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Thalictrum foliolosum

Thalictrum foliolosum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Thalictrum foliolosum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643ffe8942f69724720548
Scientific name Thalictrum foliolosum
Authority DC.
First published in Syst. Nat. 1: 175 (1817)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Thalictrum dalingo Buch.-Ham. ex DC. Syst. Nat. 1: 175 (1817)
Thalictrum villosum Jacquem. ex Lecoy. Bull. Soc. Roy. Bot. Belgique 24: 323 (1885)

Common names Top

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Language Common/alternative name
English leafy meadow-rue
Chinese 马尾连
Chinese 马尾黄连
Chinese 多叶唐松草
Chinese 金丝黄连

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

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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-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • West Himalaya
    • Indo-China
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000454082
Tropicos 27101933
KEW urn:lsid:ipni.org:names:714441-1
The Plant List kew-2512690
Open Tree Of Life 124406
NCBI Taxonomy 1277777
IPNI 714441-1
GBIF 3929091
EOL 2873978
USDA GRIN 36437
CMAUP NPO13637

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
Phenolic Compounds from Wild Plant and In Vitro Cultures of Ageratina pichichensis and Evaluation of Their Antioxidant Activity Motolinia-Alcántara EA, Franco-Vásquez AM, Nieto-Camacho A, Arreguín-Espinosa R, Rodríguez-Monroy M, Cruz-Sosa F, Román-Guerrero A Plants (Basel) 01-Mar-2023
PMCID:PMC10005229
doi:10.3390/plants12051107
PMID:36903964
Treatment Effects of Natural Products on Inflammatory Bowel Disease In Vivo and Their Mechanisms: Based on Animal Experiments Zhou Y, Wang D, Yan W Nutrients 18-Feb-2023
PMCID:PMC9967064
doi:10.3390/nu15041031
PMID:36839389
Diversity, distribution, and sustainability of traditional medicinal plants in Kaski district, western Nepal Khakurel D, Uprety Y, Ahn G, Cha JY, Kim WY, Lee SH, Rajbhandary S Front Pharmacol 20-Dec-2022
PMCID:PMC9807671
doi:10.3389/fphar.2022.1076351
PMID:36605393
Source dependent variation in phenolics, antioxidant and antimicrobial activity of Paeonia emodi in west Himalaya, India Joshi K, Adhikari P, Bhatt ID, Pande V Physiol Mol Biol Plants 28-Oct-2022
PMCID:PMC9636362
doi:10.1007/s12298-022-01242-z
PMID:36387977
Vegetation dynamics and soil nutrient availability in a temperate forest along altitudinal gradient of Nanda Devi Biosphere Reserve, Western Himalaya, India Maletha A, Maikhuri RK, Bargali SS, Sharma A, Negi VS, Rawat LS PLoS One 07-Oct-2022
PMCID:PMC9544032
doi:10.1371/journal.pone.0275051
PMID:36206256
A Sustainable Approach to a Cleaner Production of Antimicrobial and Biocompatible Protein Fibers Danila A, Costea M, Profire L, Rimbu CM, Baican M, Lupascu F, Tatarusanu SM, Profire BS, Muresan EI Polymers (Basel) 05-Aug-2022
PMCID:PMC9370899
doi:10.3390/polym14153194
PMID:35956710
Current Evidence and Future Directions of Berberine Intervention in Depression Zhu WQ, Wu HY, Sun ZH, Guo Y, Ge TT, Li BJ, Li X, Cui RJ Front Pharmacol 23-May-2022
PMCID:PMC9168319
doi:10.3389/fphar.2022.824420
PMID:35677435
Organization, Phylogenetic Marker Exploitation, and Gene Evolution in the Plastome of Thalictrum (Ranunculaceae) Xiang KL, Mao W, Peng HW, Erst AS, Yang YX, He WC, Wu ZQ Front Plant Sci 20-May-2022
PMCID:PMC9166237
doi:10.3389/fpls.2022.897843
PMID:35668810
Characterization of the complete chloroplast genome of Thalictrum foliolosum DC. 1817, a folk medicine plant in China Pu T, Zhou Z, Zhang Z, Zhang M Mitochondrial DNA B Resour 05-Apr-2022
PMCID:PMC9004500
doi:10.1080/23802359.2022.2055981
PMID:35425861
Taify Pomegranate Juice (TPJ) Abrogates Acrylamide-Induced Oxidative Stress Through the Regulation of Antioxidant Activity, Inflammation, and Apoptosis-Associated Genes El-Shehawi AM, Sayed S, Hassan MM, Al-Otaibi S, Althobaiti F, Elseehy MM, Soliman M Front Vet Sci 22-Mar-2022
PMCID:PMC8980525
doi:10.3389/fvets.2022.833605
PMID:35392110
Phytoconstituents of traditional Himalayan Herbs as potential inhibitors of Human Papillomavirus (HPV-18) for cervical cancer treatment: An In silico Approach Salaria D, Rolta R, Mehta J, Awofisayo O, Fadare OA, Kaur B, Kumar B, Araujo da Costa R, Chandel SR, Kaushik N, Choi EH, Kaushik NK PLoS One 17-Mar-2022
PMCID:PMC8929605
doi:10.1371/journal.pone.0265420
PMID:35298541
Role of Dexamethasone and Methylprednisolone Corticosteroids in Coronavirus Disease 2019 Hospitalized Patients: A Review Mehta J, Rolta R, Mehta BB, Kaushik N, Choi EH, Kaushik NK Front Microbiol 15-Feb-2022
PMCID:PMC8886296
doi:10.3389/fmicb.2022.813358
PMID:35242118
Multifarious global flora fabricated phytosynthesis of silver nanoparticles: a green nanoweapon for antiviral approach including SARS-CoV-2 Karthik C, Punnaivalavan KA, Prabha SP, Caroline DG Int Nano Lett 12-Feb-2022
PMCID:PMC8853038
doi:10.1007/s40089-022-00367-z
PMID:35194512
Jatrorrhizine: A Review of Sources, Pharmacology, Pharmacokinetics and Toxicity Zhong F, Chen Y, Chen J, Liao H, Li Y, Ma Y Front Pharmacol 13-Jan-2022
PMCID:PMC8793695
doi:10.3389/fphar.2021.783127
PMID:35095493
Distribution of Therapeutic Efficacy of Ranunculales Plants Used by Ethnic Minorities on the Phylogenetic Tree of Chinese Species Hao DC, Zhang Y, He CN, Xiao PG Evid Based Complement Alternat Med 12-Jan-2022
PMCID:PMC8769838
doi:10.1155/2022/9027727
PMID:35069772

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 / 6,6a-secoaporphines
Thaliglucinone 182266 Click to see CN(C)CCC1=CC(=C2C3=C1C=CC4=CC5=C(C(=C43)C(=O)O2)OCO5)OC 365.40 unknown via CMAUP database
> Alkaloids and derivatives / Aporphines
5-Hydroxy-4,15,16-trimethoxy-10,10-dimethyl-10-azatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadeca-1(16),2(7),3,5,13(17),14-hexaen-10-ium 5315336 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC)C 356.40 unknown https://doi.org/10.1016/0031-9422(83)80176-9
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 https://doi.org/10.1021/NP50021A003
https://doi.org/10.1016/0031-9422(83)80176-9
Magnoflorine iodide, (+)-(RG) 131664584 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)[O-])OC)C.I 469.30 unknown via CMAUP database
Thalicarpine 21470 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC5=CC(=C(C=C5CC6C7=CC(=C(C=C7CCN6C)OC)OC)OC)OC)OC)OC 696.80 unknown https://doi.org/10.1021/NP50021A003
Xanthoplanine 14262868 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC)C 356.40 unknown https://doi.org/10.1016/0031-9422(83)80176-9
> Alkaloids and derivatives / Hasubanan alkaloids
Hernandifoline 5475263 Click to see COC1C(CC23CCNC24C1(OC(C4)C5=C3C(=C(C=C5)OC)O)OC)OC(=O)C=CC6=CC(=C(C=C6)OC)O 539.60 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(11R)-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-octaene-11,17-diol 154497569 Click to see COC1=C(C=CC2=CC3=[N+](CC(C4=CC5=C(C=C43)OCO5)O)C=C21)O 338.30 unknown https://doi.org/10.1021/NP50013A008
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/10.1016/0031-9422(83)80176-9
https://doi.org/10.1021/NP50013A008
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
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-7-ium-3-ol;iodide 5459338 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)O)OC)OC.[I-] 465.30 unknown via CMAUP database
3,9,10-trimethoxy-6,8-dihydro-5H-isoquinolino[2,1-b]isoquinolin-2-ol 162867762 Click to see COC1=C(C2=C(C=C1)C=C3C4=CC(=C(C=C4CCN3C2)OC)O)OC 339.40 unknown https://doi.org/10.1016/0031-9422(83)80176-9
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/10.1021/NP50021A003
https://doi.org/10.1016/0031-9422(83)80176-9
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 https://doi.org/10.1016/0031-9422(83)80176-9
https://doi.org/10.1021/NP50013A008
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
Dihydroberberine 10217 Click to see COC1=C(C2=C(C=C1)C=C3C4=CC5=C(C=C4CCN3C2)OCO5)OC 337.40 unknown https://doi.org/10.1016/0031-9422(83)80176-9
Dihydropalmatine 1023495 Click to see COC1=C(C2=C(C=C1)C=C3C4=CC(=C(C=C4CCN3C2)OC)OC)OC 353.40 unknown https://doi.org/10.1016/0031-9422(83)80176-9
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
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/10.1016/0031-9422(83)80176-9
https://doi.org/10.1021/NP50021A003
Thalifendine 3084288 Click to see COC1=C(C=CC2=CC3=[N+](CCC4=CC5=C(C=C43)OCO5)C=C21)O 322.30 unknown https://doi.org/10.1021/NP50013A008
https://doi.org/10.1016/0031-9422(83)80176-9
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
> 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
Cryptopine 72616 Click to see CN1CCC2=CC(=C(C=C2C(=O)CC3=C(C1)C4=C(C=C3)OCO4)OC)OC 369.40 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 / Anthracenes
Palmidin A 5320384 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C5=C(C(=CC=C5)O)C(=O)C6=C4C=C(C=C6O)CO)C=C(C=C3O)O 510.50 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
Javanicin 10149 Click to see CC1=C(C(=C2C(=C1O)C(=O)C=C(C2=O)OC)O)CC(=O)C 290.27 unknown via CMAUP database
> Lignans, neolignans and related compounds
(1S,14S)-9,20,21,25-tetramethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18(33),19,21,24,26,31-dodecaen-19-ol 10627884 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)O)OC)OC 638.70 unknown via CMAUP database
6,20,21,25-Tetramethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.29,12.13,7.114,18.027,31.022,33]hexatriaconta-3(36),4,6,9(35),10,12(34),18(33),19,21,24,26,31-dodecaen-19-ol 3696942 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)O)C=C5)OC 638.70 unknown via CMAUP database
Berbamine 275182 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown via CMAUP database
CID 5458555 5458555 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC 608.70 unknown via CMAUP database
Homoaromoline 99620 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)OC)O)OC 608.70 unknown https://doi.org/10.1021/NP50021A003
https://doi.org/10.1021/NP50013A008
Isotetrandrine 5422 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown via CMAUP database
O-Methylberbamine 5351212 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown via CMAUP database
Repandine 10031631 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)OC)OC 608.70 unknown via CMAUP database
Talysopine 179390 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)O)C=C5)OC 638.70 unknown https://doi.org/10.1021/NP50021A003
https://doi.org/10.1021/NP50013A008
Thalidasine 159795 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)O3)OC)OC)C=C5)OC)OC 652.80 unknown https://doi.org/10.1021/NP50021A003
Thalmine 442366 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)O3)O)OC)C=C5)OC 608.70 unknown via CMAUP database
Thalrugosidine 5321920 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)O3)OC)OC)C=C5)O)OC 638.70 unknown https://doi.org/10.1021/NP50013A008
https://doi.org/10.1021/NP50021A003
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
Magnograndiolide 5319198 Click to see CC1(CCC2C(C3C1CCC3(C)O)OC(=O)C2=C)O 266.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(1R)-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohex-2-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol 25245095 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C 568.90 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
(12S,26S)-4,5,17,31-tetramethoxy-11,27-dimethyl-2,19,33,35-tetraoxa-11,27-diazaoctacyclo[24.10.1.114,18.120,24.03,8.07,12.030,37.032,36]nonatriaconta-1(36),3(8),4,6,14(39),15,17,20,22,24(38),30(37),31-dodecaene 5321901 Click to see CN1CCC2=C3C(=C(C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=CC(=C5)CC6C7=C(CCN6C)C(=C8C(=C7O3)OCO8)OC)OC)OC 666.80 unknown via CMAUP database
21,22,26-Trimethoxy-16,31-dimethyl-8,24-dioxa-16,31-diazaheptacyclo[23.6.2.13,7.19,13.115,19.028,32.023,34]hexatriaconta-3(36),4,6,9,11,13(35),19,21,23(34),25,27,32-dodecaen-10-ol 45356938 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=CC=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
11,12-Dimethoxy-6,8,9,15-tetrahydro[1,3]benzodioxolo[4,5-c]benzo[g]azecin-14(7H)-one 371229 Click to see COC1=C(C=C2C(=C1)CCNCC3=C(CC2=O)C=CC4=C3OCO4)OC 355.40 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydroisoquinolines
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-octaene-11,17-diol 12443385 Click to see COC1=C(C=CC2=CC3=[N+](CC(C4=CC5=C(C=C43)OCO5)O)C=C21)O 338.30 unknown https://doi.org/10.1016/0031-9422(83)80176-9
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1S)-1-[(3-hydroxy-4-methoxyphenyl)methyl]-6-methoxy-2-methyl-1H-isoquinolin-7-ol 132988891 Click to see CN1C=CC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 327.40 unknown https://doi.org/10.1016/0031-9422(83)80176-9
(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
1-[(3-hydroxy-4-methoxyphenyl)methyl]-6-methoxy-2-methyl-1H-isoquinolin-7-ol 163026942 Click to see CN1C=CC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 327.40 unknown https://doi.org/10.1016/0031-9422(83)80176-9
Reticuline 439653 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1021/NP50021A003
Rugosinone 442350 Click to see COC1=C(C(=C(C=C1)C(=O)C2=NC=CC3=CC4=C(C=C32)OCO4)O)OC 353.30 unknown https://doi.org/10.1016/0031-9422(83)80176-9
Tembetarine 167718 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC)C 344.40 unknown https://doi.org/10.1016/0031-9422(83)80176-9
Thalirugidine 44584027 Click to see CN1CCC2=C(C(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC5C6=CC(=C(C(=C6CCN5C)O)OC)OC)OC)OC)OC)O 670.80 unknown https://doi.org/10.1021/NP50013A008
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
10-Hydroxy-2,9-dimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one 102316664 Click to see COC1=CC2=C3C=C4C=CC(=C(C4=CN3CCC2=CC1=O)OC)O 323.30 unknown https://doi.org/10.1021/NP50013A008
https://doi.org/10.1016/0031-9422(83)80176-9
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/10.1016/0031-9422(83)80176-9
Noroxyhydrastinine 89047 Click to see C1CNC(=O)C2=CC3=C(C=C21)OCO3 191.18 unknown via CMAUP database
Oxyberberine 11066 Click to see COC1=C(C2=C(C=C1)C=C3C4=CC5=C(C=C4CCN3C2=O)OCO5)OC 351.40 unknown https://doi.org/10.1021/NP50013A008
> Organoheterocyclic compounds / Pteridines and derivatives
6-(2-hydroxypropanoyl)-4a,7-dihydro-1H-pteridine-2,4-dione 25200994 Click to see CC(C(=O)C1=NC2C(=NC1)NC(=O)NC2=O)O 238.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
2-[(8S)-2-oxo-8,9-dihydrofuro[2,3-h]chromen-8-yl]propan-2-yl (Z)-2-methylbut-2-enoate 53399217 Click to see CC=C(C)C(=O)OC(C)(C)C1CC2=C(O1)C=CC3=C2OC(=O)C=C3 328.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 99647392 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)O)O 676.70 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
> Phenylpropanoids and polyketides / Tannins
(-)-Thalrugosaminine 5321919 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)OC)C=C5)OC 652.80 unknown via CMAUP database
5,6,6',7,12-Pentamethoxy-2-methyl-1',2'-didehydroberbaman 494542 Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6=NCCC7=CC(=C(C=C76)OC3=C(C(=C2OC)OC)OC)OC)C=C5 636.70 unknown via CMAUP database
Hernandezine (7CI, 8CI) 362567 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)OC)OC)OC 652.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Acide tannique [French] 16133892 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2=CC(=CC(=C2O)O)C(=O)OCC3C(C(C(C(O3)OC(=O)C4=CC(=C(C(=C4)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6)OC(=O)C7=CC(=C(C(=C7)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)OC(=O)C9=CC(=C(C(=C9)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O 1701.20 unknown via CMAUP database

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