PlantaeDB Logo
Login Sign-up

Broussonetia kazinoki

Broussonetia kazinoki - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Upload a new image!

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 UUID64400ddc896a4925388918
Scientific name Broussonetia kazinoki
Authority Siebold
First published in Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 221 (1846)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Broussonetia sieboldii Blume Mus. Bot. 2(1-8): 86. 1856 [Feb 1856]
Broussonetia hanjiana M.Kim Korean J. Pl. Taxon. 39: 82 (2009)
Broussonetia kazinoki f. koreana M.Kim Korean J. Pl. Taxon. 39(2): 84 (fig. 1F-G). 2009 [30 Jun 2009]

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Arabic بروسونتة كازينوكية
Azerbaijani kazinok kağız ağacı
Japanese コウゾ
Korean 닥나무
lzh 楮
Russian Бруссонетия Казинока
Chinese 楮
Chinese 构树
Chinese 小构树叶
Chinese 小构树汁
Chinese 小構樹
Chinese 构皮麻
Chinese 谷皮树
Chinese 小构树
Chinese 一种维管植物

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000572564
UNII O6O8V6Z9BA
USDA Plants BRKA4
Tropicos 50064843
INPN 629204
KEW urn:lsid:ipni.org:names:850852-1
The Plant List kew-2683760
Open Tree Of Life 734176
NCBI Taxonomy 66380
IPNI 850852-1
iNaturalist 470727
GBIF 6358484
Freebase /m/0nbdl2c
EPPO BRNKA
EOL 2872472
USDA GRIN 312597
CMAUP NPO16111

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
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Porous Carbon Interlayer Derived from Traditional Korean Paper for Li–S Batteries Choi Y, Jang H, Kim JP, Lee J, Jeong ED, Bae JS, Shin HC Nanomaterials (Basel) 19-Feb-2024
PMCID:PMC10892281
doi:10.3390/nano14040385
PMID:38392757
Anti-Inflammatory Herbal Extracts and Their Drug Discovery Perspective in Atopic Dermatitis Lee JW, Kim EN, Jeong GS Biomol Ther (Seoul) 01-Jan-2024
PMCID:PMC10762282
doi:10.4062/biomolther.2023.102
PMID:38148551
Biological Activity of Fermented Plant Extracts for Potential Dermal Applications Herman A, Herman AP Pharmaceutics 14-Dec-2023
PMCID:PMC10748213
doi:10.3390/pharmaceutics15122775
PMID:38140115
The Genome-Level Survey of the WOX Gene Family in Melastoma dodecandrum Lour. Zheng R, Peng Y, Chen J, Zhu X, Xie K, Ahmad S, Zhao K, Peng D, Liu ZJ, Zhou Y Int J Mol Sci 11-Dec-2023
PMCID:PMC10743900
doi:10.3390/ijms242417349
PMID:38139178
Recent insights about pyrrolidine core skeletons in pharmacology Poyraz S, Döndaş HA, Döndaş NY, Sansano JM Front Pharmacol 06-Sep-2023
PMCID:PMC10512268
doi:10.3389/fphar.2023.1239658
PMID:37745071
Tyrosinase Inhibitors: A Perspective Baber MA, Crist CM, Devolve NL, Patrone JD Molecules 30-Jul-2023
PMCID:PMC10420840
doi:10.3390/molecules28155762
PMID:37570734
Nutraceuticals as Modulators of Immune Function: A Review of Potential Therapeutic Effects Medoro A, Davinelli S, Colletti A, Di Micoli V, Grandi E, Fogacci F, Scapagnini G, Cicero AF Prev Nutr Food Sci 30-Jun-2023
PMCID:PMC10321448
doi:10.3746/pnf.2023.28.2.89
PMID:37416796
Commodity risk assessment of Malus sylvestris plants from United Kingdom Bragard C, Baptista P, Chatzivassiliou E, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Zappalà L, Lucchi A, Gómez P, Urek G, Bernardo U, Bubici G, Carluccio AV, Chiumenti M, Di Serio F, Fanelli E, Marzachì C, Kaczmarek A, Mosbach‐Schulz O, Yuen J EFSA J 19-Jun-2023
PMCID:PMC10277910
doi:10.2903/j.efsa.2023.8076
PMID:37342543
Detection, Diagnosis, and Preventive Management of the Bacterial Plant Pathogen Pseudomonas syringae Yang P, Zhao L, Gao YG, Xia Y Plants (Basel) 25-Apr-2023
PMCID:PMC10181079
doi:10.3390/plants12091765
PMID:37176823
Genome-Wide Analysis of WOX Multigene Family in Sunflower (Helianthus annuus L.) Riccucci E, Vanni C, Vangelisti A, Fambrini M, Giordani T, Cavallini A, Mascagni F, Pugliesi C Int J Mol Sci 08-Feb-2023
PMCID:PMC9968055
doi:10.3390/ijms24043352
PMID:36834765
Kazinol B protects H9c2 cardiomyocytes from hypoxia/reoxygenation-induced cardiac injury by modulating the AKT/AMPK/Nrf2 signalling pathway Zhang Q, Dang YY, Luo X, Fu JJ, Zou ZC, Jia XJ, Zheng GD, Li CW Pharm Biol 05-Feb-2023
PMCID:PMC9904293
doi:10.1080/13880209.2023.2173247
PMID:36740871
A systematic analysis of anti-diabetic medicinal plants from cells to clinical trials Omale S, Amagon KI, Johnson TO, Bremner SK, Gould GW PeerJ 05-Jan-2023
PMCID:PMC9826616
doi:10.7717/peerj.14639
PMID:36627919
Drug discovery inspired by bioactive small molecules from nature Kim S, Lim SW, Choi J Anim Cells Syst (Seoul) 21-Dec-2022
PMCID:PMC9809404
doi:10.1080/19768354.2022.2157480
PMID:36605590
Spray Film-Forming systems as promising topical in situ Systems: A review Bakhrushina EO, Shumkova MM, Sergienko FS, Novozhilova EV, Demina NB Saudi Pharm J 23-Nov-2022
PMCID:PMC9845128
doi:10.1016/j.jsps.2022.11.014
PMID:36685308

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 / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
Dihydrosanguinarine 124069 Click to see CN1CC2=C(C=CC3=C2OCO3)C4=C1C5=CC6=C(C=C5C=C4)OCO6 333.30 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Quaternary benzophenanthridine alkaloids
Chelerythrine 2703 Click to see C[N+]1=C2C(=C3C=CC(=C(C3=C1)OC)OC)C=CC4=CC5=C(C=C42)OCO5 348.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see C1=CC=C(C(=C1)C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Plakoridine A 10257462 Click to see CCCCCCCCCCCCCCCCC(=O)C=C1C(C(C(N1CCC2=CC=C(C=C2)O)CCC)C(=O)OC)O 571.80 unknown https://doi.org/10.1248/CPB.45.505
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(13R)-13-[(2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]-13-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytridecan-4-one 10530062 Click to see C(CCCCC(=O)CCCOC1C(C(C(C(O1)CO)O)O)O)CCCC(C2C(C(C(N2)CO)O)O)O 523.60 unknown https://doi.org/10.3987/REV-02-551
(13R)-13-[(2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]-13-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytridecan-5-one 10506226 Click to see C(CCCC(C1C(C(C(N1)CO)O)O)O)CCCC(=O)CCCCOC2C(C(C(C(O2)CO)O)O)O 523.60 unknown https://doi.org/10.3987/REV-02-551
1-hydroxy-13-[(3R,4S,5R)-4-hydroxy-5-(hydroxymethyl)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypyrrolidin-2-yl]tridecan-5-one 3083518 Click to see C(CCCCC(=O)CCCCO)CCCC1C(C(C(N1)CO)O)OC2C(C(C(C(O2)CO)O)O)O 507.60 unknown https://doi.org/10.3987/REV-02-551
https://doi.org/10.1248/CPB.45.700
1-Hydroxy-13-[4-hydroxy-5-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypyrrolidin-2-yl]tridecan-4-one 53463013 Click to see C(CCCCC1C(C(C(N1)CO)O)OC2C(C(C(C(O2)CO)O)O)O)CCCCC(=O)CCCO 507.60 unknown https://doi.org/10.3987/REV-02-551
13-[(2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypyrrolidin-2-yl]-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytridecan-4-one 162921386 Click to see C(CCCCC1C(C(C(N1)CO)O)OC2C(C(C(C(O2)CO)O)O)O)CCCCC(=O)CCCOC3C(C(C(C(O3)CO)O)O)O 669.80 unknown https://doi.org/10.1248/CPB.48.1281
13-[(2R,3R,4S,5R)-4-hydroxy-5-(hydroxymethyl)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypyrrolidin-2-yl]-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytridecan-4-one 10462112 Click to see C(CCCCC1C(C(C(N1)CO)O)OC2C(C(C(C(O2)CO)O)O)O)CCCCC(=O)CCCOC3C(C(C(C(O3)CO)O)O)O 669.80 unknown https://doi.org/10.3987/REV-02-551
Broussonetine B 10074961 Click to see C(CCCCC(=O)CCCCO)CCCC1C(C(C(N1)CO)O)OC2C(C(C(C(O2)CO)O)O)O 507.60 unknown https://doi.org/10.3987/REV-02-551
> 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 via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 51892422 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1021/NP980281C
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
Disogluside 11827970 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)OC1 576.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 6432744 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
(24E)-24-N-Propylidenecholesterol 5281328 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
(3S,9S,10R,13R,14S,17R)-10,13-Dimethyl-17-[(E,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 16061350 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
10,13-dimethyl-17-(5-propan-2-ylhept-5-en-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86747 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
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 via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Fucosterol 5281326 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasta-5,24(28)-dien-3beta-ol, (E)- 5318567 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasta-5,24(28)-dien-3beta-ol, (Z)- 6432178 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-[7-[4-Hydroxy-5-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypyrrolidin-2-yl]heptyl]cyclohex-2-en-1-one 85363692 Click to see C1CC=C(C(=O)C1)CCCCCCCC2C(C(C(N2)CO)O)OC3C(C(C(C(O3)CO)O)O)O 487.60 unknown https://doi.org/10.3987/REV-02-551
alpha-D-Glucopyranoside, beta-D-fructofuranosyl 91692850 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
Sucrose NF 46782954 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
2-[7-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]heptyl]cyclohex-2-en-1-one 11110173 Click to see C1CC=C(C(=O)C1)CCCCCCCC2C(C(C(N2)CO)O)O 325.40 unknown https://doi.org/10.1248/CPB.49.1487
2-[7-[3,4-Dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]heptyl]cyclohex-2-en-1-one 85300694 Click to see C1CC=C(C(=O)C1)CCCCCCCC2C(C(C(N2)CO)O)O 325.40 unknown https://doi.org/10.3987/REV-02-551
Broussonetine R 10594515 Click to see C1CC(=C(C(=O)C1)CCC(C2C(C(C(N2)CO)O)O)O)CCCCO 357.40 unknown https://doi.org/10.3987/REV-02-551
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(2R,3R,4R,5R)-2-[(1R)-4-(1,7-dioxaspiro[5.5]undecan-2-yl)-1-hydroxybutyl]-5-(hydroxymethyl)pyrrolidine-3,4-diol 102120241 Click to see C1CCOC2(C1)CCCC(O2)CCCC(C3C(C(C(N3)CO)O)O)O 359.50 unknown https://doi.org/10.3987/REV-02-551
https://doi.org/10.1248/CPB.46.1048
(2R,3R,4R,5R)-2-[(1R)-5-(1,6-dioxaspiro[4.5]decan-7-yl)-1-hydroxypentyl]-5-(hydroxymethyl)pyrrolidine-3,4-diol 102120240 Click to see C1CC(OC2(C1)CCCO2)CCCCC(C3C(C(C(N3)CO)O)O)O 359.50 unknown https://doi.org/10.1248/CPB.46.1048
https://doi.org/10.3987/REV-02-551
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Kazinol D 21637680 Click to see CC(=CCC1=C2CCC(OC2=C(C=C1CCCC3=CC(=C(C=C3O)O)C(C)(C)C=C)O)(C)C)C 464.60 unknown via CMAUP database
Kazinol K 21637682 Click to see CC(=CCC1=C2C=CC(OC2=C(C=C1CCCC3=CC(=C(C=C3O)O)C(C)(C)C=C)O)(C)C)C 462.60 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines / N-acylpiperidines
Broussonetine I 10644810 Click to see CC(=O)N1CCCCC1C(C(CCCCCCC2C(C(C(N2)CO)O)O)O)O 402.50 unknown https://doi.org/10.3987/REV-02-551
Broussonetine J 10837020 Click to see CC(=O)N1CCCCC1C(C(CCCCCCC2C(C(C(N2C(=O)C)CO)O)O)O)O 444.60 unknown https://doi.org/10.3987/REV-02-551
> Organoheterocyclic compounds / Pyrrolidines
(2R,3R,4R,5R)-2-[(10S)-10,13-dihydroxytridecyl]-5-(hydroxymethyl)pyrrolidine-3,4-diol 10066288 Click to see C(CCCCC1C(C(C(N1)CO)O)O)CCCCC(CCCO)O 347.50 unknown https://doi.org/10.3987/REV-02-551
(E)-13-[(2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]-1-hydroxytridec-10-en-4-one 10337509 Click to see C(CCC=CCCC1C(C(C(N1)CO)O)O)CCC(=O)CCCO 343.50 unknown https://doi.org/10.3987/REV-02-551
(E)-13-[(2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]-1-hydroxytridec-10-en-5-one 10472623 Click to see C(CCC(=O)CCCCO)CC=CCCC1C(C(C(N1)CO)O)O 343.50 unknown https://doi.org/10.3987/REV-02-551
13-[3,4-Dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]-1,9,13-trihydroxytridecan-4-one 85267232 Click to see C(CCC(=O)CCCO)CC(CCCC(C1C(C(C(N1)CO)O)O)O)O 377.50 unknown https://doi.org/10.3987/REV-02-551
4-Tridecanone, 13-((2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)-2-pyrrolidinyl)-1,13-dihydroxy-, (13R)- 10808575 Click to see C(CCCCC(=O)CCCO)CCCC(C1C(C(C(N1)CO)O)O)O 361.50 unknown https://doi.org/10.1248/CPB.45.700
Broussonetine C 177267 Click to see C(CCCCC1C(C(C(N1)CO)O)O)CCCCC(=O)CCCO 345.50 unknown https://doi.org/10.1248/CPB.45.700
Broussonetine D 177263 Click to see C(CCCCC(=O)CCCCO)CCCC1C(C(C(N1)CO)O)O 345.50 unknown https://doi.org/10.1248/CPB.45.700
Broussonetine F 10666310 Click to see C(CCCC(C1C(C(C(N1)CO)O)O)O)CCCC(=O)CCCCO 361.50 unknown https://doi.org/10.1248/CPB.45.700
Broussonetine S 10832551 Click to see C(CCCCC(C1C(C(C(N1)CO)O)O)O)CCCC(CCCO)O 363.50 unknown https://doi.org/10.3987/REV-02-551
Broussonetine V 101096783 Click to see C(CCC=CCCC1C(C(C(N1)CO)O)O)CCC(=O)CCCO 343.50 unknown https://doi.org/10.3987/REV-02-551
https://doi.org/10.1248/CPB.49.492
Broussonetinine B 11725129 Click to see C(CCCCC(=O)CCCCO)CCCC1C(C(C(N1)CO)O)O 345.50 unknown https://doi.org/10.1248/CPB.45.700
> Organoheterocyclic compounds / Pyrrolines
Broussonetine U 101012236 Click to see C(CCCCC(=O)CCCCO)CCCC1=NC(C(C1O)O)CO 343.50 unknown https://doi.org/10.3987/REV-02-551
> Organoheterocyclic compounds / Pyrrolizidines
(10R)-10-[(3S,5R,6R,7R,8R)-6,7-dihydroxy-5-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizin-3-yl]-1,10-dihydroxydecan-5-one 9998578 Click to see C1CC(N2C1C(C(C2CO)O)O)C(CCCCC(=O)CCCCO)O 359.50 unknown https://doi.org/10.1248/CPB.48.1281
(10R)-10-[(3S,5R,6R,7R)-6,7-dihydroxy-5-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizin-3-yl]-1,10-dihydroxydecan-5-one 101096882 Click to see C1CC(N2C1C(C(C2CO)O)O)C(CCCCC(=O)CCCCO)O 359.50 unknown https://doi.org/10.3987/REV-02-551
https://doi.org/10.1248/CPB.47.907
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 2-prenylated flavans
(+)-(2R)kazinol I 46871916 Click to see CC(=CCC1=C(C(=C(C=C1C2CCC3=C(O2)C=C(C=C3)O)O)O)CC=C(C)C)C 394.50 unknown via CMAUP database
(3S)-6-[(2S)-7-hydroxy-6-(2-methylbut-3-en-2-yl)-3,4-dihydro-2H-chromen-2-yl]-2,2-dimethyl-5-(3-methylbut-2-enyl)-3,4-dihydrochromene-3,8-diol 163041826 Click to see CC(=CCC1=C2CC(C(OC2=C(C=C1C3CCC4=CC(=C(C=C4O3)O)C(C)(C)C=C)O)(C)C)O)C 478.60 unknown https://doi.org/10.1021/NP980281C
Kazinol B 480869 Click to see CC(=CCC1=C(C=C2C=CC(OC2=C1O)(C)C)C3CCC4=C(O3)C=C(C=C4)O)C 392.50 unknown https://doi.org/10.1016/S0367-326X(03)00062-5
Kazinol H 44257177 Click to see CC(=CCC1=C2C=CC(OC2=C(C=C1C3CCC4=CC(=C(C=C4O3)O)C(C)(C)C=C)O)(C)C)C 460.60 unknown https://doi.org/10.1021/NP980281C
https://doi.org/10.1248/CPB.34.1968
Kazinol Q 10600152 Click to see CC(=CCC1=CC(=C(C(=C1O)O)CC=C(C)C)C2CCC3=CC(=C(C=C3O2)O)C(C)(C)C=C)C 462.60 unknown https://doi.org/10.1021/NP980281C
Kazinol R 10838380 Click to see CC(=CCC1=C2CC(C(OC2=C(C=C1C3CCC4=CC(=C(C=C4O3)O)C(C)(C)C=C)O)(C)C)O)C 478.60 unknown https://doi.org/10.1021/NP980281C
kazinol U 46871902 Click to see CC(=CCC1=C(C=CC(=C1O)O)C2CCC3=C(O2)C=C(C=C3)O)C 326.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 3-prenylated flavones
(8R)-2-[3,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-3,5-dihydroxy-8,9,9-trimethyl-8H-furo[2,3-h]chromen-4-one 162924265 Click to see CC1C(C2=C(O1)C=C(C3=C2OC(=C(C3=O)O)C4=CC(=C(C(=C4)O)O)CC=C(C)C)O)(C)C 438.50 unknown https://doi.org/10.1021/NP010283O
Broussonol C 11743840 Click to see CC1C(C2=C(O1)C=C(C3=C2OC(=C(C3=O)O)C4=CC(=C(C(=C4)O)O)CC=C(C)C)O)(C)C 438.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
Broussonol E 10343070 Click to see CC(=CCC1=C(C(=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)O)O)C 438.50 unknown https://doi.org/10.4014/JMB.1007.07026
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
Broussonol D 10365850 Click to see CC(=CCC1=C(C(=CC(=C1)C2=C(C(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)O)O)C 438.50 unknown https://doi.org/10.1021/NP010283O
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
3,4-Dihydro-2-(4-hydroxyphenyl)-2H-1-benzopyran-7-ol 3500616 Click to see C1CC2=C(C=C(C=C2)O)OC1C3=CC=C(C=C3)O 242.27 unknown via CMAUP database
Tupichinol C 11064571 Click to see C1CC2=C(C=C(C=C2)O)OC1C3=CC=C(C=C3)O 242.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
Broussonol A 10342975 Click to see CC1(C=CC2=C(O1)C(=CC(=C2)C3=C(C(=O)C4=C(O3)C(=C(C=C4O)O)C(C)(C)C=C)O)O)C 436.50 unknown via CMAUP database
Broussonol B 10320815 Click to see CC1C(C2=C(O1)C=C(C3=C2OC(=C(C3=O)O)C4=CC5=C(C(=C4)O)OC(C=C5)(C)C)O)(C)C 436.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
2-[3-(4-Hydroxyphenyl)propyl]-5-methoxyphenol 5315502 Click to see COC1=CC(=C(C=C1)CCCC2=CC=C(C=C2)O)O 258.31 unknown via CMAUP database
Broussonin C 442289 Click to see CC(=CCC1=C(C=CC(=C1)CCCC2=C(C=C(C=C2)O)O)O)C 312.40 unknown via CMAUP database
kazinol C 21637679 Click to see CC(=CCC1=C(C(=C(C=C1CCCC2=CC(=C(C=C2O)O)C(C)(C)C=C)O)O)CC=C(C)C)C 464.60 unknown via CMAUP database
Kazinol F 184311 Click to see CC(=CCC1=C(C(=C(C=C1CCCC2=C(C=C(C=C2)O)O)O)O)CC=C(C)C)C 396.50 unknown https://doi.org/10.1021/NP010283O
Kazinol J 21637732 Click to see CC(=CCC1=C(C(=C(C=C1CCCC2=C(C=C(C=C2)O)OC)O)O)CC=C(C)C)C 410.50 unknown https://doi.org/10.1021/NP010283O
Kazinol S 44569902 Click to see CC(=CCC1=C(C(=C(C=C1CCCC2=CC(=C(C=C2O)O)C(C)(C)C=C)O)O)CC3C(O3)(C)C)C 480.60 unknown via CMAUP database

Biological Material Top ebay Auctions

Please wait .. loading items ..

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.