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.

In traditional East Asian practice, the dried tuberous root of Asparagus cochinchinensis (tian men dong) is most often infused or decocted to moisten the lungs, ease dry cough, and calm thirst. In classical Chinese texts and modern pharmacopoeial guidance, decoctions of the root are given for dryness of the throat with scanty phlegm, constipation from dryness, and as a yin tonic for the lungs and kidneys. Across mainland China and Taiwan, Li Shizhen’s Compendium of Materia Medica and the national pharmacopeia record that the root is simmered with water for throat dryness and dry cough; similar decoctions of the root are used in Korean medicine for expectorant and tonic purposes in respiratory dryness and low-grade fevers; and in Vietnam the root is prescribed in the form of infusions and syrups as a moistening tonic for pulmonary dryness and throat irritation (Compendium of Materia Medica; Chinese Pharmacopoeia 2020; Pharmacopoeia of the Socialist Republic of Vietnam; Korean Herbal Pharmacopoeia).

For a simple therapeutic tea, soak 10–15 g of the sliced dried root in cool water for 30–60 minutes, bring to a simmer, and decoct gently for 25–35 minutes to yield roughly 200 mL of liquid; strain and drink warm, 1–2 cups daily. Do not exceed the commonly cited dose range listed in official pharmacopeial monographs. Avoid in pregnancy and in acute severe cough with abundant yellow sputum, and consult a clinician if cough persists or worsens.

Well-established constituents reported for this species include steroidal saponins such as shatavarin IV and various spirostane glycosides, asparagoside derivatives, sterols and sterol glycosides, and characteristic oligosaccharides. The mucilaginous polysaccharides are notable for their hydration qualities, and the saponins are known expectorants that can help reduce throat irritation, plausibly supporting the traditional moistening and cough-soothing actions.

Modern relevance includes ongoing clinical and pharmacological investigation into its saponins and polysaccharides for respiratory health and immunomodulation, and the dried root remains available in quality herb markets and through standard formulations in Chinese herbal dispensaries, with controlled‑by‑pharmacopoeial GMP decoctions and syrups found across the region.

General Uses Top

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Common products:
- Ornamental horticulture: Asparagus cochinchinensis is cultivated and marketed as an indoor and garden ornamental for its fine, arching foliage and compact growth habit.

Food and beverages (non-medicinal):
- Young shoots and the tuberous root are used as a vegetable. The root is peeled, sliced, and boiled before being added to soups, stews, or stir‑fried dishes; the tender shoots are blanched or briefly sautéed. The plant parts employed are the tuber (root) and the aerial shoots.

Scientific/model‑organism use:
- The species has been sequenced and deposited in public databases, providing a reference transcriptome for genetic and genomic studies of the Asparagaceae family. Its genome and expressed sequence tags are employed to investigate tuber development, metabolic pathways, and phylogenetics.

Properties relevant to use:
- As an ornamental, A. cochinchinensis tolerates low to moderate light conditions and maintains a graceful, compact habit, making it suitable for indoor culture. As a food ingredient, the tuber contains a high proportion of water and starch; after boiling it softens, producing a slightly gelatinous texture that integrates well into soups and braised dishes.

Sustainability and sourcing:
- The plant is cultivated in controlled environments and field production in southern China for both ornamental and culinary markets, reducing reliance on wild harvest. Sustainable horticultural practices, including greenhouse production and regulated planting cycles, are reported in agricultural literature and help maintain the species’ availability.

Synonyms Top

Scientific name	Authority	First published in
Asparagopsis sinica	Miq.	J. Bot. Néerl. 1: 90 (1861)
Asparagus gaudichaudianus	Kunth	Enum. Pl. 5: 71 (1850)
Asparagus insularis	Hance	Ann. Sci. Nat., Bot. , sér. 5, 5: 245 (1866)
Asparagus lucidus	Lindl.	Edwards's Bot. Reg. 30(Misc.): 29 (1844)
Asparagus sinicus	C.H.Wright	J. Linn. Soc., Bot. 36: 103 (1903)
Melanthium cochinchinense	Lour.	Fl. Cochinch. 1: 216. 1790 [Sep 1790]
Asparagus lucidus var. dolichocladus	Merr. & Rolfe	Philipp. J. Sci., C 3: 96. 1908
Asparagus dauricus var. elongatus	Pamp.	Nuovo Giorn. Bot. Ital. n.s., 22: 264. 1915
Asparagus lucidus var. pygmaeus	Makino	Bot. Mag. (Tokyo) 11: 281 (1897)
Asparagus cochinchinensis var. pygmaeus	(Makino) Ohwi	Fl. Jap. ed. rev.: 1437 1965
Asparagus cochinchinensis var. longifolius	F.T.Wang & Tang	Bull. Fan Mem. Inst. Biol. Bot. 7: 291. 1937
Asparagus cochinchinensis var. dolichoclados	F.T.Wang & Tang	Bull. Fan Mem. Inst. Biol. Bot. 7: 291. 1937
Asparagus cochinchinensis f. pygmaeus	(Makino) Yamashita & M.N.Tamura	Fl. Japan 4b: 148 (2016)

Common names Top

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Filter by language:

Language	Common/alternative name
Azerbaijani	koxinxin qulançarı
Japanese	クサスギカズラ
Korean	천문동
lzh	天門冬
Vietnamese	thiên môn đông
za	denhmwnzdungh
Chinese	天门冬
Chinese	三百棒
Chinese	天冬
Chinese	天門冬
Chinese	天门冬（天冬）
Chinese	丝冬
Chinese	老虎尾巴根
Chinese	兴安天门冬
Chinese	天冬草

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
  - Hainan
  - Tibet
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Taiwan

Asia-tropical click to expand
- Indo-China
  - Cambodia
  - Laos
  - Vietnam
- Malesia
  - Philippines

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000631919
UNII	36L6R7F7P9
Tropicos	18404339
KEW	urn:lsid:ipni.org:names:531041-1
The Plant List	kew-274989
Open Tree Of Life	899697
Observations.org	283336
NCBI Taxonomy	100514
IUCN Red List	20680957
IPNI	531041-1
iNaturalist	462199
GBIF	2768772
EPPO	ASPCC
EOL	987682
Elurikkus	299905
USDA GRIN	5501
Wikipedia	Asparagus_cochinchinensis
CMAUP	NPO11694
PFAF	Asparagus cochinchinensis

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

Ginkgolide injections in meglumine, combined with edaravone, significantly increases the efficacy in acute ischemic stroke: A meta-analysis

Yan M, Wu J, Wang L, Wang K, Li L, Sun T, Zhang H, Zhang M, Zou L, Yang S, Liu J

Front Pharmacol

25-Apr-2024

PMCID:	PMC11079130
doi:	10.3389/fphar.2023.1236684
PMID:	38726464

Traditional Tibetan medicine: therapeutic potential in lung diseases

Li C, Li Y, Huang X, Li S, Sangji K, Gu R

Front Pharmacol

18-Mar-2024

PMCID:	PMC10986185
doi:	10.3389/fphar.2024.1365911
PMID:	38567353

Cutaneous Redox Senescence

Sarandy MM, Gonçalves RV, Valacchi G

Biomedicines

01-Feb-2024

PMCID:	PMC10886899
doi:	10.3390/biomedicines12020348
PMID:	38397950

Organelle Genomes of Epipogium roseum Provide Insight into the Evolution of Mycoheterotrophic Orchids

Zhao Z, Li Y, Zhai JW, Liu ZJ, Li MH

Int J Mol Sci

27-Jan-2024

PMCID:	PMC10855806
doi:	10.3390/ijms25031578
PMID:	38338856

Natural lipid nanoparticles extracted from Morus nigra L. leaves for targeted treatment of hepatocellular carcinoma via the oral route

Gao Q, Chen N, Li B, Zu M, Ma Y, Xu H, Zhu Z, Reis RL, Kundu SC, Xiao B

J Nanobiotechnology

03-Jan-2024

PMCID:	PMC10763359
doi:	10.1186/s12951-023-02286-3
PMID:	38169394

Elicitation Induced α-Amyrin Synthesis in Tylophora indica In Vitro Cultures and Comparative Phytochemical Analyses of In Vivo and Micropropagated Plants

Mamgain J, Mujib A, Bansal Y, Gulzar B, Zafar N, Syeed R, Alsughayyir A, Dewir YH

Plants (Basel)

31-Dec-2023

PMCID:	PMC10780849
doi:	10.3390/plants13010122
PMID:	38202430

Current Research Status and Implication for Further Study of Real-World Data on East Asian Traditional Medicine for Heart Failure: A Scoping Review

Park J, Bak S, Chu H, Kang S, Youn I, Jun H, Sim D, Leem J

Healthcare (Basel)

27-Dec-2023

PMCID:	PMC10779411
doi:	10.3390/healthcare12010061
PMID:	38200969

Potential mechanism of Qinggong Shoutao pill alleviating age-associated memory decline based on integration strategy

Pan G, Chai L, Chen R, Yuan Q, Song Z, Feng W, Wei J, Yang Z, Zhang Y, Xie G, Yan A, Lv Q, Wang C, Zhao Y, Wang Y

Pharm Biol

25-Dec-2023

PMCID:	PMC10763866
doi:	10.1080/13880209.2023.2291689
PMID:	38145345

Consensus statement on research and application of Chinese herbal medicine derived extracellular vesicles-like particles (2023 edition)

Zhao Q, Wang T, Wang H, Cao P, Jiang C, Qiao H, Peng L, Lin X, Jiang Y, Jin H, Zhang H, Wang S, Wang Y, Wang Y, Chen X, Fan J, Li B, Li G, Liu B, Li Z, Qi S, Zhang M, Zheng J, Zhou J, Zheng L, Zhao K

Chin Herb Med

14-Dec-2023

PMCID:	PMC10874762
doi:	10.1016/j.chmed.2023.11.002
PMID:	38375050

The traditional use, structure, and immunostimulatory activity of bioactive polysaccharides from traditional Chinese root medicines: A review

Bo S, Zhang M, Dan M

Heliyon

13-Dec-2023

PMCID:	PMC10770551
doi:	10.1016/j.heliyon.2023.e23593
PMID:	38187324

The Weissella and Periweissella genera: up-to-date taxonomy, ecology, safety, biotechnological, and probiotic potential

Fusco V, Chieffi D, Fanelli F, Montemurro M, Rizzello CG, Franz CM

Front Microbiol

11-Dec-2023

PMCID:	PMC10758620
doi:	10.3389/fmicb.2023.1289937
PMID:	38169702

The Impact and Determinants of Mountainous Topographical Factors on Soil Microbial Community Characteristics

Yu J, Li S, Sun X, Zhou W, He L, Zhao G, Chen Z, Bai X, Zhang J

Microorganisms

28-Nov-2023

PMCID:	PMC10746091
doi:	10.3390/microorganisms11122878
PMID:	38138022

Origin of purple asparagus cultivar ‘Pacific Purple’ based on the sequence of sex determination gene

Kanno A, Hirobe N, Zhang L

Front Plant Sci

16-Nov-2023

PMCID:	PMC10687405
doi:	10.3389/fpls.2023.1237433
PMID:	38034566

Effect of miR-182-5p on apoptosis in myocardial infarction

Niu N, Miao H, Ren H

Heliyon

31-Oct-2023

PMCID:	PMC10685254
doi:	10.1016/j.heliyon.2023.e21524
PMID:	38034598

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

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 / Phenols / 4-alkoxyphenols
4-[5-(4-Hydroxyphenoxy)pent-3-en-1-ynyl]phenol	53862888	Click to see	266.29	unknown	https://doi.org/10.1021/NP030370B
Asparenydiol	10084256	Click to see C1=CC(=CC=C1C#CC=CCOC2=CC=C(C=C2)O)O	266.29	unknown	https://doi.org/10.1021/NP030370B
> Benzenoids / Phenols / Methoxyphenols
3''-Methoxyasparenydiol	11738011	Click to see	296.30	unknown	https://doi.org/10.1021/NP030370B
4-[5-(4-Hydroxyphenoxy)pent-3-en-1-ynyl]-2-methoxyphenol	73080615	Click to see	296.30	unknown	https://doi.org/10.1021/NP030370B
Coniferyl Alcohol	1549095	Click to see	180.20	unknown	https://doi.org/10.1021/NP030370B
Phenol, 4-(3-hydroxy-1-propenyl)-2-methoxy-	9983	Click to see	180.20	unknown	https://doi.org/10.1021/NP030370B
> Lignans, neolignans and related compounds
(-)-Hinokiresinol	12310493	Click to see	252.31	unknown	via CMAUP database
(3S)-1,3-bis(4-hydroxyphenyl)pent-4-en-1-one	162882512	Click to see	268.31	unknown	https://doi.org/10.1021/NP030370B
1,3-Bis-di-p-hydroxyphenyl-4-penten-1-one	44575609	Click to see	268.31	unknown	https://doi.org/10.1021/NP030370B
1,3-Bis(p-hydroxyphenyl)pentane-1,4-diene	157288	Click to see	252.31	unknown	https://doi.org/10.1016/S0031-9422(96)00442-6 https://doi.org/10.1021/NP030370B
3'-Hydroxy-4'-methoxy-4'-dehydroxynyasol	21575014	Click to see	282.30	unknown	via CMAUP database
3'-Methoxynyasol	25218067	Click to see	282.30	unknown	via CMAUP database
4-[(1Z,3R)-1-(4-hydroxyphenyl)penta-1,4-dien-3-yl]-2-methoxyphenol	135750819	Click to see COC1=C(C=CC(=C1)C(C=C)C=CC2=CC=C(C=C2)O)O	282.30	unknown	https://doi.org/10.1021/NP030370B
4-[(1Z,3S)-3-(4-hydroxyphenyl)penta-1,4-dienyl]phenol	5281830	Click to see	252.31	unknown	https://doi.org/10.1016/S0031-9422(96)00442-6 https://doi.org/10.1021/NP030370B
4-[1-(4-Hydroxyphenyl)penta-1,4-dien-3-yl]-2-methoxyphenol	71429202	Click to see COC1=C(C=CC(=C1)C(C=C)C=CC2=CC=C(C=C2)O)O	282.30	unknown	https://doi.org/10.1021/NP030370B
5-[(1E)-1-(4-hydroxyphenyl)penta-1,4-dien-3-yl]-2-methoxyphenol	11312084	Click to see	282.30	unknown	via CMAUP database
5-[(1Z,3R)-1-(4-hydroxyphenyl)penta-1,4-dien-3-yl]-2-methoxyphenol	77843999	Click to see	282.30	unknown	https://doi.org/10.1021/NP030370B
5-[1-(4-Hydroxyphenyl)penta-1,4-dien-3-yl]-2-methoxyphenol	72796735	Click to see COC1=C(C=C(C=C1)C(C=C)C=CC2=CC=C(C=C2)O)O	282.30	unknown	https://doi.org/10.1021/NP030370B
cis-Hinokiresinol	6440617	Click to see C=CC(C=CC1=CC=C(C=C1)O)C2=CC=C(C=C2)O	252.31	unknown	via CMAUP database
Hinokiresinol	5377291	Click to see	252.31	unknown	via CMAUP database
Nyasol	6915833	Click to see	252.31	unknown	via CMAUP database
Nyasol	6438674	Click to see C=CC(C=CC1=CC=C(C=C1)O)C2=CC=C(C=C2)O	252.31	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(16R)-16,17-Epoxy-9beta-hydroxy-12beta-[(Z)-2-methyl-2-butenoyloxy]kauran-19-oic acid	102056177	Click to see CC=C(C)C(=O)OC1CC2(C3(CCCC(C3CCC24CC1C5(C4)CO5)(C)C(=O)O)C)O	432.50	unknown	via CMAUP database
(1S,4S,5R,9S,10R,12R,13R)-5,9-dimethyl-12-[(Z)-2-methylbut-2-enoyl]oxy-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid	102056176	Click to see CC=C(C)C(=O)OC1CC2C3(CCCC(C3CCC24CC1C(=C)C4)(C)C(=O)O)C	400.50	unknown	via CMAUP database
(1S,4S,5R,9S,10R,12R,13S,14S)-12,14-dihydroxy-5,9-dimethyl-14-[[(Z)-2-methylbut-2-enoyl]oxymethyl]tetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid	102056175	Click to see CC=C(C)C(=O)OCC1(CC23CCC4C(C2CC(C1C3)O)(CCCC4(C)C(=O)O)C)O	434.60	unknown	via CMAUP database
(1S,4S,5S,9R,10S,12R,13S,14S)-10,12,14-trihydroxy-5,9-dimethyl-14-[[(E)-2-methylbut-2-enoyl]oxymethyl]tetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid	102056179	Click to see	450.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2S,4R,6R,7S,8R,9S,12S,13S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-ol	53486207	Click to see	416.60	unknown	via CMAUP database
(3I(2),22I(2),25S)-Spirost-5-en-3-ol	53486205	Click to see	414.60	unknown	via CMAUP database
8-Hydroxy-16,16-dimethoxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one	73802025	Click to see	490.70	unknown	https://doi.org/10.1021/NP030370B
8,10-Dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-17-ene-6,2'-oxane]-16-one	72826356	Click to see	444.60	unknown	https://doi.org/10.1021/NP030370B
Asparacosin A	11385250	Click to see	444.60	unknown	https://doi.org/10.1021/NP030370B
Asparacosin B	21575013	Click to see	490.70	unknown	https://doi.org/10.1021/NP030370B
Sarsasapogenin	92095	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1	416.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(25R)-spirost-5-en-3beta-ol 3-O-alpha-L-rhamnopyranosyl-(1-2)-O-[beta-D-glucopyranosyl-(1-3)]-beta-D-glucopyranoside	52931453	Click to see	901.10	unknown	via CMAUP database
(25S)-5beta-spirostan-3beta-yl beta-D-glucoside	440454	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)OC1	578.80	unknown	https://doi.org/10.1002/PCA.2522
(2R,3R,4S,5S,6R)-2-[4-[(18R)-16-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-6-hydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	6325818	Click to see	1023.20	unknown	https://doi.org/10.1002/PCA.2522
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(1S,2S,4S,8S,9S,12S,13R,16S)-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]icosa-6,18-dien-16-yl]oxy]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol	102004851	Click to see	1031.20	unknown	via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'S,6R,7S,8R,9S,12S,13S,16S,18R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162872693	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)OC1	724.90	unknown	https://doi.org/10.1007/S12272-011-1001-7
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(1S,2S,4S,8S,9S,12S,13R)-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]icosa-6,18-dien-16-yl]oxy]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol	51346147	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC8C7C(=C(O8)CCC(C)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)CO)O)O)O	1031.20	unknown	via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2R,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-5-[(3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(1S,2S,4S,8S,9S,12S,13R)-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(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]icosa-6,18-dien-16-yl]oxy]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol	131801368	Click to see	1031.20	unknown	https://doi.org/10.1055/S-2006-962453
(2S,3R,4S,5R,6S)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'S,6R,7S,8R,9S,12S,13S,16S,18R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	44583984	Click to see	740.90	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	11968842	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1	740.90	unknown	https://doi.org/10.1002/PCA.2522
(2S,3R,4S,5S,6R)-2-[(2S,3R,4R,5R,6S)-2-[(3S,4R,5R,6S)-4,5-dihydroxy-6-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxyoxan-2-yl]methoxy]oxan-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	5320678	Click to see	1019.20	unknown	https://doi.org/10.1002/PCA.2522
(2S,3R,4S,5S,6R)-2-[(3S,4R,5R,6S)-6-[(2R,3R,4R,5S,6S)-4,5-dihydroxy-6-methyl-2-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxyoxan-3-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	11968845	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)C)O)O)OC8C(C(C(CO8)OC9C(C(C(C(O9)CO)O)O)O)O)O)C)C)C)OC1	857.00	unknown	https://doi.org/10.1002/PCA.2522
(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	1063.20	unknown	https://doi.org/10.1055/S-2006-962453
2-(Hydroxymethyl)-6-[4-hydroxy-2-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxy-5-(3,4,5-trihydroxyoxan-2-yl)oxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-3-yl]oxyoxane-3,4,5-triol	72795700	Click to see	1005.10	unknown	https://doi.org/10.1021/NP030370B
2-[4,5-Dihydroxy-2-(hydroxymethyl)-6-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162872692	Click to see	724.90	unknown	https://doi.org/10.1007/S12272-011-1001-7
26-O-b-D-glucopyranosyl-3b, 26-diol-25(R)-furost-5,20(22)-dien-3-O-a-L-rhamnopyranosyl(1&2)-O-b-D-glucopyranoside	52931426	Click to see	1047.20	unknown	via CMAUP database
3-O-(Rhaa1-4(Rhaa1-2)Glcb)-(25R)-spirost-5-en-3beta-ol	52931449	Click to see	885.10	unknown	via CMAUP database
Aspafilioside C	148363	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)OC8C(C(C(CO8)O)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O	1023.20	unknown	via CMAUP database
Asparacoside	21575006	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)O)OC9C(C(C(CO9)O)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)C)C)C)OC1	1005.10	unknown	https://doi.org/10.1021/NP030370B
Dioscin	119245	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	869.00	unknown	via CMAUP database
Protodioscin	441891	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)O	1049.20	unknown	via CMAUP database
Pseduoprotodioscin	73817989	Click to see	1031.20	unknown	https://doi.org/10.1007/S12272-011-1001-7
Pseudoprotodioscin	21637110	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC8C7C(=C(O8)CCC(C)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)CO)O)O)O	1031.20	unknown	via CMAUP database
Pseudoprotoneodioscin	163070601	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC8C7C(=C(O8)CCC(C)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)CO)O)O)O	1031.20	unknown	https://doi.org/10.1007/S12272-011-1001-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	52940117	Click to see	576.80	unknown	via CMAUP database
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	via CMAUP database
> Organic acids and derivatives / Carboximidic acids and derivatives / Carboximidic acids
Acrylamide	6579	Click to see	71.08	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Asparagine and derivatives
(2S)-4-amino-2-ammonio-4-oxobutanoate	6992089	Click to see	132.12	unknown	via CMAUP database
CID 6991971	6991971	Click to see C(C(C(=O)[O-])[NH3+])C(=O)N	132.12	unknown	via CMAUP database
> Organic acids and derivatives / Vinylogous thioesters
Acrylamide, (Z)-	6063118	Click to see CC(C)(C)SC=CC(=O)N	159.25	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
GlyTouCan:G27155FO	102436	Click to see	504.40	unknown	https://doi.org/10.1248/CPB.22.2306
Hex2ulof(?2-1)Hex2ulof(?2-1)Hex2ulof(?2-1)Hex2ulof(?2-1)Hex2ulof(?2-1)Hex2ulof(?2-1)Hex2ulof(?2-6)Hex(?1-2?)Hex2ulof	162993381	Click to see C(C1C(C(C(O1)(CO)OCC2(C(C(C(O2)CO)O)O)OCC3(C(C(C(O3)CO)O)O)OCC4(C(C(C(O4)CO)O)O)OCC5(C(C(C(O5)CO)O)O)OCC6(C(C(C(O6)CO)O)O)OCC7(C(C(C(O7)CO)O)O)OCC8C(C(C(C(O8)OC9(C(C(C(O9)CO)O)O)CO)O)O)O)O)O)O	1477.30	unknown	https://doi.org/10.1248/CPB.22.2306
Hex2ulof(?2-1)Hex2ulof(?2-1)Hex2ulof(?2-1)Hex2ulof(?2-1)Hex2ulof(?2-1)Hex2ulof(?2-6)Hex(?1-2?)Hex2ulof	162905083	Click to see	1315.10	unknown	https://doi.org/10.1248/CPB.22.2306
Hex2ulof(?2-1)Hex2ulof(?2-1)Hex2ulof(?2-1)Hex2ulof(?2-6)Hex(?1-2?)Hex2ulof	162875972	Click to see	990.90	unknown	https://doi.org/10.1248/CPB.22.2306
Hex2ulof(?2-1)Hex2ulof(?2-1)Hex2ulof(?2-6)Hex(?1-2?)Hex2ulof	162906050	Click to see	828.70	unknown	https://doi.org/10.1248/CPB.22.2306
Hex2ulof(?2-1)Hex2ulof(?2-6)Hex(?1-2?)Hex2ulof	73803788	Click to see	666.60	unknown	https://doi.org/10.1248/CPB.22.2306
L-Fruf(b2-1)L-Fruf(b2-1)L-Fruf(b2-1)L-Fruf(b2-1)L-Fruf(b2-1)L-Fruf(b2-1)L-Fruf(b2-6)Glc(a1-2b)Fruf	162993382	Click to see	1477.30	unknown	https://doi.org/10.1248/CPB.22.2306
L-Fruf(b2-1)L-Fruf(b2-1)L-Fruf(b2-1)L-Fruf(b2-1)L-Fruf(b2-1)L-Fruf(b2-6)Glc(a1-2b)Fruf	162905084	Click to see	1315.10	unknown	https://doi.org/10.1248/CPB.22.2306
L-Fruf(b2-1)L-Fruf(b2-1)L-Fruf(b2-1)L-Fruf(b2-6)Glc(a1-2b)Fruf	163194316	Click to see	990.90	unknown	https://doi.org/10.1248/CPB.22.2306
L-Fruf(b2-1)L-Fruf(b2-1)L-Fruf(b2-6)Glc(a1-2b)Fruf	162906051	Click to see	828.70	unknown	https://doi.org/10.1248/CPB.22.2306
L-Fruf(b2-1)L-Fruf(b2-6)Glc(a1-2b)Fruf	162972534	Click to see	666.60	unknown	https://doi.org/10.1248/CPB.22.2306
L-Fruf(b2-6)Glc(a1-2b)Fruf	101691507	Click to see C(C1C(C(C(O1)(CO)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)O)O)O)O	504.40	unknown	https://doi.org/10.1248/CPB.22.2306
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-(Methoxymethyl)-2-furaldehyde	74711	Click to see	140.14	unknown	via CMAUP database
5-Hydroxymethylfurfural	237332	Click to see C1=C(OC(=C1)C=O)CO	126.11	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Ferulate	54691413	Click to see	193.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Quercetin-7-olate	46906036	Click to see	301.23	unknown	via CMAUP database

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Asparagus cochinchinensis

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