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Krameria erecta

Krameria erecta - 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 UUID6440472ce567a762996309
Scientific name Krameria erecta
Authority Willd.
First published in Mant. 3: 303 (1827)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Krameria glandulosa Rose & J.H.Painter Contr. U.S. Natl. Herb. 10: 108 (1906)
Krameria imparata Britton N. Amer. Fl. 23: 199 (1930)
Krameria interior Rose & J.H.Painter Contr. U.S. Natl. Herb. 10: 108 (1906)
Krameria navae Rzed. Ciencia (Mexico) 15: 92 (1955)
Krameria palmeri Rose Contr. U.S. Natl. Herb. 1: 304 (1895)
Krameria parviflora Benth. Bot. Voy. Sulphur : 6 (1844)
Krameria rosmarinifolia Pav. ex Chodat Biblioth. Universelle Rev. Suisse , sér. 3, 24: 499 (1890)
Krameria parvifolia Benth. Bot. Voy. Sulphur : 6 (1844)
Krameria parvifolia var. glandulosa J.F.Macbr. Contr. Gray Herb. 56: 52 (1918)
Krameria parvifolia var. imparata J.F.Macbr. Contr. Gray Herb. 56: 52 (1918)

Common names Top

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Language Common/alternative name
English littleleaf ratany
Russian krameria glandulosa
Russian krameria imparata
Russian krameria parvifolia
Russian Крамерия прямостоячая

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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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southwest
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southwestern U.S.A.
      • Arizona
      • California
      • Nevada
      • Utah

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001069516
USDA Plants KRER
Tropicos 17200017
KEW urn:lsid:ipni.org:names:690418-1
The Plant List tro-17200017
Open Tree Of Life 1091850
NCBI Taxonomy 228641
Nature Serve 2.130049
IPNI 690418-1
iNaturalist 58455
GBIF 5421448
Freebase /m/04g238l
FEIS plants/shrub/kraere
EPPO KRAER
EOL 487466
Calflora (Californian flora) 4541
USDA GRIN 443734
Wikipedia Krameria_erecta
CMAUP NPO16705
CMAUP NPO315

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
The complete chloroplast genome sequence of Zygophyllum brachypterum (Zygophyllaceae) reveals its distinctive characteristics and evolutionary implication Wang X, Gao F, Li W, Zhou Y Mitochondrial DNA B Resour 08-Dec-2023
PMCID:PMC10783824
doi:10.1080/23802359.2023.2288920
PMID:38213390
Agri-silvicultures of Mexican Arid America Andablo-Reyes AD, Moreno-Calles AI, Cancio-Coyac BA, Gutiérrez-Coatecatl E, Rivero-Romero AD, Hernández-Cendejas G, Casas A J Ethnobiol Ethnomed 14-Sep-2023
PMCID:PMC10503103
doi:10.1186/s13002-023-00612-5
PMID:37710240
Mitochondrial Phylogenomics of Cuscuta (Convolvulaceae) Reveals a Potentially Functional Horizontal Gene Transfer from the Host Lin Q, Banerjee A, Stefanović S Genome Biol Evol 14-Jun-2022
PMCID:PMC9234195
doi:10.1093/gbe/evac091
PMID:35700229
Seed Menus: An integrated decision‐support framework for native plant restoration in the Mojave Desert Shryock DF, DeFalco LA, Esque TC Ecol Evol 12-Apr-2022
PMCID:PMC9005930
doi:10.1002/ece3.8805
PMID:35432931
Overview of the phytomedicine approaches against Helicobacter pylori Vale FF, Oleastro M World J Gastroenterol 21-May-2014
PMCID:PMC4024768
doi:10.3748/wjg.v20.i19.5594
PMID:24914319
Natural Products as a Source of Anti-Inflammatory Agents Associated with Inflammatory Bowel Disease Debnath T, Kim DH, Lim BO Molecules 19-Jun-2013
PMCID:PMC6270544
doi:10.3390/molecules18067253
PMID:23783459
In vitro antioxidant and antiproliferative activities of plants of the ethnopharmacopeia from northwest of Mexico Jiménez-Estrada M, Velázquez-Contreras C, Garibay-Escobar A, Sierras-Canchola D, Lapizco-Vázquez R, Ortiz-Sandoval C, Burgos-Hernández A, Robles-Zepeda RE BMC Complement Altern Med 10-Jan-2013
PMCID:PMC3547710
doi:10.1186/1472-6882-13-12
PMID:23305162
Introduction to the Arizona Sky Island Arthropod Project (ASAP): Systematics, Biogeography, Ecology, and Population Genetics of Arthropods of the Madrean Sky Islands Moore W, Meyer WM III, Eble JA, Franklin K, Wiens JF, Brusca RC Proc RMRS 01-Jan-2013
PMCID:PMC4260471
PMID:25505938
Disturbance and Plant Succession in the Mojave and Sonoran Deserts of the American Southwest Abella SR Int J Environ Res Public Health 25-Mar-2010
PMCID:PMC2872343
doi:10.3390/ijerph7041248
PMID:20617030
Lignans and neolignans from Krameria parvifolia Hans Achenbach, Wolfgang Utz, Blanca Lozano, Elsa M. Guajardo Touché, Sergio Moreno Elsevier BV 13-May-2003
doi:10.1016/S0031-9422(96)00412-8
Lignans and nor-neolignans from Krameria interior Xorge A. Dominguez, H. Sanchez V., Griselda C. Espinoza B., Julia Verde S., Hans Achenbach, Wolfgang Utz Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85205-T

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
> Benzenoids / Benzene and substituted derivatives / Benzenesulfonic acids and derivatives
Sulfanilic acid 8479 Click to see C1=CC(=CC=C1N)S(=O)(=O)O 173.19 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Tyramine 5610 Click to see C1=CC(=CC=C1CCN)O 137.18 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(1S,6R,7R)-7-[(1S)-1,2-dihydroxyethyl]-6-hydroxy-1-(4-hydroxyphenyl)-4,8-dioxaspiro[4.4]nonane-3,9-dione 193664 Click to see C1C(C2(C(C(OC2=O)C(CO)O)O)OC1=O)C3=CC=C(C=C3)O 324.28 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
(4S,5S,8R,9R)-8-[(1S)-1,2-dihydroxyethyl]-9-hydroxy-4-(4-hydroxyphenyl)-1,7-dioxaspiro[4.4]nonane-2,6-dione 92855823 Click to see C1C(C2(C(C(OC2=O)C(CO)O)O)OC1=O)C3=CC=C(C=C3)O 324.28 unknown https://doi.org/10.1016/0031-9422(90)85205-T
(4S,5S,8R,9S)-8-[(1S)-1,2-dihydroxyethyl]-9-hydroxy-4-(4-hydroxyphenyl)-1,7-dioxaspiro[4.4]nonane-2,6-dione 6711168 Click to see C1C(C2(C(C(OC2=O)C(CO)O)O)OC1=O)C3=CC=C(C=C3)O 324.28 unknown https://doi.org/10.1016/0031-9422(90)85205-T
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown via CMAUP database
> Lignans, neolignans and related compounds
4-[(1R,2R)-1-hydroxy-2-[4-[(E)-prop-1-enyl]phenoxy]propyl]phenol 14213231 Click to see CC=CC1=CC=C(C=C1)OC(C)C(C2=CC=C(C=C2)O)O 284.30 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
https://doi.org/10.1016/0031-9422(90)85205-T
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(-)-Larreatricin 26389403 Click to see CC1C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C 284.30 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
https://doi.org/10.1016/0031-9422(90)85205-T
4-[5-(4-Hydroxyphenyl)-3,4-dimethyloxolan-2-yl]phenol 14213222 Click to see CC1C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C 284.30 unknown https://doi.org/10.1016/0031-9422(90)85205-T
https://doi.org/10.1016/S0031-9422(96)00412-8
Meso-3,3'-Didemethoxynectandrin B 14213224 Click to see CC1C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C 284.30 unknown https://doi.org/10.1016/0031-9422(90)85205-T
https://doi.org/10.1016/S0031-9422(96)00412-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Illudanes and illudins / Melleolides and analogues
Armillyl orsellinate 14707323 Click to see CC1=CC(=CC(=C1C(=O)OC2CC3(C2=C(C(C4C3CC(C4)(C)C)O)CO)C)O)O 402.50 unknown https://doi.org/10.1016/0031-9422(90)85205-T
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
[(1S,3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 102444973 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)O)C)C 588.90 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
[7,7,12,16-Tetramethyl-15-(6-methylhept-5-en-2-yl)-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 163054201 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)O)C)C 588.90 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron 21883788 Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-] 116.07 unknown via CMAUP database
> Organic acids and derivatives / Keto acids and derivatives / Alpha-keto acids and derivatives
Pyruvic Acid 1060 Click to see CC(=O)C(=O)O 88.06 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline 305 Click to see C[N+](C)(C)CCO 104.17 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines / Acyl cholines
Acetylcholine 187 Click to see CC(=O)OCC[N+](C)(C)C 146.21 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucosinolates / Alkylglucosinolates
Sinigrin 6911854 Click to see C=CCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O 359.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol 11850 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Alpha carbolines
Communesin C 44575538 Click to see CC=CC=CC(=O)N1CCC23C1N4CCC25C(NC6=CC=CC=C36)NC7=CC=CC(=C57)C4C8C(O8)(C)C 494.60 unknown https://doi.org/10.1016/0031-9422(90)85205-T
https://doi.org/10.1016/S0031-9422(96)00412-8
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R)-2beta-(4-Hydroxyphenyl)-3alpha-methyl-5-(1-propenyl)-7-methoxy-2,3-dihydrobenzofuran 101612558 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC=C(C=C3)O 296.40 unknown https://doi.org/10.1016/0031-9422(90)85205-T
1,3-Benzenediol, 4-[5-(1-propenyl)-2-benzofuranyl]-, (E)- 54300595 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=C(C=C(C=C3)O)O 266.29 unknown https://doi.org/10.1016/0031-9422(90)85205-T
https://doi.org/10.1016/S0031-9422(96)00412-8
2-(2-Hydroxy-4-methoxyphenyl)-5-(3-hydroxypropyl)benzofuran 14213211 Click to see COC1=CC(=C(C=C1)C2=CC3=C(O2)C=CC(=C3)CCCO)O 298.30 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
2-(2-Methoxy-4-hydroxyphenyl)-5-[(E)-3-hydroxy-1-propenyl]benzofuran 14704570 Click to see COC1=C(C=CC(=C1)O)C2=CC3=C(O2)C=CC(=C3)C=CCO 296.30 unknown https://doi.org/10.1016/0031-9422(90)85205-T
2-(2,4-dimethoxyphenyl)-5-[(E)-prop-1-enyl]-1-benzofuran 13834121 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=C(C=C(C=C3)OC)OC 294.30 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
2-(2,4-Dimethoxyphenyl)-5-prop-1-enyl-1-benzofuran 162881980 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=C(C=C(C=C3)OC)OC 294.30 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
2-(2,4,6-Trihydroxyphenyl)-5-[(E)-1-propenyl]benzofuran 14704569 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=C(C=C(C=C3O)O)O 282.29 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
https://doi.org/10.1016/0031-9422(90)85205-T
2-(4-Hydroxyphenyl)-5-(1-propenyl)benzofuran-3-carbaldehyde 14213216 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C=O)C3=CC=C(C=C3)O 278.30 unknown https://doi.org/10.1016/0031-9422(90)85205-T
2-(4-hydroxyphenyl)-5-(E)-propenylbenzofuran 53483951 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=CC=C(C=C3)O 250.29 unknown https://doi.org/10.1016/0031-9422(90)85205-T
2-(4-Hydroxyphenyl)-5-prop-1-enyl-1-benzofuran-3-carbaldehyde 85747347 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C=O)C3=CC=C(C=C3)O 278.30 unknown https://doi.org/10.1016/0031-9422(90)85205-T
2-(4-Methoxyphenyl)-5-(1-propenyl)benzofuran 91991396 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=CC=C(C=C3)OC 264.30 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
2-(4-Methoxyphenyl)-5-prop-1-enyl-1-benzofuran 129650689 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=CC=C(C=C3)OC 264.30 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
2-(5-Prop-1-enyl-1-benzofuran-2-yl)benzene-1,3,5-triol 163009570 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=C(C=C(C=C3O)O)O 282.29 unknown https://doi.org/10.1016/0031-9422(90)85205-T
https://doi.org/10.1016/S0031-9422(96)00412-8
2-methoxy-4-[(2R,3R)-3-methyl-5-[(E)-prop-1-enyl]-2,3-dihydro-1-benzofuran-2-yl]phenol 14213227 Click to see CC=CC1=CC2=C(C=C1)OC(C2C)C3=CC(=C(C=C3)O)OC 296.40 unknown https://doi.org/10.1016/0031-9422(90)85205-T
3-Methoxy-4-(5-prop-1-enyl-1-benzofuran-2-yl)phenol 72728594 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=C(C=C(C=C3)O)OC 280.30 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
3,5-Dimethoxy-2-(5-prop-1-enyl-1-benzofuran-2-yl)phenol 86159972 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=C(C=C(C=C3OC)OC)O 310.30 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
3,5-dimethoxy-2-[5-[(E)-prop-1-enyl]-1-benzofuran-2-yl]phenol 13834119 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=C(C=C(C=C3OC)OC)O 310.30 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
4-(3-Methyl-5-prop-1-enyl-1-benzofuran-2-yl)phenol 3001232 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC=C(C=C3)O 264.30 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
https://doi.org/10.1016/0031-9422(90)85205-T
4-(3-Methyl-5-prop-1-enyl-2,3-dihydro-1-benzofuran-2-yl)phenol 70414118 Click to see CC=CC1=CC2=C(C=C1)OC(C2C)C3=CC=C(C=C3)O 266.30 unknown https://doi.org/10.1016/0031-9422(90)85205-T
https://doi.org/10.1016/S0031-9422(96)00412-8
4-(5-Prop-1-enyl-1-benzofuran-2-yl)phenol 76044967 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=CC=C(C=C3)O 250.29 unknown https://doi.org/10.1016/0031-9422(90)85205-T
4-(7-Methoxy-3-methyl-5-prop-1-enyl-1-benzofuran-2-yl)phenol 72730286 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(=C2C)C3=CC=C(C=C3)O 294.30 unknown https://doi.org/10.1016/0031-9422(90)85205-T
4-(7-Methoxy-3-methyl-5-prop-1-enyl-2,3-dihydro-1-benzofuran-2-yl)phenol 162979824 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC=C(C=C3)O 296.40 unknown https://doi.org/10.1016/0031-9422(90)85205-T
4-(7-Methoxy-5-prop-1-enyl-1-benzofuran-2-yl)phenol 162961364 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(=C2)C3=CC=C(C=C3)O 280.30 unknown https://doi.org/10.1016/0031-9422(90)85205-T
4-[(2R,3R)-5-[(2R)-2-hydroxypropyl]-3-methyl-2,3-dihydro-1-benzofuran-2-yl]phenol 163190159 Click to see CC1C(OC2=C1C=C(C=C2)CC(C)O)C3=CC=C(C=C3)O 284.30 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
4-[5-(2-Hydroxypropyl)-3-methyl-2,3-dihydro-1-benzofuran-2-yl]phenol 162962934 Click to see CC1C(OC2=C1C=C(C=C2)CC(C)O)C3=CC=C(C=C3)O 284.30 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
4-[5-(3-Hydroxyprop-1-enyl)-1-benzofuran-2-yl]-3-methoxyphenol 163070512 Click to see COC1=C(C=CC(=C1)O)C2=CC3=C(O2)C=CC(=C3)C=CCO 296.30 unknown https://doi.org/10.1016/0031-9422(90)85205-T
4-[5-(3-Hydroxypropyl)-1-benzofuran-2-yl]-5-methoxybenzene-1,3-diol 85704945 Click to see COC1=CC(=CC(=C1C2=CC3=C(O2)C=CC(=C3)CCCO)O)O 314.30 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
4-[5-[(E)-1-Propenyl]-7-methoxybenzofuran-2-yl]phenol 14352595 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(=C2)C3=CC=C(C=C3)O 280.30 unknown https://doi.org/10.1016/0031-9422(90)85205-T
4-[7-methoxy-3-methyl-5-[(E)-prop-1-enyl]-1-benzofuran-2-yl]phenol 14352596 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(=C2C)C3=CC=C(C=C3)O 294.30 unknown https://doi.org/10.1016/0031-9422(90)85205-T
4-{5-[(1E)-prop-1-en-1-yl]-1-benzofuran-2-yl}benzene-1,3-diol 10355545 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=C(C=C(C=C3)O)O 266.29 unknown https://doi.org/10.1016/0031-9422(90)85205-T
https://doi.org/10.1016/S0031-9422(96)00412-8
5-(3-Hydroxypropyl)-2-(2-methoxy-4-hydroxyphenyl)benzofuran 14213209 Click to see COC1=C(C=CC(=C1)O)C2=CC3=C(O2)C=CC(=C3)CCCO 298.30 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
5-Methoxy-2-(5-prop-1-enyl-1-benzofuran-2-yl)phenol 157488 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=C(C=C(C=C3)OC)O 280.30 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
https://doi.org/10.1016/0031-9422(90)85205-T
Conocarpan 10999992 Click to see CC=CC1=CC2=C(C=C1)OC(C2C)C3=CC=C(C=C3)O 266.30 unknown https://doi.org/10.1016/0031-9422(90)85205-T
https://doi.org/10.1016/S0031-9422(96)00412-8
Eupomatenoid 6 6261723 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC=C(C=C3)O 264.30 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
https://doi.org/10.1016/0031-9422(90)85205-T
Rataniaphenol I 6440631 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=C(C=C(C=C3)OC)O 280.30 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
https://doi.org/10.1016/0031-9422(90)85205-T
Rataniaphenol III 14213215 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=C(C=C(C=C3)O)OC 280.30 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(-)-Fustin 12310641 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O 288.25 unknown via CMAUP database
Fustin 5317435 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O 288.25 unknown via CMAUP database
Garbanzol 442410 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferide 5281666 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
Robinetin 5281692 Click to see C1=CC2=C(C=C1O)OC(=C(C2=O)O)C3=CC(=C(C(=C3)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44559826 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
Diosmin 5281613 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)O)O)O)O)O)O 608.50 unknown via CMAUP database
Hesperidin 10621 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Gossypetin hexamethyl ether 146093 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3OC)OC)OC)OC)OC 402.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
4-[2-(2-Methoxy-5-prop-1-enylphenyl)prop-2-enyl]phenol 162987643 Click to see CC=CC1=CC(=C(C=C1)OC)C(=C)CC2=CC=C(C=C2)O 280.40 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
https://doi.org/10.1016/0031-9422(90)85205-T
4-[2-[5-(2-Hydroxypropyl)-2-methoxyphenyl]prop-2-enyl]phenol 14352598 Click to see CC(CC1=CC(=C(C=C1)OC)C(=C)CC2=CC=C(C=C2)O)O 298.40 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
4-[2-[5-[(2S)-2-hydroxypropyl]-2-methoxyphenyl]prop-2-enyl]phenol 14352599 Click to see CC(CC1=CC(=C(C=C1)OC)C(=C)CC2=CC=C(C=C2)O)O 298.40 unknown https://doi.org/10.1016/S0031-9422(96)00412-8
Hermosillol 13834124 Click to see CC=CC1=CC(=C(C=C1)OC)C(=C)CC2=CC=C(C=C2)O 280.40 unknown https://doi.org/10.1016/0031-9422(90)85205-T
https://doi.org/10.1016/S0031-9422(96)00412-8

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