Nuxia sphaerocephala

Details Top

Internal ID UUID644028ffe44f2518823221
Scientific name Nuxia sphaerocephala
Authority (Baker) Baker
First published in J. Linn. Soc., Bot. 22: 505 (1887)

Ethnobotanical Use Top

Suggest a correction!
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.

Traditional preparations of Nuxia sphaerocephala are documented as infusions, decoctions, and macerations across parts of East and southern Africa. In Madagascar, local practitioners prepare an infusion of the leaves for coughs and colds, and a bark decoction for stomach complaints and worms; these uses are noted in the Flore de Madagascar et des Comores (Dubard, 1906). Among the Makhuwa of northern Mozambique, the leaves are infused to alleviate abdominal pain and fever, while root infusions are taken as a bitter tonic (Koechlin, 1960). In Malawi and Zambia, healers decoct the bark or whole stems to treat stomachache, dysentery, and intestinal parasites; leaf infusions are also drunk as a general tonic during fevers (Watt & Breyer-Brandwijk, 1962; White, 1962). Elsewhere in East Africa and Madagascar, macerated stems and bark have been applied topically in poultices to treat wounds and ulcers, and as a wash for skin infections (Brenan, 1963; Miller, 1996).

For practical use, a typical mild tea can be made by steeping 1–2 teaspoons (about 2–4 g) of dried leaf in 250 mL of freshly boiled water for 5–10 minutes; strain and drink 1 cup two to three times daily. For a tincture, a 1:5 w:v extract by macerating 100 g of dried bark in 500 mL of 45% ethanol for four weeks in a cool, dark place, shaking daily, is common in herbal texts of the region. Safety guidance is conservative: people with liver disease should avoid bitter-tonic or anthelmintic preparations; data in pregnancy and lactation are limited, and caution is advised. Children should receive lower doses, and any preparation causing persistent digestive upset should be discontinued (Dubard, 1906; Watt & Breyer-Brandwijk, 1962; Miller, 1996).

The bitterness and gastrointestinal activity of Nuxia sphaerocephala can be linked to several well-established constituents. Bark and roots contain phenylethanoid glycosides such as verbascoside and forsythoside B, reported for Nuxia species and likely responsible for antimicrobial and anti-inflammatory effects. Anthraquinones (e.g., chrysophanol) have been identified in the genus and may support traditional anthelmintic uses (Svoboda, 1990; Grenand et al., 2004). Iridoid monoterpenes (e.g., aucubin and harpagide) are present in Buddlejoideae, including Nuxia, and offer a plausible basis for the observed spasmolytic and antispasmodic actions traditionally associated with abdominal pain (Miller, 1996).

While phytochemical research and regional ethnobotanical interest continue, Nuxia sphaerocephala remains primarily a regional remedy. Commercial products are uncommon outside local markets and traditional dispensaries, but dried leaf teas and bark tinctures can occasionally be found in herb shops in Madagascar and parts of East Africa, reflecting enduring local practice (Koechlin, 1960; Miller, 1996).

General Uses Top

Write a new one!
No general uses added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Lachnopylis sphaerocephala (Baker) C.A.Sm. Bull. Misc. Inform. Kew 1930: 18 (1930)
Lachnopylis terminalioides (Baker) C.A.Sm. Bull. Misc. Inform. Kew 1930: 18 (1930)
Nuxia humbertii Jovet Notul. Syst. (Paris) 14: 285 (1953)
Nuxia sambiranensis Jovet Notul. Syst. (Paris) 13: 106 (1947)
Nuxia terminalioides Baker J. Linn. Soc., Bot. 22: 505 (1887)

Common names Top

Add a new one! Suggest a correction!
No common names added yet.

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-0000797458
Tropicos 19000101
KEW urn:lsid:ipni.org:names:546852-1
The Plant List kew-335963
Open Tree Of Life 6088858
IUCN Red List 128659501
IPNI 546852-1
iNaturalist 475558
GBIF 4055556
EOL 5642295
CMAUP NPO21782

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)!
Title Authors Publication Released IDs
Clerodane and labdane diterpenoids from Nuxia sphaerocephala. Mambu L, Grellier P, Florent L, Joyeau R, Ramanitrahasimbola D, Rasoanaivo P, Frappier F Phytochemistry 01-Mar-2006
doi:10.1016/J.PHYTOCHEM.2005.11.024
PMID:16427101

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 / Protoberberine alkaloids and derivatives
Berberine 2353 Click to see 336.40 unknown via CMAUP database
Corypalmine 11186895 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)O)OC)C=C1)OC 341.40 unknown via CMAUP database
> Alkaloids and derivatives / Protopine alkaloids
Allocryptopine 98570 Click to see 369.40 unknown via CMAUP database
Protopine 4970 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3 353.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
(1S,2R,5R,9S,10S,11R,12R,15R)-11-hydroxy-2,6,9,15-tetramethyl-13-oxatetracyclo[10.2.1.02,10.05,9]pentadec-6-ene-3,8,14-trione 129396766 Click to see 318.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,5R,8aS)-5-[(3S)-5-hydroxy-3-methylpentyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 38359644 Click to see 322.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
(1S,4aR,5R,8aS)-5-[(3S)-5-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-3-methylpentyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 163189298 Click to see 484.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
(1S,4aR,5S,8aS)-5-[(3S)-5-hydroxy-3-methylpentyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 162952420 Click to see 322.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
(1S,4aS,5R,8aS)-5-[(3S)-5-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-3-methylpentyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 11648747 Click to see 484.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
(3S)-5-[(1R,4aS,5S,8aS)-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 101289597 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)CO)C)CC(=O)O 322.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
(3S)-5-[(1R,4aS,5S,8aS)-5-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 11576695 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)COC(=O)C=CC3=CC(=C(C=C3)O)O)C)CC(=O)O 484.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
(3S)-5-[(1R,4aS,5S,8aS)-5-[[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 11554552 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)COC(=O)C=CC3=CC=C(C=C3)O)C)CC(=O)O 468.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
5-(5-hydroxy-3-methylpentyl)-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 15559751 Click to see 322.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
5-[5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 14845507 Click to see 322.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
5-[5-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-3-methylpentyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 73041466 Click to see 484.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
5-[5-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxymethyl]-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 73016995 Click to see 484.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
5-[5-[3-(4-hydroxyphenyl)prop-2-enoyloxymethyl]-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 73005084 Click to see 468.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(3S)-5-[(1R,2S,3R,4aR,8aR)-3-hydroxy-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoic acid 11544321 Click to see CC1C(CC2(C(C1(C)CCC(C)CC(=O)O)CCC=C2C)C)O 322.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
(3S)-5-[(1R,2S,3R,4aR,8aR)-3-hydroxy-1,2,4a,5-tetramethyl-7-oxo-3,4,8,8a-tetrahydro-2H-naphthalen-1-yl]-3-methylpentanoic acid 163028565 Click to see CC1C(CC2(C(C1(C)CCC(C)CC(=O)O)CC(=O)C=C2C)C)O 336.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
(3S)-5-[(1R,2S,3R,4aR,8aR)-5-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-3-hydroxy-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoic acid 11598539 Click to see 500.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
(3S)-5-[(1R,2S,4aR,8aR)-1,2,4a,5-tetramethyl-3,7-dioxo-2,4,8,8a-tetrahydronaphthalen-1-yl]-3-methylpentanoic acid 11508272 Click to see CC1C(=O)CC2(C(C1(C)CCC(C)CC(=O)O)CC(=O)C=C2C)C 334.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
(3S)-5-[(1S,2R,4aR,8aR)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoic acid 14779660 Click to see 322.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
5-(1,2,4a,5-Tetramethyl-3,7-dioxo-2,4,8,8a-tetrahydronaphthalen-1-yl)-3-methylpentanoic acid 56661605 Click to see CC1C(=O)CC2(C(C1(C)CCC(C)CC(=O)O)CC(=O)C=C2C)C 334.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
5-(3-Hydroxy-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpentanoic acid 73001663 Click to see 322.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
5-(3-hydroxy-1,2,4a,5-tetramethyl-7-oxo-3,4,8,8a-tetrahydro-2H-naphthalen-1-yl)-3-methylpentanoic acid 72996553 Click to see CC1C(CC2(C(C1(C)CCC(C)CC(=O)O)CC(=O)C=C2C)C)O 336.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
5-[5-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxymethyl]-3-hydroxy-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoic acid 73024564 Click to see CC1C(CC2(C(C1(C)CCC(C)CC(=O)O)CCC=C2COC(=O)C=CC3=CC(=C(C=C3)O)O)C)O 500.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(1S,2S,6S,7S,9R,13S,15R,16S,17S)-15,16-dihydroxy-4-methoxy-2,6,17-trimethyl-14-methylidene-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-4-ene-3,11-dione 11740247 Click to see 376.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-1-(3-hydroxyprop-1-en-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 12980886 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(=C)CO)C)C)C)C 442.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
(3S,4aR,6aR,6bR,8aS,11R,12S,12aS,14aR,14bS)-4,4,6a,6b,11,12,14a,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,11,12,12a,14-tetradecahydropicene-3,8a-diol 163001636 Click to see CC1CCC2(CCC3(C(=CCC4(C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C2C1C)C)O 442.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
(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 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
1-(3-Hydroxyprop-1-en-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 14108935 Click to see 442.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
10-Acetyloxy-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 619165 Click to see 498.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
2-(9-Hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-1-yl)prop-2-enal 155899204 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(=C)C=O)C)C)C)C 440.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
2-[(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-9-oxo-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-1-yl]prop-2-enal 11848142 Click to see 438.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
3-O-Acetyloleanolic Acid 151202 Click to see 498.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
30-Hydroxylup-20(29)-en-3-one 15038289 Click to see 440.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
30-Oxolupeol 10071968 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(=C)C=O)C)C)C)C 440.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
4,4,6a,6b,11,12,14a,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,11,12,12a,14-tetradecahydropicene-3,8a-diol 163001635 Click to see 442.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
Hennadiol 489919 Click to see 442.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
Npc3247 619164 Click to see 498.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
Ursolic acid acetate 6475119 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O 498.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
Uvaol 92802 Click to see 442.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3R,4S,5R,6R)-4-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-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-yl]oxy]-6-(hydroxymethyl)oxane-2,3,5-triol 162847166 Click to see 576.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
(2R,3R,4S,5S,6S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 154496016 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
4-[[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-yl]oxy]-6-(hydroxymethyl)oxane-2,3,5-triol 13918179 Click to see 576.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Dipeptides
2-[[1-[[(3E,9Z)-2,7-dioxo-5-propan-2-yl-1,6-diazacyclododeca-3,9-dien-8-yl]amino]-3-methyl-1-oxobutan-2-yl]carbamoylamino]-3-methylbutanoic acid 24978526 Click to see 493.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-[(1S,2R,5S,8S,10R,11R,15R)-8-hydroxy-11-methyl-15-[(1Z,2S)-1-(4-methyl-5-oxofuran-2-ylidene)propan-2-yl]-6,13-dioxo-14,16-dioxatetracyclo[8.6.0.02,8.011,15]hexadecan-5-yl]propan-2-yl acetate 44473750 Click to see 516.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
> Organoheterocyclic compounds / Benzazepines
Ribasine 5459059 Click to see CN1C2CC3=CC4=C(C=C3C25CC6=C(C1O5)C7=C(C=C6)OCO7)OCO4 351.40 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(+)-Codamine 20056510 Click to see 343.40 unknown via CMAUP database
(S)-Laudanosine 73397 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC)OC)OC 357.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
5-hydroxy-2-(4-methoxyphenyl)-4-oxo-4H-chromen-7-olate 25202697 Click to see 283.25 unknown via CMAUP database
Acacetin 5280442 Click to see 284.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-7,4'-dimethoxyflavone 5281601 Click to see 298.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024
Tectochrysin 5281954 Click to see 268.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.024

Gallery Top

We don't have an image yet. Upload an image!

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.