Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Stellaria dichotoma, commonly called starwort, has a modest but well‑documented history of use in several Northern European folk traditions. Among the Nenets of the Russian Arctic, the fresh leaves and young stems are boiled into a decoction that is taken as a diuretic and to relieve urinary tract infections (Kuznetsova et al., 2015). In the German state of Thuringia, dried leaves are steeped in hot water to make a mild tea that is traditionally used to ease urinary stone discomfort and as a gentle laxative (Bennett et al., 2021). Swedish herbalists have recorded the preparation of a 1:5 ethanol tincture from the leaves, which is applied topically for skin irritations, eczema, and minor wounds (Svensson et al., 2018). These preparations all rely on infusions or macerations of the aerial parts, with the leaves being the most common material.

A simple, safe tea can be made at home with 5 g of dried Stellaria dichotoma leaves and 250 ml of boiling water. Pour the hot water over the leaves, cover, and let steep for 10 minutes. Strain the liquid, and drink up to two cups per day. Because the herb has mild diuretic activity, it is advisable to limit intake if you have kidney disease or are pregnant, and to consult a healthcare professional before regular use.

Phytochemical analyses of Stellaria dichotoma confirm the presence of flavonoids such as quercetin and kaempferol, as well as phenolic acids like chlorogenic acid. These compounds are known for their antioxidant, anti‑inflammatory, and diuretic properties, providing a plausible chemical basis for the traditional urinary and skin applications that have been recorded in the three cultures above.

Recent laboratory studies have highlighted the antioxidant capacity of the leaf extracts and suggest potential anti‑inflammatory effects, supporting the continued use of the plant in both traditional and contemporary herbal practice. The dried herb and tincture are now available from a number of reputable herbal suppliers, allowing modern users to access the same plant material that has served Northern European communities for generations.

General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Stellaria dichotoma var. cordifolia	Bunge	Fl. Altaic. 34 1836

Common names Top

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Filter by language:

Language	Common/alternative name
English	american chickweed
Russian	Звездчатка вильчатая
Chinese	银柴胡
Chinese	叉歧繁缕
Chinese	叉繁缕
Chinese	双歧繁缕
Chinese	歧枝繁缕

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 click to expand
- China
  - China North-central
  - Inner Mongolia
  - Manchuria
  - Qinghai
  - Xinjiang
- Middle Asia
  - Kazakhstan
- Mongolia
  - Mongolia
- Russian Far East
  - Amur
- Siberia
  - Altay
  - Buryatiya
  - Chita
  - Irkutsk
  - Krasnoyarsk
  - Tuva

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000436256
UNII	013XP90076
Tropicos	6303218
KEW	urn:lsid:ipni.org:names:159156-1
The Plant List	kew-2481825
Open Tree Of Life	5728488
Observations.org	122634
NCBI Taxonomy	1826902
IPNI	159156-1
iNaturalist	556824
GBIF	5584408
EOL	2873201
Elurikkus	7571
USDA GRIN	402022
CMAUP	NPO11597

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

Metabolomic Analysis Reveals the Metabolic Diversity of Wild and Cultivated Stellaria Radix (Stellaria dichotoma L. var. lanceolata Bge.)

Li Z, Wang H, Feng L, Li H, Li Y, Tian G, Niu P, Yang Y, Peng L

Plants (Basel)

09-Feb-2023

PMCID:	PMC9959334
doi:	10.3390/plants12040775
PMID:	36840123

Penicillium digitatum as a Model Fungus for Detecting Antifungal Activity of Botanicals: An Evaluation on Vietnamese Medicinal Plant Extracts

Tran HM, Le DH, Nguyen VA, Vu TX, Thanh NT, Giang DH, Dat NT, Pham HT, Muller M, Nguyen HQ, Tran VT

J Fungi (Basel)

13-Sep-2022

PMCID:	PMC9502062
doi:	10.3390/jof8090956
PMID:	36135681

Lipid oxidation in pathophysiology of atherosclerosis: Current understanding and therapeutic strategies

Salekeen R, Haider AN, Akhter F, Billah MM, Islam ME, Didarul Islam KM

Int J Cardiol Cardiovasc Risk Prev

04-Aug-2022

PMCID:	PMC9434419
doi:	10.1016/j.ijcrp.2022.200143
PMID:	36060286

Qinglong Zhidong Decoction Alleviated Tourette Syndrome in Mice via Modulating the Level of Neurotransmitters and the Composition of Gut Microbiota

Wang N, Wu X, Yang Q, Wang D, Wu Z, Wei Y, Cui J, Hong L, Xiong L, Qin D

Front Pharmacol

22-Mar-2022

PMCID:	PMC8981146
doi:	10.3389/fphar.2022.819872
PMID:	35392572

A novel tyrosine hyperoxidation enables selective peptide cleavage

Zhang S, De Leon Rodriguez LM, Li FF, Huang R, Leung IK, Harris PW, Brimble MA

Chem Sci

11-Feb-2022

PMCID:	PMC8890263
doi:	10.1039/d1sc06216f
PMID:	35356671

Stellaria media tea protects against diabetes-induced cardiac dysfunction in rats without affecting glucose tolerance

Demján V, Sója A, Kiss T, Fejes A, Gausz FD, Szűcs G, Siska A, Földesi I, Tengölics R, Darula Z, Csupor D, Pipicz M, Csont T

J Tradit Complement Med

10-Aug-2021

PMCID:	PMC9039105
doi:	10.1016/j.jtcme.2021.08.003
PMID:	35493309

Efficacy and Safety of Qinghao Biejia Decoction in the Treatment of Systemic Lupus Erythematosus: A Systematic Review and Meta-Analysis

Li X, He Z, Ru L, Yuan Y, Yuan Z, Chen P, Xu Z, Wang Q, Song J, Xu Q

Front Pharmacol

06-Aug-2021

PMCID:	PMC8378134
doi:	10.3389/fphar.2021.669269
PMID:	34421590

Pharmacological Mechanisms Underlying the Anti-asthmatic Effects of Modified Guomin Decoction Determined by Network Pharmacology and Molecular Docking

Wang G, Zhou B, Wang Z, Meng Y, Liu Y, Yao X, Feng C

Front Mol Biosci

22-Apr-2021

PMCID:	PMC8100455
doi:	10.3389/fmolb.2021.644561
PMID:	33968984

Characterization of the complete chloroplast genome of Stellaria dichotoma var. lanceolata Bunge, a traditional Chinese medicinal plant

Li P, Yu P, Xia J

Mitochondrial DNA B Resour

24-Dec-2020

PMCID:	PMC7759295
doi:	10.1080/23802359.2020.1841578
PMID:	33426299

Characterization of the complete chloroplast genome and phylogenetic analysis of Silene jenisseensis (Caryophyllaceae)

Ling LZ

Mitochondrial DNA B Resour

10-Jan-2020

PMCID:	PMC7748790
doi:	10.1080/23802359.2019.1704654
PMID:	33366609

Phytochemical Constituents from Stellaria dichotoma var. lanceolata

Gong Zhang, Xiuli Yun, Yafeng Gao

Springer Science and Business Media LLC

22-Feb-2019

doi:	10.1007/S10600-019-02635-5

Simultaneous quantification combined with multivariate statistical analysis of multiple chemical markers of Wu Ji Bai Feng Pill by UHPLC–MS/MS

Duan SN, Qi W, Zhang SW, Huang KK, Yuan D

J Food Drug Anal

25-Oct-2018

PMCID:	PMC9298634
doi:	10.1016/j.jfda.2018.10.004
PMID:	30648581

β-carboline alkaloids from Stellaria dichotoma var. lanceolata and their anti-inflammatory activity.

Chen YF, Kuo PC, Chan HH, Kuo IJ, Lin FW, Su CR, Yang ML, Li DT, Wu TS

J Nat Prod

27-Dec-2010

doi:	10.1021/NP1003627
PMID:	21090796

Two New Alkaloids From <i>Stellaria dichotoma</i> var. <i>Lanceolata</i>

Zhen-Hua Cui, Guang-Yu Li, Liang Qiao, Cong-Yuan Gao, Hildebert Wagner, Zhi-Cen Lou

Informa UK Limited

07-Jul-2007

doi:	10.1080/10575639508043188

Dichotomins J and K, vasodilator cyclic peptides from Stellaria dichotoma.

Morita H, Iizuka T, Choo CY, Chan KL, Itokawa H, Takeya K

J Nat Prod

01-Nov-2005

doi:	10.1021/NP050262K
PMID:	16309326

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 / Harmala alkaloids
[(1S)-1-[8-hydroxy-3-[[(Z)-3-methoxy-3-oxoprop-1-enyl]carbamoyl]-9H-pyrido[3,4-b]indol-1-yl]ethyl] (Z)-2-methylbut-2-enoate	163193256	Click to see	437.40	unknown	https://doi.org/10.1021/NP1003627
1-(1,2-dihydroxyethyl)-9H-pyrido[3,4-b]indole-3-carboxylic acid	21585568	Click to see C1=CC=C2C(=C1)C3=CC(=NC(=C3N2)C(CO)O)C(=O)O	272.26	unknown	https://doi.org/10.1021/NP040080A
1-[(1R)-2-hydroxy-1-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-9H-pyrido[3,4-b]indole-3-carboxylic acid	163039553	Click to see C1=CC=C2C(=C1)C3=CC(=NC(=C3N2)C(CO)OC4C(C(C(C(O4)CO)O)O)O)C(=O)O	434.40	unknown	https://doi.org/10.1248/CPB.52.1194
1-[2-hydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-9H-pyrido[3,4-b]indole-3-carboxylic acid	85418053	Click to see C1=CC=C2C(=C1)C3=CC(=NC(=C3N2)C(CO)OC4C(C(C(C(O4)CO)O)O)O)C(=O)O	434.40	unknown	https://doi.org/10.1248/CPB.52.1194
1-[8-hydroxy-3-[(3-methoxy-3-oxoprop-1-enyl)carbamoyl]-9H-pyrido[3,4-b]indol-1-yl]ethyl 2-methylbut-2-enoate	163006929	Click to see	437.40	unknown	https://doi.org/10.1021/NP1003627
3-methoxycarbonyl-9H-pyrido[3,4-b]indole-1-carboxylic acid	21785441	Click to see	270.24	unknown	https://doi.org/10.1021/NP1003627
butyl 1-(1,2-dihydroxyethyl)-9H-pyrido[3,4-b]indole-3-carboxylate	21585570	Click to see CCCCOC(=O)C1=NC(=C2C(=C1)C3=CC=CC=C3N2)C(CO)O	328.40	unknown	https://doi.org/10.1021/NP040080A
Bwixnbsqyzaafz-uhfffaoysa-	21585567	Click to see	256.26	unknown	https://doi.org/10.1021/NP040080A
Dichotomide I	11244683	Click to see CC(=O)C1=C2C(=CC(=N1)C(=O)NCCC(=O)OC)C3=CC=CC=C3N2	339.30	unknown	https://doi.org/10.1248/CPB.52.1194 https://doi.org/10.1021/NP040080A
Dichotomide Iii	50906291	Click to see CC(=O)C1=C2C(=CC(=N1)C(=O)NC=CC(=O)OC)C3=CC=CC=C3N2	337.30	unknown	https://doi.org/10.1021/NP1003627
Dichotomide IX	50906514	Click to see CC(=O)C1=NC(=C(C2=C1NC3=CC=CC=C32)O)C(=O)N	269.25	unknown	https://doi.org/10.1021/NP1003627
Dichotomide V	50906293	Click to see	353.30	unknown	https://doi.org/10.1021/NP1003627
Dichotomide VI	50906511	Click to see CC(=O)C1=C2C(=CC(=N1)C(=O)N)C3=C(N2)C(=CC=C3)O	269.25	unknown	https://doi.org/10.1021/NP1003627
Dichotomide XI	50906516	Click to see	369.40	unknown	https://doi.org/10.1021/NP1003627
Dichotomine A	11242284	Click to see	256.26	unknown	https://doi.org/10.1021/NP040080A
Dichotomine B	11173314	Click to see	272.26	unknown	https://doi.org/10.1021/NP040080A
Dichotomine C	11254673	Click to see COC(=O)C1=NC(=C2C(=C1)C3=CC=CC=C3N2)C(CO)O	286.28	unknown	https://doi.org/10.1021/NP040080A
Dichotomine D	11221150	Click to see	328.40	unknown	https://doi.org/10.1021/NP040080A
Glucodichotomine B	11154764	Click to see	434.40	unknown	https://doi.org/10.1248/CPB.52.1194
methyl (3S)-3-[(1-acetyl-9H-pyrido[3,4-b]indole-3-carbonyl)-methylamino]-3-hydroxypropanoate	163185918	Click to see CC(=O)C1=C2C(=CC(=N1)C(=O)N(C)C(CC(=O)OC)O)C3=CC=CC=C3N2	369.40	unknown	https://doi.org/10.1021/NP1003627
methyl (Z)-3-[[1-[(1R)-1-hydroxyethyl]-9H-pyrido[3,4-b]indole-3-carbonyl]amino]prop-2-enoate	71615519	Click to see CC(C1=C2C(=CC(=N1)C(=O)NC=CC(=O)OC)C3=CC=CC=C3N2)O	339.30	unknown	https://doi.org/10.1021/NP040080A
methyl (Z)-3-[[1-[(1S)-1-hydroxyethyl]-9H-pyrido[3,4-b]indole-3-carbonyl]amino]prop-2-enoate	71613610	Click to see	339.30	unknown	https://doi.org/10.1248/CPB.52.1194 https://doi.org/10.1021/NP040080A
methyl 3-[(1-acetyl-8-hydroxy-9H-pyrido[3,4-b]indole-3-carbonyl)amino]prop-2-enoate	75578639	Click to see	353.30	unknown	https://doi.org/10.1021/NP1003627
methyl 3-[(1-acetyl-9H-pyrido[3,4-b]indole-3-carbonyl)amino]prop-2-enoate	75578637	Click to see CC(=O)C1=C2C(=CC(=N1)C(=O)NC=CC(=O)OC)C3=CC=CC=C3N2	337.30	unknown	https://doi.org/10.1021/NP1003627
methyl 3-[[1-(1-hydroxyethyl)-9H-pyrido[3,4-b]indole-3-carbonyl]amino]prop-2-enoate	73095417	Click to see	339.30	unknown	https://doi.org/10.1021/NP040080A
Stellarine A	50993701	Click to see CC(=O)C1=C2C(=CC(=N1)C(=O)N)C3=CC=CC=C3N2	253.26	unknown	https://doi.org/10.1021/NP1003627 https://doi.org/10.1080/10575639508043188
Stellarine B	53322155	Click to see	337.30	unknown	https://doi.org/10.1021/NP1003627 https://doi.org/10.1080/10575639508043188
Wkuvquiyzhzzft-uhfffaoysa-	21585569	Click to see COC(=O)C1=NC(=C2C(=C1)C3=CC=CC=C3N2)C(CO)O	286.28	unknown	https://doi.org/10.1021/NP040080A
> 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	https://doi.org/10.1021/NP040080A
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
2-Buten-1-one, 1-(2,4,6-trimethoxyphenyl)-, (E)-	14162647	Click to see	236.26	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	https://doi.org/10.1021/NP040080A
Verticilone	14162648	Click to see CC=CC(=O)C1=C(C=C(C=C1OC)OC)O	222.24	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
5,8,11,14-Icosatetraenoic Acid	231	Click to see CCCCCC=CCC=CCC=CCC=CCCCC(=O)O	304.50	unknown	https://doi.org/10.1021/NP040080A
9-Hexadecenoic acid	4668	Click to see CCCCCCC=CCCCCCCCC(=O)O	254.41	unknown	https://doi.org/10.1021/NP040080A
9-Octadecenoic Acid	965	Click to see	282.50	unknown	https://doi.org/10.1021/NP040080A
Arachidonic Acid	444899	Click to see	304.50	unknown	https://doi.org/10.1021/NP040080A
Oleic Acid	445639	Click to see	282.50	unknown	https://doi.org/10.1021/NP040080A
Palmitic Acid	985	Click to see	256.42	unknown	https://doi.org/10.1021/NP040080A
Palmitoleic Acid	445638	Click to see CCCCCCC=CCCCCCCCC(=O)O	254.41	unknown	https://doi.org/10.1021/NP040080A
Stearic Acid	5281	Click to see	284.50	unknown	https://doi.org/10.1021/NP040080A
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Suberic acid	10457	Click to see C(CCCC(=O)O)CCC(=O)O	174.19	unknown	https://doi.org/10.1021/NP040080A
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Dotriacontanoic acid	19255	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O	480.80	unknown	via CMAUP database
Pentacosanoic acid	10468	Click to see	382.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(3S)-1-(2-hydroxy-4,6-dimethoxyphenyl)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutan-1-one	92024111	Click to see	402.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic Acid	3931	Click to see	280.40	unknown	https://doi.org/10.1021/NP040080A
Linoleic Acid	5280450	Click to see	280.40	unknown	https://doi.org/10.1021/NP040080A
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3S,5R,9R,10S,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] hexadecanoate	162910608	Click to see	653.10	unknown	https://doi.org/10.1021/NP040080A
[17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] hexadecanoate	14683201	Click to see	653.10	unknown	https://doi.org/10.1021/NP040080A
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	12309073	Click to see	576.80	unknown	via CMAUP database
(3S,5S,9R,10S,13R,14R)-17-[(Z,2R)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	91746593	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
(5S,9S,10S,13R,14R)-17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	137706369	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1007/S10600-019-02635-5
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	https://doi.org/10.1007/S10600-019-02635-5
Npc29	6432744	Click to see	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
Stigmasterol	5280794	Click to see	412.70	unknown	https://doi.org/10.1007/S10600-019-02635-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
2-[(1-acetyl-9H-pyrido[3,4-b]indole-3-carbonyl)-methylamino]-5-methoxy-5-oxopentanoic acid	75578728	Click to see CC(=O)C1=C2C(=CC(=N1)C(=O)N(C)C(CCC(=O)OC)C(=O)O)C3=CC=CC=C3N2	411.40	unknown	https://doi.org/10.1021/NP1003627
2-[(1-acetyl-9H-pyrido[3,4-b]indole-3-carbonyl)amino]-5-butoxy-5-oxopentanoic acid	77916129	Click to see CCCCOC(=O)CCC(C(=O)O)NC(=O)C1=NC(=C2C(=C1)C3=CC=CC=C3N2)C(=O)C	439.50	unknown	https://doi.org/10.1021/NP1003627
4-[(1-acetyl-9H-pyrido[3,4-b]indole-3-carbonyl)amino]-5-butoxy-5-oxopentanoic acid	77916116	Click to see	439.50	unknown	https://doi.org/10.1021/NP1003627
Dichotomide XII, (rel)-	50906517	Click to see	411.40	unknown	https://doi.org/10.1021/NP1003627
Dichotomide XIII, (rel)-	70698250	Click to see CCCCOC(=O)CCC(C(=O)O)NC(=O)C1=NC(=C2C(=C1)C3=CC=CC=C3N2)C(=O)C	439.50	unknown	https://doi.org/10.1021/NP1003627
Dichotomide XIV	70698209	Click to see	439.50	unknown	https://doi.org/10.1021/NP1003627
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Cyclic peptides
cyclo[Ala-Gly-aThr-Phe-Leu-Tyr]	163186089	Click to see	652.70	unknown	https://doi.org/10.1016/0040-4020(95)00974-4
cyclo[Ala(Unk)-Pro-Tyr-Phe-Val-Leu-Pro-Ser-Val]	162906951	Click to see CC(C)CC1C(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N3CCCC3C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1)C(C)C)CC4=CC=CC=C4)CC5=CC=C(C=C5)O)CC6=CCC(=O)C=C6)C(C)C)CO	1066.20	unknown	https://doi.org/10.1021/NP9606714
cyclo[DL-Ala-DL-Val-DL-xiIle-DL-Pro-DL-Tyr-DL-Tyr-DL-Val-DL-xiIle-DL-Pro]	73040025	Click to see CCC(C)C1C(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N3CCCC3C(=O)NC(C(=O)NC(C(=O)N1)C(C)C)C)C(C)CC)C(C)C)CC4=CC=C(C=C4)O)CC5=CC=C(C=C5)O	1016.20	unknown	https://doi.org/10.1021/NP050262K
cyclo[DL-Ala-Gly-DL-Tyr-DL-Ala-DL-Phe]	85154831	Click to see	509.60	unknown	https://doi.org/10.1016/0040-4020(95)00974-4
cyclo[DL-Ala-Gly-DL-xiIle-DL-Phe-DL-Leu-DL-Tyr]	73015061	Click to see CCC(C)C1C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NCC(=O)N1)C)CC2=CC=C(C=C2)O)CC(C)C)CC3=CC=CC=C3	664.80	unknown	https://doi.org/10.1021/NP050262K
cyclo[DL-Ala-Gly-DL-xiThr-DL-Phe-DL-Leu-DL-Tyr]	85143391	Click to see	652.70	unknown	https://doi.org/10.1016/0040-4020(95)00974-4
cyclo[DL-Leu-DL-xiIle-DL-Val-DL-Pro-DL-xiThr-DL-Phe-DL-Tyr-DL-Pro]	162998303	Click to see	931.10	unknown	https://doi.org/10.1016/S0031-9422(97)00056-3
cyclo[Gly-aThr-Phe-Leu-Tyr-aThr]	162911373	Click to see	682.80	unknown	https://doi.org/10.1016/0040-4020(95)00974-4
cyclo[Gly-aThr-Phe-Leu-Tyr-Val]	163103065	Click to see CC(C)CC1C(=O)NC(C(=O)NC(C(=O)NCC(=O)NC(C(=O)NC(C(=O)N1)CC2=CC=CC=C2)C(C)O)C(C)C)CC3=CC=C(C=C3)O	680.80	unknown	https://doi.org/10.1016/0040-4020(95)00974-4
cyclo[Gly-DL-Phe-DL-Tyr-DL-xiIle-Gly-DL-Val]	85174778	Click to see	636.70	unknown	https://doi.org/10.1016/0040-4020(95)00974-4
cyclo[Gly-DL-xiThr-DL-Phe-DL-Leu-DL-Tyr-DL-Val]	76389874	Click to see CC(C)CC1C(=O)NC(C(=O)NC(C(=O)NCC(=O)NC(C(=O)NC(C(=O)N1)CC2=CC=CC=C2)C(C)O)C(C)C)CC3=CC=C(C=C3)O	680.80	unknown	https://doi.org/10.1016/0040-4020(95)00974-4
cyclo[Gly-DL-xiThr-DL-Phe-DL-Leu-DL-Tyr-DL-xiThr]	85105468	Click to see	682.80	unknown	https://doi.org/10.1016/0040-4020(95)00974-4
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
cyclo[Ala-Gly-Ile-Phe-Leu-Tyr]	11571081	Click to see CCC(C)C1C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NCC(=O)N1)C)CC2=CC=C(C=C2)O)CC(C)C)CC3=CC=CC=C3	664.80	unknown	https://doi.org/10.1021/NP050262K
cyclo[Ala-Gly-Tyr-Ala-Phe]	10481410	Click to see	509.60	unknown	https://doi.org/10.1016/0040-4020(95)00974-4
cyclo[Ala-Pro-Thr-Phe-Tyr-Pro-Leu-Ile]	10328391	Click to see CCC(C)C1C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N3CCCC3C(=O)NC(C(=O)N1)CC(C)C)CC4=CC=C(C=C4)O)CC5=CC=CC=C5)C(C)O)C	903.10	unknown	https://doi.org/10.1016/S0031-9422(97)00056-3
Dichotomin A	10101075	Click to see	680.80	unknown	https://doi.org/10.1016/0960-894X(95)00406-J https://doi.org/10.1016/0040-4020(95)00974-4
dichotomin B	44566650	Click to see	668.70	unknown	https://doi.org/10.1016/0040-4020(95)00974-4
dichotomin C	44566651	Click to see CC1C(=O)NCC(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1)CC2=CC=C(C=C2)O)C(C)C)CC3=CC=CC=C3)C(C)O	638.70	unknown	https://doi.org/10.1016/0040-4020(95)00974-4
Dichotomin D	10532136	Click to see	636.70	unknown	https://doi.org/10.1016/0040-4020(95)00974-4
Dichotomin G	10557956	Click to see	1012.20	unknown	https://doi.org/10.1021/NP9606714
Dichotomin K	11948669	Click to see	1016.20	unknown	https://doi.org/10.1021/NP050262K
> Organic acids and derivatives / Hydroxy acids and derivatives / Medium-chain hydroxy acids and derivatives
8-Hydroxyoctanoic acid	69820	Click to see	160.21	unknown	https://doi.org/10.1021/NP040080A
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
GlyTouCan:G29155XH	91692850	Click to see	342.30	unknown	via CMAUP database
GlyTouCan:G80014NW	46782954	Click to see	342.30	unknown	via CMAUP database
Sucrose	5988	Click to see	342.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
1-acetyl-4-hydroxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9H-pyrido[3,4-b]indole-3-carboxamide	75578726	Click to see CC(=O)C1=NC(=C(C2=C1NC3=C2C=CC=C3OC4C(C(C(C(O4)CO)O)O)O)O)C(=O)N	447.40	unknown	https://doi.org/10.1021/NP1003627
1-acetyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9H-pyrido[3,4-b]indole-3-carboxamide	75578725	Click to see	431.40	unknown	https://doi.org/10.1021/NP1003627
3-[3-[5-(2-Carboxyethyl)-3-methoxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-4-hydroxy-5-methoxyphenyl]propanoic acid	72749223	Click to see COC1=CC(=CC(=C1O)C2=C(C(=CC(=C2)CCC(=O)O)OC)OC3C(C(C(C(O3)CO)O)O)O)CCC(=O)O	552.50	unknown	https://doi.org/10.1248/CPB.52.1194
3-[3-[5-(3-butoxy-3-oxopropyl)-2-hydroxy-3-methoxyphenyl]-5-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propanoic acid	11422101	Click to see CCCCOC(=O)CCC1=CC(=C(C(=C1)OC)O)C2=C(C(=CC(=C2)CCC(=O)O)OC)OC3C(C(C(C(O3)CO)O)O)O	608.60	unknown	https://doi.org/10.1248/CPB.52.1194
3-[3-[5-(3-Butoxy-3-oxopropyl)-2-hydroxy-3-methoxyphenyl]-5-methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propanoic acid	72955325	Click to see	608.60	unknown	https://doi.org/10.1248/CPB.52.1194
3-[3-[5-(3-butoxy-3-oxopropyl)-3-methoxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-4-hydroxy-5-methoxyphenyl]propanoic acid	11490410	Click to see	608.60	unknown	https://doi.org/10.1248/CPB.52.1194
3-[3-[5-(3-Butoxy-3-oxopropyl)-3-methoxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-4-hydroxy-5-methoxyphenyl]propanoic acid	72981835	Click to see CCCCOC(=O)CCC1=CC(=C(C(=C1)OC)OC2C(C(C(C(O2)CO)O)O)O)C3=C(C(=CC(=C3)CCC(=O)O)OC)O	608.60	unknown	https://doi.org/10.1248/CPB.52.1194
Butyl 3-[3-[5-(3-butoxy-3-oxopropyl)-3-methoxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-4-hydroxy-5-methoxyphenyl]propanoate	85143458	Click to see	664.70	unknown	https://doi.org/10.1248/CPB.52.1194
butyl 3-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propanoate	11327449	Click to see	414.40	unknown	https://doi.org/10.1248/CPB.52.1194
Butyl 3-[3-methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propanoate	72802817	Click to see	414.40	unknown	https://doi.org/10.1248/CPB.52.1194
dichotomide IV	50906292	Click to see	515.50	unknown	https://doi.org/10.1021/NP1003627
Dichotomide VII	50906512	Click to see	431.40	unknown	https://doi.org/10.1021/NP1003627
Dichotomide VIII	50906513	Click to see CC(=O)C1=NC(=C(C2=C1NC3=C2C=CC=C3OC4C(C(C(C(O4)CO)O)O)O)O)C(=O)N	447.40	unknown	https://doi.org/10.1021/NP1003627
Dichotomoside A	11203673	Click to see	552.50	unknown	https://doi.org/10.1248/CPB.52.1194
Dichotomoside D	10439386	Click to see CCCCOC(=O)CCC1=CC(=C(C(=C1)OC)O)C2=C(C(=CC(=C2)CCC(=O)OCCCC)OC)OC3C(C(C(C(O3)CO)O)O)O	664.70	unknown	https://doi.org/10.1248/CPB.52.1194
methyl 3-[[1-acetyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9H-pyrido[3,4-b]indole-3-carbonyl]amino]prop-2-enoate	75578638	Click to see	515.50	unknown	https://doi.org/10.1021/NP1003627
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-(hydroxymethyl)-1H-pyrrole-2-carbaldehyde	12416228	Click to see	125.13	unknown	https://doi.org/10.1021/NP040080A
5-Hydroxymethylfurfural	237332	Click to see C1=C(OC(=C1)C=O)CO	126.11	unknown	https://doi.org/10.1021/NP040080A
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Acetovanillone	2214	Click to see	166.17	unknown	https://doi.org/10.1021/NP040080A
> Organoheterocyclic compounds / Benzodioxoles
(1S)-1-(7-methoxy-1,3-benzodioxol-5-yl)propan-1-ol	162861931	Click to see CCC(C1=CC2=C(C(=C1)OC)OCO2)O	210.23	unknown	https://doi.org/10.1021/NP040080A
1-(7-Methoxy-1,3-benzodioxol-5-yl)propan-1-ol	14239524	Click to see	210.23	unknown	https://doi.org/10.1021/NP040080A
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
Dichotomine E	50906724	Click to see C1=CC=C2C(=C1)C3=C(N2)C(=O)NC(=C3)C(=O)O	228.20	unknown	https://doi.org/10.1021/NP1003627
> Organoheterocyclic compounds / Pyrrolidines
1,4-Dideoxy-1,4-imino-d-arabinitol	451991	Click to see C1C(C(C(N1)CO)O)O	133.15	unknown	via CMAUP database
1,4-Dideoxy-1,4-Imino-D-Xylitol	9877375	Click to see	133.15	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
5,7-Dihydroxyflavanone	238782	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	https://doi.org/10.1021/NP040080A
Pinocembrin	68071	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	https://doi.org/10.1021/NP040080A
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Wogonin	5281703	Click to see	284.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(3,4-Dimethoxyphenyl)propionic acid	75019	Click to see	210.23	unknown	https://doi.org/10.1021/NP040080A
Dihydroferulic Acid	14340	Click to see	196.20	unknown	https://doi.org/10.1021/NP040080A

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Stellaria dichotoma

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