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
  - China South-central
  - China Southeast

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000622851
Tropicos	24000769
KEW	urn:lsid:ipni.org:names:672482-1
The Plant List	kew-2739229
Open Tree Of Life	345836
NCBI Taxonomy	282776
IPNI	672482-1
GBIF	5531204
EOL	5473936

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

The role of PI3k/AKT signaling pathway in attenuating liver fibrosis: a comprehensive review

Shamsan E, Almezgagi M, Gamah M, Khan N, Qasem A, Chuanchuan L, Haining F

Front Med (Lausanne)

25-Mar-2024

PMCID:	PMC10999701
doi:	10.3389/fmed.2024.1389329
PMID:	38590313

RNA editing events and expression profiles of mitochondrial protein-coding genes in the endemic and endangered medicinal plant, Corydalis saxicola

Li C, Liu H, Qin M, Tan YJ, Ou XL, Chen XY, Wei Y, Zhang ZJ, Lei M

Front Plant Sci

06-Feb-2024

PMCID:	PMC10876856
doi:	10.3389/fpls.2024.1332460
PMID:	38379941

Mechanisms and Therapeutic Strategies for MAFLD Targeting TLR4 Signaling Pathways

Ren G, Bai C, Yi S, Cong Q, Zhu Y

J Innate Immun

21-Dec-2023

PMCID:	PMC10783892
doi:	10.1159/000535524
PMID:	38128497

Review of the correlation between Chinese medicine and intestinal microbiota on the efficacy of diabetes mellitus

Su M, Hu R, Tang T, Tang W, Huang C

Front Endocrinol (Lausanne)

25-Jan-2023

PMCID:	PMC9905712
doi:	10.3389/fendo.2022.1085092
PMID:	36760813

Corydalis saxicola Bunting: A Review of Its Traditional Uses, Phytochemistry, Pharmacology, and Clinical Applications

Qin F, Chen Y, Wang FF, Tang SQ, Fang YL

Int J Mol Sci

13-Jan-2023

PMCID:	PMC9864617
doi:	10.3390/ijms24021626
PMID:	36675133

Bioactivity and In Silico Studies of Isoquinoline and Related Alkaloids as Promising Antiviral Agents: An Insight

Sharma D, Sharma N, Manchanda N, Prasad SK, Sharma PC, Thakur VK, Rahman MM, Dhobi M

Biomolecules

21-Dec-2022

PMCID:	PMC9856122
doi:	10.3390/biom13010017
PMID:	36671402

Role of bioactive compounds in the treatment of hepatitis: A review

Roy A, Roy M, Gacem A, Datta S, Zeyaullah M, Muzammil K, Farghaly TA, Abdellattif MH, Yadav KK, Simal-Gandara J

Front Pharmacol

21-Dec-2022

PMCID:	PMC9810990
doi:	10.3389/fphar.2022.1051751
PMID:	36618936

Investigation of the Therapeutic Effect of Total Alkaloids of Corydalis saxicola Bunting on CCl4-Induced Liver Fibrosis in Rats by LC/MS-Based Metabolomics Analysis and Network Pharmacology

Wang Q, Luo Z, Li D, Qin J, Pan Z, Guo B, Deng L, Nong Y, Huang Z, He Y, Guo H, Zhu D, Liang Y, Su Z

Metabolites

21-Dec-2022

PMCID:	PMC9866371
doi:	10.3390/metabo13010009
PMID:	36676934

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

Effects of Dietary Macleaya cordata Extract on Growth Performance, Biochemical Indices, and Intestinal Microbiota of Yellow-Feathered Broilers Subjected to Chronic Heat Stress

Wang M, Zhang J, Huang X, Liu Y, Zeng J

Animals (Basel)

26-Aug-2022

PMCID:	PMC9454434
doi:	10.3390/ani12172197
PMID:	36077916

The Traditional Uses, Phytochemistry, Pharmacokinetics, Pharmacology, Toxicity, and Applications of Corydalis saxicola Bunting: A Review

Guo Y, Zhao L, Chang B, Yu J, Bao J, Yao Q, Luo J

Front Pharmacol

16-Feb-2022

PMCID:	PMC8890665
doi:	10.3389/fphar.2022.822792
PMID:	35250571

The anti-hepatitis B virus and anti-hepatotoxic efficacies of solanopubamine, a rare alkaloid from Solanum schimperianum

Parvez MK, Al-Dosari MS, Rehman MT, Al-Rehaily AJ, Alqahtani AS, Alajmi MF

Saudi Pharm J

07-Feb-2022

PMCID:	PMC9068741
doi:	10.1016/j.jsps.2022.02.001
PMID:	35527834

Application Potential of Plant-Derived Medicines in Prevention and Treatment of Platinum-Induced Peripheral Neurotoxicity

Xu X, Jia L, Ma X, Li H, Sun C

Front Pharmacol

13-Jan-2022

PMCID:	PMC8793340
doi:	10.3389/fphar.2021.792331
PMID:	35095502

Geniposide Ameliorates Liver Fibrosis Through Reducing Oxidative Stress and Inflammatory Respose, Inhibiting Apoptosis and Modulating Overall Metabolism

Yang L, Bi L, Jin L, Wang Y, Li Y, Li Z, He W, Cui H, Miao J, Wang L

Front Pharmacol

24-Nov-2021

PMCID:	PMC8651620
doi:	10.3389/fphar.2021.772635
PMID:	34899328

Recent Progress on Biological Activity of Amaryllidaceae and Further Isoquinoline Alkaloids in Connection with Alzheimer’s Disease

Cahlíková L, Vrabec R, Pidaný F, Peřinová R, Maafi N, Mamun AA, Ritomská A, Wijaya V, Blunden G

Molecules

29-Aug-2021

PMCID:	PMC8434202
doi:	10.3390/molecules26175240
PMID:	34500673

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 / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
(+/-)-6-Acetonyldihydrosanguinarine	181538	Click to see CC(=O)CC1C2=C(C=CC3=C2OCO3)C4=C(N1C)C5=CC6=C(C=C5C=C4)OCO6	389.40	unknown	https://doi.org/10.1055/S-2007-981549
6-Acetonyl 5,6-dihydrosanguinarine	71745004	Click to see CC(=O)CC1C2=C(C=CC3=C2OCO3)C4=C(N1C)C5=CC6=C(C=C5C=C4)OCO6	389.40	unknown	https://doi.org/10.1055/S-2007-981549
Dihydrochelerythrine	485077	Click to see CN1CC2=C(C=CC(=C2OC)OC)C3=C1C4=CC5=C(C=C4C=C3)OCO5	349.40	unknown	https://doi.org/10.1055/S-2007-981549
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-2007-981549
> 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/10.1055/S-2007-981549
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/10.1055/S-2007-981549
> 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	https://doi.org/10.1007/S10600-007-0072-7
(+-)Thalictrifoline	335206	Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC5=C4OCO5)OC)OC	353.40	unknown	https://doi.org/10.1007/S10600-007-0072-7
(+/-)-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/10.1007/S10600-007-0072-7
(12S,13R)-17-methoxy-12-methyl-5,7-dioxa-1-azapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),9,14,16,18-hexaen-16-ol	101663202	Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC5=C4OCO5)OC)O	339.40	unknown	https://doi.org/10.1007/S10600-007-0072-7
(13aR)-3-methoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-2,9,10-triol	163189285	Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C(=C(C=C4)O)O)O	313.30	unknown	https://doi.org/10.1007/S10600-007-0072-7
(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/10.1007/S10600-007-0072-7
(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/10.1007/S10600-007-0072-7
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/10.1007/S10600-007-0072-7
16,17-Dimethoxy-12-methyl-5,7-dioxa-1-azapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),9,14,16,18-hexaene	3651568	Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC5=C4OCO5)OC)OC	353.40	unknown	https://doi.org/10.1055/S-2007-981549 https://doi.org/10.1007/S10600-007-0072-7
17-Methoxy-12-methyl-5,7-dioxa-1-azapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),9,14,16,18-hexaen-16-ol	74420699	Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC5=C4OCO5)OC)O	339.40	unknown	https://doi.org/10.1007/S10600-007-0072-7
2,3,10-trimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-9-ol	453215	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)O	341.40	unknown	https://doi.org/10.1007/S10600-007-0072-7
3-methoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-2,9,10-triol	144020841	Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C(=C(C=C4)O)O)O	313.30	unknown	https://doi.org/10.1007/S10600-007-0072-7
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-hexaen-24-ol	78410986	Click to see C1CN2CC3=C(C=CC4=C3OCO4)C(C2C5=CC6=C(C=C51)OCO6)O	339.30	unknown	https://doi.org/10.1007/S10600-007-0072-7
Cavidine	193148	Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC5=C4OCO5)OC)OC	353.40	unknown	https://doi.org/10.1055/S-2007-981549 https://doi.org/10.1007/S10600-007-0072-7
Cheilanthifoline	101277425	Click to see COC1=C(C=C2CCN3CC4=C(CC3C2=C1)C=CC5=C4OCO5)O	325.40	unknown	https://doi.org/10.1007/S10600-007-0072-7
Corydalin	326549	Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC	369.50	unknown	https://doi.org/10.1055/S-2007-981549
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-2007-981549
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/10.1055/S-2007-981549
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-2007-981549 https://doi.org/10.1007/S10600-007-0072-7
L-sinactine	8016594	Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C5=C(C=C4)OCO5)OC	339.40	unknown	https://doi.org/10.1007/S10600-007-0072-7
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/10.1007/S10600-007-0072-7
Sinactine	5321317	Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C5=C(C=C4)OCO5)OC	339.40	unknown	https://doi.org/10.1007/S10600-007-0072-7
Stylopin	697545	Click to see C1CN2CC3=C(CC2C4=CC5=C(C=C41)OCO5)C=CC6=C3OCO6	323.30	unknown	https://doi.org/10.1055/S-2007-981549
Stylopine	440583	Click to see C1CN2CC3=C(CC2C4=CC5=C(C=C41)OCO5)C=CC6=C3OCO6	323.30	unknown	https://doi.org/10.1007/S10600-007-0072-7
Tetrahydrocoptisine	6770	Click to see C1CN2CC3=C(CC2C4=CC5=C(C=C41)OCO5)C=CC6=C3OCO6	323.30	unknown	https://doi.org/10.1007/S10600-007-0072-7 https://doi.org/10.1055/S-2007-981549
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/10.1007/S10600-007-0072-7
Tetrahydropalmatrubine	11282465	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)O	341.40	unknown	https://doi.org/10.1007/S10600-007-0072-7
> Alkaloids and derivatives / Protopine alkaloids
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-2007-981549

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Corydalis saxicola

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top