Siraitia grosvenorii

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Scientific Literature

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Details Top

Internal ID	UUID643ffd43ce51d369502657
Scientific name	Siraitia grosvenorii
Authority	(Swingle) C.Jeffrey ex A.M.Lu & Zhi Y.Zhang
First published in	Guihaia 4: 29 (1984)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Momordica grosvenorii	Swingle	J. Arnold Arbor. 22: 198 (1941)
Thladiantha grosvenorii	(Swingle) C.Jeffrey	Kew Bull. 33: 393 (1979)

Common names Top

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Filter by language:

Language	Common/alternative name
English	monk fruit
English	monkfruit
English	arhat fruit
Bulgarian	архат
Czech	luo-chan-kuo
Czech	luo han guo
Czech	luo chan kuo
German	momordicae grosvenori fructus
German	mönchsfrucht
German	luó hàn guǒ
Esperanto	monaĥfrukto
Persian	سیرایتیا گرسونری
Hebrew	פרי הנזיר
Japanese	ラカンカ
Japanese	羅漢果
jv	luó hàn guǒ
Korean	나한과
Norwegian Bokmål	balsampære
Russian	Архат
Slovak	luo-chan-kuo
Swedish	luo han guo
Thai	หล่อฮังก๊วย
Thai	หลอฮังก๊วย
Ukrainian	архат
Vietnamese	la hán quả
za	maklozhan
Chinese	羅漢果
Chinese	光果木鳖
Chinese	罗汉果根
Chinese	罗汉果
Chinese	罗汉果叶

Subspecies (abbr. subsp./ssp.) Top

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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 South-central
  - China Southeast

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000441673
UNII	Q1W0T771NI
Tropicos	9201171
KEW	urn:lsid:ipni.org:names:914594-1
The Plant List	kew-2489947
Open Tree Of Life	532954
NCBI Taxonomy	190515
IPNI	914594-1
GBIF	3623059
Freebase	/m/08wzr5
EOL	5735528
USDA GRIN	402732
Wikipedia	Siraitia_grosvenorii

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

Abundance and diversity of fungal endophytes isolated from monk fruit (Siraitia grosvenorii) grown in a Canadian research greenhouse

Ma L, Elmhirst JF, Darvish R, Wegener LA, Henderson D

Plant Environ Interact

02-Apr-2024

PMCID:	PMC10986896
doi:	10.1002/pei3.10142
PMID:	38567203

Efficacy of botanical lozenges in the treatment of chronic pharyngitis: a randomized controlled trial

Wu Y, Zhang F, Kuang D, Li D, Yan J, Yang J, Wang Q, Wang Y, Sun J, Liu Y, Xia Y, Cao H

Front Pharmacol

14-Mar-2024

PMCID:	PMC10973001
doi:	10.3389/fphar.2024.1162883
PMID:	38549665

Multi-omics analysis reveals promiscuous O-glycosyltransferases involved in the diversity of flavonoid glycosides in Periploca forrestii (Apocynaceae)

Wang X, Wu L, Zhang W, Qiu S, Xu Z, Wan H, He J, Wang W, Wang M, Yin Q, Shi Y, Gao R, Xiang L, Yang W

Comput Struct Biotechnol J

02-Mar-2024

PMCID:	PMC10940802
doi:	10.1016/j.csbj.2024.02.028
PMID:	38495554

Mining and functional characterization of NADPH-cytochrome P450 reductases of the DNJ biosynthetic pathway in mulberry leaves

Liao Y, Du W, Wan J, Fan J, Pi J, Wu M, Wei Y, Ouyang Z

BMC Plant Biol

23-Feb-2024

PMCID:	PMC10885410
doi:	10.1186/s12870-024-04815-0
PMID:	38395770

Mogrol stimulates G-protein-coupled bile acid receptor 1 (GPBAR1/TGR5) and insulin secretion from pancreatic β-cells and alleviates hyperglycemia in mice

Tanaka C, Harada N, Teraoka Y, Urushizaki H, Shinmori Y, Onishi T, Yotsumoto Y, Ito Y, Kitakaze T, Inui T, Murata Y, Inui H, Yamaji R

Sci Rep

08-Feb-2024

PMCID:	PMC10853268
doi:	10.1038/s41598-024-53380-x
PMID:	38332164

The complete chloroplast genome sequence of Thladiantha nudiflora Hemsl. ex F.B.Forbes & Hemsl. 1887 (Cucurbitaceae)

Zhao YY, Chen MM, Duan BL, Xie QZ, Miao Q

Mitochondrial DNA B Resour

25-Jan-2024

PMCID:	PMC10812858
doi:	10.1080/23802359.2024.2305402
PMID:	38282981

Aquilaria sinensis: An Upstart Resource for Cucurbitacin Production Offers Insights into the Origin of Plant Bitter (Bi) Gene Clusters

Ding X, Yang Z, Wang H, Zeng J, Dai H, Mei W

Plants (Basel)

16-Jan-2024

PMCID:	PMC10819951
doi:	10.3390/plants13020260
PMID:	38256813

The Prebiotic Activity of a Novel Polysaccharide Extracted from Huangshui by Fecal Fermentation In Vitro

Li M, Su J, Wu J, Zhao D, Huang M, Lu Y, Zheng J, Li H

Foods

07-Dec-2023

PMCID:	PMC10743195
doi:	10.3390/foods12244406
PMID:	38137210

Evaluation of Reference Genes for Normalizing RT-qPCR and Analysis of the Expression Patterns of WRKY1 Transcription Factor and Rhynchophylline Biosynthesis-Related Genes in Uncaria rhynchophylla

Mu D, Shao Y, He J, Zhu L, Qiu D, Wilson IW, Zhang Y, Pan L, Zhou Y, Lu Y, Tang Q

Int J Mol Sci

15-Nov-2023

PMCID:	PMC10671239
doi:	10.3390/ijms242216330
PMID:	38003520

Cloning and Functional Characterization of NADPH-Cytochrome P450 Reductases in Aconitum vilmorinianum

Cheng J, Li G, Wang X, Yang C, Xu F, Qian Z, Ma X

Molecules

03-Nov-2023

PMCID:	PMC10648341
doi:	10.3390/molecules28217409
PMID:	37959828

Curcumin as an antiviral agent and immune-inflammatory modulator in COVID-19: A scientometric analysis

Liu K, Zhu Y, Cao X, Liu Y, Ying R, Huang Q, Gao P, Zhang C

Heliyon

02-Nov-2023

PMCID:	PMC10661356
doi:	10.1016/j.heliyon.2023.e21648
PMID:	38027776

Differential roles of Cassia tora 1-deoxy-D-xylulose-5-phosphate synthase and 1-deoxy-D-xylulose-5-phosphate reductoisomerase in trade-off between plant growth and drought tolerance

Tian C, Quan H, Jiang R, Zheng Q, Huang S, Tan G, Yan C, Zhou J, Liao H

Front Plant Sci

20-Oct-2023

PMCID:	PMC10623318
doi:	10.3389/fpls.2023.1270396
PMID:	37929171

Targeting Mitochondrial Sirtuins in Age-Related Neurodegenerative Diseases and Fibrosis

Xiao H, Xie Y, Xi K, Xie J, Liu M, Zhang Y, Cheng Z, Wang W, Guo B, Wu S

Aging Dis

01-Oct-2023

PMCID:	PMC10529758
doi:	10.14336/AD.2023.0203
PMID:	37196115

Tomato root-associated Sphingobium harbors genes for catabolizing toxic steroidal glycoalkaloids

Nakayasu M, Takamatsu K, Kanai K, Masuda S, Yamazaki S, Aoki Y, Shibata A, Suda W, Shirasu K, Yazaki K, Sugiyama A

mBio

29-Sep-2023

PMCID:	PMC10653915
doi:	10.1128/mbio.00599-23
PMID:	37772873

Promiscuous CYP87A enzyme activity initiates cardenolide biosynthesis in plants

Kunert M, Langley C, Lucier R, Ploss K, Rodríguez López CE, Serna Guerrero DA, Rothe E, O’Connor SE, Sonawane PD

Nat Plants

18-Sep-2023

PMCID:	PMC10581899
doi:	10.1038/s41477-023-01515-9
PMID:	37723202

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
> Alkaloids and derivatives / Aporphines
(12S)-7,17-dimethoxy-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1,6,8(20),14,16,18-hexaen-16-ol	155806685	Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C5C(=C2OC)OCO5)OC)O	355.40	unknown	https://doi.org/10.1248/YAKUSHI1947.103.11_1167 https://doi.org/10.1248/CPB.38.2030
> Benzenoids / Phenol ethers
2-(4-Formylphenoxy)acetamide	601630	Click to see C1=CC(=CC=C1C=O)OCC(=O)N	179.17	unknown	https://doi.org/10.1093/CHROMSCI/BMU012
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Isopropyl Myristate	8042	Click to see CCCCCCCCCCCCCC(=O)OC(C)C	270.50	unknown	https://doi.org/10.1093/CHROMSCI/BMU012
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl palmitate	8181	Click to see CCCCCCCCCCCCCCCC(=O)OC	270.50	unknown	https://doi.org/10.1093/CHROMSCI/BMU012
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
2-Acetoxytridecane	527409	Click to see CCCCCCCCCCCC(C)OC(=O)C	242.40	unknown	https://doi.org/10.1093/CHROMSCI/BMU012
Butyric acid, 2-tridecyl ester	551260	Click to see CCCCCCCCCCCC(C)OC(=O)CCC	270.50	unknown	https://doi.org/10.1093/CHROMSCI/BMU012
Undecyl cyclopropanecarboxylate	560134	Click to see CCCCCCCCCCCOC(=O)C1CC1	240.38	unknown	https://doi.org/10.1093/CHROMSCI/BMU012
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
2-[[9-Hydroxy-14-(hydroxymethyl)-3,10-dimethyl-6-propan-2-yl-8-tricyclo[9.3.0.03,7]tetradeca-1,6-dienyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	5088394	Click to see CC1C2CCC(C2=CC3(CCC(=C3C(C1O)OC4C(C(C(C(O4)CO)O)O)O)C(C)C)C)CO	482.60	unknown	https://doi.org/10.1248/YAKUSHI1947.103.11_1167 https://doi.org/10.1248/CPB.54.1425
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
(3S,8S,9R,10R,13R,14S,17R)-17-[(2R)-5,6-dihydroxy-6-methylheptan-2-yl]-3-hydroxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one	441813	Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CC(=O)C3(C2CC=C4C3CCC(C4(C)C)O)C)C)C	474.70	unknown	https://doi.org/10.1016/J.BMC.2011.08.030
(3S,8S,9R,10R,13R,14S,17R)-3-hydroxy-17-[(2R,5R)-6-hydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one	11093434	Click to see CC(CCC(C(C)(C)O)OC1C(C(C(C(O1)CO)O)O)O)C2CCC3(C2(CC(=O)C4(C3CC=C5C4CCC(C5(C)C)O)C)C)C	636.90	unknown	https://doi.org/10.1248/CPB.55.1082
Bryodulcosigenin	399493	Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CC(=O)C3(C2CC=C4C3CCC(C4(C)C)O)C)C)C	474.70	unknown	https://doi.org/10.1016/J.BMC.2011.08.030
Mogrol	14525327	Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CC(C3(C2CC=C4C3CCC(C4(C)C)O)C)O)C)C	476.70	unknown	https://doi.org/10.1248/YAKUSHI1947.103.11_1155
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(2R,3R,4S,5S,6R)-2-[[(1S,3R,6S,7R,8R,11R,12S,14S,15R,16R)-14-hydroxy-15-[(2S,3S)-3-hydroxy-6-methylhept-5-en-2-yl]-7,12,16-trimethyl-6-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163093940	Click to see CC(C1C(CC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)COC6C(C(C(C(O6)CO)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)O)C(CC=C(C)C)O	799.00	unknown	https://doi.org/10.1248/YAKUSHI1947.103.11_1151
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(3R,6R)-2-hydroxy-2-methyl-6-[(3S,8R,9R,10S,13R,14S,17R)-4,4,9,13,14-pentamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]heptan-3-yl]oxyoxan-2-yl]methoxy]oxane-3,4,5-triol	17752184	Click to see CC(CCC(C(C)(C)O)OC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)C3CCC4(C3(CCC5(C4CC=C6C5CCC(C6(C)C)OC7C(C(C(C(O7)CO)O)O)O)C)C)C	947.20	unknown	https://doi.org/10.1248/CPB.55.1082 https://doi.org/10.1021/NP068074X
(3S,8S,9R,10R,13R,14S,17R)-17-[(2R,5R)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-6-hydroxy-6-methylheptan-2-yl]-4,4,9,13,14-pentamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one	122706002	Click to see CC(CCC(C(C)(C)O)OC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)OC3C(C(C(C(O3)CO)O)O)O)C4CCC5(C4(CC(=O)C6(C5CC=C7C6CCC(C7(C)C)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)C)C	1285.40	unknown	https://doi.org/10.1248/CPB.38.2030
(3S,8S,9S,10R,11R,13R,14S,17R)-11-hydroxy-17-[(2R,5R)-6-hydroxy-6-methyl-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-4,4,9,13,14-pentamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,8,10,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-7-one	102086512	Click to see CC(CCC(C(C)(C)O)OC1C(C(C(C(O1)CO)O)O)O)C2CCC3(C2(CC(C4(C3C(=O)C=C5C4CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)O)C)C	815.00	unknown	https://doi.org/10.1021/NP068074X
(3S,8S,9S,10R,11R,13R,14S,17R)-17-[(2R,5R)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-6-hydroxy-6-methylheptan-2-yl]-11-hydroxy-4,4,9,13,14-pentamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-1,2,3,8,10,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-7-one	102086513	Click to see CC(CCC(C(C)(C)O)OC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)OC3C(C(C(C(O3)CO)O)O)O)C4CCC5(C4(CC(C6(C5C(=O)C=C7C6CCC(C7(C)C)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)O)C)C	1301.40	unknown	https://doi.org/10.1021/NP068074X
[(2S,3S,4R,5R,6S)-3,4,5-triacetyloxy-6-[[(3S,8R,9S,10S,11R,13R,14R,17R)-11-acetyloxy-17-[(2S,5R)-6-hydroxy-6-methyl-5-[(2R,3S,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyheptan-2-yl]-4,4,9,13,14-pentamethyl-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxan-2-yl]methyl acetate	163106770	Click to see CC(CCC(C(C)(C)O)OC1C(C(C(C(O1)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)C2CCC3(C2(CC(C4(C3CC=C5C4CCC(C5(C)C)OC6C(C(C(C(O6)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)C)OC(=O)C)C)C	1179.30	unknown	https://doi.org/10.1007/S11418-006-0130-7
11-Oxomogroside IIE	101412310	Click to see CC(CCC(C(C)(C)O)OC1C(C(C(C(O1)CO)O)O)O)C2CCC3(C2(CC(=O)C4(C3CC=C5C4CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C)C	799.00	unknown	https://doi.org/10.1248/CPB.55.1082
11-Oxomogroside III	17752183	Click to see CC(CCC(C(C)(C)O)OC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)C3CCC4(C3(CC(=O)C5(C4CC=C6C5CCC(C6(C)C)OC7C(C(C(C(O7)CO)O)O)O)C)C)C	961.10	unknown	https://doi.org/10.1248/CPB.55.1082
11-Oxomogroside IV A	17752301	Click to see CC(CCC(C(C)(C)O)OC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)C3CCC4(C3(CC(=O)C5(C4CC=C6C5CCC(C6(C)C)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O)C)C)C	1123.30	unknown	https://doi.org/10.1248/CPB.55.1082 https://doi.org/10.1021/NP068074X
17-[5-[4,5-Dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-6-hydroxy-6-methylheptan-2-yl]-11-hydroxy-4,4,9,13,14-pentamethyl-3-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-1,2,3,8,10,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-7-one	163104722	Click to see CC(CCC(C(C)(C)O)OC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)OC3C(C(C(C(O3)CO)O)O)O)C4CCC5(C4(CC(C6(C5C(=O)C=C7C6CCC(C7(C)C)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)O)C)C	1301.40	unknown	https://doi.org/10.1021/NP068074X
2-(hydroxymethyl)-6-[[3,4,5-trihydroxy-6-[2-hydroxy-6-[(9S,10R,13R,14S)-11-hydroxy-4,4,9,13,14-pentamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptan-3-yl]oxyoxan-2-yl]methoxy]oxane-3,4,5-triol	138108019	Click to see CC(CCC(C(C)(C)O)OC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)C3CCC4(C3(CC(C5(C4CC=C6C5CCC(C6(C)C)OC7C(C(C(C(O7)CO)O)O)O)C)O)C)C	963.20	unknown	https://doi.org/10.1248/CPB.38.2030
2-[[3,4-dihydroxy-6-[2-hydroxy-6-[(8S,9R,10S,13R,14S)-11-hydroxy-4,4,9,13,14-pentamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptan-3-yl]oxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	137705498	Click to see CC(CCC(C(C)(C)O)OC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)OC3C(C(C(C(O3)CO)O)O)O)C4CCC5(C4(CC(C6(C5CC=C7C6CCC(C7(C)C)OC8C(C(C(C(O8)CO)O)O)O)C)O)C)C	1125.30	unknown	https://doi.org/10.1248/CPB.38.2030
Mogroside II B	44423068	Click to see CC(CCC(C(C)(C)OC1C(C(C(C(O1)CO)O)O)O)O)C2CCC3(C2(CC(C4(C3CC=C5C4CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)O)C)C	801.00	unknown	https://doi.org/10.1021/NP068074X
Mogroside II E	133562524	Click to see CC(CCC(C(C)(C)O)OC1C(C(C(C(O1)CO)O)O)O)C2CCC3(C2(CC(C4(C3CC=C5C4CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)O)C)C	801.00	unknown	https://doi.org/10.1248/CPB.38.2030 https://doi.org/10.1248/YAKUSHI1947.103.11_1167
Mogroside III	24720988	Click to see CC(CCC(C(C)(C)O)OC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)C3CCC4(C3(CC(C5(C4CC=C6C5CCC(C6(C)C)OC7C(C(C(C(O7)CO)O)O)O)C)O)C)C	963.20	unknown	https://doi.org/10.1248/CPB.54.1425
Mogroside V	24721270	Click to see CC(CCC(C(C)(C)O)OC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)OC3C(C(C(C(O3)CO)O)O)O)C4CCC5(C4(CC(C6(C5CC=C7C6CCC(C7(C)C)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)O)C)C	1287.40	unknown	https://doi.org/10.1201/9781351074940 https://doi.org/10.1007/S11418-006-0130-7 https://doi.org/10.1248/YAKUSHI1947.103.11_1151 https://doi.org/10.1248/CPB.38.2030 https://doi.org/10.1021/JF00063A007 https://doi.org/10.1248/YAKUSHI1947.103.11_1167
MogrosideIV	145710145	Click to see CC(CCC(C(C)(C)O)OC1C(C(C(C(O1)CO)O)O)OC2C(C(C(C(O2)CO)O)O)O)C3CCC4(C3(CC(C5(C4CC=C6C5CCC(C6(C)C)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O)C)O)C)C	1125.30	unknown	https://doi.org/10.1248/YAKUSHI1947.103.11_1151 https://doi.org/10.1248/CPB.38.2030
> Organic oxygen compounds / Organic oxides
5-Ethylcyclopentene-1-carbaldehyde	580057	Click to see CCC1CCC=C1C=O	124.18	unknown	https://doi.org/10.1093/CHROMSCI/BMU012
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
Inositol	892	Click to see C1(C(C(C(C(C1O)O)O)O)O)O	180.16	unknown	https://doi.org/10.1016/0378-8741(90)90067-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal	19233	Click to see CC(C(C(C(C=O)O)O)O)O	164.16	unknown	https://doi.org/10.1016/0378-8741(90)90067-4
D-Galactose	6036	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	https://doi.org/10.1016/0378-8741(90)90067-4
L-Rhamnose	25310	Click to see CC1C(C(C(C(O1)O)O)O)O	164.16	unknown	https://doi.org/10.1016/0378-8741(90)90067-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
(2R,3S,4S)-2,3,4,5-tetrahydroxypentanal	5460291	Click to see C(C(C(C(C=O)O)O)O)O	150.13	unknown	https://doi.org/10.1016/0378-8741(90)90067-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Gavibamycin A3	85053916	Click to see CC1C(C(CC(O1)OC2C(OC3(CC2O)OC4C(OC(CC4(O3)C)OC5C(C(OC(C5OC)C)OC6C(OC(C(C6O)OC)OC7C(C8C(CO7)OC9(O8)C1C(C(C(O9)C)(C(C)O)O)OCO1)OC(=O)C(C)C)COC)O)C)C)O)OC(=O)C1=C(C(=C(C(=C1O)Cl)O)Cl)C	1392.20	unknown	https://doi.org/10.1248/YAKUSHI1947.103.11_1167
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol	6251	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	https://doi.org/10.1016/0378-8741(90)90067-4
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4-(3-Aminophenyl)-2-methyl-4-oxobutanoic acid	577816	Click to see CC(CC(=O)C1=CC(=CC=C1)N)C(=O)O	207.23	unknown	https://doi.org/10.1093/CHROMSCI/BMU012
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
4H-Pyran-4-one	7968	Click to see C1=COC=CC1=O	96.08	unknown	https://doi.org/10.1093/CHROMSCI/BMU012
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	154496827	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O	432.40	unknown	https://doi.org/10.1248/CPB.54.1425

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Siraitia grosvenorii

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