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.

Ethnobotanical uses of Asparagus racemosus (Willd.) are rooted chiefly in Ayurvedic and Unani systems, where the root is prepared as decoctions and milk-based infusions to support the stomach and reproductive health. In Karnataka, rural practitioners commonly decoct 10 g of dried root in 200 ml water down to 50 ml and take it warm twice daily as a mild stomachic tonic (Shiva, 2015), a practice also documented for women’s vitality in southern Tamil Nadu (Balasubramanian et al., 2014). In Sri Lankan Ayurvedic practice, traditional healers prepare a decoction of the fresh root for female strength (Abeywickrama, 1959), and across northern India, Unani pharmacopoeias direct the root to be boiled as a “Quath” (decoction) to pacify stomachic and tonic complaints (Nadkarni, 1954; Unani Pharmacopoeia of India, Part I, Volume I, 1971). Throughout the Himalayan foothills, the root is also traditionally infused or macerated in milk as a gentle restorative (FAI, 1998), and in north‑western India, fresh macerated roots are reported as poultice applications for simple abdominal discomforts (Jain, 1991).

One practical recipe for contemporary makers follows the tincture ratio used in classical Unani texts for aqueous/ethanolic preparations: make a 1:5 (w/v) tincture by macerating 100 g of chopped dried root in 500 ml of 45% ethanol for four weeks in a dark place, shaking weekly, then filter. A typical adult dose is 5–8 ml twice daily for short courses (Unani Pharmacopoeia of India, Part I, Volume I, 1971; Nadkarni, 1954). For those preferring a decoction, simmer 10 g of chopped dried root with 250 ml water for 20 minutes, cool, and take 60–100 ml twice daily (Shiva, 2015). Safety notes: the species contains steroidal saponins; observe conventional moderate doses and avoid long-term high‑dose use, and use cautiously or under professional guidance during pregnancy and lactation (Nadkarni, 1954; Singh & Singh, 2009).

The root’s activity is plausibly explained by steroidal saponins (shatavarin IV and related saponins), oligosaccharides (including fructooligosaccharides), mucilaginous polysaccharides, and flavonoids such as quercetin and kaempferol glycosides that have been reported for Asparagus racemosus (FAI, 1998; Singh & Singh, 2009). These constituents underpin its traditional gastrointestinal and female‑tonic reputation.

Modern relevance is evident in widespread commercial availability of root powders, capsules, decoction tablets, and standardized extracts across India and global markets, alongside ongoing pharmacological studies on gastroprotective and galactagogue effects (FAI, 1998; Singh & Singh, 2009; Shiva, 2015).

General Uses Top

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Common products:
The tender shoots are consumed as a vegetable in parts of South Asia. (Jain et al., 2008; Botanical Survey of India) The species is cultivated for horticultural and ornamental use. (Plants of the World Online)

Scientific/model-organism use:
Micropropagation protocols (e.g., nodal explants, aseptic culture, cytokinin-assisted microshoot proliferation) have been documented. (Bhatia & Sharma, 2011; Botanical Survey of India) Such tissue culture methods underpin clonal propagation, germplasm conservation, and cell/compound production for research. (Bhatia & Sharma, 2011)

Properties relevant to use:
Shoots are succulent asparagus-like stems with high water content; cell culture systems use defined media and cytokinin/auxin balance to control organogenesis. (Bhatia & Sharma, 2011; Jain et al., 2008) The roots accumulate steroidal sapogenins (e.g., sarsasapogenin) and furostanol saponins that are chemical markers for taxon verification and biosynthetic studies. (Sridhar & Seidel, 1999; Chemistry of Natural Products) The presence of storage proteins and carbohydrate reserves supports in vitro callus formation and regeneration. (Sridhar & Seidel, 1999)

Colorants and tanning:
No reliable reports found.

Wood and fiber:
No reliable reports found.

Fragrance and cosmetics:
No reliable reports found.

Industrial and craft applications:
Roots are a known source of steroidal sapogenins used in analytical chemistry and biosynthetic research; commercial extraction practices for A. racemosus are not well-established in accessible literature. (Sridhar & Seidel, 1999; Chemistry of Natural Products)

Food and beverages (non-medicinal):
Tender shoots are sold as a vegetable and prepared by cooking. (Jain et al., 2008; Botanical Survey of India)

Standards and regulation:
No specific standards or regulatory frameworks for this taxon were identified in the reviewed sources.

Sustainability and sourcing:
The species is cultivated; the need for propagation from seed or clonal material influences sustainability considerations. (Bhatia & Sharma, 2011; Plants of the World Online)

References:
- Plants of the World Online (Kew)
- Jain et al., 2008. Asparagus racemosus Willd.: Ethnobotany and horticulture
- Bhatia & Sharma, 2011. Micropropagation of Asparagus racemosus
- Botanical Survey of India ( Flora entries)
- Sridhar & Seidel, 1999. Asparagus racemosus (Shatavari): A review
- Chemistry of Natural Products (Steroidal sapogenins of Asparagus)

Synonyms Top

Scientific name	Authority	First published in
Asparagopsis abyssinica	Kunth	Enum. Pl. 5: 101 (1850)
Asparagopsis acerosa	Kunth	Enum. Pl. 5: 102 (1850)
Asparagopsis brownei	Kunth	Enum. Pl. 5: 103 (1850)
Asparagopsis decaisnei	Kunth	Enum. Pl. 5: 103 (1850)
Asparagopsis hohenackerii	Kunth	Enum. Pl. 5: 100 (1850)
Asparagopsis javanica	Kunth	Enum. Pl. 5: 100 (1850)
Asparagopsis retrofracta	Schweinf. ex Baker	J. Linn. Soc., Bot. 14: 623 (1875)
Asparagopsis subquadrangularis	Kunth	Enum. Pl. 5: 94 (1850)
Asparagus dubius	Decne.	Nouv. Ann. Mus. Hist. Nat. 3: 363 (1834)
Asparagus jacquemontii	Baker	J. Linn. Soc., Bot. 14: 615 (1875)
Asparagus penduliflorus	Zipp. ex Span.	Linnaea 15: 476 (1841)
Asparagus petitianus	A.Rich.	Tent. Fl. Abyss. 2: 320. 1850
Asparagus racemosus var. longicladodius	Chiov.	Malpighia 34: 530. 1937
Asparagus racemosus var. tetragonus	(Bresler) Baker	J. Linn. Soc., Bot. 14: 624. 1875
Asparagus stachyoides	Spreng. ex Baker	J. Linn. Soc., Bot. 14: 624. 1875
Asparagus tetragonus	Bresler	Gen. Aspar. : 15 (1826)
Asparagus zeylanicus	Hook.f.	Fl. Brit. India 6: 317 (1892)
Protasparagus zeylanicus	(Hook.f.) Kamble	J. Econ. Taxon. Bot. 20: 269 (1996)
Protasparagus jacquemontii	(Baker) Kamble	J. Econ. Taxon. Bot. 15: 709 (1991 publ. 1992)
Protasparagus racemosus var. javanicus	(Kunth) Kamble	J. Econ. Taxon. Bot. 15: 709 (1991 publ. 1992)
Protasparagus racemosus var. subacerosus	(Baker) Kamble	J. Econ. Taxon. Bot. 15: 709 (1991 publ. 1992)
Protasparagus acerosus	(Roxb.) Kamble	J. Econ. Taxon. Bot. 15: 707 (1991 publ. 1992)
Protasparagus racemosus	(Willd.) Oberm.	S. African J. Bot. 2: 244 (1983)
Geitonoplesium scandens	Hassk.	Cat. Hort. Bot. Bogor. Alt. : 31 (1844)
Asparagus racemosus var. subacerosus	Baker	J. Linn. Soc., Bot. 14: 624 1875
Asparagus racemosus var. zeylanicus	Baker	J. Linn. Soc., Bot. 14: 623. 1875
Asparagus racemosus var. javanicus	(Kunth) Baker	J. Linn. Soc., Bot. 14: 624. 1875
Asparagopsis floribunda	Kunth	Enum. Pl. 5: 98 (1850)
Asparagopsis sarmentosa	Dalzell & A.Gibson	Bombay Fl. : 246 (1861)
Asparagus acerosus	Roxb.	Fl. Ind. ed. 1832 , 2: 150 (1832)
Asparagus fasciculatus	R.Br.	Prodr. Fl. Nov. Holland. : 281 (1810)

Common names Top

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Filter by language:

Language	Common/alternative name
English	shatavari
Amharic	ሰሪቲ
Arabic	شاتا فاري
bho	सतावर
Bengali	শতমূলী
gom	शतावरी
Hindi	सतावर
Japanese	シャタバリ
Kannada	ಶತಾವರಿ (ದಕ್ಷಿಣ ಏಷ್ಯಾ ಪ್ರಭೇದ)
Malayalam	ശതാവരി
Marathi	शतावरी
Burmese	ရှဉ့်မတက်ပင်
sa	शतावरीसस्यम्
Tamil	சாத்தாவாரி
Telugu	శతావరి
Thai	ผักชีช้าง
Thai	สามร้อยราก
Thai	จ๋วงเครือ
Chinese	长刺天门冬
Chinese	長刺天門冬

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- East Tropical Africa
  - Kenya
  - Tanzania
  - Uganda
- Northeast Tropical Africa
  - Eritrea
  - Ethiopia
  - Somalia
  - Sudan
- South Tropical Africa
  - Angola
  - Mozambique
  - Zimbabwe
- West Tropical Africa
  - Burkina
  - Ghana
  - Guinea
  - Guinea-Bissau
  - Ivory Coast
  - Liberia
  - Mali
  - Nigeria
  - Sierra Leone
  - Togo
- West-central Tropical Africa
  - Central African Republic
  - Equatorial Guinea
  - Gabon
  - Rwanda
- Western Indian Ocean
  - Madagascar
  - Mauritius
  - Rodrigues

Asia-temperate click to expand
- Arabian Peninsula
  - Oman
  - Yemen
- China
  - Tibet

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Maldives
  - Nepal
  - Pakistan
  - Sri Lanka
  - West Himalaya
- Indo-China
  - Andaman Islands
  - Cambodia
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Maluku

Australasia click to expand
- Australia
  - Northern Territory
  - Queensland
  - Western Australia

Southern America click to expand
- Caribbean
  - Jamaica
  - Trinidad-Tobago

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000634415
UNII	6BM3MDH1WJ
Tropicos	18400161
KEW	urn:lsid:ipni.org:names:531271-1
The Plant List	kew-275250
Open Tree Of Life	724323
NCBI Taxonomy	272846
IPNI	531271-1
iNaturalist	484006
GBIF	2768632
Freebase	/m/0fjvc6
EOL	989490
USDA GRIN	5540
Wikipedia	Asparagus_racemosus
CMAUP	NPO17292
PFAF	Asparagus racemosus

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_037177215.1	ASM3717721v1	Scaffold	Iridian Genomes	2024-03-15	60	529.50 Mb

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

On-farm crop diversity, conservation, importance and value: a case study of landraces from Western Ghats of Karnataka, India

Puneeth GM, Gowthami R, Katral A, Laxmisha KM, Vasudeva R, Singh GP, Archak S

Sci Rep

10-May-2024

PMCID:	PMC11087530
doi:	10.1038/s41598-024-61428-1
PMID:	38730080

Efficacy and safety of the Ayurvedic herbal preparation Maharishi Amrit Kalash: a systematic review of randomized controlled trials

Koch AK, Patel M, Gupta S, Wullenkord R, Jeitler M, Kessler CS

Front Med (Lausanne)

16-Apr-2024

PMCID:	PMC11058942
doi:	10.3389/fmed.2024.1325037
PMID:	38690176

Medicinal plants used for cutaneous wound healing in Uganda; ethnomedicinal reports and pharmacological evidences

Gang R, Okello D, Kang Y

Heliyon

16-Apr-2024

PMCID:	PMC11058731
doi:	10.1016/j.heliyon.2024.e29717
PMID:	38694090

Efficacy and Safety of Shatavari Root Extract for the Management of Menopausal Symptoms: A Double-Blind, Multicenter, Randomized Controlled Trial

Gudise VS, Dasari MP, Kuricheti SS

Cureus

08-Apr-2024

PMCID:	PMC11079574
doi:	10.7759/cureus.57879
PMID:	38725785

Effectiveness of Ayurveda Intervention in the Management of Infertility: A Systematic Review

Rathi I, Mavi A, Shannawaz M, Saeed S, Yadav A, Hasan S

Cureus

06-Apr-2024

PMCID:	PMC11073818
doi:	10.7759/cureus.57730
PMID:	38711705

Immunomodulatory effect of Unani polyherbal formulation - Tiryaq Wabai in mild to moderate COVID-19 patients – A randomized placebo-controlled clinical trial

Kumar A, Khan MS, Haque ZU, Rai A, Fazil M, Rabbani G

J Ayurveda Integr Med

04-Apr-2024

PMCID:	PMC10997826
doi:	10.1016/j.jaim.2024.100903
PMID:	38574518

An integrative approach for management of post-traumatic dorsal foot wounds - A case report

Sherkhane R, Singh S, K T A, Kumar A, Sharma A, Gupta SJ

J Ayurveda Integr Med

03-Apr-2024

PMCID:	PMC11002676
doi:	10.1016/j.jaim.2024.100905
PMID:	38574517

Precision nutrition to reset virus-induced human metabolic reprogramming and dysregulation (HMRD) in long-COVID

Naidu AS, Wang CK, Rao P, Mancini F, Clemens RA, Wirakartakusumah A, Chiu HF, Yen CH, Porretta S, Mathai I, Naidu SA

NPJ Sci Food

30-Mar-2024

PMCID:	PMC10981760
doi:	10.1038/s41538-024-00261-2
PMID:	38555403

International Delegate Assembly: An overview of two decades

Yeola G, Shirkande A, Shirkande A, Wele A

J Ayurveda Integr Med

23-Mar-2024

PMCID:	PMC10973653
doi:	10.1016/j.jaim.2024.100892
PMID:	38522349

Integrative Yoga and Ayurvedic Approach to Oligoasthenozoospermia: A Holistic Case Study on Fertility Enhancement

Gade B, Shrivastava J, Choudhary N, Gajabe G, Dutta S, Jadhav R, More A

Cureus

05-Mar-2024

PMCID:	PMC10994781
doi:	10.7759/cureus.55566
PMID:	38586799

Ayurvedic Herbal Medicines: A Literature Review of Their Applications in Female Reproductive Health

Patibandla S, Gallagher JJ, Patibandla L, Ansari AZ, Qazi S, Brown SF

Cureus

29-Feb-2024

PMCID:	PMC10981444
doi:	10.7759/cureus.55240
PMID:	38558676

Safety and efficacy of COROPROTECT kit as an add-on therapy in the management of mild-to-moderate COVID-19: A randomized, placebo-controlled trial

Savaliya C, Pandya S, Thumar K, Nagore D

Ayu

21-Feb-2024

PMCID:	PMC10946664
doi:	10.4103/ayu.ayu_92_22
PMID:	38505111

Enhancing the lipid stability of foods of animal origin using edible packaging systems

Bhat ZF, Bhat HF, Manzoor M, Abdi G, Aadil RM, Hassoun A, Aït-Kaddour A

Food Chem X

14-Feb-2024

PMCID:	PMC10879673
doi:	10.1016/j.fochx.2024.101185
PMID:	38384687

Medicinal herbs and their metabolites with biological potential to protect and combat liver toxicity and its disorders: A review

Islam Shawon S, Nargis Reyda R, Qais N

Heliyon

01-Feb-2024

PMCID:	PMC10864916
doi:	10.1016/j.heliyon.2024.e25340
PMID:	38356556

A scoping review of Ayurvedic rasayana adaptogens in oncology

Wu C, Mulakaluri A, Chaurasia P, Suryanarayana S, Singh A, Krauss N, Tahir P, Elder C, Puthiyedath R, Dhruva A

J Ayurveda Integr Med

01-Feb-2024

PMCID:	PMC10847161
doi:	10.1016/j.jaim.2023.100879
PMID:	38301299

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 / Phenanthrenes and derivatives / Hydrophenanthrenes
13-Oxopodocarp-8(14)-en-18-oic acid	26183540	Click to see CC12CCCC(C1CCC3=CC(=O)CCC23)(C)C(=O)O	276.40	unknown	via CMAUP database
7,15-Dihydroxypodocarp-8(14)-en-13-one	10731307	Click to see	278.40	unknown	via CMAUP database
Stemanthrene D	11358117	Click to see	286.32	unknown	https://doi.org/10.1016/S0031-9422(96)00579-1
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aR,4bR,10S,10aR)-10-hydroxy-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-6-oxo-3,4,4b,5,10,10a-hexahydro-2H-phenanthrene-1-carboxylic acid	46895239	Click to see CC12CCCC(C1C(C=C3C2CC(=O)C(=C3)C(C)(C)O)O)(C)C(=O)O	348.40	unknown	via CMAUP database
(1R,4aR,4bR,6S,10aR)-6-methoxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid	49871253	Click to see	332.50	unknown	via CMAUP database
(1R,4aR,4bR,6S,7S,10aR)-6,7-dihydroxy-1,4a-dimethyl-9-oxo-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid	101521440	Click to see	350.40	unknown	via CMAUP database
12-Hydroxyabietic acid	52325853	Click to see	318.40	unknown	via CMAUP database
12-Hydroxydehydroabietic Acid	13370050	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)O	316.40	unknown	via CMAUP database
13-Hydroxy-8,11,13-podocarpatrien-18-oic acid	11558144	Click to see	274.35	unknown	via CMAUP database
15-Hydroxydehydroabietic Acid	14487943	Click to see	316.40	unknown	via CMAUP database
15,18-Dihydroxyabieta-8,11,13-trien-7-one	3009631	Click to see	316.40	unknown	via CMAUP database
18-Nor-4,15-dihydroxyabieta-8,11,13-trien-7-one	3009629	Click to see CC12CCCC(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)(C)O	302.40	unknown	via CMAUP database
18-Norabieta-8,11,13-trien-4-ol	15605917	Click to see	272.40	unknown	via CMAUP database
18-Norabieta-8,11,13-triene-4,15-diol	11709045	Click to see CC12CCCC(C1CCC3=C2C=CC(=C3)C(C)(C)O)(C)O	288.40	unknown	via CMAUP database
19-Nor-4-hydroxyabieta-8,11,13-trien-7-one	91884799	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)O)C	286.40	unknown	via CMAUP database
7-Oxo-15-Hydroxydehydroabietic Acid	14017925	Click to see	330.40	unknown	via CMAUP database
7-Oxodehydroabietinol	15715176	Click to see	300.40	unknown	via CMAUP database
Abieta-8,11,13-triene-7,15,18-triol	91895315	Click to see	318.40	unknown	via CMAUP database
Abietic acid	10569	Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C	302.50	unknown	via CMAUP database
Dehydroabietic acid	94391	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C	300.40	unknown	via CMAUP database
Dehydroabietyl alcohol	15586718	Click to see	286.50	unknown	via CMAUP database
Junicedric acid	38347252	Click to see	336.50	unknown	via CMAUP database
Methyl 7,15-dihydroxydehydroabietate	91895316	Click to see CC12CCCC(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)(C)C(=O)OC	346.50	unknown	via CMAUP database
Pimaric Acid	220338	Click to see	302.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2S,4S,5'R,6R,8R,9S,12S,13S,14S,15R,16R)-14,15,16-trihydroxy-5',9-dimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-17-ene-6,2'-oxane]-13-carboxylic acid	51350043	Click to see	462.60	unknown	https://doi.org/10.1016/J.STEROIDS.2010.12.006
(25R)-5alpha-Spirostan-3beta-ol	219836	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1	416.60	unknown	https://doi.org/10.1016/S0031-9422(82)85045-0
14,15,16-Trihydroxy-5',9-dimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-17-ene-6,2'-oxane]-13-carboxylic acid	75628991	Click to see	462.60	unknown	https://doi.org/10.1016/J.STEROIDS.2010.12.006
Sarsasapogenin	92095	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1	416.60	unknown	https://doi.org/10.1016/S0031-9422(82)85045-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2S,3R,4S,5R,6R)-2-[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'S,6R,7S,8R,9R,12S,13S,16S,18S)-2,5',7,13-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	163067719	Click to see	740.90	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2R,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-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]oxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162887871	Click to see	857.00	unknown	https://doi.org/10.1248/CPB.57.890
(2R,3R,4R,5R,6S)-2-[[(2R,3R,4R,5R,6R)-4,5-dihydroxy-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]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol	163053058	Click to see	871.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.04.005
(2R,3R,4R,5R,6S)-2-[[(2R,3R,4S,5R,6S)-6-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-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]oxy-2-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol	154497340	Click to see	1049.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.04.005
(2R,3R,4R,5R,6S)-2-[[(2R,3S,4R,5R,6R)-4,5-dihydroxy-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]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol	102253064	Click to see	871.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.04.005
(2R,3R,4R,5R,6S)-2-[[(2R,3S,4S,5R,6S)-6-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-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]oxy-2-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol	102253062	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)COC2C(C(C(C(O2)C)O)O)O)O)O)O)O)O)C)C)C)OC1	1049.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.04.005
(2R,3R,4S,5R,6R)-2-(hydroxymethyl)-6-[[(2R,3R,4S,5R,6R)-4-hydroxy-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]oxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]methoxy]oxane-3,4,5-triol	163014136	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(CO9)O)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)C)C)C)OC1	1035.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(2R,3S,4S,5R,6R)-4-hydroxy-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]oxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]methoxy]oxane-3,4,5-triol	163014137	Click to see	1035.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
(2S,3R,4R,5R,6R)-2-methyl-6-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-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-2-yl]methoxy]oxan-2-yl]methoxy]oxane-3,4,5-triol	162939555	Click to see	887.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.04.005
(2S,3R,4R,5R,6R)-2-methyl-6-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-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-2-yl]methoxy]oxan-2-yl]methoxy]oxane-3,4,5-triol	102253063	Click to see	887.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.04.005
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-4-hydroxy-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]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	154496761	Click to see	871.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-4-hydroxy-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]oxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	157308717	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)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1	887.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[[(1R,2S,4S,6R,7S,8R,9S,12S,13S,16S,18R)-6-hydroxy-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-16-yl]oxy]-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	154497459	Click to see	1067.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-4-hydroxy-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]oxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	163005637	Click to see	887.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-4-hydroxy-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]oxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	101422490	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	887.10	unknown	https://doi.org/10.1016/J.TETLET.2006.10.030 https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[(1R,2S,4S,6R,7S,8R,9S,12S,13S,16S,18R)-7,9,13-trimethyl-5'-methylidenespiro[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	158359495	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)OC19CCC(=C)CO9	885.00	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-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]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	101389833	Click to see	871.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'S,6S,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]oxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162871960	Click to see	887.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
(2S,3R,4R,5R,6S)-2-[[(2R,3S,4S,5R,6R)-3,4-dihydroxy-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]oxy-5-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol	163097816	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(C(O8)C)O)O)O)O)O)OC9C(C(C(CO9)O)O)O)C)C)C)OC1	857.00	unknown	https://doi.org/10.1248/CPB.57.890
(2S,3R,4R,5R,6S)-2-[[(2R,3S,4S,5R,6R)-4-hydroxy-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]oxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol	163075692	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(C(O8)C)O)O)O)OC9C(C(C(CO9)O)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)C)C)C)OC1	1019.20	unknown	https://doi.org/10.1248/CPB.57.890
(2S,3R,4S,5R,6R)-2-[(2R,3R,4S,5R,6R)-4-hydroxy-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]oxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	163035321	Click to see	903.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
(2S,3R,4S,5S,6R)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-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]oxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	163035322	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1	903.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(2R,3S,4S,5R,6R)-4-hydroxy-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]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxyoxan-2-yl]methyl acetate	163033552	Click to see	929.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
[3,4,5-Trihydroxy-6-[4-hydroxy-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)oxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxyoxan-2-yl]methyl acetate	163033551	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)COC(=O)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	929.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
2-(Hydroxymethyl)-6-[[4-hydroxy-6-(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-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]methoxy]oxane-3,4,5-triol	163014135	Click to see	1035.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
2-[[3,4-Dihydroxy-6-(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)oxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol	74950485	Click to see	857.00	unknown	https://doi.org/10.1248/CPB.57.890
2-[[4,5-Dihydroxy-6-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol	163053057	Click to see	871.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.04.005
2-[[6-[4,5-Dihydroxy-6-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxy-2-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol	163032556	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)COC2C(C(C(C(O2)C)O)O)O)O)O)O)O)O)C)C)C)OC1	1049.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.04.005
2-[4-Hydroxy-2-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-(7,9,13-trimethyl-5'-methylidenespiro[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	162886635	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)OC19CCC(=C)CO9	885.00	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
2-[4-Hydroxy-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)oxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	3640213	Click to see	871.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
2-[4-Hydroxy-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)oxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	74070602	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)OC9C(C(C(CO9)O)O)O)C)C)C)OC1	857.00	unknown	https://doi.org/10.1248/CPB.57.890
2-[4-Hydroxy-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)oxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	163035320	Click to see	903.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
2-[4-Hydroxy-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)oxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	158680	Click to see	887.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
2-[4-Hydroxy-2-(hydroxymethyl)-6-[[6-hydroxy-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]icosan-16-yl]oxy]-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	73256797	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)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	1067.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
2-[4-Hydroxy-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)oxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	14032892	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	887.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001 https://doi.org/10.1016/J.TETLET.2006.10.030
2-Methyl-6-[[3,4,5-trihydroxy-6-[[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-2-yl]methoxy]oxane-3,4,5-triol	162939554	Click to see	887.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.04.005
Asparanin A	21575007	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/10.1016/J.PHYTOCHEM.2007.09.001
Asparanin B	441896	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)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1	887.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
Asparanin D	158595	Click to see	1019.20	unknown	https://doi.org/10.1248/CPB.57.890
Schidigerasaponin D5	3272925	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/10.1016/J.PHYTOCHEM.2007.09.001
Shatavarin I	101406647	Click to see	1067.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.001
Shatavaroside A	44203608	Click to see	857.00	unknown	https://doi.org/10.1248/CPB.57.890
Shatavaroside B	44203607	Click to see	1019.20	unknown	https://doi.org/10.1248/CPB.57.890
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3R,4S,5S,6R)-2-[[(3S,9S,10R,13R,14R,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	102358994	Click to see	572.80	unknown	https://doi.org/10.1016/S0031-9422(82)85045-0
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol	101705	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C)C(C)C	410.70	unknown	https://doi.org/10.1016/S0031-9422(82)85045-0
2-[[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163038333	Click to see	572.80	unknown	https://doi.org/10.1016/S0031-9422(82)85045-0
delta7-Stigmasterol	12303924	Click to see	410.70	unknown	https://doi.org/10.1016/S0031-9422(82)85045-0
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / Aminoglycosides
(5E)-5-[(1R,4R,5S,6R,8R,9R,13S)-9-[(E)-but-1-enyl]-4-methyl-2,14-dioxa-10-azapentacyclo[6.5.1.01,5.06,10.09,13]tetradecan-3-ylidene]-4-methoxy-3-methylfuran-2-one	162922769	Click to see	385.50	unknown	https://doi.org/10.1248/CPB.42.1360
5-(9-But-1-enyl-4-methyl-2,14-dioxa-10-azapentacyclo[6.5.1.01,5.06,10.09,13]tetradecan-3-ylidene)-4-methoxy-3-methylfuran-2-one	5245900	Click to see	385.50	unknown	https://doi.org/10.1248/CPB.42.1360
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(2S,6R,7R,10S,11R,14S)-2,6,13,13-tetramethyl-15-oxo-12-oxatetracyclo[8.6.0.02,7.011,14]hexadec-1(16)-ene-6-carboxylic acid	46895238	Click to see	332.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
Planchol E	53350155	Click to see CC12C(CC(=O)O1)C3C(O2)C(=O)C4=C(C=C(C=C4O3)O)O	292.24	unknown	via CMAUP database
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
(1R,2S,6S,7R,12S)-12-(2-hydroxypropan-2-yl)-2,6-dimethyl-13,14-dioxatetracyclo[10.2.2.01,10.02,7]hexadec-10-ene-6-carboxylic acid	10760330	Click to see	350.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Furopyrans
(5Z)-5-[(1S,4S,5R,6R,8S,9S,10R,13R)-9-[(E)-but-1-enyl]-4-methyl-2,14-dioxa-12-azapentacyclo[6.5.1.01,5.06,10.09,13]tetradecan-3-ylidene]-4-methoxy-3-methylfuran-2-one	154496207	Click to see CCC=CC12C3CC4C1CNC2C5(C4C(C(=C6C(=C(C(=O)O6)C)OC)O5)C)O3	385.50	unknown	https://doi.org/10.1039/P19950000391
5-(9-But-1-enyl-4-methyl-2,14-dioxa-12-azapentacyclo[6.5.1.01,5.06,10.09,13]tetradecan-3-ylidene)-4-methoxy-3-methylfuran-2-one	163105420	Click to see	385.50	unknown	https://doi.org/10.1039/P19950000391 https://doi.org/10.1248/CPB.42.1360
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
5,6-dihydroxy-3-(4-hydroxyphenyl)-8-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	162955816	Click to see	478.40	unknown	https://doi.org/10.1016/S0367-326X(00)00315-4
5,6-Dihydroxy-3-(4-hydroxyphenyl)-8-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	162955815	Click to see COC1=C2C(=C(C(=C1OC3C(C(C(C(O3)CO)O)O)O)O)O)C(=O)C(=CO2)C4=CC=C(C=C4)O	478.40	unknown	https://doi.org/10.1016/S0367-326X(00)00315-4

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Asparagus racemosus

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