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Haplophyllum tuberculatum

Haplophyllum tuberculatum - 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 UUID64401fbc28bd1199808223
Scientific name Haplophyllum tuberculatum
Authority (Forssk.) A.Juss.
First published in Mém. Mus. Hist. Nat. 12: 528 (1825)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ruta obovata (Steud.) O.Schwartz Mitt. Inst. Allg. Bot. Hamburg 10: 125 (1939)
Ruta montbretii Viv. Pl. Aegypt. Dec. : 13 (1830)
Ruta telephiifolia Pau Trab. Mus. Ci. Nat., Ser. Bot. 14: 19 (1918)
Ruta propinqua (Spach) O.Schwartz Mitt. Inst. Allg. Bot. Hamburg 10: 125 (1939)
Ruta stocksiana (Boiss.) Burkill List Fl. Pl. Baluchistan : 17 (1909)
Ruta kotschyi Pau Trab. Mus. Ci. Nat., Ser. Bot. 14: 19 (1918)
Haplophyllum arabicum Boiss. Diagn. Pl. Orient. 8: 127 (1849)
Haplophyllum chesneyanum Boiss. Fl. Orient. 1: 941 (1867)
Haplophyllum eremophilum Boiss. & Hausskn. Fl. Orient. , Suppl.: 149 (1888)
Haplophyllum filifolium Spach ex Jaub. & Spach Ill. Pl. Orient. 3: t. 265 (1848)
Haplophyllum haussknechtii Boiss. Fl. Orient. , Suppl.: 148 (1888)
Haplophyllum kotschyi Spach Ann. Sci. Nat., Bot. , sér. 3, 11: 186 (1849)
Haplophyllum longifolium Boiss. Diagn. Pl. Orient. 8: 127 (1849)
Haplophyllum obovatum Hand.-Mazz. Verh. K. K. Zool.-Bot. Ges. Wien 63: 54 (1913)
Haplophyllum propinquum Spach Ann. Sci. Nat., Bot. , sér. 3, 11: 189 (1849)
Haplophyllum stocksianum Boiss. Diagn. Pl. Orient. , ser. 2, 1: 117 (1854)
Haplophyllum trichostylum Bunge Fl. Orient. 1: 941 (1867)
Haplophyllum vermiculare Hand.-Mazz. Verh. K. K. Zool.-Bot. Ges. Wien 63: 51 (1913)
Haplophyllum villosulum Boiss. & Hausskn. Fl. Orient. 1: 936 (1867)
Haplophyllum tuberculatum subsp. vermiculare (Hand.-Mazz.) Maire Bull. Soc. Hist. Nat. Afrique N. 32: 207 1941
Ruta tuberculata Forssk. Fl. Aegypt.-Arab. : 86 (1775)
Ruta tuberculata var. montbretti DC. Prodr. 1: 711 1824

Common names Top

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Language Common/alternative name
Arabic صنان التيس
Arabic عفنة
Arabic مسيكة
Arabic شجرات الريح
Arabic مجبينية

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
  • Africa
    • Northeast Tropical Africa
      • Chad
      • Somalia
      • Sudan
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
  • Asia-temperate
    • Arabian Peninsula
      • Kuwait
      • Oman
      • Saudi Arabia
      • Yemen
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Sinai
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000715624
Tropicos 28101396
INPN 611163
KEW urn:lsid:ipni.org:names:771339-1
Open Tree Of Life 1081353
NCBI Taxonomy 452784
NBN Atlas NHMSYS0000459212
IPNI 771339-1
iNaturalist 489421
GBIF 5834570
EPPO HAYTU
USDA GRIN 417521

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 sustainable use of diverse plants accustomed by different ethnic groups in Sibi District, Balochistan, Pakistan Maria B, Saeed S, Ahmed A, Ahmed M, Rehman A PLoS One 21-Feb-2024
PMCID:PMC10880983
doi:10.1371/journal.pone.0294989
PMID:38381718
Pharmacological activities of chemically characterized essential oils from Haplophyllum tuberculatum (Forssk.) Agour A, Mssillou I, Allali A, Chebaibi M, El Abdali Y, El Barnossi A, Bin Jardan YA, Wondmie GF, Nafidi HA, Bourhia M, Bari A, Lyoussi B, Derwich E Front Chem 06-Oct-2023
PMCID:PMC10587419
doi:10.3389/fchem.2023.1251449
PMID:37867997
Naturally occurring phenylethanoids and phenylpropanoids: antimalarial potential Abdelmohsen UR, Bayoumi SA, Mohamed NM, Mostafa YA, Ngwa CJ, Pradel G, Farag SF RSC Adv 07-Sep-2023
PMCID:PMC10483269
doi:10.1039/d3ra04242a
PMID:37692342
Chemical Composition, Larvicidal and Molluscicidal Activity of Essential Oils of Six Guava Cultivars Grown in Vietnam Luu HV, Nguyen HH, Satyal P, Vo VH, Ngo GH, Pham VT, Setzer WN Plants (Basel) 07-Aug-2023
PMCID:PMC10421063
doi:10.3390/plants12152888
PMID:37571040
Molluscicidal and Larvicidal Potency of N-Heterocylic Analogs against Biomophalaria alexandrina Snails and Schistosoma mansoni Larval Stages Sheir SK, Elmongy EI, Mohamad AH, Osman GY, Bendary SE, Ahmed AA, Binsuwaidan R, El-Sayed IE Pharmaceutics 10-Apr-2023
PMCID:PMC10142358
doi:10.3390/pharmaceutics15041200
PMID:37111685
The Type of Grain Counts: Effectiveness of Three Essential Oil-Based Nanoemulsions against Sitophilus oryzae Kavallieratos NG, Bonacucina G, Nika EP, Skourti A, Georgakopoulou SK, Filintas CS, Panariti AM, Maggi F, Petrelli R, Ferrati M, Spinozzi E, Perinelli DR, Canale A, Benelli G Plants (Basel) 11-Feb-2023
PMCID:PMC9962515
doi:10.3390/plants12040813
PMID:36840161
Antimicrobial Compounds in Food Packaging Duda-Chodak A, Tarko T, Petka-Poniatowska K Int J Mol Sci 27-Jan-2023
PMCID:PMC9917197
doi:10.3390/ijms24032457
PMID:36768788
How the volatile organic compounds emitted by corpse plant change through flowering Kang L, Kaur J, Winkeler K, Kubiak D, Hill JE Sci Rep 07-Jan-2023
PMCID:PMC9825558
doi:10.1038/s41598-022-27108-8
PMID:36611048
Phytochemical Profiling of Sambucus nigra L. Flower and Leaf Extracts and Their Antimicrobial Potential against Almond Tree Pathogens Sánchez-Hernández E, Balduque-Gil J, González-García V, Barriuso-Vargas JJ, Casanova-Gascón J, Martín-Gil J, Martín-Ramos P Int J Mol Sci 06-Jan-2023
PMCID:PMC9866908
doi:10.3390/ijms24021154
PMID:36674670
Wound Healing Properties of Natural Products: Mechanisms of Action Criollo-Mendoza MS, Contreras-Angulo LA, Leyva-López N, Gutiérrez-Grijalva EP, Jiménez-Ortega LA, Heredia JB Molecules 06-Jan-2023
PMCID:PMC9867334
doi:10.3390/molecules28020598
PMID:36677659
Active Compounds with Medicinal Potential Found in Maxillariinae Benth. (Orchidaceae Juss.) Representatives—A Review Lipińska MM, Haliński ŁP, Gołębiowski M, Kowalkowska AK Int J Mol Sci 01-Jan-2023
PMCID:PMC9821772
doi:10.3390/ijms24010739
PMID:36614181
Effect of Eucalyptus globulus oil and Ricinus communis methanolic extract as potential natural molluscicides on the reproductive biology and some antioxidant enzymes of the land snail, Theba pisana Desouky MM, Abd El-Atti MS, Elsheakh AA, Elgohary WS Heliyon 20-Dec-2022
PMCID:PMC9798189
doi:10.1016/j.heliyon.2022.e12405
PMID:36590486
Leonotis nepetifolia Flower Bud Extract Mediated Green Synthesis of Silver Nanoparticles, Their Characterization, and In Vitro Evaluation of Biological Applications Nagaraja SK, Niazi SK, Bepari A, Assiri RA, Nayaka S Materials (Basel) 16-Dec-2022
PMCID:PMC9781718
doi:10.3390/ma15248990
PMID:36556796
Effect of Bauhinia monandra Kurz Leaf Preparations on Embryonic Stages and Adult Snails of Biomphalaria glabrata (Say, 1818), Schistosoma mansoni Cercariae and Toxicity in Artemia salina Aguiar TW, Batista JJ, Ferreira SA, Sampaio MD, Pereira DR, Ferreira MR, Soares LA, Melo AM, Albuquerque MC, Aires AD, de Araújo HD, Coelho LC Molecules 05-Aug-2022
PMCID:PMC9370106
doi:10.3390/molecules27154993
PMID:35956946
Phenolic Characterization Using cLC-DAD Analysis and Evaluation of In Vitro and In Vivo Pharmacological Activities of Ruta tuberculata Forssk Saidi A, Hambaba L, Bensaad MS, Melakhessou MA, Bensouici C, Ferhat N, Kahoul MA, Helal M, Sami R, Alharthy SA, Baty RS, Alsubhi NH, Alrefaei GI, Elhakem A, Alharthi S, Elsaid FG, Shati AA Antioxidants (Basel) 11-Jul-2022
PMCID:PMC9312153
doi:10.3390/antiox11071351
PMID:35883842

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 / Benzoic acids and derivatives / Benzamides
(+)-Tuberine 9982128 Click to see CC(=O)OC(C)(C)C1CCC(O1)(C)C(COC2=CC=C(C=C2)CCNC(=O)C3=CC=CC=C3)O 469.60 unknown https://doi.org/10.3109/13880209109082895
https://doi.org/10.1016/S0031-9422(00)84923-7
https://doi.org/10.1016/0031-9422(90)87142-H
[(3R)-4-acetyloxy-1-[(2S,3S)-3-[[4-(2-benzamidoethyl)phenoxy]methyl]-2-methyloxiran-2-yl]-4-methylpentan-3-yl] acetate 163023277 Click to see CC(=O)OC(CCC1(C(O1)COC2=CC=C(C=C2)CCNC(=O)C3=CC=CC=C3)C)C(C)(C)OC(=O)C 511.60 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
[4-Acetyloxy-1-[3-[[4-(2-benzamidoethyl)phenoxy]methyl]-2-methyloxiran-2-yl]-4-methylpentan-3-yl] acetate 376181 Click to see CC(=O)OC(CCC1(C(O1)COC2=CC=C(C=C2)CCNC(=O)C3=CC=CC=C3)C)C(C)(C)OC(=O)C 511.60 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
https://doi.org/10.1021/NP50085A008
N-phenethylbenzamide 95083 Click to see C1=CC=C(C=C1)CCNC(=O)C2=CC=CC=C2 225.28 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
Tubacetine 44584601 Click to see CC(=O)OC(CCC1(C(O1)COC2=CC=C(C=C2)CCNC(=O)C3=CC=CC=C3)C)C(C)(C)OC(=O)C 511.60 unknown https://doi.org/10.1021/NP50085A008
https://doi.org/10.1016/S0031-9422(01)00041-3
Tuberine 376183 Click to see CC(=O)OC(C)(C)C1CCC(O1)(C)C(COC2=CC=C(C=C2)CCNC(=O)C3=CC=CC=C3)O 469.60 unknown https://doi.org/10.1016/S0031-9422(00)84923-7
> Benzenoids / Phenol ethers
[(3S)-4-acetyloxy-4-methyl-1-[(2S,3S)-2-methyl-3-[[4-[2-(3-methylbut-2-enoylamino)ethyl]phenoxy]methyl]oxiran-2-yl]pentan-3-yl] acetate 638662 Click to see CC(=CC(=O)NCCC1=CC=C(C=C1)OCC2C(O2)(C)CCC(C(C)(C)OC(=O)C)OC(=O)C)C 489.60 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
2-[(2S,5S)-5-[(1S)-2-[4-(2-benzamidoethyl)phenoxy]-1-hydroxyethyl]-5-methyloxolan-2-yl]propan-2-yl acetate 162845188 Click to see CC(=O)OC(C)(C)C1CCC(O1)(C)C(COC2=CC=C(C=C2)CCNC(=O)C3=CC=CC=C3)O 469.60 unknown https://doi.org/10.1016/S0031-9422(00)84923-7
Tubasenecine 44584602 Click to see CC(=CC(=O)NCCC1=CC=C(C=C1)OCC2C(O2)(C)CCC(C(C)(C)OC(=O)C)OC(=O)C)C 489.60 unknown https://doi.org/10.1021/NP50085A008
> Benzenoids / Phenol ethers / Anisoles
(Z)-N-(4-Methoxystyryl)formamide 11137672 Click to see COC1=CC=C(C=C1)C=CNC=O 177.20 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
Tuberin 5352006 Click to see COC1=CC=C(C=C1)C=CNC=O 177.20 unknown https://doi.org/10.1021/NP50085A008
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
Diphyllin 100492 Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2O)COC3=O)C4=CC5=C(C=C4)OCO5)OC 380.30 unknown https://doi.org/10.1016/0031-9422(84)83096-4
https://doi.org/10.1016/S0031-9422(01)00041-3
Justicidin A 159982 Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2OC)COC3=O)C4=CC5=C(C=C4)OCO5)OC 394.40 unknown https://doi.org/10.21608/BFSA.1999.66115
https://doi.org/10.3109/13880209109082895
https://doi.org/10.1016/0378-8741(86)90156-X
https://doi.org/10.1016/0031-9422(84)83096-4
Justicidin B 442882 Click to see COC1=CC2=CC3=C(C(=C2C=C1OC)C4=CC5=C(C=C4)OCO5)C(=O)OC3 364.30 unknown https://doi.org/10.1016/0031-9422(84)83096-4
https://doi.org/10.3109/13880209109082895
Retrochinensin 122805 Click to see COC1=C(C=C(C=C1)C2=C3C=C4C(=CC3=CC5=C2COC5=O)OCO4)OC 364.30 unknown https://doi.org/10.1016/0031-9422(84)83096-4
https://doi.org/10.3109/13880209109082895
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3S,4S)-3-(1,3-benzodioxol-5-ylmethyl)-4-[(3,4-dimethoxyphenyl)methyl]oxolan-2-one 92154432 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC4=C(C=C3)OCO4)OC 370.40 unknown https://doi.org/10.21608/BFSA.1999.66115
https://doi.org/10.1016/S0031-9422(00)82500-5
3-(1,3-Benzodioxol-5-ylmethyl)-4-[(3,4-dimethoxyphenyl)methyl]oxolan-2-one 495973 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC4=C(C=C3)OCO4)OC 370.40 unknown https://doi.org/10.1016/S0031-9422(00)82500-5
https://doi.org/10.21608/BFSA.1999.66115
> Lignans, neolignans and related compounds / Lignan glycosides
9-(1,3-benzodioxol-5-yl)-4-[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6,7-dimethoxy-1H-benzo[f][2]benzofuran-3-one 162821327 Click to see COC1=C(C=C2C(=C1)C(=C3COC(=O)C3=C2OC4C(C(CO4)(CO)O)O)C5=CC6=C(C=C5)OCO6)OC 512.50 unknown https://doi.org/10.1016/0031-9422(84)83096-4
Naphtho[2,3-c]furan-1(3H)-one, 4-(D-apio-beta-D-furanosyloxy)-9-(1,3-benzodioxol-5-yl)-6,7-dimethoxy- 13873812 Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2OC4C(C(CO4)(CO)O)O)COC3=O)C5=CC6=C(C=C5)OCO6)OC 512.50 unknown https://doi.org/10.1016/0031-9422(84)83096-4
Tuberculatin 10391676 Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2OC4C(C(CO4)(CO)O)O)COC3=O)C5=CC6=C(C=C5)OCO6)OC 512.50 unknown https://doi.org/10.1016/0031-9422(84)83096-4
> Lignans, neolignans and related compounds / Lignan lactones
(5R,5aR,8aR)-5-(1,3-benzodioxol-5-yl)-5a,8,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one 156202 Click to see C1C2COC(=O)C2C(C3=CC4=C(C=C31)OCO4)C5=CC6=C(C=C5)OCO6 352.30 unknown https://doi.org/10.1016/S0031-9422(00)82500-5
5-(1,3-benzodioxol-5-yl)-5a,8,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one 5199318 Click to see C1C2COC(=O)C2C(C3=CC4=C(C=C31)OCO4)C5=CC6=C(C=C5)OCO6 352.30 unknown https://doi.org/10.1016/S0031-9422(00)82500-5
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(3R,3'S)-3'-[(3R)-2-hydroxy-2,6-dimethylhept-5-en-3-yl]spiro[1H-quinoline-3,2'-oxirane]-2,4-dione 101124733 Click to see CC(=CCC(C1C2(O1)C(=O)C3=CC=CC=C3NC2=O)C(C)(C)O)C 329.40 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
3'-(2-hydroxy-2,6-dimethylhept-5-en-3-yl)spiro[1H-quinoline-3,2'-oxirane]-2,4-dione 73880648 Click to see CC(=CCC(C1C2(O1)C(=O)C3=CC=CC=C3NC2=O)C(C)(C)O)C 329.40 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.2000.9712045
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.2000.9712045
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[3,4,8,8a-tetramethyl-7-oxo-4-[2-(5-oxo-2H-furan-3-yl)ethyl]-2,3,4a,5,6,8-hexahydro-1H-naphthalen-1-yl] 2-methylbut-2-enoate 162949426 Click to see CC=C(C)C(=O)OC1CC(C(C2C1(C(C(=O)CC2)C)C)(C)CCC3=CC(=O)OC3)C 416.50 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
> Organoheterocyclic compounds / Furopyridines
(8R)-4,8-dimethoxy-8-(3-methylbut-2-enyl)-5,6-dihydrofuro[2,3-b]quinolin-7-one 163029165 Click to see CC(=CCC1(C(=O)CCC2=C1N=C3C(=C2OC)C=CO3)OC)C 315.40 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
4,8-Dimethoxy-8-(3-methylbut-2-enyl)-5,6-dihydrofuro[2,3-b]quinolin-7-one 14447740 Click to see CC(=CCC1(C(=O)CCC2=C1N=C3C(=C2OC)C=CO3)OC)C 315.40 unknown https://doi.org/10.3109/13880209109082895
https://doi.org/10.1021/NP50085A008
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
(R)-dyphylline 688353 Click to see CN1C2=C(C(=O)N(C1=O)C)N(C=N2)CC(CO)O 254.24 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
6-Methoxy-1-[(4-methoxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinolin-5-ol 162998075 Click to see COC1=CC=C(C=C1)CC2C3=C(CCN2)C(=C(C=C3)OC)O 299.40 unknown https://doi.org/10.21608/BFSA.1999.66115
> Organoheterocyclic compounds / Naphthofurans
8-(1,3-benzodioxol-5-yl)-5-hydroxy-6,7-dimethoxy-3H-benzo[f][2]benzofuran-1-one 162997063 Click to see COC1=C(C2=C(C=C3COC(=O)C3=C2)C(=C1OC)O)C4=CC5=C(C=C4)OCO5 380.30 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
(E,3S)-8-(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-2,6-dimethyloct-6-ene-2,3-diol 162991894 Click to see CC(=CCOC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)CCC(C(C)(C)O)O 415.50 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
(R)-1-((4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy)-3-methylbutane-2,3-diol 636924 Click to see CC(C)(C(COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)O)O 347.40 unknown https://doi.org/10.1016/0031-9422(79)83044-7
(Z,3S)-8-(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-2,6-dimethyloct-6-ene-2,3-diol 162991896 Click to see CC(=CCOC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)CCC(C(C)(C)O)O 415.50 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
8-(4,8-Dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-2,6-dimethyloct-6-ene-2,3-diol 162991892 Click to see CC(=CCOC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)CCC(C(C)(C)O)O 415.50 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
Evoxine 73416 Click to see CC(C)(C(COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)O)O 347.40 unknown https://doi.org/10.1016/0031-9422(79)83044-7
https://doi.org/10.1055/S-2007-971491
Furo(2,3-b)quinolin-7-ol, 4-methoxy-8-(3-methyl-2-butenyl)- 135743956 Click to see CC(=CCC1=C(C=CC2=C1N=C3C(=C2OC)C=CO3)O)C 283.32 unknown https://doi.org/10.1021/NP50085A008
https://doi.org/10.1016/S0031-9422(01)00041-3
gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
https://doi.org/10.1016/0031-9422(79)83044-7
https://doi.org/10.1055/S-2007-971491
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1055/S-2007-971491
https://doi.org/10.1016/0031-9422(79)83044-7
https://doi.org/10.1016/S0031-9422(01)00041-3
> Organoheterocyclic compounds / Quinolines and derivatives / Hydroquinolines
(3R)-3-(2-methylbut-3-en-2-yl)-3-(3-methylbut-2-enyl)-1H-quinoline-2,4-dione 163049490 Click to see CC(=CCC1(C(=O)C2=CC=CC=C2NC1=O)C(C)(C)C=C)C 297.40 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives
2(1H)-Quinolinone, 3-(3-methyl-2-butenyl)-4-[(3-methyl-2-butenyl)oxy]- 4556 Click to see CC(=CCC1=C(C2=CC=CC=C2NC1=O)OCC=C(C)C)C 297.40 unknown https://doi.org/10.1016/S0031-9422(00)82500-5
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
1-Methyl-2-nonylquinolin-4(1H)-one 13967189 Click to see CCCCCCCCCC1=CC(=O)C2=CC=CC=C2N1C 285.40 unknown https://doi.org/10.1016/S0031-9422(00)82500-5
Buchapine 461150 Click to see CC(=CCC1(C(=O)C2=CC=CC=C2NC1=O)C(C)(C)C=C)C 297.40 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
https://doi.org/10.1016/S0031-9422(00)82500-5
https://doi.org/10.1021/NP50085A008
Haplotubinone 636965 Click to see CC(=CCC(C1C2(O1)C(=O)C3=CC=CC=C3NC2=O)C(C)(C)O)C 329.40 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
Flindersine 68230 Click to see CC1(C=CC2=C(O1)C3=CC=CC=C3NC2=O)C 227.26 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
https://doi.org/10.1016/S0040-4020(01)98709-5
https://doi.org/10.1055/S-2007-971491
https://doi.org/10.1021/NP50085A008
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
6-Methoxykaempferol 3-O-glucoside 5319460 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O)O 478.40 unknown https://doi.org/10.1055/S-2007-971491

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