Scientific name	Authority	First published in
Ledebouria violacea	(Hutch.) W.L.Tjaden	Brit. Cactus Succ. J. 7: 11 (1989)
Scilla violacea	Hutch.	Bull. Misc. Inform. Kew 1932: 511 (1932)
Scilla socialis	Baker	Refug. Bot. 3: t. 180 (1870)
Scilla paucifolia	Baker	Refug. Bot. 3: t. 181 (1870)

Common names Top

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Filter by language:

Language	Common/alternative name
Persian	لدبوریا سوکیالیس
Hungarian	díszeslevelű csillagvirág
Swedish	syskonstjärna
Chinese	油点百合
Chinese	油点花

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

Africa click to expand
- Southern Africa
  - Cape Provinces

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000686850
Tropicos	18403091
INPN	936182
KEW	urn:lsid:ipni.org:names:537325-1
The Plant List	kew-280869
Open Tree Of Life	62296
NCBI Taxonomy	34191
IPNI	537325-1
iNaturalist	327308
GBIF	2773791
Freebase	/m/0bhbdz8
EOL	1003546
USDA GRIN	412315
Wikipedia	Ledebouria_socialis
CMAUP	NPO11998
CMAUP	NPO7198

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

Spiro-Flavonoids in Nature: A Critical Review of Structural Diversity and Bioactivity

Pecio Ł, Pecio S, Mroczek T, Oleszek W

Molecules

14-Jul-2023

PMCID:	PMC10385819
doi:	10.3390/molecules28145420
PMID:	37513292

Design and Development of COX-II Inhibitors: Current Scenario and Future Perspective

Chahal S, Rani P, Kiran, Sindhu J, Joshi G, Ganesan A, Kalyaanamoorthy S, Mayank, Kumar P, Singh R, Negi A

ACS Omega

09-May-2023

PMCID:	PMC10210234
doi:	10.1021/acsomega.3c00692
PMID:	37251190

A systematic review on mitigation of common indoor air pollutants using plant-based methods: a phytoremediation approach

Kumar R, Verma V, Thakur M, Singh G, Bhargava B

Air Qual Atmos Health

11-Mar-2023

PMCID:	PMC10005924
doi:	10.1007/s11869-023-01326-z
PMID:	37359395

Recent development on COX-2 inhibitors as promising anti-inflammatory agents: The past 10 years

Ju Z, Li M, Xu J, Howell DC, Li Z, Chen FE

Acta Pharm Sin B

11-Jan-2022

PMCID:	PMC9214066
doi:	10.1016/j.apsb.2022.01.002
PMID:	35755295

The Antiangiogenic Activity of Naturally-occurring and synthetic Homoisoflavonoids from the Hyacinthaceae (sensu APGII)

Schwikkard S, Whitmore H, Sishtla K, Sulaiman RS, Shetty T, Basavarajappa HD, Waller C, Alqahtani A, Frankemoelle L, Chapman A, Crouch N, Wetschnig W, Knirsch W, Andriantiana J, Mas-Claret E, Langat MK, Mulholland D, Corson TW

J Nat Prod

05-Apr-2019

PMCID:	PMC6771261
doi:	10.1021/acs.jnatprod.8b00989
PMID:	30951308

Inferences of biogeographical histories within subfamily Hyacinthoideae using S-DIVA and Bayesian binary MCMC analysis implemented in RASP (Reconstruct Ancestral State in Phylogenies)

Ali SS, Yu Y, Pfosser M, Wetschnig W

Ann Bot

27-Oct-2011

PMCID:	PMC3241591
doi:	10.1093/aob/mcr274
PMID:	22039008

Isolation of glycosidase-inhibiting hyacinthacines and related alkaloids from Scilla socialis.

Kato A, Kato N, Adachi I, Hollinshead J, Fleet GW, Kuriyama C, Ikeda K, Asano N, Nash RJ

J Nat Prod

01-Jun-2007

doi:	10.1021/NP0700826
PMID:	17536859

First Nuclear DNA Amounts in more than 300 Angiosperms

ZONNEVELD BJ, LEITCH IJ, BENNETT MD

Ann Bot

19-May-2005

PMCID:	PMC4246870
doi:	10.1093/aob/mci170
PMID:	15905300

Auxin Deprivation Induces Synchronous Golgi Differentiation in Suspension-Cultured Tobacco BY-2 Cells

Winicur ZM, Feng Zhang G, Andrew Staehelin L

Plant Physiol

01-Jun-1998

PMCID:	PMC34970
doi:	10.1104/pp.117.2.501
PMID:	9625703

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
> Benzenoids / Anthracenes / Anthraquinones
1-Hydroxy-6-(5-hydroxy-4-methoxy-7-methyl-9,10-dioxoanthracen-2-yl)oxy-8-methoxy-3-methylanthracene-9,10-dione	53309223	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC)OC4=CC5=C(C(=C4)OC)C(=O)C6=C(C5=O)C=C(C=C6O)C	550.50	unknown	via CMAUP database
1-Hydroxy-8-methoxy-3-methylanthracene-9,10-dione	11300144	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC	268.26	unknown	via CMAUP database
Physcione	10639	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC	284.26	unknown	via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin	3220	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O	270.24	unknown	via CMAUP database
Questin	160717	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC)O	284.26	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Protocatechuic acid, methyl ester	287064	Click to see COC(=O)C1=CC(=C(C=C1)O)O	168.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde	240	Click to see C1=CC=C(C=C1)C=O	106.12	unknown	via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Elemicin	10248	Click to see COC1=CC(=CC(=C1OC)OC)CC=C	208.25	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol	3314	Click to see COC1=C(C=CC(=C1)CC=C)O	164.20	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Cyclobutane lignans
1-[(1R,2S,3S,4R)-2,3-dimethyl-4-(2,4,5-trimethoxyphenyl)cyclobutyl]-2,4,5-trimethoxybenzene	10341859	Click to see CC1C(C(C1C2=CC(=C(C=C2OC)OC)OC)C3=CC(=C(C=C3OC)OC)OC)C	416.50	unknown	via CMAUP database
Magnosalin	10454589	Click to see CC1C(C(C1C2=CC(=C(C=C2OC)OC)OC)C3=CC(=C(C=C3OC)OC)OC)C	416.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(3R)-5-phenyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypentanoic acid	11792570	Click to see C1=CC=C(C=C1)CCC(CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O	356.40	unknown	via CMAUP database
D-Linalool 3-glucoside	10087123	Click to see CC(=CCCC(C)(C=C)OC1C(C(C(C(O1)CO)O)O)O)C	316.39	unknown	via CMAUP database
Tuberonic acid glucoside	5281204	Click to see C1CC(=O)C(C1CC(=O)O)CC=CCCOC2C(C(C(C(O2)CO)O)O)O	388.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3R)-oct-1-en-3-ol	6992244	Click to see CCCCCC(C=C)O	128.21	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linolenic Acid	5280934	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O	278.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Trilinolein	5322095	Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCC=CCCCCC)OC(=O)CCCCCCCC=CCC=CCCCCC	879.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
3,7-Dimethyl-2,6-octadien-1-al	8843	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	via CMAUP database
Citral	638011	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	via CMAUP database
Linalool, (-)-	443158	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzoic acid	10820	Click to see CC(C)C1=CC=C(C=C1)C(=O)O	164.20	unknown	via CMAUP database
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene	440968	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
(-)-Camphene	440966	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	via CMAUP database
(+)-beta-Pinene	10290825	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	via CMAUP database
alpha-CIS-BERGAMOTENE	6429303	Click to see CC1=CCC2CC1C2(C)CCC=C(C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Menthol	165675	Click to see CC1CCC(C(C1)O)C(C)C	156.26	unknown	via CMAUP database
(+)-Perillaldehyde	1548901	Click to see CC(=C)C1CCC(=CC1)C=O	150.22	unknown	via CMAUP database
(3S,4R)-3-hydroxy-4-prop-1-en-2-ylcyclohexene-1-carbaldehyde	10725727	Click to see CC(=C)C1CCC(=CC1O)C=O	166.22	unknown	via CMAUP database
[(4R)-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]methanol	11788398	Click to see CC(=C)C1CCC(=CC1)CO	152.23	unknown	via CMAUP database
l-Menthol	16666	Click to see CC1CCC(C(C1)O)C(C)C	156.26	unknown	via CMAUP database
Limonene, (-)-	439250	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Menthone	26447	Click to see CC1CCC(C(=O)C1)C(C)C	154.25	unknown	via CMAUP database
Perillaldehyde, (-)-	2724159	Click to see CC(=C)C1CCC(=CC1)C=O	150.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
2,6,6,9-Tetramethyl-cycloundeca-1,4,8-triene	6508206	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	via CMAUP database
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
Cuparene	86895	Click to see CC1=CC=C(C=C1)C2(CCCC2(C)C)C	202.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(4R)-4-prop-1-en-2-ylcyclohexen-1-yl]methoxy]oxane-3,4,5-triol	102508931	Click to see CC(=C)C1CCC(=CC1)COC2C(C(C(C(O2)CO)O)O)O	314.37	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4S)-4-prop-1-en-2-ylcyclohexene-1-carboxylate	21631012	Click to see CC(=C)C1CCC(=CC1)C(=O)OC2C(C(C(C(O2)CO)O)O)O	328.36	unknown	via CMAUP database
Perilloside A	3086657	Click to see CC(=C)C1CCC(=CC1)COC2C(C(C(C(O2)CO)O)O)O	314.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Epicorosolic acid	15917998	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	via CMAUP database
Augustic Acid	15560128	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C	472.70	unknown	via CMAUP database
Corosolic acid	6918774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	via CMAUP database
epi-Maslinic acid	25564831	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C	472.70	unknown	via CMAUP database
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	via CMAUP database
Pomolic acid	382831	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O	472.70	unknown	via CMAUP database
Tormentic acid	73193	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O	488.70	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
22,23-Dihydrobrassicasterol	5283637	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	via CMAUP database
Campesterol	173183	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids / 3-carboxy steroids
Hyptadienic acid	14605533	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=CC5(C)C)CO)C)C)C2C1(C)O)C)C(=O)O	470.70	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
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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Eucalyptosin A	123133484	Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)OC3C(C(C(C(O3)CO)O)O)O	457.40	unknown	via CMAUP database
Prunasin	119033	Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O	295.29	unknown	via CMAUP database
Sambunigrin	91434	Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O	295.29	unknown	via CMAUP database
Vicianin	656493	Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC(C#N)C3=CC=CC=C3)O)O)O)O)O)O	427.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Benzyl beta-d-glucopyranoside	188977	Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O	270.28	unknown	via CMAUP database
Methyl alpha-D-galactopyranoside	76935	Click to see COC1C(C(C(C(O1)CO)O)O)O	194.18	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-(5-methoxy-6-prop-2-enyl-1,3-benzodioxol-4-yl)oxane-3,4,5-triol	5319623	Click to see COC1=C(C2=C(C=C1CC=C)OCO2)C3C(C(C(C(O3)CO)O)O)O	354.40	unknown	via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(2-methoxy-5-prop-2-enylphenoxy)oxane-3,4,5-triol	21579141	Click to see COC1=C(C=C(C=C1)CC=C)OC2C(C(C(C(O2)CO)O)O)O	326.34	unknown	via CMAUP database
Caffeic Acid 3-beta-D-Glucoside	442776	Click to see C1=CC(=C(C=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O)O	342.30	unknown	via CMAUP database
Eugenyl glucoside	3084296	Click to see COC1=C(C=CC(=C1)CC=C)OC2C(C(C(C(O2)CO)O)O)O	326.34	unknown	via CMAUP database
Perilloside E	49855080	Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC3C(C(C(C(O3)CO)O)O)O	370.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones
3-Methyl-1-(3-methylfuran-2-yl)but-2-en-1-one	564412	Click to see CC1=C(OC=C1)C(=O)C=C(C)C	164.20	unknown	via CMAUP database
CID 169595	169595	Click to see CC(C)C=CC(=O)C1=COC=C1	164.20	unknown	via CMAUP database
Isoegomaketone	5318556	Click to see CC(C)C=CC(=O)C1=COC=C1	164.20	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
1-(3-Methylfuran-2-yl)ethan-1-one	12281224	Click to see CC1=C(OC=C1)C(=O)C	124.14	unknown	via CMAUP database
Egomaketone	42978	Click to see CC(=CCC(=O)C1=COC=C1)C	164.20	unknown	via CMAUP database
Perilla ketone	68381	Click to see CC(C)CCC(=O)C1=COC=C1	166.22	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Protocatechualdehyde	8768	Click to see C1=CC(=C(C=C1C=O)O)O	138.12	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Dillapiol	10231	Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC	222.24	unknown	via CMAUP database
Myristicin	4276	Click to see COC1=CC(=CC2=C1OCO2)CC=C	192.21	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzoxepines
5-Methoxyfuro[2,3-g][3]benzoxepin	10084612	Click to see CC(C)(C1=CC2=CC(=C3C=COC=CC3=C2O1)OC)O	272.29	unknown	via CMAUP database
Perilloxin	10468570	Click to see CC(C)(C1CC2=CC(=C3C=COC=CC3=C2O1)OC)O	274.31	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Thiamines
3-(4-Amino-2-methyl-pyrimidin-5-ylmethyl)-5-(2-hydroxy-ethyl)-4-methyl-thiazol-3-ium	1130	Click to see CC1=C(SC=[N+]1CC2=CN=C(N=C2N)C)CCO	265.36	unknown	via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
Perillene	68316	Click to see CC(=CCCC1=COC=C1)C	150.22	unknown	via CMAUP database
> Organoheterocyclic compounds / Piperidines
(2S,3R,4R,5S,6S)-2-(hydroxymethyl)-6-methylpiperidine-3,4,5-triol	162975719	Click to see CC1C(C(C(C(N1)CO)O)O)O	177.20	unknown	https://doi.org/10.1021/NP0700826
beta-1-C-ethyl-1-deoxymannojirimycin	14446759	Click to see CCC1C(C(C(C(N1)CO)O)O)O	191.22	unknown	https://doi.org/10.1021/NP0700826
> Organoheterocyclic compounds / Pyrrolizidines
(1R,2R,3R,5S,8R)-5-(3-hydroxybutyl)-3-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2-diol	16737241	Click to see CC(CCC1CCC2N1C(C(C2O)O)CO)O	245.32	unknown	https://doi.org/10.1021/NP0700826
Hyacinthacine B7	16736266	Click to see CC1CC(C2N1C(C(C2O)O)CO)O	203.24	unknown	via CMAUP database
hyacinthacine C2	16737240	Click to see C1C(N2C(C(C(C2C1O)O)O)CO)CO	219.23	unknown	https://doi.org/10.1021/NP0700826
Hyacinthacine C3	16737238	Click to see C1C(N2C(C(C(C2C1O)O)O)CO)CO	219.23	unknown	via CMAUP database
hyacinthacine C4	10608892	Click to see CC1C(C(C2N1C(C(C2O)O)CO)O)O	219.23	unknown	https://doi.org/10.1021/NP0700826
Hyacinthacine C5	16737239	Click to see CC1C(C(C2N1C(C(C2O)O)CO)O)O	219.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-3-(3,4-Dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl (E)-3-(3,4-dihydroxyphenyl)acrylate	10970786	Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O	374.30	unknown	via CMAUP database
(S)-rosmarinic acid	639655	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	360.30	unknown	via CMAUP database
[(Z)-2-(3,5-dihydroxyphenyl)ethenyl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	5316820	Click to see C1=CC(=C(C=C1C=CC(=O)OC=CC2=CC(=CC(=C2)O)O)O)O	314.29	unknown	via CMAUP database
Caffeic acid methyl ester	689075	Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O	194.18	unknown	via CMAUP database
Nepetoidin B	5316819	Click to see C1=CC(=C(C=C1C=CC(=O)OC=CC2=CC(=C(C=C2)O)O)O)O	314.29	unknown	via CMAUP database
Rosmarinic acid	5281792	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	360.30	unknown	via CMAUP database
Vinyl caffeate	11127419	Click to see C=COC(=O)C=CC1=CC(=C(C=C1)O)O	206.19	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin	5281416	Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O	178.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
6,7,3',4'-Tetrahydroxyflavone	24721539	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=CC(=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
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	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanidin 3-O-p-coumaroyl glycosides / Anthocyanidin 3-O-6-p-coumaroyl glycosides
Shisonin	5282068	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC(=C(C=C6)O)O)O)O)O)O	757.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
Cyanin	441688	Click to see C1=CC(=C(C=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O	611.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vicenin 2	442664	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O	594.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
5,6-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-1-benzopyran-7-yl 2-O-beta-D-glucopyranuronosyl-beta-D-glucopyranosiduronic acid	102158504	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O)O	638.50	unknown	via CMAUP database
Clerodendrin	5488004	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O	622.50	unknown	via CMAUP database
Luteolin 7-diglucuronide	5282153	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O)O	638.50	unknown	via CMAUP database
Luteolin 7-glucuronide	5280601	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O	462.40	unknown	via CMAUP database
methyl (2S,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate	91129494	Click to see COC(=O)C1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C=C4)O)O)O)O)O)O	476.40	unknown	via CMAUP database
Scutellarin	185617	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O	462.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one	60195926	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O	594.50	unknown	via CMAUP database
Apigetrin	5280704	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	via CMAUP database
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
Cyanidin	128861	Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2O)O)O)O)O	287.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol	5280666	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	via CMAUP database

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Ledebouria socialis

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