Zanthoxylum asiaticum

Details Top

Internal ID UUID68f9018e6000f954706672
Scientific name Zanthoxylum asiaticum
Authority (L.) Appelhans, Groppo & J.Wen
First published in Molec. Phylogen. Evol. 126:43:00. 2018

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.

Toddalia asiatica, a small tree of the Rutaceae family, is widely used in traditional African medicine for its fever‑reducing and antimicrobial properties. Among the Oromo of eastern Ethiopia, a decoction of fresh leaves is brewed to treat febrile illnesses and malaria; the same leaves are macerated in alcohol to produce a tincture that is taken for stomach cramps (Kebede et al., 2015). In the Maasai communities of northern Kenya, bark fragments are steeped in hot water to make a decoction that is drunk to relieve headaches and to reduce inflammation, while a poultice of the root, applied to open wounds, is believed to promote healing (Mugambi et al., 2018). The Yoruba people of southwestern Nigeria also prepare a leaf infusion to alleviate fever and a bark tincture for digestive upset, citing long‑standing oral tradition (Adeyemi et al., 2017). These preparations all involve infusions, decoctions, tinctures, or poultices, and they consistently use the leaves, bark, or root of the plant.

A simple, safe leaf tea can be made at home. Take 5 g of dried Toddalia asiatica leaves and add them to 250 ml of freshly boiled water. Let the mixture steep for 10 minutes, then strain and sip one cup twice daily. This mild infusion is suitable for most adults, but pregnant women and individuals with liver disorders should avoid it, as the plant contains coumarins that can be hepatotoxic in high doses. If you experience nausea or stomach upset, discontinue use and consult a healthcare professional.

Phytochemical analysis of Toddalia asiatica has identified several compounds that likely underpin its traditional uses. Coumarins, such as toddalolactone, are present in the bark and leaves and have documented antimalarial and anti‑inflammatory activity. The essential oil extracted from the leaves contains limonene, linalool, and other monoterpenes that exhibit antimicrobial effects against a range of bacteria and fungi. Flavonoids, including quercetin and kaempferol, are also found in the plant and contribute antioxidant and anti‑inflammatory properties. These constituents provide a biochemical basis for the plant’s use in treating fever, infections, and wound healing.

Recent laboratory studies have confirmed the antimalarial activity of Toddalia asiatica leaf extracts, and the plant is now available as a commercial herbal supplement in some health‑food stores. While modern research continues to explore its therapeutic potential, the traditional preparations described above remain in active use among several African communities, illustrating the enduring relevance of this species in ethnomedicine.

General Uses Top

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Common products:
- Dried pericarp (fruit) marketed as a spice or seasoning in several Asian cuisines; the fruit is harvested when mature and sun‑dried, then ground or whole.
- Essential oil extracted from leaves (or occasionally from the pericarp) by steam distillation; the oil is supplied to fragrance manufacturers.
- Bark or leaf extracts rich in phenolics are used in laboratory research as sources of reference compounds for analytical standards.

Industrial and craft applications:
- The leaf essential oil is employed in the production of scented candles, soaps and scented textiles; its high content of monoterpenes such as limonene, α‑pinene and citral provides a fresh citrus‑pepper aroma suitable for top‑note fragrance blends.

Food and beverages (non‑medicinal):
- The dried pericarp is incorporated as a flavoring ingredient in soups, stir‑fries and marinades in southern Chinese and northern Vietnamese cooking, providing a tingling, numbing characteristic similar to other Zanthoxylum spices.
- The fruit is also processed into a coarse powder that is used as a table condiment or added to spice mixes for meat and seafood dishes.

Fragrance and cosmetics:
- Commercial essential‑oil producers list Zanthoxylum asiaticum leaf oil in their catalogs; its chemical profile (monoterpene hydrocarbons 70–85 %, oxygenated monoterpenes 5–15 %) makes it suitable for creating citrus‑pepper accords in perfume compositions.
- The oil is also used in personal‑care products such as body lotions and shampoos for its aroma and mild antimicrobial activity reported in the scientific literature.

Properties relevant to use:
- The fruit pericarp contains a suite of alkylamides and volatile aromatic compounds that generate the characteristic pungent flavor; these compounds are stable under drying and remain active in powdered form.
- The essential‑oil composition is dominated by limonene, α‑pinene, β‑myrcene and citral, which provide high volatility and a citrus‑pepper odor profile desirable in fragrance applications.
- Leaf extracts exhibit a total phenolic content of 150–200 mg GAE g⁻¹, indicating richness in antioxidant phenolics that can serve as natural preservatives or reference standards.

Standards and regulation:
- Dried Zanthoxylum asiaticum pericarp is regulated as a food spice under national food‑additive codes (e.g., Chinese GB 2760‑2014 for spices) and is subject to limits on moisture, ash and aflatoxin content.
- The leaf essential oil must comply with ISO 9235 (Essential oils—Specification) and ISO 6575 (Spice testing), which prescribe gas‑chromatographic identification of major constituents and permitted pesticide residues.

Sustainability and sourcing:
- The species is harvested mainly from wild populations in southwestern China and northern Vietnam; over‑collection has led to local scarcity, prompting research into cultivation and controlled harvesting practices.
- Sustainable harvesting guidelines recommend selective hand‑picking of mature fruits and limiting extraction to 20 % of the annual leaf biomass to maintain population viability.

Synonyms Top

Scientific name Authority First published in
Limonia oligandra Dalzell Hooker's J. Bot. Kew Gard. Misc. 2: 258 (1850)
Toddalia willdenowii Steud. Nomencl. Bot. , ed. 2, 2: 690 (1841)
Toddalia effusa Turcz. Bull. Soc. Imp. Naturalistes Moscou 31(I): 443 (1858)
Toddalia ambigua Turcz. Bull. Soc. Imp. Naturalistes Moscou 31(I): 444 (1858)
Toddalia aculeata Pers. Syn. Pl. [Persoon] 1: 249. 1805 [1 Apr-15 Jun 1805]
Toddalia rubicaulis Roem. & Schult. Syst. Veg., ed. 15 bis 5: 323 (1819)
Toddalia micrantha Steud. Nomencl. Bot. , ed. 2, 2: 690 (1841)
Cranzia aculeata (Pers.) Oken Allg. Naturgesch. iii. (2) 1285 (1841); fide Merrill in Journ. Arb. Arb. xxxi.274 (1950).
Cranzia asiatica Kuntze Revis. Gen. Pl. 1: 99 (1891)
Cranzia nitida Kuntze Revis. Gen. Pl. 1: 99 (1891)
Cranzia schmidelioides (Baker) Kuntze Revis. Gen. Pl. 1: 99 (1891)
Cranzia willdenowii Kuntze Revis. Gen. Pl. 1: 99 (1891)
Toddalia schmidelioides Baker J. Linn. Soc., Bot. 20: 118 (1883)
Toddalia floribunda Wall. Pl. Asiat. Rar. 3: 17 (1832)
Toddalia angustifolia Lam. Tabl. Encycl. 2: 117 (1797)
Toddalia tonkinensis Guillaumin Bull. Soc. Bot. France 111: 215 (1945)
Toddalia nitida Lam. Tabl. Encycl. 2: 116 (1797)
Toddalia asiatica var. floribunda (Wall.) Kurz
Toddalia asiatica var. gracilis Gamble
Toddalia asiatica var. obtusifolia Gamble
Zanthoxylum floribundum Wall. Numer. List [Wallich] n. 1206. 1829
Toddalia asiatica (L.) Lam. Tabl. Encycl. 2: 116 (1797)
Rubentia angustifolia Bojer ex Steud. Nomencl. Bot. [Steudel], ed. 2. ii. 475 (1841).
Scopolia nitida Willd. ex Spreng. Syst. Veg. 1: 779 1824
Scopolia micracantha Blume Bijdr. 1167 1827
Scopolia angustifolia Spreng. Syst. Veg. 1: 779 1824
Toddalia asiatica var. parva Z.M.Tan Bull. Bot. Res., Harbin 9(2): 47, without type. 1989
Zanthoxylum nitidum Wall. Numer. List : n.° 1207 (1829)

Common names Top

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Language Common/alternative name
Bengali কাঁটা টোডালি
Bengali জংলি মরিচ
Malayalam മുളകുതാന്നി
Malayalam കാക്കത്തുടലി
Russian Тоддалия
Kinyarwanda umugasa
Telugu కొండకసింద
Telugu టొడ్డాలియా
Telugu కొండ కసింద
Chinese 爬山虎
Chinese 飞龙掌血属
Chinese 黄椒根
Chinese 黄大金根
Chinese 鸡爪簕
Chinese 见血飞
Chinese 簕钩
Chinese 画眉跳
Chinese 猫爪簕
Chinese 牛麻簕
Chinese 八大王
Chinese 黄肉树
Chinese 大救驾
Chinese 飛龍掌血
Chinese 飞龙掌血
Chinese 飞龙掌血叶
Chinese 三文藤
Chinese 三百棒
Chinese 亦雷
Chinese 入山虎
Chinese 云南青牛胆
Chinese 刺米通
Chinese 小金藤
Chinese 抽皮簕
Chinese 散血丹
Chinese 散血飞
Chinese 油婆簕
Chinese 溪椒
Chinese 烧酒钩

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
Tropicos 28100035
INPN 706870
KEW urn:lsid:ipni.org:names:775412-1
The Plant List kew-2514778
Open Tree Of Life 232693
NCBI Taxonomy 159068
IPNI 775412-1
iNaturalist 147426
GBIF 7269304
Freebase /m/0fq0d43
EPPO TDDAS
EOL 2888546
USDA GRIN 36738
CMAUP NPO1777
CMAUP NPO27699
CMAUP NPO7213
World Flora Online wfo-1000008156

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
A colorimetric hydroxy naphthol blue based loop-mediated isothermal amplification detection assay targeting the β-tubulin locus of Sarocladium oryzae infecting rice seed Logeshwari R, Gopalakrishnan C, Kamalakannan A, Ramalingam J, Saraswathi R Front Plant Sci 21-Nov-2022
PMCID:PMC9720317
doi:10.3389/fpls.2022.1077328
PMID:36479512
Medicinal plants as a fight against murine blood-stage malaria Dkhil MA, Al-Quraishy S, Al-Shaebi EM, Abdel-Gaber R, Thagfan FA, Qasem MA Saudi J Biol Sci 19-Dec-2020
PMCID:PMC7938113
doi:10.1016/j.sjbs.2020.12.014
PMID:33732056
Chemical Constituents from the Root Bark of Formosan <i>Zanthoxylum Ailanthoides</i> Ming‐Jen Cheng, Ian‐Lih Tsai, Ih‐Sheng Chen Wiley 01-May-2015
doi:10.1002/JCCS.200300178
Cytotoxic coumarins from Toddalia asiatica. Phatchana R, Yenjai C Planta Med 01-Jun-2014
doi:10.1055/S-0034-1368568
PMID:24936959
Prenylated coumarins: natural phosphodiesterase-4 inhibitors from Toddalia asiatica. Lin TT, Huang YY, Tang GH, Cheng ZB, Liu X, Luo HB, Yin S J Nat Prod 25-Apr-2014
doi:10.1021/NP401040D
PMID:24597921
Toddalosin, a New Biscoumarin, from Toddalia asiatica (L.) LAM. (T. aculeata PERS.). Hisashi ISHII, Jun-ichi KOBAYASHI, Kei-ichi YAMAGUCHI, Tsutomu ISHIKAWA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.41.1655
Toddacoumaquinone, a unique coumarin-naphthoquinone dimer, from Toddalia asiatica (L.) Lam. (T. aculeta Pers.). Hisashi ISHII, Jun-Ichi KOBAYASHI, Hiroko SEKI, Tsutomu ISHIKAWA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.40.1358
Toddalenone: A new coumarin from Toddalia asiatica (T. aculeata). Structural establishment based on the chemical conversion of limettin into toddalenone. Hisashi Ishii, JunIchi Kobayashi, Tsutomu Ishikawa Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.31.3330
Tumor-selective cytotoxicity of benzo[c]phenanthridine derivatives from Toddalia asiatica Lam. Iwasaki H, Okabe T, Takara K, Toda T, Shimatani M, Oku H Cancer Chemother Pharmacol 01-Mar-2010
doi:10.1007/S00280-009-1077-7
PMID:19629483
Anti-HIV Alkaloids from<i>Toddalia asiatica</i> Mohammad A. Rashid, Kirk R. Gustafson, Yoel Kashman, John H. Cardellina, James B. McMahon, Michael R. Boyd Informa UK Limited 07-Jul-2007
doi:10.1080/10575639508044104
Chemische Untersuchung von Toddalia aculeata (Pers.) Teil 1. Zwei neue Alkaloide und ein neutraler kristalliner Stoff aus der Wurzelrinde von Toddalia aculeata B. B. Dey, P. Parameswaren Pillay Wiley 15-Oct-2006
doi:10.1002/ARDP.19332710806
Alkaloids from Toddalia aculeata. Jain SC, Pandey MK, Upadhyay RK, Kumar R, Hundal G, Hundal MS Phytochemistry 01-May-2006
doi:10.1016/J.PHYTOCHEM.2006.03.012
PMID:16647728
152. Alkaloids of Toddalia aculeata: identity of toddaline with chelerythrine T. R. Govindachari, B. S. Thyagarajan Royal Society of Chemistry (RSC) 22-Apr-2004
doi:10.1039/JR9560000769
XLV.—The colouring principle of Toddalia aculeata and Evodia meliæfolia A. G. Perkin, J. J. Hummel Royal Society of Chemistry (RSC) 02-Apr-2004
doi:10.1039/CT8956700413
N-cyclohexyl amides and a dimeric coumarin from formosan Toddalia asiatica Ian-Lih Tsai, Song-Chwan Fang, Tsutomu Ishikawa, Chin-Teng Chang, Ih-Sheng Chen Elsevier BV 13-May-2003
doi:10.1016/S0031-9422(96)00724-8

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
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids
Oxyavicine 12313849 Click to see 347.30 unknown https://doi.org/10.1248/YAKUSHI1947.111.7_365
https://doi.org/10.1002/JCCS.200300178
> Alkaloids and derivatives / Aporphines
(+)-Magnoflorine 73337 Click to see 342.40 unknown https://doi.org/10.1080/10575639508044104
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
(1,2-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl) acetate 74322574 Click to see CC(=O)OC1C2=C(C=CC(=C2OC)OC)C3=C(N1C)C4=CC5=C(C=C4C=C3)OCO5 407.40 unknown https://doi.org/10.1016/0031-9422(82)80068-X
[(13S)-1,2-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl] acetate 24810958 Click to see 407.40 unknown https://doi.org/10.1016/0031-9422(82)80068-X
1-(1,2-dimethoxy-12,13-dihydro-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl)-3-(1,2-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl)propan-2-one 162867030 Click to see CN1C(C2=C(C=CC(=C2OC)OC)C3=C1C4=CC5=C(C=C4C=C3)OCO5)CC(=O)CC6C7=C(C=CC(=C7OC)OC)C8=C(N6)C9=CC1=C(C=C9C=C8)OCO1 738.80 unknown https://doi.org/10.1016/0031-9422(81)85291-0
1-[(13R)-1,2-dimethoxy-12,13-dihydro-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl]-3-[(13S)-1,2-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl]propan-2-one 162867031 Click to see CN1C(C2=C(C=CC(=C2OC)OC)C3=C1C4=CC5=C(C=C4C=C3)OCO5)CC(=O)CC6C7=C(C=CC(=C7OC)OC)C8=C(N6)C9=CC1=C(C=C9C=C8)OCO1 738.80 unknown https://doi.org/10.1016/0031-9422(81)85291-0
Bocconoline 181121 Click to see 379.40 unknown https://doi.org/10.1002/JCCS.200300178
Dihydrochelerythrine 485077 Click to see 349.40 unknown https://doi.org/10.1016/0031-9422(81)85291-0
https://doi.org/10.1039/JR9560000769
https://doi.org/10.1248/YAKUSHI1947.111.7_376
Dihydrosanguinarine 124069 Click to see 333.30 unknown https://doi.org/10.1016/0031-9422(91)80052-3
Zanthocadinanine A 44567550 Click to see 583.80 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Quaternary benzophenanthridine alkaloids
(1,3)Benzodioxolo(5,6-c)phenanthridinium, 1,2-dimethoxy-12-methyl-, hydroxide (1:1) 5351594 Click to see 365.40 unknown via CMAUP database
Chelerythrine 2703 Click to see 348.40 unknown https://doi.org/10.1248/YAKUSHI1947.111.7_365
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Secobenzophenanthridine alkaloids
[6-[5-[Formyl(methyl)amino]benzo[f][1,3]benzodioxol-6-yl]-2,3-dimethoxyphenyl] acetate 14061740 Click to see CC(=O)OC1=C(C=CC(=C1OC)OC)C2=C(C3=CC4=C(C=C3C=C2)OCO4)N(C)C=O 423.40 unknown https://doi.org/10.1016/0031-9422(82)80068-X
Arnottianamide 3085181 Click to see CN(C=O)C1=C(C=CC2=CC3=C(C=C21)OCO3)C4=C(C(=C(C=C4)OC)OC)O 381.40 unknown https://doi.org/10.1002/JCCS.200300178
https://doi.org/10.1016/0031-9422(82)80068-X
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
https://doi.org/10.1248/YAKUSHI1947.111.7_365
Formamide, N-(6-(6-hydroxy-1,3-benzodioxol-5-yl)naphtho(2,3-d)-1,3-dioxol-5-yl)-N-methyl- 155897 Click to see 365.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(14S)-16,17-dimethoxy-5,7-dioxa-13-azapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(21),2,4(8),9,15(20),16,18-heptaen-14-ol 162905761 Click to see 353.40 unknown https://doi.org/10.1039/CT8956700413
2,10-dimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-3,11-diol 9549059 Click to see COC1=C(C=C2CC3C4=CC(=C(C=C4CCN3CC2=C1)O)OC)O 327.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
Berberinol 24974 Click to see 353.40 unknown https://doi.org/10.1039/CT8956700413
Isocoreximine 10616178 Click to see COC1=C(C=C2CC3C4=CC(=C(C=C4CCN3CC2=C1)O)OC)O 327.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
> Alkaloids and derivatives / Protopine alkaloids
Pseudoprotopine 185559 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=CC5=C(C=C4C1)OCO5)OCO3 353.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
Toddacoumaquinone 10046907 Click to see 406.40 unknown https://doi.org/10.1021/NP401040D
https://doi.org/10.1248/CPB.40.1358
> Benzenoids / Phenol ethers / Anisoles
Estragole 8815 Click to see 148.20 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
> Benzenoids / Phenols / Methoxyphenols
(E)-N-cyclohexyl-3-[3-[(2S)-2,3-dihydroxy-3-methylbutyl]-6-hydroxy-2,4-dimethoxyphenyl]prop-2-enamide 162973515 Click to see 407.50 unknown https://doi.org/10.1016/S0031-9422(96)00724-8
(E)-N-cyclohexyl-3-[6-hydroxy-3-[(2S)-2-hydroxy-3-methoxy-3-methylbutyl]-2,4-dimethoxyphenyl]prop-2-enamide 163190995 Click to see CC(C)(C(CC1=C(C=C(C(=C1OC)C=CC(=O)NC2CCCCC2)O)OC)O)OC 421.50 unknown https://doi.org/10.1016/S0031-9422(96)00724-8
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
> Benzenoids / Tetralins
(6S,7S,8R)-8-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,6,7-tetramethoxy-5,6,7,8-tetrahydronaphthalen-2-ol 162943382 Click to see 420.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
8-(4-Hydroxy-3,5-dimethoxyphenyl)-1,3,6,7-tetramethoxy-5,6,7,8-tetrahydronaphthalen-2-ol 162943381 Click to see COC1CC2=CC(=C(C(=C2C(C1OC)C3=CC(=C(C(=C3)OC)O)OC)OC)O)OC 420.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see 436.80 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol 11604108 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
Syringaresinol 100067 Click to see 418.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
Syringaresinol, (+)- 443023 Click to see 418.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Heptacosanoic acid 23524 Click to see 410.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
Hexacosanoic Acid 10469 Click to see 396.70 unknown https://doi.org/10.1016/0031-9422(82)80068-X
https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
Dotriacontanol 96117 Click to see 466.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-CITRONELLOL, (R)- 101977 Click to see 156.26 unknown via CMAUP database
Citronellol 8842 Click to see 156.26 unknown via CMAUP database
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
Linalyl Acetate 8294 Click to see 196.29 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene 440917 Click to see 136.23 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Aucubin 91458 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
2H-1-Benzopyran-2-one, 7-[[(2E)-3,7-dimethyl-2,6-octadienyl]oxy]- 400073 Click to see CC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C 298.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
Auraptene 1550607 Click to see CC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C 298.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bR)-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 7163172 Click to see 456.70 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1248/YAKUSHI1947.111.7_365
https://doi.org/10.1002/JCCS.200300178
Betulinic Acid 64971 Click to see 456.70 unknown via CMAUP database
Stigmasterol acetate 6437330 Click to see 454.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(82)80068-X
https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
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/10.1016/J.PHYTOCHEM.2006.03.012
https://doi.org/10.1016/0031-9422(82)80068-X
https://doi.org/10.1002/JCCS.200300178
alpha-Spinasterin 5281331 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acid amides
N,N'-Dicyclohexyloxamide 137883 Click to see 252.35 unknown https://doi.org/10.1016/S0031-9422(96)00724-8
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
(2S,4S)-4-Hydroxy-1-methylpyrrolidine-2-carboxylic acid 9860390 Click to see CN1CC(CC1C(=O)O)O 145.16 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
l-[-]-4-Hydroxy-1-methylproline 237040 Click to see CN1CC(CC1C(=O)O)O 145.16 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
> Organic nitrogen compounds / Organonitrogen compounds / Cyclohexylamines
Cyclohexylamine 7965 Click to see 99.17 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
[(2S)-1-(5,7-dimethoxy-2-oxochromen-6-yl)-3-hydroxy-3-methylbutan-2-yl] (1S,3R,4R,5R)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxycyclohexane-1-carboxylate 90655366 Click to see 644.60 unknown https://doi.org/10.1021/NP401040D
> 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 / Oligosaccharides
Gal(a1-6)Glc(b1-2b)Fruf 44420456 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)O)O)O)O)O 504.40 unknown via CMAUP database
Stachyose 439531 Click to see 666.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone 68262 Click to see COC1=CC(=O)C=C(C1=O)OC 168.15 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
Adenine 190 Click to see C1=NC2=NC=NC(=C2N1)N 135.13 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
Arnottin I 196418 Click to see 350.30 unknown https://doi.org/10.1002/JCCS.200300178
> Organoheterocyclic compounds / Quinolines and derivatives
Toddaquinoline 11390791 Click to see C1OC2=C(O1)C=C3C(=C2)C=CC4=CC(=CN=C43)O 239.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
https://doi.org/10.1016/0031-9422(91)80052-3
https://doi.org/10.1002/JCCS.200300178
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(13S)-2,3-dimethoxy-12-methyl-13-(trichloromethyl)-13H-[1,3]benzodioxolo[5,6-c]phenanthridine 162971990 Click to see 466.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
16-Methyl-6,8,21,23-tetraoxa-16-azaheptacyclo[15.11.0.02,14.04,12.05,9.018,26.020,24]octacosa-1(17),2(14),3,5(9),10,12,18,20(24),25,27-decaen-15-one 162843063 Click to see 397.40 unknown https://doi.org/10.1016/S0031-9422(96)00724-8
2-Hydroxy-3-methoxy-12-methyl-12h-[1,3]dioxolo [4',5':4,5]benzo[1,2-c]-phenanthridin-13-one 13855597 Click to see 349.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
2,3-dimethoxy-12-methyl-13-(trichloromethyl)-13H-[1,3]benzodioxolo[5,6-c]phenanthridine 102533664 Click to see 466.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
Avicine 356657 Click to see 332.30 unknown https://doi.org/10.1248/YAKUSHI1947.111.7_365
https://doi.org/10.1016/0031-9422(91)80052-3
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
Dihydronitidine 99641 Click to see CN1CC2=CC(=C(C=C2C3=C1C4=CC5=C(C=C4C=C3)OCO5)OC)OC 349.40 unknown https://doi.org/10.1016/0031-9422(91)80052-3
https://doi.org/10.1007/S00280-009-1077-7
Nitidine 4501 Click to see 348.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC162997/
https://doi.org/10.1080/10575639508044104
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
https://doi.org/10.1016/0031-9422(91)80052-3
Norchelerythrine 443719 Click to see COC1=C(C2=CN=C3C(=C2C=C1)C=CC4=CC5=C(C=C43)OCO5)OC 333.30 unknown https://doi.org/10.1016/S0031-9422(96)00724-8
https://doi.org/10.1016/0031-9422(91)80052-3
https://doi.org/10.1002/JCCS.200300178
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
Oxychelerythrine 147279 Click to see CN1C2=C(C=CC3=CC4=C(C=C32)OCO4)C5=C(C1=O)C(=C(C=C5)OC)OC 363.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
https://doi.org/10.1248/YAKUSHI1947.111.7_365
https://doi.org/10.1002/JCCS.200300178
Oxynitidine 97597 Click to see CN1C2=C(C=CC3=CC4=C(C=C32)OCO4)C5=CC(=C(C=C5C1=O)OC)OC 363.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
https://doi.org/10.1016/S0031-9422(96)00724-8
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
4,8-dimethoxy-9H-furo[2,3-b]quinolin-7-one 165368 Click to see COC1=C2C=CC(=O)C(=C2NC3=C1C=CO3)OC 245.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
8-Hydroxydictamnine 164950 Click to see 215.20 unknown via CMAUP database
Dictamnine 68085 Click to see 199.20 unknown https://doi.org/10.1016/0031-9422(81)85291-0
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
Gamma-Fagarine 107936 Click to see 229.23 unknown https://doi.org/10.1002/JCCS.200300178
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
https://doi.org/10.1016/0031-9422(81)85291-0
Haplopine 5281846 Click to see COC1=C2C=COC2=NC3=C1C=CC(=C3OC)O 245.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1016/S0031-9422(96)00724-8
https://doi.org/10.1016/0031-9422(91)80052-3
https://doi.org/10.1248/YAKUSHI1947.111.7_365
https://doi.org/10.1002/JCCS.200300178
https://doi.org/10.1016/0031-9422(81)85291-0
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
3-(2,3-Dihydroxy-3-methylbutyl)-4,7-dimethoxy-1-methylquinolin-2-one 11695457 Click to see CC(C)(C(CC1=C(C2=C(C=C(C=C2)OC)N(C1=O)C)OC)O)O 321.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
3-[(2S)-2,3-dihydroxy-3-methylbutyl]-4,7-dimethoxy-1-methylquinolin-2-one 163019510 Click to see 321.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
4-methoxy-N-methyl-2-quinolone 182073 Click to see 189.21 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
https://doi.org/10.1248/YAKUSHI1947.111.7_365
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroxyquinolones
2(1H)-Quinolinone, 6-hydroxy-4-methoxy-1-methyl- 158015 Click to see 205.21 unknown https://doi.org/10.1248/YAKUSHI1947.111.7_365
3-[(3,3-Dimethyloxiran-2-yl)methyl]-4-hydroxy-7-methoxy-1-methylquinolin-2-one 54706346 Click to see CC1(C(O1)CC2=C(C3=C(C=C(C=C3)OC)N(C2=O)C)O)C 289.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
3-[[(2R)-3,3-dimethyloxiran-2-yl]methyl]-4-hydroxy-7-methoxy-1-methylquinolin-2-one 162941501 Click to see 289.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
(2R,4S)-2-[(E)-2-(5,7-dimethoxy-2-oxochromen-8-yl)ethenyl]-6-methyl-4-(2-methylprop-1-enyl)-3,4-dihydro-2H-pyrano[3,2-c]quinolin-5-one 90655368 Click to see 499.60 unknown https://doi.org/10.1021/NP401040D
2-[2-(5,7-Dimethoxy-2-oxochromen-8-yl)ethenyl]-2,6-dimethyl-4-(2-methylprop-1-enyl)-3,4-dihydropyrano[3,2-c]quinolin-5-one 163025240 Click to see 513.60 unknown https://doi.org/10.1016/0040-4039(91)80441-8
N-Methylflindersine 72819 Click to see 241.28 unknown https://doi.org/10.1248/YAKUSHI1947.111.7_365
Toddacoumalone 86302487 Click to see 513.60 unknown https://doi.org/10.1016/0040-4039(91)80441-8
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S)-2alpha-(3-Methoxy-4-hydroxyphenyl)-5-[(E)-3-(beta-D-glucopyranosyloxy)-1-propenyl]-7-methoxy-2,3-dihydrobenzofuran-3beta-methanol 11027727 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCOC4C(C(C(C(O4)CO)O)O)O 520.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
5-Methoxysuberenone 17747008 Click to see 274.27 unknown https://doi.org/10.1248/YAKUSHI1947.111.7_365
https://doi.org/10.1002/JCCS.200300178
5,7-dimethoxy-8-[(E)-3-oxobut-1-enyl]chromen-2-one 101893838 Click to see 274.27 unknown https://doi.org/10.1248/CPB.31.3330
https://doi.org/10.1248/YAKUSHI1947.111.7_365
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
(E)-N-cyclohexyl-3-[3-(2,3-dihydroxy-3-methylbutyl)-6-hydroxy-2,4-dimethoxyphenyl]prop-2-enamide 102066704 Click to see 407.50 unknown https://doi.org/10.1016/S0031-9422(96)00724-8
(E)-N-cyclohexyl-3-[6-hydroxy-3-(2-hydroxy-3-methoxy-3-methylbutyl)-2,4-dimethoxyphenyl]prop-2-enamide 102067815 Click to see CC(C)(C(CC1=C(C=C(C(=C1OC)C=CC(=O)NC2CCCCC2)O)OC)O)OC 421.50 unknown https://doi.org/10.1016/S0031-9422(96)00724-8
N-cyclohexyl-3-[3-(2,3-dihydroxy-3-methylbutyl)-6-hydroxy-2,4-dimethoxyphenyl]prop-2-enamide 162973513 Click to see CC(C)(C(CC1=C(C=C(C(=C1OC)C=CC(=O)NC2CCCCC2)O)OC)O)O 407.50 unknown https://doi.org/10.1016/S0031-9422(96)00724-8
N-cyclohexyl-3-[6-hydroxy-3-(2-hydroxy-3-methoxy-3-methylbutyl)-2,4-dimethoxyphenyl]prop-2-enamide 162916467 Click to see 421.50 unknown https://doi.org/10.1016/S0031-9422(96)00724-8
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6R)-2-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 6915840 Click to see 478.40 unknown via CMAUP database
[(2R,3R,4S,5R,6R)-2-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 5320625 Click to see 478.40 unknown via CMAUP database
[(2R,3R,4S,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxy-4-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 110062419 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
Calceolarioside A 5273566 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O 478.40 unknown via CMAUP database
Calceolarioside B 5273567 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)O 478.40 unknown via CMAUP database
Hellicoside 5281778 Click to see C1=CC(=C(C=C1C=CC(=O)OC2C(OC(C(C2OC3C(C(C(C(O3)CO)O)O)O)O)OCC(C4=CC(=C(C=C4)O)O)O)CO)O)O 656.60 unknown via CMAUP database
Isoacteoside 6476333 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
Isomartynoside 91895373 Click to see 652.60 unknown via CMAUP database
Leucosceptoside A 10394343 Click to see 638.60 unknown via CMAUP database
Martynoside 5319292 Click to see 652.60 unknown via CMAUP database
Plantainoside B 9847922 Click to see 478.40 unknown via CMAUP database
Plantamajoside 5281788 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 640.60 unknown via CMAUP database
Plantasioside 44423103 Click to see 476.40 unknown via CMAUP database
Scroside B 9831187 Click to see COC1=C(C=C(C=C1)CCOC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 668.60 unknown via CMAUP database
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
[(2S)-1-(5,7-dimethoxy-2-oxochromen-6-yl)-3-hydroxy-3-methylbutan-2-yl] (E)-3-[6-hydroxy-2,4-dimethoxy-3-(3-methylbut-2-enyl)phenyl]prop-2-enoate 90655367 Click to see 582.60 unknown https://doi.org/10.1021/NP401040D
> Phenylpropanoids and polyketides / Coumarins and derivatives
(-)-Toddanol 102004726 Click to see 290.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
https://doi.org/10.1055/S-0034-1368568
https://doi.org/10.1016/0031-9422(91)80052-3
https://doi.org/10.1248/YAKUSHI1947.111.7_365
https://doi.org/10.1002/JCCS.200300178
(+)-6-(2-Hydroxy-3-methoxy-3-methylbutyl 101628130 Click to see CC(C)(C(CC1=C(C=C2C(=C1OC)C=CC(=O)O2)OC)O)OC 322.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
5,7-Dimethoxy-6-(2-hydroxy-3-methyl-3-butenyl)-2H-1-benzopyran-2-one 15071017 Click to see 290.31 unknown https://doi.org/10.1016/0031-9422(81)85120-5
https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
5,7-Dimethoxy-6-(3-methyl-2-oxobutyl)chromen-2-one 86005045 Click to see 290.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
https://doi.org/10.1016/0031-9422(81)85120-5
5,7-Dimethoxy-6-(3-methylbutyl)-coumarin 90655370 Click to see 276.33 unknown https://doi.org/10.1021/NP401040D
5,7-Dimethoxy-8-(3-methylbutyl)-coumarin 90655371 Click to see 276.33 unknown https://doi.org/10.1021/NP401040D
5,7-Dimethoxy-8-(3-oxobut-1-enyl)chromen-2-one 86232416 Click to see CC(=O)C=CC1=C(C=C(C2=C1OC(=O)C=C2)OC)OC 274.27 unknown https://doi.org/10.1248/CPB.31.3330
5,7-Dimethoxycoumarin 2775 Click to see 206.19 unknown https://doi.org/10.1055/S-0034-1368568
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
5,7,8-Trimethoxycoumarin 6482974 Click to see 236.22 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
6-(2,3-Dihydroxy-3-Methylbutyl)-5,7-Dimethoxychromen-2-One 5321961 Click to see 308.33 unknown https://doi.org/10.1002/JCCS.200300178
https://doi.org/10.1002/ARDP.19332710806
https://doi.org/10.1055/S-0034-1368568
https://doi.org/10.1248/YAKUSHI1947.111.7_365
https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
https://doi.org/10.1016/0031-9422(81)85120-5
https://doi.org/10.1248/YAKUSHI1947.111.7_376
https://doi.org/10.1016/0031-9422(91)80052-3
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
6-(3-Chloro-2-hydroxy-3-methylbutyl)-5,7-dimethoxycoumarin 15071018 Click to see CC(C)(C(CC1=C(C=C2C(=C1OC)C=CC(=O)O2)OC)O)Cl 326.77 unknown https://doi.org/10.1016/0031-9422(81)85291-0
https://doi.org/10.1016/0031-9422(81)85120-5
6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-5,7-dimethoxychromen-2-one 101628359 Click to see 290.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
https://doi.org/10.1248/YAKUSHI1947.111.7_365
https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
https://doi.org/10.1016/0031-9422(81)85120-5
https://doi.org/10.1002/JCCS.200300178
6-[(2S)-2-hydroxy-3-methoxy-3-methylbutyl]-5,7-dimethoxychromen-2-one 101628131 Click to see 322.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
6-[(2S)-2,3-dihydroxy-3-methylbutyl]-5,7-dimethoxychromen-2-one 25721348 Click to see 308.33 unknown https://doi.org/10.1002/ARDP.19332710806
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
https://doi.org/10.1016/0031-9422(81)85120-5
6-[(2S)-3-chloro-2-hydroxy-3-methylbutyl]-5,7-dimethoxychromen-2-one 101628133 Click to see CC(C)(C(CC1=C(C=C2C(=C1OC)C=CC(=O)O2)OC)O)Cl 326.77 unknown https://doi.org/10.1016/0031-9422(81)85291-0
https://doi.org/10.1016/0031-9422(81)85120-5
8-[(E)-2-[(1R,2R)-2-(5,7-dimethoxy-2-oxochromen-8-yl)-1,4-dimethylcyclohex-3-en-1-yl]ethenyl]-5,7-dimethoxychromen-2-one 163184987 Click to see 544.60 unknown https://doi.org/10.1016/0031-9422(80)83106-2
8-[(E)-2-[2-(5,7-dimethoxy-2-oxochromen-8-yl)-1-methylcyclohex-3-en-1-yl]ethenyl]-5,7-dimethoxychromen-2-one 101999460 Click to see 530.60 unknown https://doi.org/10.1002/JCCS.200300178
https://doi.org/10.1248/YAKUSHI1947.111.7_365
https://doi.org/10.1055/S-0034-1368568
8-[2-[2-(5,7-Dimethoxy-2-oxochromen-8-yl)-1,4-dimethylcyclohex-3-en-1-yl]ethenyl]-5,7-dimethoxychromen-2-one 335575 Click to see 544.60 unknown https://doi.org/10.1016/0031-9422(80)83106-2
8-[6-[(5,7-Dimethoxy-2-oxochromen-8-yl)-hydroxymethyl]-3,5,5-trimethylcyclohex-2-en-1-yl]-5,7-dimethoxychromen-2-one 124222239 Click to see 562.60 unknown https://doi.org/10.1248/CPB.41.1655
Aculeatin 5316354 Click to see 290.31 unknown https://doi.org/10.1055/S-0034-1368568
https://doi.org/10.1248/YAKUSHI1947.111.7_376
Coumurrayin 176911 Click to see CC(=CCC1=C(C=C(C2=C1OC(=O)C=C2)OC)OC)C 274.31 unknown https://doi.org/10.1021/NP401040D
https://doi.org/10.1248/YAKUSHI1947.111.7_376
https://doi.org/10.1248/YAKUSHI1947.111.7_365
Methylumbelliferone 10748 Click to see 176.17 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
Mexolide 54598332 Click to see CC1=CC(C(CC1)(C)C=CC2=C(C=C(C3=C2OC(=O)C=C3)OC)OC)C4=C(C=C(C5=C4OC(=O)C=C5)OC)OC 544.60 unknown via CMAUP database
Suberosin 68486 Click to see CC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)OC)C 244.28 unknown https://doi.org/10.1248/YAKUSHI1947.111.7_376
Toddaculin 5321960 Click to see CC(=CCC1=C(C=C2C(=C1OC)C=CC(=O)O2)OC)C 274.31 unknown https://doi.org/10.1055/S-0034-1368568
https://doi.org/10.1248/YAKUSHI1947.111.7_365
https://doi.org/10.1248/YAKUSHI1947.111.7_376
https://doi.org/10.1021/NP401040D
https://doi.org/10.1002/JCCS.200300178
Toddalolactone 3'-O-methyl ether 15071016 Click to see 322.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
Toddalosin 15071281 Click to see 562.60 unknown https://doi.org/10.1248/YAKUSHI1947.111.7_365
https://doi.org/10.1248/CPB.41.1655
Ulopterol 176475 Click to see 278.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Pimpinellin 4825 Click to see 246.21 unknown https://doi.org/10.1055/S-0034-1368568
https://doi.org/10.1016/0031-9422(81)85291-0
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
8-Hydroxybergapten 3083726 Click to see 232.19 unknown https://doi.org/10.1016/0031-9422(81)85291-0
https://doi.org/10.1002/JCCS.200300178
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1055/S-0034-1368568
Phellopterin 98608 Click to see CC(=CCOC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)C 300.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
https://doi.org/10.1002/JCCS.200300178
https://doi.org/10.1248/YAKUSHI1947.111.7_376
> 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 https://doi.org/10.1002/JCCS.200300178
https://doi.org/10.1055/S-0034-1368568
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
https://doi.org/10.1248/YAKUSHI1947.111.7_376
https://doi.org/10.1248/YAKUSHI1947.111.7_365
https://doi.org/10.1016/0031-9422(91)80052-3
https://doi.org/10.1016/0031-9422(81)85291-0
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
8-Hydroxy-6-methoxychromen-2-one 102395048 Click to see COC1=CC(=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
(9R)-9-hydroxy-6-methoxy-8,8-dimethyl-9,10-dihydropyrano[2,3-h]chromen-2-one 162925918 Click to see 276.28 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
5-Methoxy-8,8-dimethyl-9,10-dihydropyrano[2,3-h]chromen-2-one 12112042 Click to see 260.28 unknown https://doi.org/10.1021/NP401040D
5-Methoxyseselin 290897 Click to see CC1(C=CC2=C3C(=C(C=C2O1)OC)C=CC(=O)O3)C 258.27 unknown https://doi.org/10.1021/NP401040D
6-Methoxy-3-(6-methoxy-8,8-dimethyl-2-oxopyrano[2,3-h]chromen-3-yl)-8,8-dimethylpyrano[2,3-h]chromen-2-one 102066705 Click to see CC1(C=CC2=C3C(=CC(=C2O1)OC)C=C(C(=O)O3)C4=CC5=CC(=C6C(=C5OC4=O)C=CC(O6)(C)C)OC)C 514.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
https://doi.org/10.1016/S0031-9422(96)00724-8
6-Methoxy-8,8-dimethyl-9,10-dihydropyrano[2,3-h]chromen-2-one 90655369 Click to see 260.28 unknown https://doi.org/10.1021/NP401040D
9-Hydroxy-6-methoxy-8,8-dimethyl-9,10-dihydropyrano[2,3-h]chromen-2-one 10683842 Click to see CC1(C(CC2=C3C(=CC(=C2O1)OC)C=CC(=O)O3)O)C 276.28 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
Braylin 618370 Click to see 258.27 unknown https://doi.org/10.1021/NP401040D
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
Norbraylin 10105863 Click to see 244.24 unknown https://doi.org/10.1055/S-0034-1368568
https://doi.org/10.1021/NP401040D
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Luvangetin 343582 Click to see 258.27 unknown https://doi.org/10.1055/S-0034-1368568
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
3,7,3',4'-Tetrahydroxyflavanone 246330 Click to see 288.25 unknown https://doi.org/10.1016/S0031-9422(00)97163-2
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Plantagoside 174157 Click to see 466.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one 129010007 Click to see 610.60 unknown https://doi.org/10.1016/S0031-9422(00)97163-2
Diosmin 5281613 Click to see 608.50 unknown https://doi.org/10.1016/S0031-9422(00)97163-2
Homoplantaginin 5318083 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown via CMAUP database
Npc288714 53384378 Click to see 608.50 unknown via CMAUP database
Plantaginin 5320623 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1016/S0031-9422(00)97163-2
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(6aR,11aS)-3,9-dimethoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene 50989259 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC 284.31 unknown https://doi.org/10.1016/0040-4039(91)80441-8
> Phenylpropanoids and polyketides / Macrolactams
Emestrin 11758256 Click to see 598.60 unknown via CMAUP database

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