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Lepidium meyenii

Lepidium meyenii - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

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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No description added yet. Help us by writing one.

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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Language Common/alternative name
English maca
Spanish maca
Spanish maca - lepidium meyenii
Arabic عشبة الماكا
ba Ҡандалагөл
Czech řeřicha peruánská
German peruanischer ginseng
German maca
German maca-pflanze
German maca (pflanze)
Greek Μάκα
Persian جینسینگ پرویی
Finnish andienkrassi
Finnish maca-juuri
French maca
Hungarian perui ginzeng
Hungarian maca
Italian maca
Japanese maca
Japanese マカ
Korean 마카
Lithuanian peruvinė pipirnė
Lithuanian maca
Macedonian Мака
Portuguese maca peruana
Quechua maka
Quechua hayaq willk'u
Quechua ayaq chichira
Quechua anu kara
Quechua maca
Romanian maca
Russian Клоповник Мейена
Russian Мака перуанская
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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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.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • 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
Non-invasive prediction of maca powder adulteration using a pocket-sized spectrophotometer and machine learning techniques Zaukuu JL, Adams ZS, Donkor-Boateng NA, Mensah ET, Bimpong D, Amponsah LA Sci Rep 07-May-2024
PMCID:PMC11076633
doi:10.1038/s41598-024-61220-1
PMID:38714752
Ameliorative effects of elderberry (Sambucus nigra L.) extract and extract-derived monosaccharide-amino acid on H2O2-induced decrease in testosterone-deficiency syndrome in a TM3 Leydig cell Lee S, Kim J, Kong H, Kim YS PLoS One 25-Apr-2024
PMCID:PMC11045058
doi:10.1371/journal.pone.0302403
PMID:38662754
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
Influence of dietary supplementation with Lepidium meyenii (Maca) on sperm quality in dogs Gattuso DT, Polisca A, Interlandi CD, Rizzo M, Tabbì M, Giudice E, Cristarella S, Rifici C, Quartuccio M, Zappone V Front Vet Sci 29-Feb-2024
PMCID:PMC10937364
doi:10.3389/fvets.2024.1375146
PMID:38487706
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
Exploring the chemical and pharmacological variability of Lepidium meyenii: a comprehensive review of the effects of maca Ulloa del Carpio N, Alvarado-Corella D, Quiñones-Laveriano DM, Araya-Sibaja A, Vega-Baudrit J, Monagas-Juan M, Navarro-Hoyos M, Villar-López M Front Pharmacol 19-Feb-2024
PMCID:PMC10910417
doi:10.3389/fphar.2024.1360422
PMID:38440178
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
In vitro immune-enhancing effects of Platycodon grandiflorum combined with Salvia plebeian via MAPK and NF-κB signaling in RAW264.7 cells Jang AY, Kim M, Rod-in W, Nam YS, Yoo TY, Park WJ PLoS One 02-Feb-2024
PMCID:PMC10836713
doi:10.1371/journal.pone.0297512
PMID:38306362
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
Bioactive compounds as potential alternative treatments to prevent cancer therapy-induced male infertility Simón L, Mariotti-Celis MS Front Endocrinol (Lausanne) 18-Jan-2024
PMCID:PMC10831851
doi:10.3389/fendo.2023.1293780
PMID:38303979
Is there a difference between the effects of phytoestrogens and non-phytoestrogens medicinal plants on sexual health? A systematic review and meta-analysis Sayahi M, Keramat A, Nourimand1 Ph.D. Candidate F, Mohammadzadeh H Int J Reprod Biomed 19-Dec-2023
PMCID:PMC10823120
doi:10.18502/ijrm.v21i11.14652
PMID:38292511
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

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
Elaidolinolenic 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
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
> 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
Isofucosterol 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-Methoxy-3-indolylmethyl glucosinolate 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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