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Corydalis ternata

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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 UUID644013ba66efc676844445
Scientific name Corydalis ternata
Authority (Nakai) Nakai
First published in Bot. Mag. (Tokyo) 28: 29 (1914)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 三裂延胡索

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000622960
Tropicos 50154449
KEW urn:lsid:ipni.org:names:672538-1
Open Tree Of Life 7591082
NCBI Taxonomy 2902606
IPNI 672538-1
iNaturalist 493385
GBIF 7314820
Elurikkus 587397
USDA GRIN 423647
CMAUP NPO25345

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
In Vivo Genotoxicity Evaluation of a No-Pain Pharmacopuncture Extract Using the Micronucleus Test Hwang JH, Jung C J Pharmacopuncture 31-Dec-2023
PMCID:PMC10739474
doi:10.3831/KPI.2023.26.4.366
PMID:38162468
GC-MS/MS Method for Determination of Polycyclic Aromatic Hydrocarbons in Herbal Medicines Park J, Kim K, Ryu D, Whang JH, Mah JH Molecules 02-May-2023
PMCID:PMC10179879
doi:10.3390/molecules28093853
PMID:37175264
Phytochemicals as alternative fungicides for controlling plant diseases: A comprehensive review of their efficacy, commercial representatives, advantages, challenges for adoption, and possible solutions Deresa EM, Diriba TF Heliyon 17-Feb-2023
PMCID:PMC9984788
doi:10.1016/j.heliyon.2023.e13810
PMID:36879959
Extensive reorganization of the chloroplast genome of Corydalis platycarpa: A comparative analysis of their organization and evolution with other Corydalis plastomes Raman G, Nam GH, Park S Front Plant Sci 09-Dec-2022
PMCID:PMC10115153
doi:10.3389/fpls.2022.1043740
PMID:37090468
Evaluation of Genotoxicity of SU-Eohyeol Pharmacopuncture Using an In Vitro Chromosome Aberration Test in Chinese Hamster Lung Cell Ku J, Hwang JH J Pharmacopuncture 30-Sep-2022
PMCID:PMC9510136
doi:10.3831/KPI.2022.25.3.290
PMID:36186089
A Comprehensive Review on the Chemical Properties, Plant Sources, Pharmacological Activities, Pharmacokinetic and Toxicological Characteristics of Tetrahydropalmatine Du Q, Meng X, Wang S Front Pharmacol 26-Apr-2022
PMCID:PMC9086320
doi:10.3389/fphar.2022.890078
PMID:35559252
East Asian Herbal Medicine to Reduce Primary Pain and Adverse Events in Cancer Patients : A Systematic Review and Meta-Analysis With Association Rule Mining to Identify Core Herb Combination Jo HG, Seo J, Choi S, Lee D Front Pharmacol 17-Jan-2022
PMCID:PMC8802093
doi:10.3389/fphar.2021.800571
PMID:35111066
Pharmacodynamic Evaluation of the Gexia Zhuyu Decoction in the Treatment of NAFLD and the Molecular Mechanism Underlying the TRPM4 Pathway Regulation Zhao YW, Yang J, Niu J, Wang T, Liang XD, Ren Y, Wang R Evid Based Complement Alternat Med 30-Nov-2021
PMCID:PMC8651363
doi:10.1155/2021/3364579
PMID:34887931
Herbal drugs and natural bioactive products as potential therapeutics: A review on pro-cognitives and brain boosters perspectives Halder S, Anand U, Nandy S, Oleksak P, Qusti S, Alshammari EM, El-Saber Batiha G, Koshy EP, Dey A Saudi Pharm J 15-Jul-2021
PMCID:PMC8363108
doi:10.1016/j.jsps.2021.07.003
PMID:34408548
Role of natural products in mitigation of toxic effects of methamphetamine: A review of in vitro and in vivo studies Moshiri M, Roohbakhsh A, Talebi M, Iranshahy M, Etemad L Avicenna J Phytomed 01-Jul-2020
PMCID:PMC7430958
PMID:32850291
Determination of Selected Isoquinoline Alkaloids from Mahonia aquifolia; Meconopsis cambrica; Corydalis lutea; Dicentra spectabilis; Fumaria officinalis; Macleaya cordata Extracts by HPLC-DAD and Comparison of Their Cytotoxic Activity Petruczynik A, Plech T, Tuzimski T, Misiurek J, Kaproń B, Misiurek D, Szultka-Młyńska M, Buszewski B, Waksmundzka-Hajnos M Toxins (Basel) 02-Oct-2019
PMCID:PMC6832497
doi:10.3390/toxins11100575
PMID:31581717
Neuroprotective Potential of Secondary Metabolites from Melicope lunu-ankenda (Rutaceae) Abdulwanis Mohamed Z, Mohamed Eliaser E, Mazzon E, Rollin P, Cheng Lian Ee G, Abdull Razis AF Molecules 27-Aug-2019
PMCID:PMC6749319
doi:10.3390/molecules24173109
PMID:31461914
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
Shaofu Zhuyu decoction ameliorates obesity-mediated hepatic steatosis and systemic inflammation by regulating metabolic pathways Hong M, Jung J, Park HS, Lee SM, Jeong NJ, Kim SH, Lee KW, Lee JA, Kim MS PLoS One 01-Jun-2017
PMCID:PMC5453538
doi:10.1371/journal.pone.0178514
PMID:28570676
<I>Untersuchungen über koreanische Corydalis-Knolle. I</I>. Jo Go Pharmaceutical Society of Japan 20-Apr-2017
doi:10.1248/YAKUSHI1881.49.9_801

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 / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
Crinamine,6-methoxy- 622672 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)OC)O 331.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.035
> Alkaloids and derivatives / Aporphines
(-)-Corydine 6993625 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)O)OC 341.40 unknown https://doi.org/10.1248/YAKUSHI1881.49.9_801
(+/-)-Corydine 111119 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)O)OC 341.40 unknown https://doi.org/10.1248/YAKUSHI1881.49.9_801
(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
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
Artabotrine 48704 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC 341.40 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 via CMAUP database
Glaucine 16754 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC 355.40 unknown via CMAUP database
Isocorydine 10143 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC 341.40 unknown via CMAUP database
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 via CMAUP database
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 via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
(23S)-23-ethoxy-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)-octaene 86310874 Click to see CCOC1C2=C(C=CC3=C2OCO3)C4=C(N1C)C5=CC6=C(C=C5C=C4)OCO6 377.40 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Quaternary benzophenanthridine alkaloids
Chelerythrine 2703 Click to see C[N+]1=C2C(=C3C=CC(=C(C3=C1)OC)OC)C=CC4=CC5=C(C=C42)OCO5 348.40 unknown via CMAUP database
Sanguinarium 5154 Click to see C[N+]1=C2C(=C3C=CC4=C(C3=C1)OCO4)C=CC5=CC6=C(C=C52)OCO6 332.30 unknown via CMAUP database
> Alkaloids and derivatives / Phthalide isoquinolines
(-)-Adlumine 638255 Click to see CN1CCC2=CC(=C(C=C2C1C3C4=C(C5=C(C=C4)OCO5)C(=O)O3)OC)OC 383.40 unknown via CMAUP database
(+)-Adlumine 442155 Click to see CN1CCC2=CC(=C(C=C2C1C3C4=C(C5=C(C=C4)OCO5)C(=O)O3)OC)OC 383.40 unknown via CMAUP database
(+)-Corlumine 5316069 Click to see CN1CCC2=CC(=C(C=C2C1C3C4=C(C5=C(C=C4)OCO5)C(=O)O3)OC)OC 383.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(-)-13beta-Hydroxystylopine 6452886 Click to see C1CN2CC3=C(C=CC4=C3OCO4)C(C2C5=CC6=C(C=C51)OCO6)O 339.30 unknown via CMAUP database
(-)-Corydaline 638256 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC 369.50 unknown via CMAUP database
(-)-Corydalmine 161665 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C(=C(C=C4)O)OC)OC 341.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.035
(+)-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
(+/-)-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
(+/-)-Isocorypalmine 10220 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)OC 341.40 unknown via CMAUP database
(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
(13aS)-2,3-dimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-9,10-diol 101663205 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C(=C(C=C4)O)O)OC 327.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.035
(13aS)-2,3,10-trimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-11-ol 46919623 Click to see COC1=C(C=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)O)OC 341.40 unknown via CMAUP database
(1R,24S)-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 14315597 Click to see CC1C2C3=CC4=C(C=C3CCN2CC5=C1C=CC6=C5OCO6)OCO4 337.40 unknown via CMAUP database
(7S,13aS)-2,10-dimethoxy-7-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium-3,9-diol 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
(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 https://doi.org/10.1016/J.BMCL.2010.06.035
(S)-Cheilanthifoline 440582 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C5=C(C=C4)OCO5)O 325.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.035
(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 via CMAUP database
12H-Benzo[a]-1,3-benzodioxolo[4,5-g]quinolizin-9-ol, 6,6a,11,14-tetrahydro-8-methoxy- 590762 Click to see COC1=C(C=C2CCN3CC4=C(CC3C2=C1)C=CC5=C4OCO5)O 325.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.035
16-Methoxy-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-octaen-17-olate 10426199 Click to see COC1=C(C=CC2=CC3=[N+](CCC4=CC5=C(C=C43)OCO5)C=C21)[O-] 321.30 unknown https://doi.org/10.1016/J.BMCL.2010.06.035
17-Methoxy-5,7-dioxa-1-azoniapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-1(13),2,4(8),9,11,14,16,18-octaen-16-ol 45490416 Click to see COC1=C(C=C2C(=C1)CC[N+]3=C2C=C4C=CC5=C(C4=C3)OCO5)O 322.30 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/10.1016/J.BMCL.2010.06.035
Berberine Chloride 12456 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC.[Cl-] 371.80 unknown via CMAUP database
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.BMCL.2010.06.035
Chelianthifoline 5117621 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C5=C(C=C4)OCO5)O 325.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.035
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 via CMAUP database
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/10.1016/J.BMCL.2010.06.035
Coptisine Chloride 72321 Click to see C1C[N+]2=C(C=C3C=CC4=C(C3=C2)OCO4)C5=CC6=C(C=C51)OCO6.[Cl-] 355.80 unknown via CMAUP database
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 via CMAUP database
Corydaline 101301 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC 369.50 unknown via CMAUP database
Corypalmine 11186895 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)O)OC)C=C1)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 via CMAUP database
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 via CMAUP database
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 via CMAUP database
Demethylcorydalmine 14138277 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C(=C(C=C4)O)O)OC 327.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.035
DL-Tetrahydropalmatine 5417 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown via CMAUP database
Epiberberine 160876 Click to see COC1=C(C=C2C(=C1)CC[N+]3=C2C=C4C=CC5=C(C4=C3)OCO5)OC 336.40 unknown via CMAUP database
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 https://doi.org/10.1016/J.BMCL.2010.06.035
Ophiocarpine 12313750 Click to see COC1=C(C2=C(C=C1)C(C3C4=CC5=C(C=C4CCN3C2)OCO5)O)OC 355.40 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 via CMAUP database
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
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 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 via CMAUP database
Thalifendine chloride 5321913 Click to see COC1=C(C=CC2=CC3=[N+](CCC4=CC5=C(C=C43)OCO5)C=C21)O.[Cl-] 357.80 unknown via CMAUP database
Xylopinine 226520 Click to see COC1=C(C=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)OC)OC 355.40 unknown via CMAUP database
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://doi.org/10.1248/YAKUSHI1881.49.9_801
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/10.1016/J.BMCL.2010.06.035
https://doi.org/10.1055/S-1999-13983
Pseudoprotopine 185559 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=CC5=C(C=C4C1)OCO5)OCO3 353.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.035
> 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
> 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 https://doi.org/10.1016/J.BMCL.2010.06.035
2,3-Dihydroxy-6-(5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-5-ylmethyl)benzoic acid 162975698 Click to see C1CNC(C2=CC3=C(C=C21)OCO3)CC4=C(C(=C(C=C4)O)O)C(=O)O 343.30 unknown https://doi.org/10.1016/J.BMCL.2010.06.035
2,3-dihydroxy-6-[[(5R)-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]benzoic acid 162975700 Click to see C1CNC(C2=CC3=C(C=C21)OCO3)CC4=C(C(=C(C=C4)O)O)C(=O)O 343.30 unknown https://doi.org/10.1016/J.BMCL.2010.06.035
2,3-dihydroxy-6-[[(5S)-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]benzoic acid 162975699 Click to see C1CNC(C2=CC3=C(C=C21)OCO3)CC4=C(C(=C(C=C4)O)O)C(=O)O 343.30 unknown https://doi.org/10.1016/J.BMCL.2010.06.035
Coryternatine B 49862537 Click to see COC1=C(C(=C(C=C1)CC2C3=CC4=C(C=C3CCN2)OCO4)C(=O)O)OC 371.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.035
Coryternatine C 49862538 Click to see COC1=C(C(=C(C=C1)CC2C3=CC4=C(C=C3CCN2)OCO4)C(=O)O)OC 371.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.035
Reticulin 10233 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.035
Reticuline 439653 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.035
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
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 / Tetrahydroisoquinolines
5-(5,6,7,8-Tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-5-ylmethyl)-1,3-benzodioxole-4-carboxylic acid 75251435 Click to see C1CNC(C2=CC3=C(C=C21)OCO3)CC4=C(C5=C(C=C4)OCO5)C(=O)O 355.30 unknown https://doi.org/10.1016/J.BMCL.2010.06.035
Corypalline 280225 Click to see CN1CCC2=CC(=C(C=C2C1)O)OC 193.24 unknown via CMAUP database
Coryternatine A 46911013 Click to see C1CNC(C2=CC3=C(C=C21)OCO3)CC4=C(C5=C(C=C4)OCO5)C(=O)O 355.30 unknown https://doi.org/10.1016/J.BMCL.2010.06.035
Epi-Coryximine 49862477 Click to see CN1CCC2=CC3=C(C=C2C1CC4=C(C5=C(C=C4)OCO5)C(=O)O)OCO3 369.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.035

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