Liriope muscari is a species of flowering plant native to East Asia. It is commonly known as big blue lilyturf, lilyturf, border grass, or monkey grass. This small perennial plant has grass-like evergreen leaves and produces lilac-purple flowers in late summer, followed by single-seeded berries in the fall. It is often used as a groundcover in landscaping, but it is considered invasive in North America and can be harmful to native wildlife. Liriope muscari is easy to grow and can tolerate a wide range of conditions, but it is best suited for moist, fertile soils with partial shade. It can be propagated through division or seeds, but the latter can be difficult due to the plant's dormancy and short storage life. While it has gained popularity as a landscaping plant, some argue that it has been overused and suggest using native alternatives. In traditional Chinese medicine, the roots of this plant are used for medicinal purposes.

Synonyms Top

Scientific name	Authority	First published in
Ophiopogon muscari	Decne.	Ann. Gén. Hort. 17: 181 (1867)
Liriope gigantea	H.H.Hume	Baileya 9: 148 (1961)
Liriope exiliflora	(L.H.Bailey) H.H.Hume	Baileya 9: 144 (1961)
Liriope platyphylla	F.T.Wang & Tang	Acta Phytotax. Sin. 1: 332 (1951)
Liriope muscari f. variegata	(L.H.Bailey) H.Hara	J. Jap. Bot. 59: 37 (1984)
Liriope muscari f. latifolia	(Makino) H.Hara	J. Jap. Bot. 59: 37 (1984)
Liriope muscari f. exiliflora	(L.H.Bailey) H.Hara	J. Jap. Bot. 59: 37 (1984)
Liriope yingdeensis	R.H.Miao	Acta Sci. Nat. Univ. Sunyatseni 1982(3): 75 (1982)
Ophiopogon spicatus var. communis	Maxim.	Bull. Acad. Imp. Sci. Saint-Pétersbourg 15: 85 1871
Liriope graminifolia var. densifolia	Maxim. ex Baker	J. Linn. Soc., Bot. 17: 500 1879
Liriope spicata var. latifolia	Franch.	Nouv. Arch. Mus. Hist. Nat. sér. 2, 7: 104. 1884
Liriope spicata var. densiflora	(Maxim. ex Baker) C.H.Wright	J. Linn. Soc., Bot. 36: 79 1903
Liriope muscari var. communis	(Maxim.) Nakai	Bot. Mag. (Tokyo) 43: 776 1934
Liriope muscari var. exiliflora	L.H.Bailey	Gentes Herb. 2: 37 1929
Liriope graminifolia var. latifolia	Makino	Yagaihakubutsu 3: 165 1933
Liriope muscari var. variegata	L.H.Bailey	Gentes Herb. 2: 35 1929
Liriope graminifolia var. variegata	(L.H.Bailey) Makino	Engei-Shokub. 3: 1065 1940
Liriope platyphylla f. variegata	(L.H.Bailey) Ishii & Hosaka	Engei-Shokub.-Zufu 3: 381 1956
Liriope graminifolia var. praealba	Makino	J. Jap. Bot. 5: 22. 1928
Liriope muscari f. praealba	(Makino) Nemoto	Fl. Jap. Suppl. 1066 1936
Liriope muscari f. albiflora	(Makino) Nemoto	Fl. Jap. Suppl. 1066 1936
Liriope graminifolia var. albiflora	Makino	J. Jap. Bot. 3: 38. 1926
Liriope platyphylla var. albiflora	(Makino) Honda	Nom. Pl. Jap. ed. emend.: 380 1957
Liriope muscari var. communis	(Maxim.) P.S.Hsu & L.Chu Li	Acta Phytotax. Sin. 19(4): 460. 1981 [18 Nov 1981]
Liriope spicata var. densifolia	(Maxim. ex Baker) C.H.Wright	J. Linn. Soc., Bot. 36(250): 79–80 1903

Common names Top

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Filter by language:

Language	Common/alternative name
English	big blue lilyturf'
English	border grass
English	lilyturf
English	monkey grass
English	big blue lilyturf
Arabic	ليريوبية موسكارية
Esperanto	simia herbo
Esperanto	lilia gozono
Japanese	藪蘭
Japanese	サマームスカリ
Japanese	ヤブラン
Korean	맥문동
Russian	Лириопа мускари
Russian	Комнатный мышиный гиацинт
Russian	Лириопе плосколистная
Russian	Лириопе мускари
Chinese	短莛山麦冬
Chinese	阔叶山麦冬
Chinese	阔叶山麦冬（短葶山冬麦）
Chinese	阔叶麦冬
Chinese	闊葉山麥冬
Chinese	土麦冬

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Taiwan

Northern America click to expand
- Southeastern U.S.A.
  - Alabama
  - Florida

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000681593
UNII	71H518MIV2
Florida Plant Atlas	4336
Flora of Alabama	4448
USDA Plants	LIMU6
Tropicos	18405500
INPN	913715
KEW	urn:lsid:ipni.org:names:537868-1
The Plant List	kew-280317
Plantarium	72617
Missouri Botanical Garden	282388
Open Tree Of Life	1023700
Observations.org	206259
NCBI Taxonomy	39529
Nature Serve	2.148654
IPNI	537868-1
iNaturalist	223938
GBIF	5549949
Freebase	/m/06wbhr7
EPPO	LRIMU
EOL	1002997
Elurikkus	5510
USDA GRIN	410578
Wikipedia	Liriope_muscari
CMAUP	NPO5275

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

Designing combinational herbal drugs based on target space analysis

Woyessa AM, Bultum LE, Lee D

BMC Complement Med Ther

01-May-2024

PMCID:	PMC11064244
doi:	10.1186/s12906-024-04455-9
PMID:	38693521

Examining the Pathogenesis of MAFLD and the Medicinal Properties of Natural Products from a Metabolic Perspective

Fu Y, Wang Z, Qin H

Metabolites

12-Apr-2024

PMCID:	PMC11052500
doi:	10.3390/metabo14040218
PMID:	38668346

Study of summer microclimate and PM2.5 concentration in campus plant communities

Jiang Y, Liu C, Wen C, Long Y

Sci Rep

09-Feb-2024

PMCID:	PMC10853255
doi:	10.1038/s41598-024-52508-3
PMID:	38332000

Saengmaeksan, a traditional polyherbal formulation containing Panax ginseng, improves energy metabolism during exercise

Baek S, Kim J, Nam MH, Park SM, Lee TS, Kang SY, Kim JY, Yoon HJ, Kwon SH, Park J, Lee SJ, Oh SJ, Lim K, Kim BS, Lee KP, Moon BS

PLoS One

29-Jan-2024

PMCID:	PMC10824426
doi:	10.1371/journal.pone.0296487
PMID:	38285695

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

Anti-Inflammatory Effects of the LK5 Herbal Complex on LPS- and IL-4/IL-13-Stimulated HaCaT Cells and a DNCB-Induced Animal Model of Atopic Dermatitis in BALB/c Mice

Kim HJ, Kim SY, Bae HJ, Choi YY, An JY, Cho YE, Cho SY, Lee SJ, Lee S, Sin M, Yun YM, Lee JR, Park SJ

Pharmaceutics

27-Dec-2023

PMCID:	PMC10821371
doi:	10.3390/pharmaceutics16010040
PMID:	38258052

Comparison of the Metabolomics of Different Dendrobium Species by UPLC-QTOF-MS

Zhang T, Yang X, Wang F, Liu P, Xie M, Lu C, Liu J, Sun J, Fan B

Int J Mol Sci

05-Dec-2023

PMCID:	PMC10742841
doi:	10.3390/ijms242417148
PMID:	38138977

Latin American Plants against Microorganisms

Cuevas-Cianca SI, Romero-Castillo C, Gálvez-Romero JL, Sánchez-Arreola E, Juárez ZN, Hernández LR

Plants (Basel)

28-Nov-2023

PMCID:	PMC10708099
doi:	10.3390/plants12233997
PMID:	38068631

Complement C3-Deficiency-Induced Constipation in FVB/N-C3em1Hlee/Korl Knockout Mice Was Significantly Relieved by Uridine and Liriope platyphylla L. Extracts

Song HJ, Kim JE, Jin YJ, Roh YJ, Seol A, Kim TR, Park KH, Park ES, An BS, Yang SY, Seo S, Jo SM, Jung YS, Hwang DY

Int J Mol Sci

30-Oct-2023

PMCID:	PMC10649790
doi:	10.3390/ijms242115757
PMID:	37958740

Altered synaptic currents, mitophagy, mitochondrial dynamics in Alzheimer's disease models and therapeutic potential of Dengzhan Shengmai capsules intervention

Zhao B, Wei D, Long Q, Chen Q, Wang F, Chen L, Li Z, Li T, Ma T, Liu W, Wang L, Yang C, Zhang X, Wang P, Zhang Z

J Pharm Anal

28-Oct-2023

PMCID:	PMC11010627
doi:	10.1016/j.jpha.2023.10.006
PMID:	38618251

Synthetic and Natural Bioactive Molecules in Balancing the Crosstalk among Common Signaling Pathways in Alzheimer’s Disease: Understanding the Neurotoxic Mechanisms for Therapeutic Intervention

Shah AJ, Mir PA, Adnan M, Patel M, Maqbool M, Mir RH, Masoodi MH

ACS Omega

20-Oct-2023

PMCID:	PMC10620788
doi:	10.1021/acsomega.3c05662
PMID:	37929080

Anti-Inflammatory and Antioxidant Activities of Lipophilic Fraction from Liriope platyphylla Seeds Using Network Pharmacology, Molecular Docking, and In Vitro Experiments

Truong VL, Bae YJ, Rarison RH, Bang JH, Park SY, Jeong WS

Int J Mol Sci

06-Oct-2023

PMCID:	PMC10573744
doi:	10.3390/ijms241914958
PMID:	37834406

Advance in vasculogenic mimicry in ovarian cancer (Review)

Tian X, Si Q, Liu M, Shi J, Zhao R, Xiong Y, Yu L, Cui H, Guan H

Oncol Lett

05-Sep-2023

PMCID:	PMC10509778
doi:	10.3892/ol.2023.14043
PMID:	37736556

Phytochemicals targeting glycolysis in colorectal cancer therapy: effects and mechanisms of action

Zhan L, Su F, Li Q, Wen Y, Wei F, He Z, Chen X, Yin X, Wang J, Cai Y, Gong Y, Chen Y, Ma X, Zeng J

Front Pharmacol

24-Aug-2023

PMCID:	PMC10484417
doi:	10.3389/fphar.2023.1257450
PMID:	37693915

Efficacy and Safety of Woohwangchungsimwon Combined with Donepezil in Behavioral and Psychological Symptoms of Dementia in Patients with Probable Alzheimer’s Disease: Study Protocol for a Randomized Controlled Trial

Kim MG, Hyun MS, Park SG, Cho E, Kim J, Choi HK, Son KL, Lim CY, Kim KK, Koo BS

Healthcare (Basel)

16-Jul-2023

PMCID:	PMC10378906
doi:	10.3390/healthcare11142036
PMID:	37510478

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Pentyl benzoate	16296	Click to see CCCCCOC(=O)C1=CC=CC=C1	192.25	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol	244	Click to see C1=CC=C(C=C1)CO	108.14	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3S,4S,5S,6S)-2-[[(1R,2S,4aR,5R,8aR)-5-hydroxy-4a,8-dimethyl-2-propan-2-yl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162898270	Click to see CC1=CCC(C2(C1C(C(CC2)C(C)C)OC3C(C(C(C(O3)CO)O)O)O)C)O	400.50	unknown	https://doi.org/10.1021/NP049864E
2-[(5-hydroxy-4a,8-dimethyl-2-propan-2-yl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-1-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	14164915	Click to see CC1=CCC(C2(C1C(C(CC2)C(C)C)OC3C(C(C(C(O3)CO)O)O)O)C)O	400.50	unknown	https://doi.org/10.1021/NP049864E
Liriopeoside A	21589805	Click to see CC1=CCC(C2(C1C(C(CC2)C(C)C)OC3C(C(C(C(O3)CO)O)O)O)C)O	400.50	unknown	https://doi.org/10.1021/NP049864E
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
2,6,10,14,19,23,27,31-Octamethyldotriaconta-2,6,10,12,14,16,18,22,26,30-decaene	94171	Click to see CC(=CCCC(=CCCC(=CCCC(=CC=CC=C(C)C=CC=C(C)CCC=C(C)CCC=C(C)C)C)C)C)C	542.90	unknown	via CMAUP database
Beta-Carotene	5280489	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C	536.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Torularhodin	5281248	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)C=CC=C(C)C(=O)O)C)C	564.80	unknown	via CMAUP database
> 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
(5'S,9S,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14,16-diol	24893327	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)O)C)C)C)OC1	430.60	unknown	via CMAUP database
3-Hydroxyolean-12-en-28-oic acid	619166	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	https://doi.org/10.1021/NP049864E
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	https://doi.org/10.1021/NP049864E
Ruscogenin	441893	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)O)C)C)C)OC1	430.60	unknown	via CMAUP database
Ursolic acid acetate	6475119	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O	498.70	unknown	https://doi.org/10.1021/NP049864E
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2R,3R,4S,5R)-2-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(5'S,7S,9S,13R,14R,16R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxyoxan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxyoxane-3,4,5-triol	11968386	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)O)C)C)C)OC1	887.00	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[(2S)-4-[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-6,16-dihydroxy-14-[(2R,3R,4S,5S,6R)-5-hydroxy-6-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	101899809	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(C(O6)C)O)OC7C(C(C(CO7)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O	1051.20	unknown	via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-4,5-dihydroxy-2-[(14R,16R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-6-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol	11968813	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1	722.90	unknown	https://doi.org/10.1142/S0192415X15500275
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-2-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-6-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol	71307569	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1	722.90	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5R,6R)-4,5-dihydroxy-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-6-methyloxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	162957846	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1	738.90	unknown	https://doi.org/10.1248/CPB.38.1931
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-5-hydroxy-2-[(14R,16R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-6-methyl-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-4-yl]oxy-6-methyloxane-3,4,5-triol	5320302	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)C)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	869.00	unknown	https://doi.org/10.1142/S0192415X15500275
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-5-hydroxy-2-[(1R,2S,4R,5'R,6R,7S,8S,9S,12S,13R,14R,16R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	162982405	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1	871.00	unknown	https://doi.org/10.1248/CPB.38.1931
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R)-2-[(2R,3R,4S,5S,6R)-3,5-dihydroxy-2-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-6-methyloxan-4-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	162887536	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(CO8)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)C)C)C)OC1	871.00	unknown	https://doi.org/10.1211/0022357011775802
(2S,3R,4S,5S,6R)-2-[(3R,4S,5S,6R)-5-hydroxy-2-[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	101514160	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1	871.00	unknown	via CMAUP database
(3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[[(1S,2S,4S,7S,8R,9S,12S,13R,16S)-6-methoxy-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	123134748	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC	1063.20	unknown	https://doi.org/10.1248/CPB.31.1980
(3R,4S,5R,6S)-2-[(3R,4R,5S,6R)-4,5-dihydroxy-2-[(1S,2S,4S,5'R,7S,8R,9S,12S,13R,14R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-6-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol	53486206	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1	722.90	unknown	via CMAUP database
[(2S,3R,4R,5S,6S)-2-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-2-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-6-methyloxan-3-yl]oxy-3,5-dihydroxy-6-methyloxan-4-yl] acetate	91668492	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)O)OC8C(C(C(C(O8)C)O)OC(=O)C)O)C)C)C)OC1	764.90	unknown	via CMAUP database
[(2S,3R,4R,5S,6S)-2-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-2-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13S,14R,16R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-6-methyloxan-3-yl]oxy-3,5-dihydroxy-6-methyloxan-4-yl] acetate	91798589	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)O)OC8C(C(C(C(O8)C)O)OC(=O)C)O)C)C)C)OC1	764.90	unknown	via CMAUP database
2-[2-[3,5-Dihydroxy-2-(16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl)oxy-6-methyloxan-4-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	162887535	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(CO8)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)C)C)C)OC1	871.00	unknown	https://doi.org/10.1211/0022357011775802
2-[4,5-Dihydroxy-2-(16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl)oxy-6-methyloxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	14682471	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1	738.90	unknown	https://doi.org/10.1248/CPB.38.1931
3-Hydroxyspirost-5-en-1-yl 6-deoxy-2-O-(6-deoxyhexopyranosyl)hexopyranoside	3081483	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1	722.90	unknown	via CMAUP database
Cixiophiopogon A	102004869	Click to see CC1CCC2(C(C3(C(O2)CC4(C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)O)O)C)OC1	887.00	unknown	via CMAUP database
Liriope muscari baily Saponins	14682474	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1	871.00	unknown	https://doi.org/10.1248/CPB.38.1931
Liriopesides B	21630160	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)OC7C(C(C(C(O7)C)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1	722.90	unknown	via CMAUP database
Ophiopogonin A	46173858	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)O)OC8C(C(C(C(O8)C)O)OC(=O)C)O)C)C)C)OC1	764.90	unknown	via CMAUP database
Ophiopogonin B	46173857	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1	722.90	unknown	via CMAUP database
Ophiopogonin D	46173859	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	855.00	unknown	via CMAUP database
ophiopojaponin C	90477999	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)OC(=O)C)OC7C(C(C(C(O7)C)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	897.10	unknown	via CMAUP database
Spicatoside A	21630001	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1	871.00	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Hydroxymethylfurfural	237332	Click to see C1=C(OC(=C1)C=O)CO	126.11	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Dialkyl ethers
2-Ethylhexyl 3-aminopropyl ether	21499	Click to see CCCCC(CC)COCCCN	187.32	unknown	via CMAUP database
Ethylene glycol dibutyl ether	8188	Click to see CCCCOCCOCCCC	174.28	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Hydroxypyrimidines
5-methylpyrimidine-2,4-diol	5274265	Click to see CC1=CN=C(N=C1O)O	126.11	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Maltol	8369	Click to see CC1=C(C(=O)C=CO1)O	126.11	unknown	via CMAUP database
> Organophosphorus compounds / Organic phosphines and derivatives
Triethylphosphine	27365	Click to see CCP(CC)CC	118.16	unknown	https://doi.org/10.1142/S0192415X15500275
> Organosulfur compounds / Thioacetals / Monothioacetals
Carbonodithioic acid, S-ethyl O-(1-methylethyl) ester	539987	Click to see CCSC(=S)OC(C)C	164.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
cis-N-p-coumaroyltyramine	13939145	Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O	283.32	unknown	https://doi.org/10.1021/NP049864E
> Phenylpropanoids and polyketides / Coumarins and derivatives
N-[2-(4-hydroxyphenyl)ethyl]-2-oxochromene-4-carboxamide	162910243	Click to see C1=CC=C2C(=C1)C(=CC(=O)O2)C(=O)NCCC3=CC=C(C=C3)O	309.30	unknown	https://doi.org/10.1021/NP049864E
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Delphinidin 3-(6-rhamnosylglucosuide)	44256887	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O)O)O)O	611.50	unknown	via CMAUP database
Tulipanin	5492231	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O)O)O)O	611.50	unknown	https://doi.org/10.1142/S0192415X15500275
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
3-(1,3-Benzodioxol-5-ylmethyl)-5,7-dihydroxy-6,8-dimethyl-2,3-dihydrochromen-4-one	5319741	Click to see CC1=C(C(=C2C(=C1O)C(=O)C(CO2)CC3=CC4=C(C=C3)OCO4)C)O	342.30	unknown	via CMAUP database
6-Aldehydoisoophiopogonanone A	71584762	Click to see CC1=C(C(=C(C2=C1OCC(C2=O)CC3=CC4=C(C=C3)OCO4)O)C=O)O	356.30	unknown	via CMAUP database
Methylophiopogonanone B	46886723	Click to see CC1=C(C(=C2C(=C1O)C(=O)C(CO2)CC3=CC=C(C=C3)OC)C)O	328.40	unknown	via CMAUP database
Ophiopogonanone A	9996586	Click to see CC1=C(C2=C(C=C1O)OCC(C2=O)CC3=CC4=C(C=C3)OCO4)O	328.30	unknown	via CMAUP database
Ophiopogonanone D	11003181	Click to see CC1=C(C(=C2C(=C1OC)C(=O)C(CO2)CC3=CC4=C(C=C3)OCO4)C=O)O	370.40	unknown	via CMAUP database
Ophiopogonanone E	5316797	Click to see CC1=C(C2=C(C(=C1O)OC)OCC(C2=O)CC3=C(C=C(C=C3)OC)O)O	360.40	unknown	via CMAUP database
Ophiopogonanone F	5318201	Click to see CC1=C(C(=C2C(=C1OC)C(=O)C(CO2)CC3=C(C=C(C=C3)OC)O)OC)O	374.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavones
Methylophiopogonone A	10065830	Click to see CC1=C(C(=C2C(=C1O)C(=O)C(=CO2)CC3=CC4=C(C=C3)OCO4)C)O	340.30	unknown	https://doi.org/10.1016/J.LFS.2004.04.039
Methylophiopogonone B	23259413	Click to see CC1=C(C(=C2C(=C1O)C(=O)C(=CO2)CC3=CC=C(C=C3)OC)C)O	326.30	unknown	via CMAUP database
Ophiopogonone A	10087732	Click to see CC1=C(C2=C(C=C1O)OC=C(C2=O)CC3=CC4=C(C=C3)OCO4)O	326.30	unknown	https://doi.org/10.1016/J.LFS.2004.04.039
Ophiopogonone C	11142766	Click to see CC1=C(C(=C2C(=C1O)C(=O)C(=CO2)CC3=CC4=C(C=C3)OCO4)C=O)O	354.30	unknown	via CMAUP database

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Liriope muscari

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