Corydalis incisa, also known as incised fumewort, is a plant in the poppy family that can grow as an annual or biennial herb. It is native to Japan, Korea, Taiwan, and China and is commonly found in forests, clearings, and irrigation channels. In the United States, it has been introduced and can be found in several states, including New York, Pennsylvania, and North Carolina. The plant is known for its explosive seed dispersal, aided by an elaiosome that attracts ants. It has been reported to thrive in alluvial sediments and can form dense stands that outcompete other plants in riparian areas.

Synonyms Top

Scientific name	Authority	First published in
Capnoides incisa	Kuntze	Revis. Gen. Pl. 1: 14 (1891)
Corydalis incisa var. alba	S.Y.Wang	Fl. Henan 2: 12 (1988)
Corydalis incisa f. bicolor	Hayashi	J. Geobot. 22(1): 5. 1974
Corydalis incisa f. candida	Hiyama	J. Jap. Bot. 33: 189 1958
Corydalis incisa f. liuchiuensis	Nakai	Bot. Mag. (Tokyo) 25: 64 1911
Corydalis incisa f. pallescens	Makino	Bot. Mag. (Tokyo) 23: 251 1909
Fumaria incisa	Thunb.	Nova Acta Acad. Sci. Imp. Petrop. Hist. Acad. 12: 104 (1801)
Corydalis incisa var. koreana	Fedde	Repert. Spec. Nov. Regni Veg. 17: 197 1921
Corydalis incisa var. pseudomakinoana	Fedde	Repert. Spec. Nov. Regni Veg. 17: 197 1921
Corydalis incisa var. tschekiangensis	Fedde	Repert. Spec. Nov. Regni Veg. 17: 197 1921

Common names Top

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Filter by language:

Language	Common/alternative name
Upper Sorbian	cuzy kokorč
Japanese	紫華鬘
Japanese	ムラサキケマン
Korean	자주괴불주머니
Chinese	刻叶紫堇
Chinese	刻葉紫菫
Chinese	刻裂紫堇
Chinese	紫花鱼灯草
Chinese	地锦苗
Chinese	断肠草
Chinese	烫伤草
Chinese	羊不吃

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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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 click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Taiwan

Northern America click to expand
- Northeastern U.S.A.
  - New York
- Southeastern U.S.A.
  - Maryland

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000622464
USDA Plants	COIN21
Tropicos	24001069
KEW	urn:lsid:ipni.org:names:672291-1
The Plant List	kew-2738853
PFAF	Corydalis incisa
Open Tree Of Life	900631
NCBI Taxonomy	404570
IPNI	672291-1
iNaturalist	447077
GBIF	7314981
Freebase	/m/0nbgn9j
EPPO	COYIS
EOL	5473619
Wikipedia	Corydalis_incisa
CMAUP	NPO6328

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

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

In Vitro Screening of East Asian Plant Extracts for Potential Use in Reducing Ruminal Methane Production

Bharanidharan R, Arokiyaraj S, Baik M, Ibidhi R, Lee SJ, Lee Y, Nam IS, Kim KH

Animals (Basel)

04-Apr-2021

PMCID:	PMC8066825
doi:	10.3390/ani11041020
PMID:	33916571

A higher-rank classification for rust fungi, with notes on genera

Aime MC, McTaggart AR

Fungal Syst Evol

13-Nov-2020

PMCID:	PMC8165960
doi:	10.3114/fuse.2021.07.02
PMID:	34124616

Regulation of Anti-Oxidative, Anti-Inflammatory, and Anti-Apoptotic Activity of Advanced Cooling Composition (ACC) in UVB-Irradiated Human HaCaT Keratinocytes

Park J, Woo YK, Cho HJ

Int J Mol Sci

07-Sep-2020

PMCID:	PMC7555985
doi:	10.3390/ijms21186527
PMID:	32906658

Quantitative comparison of flowering phenology traits among trees, perennial herbs, and annuals in a temperate plant community

Nagahama A, Yahara T

Am J Bot

14-Nov-2019

PMCID:	PMC6973048
doi:	10.1002/ajb2.1387
PMID:	31724169

Ultrahigh Performance Liquid Chromatography–Electrospray Ionization Tandem Mass Spectrometry Method for Qualitative and Quantitative Analyses of Constituents of Corydalis bungeana Turcz Extract

Tian M, Yang C, Yang J, Dong H, Liu L, Ren Y, Wang Z

Molecules

24-Sep-2019

PMCID:	PMC6803914
doi:	10.3390/molecules24193463
PMID:	31554239

Traditional knowledge on herbal drinks among indigenous communities in Azad Jammu and Kashmir, Pakistan

Rashid N, Gbedomon RC, Ahmad M, Salako VK, Zafar M, Malik K

J Ethnobiol Ethnomed

21-Feb-2018

PMCID:	PMC5822664
doi:	10.1186/s13002-018-0217-8
PMID:	29467005

Corrigendum: In silico identification of anti-cancer compounds and plants from traditional Chinese medicine database

Dai SX, Li WX, Han FF, Guo YC, Zheng JJ, Liu JQ, Wang Q, Gao YD, Li GH, Huang JF

Sci Rep

10-Oct-2016

PMCID:	PMC5056451
doi:	10.1038/srep34972
PMID:	27721399

In silico identification of anti-cancer compounds and plants from traditional Chinese medicine database

Dai SX, Li WX, Han FF, Guo YC, Zheng JJ, Liu JQ, Wang Q, Gao YD, Li GH, Huang JF

Sci Rep

05-May-2016

PMCID:	PMC4857115
doi:	10.1038/srep25462
PMID:	27145869

Does Plant Origin Influence the Fitness Impact of Flower Damage? A Meta-Analysis

González-Browne C, Murúa MM, Navarro L, Medel R

PLoS One

19-Jan-2016

PMCID:	PMC4718695
doi:	10.1371/journal.pone.0146437
PMID:	26785039

Zygomorphy evolved from disymmetry in Fumarioideae (Papaveraceae, Ranunculales): new evidence from an expanded molecular phylogenetic framework

Sauquet H, Carrive L, Poullain N, Sannier J, Damerval C, Nadot S

Ann Bot

26-Mar-2015

PMCID:	PMC4407061
doi:	10.1093/aob/mcv020
PMID:	25814061

Studien iiber die Alkaloide der Papaveraceen. XVIII. Die Alkaloide von Corydalis incisa (11). Uber die Struktur des Corydamins

NARAO TAKAO, KINUKO IWASA

Pharmaceutical Society of Japan

08-Dec-2011

doi:	10.1248/CPB.21.1587

Alkaloids of Corydalis incisa PERS. III. The Structures of Corydamine Hydrochloride and N-Formyl Corydamine

GENICHIRO NONAKA, ITSUO NISHIOKA

Pharmaceutical Society of Japan

08-Dec-2011

doi:	10.1248/CPB.21.1410

Alkaloids of Corydalis incisa pers. VI. The structures of benzo(c)phenanthridine-type alkaloids, 12-hydroxycorynoline and 11-epicorynoline.

GENICHIRO NONAKA, ITSUO NISHIOKA

Pharmaceutical Society of Japan

08-Dec-2011

doi:	10.1248/CPB.23.521

Alkaloids of Corydalis incisa PERS. V. The structures of corydalispirone and corydalisol.

GENICHIRO NONAKA, ITSUO NISHIOKA

Pharmaceutical Society of Japan

08-Dec-2011

doi:	10.1248/CPB.23.294

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
Bulbocapnine	12441	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)OC)O)OCO3	325.40	unknown	https://doi.org/10.1016/S0367-326X(99)00045-3
Corytuberine	160500	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC	327.40	unknown	https://doi.org/10.1016/S0367-326X(99)00045-3
Corytuberine, pentahydrate	347379	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC	327.40	unknown	https://doi.org/10.1016/S0367-326X(99)00045-3
d-Bulbocapnine	9276	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)OC)O)OCO3	325.40	unknown	https://doi.org/10.1016/S0367-326X(99)00045-3
> 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/S0367-326X(99)00045-3
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Hexahydrobenzophenanthridine alkaloids
(11alpha)-13-Methylchelidonine	185284	Click to see CC12C(CC3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)O	367.40	unknown	https://doi.org/10.1016/S0031-9422(00)86453-5 https://doi.org/10.1248/CPB.23.521 https://doi.org/10.1007/BF02975246
(12S)-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-12-ol	5316101	Click to see CC12C(CC3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)O	367.40	unknown	https://doi.org/10.1016/S0367-326X(99)00045-3 https://doi.org/10.1021/NP50102A005 https://doi.org/10.1007/BF02975246 https://doi.org/10.1007/BF02976997
(13,24-Dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-12-yl) acetate	13909033	Click to see CC(=O)OC1CC2=CC3=C(C=C2C4C1(C5=C(CN4C)C6=C(C=C5)OCO6)C)OCO3	409.40	unknown	https://doi.org/10.1016/S0031-9422(00)86453-5
(13,24-Dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-12-yl) hydrogen sulfate	73806753	Click to see CC12C(CC3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)OS(=O)(=O)O	447.50	unknown	https://doi.org/10.1016/0031-9422(79)80194-6
(1R,11R,12R,13R)-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-2,4(8),9,14(22),15,17(21)-hexaene-11,12-diol	146167747	Click to see CC12C(C(C3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)O)O	383.40	unknown	https://doi.org/10.1248/CPB.23.521
(1R,12R,13R)-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-12-ol	102428394	Click to see CC12C(CC3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)O	367.40	unknown	https://doi.org/10.1248/CPB.23.521
(1R,12R,13S)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one	163059376	Click to see CC12C(CC3=CC4=C(C=C3C1N(C(=O)C5=C2C=CC6=C5OCO6)C)OCO4)O	381.40	unknown	https://doi.org/10.1007/BF02975246
(1R,12S,13R,23S)-23-(hydroxymethyl)-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-12-ol	102059838	Click to see CC12C(CC3=CC4=C(C=C3C1N(C(C5=C2C=CC6=C5OCO6)CO)C)OCO4)O	397.40	unknown	https://doi.org/10.1016/0031-9422(79)80194-6
(1R,12S,13R)-12-hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one	132558697	Click to see CC12C(CC3=CC4=C(C=C3C1N(C(=O)C5=C2C=CC6=C5OCO6)C)OCO4)O	381.40	unknown	https://doi.org/10.1248/CPB.23.521
(1R,14S,24R)-24,25-dimethyl-5,7,13,17,19-pentaoxa-25-azaheptacyclo[12.10.1.02,10.04,8.012,24.015,23.016,20]pentacosa-2,4(8),9,15(23),16(20),21-hexaene	101324793	Click to see CC12C3CC4=CC5=C(C=C4C1N(C(O3)C6=C2C=CC7=C6OCO7)C)OCO5	365.40	unknown	https://doi.org/10.1016/S0367-326X(99)00045-3 https://doi.org/10.1021/NP50102A005
(1S,12R,13S)-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-12-ol	21768978	Click to see CC12C(CC3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)O	367.40	unknown	https://doi.org/10.1016/S0031-9422(00)86453-5
(1S,12R,14R,24S)-24,25-dimethyl-5,7,13,17,19-pentaoxa-25-azaheptacyclo[12.10.1.02,10.04,8.012,24.015,23.016,20]pentacosa-2,4(8),9,15(23),16(20),21-hexaene	162848218	Click to see CC12C3CC4=CC5=C(C=C4C1N(C(O3)C6=C2C=CC7=C6OCO7)C)OCO5	365.40	unknown	https://doi.org/10.1016/S0031-9422(00)86453-5
[(1R,12S,13R)-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-12-yl] hydrogen sulfate	163008771	Click to see CC12C(CC3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)OS(=O)(=O)O	447.50	unknown	https://doi.org/10.1016/0031-9422(79)80194-6
[(1S,12R,13S)-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-12-yl] acetate	124396470	Click to see CC(=O)OC1CC2=CC3=C(C=C2C4C1(C5=C(CN4C)C6=C(C=C5)OCO6)C)OCO3	409.40	unknown	https://doi.org/10.1016/S0031-9422(00)86453-5
[(1S)-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-12-yl] acetate	5315913	Click to see CC(=O)OC1CC2=CC3=C(C=C2C4C1(C5=C(CN4C)C6=C(C=C5)OCO6)C)OCO3	409.40	unknown	via CMAUP database
12-Hydroxy-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-23-one	163059374	Click to see CC12C(CC3=CC4=C(C=C3C1N(C(=O)C5=C2C=CC6=C5OCO6)C)OCO4)O	381.40	unknown	https://doi.org/10.1248/CPB.23.521
12-Hydroxycorynoline	101806253	Click to see CC12C(C(C3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)O)O	383.40	unknown	via CMAUP database
13,24-Dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-2,4(8),9,14(22),15,17(21)-hexaene-11,12-diol	73833898	Click to see CC12C(C(C3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)O)O	383.40	unknown	https://doi.org/10.1248/CPB.23.521
23-(Hydroxymethyl)-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-12-ol	162979285	Click to see CC12C(CC3=CC4=C(C=C3C1N(C(C5=C2C=CC6=C5OCO6)CO)C)OCO4)O	397.40	unknown	https://doi.org/10.1016/0031-9422(79)80194-6
24,25-Dimethyl-5,7,13,17,19-pentaoxa-25-azaheptacyclo[12.10.1.02,10.04,8.012,24.015,23.016,20]pentacosa-2,4(8),9,15(23),16(20),21-hexaene	5316102	Click to see CC12C3CC4=CC5=C(C=C4C1N(C(O3)C6=C2C=CC7=C6OCO7)C)OCO5	365.40	unknown	https://doi.org/10.1016/S0031-9422(00)86453-5 https://doi.org/10.1007/BF02975246 https://doi.org/10.1016/S0367-326X(99)00045-3 https://doi.org/10.1021/NP50102A005
5b,6,7,12balpha,13,14-Hexahydro-5balpha,13-dimethyl-6,14-epoxy[1,3]benzodioxolo[5,6-c]-1,3-dioxolo[4,5-i]phenanthridine	9885447	Click to see CC12C3CC4=CC5=C(C=C4C1N(C(O3)C6=C2C=CC7=C6OCO7)C)OCO5	365.40	unknown	via CMAUP database
Acetylcorynoline	177015	Click to see CC(=O)OC1CC2=CC3=C(C=C2C4C1(C5=C(CN4C)C6=C(C=C5)OCO6)C)OCO3	409.40	unknown	https://doi.org/10.1007/BF02975246 https://doi.org/10.1016/S0367-326X(99)00045-3
Chelidonine-6,6,12-d3, 13-methyl-, (12alpha,14beta)-(+-)-	6913599	Click to see CC12C(CC3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)O	370.40	unknown	via CMAUP database
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
Corynoline	177014	Click to see CC12C(CC3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)O	367.40	unknown	https://doi.org/10.1007/BF02976997 https://doi.org/10.1021/NP50102A005 https://doi.org/10.1016/S0367-326X(99)00045-3
Corynoloxine	146167748	Click to see CC12C3CC4=CC5=C(C=C4C1N(C(O3)C6=C2C=CC7=C6OCO7)C)OCO5	365.40	unknown	https://doi.org/10.1007/BF02975246
> 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
Chelerythrine hydroxide	5351594	Click to see C[N+]1=C2C(=C3C=CC(=C(C3=C1)OC)OC)C=CC4=CC5=C(C=C42)OCO5.[OH-]	365.40	unknown	via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
Cytisine, N-formyl-	589870	Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)C=O	218.25	unknown	via CMAUP database
> Alkaloids and derivatives / Morphinans
(1R,9S,10S)-4-acetyl-3-hydroxy-12-methoxy-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2(7),3,5,11-tetraen-13-one	57339442	Click to see CC(=O)C1=C(C2=C(CC3C4C2(CCN3C)CC(=O)C(=C4)OC)C=C1)O	341.40	unknown	via CMAUP database
> Alkaloids and derivatives / Phthalide isoquinolines
6-(6-Methyl-5,6,7,8-tetrahydro[1,3]dioxolo[4,5-g]isoquinolin-5-yl)furo[3,4-E][1,3]benzodioxol-8(6H)-one	2376	Click to see CN1CCC2=CC3=C(C=C2C1C4C5=C(C6=C(C=C5)OCO6)C(=O)O4)OCO3	367.40	unknown	https://doi.org/10.1021/JA01163A114
Adlumidine	120734	Click to see CN1CCC2=CC3=C(C=C2C1C4C5=C(C6=C(C=C5)OCO6)C(=O)O4)OCO3	367.40	unknown	https://doi.org/10.1021/JA01163A114
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(+)-Coreximine	7037181	Click to see COC1=C(C=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)O)O	327.40	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
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
Capaurine	94149	Click to see COC1=C(C2=C(CC3C4=C(C(=C(C=C4CCN3C2)OC)OC)O)C=C1)OC	371.40	unknown	https://doi.org/10.1016/S0367-326X(99)00045-3
Chelianthifoline	5117621	Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C5=C(C=C4)OCO5)O	325.40	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	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	https://doi.org/10.1016/S0367-326X(99)00045-3
Mecambridine	161692	Click to see COC1=C(C(=C2CC3C4=C(C5=C(C=C4CCN3CC2=C1)OCO5)OC)CO)OC	399.40	unknown	https://doi.org/10.1016/S0367-326X(99)00045-3
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/10.1002/CBDV.200890121
Worenine	20055073	Click to see CC1=C2C3=CC4=C(C=C3CC[N+]2=CC5=CC6=C(C=C15)OCO6)OCO4	334.30	unknown	via CMAUP database
> Alkaloids and derivatives / Protopine alkaloids
Corycavamine	12304036	Click to see CC1C2=C(CN(CCC3=CC4=C(C=C3C1=O)OCO4)C)C5=C(C=C2)OCO5	367.40	unknown	https://doi.org/10.1021/NP50102A005 https://doi.org/10.1016/S0031-9422(00)86453-5
Corycavine	276145	Click to see CC1C2=C(CN(CCC3=CC4=C(C=C3C1=O)OCO4)C)C5=C(C=C2)OCO5	367.40	unknown	https://doi.org/10.1016/S0031-9422(00)86453-5
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/S0031-9422(00)86453-5
> Benzenoids / Phenanthrenes and derivatives
5-Hydroxy-4,13-dimethoxy-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2,4,6,10,13-pentaen-12-one	5320383	Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=CC(=C(C=C34)OC)O)OC	327.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(E)-6,9,10-trihydroxyoctadec-7-enoic acid	5321100	Click to see CCCCCCCCC(C(C=CC(CCCCC(=O)O)O)O)O	330.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hentriacontanol	68345	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO	452.80	unknown	https://doi.org/10.1248/YAKUSHI1947.90.10_1327
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
[(1S,3S,4S,6S,10S,11S,12R,13R)-3,6,12-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	5315330	Click to see CC(=O)OC1C(C2CC3(C1C4(CCC(C(C4C(C3)O)(C)C)O)C)C(=O)C2=C)O	392.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Epicurzerenone	5317062	Click to see CC1=COC2=C1C(=O)C(C(C2)(C)C=C)C(=C)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
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines
Hinckdentine A	15924024	Click to see C1CNC(=O)CC2C13C4=C(C=CC(=C4)Br)N=CN3C5=C2C=C(C=C5Br)Br	540.00	unknown	via CMAUP database
> 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 / Indolizidines
Corynoxeine	44568160	Click to see COC=C(C1CC2C3(CCN2CC1C=C)C4=CC=CC=C4NC3=O)C(=O)OC	382.50	unknown	via CMAUP database
methyl (E)-2-[(6'R,7'S)-6'-ethenyl-2-oxospiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-7'-yl]-3-methoxyprop-2-enoate	5316103	Click to see COC=C(C1CC2C3(CCN2CC1C=C)C4=CC=CC=C4NC3=O)C(=O)OC	382.50	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	https://doi.org/10.1248/CPB.21.1587 https://doi.org/10.1248/CPB.21.1410
N-[2-[6-([1,3]dioxolo[4,5-h]isoquinolin-7-yl)-1,3-benzodioxol-5-yl]ethyl]-N-methylformamide	5317376	Click to see CN(CCC1=CC2=C(C=C1C3=NC=C4C(=C3)C=CC5=C4OCO5)OCO2)C=O	378.40	unknown	https://doi.org/10.1248/CPB.21.1410
> 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
Reticuline	439653	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
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/S0367-326X(99)00045-3
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
CID 5458757	5458757	Click to see CC(=C)C1C2CC3(C4(CO4)C5C(C3(C1C(=O)O2)O)O5)C	278.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
Palmarin	442068	Click to see CC12CCC3C(=O)OC(CC3(C1C4C5C(C2(C(=O)O4)O)O5)C)C6=COC=C6	374.40	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 / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(+)-Luguine	442317	Click to see C1C(C2=C3C=CC4=C(C3=CN=C2C5=CC6=C(C=C51)OCO6)OCO4)O	335.30	unknown	https://doi.org/10.1007/BF02975246
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(5S)-6-methylspiro[7,8-dihydro-[1,3]dioxolo[4,5-g]isoquinoline-5,7'-9H-[1,3]dioxolo[4,5-h]isochromene]-6'-one	101919125	Click to see CN1CCC2=CC3=C(C=C2C14C(=O)C5=C(CO4)C6=C(C=C5)OCO6)OCO3	367.40	unknown	https://doi.org/10.1248/CPB.23.294
[5-[(6-methyl-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl)methyl]-1,3-benzodioxol-4-yl]methanol	13997260	Click to see CN1CCC2=CC3=C(C=C2C1CC4=C(C5=C(C=C4)OCO5)CO)OCO3	355.40	unknown	https://doi.org/10.1248/CPB.23.294
[5-[[(5R)-6-methyl-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]-1,3-benzodioxol-4-yl]methanol	11089560	Click to see CN1CCC2=CC3=C(C=C2C1CC4=C(C5=C(C=C4)OCO5)CO)OCO3	355.40	unknown	https://doi.org/10.1248/CPB.23.294
Hypecorinine	13997263	Click to see CN1CCC2=CC3=C(C=C2C14C(=O)C5=C(CO4)C6=C(C=C5)OCO6)OCO3	367.40	unknown	https://doi.org/10.1248/CPB.23.294
methyl 2-[6-(6,8-dimethyl-7,9-dihydro-6H-[1,3]dioxolo[4,5-h]isoquinolin-7-yl)-1,3-benzodioxol-5-yl]acetate	5316091	Click to see CC1C(N(CC2=C1C=CC3=C2OCO3)C)C4=CC5=C(C=C4CC(=O)OC)OCO5	397.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
(1R,4Z,6R,7R)-4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6-methyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione	12311394	Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(CO)O)C	351.40	unknown	via CMAUP database

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Corydalis incisa

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