Scientific name	Authority	First published in
Pistolochia turtschaninovii	(Besser) Holub	Folia Geobot. Phytotax. 8: 172 (1973)
Corydalis remota	Fisch. ex Maxim.	Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 9: 37 (1859)
Corydalis remota f. non-apiculata	(Ohwi) C.Y.Wu & Z.Y.Su	Acta Bot. Yunnan. 7(3): 269. 1985
Corydalis remota f. papillosa	(Kitag.) C.Y.Wu & Z.Y.Su	Acta Bot. Yunnan. 7: 268 (1985)
Corydalis remota var. rotundiloba	Maxim.	Prim. Fl. Amur. 38 1859
Corydalis ternata f. yanhusuo	(Y.H.Chou & Chun C.Hsu) Y.C.Zhu	in Pl. Medic. Chinae Bor.-orient. (ed. Zhu You Chang) 442 (1989):.
Corydalis turtschaninovii f. multisecta	P.Y.Fu	Bull. Bot. Res., Harbin 15(3): 330. 1995
Corydalis turtschaninovii var. non-apiculata	Ohwi	Acta Phytotax. Geobot. 9: 262 1942
Corydalis turtschaninovii var. papillosa	Kitag.	Rep. Inst. Sci. Res. Manchoukou 2: 294 1938
Corydalis turtschaninovii f. papillosa	(Kitag.) Y.C.Zhu	in Pl. Medic. Chinae Bor.-orient. (ed. Zhu You Chang) 445 (1989):.
Corydalis bulbosa f. ternata	Nakai	Bot. Mag. (Tokyo) 26: 91, 94 1912
Corydalis solida subsp. remota	(Fisch. ex Maxim.) Korsh.	Mém. Acad. Imp. Sci. St.-Pétersbourg, Divers Savans 1892: 306 1892
Corydalis turtschaninovii var. ternata	(Nakai) Ohwi	Acta Phytotax. Geobot. 17: 262 1942
Pistolochia remota	(Fisch. ex Maxim.) Soják	Cas. Nár. Mus., Odd. Prír. 140: 129 (1972)
Corydalis remota var. punctata	Skvortsov
Corydalis woroschilovii	Urusov	Khorol. Taxon. Rast. Sovetsk. Dal'nego Vostoka : 105 (1990)

Common names Top

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Filter by language:

Language	Common/alternative name
Japanese	エンゴサク
Korean	조선현호색
Chinese	毛黄堇
Chinese	齿瓣延胡索
Chinese	蓝花莱
Chinese	蓝雀花

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Corydalis turtschaninovii subsp. vernyi	(Franch. & Sav.) Lidén	Willdenowia 26: 28 (1996)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - Inner Mongolia
  - Manchuria
- Eastern Asia
  - Japan
  - Korea
- Russian Far East
  - Amur
  - Khabarovsk
  - Primorye
- Siberia
  - Chita

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000623001
Tropicos	50154705
KEW	urn:lsid:ipni.org:names:672558-1
The Plant List	kew-2739374
Open Tree Of Life	5727965
NCBI Taxonomy	1577077
IPNI	672558-1
iNaturalist	491319
GBIF	7314740
EOL	5474057
USDA GRIN	419522
CMAUP	NPO13962
CMAUP	NPO28698

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

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

Berberine and Its Study as an Antidiabetic Compound

Utami AR, Maksum IP, Deawati Y

Biology (Basel)

08-Jul-2023

PMCID:	PMC10376565
doi:	10.3390/biology12070973
PMID:	37508403

Natural Inhibitors of Cholinesterases: Chemistry, Structure–Activity and Methods of Their Analysis

Smyrska-Wieleba N, Mroczek T

Int J Mol Sci

01-Feb-2023

PMCID:	PMC9916849
doi:	10.3390/ijms24032722
PMID:	36769043

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

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

UHPLC-Q-Orbitrap-MS-Based Metabolomics Reveals Chemical Variations of Two Types of Rhizomes of Polygonatum sibiricum

Luo G, Lin J, Cheng W, Liu Z, Yu T, Yang B

Molecules

22-Jul-2022

PMCID:	PMC9331047
doi:	10.3390/molecules27154685
PMID:	35897876

Hidden Agenda - The Involvement of Endoplasmic Reticulum Stress and Unfolded Protein Response in Inflammation-Induced Muscle Wasting

Kny M, Fielitz J

Front Immunol

09-May-2022

PMCID:	PMC9124858
doi:	10.3389/fimmu.2022.878755
PMID:	35615361

Insecticidal Activity of Extracts, Fractions, and Pure Molecules of Cissampelos pareira Linnaeus against Aphid, Aphis craccivora Koch

Kumari S, Dolma SK, Anmol, Sharma U, Reddy SG

Molecules

19-Jan-2022

PMCID:	PMC8838119
doi:	10.3390/molecules27030633
PMID:	35163898

Antibacterial Activity and Multi-Targeting Mechanism of Dehydrocorydaline From Corydalis turtschaninovii Bess. Against Listeria monocytogenes

Kim G, Xu Y, Zhang J, Sui Z, Corke H

Front Microbiol

11-Jan-2022

PMCID:	PMC8787222
doi:	10.3389/fmicb.2021.799094
PMID:	35087499

Processing and Compatibility of Corydalis yanhusuo: Phytochemistry, Pharmacology, Pharmacokinetics, and Safety

Wu L, Yang Y, Mao Z, Wu J, Ren D, Zhu B, Qin L

Evid Based Complement Alternat Med

30-Dec-2021

PMCID:	PMC8739176
doi:	10.1155/2021/1271953
PMID:	35003289

8-, 9-, and 11-Aryloxy Dimeric Aporphines and Their Pharmacological Activities

Ali G, Cuny GD

Molecules

27-Jul-2021

PMCID:	PMC8347945
doi:	10.3390/molecules26154521
PMID:	34361671

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

Nutraceuticals in the Prevention and Treatment of the Muscle Atrophy

Wang Y, Liu Q, Quan H, Kang SG, Huang K, Tong T

Nutrients

02-Jun-2021

PMCID:	PMC8227811
doi:	10.3390/nu13061914
PMID:	34199575

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

Biologically Active Isoquinoline Alkaloids covering 2014-2018

Shang XF, Yang CJ, Morris-Natschke SL, Li JC, Yin XD, Liu YQ, Guo X, Peng JW, Goto M, Zhang JY, Lee KH

Med Res Rev

29-Jul-2020

PMCID:	PMC7554109
doi:	10.1002/med.21703
PMID:	32729169

Phytochemical Profile Top

Add a new one!

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)-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
[6aS,(+)]-5,6,6a,7-Tetrahydro-1,2,9,10-tetramethoxy-4H-dibenzo[de,g]quinoline	11348415	Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)OC)NCCC3=C1)OC	341.40	unknown	https://doi.org/10.1055/S-0030-1249972
1,2,10-Trimethoxy-5,6,6a,7-tetrahydro-4h-dibenzo[de,g]quinolin-9-ol	267400	Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)OC	327.40	unknown	https://doi.org/10.1055/S-0030-1249972
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-6,7-dimethyl-5,6-dihydro-4h-dibenzo[de,g]quinoline	53073	Click to see CC1=C2C3=C(C4=CC(=C(C=C14)OC)OC)C(=C(C=C3CCN2C)OC)OC	367.40	unknown	https://doi.org/10.1055/S-0030-1249972
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
5,15,16-Trimethoxy-10-methyl-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1,3,5,7,9(17),13,15-heptaen-4-ol	49871020	Click to see CN1CCC2=CC(=C(C3=C4C=C(C(=CC4=CC1=C23)OC)O)OC)OC	339.40	unknown	https://doi.org/10.1055/S-0030-1249972
7-Hydroxydehydroglaucine	10317002	Click to see CN1CCC2=CC(=C(C3=C2C1=C(C4=CC(=C(C=C43)OC)OC)O)OC)OC	369.40	unknown	https://doi.org/10.1055/S-0030-1249972
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://doi.org/10.1055/S-0030-1249972
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-0030-1249972
ethyl 4-[(6aS)-1,2,9,10-tetramethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-yl]-4-oxobutanoate	49871019	Click to see CCOC(=O)CCC(=O)N1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC	469.50	unknown	https://doi.org/10.1055/S-0030-1249972
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-0030-1249972 https://doi.org/10.1248/BPB.17.262
Isocorydine	10143	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC	341.40	unknown	via CMAUP database
Laurotetanine	31415	Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)OC	327.40	unknown	https://doi.org/10.1055/S-0030-1249972
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
methyl 4-[(6aS)-1,2,9,10-tetramethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-yl]-4-oxobutanoate	163059303	Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)OC)N(CCC3=C1)C(=O)CCC(=O)OC)OC	455.50	unknown	https://doi.org/10.1055/S-0030-1249972
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	https://doi.org/10.1055/S-0030-1249972
Nantenine	197001	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC5=C(C=C43)OCO5)OC)OC	339.40	unknown	via CMAUP database
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/10.1055/S-0030-1249972
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/10.1055/S-0030-1249972
> 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://doi.org/10.1055/S-0030-1249972
(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
(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/10.1248/BPB.27.1270
(R)-Corytenchine	101503694	Click to see COC1=C(C=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)O)OC	341.40	unknown	via CMAUP database
(RS)-Nandinine	261619	Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)O	325.40	unknown	https://doi.org/10.1055/S-0030-1249972
(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/10.1055/S-0030-1249972
(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://doi.org/10.1055/S-0030-1249972
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
2,3,9-trimethoxy-13-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-10-ol	5315412	Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)O)OC)OC	355.40	unknown	https://doi.org/10.1248/BPB.27.1270 https://doi.org/10.1055/S-0030-1249972
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/10.1248/BPB.27.1270 https://doi.org/10.1055/S-0030-1249972
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/10.1002/JCCS.199700053
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/10.1055/S-0030-1249972 https://doi.org/10.1248/BPB.27.1270
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/10.1002/JCCS.199700053
Corybulbine	10316181	Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)O)OC	355.40	unknown	https://doi.org/10.1248/BPB.27.1270 https://doi.org/10.1055/S-0030-1249972
Corydalin	326549	Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC	369.50	unknown	https://doi.org/10.1248/BPB.27.1270 https://doi.org/10.1055/S-0030-1249972
Corydaline	101301	Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC	369.50	unknown	https://doi.org/10.1055/S-0030-1249972 https://doi.org/10.1248/BPB.27.1270
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	https://doi.org/10.1055/S-0030-1249972
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/10.1002/JCCS.199700053
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/10.1248/BPB.20.431
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
Discretinine	11186895	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)O)OC)C=C1)OC	341.40	unknown	https://doi.org/10.1055/S-0030-1249972
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/10.1055/S-0030-1249972 https://doi.org/10.1248/BPB.27.1270
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
Isocorybulbine	12310873	Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)O	355.40	unknown	https://doi.org/10.1055/S-0030-1249972
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
Nandinine	12313091	Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)O	325.40	unknown	https://doi.org/10.1055/S-0030-1249972
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/10.1002/JCCS.199700053
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	https://doi.org/10.1055/S-0030-1249972
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-0030-1249972 https://doi.org/10.1248/BPB.17.262
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://doi.org/10.1055/S-0030-1249972 https://doi.org/10.1248/BPB.27.1270
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	via CMAUP database
Yuanhunine	128558	Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)O)OC)OC	355.40	unknown	https://doi.org/10.1248/BPB.27.1270 https://doi.org/10.1055/S-0030-1249972
> 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	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	via CMAUP database
Pseudoprotopine	185559	Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=CC5=C(C=C4C1)OCO5)OCO3	353.40	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
Flaccidin	14235431	Click to see COC1=C(C2=C3C(=C1)CCC4=C3C(=CC(=C4)O)OC2)O	270.28	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
(3Z,18Z)-henicosa-3,18-dien-1,8,10,20-tetrayne	10636218	Click to see C#CC=CCCCCCCC#CC#CCCCC=CC#C	276.40	unknown	via CMAUP database
Callypentayne	10778600	Click to see C#CC=CCCCCC=CC#CC#CCCCC#CC#C	272.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
callysponginol sulfonic acid A	11123673	Click to see CCCCCCC=CCCCCCCCCCCCCC#CC(C(=O)O)OS(=O)(=O)O	458.70	unknown	via CMAUP database
Callyspongynic Acid	636783	Click to see C#CC(C=CCCCCCC#CC#CCCCC#CCCCC#CCCCCCC#CC(=O)O)O	470.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
Siphonodiol	11151732	Click to see C#CC=CCCCCC=CC#CC#CCCCC#CC#CC(CO)O	332.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Excisanin H	10066342	Click to see CC1(CCC(C23C1CC(C45C2CCC(C4(OC3)O)C(=C)C5=O)O)O)C	348.40	unknown	https://doi.org/10.1055/S-0030-1249972
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
Callystatin A	5471086	Click to see CCC(C)C(C(C)C(=O)C(C)C=C(C)C=CCC(C)C=C(CC)C=CC1CC=CC(=O)O1)O	456.70	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
> 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
4-hydroxy-N-[(3S,5R)-3-[(4-hydroxyphenyl)methyl]-2-oxo-1,4-diazocan-5-yl]benzamide	101562583	Click to see C1CC(NC(C(=O)NC1)CC2=CC=C(C=C2)O)NC(=O)C3=CC=C(C=C3)O	369.40	unknown	https://doi.org/10.1016/J.TETLET.2012.01.043
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Dipeptides
Spumigin E	71449303	Click to see CC1CC(N(C1)C(=O)C(CCC2=CC=C(C=C2)O)NC(=O)C(CC3=CC=C(C=C3)O)O)C(=O)NC(CCCN=C(N)N)C=O	610.70	unknown	https://doi.org/10.1055/S-0030-1249972
> Organic acids and derivatives / Organic sulfuric acids and derivatives / Sulfuric acid esters / Sulfuric acid monoesters
[(2R,14Z,20Z)-1-sulfooxytricosa-14,20-dien-3,5,10,12,22-pentayn-2-yl] hydrogen sulfate	5470011	Click to see C#CC=CCCCCC=CC#CC#CCCCC#CC#CC(COS(=O)(=O)O)OS(=O)(=O)O	492.60	unknown	via CMAUP database
[(2R,14Z,20Z)-2-hydroxytricosa-14,20-dien-3,5,10,12,22-pentaynyl] hydrogen sulfate	21774473	Click to see C#CC=CCCCCC=CC#CC#CCCCC#CC#CC(COS(=O)(=O)O)O	412.50	unknown	via CMAUP database
> 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
> 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

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Corydalis turtschaninovii

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