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Toddalia asiatica

Toddalia asiatica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643ffea881001691094577
Scientific name Toddalia asiatica
Authority (L.) Lam.
First published in Tabl. Encycl. 2: 116 (1797)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aralia labordei H.Lév. Bull. Acad. Int. Géogr. Bot. 24: 144 (1914)
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)
Paullinia asiatica L. Sp. Pl. : 365 (1753)
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 rubricaulis Schult. Syst. Veg., ed. 15 bis 5: 323 (1819)
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

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000455337
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

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
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
Toddacoumalone, a novel mixed dimer of coumarin and quinolone from Toddalia asiatica (L.) Lam. (T. aculeata pers.) Hisashi Ishii, Jun-Ichi Kobayashi, Tsutomu Ishikawa Elsevier BV 25-Jul-2002
doi:10.1016/0040-4039(91)80441-8

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 CN1C2=C(C=CC3=CC4=C(C=C32)OCO4)C5=CC6=C(C=C5C1=O)OCO6 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 C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC)C 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 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
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 CN1C(C2=C(C=CC(=C2OC)OC)C3=C1C4=CC5=C(C=C4C=C3)OCO5)CO 379.40 unknown https://doi.org/10.1002/JCCS.200300178
Dihydrochelerythrine 485077 Click to see CN1CC2=C(C=CC(=C2OC)OC)C3=C1C4=CC5=C(C=C4C=C3)OCO5 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 CN1CC2=C(C=CC3=C2OCO3)C4=C1C5=CC6=C(C=C5C=C4)OCO6 333.30 unknown https://doi.org/10.1016/0031-9422(91)80052-3
Zanthocadinanine A 44567550 Click to see CC(C)C1CCC(C2C1C=C(CC2)CC3C4=C(C=CC(=C4OC)OC)C5=C(N3C)C6=CC7=C(C=C6C=C5)OCO7)(C)OC 583.80 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Quaternary benzophenanthridine alkaloids
Chelerythrine 2703 Click to see C[N+]1=C2C(=C3C=CC(=C(C3=C1)OC)OC)C=CC4=CC5=C(C=C42)OCO5 348.40 unknown https://doi.org/10.1248/YAKUSHI1947.111.7_365
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
Chelerythrine hydroxide 5351594 Click to see C[N+]1=C2C(=C3C=CC(=C(C3=C1)OC)OC)C=CC4=CC5=C(C=C42)OCO5.[OH-] 365.40 unknown via CMAUP database
> 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 CN(C=O)C1=C(C=CC2=CC3=C(C=C21)OCO3)C4=CC5=C(C=C4O)OCO5 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 COC1=C(C2=C(C=C1)C=C3C4=CC5=C(C=C4CCN3C2O)OCO5)OC 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/
9,10-Dimethoxy-2,3-(methylenedioxy)-13,13a-didehydro-8-berbinol 24974 Click to see COC1=C(C2=C(C=C1)C=C3C4=CC5=C(C=C4CCN3C2O)OCO5)OC 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 CC1=CC(=C2C(=C1)C(=O)C=C(C2=O)OC)C3=C(C=C(C4=C3OC(=O)C=C4)OC)OC 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 COC1=CC=C(C=C1)CC=C 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 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
(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 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/
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 CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 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 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, (+)- 443023 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/
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Heptacosanoic acid 23524 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 410.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
Hexacosanoic acid 10469 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 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 CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 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, (+/-)- 8842 Click to see CC(CCC=C(C)C)CCO 156.26 unknown via CMAUP database
beta-CITRONELLOL, (R)- 101977 Click to see CC(CCC=C(C)C)CCO 156.26 unknown via CMAUP database
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
Linalyl acetate 8294 Click to see CC(=CCCC(C)(C=C)OC(=O)C)C 196.29 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 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 CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene 6451618 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)- 17868 Click to see CC1=CCC2(C1C2)C(C)C 136.23 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 CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0367-326X(98)00002-1
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 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
(1S,2R,4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid 7163172 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
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 CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
Stigmasterol acetate 6437330 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C 454.70 unknown via CMAUP database
Ursolic Acid 64945 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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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 CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 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
Beta-Sitosterol 222284 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
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 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 C1CCC(CC1)NC(=O)C(=O)NC2CCCCC2 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 C1CCC(CC1)N 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 CC(C)(C(CC1=C(C=C2C(=C1OC)C=CC(=O)O2)OC)OC(=O)C3(CC(C(C(C3)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 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 C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 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 C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3C(C(C(C(O3)OC4(C(C(C(O4)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O 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 COC1=C(C2=C(C=C1)C3=C(C4=CC5=C(C=C4C=C3)OCO5)OC2=O)OC 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 CN1C(C2=CC(=C(C=C2C3=C1C4=CC5=C(C=C4C=C3)OCO5)OC)OC)C(Cl)(Cl)Cl 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 CN1C2=C(C=CC3=CC4=C(C=C32)OCO4)C5=C(C1=O)C=C6C=CC7=C(C6=C5)OCO7 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 CN1C2=C(C=CC3=CC4=C(C=C32)OCO4)C5=CC(=C(C=C5C1=O)O)OC 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 CN1C(C2=CC(=C(C=C2C3=C1C4=CC5=C(C=C4C=C3)OCO5)OC)OC)C(Cl)(Cl)Cl 466.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
Avicine 356657 Click to see C[N+]1=CC2=CC3=C(C=C2C4=C1C5=CC6=C(C=C5C=C4)OCO6)OCO3 332.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
https://doi.org/10.1016/0031-9422(91)80052-3
https://doi.org/10.1248/YAKUSHI1947.111.7_365
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/10.1007/S00280-009-1077-7
https://doi.org/10.1016/0031-9422(91)80052-3
Nitidine 4501 Click to see C[N+]1=CC2=CC(=C(C=C2C3=C1C4=CC5=C(C=C4C=C3)OCO5)OC)OC 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/10.1002/JCCS.200300178
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
https://doi.org/10.1016/0031-9422(91)80052-3
https://doi.org/10.1016/S0031-9422(96)00724-8
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/10.1002/JCCS.200300178
https://doi.org/10.1248/YAKUSHI1947.111.7_365
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/
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 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 COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown https://doi.org/10.1016/0031-9422(81)85291-0
https://doi.org/10.1002/JCCS.200300178
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
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/
Robustine 164950 Click to see COC1=C2C=COC2=NC3=C1C=CC=C3O 215.20 unknown via CMAUP database
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1002/JCCS.200300178
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
https://doi.org/10.1016/S0031-9422(96)00724-8
> 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 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
4-Methoxy-1-methylquinolin-2-one 182073 Click to see CN1C2=CC=CC=C2C(=CC1=O)OC 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 CN1C2=C(C=C(C=C2)O)C(=CC1=O)OC 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 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
> 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 CC(=CC1CC(OC2=C1C(=O)N(C3=CC=CC=C32)C)C=CC4=C(C=C(C5=C4OC(=O)C=C5)OC)OC)C 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 CC(=CC1CC(OC2=C1C(=O)N(C3=CC=CC=C32)C)(C)C=CC4=C(C=C(C5=C4OC(=O)C=C5)OC)OC)C 513.60 unknown https://doi.org/10.1016/0040-4039(91)80441-8
N-Methylflindersine 72819 Click to see CC1(C=CC2=C(O1)C3=CC=CC=C3N(C2=O)C)C 241.28 unknown https://doi.org/10.1248/YAKUSHI1947.111.7_365
Toddacoumalone 86302487 Click to see CC(=CC1CC(OC2=C1C(=O)N(C3=CC=CC=C32)C)(C)C=CC4=C(C=C(C5=C4OC(=O)C=C5)OC)OC)C 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 CC(=O)C=CC1=C(C=C2C(=C1OC)C=CC(=O)O2)OC 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 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
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 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
(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 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
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(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 C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O 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 CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)OC)O)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O)O)O)O 652.60 unknown via CMAUP database
Leucosceptoside A 10394343 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 638.60 unknown via CMAUP database
Martynoside 5319292 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)OC)O)O)O)O)O 652.60 unknown via CMAUP database
Plantainoside B 9847922 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O 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 C1C(OC2C(C(C(OC2O1)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)C4=CC(=C(C=C4)O)O 476.40 unknown via CMAUP database
Sanangoside 6915840 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O 478.40 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 CC(=CCC1=C(C=C(C(=C1OC)C=CC(=O)OC(CC2=C(C=C3C(=C2OC)C=CC(=O)O3)OC)C(C)(C)O)O)OC)C 582.60 unknown https://doi.org/10.1021/NP401040D
> Phenylpropanoids and polyketides / Coumarins and derivatives
(-)-Toddanol 102004726 Click to see CC(=C)C(CC1=C(C=C2C(=C1OC)C=CC(=O)O2)OC)O 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 CC(=C)C(CC1=C(C=C2C(=C1OC)C=CC(=O)O2)OC)O 290.31 unknown 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
5,7-Dimethoxy-6-(3-methyl-2-oxobutyl)chromen-2-one 86005045 Click to see CC(C)C(=O)CC1=C(C=C2C(=C1OC)C=CC(=O)O2)OC 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 CC(C)CCC1=C(C=C2C(=C1OC)C=CC(=O)O2)OC 276.33 unknown https://doi.org/10.1021/NP401040D
5,7-Dimethoxy-8-(3-methylbutyl)-coumarin 90655371 Click to see CC(C)CCC1=C(C=C(C2=C1OC(=O)C=C2)OC)OC 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 COC1=CC2=C(C=CC(=O)O2)C(=C1)OC 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 COC1=CC(=C(C2=C1C=CC(=O)O2)OC)OC 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 CC(C)(C(CC1=C(C=C2C(=C1OC)C=CC(=O)O2)OC)O)O 308.33 unknown 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/
https://doi.org/10.1002/ARDP.19332710806
https://doi.org/10.1002/JCCS.200300178
https://doi.org/10.1016/0031-9422(81)85120-5
https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
https://doi.org/10.1248/YAKUSHI1947.111.7_365
https://doi.org/10.1055/S-0034-1368568
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 CC(=C)C(CC1=C(C=C2C(=C1OC)C=CC(=O)O2)OC)O 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 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/
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
7-Methoxycoumarin 10748 Click to see COC1=CC2=C(C=C1)C=CC(=O)O2 176.17 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.012
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 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 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 CC1(CCC=CC1C2=C(C=C(C3=C2OC(=O)C=C3)OC)OC)C=CC4=C(C=C(C5=C4OC(=O)C=C5)OC)OC 530.60 unknown https://doi.org/10.1055/S-0034-1368568
https://doi.org/10.1248/YAKUSHI1947.111.7_365
https://doi.org/10.1002/JCCS.200300178
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 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 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 CC1=CC(C(C(C1)(C)C)C(C2=C(C=C(C3=C2OC(=O)C=C3)OC)OC)O)C4=C(C=C(C5=C4OC(=O)C=C5)OC)OC 562.60 unknown https://doi.org/10.1248/CPB.41.1655
Aculeatin 5316354 Click to see CC1(C(O1)CC2=C(C=C3C(=C2OC)C=CC(=O)O3)OC)C 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
Ent-toddalolactone 25721348 Click to see CC(C)(C(CC1=C(C=C2C(=C1OC)C=CC(=O)O2)OC)O)O 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
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 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/
Toddalosin 15071281 Click to see CC1=CC(C(C(C1)(C)C)C(C2=C(C=C(C3=C2OC(=O)C=C3)OC)OC)O)C4=C(C=C(C5=C4OC(=O)C=C5)OC)OC 562.60 unknown https://doi.org/10.1248/CPB.41.1655
https://doi.org/10.1248/YAKUSHI1947.111.7_365
Ulopterol 176475 Click to see CC(C)(C(CC1=C(C=C2C(=C1)C=CC(=O)O2)OC)O)O 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 COC1=C(C2=C(C=CO2)C3=C1C=CC(=O)O3)OC 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 COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)O 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 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/
5-Methoxy-8,8-dimethyl-9,10-dihydropyrano[2,3-h]chromen-2-one 12112042 Click to see CC1(CCC2=C3C(=C(C=C2O1)OC)C=CC(=O)O3)C 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 CC1(CCC2=C3C(=CC(=C2O1)OC)C=CC(=O)O3)C 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 CC1(C=CC2=C3C(=CC(=C2O1)OC)C=CC(=O)O3)C 258.27 unknown https://doi.org/10.1021/NP401040D
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720317/
Norbraylin 10105863 Click to see CC1(C=CC2=C3C(=CC(=C2O1)O)C=CC(=O)O3)C 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 CC1(C=CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)OC)C 258.27 unknown https://doi.org/10.1055/S-0034-1368568
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Tetrahydroxyflavanone 246330 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O 288.25 unknown https://doi.org/10.1016/S0031-9422(00)97163-2
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 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 C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Plantagoside 174157 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C(=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O 466.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 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 CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown https://doi.org/10.1016/S0031-9422(00)97163-2
5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 53384378 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 608.50 unknown via CMAUP database
Diosmin 5281613 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 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
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 CN1C(=O)C23C(C4=COC=CC5C4N2C(=O)C1(C(C6=CC(=C(C=C6)O)OC7=C(C=CC(=C7)C(=O)O5)OC)O)SS3)O 598.60 unknown via CMAUP database

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