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.

Ophiopogon japonicus, commonly known as “Maidong,” has a long history of use in East Asian traditional medicine. In Chinese folk practice, the dried root is boiled into a decoction to treat cough, asthma, and fever, a method described by Li et al. (2015) and still taught in modern Chinese herbal schools. Korean practitioners use a similar root decoction, often combined with ginseng, to relieve sore throat and chronic bronchitis; this practice is documented in Kim et al. (2018). In Japan, the root is also brewed as a mild tea to soothe sore throats and to calm the nervous system, a use noted by Tanaka (2016). In all three cultures, the root is the primary material; leaves and rhizomes are occasionally used in poultices for skin inflammation, but the most common preparations are infusions and decoctions of the root.

A simple, safe recipe for a Maidong tea is as follows: take 10 g of dried root, place it in a pot with 500 ml of water, bring to a boil, then reduce the heat and simmer for 30 minutes. Strain the liquid, discard the solids, and drink the tea 2–3 times a day, preferably after meals. If you are pregnant, nursing, or have liver disease, consult a healthcare professional before using this tea, as some studies have reported mild hepatotoxicity at high doses. The decoction can be stored in the refrigerator for up to 48 hours and re‑heated gently before consumption.

The therapeutic effects of Maidong are largely attributed to its saponins, polysaccharides, and flavonoids. Saponins such as ophiopogonin D have been shown to possess anti‑inflammatory and bronchodilatory properties, while the polysaccharides contribute to immune modulation. Flavonoids, including luteolin and apigenin, provide antioxidant activity that may underlie the plant’s traditional use for cough and fever. These constituents have been isolated and characterized in several peer‑reviewed studies, providing a biochemical basis for the observed medicinal effects.

Contemporary research continues to explore Maidong’s potential. Recent clinical trials have investigated its efficacy in chronic obstructive pulmonary disease and as an adjunct in cancer therapy, while commercial herbal manufacturers now offer standardized Maidong extracts and teas. The plant remains a staple in traditional East Asian medicine, and its continued study bridges ancient practice with modern pharmacology.

General Uses Top

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Common products:
Ophiopogon japonicus is cultivated for the ornamental nursery trade as whole plants, plug trays, or sod. The species is marketed as a low‑maintenance, evergreen groundcover for residential, commercial, and public landscapes and as an indoor terrarium plant. Major nursery catalogs and the USDA PLANTS database list it as a commonly sold ornamental.

Fragrance and cosmetics:
The root extract (Ophiopogon japonicus root extract) is listed in the International Nomenclature of Cosmetic Ingredients (INCI) as a skin‑conditioning agent. Commercial creams, lotions, and serums incorporate the extract for its moisture‑retaining properties, and it appears in ingredient lists of mass‑market and boutique brands.

Scientific and model organism uses:
A chromosome‑level genome of Ophiopogon japonicus was published (Wang et al., 2022, Plant Biotechnology Journal), providing a reference for phylogenetic studies within Asparagaceae and comparative genomics of monocots. The species serves as a model for rhizome development, evergreen leaf physiology, and secondary metabolite biosynthesis; genomic data are deposited in NCBI GenBank and accessible via community resources (e.g., CoGe, Phytozome).

Properties relevant to use:
The plant forms a dense, shallow rhizome mat that creates a continuous groundcover, reducing soil erosion and suppressing weeds. Its evergreen foliage retains colour through winter, it tolerates partial shade and moderate foot traffic, and its compact stature (15–30 cm) suits low‑maintenance landscape applications.

Standards and regulation:
As an ornamental plant, O. japonicus must meet national plant‑health regulations (e.g., USDA‑APHIS import rules for non‑quarantine species in the United States; EU Plant Health Directive 2000/29/EC). The INCI listing of the root extract obligates compliance with the European Cosmetic Regulation (EC) No 1223/2009 and U.S. FDA cosmetic labeling requirements.

Sustainability and sourcing:
Propagation is achieved vegetatively by dividing mature clumps, allowing rapid, resource‑efficient production without seed‑generated variation. The species requires low water and minimal chemical inputs, supporting sustainable landscaping. Commercial cultivation typically occurs in temperate greenhouses, limiting land‑use pressure compared with annual field crops.

Synonyms Top

Scientific name	Authority	First published in
Ophiopogon gracilis	Kunth	Enum. Pl. 5: 298 (1850)
Slateria coerulea	Siebold ex Miq.	Ann. Mus. Bot. Lugduno-Batavi 3: 143 (1867)
Slateria japonica	(Thunb.) Desv.	J. Bot. (Desvaux) 1: 244 (1809)
Liriope gracilis	(Kunth) Nakai	Index Seminum (TI, Tokyo) 1919-1920: 33 (1920)
Mondo gracile	(Kunth) Koidz.	Acta Phytotax. Geobot. 3: 148 (1934)
Mondo longifolium	Ohwi	Repert. Spec. Nov. Regni Veg. 36: 45 (1934)
Mondo japonicum	(Thunb.) Farw.	Amer. Midl. Naturalist 7: 42 (1921)
Mondo stolonifer	(H.Lév. & Vaniot) Farw.	Amer. Midl. Naturalist 7: 42 (1921)
Ophiopogon stolonifer	H.Lév. & Vaniot	Liliac. & C.Chine : 16 (1905)
Ophiopogon merrillii	Masam.	Bull. Soc. Bot. France 84: 90 (1937)
Ophiopogon ohwii	Okuyama	J. Jap. Bot. 13: 35 (1937)
Ophiopogon argyi	H.Lév.	Repert. Spec. Nov. Regni Veg. 9: 77 (1910)
Ophiopogon chekiangensis	Koiti Kimura & Migo	J. Jap. Bot. 57: 313 (1982)
Polygonastrum compressum	Moench	Suppl. Meth. : 268 (1802)
Tricoryne caulescens	D.Dietr.	Syn. Pl. 2: 1152 (1840)
Tricoryne acaulis	D.Dietr.	Syn. Pl. 2: 1152 (1840)
Ophiopogon japonicus var. elevatus	Kuntze	Revis. Gen. Pl. 2: 699. 1891
Anemarrhena cavaleriei	H.Lév.	Bull. Acad. Int. Géogr. Bot. 24: 37. 1915 (1915)
Convallaria graminifolia	Salisb.	Prodr. Stirp. Chap. Allerton : 254 (1796)
Convallaria japonica	Thunb.	Nova Acta Regiae Soc. Sci. Upsal. , ser. 2, 3: 208 (1780)
Flueggea anceps	Raf.	Fl. Tellur. 4: 18. 1838 [1836 publ. mid-1838]
Flueggea japonica	(Thunb.) Rich.	Neues J. Bot. ii. (1807) 9.
Convallaria japonica var. minor	Thunb.	Fl. Jap. 253. 1784
Ophiopogon japonicus var. umbrosus	Maxim.	Mélanges Biol. Bull. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 7: 327. 1869
Mondo gracile var. brevipedicellatum	Koidz.	Acta Phytotax. Geobot. 3: 148. 1934
Ophiopogon gracilis var. brevipedicellatus	(Koidz.) Nemoto	Fl. Japan, Suppl. 1067 1936
Ophiopogon japonicus var. caespitosus	Okuyama	J. Jap. Bot. 26: 318. 1951
Convallaria japonica	L.f.	Suppl. Pl. 204. 1782 [1781 publ. Apr 1782]
Flueggea angulata	Raf.	Fl. Tellur. 4: 18. 1838 [1836 publ. mid-1838]

Common names Top

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Filter by language:

Language	Common/alternative name
English	dwarf mondograss
English	dwarf mondo grass
English	dwarf lilyturf
English	mondo grass
English	fountainplant
English	mondograss
English	monkeygrass
Azerbaijani	yapon ofiopoqonu
Esperanto	nana mondo herbo
Persian	افیوپگن جاپنیکا
French	muguet du japon
Indonesian	rumput kucai
Japanese	リュウノヒゲ
Japanese	ジャノヒゲ
Slovenian	japonska kačja brada
Thai	แบะหมึ่งตง
Vietnamese	mạch môn
Chinese	绣墩草
Chinese	沿階草
Chinese	書帶草
Chinese	麦冬（沿阶草）
Chinese	沿阶草
Chinese	麦门冬
Chinese	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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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

Asia-tropical click to expand
- Indo-China
  - Vietnam
- Malesia
  - Jawa
  - Philippines

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

Pacific click to expand
- Northwestern Pacific
  - Marianas

Southern America click to expand
- Southern South America
  - Argentina Northeast

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000673577
UNII	2983RA66TS
Florida Plant Atlas	4933
Flora of Alabama	5278
USDA Plants	OPJA
Tropicos	18404334
INPN	447838
Flora of Italy	8535
KEW	urn:lsid:ipni.org:names:429781-1
The Plant List	kew-279475
Missouri Botanical Garden	282276
PFAF	Ophiopogon japonicus
Open Tree Of Life	725826
NCBI Taxonomy	100506
IPNI	429781-1
iNaturalist	200061
GBIF	2774158
Freebase	/m/04wtjp
EPPO	OPPJA
EOL	1002097
USDA GRIN	25788
Wikipedia	Ophiopogon_japonicus
CMAUP	NPO29403
CMAUP	NPO9261

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

Efficacy and safety of herbal medicine combined with acupuncture in pediatric epilepsy treatment: A meta-analysis of randomized controlled trials

Su HW, Chen HT, Kao CL, Hung KC, Lin YT, Liu PH, Lin CM, Chen IW

PLoS One

09-May-2024

PMCID:	PMC11081325
doi:	10.1371/journal.pone.0303201
PMID:	38723054

Potential Effects of Traditional Chinese Medicine in Anti-Aging and Aging-Related Diseases: Current Evidence and Perspectives

Ding X, Ma X, Meng P, Yue J, Li L, Xu L

Clin Interv Aging

01-May-2024

PMCID:	PMC11070163
doi:	10.2147/CIA.S447514
PMID:	38706635

Lipid metabolism disorder in diabetic kidney disease

Han YZ, Du BX, Zhu XY, Wang YZ, Zheng HJ, Liu WJ

Front Endocrinol (Lausanne)

29-Apr-2024

PMCID:	PMC11089115
doi:	10.3389/fendo.2024.1336402
PMID:	38742197

Efficacy of Shensong Yangxin capsule combined with dronedarone in paroxysmal atrial fibrillation after ablation

Zhou T, Gong P, Xu M, Yan L, Zhang Y

Medicine (Baltimore)

26-Apr-2024

PMCID:	PMC11049715
doi:	10.1097/MD.0000000000037918
PMID:	38669399

Potential Targets of Natural Products for Improving Cardiac Ischemic Injury: The Role of Nrf2 Signaling Transduction

Wang H, Han J, Dmitrii G, Zhang XA

Molecules

26-Apr-2024

PMCID:	PMC11085255
doi:	10.3390/molecules29092005
PMID:	38731496

Research advances on molecular mechanism and natural product therapy of iron metabolism in heart failure

Zhang T, Luo L, He Q, Xiao S, Li Y, Chen J, Qin T, Xiao Z, Ge Q

Eur J Med Res

24-Apr-2024

PMCID:	PMC11044586
doi:	10.1186/s40001-024-01809-4
PMID:	38659000

TCM targets ferroptosis: potential treatments for cancer

Qin L, Zhong Y, Li Y, Yang Y

Front Pharmacol

22-Apr-2024

PMCID:	PMC11082647
doi:	10.3389/fphar.2024.1360030
PMID:	38738174

Active metabolites combination therapies: towards the next paradigm for more efficient and more scientific Chinese medicine

Gao Q, Wu H, Chen M, Gu X, Wu Q, Xie T, Sui X

Front Pharmacol

18-Apr-2024

PMCID:	PMC11063311
doi:	10.3389/fphar.2024.1392196
PMID:	38698817

Dietary supplementation of Chinese herbal medicines enhances the immune response and resistance of rainbow trout (Oncorhynchus mykiss) to infectious hematopoietic necrosis virus

Wang Q, Pan Y, Huang J, Li Y, Wu S, Zhao L, Sun T, Kang Y, Liu Z

Front Vet Sci

17-Apr-2024

PMCID:	PMC11062137
doi:	10.3389/fvets.2024.1341920
PMID:	38694480

Research on the metabolic regulation mechanism of Yangyin Qingfei decoction plus in severe pneumonia caused by Mycoplasma pneumoniae in mice

Zhang T, Zhao X, Zhang X, Liang X, Guan Z, Wang G, Liu G, Wu Z

Front Pharmacol

17-Apr-2024

PMCID:	PMC11061391
doi:	10.3389/fphar.2024.1376812
PMID:	38694915

Exploring the Mechanism of Yiwei Decoction in the Intervention of a Premature Ovarian Insufficiency Rat Based on Network Pharmacology and the miRNA-mRNA Regulatory Network

Fan W, Lei H, Li X, Zhao Y, Zhang Y, Li Y

ACS Omega

17-Apr-2024

PMCID:	PMC11064180
doi:	10.1021/acsomega.3c09551
PMID:	38708213

The gut-liver axis in fatty liver disease: role played by natural products

Ming Z, Ruishi X, Linyi X, Yonggang Y, Haoming L, Xintian L

Front Pharmacol

15-Apr-2024

PMCID:	PMC11056694
doi:	10.3389/fphar.2024.1365294
PMID:	38686320

Aroplectrus dimerus (Hymenoptera: Eulophidae), Ectoparasitoid of the Nettle Caterpillar, Oxyplax pallivitta (Lepidoptera: Limacodidae): Evaluation in the Hawaiian Islands

Yalemar JA, Nagamine WT, Bautista RC, Cho DY, Nakahara LM, Ramadan MM

Life (Basel)

15-Apr-2024

PMCID:	PMC11051351
doi:	10.3390/life14040509
PMID:	38672779

A relatively rare traditional Chinese medicine pattern of primary Sjögren syndrome: A case report

Chen Q, Chen X, Zhu Y, Yu X

Medicine (Baltimore)

12-Apr-2024

PMCID:	PMC11018238
doi:	10.1097/MD.0000000000037744
PMID:	38608118

The potential of astragalus polysaccharide for treating diabetes and its action mechanism

Liu S, Wang L, Zhang Z, Leng Y, Yang Y, Fu X, Xie H, Gao H, Xie C

Front Pharmacol

10-Apr-2024

PMCID:	PMC11039829
doi:	10.3389/fphar.2024.1339406
PMID:	38659573

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
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol	244	Click to see	108.14	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
Orchinol	181686	Click to see COC1=CC2=C(C3=C(CC2)C=C(C=C3)O)C(=C1)OC	256.30	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Feruloyltyramine	5280537	Click to see	313.30	unknown	via CMAUP database
> Hydrocarbons / Polycyclic hydrocarbons
beta-Patchoulene	101731	Click to see	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Tianshic acid	5321949	Click to see	330.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
methyl (1S,4aR,4bS,7E,8R,8aS,9R,10aR)-9-hydroxy-7-[2-[2-hydroxyethyl(methyl)amino]-2-oxoethylidene]-1,4a,8-trimethyl-10-oxo-2,3,4,4b,5,6,8,8a,9,10a-decahydrophenanthrene-1-carboxylate	101710278	Click to see CC1C2C(CCC1=CC(=O)N(C)CCO)C3(CCCC(C3C(=O)C2O)(C)C(=O)OC)C	435.60	unknown	https://doi.org/10.1080/14786411003762051
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
CID 44630107	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)83615-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(-)-Borneol glucoside	21631069	Click to see	316.39	unknown	https://doi.org/10.1248/CPB.41.566
(2R,3S,4S,5R,6R)-2-[[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[[(1R,2S,4R)-1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl]oxy]oxane-3,4,5-triol	14526912	Click to see CC1(C2CCC1(C(C2)OC3C(C(C(C(O3)COC4C(C(C(O4)CO)O)O)O)O)O)C)C	448.50	unknown	https://doi.org/10.1016/0031-9422(90)80151-6
(2R,3S,4S,5S,6S)-2-[[(1R,2S,4aR,5R,8S,8aR)-5,8-dihydroxy-4a,8-dimethyl-2-propan-2-yl-1,2,3,4,5,6,7,8a-octahydronaphthalen-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162973703	Click to see	418.50	unknown	https://doi.org/10.1021/NP049864E
2-[(5,8-Dihydroxy-4a,8-dimethyl-2-propan-2-yl-1,2,3,4,5,6,7,8a-octahydronaphthalen-1-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	73808182	Click to see	418.50	unknown	https://doi.org/10.1021/NP049864E
2-[[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl)oxy]oxane-3,4,5-triol	14526911	Click to see	448.50	unknown	https://doi.org/10.1016/0031-9422(90)80151-6
Ophiopogonoside A	21589806	Click to see CC(C)C1CCC2(C(CCC(C2C1OC3C(C(C(C(O3)CO)O)O)O)(C)O)O)C	418.50	unknown	https://doi.org/10.1021/NP049864E
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(25s)-Spirost-5-ene-1beta,3beta-diol	12315113	Click to see	430.60	unknown	https://doi.org/10.1248/BPB.29.1267
(3I(2),22I(2),25S)-Spirost-5-en-3-ol	53486205	Click to see	414.60	unknown	via CMAUP database
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	51892422	Click to see	456.70	unknown	https://doi.org/10.1021/NP049864E
(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	430.60	unknown	via CMAUP database
Oleanolic Acid	10494	Click to see	456.70	unknown	via CMAUP database
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
Spirost-5-en-1,3-diol	3842686	Click to see	430.60	unknown	https://doi.org/10.1248/BPB.29.1267
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(25R)-Ruscogenin-3-yl \|A-L-rhamnopyranosyl-(1 inverted exclamation marku2)-[\|A-D-xylopyranosyl-(1 inverted exclamation marku4)]-\|A-D-glucopyranoside	45258032	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(CO8)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)O)C)C)C)OC1	871.00	unknown	https://doi.org/10.1002/HLCA.200900165
(25S)-1beta-(6-Deoxy-beta-D-galactopyranosyloxy)-3beta-(alpha-L-rhamnopyranosyloxy)spirost-5-ene	21630160	Click to see	722.90	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
(2R,3S,4R,5R,6S)-2-[(2S,3S,4R,5R,6S)-2-[(1R,2R,4R,5'S,6S,7S,8R,9R,12R,13S,16R)-2,8-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162899088	Click to see CC1CCC2(C(C3(C(O2)CC4(C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)O)O)C)OC1	754.90	unknown	https://doi.org/10.1016/0031-9422(90)80151-6
(2S,3R,4R,5R,6R)-2-methyl-6-[(1S,2S,4S,5'S,6S,7S,8R,9S,12S,13R,14R,16R)-5',7,9,13-tetramethyl-14-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxane-3,4,5-triol	162905796	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	https://doi.org/10.1002/JLAC.199519950380
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-2-[(2R,5'R,6R,7S,8S)-2,8-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	11968811	Click to see	887.00	unknown	via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-2-[(2R,5'R,6R,7S,8S)-2,8-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-6-(hydroxymethyl)-5-[(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-3-yl]oxy-6-methyloxane-3,4,5-triol	11968812	Click to see	1049.20	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/10.1248/CPB.41.566 https://doi.org/10.1248/CPB.32.3994
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-4,5-dihydroxy-2-[(1R,2S,4S,5'S,6R,7S,8R,9S,12R,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	162932615	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/10.1248/CPB.41.566
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-4,5-dihydroxy-2-[(1S,2S,4S,5'R,6R,7S,8R,9S,12R,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	163187433	Click to see	722.90	unknown	https://doi.org/10.1248/CPB.41.566
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-methyl-2-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,14R)-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-6-methyloxane-3,4,5-triol	162977228	Click to see	706.90	unknown	https://doi.org/10.1248/CPB.20.1729
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-2-[(1R,2R,4S,5'R,6R,7S,8S,9S,12R,13R,16S)-2,8-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162899089	Click to see	754.90	unknown	https://doi.org/10.1016/0031-9422(90)80151-6
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-5-hydroxy-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,12R,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-methyloxane-3,4,5-triol	162916910	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	https://doi.org/10.1248/CPB.41.566
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-5-hydroxy-2-[(1R,2S,4S,5'S,6R,7S,8R,9S,12R,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-methyloxane-3,4,5-triol	162916914	Click to see	855.00	unknown	https://doi.org/10.1248/CPB.41.566
(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	https://doi.org/10.1248/CPB.32.3994 https://doi.org/10.1248/CPB.41.566
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5S)-5-hydroxy-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-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	11158720	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	841.00	unknown	https://doi.org/10.1080/14786411003762051
(2S,3R,4S,5R,6R)-2-[(1S,2R,3'S,4R,4'S,5'S,6S,7S,8R,9S,12S,13R,14R,16R)-3',16-dihydroxy-14-[(2S,3R,4S,5S)-5-hydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-4'-yl]oxy-6-methyloxane-3,4,5-triol	162844901	Click to see CC1COC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)C(C1OC1C(C(C(C(O1)C)O)O)O)O	1019.10	unknown	https://doi.org/10.1248/CPB.41.566
(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	869.00	unknown	https://doi.org/10.1248/CPB.41.566 https://doi.org/10.1248/CPB.32.3994
(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
[(2R,3R,4R,5R,6R)-4-hydroxy-6-[(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-2-methyl-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] hydrogen sulfate	162947072	Click to see	803.00	unknown	https://doi.org/10.1248/CPB.32.3994
[(2R,3R,4R,5R,6R)-6-[[(1S,2S,4S,6S,7S,8R,9S,12S,13R,14R,16R)-6,16-dihydroxy-7,9,13-trimethyl-6-[(3R)-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-14-yl]oxy]-4-hydroxy-2-methyl-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] hydrogen sulfate	163073461	Click to see	983.10	unknown	https://doi.org/10.1248/CPB.32.3994
[(2S,3R,4R,5R,6S)-4,5-dihydroxy-2-[(2R,3R,4S,5S,6R)-4-hydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'R,6R,7S,8S,9S,12S,13R,16S)-8-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxan-3-yl] acetate	45258132	Click to see CC1CCC2(C(C3(C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(CO8)O)O)O)O)OC9C(C(C(C(O9)C)O)O)OC(=O)C)C)C)O)C)OC1	913.10	unknown	https://doi.org/10.1002/HLCA.200900165
[(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	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
[(2S,3R,4S,5R,6S)-6-[(2S,3R,4S,5S)-2-[(1S,2R,3'S,4S,4'S,5'S,6S,7S,8R,9S,12R,13R,14R,16R)-3',16-dihydroxy-5',7,9,13-tetramethyl-4'-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-5-hydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate	162988749	Click to see CC1COC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)OC(=O)C)O)O)C)C)C)C(C1OC1C(C(C(C(O1)C)O)O)O)O	1061.20	unknown	https://doi.org/10.1248/CPB.41.566
[(2S,3S,4R,5R,6S)-4,5-diacetyloxy-6-[(2S,3R,4S,5S)-2-[(1S,2S,3'S,4S,4'S,5'S,6S,7S,8R,9S,12S,13R,14R,16R)-3',16-dihydroxy-5',7,9,13-tetramethyl-4'-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-5-hydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-2-methyloxan-3-yl] acetate	10034225	Click to see CC1COC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)OC(=O)C)OC(=O)C)OC(=O)C)C)C)C)C(C1OC1C(C(C(C(O1)C)O)O)O)O	1145.20	unknown	https://doi.org/10.1248/CPB.41.566
[(3S,4R,5R,6S)-4-hydroxy-6-[(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-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] hydrogen sulfate	102317037	Click to see	788.90	unknown	https://doi.org/10.1248/CPB.32.3994
[4-Hydroxy-6-(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-2-methyl-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] hydrogen sulfate	131863897	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)OS(=O)(=O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1	803.00	unknown	https://doi.org/10.1248/CPB.32.3994
[4-Hydroxy-6-(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-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] hydrogen sulfate	163049230	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)OS(=O)(=O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1	788.90	unknown	https://doi.org/10.1248/CPB.32.3994
[4,5-Diacetyloxy-6-[2-[3',16-dihydroxy-5',7,9,13-tetramethyl-4'-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-5-hydroxy-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-2-methyloxan-3-yl] acetate	85099349	Click to see	1145.20	unknown	https://doi.org/10.1248/CPB.41.566
[4,5-Dihydroxy-2-[4-hydroxy-6-(hydroxymethyl)-2-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxan-3-yl] acetate	75104289	Click to see	897.10	unknown	https://doi.org/10.1002/HLCA.200900165
[4,5-Dihydroxy-2-[4-hydroxy-6-(hydroxymethyl)-2-(8-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxan-3-yl] acetate	75104290	Click to see CC1CCC2(C(C3(C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(CO8)O)O)O)O)OC9C(C(C(C(O9)C)O)O)OC(=O)C)C)C)O)C)OC1	913.10	unknown	https://doi.org/10.1002/HLCA.200900165
[6-[[6,16-Dihydroxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-4-hydroxy-2-methyl-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] hydrogen sulfate	163073460	Click to see	983.10	unknown	https://doi.org/10.1248/CPB.32.3994
[6-[2-[3',16-Dihydroxy-5',7,9,13-tetramethyl-4'-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-5-hydroxy-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate	85118713	Click to see	1061.20	unknown	https://doi.org/10.1248/CPB.41.566
2-[2-(2,8-Dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxy-5-hydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162950637	Click to see	917.00	unknown	https://doi.org/10.1080/14786411003762051
2-[2-(2,8-Dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxy-6-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	5320299	Click to see CC1CCC2(C(C3(C(O2)CC4(C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)O)O)C)OC1	1049.20	unknown	https://doi.org/10.1080/14786411003762051
2-[3',16-Dihydroxy-14-[5-hydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-4'-yl]oxy-6-methyloxane-3,4,5-triol	85099225	Click to see	1019.10	unknown	https://doi.org/10.1248/CPB.41.566
2-[4-Hydroxy-6-(hydroxymethyl)-2-(14-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	75104240	Click to see	871.00	unknown	https://doi.org/10.1002/HLCA.200900165
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-methyloxane-3,4,5-triol	12313751	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/10.1248/CPB.41.566 https://doi.org/10.1248/CPB.32.3994
2-[4,5-Dihydroxy-6-methyl-2-(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-6-methyloxane-3,4,5-triol	162977227	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CCC6)OC7C(C(C(C(O7)C)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1	706.90	unknown	https://doi.org/10.1248/CPB.20.1729
2-[5-Hydroxy-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-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	72832607	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	841.00	unknown	https://doi.org/10.1080/14786411003762051
2''-O-Acetylsprengerinin C	45258131	Click to see	897.10	unknown	https://doi.org/10.1002/HLCA.200900165
3-Hydroxyspirost-5-en-1-yl 6-deoxy-2-O-(6-deoxyhexopyranosyl)hexopyranoside	3081483	Click to see	722.90	unknown	via CMAUP database
cixi-ophiopogon B	162997911	Click to see	1049.20	unknown	https://doi.org/10.1080/14786411003762051
cixi-ophiopogon C	162950638	Click to see	917.00	unknown	https://doi.org/10.1080/14786411003762051
Cixiophiopogon A	102004869	Click to see	887.00	unknown	via CMAUP database
Ojv-VI	12314417	Click to see	855.00	unknown	https://doi.org/10.1248/CPB.41.566 https://doi.org/10.1271/BBB.110066 https://doi.org/10.1248/BPB.29.1267 https://doi.org/10.1248/CPB.32.3994
Ophiogenin-3-O-alpha-L-rhaMnopyranosyl-(1-->2)-beta-D-glucopyranoside	14526906	Click to see	754.90	unknown	https://doi.org/10.1016/0031-9422(90)80151-6
Ophiogenin-3-O-alpha-L-rhaMnopyranosyl(1-->2)[beta-D-xylopyranosyl(1-->3)]-beta-D-glucopyranoside	73157236	Click to see	887.00	unknown	https://doi.org/10.1080/14786411003762051
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	722.90	unknown	https://doi.org/10.1248/CPB.32.3994
Ophiopogonin D'	46173859	Click to see	855.00	unknown	https://doi.org/10.1248/CPB.41.566 https://doi.org/10.1271/BBB.110066 https://doi.org/10.1248/BPB.29.1267 https://doi.org/10.1248/CPB.32.3994
ophiopojaponin C	90477999	Click to see	897.10	unknown	via CMAUP database
Prosapogenin A	11061578	Click to see	722.90	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
spicatosideB	14682457	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	https://doi.org/10.1002/JLAC.199519950380
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	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	https://doi.org/10.1248/CPB.32.3994
Npc196776	50930798	Click to see	410.70	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	https://doi.org/10.1248/CPB.32.3994
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one	6802	Click to see	283.24	unknown	via CMAUP database
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
1-((2r,5r)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-1h-pyrimidine-2,4-dione	45356795	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
L-Pyroglutamic Acid	7405	Click to see	129.11	unknown	https://doi.org/10.1007/BF02978205
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Azetidinecarboxylic Acid	17288	Click to see	101.10	unknown	https://doi.org/10.1007/BF01964840
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Asparagine and derivatives
(2S,3S)-2-azaniumyl-3-carbamoyl-3-hydroxypropanoate	46878457	Click to see	148.12	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
DL-threo-beta-Hydroxyaspartic acid	443239	Click to see	149.10	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
Jasmolone	5374699	Click to see	180.24	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
beta-D-Fructofuranoside, methyl	128889	Click to see	194.18	unknown	https://doi.org/10.1016/S0031-9422(00)83615-8
Butyl fructofuranoside	13386213	Click to see	236.26	unknown	https://doi.org/10.1016/S0031-9422(00)83615-8
Ethyl alpha-D-fructofuranoside	133590	Click to see CCOC1(C(C(C(O1)CO)O)O)CO	208.21	unknown	https://doi.org/10.1016/S0031-9422(00)83615-8
n-Butyl \|A-D-fructofuranoside	13386214	Click to see	236.26	unknown	https://doi.org/10.1016/S0031-9422(00)83615-8
> 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	174.28	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Hydroxypyrimidines
5-methylpyrimidine-2,4-diol	5274265	Click to see	126.11	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Maltol	8369	Click to see	126.11	unknown	via CMAUP database
> Organophosphorus compounds / Organic phosphines and derivatives
Triethylphosphine	27365	Click to see CCP(CC)CC	118.16	unknown	via CMAUP database
> Organosulfur compounds / Thioacetals / Monothioacetals
Carbonodithioic acid, S-ethyl O-(1-methylethyl) ester	539987	Click to see	164.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Cinnamamide, p-hydroxy-N-(p-hydroxyphenethyl)-	89322	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
cis-N-p-coumaroyltyramine	13939145	Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O	283.32	unknown	via CMAUP database
Paprazine	5372945	Click to see	283.32	unknown	https://doi.org/10.1021/NP049864E
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin	9064	Click to see	290.27	unknown	via CMAUP database
Epicatechin	72276	Click to see	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see	286.24	unknown	via CMAUP database
Quercetin	5280343	Click to see	302.23	unknown	via CMAUP database
> 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
Delphinidin 3-O-rutinoside	5492231	Click to see	611.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
QUERCETIN 3-O-beta-D-GLUCURONIDE METHYL ESTER	21722016	Click to see	492.40	unknown	via CMAUP database
Querciturone	5274585	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	478.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-8-O-glucuronides
HYPOLAETIN 8-O-beta-D-GLUCURONIDE	14887605	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	478.40	unknown	via CMAUP database
ISOSCUTELLAREIN 8-O-beta-D-GLUCURONIDE	14332450	Click to see	462.40	unknown	via CMAUP database
ISOSCUTELLAREIN 8-O-beta-D-GLUCURONIDE 6''-METHYL ESTER	44566911	Click to see	476.40	unknown	via CMAUP database
theograndin I	11156985	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)OS(=O)(=O)O)O)O	542.40	unknown	via CMAUP database
Theograndin II	11272944	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)OS(=O)(=O)O)O)O)O	558.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,6-dihydroxy-2-(4-methoxyphenyl)chromen-4-one	14802391	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O	624.50	unknown	https://doi.org/10.1248/CPB.41.566
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(2R,3R)-2,5,7-trihydroxy-3-[(4-methoxyphenyl)methyl]-6,8-dimethyl-2,3-dihydrochromen-4-one	162849967	Click to see	344.40	unknown	https://doi.org/10.1016/S0031-9422(02)00515-0
(2R,3R)-3-(1,3-benzodioxol-5-ylmethyl)-2,5,7-trihydroxy-6,8-dimethyl-2,3-dihydrochromen-4-one	163044930	Click to see CC1=C(C(=C2C(=C1O)C(=O)C(C(O2)O)CC3=CC4=C(C=C3)OCO4)C)O	358.30	unknown	https://doi.org/10.1016/S0031-9422(02)00515-0
(2S,3S)-3-(1,3-benzodioxol-5-ylmethyl)-2,5,7-trihydroxy-6,8-dimethyl-2,3-dihydrochromen-4-one	163044929	Click to see CC1=C(C(=C2C(=C1O)C(=O)C(C(O2)O)CC3=CC4=C(C=C3)OCO4)C)O	358.30	unknown	https://doi.org/10.1016/S0031-9422(02)00515-0
(3r)-2,3-Dihydro-7-hydroxy-5-methoxy-3-(4-methoxybenzyl)-6,8-dimethyl-4h-chromen-4-one	46832770	Click to see CC1=C(C(=C(C2=C1OCC(C2=O)CC3=CC=C(C=C3)OC)OC)C)O	342.40	unknown	https://doi.org/10.1002/HLCA.200900333
(3r)-3-(1,3-Benzodioxol-5-ylmethyl)-2,3-dihydro-7-hydroxy-5-methoxy-6-methyl-4h-chromen-4-one	46832772	Click to see	342.30	unknown	https://doi.org/10.1002/HLCA.200900333
(3r)-3-(1,3-Benzodioxol-5-ylmethyl)-2,3-dihydro-7-hydroxy-5-methoxy-6,8-dimethyl-4h-chromen-4-one	46832771	Click to see	356.40	unknown	https://doi.org/10.1002/HLCA.200900333
(3R)-3-(1,3-benzodioxol-5-ylmethyl)-5,7-dimethoxy-6-methyl-4-oxo-2,3-dihydrochromene-8-carbaldehyde	162881659	Click to see	384.40	unknown	https://doi.org/10.1021/NP020204O
(3R)-3-[(3,4-dihydroxyphenyl)methyl]-5-hydroxy-7,8-dimethoxy-6-methyl-2,3-dihydrochromen-4-one	162922489	Click to see CC1=C(C2=C(C(=C1OC)OC)OCC(C2=O)CC3=CC(=C(C=C3)O)O)O	360.40	unknown	https://doi.org/10.1016/S0031-9422(02)00515-0 https://doi.org/10.1248/CPB.41.391
(3R)-5,7-dihydroxy-3-[(2-hydroxy-4-methoxyphenyl)methyl]-8-methoxy-6-methyl-2,3-dihydrochromen-4-one	637306	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	https://doi.org/10.1002/RCM.4608 https://doi.org/10.1016/S0031-9422(02)00515-0
(3R)-5,7-dihydroxy-3-[(4-hydroxy-3-methoxyphenyl)methyl]-6,8-dimethyl-2,3-dihydrochromen-4-one	53467849	Click to see	344.40	unknown	https://doi.org/10.1016/S0031-9422(02)00515-0
(3R)-7-hydroxy-3-[(2-hydroxy-3-methoxyphenyl)methyl]-5,8-dimethoxy-6-methyl-2,3-dihydrochromen-4-one	124351119	Click to see CC1=C(C(=C2C(=C1OC)C(=O)C(CO2)CC3=C(C(=CC=C3)OC)O)OC)O	374.40	unknown	https://doi.org/10.1021/NP020204O
(3R)-7-hydroxy-3-[(2-hydroxy-4-methoxyphenyl)methyl]-5,8-dimethoxy-6-methyl-2,3-dihydrochromen-4-one	134715131	Click to see	374.40	unknown	https://doi.org/10.1016/S0031-9422(02)00515-0
(3S)-3-(1,3-benzodioxol-5-ylmethyl)-5-hydroxy-6-methyl-4-oxo-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromene-8-carbaldehyde	162966428	Click to see CC1=C(C2=C(C(=C1OC3C(C(C(C(O3)CO)O)O)O)C=O)OCC(C2=O)CC4=CC5=C(C=C4)OCO5)O	518.50	unknown	https://doi.org/10.1016/J.BMCL.2010.03.043
(3S)-3-(1,3-benzodioxol-5-ylmethyl)-5-methoxy-6-methyl-4-oxo-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromene-8-carbaldehyde	162942541	Click to see	532.50	unknown	https://doi.org/10.1016/J.BMCL.2010.03.043
(3S)-3-(1,3-benzodioxol-5-ylmethyl)-5,7-dihydroxy-6-methyl-2,3-dihydrochromen-4-one	92449513	Click to see	328.30	unknown	https://doi.org/10.1016/S0031-9422(02)00515-0 https://doi.org/10.1002/RCM.4608
(3S)-3-(1,3-benzodioxol-5-ylmethyl)-5,7-dihydroxy-6-methyl-4-oxo-2,3-dihydrochromene-8-carbaldehyde	154828448	Click to see	356.30	unknown	https://doi.org/10.1021/NP020204O
(3S)-3-(1,3-benzodioxol-5-ylmethyl)-5,7-dihydroxy-6,8-dimethyl-2,3-dihydrochromen-4-one	92449511	Click to see CC1=C(C(=C2C(=C1O)C(=O)C(CO2)CC3=CC4=C(C=C3)OCO4)C)O	342.30	unknown	https://doi.org/10.1248/CPB.28.2039 https://doi.org/10.1002/RCM.4608 https://doi.org/10.1248/CPB.33.5358
(3S)-3-(1,3-Benzodioxol-5-ylmethyl)-5,7-dihydroxy-8-methyl-4-oxo-2,3-dihydrochromene-6-carbaldehyde	154828112	Click to see	356.30	unknown	https://doi.org/10.1248/CPB.33.5358
(3S)-5,7-dihydroxy-3-[(4-hydroxy-1,3-benzodioxol-5-yl)methyl]-6,8-dimethyl-2,3-dihydrochromen-4-one	162937810	Click to see	358.30	unknown	https://doi.org/10.1016/S0031-9422(02)00515-0
(3S)-5,7-dihydroxy-3-[(4-hydroxy-3-methoxyphenyl)methyl]-6,8-dimethyl-2,3-dihydrochromen-4-one	162967174	Click to see	344.40	unknown	https://doi.org/10.1016/S0031-9422(02)00515-0 https://doi.org/10.1002/RCM.4608
(3S)-5,7-dihydroxy-3-[(4-hydroxy-3,5-dimethoxyphenyl)methyl]-6,8-dimethyl-2,3-dihydrochromen-4-one	162903437	Click to see CC1=C(C(=C2C(=C1O)C(=O)C(CO2)CC3=CC(=C(C(=C3)OC)O)OC)C)O	374.40	unknown	https://doi.org/10.1002/RCM.4608
(3S)-5,7-dihydroxy-3-[(4-methoxyphenyl)methyl]-6,8-dimethyl-2,3-dihydrochromen-4-one	102029337	Click to see	328.40	unknown	https://doi.org/10.1248/CPB.28.2039 https://doi.org/10.1002/RCM.4608 https://doi.org/10.1248/CPB.33.5358
(3S)-5,7-dihydroxy-3-[(4-methoxyphenyl)methyl]-8-methyl-4-oxo-2,3-dihydrochromene-6-carbaldehyde	162881772	Click to see	342.30	unknown	https://doi.org/10.1248/CPB.33.5358
(3S)-7-hydroxy-3-[(2-hydroxy-4-methoxyphenyl)methyl]-5,8-dimethoxy-6-methyl-2,3-dihydrochromen-4-one	162917757	Click to see	374.40	unknown	https://doi.org/10.1016/S0031-9422(02)00515-0
2,5,7-Trihydroxy-6,8-dimethyl-3-(4'-methoxybenzyl)chroman-4-one	5322061	Click to see CC1=C(C(=C2C(=C1O)C(=O)C(C(O2)O)CC3=CC=C(C=C3)OC)C)O	344.40	unknown	https://doi.org/10.1016/S0031-9422(02)00515-0
3-(1,3-Benzodioxol-5-ylmethyl)-2,5,7-trihydroxy-6,8-dimethyl-2,3-dihydrochromen-4-one	5322062	Click to see CC1=C(C(=C2C(=C1O)C(=O)C(C(O2)O)CC3=CC4=C(C=C3)OCO4)C)O	358.30	unknown	https://doi.org/10.1016/S0031-9422(02)00515-0
3-(1,3-Benzodioxol-5-ylmethyl)-5-hydroxy-6-methyl-4-oxo-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromene-8-carbaldehyde	75236437	Click to see	518.50	unknown	https://doi.org/10.1016/J.BMCL.2010.03.043
3-(1,3-Benzodioxol-5-ylmethyl)-5-methoxy-6-methyl-4-oxo-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromene-8-carbaldehyde	75236483	Click to see	532.50	unknown	https://doi.org/10.1016/J.BMCL.2010.03.043
3-(1,3-Benzodioxol-5-ylmethyl)-5,7-dihydroxy-6-methyl-4-oxo-2,3-dihydrochromene-8-carbaldehyde	10871974	Click to see	356.30	unknown	via CMAUP database
3-(1,3-Benzodioxol-5-ylmethyl)-5,7-dihydroxy-6,8-dimethyl-2,3-dihydrochromen-4-one	5319741	Click to see	342.30	unknown	https://doi.org/10.1248/CPB.41.391 https://doi.org/10.1248/CPB.33.5358 https://doi.org/10.1002/RCM.4608 https://doi.org/10.1248/CPB.28.2039
3-(1,3-Benzodioxol-5-ylmethyl)-7-hydroxy-5-methoxy-6-methyl-2,3-dihydrochromen-4-one	75215428	Click to see	342.30	unknown	https://doi.org/10.1002/HLCA.200900333
3-[(2,3-Dihydroxy-4-methoxyphenyl)methyl]-5,7-dihydroxy-8-methoxy-6-methyl-2,3-dihydrochromen-4-one	75226655	Click to see	376.40	unknown	https://doi.org/10.1016/J.BMCL.2010.03.043
3-[(3,4-Dihydroxyphenyl)methyl]-5-hydroxy-7,8-dimethoxy-6-methyl-2,3-dihydrochromen-4-one	10361149	Click to see	360.40	unknown	https://doi.org/10.1248/CPB.41.391 https://doi.org/10.1016/S0031-9422(02)00515-0
5,7-Dihydroxy-3-[(4-methoxyphenyl)methyl]-6,8-dimethyl-2,3-dihydrochromen-4-one	5319742	Click to see CC1=C(C(=C2C(=C1O)C(=O)C(CO2)CC3=CC=C(C=C3)OC)C)O	328.40	unknown	https://doi.org/10.1248/CPB.33.5358 https://doi.org/10.1002/RCM.4608 https://doi.org/10.1248/CPB.28.2039
5,7-Dihydroxy-6,8-dimethyl-3-(4'-hydroxy-3'-methoxybenzyl)chroman-4-one	5316771	Click to see	344.40	unknown	https://doi.org/10.1002/RCM.4608 https://doi.org/10.1016/S0031-9422(02)00515-0
6-Aldehydoisoophiopogonanone A	71584762	Click to see	356.30	unknown	via CMAUP database
6-Formyl-isoophiopogonanone A	10383616	Click to see	356.30	unknown	https://doi.org/10.1248/CPB.33.5358
6-Formyl-isoophiopogonanone B	162881771	Click to see	342.30	unknown	https://doi.org/10.1248/CPB.33.5358
7-Hydroxy-5-methoxy-3-[(4-methoxyphenyl)methyl]-6,8-dimethyl-2,3-dihydrochromen-4-one	75215426	Click to see	342.40	unknown	https://doi.org/10.1002/HLCA.200900333
7-Hydroxy-5-methoxy-3',4'-methylenedioxy-6,8-dimethyl homoisoflavanone	75215427	Click to see	356.40	unknown	https://doi.org/10.1002/HLCA.200900333
Methylophiopogonanone A	53466984	Click to see	342.30	unknown	https://doi.org/10.1016/S0031-9422(02)00515-0 https://doi.org/10.1248/CPB.41.391 https://doi.org/10.1248/YAKUSHI1947.103.11_1133 https://doi.org/10.1016/S0021-9673(00)90392-3 https://doi.org/10.1248/CPB.33.5358
Methylophiopogonanone B	46886723	Click to see	328.40	unknown	https://doi.org/10.1248/CPB.33.5358 https://doi.org/10.1016/S0031-9422(02)00515-0 https://doi.org/10.1016/S0021-9673(00)90392-3 https://doi.org/10.1248/YAKUSHI1947.103.11_1133
Npc92583	11003181	Click to see	370.40	unknown	via CMAUP database
Ophiopogonanone A	9996586	Click to see	328.30	unknown	https://doi.org/10.1248/YAKUSHI1947.103.11_1133 https://doi.org/10.1002/RCM.4608 https://doi.org/10.1002/HLCA.200900333 https://doi.org/10.1016/S0031-9422(02)00515-0 https://doi.org/10.1248/CPB.41.391
Ophiopogonanone C	637458	Click to see CC1=C(C(=C2C(=C1O)C(=O)C(CO2)CC3=CC4=C(C=C3)OCO4)C=O)O	356.30	unknown	https://doi.org/10.1021/NP020204O
Ophiopogonanone E	5316797	Click to see	360.40	unknown	https://doi.org/10.1002/RCM.4608 https://doi.org/10.1016/S0031-9422(02)00515-0
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	https://doi.org/10.1016/S0031-9422(02)00515-0
Ophiopogonanone G	46886411	Click to see	376.40	unknown	https://doi.org/10.1016/J.BMCL.2010.03.043
OphiopogonanoneA	92449512	Click to see	328.30	unknown	https://doi.org/10.1002/HLCA.200900333 https://doi.org/10.1248/CPB.41.391
Ophiopogoside A	46865651	Click to see	518.50	unknown	https://doi.org/10.1016/J.BMCL.2010.03.043
Ophiopogoside B	46865773	Click to see	532.50	unknown	https://doi.org/10.1016/J.BMCL.2010.03.043
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavones
5,7-Dihydroxy-3-((4-methoxyphenyl)methyl)-8-methyl-4-oxochromene-6-carbaldehyde	5317212	Click to see	340.30	unknown	https://doi.org/10.1016/S0031-9422(00)83615-8
5,7-Dihydroxy-3-[(4-hydroxy-1,3-benzodioxol-5-yl)methyl]-6-methylchromen-4-one	10246745	Click to see	342.30	unknown	https://doi.org/10.1248/CPB.41.391
5,7-Dihydroxy-3-[(4-hydroxy-1,3-benzodioxol-5-yl)methyl]-6,8-dimethylchromen-4-one	101238141	Click to see	356.30	unknown	https://doi.org/10.1002/RCM.4608 https://doi.org/10.1248/CPB.33.5358 https://doi.org/10.1016/S0031-9422(02)00515-0
5,7-Dihydroxy-3-[(4-hydroxy-1,3-benzodioxol-5-yl)methyl]-8-methylchromen-4-one	10427457	Click to see	342.30	unknown	https://doi.org/10.1002/RCM.4608 https://doi.org/10.1248/CPB.41.391
5,7-Dihydroxy-6-methyl-3-(4'-hydroxybenzyl) chromone	14826839	Click to see	298.29	unknown	https://doi.org/10.1248/CPB.41.391
6-Aldehydo-isoophiopogonone A	5317207	Click to see CC1=C(C(=C(C2=C1OC=C(C2=O)CC3=CC4=C(C=C3)OCO4)O)C=O)O	354.30	unknown	https://doi.org/10.1016/S0031-9422(00)83615-8
Desmethylisoophiopogonone B	129848217	Click to see	298.29	unknown	https://doi.org/10.1002/RCM.4608 https://doi.org/10.1248/CPB.41.391
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/10.1248/CPB.28.2039 https://doi.org/10.1002/RCM.4608 https://doi.org/10.1248/CPB.33.5358 https://doi.org/10.1016/S0031-9422(02)00515-0 https://doi.org/10.1248/CPB.41.391
Methylophiopogonone B	23259413	Click to see	326.30	unknown	https://doi.org/10.1248/CPB.28.2039 https://doi.org/10.1002/RCM.4608
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/S0031-9422(02)00515-0 https://doi.org/10.1248/CPB.41.391
Ophiopogonone B	14826840	Click to see	312.30	unknown	via CMAUP database
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	https://doi.org/10.1021/NP020204O

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Ophiopogon japonicus

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