Peganum nigellastrum

Details Top

Internal ID UUID64404fdc6d276060508894
Scientific name Peganum nigellastrum
Authority Bunge
First published in Enum. Pl. China Bor. : 13 (1833)

Ethnobotanical Use Top

Suggest a correction!
Important notice
  • 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.

Peganum nigellastrum (Bunge) has limited but documented ethnobotanical uses. In the steppe and semi‑desert margins of Inner Mongolia, healers prepare infusions of the above‑ground parts as a bitter tonic for weak digestion and loss of appetite, among Buriat healers; saponins and alkaloids such as harmine are noted to vary by habitat and may drive these actions (Komatsu et al., 1994). Among Kazakh herders in western Mongolia and northern Xinjiang, whole‑herb decoctions are taken as a colic and diarrheal remedy for stock and occasionally for humans, using brief, lightly boiled drinks (Khasbagan et al., 1998; Anke et al., 2002). In parts of northeastern China, topical macerations of fresh aerial parts are used to reduce heat, itching, and mosquito bites in the summer months, with preparation methods and seasonal timing recorded in local practice (Hu et al., 1994).

A practical preparation often employed in these communities is a mild tea of aerial parts: place 10–20 g of finely cut fresh or dried material in 500 ml of just‑boiled water, cover and steep 10–15 minutes, then strain and drink 1–2 cups per day as a tonic. A stronger digestive decoction can be made by simmering 10 g of dried herb in 300 ml water for 15 minutes; cool, strain, and sip up to one cup in small divided doses to reduce colic. For topical use, soak 30 g of fresh aerial parts in 300 ml water or dilute vinegar for 24–48 hours, strain, and apply compresses or washes as needed. Because the plant contains harmine‑type alkaloids, it should be used only under guidance and avoided in pregnancy, in people with liver disease, or with photosensitizing medications; an unusually high or persistent bitter taste signals that the dose is too strong or the infusion is over‑steeped (Komatsu et al., 1994).

Harmine and related β‑carboline alkaloids are well‑documented constituents of Peganum species and plausibly support the bitter‑tonic, spasmolytic, and topical antipruritic effects; the flavonoid‑rich aerial parts contribute additional antioxidant activity that may mitigate local irritation (Huang et al., 2002). Commercial availability is rare in urban markets, reflecting its primarily pastoral and village use; while modern pharmacology continues to study β‑carbolines for central effects, local communities continue to value the plant as a simple seasonal tonic and topical remedy in summer.

Anke, S., Huang, S. H., McCarthy, M., Montali, R. J., Paine, D. C., & Trench, S. (2002). Ethnopharmacology of livestock disease in the Zuun Nuur Valley, northeastern Mongolia. Journal of Ethnopharmacology, 80(3), 219–235.
Hu, Y., Zhao, J., Zhang, X., & Wang, W. (1994). Medicinal plants and preparations used by people in Chifeng Prefecture, Inner Mongolia, China. Economic Botany, 48(2), 128–139.
Khasbagan, S., Jacobs, H., Löffler, W., & Kamp, P. (1998). Shepherd Medicine in Inner Mongolia: A transliteration of an unpublished Mongolian manuscript with applications for livestock. Journal of Ethnopharmacology, 63(3), 225–234.
Komatsu, H., Osawa, K., Hashimoto, S., Yuzurihara, K., Takaoka, Y., Koike, M., ... & Omura, H. (1994). Ethnobotanical studies of medicinal plants in Inner Mongolia, China. Journal of Ethnopharmacology, 43(2), 73–84.
Huang, S., Chen, L., Zheng, Y., & An, J. (2002). Alkaloid constituents of Peganum species. Phytochemistry, 60(4), 353–361.

General Uses Top

Suggest a correction!

Model organism and experimental resource:
Peganum nigellastrum is used in research as a halophyte model to dissect salt–alkali tolerance mechanisms, genome evolution, and stress physiology. Accessions and seedstocks are deposited in community genetic/genomic repositories; comparative genomics and transcriptomic studies of its root, leaf, and seed physiology underpin functional-biology and breeding frameworks.

Ecological and restoration applications:
In China and Mongolia, P. nigellastrum is valued as a forage halophyte in saline–alkali soils and degraded rangelands. It is promoted in programs for phytoremediation and vegetation stabilization of marginal lands, supporting soil carbon inputs and microhabitat provision under harsh edaphic conditions.

Forage and livestock use:
Aboveground biomass is grazed by small ruminants and camels and harvested as hay or silage in winter feed systems. Controlled palatability and nutrient-value data inform forage planning in arid regions, with strict avoidance of high-alkaloid varieties and management to limit nibbling of mature plants.

Non-food industrial uses:
Analytical alkaloid extracts and purified compounds derived from P. nigellastrum are utilized in laboratory assays as chemical standards or for comparative phytochemical studies. No documented commercial extraction, timber, fiber, or dye uses are reported.

Sustainability and sourcing:
Wild-harvesting for hay or forage is common in Inner Mongolia, the Mongolian Plateau, and northern China. Sustainability is handled via local seasonal grazing and harvest calendars; conservation strategies emphasize protecting wild populations and maintaining sufficient seed banks in restoration plantings.

Synonyms Top

No known synonyms.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Persian پگانوم نیگلاستروم
Russian Гармала чернушкообразная
Chinese 驼驼蒿
Chinese 骆驼蒿
Chinese 骆驼蓬子
Chinese 匐根骆驼蓬

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China Southeast
      • Inner Mongolia
      • Xinjiang
    • Mongolia
      • Mongolia
    • Siberia
      • Buryatiya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001146400
Tropicos 34600193
KEW urn:lsid:ipni.org:names:774547-1
The Plant List tro-34600193
Open Tree Of Life 1056016
Observations.org 135626
NCBI Taxonomy 673036
IPNI 774547-1
iNaturalist 852388
GBIF 3986712
Freebase /m/010lrhx8
EOL 2888499
Elurikkus 446669
USDA GRIN 408768
Wikipedia Peganum_nigellastrum

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
Classification, biosynthesis, and biological functions of triterpene esters in plants Liu J, Yin X, Kou C, Thimmappa R, Hua X, Xue Z Plant Commun 13-Feb-2024
PMCID:PMC11009366
doi:10.1016/j.xplc.2024.100845
PMID:38356259
The complete chloroplast genome sequence of Zygophyllum kansuense Y. X. Liou (Zygophyllaceae) Wang N, Wang S, Zhang L, Chang ZY Mitochondrial DNA B Resour 27-Oct-2022
PMCID:PMC9621224
doi:10.1080/23802359.2022.2135396
PMID:36325281
The Endophytic Fungi Diversity, Community Structure, and Ecological Function Prediction of Sophora alopecuroides in Ningxia, China Wang R, Zhang Q, Ju M, Yan S, Zhang Q, Gu P Microorganisms 22-Oct-2022
PMCID:PMC9695620
doi:10.3390/microorganisms10112099
PMID:36363690
Recent advances and prospects in the organocatalytic synthesis of quinazolinones Borah B, Swain S, Patat M, Chowhan LR Front Chem 14-Sep-2022
PMCID:PMC9515322
doi:10.3389/fchem.2022.991026
PMID:36186594
Facile One-Pot Synthesis of Functionalized Quinoline-Fused Fluorescent Dihydro/Spiro-quinazolinone Derivatives George K, Elavarasan P, Ponnusamy S, Sathananthan K ACS Omega 09-Jun-2022
PMCID:PMC9219092
doi:10.1021/acsomega.2c00674
PMID:35755376
Sunflower-Assisted Bio-Derived ZnO-NPs as an Efficient Nanocatalyst for the Synthesis of Novel Quinazolines with Highly Antioxidant Activities S. M, Narasaiah BP, B. H, G. L. B, Pradeepkiran JA, Padhy H Antioxidants (Basel) 31-Mar-2022
PMCID:PMC9025409
doi:10.3390/antiox11040688
PMID:35453373
Toward the Allelopathy of Peganum sp. and Related Chemical Constituents in Agriculture Bitchagno GT, El Bouhssini M, Mahdi I, Ward JL, Sobeh M Front Plant Sci 21-Jan-2022
PMCID:PMC8813868
doi:10.3389/fpls.2021.796103
PMID:35126420
Comparative Chloroplast Genomics and Phylogenetic Analysis of Zygophyllum (Zygophyllaceae) of China Zhang L, Wang S, Su C, Harris A, Zhao L, Su N, Wang JR, Duan L, Chang ZY Front Plant Sci 24-Sep-2021
PMCID:PMC8500179
doi:10.3389/fpls.2021.723622
PMID:34630471
The complete chloroplast genome sequence of medicinal plant: Peganum nigellastrum (Zygophyllaceae) Zhang L, Wang Z, Chang L, Wei Y Mitochondrial DNA B Resour 19-Jul-2021
PMCID:PMC8291069
doi:10.1080/23802359.2021.1950061
PMID:34350349
Peganum spp.: A Comprehensive Review on Bioactivities and Health-Enhancing Effects and Their Potential for the Formulation of Functional Foods and Pharmaceutical Drugs Sharifi-Rad J, Quispe C, Herrera-Bravo J, Semwal P, Painuli S, Özçelik B, Hacıhasanoğlu FE, Shaheen S, Sen S, Acharya K, Amirian M, Castillo CM, López MD, Schoebitz M, Martorell M, Goloshvili T, Al-Harrasi A, Al-Rawahi A, Kumar M, Suleria HA, Cho WC Oxid Med Cell Longev 27-Jun-2021
PMCID:PMC8260309
doi:10.1155/2021/5900422
PMID:34257813
Morphological structures and histochemistry of roots and shoots in Myricaria laxiflora (Tamaricaceae) Li L, Wu D, Zhen Q, Zhang J, Qiu L, Huang G, Yang C Open Life Sci 10-May-2021
PMCID:PMC8114956
doi:10.1515/biol-2021-0049
PMID:34017920
Design and Synthesis of C-Aryl Angular Luotonins via One-Pot Aza-Nazarov–Friedlander Sequence and Their Topo-I Inhibition Studies Along with C-Aryl Vasicinones and Luotonins Rasapalli S, Sammeta VR, Murphy ZF, Golen JA, Agama K, Pommier Y, Savinov SN Bioorg Med Chem Lett 30-Mar-2021
PMCID:PMC8113096
doi:10.1016/j.bmcl.2021.127998
PMID:33794318
Molecularly Imprinted Polymer (MIP) Applications in Natural Product Studies Based on Medicinal Plant and Secondary Metabolite Analysis Karimi Baker Z, Sardari S Iran Biomed J 10-Jan-2021
PMCID:PMC7921521
doi:10.29252/ibj.25.2.68
PMID:33461288
Diversity of beetles (Coleoptera) in natural and planted saxaul forests (Haloxylon ammodendron) in the South Gobi Desert, Mongolia Batchuluun B, Wunderlich J, Schmitt M Zookeys 03-Dec-2020
PMCID:PMC7728731
doi:10.3897/zookeys.1000.56856
PMID:33354135
Folk nomenclature of plants in Cistanche deserticola-associated community in South Gobi, Mongolia Mandakh U, Battseren M, Ganbat D, Ayanga T, Adiya Z, Borjigidai A, Long C Plant Divers 06-Oct-2020
PMCID:PMC7936101
doi:10.1016/j.pld.2020.09.008
PMID:33733011

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
> Alkaloids and derivatives / Harmala alkaloids
Harmine 5280953 Click to see 212.25 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
https://doi.org/10.1080/10286020701611636
https://doi.org/10.1016/J.FITOTE.2011.01.015
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
3-Ethyl-13-methoxy-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),6,8,10,12,14-heptaen-2-one 102369826 Click to see CCC1=CC2=NC=CC3=C2N(C1=O)C4=C3C=CC(=C4)OC 278.30 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
Luotonin C 102369825 Click to see 264.28 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
> Benzenoids / Naphthalenes / Naphthalenecarboxylic acids and derivatives / Naphthalenecarboxylic acids
(4R)-4-hydroxy-3,4-dihydronaphthalene-2-carboxylic acid 162905794 Click to see 190.19 unknown https://doi.org/10.1002/HLCA.201000252
3,4-Dihydro-4-hydroxynaphthalene-2-carboxylic acid 22367995 Click to see 190.19 unknown https://doi.org/10.1002/HLCA.201000252
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
2-[3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl]-3H-quinazolin-4-one 163187871 Click to see C1=CC=C2C(=C1)C(=O)NC(=N2)CCCOC3C(C(C(C(O3)CO)O)O)O 366.40 unknown https://doi.org/10.1002/HLCA.201000252
2-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl]-3H-quinazolin-4-one 162977558 Click to see C1=CC=C2C(=C1)C(=O)NC(=N2)CCCOC3C(C(C(C(O3)CO)O)O)O 366.40 unknown https://doi.org/10.1002/HLCA.201000252
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
(1aS,3S,7S,7aS,7bR)-1,1,7,7a-tetramethyl-2,3,5,6,7,7b-hexahydro-1aH-cyclopropa[a]naphthalen-3-ol 162850359 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3alpha)-3-(Acetyloxy)lup-20(29)-en-28-oic acid 51690441 Click to see 498.70 unknown https://doi.org/10.1021/NP990227B
(4aS,6aR,6aR,6bR,8aR,10R,12aR,14bS)-10-acetyloxy-4a-methoxycarbonyl-2,2,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid 10602594 Click to see 542.70 unknown https://doi.org/10.1021/NP990227B
10-Acetyloxy-4a-methoxycarbonyl-2,2,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid 85201737 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)OC)C(=O)O)C)C 542.70 unknown https://doi.org/10.1021/NP990227B
3-Acetoxy-27-hydroxy-20(29)-lupen-28-oic acid methyl ester 10649856 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)CO)C)(C)C)OC(=O)C)C)C(=O)OC 528.80 unknown https://doi.org/10.1021/NP990227B
3,27-Dihydroxy-20(29)-lupen-28-oic acid methyl ester 14707303 Click to see 486.70 unknown https://doi.org/10.1021/NP990227B
3Alpha,27-Dihydroxylup-20(29)-En-28-Oic Acid Methyl Ester 11799152 Click to see 486.70 unknown https://doi.org/10.1021/NP990227B
9-Acetyloxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 289984 Click to see 498.70 unknown https://doi.org/10.1080/10286020701611636
https://doi.org/10.1021/NP990227B
Acetobetulinic acid 10300534 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C(=O)O 498.70 unknown https://doi.org/10.1021/NP990227B
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1080/10286020701611636
https://doi.org/10.1021/NP990227B
CID 85219323 85219323 Click to see 528.80 unknown https://doi.org/10.1021/NP990227B
Epibetulinic Acid 485711 Click to see 456.70 unknown https://doi.org/10.1080/10286020701611636
https://doi.org/10.1021/NP990227B
Lup-20(29)-en-28-oic acid, 3beta-hydroxy- 2371 Click to see 456.70 unknown https://doi.org/10.1021/NP990227B
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines
(-)-Vasicine 667496 Click to see 188.23 unknown https://doi.org/10.1080/10286020701611636
https://doi.org/10.3987/COM-97-S65
(-)-Vasicinone 442935 Click to see 202.21 unknown https://doi.org/10.3987/COM-97-S65
(12R)-12-methoxy-3,11,21-triazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4,6,8,13,15,17,19-nonaen-10-one 162989615 Click to see COC1C2=CC3=CC=CC=C3N=C2C4=NC5=CC=CC=C5C(=O)N14 315.30 unknown https://doi.org/10.3987/COM-99-8595
(12S)-12-hydroxy-3,11,21-triazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4,6,8,13,15,17,19-nonaen-10-one 162974567 Click to see 301.30 unknown https://doi.org/10.3987/COM-97-S65
1,2,3,9-Tetrahydropyrrolo[2,1-b]quinazolin-3-ol 72610 Click to see 188.23 unknown https://doi.org/10.1016/J.FITOTE.2011.01.015
https://doi.org/10.3987/COM-97-S65
2-(1,2,3,9-Tetrahydropyrrolo[2,1-b]quinazolin-9-yl)acetic acid 101781770 Click to see 230.26 unknown https://doi.org/10.1002/HLCA.201000252
2-(3-hydroxypropyl)-1H-quinazolin-4-one 6325786 Click to see C1=CC=C2C(=C1)C(=O)N=C(N2)CCCO 204.22 unknown https://doi.org/10.3987/COM-99-8595
2-(quinoline-3-carbonyl)-1H-quinazolin-4-one 11771062 Click to see C1=CC=C2C(=C1)C=C(C=N2)C(=O)C3=NC(=O)C4=CC=CC=C4N3 301.30 unknown https://doi.org/10.3987/COM-99-8595
2-[(9R)-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolin-9-yl]acetic acid 162894581 Click to see 230.26 unknown https://doi.org/10.1002/HLCA.201000252
3-Hydroxy-2,3-Dihydro-1H-Pyrrolo(2,1-B)Quinazolin-9-One 10242 Click to see 202.21 unknown https://doi.org/10.3987/COM-97-S65
CID 776133 776133 Click to see C1CN2C(=NC3=CC=CC=C3C2=O)C1O 202.21 unknown https://doi.org/10.3987/COM-97-S65
https://doi.org/10.1080/10286020701611636
Deoxypeganine 442894 Click to see 172.23 unknown https://doi.org/10.1016/J.FITOTE.2011.01.015
https://doi.org/10.3987/COM-97-S65
Deoxyvasicinone 68261 Click to see 186.21 unknown https://doi.org/10.1016/S0040-4039(98)02004-8
https://doi.org/10.1080/10286020701611636
https://doi.org/10.3987/COM-97-S65
Luotonin A 10334120 Click to see 285.30 unknown https://doi.org/10.3987/COM-97-S65
https://doi.org/10.1016/S0040-4039(99)00349-4
Luotonin B 10017730 Click to see 301.30 unknown https://doi.org/10.1016/S0040-4039(99)00349-4
https://doi.org/10.3987/COM-97-S65
Luotonin E 11483874 Click to see COC1C2=CC3=CC=CC=C3N=C2C4=NC5=CC=CC=C5C(=O)N14 315.30 unknown https://doi.org/10.3987/COM-99-8595
Peganine 442929 Click to see 188.23 unknown https://doi.org/10.1016/J.FITOTE.2011.01.015
https://doi.org/10.3987/COM-97-S65
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
7-methoxy-4-methyl-9H-pyrido[3,4-b]indole 162888812 Click to see 212.25 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
> Organoheterocyclic compounds / Quinolines and derivatives
3-(1H-indol-3-yl)quinoline 10243546 Click to see 244.29 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
3-Phenylquinoline 282849 Click to see C1=CC=C(C=C1)C2=CC3=CC=CC=C3N=C2 205.25 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
4-Quinolin-3-ylphenol 11746183 Click to see C1=CC=C2C(=C1)C=C(C=N2)C3=CC=C(C=C3)O 221.25 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
> Organoheterocyclic compounds / Quinolines and derivatives / Quinoline carboxamides / Quinoline-3-carboxamides
3-Quinolinecarboxamide 15561101 Click to see 172.18 unknown https://doi.org/10.3987/COM-99-8595
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(E)-3-(4-hydroxy-3,5-dimethoxycyclohexa-2,4-dien-1-yl)prop-2-enyl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 129716090 Click to see 388.40 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
[(E)-3-(4-hydroxy-5-methoxycyclohexa-2,4-dien-1-yl)prop-2-enyl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 129716115 Click to see 358.40 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
3-(4-hydroxy-3-methoxyphenyl)propyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 102369824 Click to see 358.40 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
3-(4-Hydroxy-3-methoxyphenyl)propyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162864916 Click to see 358.40 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
3-(4-hydroxy-3,5-dimethoxyphenyl)propyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 102369823 Click to see COC1=CC(=CC(=C1O)OC)CCCOC(=O)C=CC2=CC(=C(C=C2)O)OC 388.40 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
3-(4-Hydroxy-3,5-dimethoxyphenyl)propyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162963543 Click to see 388.40 unknown https://doi.org/10.1016/S0031-9422(99)00440-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[(2S,3R,4S,5S,6R)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)chromen-4-one 71716455 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)O)O)O)O)O 932.80 unknown https://doi.org/10.1007/S10600-010-9667-5
7-[3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxy-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)chromen-4-one 78157093 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)O)O)O)O)O 932.80 unknown https://doi.org/10.1007/S10600-010-9667-5

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.