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Pseudostellaria heterophylla

Pseudostellaria heterophylla - 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 UUID643ff7ed792e9893083801
Scientific name Pseudostellaria heterophylla
Authority (Miq.) Pax
First published in Nat. Pflanzenfam. ed. 2 , 16c: 318 (1934)

Description Top

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Synonyms Top

Scientific name Authority First published in
Krascheninikovia heterophylla Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 187 (1867)
Pseudostellaria rhaphanorrhiza (Hemsl.) Pax Nat. Pflanzenfam. ed. 2 , 16c: 318 (1934)
Stellaria heterophylla Hemsl. ex F.B.Forbes & Hemsl. J. Linn. Soc., Bot. 23: 68 (1886)
Stellaria rhaphanorrhiza Hemsl. J. Linn. Soc., Bot. 23: 69 (1886)
Krascheninikovia rhaphanorrhiza (Hemsl.) Korsh. Izv. Imp. Akad. Nauk , ser. 5, 9: 39 (1898)

Common names Top

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Language Common/alternative name
English hai er shen
English tai zi shen
Arabic نجمية كاذبة متباينة الورق
Japanese ワダソウ
Korean 개별꽃
Chinese 孩儿参
Chinese 孩儿参（太子参）
Chinese 太子参
Chinese 异叶假繁缕
Chinese 孩兒參

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
      • Qinghai
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Primorye

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000395657
UNII 2E0DVE4XPS
Tropicos 6302943
KEW urn:lsid:ipni.org:names:156276-1
The Plant List kew-2409729
Open Tree Of Life 698777
Observations.org 127917
NCBI Taxonomy 418402
IPNI 156276-1
iNaturalist 565423
GBIF 3815617
Freebase /m/02qhft1
EPPO QSTHP
EOL 2873188
Elurikkus 418074
USDA GRIN 423510
Wikipedia Pseudostellaria_heterophylla
CMAUP NPO6715

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
Metabolomics analysis reveals the metabolite profiles of Rheum tanguticum grown under different altitudinal gradients Wang L, Zhao S, Li J, Zhou G BMC Plant Biol 28-Mar-2024
PMCID:PMC10976683
doi:10.1186/s12870-024-04933-9
PMID:38539101
A review of chemotherapeutic drugs-induced arrhythmia and potential intervention with traditional Chinese medicines Li W, Cheng X, Zhu G, Hu Y, Wang Y, Niu Y, Li H, Aierken A, Li J, Feng L, Liu G Front Pharmacol 20-Mar-2024
PMCID:PMC10987752
doi:10.3389/fphar.2024.1340855
PMID:38572424
A multi-center cross-sectional study of Chinese Herbal Medicine-Drug adverse reactions using active surveillance in Singapore’s Traditional Chinese Medicine clinics Ng CY, Zhao Y, Wang N, Chia KL, Teo CH, Peh W, Yeo P, Zhong LL Chin Med 07-Mar-2024
PMCID:PMC10918936
doi:10.1186/s13020-024-00915-z
PMID:38454483
Traditional Chinese medicine treats ulcerative colitis by regulating gut microbiota, signaling pathway and cytokine: Future novel method option for pharmacotherapy Wang T, Liu X, Zhang W, Wang J, Wang T, Yue W, Ming L, Cheng J, Sun J Heliyon 06-Mar-2024
PMCID:PMC10945194
doi:10.1016/j.heliyon.2024.e27530
PMID:38501018
Antitumour mechanisms of traditional Chinese medicine elicited by regulating tumour-associated macrophages in solid tumour microenvironments Gao J, Tan W, Yuan L, Wang H, Wen J, Sun K, Chen X, Wang S, Deng W Heliyon 02-Mar-2024
PMCID:PMC10923716
doi:10.1016/j.heliyon.2024.e27220
PMID:38463777
A Prospective, Multicentered, Randomized, Double-Blind, Placebo-Controlled Clinical Trial of Keluoxin Capsules in the Treatment of Microalbuminuria in Patients with Type 2 Early Diabetic Kidney Disease Zhao J, Wang S, Li X, Zhang G, Xu Y, Zheng X, Guo J, Zhang Z J Integr Complement Med 14-Feb-2024
PMCID:PMC10884549
doi:10.1089/jicm.2022.0809
PMID:37733303
Synergistic Effects of Oligochitosan and Pyraclostrobin in Controlling Leaf Spot Disease in Pseudostellaria heterophylla Zhang C, Tang C, Wang Q, Su Y, Zhang Q Antibiotics (Basel) 27-Jan-2024
PMCID:PMC10886130
doi:10.3390/antibiotics13020128
PMID:38391514
Bioactive peptides: an alternative therapeutic approach for cancer management Ghadiri N, Javidan M, Sheikhi S, Taştan Ö, Parodi A, Liao Z, Tayybi Azar M, Ganjalıkhani-Hakemi M Front Immunol 24-Jan-2024
PMCID:PMC10847386
doi:10.3389/fimmu.2024.1310443
PMID:38327525
Recent advances in the extraction, purification, structural-property correlations, and antiobesity mechanism of traditional Chinese medicine-derived polysaccharides: a review Zhi N, Chang X, Wang X, Guo J, Chen J, Gui S Front Nutr 17-Jan-2024
PMCID:PMC10828026
doi:10.3389/fnut.2023.1341583
PMID:38299183
Medicine for chronic atrophic gastritis: a systematic review, meta- and network pharmacology analysis Weng J, Wu XF, Shao P, Liu XP, Wang CX Ann Med 03-Jan-2024
PMCID:PMC10769149
doi:10.1080/07853890.2023.2299352
PMID:38170849
The Role of AMPK Signaling in Ulcerative Colitis Yuan Y, Wang F, Liu X, Shuai B, Fan H Drug Des Devel Ther 29-Dec-2023
PMCID:PMC10759424
doi:10.2147/DDDT.S442154
PMID:38170149
Extraction of Polysaccharides from Root of Pseudostellaria heterophylla (Miq.) Pax. and the Effects of Ultrasound Treatment on Its Properties and Antioxidant and Immune Activities Li H, Liu Z, Liu Q, Zhang X, Li S, Tang F, Zhang L, Yang Q, Wang Q, Yang S, Huang L, Ba Y, Du X, Yang F, Feng H Molecules 26-Dec-2023
PMCID:PMC10779800
doi:10.3390/molecules29010142
PMID:38202725
An exploration of the effect of Chinese herbal compound on the occurrence and development of large intestine cancer and intestinal flora Liu P, Ying J, Guo X, Tang X, Zou W, Wang T, Xu X, Zhao B, Song N, Cheng J Heliyon 10-Dec-2023
PMCID:PMC10761579
doi:10.1016/j.heliyon.2023.e23533
PMID:38173486
In Vitro Studies of Endophytic Bacteria Isolated from Ginger (Zingiber officinale) as Potential Plant-Growth-Promoting and Biocontrol Agents against Botrytis cinerea and Colletotrichum acutatum Bódalo A, Borrego R, Garrido C, Bolivar-Anillo HJ, Cantoral JM, Vela-Delgado MD, González-Rodríguez VE, Carbú M Plants (Basel) 30-Nov-2023
PMCID:PMC10708395
doi:10.3390/plants12234032
PMID:38068667
A Probiotic Bacillus amyloliquefaciens D-1 Strain Is Responsible for Zearalenone Detoxifying in Coix Semen Deng T, Chen Y, Zhang J, Gao Y, Yang C, Jiang W, Ou X, Wang Y, Guo L, Zhou T, Yuan QS Toxins (Basel) 28-Nov-2023
PMCID:PMC10747864
doi:10.3390/toxins15120674
PMID:38133178

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 / Tropane alkaloids
Apoatropine 64695 Click to see CN1C2CCC1CC(C2)OC(=O)C(=C)C3=CC=CC=C3 271.35 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 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
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
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 / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see C1=CC=C(C(=C1)C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1021/NP50060A030
https://doi.org/10.1007/978-3-7091-1084-3_4
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Glyceryl monolinoleate 5283469 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC(CO)O 354.50 unknown https://doi.org/10.1021/NP50060A030
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1021/NP50060A030
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Tripalmitin 11147 Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC 807.30 unknown https://doi.org/10.1007/978-3-7091-1084-3_4
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(+)-Taraxerol 42608290 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown via CMAUP database
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown via CMAUP database
Taraxerol acetate 94225 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
3-butyl-6-[(3S,4E,7E,10E,12E,15R,16R,17S,18E)-3,15,17-trihydroxy-4,8,10,12,16,18-hexamethylicosa-4,7,10,12,18-pentaen-2-yl]pyran-2-one 101692352 Click to see CCCCC1=CC=C(OC1=O)C(C)C(C(=CCC=C(C)CC(=CC(=CCC(C(C)C(C(=CC)C)O)O)C)C)C)O 554.80 unknown https://doi.org/10.1016/S0040-4020(01)81333-8
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(10R)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45358157 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
(1S,2R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45483617 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
3beta-Hydroxy-1,11-dioxo-ergosta-8,24(28)-diene-4alpha-carboxylic acid 9982179 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CC(=O)C3=C2CCC4C3(C(=O)CC(C4C(=O)O)O)C)C 470.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 6432744 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
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
> 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
> 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 / Alpha amino acids and derivatives / Alanine and derivatives
DL-Alanine 602 Click to see CC(C(=O)O)N 89.09 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acid esters
Methyl 4-hydroxy-5-oxopyrrolidine-2-carboxylate 54154956 Click to see COC(=O)C1CC(C(=O)N1)O 159.14 unknown https://doi.org/10.1002/HLCA.200390280
Methyl 5-oxo-L-prolinate 78646 Click to see COC(=O)C1CCC(=O)N1 143.14 unknown https://doi.org/10.1002/HLCA.200390280
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
DL-Glutamine 738 Click to see C(CC(=O)N)C(C(=O)O)N 146.14 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
Lysine, DL- 866 Click to see C(CCN)CC(C(=O)O)N 146.19 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
N,N-Dimethylglycine 673 Click to see CN(C)CC(=O)O 103.12 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Arginine and derivatives
DL-Arginine 232 Click to see C(CC(C(=O)O)N)CN=C(N)N 174.20 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Asparagine and derivatives
DL-Asparagine 236 Click to see C(C(C(=O)O)N)C(=O)N 132.12 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
DL-Glutamic acid 611 Click to see C(CC(=O)O)C(C(=O)O)N 147.13 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Histidine and derivatives
DL-Histidine 773 Click to see C1=C(NC=N1)CC(C(=O)O)N 155.15 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Leucine and derivatives
DL-Leucine 857 Click to see CC(C)CC(C(=O)O)N 131.17 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
DL-Phenylalanine 994 Click to see C1=CC=C(C=C1)CC(C(=O)O)N 165.19 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
(2S)-4-Hydroxy-5-oxopyrrolidine-2-carboxylic acid 45082769 Click to see C1C(C(=O)NC1C(=O)O)O 145.11 unknown https://doi.org/10.1002/HLCA.200390280
DL-Pyroglutamic acid 499 Click to see C1CC(=O)NC1C(=O)O 129.11 unknown https://doi.org/10.1002/HLCA.200390280
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
DL-Tyrosine 1153 Click to see C1=CC(=CC=C1CC(C(=O)O)N)O 181.19 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Valine and derivatives
DL-Valine 1182 Click to see CC(C)C(C(=O)O)N 117.15 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Gamma amino acids and derivatives
Gamma-Aminobutyric Acid 119 Click to see C(CC(=O)O)CN 103.12 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Cyclic peptides
cyclo[DL-Ala-Gly-DL-Pro-DL-Val-DL-Tyr] 85937010 Click to see CC1C(=O)NCC(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)N1)CC3=CC=C(C=C3)O)C(C)C 487.50 unknown https://doi.org/10.1002/HLCA.200390280
cyclo[Gly-aThr-D-Leu-Pro-Ser-D-Pro-D-Phe-Leu] 162970182 Click to see CC(C)CC1C(=O)NCC(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)N3CCCC3C(=O)NC(C(=O)N1)CC4=CC=CC=C4)CO)CC(C)C)C(C)O 813.00 unknown https://doi.org/10.1016/S0040-4020(01)81333-8
cyclo[Gly-aThr-D-Leu-Pro-Ser-Pro-D-Phe-Ile] 163188846 Click to see CCC(C)C1C(=O)NCC(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)N3CCCC3C(=O)NC(C(=O)N1)CC4=CC=CC=C4)CO)CC(C)C)C(C)O 813.00 unknown https://doi.org/10.1016/S0040-4020(01)89612-5
cyclo[Gly-DL-xiThr-DL-Leu-DL-Pro-DL-Ser-DL-Pro-DL-Phe-DL-xiIle] 163019554 Click to see CCC(C)C1C(=O)NCC(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)N3CCCC3C(=O)NC(C(=O)N1)CC4=CC=CC=C4)CO)CC(C)C)C(C)O 813.00 unknown https://doi.org/10.1016/S0040-4020(01)81333-8
https://doi.org/10.1016/S0040-4020(01)89612-5
cyclo[Gly-Gly-DL-Tyr-DL-Leu-DL-Pro-DL-Pro-DL-Leu-DL-Ser] 73826615 Click to see CC(C)CC1C(=O)NC(C(=O)NCC(=O)NCC(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)N3CCCC3C(=O)N1)CC(C)C)CC4=CC=C(C=C4)O)CO 784.90 unknown https://doi.org/10.1016/S0040-4020(01)89612-5
cyclo[Gly-Gly-DL-Tyr-DL-Pro-DL-Leu-DL-xiIle-DL-Leu] 73657322 Click to see CCC(C)C1C(=O)NC(C(=O)NCC(=O)NCC(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)N1)CC(C)C)CC3=CC=C(C=C3)O)CC(C)C 713.90 unknown https://doi.org/10.1016/S0040-4020(01)89612-5
cyclo[Gly-Gly-Tyr-D-Leu-Pro-Pro-D-Leu-Ser] 163190951 Click to see CC(C)CC1C(=O)NC(C(=O)NCC(=O)NCC(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)N3CCCC3C(=O)N1)CC(C)C)CC4=CC=C(C=C4)O)CO 784.90 unknown https://doi.org/10.1016/S0040-4020(01)89612-5
cyclo[Gly-Gly-Tyr-Pro-Leu-D-aIle-Leu] 162925294 Click to see CCC(C)C1C(=O)NC(C(=O)NCC(=O)NCC(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)N1)CC(C)C)CC3=CC=C(C=C3)O)CC(C)C 713.90 unknown https://doi.org/10.1016/S0040-4020(01)89612-5
cyclo[Gly-Gly-Tyr-Pro-Leu-D-Ile-Leu] 162925295 Click to see CCC(C)C1C(=O)NC(C(=O)NCC(=O)NCC(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)N1)CC(C)C)CC3=CC=C(C=C3)O)CC(C)C 713.90 unknown https://doi.org/10.1016/S0040-4020(01)89612-5
cyclo[Gly-Ile-Thr-Pro-Val-Ile-Phe] 163041584 Click to see CCC(C)C1C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NCC(=O)N1)CC3=CC=CC=C3)C(C)CC)C(C)C)C(C)O 727.90 unknown https://doi.org/10.1016/S0031-9422(00)95114-8
Pseudostellarin H 10463302 Click to see CC(C)CC1C(=O)NC(C(=O)NC(C(=O)NCC(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)N3CCCC3C(=O)N1)C(C)O)C(C)O)CC4=CC=CC=C4)CC5=CC=CC=C5 861.00 unknown https://doi.org/10.1021/NP50120A021
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
(2S)-N-[(1S)-1-[[(1S)-1-(acetylcarbamoyl)-4-guanidino-butyl]carbamoyl]-4-guanidino-butyl]-5-guanidino-2-[[(2S)-5-guanidino-2-[[(2S)-5-guanidino-2-[[(2S)-5-guanidino-2-[[(2S)-5-guanidino-2-[[(2S)-5-guanidino-2-[[(2S)-5-guanidino-2-hydroxy-pentanoyl]amino]pentanoyl]amino]pentanoyl]amino]pentanoyl]amino]pentanoyl]amino]pentanoyl]amino]pentanamide 49769220 Click to see CC(=O)NC(=O)C(CCCN=C(N)N)NC(=O)C(CCCN=C(N)N)NC(=O)C(CCCN=C(N)N)NC(=O)C(CCCN=C(N)N)NC(=O)C(CCCN=C(N)N)NC(=O)C(CCCN=C(N)N)NC(=O)C(CCCN=C(N)N)NC(=O)C(CCCN=C(N)N)NC(=O)C(CCCN=C(N)N)O 1465.70 unknown via CMAUP database
cyclo(Gly-Tyr-Gly-Pro-Leu-Ile-Leu-) 10055626 Click to see CCC(C)C1C(=O)NC(C(=O)NCC(=O)NC(C(=O)NCC(=O)N2CCCC2C(=O)NC(C(=O)N1)CC(C)C)CC3=CC=C(C=C3)O)CC(C)C 713.90 unknown via CMAUP database
cyclo[Ala-Gly-Pro-Tyr-aIle] 162907094 Click to see CCC(C)C1C(=O)NC(C(=O)NCC(=O)N2CCCC2C(=O)NC(C(=O)N1)CC3=CC=C(C=C3)O)C 501.60 unknown https://doi.org/10.1021/NP50120A021
cyclo[Ala-Pro-Phe-Ser-Phe-Gly-Pro-Ile] 163103792 Click to see CCC(C)C1C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NCC(=O)N3CCCC3C(=O)N1)CC4=CC=CC=C4)CO)CC5=CC=CC=C5)C 816.90 unknown https://doi.org/10.1021/NP50120A021
cyclo[DL-Ala-DL-Pro-DL-Phe-DL-Ser-DL-Phe-Gly-DL-Pro-DL-xiIle] 163103791 Click to see CCC(C)C1C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NCC(=O)N3CCCC3C(=O)N1)CC4=CC=CC=C4)CO)CC5=CC=CC=C5)C 816.90 unknown https://doi.org/10.1016/S0040-4039(00)73238-2
cyclo[Gly-D-Thr-D-Pro-D-aThr-Pro-D-aIle-D-Phe-Phe] 163086074 Click to see CCC(C)C1C(=O)NC(C(=O)NC(C(=O)NCC(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)N3CCCC3C(=O)N1)C(C)O)C(C)O)CC4=CC=CC=C4)CC5=CC=CC=C5 861.00 unknown https://doi.org/10.1021/NP50120A021
cyclo[Gly-Gly-Tyr-Ile-Pro-Pro-Ile-Ser] 163105715 Click to see CCC(C)C1C(=O)NC(C(=O)NCC(=O)NCC(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)N3CCCC3C(=O)N1)C(C)CC)CC4=CC=C(C=C4)O)CO 784.90 unknown https://doi.org/10.1021/NP50120A021
cyclo[Gly-Pro-aIle-D-aIle-aIle-Gly-Tyr] 163105268 Click to see CCC(C)C1C(=O)NC(C(=O)NC(C(=O)NCC(=O)NC(C(=O)NCC(=O)N2CCCC2C(=O)N1)CC3=CC=C(C=C3)O)C(C)CC)C(C)CC 713.90 unknown https://doi.org/10.1021/NP50120A021
cyclo[Gly-Pro-Pro-Ile-Gly-Pro-Val-Ile-Phe] 163067501 Click to see CCC(C)C1C(=O)NCC(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NCC(=O)N3CCCC3C(=O)N4CCCC4C(=O)N1)CC5=CC=CC=C5)C(C)CC)C(C)C 878.10 unknown https://doi.org/10.1021/NP50120A021
cyclo[Gly-Thr-Ile-Pro-Ser-Pro-Phe-Ile] 163104611 Click to see CCC(C)C1C(=O)NCC(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)N3CCCC3C(=O)NC(C(=O)N1)CC4=CC=CC=C4)CO)C(C)CC)C(C)O 813.00 unknown https://doi.org/10.1021/NP50120A021
Heterophyllin B 102022989 Click to see CCC(C)C1C(=O)NC(C(=O)NCC(=O)NCC(=O)NC(C(=O)N2CCCC2C(=O)N3CCCC3C(=O)N4CCCC4C(=O)N1)CC(C)C)CC5=CC=CC=C5 778.90 unknown https://doi.org/10.1016/S0031-9422(00)95114-8
https://doi.org/10.1002/HLCA.200390280
Pseudostellarin A 10391309 Click to see CC1C(=O)NCC(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)N1)CC(C)C)CC3=CC=C(C=C3)O 501.60 unknown https://doi.org/10.1016/S0040-4020(01)81333-8
Pseudostellarin B 10078303 Click to see CCC(C)C1C(=O)NCC(=O)NCC(=O)NCC(=O)N2CCCC2C(=O)N3CCCC3C(=O)NC(C(=O)NCC(=O)N1)CC4=CC=CC=C4 682.80 unknown https://doi.org/10.1016/S0040-4020(01)81333-8
https://doi.org/10.1002/HLCA.200390280
https://doi.org/10.1021/NP50120A021
Pseudostellarin C 10328048 Click to see CC(C)CC1C(=O)NCC(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)N3CCCC3C(=O)NC(C(=O)N1)CC4=CC=CC=C4)CO)CC(C)C)C(C)O 813.00 unknown https://doi.org/10.1016/S0040-4020(01)81333-8
Pseudostellarin D 164508 Click to see CCC(C)C1C(=O)NC(C(=O)NCC(=O)NC(C(=O)NCC(=O)N2CCCC2C(=O)NC(C(=O)N1)CC(C)C)CC3=CC=C(C=C3)O)CC(C)C 713.90 unknown https://doi.org/10.1021/NP50120A021
Pseudostellarin E 10033610 Click to see CCC(C)C1C(=O)NC(C(=O)NCC(=O)N2CCCC2C(=O)N3CCCC3C(=O)NC(C(=O)NCC(=O)N4CCCC4C(=O)NC(C(=O)N1)C(C)C)CC(C)C)CC5=CC=CC=C5 878.10 unknown https://doi.org/10.1016/S0040-4020(01)89612-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Fumaric Acid 444972 Click to see C(=CC(=O)O)C(=O)O 116.07 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
Succinic Acid 1110 Click to see C(CC(=O)O)C(=O)O 118.09 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Organic acids and derivatives / Hydroxy acids and derivatives / Alpha hydroxy acids and derivatives
Lactic Acid 612 Click to see CC(C(=O)O)O 90.08 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Organic acids and derivatives / Keto acids and derivatives / Short-chain keto acids and derivatives
3-Methyl-2-oxobutanoic acid 49 Click to see CC(C)C(=O)C(=O)O 116.11 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
Acetoacetic acid 96 Click to see CC(=O)CC(=O)O 102.09 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Organic acids and derivatives / Organic sulfonic acids and derivatives / Organosulfonic acids and derivatives / Organosulfonic acids
Taurine 1123 Click to see C(CS(=O)(=O)O)N 125.15 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
alpha-D-Glucopyranoside, beta-D-fructofuranosyl 91692850 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
alpha-Sophorose 88719 Click to see C(C1C(C(C(C(O1)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O 342.30 unknown https://doi.org/10.1007/978-3-7091-1084-3_4
Gal(a1-4)a-Ido 131632347 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1007/978-3-7091-1084-3_4
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1007/978-3-7091-1084-3_4
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
Sucrose NF 46782954 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown via CMAUP database
Grape sugar 79025 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Raffinose 439242 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)O)O)O)O)O 504.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Organoheterocyclic compounds / Pyrroles / Pyrrole carboxylic acids and derivatives
Furan-3-ylmethyl 1H-pyrrole-2-carboxylate 189695 Click to see C1=CNC(=C1)C(=O)OCC2=COC=C2 191.18 unknown https://doi.org/10.1021/NP50060A030
> Organoheterocyclic compounds / Pyrroles / Pyrrole carboxylic acids and derivatives / Pyrrole carboxylic acids / Pyrrole 2-carboxylic acids
3-(furan-2-ylmethyl)-1H-pyrrole-2-carboxylic acid 90865811 Click to see C1=COC(=C1)CC2=C(NC=C2)C(=O)O 191.18 unknown https://doi.org/10.1021/NP50060A030
Pyrrole-2-carboxylic acid 12473 Click to see C1=CNC(=C1)C(=O)O 111.10 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Salvianolic acid B 6451084 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)OC(CC5=CC(=C(C=C5)O)O)C(=O)O)O)O 718.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown via CMAUP database
cis-Cinnamic acid 5372954 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 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 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273876/
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(4-Hydroxy-3-methoxyphenyl)propionic acid 14340 Click to see COC1=C(C=CC(=C1)CCC(=O)O)O 196.20 unknown via CMAUP database

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