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Haplophyllum tuberculatum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
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)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Haplophyllum tuberculatum (Forssk.) A.Juss. has been used in desert and semi‑desert regions as a fragrant, stomachic, and respiratory remedy, with preparations made from leaves or aerial parts by infusion, decoction, poultice, or maceration in oil or water. Among Bedouin pastoralists in the Arabian Peninsula, an infusion of the leaves is taken after meals to aid digestion and relieve colic (Ghazanfar, 1994). In northeastern Iran’s Sistan and Baluchestan, communities similarly prepare a mild decoction of leaves as a carminative and fever reducer (Mozafarian, 1996). Bedouin healers in Jordan also value the aerial parts, simmering them in water for coughs and respiratory complaints, while in Morocco’s Anti‑Atlas, a poultice of crushed aerial parts or fresh leaves is applied to wounds and skin infections (Bellakhdar, 1997).

The preparation methods are simple and consistent across regions: for a mild digestive tea, pour approximately 250 mL of just‑boiled water over 1–2 g (about 1 small handful) of dried leaves and aerial parts, steep 5–10 minutes, strain, and sip a cup after meals; for a topical poultice, lightly crush 10–20 g of fresh aerial parts to a mash, apply directly to the affected area, cover, and renew twice daily; for a hydroalcoholic tincture (1:5 by weight), macerate 100 g of dried aerial parts in 500 mL of 45% ethanol for 2–4 weeks in a dark place, shaking occasionally, then press and filter. Safety notes are important: aerial parts contain furanocoumarins and quinoline alkaloids that can cause phototoxicity or skin irritation, and the plant should not be used during pregnancy; the tea should be limited to 1–2 cups per day and avoided by individuals with known photosensitivity.

Phytochemistry supports these uses: the aerial parts contain essential oils rich in α‑ and β‑pinene, limonene, and camphor, and notable furanocoumarins such as psoralen and isopimpinellin; quinoline alkaloids (including haplophylline) and tetranortriterpenoids (such as haplophytin) are also reported (Ulubelen et al., 2000). The antimicrobial and carminative actions plausibly relate to the essential oils and the photoactive furanocoumarins, while the antispasmodic effect aligns with the alkaloidal constituents.

Modern relevance remains modest yet steady: small batches of dried aerial parts are sold in regional herb markets, while ethanolic extracts and essential‑oil preparations occasionally appear in niche cosmetics and aromatherapy products; active research continues to probe antimicrobial, anti‑inflammatory, and antispasmodic activities, which dovetails with documented traditional applications in digestive and respiratory care (Ulubelen et al., 2000).

General Uses 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 dichotoma DC. Prodr. 1: 711 (1824)
Ruta montbretii Viv. Pl. Aegypt. Dec. : 13 (1830)
Ruta glabra DC. Prodr. 1: 711 (1824)
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 candolleanum Spach ex Jaub. & Spach Ill. Pl. Orient. 3: t. 270 (1848)
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 glabrum Bornm. Beih. Bot. Centralbl., Abt. 2. 31(2): 168. 1911
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
Haplophyllum dichotomum (DC.) G.Don Gen. Hist. 1: 780 (1831)
Haplophyllum glabrum G.Don Gen. Hist. 1: 780 (1831)

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

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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
An efficient in vitro organogenesis protocol for the endangered relic tree species Bretschneidera sinensis and genetic fidelity assessment using DNA markers Yan X, Zheng K, Li P, Zhong X, Zhu Z, Zhou H, Zhu M Front Plant Sci 10-Apr-2024
PMCID:PMC11039884
doi:10.3389/fpls.2024.1259925
PMID:38660444
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
A critical overview of challenging roles of medicinal plants in improvement of wound healing technology Pathak D, Mazumder A Daru 15-Jan-2024
PMCID:PMC11087437
doi:10.1007/s40199-023-00502-x
PMID:38225520
Molecular Evidence of Breast Cancer Cell Proliferation Inhibition by a Combination of Selected Qatari Medicinal Plants Crude Extracts Alateyah N, Alsafran M, Usman K, Ouhtit A Nutrients 07-Oct-2023
PMCID:PMC10574548
doi:10.3390/nu15194276
PMID:37836560
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
Essential Oils as Nematicides in Plant Protection—A Review Catani L, Manachini B, Grassi E, Guidi L, Semprucci F Plants (Basel) 22-Mar-2023
PMCID:PMC10058003
doi:10.3390/plants12061418
PMID:36987106
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

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides
[(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 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
2-[5-[2-[4-(2-Benzamidoethyl)phenoxy]-1-hydroxyethyl]-5-methyloxolan-2-yl]propan-2-yl acetate 376183 Click to see 469.60 unknown https://doi.org/10.1016/S0031-9422(00)84923-7
N-Phenethylbenzamide 95083 Click to see 225.28 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
Tubacetine 44584601 Click to see 511.60 unknown https://doi.org/10.1021/NP50085A008
https://doi.org/10.1016/S0031-9422(01)00041-3
Tuberine, (+)- 9982128 Click to see 469.60 unknown https://doi.org/10.1016/0031-9422(90)87142-H
https://doi.org/10.1016/S0031-9422(00)84923-7
https://doi.org/10.3109/13880209109082895
> Benzenoids / Phenol ethers
[(3S)-4-acetyloxy-4-methyl-1-[(2S,3R)-2-methyl-3-[[4-[2-(3-methylbut-2-enoylamino)ethyl]phenoxy]methyl]oxiran-2-yl]pentan-3-yl] acetate 44584602 Click to see 489.60 unknown https://doi.org/10.1021/NP50085A008
[(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 469.60 unknown https://doi.org/10.1016/S0031-9422(00)84923-7
> 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
9-(1,3-Benzodioxol-5-yl)-4-hydroxy-6,7-dimethoxynaphtho(2,3-c)furan-1(3H)-one 100492 Click to see 380.30 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
https://doi.org/10.1016/0031-9422(84)83096-4
9-(3,4-Dimethoxy-phenyl)-8-H-furo(3',4':6,7)naphtho(2,3-d)(1,3)dioxol-6-one 122805 Click to see 364.30 unknown https://doi.org/10.1016/0031-9422(84)83096-4
https://doi.org/10.3109/13880209109082895
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/10.1016/0031-9422(84)83096-4
https://doi.org/10.1016/0378-8741(86)90156-X
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/10.3109/13880209109082895
https://doi.org/10.1016/0031-9422(84)83096-4
> 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/10.1016/S0031-9422(00)82500-5
https://doi.org/10.21608/BFSA.1999.66115
3-(1,3-Benzodioxol-5-ylmethyl)-4-[(3,4-dimethoxyphenyl)methyl]oxolan-2-one 495973 Click to see 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 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 512.50 unknown https://doi.org/10.1016/0031-9422(84)83096-4
> Lignans, neolignans and related compounds / Lignan lactones
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
Polygamain 156202 Click to see 352.30 unknown https://doi.org/10.1016/S0031-9422(00)82500-5
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1080/10412905.2000.9712045
(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
> 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 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 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 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 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 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 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 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 283.32 unknown https://doi.org/10.1016/S0031-9422(01)00041-3
https://doi.org/10.1021/NP50085A008
Gamma-Fagarine 107936 Click to see 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/10.1016/S0031-9422(01)00041-3
https://doi.org/10.1055/S-2007-971491
https://doi.org/10.1016/0031-9422(79)83044-7
> 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 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-nonyl-4(1H)-quinolone 13967189 Click to see 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 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 227.26 unknown https://doi.org/10.1016/S0040-4020(01)98709-5
https://doi.org/10.1055/S-2007-971491
https://doi.org/10.1016/S0031-9422(01)00041-3
https://doi.org/10.1021/NP50085A008
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
6-Methoxykaempferol 3-glucoside 5319460 Click to see 478.40 unknown https://doi.org/10.1055/S-2007-971491

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