Language	Common/alternative name
English	mioga ginger
English	japanese ginger
English	myoga ginger
Azerbaijani	yapon zəncəfili
azb	ژاپون زنجفیلی
German	myoga
German	japanischer ingwer
Esperanto	miogo
Japanese	蘘荷
Japanese	鈍根草
Japanese	茗荷
Japanese	みょうが
Japanese	ミョウガ
Korean	양애
Korean	양하
lzh	蘘荷
Dutch	japanse gember
Polish	imbir japoński
Polish	imbir mioga
Portuguese	myoga
Thai	ขิงญี่ปุ่น
Vietnamese	myōga
Vietnamese	myoga
Chinese	茗荷
Chinese	野姜
Chinese	蘘荷花
Chinese	蘘荷子
Chinese	蘘荷

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name	Authority	First published in
Zingiber mioga var. variegatum	Makino	J. Jap. Bot. 6: 10. 1929

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Taiwan

Asia-tropical click to expand
- Indo-China
  - Vietnam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000617153
USDA Plants	ZIMI4
Tropicos	34500017
KEW	urn:lsid:ipni.org:names:798364-1
The Plant List	kew-273338
Open Tree Of Life	777753
NCBI Taxonomy	136225
IPNI	798364-1
iNaturalist	151801
GBIF	2757086
Freebase	/m/02c66f
EPPO	ZINMI
EOL	888221
USDA GRIN	42253
Wikipedia	Myoga

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

A journey from molecule to physiology and in silico tools for drug discovery targeting the transient receptor potential vanilloid type 1 (TRPV1) channel

Amaya-Rodriguez CA, Carvajal-Zamorano K, Bustos D, Alegría-Arcos M, Castillo K

Front Pharmacol

24-Jan-2024

PMCID:	PMC10847257
doi:	10.3389/fphar.2023.1251061
PMID:	38328578

The complete chloroplast genome of Hedychium flavum Roxb., an ornamental, edible and medicinal plant

Li MF, Xiao T, Zhang YH

Mitochondrial DNA B Resour

15-Nov-2023

PMCID:	PMC10653761
doi:	10.1080/23802359.2023.2281029
PMID:	38026495

The complete chloroplast genome sequence of Zingiber teres S. Q. Tong & Y. M. Xia (Zingiberaceae)

Wang X, Tian S, Wang H, Yang L, Zou X, Baskaran XR, Li Q, Xing H, Li HL

Mitochondrial DNA B Resour

25-Jun-2023

PMCID:	PMC10294729
doi:	10.1080/23802359.2023.2226256
PMID:	37383606

Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China

Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C

J Ethnobiol Ethnomed

30-May-2023

PMCID:	PMC10230803
doi:	10.1186/s13002-023-00594-4
PMID:	37254191

Modulating Effects of Zingiberaceae Phenolic Compounds on Neurotrophic Factors and Their Potential as Neuroprotectants in Brain Disorders and Age-Associated Neurodegenerative Disorders: A Review

Razak AM, Tan JK, Mohd Said M, Makpol S

Nutrients

30-May-2023

PMCID:	PMC10255673
doi:	10.3390/nu15112564
PMID:	37299526

Metabolomic responses to the mechanical wounding of Catharanthus roseus’ upper leaves

Chen Q, Jin Y, Guo X, Xu M, Wei G, Lu X, Tang Z

PeerJ

20-Mar-2023

PMCID:	PMC10035419
doi:	10.7717/peerj.14539
PMID:	36968002

Changes in homegardens in relocation villages, a case study in the Baiku Yao area in Southern China

Hu R, Xu C, Nong Y, Luo B

J Ethnobiol Ethnomed

27-Feb-2023

PMCID:	PMC9972620
doi:	10.1186/s13002-023-00578-4
PMID:	36849896

Healthy Zerumbone: From Natural Sources to Strategies to Improve Its Bioavailability and Oral Administration

Ibáñez MD, Sánchez-Ballester NM, Blázquez MA

Plants (Basel)

20-Dec-2022

PMCID:	PMC9823342
doi:	10.3390/plants12010005
PMID:	36616138

Biogeochemical niche conservatism relates to plant species diversification and life form evolution in a subtropical montane evergreen broad‐leaved forest

Bai K, Zhou X, Lv S, Wei S, Deng L, Tan Y

Ecol Evol

03-Dec-2022

PMCID:	PMC9719084
doi:	10.1002/ece3.9587
PMID:	36479033

Plants as Modulators of Melanogenesis: Role of Extracts, Pure Compounds and Patented Compositions in Therapy of Pigmentation Disorders

Merecz-Sadowska A, Sitarek P, Stelmach J, Zajdel K, Kucharska E, Zajdel R

Int J Mol Sci

26-Nov-2022

PMCID:	PMC9736547
doi:	10.3390/ijms232314787
PMID:	36499134

Advancements and future prospective of DNA barcodes in the herbal drug industry

Mahima K, Sunil Kumar KN, Rakhesh KV, Rajeswaran PS, Sharma A, Sathishkumar R

Front Pharmacol

21-Oct-2022

PMCID:	PMC9635000
doi:	10.3389/fphar.2022.947512
PMID:	36339543

An overview of remote monitoring methods in biodiversity conservation

Kerry RG, Montalbo FJ, Das R, Patra S, Mahapatra GP, Maurya GK, Nayak V, Jena AB, Ukhurebor KE, Jena RC, Gouda S, Majhi S, Rout JR

Environ Sci Pollut Res Int

05-Oct-2022

PMCID:	PMC9534007
doi:	10.1007/s11356-022-23242-y
PMID:	36197618

Synergistic Hypolipidemic Effects and Mechanisms of Phytochemicals: A Review

Liu Y, Liu C, Kou X, Wang Y, Yu Y, Zhen N, Jiang J, Zhaxi P, Xue Z

Foods

09-Sep-2022

PMCID:	PMC9497508
doi:	10.3390/foods11182774
PMID:	36140902

Plants of the Genus Zingiber: A Review of Their Ethnomedicine, Phytochemistry and Pharmacology

Deng M, Yun X, Ren S, Qing Z, Luo F

Molecules

29-Apr-2022

PMCID:	PMC9103766
doi:	10.3390/molecules27092826
PMID:	35566177

Identification of Inhibitory Activities of Dietary Flavonoids against URAT1, a Renal Urate Re-Absorber: In Vitro Screening and Fractional Approach Focused on Rooibos Leaves

Toyoda Y, Takada T, Saito H, Hirata H, Ota-Kontani A, Tsuchiya Y, Suzuki H

Nutrients

28-Jan-2022

PMCID:	PMC8839210
doi:	10.3390/nu14030575
PMID:	35276934

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 / Benzene and substituted derivatives
Phenylethyl Alcohol	6054	Click to see C1=CC=C(C=C1)CCO	122.16	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Benzenoids / Benzene and substituted derivatives / Toluenes
Toluene	1140	Click to see CC1=CC=CC=C1	92.14	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Benzenoids / Benzene and substituted derivatives / Xylenes / m-Xylenes
m-Xylene	7929	Click to see CC1=CC(=CC=C1)C	106.16	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Phenol	996	Click to see C1=CC=C(C=C1)O	94.11	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Benzenoids / Phenols / Methoxyphenols
Eugenol	3314	Click to see COC1=C(C=CC(=C1)CC=C)O	164.20	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Pentadecane	12391	Click to see CCCCCCCCCCCCCCC	212.41	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl dodecanoate	7800	Click to see CCCCCCCCCCCC(=O)OCC	228.37	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexanol	8103	Click to see CCCCCCO	102.17	unknown	https://doi.org/10.1271/BBB1961.55.1655
1-Hydroxyheptan-2-one	12691664	Click to see CCCCCC(=O)CO	130.18	unknown	https://doi.org/10.1271/BBB1961.55.1655
1-Octanol	957	Click to see CCCCCCCCO	130.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
2-Methylhexan-1-ol	43858	Click to see CCCCC(C)CO	116.20	unknown	https://doi.org/10.1271/BBB1961.55.1655
2-Nonanol	12367	Click to see CCCCCCCC(C)O	144.25	unknown	https://doi.org/10.1271/BBB1961.55.1655
2-Tridecanol	15449	Click to see CCCCCCCCCCCC(C)O	200.36	unknown	https://doi.org/10.1271/BBB1961.55.1655
2-Undecanol	15448	Click to see CCCCCCCCCC(C)O	172.31	unknown	https://doi.org/10.1271/BBB1961.55.1655
3-Octanol	11527	Click to see CCCCCC(CC)O	130.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Lipids and lipid-like molecules / Glycerolipids / Diradylglycerols / Diacylglycerols / 1,2-diacylglycerols
(2-Acetyloxy-3-hydroxypropyl) 3-methyl-5-(1,2,5,5-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-1-yl)pentanoate	73815547	Click to see CC1CCC2C(=CCCC2(C)C)C1(C)CCC(C)CC(=O)OCC(CO)OC(=O)C	422.60	unknown	https://doi.org/10.1271/BBB.66.2698
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2E)-2-[2-[(1S,2S,4aS,8aR)-2-formyl-5,5,8a-trimethyl-1,2,3,4,4a,6,7,8-octahydronaphthalen-1-yl]ethylidene]butanedial	11857930	Click to see CC1(CCCC2(C1CCC(C2CC=C(CC=O)C=O)C=O)C)C	318.40	unknown	https://doi.org/10.1271/BBB.60226
2-[2-(2-Formyl-5,5,8a-trimethyl-1,2,3,4,4a,6,7,8-octahydronaphthalen-1-yl)ethylidene]butanedial	73128902	Click to see CC1(CCCC2(C1CCC(C2CC=C(CC=O)C=O)C=O)C)C	318.40	unknown	https://doi.org/10.1271/BBB.60226
2-[2-(5,5,8a-trimethylspiro[3,4,4a,6,7,8-hexahydro-1H-naphthalene-2,2'-oxirane]-1-yl)ethylidene]butanedial	73819354	Click to see CC1(CCCC2(C1CCC3(C2CC=C(CC=O)C=O)CO3)C)C	318.40	unknown	https://doi.org/10.1271/BBB.60226 https://doi.org/10.1271/BBB.66.2698
8b,17-Epoxy-12E-labdene-15,16-dial	131752056	Click to see CC1(CCCC2(C1CCC3(C2CC=C(CC=O)C=O)CO3)C)C	318.40	unknown	https://doi.org/10.1271/BBB.66.2698
Aframodial	21668974	Click to see CC1(CCCC2(C1CCC3(C2CC=C(CC=O)C=O)CO3)C)C	318.40	unknown	https://doi.org/10.1271/BBB.60226 https://doi.org/10.1271/BBB.66.2698
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
2,6,11,15-Tetramethylhexadeca-2,7,10,14-tetraen-6-ol	71317439	Click to see CC(=CCCC(=CCC=CC(C)(CCC=C(C)C)O)C)C	290.50	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)-	5281553	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
beta-Ocimene, (3Z)-	5320250	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
Geranylacetone	1549778	Click to see CC(=CCCC(=CCCC(=O)C)C)C	194.31	unknown	https://doi.org/10.1271/BBB1961.55.1655
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1271/BBB1961.55.1655
Linalyl acetate	8294	Click to see CC(=CCCC(C)(C=C)OC(=O)C)C	196.29	unknown	https://doi.org/10.1271/BBB1961.55.1655
Methyl geranate	5365910	Click to see CC(=CCCC(=CC(=O)OC)C)C	182.26	unknown	https://doi.org/10.1271/BBB1961.55.1655
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
Neral	643779	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1271/BBB1961.55.1655
Thymol	6989	Click to see CC1=CC(=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1271/BBB1961.55.1655
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
Camphor	2537	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
Fenchol	15406	Click to see CC1(C2CCC(C2)(C1O)C)C	154.25	unknown	https://doi.org/10.1271/BBB1961.55.1655
Fenchone	14525	Click to see CC1(C2CCC(C2)(C1=O)C)C	152.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
Myrtenal	61130	Click to see CC1(C2CC=C(C1C2)C=O)C	150.22	unknown	https://doi.org/10.1271/BBB1961.55.1655
Myrtenol	10582	Click to see CC1(C2CC=C(C1C2)CO)C	152.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
Pinocarveol	102667	Click to see CC1(C2CC1C(=C)C(C2)O)C	152.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
trans-Borneol	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol	94221	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
2-Cyclohexen-1-one, 6-methyl-3-(1-methylethyl)-	10363	Click to see CC1CCC(=CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1271/BBB1961.55.1655
Beta-Phellandrene	11142	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
beta-Terpineol	8748	Click to see CC(=C)C1CCC(CC1)(C)O	154.25	unknown	https://doi.org/10.1271/BBB1961.55.1655
Carvone, (+/-)-	7439	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	https://doi.org/10.1271/BBB1961.55.1655
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
p-Menth-3-en-1-ol	11468	Click to see CC(C)C1=CCC(CC1)(C)O	154.25	unknown	https://doi.org/10.1271/BBB1961.55.1655
Perillaldehyde	16441	Click to see CC(=C)C1CCC(=CC1)C=O	150.22	unknown	https://doi.org/10.1271/BBB1961.55.1655
Piperitone	6987	Click to see CC1=CC(=O)C(CC1)C(C)C	152.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3R,6E)-nerolidol	11241545	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1271/BBB1961.55.1655
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane	6432312	Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C	204.35	unknown	https://doi.org/10.1271/BBB1961.55.1655
alpha-Cadinol	10398656	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1271/BBB1961.55.1655
beta-Ionone	638014	Click to see CC1=C(C(CCC1)(C)C)C=CC(=O)C	192.30	unknown	https://doi.org/10.1271/BBB1961.55.1655
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1271/BBB1961.55.1655
delta-Elemene	12309449	Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C	204.35	unknown	https://doi.org/10.1271/BBB1961.55.1655
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene	44583886	Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C	204.35	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1R,2R,3R,6R)-3-ethenyl-3,7,7-trimethyl-2-prop-1-en-2-ylbicyclo[4.1.0]heptane	101973934	Click to see CC(=C)C1C2C(C2(C)C)CCC1(C)C=C	204.35	unknown	https://doi.org/10.1271/BBB1961.55.1655
Beta-Elemene	6918391	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene	91723653	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Caryophyllene formate	93947	Click to see CC1(CC2C1CCC3(CCCC2(C3)OC=O)C)C	250.38	unknown	https://doi.org/10.1271/BBB1961.55.1655
Ethyl Acetate	8857	Click to see CCOC(=O)C	88.11	unknown	https://doi.org/10.1271/BBB1961.55.1655
Isoamyl acetate	31276	Click to see CC(C)CCOC(=O)C	130.18	unknown	https://doi.org/10.1271/BBB1961.55.1655
Propyl acetate	7997	Click to see CCCOC(=O)C	102.13	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Organic oxygen compounds / Organic oxides
(4aS,6aS,11aS,11bR)-4,4,11b-trimethyl-2,3,4a,5,6,6a,11,11a-octahydro-1H-cyclohepta[a]naphthalene-8,9-dicarbaldehyde	102479664	Click to see CC1(CCCC2(C1CCC3C2CC=C(C(=C3)C=O)C=O)C)C	300.40	unknown	https://doi.org/10.1271/BBB.80347
4,4,11b-trimethyl-2,3,4a,5,6,6a,11,11a-octahydro-1H-cyclohepta[a]naphthalene-8,9-dicarbaldehyde	162930383	Click to see CC1(CCCC2(C1CCC3C2CC=C(C(=C3)C=O)C=O)C)C	300.40	unknown	https://doi.org/10.1271/BBB.80347
beta-Cyclocitral	9895	Click to see CC1=C(C(CCC1)(C)C)C=O	152.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
1-Pentanol	6276	Click to see CCCCCO	88.15	unknown	https://doi.org/10.1271/BBB1961.55.1655
Isoamyl alcohol	31260	Click to see CC(C)CCO	88.15	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(6aS,11aR,11bS)-7-hydroxy-4,4,11b-trimethyl-1,2,3,4a,5,6,7,8,11,11a-decahydrocyclohepta[a]naphthalene-6a,9-dicarbaldehyde	5317450	Click to see CC1(CCCC2(C1CCC3(C2CC=C(CC3O)C=O)C=O)C)C	318.40	unknown	https://doi.org/10.1271/BBB.66.2698
1-Penten-3-OL	12020	Click to see CCC(C=C)O	86.13	unknown	https://doi.org/10.1271/BBB1961.55.1655
3-Pentanol	11428	Click to see CCC(CC)O	88.15	unknown	https://doi.org/10.1271/BBB1961.55.1655
7-Hydroxy-4,4,11b-trimethyl-1,2,3,4a,5,6,7,8,11,11a-decahydrocyclohepta[a]naphthalene-6a,9-dicarbaldehyde	14330184	Click to see CC1(CCCC2(C1CCC3(C2CC=C(CC3O)C=O)C=O)C)C	318.40	unknown	https://doi.org/10.1271/BBB.66.2698 https://doi.org/10.1271/BBB.80347
Galanal A	3050416	Click to see CC1(CCCC2(C1CCC3(C2CC=C(CC3O)C=O)C=O)C)C	318.40	unknown	https://doi.org/10.1271/BBB.66.2698 https://doi.org/10.1271/BBB.80347
Galanal B	3086504	Click to see CC1(CCCC2(C1CCC3(C2CC=C(CC3O)C=O)C=O)C)C	318.40	unknown	https://doi.org/10.1271/BBB.66.2698 https://doi.org/10.1271/BBB.80347
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
4-Isopropylcyclohexanol	20739	Click to see CC(C)C1CCC(CC1)O	142.24	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
2-Methyl-3-buten-2-OL	8257	Click to see CC(C)(C=C)O	86.13	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Heptanal	8130	Click to see CCCCCCC=O	114.19	unknown	https://doi.org/10.1271/BBB1961.55.1655
Hexanal	6184	Click to see CCCCCC=O	100.16	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Cyclohexanone	7967	Click to see C1CCC(=O)CC1	98.14	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
10-Undecen-2-one	118928	Click to see CC(=O)CCCCCCCC=C	168.28	unknown	https://doi.org/10.1271/BBB1961.55.1655
2-Decanone	12741	Click to see CCCCCCCCC(=O)C	156.26	unknown	https://doi.org/10.1271/BBB1961.55.1655
2-Dodecanone	22556	Click to see CCCCCCCCCCC(=O)C	184.32	unknown	https://doi.org/10.1271/BBB1961.55.1655
2-Heptanone	8051	Click to see CCCCCC(=O)C	114.19	unknown	https://doi.org/10.1271/BBB1961.55.1655
2-Nonanone	13187	Click to see CCCCCCCC(=O)C	142.24	unknown	https://doi.org/10.1271/BBB1961.55.1655
2-Tetradecanone	75364	Click to see CCCCCCCCCCCCC(=O)C	212.37	unknown	https://doi.org/10.1271/BBB1961.55.1655
2-Tridecanone	11622	Click to see CCCCCCCCCCCC(=O)C	198.34	unknown	https://doi.org/10.1271/BBB1961.55.1655
2-Undecanone	8163	Click to see CCCCCCCCCC(=O)C	170.29	unknown	https://doi.org/10.1271/BBB1961.55.1655
3-Octanone	246728	Click to see CCCCCC(=O)CC	128.21	unknown	https://doi.org/10.1271/BBB1961.55.1655
3-Pentanone	7288	Click to see CCC(=O)CC	86.13	unknown	https://doi.org/10.1271/BBB1961.55.1655
6-Methyl-5-hepten-2-one	9862	Click to see CC(=CCCC(=O)C)C	126.20	unknown	https://doi.org/10.1271/BBB1961.55.1655
Methyl isobutyl ketone	7909	Click to see CC(C)CC(=O)C	100.16	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Organoheterocyclic compounds / Benzothiazoles
Benzothiazole	7222	Click to see C1=CC=C2C(=C1)N=CS2	135.19	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Organoheterocyclic compounds / Diazines / Pyrazines / Methoxypyrazines
2-sec-Butyl-3-methoxypyrazine	520098	Click to see CCC(C)C1=NC=CN=C1OC	166.22	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Organoheterocyclic compounds / Dioxanes / 1,4-dioxanes
Dioxane	31275	Click to see C1COCCO1	88.11	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Organoheterocyclic compounds / Epoxides
2,2-Dimethyl-3-(3-methylenepent-4-enyl)oxirane	122371	Click to see CC1(C(O1)CCC(=C)C=C)C	152.23	unknown	https://doi.org/10.1271/BBB1961.55.1655
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Indole	798	Click to see C1=CC=C2C(=C1)C=CN2	117.15	unknown	https://doi.org/10.1271/BBB1961.55.1655

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Zingiber mioga

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