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Sophora stenophylla

Sophora stenophylla - 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 UUID643fd764c20db729042181
Scientific name Sophora stenophylla
Authority A.Gray
First published in J.C.Ives, Rep. Colorado R.4: 10 (1861)

Description Top

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Synonyms Top

Scientific name Authority First published in
Vexibia stenophylla (A.Gray) W.A.Weber Phytologia62: 438 (1987)

Common names Top

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Language Common/alternative name
English fringeleaf necklacepod
Arabic صفيراء ضيقة الأوراق

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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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
    • South-central U.S.A.
      • New Mexico
    • Southwestern U.S.A.
      • Arizona
      • Utah

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000174273
USDA Plants SOST4
Tropicos 13033025
KEW urn:lsid:ipni.org:names:1185410-2
The Plant List ild-20394
Open Tree Of Life 193921
NCBI Taxonomy 1151082
Nature Serve 2.134273
IPNI 1185410-2
iNaturalist 148926
GBIF 2959026
Freebase /m/011spc5v
EOL 640533
USDA GRIN 448257
Wikipedia Sophora_stenophylla

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
Phenolic Compounds Isolated from the Roots of Sophora stenophylla. Masayoshi OHYAMA, Toshiyuki TANAKA, Munekazu IINUMA, Charles L. BURANDT Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.46.663
Complete plastid genome sequence of the chickpea (Cicer arietinum) and the phylogenetic distribution of rps12 and clpP intron losses among legumes (Leguminosae) Jansen RK, Wojciechowski MF, Sanniyasi E, Lee SB, Daniell H Mol Phylogenet Evol 27-Jun-2008
PMCID:PMC2586962
doi:10.1016/j.ympev.2008.06.013
PMID:18638561

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
> 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/10.1248/CPB.46.663
> Organoheterocyclic compounds / Naphthofurans
(5S,5aS,8S,9aS,9bS)-5,8,9b-trihydroxy-6,6,9a-trimethyl-3,5,5a,7,8,9-hexahydrobenzo[g][2]benzofuran-1-one 163061205 Click to see CC1(CC(CC2(C1C(C=C3C2(C(=O)OC3)O)O)C)O)C 282.33 unknown https://doi.org/10.1248/CPB.46.663
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
16146988 Click to see C1=CC(=O)C=CC1=C2C(C3=C4C(C(OC4=CC(=C3)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)C7C(C8=C(C=C(C=C8O)O)C9C(OC1=CC(=CC7=C91)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O 904.90 unknown https://doi.org/10.1248/CPB.46.663
(-)-Canaliculatol 189198 Click to see C1=CC(=CC=C1C2C3C(C(C4=C(C=C(C=C4O)O)C5C(OC6=CC(=CC3=C56)O)C7=CC=C(C=C7)O)C8=CC=C(C=C8)O)C9=C2C(=CC(=C9)O)O)O 680.70 unknown https://doi.org/10.1248/CPB.46.663
(-)-Hopeaphenol 44334030 Click to see C1=CC(=CC=C1C2C(C3=C4C(C(OC4=CC(=C3)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)C7C(C8=C(C=C(C=C8O)O)C9C(OC1=CC(=CC7=C91)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O 906.90 unknown https://doi.org/10.1248/CPB.46.663
(1R,4S,5S,11R,12R,15S,16S,22R)-4,15-bis(3,5-dihydroxyphenyl)-5,11,16,22-tetrakis(4-hydroxyphenyl)-6,17-dioxahexacyclo[10.10.0.02,10.03,7.013,21.014,18]docosa-2(10),3(7),8,13(21),14(18),19-hexaene-9,20-diol 10795822 Click to see C1=CC(=CC=C1C2C3C(C(C4=C3C5=C(C=C4O)OC(C5C6=CC(=CC(=C6)O)O)C7=CC=C(C=C7)O)C8=CC=C(C=C8)O)C9=C2C(=CC1=C9C(C(O1)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O)O 906.90 unknown https://doi.org/10.1248/CPB.46.663
(2S,9S)-2-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]-5-hydroxy-8,8-dimethyl-9-(3-methylbut-2-enyl)-2,3,9,10-tetrahydropyrano[2,3-h]chromen-4-one 162935913 Click to see CC(=CCC1CC2=C(C=C(C3=C2OC(CC3=O)C4=CC5=C(C=C4O)OC(C5C6=CC(=CC(=C6)O)O)C7=CC=C(C=C7)O)O)OC1(C)C)C 650.70 unknown https://doi.org/10.1248/CPB.46.663
(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/10.1248/CPB.46.663
(8R,9S,16R)-8,16-bis(4-hydroxyphenyl)-9-[(8R,9S,16R)-4,6,12-trihydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaen-9-yl]-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaene-4,6,12-triol 101945536 Click to see C1=CC(=CC=C1C2C(C3=C4C(C(OC4=CC(=C3)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)C7C(C8=C(C=C(C=C8O)O)C9C(OC1=CC(=CC7=C91)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O 906.90 unknown https://doi.org/10.1248/CPB.46.663
(9S,16R)-6,12-dihydroxy-8,16-bis(4-hydroxyphenyl)-9-[(8R,9S,16R)-4,6,12-trihydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaen-9-yl]-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2,5,7,10(17),11,13-hexaen-4-one 101945537 Click to see C1=CC(=CC=C1C2C(C3=C4C(C(OC4=CC(=C3)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)C7C8=C9C(C(OC9=CC(=C8)O)C1=CC=C(C=C1)O)C1=CC(=O)C=C(C1=C7C1=CC=C(C=C1)O)O)O 904.90 unknown https://doi.org/10.1248/CPB.46.663
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/10.1248/CPB.46.663
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/10.1248/CPB.46.663
4,15-Bis(3,5-dihydroxyphenyl)-5,11,16,22-tetrakis(4-hydroxyphenyl)-6,17-dioxahexacyclo[10.10.0.02,10.03,7.013,21.014,18]docosa-2(10),3(7),8,13(21),14(18),19-hexaene-9,20-diol 73800070 Click to see C1=CC(=CC=C1C2C3C(C(C4=C3C5=C(C=C4O)OC(C5C6=CC(=CC(=C6)O)O)C7=CC=C(C=C7)O)C8=CC=C(C=C8)O)C9=C2C(=CC1=C9C(C(O1)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O)O 906.90 unknown https://doi.org/10.1248/CPB.46.663
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/10.1248/CPB.46.663
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/10.1248/CPB.46.663
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/10.1248/CPB.46.663
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/10.1248/CPB.46.663
Hopeaphenol 495605 Click to see C1=CC(=CC=C1C2C(C3=C4C(C(OC4=CC(=C3)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)C7C(C8=C(C=C(C=C8O)O)C9C(OC1=CC(=CC7=C91)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O 906.90 unknown https://doi.org/10.1248/CPB.46.663
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/10.1248/CPB.46.663
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/10.1248/CPB.46.663
Stenophyllol B 10794663 Click to see C1=CC(=CC=C1C2C3C(C(C4=C(C=C(C=C4O)O)C5C(OC6=CC(=CC3=C56)O)C7=CC=C(C=C7)O)C8=CC=C(C=C8)O)C9=C2C(=CC(=C9)O)O)O 680.70 unknown https://doi.org/10.1248/CPB.46.663
Stenophyllol C 49866363 Click to see C1=CC(=CC=C1C2C3C(C(C4=C3C5=C(C=C4O)OC(C5C6=CC(=CC(=C6)O)O)C7=CC=C(C=C7)O)C8=CC=C(C=C8)O)C9=C2C(=CC1=C9C(C(O1)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O)O 906.90 unknown https://doi.org/10.1248/CPB.46.663
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 6565899 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/10.1248/CPB.46.663
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/10.1248/CPB.46.663
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/10.1248/CPB.46.663
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/10.1248/CPB.46.663
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/10.1248/CPB.46.663
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2S,3S,4R,5S,6S)-2-[(2S,3S,4S,5R,6S)-4,5-dihydroxy-2-[5-hydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxy-6-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-3-yl]oxy-3,5-dihydroxy-6-methyloxan-4-yl] acetate 162899284 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)OC(=O)C)O 796.70 unknown https://doi.org/10.1248/CPB.46.663
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(1R,12R)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaene-16,17-diol 11472095 Click to see C1C2C(C3=C(O1)C(=C(C=C3)O)O)OC4=CC5=C(C=C24)OCO5 300.26 unknown https://doi.org/10.1248/CPB.46.663
3,4-Dihydroxy-8,9-methylenedioxypterocarpan 24013844 Click to see C1C2C(C3=C(O1)C(=C(C=C3)O)O)OC4=CC5=C(C=C24)OCO5 300.26 unknown https://doi.org/10.1248/CPB.46.663

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