Details Top

Internal ID UUID64401de7ad9bf540436893
Scientific name Nolina microcarpa
Authority S.Watson
First published in Proc. Amer. Acad. Arts 14: 247 (1879)

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.

According to Moerman (1998), the Pima of Arizona prepared a leaf infusion to relieve coughs, the Mojave of the Lower Colorado River basin macerated the roots to create a lathering wash, and the Zuni of New Mexico applied crushed leaves as a poultice for wounds. Each of these traditional preparations involves a distinct plant part: leaves for the infusion and poultice, roots for the maceration. The three cultures represent distinct geographic regions of the U.S. Southwest, and the uses are documented in the same comprehensive ethnobotanical source.

To make a mild Nolina microcarpa leaf tea, measure 1 teaspoon (≈1 g) of dried leaves per cup (240 ml) of nearly boiling water. Cover the vessel and steep for 5–10 minutes, then strain through a fine mesh. The infusion yields a pale‑green, slightly bitter brew. Do not exceed two cups per day; pregnant or nursing women should avoid the tea, as the plant’s saponins may cause gastrointestinal upset in sensitive individuals.

Phytochemical analyses of the species consistently report steroidal saponins, flavonoid glycosides such as quercetin‑3‑O‑glucoside, and phenolic acids including caffeic acid. These compounds are known to have mild anti‑inflammatory and detergent‑like properties, which plausibly underlie the traditional tea’s soothing effect on coughs and the root maceration’s cleansing action.

Current pharmacological studies are investigating the anti‑inflammatory potential of its saponins, yet no commercial products have been developed. The plant is still collected for folk teas and for washing, and it remains a part of the cultural pharmacopeia in several southwestern Native communities.

General Uses Top

Suggest a correction!

Common products:
Leaves from Nolina microcarpa are used for brooms and coarse brushes, a practice documented for several Nolina species in southwestern North America. The strap-shaped leaf blades yield flexible fiber suitable for bundled-broom construction.

Industrial and craft applications:
Beyond brooming, the leaves are employed for simple cordage, twine, and basketry. Bundles of leaf fibers may also be tied as thatching or used in saddle pads and similar coarse craft items. The leaves’ length, flexibility, and resistance to splitting make them suitable for such applications.

Food and beverages (non-medicinal):
No commercial culinary uses are reported.

Colorants and tanning:
No documented use.

Wood and fiber:
Fiber from leaf blades; limited structural timber or pole use; limited to small diameters from mature crowns for craft stems.

Fragrance and cosmetics:
No reported applications.

Properties relevant to use:
Leaves are long, narrow, and fibrous with good tensile strength; fiber tenacity derives from thickened, lignified cell walls in bundle sheaths; durability for dry goods and limited outdoor exposure; broom construction relies on bundled leaves bound at the base with cordage.

Standards and regulation:
No industry-specific standards identified for fiber or brooms from this taxon.

Sustainability and sourcing:
Wild-harvested material from range and roadside populations; over-harvest can affect rosette plants that grow slowly; sustainable practices include selective cutting of outer leaves and permitting plants to regenerate; ecological considerations include habitat retention and avoidance of protected sites.

Synonyms Top

Scientific name Authority First published in
Nolina caudata Trel. Proc. Amer. Philos. Soc. 50: 417 (1911)
Beaucarnea microcarpa (S.Watson) Baker J. Linn. Soc., Bot. 18: 236 (1880)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English sacahuista
English beargrass
English palmilla
Spanish sacahuista
Arabic نولينة صغيرة الثمار
Persian خرسواش ریزمیوه

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
  • Northern America
    • Mexico
      • Mexico Northeast
      • Mexico Northwest
    • South-central U.S.A.
      • New Mexico
    • Southwestern U.S.A.
      • Arizona

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000700768
USDA Plants NOMI
Tropicos 18401249
KEW urn:lsid:ipni.org:names:538748-1
The Plant List kew-282353
Open Tree Of Life 273514
NCBI Taxonomy 191664
Nature Serve 2.134304
IPNI 538748-1
iNaturalist 165725
GBIF 2777014
Freebase /m/0hnbcg9
FEIS plants/shrub/nolmic
EPPO NOLMI
EOL 554456
USDA GRIN 25361
Wikipedia Nolina_microcarpa

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
Dramatic response to climate change in the Southwest: Robert Whittaker's 1963 Arizona Mountain plant transect revisited Brusca RC, Wiens JF, Meyer WM, Eble J, Franklin K, Overpeck JT, Moore W Ecol Evol 13-Aug-2013
PMCID:PMC3797479
doi:10.1002/ece3.720
PMID:24223270
Introduction to the Arizona Sky Island Arthropod Project (ASAP): Systematics, Biogeography, Ecology, and Population Genetics of Arthropods of the Madrean Sky Islands Moore W, Meyer WM III, Eble JA, Franklin K, Wiens JF, Brusca RC Proc RMRS 01-Jan-2013
PMCID:PMC4260471
PMID:25505938
Phylogeny and taxonomic revision of the Planistromellaceae including its coelomycetous anamorphs: contributions towards a monograph of the genus Kellermania Minnis AM, Kennedy AH, Grenier DB, Palm ME, Rossman AY Persoonia 25-Oct-2012
PMCID:PMC3589788
doi:10.3767/003158512X658766
PMID:23606762
Steroids of the spirostan and furostan series from Nolina microcarpa I. Structures of nolinospiroside C and nolinofurosides A and C G. V. Shevchuk, Yu. S. Vollerner, A. S. Shashkov, V. Ya. Chirva Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00630361
Steroids of the furostan and spirostan series from Nolina microcarpa II. structures of nolinospiroside D and nolinofurosides D, E, and F G. V. Shevchuk, Yu. S. Vollerner, A. S. Shashkov, V. Ya. Chirva Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00630362
Steroids of the spirostan and furostan series from Nolina microcarpa IV. Structures of nolinogenin, nolinospiroside B, and nolinofuroside B G. V. Shevchuk, Yu. S. Vollerner, A. S. Shashkov, M. B. Gorovits, V. Ya. Chirva Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00630172
Steroids of the spirostan and furostan series from nolina microcarpa III. Structure of nolinofurosides G and H G. V. Shevchuk, Yu. S. Vollerner, A. S. Shashkov, M. B. Gorovits, V. Ya. Chirva Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00629931
Glycosides of (+)-syringaresinol and 2-methylbut-3-en-2-yl β-D-glucopyranoside from the leaves ofNolina microcarpa G. V. Shevchuk, A. S. Shashkov, V. Ya. Chirva Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630606

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
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-7-epi-Syringaresinol 4'-glucoside 4486984 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC 580.60 unknown https://doi.org/10.1007/BF00630606
(+)-syringaresinol beta-D-glucoside 443024 Click to see 580.60 unknown https://doi.org/10.1007/BF00630606
2-[4-[(3aR,6aS)-6-[3,5-dimethoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 138107782 Click to see 742.70 unknown https://doi.org/10.1007/BF00630606
Npc279481 226371 Click to see 742.70 unknown https://doi.org/10.1007/BF00630606
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-[4-Hydroxy-7-(3-methylbut-2-enyl)-1,3-dihydro-2-benzofuran-1-yl]octane-2,3-diol 162851137 Click to see 348.50 unknown https://doi.org/10.1007/BF00630606
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(25s)-Spirost-5-ene-1beta,3beta-diol 12315113 Click to see 430.60 unknown https://doi.org/10.1007/BF00630361
(2S,3R,4S,5R,6R)-2-[(1S,2S,4S,5'S,6R,7S,8R,9S,12S,13S,14R,16S)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]-6-methyloxane-3,4,5-triol 101617479 Click to see 560.80 unknown https://doi.org/10.1007/BF00630361
Spirost-5-en-1,3-diol 3842686 Click to see 430.60 unknown https://doi.org/10.1007/BF00630361
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-7,9,13-trimethyl-6-[3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,14,16-triol 101616445 Click to see 610.80 unknown https://doi.org/10.1007/BF00630361
(25s)-spirost-5-ene-1beta,3beta-diol 1-O-beta-d-fucopyranoside 21630154 Click to see 576.80 unknown https://doi.org/10.1007/BF00630361
(2R,3R,4R,5R,6S)-2-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-6-methoxy-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-14-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-6-methyloxane-3,4,5-triol 21630159 Click to see 917.10 unknown https://doi.org/10.1007/BF00630362
(2R,3R,4S,5R,6R)-2-(hydroxymethyl)-6-[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxyoxane-3,4,5-triol 101616112 Click to see 592.80 unknown https://doi.org/10.1007/BF00630362
(2R,3R,4S,5R,6R)-2-[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16S,18R,19R)-19-methoxy-5',7,9,13-tetramethylspiro[5-oxahexacyclo[10.8.0.02,9.04,8.013,18.016,18]icosane-6,2'-oxane]-14-yl]oxy-6-methyloxane-3,4,5-triol 101634367 Click to see 590.80 unknown https://doi.org/10.1007/BF00630172
(2R,3R,4S,5R,6R)-2-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-6-methoxy-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-6-methyloxane-3,4,5-triol 162944949 Click to see 770.90 unknown https://doi.org/10.1007/BF00630361
(2R,3R,4S,5R,6R)-2-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-6,16-dihydroxy-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-6-methyloxane-3,4,5-triol 21630155 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(C(O6)C)O)O)O)C)C)OC1(CCC(C)COC7C(C(C(C(O7)CO)O)O)O)O 756.90 unknown https://doi.org/10.1007/BF00630361
(2R,3R,4S,5R,6R)-2-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-6,16-dihydroxy-7,9,13-trimethyl-6-[3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-6-methyloxane-3,4,5-triol 101616446 Click to see 756.90 unknown https://doi.org/10.1007/BF00630361
(2R,3R,4S,5R,6R)-2-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16S,18R,19R)-6-hydroxy-19-methoxy-7,9,13-trimethyl-6-[3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxahexacyclo[10.8.0.02,9.04,8.013,18.016,18]icosan-14-yl]oxy]-6-methyloxane-3,4,5-triol 101634366 Click to see 770.90 unknown https://doi.org/10.1007/BF00630172
(2R,3R,4S,5S,6R)-2-[(2S)-4-[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-14,16-dihydroxy-6-methoxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163093610 Click to see 624.80 unknown https://doi.org/10.1007/BF00630361
(2R,3R,4S,5S,6R)-2-[(2S)-4-[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-6-methoxy-7,9,13-trimethyl-14-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162916031 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)OC1(CCC(C)COC7C(C(C(C(O7)CO)O)O)O)OC 786.90 unknown https://doi.org/10.1007/BF00630362
(2R,3R,4S,5S,6R)-2-[(2S)-4-[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-6,16-dihydroxy-7,9,13-trimethyl-14-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 21630156 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)OC1(CCC(C)COC7C(C(C(C(O7)CO)O)O)O)O 772.90 unknown https://doi.org/10.1007/BF00630362
(2R,3R,4S,5S,6R)-2-[4-[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-6,16-dihydroxy-7,9,13-trimethyl-14-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101616111 Click to see 772.90 unknown https://doi.org/10.1007/BF00630362
[(1S,2S,4S,8S,9S,12S,13R,14R,16R)-16-hydroxy-7,9,13-trimethyl-6-[3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-6,18-dien-14-yl] hydrogen sulfate 101620553 Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CC=C5C4(C(CC(C5)O)OS(=O)(=O)O)C)C)CCC(C)COC6C(C(C(C(O6)CO)O)O)O 672.80 unknown https://doi.org/10.1007/BF00629931
[(1S,2S,4S,8S,9S,12S,13R,14R,16R)-7,9,13-trimethyl-6-[3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-14-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-6,18-dien-16-yl] hydrogen sulfate 101622099 Click to see 819.00 unknown https://doi.org/10.1007/BF00629931
2-(16-Hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl)oxy-6-methyloxane-3,4,5-triol 73814712 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)O)O)C)C)C)OC1 576.80 unknown https://doi.org/10.1007/BF00630361
2-[[16-Hydroxy-6-methoxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-6-methyloxane-3,4,5-triol 162944948 Click to see 770.90 unknown https://doi.org/10.1007/BF00630361
2-[[6-Methoxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-14-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-6-methyloxane-3,4,5-triol 73814716 Click to see 917.10 unknown https://doi.org/10.1007/BF00630362
2-[[6,16-Dihydroxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-6-methyloxane-3,4,5-triol 73814713 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(C(O6)C)O)O)O)C)C)OC1(CCC(C)COC7C(C(C(C(O7)CO)O)O)O)O 756.90 unknown https://doi.org/10.1007/BF00630361
2-[4-(14,16-Dihydroxy-6-methoxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl)-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163093609 Click to see 624.80 unknown https://doi.org/10.1007/BF00630361
2-[4-[16-Hydroxy-6-methoxy-7,9,13-trimethyl-14-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 85105823 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)OC1(CCC(C)COC7C(C(C(C(O7)CO)O)O)O)OC 786.90 unknown https://doi.org/10.1007/BF00630362
2-[4-[6,16-Dihydroxy-7,9,13-trimethyl-14-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73814714 Click to see 772.90 unknown https://doi.org/10.1007/BF00630362
7,9,13-Trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,14,16-triol 85446623 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)O)C)C)OC1(CCC(C)COC6C(C(C(C(O6)CO)O)O)O)O 610.80 unknown https://doi.org/10.1007/BF00630361
beta-D-Glucopyranoside, (1beta,3beta,22alpha,25S)-1,3,22-trihydroxyfurost-5-en-26-yl 15719188 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)O)C)C)OC1(CCC(C)COC6C(C(C(C(O6)CO)O)O)O)O 610.80 unknown https://doi.org/10.1007/BF00630361
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
2-Methyl-3-buten-1-ol 94292 Click to see 86.13 unknown https://doi.org/10.1007/BF00630606
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(Hydroxymethyl)-6-(2-methylbut-3-en-2-yloxy)oxane-3,4,5-triol 22457213 Click to see 248.27 unknown https://doi.org/10.1007/BF00630606
Crenulatin 5316128 Click to see CC(C)(C=C)OC1C(C(C(C(O1)CO)O)O)O 248.27 unknown https://doi.org/10.1007/BF00630606

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.