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Sophora davidii

Sophora davidii - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Sophora davidii - 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 UUID643fdeacb63e6979318211
Scientific name Sophora davidii
Authority (Franch.) Pavol.

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Sophora viciaefolia Hance
Caragana chamlago B.Mey.
Sophora moorcroftiana subsp. viciifolia (Hance) Yakovlev

Common names Top

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Language Common/alternative name
Arabic صفيراء داودية
Chinese 苦豆子
Chinese 白刺花
Chinese 白刺槐
Chinese 白刺花叶
Chinese 白刺花果
Chinese 白刺花根
Chinese 苦刺花
Chinese 狼牙刺
Chinese 狼牙槐
Chinese 白刻针
Chinese 铁马胡烧
Chinese 马蹄针
Chinese 马鞭采

Subspecies (abbr. subsp./ssp.) Top

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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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000212090
USDA Plants SODA3
Tropicos 13044680
KEW urn:lsid:ipni.org:names:518822-1
The Plant List ild-7167
Missouri Botanical Garden 280550
Open Tree Of Life 33319
NCBI Taxonomy 49839
IPNI 518823-1
iNaturalist 135411
GBIF 2959090
EPPO SOBDA
EOL 702855
USDA GRIN 34952

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
Transcriptome analysis of Gossypium reveals the molecular mechanisms of Ca2+ signaling pathway on arsenic tolerance induced by arbuscular mycorrhizal fungi Gong M, Bai N, Su J, Wang Y, Wei Y, Zhang Q Front Microbiol 25-Mar-2024
PMCID:PMC11000422
doi:10.3389/fmicb.2024.1362296
PMID:38591035
Effects of acid and aluminum stress on seed germination and physiological characteristics of seedling growth in Sophora davidii Long S, Xie W, Zhao W, Liu D, Wang P, Zhao L Plant Signal Behav 20-Mar-2024
PMCID:PMC10956626
doi:10.1080/15592324.2024.2328891
PMID:38506438
Transcriptome data analysis provides insights into the conservation of Michelia lacei, a plant species with extremely small populations distributed in Yunnan province, China Liu Y, Cai L, Sun W BMC Plant Biol 19-Mar-2024
PMCID:PMC10949798
doi:10.1186/s12870-024-04892-1
PMID:38500068
The complete chloroplast genome sequence of Ammodendron bifolium (Fabaceae), an endangered desert shrub from China Tian H, Zhu X, Qiu J, Zhang H, Shi X Mitochondrial DNA B Resour 03-Mar-2024
PMCID:PMC10913713
doi:10.1080/23802359.2024.2324922
PMID:38450410
Exploration of Ginkgo biloba leaves on non-small cell lung cancer based on network pharmacology and molecular docking Wang M, Li R, Bai M, Zhou X Medicine (Baltimore) 01-Mar-2024
PMCID:PMC10906577
doi:10.1097/MD.0000000000037218
PMID:38428907
The Impact of Water Potential and Temperature on Native Species’ Capability for Seed Germination in the Loess Plateau Region, China Hu G, He X, Wang N, Liu J, Zhou Z Plants (Basel) 29-Feb-2024
PMCID:PMC10934695
doi:10.3390/plants13050693
PMID:38475540
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
Rapidly mining candidate cotton drought resistance genes based on key indicators of drought resistance Geng S, Gao W, Li S, Chen Q, Jiao Y, Zhao J, Wang Y, Wang T, Qu Y, Chen Q BMC Plant Biol 21-Feb-2024
PMCID:PMC10880307
doi:10.1186/s12870-024-04801-6
PMID:38383284
Shifting patterns in fine root distribution of four xerophytic species across soil structural gradients and years of growth Hu H, Bao W, Huang L, Li F Ecol Evol 07-Feb-2024
PMCID:PMC10850925
doi:10.1002/ece3.10889
PMID:38333099
Integrated physiological, transcriptomic, and metabolomic analyses of drought stress alleviation in Ehretia macrophylla Wall. seedlings by SiO2 NPs (silica nanoparticles) Chen M, Jiao SQ, Xie L, Geng X, Qi S, Fan J, Cheng S, Shi J, Cao X Front Plant Sci 02-Feb-2024
PMCID:PMC10869631
doi:10.3389/fpls.2024.1260140
PMID:38371410
A trade-off between leaf hydraulic efficiency and safety across three xerophytic species in response to increased rock fragment content Zhang X, Ma S, Hu H, Li F, Bao W, Huang L Tree Physiol 20-Jan-2024
PMCID:PMC10918055
doi:10.1093/treephys/tpae010
PMID:38245807
Juvenile Plant–Microbe Interactions Modulate the Adaptation and Response of Forest Seedlings to Rapid Climate Change Sanhueza T, Hernández I, Sagredo-Sáez C, Villanueva-Guerrero A, Alvarado R, Mujica MI, Fuentes-Quiroz A, Menendez E, Jorquera-Fontena E, Valadares RB, Herrera H Plants (Basel) 09-Jan-2024
PMCID:PMC10819047
doi:10.3390/plants13020175
PMID:38256729
Preliminary exploration of herbal tea products based on traditional knowledge and hypotheses concerning herbal tea selection: a case study in Southwest Guizhou, China Long X, Ranjitkar S, Waldstein A, Wu H, Li Q, Geng Y J Ethnobiol Ethnomed 02-Jan-2024
PMCID:PMC10763305
doi:10.1186/s13002-023-00645-w
PMID:38169414
Characteristics of Soil Arsenic Contamination and the Potential of Pioneer Plants for Arsenic Remediation in Gold Mine Tailings Han L, Zhai Y, Chen R, Fan Y, Liu Z, Zhao Y, Li R, Xia L Toxics 16-Dec-2023
PMCID:PMC10747858
doi:10.3390/toxics11121025
PMID:38133426
Phytohormone Response of Drought-Acclimated Illicium difengpi (Schisandraceae) Wu C, Liu B, Zhang X, Wang M, Liang H Int J Mol Sci 17-Nov-2023
PMCID:PMC10671654
doi:10.3390/ijms242216443
PMID:38003632

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 / Lupin alkaloids / Cytisine and derivatives
(+)-Cytisine 683511 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
(1S,5R)-3,4,5,6-tetrahydro-1H-1,5-methanopyrido[1,2-a][1,5]diazocin-8(2H)-one 6713952 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
Citizin 22407 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
Cytisinicline 10235 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
> Alkaloids and derivatives / Lupin alkaloids / Matrine alkaloids
(+)-Matrine 285698 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
(1R,2R,5S,9R,17S)-5-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 5318253 Click to see C1CC2CN3C(CCC(C3=O)O)C4C2N(C1)CCC4 264.36 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
(1R,2R,5S,9S,17S)-5-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 10659287 Click to see C1CC2CN3C(CCC(C3=O)O)C4C2N(C1)CCC4 264.36 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
(1R,2R,9S,15S,17R)-15-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 154495892 Click to see C1CC2C3CC(CN4C3C(CCC4)CN2C(=O)C1)O 264.36 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
(1R,2R,9S,15S,17S)-15-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 12133310 Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CC(C4)O 262.35 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
(1R,2S,9R,17S)-13-oxido-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 129316889 Click to see C1CC2CN3C(CC=CC3=O)C4C2[N+](C1)(CCC4)[O-] 262.35 unknown https://doi.org/10.1002/MCS.1046
(1S,2S,3R,9S,17S)-3-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 12133309 Click to see C1CC2CN3C(C4C2N(C1)CCC4)C(C=CC3=O)O 262.35 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
15-Hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 78385078 Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CC(C4)O 262.35 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
15-Hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 73193574 Click to see C1CC2C3CC(CN4C3C(CCC4)CN2C(=O)C1)O 264.36 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
3-Hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 75021824 Click to see C1CC2CN3C(C4C2N(C1)CCC4)C(C=CC3=O)O 262.35 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
5-Hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 78385079 Click to see C1CC2CN3C(CCC(C3=O)O)C4C2N(C1)CCC4 264.36 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
7,13-Diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 618867 Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CCC4 246.35 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
9alpha-Hydroxymatrine 15385684 Click to see C1CC2C3CC(CN4C3C(CCC4)CN2C(=O)C1)O 264.36 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
Ammothamnine 114850 Click to see C1CC2C3CCC[N+]4(C3C(CCC4)CN2C(=O)C1)[O-] 264.36 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
Matrine 91466 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
Matrine oxide 24864132 Click to see C1CC2C3CCC[N+]4(C3C(CCC4)CN2C(=O)C1)[O-] 264.36 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
N-Oxysophocarpine 618688 Click to see C1CC2CN3C(CC=CC3=O)C4C2[N+](C1)(CCC4)[O-] 262.35 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
Sophocarpidine 24721085 Click to see C1CC2CN3C(CC=CC3=O)C4C2[N+](C1)(CCC4)[O-] 262.35 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
Sophocarpine 115269 Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CCC4 246.35 unknown https://doi.org/10.1002/MCS.1046
https://doi.org/10.1016/S0031-9422(98)00486-5
Sophoridine 165549 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown https://doi.org/10.1002/MCS.1046
https://doi.org/10.1016/S0031-9422(98)00486-5
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(1R,2R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 163184988 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
(1R,2R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 6575009 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
(1R,2R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 442956 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
(1R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-6-one 51018075 Click to see C1CCN2CC3CC(C2C1)CN4C3=CCCC4=O 246.35 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
https://doi.org/10.1016/0031-9422(91)80112-E
(1R,9R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-6-one 163185252 Click to see C1CCN2CC3CC(C2C1)CN4C3=CCCC4=O 246.35 unknown https://doi.org/10.1016/0031-9422(91)80112-E
(1S,2R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadecan-8-one 12306750 Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3CCCC4 248.36 unknown https://doi.org/10.1016/0031-9422(91)80112-E
5,6-Dehydrolupanine 520559 Click to see C1CCN2CC3CC(C2C1)CN4C3=CCCC4=O 246.35 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
alpha-Isolupanine 119201 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
CID 442940 442940 Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3CCCC4 248.36 unknown https://doi.org/10.1016/0031-9422(91)80112-E
Lupanine 91471 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
2,2,6a,6b,9,9,12a-heptamethyl-4-(2-methylbutanoyloxy)-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-4a-carboxylic acid 73657148 Click to see CCC(C)C(=O)OC1CC(CC2C1(CCC3(C2=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C(=O)O)(C)C 554.80 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
> Organoheterocyclic compounds / Diazanaphthalenes / Naphthyridines
Neosophoramine 618327 Click to see C1CC2CN3C(=O)C=CC=C3C4C2N(C1)CCC4 244.33 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
Sophoramine 169014 Click to see C1CC2CN3C(=O)C=CC=C3C4C2N(C1)CCC4 244.33 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
> Organoheterocyclic compounds / Isobenzofurans
[(1S,5R,6R)-5-[[(1R,3aR,7R,7aS)-7-hydroxy-3a,7-dimethyl-3-oxo-4,5,6,7a-tetrahydro-1H-2-benzofuran-1-yl]methyl]-7-methylidene-4-oxo-6-bicyclo[3.2.1]oct-2-enyl] acetate 162904392 Click to see CC(=O)OC1C(=C)C2CC1(C(=O)C=C2)CC3C4C(CCCC4(C)O)(C(=O)O3)C 388.50 unknown https://doi.org/10.1016/S0031-9422(98)00486-5
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(1R,2S,3S,9S,10S,17S)-2-(3,5-dihydroxyphenyl)-3,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 11614520 Click to see C1=CC(=CC=C1C2C(C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C2C(=C6)O)C7=CC=C(C=C7)O)C8=CC=C(C=C8)O)C9=CC(=CC(=C9)O)O)O 680.70 unknown https://doi.org/10.1016/0040-4039(96)01078-7
https://doi.org/10.1016/S0031-9422(00)00016-9
(1R,2S,3S)-2-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-1-[(S)-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-5-yl]-(4-hydroxyphenyl)methyl]-3-(4-hydroxyphenyl)-2,3-dihydro-1H-indene-4,6-diol 163187664 Click to see C1=CC(=CC=C1C=CC2=C(C(=CC3=C2C(C(O3)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O)C(C6C(C(C7=C6C=C(C=C7O)O)C8=CC=C(C=C8)O)C9=C1C(C(OC1=CC(=C9)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)C1=CC=C(C=C1)O)O 1135.20 unknown https://doi.org/10.1016/0040-4039(96)01078-7
(1S,2R,3R,9R,10R,17R)-2-(3,5-dihydroxyphenyl)-3,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 101383933 Click to see C1=CC(=CC=C1C2C(C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C2C(=C6)O)C7=CC=C(C=C7)O)C8=CC=C(C=C8)O)C9=CC(=CC(=C9)O)O)O 680.70 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
(1S,2R,3S)-2-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-1-[(R)-hydroxy-(4-hydroxyphenyl)methyl]-3-(4-hydroxyphenyl)-2,3-dihydro-1H-indene-4,6-diol 162907359 Click to see C1=CC(=CC=C1C2C(C(C3=C2C(=CC(=C3)O)O)C(C4=CC=C(C=C4)O)O)C5=C6C(C(OC6=CC(=C5)O)C7=CC=C(C=C7)O)C8=CC(=CC(=C8)O)O)O 698.70 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
(1S,2S,3R,9R,10R,17R)-2-(3,5-dihydroxyphenyl)-3,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 154496441 Click to see C1=CC(=CC=C1C2C(C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C2C(=C6)O)C7=CC=C(C=C7)O)C8=CC=C(C=C8)O)C9=CC(=CC(=C9)O)O)O 680.70 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
(2R,3R,10R,11S,18R,19R,23R,24R)-23-(3,5-dihydroxyphenyl)-3,11,19,24-tetrakis(4-hydroxyphenyl)-4,12,20,25-tetraoxaoctacyclo[16.9.1.12,5.110,13.021,28.022,26.09,30.017,29]triaconta-1(27),5,7,9(30),13,15,17(29),21(28),22(26)-nonaene-7,15-diol 102460760 Click to see C1=CC(=CC=C1C2C(C3=C(O2)C=C4C5C(OC6=CC(=CC(=C56)C7C(OC8=CC(=CC(=C78)C9C4=C3OC9C1=CC=C(C=C1)O)O)C1=CC=C(C=C1)O)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O 904.90 unknown https://doi.org/10.1016/0040-4039(96)01078-7
https://doi.org/10.1016/S0031-9422(00)00016-9
(2R,3R,10R,11S,18S,19S)-3,11,19-tris(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.12,5.110,13.021,25.09,27.017,26]heptacosa-1(25),5,7,9(27),13,15,17(26),21,23-nonaene-7,15,23-triol 162863065 Click to see C1=CC(=CC=C1C2C3C4=C5C(C(OC5=CC(=C4)O)C6=CC=C(C=C6)O)C7=C8C(C(OC8=CC(=C7)O)C9=CC=C(C=C9)O)C1=C3C(=CC(=C1)O)O2)O 678.70 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
(2R,3R,10S,11S,18R,19R,23S,24S)-23-(3,5-dihydroxyphenyl)-3,11,19,24-tetrakis(4-hydroxyphenyl)-4,12,20,25-tetraoxaoctacyclo[16.9.1.12,5.110,13.021,28.022,26.09,30.017,29]triaconta-1(27),5,7,9(30),13,15,17(29),21(28),22(26)-nonaene-7,15-diol 162956045 Click to see C1=CC(=CC=C1C2C(C3=C(O2)C=C4C5C(OC6=CC(=CC(=C56)C7C(OC8=CC(=CC(=C78)C9C4=C3OC9C1=CC=C(C=C1)O)O)C1=CC=C(C=C1)O)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O 904.90 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
(2R,3S,10R,11R,18S,19R,23S,24S)-23-(3,5-dihydroxyphenyl)-3,11,19,24-tetrakis(4-hydroxyphenyl)-4,12,20,25-tetraoxaoctacyclo[16.9.1.12,5.110,13.021,28.022,26.09,30.017,29]triaconta-1(27),5,7,9(30),13,15,17(29),21(28),22(26)-nonaene-7,15-diol 162956044 Click to see C1=CC(=CC=C1C2C(C3=C(O2)C=C4C5C(OC6=CC(=CC(=C56)C7C(OC8=CC(=CC(=C78)C9C4=C3OC9C1=CC=C(C=C1)O)O)C1=CC=C(C=C1)O)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O 904.90 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
(2S,10R,18S)-3,11,19-tris(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.12,5.110,13.021,25.09,27.017,26]heptacosa-1(25),5,7,9(27),13,15,17(26),21,23-nonaene-7,15,23-triol 138113868 Click to see C1=CC(=CC=C1C2C3C4=C5C(C(OC5=CC(=C4)O)C6=CC=C(C=C6)O)C7=C8C(C(OC8=CC(=C7)O)C9=CC=C(C=C9)O)C1=C3C(=CC(=C1)O)O2)O 678.70 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
(2S,3R,10R,11R,18S,19S)-3,11,19-tris(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.12,5.110,13.021,25.09,27.017,26]heptacosa-1(25),5,7,9(27),13,15,17(26),21,23-nonaene-7,15,23-triol 97182160 Click to see C1=CC(=CC=C1C2C3C4=C5C(C(OC5=CC(=C4)O)C6=CC=C(C=C6)O)C7=C8C(C(OC8=CC(=C7)O)C9=CC=C(C=C9)O)C1=C3C(=CC(=C1)O)O2)O 678.70 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
(2S)-2-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]-5,7-dihydroxy-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 154804589 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC4=C(C=C3O)OC(C4C5=CC(=CC(=C5)O)O)C6=CC=C(C=C6)O)C(=C)C)C 650.70 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
(2S)-2-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]-5,7-dihydroxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 162863174 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC4=C(C=C3O)OC(C4C5=CC(=CC(=C5)O)O)C6=CC=C(C=C6)O)C(=C)C)C 650.70 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
(2S)-2-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrobenzofuran-5-yl]-5,7-dihydroxy-8-(3-methylbut-2-enyl)chroman-4-one 484589 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC4=C(C=C3O)OC(C4C5=CC(=CC(=C5)O)O)C6=CC=C(C=C6)O)C 582.60 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
(2S)-2-[(2S,3S)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]-5,7-dihydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 162914215 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC4=C(C=C3O)OC(C4C5=CC(=CC(=C5)O)O)C6=CC=C(C=C6)O)C 582.60 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
2-[(2R,3R)-3-(3,5-Dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]-5,7-dihydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 134715105 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC4=C(C=C3O)OC(C4C5=CC(=CC(=C5)O)O)C6=CC=C(C=C6)O)C 582.60 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
2-[[(2S)-2-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrobenzofuran-5-yl]-5,7-dihydroxy-4-oxo-chroman-8-yl]methyl]-5-methyl-hex-4-enoic acid 484590 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC4=C(C=C3O)OC(C4C5=CC(=CC(=C5)O)O)C6=CC=C(C=C6)O)C(=O)O)C 654.70 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
2-[3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-1-[[3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-5-yl]-(4-hydroxyphenyl)methyl]-3-(4-hydroxyphenyl)-2,3-dihydro-1H-indene-4,6-diol 101994134 Click to see C1=CC(=CC=C1C=CC2=C(C(=CC3=C2C(C(O3)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O)C(C6C(C(C7=C6C=C(C=C7O)O)C8=CC=C(C=C8)O)C9=C1C(C(OC1=CC(=C9)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)C1=CC=C(C=C1)O)O 1135.20 unknown https://doi.org/10.1016/0040-4039(96)01078-7
2-[3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-1-[[3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-4-[2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-5-yl]-(4-hydroxyphenyl)methyl]-3-(4-hydroxyphenyl)-2,3-dihydro-1H-indene-4,6-diol 163029186 Click to see C1=CC(=CC=C1C=CC2=C(C(=CC3=C2C(C(O3)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O)C(C6C(C(C7=C6C=C(C=C7O)O)C8=CC=C(C=C8)O)C9=C1C(C(OC1=CC(=C9)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)C1=CC=C(C=C1)O)O 1135.20 unknown https://doi.org/10.1016/0040-4039(96)01078-7
2-[3-(3,5-Dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrobenzofuran-5-yl]-5,7-dihydroxy-8-(3-methylbut-2-enyl)chroman-4-one 500116 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC4=C(C=C3O)OC(C4C5=CC(=CC(=C5)O)O)C6=CC=C(C=C6)O)C 582.60 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
23-(3,5-Dihydroxyphenyl)-3,11,19,24-tetrakis(4-hydroxyphenyl)-4,12,20,25-tetraoxaoctacyclo[16.9.1.12,5.110,13.021,28.022,26.09,30.017,29]triaconta-1(27),5,7,9(30),13,15,17(29),21(28),22(26)-nonaene-7,15-diol 162956043 Click to see C1=CC(=CC=C1C2C(C3=C(O2)C=C4C5C(OC6=CC(=CC(=C56)C7C(OC8=CC(=CC(=C78)C9C4=C3OC9C1=CC=C(C=C1)O)O)C1=CC=C(C=C1)O)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O 904.90 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
5-[(2R,3R)-6-hydroxy-4-[(2R,3R)-6-hydroxy-2-(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 163186865 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=C6C(C(OC6=CC(=C5)O)C7=CC=C(C=C7)O)C8=CC(=CC(=C8)O)O)O 680.70 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
5-[(2S,3R)-6-hydroxy-4-[(2R,3S)-6-hydroxy-2-(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 160649591 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=C6C(C(OC6=CC(=C5)O)C7=CC=C(C=C7)O)C8=CC(=CC(=C8)O)O)O 680.70 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
5-[6-Hydroxy-2-(4-hydroxyphenyl)-4-[2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 366354 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
5-[6-Hydroxy-4-[6-hydroxy-2-(4-hydroxyphenyl)-4-[2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 366355 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=C6C(C(OC6=CC(=C5)O)C7=CC=C(C=C7)O)C8=CC(=CC(=C8)O)O)O 680.70 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
CID 134715106 134715106 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC4=C(C=C3O)OC(C4C5=CC(=CC(=C5)O)O)C6=CC=C(C=C6)O)C(=C)C)C 650.70 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
CID 375682 375682 Click to see C1=CC(=CC=C1C2C3C4=C5C(C(OC5=CC(=C4)O)C6=CC=C(C=C6)O)C7=C8C(C(OC8=CC(=C7)O)C9=CC=C(C=C9)O)C1=C3C(=CC(=C1)O)O2)O 678.70 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
Davidiol B 101945535 Click to see C1=CC(=CC=C1C2C(C(C3=C2C(=CC(=C3)O)O)C(C4=CC=C(C=C4)O)O)C5=C6C(C(OC6=CC(=C5)O)C7=CC=C(C=C7)O)C8=CC(=CC(=C8)O)O)O 698.70 unknown https://doi.org/10.1016/0040-4039(96)01078-7
https://doi.org/10.1016/S0031-9422(00)00016-9
Epsilon-viniferin 5281728 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
Sophoraflavanone H 372582 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC4=C(C=C3O)OC(C4C5=CC(=CC(=C5)O)O)C6=CC=C(C=C6)O)C 582.60 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
Sophoraflavanone I 15081162 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC4=C(C=C3O)OC(C4C5=CC(=CC(=C5)O)O)C6=CC=C(C=C6)O)C(=C)C)C 650.70 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
Viniferol D 182979 Click to see C1=CC(=CC=C1C2C(C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C2C(=C6)O)C7=CC=C(C=C7)O)C8=CC=C(C=C8)O)C9=CC(=CC(=C9)O)O)O 680.70 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 1711996 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 424.50 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
(2R)-5,7-dihydroxy-2-(4-hydroxy-2-methoxyphenyl)-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 124355877 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C 438.50 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
Isokurarinone 5318581 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C 438.50 unknown https://doi.org/10.1021/NP990567X
https://doi.org/10.1016/S0031-9422(00)00016-9
Leachianone A 44593449 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C 438.50 unknown https://doi.org/10.1016/S0031-9422(00)00016-9
Marini 73198 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 424.50 unknown https://doi.org/10.1016/S0944-7113(00)80089-6
https://doi.org/10.1016/S0031-9422(00)00016-9
Sophoraflavanone G 72936 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 424.50 unknown https://doi.org/10.1016/S0031-9422(00)00016-9

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