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Tephroseris kirilowii

Tephroseris kirilowii - 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 UUID643fc6dc1d5af578808125
Scientific name Tephroseris kirilowii
Authority (DC.) Holub
First published in Folia Geobot. Phytotax. 12(4): 429 (1977)

Description Top

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Synonyms Top

Scientific name Authority First published in
Senecio integrifolius f. pseudo-pratensis Cufod. Repertorium Specierum Novarum Regni Vegetabilis, Beihefte 70: 60 1933
Senecio integrifolius var. spathulata (Miq.) Hara Enum. Sperm. Jap. 2: 254 (1952)
Senecio kirilowii Turcz. ex DC. Prodr. 6: 361 (1838)
Senecio integrifolius var. spathulifolius (Miq.) Hara Enumeratio Spermatophytarum Japonicarum 2: 254 1952
Senecio integrifolius subsp. kirilowii (Turcz. ex DC.) Kitag. Report of the Institute of Scientific Research, Manchoukuo 3(Append. 1): 469 1939
Senecio integrifolius subsp. fauriei Kitam. Acta Phytotax. Geobot. 6: 272 (1937)
Senecio aurantiacus var. spathulata Miq. Ann. Mus. Bot. Lugd.-Bat. 2: 181 (1866)
Senecio integrifolius subsp. amurensis (Schischk.) Vorosch.
Senecio campestris var. tomentosus Franch. Nouvelles archives du museum d'histoire naturelle, ser. 2 6: 54 1883
Senecio aurantiacus var. spathulifolius Miq. Annales Museum Botanicum Lugduno-Batavi 2: 181 1866
Tephroseris integrifolia subsp. kirilowii (Turcz. ex DC.) B.Nord. Opera Bot. 44: 45 (1978)
Senecio amurensis Schischk. Fl. URSS 26: 757, 883. 1961
Senecio tashiroi Hayata Icon. Pl. Formosan. 8: 68 (1919)
Senecio campestris subsp. kirilowii (Turcz. ex DC.) Kitag. Neolin. Fl. Manshur. : 678 (1979)

Common names Top

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Language Common/alternative name
Japanese オカオグルマ
Korean 솜방망이
Polish senecio integrifolius
Polish starzec polny
Chinese 狗舌草
Chinese 桑螵蛸
Chinese 狗舌头草

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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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
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
    • Siberia
      • Altay
      • Chita
      • Irkutsk
      • West Siberia
      • Yakutskiya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000009776
Tropicos 50157131
KEW urn:lsid:ipni.org:names:255231-1
The Plant List gcc-109470
Open Tree Of Life 567890
Observations.org 130331
NCBI Taxonomy 186974
IPNI 255231-1
iNaturalist 482934
GBIF 3131094
Freebase /m/0nbdc0g
CMAUP NPO13737

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
Flavonoids as promising molecules in the cancer therapy: An insight Mir SA, Dar A, Hamid L, Nisar N, Malik JA, Ali T, Bader GN Curr Res Pharmacol Drug Discov 08-Dec-2023
PMCID:PMC10733705
doi:10.1016/j.crphar.2023.100167
PMID:38144883
Natural products targeting inflammation-related metabolic disorders: A comprehensive review Nainu F, Frediansyah A, Mamada SS, Permana AD, Salampe M, Chandran D, Emran TB, Simal-Gandara J Heliyon 02-Jun-2023
PMCID:PMC10279840
doi:10.1016/j.heliyon.2023.e16919
PMID:37346355
Traditional Mongolian medicine: Past, present and future Bai L, Fu M Chin Herb Med 29-Jun-2022
PMCID:PMC9476767
doi:10.1016/j.chmed.2022.06.001
PMID:36118004
Flavonoids Targeting the mTOR Signaling Cascades in Cancer: A Potential Crosstalk in Anti-Breast Cancer Therapy Hussain Y, Khan H, Alam W, Aschner M, Abdullah, Alsharif KF, Saso L Oxid Med Cell Longev 27-Jun-2022
PMCID:PMC9252758
doi:10.1155/2022/4831833
PMID:35795855
Promoting Apoptosis, a Promising Way to Treat Breast Cancer With Natural Products: A Comprehensive Review Yuan L, Cai Y, Zhang L, Liu S, Li P, Li X Front Pharmacol 28-Jan-2022
PMCID:PMC8836889
doi:10.3389/fphar.2021.801662
PMID:35153757
Bioactive Phytochemicals with Anti-Aging and Lifespan Extending Potentials in Caenorhabditis elegans Okoro NO, Odiba AS, Osadebe PO, Omeje EO, Liao G, Fang W, Jin C, Wang B Molecules 02-Dec-2021
PMCID:PMC8658929
doi:10.3390/molecules26237323
PMID:34885907
Overview of the Antioxidant and Anti-Inflammatory Activities of Selected Plant Compounds and Their Metal Ions Complexes Mucha P, Skoczyńska A, Małecka M, Hikisz P, Budzisz E Molecules 12-Aug-2021
PMCID:PMC8398118
doi:10.3390/molecules26164886
PMID:34443474
The polyphenol/saponin-rich Rhus tripartita extract has an apoptotic effect on THP-1 cells through the PI3K/AKT/mTOR signaling pathway Tlili H, Macovei A, Buonocore D, Lanzafame M, Najjaa H, Lombardi A, Pagano A, Dossena M, Verri M, Arfa AB, Neffati M, Doria E BMC Complement Med Ther 27-May-2021
PMCID:PMC8161611
doi:10.1186/s12906-021-03328-9
PMID:34044827
ROCK1 activation-mediated mitochondrial translocation of Drp1 and cofilin are required for arnidiol-induced mitochondrial fission and apoptosis Hu J, Zhang H, Li J, Jiang X, Zhang Y, Wu Q, Shen L, Shi J, Gao N J Exp Clin Cancer Res 19-Feb-2020
PMCID:PMC7031977
doi:10.1186/s13046-020-01545-7
PMID:32075676
Flavonoids inhibit cell proliferation and induce apoptosis and autophagy through downregulation of PI3Kγ mediated PI3K/AKT/mTOR/p70S6K/ULK signaling pathway in human breast cancer cells Zhang HW, Hu JJ, Fu RQ, Liu X, Zhang YH, Li J, Liu L, Li YN, Deng Q, Luo QS, Ouyang Q, Gao N Sci Rep 26-Jul-2018
PMCID:PMC6062549
doi:10.1038/s41598-018-29308-7
PMID:30050147
Fast-cycling unit of root turnover in perennial herbaceous plants in a cold temperate ecosystem Sun K, Luke McCormack M, Li L, Ma Z, Guo D Sci Rep 21-Jan-2016
PMCID:PMC4726329
doi:10.1038/srep19698
PMID:26791578

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
Anolobine 164710 Click to see C1CNC2CC3=C(C=CC(=C3)O)C4=C2C1=CC5=C4OCO5 281.30 unknown via CMAUP database
Anonaine 160597 Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5 265.31 unknown via CMAUP database
Asimilobine 160875 Click to see COC1=C(C=C2CCNC3C2=C1C4=CC=CC=C4C3)O 267.32 unknown via CMAUP database
Atherospermidine 77514 Click to see COC1=C2C(=C3C4=CC=CC=C4C(=O)C5=NC=CC1=C35)OCO2 305.30 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
Dicentrinone 177744 Click to see COC1=C(C=C2C(=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O)OC 335.30 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
Lanuginosine 97622 Click to see COC1=CC2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O 305.30 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 via CMAUP database
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown via CMAUP database
Lysicamine 122691 Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC=CC=C42)OC 291.30 unknown via CMAUP database
Norisocorydine 12313549 Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)OC)OC)C=C1)O 327.40 unknown via CMAUP database
Norstephalagine 133381 Click to see COC1=C2C(=C3C4=CC=CC=C4CC5C3=C1CCN5)OCO2 295.30 unknown via CMAUP database
O-Nornuciferine 197017 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=CC=C43)OC)O 281.30 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
Romucosine 10734687 Click to see COC(=O)N1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 323.30 unknown via CMAUP database
Romucosine H 5320994 Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3C(=O)OC)OC)OC)C=C1)O 385.40 unknown via CMAUP database
Xylopine 160503 Click to see COC1=CC2=C(C=C1)C3=C4C(C2)NCCC4=CC5=C3OCO5 295.30 unknown via CMAUP database
> Alkaloids and derivatives / Aporphines / Hydroxy-7-aporphines
Michelalbine 10378981 Click to see C1CNC2C(C3=CC=CC=C3C4=C2C1=CC5=C4OCO5)O 281.30 unknown via CMAUP database
Ushinsunine 197018 Click to see CN1CCC2=CC3=C(C4=C2C1C(C5=CC=CC=C54)O)OCO3 295.30 unknown via CMAUP database
> Alkaloids and derivatives / Proaporphines
(4S)-10,11-dimethoxyspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohexa-2,5-diene]-1'-one 830726 Click to see COC1=C(C2=C3C(CC24C=CC(=O)C=C4)NCCC3=C1)OC 297.30 unknown via CMAUP database
Pronuciferine, (-)- 793841 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)OC)OC 311.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Halobenzoic acids and derivatives / Halobenzoic acids
3-Chlorobenzoic acid 447 Click to see C1=CC(=CC(=C1)Cl)C(=O)O 156.56 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
3,4,5-Trimethoxybenzoic acid 8357 Click to see COC1=CC(=CC(=C1OC)OC)C(=O)O 212.20 unknown via CMAUP database
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Methyl vanillate 19844 Click to see COC1=C(C=CC(=C1)C(=O)OC)O 182.17 unknown via CMAUP database
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3-Hydroxy-4-methoxybenzoic acid 12575 Click to see COC1=C(C=C(C=C1)C(=O)O)O 168.15 unknown via CMAUP database
Methyl 3-hydroxy-4-methoxybenzoate 4056967 Click to see COC1=C(C=C(C=C1)C(=O)OC)O 182.17 unknown via CMAUP database
Methyl 4-methoxybenzoate 8499 Click to see COC1=CC=C(C=C1)C(=O)OC 166.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see COC(=O)C1=CC=C(C=C1)O 152.15 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
(2S)-3-(4-hydroxy-3,5-dimethoxyphenyl)propane-1,2-diol 86330909 Click to see COC1=CC(=CC(=C1O)OC)CC(CO)O 228.24 unknown via CMAUP database
Isovanillin 12127 Click to see COC1=C(C=C(C=C1)C=O)O 152.15 unknown via CMAUP database
n-Dihydroferuloyltyramine 16119667 Click to see COC1=C(C=CC(=C1)CCC(=O)NCCC2=CC=C(C=C2)O)O 315.40 unknown via CMAUP database
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown via CMAUP database
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(+)-Lirioresinol C 11796268 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
Episyringaresinol 12309694 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
Syringaresinol, (+)- 443023 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
Acanthoside D 21603207 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC 742.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(16R)-17-Hydroxykaura-18-oic acid 44575990 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)CO)(C)C(=O)O 320.50 unknown via CMAUP database
(1S,4R,9R,10R,13R,14S)-14-(hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecan-14-ol 12112093 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(CO)O)C)C 306.50 unknown via CMAUP database
(1S,4S,5R,9S,10R,13R,14R)-14-(dimethoxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 46210308 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)C(OC)OC)(C)C(=O)O 364.50 unknown via CMAUP database
(4R)-17-Acetoxykauran-18-oic acid 102425890 Click to see CC(=O)OCC1CC23CCC4C(C2CCC1C3)(CCCC4(C)C(=O)O)C 362.50 unknown via CMAUP database
[(1S,4S,5R,9S,10R,13R,14R)-5-(hydroxymethyl)-5,9-dimethyl-14-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methanol 46210166 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)CO)C)CO 306.50 unknown via CMAUP database
16alphaH-17,19-ent-kauranediol 102594837 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)CO)C)CO 306.50 unknown via CMAUP database
16beta,17-Dihydroxy-ent-kaurane-19-oic acid 469209 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)(CO)O)(C)C(=O)O 336.50 unknown via CMAUP database
17-Hydroxykaura-18-oic acid 46210307 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)CO)(C)C(=O)O 320.50 unknown via CMAUP database
Diterpenoid SP-II 442023 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)(CO)O)(C)C(=O)O 336.50 unknown via CMAUP database
ent-Kauran-16-beta-ol 21593607 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(C)O)C)C 290.50 unknown via CMAUP database
Kaurane-16alpha,17-diol 13816761 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(CO)O)C)C 306.50 unknown via CMAUP database
Kaurenoic acid 73062 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown via CMAUP database
Methyl 16alpha,17-dihydroxy-ent-kauran-19-oate 46233487 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)(CO)O)(C)C(=O)OC 350.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(5beta,8alpha,9beta,10alpha,12alpha,16R)-16,17-Dihydroxyatisane-18-oic acid methyl ester 25006930 Click to see CC12CCCC(C1CCC34C2CC(CC3)C(C4)(CO)O)(C)C(=O)OC 350.50 unknown via CMAUP database
methyl (1S,4S,5R,9S,10R,12S,13R)-13-(acetyloxymethyl)-13-hydroxy-5,9-dimethyltetracyclo[10.2.2.01,10.04,9]hexadecane-5-carboxylate 25006927 Click to see CC(=O)OCC1(CC23CCC1CC2C4(CCCC(C4CC3)(C)C(=O)OC)C)O 392.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
Sitoindoside I 9832350 Click to see CCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O 815.30 unknown via CMAUP database
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasterol glucoside 6602508 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
9-beta-d-Arabinofuranosylade-nine 12358320 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Uridine 6029 Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O 244.20 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Cherimolacyclopeptide A 11205172 Click to see CCC(C)C1C(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)NCC(=O)NC(C(=O)NC(C(=O)N3CCCC3C(=O)N1)CC(C)C)CCSC)C(C)O)CCC(=O)N 838.00 unknown via CMAUP database
Cherimolacyclopeptide C 11216146 Click to see CCC(C)C1C(=O)N2CCCC2C(=O)N3CCCC3C(=O)NCC(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1)CC4=CNC5=CC=CC=C54)C)C 692.80 unknown via CMAUP database
Cherimolacyclopeptide D 11599937 Click to see CC1C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NCC(=O)NC(C(=O)NC(C(=O)N1)CC(=O)N)CC(C)C)C(C)O)C(C)C 652.70 unknown via CMAUP database
Cherimolacyclopeptide F 101773878 Click to see CCC(C)C1C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)N3CCCC3C(=O)NCC(=O)NC(C(=O)NCC(=O)N1)CCSC)CCSC)CC(C)C)CC4=CC=C(C=C4)O 960.20 unknown via CMAUP database
cyclo[Ala-Pro-Gly-Ala-Val-Pro-Ile-Tyr] 11585828 Click to see CCC(C)C1C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NCC(=O)NC(C(=O)NC(C(=O)N3CCCC3C(=O)N1)C(C)C)C)C)CC4=CC=C(C=C4)O 768.90 unknown via CMAUP database
cyclo[Gly-Leu-Gly-Phe-Tyr-Pro] 71608845 Click to see CC(C)CC1C(=O)NCC(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NCC(=O)N1)CC3=CC=C(C=C3)O)CC4=CC=CC=C4 634.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Koaburaside monomethyl ether 636454 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)CO)O)O)O 346.33 unknown via CMAUP database
Thalictoside 21629843 Click to see C1=CC(=CC=C1CC[N+](=O)[O-])OC2C(C(C(C(O2)CO)O)O)O 329.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone 68262 Click to see COC1=CC(=O)C=C(C1=O)OC 168.15 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
Cheritamine 101428698 Click to see CCCCC=CCCCCCCCCCCCCCCCCCCCCCCCC(=O)NCCC1=CNC2=CC=CC=C21 593.00 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(R)-1-[(4-Hydroxyphenyl)methyl]-5,6-dimethoxy-1,2,3,4-tetrahydroisoquinolin-7-ol 101687011 Click to see COC1=C2CCNC(C2=CC(=C1OC)O)CC3=CC=C(C=C3)O 315.40 unknown via CMAUP database
1-[Hydroxy(4-hydroxyphenyl)methyl]-6-methoxyisoquinolin-7-ol 637078 Click to see COC1=C(C=C2C(=C1)C=CN=C2C(C3=CC=C(C=C3)O)O)O 297.30 unknown via CMAUP database
1alpha-(3-Methoxy-4-hydroxybenzyl)-2-methyl-1,2,3,4-tetrahydro-6-methoxyisoquinoline-7-ol 14357385 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)O)OC)O)OC 329.40 unknown via CMAUP database
Annocherine B 5319094 Click to see COC1=C(C=C2C(=C1)C=CN=C2C(C3=CC=C(C=C3)O)OC)O 311.30 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
7-Hydroxy-6-methoxy-2-methylisoquinolin-1-one 59620302 Click to see CN1C=CC2=CC(=C(C=C2C1=O)O)OC 205.21 unknown via CMAUP database
Cherianoine 5315819 Click to see CN1C=CC2=CC(=C(C(=C2C1=O)OC)O)OC 235.24 unknown via CMAUP database
Thalifoline 89048 Click to see CN1CCC2=CC(=C(C=C2C1=O)O)OC 207.23 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Plaunol B 442074 Click to see C=C1CC2C3(C(C14CC(OC4=O)C5=COC=C5)CCC=C3C(=O)O2)CO 356.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Nicotinic acid 938 Click to see C1=CC(=CN=C1)C(=O)O 123.11 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines / Pyrrolidine carboxylic acids and derivatives / Pyrrolidinecarboxamides
2-Oxopyrrolidine-1-carboxamide 326996 Click to see C1CC(=O)N(C1)C(=O)N 128.13 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
4H-pyrano[3,4-c]quinolin-4-one 638628 Click to see C1=CC=C2C(=C1)C3=C(C=N2)C(=O)OC=C3 197.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
3-(3,4-Dihydroxyphenyl)-N-phenethylpropenamide, (E)- 11391937 Click to see C1=CC=C(C=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)O 283.32 unknown via CMAUP database
cis-Caffeoyltyramine 16119508 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC(=C(C=C2)O)O)O 299.32 unknown via CMAUP database
FERULOYL-beta-PHENETHYLAMINE 11162295 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=CC=C2)O 297.30 unknown via CMAUP database
n-cis-Feruloyltyramine 6440659 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown via CMAUP database
N-Feruloyl-3-methoxytyramine, (Z)- 5322166 Click to see COC1=C(C=CC(=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)OC)O 343.40 unknown via CMAUP database
N-trans-feruloylmethoxytyramine 5352115 Click to see COC1=C(C=CC(=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)OC)O 343.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Paprazine 5372945 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
methyl (2Z)-3-(4-hydroxyphenyl)acrylate 12343877 Click to see COC(=O)C=CC1=CC=C(C=C1)O 178.18 unknown via CMAUP database
Methyl 4-hydroxycinnamate 5319562 Click to see COC(=O)C=CC1=CC=C(C=C1)O 178.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
(1R,4Z,6R,7S,11R,17S)-4-ethylidene-7-hydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadecane-3,8-dione 11900051 Click to see CC=C1CC(C(C(=O)OCC2CCN3C2C(CC3)OC1=O)(C)O)C 337.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(4-Hydroxyphenyl)propionic acid 10394 Click to see C1=CC(=CC=C1CCC(=O)O)O 166.17 unknown via CMAUP database

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