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Corydalis yanhusuo

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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 UUID644013be33724648261056
Scientific name Corydalis yanhusuo
Authority (Y.H.Chou & Chun C.Hsu) W.T.Wang ex Z.Y.Su & C.Y.Wu
First published in Acta Bot. Yunnan. 7: 269 (1985)

Description Top

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Synonyms Top

Scientific name Authority First published in
Corydalis turtschaninovii f. yanhusuo Y.H.Chou & Chun C.Hsu Acta Phytotax. Sin. 15(2): 82 (1977)

Common names Top

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Language Common/alternative name
English yan hu suo
Japanese エンゴサク
Japanese 延胡索
lzh 延胡索
Dutch yan hu suo
Chinese 延胡索
Chinese 山延胡索
Chinese 元胡
Chinese 元胡索
Chinese 玄胡
Chinese 玄胡索

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000623057
UNII DX4V4VDT5J
Tropicos 24000814
KEW urn:lsid:ipni.org:names:929107-1
The Plant List kew-2739428
Open Tree Of Life 300823
NCBI Taxonomy 458692
IPNI 929107-1
iNaturalist 491317
GBIF 5531937
Freebase /m/010lw_pw
EOL 5474105
USDA GRIN 402560
Wikipedia Corydalis_yanhusuo
CMAUP NPO827

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
Chinese herbal medicine decreases incidence of hepatocellular carcinoma in diabetes mellitus patients with regular insulin management Lai HC, Cheng JC, Yip HT, Jeng LB, Huang ST World J Gastrointest Oncol 15-Mar-2024
PMCID:PMC10989382
doi:10.4251/wjgo.v16.i3.716
PMID:38577471
Traditional Chinese medicine treats ulcerative colitis by regulating gut microbiota, signaling pathway and cytokine: Future novel method option for pharmacotherapy Wang T, Liu X, Zhang W, Wang J, Wang T, Yue W, Ming L, Cheng J, Sun J Heliyon 06-Mar-2024
PMCID:PMC10945194
doi:10.1016/j.heliyon.2024.e27530
PMID:38501018
Efficacy and safety of Wuhu oral liquid in treating acute soft tissue injuries: a multicenter, randomized, double-blind, double-dummy, parallel-controlled trial Zhu WH, Shen Y, Xiao Y, Shi Q, Fan ZX, Feng YQ, Wan HB, Qu B, Zhao J, Zhang WQ, Xu GH, Wu XQ, Tang DZ Front Pharmacol 23-Feb-2024
PMCID:PMC10921885
doi:10.3389/fphar.2024.1335182
PMID:38464733
Usage Patterns of Traditional Chinese Medicine for Patients with Bipolar Disorder: A Population-Based Study in Taiwan Chen SP, Yang ST, Hu KC, Satyanarayanan SK, Su KP Healthcare (Basel) 18-Feb-2024
PMCID:PMC10888309
doi:10.3390/healthcare12040490
PMID:38391865
Extreme Reconfiguration of Plastid Genomes in Papaveraceae: Rearrangements, Gene Loss, Pseudogenization, IR Expansion, and Repeats Cao J, Wang H, Cao Y, Kan S, Li J, Liu Y Int J Mol Sci 14-Feb-2024
PMCID:PMC10888665
doi:10.3390/ijms25042278
PMID:38396955
Regulation of intestinal flora in patients with chronic atrophic gastritis by modified Chai Shao Liu Jun Zi decoction based on 16S rRNA sequencing Xing C, Liu Y, Wang S, Zhang J, Liu G, Li N, Leng Y, Ying D, Xu C Medicine (Baltimore) 09-Feb-2024
PMCID:PMC10860994
doi:10.1097/MD.0000000000037053
PMID:38335441
Three-tiered authentication of herbal traditional Chinese medicine ingredients used in women’s health provides progressive qualitative and quantitative insight Mück F, Scotti F, Mauvisseau Q, Thorbek BL, Wangensteen H, de Boer HJ Front Pharmacol 05-Feb-2024
PMCID:PMC10875096
doi:10.3389/fphar.2024.1353434
PMID:38375033
Metabolomics study of graphene nuangong acupoint plaster for primary dysmenorrhea Liu W, Zhang T, Hu Z, Li X, Wang F, Peng R Heliyon 01-Feb-2024
PMCID:PMC10847914
doi:10.1016/j.heliyon.2024.e25268
PMID:38327403
Acupoint herbal patching for postherpetic neuralgia: A systematic review and meta-analysis Pu B, Lu X, Yu P, Wang C, Li J, Yang D, Wang J Medicine (Baltimore) 26-Jan-2024
PMCID:PMC10817132
doi:10.1097/MD.0000000000037029
PMID:38277557
Modern pharmacological research and application of medicinal insect Coridius chinensis Xiong K, Zeng F, Lei X, Wei Y, Zhou X, Hou X Heliyon 13-Jan-2024
PMCID:PMC10830530
doi:10.1016/j.heliyon.2024.e24613
PMID:38304792
Mechanistic insights into the ameliorative effects of hypoxia-induced myocardial injury by Corydalis yanhusuo total alkaloids: based on network pharmacology and experiment verification Qi J, Li H, Yang Y, Sun X, Wang J, Han X, Chu X, Sun Z, Chu L Front Pharmacol 11-Jan-2024
PMCID:PMC10808789
doi:10.3389/fphar.2023.1275558
PMID:38273838
The CYP80A and CYP80G Are Involved in the Biosynthesis of Benzylisoquinoline Alkaloids in the Sacred Lotus (Nelumbo nucifera) Hao C, Yu Y, Liu Y, Liu A, Chen S Int J Mol Sci 05-Jan-2024
PMCID:PMC10815925
doi:10.3390/ijms25020702
PMID:38255776
Medicine for chronic atrophic gastritis: a systematic review, meta- and network pharmacology analysis Weng J, Wu XF, Shao P, Liu XP, Wang CX Ann Med 03-Jan-2024
PMCID:PMC10769149
doi:10.1080/07853890.2023.2299352
PMID:38170849
Haplotype-resolved genome assembly of Corydalis yanhusuo, a traditional Chinese medicine with unusual telomere motif Xu D, Ye Z, Huang Y, Zhu K, Xu H, Yu J, Feng Y, Zhao X, Wang L, Xu H, Li Q, Qin M, Tang Y, Zhang X, Zhao Y Hortic Res 02-Jan-2024
PMCID:PMC10894459
doi:10.1093/hr/uhad296
PMID:38404592
Blockade of spinal dopamine D1/D2 receptor heteromers by levo-Corydalmine suppressed calcium signaling cascade in spinal neurons to alleviate bone cancer pain in rats Ma XN, Yao CH, Yang YJ, Li X, Zhou MY, Yang J, Zhang S, Yu BY, Dai WL, Liu JH J Cancer 01-Jan-2024
PMCID:PMC10788731
doi:10.7150/jca.91129
PMID:38230224

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
(+/-)-Corydine 111119 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)O)OC 341.40 unknown via CMAUP database
(R)-5,6,6a,7-Tetrahydro-1,2,9,10-tetramethoxy-6-methyl-4H-dibenzo(de,g)quinoline 1078819 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC 355.40 unknown via CMAUP database
(R)-nantenine 46225255 Click to see CC(=O)C1=C(C2=C3C(CC4=CC5=C(C=C42)OCO5)N(CCC3=C1)C)C(=O)C 363.40 unknown via CMAUP database
(S)-nantenine 46225254 Click to see CC(=O)C1=C(C2=C3C(CC4=CC5=C(C=C42)OCO5)N(CCC3=C1)C)C(=O)C 363.40 unknown via CMAUP database
1,2,10-Trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-11-ol 48704 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC 341.40 unknown via CMAUP database
1,2,9,10-Tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline 10145 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC 355.40 unknown via CMAUP database
11,12-Dimethoxy-7-methyl-6,7,7a,8-tetrahydro-5h-[1,3]benzodioxolo[6,5,4-de]benzo[g]quinoline 273033 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)OC)OC)OCO3 339.40 unknown via CMAUP database
4,15,16-Trimethoxy-10-azatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadeca-1(16),2,4,6,13(17),14-hexaen-3-ol 5320211 Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)OC)OC)C=C1)O 327.40 unknown via CMAUP database
Boldine 2-methyl ether 16573 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC 341.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4158457/
Corytuberine, pentahydrate 347379 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC 327.40 unknown via CMAUP database
Dehydroglaucine 398788 Click to see CN1CCC2=CC(=C(C3=C4C=C(C(=CC4=CC1=C23)OC)OC)OC)OC 353.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263280/
Glaucine 16754 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC 355.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4158457/
https://doi.org/10.1248/CPB.33.5369
https://doi.org/10.1055/S-2006-962324
https://doi.org/10.1016/0031-9422(93)85312-F
Isocorydine 10143 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC 341.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4158457/
Litseglutine B 12016618 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)OC)O 341.40 unknown via CMAUP database
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
N-Methyllaurotetanine; NSC 247506; NSC 247564 631015 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC 341.40 unknown via CMAUP database
Nantenine 197001 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC5=C(C=C43)OCO5)OC)OC 339.40 unknown https://doi.org/10.1016/0031-9422(93)85312-F
Norglaucin 30835 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)OC)NCCC3=C1)OC 341.40 unknown https://doi.org/10.1016/0031-9422(93)85312-F
O-Methylbulbocapnine 10246564 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)OC)OC)OCO3 339.40 unknown via CMAUP database
Oxoglaucine 97662 Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC(=C(C=C42)OC)OC)OC 351.40 unknown https://doi.org/10.1016/J.JEP.2008.05.041
Thaliporphine 6992288 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)O)OC 341.40 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Hexahydrobenzophenanthridine alkaloids
Chelidonine, 13-methyl-, (14beta)- 56842002 Click to see CC12C(CC3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)O 367.40 unknown via CMAUP database
> Alkaloids and derivatives / Phthalide isoquinolines
6-[(5S)-6-methyl-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]-6H-furo[3,4-g][1,3]benzodioxol-8-one 6710622 Click to see CN1CCC2=CC3=C(C=C2C1C4C5=C(C6=C(C=C5)OCO6)C(=O)O4)OCO3 367.40 unknown via CMAUP database
Bicuculline 10237 Click to see CN1CCC2=CC3=C(C=C2C1C4C5=C(C6=C(C=C5)OCO6)C(=O)O4)OCO3 367.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(-)-Corydaline 638256 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC 369.50 unknown via CMAUP database
(+)-Corypalmine 12304090 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)O)OC)C=C1)OC 341.40 unknown via CMAUP database
(+)-Isocorypalmine 71261649 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)OC 341.40 unknown via CMAUP database
(+)-Xylopinine 1023518 Click to see COC1=C(C=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)OC)OC 355.40 unknown via CMAUP database
(+/-)-Isocorypalmine 10220 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)OC 341.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263280/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271193/
(13aR)-2,3,9,10-tetramethoxy-13-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline 5316092 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC 369.50 unknown https://doi.org/10.1055/S-2006-962324
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4158457/
https://doi.org/10.1055/S-2001-18853
(13aR)-3,10-dimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-2,9-diol 1152279 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O 327.40 unknown via CMAUP database
(13R)-2,3,9,10-tetramethoxy-13-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline 9864127 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC 369.50 unknown via CMAUP database
(13S)-2,3,9-trimethoxy-13-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-10-ol 11291216 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)O)OC)OC 355.40 unknown via CMAUP database
(R)-Canadine 443422 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown via CMAUP database
(R)-Corytenchine 101503694 Click to see COC1=C(C=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)O)OC 341.40 unknown via CMAUP database
(S)-Canadine 21171 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown via CMAUP database
(S)-Scoulerine 439654 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O 327.40 unknown via CMAUP database
(S)-Tetrahydrocolumbamine 440229 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)OC 341.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263280/
https://doi.org/10.1248/CPB.33.5369
https://doi.org/10.1055/S-2006-962324
16,17-Dimethoxy-6-tritio-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(13),2,4(8),9,14,16,18,20-octaene 10246509 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC 338.40 unknown via CMAUP database
24-Methyl-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.02,10.04,8.015,23.016,20]tetracosa-2,4(8),9,15(23),16(20),21-hexaene 5321847 Click to see CC1C2C3=CC4=C(C=C3CCN2CC5=C1C=CC6=C5OCO6)OCO4 337.40 unknown via CMAUP database
Berberine 2353 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC 336.40 unknown https://doi.org/10.1248/CPB.33.5369
beta-Norcoralydine 10653 Click to see COC1=C(C=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)OC)OC 355.40 unknown via CMAUP database
Canadine 34458 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown https://doi.org/10.1016/J.TALANTA.2008.12.002
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4158457/
CID 59819 59819 Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=CC(=C(C=C4C2)OC)O)O)OC 342.40 unknown via CMAUP database
Columbamine 72310 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)O)OC 338.40 unknown https://doi.org/10.1248/CPB.33.5369
Coptisine 72322 Click to see C1C[N+]2=C(C=C3C=CC4=C(C3=C2)OCO4)C5=CC6=C(C=C51)OCO6 320.30 unknown https://doi.org/10.1248/CPB.33.5369
Corybulbine 10316181 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)O)OC 355.40 unknown via CMAUP database
Corydalin 326549 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC 369.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263280/
Corydaline 101301 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC 369.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263280/
https://doi.org/10.1248/CPB.33.5369
https://doi.org/10.1055/S-2001-18853
https://doi.org/10.1055/S-2006-962324
Corydalmine 161665 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C(=C(C=C4)O)OC)OC 341.40 unknown via CMAUP database
Corypalmine 185605 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)O)OC)C=C1)OC 341.40 unknown via CMAUP database
Corytenchine 46919623 Click to see COC1=C(C=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)O)OC 341.40 unknown via CMAUP database
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
D-Tetrahydropalmatine 969488 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown https://doi.org/10.1248/CPB.33.5369
Dehydrocorybulbine 5316439 Click to see CC1=C2C=CC(=C(C2=C[N+]3=C1C4=CC(=C(C=C4CC3)O)OC)OC)OC 352.40 unknown via CMAUP database
Dehydrocorydaline 34781 Click to see CC1=C2C=CC(=C(C2=C[N+]3=C1C4=CC(=C(C=C4CC3)OC)OC)OC)OC 366.40 unknown https://doi.org/10.1055/S-2006-962324
https://doi.org/10.1248/CPB.33.5369
Dehydrocorydalmine 3083983 Click to see COC1=C(C=C2C(=C1)CC[N+]3=C2C=C4C=CC(=C(C4=C3)OC)O)OC 338.40 unknown https://doi.org/10.1093/CHROMSCI/48.6.441
Discretinine 11186895 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)O)OC)C=C1)OC 341.40 unknown via CMAUP database
DL-Tetrahydropalmatine 5417 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263280/
Epiberberine 160876 Click to see COC1=C(C=C2C(=C1)CC[N+]3=C2C=C4C=CC5=C(C4=C3)OCO5)OC 336.40 unknown https://doi.org/10.1016/J.JEP.2008.05.041
Jatrorrhizine 72323 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)O)OC)OC 338.40 unknown via CMAUP database
Kikemanin 5316093 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C(=C(C=C4)O)OC)OC 341.40 unknown via CMAUP database
Palmatine 19009 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)OC)OC 352.40 unknown https://doi.org/10.1248/CPB.33.5369
Phellodendrine 3081405 Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=CC(=C(C=C4C2)OC)O)O)OC 342.40 unknown via CMAUP database
Pseudoberberine 14707273 Click to see COC1=C(C=C2C=[N+]3CCC4=CC5=C(C=C4C3=CC2=C1)OCO5)OC.[Cl-] 371.80 unknown via CMAUP database
Pseudocoptisine 15520811 Click to see C1C[N+]2=CC3=CC4=C(C=C3C=C2C5=CC6=C(C=C51)OCO6)OCO4 320.30 unknown via CMAUP database
Pseudopalmatine 644002 Click to see COC1=C(C=C2C(=C1)CC[N+]3=CC4=CC(=C(C=C4C=C23)OC)OC)OC 352.40 unknown via CMAUP database
Scoulerine 22955 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O 327.40 unknown via CMAUP database
Stepharanine 10358881 Click to see COC1=C(C=C2C(=C1)CC[N+]3=C2C=C4C=CC(=C(C4=C3)OC)O)O 324.30 unknown via CMAUP database
Steponine 15432819 Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=C(C2)C(=C(C=C4)OC)O)OC)O 342.40 unknown via CMAUP database
Stylopin 697545 Click to see C1CN2CC3=C(CC2C4=CC5=C(C=C41)OCO5)C=CC6=C3OCO6 323.30 unknown via CMAUP database
Stylopine 440583 Click to see C1CN2CC3=C(CC2C4=CC5=C(C=C41)OCO5)C=CC6=C3OCO6 323.30 unknown via CMAUP database
Tetrahydrocoptisine 6770 Click to see C1CN2CC3=C(CC2C4=CC5=C(C=C41)OCO5)C=CC6=C3OCO6 323.30 unknown https://doi.org/10.1055/S-2006-962324
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245449/
Tetrahydrocorysamine 14315597 Click to see CC1C2C3=CC4=C(C=C3CCN2CC5=C1C=CC6=C5OCO6)OCO4 337.40 unknown via CMAUP database
Tetrahydropalmatine 72301 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263280/
Tetrahydropalmatine hydrochloride 6602555 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC.Cl 391.90 unknown via CMAUP database
Xylopinine 226520 Click to see COC1=C(C=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)OC)OC 355.40 unknown https://doi.org/10.1016/J.JEP.2008.05.041
Yuanhunine 128558 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)O)OC)OC 355.40 unknown via CMAUP database
> Alkaloids and derivatives / Protopine alkaloids
Allocryptopine 98570 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C(=C(C=C4)OC)OC)OCO3 369.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271193/
Corycavine 276145 Click to see CC1C2=C(CN(CCC3=CC4=C(C=C3C1=O)OCO4)C)C5=C(C=C2)OCO5 367.40 unknown via CMAUP database
Protopine 4970 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3 353.40 unknown https://doi.org/10.1055/S-2006-962324
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263280/
Pseudoprotopine 185559 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=CC5=C(C=C4C1)OCO5)OCO3 353.40 unknown via CMAUP database
> Alkaloids and derivatives / Rhoeadine alkaloids
(1R,11S,13S)-11,16,17-trimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.02,10.05,9.014,19]docosa-2(10),3,5(9),14,16,18-hexaene 12309553 Click to see CN1CCC2=CC(=C(C=C2C3C1C4=C(C(O3)OC)C5=C(C=C4)OCO5)OC)OC 399.40 unknown via CMAUP database
> Benzenoids / Anthracenes
Palmidin A 5320384 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C5=C(C(=CC=C5)O)C(=O)C6=C4C=C(C=C6O)CO)C=C(C=C3O)O 510.50 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,3,5-Trihydroxy-9,10-dioxoanthracene-2-carbaldehyde 5320212 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=CC(=C(C(=C3C2=O)O)C=O)O 284.22 unknown via CMAUP database
> Benzenoids / Indanes / Indanones
Isocrotonylpterosin B 5318536 Click to see CC=CC(=O)OCCC1=C(C2=C(CC(C2=O)C)C=C1C)C 286.40 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthols and derivatives
Stypandrol 188516 Click to see CC1=CC2=C(C(=C(C=C2)C3=C(C4=C(C=C3)C=C(C(=C4O)C(=O)C)C)O)O)C(=C1C(=O)C)O 430.40 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
(S,S)-tramadol(1+) 6919029 Click to see C[NH+](C)CC1CCCCC1(C2=CC(=CC=C2)OC)O 264.38 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3aS,6aR,9aR,9bR)-3,6,9-trimethylidene-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one 11673075 Click to see C=C1CCC2C(C3C1CCC3=C)OC(=O)C2=C 230.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
Corchorozide A 56840797 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)O 534.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1016/0031-9422(93)85312-F
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / D-alpha-amino acids
(R)-2-Amino-4-(aminooxy)butanoic acid 10176161 Click to see C(CON)C(C(=O)O)N 134.13 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron 21883788 Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-] 116.07 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
2-[(1R,2S,3R,4R,5S,6R)-3-(diaminomethylideneamino)-4-[(2R,5S)-3-[(3S,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-(methylamino)oxan-2-yl]-4-formyl-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2,5,6-trihydroxycyclohexyl]guanidine 11968896 Click to see CNC1C(C(C(OC1C2C(OC(C2(C=O)O)CO)OC3C(C(C(C(C3O)O)N=C(N)N)O)N=C(N)N)CO)O)O 581.60 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
5-(3,4-Methylenedioxyphenyl)pentanoic acid 5321853 Click to see C1OC2=C(O1)C=C(C=C2)CCCCC(=O)O 222.24 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
2,2-Dimethyl-5,7-dimethoxy-6-(1-methoxyethyl)-2H-1-benzopyran 5319700 Click to see CC(C1=C(C=C2C(=C1OC)C=CC(O2)(C)C)OC)OC 278.34 unknown via CMAUP database
> Organoheterocyclic compounds / Dibenzazecins
7,8-Dimethoxy-12-methyl-17,19-dioxa-12-azatetracyclo[12.7.0.04,9.016,20]henicosa-1(21),4(9),5,7,14,16(20)-hexaen-2-one 163090641 Click to see CN1CCC2=C(CC(=O)C3=CC4=C(C=C3C1)OCO4)C=CC(=C2OC)OC 369.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263280/
> Organoheterocyclic compounds / Dihydrofurans
Tetrahydrocyperaquinone 5321848 Click to see CC1COC2=C1C(=O)C3=C(C2=O)OC(C3)C(=C)C 246.26 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
Yuehchukene 126009 Click to see CC1=CC2C(C(C3=C2C4=CC=CC=C4N3)C5=CNC6=CC=CC=C65)C(C1)(C)C 366.50 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives
Corydamine 5316094 Click to see CNCCC1=CC2=C(C=C1C3=NC=C4C(=C3)C=CC5=C4OCO5)OCO2 350.40 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(R)-Reticuline 440586 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
2,9,10-Trimethoxy-13-methyl-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one 72715158 Click to see CC1=C2C=CC(=C(C2=CN3C1=C4C=C(C(=O)C=C4CC3)OC)OC)OC 351.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245449/
8-Oxocoptisine 5245667 Click to see C1CN2C(=CC3=C(C2=O)C4=C(C=C3)OCO4)C5=CC6=C(C=C51)OCO6 335.30 unknown via CMAUP database
Noroxyhydrastinine 89047 Click to see C1CNC(=O)C2=CC3=C(C=C21)OCO3 191.18 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
2,9,10-Trimethoxy-4a,8,11,13a-tetrahydro-5H-isoquinolino[2,3-a]quinolin-3-ol 3083926 Click to see COC1=C(CC2=CN3C4C=C(C(=CC4CC=C3C=C2C1)O)OC)OC 341.40 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(1R,8'S)-6,7-dimethoxy-2-methyl-spiro[3,4-dihydroisoquinoline-1,7'-6,8-dihydrocyclopenta[g][1,3]benzodioxole]-8'-ol 442236 Click to see CN1CCC2=CC(=C(C=C2C13CC4=C(C3O)C5=C(C=C4)OCO5)OC)OC 369.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Plantalloside 13962915 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
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
2-[(8S)-2-oxo-8,9-dihydrofuro[2,3-h]chromen-8-yl]propan-2-yl (Z)-2-methylbut-2-enoate 53399217 Click to see CC=C(C)C(=O)OC(C)(C)C1CC2=C(O1)C=CC3=C2OC(=O)C=C3 328.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Corylidin 5316096 Click to see CC1(C(C(C2=C(O1)C=C3C(=C2)C4=C(C5=C(O4)C=C(C=C5)O)C(=O)O3)O)O)C 368.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Leonticine 12314123 Click to see CN(C)CCC1=C(C(=C(C=C1)OC)O)C=CC2=CC=C(C=C2)OC 327.40 unknown via CMAUP database

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