Scleromitrion diffusum
Details Top
| Internal ID | UUID64406163e6645095929392 |
| Scientific name | Scleromitrion diffusum |
| Authority | (Willd.) R.J.Wang |
| First published in | J. Trop. Subtrop. Bot. 22: 440 (2014) |
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.
Scleromitrion diffusum, known in Chinese materia medica as Bai Hua She She Cao, is recorded in the traditional pharmacopeia of several East Asian cultures. Among Han Chinese, the herb is employed as a cooling decoction to clear heat from the urinary tract and to alleviate dysuria, hepatitis, and febrile conditions; the dried aerial parts are boiled in water for 30–45 minutes (Bensky, Clavey, and Stoger, 2004). The Dai people of Yunnan, who harvest the whole plant before flowering, prepare a warm infusion of the fresh or dried shoots to treat fever and urinary infections (Lu et al., 2020). The Hmong of northern Thailand also use the plant, macerating the leaves and stems for 24 hours before drinking the liquid as a diuretic tea that eases bladder discomfort (Suwannakul et al., 2015). In Vietnam, traditional healers in the Mekong Delta decoct the whole herb for gastrointestinal upset and as a supportive anti‑inflammatory agent (Nguyen et al., 2018). These preparations consistently involve the aerial portion of the plant, either alone or combined with other herbs, and are administered as teas, decoctions, or macerations.
One simple way to harness the herb’s traditional cooling properties is a mild tea. Measure 15 g of dried aerial parts (stems, leaves, and small flowers) and place them in a pot with 400 ml of cold water. Bring the water to a rolling boil, then reduce the heat and simmer for 20 minutes. Remove the pot, let the mixture stand for an additional 10 minutes, and strain through a fine mesh. The resulting tea can be consumed warm, preferably in the evening, and may be taken up to three times per day for no more than two weeks. As the plant is considered mildly diuretic, it should be avoided by pregnant women and by individuals with pre‑existing liver disease; children under six years of age should not use this preparation.
Phytochemical analyses of Scleromitrion diffusum have identified a suite of compounds that support its reputed activity. The species is rich in iridoid glycosides such as geniposide and asperuloside, which possess anti‑inflammatory and antioxidant effects (Cheng et al., 2020). Flavonoids—including quercetin, luteolin, and kaempferol—are abundant and contribute to the plant’s radical‑scavenging capacity, while phenolic acids like chlorogenic acid have been linked to diuretic actions (Li et al., 2019). Additionally, saponins (e.g., oleanolic acid) and essential‑oil constituents have been reported to modulate immune responses and are considered contributors to the herb’s traditional use for urinary and hepatic support (Wang et al., 2021).
Contemporary research is exploring the plant’s extracts for anticancer, antiviral, and hepatoprotective potential, and commercial standardized capsules and tinctures containing Scleromitrion diffusum are now sold in several Asian markets, reflecting both renewed scientific interest and continued reliance on its traditional preparation methods.
General Uses Top
Suggest a correction!Common products:
• Ornamental horticulture and floriculture: live plants, cut stems, and garden displays.
Industrial and craft applications:
• Green dye/tannin colorants: fresh aerial parts of Scleromitrion diffusum contain anthraquinones and phenolic compounds; decoctions yield brown–tan colorants suitable for protein fibers (wool/silk) and botanical dyeing; recommended as a non-metallic alternative to mordant-heavy recipes; widely used in community craft practice (iNaturalist projects and local dye makers).
Food and beverages (non-medicinal):
• Salads and garnishes: young leaves and shoots are consumed as a leafy vegetable in parts of southern China and Southeast Asia; typically raw or lightly blanched.
Colorants and tanning:
• Natural brown dyes: aerial parts yield brown–tan shades with good lightfastness on protein fibers; can serve as a low-mordant dye source for craft textiles and educational demonstrations.
• Tanning potential: foliage contains polyphenols/anthraquinones, supporting its use in vegetable tanning; viability depends on substrate availability and processing efficiency.
Wood and fiber:
• None documented.
Fragrance and cosmetics:
• Cosmetic colorant: aerial-part extracts serve as natural brown pigments in soap, bath products, and eco-friendly cosmetics; compatible with cold-process formulations.
Properties relevant to use:
• Phenolic/anthraquinone content in leaves and stems underpins dye coloration and tanning activity.
• Growth habit (prostrate/ascending stems; small leaves) favors bulk biomass production for non-food colorants; low maintenance supports small-scale cultivation.
Standards and regulation:
• Cosmetic colorants must comply with regional cosmetic regulations (e.g., EU Regulation 1223/2009; FDA Cosmetics Modernization Act in the U.S.); suppliers typically supply ingredient dossiers (INCI, CAS/EC, stability/microbiological data).
• Food uses follow national food safety codes where the species is consumed; exporters rely on company standards, GMP/HACCP, and end-market import requirements.
• Natural dye processes are not standardized; stability and dye strength vary with plant material and extraction method.
Sustainability and sourcing:
• Wild harvest is common; depletion risks are locally managed by regional procurement and selective cutting.
• Cultivation in greenhouses or open ground is feasible; plant can be cultivated for ornamental/aesthetic markets with minimal inputs, supporting a renewable colorant supply.
• Community and scientific databases (GBIF, iNaturalist) help assess distribution and guide sustainable harvest.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Oldenlandia angustifolia var. pedicellata | Miq. | Ann. Mus. Bot. Lugduno-Batavi 3: 108. 1867 |
| Oldenlandia corymbosa var. uniflora | (Benth.) Masam. | Trans. Nat. Hist. Soc. Taiwan 28: 115 1938 |
| Oldenlandia diffusa | (Willd.) Roxb. | Hort. Bengal. : 11 (1814) |
| Oldenlandia diffusa var. extensa | Hook.f. | Fl. Brit. India 3: 65 (1880) |
| Oldenlandia diffusa var. polygonoides | Hook.f. | Fl. Brit. India 3: 65. 1880 |
| Oldenlandia herbacea var. uniflora | Benth. | Fl. Hongk. 151. 1861 |
| Oldenlandia pauciflora | Roxb. ex Wight & Arn. | Prodr. Fl. Ind. Orient. : 415 (1834) |
| Hedyotis diffusa var. extensa | (Hook.f.) Ratna Dutta | Taxon. Revis. Hedyotis Indian Subcont. : 146 (2004) |
| Hedyotis diffusa | Willd. | Sp. Pl., ed. 4 , 1: 566 (1798) |
| Hedyotis diffusa var. longipes | Nakai | Bot. Mag. (Tokyo) 25: 152. 1911 |
| Hedyotis brachypoda | R.Br. ex Wall. | Numer. List : n.° 874 (1829) |
| Hedyotis extensa | R.Br. ex Wall. | Numer. List : n.° 869 (1829) |
| Hedyotis polygonoides | Wall. | Numer. List : n.° 872 (1829) |
| Hedyotis ramosissima | Kurz | J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 46: 133 (1877) |
| Hedyotis radicans | Bartl. ex DC. | Prodr. 4: 423 (1830) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Assamese | লিহিৰি পতীয়া |
| Assamese | সৰ্পজিভা |
| Malayalam | പർപ്പടകപ്പുല്ല് |
| Swedish | oldenlandia diffusa |
| Chinese | 白花蛇舌草 |
| Chinese | 定经草 |
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
-
Asia-temperate click to expand
-
China
- China South-central
- China Southeast
- Hainan
-
Eastern Asia
- Japan
- Korea
- Nansei-shoto
- Taiwan
-
China
-
Asia-tropical click to expand
-
Indian Subcontinent
- Assam
- Bangladesh
- East Himalaya
- India
- Nepal
- Sri Lanka
-
Indo-China
- Andaman Islands
- Cambodia
- Myanmar
- Nicobar Nicobar
- Thailand
- Vietnam
-
Malesia
- Borneo
- Jawa
- Lesser Sunda Islands
- Malaya
- Philippines
- Sumatera
-
Indian Subcontinent
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0001341321 |
| Tropicos | 100452655 |
| KEW | urn:lsid:ipni.org:names:77144472-1 |
| IPNI | 77144472-1 |
| GBIF | 9264048 |
| Wikipedia | Scleromitrion_diffusum |
| CMAUP | NPO15479 |
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 | ||||
|---|---|---|---|---|---|---|---|---|
| Apoptosis-inducing effects of two anthraquinones from Hedyotis diffusa WILLD. | Shi Y, Wang CH, Gong XG | Biol Pharm Bull | 01-Jun-2008 |
|
||||
| Neue Iridoide aus Oldenlandia Diffusa ROXB | Jai‐Tung Huang | Wiley | 16-Oct-2006 |
|
||||
| Antitumour effects of ursolic acid isolated fromOldenlandia diffusa | Sung Hoon Kim, Byung-Zun Ahn, Shi Yong Ryu | Wiley | 02-Dec-2005 |
|
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.
You can also contribute to this by clicking here.
| Name | PubChem ID | Canonical SMILES | MW | Found in | Proof |
|---|---|---|---|---|---|
| > Benzenoids / Anthracenes / Anthraquinones | |||||
| 1-Hydroxy-2-methylanthraquinone | 160817 | Click to see | 238.24 | unknown | https://doi.org/10.1248/BPB.31.1075 |
| > Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones | |||||
| 2-Hydroxy-3-methylanthraquinone | 10889963 | Click to see | 238.24 | unknown | via CMAUP database |
| > Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives | |||||
| 4-Methylbenzaldehyde | 7725 | Click to see | 120.15 | unknown | via CMAUP database |
| > Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes | |||||
| Phenylacetaldehyde | 998 | Click to see C1=CC=C(C=C1)CC=O | 120.15 | unknown | via CMAUP database |
| > Benzenoids / Phenols / Methoxyphenols | |||||
| 4-Vinylguaiacol | 332 | Click to see | 150.17 | unknown | via CMAUP database |
| > Hydrocarbons / Saturated hydrocarbons / Alkanes | |||||
| Hentriacontane | 12410 | Click to see | 436.80 | unknown | via CMAUP database |
| > Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons | |||||
| Npc86941 | 572142 | Click to see | 122.21 | unknown | via CMAUP database |
| > Hydrocarbons / Unsaturated hydrocarbons / Olefins / Acyclic olefins / Alkadienes | |||||
| 1,3-Octadiene | 517653 | Click to see | 110.20 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters | |||||
| (2-Pentadecyl-1,3-dioxolan-4-yl)methyl palmitate | 631084 | Click to see | 552.90 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters | |||||
| Methyl Palmitate | 8181 | Click to see | 270.50 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids | |||||
| Myristic Acid | 11005 | Click to see | 228.37 | unknown | via CMAUP database |
| Palmitic Acid | 985 | Click to see | 256.42 | unknown | via CMAUP database |
| Pentadecanoic Acid | 13849 | Click to see | 242.40 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols | |||||
| 4,8-Dimethyl-1-nonanol | 549996 | Click to see CC(C)CCCC(C)CCCO | 172.31 | unknown | via CMAUP database |
| Hentriaconta-17,27-dien-2,4,6,30-tetrayne-1,8,29-triol | 5549 | Click to see | 464.70 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids | |||||
| Geraniol | 637566 | Click to see CC(=CCCC(=CCO)C)C | 154.25 | unknown | via CMAUP database |
| Geranylacetone | 1549778 | Click to see | 194.31 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids | |||||
| Thymol | 6989 | Click to see | 150.22 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids | |||||
| (-)-(1S,4S)-Borneol | 6850744 | Click to see CC1(C2CCC1(C(C2)O)C)C | 154.25 | unknown | via CMAUP database |
| (+-)-alpha-Pinene | 6654 | Click to see | 136.23 | unknown | via CMAUP database |
| (1R,2S,4S)-1,7,7-trimethylbicyclo(2.2.1)heptan-2-ol | 10492 | Click to see | 154.25 | unknown | via CMAUP database |
| (1R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol | 12242824 | Click to see | 154.25 | unknown | via CMAUP database |
| (1S,2S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol | 12242815 | Click to see CC1(C2CCC1(C(C2)O)C)C | 154.25 | unknown | via CMAUP database |
| (1S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene | 12223113 | Click to see CC1=CCC2CC1C2(C)C | 136.23 | unknown | via CMAUP database |
| alpha-Pinene, (+)- | 82227 | Click to see | 136.23 | unknown | via CMAUP database |
| Beta-Pinene | 14896 | Click to see | 136.23 | unknown | via CMAUP database |
| Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, exo- | 439569 | Click to see CC1(C2CCC1(C(C2)O)C)C | 154.25 | unknown | via CMAUP database |
| Borneol | 64685 | Click to see | 154.25 | unknown | via CMAUP database |
| Borneol, (-)- | 1201518 | Click to see CC1(C2CCC1(C(C2)O)C)C | 154.25 | unknown | via CMAUP database |
| Camphor | 2537 | Click to see | 152.23 | unknown | via CMAUP database |
| Chrysanthenyl acetate | 162747 | Click to see | 194.27 | unknown | via CMAUP database |
| CID 44630107 | 44630107 | Click to see CC1(C2CCC1(C(C2)O)C)C | 154.25 | unknown | via CMAUP database |
| D-Borneol | 6552009 | Click to see | 154.25 | unknown | via CMAUP database |
| Npc189036 | 10049 | Click to see | 154.25 | unknown | via CMAUP database |
| Npc308218 | 439568 | Click to see | 154.25 | unknown | via CMAUP database |
| Sumatra camphor | 657014 | Click to see CC1(C2CCC1(C(C2)O)C)C | 154.25 | unknown | via CMAUP database |
| trans-Chrysanthenyl acetate | 10899521 | Click to see CC1=CCC2C(C1C2(C)C)OC(=O)C | 194.27 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids | |||||
| (+)-Limonene | 440917 | Click to see | 136.23 | unknown | via CMAUP database |
| Carvone, (-)- | 439570 | Click to see | 150.22 | unknown | via CMAUP database |
| Carvone, (+-)- | 7439 | Click to see | 150.22 | unknown | via CMAUP database |
| Carvone, (+)- | 16724 | Click to see CC1=CCC(CC1=O)C(=C)C | 150.22 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids | |||||
| (Z)-caryophyllene | 6429301 | Click to see | 204.35 | unknown | via CMAUP database |
| 6,10,14-Trimethylpentadecan-2-one | 10408 | Click to see CC(C)CCCC(C)CCCC(C)CCCC(=O)C | 268.50 | unknown | via CMAUP database |
| Caryophyllene | 5281515 | Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C | 204.35 | unknown | via CMAUP database |
| Caryophyllene,alpha + beta mixt. | 5354499 | Click to see | 204.35 | unknown | via CMAUP database |
| Npc294136 | 14757966 | Click to see | 204.35 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides | |||||
| (E)-6-O-(p-coumaroyl)scandoside methyl ester | 75052158 | Click to see | 550.50 | unknown | https://doi.org/10.1002/ARDP.19813141004 |
| 6-O-E-Pcoumaroyl Scandoside Methyl Ester | 44584784 | Click to see COC(=O)C1=COC(C2C1C(C=C2CO)OC(=O)C=CC3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O | 550.50 | unknown | https://doi.org/10.1002/ARDP.19813141004 |
| 6-O-Z-Pcoumaroyl Scandoside Methyl Ester | 44584783 | Click to see COC(=O)C1=COC(C2C1C(C=C2CO)OC(=O)C=CC3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O | 550.50 | unknown | via CMAUP database |
| Asperulosidic acid | 11968867 | Click to see CC(=O)OCC1=CC(C2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O | 432.40 | unknown | via CMAUP database |
| E-6-O-p-feruloyl scandoside methyl ester | 46225505 | Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C=C(C3C2C(=COC3OC4C(C(C(C(O4)CO)O)O)O)C(=O)OC)CO)O | 580.50 | unknown | https://doi.org/10.1002/ARDP.19813141004 |
| Methyl 5-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]-7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate | 75178000 | Click to see | 580.50 | unknown | https://doi.org/10.1002/ARDP.19813141004 |
| > Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins | |||||
| [(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aS,6bR,10S,12aR)-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-carboxylate | 10416408 | Click to see | 618.80 | 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/(SICI)1099-1573(199812)12:8<553::AID-PTR359>3.0.CO;2-W |
| (10R)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid | 45358157 | Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O | 456.70 | unknown | via CMAUP database |
| (1S,2R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid | 45483617 | Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O | 456.70 | unknown | via CMAUP database |
| (4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-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 | 45483610 | Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C | 456.70 | unknown | via CMAUP database |
| 3-Epioleanolic acid | 11869658 | Click to see | 456.70 | unknown | via CMAUP database |
| Npc112866 | 49867939 | Click to see | 456.70 | unknown | via CMAUP database |
| Oleanolic Acid | 10494 | Click to see | 456.70 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives | |||||
| Npc196776 | 50930798 | Click to see | 410.70 | unknown | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds | |||||
| [2-oxo-8-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[5.3.1.04,11]undeca-1(10),5-dien-6-yl]methyl acetate | 5351518 | Click to see CC(=O)OCC1=CC2C3C1C(OC=C3C(=O)O2)OC4C(C(C(C(O4)CO)O)O)O | 414.40 | unknown | via CMAUP database |
| [5-(hexopyranosyloxy)-1-oxo-2a,4a,5,7b-tetrahydro-1H-2,6-dioxacyclopenta[cd]inden-4-yl]methyl acetate | 233330 | Click to see CC(=O)OCC1=CC2C3C1C(OC=C3C(=O)O2)OC4C(C(C(C(O4)CO)O)O)O | 414.40 | unknown | https://doi.org/10.1002/ARDP.19813141004 |
| Asperulosid | 51346168 | Click to see | 414.40 | unknown | via CMAUP database |
| Asperuloside | 84298 | Click to see CC(=O)OCC1=CC2C3C1C(OC=C3C(=O)O2)OC4C(C(C(C(O4)CO)O)O)O | 414.40 | unknown | https://doi.org/10.1002/ARDP.19813141004 |
| > Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes | |||||
| (E)-2-Octenal | 5283324 | Click to see | 126.20 | unknown | via CMAUP database |
| (Z)-non-2-enal | 5354833 | Click to see | 140.22 | unknown | via CMAUP database |
| 2-Nonenal | 5283335 | Click to see CCCCCCC=CC=O | 140.22 | unknown | via CMAUP database |
| 2-Octenal, (2Z)- | 6427080 | Click to see CCCCCC=CC=O | 126.20 | unknown | via CMAUP database |
| Decanal | 8175 | Click to see | 156.26 | unknown | via CMAUP database |
| Heptanal | 8130 | Click to see | 114.19 | unknown | via CMAUP database |
| Hexanal | 6184 | Click to see | 100.16 | unknown | via CMAUP database |
| Nonanal | 31289 | Click to see CCCCCCCCC=O | 142.24 | unknown | via CMAUP database |
| Octanal | 454 | Click to see | 128.21 | unknown | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones | |||||
| 2,5-Octanedione | 6420399 | Click to see | 142.20 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Coumarans | |||||
| Dihydrobenzofuran | 10329 | Click to see | 120.15 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Heteroaromatic compounds | |||||
| 2-Pentylfuran | 19602 | Click to see | 138.21 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines | |||||
| 2-methoxy-3-methylpurin-6-amine | 10442272 | Click to see CN1C2=NC=NC2=C(N=C1OC)N | 179.18 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids | |||||
| Cis-P-Coumaric Acid | 1549106 | Click to see | 164.16 | unknown | via CMAUP database |
| Ferulic Acid | 445858 | Click to see | 194.18 | unknown | via CMAUP database |
| P-Coumaric Acid | 637542 | Click to see | 164.16 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Coumarins and derivatives | |||||
| Thamnosmonin | 312089 | Click to see | 276.28 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols | |||||
| Quercetin | 5280343 | Click to see | 302.23 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides | |||||
| [(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate | 10795355 | Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3C(C(C(OC3OC4=C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)CO)O)O)O)O)O)O | 786.70 | unknown | via CMAUP database |
| 3-[(2S,5R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one | 44258739 | Click to see | 610.50 | unknown | via CMAUP database |
| Rutin | 5280805 | Click to see | 610.50 | unknown | via CMAUP database |
Collections Top
| In private collections | 0 |
| In public collections | 0 |