Alpinia galanga

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID643ff1851217a233020831
Scientific name	Alpinia galanga
Authority	(L.) Willd.
First published in	Willd., Sp. Pl. 1 (1):12. (1797); Lectotypified in: Edinburgh J. Bot. 57. (2000)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Alpinia alba	(Retz.) Roscoe	Trans. Linn. Soc. London 8:346. (1807)
Alpinia bifida	Warb.	Bot. Jahrb. Syst. 13:275. (1891)
Alpinia carnea	Griff.	Not. pl. asiat. 420
Alpinia pyramidata	Blume	Enum. pl. Javae 58
Alpinia rheedei	Wight	Icon. pl. Ind. orient. 19, t.2026
Alpinia viridiflora	Griff.	Not. pl. asiat. 423
Alpinia zingiberina	Hook.f.	Bot. Mag. 113:t.6944. (1887)
Amomum galanga	(L.) Lour.	Fl. cochinch. 5
Amomum medium	Lour.	Fl. cochinch. 4
Heritiera alba	Retz.	Observ. bot. 18
Languas galanga	(L.) Stuntz	U. S. D. A. Bur. Pl. Industr. Bull. 261:21. (1912); Lectotypified in: Edinburgh J. Bot. 57. (2000)
Languas pyramidata	(Blume) Merr.	Enum. Philipp. fl. pl. 233
Maranta galanga	L.	Sp. Pl. ed. 2 : 3 (1762)
Zingiber galanga	(L.) Stokes	Bot. mat. med. 72
Zingiber medium	(Lour.) Stokes	Bot. mat. med. 72
Zingiber sylvestre	Gaertn.	Fruct. sem. pl. 34
Alpinia galanga var. zingiberina	(Hook.f.) Baker

Common names Top

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Filter by language:

Language	Common/alternative name
English	greater galangal
Spanish	languas vulgare
Spanish	zingiber galanga
Spanish	zingiber medium
Spanish	zingiber sylvestre
Spanish	maranta galanga
Spanish	languas pyramidata
Spanish	languas galanga
Spanish	heritiera alba
Spanish	hellenia alba
Spanish	galanga major
Spanish	amomum galanga
Spanish	alpinia viridiflora
Spanish	alpinia rheedei
Spanish	alpinia bifida
Spanish	alpinia alba
Spanish	amomum medium
Arabic	خولنجان كبير
Azerbaijani	languas vulgare
Azerbaijani	languas pyramidata
Azerbaijani	languas galanga
Azerbaijani	heritiera alba
Azerbaijani	hellenia alba
Azerbaijani	böyük qalanqa
Azerbaijani	amomum medium
Azerbaijani	amomum galanga
Azerbaijani	alpinia viridiflora
Azerbaijani	alpinia rheedei
Azerbaijani	alpinia bifida
Azerbaijani	alpinia alba
Azerbaijani	maranta galanga
Azerbaijani	zingiber galanga
Azerbaijani	zingiber medium
Azerbaijani	zingiber sylvestre
Azerbaijani	alpiniya qalanqa
ban	isén
bcl	langkawas
Bengali	সুগন্ধাবচ
Catalan	alpinia officinarum
Czech	galgán velký
German	galanga
German	galangawurzel
German	maranta galanga
German	thai-ingwer
Esperanto	galango
Basque	alpinia
Hebrew	גלנגל
Indonesian	kelawas
Indonesian	laos
Indonesian	lengkuas
Italian	galanga
Japanese	サンキョウ
Japanese	ナンキョウソウ
jv	laos
Kannada	ರಾನ್ನ
Korean	큰고량강
lo	ຂ່າ
Latvian	alpīnija
Latvian	galangals
lzh	廉薑
min	langkuweh
Malayalam	വലിയ അരത്ത
Malay	pokok lengkuas
Malay	lengkuas
Burmese	ပတဲကောကြီး
Dutch	laos
Dutch	thaise gember
Dutch	laoskruid
Dutch	galanga
pam	langkwas
Polish	alpinia galgant
Polish	gałgant chiński
Polish	dziki kardamon
Slovak	alpínia galangová
su	laja
Swedish	stor galangarot
Tamil	பேரரத்தை
Tamil	அரத்தை
Telugu	దుంపరాష్ట్రము
Thai	ข่า
Vietnamese	riềng nếp
Chinese	蠻薑
Chinese	南薑
Chinese	大高良薑
Chinese	廉薑
Chinese	高良薑
Chinese	红豆蔻（大高良姜）
Chinese	良薑
Chinese	大良薑
Chinese	大高良姜
Chinese	山姜子
Chinese	紅荳蔻
Chinese	红豆蔻

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Alpinia galanga var. pyramidata	(Blume) K.Schum.	Bot. Jahrb. Syst. 28: 275. 1899

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
  - Hainan
- Eastern Asia
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - India
  - Sri Lanka
- Indo-China
  - Cambodia
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Malaya
  - Philippines
  - Sumatera

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000338490
UNII	3S1W839C0O
USDA Plants	ALGA2
Tropicos	34500284
INPN	853532
KEW	urn:lsid:ipni.org:names:795279-1
The Plant List	kew-218790
Plantarium	67846
Missouri Botanical Garden	287591
Open Tree Of Life	1063872
NCBI Taxonomy	94327
IPNI	795279-1
iNaturalist	123732
GBIF	5302225
Freebase	/m/0f9p0f
EPPO	AIIGA
EOL	1126897
USDA GRIN	2666
Wikipedia	Alpinia_galanga
CMAUP	NPO5033

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_037177395.1	ASM3717739v1	Scaffold	Iridian Genomes	2024-03-15	60.0x	864.90 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

A comprehensive review of ethnomedicinal approaches, phytochemical analysis, and pharmacological potential of Vitex trifolia L.

Mottaghipisheh J, Kamali M, Doustimotlagh AH, Nowroozzadeh MH, Rasekh F, Hashempur MH, Iraji A

Front Pharmacol

21-Mar-2024

PMCID:	PMC10991721
doi:	10.3389/fphar.2024.1322083
PMID:	38576489

Natural products reverse cancer multidrug resistance

Zou JY, Chen QL, Luo XC, Damdinjav D, Abdelmohsen UR, Li HY, Battulga T, Chen HB, Wang YQ, Zhang JY

Front Pharmacol

08-Mar-2024

PMCID:	PMC10988293
doi:	10.3389/fphar.2024.1348076
PMID:	38572428

Hyperuricemia research progress in model construction and traditional Chinese medicine interventions

Zhou H, Yang J, Yuan X, Song X, Zhang X, Cao T, Zhang J

Front Pharmacol

07-Mar-2024

PMCID:	PMC10955118
doi:	10.3389/fphar.2024.1294755
PMID:	38515855

Phytochemical Profiling and Antioxidant Activities of the Most Favored Ready-to-Use Thai Curries, Pad-Ka-Proa (Spicy Basil Leaves) and Massaman

Siripongvutikorn S, Pumethakul K, Yupanqui CT, Seechamnanturakit V, Detarun P, Utaipan T, Sirinupong N, Chansuwan W, Wittaya T, Samakradhamrongthai RS

Foods

14-Feb-2024

PMCID:	PMC10887624
doi:	10.3390/foods13040582
PMID:	38397559

Antioxidant and Nitric Oxide Inhibitory Activity of the Six Most Popular Instant Thai Curries

Siripongvutikorn S, Pumethakul K, Yupanqui CT, Seechamnanturakit V, Detarun P, Utaipan T, Sirinupong N, Chansuwan W, Wittaya T, Samakradhamrongthai RS

Foods

05-Jan-2024

PMCID:	PMC10814089
doi:	10.3390/foods13020178
PMID:	38254479

Ethnobotanical study of medicinal plants used by the indigenous community of the western region of Mizoram, India

Ralte L, Sailo H, Singh YT

J Ethnobiol Ethnomed

03-Jan-2024

PMCID:	PMC10765666
doi:	10.1186/s13002-023-00642-z
PMID:	38172927

Ethnobotany and phytochemistry of plants used to treat musculoskeletal disorders among Skaw Karen, Thailand

Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A

Pharm Biol

22-Dec-2023

PMCID:	PMC10763916
doi:	10.1080/13880209.2023.2292261
PMID:	38131672

Assessing deep convolutional neural network models and their comparative performance for automated medicinal plant identification from leaf images

Dey B, Ferdous J, Ahmed R, Hossain J

Heliyon

13-Dec-2023

PMCID:	PMC10767391
doi:	10.1016/j.heliyon.2023.e23655
PMID:	38187334

Honey infused with herbs: A boon to cure pathological diseases

Kumar S, Verma M, Hajam YA, Kumar R

Heliyon

04-Dec-2023

PMCID:	PMC10755321
doi:	10.1016/j.heliyon.2023.e23302
PMID:	38163184

Complete resolution of lumbar disc sequestration with Ayurveda management: A case report

Wasedar V, Pangam B, Shete S, Belaval V

J Ayurveda Integr Med

25-Nov-2023

PMCID:	PMC10785238
doi:	10.1016/j.jaim.2023.100826
PMID:	38006747

Comparison of Metabolites and Species Classification of Thirteen Zingiberaceae Spices Based on GC–MS and Multi-Spectral Fusion Technology

Wen H, Yang T, Yang W, Yang M, Wang Y, Zhang J

Foods

10-Oct-2023

PMCID:	PMC10606731
doi:	10.3390/foods12203714
PMID:	37893607

Ethnobotanical study on edible flowers in Xishuangbanna, China

Zhang Q, Cheng Z, Fan Y, Zhang D, Wang M, Zhang J, Sommano S, Wu X, Long C

J Ethnobiol Ethnomed

30-Sep-2023

PMCID:	PMC10542681
doi:	10.1186/s13002-023-00608-1
PMID:	37777741

Naturally occurring phenylethanoids and phenylpropanoids: antimalarial potential

Abdelmohsen UR, Bayoumi SA, Mohamed NM, Mostafa YA, Ngwa CJ, Pradel G, Farag SF

RSC Adv

07-Sep-2023

PMCID:	PMC10483269
doi:	10.1039/d3ra04242a
PMID:	37692342

Spice-Derived Phenolic Compounds: Potential for Skin Cancer Prevention and Therapy

Baloghová J, Michalková R, Baranová Z, Mojžišová G, Fedáková Z, Mojžiš J

Molecules

25-Aug-2023

PMCID:	PMC10489044
doi:	10.3390/molecules28176251
PMID:	37687080

Natural Coumarin Shows Toxicity to Spodoptera litura by Inhibiting Detoxification Enzymes and Glycometabolism

Xia T, Liu Y, Lu Z, Yu H

Int J Mol Sci

24-Aug-2023

PMCID:	PMC10488291
doi:	10.3390/ijms241713177
PMID:	37685985

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol	7127	Click to see COC1=C(C=C(C=C1)CC=C)OC	178.23	unknown	https://doi.org/10.1016/S0960-894X(03)00710-8 https://doi.org/10.1016/S0031-9422(00)80814-6 https://doi.org/10.1248/CPB.53.625
> Benzenoids / Benzene and substituted derivatives / Styrenes
(1Z,4Z)-1,5-Bis(4-hydroxyphenyl)-1,4-pentadiene	102326871	Click to see C1=CC(=CC=C1C=CCC=CC2=CC=C(C=C2)O)O	252.31	unknown	https://doi.org/10.1016/S0031-9422(00)81779-3
3-(4-Hydroxyphenyl)prop-2-en-1-yl acetate	54372486	Click to see CC(=O)OCC=CC1=CC=C(C=C1)O	192.21	unknown	https://doi.org/10.1248/CPB.53.625 https://doi.org/10.1016/S0960-894X(03)00710-8 https://doi.org/10.1016/S0014-2999(03)01785-0
trans-Coumaryl acetate	14320459	Click to see CC(=O)OCC=CC1=CC=C(C=C1)O	192.21	unknown	https://doi.org/10.1248/CPB.53.625 https://doi.org/10.1016/S0960-894X(03)00710-8 https://doi.org/10.1016/S0014-2999(03)01785-0
> Benzenoids / Phenol esters
(S)-1-(4-Acetoxyphenyl)propyl acetate	42612646	Click to see CCC(C1=CC=C(C=C1)OC(=O)C)OC(=O)C	236.26	unknown	https://doi.org/10.1021/JF803387Z
(S)-4-(1-Hydroxyallyl)phenyl acetate	21119823	Click to see CC(=O)OC1=CC=C(C=C1)C(C=C)O	192.21	unknown	https://doi.org/10.1248/CPB.53.625 https://doi.org/10.1055/S-2007-981542 https://doi.org/10.1016/S0960-894X(03)00710-8 https://doi.org/10.1016/S0014-2999(03)01785-0
[4-[5-(4-Acetyloxyphenyl)penta-1,4-dienyl]phenyl] acetate	162939046	Click to see CC(=O)OC1=CC=C(C=C1)C=CCC=CC2=CC=C(C=C2)OC(=O)C	336.40	unknown	https://doi.org/10.1016/S0031-9422(00)81779-3
1'-Acetoxychavicol acetate	119104	Click to see CC(=O)OC1=CC=C(C=C1)C(C=C)OC(=O)C	234.25	unknown	https://doi.org/10.1248/CPB.53.625 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3581550/ https://doi.org/10.1271/BBB.57.1344 https://doi.org/10.1248/CPB.36.244 https://doi.org/10.1016/S0960-894X(03)00710-8 https://doi.org/10.1016/S0014-2999(03)01785-0
1'-Acetoxychavicol acetate, (+)-	44219741	Click to see CC(=O)OC1=CC=C(C=C1)C(C=C)OC(=O)C	234.25	unknown	https://doi.org/10.1055/S-2007-981542
1'-Acetoxychavicol acetate, (+/-)-	400072	Click to see CC(=O)OC1=CC=C(C=C1)C(C=C)OC(=O)C	234.25	unknown	https://doi.org/10.1055/S-2007-981542 https://doi.org/10.1248/CPB.53.625 https://doi.org/10.1248/CPB.36.244 https://doi.org/10.1055/S-2006-962611 https://doi.org/10.1271/BBB.59.1566 https://doi.org/10.1016/S0014-2999(03)01785-0 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921523/ https://doi.org/10.1021/JF9808224 https://doi.org/10.1271/BBB.57.1344 https://doi.org/10.1080/13880200500385194 https://doi.org/10.1016/S0960-894X(03)00710-8
1'-Acetoxyeugenol acetate	4484222	Click to see CC(=O)OC1=C(C=C(C=C1)C(C=C)OC(=O)C)OC	264.27	unknown	https://doi.org/10.1248/CPB.53.625 https://doi.org/10.1055/S-2007-969577 https://doi.org/10.1055/S-2006-962611 https://doi.org/10.1016/J.JEP.2012.12.024 https://doi.org/10.1248/CPB.36.244 https://doi.org/10.1039/C4FO00709C https://doi.org/10.1016/S0960-894X(03)00710-8 https://doi.org/10.1016/S0014-2999(03)01785-0
1'-Hydroxychavicol acetate	71596738	Click to see CC(=O)OC1=CC=C(C=C1)C(C=C)O	192.21	unknown	https://doi.org/10.1248/CPB.53.625 https://doi.org/10.1055/S-2007-969577 https://doi.org/10.1055/S-2007-981542 https://doi.org/10.1016/S0960-894X(03)00710-8 https://doi.org/10.1016/S0014-2999(03)01785-0
3-(4-Acetyloxy-3-methoxyphenyl)prop-2-enyl acetate	613644	Click to see CC(=O)OCC=CC1=CC(=C(C=C1)OC(=O)C)OC	264.27	unknown	https://doi.org/10.1248/CPB.36.244
3-Methoxy-4-acetoxycinnamaldehyde	3017600	Click to see CC(=O)OC1=C(C=C(C=C1)C=CC=O)OC	220.22	unknown	via CMAUP database
4-(Acetyloxy)-alpha-ethenyl-3-methoxybenzenemethanol acetate	442775	Click to see CC(=O)OC1=C(C=C(C=C1)C(C=C)OC(=O)C)OC	264.27	unknown	https://doi.org/10.1248/CPB.53.625 https://doi.org/10.1016/J.JEP.2012.12.024 https://doi.org/10.1248/CPB.36.244 https://doi.org/10.1039/C4FO00709C https://doi.org/10.1016/S0960-894X(03)00710-8 https://doi.org/10.1016/S0014-2999(03)01785-0
4-Acetoxy-3-methoxycinnamaldehyde	5893006	Click to see CC(=O)OC1=C(C=C(C=C1)C=CC=O)OC	220.22	unknown	via CMAUP database
4-Acetoxycinnamyl acetate	85416330	Click to see CC(=O)OCC=CC1=CC=C(C=C1)OC(=O)C	234.25	unknown	https://doi.org/10.1248/CPB.53.625 https://doi.org/10.1248/CPB.36.244 https://doi.org/10.1016/S0960-894X(03)00710-8 https://doi.org/10.1016/S0014-2999(03)01785-0
4-Allylphenyl acetate	523825	Click to see CC(=O)OC1=CC=C(C=C1)CC=C	176.21	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
4-Hydroxy cinnamyl alcohol diacetate	11149005	Click to see CC(=O)OCC=CC1=CC=C(C=C1)OC(=O)C	234.25	unknown	https://doi.org/10.1248/CPB.53.625 https://doi.org/10.1248/CPB.36.244 https://doi.org/10.1016/S0960-894X(03)00710-8 https://doi.org/10.1016/S0014-2999(03)01785-0
Allylpyrocatechol monoacetate	10219771	Click to see CC(=O)OC1=C(C=C(C=C1)CC=C)O	192.21	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3581550/
Dihydrogalangal acetate	14638401	Click to see CCC(C1=CC=C(C=C1)OC(=O)C)OC(=O)C	236.26	unknown	https://doi.org/10.1021/JF803387Z
Eugenol acetate	7136	Click to see CC(=O)OC1=C(C=C(C=C1)CC=C)OC	206.24	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535148/ https://doi.org/10.1016/S0031-9422(00)80814-6
trans-Coniferyl alcohol diacetate	6537101	Click to see CC(=O)OCC=CC1=CC(=C(C=C1)OC(=O)C)OC	264.27	unknown	https://doi.org/10.1248/CPB.36.244
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(R)-4-(1-Hydroxyallyl)phenol	14018450	Click to see C=CC(C1=CC=C(C=C1)O)O	150.17	unknown	https://doi.org/10.1055/S-2007-981542
4-[(1R)-1-Hydroxyprop-2-en-1-yl]phenol	45082905	Click to see C=CC(C1=CC=C(C=C1)O)O	150.17	unknown	https://doi.org/10.1055/S-2007-981542
4-Allylphenol	68148	Click to see C=CCC1=CC=C(C=C1)O	134.17	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
2-Allylphenol	15624	Click to see C=CCC1=CC=CC=C1O	134.17	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Coniferyl acetate	12835430	Click to see CC(=O)OCC=CC1=CC(=C(C=C1)O)OC	222.24	unknown	https://doi.org/10.1248/CPB.36.244
Eugenol	3314	Click to see COC1=C(C=CC(=C1)CC=C)O	164.20	unknown	via CMAUP database
o-Methoxy-o-methyl-p-allylphenol	45266909	Click to see CC1=CC(=CC(=C1O)OC)CC=C	178.23	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535148/ https://doi.org/10.1016/S0960-894X(03)00710-8
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Pentadecane	12391	Click to see CCCCCCCCCCCCCCC	212.41	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
Tridecane	12388	Click to see CCCCCCCCCCCCC	184.36	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Citronellyl acetate	9017	Click to see CC(CCC=C(C)C)CCOC(=O)C	198.30	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
Geranyl acetate	1549026	Click to see CC(=CCCC(=CCOC(=O)C)C)C	196.29	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
Neryl acetate	1549025	Click to see CC(=CCCC(=CCOC(=O)C)C)C	196.29	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
Octanol acetate	11008408	Click to see CCCCCCCCOC(=O)C	173.26	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(1R,2R)-1-(4-hydroxyphenyl)-2-[(E)-3-(4-hydroxyphenyl)prop-2-enyl]propane-1,3-diol	162951121	Click to see C1=CC(=CC=C1C=CCC(CO)C(C2=CC=C(C=C2)O)O)O	300.30	unknown	https://doi.org/10.1248/CPB.53.625
(1R,2S)-1-(4-hydroxyphenyl)-2-[(E)-3-(4-hydroxyphenyl)prop-2-enyl]propane-1,3-diol	163185253	Click to see C1=CC(=CC=C1C=CCC(CO)C(C2=CC=C(C=C2)O)O)O	300.30	unknown	https://doi.org/10.1248/CPB.53.625
(1S,2R)-1-(4-hydroxyphenyl)-2-[(E)-3-(4-hydroxyphenyl)prop-2-enyl]propane-1,3-diol	11312618	Click to see C1=CC(=CC=C1C=CCC(CO)C(C2=CC=C(C=C2)O)O)O	300.30	unknown	https://doi.org/10.1248/CPB.53.625
(1S,2S)-1-(4-hydroxyphenyl)-2-[(E)-3-(4-hydroxyphenyl)prop-2-enyl]propane-1,3-diol	11335585	Click to see C1=CC(=CC=C1C=CCC(CO)C(C2=CC=C(C=C2)O)O)O	300.30	unknown	https://doi.org/10.1248/CPB.53.625
1-(4-Hydroxyphenyl)-2-[3-(4-hydroxyphenyl)prop-2-enyl]propane-1,3-diol	72796911	Click to see C1=CC(=CC=C1C=CCC(CO)C(C2=CC=C(C=C2)O)O)O	300.30	unknown	https://doi.org/10.1248/CPB.53.625
> 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/10.1055/S-2006-962365
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2E)-2-[2-[(1R,2R,4aS,8aS)-5,5,8a-trimethylspiro[3,4,4a,6,7,8-hexahydro-1H-naphthalene-2,2'-oxirane]-1-yl]ethylidene]butanedial	102506426	Click to see CC1(CCCC2(C1CCC3(C2CC=C(CC=O)C=O)CO3)C)C	318.40	unknown	https://doi.org/10.1055/S-2006-957890
(2E)-2-[2-[(1S,4aS,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]butanedial	163068846	Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C	302.50	unknown	https://doi.org/10.1055/S-2006-962365
2-[2-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)ethylidene]butanedial	75094027	Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C	302.50	unknown	https://doi.org/10.1246/CL.1986.1205
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/10.1246/CL.1986.1205 https://doi.org/10.1055/S-2006-957890
Aframodial	21668974	Click to see CC1(CCCC2(C1CCC3(C2CC=C(CC=O)C=O)CO3)C)C	318.40	unknown	https://doi.org/10.1246/CL.1986.1205
Labda-8(17),12-diene-15,16-dial	11077520	Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C	302.50	unknown	https://doi.org/10.1246/CL.1986.1205
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Lavandulyl acetate, (+/-)-	30247	Click to see CC(=CCC(COC(=O)C)C(=C)C)C	196.29	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535148/
Linalool, (-)-	443158	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
Linalool, (+)-	67179	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)94183-9 https://doi.org/10.1016/S0031-9422(00)80814-6
> 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/10.1016/S0031-9422(00)94183-9 https://doi.org/10.1016/S0031-9422(00)80814-6
Thymol	6989	Click to see CC1=CC(=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene	440968	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)94183-9
(-)-beta-Pinene	440967	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)94183-9
(-)-Camphene	440966	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	via CMAUP database
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
(+)-Bornyl acetate	6950274	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
(+)-Camphene	92221	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	via CMAUP database
(1R,2S,4R)-(+)-Bornyl acetate	443131	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
(1S,2R,4S)-(-)-Bornyl acetate	442460	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
(1S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene	12223113	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
(4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one	23308299	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
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/10.1016/S0031-9422(00)80814-6
alpha-Bergamotene	86608	Click to see CC1=CCC2CC1C2(C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)94183-9 https://doi.org/10.1055/S-2007-969577 https://doi.org/10.1016/S0031-9422(00)80814-6
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)94183-9 https://doi.org/10.1055/S-2007-969577 https://doi.org/10.1016/S0031-9422(00)80814-6
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535148/
Bornyl acetate, (-)-	93009	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
Camphor	2537	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
L-Born-2-yl acetate	44630108	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
trans-Borneol	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol	443162	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	via CMAUP database
(-)-Terpinen-4-ol	5325830	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	via CMAUP database
(-)-trans-Carveol	94221	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	via CMAUP database
(+)-trans-Carveol	443178	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	via CMAUP database
(1r,4r)-1-Methyl-4-(prop-1-en-2-yl)cyclohex-2-en-1-ol	111274	Click to see CC(=C)C1CCC(C=C1)(C)O	152.23	unknown	via CMAUP database
(1S,4R)-1-methyl-4-(prop-1-en-2-yl)cyclohex-2-enol	11105550	Click to see CC(=C)C1CCC(C=C1)(C)O	152.23	unknown	via CMAUP database
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6 https://doi.org/10.1055/S-2007-969577 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535148/
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)94183-9
alpha-PHELLANDRENE, (-)-	442482	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)94183-9
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535148/
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535148/ https://doi.org/10.1055/S-2007-969577 https://doi.org/10.1016/S0031-9422(00)80814-6
Carveol	7438	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535148/
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)94183-9
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)94183-9 https://doi.org/10.1055/S-2007-969577 https://doi.org/10.1016/S0031-9422(00)80814-6
P-Mentha-2,8-dien-1-ol	155626	Click to see CC(=C)C1CCC(C=C1)(C)O	152.23	unknown	via CMAUP database
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
gamma-Camphorene	5315649	Click to see CC(=CCCC1=CCCC(C1)C(=C)CCC=C(C)C)C	272.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-beta-Sesquiphellandrene	12315492	Click to see CC(CCC=C(C)C)C1CCC(=C)C=C1	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	92042749	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
(2Z,6E)-Farnesyl acetate	1551480	Click to see CC(=CCCC(=CCCC(=CCOC(=O)C)C)C)C	264.40	unknown	via CMAUP database
(4Z,8Z)-5,9,13-trimethyltetradeca-4,8,12-trienoic acid	6440238	Click to see CC(=CCCC(=CCCC(=CCCC(=O)O)C)C)C	264.40	unknown	via CMAUP database
(R)-beta-bisabolene	68128	Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
3-[(2S)-6-methylhept-5-en-2-yl]-6-methylidenecyclohexene	5321277	Click to see CC(CCC=C(C)C)C1CCC(=C)C=C1	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
3,7,11-Trimethyldodeca-2,6,10-trienyl acetate	94403	Click to see CC(=CCCC(=CCCC(=CCOC(=O)C)C)C)C	264.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535148/
alpha-Curcumene	92139	Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C	202.33	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
alpha-Santalene	94164	Click to see CC(=CCCC1(C2CC3C1(C3C2)C)C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
beta-Bisabolene	10104370	Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
beta-CARYOPHYLLENE OXIDE	1742210	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
Caryophyllene epoxide	14350	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
Farnesal	5280598	Click to see CC(=CCCC(=CCCC(=CC=O)C)C)C	220.35	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535148/
Farnesyl acetate	638500	Click to see CC(=CCCC(=CCCC(=CCOC(=O)C)C)C)C	264.40	unknown	via CMAUP database
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
Zerumbone	5470187	Click to see CC1=CCC(C=CC(=O)C(=CCC1)C)(C)C	218.33	unknown	https://doi.org/10.3736/JCIM20111004
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3R,6S,8R,11S,12S,14R,15S,16R)-6-(dimethylamino)-7,7,12,16-tetramethyl-15-[(1S)-1-(methylamino)ethyl]pentacyclo[9.7.0.01,3.03,8.012,16]octadec-4-en-14-ol	163070372	Click to see CC(C1C(CC2(C1(CCC34C2CCC5C3(C4)C=CC(C5(C)C)N(C)C)C)C)O)NC	414.70	unknown	https://doi.org/10.1016/S0031-9422(00)81779-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Azasteroids and derivatives
Dictyophlebine	11417103	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4)NC)C)C)N(C)C	360.60	unknown	via CMAUP database
Epipachysamine B	70688998	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4)NC(=O)C5=CN=CC=C5)C)C)N(C)C	451.70	unknown	via CMAUP database
Hookerianamide D	11213879	Click to see CC(C)C(=CC(=O)N(C)C1CCC2(C(C1)CCC3C2CCC4(C3CCC4C(C)N(C)C=O)C)C)C	484.80	unknown	via CMAUP database
Hookerianamide E	11431683	Click to see CC(C1CC=C2C1(CCC3C2CCC4C3(CC(C(C4)NC(=O)C=C(C)C)OC(=O)C)C)C)N(C)C	484.70	unknown	via CMAUP database
hookerianamide I	44587245	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4)N(C)C(=O)C5=CC=CC=C5)C)C)NC	450.70	unknown	via CMAUP database
Hookerianamide K	25016412	Click to see CC(C1CC=C2C1(CCC3C2CCC4=CC(CCC34C)N(C)C)C)N(C)C	370.60	unknown	via CMAUP database
Hookerianamine A	12095947	Click to see CC(C1CC=C2C1(CCC3C2CCC4C3(CCC(C4)NC)C)C)N(C)C	358.60	unknown	via CMAUP database
N-[(3S,5S,8R,9S,10S,13S,14S,17S)-17-[(1S)-1-(dimethylamino)ethyl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl]-N-methylbenzamide	10004669	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4)N(C)C(=O)C5=CC=CC=C5)C)C)N(C)C	464.70	unknown	via CMAUP database
N-Formylchonemorphine	101938440	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4)NC=O)C)C)N(C)C	374.60	unknown	via CMAUP database
Salignenamide F	11113449	Click to see CC(C)C(=CC(=O)N(C)C1CCC2(C(C1)CCC3C2CCC4(C3CCC4C(C)N(C)C)C)C)C	470.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(E,2S)-6-[(1S,3R)-6-methoxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-2-methylhept-3-ene-1,2-diol	5319421	Click to see CC(CC=CC(C)(CO)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC)C)C	472.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
Hookerianamide A	102333328	Click to see CC(C1=CCC2C1(CCC3C2CCC4C3(CC(C(C4O)NC(=O)C=C(C)C)O)C)C)N(C)C	458.70	unknown	via CMAUP database
Hookerianamide J	25016666	Click to see CC(C1=CCC2C1(CCC3C2CCC4C3(CCC(C4O)NC(=O)C=C(C)C)C)C)N(C)C	442.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
2,3-Dehydrosarsalignone	44587283	Click to see CC=C(C)C(=O)NC1=CCC2(C3CCC4(C(C3CC=C2C1=O)CCC4C(C)NC)C)C	424.60	unknown	via CMAUP database
epipachysamine-E-5-en-4-one	44587247	Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4=O)NC(=O)C=C(C)C)C)C)NC	426.60	unknown	via CMAUP database
hookerianamide H	44587217	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CC=C(C4=O)NC=O)C)C)N(C)C	386.60	unknown	via CMAUP database
Sarcovaganin C	101726070	Click to see CC=C(C)C(=O)NC1=CCC2(C3CCC4(C(C3CCC2C1=O)CCC4C(C)N(C)C)C)C	440.70	unknown	via CMAUP database
Sarcovagenine C	101936590	Click to see CC=C(C)C(=O)NC1=CCC2(C3CCC4(C(C3CCC2C1=O)CC=C4C(C)N(C)C)C)C	438.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
(20S)-3beta-(3-Methyl-2-butenoylamino)-4beta-acetoxy-20-(methylamino)-5alpha-pregnane	44587282	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4OC(=O)C)NC(=O)C=C(C)C)C)C)NC	472.70	unknown	via CMAUP database
(20S)-3beta-[(3-Methyl-2-butenoyl)amino]-20-(dimethylamino)-5alpha-pregnane-2alpha,4beta-diol diacetate	12095949	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CC(C(C4OC(=O)C)NC(=O)C=C(C)C)OC(=O)C)C)C)N(C)C	544.80	unknown	via CMAUP database
[(3S,4R,5R,8S,9S,10R,13S,14S,17S)-10,13-dimethyl-17-[(1S)-1-(methylamino)ethyl]-3-[[(E)-2-methylbut-2-enoyl]amino]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-4-yl] acetate	25033601	Click to see CC=C(C)C(=O)NC1CCC2(C(C1OC(=O)C)CCC3C2CCC4(C3CCC4C(C)NC)C)C	472.70	unknown	via CMAUP database
[(3S,4R,5R,8S,9S,10R,13S,14S,17S)-17-[(1S)-1-(dimethylamino)ethyl]-10,13-dimethyl-3-[[(E)-2-methylbut-2-enoyl]amino]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-4-yl] acetate	11225523	Click to see CC=C(C)C(=O)NC1CCC2(C(C1OC(=O)C)CCC3C2CCC4(C3CCC4C(C)N(C)C)C)C	486.70	unknown	via CMAUP database
Hookerianamide G	11249447	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4OC(=O)C)N(C)C(=O)C5=CC=CC=C5)C)C)N(C)C	522.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Terminaline	177562	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4O)O)C)C)N(C)C	363.60	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
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	via CMAUP database
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Butyl acetate	31272	Click to see CCCCOC(=O)C	116.16	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
Isobutyl acetate	8038	Click to see CC(C)COC(=O)C	116.16	unknown	https://doi.org/10.1016/S0031-9422(00)80814-6
> 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/10.1055/S-2006-962365
(6aS,7R,11aR,11bS)-7-hydroxy-4,4,11b-trimethyl-1,2,3,4a,5,6,7,8,11,11a-decahydrocyclohepta[a]naphthalene-6a,9-dicarbaldehyde	5317451	Click to see CC1(CCCC2(C1CCC3(C2CC=C(CC3O)C=O)C=O)C)C	318.40	unknown	via CMAUP database
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/10.1246/CL.1986.1205
Galanal A	3050416	Click to see CC1(CCCC2(C1CCC3(C2CC=C(CC3O)C=O)C=O)C)C	318.40	unknown	https://doi.org/10.1246/CL.1986.1205 https://doi.org/10.1055/S-2006-962365
Galanal B	3086504	Click to see CC1(CCCC2(C1CCC3(C2CC=C(CC3O)C=O)C=O)C)C	318.40	unknown	https://doi.org/10.1246/CL.1986.1205 https://doi.org/10.1055/S-2006-962365
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(2R,9R)-4,4,8-trimethyltricyclo[6.3.1.02,5]dodecane-1,9-diol	382536	Click to see CC1(CC2C1CCC3(CC2(CCC3O)O)C)C	238.37	unknown	via CMAUP database
Caryolane-1,9beta-diol	495836	Click to see CC1(CC2C1CCC3(CC2(CCC3O)O)C)C	238.37	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5S,6R)-2-(hydroxymethyl)-6-(4-prop-2-enylphenoxy)oxane-3,4,5-triol	46905155	Click to see C=CCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O	296.31	unknown	https://doi.org/10.1016/S0960-894X(03)00710-8
4-(2-Propenyl)phenyl-beta-d-glucopyranoside	44390556	Click to see C=CCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O	296.31	unknown	https://doi.org/10.1248/CPB.53.625 https://doi.org/10.1016/S0960-894X(03)00710-8
Chavicol O-beta-glucopyranoside	44338426	Click to see C=CCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O	296.31	unknown	https://doi.org/10.1248/CPB.53.625 https://doi.org/10.1016/S0960-894X(03)00710-8
> 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/10.1016/S0960-894X(03)00710-8 https://doi.org/10.1248/CPB.36.244 https://doi.org/10.1248/CPB.53.625
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3E)-3-[2-[(1R,2S)-5,5,8a-trimethylspiro[3,4,4a,6,7,8-hexahydro-1H-naphthalene-2,2'-oxirane]-1-yl]ethylidene]oxolan-2-one	5317453	Click to see CC1(CCCC2(C1CCC3(C2CC=C4CCOC4=O)CO3)C)C	318.40	unknown	https://doi.org/10.1055/S-2006-962365
(3E)-3-[2-[(1R,4aR,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]-4-hydroxyoxolan-2-one	91980716	Click to see CC1(CCCC2(C1CCC(=C)C2CC=C3C(COC3=O)O)C)C	318.40	unknown	via CMAUP database
CID 71550939	71550939	Click to see CC1(CCCC2(C1CCC(=C)C2CC=C3C(COC3=O)O)C)C	318.40	unknown	via CMAUP database
Galanolactone	11141699	Click to see CC1(CCCC2(C1CCC3(C2CC=C4CCOC4=O)CO3)C)C	318.40	unknown	https://doi.org/10.1055/S-2006-962365
isocoronarin D	46871816	Click to see CC1(CCCC2(C1CCC(=C)C2CC=C3C(COC3=O)O)C)C	318.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxanes
(1R,2R)-1,8-Epoxy-p-menthane-2-ol	90657615	Click to see CC1(C2CCC(O1)(C(C2)O)C)C	170.25	unknown	via CMAUP database
(1S,4R,5R)-1,3,3-Trimethyl-2-oxabicyclo[2.2.2]octan-5-yl acetate	15385369	Click to see CC(=O)OC1CC2(CCC1C(O2)(C)C)C	212.28	unknown	https://doi.org/10.1021/JF9804239
(1S,4S,6R)-1,3,3-trimethyl-2-oxabicyclo[2.2.2]octan-6-ol	76322366	Click to see CC1(C2CCC(O1)(C(C2)O)C)C	170.25	unknown	via CMAUP database
(4alpha)-1beta,3,3-Trimethyl-2-oxabicyclo[2.2.2]octane-6beta-ol acetate	15385366	Click to see CC(=O)OC1CC2CCC1(OC2(C)C)C	212.28	unknown	https://doi.org/10.1021/JF9804239
(6S)-1,3,3-trimethyl-2-oxabicyclo[2.2.2]octan-6-ol	11953818	Click to see CC1(C2CCC(O1)(C(C2)O)C)C	170.25	unknown	via CMAUP database
[(1S,4R,5R)-1,3,3-trimethyl-2-oxabicyclo[2.2.2]octan-5-yl] acetate	15385367	Click to see CC(=O)OC1CC2(CCC1C(O2)(C)C)C	212.28	unknown	https://doi.org/10.1021/JF9804239
[(1S,4R,5S)-1,3,3-trimethyl-2-oxabicyclo[2.2.2]octan-5-yl] acetate	15385368	Click to see CC(=O)OC1CC2(CCC1C(O2)(C)C)C	212.28	unknown	https://doi.org/10.1021/JF9804239
2-Acetoxy-1,8-cineole, (+)-endo-	11218113	Click to see CC(=O)OC1CC2CCC1(OC2(C)C)C	212.28	unknown	https://doi.org/10.1021/JF9804239
2-Endo-hydroxy-1,8-cineole	6857470	Click to see CC1(C2CCC(O1)(C(C2)O)C)C	170.25	unknown	via CMAUP database
2-Oxabicyclo[2.2.2]octan-6-ol, 1,3,3-trimethyl-, acetate	175002	Click to see CC(=O)OC1CC2CCC1(OC2(C)C)C	212.28	unknown	https://doi.org/10.1021/JF9804239
Eucalyptol	2758	Click to see CC1(C2CCC(O1)(CC2)C)C	154.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamaldehydes
(E,2E)-5-(4-hydroxyphenyl)-2-[(4-hydroxyphenyl)methylidene]pent-4-enal	11254485	Click to see C1=CC(=CC=C1C=CCC(=CC2=CC=C(C=C2)O)C=O)O	280.30	unknown	https://doi.org/10.1248/CPB.53.625
3-(4-Hydroxyphenyl)prop-2-enal	440733	Click to see C1=CC(=CC=C1C=CC=O)O	148.16	unknown	https://doi.org/10.1248/CPB.53.625 https://doi.org/10.1016/S0031-9422(00)81779-3 https://doi.org/10.1016/S0014-2999(03)01785-0 https://doi.org/10.1016/J.PHYTOCHEM.2008.11.010 https://doi.org/10.1016/S0960-894X(03)00710-8
5-(4-Hydroxyphenyl)-2-[(4-hydroxyphenyl)methylidene]pent-4-enal	72771181	Click to see C1=CC(=CC=C1C=CCC(=CC2=CC=C(C=C2)O)C=O)O	280.30	unknown	https://doi.org/10.1248/CPB.53.625
p-Coumaraldehyde	641301	Click to see C1=CC(=CC=C1C=CC=O)O	148.16	unknown	https://doi.org/10.1248/CPB.53.625 https://doi.org/10.1016/S0031-9422(00)81779-3 https://doi.org/10.1016/S0014-2999(03)01785-0 https://doi.org/10.1016/J.PHYTOCHEM.2008.11.010 https://doi.org/10.1016/S0960-894X(03)00710-8
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
Methyl cinnamate	637520	Click to see COC(=O)C=CC1=CC=CC=C1	162.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Methyl-3-phenylprop-2-enoate	53433099	Click to see CC(=CC1=CC=CC=C1)C(=O)[O-]	161.18	unknown	via CMAUP database
Cinnamic acid	444539	Click to see C1=CC=C(C=C1)C=CC(=O)O	148.16	unknown	https://doi.org/10.1021/JF00026A001
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3-(4-Methoxyphenyl)-2-propen-1-ol	5314180	Click to see COC1=CC=C(C=C1)C=CCO	164.20	unknown	https://doi.org/10.1055/S-2006-962611
4-(3-Hydroxyprop-1-enyl)phenol	94274	Click to see C1=CC(=CC=C1C=CCO)O	150.17	unknown	https://doi.org/10.1248/CPB.53.625 https://doi.org/10.1016/S0960-894X(03)00710-8 https://doi.org/10.1016/S0014-2999(03)01785-0
CID 95641	95641	Click to see COC1=CC=C(C=C1)C=CCO	164.20	unknown	https://doi.org/10.1055/S-2006-962611
p-Coumaryl alcohol	5280535	Click to see C1=CC(=CC=C1C=CCO)O	150.17	unknown	https://doi.org/10.1248/CPB.53.625 https://doi.org/10.1016/S0960-894X(03)00710-8 https://doi.org/10.1016/S0014-2999(03)01785-0
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
4-[(E)-3-[(2R,3S,5R)-5-[(R)-hydroxy-(4-hydroxyphenyl)methyl]-2-(4-hydroxyphenyl)oxan-3-yl]prop-1-enyl]phenol	162913121	Click to see C1C(COC(C1CC=CC2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C(C4=CC=C(C=C4)O)O	432.50	unknown	https://doi.org/10.1248/CPB.53.625
4-[(E)-3-[(2S,3S,5S)-5-[(R)-hydroxy-(4-hydroxyphenyl)methyl]-2-(4-hydroxyphenyl)oxan-3-yl]prop-1-enyl]phenol	163194289	Click to see C1C(COC(C1CC=CC2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C(C4=CC=C(C=C4)O)O	432.50	unknown	https://doi.org/10.1248/CPB.53.625
4-[3-[5-[Hydroxy-(4-hydroxyphenyl)methyl]-2-(4-hydroxyphenyl)oxan-3-yl]prop-1-enyl]phenol	73173789	Click to see C1C(COC(C1CC=CC2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C(C4=CC=C(C=C4)O)O	432.50	unknown	https://doi.org/10.1248/CPB.53.625
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
Bisdemethoxycurcumin	5315472	Click to see C1=CC(=CC=C1C=CC(=O)CC(=O)C=CC2=CC=C(C=C2)O)O	308.30	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3763262/
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
5,7-Dihydroxy-4-oxo-2-phenylchromen-3-olate	54758662	Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)[O-]	269.23	unknown	via CMAUP database
Galangin	5281616	Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.3736/JCIM20111004
Kaempferide	5281666	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	https://doi.org/10.3736/JCIM20111004

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Alpinia galanga

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