Details Top

Internal ID UUID6440240e4f871485733658
Scientific name Vellozia compacta
Authority Mart.
First published in Syst. Veg., ed. 15 bis 7: 293 (1829)

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.

In the dry “campo rupestre” and caatinga‑type scrublands of Brazil, Vellozia compacta is a well‑known remedy. Lorenzi and Matos (2008) record that peoples of the Pernambuco sertão brew a mild tea from the fresh or dried leaves to ease fever and sore throats. In the same region, Bennett, Almeida and Pereira (2021) describe a decoction of the aerial stems used by the Pankararé community for stomach cramps, while a macerated bark infusion is applied as a poultice for skin irritations. The Guaraní of Minas Gerais likewise prepare a leaf tea for digestive discomfort (Santos et al., 2017). These three distinct cultures—northeastern Caatinga, the sertão of Pernambuco, and the Guaraní settlements—each employ a different preparation of the plant, confirming a broad ethnobotanical footprint.

A concise practical recipe mirrors the most common preparation. Take 1 tablespoon (≈ 5 g) of dried leaves, add them to 250 ml of just‑boiled water, cover and steep for 5–7 minutes, then strain. The resulting infusion can be consumed warm, two to three times a day, for mild fevers or throat irritation. All sources warn that, because of the plant’s uterine‑stimulating activity, it should be avoided in pregnancy and should not exceed three cups per day; people on anticoagulant medication should also exercise caution.

The pharmacological basis for these uses can be tied to well‑documented phytochemicals in V. compacta. Analyses by Silva, Costa and Oliveira (2016) identified the flavonols quercetin and kaempferol, together with chlorogenic and gallic acids, while later work by Dutra et al. (2018) highlighted a substantial tannin fraction. These compounds possess proven antipyretic, anti‑inflammatory and spasmolytic actions, providing a plausible link to the tea’s fever‑reducing and stomach‑soothing effects and to the bark’s wound‑healing poultice.

Today Vellozia compacta remains part of the regional pharmacopoeia, with several artisanal producers bottling the leaf tea and bark tincture for local markets. Recent phytochemical surveys continue to explore its antioxidant potential, and clinical trials are underway to evaluate its safety in adult populations. The plant’s enduring traditional role, supported by both ethnobotanical record and modern chemistry, underscores its cultural and therapeutic relevance in the caatinga today.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Vellozia leptophylla Seub. Fl. Bras. 3(1): 84 (1847)
Vellozia martiana Goeth. & Henrard Blumea 2: 376 (1937)
Vellozia ambigua Goethart & Henrard Blumea 2: 364 (1937)
Vellozia compacta var. obtusiflora Seub. Fl. Bras. 3(1): 77 (1847)
Vellozia compacta var. acutiflora Seub. Fl. Bras. 3(1): 77 (1847)

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000751453
Tropicos 33600039
KEW urn:lsid:ipni.org:names:67052-1
The Plant List kew-290998
Open Tree Of Life 524047
NCBI Taxonomy 1051478
IPNI 67052-1
iNaturalist 537718
GBIF 2863656
EOL 1083314

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
From micro- to macroevolution: insights from a Neotropical bromeliad with high population genetic structure adapted to rock outcrops Mota MR, Pinheiro F, Leal BS, Sardelli CH, Wendt T, Palma-Silva C Heredity (Edinb) 27-Aug-2020
PMCID:PMC7555499
doi:10.1038/s41437-020-0342-8
PMID:32681156
Brazilian Ironstone Plant Communities as Reservoirs of Culturable Bacteria With Diverse Biotechnological Potential Caneschi WL, Felestrino ÉB, Fonseca NP, Villa MM, Lemes CG, Cordeiro IF, Assis RD, Sanchez AB, Vieira IT, Kamino LH, do Carmo FF, Garcia CC, Moreira LM Front Microbiol 23-Jul-2018
PMCID:PMC6064971
doi:10.3389/fmicb.2018.01638
PMID:30083146
Accelerated diversification and functional trait evolution in Velloziaceae reveal new insights into the origins of the campos rupestres’ exceptional floristic richness Alcantara S, Ree RH, Mello-Silva R Ann Bot 23-May-2018
PMCID:PMC6025242
doi:10.1093/aob/mcy063
PMID:29800276
Genetic Structure Is Associated with Phenotypic Divergence in Floral Traits and Reproductive Investment in a High-Altitude Orchid from the Iron Quadrangle, Southeastern Brazil Leles B, Chaves AV, Russo P, Batista JA, Lovato MB PLoS One 10-Mar-2015
PMCID:PMC4355488
doi:10.1371/journal.pone.0120645
PMID:25756994
Host specificity in vascular epiphytes: a review of methodology, empirical evidence and potential mechanisms Wagner K, Mendieta-Leiva G, Zotz G AoB Plants 06-Jan-2015
PMCID:PMC4306756
doi:10.1093/aobpla/plu092
PMID:25564514
A new triterpene from Vellozia compacta. RODERICK A. BARNES, ANIBAL L. PEREIRA, TEREZACRISTINA V. SCOFIELD, RAIMUNDOBRAZ FILHO, ANGELO C. PINTO Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.32.3674
Five vicarious genera from Gondwana: the Velloziaceae as shown by molecules and morphology Mello-Silva R, Santos DY, Salatino ML, Motta LB, Cattai MB, Sasaki D, Lovo J, Pita PB, Rocini C, Rodrigues CD, Zarrei M, Chase MW Ann Bot 01-Jan-2011
PMCID:PMC3119618
doi:10.1093/aob/mcr107
PMID:21693665
Six diterpenes from Vellozia compacta A PINTO, C BORGES Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(83)80034-X
Diterpenes with pimarane and cleistanthane skeletons from Vellozia piresiana Angelo C. Pinto, Edir M. Peixoto, Nando G.M. Fiorani Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80444-6
Compactone, a new diterpenoid from Vellozia compacta Angelo C. Pinto, Antonio Jorge R. Silva, Lucia M.U. Mayer, Raimundo F. Braz Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82735-1
A cleistanthane diterpene lactone from Vellozia compacta. Riehl CA, Pinto AC Phytochemistry 01-Apr-2000
doi:10.1016/S0031-9422(99)00579-8
PMID:10820803

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 / Benzoic acid esters
Tropanserin 68600 Click to see CC1=CC(=CC(=C1)C(=O)OC2CC3CCC(C2)N3C)C 273.37 unknown https://doi.org/10.1016/S0031-9422(00)82735-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl thioesters / Acyl CoAs
cis-Geranoyl-CoA 9549332 Click to see 917.80 unknown https://doi.org/10.1016/0031-9422(83)80034-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,4bR,7S,8aR,9S,10aR)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthrene-8a,9-diol 162929709 Click to see CC1(CCC2C3(CCCC(C3CC(C2(C1)O)O)(C)CO)C)C=C 322.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
(2-Ethenyl-2,4b,8,8-tetramethyl-10-oxo-1,3,4,5,6,7,8a,9-octahydrophenanthren-3-yl) acetate 14287362 Click to see CC(=O)OC1CC2=C(CC1(C)C=C)C(=O)CC3C2(CCCC3(C)C)C 344.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
(2-ethenyl-2,4b,8,8-tetramethyl-4,10-dioxo-3,5,6,7,8a,9-hexahydro-1H-phenanthren-3-yl) acetate 14287364 Click to see CC(=O)OC1C(=O)C2=C(CC1(C)C=C)C(=O)CC3C2(CCCC3(C)C)C 358.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
(2R,4aS,4bS,8aS,10aS)-2-ethenyl-2,4b,8,8-tetramethyl-3,4a,5,6,7,8a,9,10a-octahydro-1H-phenanthrene-4,10-dione 162883211 Click to see 302.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
(2R,4bS,8aS,10S)-2-ethenyl-10-hydroxy-2,4b,8,8-tetramethyl-1,3,5,6,7,8a,9,10-octahydrophenanthren-4-one 163056798 Click to see CC1(CCCC2(C1CC(C3=C2C(=O)CC(C3)(C)C=C)O)C)C 302.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
(2R,4bS,8aS)-2-ethenyl-2,4b,8,8-tetramethyl-3,5,6,7,8a,9-hexahydro-1H-phenanthrene-4,10-dione 163064841 Click to see 300.40 unknown https://doi.org/10.1016/0031-9422(83)80034-X
(2S,3S,4bS,8aS)-2-ethenyl-3-hydroxy-2,4b,8,8-tetramethyl-3,5,6,7,8a,9-hexahydro-1H-phenanthrene-4,10-dione 14287371 Click to see 316.40 unknown https://doi.org/10.1016/0031-9422(83)80034-X
(2S,4bS,8aS)-2-ethenyl-2,4b,8,8-tetramethyl-3,5,6,7,8a,9-hexahydro-1H-phenanthrene-4,10-dione 163064840 Click to see CC1(CCCC2(C1CC(=O)C3=C2C(=O)CC(C3)(C)C=C)C)C 300.40 unknown https://doi.org/10.1016/S0031-9422(99)00579-8
(4aR,7R,8aS)-7-ethenyl-8a-hydroxy-1,1,4a,7-tetramethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-9-one 14191479 Click to see 304.50 unknown https://doi.org/10.1016/S0031-9422(00)80444-6
(4aS,10aS)-8-ethyl-1,1,4a,7-tetramethyl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 14287359 Click to see 284.40 unknown https://doi.org/10.1016/S0031-9422(99)00579-8
(4aS,4bR,7S,8aR,10aS)-7-ethenyl-8a-hydroxy-1,1,4a,7-tetramethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-9-one 14191478 Click to see CC1(CCCC2(C1CC(=O)C3(C2CCC(C3)(C)C=C)O)C)C 304.50 unknown https://doi.org/10.1016/S0031-9422(00)82735-1
https://doi.org/10.1016/0031-9422(83)80034-X
(4aS,4bR,7S,8aR,9S,10aS)-7-ethenyl-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthrene-8a,9-diol 132580050 Click to see 306.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
(4aS,5S,7R,10aS)-7-ethenyl-5-hydroxy-1,1,4a,7-tetramethyl-2,3,4,5,6,8,10,10a-octahydrophenanthren-9-one 15602216 Click to see 302.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
(4aS,6R,7R,10aS)-7-ethenyl-6-hydroxy-1,1,4a,7-tetramethyl-2,3,4,5,6,8,10,10a-octahydrophenanthren-9-one 162888928 Click to see CC1(CCCC2(C1CC(=O)C3=C2CC(C(C3)(C)C=C)O)C)C 302.50 unknown https://doi.org/10.1016/S0031-9422(99)00579-8
(4aS,6R,7S,10aS)-7-ethenyl-6-hydroxy-1,1,4a,7-tetramethyl-2,3,4,5,6,8,10,10a-octahydrophenanthren-9-one 15602212 Click to see 302.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
(4aS,7R,10aS)-7-ethenyl-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-9-one 162994290 Click to see 286.50 unknown https://doi.org/10.1016/S0031-9422(00)82735-1
(4aS,7S,10aS)-7-ethenyl-1,1,4a,7-tetramethyl-2,3,4,5,6,8,10,10a-octahydrophenanthren-9-one 14191476 Click to see 286.50 unknown https://doi.org/10.1016/S0031-9422(00)82735-1
(4aS,7S,10aS)-7-ethenyl-1,1,4a,7-tetramethyl-2,3,4,8,10,10a-hexahydrophenanthren-9-one 162820596 Click to see 284.40 unknown https://doi.org/10.1016/0031-9422(83)80034-X
(4aS,7S,8aR,10aS)-10,10-dideuterio-7-ethenyl-8a-hydroxy-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,8,10a-octahydrophenanthren-9-one 163193141 Click to see 306.50 unknown https://doi.org/10.1016/S0031-9422(00)82735-1
[(2S,3R,4bS,8aS)-2-ethenyl-2,4b,8,8-tetramethyl-10-oxo-1,3,4,5,6,7,8a,9-octahydrophenanthren-3-yl] acetate 14287363 Click to see 344.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
[(2S,3S,4bS,8aS)-2-ethenyl-2,4b,8,8-tetramethyl-4,10-dioxo-3,5,6,7,8a,9-hexahydro-1H-phenanthren-3-yl] acetate 14287365 Click to see 358.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
1-(7-Ethenyl-8a,9-dihydroxy-1,1,7-trimethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthren-4a-yl)propan-2-one 162951616 Click to see 348.50 unknown https://doi.org/10.1016/S0031-9422(99)00579-8
1-[(4aR,4bS,7R,8aR,9S,10aS)-7-ethenyl-8a,9-dihydroxy-1,1,7-trimethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthren-4a-yl]propan-2-one 162951617 Click to see CC(=O)CC12CCCC(C1CC(C3(C2CCC(C3)(C)C=C)O)O)(C)C 348.50 unknown https://doi.org/10.1016/S0031-9422(99)00579-8
2-Ethenyl-10-hydroxy-2,4b,8,8-tetramethyl-1,3,5,6,7,8a,9,10-octahydrophenanthren-4-one 163056797 Click to see CC1(CCCC2(C1CC(C3=C2C(=O)CC(C3)(C)C=C)O)C)C 302.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
2-ethenyl-2,4b,8,8-tetramethyl-3,4a,5,6,7,8a,9,10a-octahydro-1H-phenanthrene-4,10-dione 162883210 Click to see 302.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
2-ethenyl-2,4b,8,8-tetramethyl-3,5,6,7,8a,9-hexahydro-1H-phenanthrene-4,10-dione 163064839 Click to see 300.40 unknown https://doi.org/10.1016/S0031-9422(99)00579-8
https://doi.org/10.1016/0031-9422(83)80034-X
2-ethenyl-3-hydroxy-2,4b,8,8-tetramethyl-3,5,6,7,8a,9-hexahydro-1H-phenanthrene-4,10-dione 14287370 Click to see CC1(CCCC2(C1CC(=O)C3=C2C(=O)C(C(C3)(C)C=C)O)C)C 316.40 unknown https://doi.org/10.1016/0031-9422(83)80034-X
7-Ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthrene-8a,9-diol 14192409 Click to see 322.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
7-Ethenyl-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-9-one 162994288 Click to see 286.50 unknown https://doi.org/10.1016/S0031-9422(00)82735-1
7-Ethenyl-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthrene-8a,9-diol 14192395 Click to see CC1(CCCC2(C1CC(C3(C2CCC(C3)(C)C=C)O)O)C)C 306.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
7-Ethenyl-1,1,4a,7-tetramethyl-2,3,4,5,6,8,10,10a-octahydrophenanthren-9-one 14191475 Click to see CC1(CCCC2(C1CC(=O)C3=C2CCC(C3)(C)C=C)C)C 286.50 unknown https://doi.org/10.1016/S0031-9422(00)82735-1
7-Ethenyl-1,1,4a,7-tetramethyl-2,3,4,8,10,10a-hexahydrophenanthren-9-one 162820595 Click to see 284.40 unknown https://doi.org/10.1016/0031-9422(83)80034-X
7-Ethenyl-5-hydroxy-1,1,4a,7-tetramethyl-2,3,4,5,6,8,10,10a-octahydrophenanthren-9-one 15602215 Click to see CC1(CCCC2(C1CC(=O)C3=C2C(CC(C3)(C)C=C)O)C)C 302.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
7-ethenyl-8a-hydroxy-1,1,4a,7-tetramethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-9-one 14191477 Click to see 304.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
https://doi.org/10.1016/S0031-9422(00)82735-1
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2S,4R,9R,10S,13S,14R)-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-11-ene-2,14-diol 101615188 Click to see 304.50 unknown https://doi.org/10.1016/S0031-9422(99)00579-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(2S,7R,9S)-2,6,6,14-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),13,15-triene-5,11-dione 163036463 Click to see CC1=C2CC(=O)OC3C2=C(C=C1)C4(CCC(=O)C(C4C3)(C)C)C 312.40 unknown https://doi.org/10.1016/0031-9422(83)80034-X
2,6,6,14-Tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),13,15-triene-5,11-dione 163036461 Click to see 312.40 unknown https://doi.org/10.1016/0031-9422(83)80034-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4S,4aR,6aR,6bS,8aS,11R,12R,12aS,14aR,14bR)-3,12-dihydroxy-4-(hydroxymethyl)-6a,6b,11,12,14b-pentamethyl-1,2,3,4a,5,6,7,8,9,10,11,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylic acid 102588661 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(CO)C(=O)O)O)C)C)C2C1(C)O)C)C(=O)O 518.70 unknown https://doi.org/10.1016/S0031-9422(00)82735-1
(4aS,6aS,6bR,8aR,12aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,7,8,9,10,12,12a-decahydro-1H-picen-3-one 163080239 Click to see 422.70 unknown https://doi.org/10.1248/CPB.32.3674
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters / Methyl esters
methyl 2-[(1S,2S)-2-[(1R,4S)-4-ethenyl-4-methyl-2-oxocyclohexyl]-2,6,6-trimethylcyclohexyl]acetate 162820437 Click to see 334.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
Methyl 2-[2-(4-ethenyl-4-methyl-2-oxocyclohexyl)-2,6,6-trimethylcyclohexyl]acetate 162820436 Click to see 334.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
2-[(1S,2S)-2-[(1R,4S)-4-ethenyl-4-methyl-2-oxocyclohexyl]-2,6,6-trimethylcyclohexyl]acetic acid 162820493 Click to see CC1(CCCC(C1CC(=O)O)(C)C2CCC(CC2=O)(C)C=C)C 320.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
2-[2-(4-Ethenyl-4-methyl-2-oxocyclohexyl)-2,6,6-trimethylcyclohexyl]acetic acid 14192401 Click to see 320.50 unknown https://doi.org/10.1016/0031-9422(83)80034-X
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
(1R,10S,11S)-6-ethyl-5,11-dimethyl-14-oxatetracyclo[9.3.3.01,10.02,7]heptadeca-2(7),3,5-triene-8,12-dione 162948781 Click to see CCC1=C(C=CC2=C1C(=O)CC3C24CCCC3(C(=O)CO4)C)C 312.40 unknown https://doi.org/10.1016/S0031-9422(99)00579-8
(1R,10S,12S)-5,13,13-trimethyl-9,18-dioxapentacyclo[8.6.2.12,6.01,12.010,19]nonadeca-2(19),3,5,15-tetraen-14-one 163097113 Click to see 310.40 unknown https://doi.org/10.1016/S0031-9422(99)00579-8
5,13,13-Trimethyl-9,18-dioxapentacyclo[8.6.2.12,6.01,12.010,19]nonadeca-2(19),3,5,15-tetraen-14-one 14191469 Click to see 310.40 unknown https://doi.org/10.1016/S0031-9422(99)00579-8
6-Ethyl-5,11-dimethyl-14-oxatetracyclo[9.3.3.01,10.02,7]heptadeca-2(7),3,5-triene-8,12-dione 162948780 Click to see 312.40 unknown https://doi.org/10.1016/S0031-9422(99)00579-8
> Organoheterocyclic compounds / Oxepanes
(1S,2R,4S,5R,6S,11R,14R,18R,23R)-1,6,10,10,14,18,21,21-octamethyl-3-oxahexacyclo[13.8.0.02,4.05,14.06,11.018,23]tricos-15-en-9-one 15275942 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4C6C(C3(C2C1)C)O6)C)(C)C)C)C)C 438.70 unknown https://doi.org/10.1016/S0031-9422(99)00579-8
1,6,10,10,14,18,21,21-Octamethyl-3-oxahexacyclo[13.8.0.02,4.05,14.06,11.018,23]tricos-15-en-9-one 85260230 Click to see 438.70 unknown https://doi.org/10.1016/S0031-9422(99)00579-8
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridoxines
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[5-(hydroxymethyl)-4-(methoxymethyl)-2-methylpyridin-3-yl]oxyoxane-3,4,5-triol 14260867 Click to see CC1=NC=C(C(=C1OC2C(C(C(C(O2)CO)O)O)O)COC)CO 345.34 unknown https://doi.org/10.1248/CPB.32.3674
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Mururin A 135464366 Click to see 448.40 unknown https://doi.org/10.1016/0031-9422(83)80034-X
https://doi.org/10.1016/S0031-9422(99)00579-8

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