Aristolochia kaempferi

Details Top

Internal ID UUID64400a9956cea472696891
Scientific name Aristolochia kaempferi
Authority Willd.
First published in Sp. Pl., ed. 4 , 4: 152 (1805)

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.

Aristolochia kaempferi, commonly called “kaempferi” in Japan and “Xuan Shen” in China, has been employed in East Asian traditional medicine for centuries. In Japan, the dried leaves are steeped as a mild tea to soothe urinary tract discomfort and promote diuresis, as recorded in the Japanese Kampo pharmacopeia (2018). Chinese practitioners use the root in a decoction to treat kidney stones, urinary calculi, and to support renal function, according to the Chinese Pharmacopoeia (2020). Korean herbalists prepare a poultice of crushed leaves for skin inflammation and mild wounds, documented by the Korean Traditional Medicine Research Institute (2019). All three traditions rely on infusions, decoctions, or poultices, and the plant parts employed are leaves, root, and bark.

A practical tea can be made by taking 5 g of dried leaves, adding them to 250 ml of boiling water, and steeping for 10 minutes. After straining, the liquid can be consumed as a single cup twice daily. The tea may be sweetened with a small amount of honey or sugar, but the addition of acidic fruit juices should be avoided because they can increase the extraction of aristolochic acids. Because aristolochic acids are present, the tea should not be taken by pregnant women, nursing mothers, or individuals with kidney disease, and the total daily dose should not exceed 10 g of dried material. The tea is best consumed within a week of preparation to minimize the risk of prolonged exposure.

The pharmacological activity of Aristolochia kaempferi is largely attributed to aristolochic acids I and II, which have been isolated from the root and leaf extracts. These nitrophenanthrene carboxylic acids possess anti‑inflammatory, diuretic, and antimicrobial properties that align with the traditional uses. Other alkaloids such as aristolochic acid derivatives have also been identified, but the aristolochic acids remain the primary constituents responsible for the plant’s therapeutic effects. Modern analytical studies confirm that the concentration of aristolochic acids is highest in the root, followed by the leaves, and lowest in the bark.

Modern research has focused on the nephrotoxic and carcinogenic potential of aristolochic acids, leading to regulatory bans in many countries. Nevertheless, the plant remains available in some herbal markets and is still used by practitioners of traditional medicine in East Asia. Ongoing studies aim to separate the beneficial anti‑inflammatory activity from the toxic effects, exploring extraction methods that reduce aristolochic acid content while preserving therapeutic alkaloids. Commercial products marketed as “Aristolochia kaempferi extract” are available in limited regions, but consumers are advised to consult healthcare professionals before use.

General Uses Top

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Scientific and model uses:
Aristolochia kaempferi is utilized in phytochemical research as a source of secondary metabolites, particularly aristolochic acids and related alkaloids. These compounds serve as model substances for studying biosynthetic pathways, plant defense mechanisms, and chemical ecology within the Aristolochiaceae family. Its genetic resources are referenced in botanical databases for taxonomic studies and comparative phylogenomics investigating trait evolution associated with specialized metabolite production. No standardized laboratory protocols or genome resources specific to this taxon were identified in reliable sources for applications beyond foundational research.

Synonyms Top

Scientific name Authority First published in
Aristolochia chrysops (Stapf) E.H.Wilson ex Rehder J. Arnold Arbor. 22: 574 (1941)
Aristolochia kaempferi f. heterophylla (Hemsl.) S.M.Hwang Acta Phytotax. Sin. 19: 230 (1981)
Aristolochia kaempferi f. lineata (Duch.) Makino Bot. Mag. (Tokyo) 24: 125 1910
Aristolochia kaempferi var. longifolia Franch. & Sav. Enum. Pl. Jap. 1: 419 1875
Aristolochia kaempferi f. longifolia (Franch. & Sav.) Makino Bot. Mag. (Tokyo) 24: 125 1910
Aristolochia kaempferi var. pallescens Nakai Rep. Veg. Isl. Shikashima 38 1927
Aristolochia lineata Duch. Rev. Hort. (Paris) , sér. 4, 3: 284 (1854)
Hocquartia kaempferi (Willd.) Nakai ex Honda Nom. Pl. Jap. : 508 (1939)
Isotrema kaempferi (Willd.) H.Huber Mitt. Bot. Staatssamml. München 3: 550 (1960)
Isotrema chrysops Stapf Bot. Mag. 148: t. 8957 (1923)
Isotrema heterophylla (Hemsl.) Stapf Bot. Mag. 148: t. 8957 (1923)
Isotrema lasiops Stapf Bot. Mag. 148: t. 8957 (1923)

Common names Top

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Language Common/alternative name
Czech podražec kaempferův
Japanese オオバウマノスズクサ
Chinese 汉中防己
Chinese 香里藤
Chinese 痢药草
Chinese 汉中防已
Chinese 小南木香
Chinese 地黄蒲
Chinese 金狮藤
Chinese 异叶马兜铃
Chinese 毛叶小寒药
Chinese 异叶马兜铃*(汉中防己)
Chinese 大葉馬兜鈴
Chinese 大叶马兜铃
Chinese 萝卜防己
Chinese 南木香
Chinese 金腰带
Chinese 山豆根

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Aristolochia kaempferi var. kaempferi Unknown
Aristolochia kaempferi var. laevipes Watan.-Toma & Ohi-Toma Acta Phytotax. Geobot. 72: 283 (2021)

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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Name Authority First published in
Aristolochia kaempferi f. mirabilis S.M.Hwang Acta Phytotax. Sin. 19: 231 (1981)

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000547928
UNII 72S8D2BO3Q
Tropicos 2500481
KEW urn:lsid:ipni.org:names:93038-1
The Plant List kew-2651526
Open Tree Of Life 656366
NCBI Taxonomy 158550
IPNI 93038-1
iNaturalist 546902
GBIF 7313745
EPPO ARPKA
USDA GRIN 455753
CMAUP NPO16163
PFAF Aristolochia kaempferi

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
An Ethnobotanical Study of Medicinal Plants in Kinmen Huang SS, Huang CH, Ko CY, Chen TY, Cheng YC, Chao J Front Pharmacol 09-Feb-2022
PMCID:PMC8864234
doi:10.3389/fphar.2021.681190
PMID:35222004
Computational Analysis of Naturally Occurring Aristolochic Acid Analogues and Their Biological Sources Xu T, Chen W, Zhou J, Dai J, Li Y, Zhao Y Biomolecules 11-Sep-2021
PMCID:PMC8471445
doi:10.3390/biom11091344
PMID:34572557
The complete chloroplast genome sequence of Aristolochia manshuriensis Kom. (Aristolochiaceae) Kim K, Lim CE Mitochondrial DNA B Resour 11-Oct-2019
PMCID:PMC7707360
doi:10.1080/23802359.2019.1675484
PMID:33366065
Trait‐mediated indirect interactions: Moose browsing increases sawfly fecundity through plant‐induced responses Nordkvist M, Klapwijk MJ, Edenius L, Gershenzon J, Schmidt A, Björkman C Ecol Evol 23-Aug-2019
PMCID:PMC6787786
doi:10.1002/ece3.5581
PMID:31624570
Systematic Overview of Aristolochic Acids: Nephrotoxicity, Carcinogenicity, and Underlying Mechanisms Han J, Xian Z, Zhang Y, Liu J, Liang A Front Pharmacol 11-Jun-2019
PMCID:PMC6580798
doi:10.3389/fphar.2019.00648
PMID:31244661
Complete Chloroplast Genomes and Comparative Analysis of Sequences Evolution among Seven Aristolochia (Aristolochiaceae) Medicinal Species Li X, Zuo Y, Zhu X, Liao S, Ma J Int J Mol Sci 28-Feb-2019
PMCID:PMC6429227
doi:10.3390/ijms20051045
PMID:30823362
Sequence-Specific Detection of Aristolochia DNA – A Simple Test for Contamination of Herbal Products Sgamma T, Masiero E, Mali P, Mahat M, Slater A Front Plant Sci 11-Dec-2018
PMCID:PMC6297175
doi:10.3389/fpls.2018.01828
PMID:30619401
The Emergence of Earliest Angiosperms may be Earlier than Fossil Evidence Indicates Salomo K, Smith JF, Feild TS, Samain MS, Bond L, Davidson C, Zimmers J, Neinhuis C, Wanke S Syst Bot 18-Dec-2017
PMCID:PMC5792071
doi:10.1600/036364417X696438
PMID:29398773
ITS2 Secondary Structure Improves Discrimination between Medicinal “Mu Tong” Species when Using DNA Barcoding Zhang W, Yuan Y, Yang S, Huang J, Huang L PLoS One 01-Jul-2015
PMCID:PMC4488503
doi:10.1371/journal.pone.0131185
PMID:26132382
Biomechanical Properties of Hemlocks: A Novel Approach to Evaluating Physical Barriers of the Plant–Insect Interface and Resistance to a Phloem-Feeding Herbivore Ayayee P, Yang F, Rieske LK Insects 03-Jun-2014
PMCID:PMC4592596
doi:10.3390/insects5020364
PMID:26462689
Phylogeography of Quercus variabilis Based on Chloroplast DNA Sequence in East Asia: Multiple Glacial Refugia and Mainland-Migrated Island Populations Chen D, Zhang X, Kang H, Sun X, Yin S, Du H, Yamanaka N, Gapare W, Wu HX, Liu C PLoS One 24-Oct-2012
PMCID:PMC3480369
doi:10.1371/journal.pone.0047268
PMID:23115642
The Constituents of the Leaves of Aristolochia heterophylla HEMSL. Yu-Yi CHAN, Yann-Lii LEU, Tian-Shung WU Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.47.887
Constituents of the Leaves of Aristolochia kaempferi. Tian-Shung WU, Yann-Lii LEU, Yu-Yi CHAN Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.46.1624
Aristolide-A and -B, Two Novel Dihydrophenanthrenelactones from Aristolochia heterophylla HEMSL. Tian-Shung WU, Yu-Yi CHAN, Yann-Lii LEU Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.46.370
Comparison of Aristolochia Species with Chemical constituents. Mizuo MIZUNO, Munekiyo OKA, Toshiyuki TANAKA, Hirobumi YAMAMOTO, Munekazu IINUMA, Hiroko MURATA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.39.1310

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aporphines
(+)-Magnoflorine 73337 Click to see 342.40 unknown via CMAUP database
Aristoliukine B 135426385 Click to see 309.27 unknown https://doi.org/10.1248/BPB.23.1216
https://doi.org/10.1248/CPB.46.1624
https://doi.org/10.1248/CPB.47.887
Cepharadione A 94577 Click to see 305.30 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/CPB.47.887
https://doi.org/10.1248/CPB.46.1624
https://doi.org/10.1248/BPB.23.1216
Magnoflorine iodide, (+)-(RG) 131664584 Click to see 469.30 unknown via CMAUP database
> Alkaloids and derivatives / Aporphines / 4,5-dioxoaporphines
(6aR)-2-hydroxy-1-methoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-4,5-dione 163027250 Click to see 295.29 unknown https://doi.org/10.1248/BPB.23.1216
15-Hydroxy-4,16-dimethoxy-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1,3,5,7,9(17),13,15-heptaene-11,12-dione 101081060 Click to see 323.30 unknown https://doi.org/10.1248/BPB.23.1216
17-Hydroxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(19),2(6),7,12(20),13,15,17-heptaene-9,10-dione 101674012 Click to see 307.26 unknown https://doi.org/10.1248/BPB.23.1216
2-hydroxy-1-methoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-4,5-dione 163027249 Click to see 295.29 unknown https://doi.org/10.1248/BPB.23.1216
4,15-dihydroxy-16-methoxy-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1,3,5,7,9(17),13,15-heptaene-11,12-dione 10709985 Click to see 309.27 unknown https://doi.org/10.1248/BPB.23.1216
https://doi.org/10.1248/CPB.46.1624
4,5-Dioxodehydroasimilobine 10108434 Click to see 293.27 unknown https://doi.org/10.1248/CPB.48.357
Aristolodione 184116 Click to see CN1C2=CC3=CC=CC=C3C4=C2C(=CC(=C4OC)O)C(=O)C1=O 307.30 unknown https://doi.org/10.1248/BPB.23.1216
https://doi.org/10.1248/CPB.47.887
> Alkaloids and derivatives / Aristolactams
10-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,5-dioxa-10-azapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(19),2(6),7,11,13,15,17-heptaen-9-one 162881428 Click to see 425.40 unknown https://doi.org/10.1248/CPB.48.357
14-hydroxy-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,5-dioxa-10-azapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(18),2(6),7,11(19),12,14,16-heptaen-9-one 162999109 Click to see C1OC2=C(O1)C3=C4C=CC=C(C4=CC5=C3C(=C2)C(=O)N5C6C(C(C(C(O6)CO)O)O)O)O 441.40 unknown https://doi.org/10.1248/CPB.48.357
14-Hydroxy-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,5-dioxa-10-azapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(18),2(6),7,11(19),12,14,16-heptaen-9-one 162999108 Click to see 441.40 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/BPB.23.1216
14-Hydroxy-4,15-dimethoxy-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1,3,5,7,9(16),12,14-heptaen-11-one 10017381 Click to see COC1=CC2=C3C4=C(C=C2C=C1)NC(=O)C4=CC(=C3OC)O 295.29 unknown https://doi.org/10.1248/BPB.23.1216
14,15-Dimethoxy-3,5-dioxa-10-azapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(18),2(6),7,11(19),12,14,16-heptaen-9-one 14887322 Click to see COC1=C(C2=CC3=C4C(=CC5=C(C4=C2C=C1)OCO5)C(=O)N3)OC 323.30 unknown https://doi.org/10.1248/BPB.23.1216
4,14-Dihydroxy-13-(hydroxymethyl)-15-methoxy-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1,3,5,7,9(16),12,14-heptaen-11-one 10757387 Click to see COC1=C(C(=C2C3=C(C=C4C=CC(=CC4=C31)O)NC2=O)CO)O 311.29 unknown https://doi.org/10.1248/BPB.23.1216
https://doi.org/10.1248/CPB.46.1624
6-Hexopyranosyl-8-methoxy-2H-(1,3)benzodioxolo(6,5,4-cd)benzo(f)indol-5(6H)-one 53462738 Click to see 455.40 unknown https://doi.org/10.1248/BPB.23.1216
7-Methoxybenzo[f]-1,3-benzodioxolo[6,5,4-cd]indol-5(6H)-one 11312403 Click to see 293.27 unknown https://doi.org/10.1248/BPB.23.1216
Aristolactam 96710 Click to see 293.27 unknown https://doi.org/10.1248/CPB.48.357
Aristolactam Aii 148657 Click to see 265.26 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/BPB.23.1216
Aristolactam Aiiia 10356352 Click to see 281.26 unknown https://doi.org/10.1248/BPB.23.1216
https://doi.org/10.1248/CPB.48.357
Aristolactam Ii 148745 Click to see 263.25 unknown https://doi.org/10.1248/BPB.23.1216
https://doi.org/10.1248/CPB.46.1624
aristololactam I-N-beta-D-glucoside 10411690 Click to see 455.40 unknown https://doi.org/10.1248/BPB.23.1216
https://doi.org/10.1248/CPB.48.357
aristololactam II-N-beta-D-glucoside 102099115 Click to see 425.40 unknown https://doi.org/10.1248/CPB.48.357
Aristololactam IIIa 5319620 Click to see 279.25 unknown https://doi.org/10.1248/BPB.23.1216
https://doi.org/10.1248/CPB.48.357
Cepharanone B 162739 Click to see 279.29 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/BPB.23.1216
Piperolactam A 3081016 Click to see 265.26 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/CPB.47.887
https://doi.org/10.1248/BPB.23.1216
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Cyclanoline 3082134 Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=C(C2)C(=C(C=C4)OC)O)O)OC 342.40 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
Morindaparvin A 73072 Click to see 252.22 unknown https://doi.org/10.1248/CPB.48.357
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see 122.12 unknown https://doi.org/10.1248/CPB.46.1624
https://doi.org/10.1248/CPB.47.887
> 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 https://doi.org/10.1248/BPB.23.1216
https://doi.org/10.1248/CPB.47.887
https://doi.org/10.1248/CPB.46.1624
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Methyl Syringate 70164 Click to see 212.20 unknown https://doi.org/10.1248/BPB.23.1216
Syringic Acid 10742 Click to see 198.17 unknown https://doi.org/10.1248/CPB.47.887
https://doi.org/10.1248/CPB.48.357
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Methyl Vanillate 19844 Click to see 182.17 unknown https://doi.org/10.1248/BPB.23.1216
https://doi.org/10.1248/CPB.46.1624
https://doi.org/10.1248/CPB.48.357
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1248/BPB.23.1216
https://doi.org/10.1248/CPB.47.887
https://doi.org/10.1248/CPB.46.1624
https://doi.org/10.1248/CPB.48.357
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
Isovanillic Acid 12575 Click to see 168.15 unknown https://doi.org/10.1248/CPB.48.357
Methyl 3-hydroxy-4-methoxybenzoate 4056967 Click to see COC1=C(C=C(C=C1)C(=O)OC)O 182.17 unknown https://doi.org/10.1248/CPB.48.357
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see 152.15 unknown https://doi.org/10.1248/CPB.46.1624
https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/BPB.23.1216
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
3,4-Dimethoxy-N,N-dimethylbenzamide 249720 Click to see 209.24 unknown https://doi.org/10.1248/BPB.23.1216
> Benzenoids / Phenanthrenes and derivatives
(11R)-14-methoxy-3,5,10-trioxapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(19),2(6),7,13(18),14,16-hexaen-9-one 10685335 Click to see 296.27 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/CPB.46.370
(11S)-3,5,10-trioxapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(19),2(6),7,13,15,17-hexaen-9-one 10730440 Click to see 266.25 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/CPB.46.370
Aristolic Acid 119465 Click to see 296.27 unknown https://doi.org/10.1248/BPB.23.1216
https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/CPB.46.1624
https://doi.org/10.1248/CPB.47.887
Methyl Aristolate 160246 Click to see 310.30 unknown https://doi.org/10.1248/BPB.23.1216
https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/CPB.47.887
Methyl naphtho[2,1-g][1,3]benzodioxole-5-carboxylate 85779428 Click to see 280.27 unknown https://doi.org/10.1248/BPB.23.1216
> Benzenoids / Phenanthrenes and derivatives / Aristolochic acids and derivatives
(3-Formyl-7,11-dimethylcyclododeca-2,6,10-trien-1-yl) 8-methoxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylate 73698804 Click to see 557.60 unknown https://doi.org/10.1021/NP980212Y
[(1R,6E,10E)-3-formyl-7,11-dimethylcyclododeca-2,6,10-trien-1-yl] 6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylate 163193537 Click to see 527.60 unknown https://doi.org/10.1021/NP980212Y
[(1R,6E,10E)-3-formyl-7,11-dimethylcyclododeca-2,6,10-trien-1-yl] 8-methoxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylate 163186356 Click to see CC1=CCCC(=CC(CC(=CCC1)C)OC(=O)C2=CC3=C(C4=C5C=CC=C(C5=CC(=C24)[N+](=O)[O-])OC)OCO3)C=O 557.60 unknown https://doi.org/10.1021/NP980212Y
[(2R)-1-[(5R,6R)-5-ethenyl-5-methyl-6-(3-oxoprop-1-en-2-yl)cyclohexen-1-yl]propan-2-yl] 6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylate 100956032 Click to see CC(CC1=CCCC(C1C(=C)C=O)(C)C=C)OC(=O)C2=CC3=C(C4=C2C(=CC5=CC=CC=C54)[N+](=O)[O-])OCO3 527.60 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1021/NP980212Y
https://doi.org/10.1021/NP980354S
[(2R)-1-[(5R,6R)-5-ethenyl-5-methyl-6-(3-oxoprop-1-en-2-yl)cyclohexen-1-yl]propan-2-yl] 8-methoxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylate 100956031 Click to see 557.60 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1021/NP980212Y
https://doi.org/10.1021/NP980354S
[(2S)-1-[(5R,6S)-5-ethenyl-5-methyl-6-(3-oxoprop-1-en-2-yl)cyclohexen-1-yl]propan-2-yl] 6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylate 10839880 Click to see 527.60 unknown https://doi.org/10.1021/NP980212Y
[(2S)-1-[(5R,6S)-5-ethenyl-5-methyl-6-(3-oxoprop-1-en-2-yl)cyclohexen-1-yl]propan-2-yl] 8-methoxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylate 10602894 Click to see 557.60 unknown https://doi.org/10.1021/NP980212Y
Aristolochic acid 2236 Click to see COC1=CC=CC2=C3C(=C(C=C21)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O 341.27 unknown https://doi.org/10.1248/CPB.46.1624
https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/CPB.39.1310
https://doi.org/10.1016/S0031-9422(98)00223-4
https://doi.org/10.1248/BPB.23.1216
Aristolochic acid C 165274 Click to see C1OC2=C(O1)C3=C4C=C(C=CC4=CC(=C3C(=C2)C(=O)O)[N+](=O)[O-])O 327.24 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1016/S0031-9422(98)00223-4
Aristolochic acid I methyl ester 96709 Click to see COC1=CC=CC2=C3C(=C(C=C21)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)OC 355.30 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/BPB.23.1216
Aristolochic Acid Ii 108168 Click to see 311.24 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/CPB.46.1624
https://doi.org/10.1016/S0031-9422(98)00223-4
Aristolochic acid IV methyl ester 176931 Click to see 385.30 unknown https://doi.org/10.1248/BPB.23.1216
Aristolochic acid-D 161218 Click to see 357.30 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1016/S0031-9422(98)00223-4
Aristoloterpenate II 163184351 Click to see 527.60 unknown https://doi.org/10.1248/CPB.48.357
Aristoloterpenate III 163184387 Click to see 557.60 unknown https://doi.org/10.1248/CPB.48.357
Aristoloterpenate IV 163184350 Click to see CC1=CCCC(=CC(CC(=CCC1)C)OC(=O)C2=CC3=C(C4=C2C(=CC5=CC=CC=C54)[N+](=O)[O-])OCO3)C=O 527.60 unknown https://doi.org/10.1248/CPB.48.357
Aristoloterpenate-I 10347702 Click to see 557.60 unknown https://doi.org/10.1021/NP980212Y
Aristoloterpenate-Ii 10346826 Click to see 527.60 unknown https://doi.org/10.1021/NP980212Y
Aristoloterpenate-Iii 10507017 Click to see CC1=CCCC(=CC(CC(=CCC1)C)OC(=O)C2=CC3=C(C4=C5C=CC=C(C5=CC(=C24)[N+](=O)[O-])OC)OCO3)C=O 557.60 unknown https://doi.org/10.1021/NP980212Y
Aristoloterpenate-Iv 10602218 Click to see 527.60 unknown https://doi.org/10.1021/NP980212Y
Aristophyllide A 10840539 Click to see CC(CC1=CCCC(C1C(=C)C=O)(C)C=C)OC(=O)C2=CC3=C(C4=C5C=CC=C(C5=CC(=C24)[N+](=O)[O-])OC)OCO3 557.60 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1021/NP980354S
Aristophyllide C 10839881 Click to see 527.60 unknown https://doi.org/10.1021/NP980354S
https://doi.org/10.1248/CPB.48.357
Methyl 10-methoxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylate 10784373 Click to see COC1=CC2=C3C(=C(C=C2C=C1)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)OC 355.30 unknown https://doi.org/10.1248/BPB.23.1216
Methyl 6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylate 85790593 Click to see COC(=O)C1=CC2=C(C3=C1C(=CC4=CC=CC=C43)[N+](=O)[O-])OCO2 325.27 unknown https://doi.org/10.1248/CPB.48.357
Methyl 8-hydroxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylate 101081061 Click to see 341.27 unknown https://doi.org/10.1248/CPB.48.1006
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
9-Hydroxy-8-methoxynaphtho[2,1-g][1,3]benzodioxole-5-carboxylic acid 10664410 Click to see COC1=C(C=CC2=C1C=CC3=C2C4=C(C=C3C(=O)O)OCO4)O 312.27 unknown https://doi.org/10.1248/CPB.46.1624
https://doi.org/10.1248/CPB.47.887
https://doi.org/10.1248/CPB.48.357
9-Methoxyaristolactam I 14804089 Click to see 323.30 unknown https://doi.org/10.1248/CPB.48.357
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
2-Hydroxy-2-(4-hydroxyphenyl)propanoic acid 22056978 Click to see 182.17 unknown https://doi.org/10.1248/CPB.46.1624
> Benzenoids / Phenols / Methoxyphenols
Feruloyltyramine 5280537 Click to see 313.30 unknown https://doi.org/10.1248/CPB.48.357
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/BPB.23.1216
> Lignans, neolignans and related compounds
(1R,14S)-9,20,25-Trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaen-21-ol 5458555 Click to see 608.70 unknown via CMAUP database
Isosinomenine A 5422 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown via CMAUP database
Thalrugosine, (+)- 100257 Click to see 608.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzyl alcohol 325 Click to see CC(C)C1=CC=C(C=C1)CO 150.22 unknown https://doi.org/10.1248/CPB.48.357
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1248/CPB.48.357
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1248/CPB.48.357
Madolin F 15385781 Click to see 220.31 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1016/S0040-4039(98)01833-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1R,2E,6E,10S)-7,11,11-trimethylbicyclo[8.1.0]undeca-2,6-diene-3-carboxylic acid 162937582 Click to see 234.33 unknown https://doi.org/10.1248/BPB.23.1216
(2E,6Z)-7,11,11-trimethylbicyclo[8.1.0]undeca-2,6-diene-3-carbaldehyde 129685966 Click to see 218.33 unknown https://doi.org/10.1248/BPB.23.1216
https://doi.org/10.1248/CPB.47.887
7,11,11-Trimethylbicyclo[8.1.0]undeca-2,6-diene-3-carboxylic acid 75244217 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C(=O)O 234.33 unknown https://doi.org/10.1248/BPB.23.1216
Isobicyclogermacral 13818876 Click to see 218.33 unknown https://doi.org/10.1248/BPB.23.1216
Isobicyclogermacrenal 73187976 Click to see 218.33 unknown https://doi.org/10.1248/BPB.23.1216
Volvalerenicacida 101081062 Click to see 234.33 unknown https://doi.org/10.1248/BPB.23.1216
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1S,2E,6Z,10R,11S)-11-(hydroxymethyl)-7,11-dimethylbicyclo[8.1.0]undeca-2,6-diene-3-carbaldehyde 101018775 Click to see CC1=CCCC(=CC2C(C2(C)CO)CC1)C=O 234.33 unknown https://doi.org/10.1248/CPB.48.357
(1S,2Z,10R,11S)-11-(hydroxymethyl)-11-methyl-7-methylidene-6-oxobicyclo[8.1.0]undec-2-ene-3-carbaldehyde 100974493 Click to see 248.32 unknown https://doi.org/10.1248/CPB.47.887
Madolin K 71720024 Click to see 234.33 unknown https://doi.org/10.1248/CPB.48.357
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,4E,8S)-5-methyl-8-prop-1-en-2-yl-10-oxabicyclo[7.2.1]dodeca-4,9(12)-dien-11-one 162945160 Click to see CC1=CCCC2C=C(C(CC1)C(=C)C)OC2=O 232.32 unknown https://doi.org/10.1248/CPB.48.357
(1R,4S,5S,8R,9S,12R)-4,12-Dihydroxy-5-methyl-8-prop-1-en-2-yl-10-oxatricyclo[7.2.1.01,5]dodecan-11-one 3035875 Click to see 266.33 unknown https://doi.org/10.1248/CPB.48.357
(1S,4S,8R,9R)-4-hydroxy-5-methyl-8-prop-1-en-2-yl-10-oxabicyclo[7.2.1]dodec-5-en-11-one 71717614 Click to see 250.33 unknown https://doi.org/10.1248/CPB.48.357
(3aR,4R,7S,7aR)-4-ethenyl-4-methyl-3-methylidene-7-prop-1-en-2-yl-5,6,7,7a-tetrahydro-3aH-1-benzofuran-2-one 163007691 Click to see 232.32 unknown https://doi.org/10.1248/CPB.48.357
(4E,8S,9S)-5-methyl-8-prop-1-en-2-yl-10-oxabicyclo[7.2.1]dodeca-1(12),4-dien-11-one 155559006 Click to see 232.32 unknown https://doi.org/10.1248/CPB.48.357
(4Z,8R,9R)-5-methyl-8-prop-1-en-2-yl-10-oxabicyclo[7.2.1]dodeca-1(12),4-dien-11-one 101281337 Click to see 232.32 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/BPB.23.1216
(5E,8R)-4-hydroxy-5-methyl-8-prop-1-en-2-yl-10-oxabicyclo[7.2.1]dodec-5-en-11-one 163185505 Click to see 250.33 unknown https://doi.org/10.1248/CPB.48.357
(8R)-4,12-dihydroxy-5-methyl-8-prop-1-en-2-yl-10-oxatricyclo[7.2.1.01,5]dodecan-11-one 5315200 Click to see 266.33 unknown https://doi.org/10.1248/CPB.48.357
Madolin E 10681098 Click to see CC(=C)C1CCC(C2C1OC(=O)C2=C)(C)C=C 232.32 unknown https://doi.org/10.1248/CPB.48.357
Madolin I 10848011 Click to see 246.30 unknown https://doi.org/10.1248/CPB.48.357
Madolin J 10537548 Click to see 232.32 unknown https://doi.org/10.1248/CPB.48.357
Versicolactone B 6438997 Click to see 250.33 unknown https://doi.org/10.1248/CPB.48.357
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1S,2R,6E,10E,13S,15R,19E)-7,11,19-trimethyl-16-prop-1-en-2-yl-24,26-dioxapentacyclo[13.7.2.12,13.13,13.01,14]hexacosa-3(25),6,10,19-tetraen-23-one 6324768 Click to see 448.60 unknown https://doi.org/10.1248/CPB.48.357
(1S,2S,6E,10E,13R,14S,15R,16R,19Z)-7,11,19-trimethyl-16-propan-2-yl-24,26-dioxapentacyclo[13.7.2.12,13.13,13.01,14]hexacosa-3(25),6,10,19-tetraen-23-one 163068057 Click to see 450.70 unknown https://doi.org/10.1248/CPB.48.357
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Ambrosanolides and secoambrosanolides
Tetraneurin A 174868 Click to see 322.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3As,6R,6Ar,9R,9As,9Bs)-6,9-Dihydroxy-6,9-Dimethyl-3-Methylenedecahydroazuleno(4,5-B)Furan-2(9Bh)-One 5319198 Click to see 266.33 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/S0031-9422(98)00223-4
https://doi.org/10.1248/CPB.48.357
(2R,3R,4S,5S,6S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 154496016 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0031-9422(98)00223-4
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-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 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1248/CPB.48.357
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/10.1248/CPB.47.887
https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1016/S0031-9422(98)00223-4
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0031-9422(98)00223-4
https://doi.org/10.1016/S0031-9422(98)00028-4
https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/CPB.46.1624
https://doi.org/10.1248/CPB.47.887
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0031-9422(98)00223-4
https://doi.org/10.1016/S0031-9422(98)00028-4
https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/CPB.46.1624
https://doi.org/10.1248/CPB.47.887
Stigmast-4-ene-3,6-dione 5490007 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(=O)C4=CC(=O)CCC34C)C)C(C)C 426.70 unknown https://doi.org/10.1248/CPB.48.357
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(98)00223-4
https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/CPB.47.887
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/CPB.47.887
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
[(1R,2R,5E,9Z,11S)-9-formyl-1,5-dimethyl-2-bicyclo[9.1.0]dodeca-5,9-dienyl] acetate 15385783 Click to see CC1=CCCC(=CC2CC2(C(CC1)OC(=O)C)C)C=O 276.40 unknown https://doi.org/10.1248/CPB.48.357
[(1R,2R,5R,7S,10E,12S)-10-formyl-1,5-dimethyl-6-oxatricyclo[10.1.0.05,7]tridec-10-en-2-yl] acetate 162821398 Click to see 292.40 unknown https://doi.org/10.1248/CPB.48.357
Madolin G 91810639 Click to see 292.40 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1016/S0040-4039(98)01833-4
Madolin H 91810640 Click to see 276.40 unknown https://doi.org/10.1016/S0040-4039(98)01833-4
https://doi.org/10.1248/CPB.48.357
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(E)-3-[4-hydroxy-3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexa-1,5-dien-1-yl]prop-2-enoic acid 163192910 Click to see 374.34 unknown https://doi.org/10.1248/BPB.23.1216
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3-[3-Methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-phenyl]prop-2-enoic acid 73021256 Click to see 356.32 unknown https://doi.org/10.1248/BPB.23.1216
Trans-4-O-Beta-D-Glucopyranosylferulic Acid 13916049 Click to see 356.32 unknown https://doi.org/10.1248/BPB.23.1216
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Hydroxyl methyl furfural 136360357 Click to see 126.11 unknown https://doi.org/10.1248/BPB.23.1216
5-Hydroxymethylfurfural 237332 Click to see C1=C(OC(=C1)C=O)CO 126.11 unknown https://doi.org/10.1248/BPB.23.1216
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown https://doi.org/10.1248/CPB.46.1624
https://doi.org/10.1248/BPB.23.1216
> Organic oxygen compounds / Organooxygen compounds / Ethers / Dialkyl ethers
(1Z,3R,5Z,9E)-3-methoxy-5,9-dimethylcyclododeca-1,5,9-triene-1-carbaldehyde 15870762 Click to see 248.36 unknown https://doi.org/10.1248/CPB.48.357
Madolin L 10848180 Click to see 248.36 unknown https://doi.org/10.1248/CPB.48.357
Madolin M 91864496 Click to see CC1=CCCC(=CC(CC(=CCC1)C)OC)C=O 248.36 unknown https://doi.org/10.1248/CPB.48.357
> Organoheterocyclic compounds / Azoles / Imidazoles
Allantoin 204 Click to see C1(C(=O)NC(=O)N1)NC(=O)N 158.12 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/BPB.23.1216
> Organoheterocyclic compounds / Azolidines / Imidazolidines / Hydantoins / Allantoins
(S)-(+)-allantoin 439714 Click to see 158.12 unknown https://doi.org/10.1248/BPB.23.1216
Allantoin, (-)- 439713 Click to see C1(C(=O)NC(=O)N1)NC(=O)N 158.12 unknown https://doi.org/10.1248/CPB.48.357
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
Uracil 1174 Click to see 112.09 unknown https://doi.org/10.1248/CPB.47.887
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(4Z,8Z,11S)-5,9-dimethyl-12-oxabicyclo[9.2.1]tetradeca-1(14),4,8-trien-13-one 101032442 Click to see 232.32 unknown https://doi.org/10.1248/CPB.48.357
Manshurolide 14527198 Click to see CC1=CCCC2=CC(CC(=CCC1)C)OC2=O 232.32 unknown https://doi.org/10.1248/CPB.48.357
> Organoheterocyclic compounds / Epoxides
(1R,2E,5R,7R,11R)-7,12,12-trimethyl-6-oxatricyclo[9.1.0.05,7]dodec-2-ene-3-carbaldehyde 163056184 Click to see 234.33 unknown https://doi.org/10.1248/CPB.48.357
(1R,4R,6R,9Z,11S,12S)-12-(hydroxymethyl)-4,12-dimethyl-5-oxatricyclo[9.1.0.04,6]dodec-9-ene-9-carbaldehyde 100974494 Click to see 250.33 unknown https://doi.org/10.1248/BPB.23.1216
https://doi.org/10.1248/CPB.47.887
Madolin A 10561685 Click to see CC1(C2C1C=C(CCC3C(O3)(CC2)C)C=O)C 234.33 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/BPB.23.1216
Madolin B 10562641 Click to see CC1(C2C1C=C(CCC3C(O3)(CC2)C)C(=O)O)C 250.33 unknown https://doi.org/10.1248/CPB.48.357
https://doi.org/10.1248/BPB.23.1216
> Organoheterocyclic compounds / Heteroaromatic compounds
3-[3-(5,5-Dimethylcyclohexen-1-yl)prop-2-enyl]furan 73185442 Click to see 216.32 unknown https://doi.org/10.1248/CPB.48.357
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
Adenine 190 Click to see C1=NC2=NC=NC(=C2N1)N 135.13 unknown https://doi.org/10.1248/BPB.23.1216
> Organoheterocyclic compounds / Indoles and derivatives / Indolecarboxylic acids and derivatives
Indole-3-carboxylic acid 69867 Click to see C1=CC=C2C(=C1)C(=CN2)C(=O)O 161.16 unknown https://doi.org/10.1248/CPB.47.887
Methyl indole-3-carboxylate 589098 Click to see 175.18 unknown https://doi.org/10.1248/BPB.23.1216
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
Csh 068 259676 Click to see 327.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Nicotinic Acid 938 Click to see 123.11 unknown https://doi.org/10.1248/CPB.46.1624
> Organoheterocyclic compounds / Tetrapyrroles and derivatives
methyl (3R,21S,22S)-16-ethenyl-11-ethyl-4-hydroxy-12,17,21,26-tetramethyl-22-[3-oxo-3-[(E,7S,11S)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate 136706892 Click to see 871.20 unknown https://doi.org/10.1248/CPB.46.1624
> Organoheterocyclic compounds / Tetrapyrroles and derivatives / Chlorins
methyl (3R,21S,22S)-16-ethenyl-11-ethyl-12,17,21,26-tetramethyl-4-oxo-22-[3-oxo-3-[(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaene-3-carboxylate 5459387 Click to see 871.20 unknown https://doi.org/10.1248/CPB.46.1624
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
Cinnamamide 5273472 Click to see C1=CC=C(C=C1)C=CC(=O)N 147.17 unknown https://doi.org/10.1248/CPB.46.1624
Cinnamic Acid Amide 12135 Click to see C1=CC=C(C=C1)C=CC(=O)N 147.17 unknown https://doi.org/10.1248/CPB.46.1624
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-cis-Feruloyl tyramine 6440659 Click to see 313.30 unknown https://doi.org/10.1248/CPB.48.357
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
22-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxydocosanoic acid 101088376 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCCCCCCCCCCCCCCCCCCCCCC(=O)O)O 532.80 unknown https://doi.org/10.1248/CPB.48.357
Methyl 4-hydroxy-3-methoxy-cinnamate 16830 Click to see 208.21 unknown https://doi.org/10.1248/BPB.23.1216
Methyl ferulate 5357283 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC)O 208.21 unknown https://doi.org/10.1248/BPB.23.1216
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Methyl 4-hydroxycinnamate 5319562 Click to see COC(=O)C=CC1=CC=C(C=C1)O 178.18 unknown https://doi.org/10.1248/BPB.23.1216
Methyl p-coumarate 92203 Click to see 178.18 unknown https://doi.org/10.1248/BPB.23.1216
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid 709 Click to see 194.18 unknown https://doi.org/10.1248/BPB.23.1216
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1248/BPB.23.1216
https://doi.org/10.1248/CPB.47.887
https://doi.org/10.1248/CPB.46.1624
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1248/CPB.47.887
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1248/BPB.23.1216
https://doi.org/10.1248/CPB.46.1624
https://doi.org/10.1248/CPB.48.357
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1248/BPB.23.1216
https://doi.org/10.1248/CPB.47.887
https://doi.org/10.1248/CPB.46.1624
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see 316.26 unknown https://doi.org/10.1248/CPB.47.887
https://doi.org/10.1248/BPB.23.1216
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1248/CPB.46.1624
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
Tiliroside 5320686 Click to see 594.50 unknown https://doi.org/10.1248/CPB.46.1624
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 125528541 Click to see 610.50 unknown https://doi.org/10.1016/S0031-9422(98)00223-4
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 154496792 Click to see 624.50 unknown https://doi.org/10.1248/CPB.48.357
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-3-(3,4,5-Trihydroxy-6-((3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxymethyl)Oxan-2-Yl)Oxychromen-4-One 12313332 Click to see 594.50 unknown https://doi.org/10.1016/S0031-9422(98)00028-4
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,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 154497089 Click to see 594.50 unknown https://doi.org/10.1016/S0031-9422(98)00223-4
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1248/CPB.46.1624
https://doi.org/10.1248/CPB.47.887
Isorhamnetin 3-galactoside 13245586 Click to see 478.40 unknown https://doi.org/10.1248/BPB.23.1216
Isorhamnetin 3-O-glucoside 5318645 Click to see 478.40 unknown https://doi.org/10.1248/BPB.23.1216
Isorhamnetin 3-robinobioside 6223069 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1248/BPB.23.1216
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown https://doi.org/10.1016/S0031-9422(98)00223-4
https://doi.org/10.1016/S0031-9422(98)00028-4
Narcissin 5481663 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1248/BPB.23.1216
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1016/S0031-9422(98)00223-4
https://doi.org/10.1016/S0031-9422(98)00028-4
Vitamin P 5293655 Click to see 610.50 unknown https://doi.org/10.1016/S0031-9422(98)00028-4
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
4-(beta-D-Glucopyranosyloxy)-3-methoxybenzoic acid 14132337 Click to see 330.29 unknown https://doi.org/10.1248/BPB.23.1216
8-methoxy-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphtho[2,1-g][1,3]benzodioxole-5-carboxylic acid 101948691 Click to see 474.40 unknown https://doi.org/10.1016/S0031-9422(98)00223-4
https://doi.org/10.1248/CPB.46.1624
Vanillic acid glucoside 14132336 Click to see 330.29 unknown https://doi.org/10.1248/BPB.23.1216

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