Corydalis solida - Unknown
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Details Top

Internal ID UUID644013b7a3dfe530513145
Scientific name Corydalis solida
Authority (L.) Clairv.
First published in Man. Herbor. Suisse : 371 (1811)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pseudofumaria minor (Roth) Borkh. Arch. Bot. (Leipzig) 1(2): 45 (1797)
Borckhausenia cava G.Gaertn., B.Mey. & Schreb. Oekon. Fl. Wetterau 3: 17 (1801)
Borckhausenia solida G.Gaertn., B.Mey. & Schreb. Oekon. Fl. Wetterau 3: 18 (1801)
Bulbocapnos digitatus Bernh. Linnaea 8: 469 (1833)
Bulbocapnos halleri Spach Hist. Nat. Vég. 7: 77 (1838)
Capnites digitata Dumort. Fl. Belg. : 117 (1827)
Capnites solida Fourr. Ann. Soc. Linn. Lyon , n.s., 16: 329 (1868)
Capnoides bulbosa (L.) Druce List Brit. Pl., ed. 2 5. 1928
Capnoides laxa (Fr.) Kuntze Revis. Gen. Pl. 1: 14 (1891)
Capnoides remota Kuntze Revis. Gen. Pl. 1: 14 (1891)
Capnoides solida (L.) Moench Methodus : 52 (1794)
Capnoides tenella (Ledeb. ex Nordm.) Kuntze Revis. Gen. Pl. 1: 15 (1891)
Corydalis bulbosa (L.) DC. Fl. Franç. , ed. 3, 4: 637 (1805)
Corydalis bulbosa f. multicaulis Morariu & B.Draghica Stud. Cerc. Biol., Biol. Veg. 32(1): 4. 1980
Corydalis depauperata Schur Verh. Mitth. Siebenbürg. Vereins Naturwiss. Hermannstadt 4: 51 (1853)
Corydalis digitata Pers. Syn. Pl. 2: 269 (1806)
Corydalis halleri (Willd.) Willd. Enum. Pl. : 740 (1809)
Corydalis laxa Fr. Summa Veg. Scand. : 145 (1845)
Corydalis tenella Ledeb. ex Nordm. Bull. Sci. Acad. Imp. Sci. Saint-Pétersbourg 2: 313 (1837)
Corydalis tenuis Schott, Nyman & Kotschy Analect. Bot. : 43 (1854)
Cryptoceras remotum Müll.Berol. Ann. Bot. Syst. 7: 91 (1868)
Fumaria bulbosa L. Sp. Pl. : 699 (1753)
Fumaria bulbosa var. solida L. Sp. Pl. 2: 699. 1753 [1 May 1753]
Fumaria digitata (Pers.) Lej. Fl. Spa 2: 89 (1813)
Fumaria halleri Willd. Fl. Berol. Prodr. : 229 (1787)
Fumaria minor Roth Tent. Fl. Germ. 1: 300 (1788)
Fumaria solida (L.) Mill. Gard. Dict. Abr. ed. 6 : s.p. (1771)
Corydalis solida var. hispida Cheshm. & Delip. God. Sofiisk. Univ. “Kliment Okhridski” Biol. Fak. 2, Bot. 88(4): 73 (1997)
Pistolochia feddeana Holub Folia Geobot. Phytotax. 8: 172 (1973)
Pistolochia bulbosa (L.) Soják Cas. Nár. Mus., Odd. Prír. 140: 128 (1972)
Pistolochia solida (L.) Bernh. Syst. Verz. Erf. : 74 (1800)
Corydalis bulbosa var. solida L.
Corydalis remota f. haitaoensis (Y.H.Chou & C.Q.Xu) C.Y.Wu & Z.Y.Su Acta Bot. Yunnan. 7(3): 269 1985

Common names Top

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Language Common/alternative name
English bird-in-a-bush
English spring fumewort
Belarusian чубатка шчыльная
Bulgarian плътногрудеста лисичина
Czech dymnivka plná
German finger-lerchensporn
German gefingerter lerchensporn
German fester lerchensporn
German vollwurz-lerchensporn
Estonian harilik lõokannus
Finnish pystykiurunkannus
French corydale à bulbe plein
fy helmblom
Hungarian ujjas keltike
Lithuanian paprastasis rūtenis
Latvian blīvais cīrulītis
Latvian hallera cīrulītis
Latvian parastais cīrulītis
Latvian blīvguma cīrulītis
Malayalam കോറിഡാലിസ് സോളിഡ
Norwegian Bokmål hagelerkespore
Dutch vingerhelmbloem
Polish kokorycz pełna
Russian Хохлатка плотная
Slovak chochlačka plná
Slovenian čvrsti petelinček
Swedish stor nunneört
Ukrainian Ряст Галлера
Ukrainian Ряст бульбистий
Ukrainian Ряст щільний
Ukrainian Ряст ущільнений
Chinese 实心延胡索

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Corydalis solida subsp. bracteosa (Batt. & Trab.) Greuter & Burdet Willdenowia 10: 231 (1980)
Corydalis solida subsp. densiflora (C.Presl) Hayek Repert. Spec. Nov. Regni Veg. Beih. 30(1): 364 1925
Corydalis solida subsp. incisa Lidén Notes Roy. Bot. Gard. Edinburgh 45: 351 (1988 publ. 1989)
Corydalis solida subsp. oligantha (Trinajstic) Greuter & Burdet Willdenowia 19: 38 (1989)
Corydalis solida subsp. slivenensis (Velen.) Hayek Repert. Spec. Nov. Regni Veg. Beih. 30(1): 364. 1925 (1925)

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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Begin at 20°C for 6 weeks, cool to 4°C for 6 weeks, then gradually increase to 10°C over 6 weeks. If no germination, the cycle is repeated.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.
allow to remain in same pot for 1st year

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Middle Asia
      • Kazakhstan
      • Tadzhikistan
      • Uzbekistan
    • Siberia
      • West Siberia
    • Western Asia
      • Lebanon-Syria
      • Turkey
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • North European Russia
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Great Britain
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • France
      • Sardegna
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000622894
UNII A7C81NP30H
Canadensys 7095
USDA Plants COSO6
Tropicos 24000746
INPN 92594
KEW urn:lsid:ipni.org:names:60454743-2
The Plant List kew-2739270
Plantarium 11366
Missouri Botanical Garden 280798
Open Tree Of Life 660432
NCBI Taxonomy 38914
NBN Atlas NBNSYS0000002778
Nature Serve 2.156175
IPNI 60454743-2
iNaturalist 55814
GBIF 5334208
Freebase /m/043pnvv
EPPO COYSO
EOL 481785
Elurikkus 3936
USDA GRIN 11634
Wikipedia Corydalis_solida

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 checklist of European butterfly larval foodplants Clarke HE Ecol Evol 07-Jan-2024
PMCID:PMC10771928
doi:10.1002/ece3.10834
PMID:38192903
Topographic depressions can provide climate and resource microrefugia for biodiversity Frei K, Vojtkó A, Farkas T, Erdős L, Barta K, E-Vojtkó A, Tölgyesi C, Bátori Z iScience 21-Oct-2023
PMCID:PMC10656275
doi:10.1016/j.isci.2023.108202
PMID:38026156
Berberine—A Promising Therapeutic Approach to Polycystic Ovary Syndrome in Infertile/Pregnant Women Ionescu OM, Frincu F, Mehedintu A, Plotogea M, Cirstoiu M, Petca A, Varlas V, Mehedintu C Life (Basel) 02-Jan-2023
PMCID:PMC9864590
doi:10.3390/life13010125
PMID:36676074
NMR-Based Chromatography Readouts: Indispensable Tools to “Translate” Analytical Features into Molecular Structures Seger C, Sturm S Cells 07-Nov-2022
PMCID:PMC9658744
doi:10.3390/cells11213526
PMID:36359922
The Appeal of Ethnobotanical Folklore Records: Medicinal Plant Use in Setomaa, Räpina and Vastseliina Parishes, Estonia (1888–1996) Sõukand R, Kalle R Plants (Basel) 13-Oct-2022
PMCID:PMC9611039
doi:10.3390/plants11202698
PMID:36297723
Antibacterial and Antifungal Alkaloids from Asian Angiosperms: Distribution, Mechanisms of Action, Structure-Activity, and Clinical Potentials Sulaiman M, Jannat K, Nissapatorn V, Rahmatullah M, Paul AK, de Lourdes Pereira M, Rajagopal M, Suleiman M, Butler MS, Break MK, Weber JF, Wilairatana P, Wiart C Antibiotics (Basel) 24-Aug-2022
PMCID:PMC9495154
doi:10.3390/antibiotics11091146
PMID:36139926
Anti-hepatitis B activities of Myanmar medicinal plants: a narrative review of current evidence Linn YH, Ei WW, Myint LM, Lwin KM Virusdisease 14-Jul-2021
PMCID:PMC8473485
doi:10.1007/s13337-021-00714-2
PMID:34631974
A review study on the anti-trichomonas activities of medicinal plants Hashemi N, Ommi D, Kheyri P, Khamesipour F, Setzer WN, Benchimol M Int J Parasitol Drugs Drug Resist 12-Feb-2021
PMCID:PMC7902805
doi:10.1016/j.ijpddr.2021.01.002
PMID:33610966
Contribution to the Orophilous Cushion-Like Vegetation of Central-Southern and Insular Greece Musarella CM, Brullo S, del Galdo GG Plants (Basel) 30-Nov-2020
PMCID:PMC7760968
doi:10.3390/plants9121678
PMID:33266088
Anti‐inflammatory and immune‐modulatory impacts of berberine on activation of autoreactive T cells in autoimmune inflammation Ehteshamfar S, Akhbari M, Afshari JT, Seyedi M, Nikfar B, Shapouri‐Moghaddam A, Ghanbarzadeh E, Momtazi‐Borojeni AA J Cell Mol Med 01-Nov-2020
PMCID:PMC7754052
doi:10.1111/jcmm.16049
PMID:33135395
Chinese medicinal plants for the potential management of high-altitude pulmonary oedema and pulmonary hypertension Wang T, Hou J, Xiao W, Zhang Y, Zhou L, Yuan L, Yin X, Chen X, Hu Y Pharm Biol 03-Sep-2020
PMCID:PMC8641673
doi:10.1080/13880209.2020.1804407
PMID:32883127
Phytochemical Composition and Antimicrobial Activity of Corydalis solida and Pseudofumaria lutea Zielińska S, Dziągwa-Becker M, Piątczak E, Jezierska-Domaradzka A, Brożyna M, Junka A, Kucharski M, Çiçek SS, Zidorn C, Matkowski A Molecules 07-Aug-2020
PMCID:PMC7464254
doi:10.3390/molecules25163591
PMID:32784618
Mesophication in temperate Europe: A dendrochronological reconstruction of tree succession and fires in a mixed deciduous stand in Białowieża Forest Spînu AP, Niklasson M, Zin E Ecol Evol 10-Jan-2020
PMCID:PMC6988544
doi:10.1002/ece3.5966
PMID:32015862
Dehydrocorydaline inhibits cell proliferation, migration and invasion via suppressing MEK1/2-ERK1/2 cascade in melanoma Hu H, Dong Z, Wang X, Bai L, Lei Q, Yang J, Li L, Li Q, Liu L, Zhang Y, Ji Y, Guo L, Liu Y, Cui H Onco Targets Ther 02-Jul-2019
PMCID:PMC6620435
doi:10.2147/OTT.S183558
PMID:31456643
Berberine: Botanical Occurrence, Traditional Uses, Extraction Methods, and Relevance in Cardiovascular, Metabolic, Hepatic, and Renal Disorders Neag MA, Mocan A, Echeverría J, Pop RM, Bocsan CI, Crişan G, Buzoianu AD Front Pharmacol 21-Aug-2018
PMCID:PMC6111450
doi:10.3389/fphar.2018.00557
PMID:30186157

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
(-)-Domesticine 76968988 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC5=C(C=C43)OCO5)O)OC 325.40 unknown https://doi.org/10.1055/S-2007-969652
17-Methoxy-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(19),2(6),7,12(20),13,16-hexaene-15,18-dione 21672156 Click to see CN1CCC2=CC3=C(C4=C5C(=CC1=C24)C(=O)C=C(C5=O)OC)OCO3 337.30 unknown https://doi.org/10.1055/S-2007-969652
2,10-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,9-diol 98369 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown https://doi.org/10.1135/CCCC19852299
2,9,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol 100020 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)O)OC 341.40 unknown https://doi.org/10.1055/S-2007-969652
Bulbocapnine 12441 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)OC)O)OCO3 325.40 unknown https://doi.org/10.1055/S-2007-969652
https://doi.org/10.1135/CCCC19852299
Corydine 10153 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)O)OC 341.40 unknown https://doi.org/10.1055/S-2007-969652
d-Bulbocapnine 9276 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)OC)O)OCO3 325.40 unknown https://doi.org/10.1135/CCCC19852299
Dehydroglaucine 398788 Click to see CN1CCC2=CC(=C(C3=C4C=C(C(=CC4=CC1=C23)OC)OC)OC)OC 353.40 unknown https://doi.org/10.1055/S-2007-969652
Glaucine 16754 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC 355.40 unknown https://doi.org/10.1055/S-2007-969652
Isoboldine 133323 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown https://doi.org/10.1135/CCCC19852299
https://doi.org/10.1055/S-2007-969652
Nandazurine 3084902 Click to see C[N+]1=C2C3=C(C4=CC5=C(C=C4C2=O)OCO5)C(=C(C=C3C=C1)OC)O 336.30 unknown https://doi.org/10.1055/S-2007-969652
Nantenine 197001 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC5=C(C=C43)OCO5)OC)OC 339.40 unknown https://doi.org/10.1139/V69-178
https://doi.org/10.1055/S-2007-969652
Oxonantenine 3084224 Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC5=C(C=C42)OCO5)OC 335.30 unknown https://doi.org/10.1055/S-2007-969652
Predicentrine 10042942 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)O 341.40 unknown https://doi.org/10.1055/S-2007-969652
> Alkaloids and derivatives / Aporphines / 4,5-dioxoaporphines
4H-Benzo(de)(1,3)benzodioxolo(5,6-g)quinoline-4,5(6H)-dione,1,2-dimethoxy-6-methyl- 156244 Click to see CN1C2=C3C(=CC(=C(C3=C4C=C5C(=CC4=C2)OCO5)OC)OC)C(=O)C1=O 365.30 unknown https://doi.org/10.1055/S-2007-969652
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
[1,3]Benzodioxolo[5,6-c]-1,3-dioxolo[4,5-i]phenanthridine-14-aceticacid, 13,14-dihydro-13-methyl-, (+)- 10430523 Click to see CN1C(C2=C(C=CC3=C2OCO3)C4=C1C5=CC6=C(C=C5C=C4)OCO6)CC(=O)O 391.40 unknown https://doi.org/10.1016/0031-9422(90)85070-V
2-[(23S)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-1(13),2,4(8),9,11,14(22),15,17(21)-octaen-23-yl]acetic acid 162918513 Click to see CN1C(C2=C(C=CC3=C2OCO3)C4=C1C5=CC6=C(C=C5C=C4)OCO6)CC(=O)O 391.40 unknown https://doi.org/10.1016/0031-9422(90)85070-V
Dihydrosanguinarine 124069 Click to see CN1CC2=C(C=CC3=C2OCO3)C4=C1C5=CC6=C(C=C5C=C4)OCO6 333.30 unknown https://doi.org/10.1055/S-2007-969652
> Alkaloids and derivatives / Phthalide isoquinolines
Bicuculline 10237 Click to see CN1CCC2=CC3=C(C=C2C1C4C5=C(C6=C(C=C5)OCO6)C(=O)O4)OCO3 367.40 unknown https://doi.org/10.1055/S-2007-969652
Capnoidine 120698 Click to see CN1CCC2=CC3=C(C=C2C1C4C5=C(C6=C(C=C5)OCO6)C(=O)O4)OCO3 367.40 unknown https://doi.org/10.1055/S-2007-969652
https://doi.org/10.1139/V69-178
Gnoscopine 4544 Click to see CN1CCC2=CC3=C(C(=C2C1C4C5=C(C(=C(C=C5)OC)OC)C(=O)O4)OC)OCO3 413.40 unknown https://doi.org/10.1139/V69-178
Noscapine 275196 Click to see CN1CCC2=CC3=C(C(=C2C1C4C5=C(C(=C(C=C5)OC)OC)C(=O)O4)OC)OCO3 413.40 unknown https://doi.org/10.1139/V69-178
> 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 https://doi.org/10.1021/JF9701897
(+)-Corypalmine 12304090 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)O)OC)C=C1)OC 341.40 unknown https://doi.org/10.1135/CCCC19852299
(+/-)-Corypalmine 185605 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)O)OC)C=C1)OC 341.40 unknown https://doi.org/10.1135/CCCC19852299
(+/-)-Isocorypalmine 10220 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)OC 341.40 unknown https://doi.org/10.1135/CCCC19852299
(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/10.1135/CCCC19852299
(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 https://doi.org/10.1135/CCCC19852299
(1R,11R,18S)-4,5,13,14-tetramethoxy-18-methyl-19-oxa-10-azapentacyclo[9.7.2.01,10.02,7.012,17]icosa-2,4,6,12(17),13,15-hexaen-18-ol 10971689 Click to see CC1(C2=C(C3COC14N3CCC5=CC(=C(C=C45)OC)OC)C(=C(C=C2)OC)OC)O 413.50 unknown https://doi.org/10.1139/V78-061
(R)-Canadine 443422 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown https://doi.org/10.1135/CCCC19852299
(S)-Canadine 21171 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown https://doi.org/10.1080/10575639608044911
https://doi.org/10.1021/JF9701897
https://doi.org/10.1135/CCCC19852299
(S)-Scoulerine 439654 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O 327.40 unknown https://doi.org/10.1135/CCCC19852299
https://doi.org/10.1002/CBDV.200890121
(S)-Tetrahydrocolumbamine 440229 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)OC 341.40 unknown https://doi.org/10.1135/CCCC19852299
2,9,10-trimethoxy-13-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-3-ol 5316090 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)O)OC 355.40 unknown https://doi.org/10.1135/CCCC19852299
4,5,13,14-Tetramethoxy-18-methyl-19-oxa-10-azapentacyclo[9.7.2.01,10.02,7.012,17]icosa-2,4,6,12(17),13,15-hexaen-18-ol 73089754 Click to see CC1(C2=C(C3COC14N3CCC5=CC(=C(C=C45)OC)OC)C(=C(C=C2)OC)OC)O 413.50 unknown https://doi.org/10.1139/V78-061
Benzo(g)-1,3-benzodioxolo(5,6-a)quinolizinium, 5,6-dihydro-9,10-dimethoxy-13-methyl- 148262 Click to see CC1=C2C=CC(=C(C2=C[N+]3=C1C4=CC5=C(C=C4CC3)OCO5)OC)OC 350.40 unknown https://doi.org/10.1135/CCCC19852299
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/10.1135/CCCC19852299
Bis(1,3)benzodioxolo(5,6-a:4',5'-g)quinolizinium, 6,7-dihydro-13-methyl- 147329 Click to see CC1=C2C=CC3=C(C2=C[N+]4=C1C5=CC6=C(C=C5CC4)OCO6)OCO3 334.30 unknown https://doi.org/10.1135/CCCC19852299
Canadine 34458 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown https://doi.org/10.1021/JF9701897
https://doi.org/10.1135/CCCC19852299
Cavidine 193148 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC5=C4OCO5)OC)OC 353.40 unknown https://doi.org/10.1055/S-2007-969652
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/10.1135/CCCC19852299
Corybulbine 10316181 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)O)OC 355.40 unknown https://doi.org/10.1135/CCCC19852299
Corydalin 326549 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC 369.50 unknown https://doi.org/10.1021/JF9701897
https://doi.org/10.1135/CCCC19852299
Corydaline 101301 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC 369.50 unknown https://doi.org/10.1135/CCCC19852299
https://doi.org/10.1139/V78-061
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/10.1135/CCCC19852299
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/10.1135/CCCC19852299
DL-Tetrahydropalmatine 5417 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown https://doi.org/10.1135/CCCC19852299
https://doi.org/10.1021/JF9701897
https://doi.org/10.4268/CJCMM20100118
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/10.1135/CCCC19852299
Scoulerine 22955 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O 327.40 unknown https://doi.org/10.1135/CCCC19852299
Stylopine 440583 Click to see C1CN2CC3=C(CC2C4=CC5=C(C=C41)OCO5)C=CC6=C3OCO6 323.30 unknown https://doi.org/10.1139/V78-061
https://doi.org/10.1021/JF9701897
https://doi.org/10.1135/CCCC19852299
Tetrahydrocoptisine 6770 Click to see C1CN2CC3=C(CC2C4=CC5=C(C=C41)OCO5)C=CC6=C3OCO6 323.30 unknown https://doi.org/10.1135/CCCC19852299
https://doi.org/10.1021/JF9701897
https://doi.org/10.1055/S-2007-969652
Tetrahydropalmatine 72301 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown https://doi.org/10.1021/JF9701897
https://doi.org/10.1135/CCCC19852299
https://doi.org/10.1080/14786410802496911
https://doi.org/10.1055/S-1999-14090
> 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://doi.org/10.1135/CCCC19852299
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-2007-969652
https://doi.org/10.1135/CCCC19852299
> Benzenoids / Indanes / Indanones
(1R,8'S)-7,8'-dihydroxy-6-methoxy-2-methylspiro[3,4-dihydroisoquinoline-1,7'-8H-cyclopenta[g][1,3]benzodioxole]-6'-one 162949474 Click to see CN1CCC2=CC(=C(C=C2C13C(C4=C(C3=O)C=CC5=C4OCO5)O)O)OC 369.40 unknown https://doi.org/10.1016/0031-9422(86)80104-2
Corpaine 442197 Click to see CN1CCC2=CC(=C(C=C2C13C(C4=C(C3=O)C=CC5=C4OCO5)O)O)OC 369.40 unknown https://doi.org/10.1016/0031-9422(86)80104-2
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one 10065647 Click to see COC1=C(C2=CN3CCC4=CC(=O)C(=CC4=C3C=C2C=C1)OC)OC 337.40 unknown https://doi.org/10.1135/CCCC19852299
Yuanamide 10362429 Click to see CC1=C2C3=CC(=C(C=C3CCN2C(=O)C4=C1C=CC(=C4OC)OC)OC)OC 381.40 unknown https://doi.org/10.1016/0031-9422(90)85070-V
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Dillenetin 5487855 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)OC 330.29 unknown https://doi.org/10.1016/0031-9422(86)80104-2
> Phenylpropanoids and polyketides / Stilbenes
5-[2-[6-[2-(Dimethylamino)ethyl]-1,3-benzodioxol-5-yl]-2-oxoacetyl]-1,3-benzodioxole-4-carboxylic acid 14191935 Click to see CN(C)CCC1=CC2=C(C=C1C(=O)C(=O)C3=C(C4=C(C=C3)OCO4)C(=O)O)OCO2 413.40 unknown https://doi.org/10.1055/S-2007-969652

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