Glycosmis parviflora

Details Top

Internal ID UUID64401e2dd7101974353185
Scientific name Glycosmis parviflora
Authority (Sims) Little
First published in Phytologia 2: 463 (1948)

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.

Ethnobotanical Uses

Documented medicinal and culinary preparations of Glycosmis parviflora center on leaf infusions or decoctions, with occasional poultices of crushed leaves. Among the Mapuche of southern Chile, the plant is not part of their tradition. Across mainland Southeast Asia, especially among Thai and Lao hill peoples in northern Thailand and Laos, fresh or dried leaf infusions have been used as a bitter tonic and for colds, fevers, and digestive complaints (Perry and Metzger, 1980; Bundit et al., 1999). In Bangladesh and India’s Northeast, preparations of the leaves are taken as mild teas for fever and general weakness (Kumar, 2009). In Malaysia, crushed leaf poultices are applied to wounds and inflamed skin (Perry and Metzger, 1980).

In these regions the whole leaf—fresh when available or dried for storage—is the standard plant part, and the preparations are short, simple teas or decoctions. On the coast of southern China and northern Vietnam, comparable uses as a febrifuge have been recorded as cold macerations or decoctions of fresh leaves (Hu, 2005). Typical quantities reported in ethnobotanical surveys are a small handful of fresh leaves or one to two tablespoonfuls of dried leaf per liter of water, infused or briefly boiled (Kumar, 2009). In clinical and ethnobotanical contexts the product is commonly referred to as a mild tea, and the same plant part is used for poultices (Perry and Metzger, 1980; Hu, 2005).

A practical, one-time preparation for a mild leaf tea is straightforward. Use about 8–10 fresh leaves or 1–2 teaspoons of dried, crumbled leaf; pour 250 mL of just-boiled water over the plant material and steep 5–10 minutes. Strain and drink 1 cup as needed, no more than twice daily. While toxicity data for Glycosmis parviflora are limited, bitter preparations are not recommended for pregnancy or for individuals with known sensitivity to Rutaceae; if signs of irritation occur, discontinue use (Vasisht et al., 1999; JASAN, 2005).

Well-established constituents of Rutaceae leaves include limonoids such as limonin and obacunone, coumarins such as scopoletin and umbelliferone, and flavonoids such as quercetin and kaempferol glycosides, with furanocoumarins occasionally reported (Li and Sze, 2004; Shukla et al., 2009). These compounds provide a plausible biochemical basis for the documented uses as a bitter tonic, febrifuge, and topical anti-inflammatory.

The tea continues to be prepared at household level in parts of mainland Southeast Asia and Northeast India, with pharmacognostic and phytochemical work focused on the leaf’s alkaloids and limonoids (Li and Sze, 2004; Shukla et al., 2009).

General Uses Top

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Common products:
Edible uses are not documented for this taxon.

Industrial and craft applications:
No industrial or craft uses are documented.

Food and beverages (non-medicinal):
No beverage or food uses are documented for this taxon.

Colorants and tanning:
No tannin-based tanning or natural dye use is documented.

Wood and fiber:
No timber, fiber, or pulp uses are documented.

Fragrance and cosmetics:
No essential oil, perfume, or cosmetic ingredient uses are documented.

Properties relevant to use:
No physical or chemical properties relevant to commercial use are documented for this taxon.

Standards and regulation:
No relevant standards or regulatory frameworks are documented for this taxon.

Sustainability and sourcing:
No sustainable harvesting or conservation context is documented for this taxon.

Synonyms Top

Scientific name Authority First published in
Murraya cerasiformis Blanco Fl. Filip. : 363 (1837)
Amyris axilliflora Griseb. Cat. Pl. Cub. : 66 (1866)
Glycosmis americana Sagot ex Oliv. J. Proc. Linn. Soc., Bot. 5(Suppl. 2): 37 (1861)
Glycosmis citrifolia Lindl. Trans. Hort. Soc. London 6: 72 (1825)
Glycosmis heterophylla A.Rich. Hist. Fis. Cuba, Bot. 10: 231 (1845)
Glycosmis obtusa Miq. Ann. Mus. Bot. Lugduno-Batavi 1: 211 (1864)
Glycosmis parviflora var. obtusa (Miq.) B.C.Stone Proc. Acad. Nat. Sci. Philadelphia 137(2): 15 (1985)
Glycosmis pentaphylla var. citrifolia (Willd.) Bakh.f. Blumea 6: 366 1950
Limonia parviflora Sims Bot. Mag. 50: t. 2416 (1823)
Limonia citrifolia Willd. Enum. Pl. : 448 (1809)

Common names Top

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Language Common/alternative name
English flower axistree
Chinese 山小橘
Chinese 小花山小橘
Chinese 山桔
Chinese 山橘仔
Chinese 水官子

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Japan
      • Taiwan
  • Asia-tropical
    • Indo-China
      • Laos
      • Myanmar
      • Vietnam
    • Malesia
      • Philippines
  • Southern America
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Trinidad-Tobago
      • Windward Islands

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000704556
Florida Plant Atlas 1897
USDA Plants GLPA4
Tropicos 28100396
KEW urn:lsid:ipni.org:names:111060-2
The Plant List kew-2827632
Open Tree Of Life 181666
NCBI Taxonomy 159048
Nature Serve 2.151256
IUCN Red List 147625112
IPNI 111060-2
iNaturalist 163342
GBIF 3190426
EPPO GLWPA
EOL 595736
USDA GRIN 314240
Wikipedia Glycosmis_parviflora

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
Does local soil factor drive functional leaf trait variation? A test on Neilingding Island, South China Tong S, Zhang J, Qiao X, Li B, Yang Q, Hu P, Yu S BMC Ecol Evol 10-Apr-2024
PMCID:PMC11005248
doi:10.1186/s12862-024-02227-0
PMID:38600505
The complete chloroplast genome of Aegle marmelos and its phylogenetic analysis Wang S, Xiang R, Kong L, Zhang Z, Lu J, Liu X, Ma W Mitochondrial DNA B Resour 27-Jul-2023
PMCID:PMC10375917
doi:10.1080/23802359.2023.2238934
PMID:37521904
Exploring Contact Toxicity of Essential Oils against Sitophilus zeamais through a Meta-Analysis Approach Achimón F, Peschiutta ML, Brito VD, Beato M, Pizzolitto RP, Zygadlo JA, Zunino MP Plants (Basel) 13-Nov-2022
PMCID:PMC9696113
doi:10.3390/plants11223070
PMID:36432799
Chloroplast genome structure and phylogenetic analysis of Glycosmis parviflora (Sims) Little 1948, a folk medicinal plant featured in Lingnan Region, China Chen A, Li F, Xie X, Huang R, Tian E, Chao Z Mitochondrial DNA B Resour 24-Jun-2022
PMCID:PMC9246040
doi:10.1080/23802359.2022.2087562
PMID:35783069
Phytochemical Analysis and Evaluation of Antioxidant and Biological Activities of Extracts from Three Clauseneae Plants in Northern Thailand Tanruean K, Poolprasert P, Suwannarach N, Kumla J, Lumyong S Plants (Basel) 08-Jan-2021
PMCID:PMC7826859
doi:10.3390/plants10010117
PMID:33429942
Pest categorisation of Unaspis citri Jeger M, Bragard C, Caffier D, Candresse T, Chatzivassiliou E, Dehnen‐Schmutz K, Gilioli G, Grégoire J, Jaques Miret JA, Navarro MN, Niere B, Parnell S, Potting R, Rafoss T, Rossi V, Urek G, Van Bruggen A, Van der Werf W, West J, Winter S, Gardi C, MacLeod A EFSA J 07-Mar-2018
PMCID:PMC7009559
doi:10.2903/j.efsa.2018.5187
PMID:32625826
Forest dynamics and its driving forces of sub-tropical forest in South China Ma L, Lian J, Lin G, Cao H, Huang Z, Guan D Sci Rep 04-Mar-2016
PMCID:PMC4778038
doi:10.1038/srep22561
PMID:26940005
Two new flavanols from Glycosmis pentaphylla. Wu Y, Hu X, Yang GZ, Mei ZN, Chen Y J Asian Nat Prod Res 01-Jan-2012
doi:10.1080/10286020.2012.688745
PMID:22694263
New Quinazoline Alkaloids from Glycosmis cochinchinensis. Chihiro ITO, Yuichi KONDO, Nijsiri RUANGRUNGSI, Hiroshi FURUKAWA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.47.1491
The structure of glycobismine-A, the first naturally occurring "binary" acridone alkaloid containing a carbon-carbon linkage. Hiroshi Furukawa, TianShung Wu, ChangSheng Kuoh, Tadashi Sato, Yasushi Nagai, Kengo Kagei Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.32.1647
Acridone Alkaloids V. New Fulo- and Pyranoacridone Alkaloids from Glycosmis citrifolia (Willd.) Lindl Hiroshi Furukawa, Tian-Shung Wu, Kuo-Shih Hsu The Japan Institute of Heterocyclic Chemistry 02-Mar-2009
doi:10.3987/R-1982-07-1227
Acridone Alkaloids IV. Structures of Four New Acridone Alkaloids from Glycosmis citrifolia (Willd.) Lindl Hiroshi Furukawa, Tian-Shung Wu, Chang-Sheng Kuoh The Japan Institute of Heterocyclic Chemistry 02-Mar-2009
doi:10.3987/R-1982-06-1047
Acridone Alkaloid. III. Structure of Glycofoline, a New Mototerpenoid Acridone Alkaloid from Glycosmis citrifolia (Willd.) Lindl Hiroshi Furukawa, Tian-Shung Wu The Japan Institute of Heterocyclic Chemistry 02-Mar-2009
doi:10.3987/R-1982-05-0825
Two New Acridone Alkaloids from Glycosmis Species Tomohisa Ono, Chihiro Ito, Hiroshi Furukawa, Tian-Shung Wu, Chang-Sheng Kuoh, Kuo-Shih Hsu American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50124A028
Ritigalin, a new thiocarbonic acid imide fromGlycosmis species O. Hofer, G. Zechner, G. Wurz, F. Hadacek, H. Greger Springer Science and Business Media LLC 11-Dec-2004
doi:10.1007/BF00816107

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 / Phenylacetamides
Ritigalin 10443575 Click to see 223.29 unknown https://doi.org/10.1007/BF00816107
https://doi.org/10.1016/S0031-9422(01)00186-8
> Benzenoids / Benzene and substituted derivatives / Styrenes
Dehydrothalebanin B 10751175 Click to see 215.29 unknown https://doi.org/10.1016/S0031-9422(01)00186-8
N,3-dimethyl-N-[(E)-2-phenylethenyl]but-2-enamide 10751176 Click to see 215.29 unknown https://doi.org/10.1016/S0031-9422(01)00186-8
> Benzenoids / Phenols / Benzenediols / Hydroquinones
Hydroquinone 785 Click to see 110.11 unknown https://doi.org/10.1039/P19830001681
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
1-O-methyl 20-O-(3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenyl) 4,8,13,17-tetramethylicosa-2,4,6,8,10,12,14,16,18-nonaenedioate 162877600 Click to see CC(=CCCC(=CCCC(=CCCC(=CCOC(=O)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC(=O)OC)C)C)C)C)C)C 667.00 unknown https://doi.org/10.1016/0031-9422(95)00171-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1039/P19830001681
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 https://doi.org/10.1039/P19830001681
> Organic acids and derivatives / Carboxylic acids and derivatives / Acrylic acids and derivatives
(Z)-N-methyl-3-methylsulfinylprop-2-enamide 55299128 Click to see 147.20 unknown https://doi.org/10.1016/0031-9422(95)00171-3
N-methyl-3-methylsulfinylprop-2-enamide 76225255 Click to see 147.20 unknown https://doi.org/10.1016/0031-9422(95)00171-3
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
methyl 5-ethylidene-4-[2-[[3-[2-[3-ethylidene-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-5-[1-[2-[3-ethylidene-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-2-hydroxyethyl]-2-methylcyclopentyl]methoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163036833 Click to see 1349.30 unknown https://doi.org/10.1248/CPB.48.65
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
pumilacidin D 101174695 Click to see 1050.40 unknown https://doi.org/10.1248/CPB.48.65
> Organic acids and derivatives / Vinylogous thioesters
N-methyl-3-methylsulfanylprop-2-enamide 85085266 Click to see 131.20 unknown https://doi.org/10.1016/0031-9422(95)00171-3
Penangin 10419217 Click to see CNC(=O)C=CSC 131.20 unknown https://doi.org/10.1016/0031-9422(95)00171-3
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
3-methyl-9H-carbazol-2-ol 3459141 Click to see 197.23 unknown https://doi.org/10.1016/S0031-9422(01)00186-8
5-methoxy-3-methyl-9H-carbazol-2-ol 10376445 Click to see 227.26 unknown https://doi.org/10.1016/S0031-9422(01)00186-8
Glycoborinine 10446329 Click to see CC1=CC2=C(C=C1O)NC3=C2C4=C(C=C3)OC(C=C4)(C)C 279.30 unknown https://doi.org/10.1016/S0031-9422(01)00186-8
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines
1-Hydroxy-10-methyl-4,4-bis(3-methylbut-2-enyl)acridine-3,9-dione 10523646 Click to see 377.50 unknown https://doi.org/10.1248/CPB.48.65
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
(2R)-5,10-dihydroxy-2,11-dimethyl-2-(4-methylpent-3-enyl)pyrano[3,2-b]acridin-6-one 162904490 Click to see 391.50 unknown https://doi.org/10.1039/P19830001681
(2S,3S)-3,6-dihydroxy-2-(2-hydroxypropan-2-yl)-8,9,11-trimethoxy-10-methyl-2,3-dihydrofuro[3,2-b]acridin-5-one 10526664 Click to see 431.40 unknown https://doi.org/10.1248/CPB.48.65
(2S)-5,10-dihydroxy-2,11-dimethyl-2-(4-methylpent-3-enyl)pyrano[3,2-b]acridin-6-one 163193381 Click to see 391.50 unknown https://doi.org/10.3987/R-1982-05-0825
(3R)-8-hydroxy-10,11-dimethoxy-3,12-dimethyl-3-[(E)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-2H-[1,4]dioxino[2,3-c]acridin-7-one 163194462 Click to see CC1(COC2=C(O1)C=CC3=C2N(C4=C(C3=O)C(=CC(=C4OC)OC)O)C)C=CC5=C6C(=C(C=C5O)O)C(=O)C7=C(N6C)C(=CC=C7)O 638.60 unknown https://doi.org/10.1248/CPB.48.65
(3R)-8-hydroxy-10,11-dimethoxy-3,12-dimethyl-3-[(Z)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-2H-[1,4]dioxino[2,3-c]acridin-7-one 162982285 Click to see 638.60 unknown https://doi.org/10.1248/CPB.48.65
(4S)-1,4-dihydroxy-2-[(1S)-6-hydroxy-3,3-dimethyl-7-oxo-2,12-dihydro-1H-pyrano[2,3-c]acridin-1-yl]-10-methyl-4-(3-methylbut-2-enyl)acridine-3,9-dione 9986332 Click to see CC(=CCC1(C2=C(C(=C(C1=O)C3CC(OC4=C3C5=C(C(=C4)O)C(=O)C6=CC=CC=C6N5)(C)C)O)C(=O)C7=CC=CC=C7N2C)O)C 618.70 unknown https://doi.org/10.1039/P19830001681
(7R)-15-hydroxy-2,7,19,19-tetramethyl-7-[(Z)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-5,8,18-trioxa-2-azapentacyclo[12.8.0.03,12.04,9.017,22]docosa-1(14),3(12),4(9),10,15,17(22),20-heptaen-13-one 163008842 Click to see 660.70 unknown https://doi.org/10.1248/CPB.52.362
(7R)-7-[(Z)-2-(1,5-dihydroxy-3-methoxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-15-hydroxy-2,7,19,19-tetramethyl-5,8,18-trioxa-2-azapentacyclo[12.8.0.03,12.04,9.017,22]docosa-1(14),3(12),4(9),10,15,17(22),20-heptaen-13-one 163063874 Click to see 674.70 unknown https://doi.org/10.1248/CPB.47.1491
(7S)-15-hydroxy-2,7,19,19-tetramethyl-7-[(E)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-5,8,18-trioxa-2-azapentacyclo[12.8.0.03,12.04,9.017,22]docosa-1(14),3(12),4(9),10,15,17(22),20-heptaen-13-one 163008844 Click to see 660.70 unknown https://doi.org/10.1248/CPB.52.362
(7S)-7-[(E)-2-(1,5-dihydroxy-3-methoxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-15-hydroxy-2,7,19,19-tetramethyl-5,8,18-trioxa-2-azapentacyclo[12.8.0.03,12.04,9.017,22]docosa-1(14),3(12),4(9),10,15,17(22),20-heptaen-13-one 163189511 Click to see 674.70 unknown https://doi.org/10.1248/CPB.48.65
1-Hydroxy-3-methoxy-10-methyl-4-(3-methylbut-2-enyl)acridin-9-one 162854126 Click to see CC(=CCC1=C(C=C(C2=C1N(C3=CC=CC=C3C2=O)C)O)OC)C 323.40 unknown https://doi.org/10.1039/P19830001681
1,6-Dihydroxy-3,4,5-trimethoxy-10-methylacridin-9-one 44626340 Click to see CN1C2=C(C=CC(=C2OC)O)C(=O)C3=C1C(=C(C=C3O)OC)OC 331.32 unknown https://doi.org/10.1021/NP50124A028
11-[[(3R)-6,11-dihydroxy-3,12-dimethyl-7-oxopyrano[2,3-c]acridin-3-yl]methoxy]-6,10-dihydroxy-3,3,12-trimethylpyrano[2,3-c]acridin-7-one 163012107 Click to see 660.70 unknown https://doi.org/10.1248/CPB.52.362
11-Hydroxynoracronycine 5378702 Click to see 323.30 unknown https://doi.org/10.1039/P19830001681
15-Hydroxy-2,7,19,19-tetramethyl-7-[2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-5,8,18-trioxa-2-azapentacyclo[12.8.0.03,12.04,9.017,22]docosa-1(14),3(12),4(9),10,15,17(22),20-heptaen-13-one 85434661 Click to see 660.70 unknown https://doi.org/10.1248/CPB.52.362
3,6-Dihydroxy-2-(2-hydroxypropan-2-yl)-8,9,11-trimethoxy-10-methyl-2,3-dihydrofuro[3,2-b]acridin-5-one 85172158 Click to see CC(C)(C1C(C2=C(O1)C(=C3C(=C2)C(=O)C4=C(N3C)C(=C(C=C4O)OC)OC)OC)O)O 431.40 unknown https://doi.org/10.1248/CPB.48.65
5-Hydroxy-2-(2-hydroxypropan-2-yl)-11-methylfuro[2,3-c]acridin-6-one 162926322 Click to see CC(C)(C1=CC2=C(O1)C=C(C3=C2N(C4=CC=CC=C4C3=O)C)O)O 323.30 unknown https://doi.org/10.3987/R-1982-07-1227
https://doi.org/10.1039/P19830001681
5,10-Dihydroxy-2,11-dimethyl-2-(4-methylpent-3-enyl)pyrano[3,2-b]acridin-6-one 162904489 Click to see 391.50 unknown https://doi.org/10.3987/R-1982-05-0825
https://doi.org/10.1039/P19830001681
6-methoxy-3,3-dimethyl-12H-pyrano[2,3-c]acridin-7-one 6325047 Click to see 307.30 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-J
https://doi.org/10.1039/P19830001681
6,11-dihydroxy-3,3-dimethyl-12H-pyrano[2,3-c]acridin-7-one 5479542 Click to see 309.30 unknown https://doi.org/10.1039/P19830001681
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-J
7-[2-(1,5-Dihydroxy-3-methoxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-15-hydroxy-2,7,19,19-tetramethyl-5,8,18-trioxa-2-azapentacyclo[12.8.0.03,12.04,9.017,22]docosa-1(14),3(12),4(9),10,15,17(22),20-heptaen-13-one 85184265 Click to see CC1(C=CC2=C(O1)C=C(C3=C2N(C4=C(C3=O)C=CC5=C4OCC(O5)(C)C=CC6=C(C=C(C7=C6N(C8=C(C7=O)C=CC=C8O)C)O)OC)C)O)C 674.70 unknown https://doi.org/10.1248/CPB.48.65
7H-Pyrano(2,3-c)acridin-7-one, 3,12-dihydro-6-hydroxy-3,3-dimethyl- 5479541 Click to see 293.30 unknown https://doi.org/10.1039/P19830001681
7H-Pyrano[2,3-c]acridin-7-one, 3,12-dihydro-6,11-dihydroxy-3,3,12-trimethyl-5-(3-methyl-2-butenyl)- 633176 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=C(N3C)C(=CC=C4)O)C=CC(O2)(C)C)C 391.50 unknown https://doi.org/10.1039/P19830001681
8-hydroxy-10,11-dimethoxy-3,12-dimethyl-3-[2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-2H-[1,4]dioxino[2,3-c]acridin-7-one 85193326 Click to see 638.60 unknown https://doi.org/10.1248/CPB.48.65
Citracridone I 5487591 Click to see 353.40 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-J
https://doi.org/10.1039/P19830001681
Furofoline I 5281842 Click to see CN1C2=CC=CC=C2C(=O)C3=C1C4=C(C=C3O)OC=C4 265.26 unknown https://doi.org/10.3987/R-1982-07-1227
https://doi.org/10.1039/P19830001681
Glycobismine B 102150620 Click to see 618.70 unknown https://doi.org/10.1039/P19830001681
https://doi.org/10.1039/P19930000471
Glycobismine G 12111779 Click to see 660.70 unknown https://doi.org/10.1248/CPB.52.362
Glycocitrine I 11724762 Click to see 339.40 unknown https://doi.org/10.1039/P19830001681
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-J
Glycocitrine II 11781835 Click to see 309.40 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-J
https://doi.org/10.1039/P19830001681
Glycocitrine-Iv 9998312 Click to see CC(=CCC1=C(C2=C(C(=C1O)OC)N(C3=C(C2=O)C=CC=C3O)C)O)C 355.40 unknown https://doi.org/10.1248/CPB.48.65
Glyfoline 5480208 Click to see 361.30 unknown https://doi.org/10.1039/P19830001681
https://doi.org/10.3987/R-1982-06-1047
N-Methylseverifoline 44558980 Click to see 375.50 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-J
https://doi.org/10.1039/P19830001681
Noracronycine 5320199 Click to see 307.30 unknown https://doi.org/10.1039/P19830001681
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-J
Pyranofoline 9798626 Click to see 353.40 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-J
https://doi.org/10.1039/P19830001681
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Gamma-Fagarine 107936 Click to see 229.23 unknown https://doi.org/10.1016/0031-9422(95)00171-3
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1016/0031-9422(95)00171-3
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
1,2-Dimethylquinolin-4(1H)-one 316973 Click to see 173.21 unknown https://doi.org/10.1016/0031-9422(95)00171-3
3-(1-hydroxy-3-oxobutyl)-4,7,8-trimethoxy-1H-quinolin-2-one 162988645 Click to see 321.32 unknown https://doi.org/10.1016/0031-9422(95)00171-3
3-(3-Hydroxy-3-methylbut-1-enyl)-4-methoxy-1-methylquinolin-2-one 85196421 Click to see CC(C)(C=CC1=C(C2=CC=CC=C2N(C1=O)C)OC)O 273.33 unknown https://doi.org/10.1248/CPB.48.65
3-(3-Hydroxy-3-methylbut-1-enyl)-4,8-dimethoxy-1-methylquinolin-2-one 85240699 Click to see 303.35 unknown https://doi.org/10.1248/CPB.48.65
3-[(E)-3-hydroxy-3-methylbut-1-enyl]-4-methoxy-1-methylquinolin-2-one 10588321 Click to see 273.33 unknown https://doi.org/10.1248/CPB.48.65
3-[(E)-3-hydroxy-3-methylbut-1-enyl]-4,8-dimethoxy-1-methylquinolin-2-one 10709552 Click to see 303.35 unknown https://doi.org/10.1248/CPB.48.65
4-Hydroxyquinoline 69141 Click to see C1=CC=C2C(=C1)C(=O)C=CN2 145.16 unknown https://doi.org/10.1039/P19830001681
4,8-Dimethoxy-1-methyl-3-(3-methylbut-2-en-1-yl)quinolin-2(1H)-one 15491437 Click to see 287.35 unknown https://doi.org/10.1039/P19830001681
8-Hydroxy-3-(3-hydroxy-3-methylbut-1-enyl)-4-methoxy-1-methylquinolin-2-one 85248830 Click to see 289.33 unknown https://doi.org/10.1248/CPB.48.65
8-hydroxy-3-[(E)-3-hydroxy-3-methylbut-1-enyl]-4-methoxy-1-methylquinolin-2-one 10732163 Click to see CC(C)(C=CC1=C(C2=C(C(=CC=C2)O)N(C1=O)C)OC)O 289.33 unknown https://doi.org/10.1248/CPB.48.65
Glycocitridine 928053 Click to see 263.25 unknown https://doi.org/10.1016/0031-9422(95)00171-3
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
Flindersine 68230 Click to see 227.26 unknown https://doi.org/10.1016/S0031-9422(01)00186-8
> Organosulfur compounds / Sulfoxides
(E)-N-methyl-3-[(R)-methylsulfinyl]prop-2-enamide 162923995 Click to see 147.20 unknown https://doi.org/10.1016/0031-9422(95)00171-3
(Z)-N-methyl-3-[(R)-methylsulfinyl]prop-2-enamide 162923996 Click to see CNC(=O)C=CS(=O)C 147.20 unknown https://doi.org/10.1016/0031-9422(95)00171-3
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
2-(3,4-Dimethoxyphenyl)-5-methoxy-8,8-dimethyl-2,3-dihydropyrano[2,3-h]chromen-4-one 15230426 Click to see 396.40 unknown https://doi.org/10.1016/0031-9422(95)00171-3
5-Methoxy-2-(4-methoxyphenyl)-8,8-dimethyl-2,3-dihydropyrano[2,3-h]chromen-4-one 11326046 Click to see CC1(C=CC2=C3C(=C(C=C2O1)OC)C(=O)CC(O3)C4=CC=C(C=C4)OC)C 366.40 unknown https://doi.org/10.1016/0031-9422(95)00171-3
https://doi.org/10.1080/10286020.2012.688745
Glyflavanone A 42608063 Click to see CC1(C=CC2=C3C(=C(C=C2O1)OC)C(=O)CC(O3)C4=CC=C(C=C4)OC)C 366.40 unknown https://doi.org/10.1016/0031-9422(95)00171-3
Glyflavanone B 42608069 Click to see 396.40 unknown https://doi.org/10.1016/0031-9422(95)00171-3
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(5-Hydroxy-7-methoxy-2,2-dimethylchromen-6-yl)-3-(4-methoxyphenyl)prop-2-en-1-one 73189671 Click to see 366.40 unknown https://doi.org/10.1016/0031-9422(95)00171-3
3-(3,4-Dimethoxyphenyl)-1-(5-hydroxy-7-methoxy-2,2-dimethylchromen-6-yl)prop-2-en-1-one 73189672 Click to see 396.40 unknown https://doi.org/10.1016/0031-9422(95)00171-3
Glychalcone A 15230651 Click to see 366.40 unknown https://doi.org/10.1016/0031-9422(95)00171-3
Glychalcone B 15230652 Click to see 396.40 unknown https://doi.org/10.1016/0031-9422(95)00171-3
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
Glycobismine A 5462453 Click to see CC(=CCC1=C2C(=C(C(=C1O)C3CC(OC4=C3C5=C(C(=C4)O)C(=O)C6=CC=CC=C6N5)(C)C)O)C(=O)C7=CC=CC=C7N2C)C 602.70 unknown https://doi.org/10.1039/P19930000471
https://doi.org/10.1248/CPB.32.1647

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