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Aristolochia manshuriensis

Aristolochia manshuriensis - 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 UUID64400a9f51707707288140
Scientific name Aristolochia manshuriensis
Authority Kom.
First published in Trudy Imp. S.-Peterburgsk. Bot. Sada 22: 112 (1904)

Description Top

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Synonyms Top

Scientific name Authority First published in
Hocquartia manshuriensis (Kom.) Nakai Fl. Sylv. Kor. 21: 27 (1936)
Isotrema manshuriensis (Kom.) H.Huber Mitt. Bot. Staatssamml. München 3: 550 1960

Common names Top

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Language Common/alternative name
Bulgarian манджурска вълча ябълка
Czech podražec mandžuský
Korean 등칡
Lithuanian mandžiūrinė kartuolė
Polish kokornak mandżurski
Russian кирказон маньчжурский
Russian кирказон манчжурский
Chinese 关木通
Chinese 木通馬兜铃
Chinese 东北马兜铃
Chinese 八月札
Chinese 木通根
Chinese 马木通
Chinese 恺木香
Chinese 东北木通
Chinese 木通马兜铃*(东北马兜铃、关木通）
Chinese 木通马兜铃
Chinese 木通
Chinese 万年藤

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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No forms added yet.

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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Manchuria
    • Eastern Asia
      • Korea
    • Russian Far East
      • Primorye

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000548038
UNII JT0WP9ML3G
Tropicos 2500345
KEW urn:lsid:ipni.org:names:93111-1
The Plant List kew-2651629
Missouri Botanical Garden 241860
Open Tree Of Life 656376
NCBI Taxonomy 158555
IPNI 93111-1
iNaturalist 501104
GBIF 3588911
Freebase /m/0nbh990
EPPO ARPMA
USDA GRIN 4100
CMAUP NPO18443

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
Growing attention on the toxicity of Chinese herbal medicine: a bibliometric analysis from 2013 to 2022 Zhu KX, Wu M, Bian ZL, Han SL, Fang LM, Ge FF, Wang XZ, Xie SF Front Pharmacol 01-Feb-2024
PMCID:PMC10867220
doi:10.3389/fphar.2024.1293468
PMID:38362153
Traditional Chinese medicine Zhusha Anshen Wan: protective effects on liver, kidney, and intestine of the individual drugs using 1H NMR metabolomics Wang D, Yu C, Liu B, Wang H Front Pharmacol 29-Jan-2024
PMCID:PMC10871036
doi:10.3389/fphar.2024.1353325
PMID:38370476
Natural Substances vs. Approved Drugs in the Treatment of Main Cardiovascular Disorders—Is There a Breakthrough? Grujić-Milanović J, Rajković J, Milanović S, Jaćević V, Miloradović Z, Nežić L, Novaković R Antioxidants (Basel) 07-Dec-2023
PMCID:PMC10740850
doi:10.3390/antiox12122088
PMID:38136208
Biosynthesis of Functional Silver Nanoparticles Using Callus and Hairy Root Cultures of Aristolochia manshuriensis Yugay YA, Sorokina MR, Grigorchuk VP, Rusapetova TV, Silant’ev VE, Egorova AE, Adedibu PA, Kudinova OD, Vasyutkina EA, Ivanov VV, Karabtsov AA, Mashtalyar DV, Degtyarenko AI, Grishchenko OV, Kumeiko VV, Bulgakov VP, Shkryl YN J Funct Biomater 01-Sep-2023
PMCID:PMC10532211
doi:10.3390/jfb14090451
PMID:37754865
Enhanced Production of Nitrogenated Metabolites with Anticancer Potential in Aristolochia manshuriensis Hairy Root Cultures Shkryl YN, Tchernoded GK, Yugay YA, Grigorchuk VP, Sorokina MR, Gorpenchenko TY, Kudinova OD, Degtyarenko AI, Onishchenko MS, Shved NA, Kumeiko VV, Bulgakov VP Int J Mol Sci 08-Jul-2023
PMCID:PMC10379662
doi:10.3390/ijms241411240
PMID:37511000
Horizon scan of DNA-based methods for quality control and monitoring of herbal preparations Raclariu-Manolică AC, Mauvisseau Q, de Boer HJ Front Pharmacol 03-May-2023
PMCID:PMC10193163
doi:10.3389/fphar.2023.1179099
PMID:37214460
Isolation of oleanolic acid from Clematis armandii for differentiation it from adulterants by HPTLC/HPLC Ha Minh H, Huynh Ngoc Thuy T, Tran Viet H Heliyon 13-Apr-2023
PMCID:PMC10133656
doi:10.1016/j.heliyon.2023.e15008
PMID:37123914
Prostaglandin F2α Regulates Adipogenesis by Modulating Extracellular Signal-Regulated Kinase Signaling in Graves’ Ophthalmopathy Zhu R, Wang XH, Wang BW, Ouyang X, You YY, Xie HT, Zhang MC, Jiang FG Int J Mol Sci 10-Apr-2023
PMCID:PMC10138945
doi:10.3390/ijms24087012
PMID:37108173
DNA barcoding in herbal medicine: Retrospective and prospective Chen S, Yin X, Han J, Sun W, Yao H, Song J, Li X J Pharm Anal 05-Apr-2023
PMCID:PMC10257146
doi:10.1016/j.jpha.2023.03.008
PMID:37305789
De novo Assembly and Comparative Analyses of Mitochondrial Genomes in Piperales Yu R, Chen X, Long L, Jost M, Zhao R, Liu L, Mower JP, dePamphilis CW, Wanke S, Jiao Y Genome Biol Evol 10-Mar-2023
PMCID:PMC10036691
doi:10.1093/gbe/evad041
PMID:36896589
Gut microbiota: The key to the treatment of metabolic syndrome in traditional Chinese medicine – a case study of diabetes and nonalcoholic fatty liver disease Bao Y, Han X, Liu D, Tan Z, Deng Y Front Immunol 23-Dec-2022
PMCID:PMC9816483
doi:10.3389/fimmu.2022.1072376
PMID:36618372
Safety of prescribed herbal medicines for hepatic and renal function of polypharmacy patients with stroke: A single-center retrospective study Kim J, Jang W Medicine (Baltimore) 02-Dec-2022
PMCID:PMC9726389
doi:10.1097/MD.0000000000032147
PMID:36482592
Advancements and future prospective of DNA barcodes in the herbal drug industry Mahima K, Sunil Kumar KN, Rakhesh KV, Rajeswaran PS, Sharma A, Sathishkumar R Front Pharmacol 21-Oct-2022
PMCID:PMC9635000
doi:10.3389/fphar.2022.947512
PMID:36339543
Promising effects of herbal compounds against strongyloidiasis: a systematic review Soleimani A, Keivani N, Lotfipour S, Abolhasani S, Valizadeh S, Behniafar H J Parasit Dis 21-Sep-2022
PMCID:PMC9606197
doi:10.1007/s12639-022-01532-z
PMID:36457765
Mutational signature and clonal relatedness of recurrent urothelial carcinomas with aristolochic acid Zhu J, Ai Q, Cheng Q, Shen D, Dong Z, Li J, Shen D, Wang W, Zhang X, Li H Front Oncol 14-Sep-2022
PMCID:PMC9516318
doi:10.3389/fonc.2022.990023
PMID:36185218

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
16-Hydroxy-4,15-dimethoxy-10-methyl-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1,4,7,9(17),13,15-hexaene-3,6-dione 162843626 Click to see CN1CCC2=CC(=C(C3=C4C(=CC1=C23)C(=O)C=C(C4=O)OC)O)OC 339.30 unknown https://doi.org/10.1021/NP0301238
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 via CMAUP database
Magnoflorine iodide, (+)-(RG) 131664584 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)[O-])OC)C.I 469.30 unknown via CMAUP database
> Alkaloids and derivatives / Aristolactams
Aristolactam AII 148657 Click to see COC1=C(C=C2C3=C1C4=CC=CC=C4C=C3NC2=O)O 265.26 unknown https://doi.org/10.1021/NP0301238
Aristolactam AIIIa 10356352 Click to see COC1=C(C=C2C3=C(C=C4C=CC(=CC4=C31)O)NC2=O)O 281.26 unknown https://doi.org/10.1016/J.BMCL.2010.01.018
Aristolactam BII 162739 Click to see COC1=C(C2=C3C(=C1)C(=O)NC3=CC4=CC=CC=C42)OC 279.29 unknown https://doi.org/10.1248/CPB.39.1310
Aristolactam II 148745 Click to see C1OC2=C(O1)C3=C4C(=C2)C(=O)NC4=CC5=CC=CC=C53 263.25 unknown https://doi.org/10.1248/CPB.39.1310
Aristololactam 96710 Click to see COC1=CC=CC2=C3C4=C(C=C21)NC(=O)C4=CC5=C3OCO5 293.27 unknown https://doi.org/10.1248/CPB.39.1310
Manshurienine B 46232738 Click to see C1OC2=C(O1)C3=C4C=CC=C(C4=CC5=C3C(=C2)C(=O)N5)OC6C(C(C(C(O6)CO)O)O)O 441.40 unknown https://doi.org/10.1016/J.BMCL.2010.01.018
> 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/10.1021/NP0301238
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Methyl vanillate 19844 Click to see COC1=C(C=CC(=C1)C(=O)OC)O 182.17 unknown https://doi.org/10.1021/NP0301238
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1021/NP0301238
> Benzenoids / Naphthalenes / Naphthoquinones
2H-Naphtho[1,8-bc]furan-6,7-dione, 3-hydroxy-2,2,5,8-tetramethyl- 621021 Click to see CC1=CC(=C2C3=C1C(=O)C(=O)C(=C3OC2(C)C)C)O 258.27 unknown https://doi.org/10.1021/NP0301238
> Benzenoids / Phenanthrenes and derivatives
2-(8-Methoxy-6-nitronaphtho[2,1-g][1,3]benzodioxol-5-yl)acetic acid 5316406 Click to see COC1=CC=CC2=C3C(=C(C=C21)[N+](=O)[O-])C(=CC4=C3OCO4)CC(=O)O 355.30 unknown https://doi.org/10.1007/978-1-4615-8819-1_17
https://doi.org/10.1021/NP50024A001
Aristolamide 53320351 Click to see COC1=CC=CC2=C1C=CC3=C2C4=C(C=C3C(=O)N)OCO4 295.29 unknown via CMAUP database
Aristolamide Ii 51346765 Click to see C1OC2=C(O1)C3=C(C=CC4=CC=CC=C43)C(=C2)C(=O)N 265.26 unknown via CMAUP database
Demethylaristofolin E 11780432 Click to see C1OC2=C(O1)C3=C(C=CC4=CC=CC=C43)C(=C2)C(=O)O 266.25 unknown https://doi.org/10.1021/NP0301238
Methyl aristolate 160246 Click to see COC1=CC=CC2=C1C=CC3=C2C4=C(C=C3C(=O)OC)OCO4 310.30 unknown via CMAUP database
Methyl naphtho[2,1-g][1,3]benzodioxole-5-carboxylate 85779428 Click to see COC(=O)C1=CC2=C(C3=C1C=CC4=CC=CC=C43)OCO2 280.27 unknown https://doi.org/10.1021/NP0301238
Naphtho(2,1-g)(1,3)benzodioxole-5-carboxylic acid, 8,10-dimethoxy-, methyl ester 182432 Click to see COC1=CC2=C(C=CC3=C2C4=C(C=C3C(=O)OC)OCO4)C(=C1)OC 340.30 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Aristolochic acids and derivatives
Ariskanin A 5320068 Click to see COC1=C(C2=C(C(=C1)C(=O)OC)C(=CC3=CC=CC=C32)[N+](=O)[O-])OC 341.30 unknown via CMAUP database
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/10.1016/S0378-8741(98)00123-8
https://doi.org/10.1021/NP0301238
https://doi.org/10.1007/S10600-011-9794-7
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 via CMAUP database
Aristolochic acid d 161218 Click to see COC1=CC(=CC2=C3C(=C(C=C12)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O)O 357.30 unknown via CMAUP database
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 via CMAUP database
Aristolochic acid II 108168 Click to see C1OC2=C(O1)C3=C(C(=C2)C(=O)O)C(=CC4=CC=CC=C43)[N+](=O)[O-] 311.24 unknown https://doi.org/10.1021/NP0301238
https://doi.org/10.1007/S10600-011-9794-7
https://doi.org/10.1016/S0378-8741(98)00123-8
Aristolochic acid II methyl ester 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/10.1021/NP0301238
Aristolochic acid IV 167493 Click to see COC1=CC2=C3C(=C(C=C2C(=C1)OC)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O 371.30 unknown https://doi.org/10.1021/NP50024A001
https://doi.org/10.1007/978-1-4615-8819-1_17
https://doi.org/10.1007/S10600-011-9794-7
Aristolochic acid IV methyl ester 176931 Click to see COC1=CC2=C3C(=C(C=C2C(=C1)OC)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)OC 385.30 unknown https://doi.org/10.1021/NP0301238
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
12,14-Dimethoxy-3,5-dioxa-10-azapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(19),2(6),7,11,13(18),14,16-heptaen-9-one 14804089 Click to see COC1=CC=CC2=C1C(=C3C4=C2C5=C(C=C4C(=O)N3)OCO5)OC 323.30 unknown https://doi.org/10.1021/NP0301238
> Benzenoids / Phenols / Methoxyphenols
N-Trans-feruloyltramine 5280537 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoalkylglycerols
3-Octacosoxypropane-1,2-diol 139785015 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCOCC(CO)O 484.80 unknown https://doi.org/10.1007/S10600-011-9794-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
Isobicyclogermacral 13818876 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C=O 218.33 unknown via CMAUP database
Isobicyclogermacrenal 129685966 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C=O 218.33 unknown https://doi.org/10.1016/S0031-9422(00)81852-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aS,6bR,10S,12aR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 10416408 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 618.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,9R,10S,12aR,14bR)-10-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 53487826 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Cauloside A 441928 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)O)C)C)C2C1)C)C(=O)O)C 604.80 unknown via CMAUP database
Hederagenin 73299 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Oleanolic Acid (Caryophyllin) 49867939 Click to see CC1(CC2C(CCC3(C2=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(C1)C(=O)O)C 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
16-(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 53399246 Click to see CCC(CCC(C)C1CC2C3CC=C4CC(CCC4(C3CCC2(C1)C)C)O)C(C)C 414.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8R,9R,10S,13R,14R,17R)-17-[(E,2R,5R)-5-ethyl-6-methylhept-3-en-2-yl]-3,10,13-trimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene 50930798 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)C)C)C)C(C)C 410.70 unknown via CMAUP database
(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/10.1021/NP0301238
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/10.1007/S10600-011-9794-7
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/S10600-011-9794-7
6-Hydroxystigmast-4-en-3-one 71307329 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C 428.70 unknown https://doi.org/10.1007/S10600-011-9794-7
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/10.1021/NP0301238
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/10.1007/S10600-011-9794-7
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/10.1007/S10600-011-9794-7
> Organic acids and derivatives / Keto acids and derivatives / Alpha-keto acids and derivatives
2-(4-Methoxycyclohexa-1,3-dien-1-yl)-2-oxoacetic acid 29927927 Click to see COC1=CC=C(CC1)C(=O)C(=O)O 182.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Aristomanoside 11028762 Click to see COC1=C(C=CC(=C1)CCNC(=O)C=CC2=CC(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)OC)OC4C(C(C(C(O4)CO)O)O)O 667.70 unknown https://doi.org/10.1021/NP0301238
> 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 CC1=CCCC2=CC(CC(=CCC1)C)OC2=O 232.32 unknown https://doi.org/10.1016/0031-9422(90)80062-L
Manshurolide 14527198 Click to see CC1=CCCC2=CC(CC(=CCC1)C)OC2=O 232.32 unknown https://doi.org/10.1016/0031-9422(90)80062-L
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Pyridinones
Aristopyridinone A 53322330 Click to see C1=CC(=CC=C1CCC2=C(C=CNC2=O)CO)O 245.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-trans-feruloylmethoxytyramine 5352115 Click to see COC1=C(C=CC(=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)OC)O 343.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
cis-N-p-coumaroyltyramine 13939145 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown via CMAUP database
Paprazine 5372945 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown https://doi.org/10.1021/NP0301238
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1007/S10600-011-9794-7
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1021/NP0301238
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1021/NP0301238
https://doi.org/10.1007/S10600-011-9794-7
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Aristoloside 128576 Click to see COC1=CC(=CC2=C3C(=C(C=C12)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O)OC5C(C(C(C(O5)CO)O)O)O 519.40 unknown https://doi.org/10.1021/NP0301238
https://doi.org/10.1007/978-1-4615-8819-1_17
https://doi.org/10.1021/NP50024A001

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