] acetate	101267306	Click to see CC(C(CC(C=CC1C(C(CC(=O)O1)OC)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C	458.50	unknown	https://doi.org/10.1021/JF020280X
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(2S)-2-Hydroxybutanedioic acid	222656	Click to see C(C(C(=O)O)O)C(=O)O	134.09	unknown	https://doi.org/10.1021/JF020280X
Malic Acid	525	Click to see C(C(C(=O)O)O)C(=O)O	134.09	unknown	https://doi.org/10.1021/JF020280X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucosinolates / Alkylglucosinolates
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1E)-2-(3-methoxyphenyl)-N-sulfooxyethanimidothioate	9548725	Click to see COC1=CC=CC(=C1)CC(=NOS(=O)(=O)O)SC2C(C(C(C(O2)CO)O)O)O	439.50	unknown	https://doi.org/10.1021/JF020280X
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1E)-N-sulfooxyhex-5-enimidothioate	14390051	Click to see C=CCCCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O	387.40	unknown	https://doi.org/10.1007/BF02864563
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 2-(3-methoxyphenyl)-N-sulfooxyethanimidothioate	4479903	Click to see COC1=CC=CC(=C1)CC(=NOS(=O)(=O)O)SC2C(C(C(C(O2)CO)O)O)O	439.50	unknown	https://doi.org/10.1021/JF020280X
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 2-phenyl-N-sulfooxyethanimidothioate	437038	Click to see C1=CC=C(C=C1)CC(=NOS(=O)(=O)O)SC2C(C(C(C(O2)CO)O)O)O	409.40	unknown	https://doi.org/10.1021/JF020280X
{[(E)-(2-phenyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene)amino]oxy}sulfonic acid	9573945	Click to see C1=CC=C(C=C1)CC(=NOS(=O)(=O)O)SC2C(C(C(C(O2)CO)O)O)O	409.40	unknown	https://doi.org/10.1016/S0305-1978(02)00058-3
3-Indolylmethyl glucosinolate	6602378	Click to see C1=CC=C2C(=C1)C(=CN2)CC(=NOS(=O)(=O)O)SC3C(C(C(C(O3)CO)O)O)O	448.50	unknown	https://doi.org/10.1007/BF02864563
4-Methoxyglucobrassicin	9576738	Click to see COC1=CC=CC2=C1C(=CN2)CC(=NOS(=O)(=O)O)SC3C(C(C(C(O3)CO)O)O)O	478.50	unknown	https://doi.org/10.1007/BF02864563
4-Pentenylglucosinolate	9548628	Click to see C=CCCCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O	387.40	unknown	https://doi.org/10.1007/BF02864563
beta-D-Glucopyranose, 1-thio-, 1-(6-(methylsulfinyl)-N-(sulfooxy)hexanimidate)	9589398	Click to see CS(=O)CCCCCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O	451.50	unknown	https://doi.org/10.1007/BF02864563
Glucobrassicin	9601691	Click to see C1=CC=C2C(=C1)C(=CN2)CC(=NOS(=O)(=O)O)SC3C(C(C(C(O3)CO)O)O)O	448.50	unknown	https://doi.org/10.1007/BF02864563
Glucotropaeolin	9548605	Click to see C1=CC=C(C=C1)CC(=NOS(=O)(=O)O)SC2C(C(C(C(O2)CO)O)O)O	409.40	unknown	https://doi.org/10.1007/BF02864563
Glucotropeolin	6537197	Click to see C1=CC=C(C=C1)CC(=NOS(=O)(=O)O)SC2C(C(C(C(O2)CO)O)O)O	409.40	unknown	https://doi.org/10.1021/JF020280X
p-Hydroxybenzyl glucosinolate	9573049	Click to see C1=CC(=CC=C1CC(=NOS(=O)(=O)O)SC2C(C(C(C(O2)CO)O)O)O)O	425.40	unknown	https://doi.org/10.1007/BF02864563
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
alpha-Maltose	439341	Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O	342.30	unknown	https://doi.org/10.1016/J.FOODCHEM.2008.09.076
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
Mesityl oxide	8858	Click to see CC(=CC(=O)C)C	98.14	unknown	https://doi.org/10.1016/S0031-9422(02)00208-X
> Organoheterocyclic compounds / Azoles / Imidazoles / Substituted imidazoles / N-substituted imidazoles
1,3-Dibenzyl-2,4,5-trimethylimidazol-1-ium	9862175	Click to see CC1=C([N+](=C(N1CC2=CC=CC=C2)C)CC3=CC=CC=C3)C	291.40	unknown	https://doi.org/10.1016/S0031-9422(98)00275-1
1,3-Dibenzyl-4,5-dimethylimidazol-1-ium	404703	Click to see CC1=C([N+](=CN1CC2=CC=CC=C2)CC3=CC=CC=C3)C	277.40	unknown	https://doi.org/10.1016/S0031-9422(98)00275-1
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Indole	798	Click to see C1=CC=C2C(=C1)C=CN2	117.15	unknown	https://doi.org/10.1016/S0031-9422(02)00208-X
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Dihydropyridines
Macaridine	636583	Click to see C1C(=C(C=CN1O)C=O)CC2=CC=CC=C2	215.25	unknown	https://doi.org/10.1016/S0031-9422(01)00395-8

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Lepidium meyenii

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