Gastrodia elata is a saprophytic perennial herb in the family Orchidaceae. It is found in Nepal, Bhutan, India, Japan, Korea, Siberia, Taiwan, and China, growing at elevations of 400–3,200 m (1,300–10,500 ft), at the edge of forests. It has an 8–12 cm long elliptical underground rhizome with a diameter of 3–5 cm, an erect stem of 0.3–1 m up to 2 m, and pale olivine or orange red flowers. It grows in symbiosis with the fungus Armillaria mellea on rotting wood, depending on the hypha of the fungus to invade the root system so that the plant can absorb nutrients from A. mellea. It produces 4-Hydroxybenzaldehyde and gastrodin, as well as 2,4-Bis(4-hydroxybenzyl) phenol, gastrol, gastrodigenin and other related compounds. It is used in traditional Chinese medicine and Sichuan cuisine, and has been shown to exert novel pain relief and inflammatory-mediating activities, as well as in vivo and in vitro inhibitory activity on nitric oxide

Synonyms Top

Scientific name	Authority	First published in
Gastrodia elata f. viridis	(Makino) Makino	Ill. Fl. Jap. 692 1940
Gastrodia elata var. pallens	Kitag.	Lin. Fl. Manshur. 151. 1939
Gastrodia elata var. viridis	(Makino) Makino	J. Jap. Bot. 1: 10 1916
Gastrodia elata f. alba	S.Chow	Acta Bot. Yunnan. 5: 366 (1983)
Gastrodia elata f. flavida	S.Chow	Acta Bot. Yunnan. 5: 366 (1983)
Gastrodia elata f. glauca	S.Chow	Acta Bot. Yunnan. 5: 365 (1983)
Gastrodia elata var. gracilis	Pamp.	Nuovo Giorn. Bot. Ital. n.s., 22: 271. 1915
Gastrodia elata f. pilifera	Tuyama	J. Jap. Bot. 17: 582 1941
Gastrodia mairei	Schltr.	Repert. Spec. Nov. Regni Veg. 12: 105 (1913)
Gastrodia viridis	Makino	Bot. Mag. (Tokyo) 16: 178 (1902)
Gastrodia elata var. obovata	Yue J.Zhang	Acta Bot. Boreal.-Occid. Sin. 30: 1277 (2010)

Common names Top

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Filter by language:

Language	Common/alternative name
English	tall gastrodia
English	orchid(orchidaceae)
Azerbaijani	hündür şişkinot
azb	هۆندور شیشکینوت
Japanese	オニノヤガラ
Korean	천마 (식물)
Korean	천마
lzh	赤箭
Russian	Гастродия высокая
Chinese	独摇
Chinese	離母
Chinese	赤箭脂
Chinese	自動草
Chinese	自动草
Chinese	离母
Chinese	獨搖芝
Chinese	獨搖
Chinese	独摇芝
Chinese	天麻
Chinese	水洋芋
Chinese	明天麻
Chinese	定风草
Chinese	定風草
Chinese	合離草
Chinese	合离草
Chinese	赤箭
Chinese	高赤箭
Chinese	还筒子

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 North-central
  - China South-central
  - China Southeast
  - Inner Mongolia
  - Manchuria
  - Tibet
- Eastern Asia
  - Japan
  - Korea
  - Taiwan
- Russian Far East
  - Khabarovsk
  - Kuril Islands
  - Primorye
  - Sakhalin

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - East Himalaya
  - Nepal

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000971542
UNII	ZK2B063E7Q
Tropicos	23507520
KEW	urn:lsid:ipni.org:names:635522-1
The Plant List	kew-88817
PFAF	Gastrodia elata
Open Tree Of Life	643482
NCBI Taxonomy	91201
IUCN Red List	46671
IPNI	635522-1
iNaturalist	429605
GBIF	2813351
Freebase	/m/02x98jm
EPPO	GSAEL
EOL	1112803
USDA GRIN	402591
Wikipedia	Gastrodia_elata
CMAUP	NPO22309

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_016760335.1	NIFOS_GasEla_1.0	Chromosome	National Institute of Forest Science, South Korea	2021-01-28	95.0x	0.97 Gb

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

Assembly and comparative analysis of the complete multichromosomal mitochondrial genome of Cymbidium ensifolium, an orchid of high economic and ornamental value

Shen B, Shen A, Liu L, Tan Y, Li S, Tan Z

BMC Plant Biol

09-Apr-2024

PMCID:	PMC11003039
doi:	10.1186/s12870-024-04962-4
PMID:	38594641

Oxidative Stress in Spinocerebellar Ataxia Type 3 and Its Attenuation by Herbal Remedies in Traditional Chinese Medicine: A Systematic Review

Mohd Hisam NS, Wong KH

Antioxidants (Basel)

19-Mar-2024

PMCID:	PMC10968558
doi:	10.3390/antiox13030375
PMID:	38539908

Comparative transcriptomics and proteomics analysis of the symbiotic germination of Paphiopedilum barbigerum with Epulorhiza sp. FQXY019

Tian F, Wang J, Ding F, Wang L, Yang Y, Bai X, Tan C, Liao X

Front Microbiol

18-Mar-2024

PMCID:	PMC10982344
doi:	10.3389/fmicb.2024.1358137
PMID:	38562471

The impact of thermal pretreatment on phytochemical profiles and bioactivity of freeze-dried lily bulbs (Lilium lancifolium)

Cai Y, Quan H, Liu Y, Han X, Lu Y, Lan X, Guo X

Food Chem X

15-Mar-2024

PMCID:	PMC10966175
doi:	10.1016/j.fochx.2024.101284
PMID:	38544934

The host sex contributes to the endophytic bacterial community in Sargassum thunbergii and their receptacles

Zhao Y, Sun T, Li Y, Yang Z, Chen J, Wang J, Yu X, Tang X, Xiao H

Front Microbiol

15-Mar-2024

PMCID:	PMC10978810
doi:	10.3389/fmicb.2024.1334918
PMID:	38559345

Chinese patent medicine combined with calcium channel blockers in the treatment of essential hypertension:a Bayes network meta-analysis and systematic review

Cui L, Liu X, Li Y, Jing T, Liu D, Ren C, Yin T, Wang Y, Zhao Z, Wang J, Han X, Wang L

Front Pharmacol

15-Mar-2024

PMCID:	PMC10978809
doi:	10.3389/fphar.2024.1321405
PMID:	38560355

Isolation, Bioactivity, and Molecular Docking of a Rare Gastrodin Isocitrate and Diverse Parishin Derivatives from Gastrodia elata Blume

Zhou J, Chen JQ, Gong S, Ban YJ, Zhang L, Liu Y, Wu JL, Li N

ACS Omega

14-Mar-2024

PMCID:	PMC10976414
doi:	10.1021/acsomega.4c00436
PMID:	38559968

Exploring the microbial ecosystem of Berchemia polyphylla var. leioclada: a comprehensive analysis of endophytes and rhizospheric soil microorganisms

Tang Y, Zhou S, Xiao Y, Zhang T, Tao X, Shi K, Lu Y, Yang Y, Zhao Y, Zhao T

Front Microbiol

13-Mar-2024

PMCID:	PMC10965698
doi:	10.3389/fmicb.2024.1338956
PMID:	38544861

Gut microbiota and its metabolites in Alzheimer’s disease: from pathogenesis to treatment

Zou X, Zou G, Zou X, Wang K, Chen Z

PeerJ

13-Mar-2024

PMCID:	PMC10944166
doi:	10.7717/peerj.17061
PMID:	38495755

A multi-center cross-sectional study of Chinese Herbal Medicine-Drug adverse reactions using active surveillance in Singapore’s Traditional Chinese Medicine clinics

Ng CY, Zhao Y, Wang N, Chia KL, Teo CH, Peh W, Yeo P, Zhong LL

Chin Med

07-Mar-2024

PMCID:	PMC10918936
doi:	10.1186/s13020-024-00915-z
PMID:	38454483

Interactions Between the Ubiquitin–Proteasome System, Nrf2, and the Cannabinoidome as Protective Strategies to Combat Neurodegeneration: Review on Experimental Evidence

Monsalvo-Maraver LA, Ovalle-Noguez EA, Nava-Osorio J, Maya-López M, Rangel-López E, Túnez I, Tinkov AA, Tizabi Y, Aschner M, Santamaría A

Neurotox Res

23-Feb-2024

PMCID:	PMC10891226
doi:	10.1007/s12640-024-00694-3
PMID:	38393521

Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China

Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X

J Ethnobiol Ethnomed

23-Feb-2024

PMCID:	PMC10893717
doi:	10.1186/s13002-024-00656-1
PMID:	38395900

First report of the complete mitochondrial genome of 3 beetles (Coleoptera: Scarabaeidae) harming Gastrodia elata (Asparagales: Orchidaceae)

Long T, Zhu W, Yang L, Long J, Chang Z, Chen X

J Insect Sci

22-Feb-2024

PMCID:	PMC10883712
doi:	10.1093/jisesa/ieae009
PMID:	38387434

Fungal communities associated with early immature tubers of wild Gastrodia elata

Li D, Jin X, Li Y, Wang Y, He H, Zhang H

Ecol Evol

21-Feb-2024

PMCID:	PMC10881901
doi:	10.1002/ece3.11004
PMID:	38389997

Austin-Type Meroterpenoids from Fungi Reported in the Last Five Decades: A Review

He JL, Chen CJ, Liu YH, Gao CH, Wang RP, Zhang WF, Bai M

J Fungi (Basel)

19-Feb-2024

PMCID:	PMC10890278
doi:	10.3390/jof10020162
PMID:	38392834

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 / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
14-Ethoxy-13-methyl-13,14-dihydro-[1,3]dioxolo[4',5':4,5]benzo[1,2-c][1,3]dioxolo[4,5-i]phenanthridine	5317235	Click to see CCOC1C2=C(C=CC3=C2OCO3)C4=C(N1C)C5=CC6=C(C=C5C=C4)OCO6	377.40	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
3-Hydroxybenzoate	54675842	Click to see C1=CC(=CC(=C1)[O-])C(=O)O	137.11	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	https://doi.org/10.1007/BF02973905
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
4-Hydroxybenzyl alcohol	125	Click to see C1=CC(=CC=C1CO)O	124.14	unknown	https://doi.org/10.1007/BF02980077 https://doi.org/10.1055/S-2001-18844 https://doi.org/10.1055/S-2006-957892 https://doi.org/10.1081/AL-100002599 https://doi.org/10.1007/BF02973905 https://doi.org/10.1248/CPB.29.55 https://doi.org/10.1007/BF02975302 https://doi.org/10.1016/J.PHYMED.2008.02.012 https://doi.org/10.1016/S0031-9422(02)00008-0 https://doi.org/10.1039/B103653J https://doi.org/10.1248/CPB.54.1720 https://doi.org/10.1093/CHROMSCI/39.6.251 https://doi.org/10.1081/JLC-100103395 https://doi.org/10.1016/0031-9422(95)00051-8 https://doi.org/10.1021/NP0605182 https://doi.org/10.1016/S0021-9673(99)00534-8
4-Methoxybenzyl alcohol	7738	Click to see COC1=CC=C(C=C1)CO	138.16	unknown	via CMAUP database
Benzyl Alcohol	244	Click to see C1=CC=C(C=C1)CO	108.14	unknown	https://doi.org/10.1007/BF02973905
> Benzenoids / Benzene and substituted derivatives / Benzyl sulfoxides / Benzyl alkyl sulfoxides
4,4'-[Sulfinylbis(methylene)]diphenol	54226032	Click to see C1=CC(=CC=C1CS(=O)CC2=CC=C(C=C2)O)O	262.33	unknown	https://doi.org/10.1016/S0031-9422(02)00008-0 https://doi.org/10.1021/NP0605182
> Benzenoids / Benzene and substituted derivatives / Benzylethers
4-(4'-Hydroxybenzyloxy)benzyl methyl ether	5318157	Click to see COCC1=CC=C(C=C1)OCC2=CC=C(C=C2)O	244.28	unknown	https://doi.org/10.1007/BF02973905 https://doi.org/10.1248/CPB.29.55
4-(Ethoxymethyl)phenol	93781	Click to see CCOCC1=CC=C(C=C1)O	152.19	unknown	https://doi.org/10.1021/NP0605182
4-(Methoxymethyl)phenol	79310	Click to see COCC1=CC=C(C=C1)O	138.16	unknown	https://doi.org/10.1007/BF02980077 https://doi.org/10.1021/NP0605182 https://doi.org/10.1007/BF02975302 https://doi.org/10.1248/CPB.29.55 https://doi.org/10.1016/S0031-9422(02)00008-0 https://doi.org/10.1055/S-2007-981619
5-[(4-Hydroxybenzyl)oxy]methyl-2-furaldehyde	53483405	Click to see C1=CC(=CC=C1COCC2=CC=C(O2)C=O)O	232.23	unknown	https://doi.org/10.1055/S-2007-981619
Benzyl methyl ether	10869	Click to see COCC1=CC=CC=C1	122.16	unknown	https://doi.org/10.1007/BF02973905
Bis-(4-hydroxybenzyl)ether	5315477	Click to see C1=CC(=CC=C1COCC2=CC=C(C=C2)O)O	230.26	unknown	https://doi.org/10.1016/S0031-9422(02)00008-0 https://doi.org/10.1021/NP0605182 https://doi.org/10.1007/BF02980077 https://doi.org/10.1016/0031-9422(95)00051-8
Phenol, 4-[[4-(ethoxymethyl)phenoxy]methyl]-	5317234	Click to see CCOCC1=CC=C(C=C1)OCC2=CC=C(C=C2)O	258.31	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
4-(4-Hydroxybenzyl)-2-methoxyphenol	15593817	Click to see COC1=C(C=CC(=C1)CC2=CC=C(C=C2)O)O	230.26	unknown	via CMAUP database
4-(Hydroxymethyl)-2-[(4-hydroxyphenyl)methyl]phenol	13699757	Click to see C1=CC(=CC=C1CC2=C(C=CC(=C2)CO)O)O	230.26	unknown	https://doi.org/10.1016/S0031-9422(02)00008-0
4-Hydroxy-3-[(4-hydroxyphenyl)methyl]benzaldehyde	11276243	Click to see C1=CC(=CC=C1CC2=C(C=CC(=C2)C=O)O)O	228.24	unknown	via CMAUP database
4,4'-Methanediylbis(2-methoxyphenol)	235387	Click to see COC1=C(C=CC(=C1)CC2=CC(=C(C=C2)O)OC)O	260.28	unknown	via CMAUP database
4,4'-Methylenediphenol	12111	Click to see C1=CC(=CC=C1CC2=CC=C(C=C2)O)O	200.23	unknown	https://doi.org/10.1016/S0031-9422(02)00008-0 https://doi.org/10.1007/BF02975302 https://doi.org/10.1007/BF02973905 https://doi.org/10.1016/0031-9422(95)00051-8
Gastrol	636636	Click to see C1=CC(=CC=C1CC2=C(C=CC(=C2)COCC3=CC=C(C=C3)O)O)O	336.40	unknown	https://doi.org/10.1016/S0031-9422(02)00008-0
> Benzenoids / Benzene and substituted derivatives / Phenylmethylamines
4-Hydroxybenzylamine	97472	Click to see C1=CC(=CC=C1CN)O	123.15	unknown	via CMAUP database
> Benzenoids / Phenol ethers
4-[(4-Hydroxybenzyl)oxy]benzyl alcohol	5318319	Click to see C1=CC(=CC=C1CO)OCC2=CC=C(C=C2)O	230.26	unknown	https://doi.org/10.1016/S0031-9422(02)00008-0
4-[[4-(Phenoxymethyl)phenoxy]methyl]phenol	163192565	Click to see C1=CC=C(C=C1)OCC2=CC=C(C=C2)OCC3=CC=C(C=C3)O	306.40	unknown	https://doi.org/10.1016/S0031-9422(02)00008-0
4-[[4-[[4-(Hydroxymethyl)phenoxy]methyl]phenoxy]methyl]phenol	101182041	Click to see C1=CC(=CC=C1CO)OCC2=CC=C(C=C2)OCC3=CC=C(C=C3)O	336.40	unknown	https://doi.org/10.1016/S0031-9422(02)00008-0
4-Ethoxybenzyl alcohol	80345	Click to see CCOC1=CC=C(C=C1)CO	152.19	unknown	via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-[[Hydroxy-[(4-hydroxyphenyl)methyl]amino]methyl]phenol	5317532	Click to see C1=CC(=CC=C1CN(CC2=CC=C(C=C2)O)O)O	245.27	unknown	via CMAUP database
Bis-(4-hydroxybenzyl)sulfide	23651847	Click to see C1=CC(=CC=C1CSCC2=CC=C(C=C2)O)O	246.33	unknown	https://doi.org/10.1021/NP0605182
> Benzenoids / Phenols / Benzenediols / Hydroquinones
Hydroquinone	785	Click to see C1=CC(=CC=C1O)O	110.11	unknown	https://doi.org/10.1021/NP0605182
> Benzenoids / Phenols / Methoxyphenols
2,3,6-Trideuterio-4-hydroxy-5-methoxybenzaldehyde	11389509	Click to see COC1=C(C=CC(=C1)C=O)O	155.17	unknown	via CMAUP database
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	https://doi.org/10.1055/S-2001-18844 https://doi.org/10.1016/S0021-9673(99)00534-8 https://doi.org/10.1007/BF02973905 https://doi.org/10.1039/B103653J https://doi.org/10.1007/BF02979066
Vanillyl alcohol	62348	Click to see COC1=C(C=CC(=C1)CO)O	154.16	unknown	https://doi.org/10.1007/BF02973905 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269714/ https://doi.org/10.1016/S0021-9673(99)00534-8 https://doi.org/10.1039/B103653J
> Benzenoids / Phenols / Tyrosols and derivatives
p-Hydroxybenzylmethylether	23050675	Click to see C1=CC(=CC=C1CCOCCC2=CC=C(C=C2)O)O	258.31	unknown	https://doi.org/10.1016/S0031-9422(02)00008-0 https://doi.org/10.1007/BF02980077 https://doi.org/10.1007/BF02975302
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Suchilactone	10915582	Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2=CC3=CC4=C(C=C3)OCO4)OC	368.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3S,4R,5S)-2-[[(1R,2S,3S)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol	9985078	Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(CO4)O)O)O	552.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	https://doi.org/10.1248/CPB.29.55
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
trimethyl 2-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropane-1,2,3-tricarboxylate	16097950	Click to see COC(=O)CC(CC(=O)OC)(C(=O)OC)OC1C(C(C(C(O1)CO)O)O)O	396.34	unknown	https://doi.org/10.1248/CPB.54.1720
Trimethyl 2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropane-1,2,3-tricarboxylate	162908618	Click to see COC(=O)CC(CC(=O)OC)(C(=O)OC)OC1C(C(C(C(O1)CO)O)O)O	396.34	unknown	https://doi.org/10.1248/CPB.54.1720
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Pseudolaric acid D	91895324	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C4)C(=O)O)C)CO	318.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids
[(1S,4S,5R,6R,9S,14R)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxo-7-tetracyclo[7.5.1.01,5.010,12]pentadeca-2,7-dienyl]methyl hexadecanoate	5318035	Click to see CCCCCCCCCCCCCCCC(=O)OCC1=CC2C3C(C3(C)C)CC(C4(C2=O)C=C(C(C4(C1O)O)O)C)C	586.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(R)-(+)-Citronellal	75427	Click to see CC(CCC=C(C)C)CC=O	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Illudanes and illudins / Melleolides and analogues
Armillarin	134206	Click to see CC1=CC(=CC(=C1C(=O)OC2CC3(C2(C(=CC4C3CC(C4)(C)C)C=O)O)C)O)OC	414.50	unknown	https://doi.org/10.1093/ACPROF:OSO/9780198570769.003.0002
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,3'R,4R,5R,6R,8S,10R,12S,13S,16R,21R,25R)-25-hydroxy-3',4,6,12,17,17-hexamethylspiro[9,18,22,23-tetraoxahexacyclo[14.7.2.01,13.04,12.05,10.021,25]pentacosane-8,5'-oxolane]-2',19-dione	21595102	Click to see CC1CC2(CC(C(=O)O2)C)OC3C1C4(CCC56CC7(C(CCC5C4(C3)C)C(OC(=O)CC7OO6)(C)C)O)C	532.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
deacetylpseudolaric acid A	11977243	Click to see CC1=CCC23CCC(C2(CC1)O)C(OC3=O)(C)C=CC=C(C)C(=O)O	346.40	unknown	via CMAUP database
Demethoxydeacetoxypseudolaric acid B	6475946	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(=CC3)C(=O)O)O)C(=O)O1)C)C(=O)O	376.40	unknown	via CMAUP database
Methyl pseudolarate A	91885219	Click to see CC1=CCC23CCC(C2(CC1)OC(=O)C)C(OC3=O)(C)C=CC=C(C)C(=O)OC	402.50	unknown	via CMAUP database
Methyl pseudolarate B	6475944	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(=CC3)C(=O)OC)OC(=O)C)C(=O)O1)C)C(=O)OC	446.50	unknown	via CMAUP database
Pseudolaric acid A	6436278	Click to see CC1=CCC23CCC(C2(CC1)OC(=O)C)C(OC3=O)(C)C=CC=C(C)C(=O)O	388.50	unknown	via CMAUP database
Pseudolaric acid B	6475943	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(=CC3)C(=O)OC)OC(=O)C)C(=O)O1)C)C(=O)O	432.50	unknown	via CMAUP database
Pseudolaric acid B-O-beta-D-glucopyranoside	10031398	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(=CC3)C(=O)OC)OC(=O)C)C(=O)O1)C)C(=O)OC4C(C(C(C(O4)CO)O)O)O	594.60	unknown	via CMAUP database
Pseudolaric acid C	6440704	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(=CC3)C(=O)OC)O)C(=O)O1)C)C(=O)O	390.40	unknown	via CMAUP database
pseudolaric acid C2	6475945	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(=CC3)C(=O)O)OC(=O)C)C(=O)O1)C)C(=O)O	418.40	unknown	via CMAUP database
Pseudolaric acid F	636647	Click to see CC1=CCC2(C3CCC2(CC1=O)C(=O)OC3(C)C=CC=C(C)C(=O)O)OC(=O)C	402.40	unknown	via CMAUP database
pseudolaric acid G	10894737	Click to see CC1=CCC2(C3CCC2(CC1O)C(=O)OC3(C)C=CC=C(C)C(=O)O)OC(=O)C	404.50	unknown	via CMAUP database
Pseudolaric acid H	11783999	Click to see CC1=CCC2(C3CCC2(C=C1)C(=O)OC3(C)C=CC=C(C)C(=O)O)OC(=O)C	386.40	unknown	via CMAUP database
PseudolaricacidAbeta-D-glucoside	44566375	Click to see CC1=CCC23CCC(C2(CC1)OC(=O)C)C(OC3=O)(C)C=CC=C(C)C(=O)OC4C(C(C(C(O4)CO)O)O)O	550.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Diosgenin	99474	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1	414.60	unknown	via CMAUP database
Pseudolarolide C	21592338	Click to see CC1CC2(CC(C(=O)O2)C)OC3C1C4(CCC56CC5(C(CCC6C4(C3)C)C(C)(C)O)CCC(=O)OC)C	516.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
3,23-Dioxocycloart-24-en-26-oic acid	21593999	Click to see CC(CC(=O)C=C(C)C(=O)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C	468.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	6432744	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
(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 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
(3S,8R,9R,10S,13R,14S,17R)-17-[(2R,5S)-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-ol	636741	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
17-(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-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1248/CPB.29.55 https://doi.org/10.1007/BF02975302 https://doi.org/10.1055/S-2007-981619
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1007/BF02975302 https://doi.org/10.1080/10286020290019730
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1055/S-2007-981619
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/10.1055/S-2007-981619
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/10.1055/S-2007-981619
> Nucleosides, nucleotides, and analogues / Purine nucleosides
(2R,3R,4S,5R)-2-(6-aminopurin-9-yl)-5-(hydroxymethyl)-2-[(4-hydroxyphenyl)methyl]oxolane-3,4-diol	66589628	Click to see C1=CC(=CC=C1CC2(C(C(C(O2)CO)O)O)N3C=NC4=C(N=CN=C43)N)O	373.40	unknown	https://doi.org/10.1002/JSSC.200600469
2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol	191	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	unknown	https://doi.org/10.1021/NP0605182
2-(Hydroxymethyl)-5-[6-[(4-hydroxyphenyl)methylamino]purin-9-yl]oxolane-3,4-diol	59690894	Click to see C1=CC(=CC=C1CNC2=C3C(=NC=N2)N(C=N3)C4C(C(C(O4)CO)O)O)O	373.40	unknown	https://doi.org/10.1021/NP0605182
2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)-2-[(4-hydroxyphenyl)methyl]oxolan-2-yl]-1H-purin-6-one	163187977	Click to see C1=CC(=CC=C1CC2(C(C(C(O2)CO)O)O)N3C=NC4=C3N=C(NC4=O)N)O	389.40	unknown	https://doi.org/10.1002/JSSC.200600469
2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one	6802	Click to see C1=NC2=C(N1C3C(C(C(O3)CO)O)O)NC(=NC2=O)N	283.24	unknown	via CMAUP database
9-alpha-Ribofuranosyladenine	448378	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	unknown	https://doi.org/10.1021/NP0605182
Adenosine	60961	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	unknown	https://doi.org/10.1021/NP0605182
N6-(4-Hydroxybenzyl)-adenosine	10474479	Click to see C1=CC(=CC=C1CNC2=C3C(=NC=N2)N(C=N3)C4C(C(C(O4)CO)O)O)O	373.40	unknown	https://doi.org/10.1021/NP0605182
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Uridine	6029	Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O	244.20	unknown	https://doi.org/10.1021/NP0605182
Yridine	7059438	Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O	244.20	unknown	https://doi.org/10.1021/NP0605182
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Glycine, N-[N-L-g-glutamyl-S-[(4-hydroxyphenyl)methyl]-L-cysteinyl]-	53865860	Click to see C1=CC(=CC=C1CSCC(C(=O)NCC(=O)O)NC(=O)CCC(C(=O)O)N)O	413.40	unknown	https://doi.org/10.1016/0031-9422(94)00771-K
S-(4-Hydroxybenzyl)glutathione	10364396	Click to see C1=CC(=CC=C1CSCC(C(=O)NCC(=O)O)NC(=O)CCC(C(=O)O)N)O	413.40	unknown	https://doi.org/10.1016/0031-9422(94)00771-K
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Butanedioate;hydron	21952380	Click to see [H+].[H+].C(CC(=O)[O-])C(=O)[O-]	118.09	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(2S,3S,4R)-4-methoxy-6-oxo-2-[(E,3S,5R,6S)-3,5,6-triacetyloxyhept-1-enyl]oxan-3-yl] acetate	101267306	Click to see CC(C(CC(C=CC1C(C(CC(=O)O1)OC)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C	458.50	unknown	https://doi.org/10.1021/NP0605182
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron	88113319	Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O	192.12	unknown	via CMAUP database
Trimethyl citrate	74112	Click to see COC(=O)CC(CC(=O)OC)(C(=O)OC)O	234.20	unknown	https://doi.org/10.1021/NP0605182
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
alpha-D-Glucopyranoside, beta-D-fructofuranosyl	91692850	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	via CMAUP database
D-Alt(a1-2a)L-Psif	53301851	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	via CMAUP database
Sucrose	5988	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	https://doi.org/10.1093/CHROMSCI/39.6.251 https://doi.org/10.1039/B103653J
Sucrose NF	46782954	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[4-(hydroxymethyl)phenoxy]oxane-3,4,5-triol	154496023	Click to see C1=CC(=CC=C1CO)OC2C(C(C(C(O2)CO)O)O)O	286.28	unknown	https://doi.org/10.1021/NP0605182
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-(methoxymethyl)phenoxy]oxane-3,4,5-triol	91166794	Click to see COCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O	300.30	unknown	https://doi.org/10.1021/NP0605182
(3R)-3-hydroxy-5-oxo-5-[[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methoxy]-3-[[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methoxycarbonyl]pentanoic acid	162861016	Click to see C1=CC(=CC=C1COC(=O)CC(CC(=O)O)(C(=O)OCC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	728.60	unknown	https://doi.org/10.1016/0031-9422(95)00955-8
1,3-bis(4-(D-glucopyranosyloxy)benzyl)citrate	75144772	Click to see C1=CC(=CC=C1COC(=O)CC(CC(=O)OCC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)(C(=O)O)O)OC4C(C(C(C(O4)CO)O)O)O	728.60	unknown	https://doi.org/10.1016/0031-9422(95)00955-8
2-(Hydroxymethyl)-6-[4-(hydroxymethyl)phenoxy]oxane-3,4,5-triol	3645183	Click to see C1=CC(=CC=C1CO)OC2C(C(C(C(O2)CO)O)O)O	286.28	unknown	https://doi.org/10.1055/S-2006-957892 https://doi.org/10.1021/NP0605182 https://doi.org/10.1248/CPB.29.55 https://doi.org/10.1055/S-2007-981619
2-(Hydroxymethyl)-6-[4-(methoxymethyl)phenoxy]oxane-3,4,5-triol	156343008	Click to see COCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O	300.30	unknown	https://doi.org/10.1021/NP0605182
2-(Hydroxymethyl)-6-[4-[(4-hydroxyphenyl)methoxymethyl]phenoxy]oxane-3,4,5-triol	73157714	Click to see C1=CC(=CC=C1COCC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O	392.40	unknown	https://doi.org/10.1248/CPB.29.55
2-hydroxy-4-oxo-2-[2-oxo-2-[[4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methoxy]ethyl]-4-[[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methoxy]butanoic acid	46173915	Click to see C1=CC(=CC=C1COC(=O)CC(CC(=O)OCC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)(C(=O)O)O)OC4C(C(C(C(O4)CO)O)O)O	728.60	unknown	via CMAUP database
2-O-[4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl] 1-O-[[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl] 3-O-[[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]methyl] 2-hydroxypropane-1,2,3-tricarboxylate	44421666	Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)COC(=O)CC(CC(=O)OCC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)(C(=O)OC5=CC=C(C=C5)OC6C(C(C(C(O6)CO)O)O)O)O)O)O)O	966.90	unknown	via CMAUP database
3-Hydroxy-5-oxo-5-[[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methoxy]-3-[[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methoxycarbonyl]pentanoic acid	75061243	Click to see C1=CC(=CC=C1COC(=O)CC(CC(=O)O)(C(=O)OCC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	728.60	unknown	https://doi.org/10.1016/0031-9422(95)00955-8
Citricacidtris(p-beta-D-glucopyranosyloxybenzyl)ester	85185120	Click to see C1=CC(=CC=C1COC(=O)CC(CC(=O)OCC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)(C(=O)OCC4=CC=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)O)OC6C(C(C(C(O6)CO)O)O)O	996.90	unknown	https://doi.org/10.1016/S0021-9673(98)00120-4 https://doi.org/10.1016/S0021-9673(98)00036-3 https://doi.org/10.1016/0031-9422(95)00955-8 https://doi.org/10.1007/BF02976550 https://doi.org/10.1248/CPB.29.55
Gastrodin	115067	Click to see C1=CC(=CC=C1CO)OC2C(C(C(C(O2)CO)O)O)O	286.28	unknown	https://doi.org/10.1007/BF02980077 https://doi.org/10.1055/S-2006-957892 https://doi.org/10.1081/AL-100002599 https://doi.org/10.1248/CPB.29.55 https://doi.org/10.1016/J.PHYMED.2008.02.012 https://doi.org/10.1007/BF02976550 https://doi.org/10.1039/B103653J https://doi.org/10.1093/CHROMSCI/39.6.251 https://doi.org/10.1081/JLC-100103395 https://doi.org/10.1055/S-2007-981619 https://doi.org/10.1021/NP0605182 https://doi.org/10.1016/S0021-9673(99)00534-8
Gastrodioside	11972303	Click to see C1=CC(=CC=C1COCC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O	392.40	unknown	https://doi.org/10.1248/CPB.29.55
Parishin	10557926	Click to see C1=CC(=CC=C1COC(=O)CC(CC(=O)OCC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)(C(=O)OCC4=CC=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)O)OC6C(C(C(C(O6)CO)O)O)O	996.90	unknown	https://doi.org/10.1016/0031-9422(95)00955-8 https://doi.org/10.1021/NP0605182 https://doi.org/10.1248/CPB.29.55
Parishin B	44715528	Click to see C1=CC(=CC=C1COC(=O)CC(CC(=O)O)(C(=O)OCC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	728.60	unknown	via CMAUP database
Parishin C	10676408	Click to see C1=CC(=CC=C1COC(=O)CC(CC(=O)OCC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)(C(=O)O)O)OC4C(C(C(C(O4)CO)O)O)O	728.60	unknown	https://doi.org/10.1016/0031-9422(95)00955-8
Parishin E	91973797	Click to see C1=CC(=CC=C1COC(=O)CC(CC(=O)O)(C(=O)O)O)OC2C(C(C(C(O2)CO)O)O)O	460.40	unknown	https://doi.org/10.1002/JSSC.200600469
Suffruticoside A	9986231	Click to see CC(=O)C1=C(C=C(C=C1)OC)OC2C(C(C(C(O2)COC3C(C(CO3)(COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)O)O	612.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-(-)-Fructose	5984	Click to see C(C(C(C(C(=O)CO)O)O)O)O	180.16	unknown	https://doi.org/10.1093/CHROMSCI/39.6.251 https://doi.org/10.1039/B103653J
D-Fructose	2723872	Click to see C1C(C(C(C(O1)(CO)O)O)O)O	180.16	unknown	https://doi.org/10.1093/CHROMSCI/39.6.251 https://doi.org/10.1039/B103653J
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal	107526	Click to see C(C(C(C(C(C=O)O)O)O)O)O	180.16	unknown	https://doi.org/10.1039/B103653J
D-Glucose	5793	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	https://doi.org/10.1093/CHROMSCI/39.6.251 https://doi.org/10.1039/B103653J
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Glycoprotein	439212	Click to see CC(=O)NC1C(C(C(OC1NC(=O)CC(C(=O)N)NC(=O)C)CO)OC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)CO)O)O)O)O)NC(=O)C)O	741.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269714/
> 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	https://doi.org/10.1055/S-2007-981619 https://doi.org/10.1021/NP0605182
5,5'-Oxybis(5-methylene-2-furaldehyde)	12366272	Click to see C1=C(OC(=C1)C=O)COCC2=CC=C(O2)C=O	234.20	unknown	https://doi.org/10.1007/BF02980077
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
1-Furan-2-yl-2-(4-hydroxyphenyl)-ethanone	80097762	Click to see C1=COC(=C1)C(=O)CC2=CC=C(C=C2)O	202.21	unknown	https://doi.org/10.1055/S-2007-981619
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde	126	Click to see C1=CC(=CC=C1C=O)O	122.12	unknown	https://doi.org/10.1248/CPB.29.55 https://doi.org/10.1016/S0031-9422(02)00008-0 https://doi.org/10.1093/CHROMSCI/39.6.251 https://doi.org/10.1055/S-2001-18844 https://doi.org/10.1016/S0021-9673(99)00534-8 https://doi.org/10.1081/JLC-100103395 https://doi.org/10.1007/BF02973905 https://doi.org/10.1016/J.PHYMED.2008.02.012 https://doi.org/10.1039/B103653J https://doi.org/10.1007/BF02980077 https://doi.org/10.1007/BF02979066 https://doi.org/10.1007/BF02975302 https://doi.org/10.1021/NP0605182
p-Hydroxybenzaldehyde-d5	10701848	Click to see C1=CC(=CC=C1C=O)O	127.15	unknown	via CMAUP database
Protocatechualdehyde	8768	Click to see C1=CC(=C(C=C1C=O)O)O	138.12	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrazines
2,3,5,6-Tetramethylpyrazine	14296	Click to see CC1=C(N=C(C(=N1)C)C)C	136.19	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Hydroxypyrimidines
5-methylpyrimidine-2,4-diol	5274265	Click to see CC1=CN=C(N=C1O)O	126.11	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
Cytosine	597	Click to see C1=C(NC(=O)N=C1)N	111.10	unknown	via CMAUP database
Uracil	1174	Click to see C1=CNC(=O)NC1=O	112.09	unknown	via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
Adenine	190	Click to see C1=NC2=NC=NC(=C2N1)N	135.13	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
4-[[(1R)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-2-[4-[(6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenoxy]phenol	45358120	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC5C6=CC(=C(C=C6CCN5C)OC)OC)O)OC)OC	624.80	unknown	via CMAUP database
> Organoheterocyclic compounds / Pteridines and derivatives / Pterins and derivatives / Biopterins and derivatives
2-amino-6-(1,2-dihydroxypropyl)-1,8-dihydropteridine-4,7-dione	6325360	Click to see CC(C(C1=NC2=C(NC1=O)NC(=NC2=O)N)O)O	253.22	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Aurone flavonoids / Auronols
(2S)-2-[(3,5-dihydroxy-4-methoxyphenyl)methyl]-2,4,6-trihydroxy-1-benzofuran-3-one	92298899	Click to see COC1=C(C=C(C=C1O)CC2(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	334.28	unknown	via CMAUP database
(2S)-2,4,6-trihydroxy-2-[(3,4,5-trihydroxyphenyl)methyl]-1-benzofuran-3-one	92299930	Click to see C1=C(C=C(C(=C1O)O)O)CC2(C(=O)C3=C(C=C(C=C3O2)O)O)O	320.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Depsides and depsidones
[4-[4-[2-[2-[4-[4-(4-Hydroxybenzoyl)oxybenzoyl]oxyphenyl]ethoxy]ethyl]phenoxy]carbonylphenyl] 4-hydroxybenzoate	163192600	Click to see C1=CC(=CC=C1CCOCCC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OC(=O)C4=CC=C(C=C4)O)OC(=O)C5=CC=C(C=C5)OC(=O)C6=CC=C(C=C6)O	738.70	unknown	https://doi.org/10.1007/BF02980077
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
2,4-Bis(4-hydroxybenzyl)phenol	193195	Click to see C1=CC(=CC=C1CC2=CC(=C(C=C2)O)CC3=CC=C(C=C3)O)O	306.40	unknown	https://doi.org/10.1016/S0031-9422(02)00008-0 https://doi.org/10.1016/0031-9422(95)00051-8
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
4,4'-Dihydroxybibenzyl	80152	Click to see C1=CC(=CC=C1CCC2=CC=C(C=C2)O)O	214.26	unknown	https://doi.org/10.1021/NP0605182

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Gastrodia elata

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