Ephedra equisetina - Unknown
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Details Top

Internal ID UUID644028c354c01156856155
Scientific name Ephedra equisetina
Authority Bunge
First published in Beitr. Fl. Russl. : 324 (1852)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ephedra equisetina var. monoica Y.Yang Acta Phytotax. Sin. 38: 385 (2000)
Ephedra nebrodensis subsp. equisetina (Bunge) Breistr. ex Greuter & Burdet Willdenowia 13: 278 (1983 publ. 1984)
Ephedra shennungiana T.H.Tang J. Amer. Pharm. Assoc. 17: 339 (1928)

Common names Top

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Language Common/alternative name
English ma huang
Azerbaijani qatırquyruğuyabənzər acılıqotu
Czech chvojník přesličkovitý
Japanese 木賊麻黄
Japanese モクゾクマオウ
Kazakh Қырықбуынды қылша
mn Морин зээргэнэ
Polish przęśl skrzypowata
Russian Эфедра хвощевая
Russian Хвойник хвощевый
Ukrainian Ефедра гірська
Chinese 木麻黄
Chinese 山麻黄
Chinese 木贼麻黄
Chinese 麻黄根
Chinese 麻黄
Chinese 苡芭菊

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
  • Asia-temperate
    • Caucasus
      • North Caucasus
    • China
      • China North-central
      • Inner Mongolia
      • Qinghai
      • Xinjiang
    • Middle Asia
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Primorye
    • Siberia
      • Altay
      • Krasnoyarsk
      • Tuva
      • West Siberia
    • Western Asia
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000794353
UNII L49PWN69DY
USDA Plants EPEQ2
Tropicos 14300094
KEW urn:lsid:ipni.org:names:928049-1
The Plant List kew-332918
Open Tree Of Life 878619
Observations.org 124425
NCBI Taxonomy 173280
IPNI 928049-1
iNaturalist 135495
GBIF 2653316
EPPO EPEEQ
EOL 1156283
US Library of Congress sh85044253
USDA GRIN 15221
CMAUP NPO28125

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
Distribution Pattern of Suitable Areas and Corridor Identification of Endangered Ephedra Species in China Zhang H, Li J, Zou H, Wang Z, Zhu X, Zhang Y, Liu Z Plants (Basel) 20-Mar-2024
PMCID:PMC10975542
doi:10.3390/plants13060890
PMID:38592953
Integrating artificial intelligence into the modernization of traditional Chinese medicine industry: a review Zhou E, Shen Q, Hou Y Front Pharmacol 23-Feb-2024
PMCID:PMC10921893
doi:10.3389/fphar.2024.1181183
PMID:38464717
Feed plants, ethnoveterinary medicine, and biocultural values: insights on the Luchuan pig from Hakka communities in China Liufu Y, Zhou J, Fu Q, Shao M, Xie Y, Luo B J Ethnobiol Ethnomed 15-Sep-2023
PMCID:PMC10502998
doi:10.1186/s13002-023-00613-4
PMID:37710305
Potential herb–drug interactions between anti-COVID-19 drugs and traditional Chinese medicine Ye L, Fan S, Zhao P, Wu C, Liu M, Hu S, Wang P, Wang H, Bi H Acta Pharm Sin B 05-Jun-2023
PMCID:PMC10239737
doi:10.1016/j.apsb.2023.06.001
PMID:37360014
Study on wild medicinal plant resources and their applied ethnology in multiethnic areas of the Gansu–Ningxia–Inner Mongolia intersection zone Xie J, Luo C, Yang X, Ren Y, Zhang X, Chen H, Zhao Y, Liu S, Wu F J Ethnobiol Ethnomed 20-May-2023
PMCID:PMC10199607
doi:10.1186/s13002-023-00585-5
PMID:37210577
The use of Ephedra herbs in the treatment of COVID-19 Sadeghi Dousari A, Karimian Amroabadi M, Soofi Neyestani Z, Taati Moghadam M, Satarzadeh N Avicenna J Phytomed 01-May-2023
PMCID:PMC10465882
doi:10.22038/AJP.2022.21607
PMID:37654998
Addressing the Relationship between Leaf Nitrogen and Carbon Isotope Discrimination from the Three Levels of Community, Population and Individual Wang S, Han Y, Jia Y, Chen Z, Wang G Plants (Basel) 04-Apr-2023
PMCID:PMC10097192
doi:10.3390/plants12071551
PMID:37050177
Modeling for Predicting the Potential Geographical Distribution of Three Ephedra Herbs in China Guo L, Gao Y, He P, He Y, Meng F Plants (Basel) 09-Feb-2023
PMCID:PMC9963152
doi:10.3390/plants12040787
PMID:36840134
Interaction between Chinese medicine and digoxin: Clinical and research update Zhuang W, He T, Jia BB, Wang ZZ, Zhang L, Dong XZ, Xi SY Front Pharmacol 07-Feb-2023
PMCID:PMC9941676
doi:10.3389/fphar.2023.1040778
PMID:36825153
Ephedrae Herba: A Review of Its Phytochemistry, Pharmacology, Clinical Application, and Alkaloid Toxicity Tang S, Ren J, Kong L, Yan G, Liu C, Han Y, Sun H, Wang XJ Molecules 09-Jan-2023
PMCID:PMC9863261
doi:10.3390/molecules28020663
PMID:36677722
Tackling the Future Pandemics: Broad-Spectrum Antiviral Agents (BSAAs) Based on A-Type Proanthocyanidins Maffei ME, Salata C, Gribaudo G Molecules 30-Nov-2022
PMCID:PMC9736452
doi:10.3390/molecules27238353
PMID:36500445
Traditional Chinese Medicine in Treatment of COVID-19 and Viral Disease: Efficacies and Clinical Evidence Ding X, Fan LL, Zhang SX, Ma XX, Meng PF, Li LP, Huang MY, Guo JL, Zhong PZ, Xu LR Int J Gen Med 28-Nov-2022
PMCID:PMC9718497
doi:10.2147/IJGM.S386375
PMID:36465269
An Amide Alkaloid Isolated from Ephedra sinica Ameliorates OVA-Induced Allergic Asthma by Inhibiting Mast Cell Activation and Dendritic Cell Maturation Jia J, Zeng M, Zhu D, Jiao X, Zhang B, Yang R, Feng W, Zheng X Int J Mol Sci 04-Nov-2022
PMCID:PMC9655655
doi:10.3390/ijms232113541
PMID:36362328
Comparative chloroplast genome analysis of Ficus (Moraceae): Insight into adaptive evolution and mutational hotspot regions Zhang ZR, Yang X, Li WY, Peng YQ, Gao J Front Plant Sci 15-Sep-2022
PMCID:PMC9521400
doi:10.3389/fpls.2022.965335
PMID:36186045
Successful Intervention with Traditional Chinese Medicine for Severe Coronavirus Disease 2019: A Case Report Lu W, Zhang W, Xu X, Guo Q, Fang B 19-Aug-2022
PMCID:PMC9549768
doi:10.4103/2773-0387.348715

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown https://doi.org/10.1007/BF00563959
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1007/BF00563959
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1007/BF00563959
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1007/BF00563959
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
(-)-Ephedrinium 6922965 Click to see CC(C(C1=CC=CC=C1)O)[NH2+]C 166.24 unknown via CMAUP database
(-)-Norephedrine 10297 Click to see CC(C(C1=CC=CC=C1)O)N 151.21 unknown via CMAUP database
(-)-Pseudoephedrine 62946 Click to see CC(C(C1=CC=CC=C1)O)NC 165.23 unknown via CMAUP database
(+)-N-Methylephedrine 102023 Click to see CC(C(C1=CC=CC=C1)O)N(C)C 179.26 unknown via CMAUP database
(+)-N-Methylpseudoephedrine 7059596 Click to see CC(C(C1=CC=CC=C1)O)N(C)C 179.26 unknown via CMAUP database
(1R,2R)-2-(dimethylamino)-1-phenylpropan-1-ol 5706040 Click to see CC(C(C1=CC=CC=C1)O)N(C)C 179.26 unknown via CMAUP database
(1r,2s)-n-Methylephedrine 6918907 Click to see CC(C(C1=CC=CC=C1)O)[NH+](C)C 180.27 unknown via CMAUP database
(1S,2S)-(+)-norpseudoephedrine 6918945 Click to see CC(C(C1=CC=CC=C1)O)[NH3+] 152.21 unknown via CMAUP database
(1S)-1-Phenyl-2-(methylamino)-1-propanol 11972440 Click to see CC(C(C1=CC=CC=C1)O)NC 165.23 unknown via CMAUP database
(2S)-2-amino-1-((1,2,3,4,5,6-14C6)cyclohexatrienyl)propan-1-ol 10080695 Click to see CC(C(C1=CC=CC=C1)O)N 163.16 unknown via CMAUP database
[(1R,2S)-1-hydroxy-1-phenylpropan-2-yl]-dimethylazanium;chloride 11954231 Click to see CC(C(C1=CC=CC=C1)O)[NH+](C)C.[Cl-] 215.72 unknown via CMAUP database
1-Phenyl-1,2-propanedione 11363 Click to see CC(=O)C(=O)C1=CC=CC=C1 148.16 unknown via CMAUP database
Besan 25137849 Click to see [H+].CC(C(C1=CC=CC=C1)O)NC.[Cl-] 201.69 unknown via CMAUP database
Cathine 441457 Click to see CC(C(C1=CC=CC=C1)O)N 151.21 unknown via CMAUP database
d-Ephedrine 9457 Click to see CC(C(C1=CC=CC=C1)O)NC 165.23 unknown via CMAUP database
DL-Methylephedrine saccharinate 9851505 Click to see CC(C(C1=CC=CC=C1)O)N(C)C 179.26 unknown via CMAUP database
Ephedrine 9294 Click to see CC(C(C1=CC=CC=C1)O)NC 165.23 unknown https://doi.org/10.1007/BF00596651
https://doi.org/10.1007/S11418-011-0528-8
Methylephedrine 64782 Click to see CC(C(C1=CC=CC=C1)O)N(C)C 179.26 unknown via CMAUP database
N-Methylephedrine 4374 Click to see CC(C(C1=CC=CC=C1)O)N(C)C 179.26 unknown via CMAUP database
Norpseudoephedrine 162265 Click to see CC(C(C1=CC=CC=C1)O)N 151.21 unknown via CMAUP database
Phenylpropanolamine 26934 Click to see CC(C(C1=CC=CC=C1)O)N 151.21 unknown via CMAUP database
Propadrine 4786 Click to see CC(C(C1=CC=CC=C1)O)N 151.21 unknown via CMAUP database
Pseudoephedrine 7028 Click to see CC(C(C1=CC=CC=C1)O)NC 165.23 unknown https://doi.org/10.1007/BF00596651
Racephedrine 5032 Click to see CC(C(C1=CC=CC=C1)O)NC 165.23 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
4-Methoxystyrene 12507 Click to see COC1=CC=C(C=C1)C=C 134.17 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(-)-Synephrine 854067 Click to see CNCC(C1=CC=C(C=C1)O)O 167.20 unknown via CMAUP database
(+)-Synephrine 667452 Click to see CNCC(C1=CC=C(C=C1)O)O 167.20 unknown via CMAUP database
(R)-synephrine 6951208 Click to see C[NH2+]CC(C1=CC=C(C=C1)O)O 168.21 unknown via CMAUP database
Synephrine 7172 Click to see CNCC(C1=CC=C(C=C1)O)O 167.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl butyrate 12180 Click to see CCCC(=O)OC 102.13 unknown via CMAUP database
Methyl Stearate 8201 Click to see CCCCCCCCCCCCCCCCCC(=O)OC 298.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
1,4-Cineole 10106 Click to see CC(C)C12CCC(O1)(CC2)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol 443162 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Alpha-Tocopherol 14985 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown https://doi.org/10.1007/BF02236284
Covi-ox 6560141 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown https://doi.org/10.1007/BF02236284
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
[(1R,2S,5R,6R,7R,9R)-7-acetyloxy-5-hydroxy-6-(hydroxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-8-yl] benzoate 6325577 Click to see CC1CCC(C2(C13CC(C(C2OC(=O)C)OC(=O)C4=CC=CC=C4)C(O3)(C)C)CO)O 432.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
[(1S,4aR,7S,7aS)-7-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-5-yl] 4-hydroxybenzoate 6325359 Click to see CC1(CC(C2C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C4=CC=C(C=C4)O)O 468.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3R,4R,5R,6S)-2-[(2R,3S,4R,5R,6R)-6-[[3,12-dihydroxy-17-[(5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-yl]oxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 6325857 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3CC4(C(CC(C5C4(CCC5C6(CCC(O6)C(C)(C)O)C)C)O)C7(C3C(C(CC7)O)(C)C)C)C)CO)O)O)O 801.00 unknown via CMAUP database
2alpha,3alpha,19,24-Tetrahydroxyurs-12-ene-28-oic acid beta-D-glucopyranosyl ester 100956042 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O 666.80 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 https://doi.org/10.1007/BF02236284
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(5aR,9S,11aS,13bR)-9-methoxy-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-2,3,4,5,5b,6,7,7a,9,10,11,13b-dodecahydro-1H-cyclopenta[a]chrysen-13-one 5320321 Click to see CC(C)C1CCC2C1(CCC3(C2(C(=O)C=C4C3CCC5C4(CCC(C5(C)C)OC)C)C)C)C 454.70 unknown via CMAUP database
24-Hydroxytormentic acid 14055737 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1(C)O)C)C(=O)O 504.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1007/BF02236284
methyl 6-[(10S,13R,17R)-7,15-dihydroxy-4,4,10,13,14-pentamethyl-3,11-dioxo-2,5,6,7,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methyl-4-oxoheptanoate 5319630 Click to see CC(CC(=O)CC(C)C(=O)OC)C1CC(C2(C1(CC(=O)C3=C2C(CC4C3(CCC(=O)C4(C)C)C)O)C)C)O 530.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol 5997 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown https://doi.org/10.1007/BF02236284
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
(3S,8R,9S,13R)-9-ethyl-4,4,13,14-tetramethyl-17-(6-methylheptan-2-yl)-2,3,5,6,7,8,10,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 5316233 Click to see CCC12CCC3(C(CCC3(C1CCC4C2CCC(C4(C)C)O)C)C(C)CCCC(C)C)C 444.80 unknown https://doi.org/10.1007/BF02236284
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 145925700 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://doi.org/10.1007/BF02236284
Cycloartanol 12760132 Click to see CC(C)CCCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 428.70 unknown https://doi.org/10.1007/BF02236284
Cycloartenol 92110 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://doi.org/10.1007/BF02236284
> 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/10.1007/BF02236284
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/10.1007/BF02236284
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 6-hydroxysteroids
2-(methylamino)ethyl (2E)-2-(8-formyl-7,10-dihydroxy-1,4b,8-trimethyl-3,4,4a,5,6,7,8a,9,10,10a-decahydro-1H-phenanthren-2-ylidene)acetate 5476322 Click to see CC1C2C(CCC1=CC(=O)OCCNC)C3(CCC(C(C3CC2O)(C)C=O)O)C 407.50 unknown via CMAUP database
> 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/BF02236284
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/BF02236284
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/10.1007/BF02236284
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
2-Oxo-2-oxonioacetate 18676629 Click to see [H+].[H+].C(=O)(C(=O)[O-])[O-] 90.03 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
Hydron;2-hydroxybutanedioate 20130941 Click to see [H+].[H+].C(C(C(=O)[O-])O)C(=O)[O-] 134.09 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Tertiary amines / Trialkylamines
N,N-Dimethylisopropylamine 70452 Click to see CC(C)N(C)C 87.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
((2R,3S,4S,5R,6S)-3,4,5-Trihydroxy-6-(2,4,6-trimethoxyphenoxy)tetrahydro-2H-pyran-2-yl)methyl 3,4,5-trihydroxybenzoate 21670002 Click to see COC1=CC(=C(C(=C1)OC)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)OC 498.40 unknown via CMAUP database
(2R,3S,4S,5R,6S)-2-(Hydroxymethyl)-6-(2,4,6-trimethoxyphenoxy)tetrahydro-2H-pyran-3,4,5-triol 23259943 Click to see COC1=CC(=C(C(=C1)OC)OC2C(C(C(C(O2)CO)O)O)O)OC 346.33 unknown via CMAUP database
4-O-beta-D-glucosyl-4-coumaric acid 9840292 Click to see C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
Cibarin 322363 Click to see C(C[N+](=O)[O-])C(=O)OCC1C(C(C(C(O1)OC(=O)CC[N+](=O)[O-])O)O)O 382.28 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(+)-Cathinone 149798 Click to see CC(C(=O)C1=CC=CC=C1)N 149.19 unknown via CMAUP database
(Z)-1-(2,6-dihydroxy-4-methoxyphenyl)oct-5-en-1-one 11957912 Click to see CCC=CCCCC(=O)C1=C(C=C(C=C1O)OC)O 264.32 unknown via CMAUP database
1-(2,6-Dihydroxy-4-methoxyphenyl)-1-hexanone 11957913 Click to see CCCCCC(=O)C1=C(C=C(C=C1O)OC)O 238.28 unknown via CMAUP database
2-Aminopropiophenone 107786 Click to see CC(C(=O)C1=CC=CC=C1)N 149.19 unknown via CMAUP database
Cathinone 62258 Click to see CC(C(=O)C1=CC=CC=C1)N 149.19 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(2R,3S,4R,5R)-2-butoxy-2-(hydroxymethyl)oxane-3,4,5-triol 50914217 Click to see CCCCOC1(C(C(C(CO1)O)O)O)CO 236.26 unknown via CMAUP database
> Organoheterocyclic compounds / Azolidines / Oxazolidines / Oxazolidinones
3,4-Dimethyl-5-phenyl-1,3-oxazolidin-2-one 237192 Click to see CC1C(OC(=O)N1C)C2=CC=CC=C2 191.23 unknown via CMAUP database
Ephedroxane 161171 Click to see CC1C(OC(=O)N1C)C2=CC=CC=C2 191.23 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrazines
2,3,5,6-Tetramethylpyrazine 14296 Click to see CC1=C(N=C(C(=N1)C)C)C 136.19 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
5,6,8-trihydroxy-2-methylbenzo[g]chromen-4-one 5320218 Click to see CC1=CC(=O)C2=C(C3=C(C=C(C=C3C=C2O1)O)O)O 258.23 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Dihydrofuranoquinolines
O-Methylptelefolonium 148759 Click to see CC(=C)C1CC2=C(C3=C(C(=CC(=C3)OC)OC)[N+](=C2O1)C)OC 316.40 unknown via CMAUP database
> Organosulfur compounds / Thioethers / Aryl thioethers
N4,N6-dicyclopentyl-2-(methylthio)-5-nitropyrimidine-4,6-diamine 6604928 Click to see CSC1=NC(=C(C(=N1)NC2CCCC2)[N+](=O)[O-])NC3CCCC3 337.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1007/BF00563959
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1007/BF00563959
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1007/BF00563959
> Phenylpropanoids and polyketides / Cinnamyl alcohols
1-Dideuterio-3-phenylprop-2-en-1-ol 10534709 Click to see C1=CC=C(C=C1)C=CCO 136.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
(-)-Epiafzelechin 443639 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC=C(C=C3)O)O 274.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Myricitrin 5281673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown via CMAUP database
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Protocatechuic acid 3-glucoside 11972438 Click to see C1=CC(=C(C=C1C(=O)O)OC2C(C(C(C(O2)CO)O)O)O)O 316.26 unknown via CMAUP database

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