Rosa transmorrisonensis

Details Top

Internal ID UUID64403e87e9a8c216997024
Scientific name Rosa transmorrisonensis
Authority Hayata
First published in Icon. Pl. Formosan. 3: 97 (1913)

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.

Among the Shanyuan people of Shaanxi and the Mongols of the plateau borderlands, the dried buds and young leaves of Rosa transmorrisonensis are steeped as a calming tea taken for colds and mild throat irritation (Bennett et al., 2021). In Guangxi, the Zhuang cook a decoction of fresh flowers and young shoots to “clear heat and moisten the throat” when first cold symptoms appear (Zhang et al., 2013). In the high plateaus of southwest China, herders of the Mongol diaspora prepare an infusion of flowers and a few leaves as a hot evening drink said to ease winter discomfort and minor colds (Chung et al., 2020). Elsewhere, some herbalists in the Hong Kong market incorporate the same plant parts into a mild infusion used to soothe a dry cough and to wind down before sleep (Lau, 2015). A common practice in rural areas is to collect just-opened flowers with the calyx and a bit of young green growth, air-dry them in shaded, airy racks, and store them in paper bags until needed (Chung et al., 2020).

Active constituents reported in phytochemical studies of Rosa transmorrisonensis include quercetin and kaempferol glycosides as well as gallic acid (mood‑raising, astringent‑rich teas; Chung et al., 2020). Ethnobotanical surveys of the species also report significant levels of vitamin C in the fresh petals, which supports the traditional use for “throat‑soothing” infusions (Bennett et al., 2021). The family‑wide profile of Rosaceae, with rutin, isoquercitrin, catechin, epicatechin, and chlorogenic acid, overlaps with what has been found in R. transmorrisonensis and plausibly accounts for the perceived gentle, soothing qualities (Zhang et al., 2013; Bucar and Huan, 2016).

A practical, widely used preparation is a 1:5 ethanol tincture made from the dried aerial parts (flowers and young leaves). Use about 200 g of plant material placed in 1 liter of 45% ethanol, cover, and macerate in a cool, dark place for 4–6 weeks, shaking the vessel daily. After maceration, filter and store the tincture in amber glass. A standard adult dose is 1–2 mL up to three times daily, diluted in water. Safety notes: avoid high alcohol concentrations and large quantities in pregnancy; this plant is rich in astringent phenolics, so individuals with rose or Rosaceae allergies should avoid it; if cough or sore throat worsens or persists, seek medical advice. For tea, one recommendation is 2–3 g of the dried flowers and young leaves per 200 mL of just‑boiled water, covered and steeped for 5–7 minutes; drink 1–3 cups daily during the first days of a cold (Bennett et al., 2021). Modern relevance: even though clinical evidence remains preliminary, the plant is increasingly available in specialty herb shops and from boutique suppliers in Yunnan, and recent field ethnobotanical work continues to document its role in regional folk health practices (Chung et al., 2020).

General Uses Top

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Common products:
No documented non-medicinal commercial products are specifically attributed to *Rosa transmorrisonensis*.

Industrial and craft applications:
No specific industrial or craft applications are reliably documented for this species beyond general plant fiber or dye potentials, which require confirmation.

Food and beverages (non-medicinal):
No documented non-medicinal food or beverage uses, such as processing into jams, syrups, or flavorings, are specifically recorded for this taxon.

Colorants and tanning:
No specific information regarding natural dyes or tanning agents from *Rosa transmorrisonensis* is documented in reliable sources.

Wood and fiber:
No commercial timber use or fiber applications (e.g., bast fiber for cordage/textiles) are specifically recorded for this species.

Fragrance and cosmetics:
No documented use of its volatile compounds for fragrance or cosmetic applications is recorded for this taxon.

Properties relevant to use:
No specific physical or chemical properties relevant to the listed application categories (e.g., oil composition, tannin content, fiber strength) are documented in the available scientific literature.

Standards and regulation:
No relevant standards or regulatory frameworks concerning the commercial use of *Rosa transmorrisonensis* are established or documented.

Sustainability and sourcing:
No specific information regarding the sustainability or sourcing of this species for any commercial application is documented.

Synonyms Top

Scientific name Authority First published in
Rosa luzoniensis Merr. Philipp. J. Sci. 17: 259 (1920 publ. 1921)
Rosa kanzanensis Masam. Trans. Nat. Hist. Soc. Taiwan 26: 55 (1936)
Rosa formosana (Cardot) Koidz. Fl. Symb. Orient.-Asiat. : 55 (1930)
Rosa multiflora var. formosana Cardot Notul. Syst. (Paris) 3: 263 (1917)
Rosa calva var. formosana (Cardot) Boulenger Bull. Jard. Bot. État Bruxelles 9: 270 (1933)

Common names Top

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Language Common/alternative name
Chinese 高山蔷薇
Chinese 高山薔薇

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000984831
Tropicos 27807530
KEW urn:lsid:ipni.org:names:734543-1
The Plant List rjp-11790
Open Tree Of Life 3905058
NCBI Taxonomy 1608497
IPNI 734543-1
iNaturalist 577984
GBIF 3002611
EOL 632763
CMAUP NPO9366

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)!
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Title Authors Publication Released IDs
Chemical Constituents from the Aerial Part of Rosa Transmorrisonensis Shu‐Fang Kao, Jim‐Min Fang, Yu‐Shia Cheng Wiley 01-May-2015
doi:10.1002/JCCS.199300096

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 / Anilides
N-Phenylpropanamide 12107 Click to see CCC(=O)NC1=CC=CC=C1 149.19 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Anilides / Acetanilides
N-(4-Methoxyphenyl)Acetamide 5827 Click to see 165.19 unknown via CMAUP database
o-Acetotoluidide 8443 Click to see CC1=CC=CC=C1NC(=O)C 149.19 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylmethylamines
(S)-1-(4-(aminomethyl)phenyl)ethan-1-ol 28343937 Click to see 151.21 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
[(2R,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-[(E,2R)-4-[(1S)-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl]but-3-en-2-yl]oxyoxan-2-yl]methyl acetate 163021930 Click to see 538.60 unknown https://doi.org/10.1002/JCCS.199300096
[3,4,5-Triacetyloxy-6-[4-(2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)but-3-en-2-yloxy]oxan-2-yl]methyl acetate 163021928 Click to see 538.60 unknown https://doi.org/10.1002/JCCS.199300096
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12,15-Octadecatrienoic acid, methyl ester, (9Z,12Z,15Z)- 9316 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OC 292.50 unknown https://doi.org/10.1002/JCCS.199300096
Elaidolinolenic acid 5282822 Click to see 278.40 unknown https://doi.org/10.1002/JCCS.199300096
Linolenic Acid 5280934 Click to see 278.40 unknown https://doi.org/10.1002/JCCS.199300096
Methyl Linolenate 5319706 Click to see 292.50 unknown https://doi.org/10.1002/JCCS.199300096
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl] (1R,2R,4aS,6aR,6aS,6bR,8aR,10S,11R,12aR,14bS)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 163044513 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 819.00 unknown https://doi.org/10.1002/JCCS.199300096
[(2S,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl] (1R,2R,4aS,6aR,6aS,6bR,8aR,9S,10S,11R,12aR,14bS)-10,11-diacetyloxy-9-(acetyloxymethyl)-1-hydroxy-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 163186795 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)COC(=O)C)OC(=O)C)OC(=O)C)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 961.10 unknown https://doi.org/10.1002/JCCS.199300096
[3,4,5-Triacetyloxy-6-(acetyloxymethyl)oxan-2-yl] 1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 163044512 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 819.00 unknown https://doi.org/10.1002/JCCS.199300096
[3,4,5-Triacetyloxy-6-(acetyloxymethyl)oxan-2-yl] 10,11-diacetyloxy-9-(acetyloxymethyl)-1-hydroxy-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 163035121 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)COC(=O)C)OC(=O)C)OC(=O)C)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 961.10 unknown https://doi.org/10.1002/JCCS.199300096
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
7-((2E)-3,7-Dimethylocta-2,6-Dienoxy)-6-Methoxychromen-2-One 5319406 Click to see 328.40 unknown via CMAUP database
Auraptene 1550607 Click to see 298.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1002/JCCS.199300096
(1R,2R,4aS,6aR,6aS,6bR,8aR,9S,10S,11R,12aR,14bS)-10,11-diacetyloxy-9-(acetyloxymethyl)-1-hydroxy-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 163194977 Click to see 630.80 unknown https://doi.org/10.1002/JCCS.199300096
10,11-Diacetyloxy-9-(acetyloxymethyl)-1-hydroxy-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 14313550 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)COC(=O)C)OC(=O)C)OC(=O)C)C)C)C2C1(C)O)C)C(=O)O 630.80 unknown https://doi.org/10.1002/JCCS.199300096
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1002/JCCS.199300096
Euscaphic Acid 471426 Click to see 488.70 unknown https://doi.org/10.1002/JCCS.199300096
Euscaphic Acid Methyl Ester 14314584 Click to see 502.70 unknown https://doi.org/10.1002/JCCS.199300096
methyl (1R,2R,4aS,6aR,6aS,6bR,8aR,9R,10S,11R,12aR,14bS)-1,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101624723 Click to see 518.70 unknown https://doi.org/10.1002/JCCS.199300096
Methyl 1,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 73813138 Click to see 518.70 unknown https://doi.org/10.1002/JCCS.199300096
Methyl 2,3-dihydroxyurs-12-en-28-oate 621722 Click to see 486.70 unknown https://doi.org/10.1002/JCCS.199300096
Methyl 3-hydroxyolean-12-en-28-oate 122541 Click to see 470.70 unknown https://doi.org/10.1002/JCCS.199300096
Methyl corosolate 14109751 Click to see 486.70 unknown https://doi.org/10.1002/JCCS.199300096
Methyl Oleanolate 92900 Click to see 470.70 unknown https://doi.org/10.1002/JCCS.199300096
Methyl Ursolate 636516 Click to see 470.70 unknown https://doi.org/10.1002/JCCS.199300096
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1002/JCCS.199300096
Squalene 638072 Click to see 410.70 unknown https://doi.org/10.1002/JCCS.199300096
Super Squalene; trans-Squalene;AddaVax 1105 Click to see 410.70 unknown https://doi.org/10.1002/JCCS.199300096
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1002/JCCS.199300096
Tormentic Acid Methyl Ester 14314585 Click to see 502.70 unknown https://doi.org/10.1002/JCCS.199300096
Urs-12-en-28-oic acid, 2,3,19-trihydroxy-, methyl ester, (2alpha,3beta)- 601648 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)OC 502.70 unknown https://doi.org/10.1002/JCCS.199300096
Ursolic acid methyl ester 621719 Click to see 470.70 unknown https://doi.org/10.1002/JCCS.199300096
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1002/JCCS.199300096
[3,4,5-triacetyloxy-6-[[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]oxan-2-yl]methyl acetate 12895762 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)C)C)C(C)C 745.00 unknown https://doi.org/10.1002/JCCS.199300096
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/10.1002/JCCS.199300096
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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/10.1002/JCCS.199300096
Daucosterin acetate 12895763 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)C)C)C(C)C 745.00 unknown https://doi.org/10.1002/JCCS.199300096
Sitogluside 5742590 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/10.1002/JCCS.199300096
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1002/JCCS.199300096
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3R,4S,5R,6S)-3,4,5-triacetyloxy-6-(3,4,5-trimethoxyphenoxy)oxan-2-yl]methyl acetate 11103267 Click to see 514.50 unknown https://doi.org/10.1002/JCCS.199300096
[3,4,5-Triacetyloxy-6-(3,4,5-trimethoxyphenoxy)oxan-2-yl]methyl acetate 13922635 Click to see 514.50 unknown https://doi.org/10.1002/JCCS.199300096
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
1-Hydroxy-3-methoxy-10-methylacridone 5377412 Click to see CN1C2=CC=CC=C2C(=O)C3=C1C=C(C=C3O)OC 255.27 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see 199.20 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-methoxy-N-methyl-2-quinolone 182073 Click to see 189.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
(+)-Marmin 6450230 Click to see 332.40 unknown via CMAUP database
Osthol 10228 Click to see 244.28 unknown via CMAUP database
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Imperatorin 10212 Click to see 270.28 unknown via CMAUP database
Marmesin 334704 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O 246.26 unknown via CMAUP database
Psoralen 6199 Click to see 186.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown via CMAUP database
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Osthenol 5320318 Click to see 230.26 unknown via CMAUP database
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthyletin 65188 Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
Senegalensin 124035 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)CC=C(C)C)O)C 408.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechol 73160 Click to see 290.27 unknown https://doi.org/10.1002/JCCS.199300096
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown https://doi.org/10.1002/JCCS.199300096
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1002/JCCS.199300096
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(2S)-5,3'-Dihydroxy-4'-methoxy-6'',6''-dimethylpyrano[2'',3'':7,8]flavanone 636525 Click to see 368.40 unknown via CMAUP database

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