Curcuma aromatica

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Distribution

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Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID643ff4bca853b327038843
Scientific name	Curcuma aromatica
Authority	Salisb.
First published in	Parad. lond. t.96. (1807); Lectotypified in: Taxon 59 (1). (2010) by Leong-Škorničková J., Šída O. & Marhold K.

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Synonyms Top

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Common names Top

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Language	Common/alternative name
ban	temu agung
Bulgarian	ароматна куркума
Hindi	van haldi
Japanese	キョウオウ
Kannada	ಕಾಡು ಅರಿಸಿನ
Korean	강황
lzh	鬱金
Malayalam	കസ്തൂരി മഞ്ഞൾ
Malayalam	കസ്തൂരിമഞ്ഞൾ
Russian	куркума ароматная
Tamil	கத்தூரி மஞ்சள்
Thai	ว่านนางคำ
Ukrainian	Куркума ароматна
Vietnamese	nghệ trắng
Vietnamese	nghệ rừng
za	gohinghenj
Chinese	鬱金
Chinese	毛郁金
Chinese	郁金（毛郁金）^
Chinese	姜黄
Chinese	郁金
Chinese	莪术

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan
  - Tibet

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Sri Lanka
- Indo-China
  - Cambodia
  - Myanmar
  - Thailand
  - Vietnam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000365436
UNII	RIV999L6M8
USDA Plants	CUAR3
Tropicos	34500306
KEW	urn:lsid:ipni.org:names:796426-1
The Plant List	kew-235193
Open Tree Of Life	1081978
NCBI Taxonomy	136209
IPNI	796426-1
iNaturalist	347672
GBIF	2757544
Freebase	/m/0gtvlyr
EPPO	CURAR
USDA GRIN	400160
Wikipedia	Curcuma_aromatica
CMAUP	NPO25209

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

Efficacy and safety of herbal medicine combined with acupuncture in pediatric epilepsy treatment: A meta-analysis of randomized controlled trials

Su HW, Chen HT, Kao CL, Hung KC, Lin YT, Liu PH, Lin CM, Chen IW

PLoS One

09-May-2024

PMCID:	PMC11081325
doi:	10.1371/journal.pone.0303201
PMID:	38723054

A comprehensive review on the hepatotoxicity of herbs used in the Indian (Ayush) systems of alternative medicine

Philips CA, Theruvath AH

Medicine (Baltimore)

19-Apr-2024

PMCID:	PMC11029936
doi:	10.1097/MD.0000000000037903
PMID:	38640296

Mechanisms of Sepsis-Induced Acute Lung Injury and Advancements of Natural Small Molecules in Its Treatment

Xu Y, Xin J, Sun Y, Wang X, Sun L, Zhao F, Niu C, Liu S

Pharmaceuticals (Basel)

08-Apr-2024

PMCID:	PMC11054595
doi:	10.3390/ph17040472
PMID:	38675431

Progress of medicinal plants and their active metabolites in ischemia-reperfusion injury of stroke: a novel therapeutic strategy based on regulation of crosstalk between mitophagy and ferroptosis

Zhang G, Wang Q, Jiang B, Yao L, Wu W, Zhang X, Wan D, Gu Y

Front Pharmacol

08-Apr-2024

PMCID:	PMC11033413
doi:	10.3389/fphar.2024.1374445
PMID:	38650626

Bio-clay: Antioxidant-rich and stable for body mud scrubs

Maneetong S, Thuadaij P

Heliyon

03-Apr-2024

PMCID:	PMC11004215
doi:	10.1016/j.heliyon.2024.e29122
PMID:	38601526

Mechanisms of ferroptosis in nonalcoholic fatty liver disease and therapeutic effects of traditional Chinese medicine: a review

Wang N, Que H, Luo Q, Zheng W, Li H, Wang Q, Gu J

Front Med (Lausanne)

25-Mar-2024

PMCID:	PMC10999571
doi:	10.3389/fmed.2024.1356225
PMID:	38590315

Maximizing Curcuminoid Extraction from Curcuma aromatica Salisb. Rhizomes via Environmentally Friendly Microwave-Assisted Extraction Technique Using Full Factorial Design

Suksaeree J, Monton C

Int J Food Sci

25-Mar-2024

PMCID:	PMC10985645
doi:	10.1155/2024/4566123
PMID:	38566754

Elucidating phylogenetic relationships within the genus Curcuma through the comprehensive analysis of the chloroplast genome of Curcuma viridiflora Roxb. 1810 (Zingiberaceae)

Lin L, Hao Z, Zhou L, Liu W, Liu N, Wang K, Jia R

Mitochondrial DNA B Resour

20-Mar-2024

PMCID:	PMC10962285
doi:	10.1080/23802359.2024.2329674
PMID:	38529111

Efficacy and safety of adjuvant topical application of botanicals in the treatment of melasma: A systematic review and meta-analysis

Guo L, Zhang Y, Wu S, Bai M, Tian S, Miao M

Heliyon

15-Mar-2024

PMCID:	PMC10966692
doi:	10.1016/j.heliyon.2024.e28096
PMID:	38545140

Comparative Pharmacokinetics Research of 13 Bioactive Components of Jieyu Pills in Control and Attention Deficit Hyperactivity Disorder Model Rats Based on UPLC-Orbitrap Fusion MS

Liu X, Wan Y, Sun S, Wang T, Li T, Sun Q, Zhang W, Zhao D, Tian Y, Feng S

Molecules

10-Mar-2024

PMCID:	PMC10976160
doi:	10.3390/molecules29061230
PMID:	38542867

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

Two-Phase Fermentation Systems for Microbial Production of Plant-Derived Terpenes

Li T, Liu X, Xiang H, Zhu H, Lu X, Feng B

Molecules

02-Mar-2024

PMCID:	PMC10934027
doi:	10.3390/molecules29051127
PMID:	38474639

Integrated 16S rRNA sequencing and metabolomic analysis reveals the potential protective mechanism of Germacrone on diabetic nephropathy in mice: Germacrone ameliorates DN via microbiota regulation

Wang Y, He X, Xue M, Yu H, He Q, Jin J

Acta Biochim Biophys Sin (Shanghai)

01-Mar-2024

PMCID:	PMC10984863
doi:	10.3724/abbs.2024021
PMID:	38429975

Effectiveness of adjuvant traditional Chinese medicine on macrovascular invasion in patients with hepatocellular carcinoma: a real-world propensity score-matched study

Yan H, Wang X, Yu L, Liu X, Yan F, Xie Y, Pu Q, Yang Z

Front Pharmacol

23-Feb-2024

PMCID:	PMC10923102
doi:	10.3389/fphar.2024.1353720
PMID:	38464727

Hu-Qi-Zheng-Xiao Decoction Inhibits the Metastasis of Hepatocellular Carcinoma Cells by Suppressing the HIF-1α Signaling Pathway to Inhibit EMT, LCSC, and Angiogenic Process

Wang X, Yin L, Chai M, Kou B, Liu X, Wang X

Integr Cancer Ther

22-Feb-2024

PMCID:	PMC10893843
doi:	10.1177/15347354231226126
PMID:	38385348

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Cumenes
o-Cymene	10703	Click to see CC1=CC=CC=C1C(C)C	134.22	unknown	https://doi.org/10.1002/PCA.1296
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
4-[2,4-Dinitro-5-(2,4,6-trimethylphenoxy)anilino]benzonitrile	49777919	Click to see CC1=CC(=C(C(=C1)C)OC2=C(C=C(C(=C2)NC3=CC=C(C=C3)C#N)[N+](=O)[O-])[N+](=O)[O-])C	418.40	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Toluenes
(+)-Curcumene ether	11276006	Click to see CC1=CC=C(C=C1)C2(CCCC(O2)(C)C)C	218.33	unknown	via CMAUP database
> Lignans, neolignans and related compounds
10,24-Dimethoxy-15,29-dimethyl-7,22-dioxa-15,29-diazaheptacyclo[21.6.2.23,6.218,21.18,12.026,30.016,34]hexatriaconta-3(36),4,6(35),8(34),9,11,18,20,23,25,30,32-dodecaene-9,20-diol	626934	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC(=C(O3)C=C7)O)N(CCC6=CC(=C5O)OC)C)OC	594.70	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(+)-Talaumidin	11256357	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)O)OC)C	342.40	unknown	https://doi.org/10.1248/CPB.39.843 https://doi.org/10.1248/CPB.39.854
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Acyl carnitines
L-Octanoylcarnitine	11953814	Click to see CCCCCCCC(=O)OC(CC(=O)[O-])C[N+](C)(C)C	287.39	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
2-Octanol	20083	Click to see CCCCCCC(C)O	130.23	unknown	https://doi.org/10.1016/J.JPBA.2005.07.050
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,2R,8aS)-1-[(3R)-3-hydroxy-3-methylpent-4-enyl]-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol	73114	Click to see CC1(CCCC2(C1CCC(C2CCC(C)(C=C)O)(C)O)C)C	308.50	unknown	https://doi.org/10.1002/PCA.1296
(1S,2R,4bS,8aS,9S,10S)-2-ethenyl-2,4b,8,8-tetramethyl-3,4,5,6,7,8a,9,10-octahydro-1H-phenanthrene-1,9,10-triol	24882250	Click to see CC1(CCCC2(C1C(C(C3=C2CCC(C3O)(C)C=C)O)O)C)C	320.50	unknown	https://doi.org/10.1002/HLCA.200890100
[(2S,3R)-1-[(1R,2S,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-3-oxo-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-4-en-2-yl] acetate	163189148	Click to see CC(C=C)C(CC1C2(CCCC(C2CC(=O)C1(C)O)(C)C)C)OC(=O)C	364.50	unknown	https://doi.org/10.1002/HLCA.200890100
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(6R)-6-ethenyl-3,6-dimethyl-5-prop-1-en-2-yl-5,7-dihydro-1-benzofuran-4-one	137705001	Click to see CC1=COC2=C1C(=O)C(C(C2)(C)C=C)C(=C)C	230.30	unknown	https://doi.org/10.1002/FFJ.2730040106
(6S)-6-ethenyl-3,6-dimethyl-5-prop-1-en-2-yl-5,7-dihydro-1-benzofuran-4-one	5316218	Click to see CC1=COC2=C1C(=O)C(C(C2)(C)C=C)C(=C)C	230.30	unknown	https://doi.org/10.1002/FFJ.2730040106
Benzofuran, 6-ethenyl-4,5,6,7-tetrahydro-3,6-dimethyl-5-isopropenyl-, trans-	12305301	Click to see CC1=COC2=C1CC(C(C2)(C)C=C)C(=C)C	216.32	unknown	https://doi.org/10.1002/FFJ.2730040106
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Camphene	440966	Click to see CC1(C2CCC(C2)C1=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
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	via CMAUP database
Camphor	2537	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
CID 44630107	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
exo-Bornyl isovalerate	76957121	Click to see CC(C)CC(=O)OC1CC2CCC1(C2(C)C)C	238.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-beta-Phellandrene	443161	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	via CMAUP database
Carvone, (+)-	16724	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	via CMAUP database
Carvone, (+/-)-	7439	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	via CMAUP database
p-Menth-3-en-1-ol	11468	Click to see CC(C)C1=CCC(CC1)(C)O	154.25	unknown	https://doi.org/10.1002/PCA.1296
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
m-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
(1R,4S,7S,10R)-1,7-dimethyl-4-propan-2-yl-11-oxabicyclo[8.1.0]undecane-3,6-dione	101601372	Click to see CC1CCC2C(O2)(CC(=O)C(CC1=O)C(C)C)C	252.35	unknown	https://doi.org/10.1248/CPB.39.843
(1S,7R)-1-methyl-7-(3-oxobutyl)-4-propan-2-ylidenebicyclo[4.1.0]heptan-3-one	42608155	Click to see CC(=C1CC2C(C2(CC1=O)C)CCC(=O)C)C	234.33	unknown	https://doi.org/10.1248/CPB.35.53
(1S,8aS)-1-hydroxy-1,4-dimethyl-7-propan-2-ylidene-2,3,8,8a-tetrahydroazulene-5,6-dione	101720148	Click to see CC1=C2CCC(C2CC(=C(C)C)C(=O)C1=O)(C)O	248.32	unknown	https://doi.org/10.1271/BBB.67.911
(1S)-7-Isopropylidene-1,2,3,5,6,7,8,8abeta-octahydro-1beta-hydroxy-1,4-dimethylazulen-6-one	14543199	Click to see CC1=C2CCC(C2CC(=C(C)C)C(=O)C1)(C)O	234.33	unknown	https://doi.org/10.1248/CPB.38.55
(3R,3aR)-3-hydroxy-3,8-dimethyl-5-propan-2-ylidene-2,3a,4,7-tetrahydro-1H-azulen-6-one	133562028	Click to see CC1=C2CCC(C2CC(=C(C)C)C(=O)C1)(C)O	234.33	unknown	https://doi.org/10.1248/CPB.38.55
(4R)-3-methyl-4-(3-oxobutyl)-7-propan-2-ylidenecyclohept-2-en-1-one	163004064	Click to see CC1=CC(=O)C(=C(C)C)CCC1CCC(=O)C	234.33	unknown	https://doi.org/10.1248/CPB.38.55
(6S)-6-methyl-5-(3-oxobutyl)-2-propan-2-ylidenecyclohept-4-en-1-one	21769417	Click to see CC1CC(=O)C(=C(C)C)CC=C1CCC(=O)C	234.33	unknown	https://doi.org/10.1248/CPB.38.55
(S)-Turmerone	14367555	Click to see CC1=CCC(=CC1)C(C)CC(=O)C=C(C)C	218.33	unknown	via CMAUP database
1-Hydroxy-1,4-dimethyl-7-propan-2-ylidene-2,3,8,8a-tetrahydroazulene-5,6-dione	163078119	Click to see CC1=C2CCC(C2CC(=C(C)C)C(=O)C1=O)(C)O	248.32	unknown	https://doi.org/10.1271/BBB.67.911
3-Methyl-4-(3-oxobutyl)-7-propan-2-ylidenecyclohept-2-en-1-one	14543213	Click to see CC1=CC(=O)C(=C(C)C)CCC1CCC(=O)C	234.33	unknown	https://doi.org/10.1248/CPB.38.55
4,7-Dimethyl-7-(4-methylpent-3-enyl)bicyclo[2.2.1]heptan-3-ol	5315645	Click to see CC(=CCCC1(C2CCC1(C(C2)O)C)C)C	222.37	unknown	via CMAUP database
5-methyl-2-[(2R)-6-methylhept-5-en-2-yl]phenol	360253	Click to see CC1=CC(=C(C=C1)C(C)CCC=C(C)C)O	218.33	unknown	https://doi.org/10.1002/FFJ.2730040106
alpha-Zingiberene	11127403	Click to see CC1=CCC(C=C1)C(C)CCC=C(C)C	204.35	unknown	via CMAUP database
Ar-Curcumene	3083834	Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C	202.33	unknown	via CMAUP database
Bicyclo(4.1.0)heptan-3-one, 1-methyl-4-(1-methylethylidene)-7-(3-oxobutyl)-, (1S,6R,7R)-	153845	Click to see CC(=C1CC2C(C2(CC1=O)C)CCC(=O)C)C	234.33	unknown	https://doi.org/10.1248/CPB.35.53
Caryophyllene,alpha + beta mixt.	5354499	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
Curcumadione	14543212	Click to see CC1CC(=O)C(=C(C)C)CC=C1CCC(=O)C	234.33	unknown	https://doi.org/10.1248/CPB.38.55
Curcumenone	14632994	Click to see CC(=C1CC2C(C2(CC1=O)C)CCC(=O)C)C	234.33	unknown	https://doi.org/10.1248/CPB.35.53
delta-Elemene	12309449	Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C	204.35	unknown	via CMAUP database
Neoprocurcumenol	14543200	Click to see CC1=C2CCC(C2CC(=C(C)C)C(=O)C1)(C)O	234.33	unknown	https://doi.org/10.1248/CPB.38.55
Turricolol E	5281861	Click to see CC(=CCCC(=CCCC(=CCC1=C(C=CC(=C1)O)O)C)CO)C	330.50	unknown	via CMAUP database
Xanthorrhizol	93135	Click to see CC1=C(C=C(C=C1)C(C)CCC=C(C)C)O	218.33	unknown	https://doi.org/10.1002/FFJ.2730040106
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(+)-Curdione	518796	Click to see CC1CCC=C(CC(=O)C(CC1=O)C(C)C)C	236.35	unknown	https://doi.org/10.1248/CPB.35.53 https://doi.org/10.1248/BPB.26.1135 https://doi.org/10.1248/CPB.39.843 https://doi.org/10.1271/BBB.67.911
(1R,6E,10S)-6,10-dimethyl-3-propan-2-ylidene-11-oxabicyclo[8.1.0]undec-6-en-4-one	163003032	Click to see CC1=CCCC2(C(O2)CC(=C(C)C)C(=O)C1)C	234.33	unknown	https://doi.org/10.1248/CPB.35.53 https://doi.org/10.1248/CPB.37.233
(1S,3E,6E,10S)-3-(1-hydroxypropan-2-ylidene)-6,10-dimethyl-11-oxabicyclo[8.1.0]undec-6-en-4-one	162856909	Click to see CC1=CCCC2(C(O2)CC(=C(C)CO)C(=O)C1)C	250.33	unknown	https://doi.org/10.1248/CPB.38.55
(1Z,3R,5S,8S,10R,12S)-5,10,15,15-tetramethyl-4,9,13,14-tetraoxatetracyclo[10.3.0.03,5.08,10]pentadec-1-en-12-ol	101603568	Click to see CC1(C2=CC3C(O3)(CCC4C(O4)(CC2(OO1)O)C)C)C	282.33	unknown	https://doi.org/10.1248/CPB.39.854
(1Z,3S,5S,8S,10S,12S)-5,10,15,15-tetramethyl-4,9,13,14-tetraoxatetracyclo[10.3.0.03,5.08,10]pentadec-1-en-12-ol	21769359	Click to see CC1(C2=CC3C(O3)(CCC4C(O4)(CC2(OO1)O)C)C)C	282.33	unknown	https://doi.org/10.1248/CPB.39.854
(3E,6E,10S)-3-(1-hydroxypropan-2-ylidene)-6,10-dimethylcyclodec-6-ene-1,4-dione	21769413	Click to see CC1CCC=C(CC(=O)C(=C(C)CO)CC1=O)C	250.33	unknown	https://doi.org/10.1248/CPB.38.55
(3R,6E,10S)-6,10-Dimethyl-3-propan-2-ylcyclodec-6-ene-1,4-dione	10466651	Click to see CC1CCC=C(CC(=O)C(CC1=O)C(C)C)C	236.35	unknown	https://doi.org/10.1248/CPB.35.53 https://doi.org/10.1248/CPB.39.843 https://doi.org/10.1271/BBB.67.911
(3Z,7E,10Z)-10-(1-hydroxypropan-2-ylidene)-3,7-dimethylcyclodeca-3,7-dien-1-one	139031767	Click to see CC1=CCC(=C(C)CO)C(=O)CC(=CCC1)C	234.33	unknown	https://doi.org/10.1248/CPB.38.55
(6E,10S)-6,10-dimethyl-3-propan-2-ylidenecyclodec-6-ene-1,4-dione	10421549	Click to see CC1CCC=C(CC(=O)C(=C(C)C)CC1=O)C	234.33	unknown	https://doi.org/10.1248/CPB.35.53
(6E)-3-[(E)-1-(Acetoxymethyl)ethylidene]-6,10alpha-dimethyl-6-cyclodecene-1,4-dione	21769412	Click to see CC1CCC=C(CC(=O)C(=C(C)COC(=O)C)CC1=O)C	292.40	unknown	https://doi.org/10.1248/CPB.38.55
(6E)-6,10-dimethyl-3-propan-2-ylcyclodec-6-ene-1,4-dione	5316216	Click to see CC1CCC=C(CC(=O)C(CC1=O)C(C)C)C	236.35	unknown	https://doi.org/10.1248/CPB.35.53 https://doi.org/10.1248/CPB.39.843
(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/10.1002/FFJ.2730040106
[(2E)-2-[(1S,6E,10S)-6,10-dimethyl-4-oxo-11-oxabicyclo[8.1.0]undec-6-en-3-ylidene]propyl] acetate	101528955	Click to see CC1=CCCC2(C(O2)CC(=C(C)COC(=O)C)C(=O)C1)C	292.40	unknown	https://doi.org/10.1248/CPB.38.55
[(2S)-2-[(1R,4E,8S)-4,8-dimethyl-2,9-dioxocyclodec-4-en-1-yl]propyl] acetate	162962858	Click to see CC1CCC=C(CC(=O)C(CC1=O)C(C)COC(=O)C)C	294.40	unknown	https://doi.org/10.1248/CPB.38.55
[(2Z)-2-[(1S,6E,10S)-6,10-dimethyl-4-oxo-11-oxabicyclo[8.1.0]undec-6-en-3-ylidene]propyl] acetate	14543206	Click to see CC1=CCCC2(C(O2)CC(=C(C)COC(=O)C)C(=O)C1)C	292.40	unknown	https://doi.org/10.1248/CPB.38.55
10-(1-Hydroxypropan-2-ylidene)-3,7-dimethylcyclodeca-3,7-dien-1-one	74329201	Click to see CC1=CCC(=C(C)CO)C(=O)CC(=CCC1)C	234.33	unknown	https://doi.org/10.1248/CPB.38.55
13-Hydroxygermacrone	10399140	Click to see CC1=CCC(=C(C)CO)C(=O)CC(=CCC1)C	234.33	unknown	https://doi.org/10.1248/CPB.38.55
2-(4,8-Dimethyl-2,9-dioxocyclodec-4-en-1-yl)propyl acetate	72732663	Click to see CC1CCC=C(CC(=O)C(CC1=O)C(C)COC(=O)C)C	294.40	unknown	https://doi.org/10.1248/CPB.38.55
2-(4,8-Dimethyl-2,9-dioxocyclodec-4-en-1-ylidene)propyl acetate	73834006	Click to see CC1CCC=C(CC(=O)C(=C(C)COC(=O)C)CC1=O)C	292.40	unknown	https://doi.org/10.1248/CPB.38.55
2-(6,10-Dimethyl-4-oxo-11-oxabicyclo[8.1.0]undec-6-en-3-ylidene)propyl acetate	73834009	Click to see CC1=CCCC2(C(O2)CC(=C(C)COC(=O)C)C(=O)C1)C	292.40	unknown	https://doi.org/10.1248/CPB.38.55
3-(1-Hydroxypropan-2-ylidene)-6,10-dimethyl-11-oxabicyclo[8.1.0]undec-6-en-4-one	73834008	Click to see CC1=CCCC2(C(O2)CC(=C(C)CO)C(=O)C1)C	250.33	unknown	https://doi.org/10.1248/CPB.38.55
3-(1-Hydroxypropan-2-ylidene)-6,10-dimethylcyclodec-6-ene-1,4-dione	73834007	Click to see CC1CCC=C(CC(=O)C(=C(C)CO)CC1=O)C	250.33	unknown	https://doi.org/10.1248/CPB.38.55
3,7-Cyclodecadien-1-one, 3,7-dimethyl-10-(1-methylethylidene)-, (Z,E)-	81323	Click to see CC1=CCC(=C(C)C)C(=O)CC(=CCC1)C	218.33	unknown	https://doi.org/10.1248/CPB.35.53 https://doi.org/10.1248/BPB.26.1135
4,11-Dimethyl-8-propan-2-ylidene-5-oxatricyclo[9.1.0.04,6]dodecan-9-one	162870774	Click to see CC(=C1CC2C(O2)(CCC3CC3(CC1=O)C)C)C	248.36	unknown	https://doi.org/10.1002/HLCA.200900059
5,10,15,15-Tetramethyl-4,9,13,14-tetraoxatetracyclo[10.3.0.03,5.08,10]pentadec-1-en-12-ol	73657400	Click to see CC1(C2=CC3C(O3)(CCC4C(O4)(CC2(OO1)O)C)C)C	282.33	unknown	https://doi.org/10.1248/CPB.39.854
6,10-Dimethyl-3-propan-2-ylidene-11-oxabicyclo[8.1.0]undec-6-en-4-one	73037839	Click to see CC1=CCCC2(C(O2)CC(=C(C)C)C(=O)C1)C	234.33	unknown	https://doi.org/10.1248/CPB.35.53 https://doi.org/10.1248/CPB.39.843 https://doi.org/10.1002/HLCA.200900059
6,10-Dimethyl-3-propan-2-ylidenecyclodec-6-ene-1,4-dione	78173043	Click to see CC1CCC=C(CC(=O)C(=C(C)C)CC1=O)C	234.33	unknown	https://doi.org/10.1248/CPB.35.53
CID 131675179	131675179	Click to see CC1CCC=C(CC(=O)C(CC1=O)C(C)C)C	236.35	unknown	https://doi.org/10.1248/CPB.35.53 https://doi.org/10.1016/J.BSE.2009.09.008 https://doi.org/10.1248/CPB.39.843
Dehydrocurdione	14191392	Click to see CC1CCC=C(CC(=O)C(=C(C)C)CC1=O)C	234.33	unknown	https://doi.org/10.1248/CPB.35.53
Germacr-1(10)-ene-5,8-dione	6441391	Click to see CC1CCC=C(CC(=O)C(CC1=O)C(C)C)C	236.35	unknown	https://doi.org/10.1248/CPB.35.53 https://doi.org/10.1248/BPB.26.1135 https://doi.org/10.1248/CPB.39.843 https://doi.org/10.1248/CPB.20.987 https://doi.org/10.1002/HLCA.200900059
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730040106
Germacrone	6436348	Click to see CC1=CCC(=C(C)C)C(=O)CC(=CCC1)C	218.33	unknown	https://doi.org/10.1002/FFJ.2730040106 https://doi.org/10.1248/CPB.35.53
Neocurdione	24836956	Click to see CC1CCC=C(CC(=O)C(CC1=O)C(C)C)C	236.35	unknown	https://doi.org/10.1248/CPB.35.53 https://doi.org/10.1016/J.BSE.2009.09.008 https://doi.org/10.1248/CPB.39.843 https://doi.org/10.1271/BBB.67.911
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(1S,2S,5S,9R)-2-methyl-6-methylidene-9-propan-2-yl-11-oxatricyclo[6.2.1.01,5]undecan-8-ol	57336521	Click to see CC1CCC2C13CC(C(O3)(CC2=C)O)C(C)C	236.35	unknown	via CMAUP database
(1S,3abeta,8abeta)-Octahydro-1beta,4beta-dihydroxy-7-isopropylidene-1,4-dimethylazulen-6(5H)-one	14632999	Click to see CC(=C1CC2C(CCC2(C)O)C(CC1=O)(C)O)C	252.35	unknown	https://doi.org/10.1248/CPB.35.53
(1S,5R,8R)-2-methyl-6-methylidene-9-propan-2-yl-11-oxatricyclo[6.2.1.01,5]undecan-8-ol	138107810	Click to see CC1CCC2C13CC(C(O3)(CC2=C)O)C(C)C	236.35	unknown	https://doi.org/10.1016/J.BSE.2009.09.008
(3R,3aR,8aS)-3-hydroxy-3,8-dimethyl-5-propan-2-ylidene-2,3a,4,8a-tetrahydro-1H-azulen-6-one	97289691	Click to see CC1=CC(=O)C(=C(C)C)CC2C1CCC2(C)O	234.33	unknown	https://doi.org/10.1248/CPB.35.53
(3S,3aS,8aR)-3-hydroxy-3-methyl-8-methylidene-5-propan-2-ylidene-2,3a,4,8a-tetrahydro-1H-azulen-6-one	14543198	Click to see CC(=C1CC2C(CCC2(C)O)C(=C)CC1=O)C	234.33	unknown	https://doi.org/10.1248/CPB.38.55
(5S,8S)-2-methyl-6-methylidene-9-propan-2-yl-11-oxatricyclo[6.2.1.01,5]undecan-8-ol	5316215	Click to see CC1CCC2C13CC(C(O3)(CC2=C)O)C(C)C	236.35	unknown	https://doi.org/10.1248/CPB.32.3783
2-Methyl-6-methylidene-9-(propan-2-yl)-11-oxatricyclo[6.2.1.0^{1,5}]undecan-8-ol	3559861	Click to see CC1CCC2C13CC(C(O3)(CC2=C)O)C(C)C	236.35	unknown	https://doi.org/10.1248/CPB.39.843
3-Hydroxy-3,8-dimethyl-5-(propan-2-ylidene)-1,2,3,3a,4,5,6,8a-octahydroazulen-6-one	5320710	Click to see CC1=CC(=O)C(=C(C)C)CC2C1CCC2(C)O	234.33	unknown	https://doi.org/10.1248/CPB.35.53 https://doi.org/10.1248/CPB.38.55
3-Hydroxy-8-methoxy-3,8-dimethyl-5-propan-2-ylidene-1,2,3a,4,7,8a-hexahydroazulen-6-one	73813177	Click to see CC(=C1CC2C(CCC2(C)O)C(CC1=O)(C)OC)C	266.38	unknown	https://doi.org/10.1248/CPB.35.53
4,10-Epizedoarondiol	24834047	Click to see CC(=C1CC2C(CCC2(C)O)C(CC1=O)(C)O)C	252.35	unknown	https://doi.org/10.1248/CPB.35.53
ent-Isozedoaronediol	25754115	Click to see CC(=C1CC2C(CCC2(C)O)C(CC1=O)(C)O)C	252.35	unknown	https://doi.org/10.1248/CPB.35.53
Epiprocurcumenol	10263440	Click to see CC1=CC(=O)C(=C(C)C)CC2C1CCC2(C)O	234.33	unknown	https://doi.org/10.1248/CPB.38.55
Isoprocurcumenol	14543197	Click to see CC(=C1CC2C(CCC2(C)O)C(=C)CC1=O)C	234.33	unknown	https://doi.org/10.1248/CPB.38.55
Isozedoarondiol	14632998	Click to see CC(=C1CC2C(CCC2(C)O)C(CC1=O)(C)O)C	252.35	unknown	https://doi.org/10.1248/CPB.35.53
Methylzedoarondiol	21626407	Click to see CC(=C1CC2C(CCC2(C)O)C(CC1=O)(C)OC)C	266.38	unknown	https://doi.org/10.1248/CPB.35.53
Procurcumenol	189061	Click to see CC1=CC(=O)C(=C(C)C)CC2C1CCC2(C)O	234.33	unknown	https://doi.org/10.1248/CPB.35.53
Zedoarondiol	14632997	Click to see CC(=C1CC2C(CCC2(C)O)C(CC1=O)(C)O)C	252.35	unknown	https://doi.org/10.1248/CPB.35.53
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(5Z,9E,11aR)-11a-hydroxy-3,6,10-trimethyl-8,11-dihydro-7H-cyclodeca[b]furan-2,4-dione	101492101	Click to see CC1=CC(=O)C2=C(C(=O)OC2(CC(=CCC1)C)O)C	262.30	unknown	https://doi.org/10.1002/HLCA.200900059
(6S,11aS)-11a-hydroxy-3,6,10-trimethyl-6,7,8,11-tetrahydro-4H-cyclodeca[b]furan-2,5-dione	162961717	Click to see CC1CCC=C(CC2(C(=C(C(=O)O2)C)CC1=O)O)C	264.32	unknown	https://doi.org/10.1016/J.FITOTE.2009.05.004
(6S,9E,11aR)-11a-hydroxy-3,6,10-trimethyl-6,7,8,11-tetrahydro-4H-cyclodeca[b]furan-2,5-dione	44254209	Click to see CC1CCC=C(CC2(C(=C(C(=O)O2)C)CC1=O)O)C	264.32	unknown	https://doi.org/10.1002/HLCA.200900059
(6S,9E,11aR)-3,6,10-trimethyl-4,6,7,8,11,11a-hexahydrocyclodeca[b]furan-2,5-dione	44254211	Click to see CC1CCC=C(CC2C(=C(C(=O)O2)C)CC1=O)C	248.32	unknown	https://doi.org/10.1002/HLCA.200900059
11a-Hydroxy-3,6,10-trimethyl-4,7,8,11-tetrahydrocyclodeca[b]furan-2-one	137796297	Click to see CC1=CCC2=C(C(=O)OC2(CC(=CCC1)C)O)C	248.32	unknown	https://doi.org/10.1002/HLCA.200900059
3,6,10-Trimethyl-4,6,7,8,11,11a-hexahydrocyclodeca[b]furan-2,5-dione	74975743	Click to see CC1CCC=C(CC2C(=C(C(=O)O2)C)CC1=O)C	248.32	unknown	https://doi.org/10.1002/HLCA.200900059
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
Androstenedione	6128	Click to see CC12CCC(=O)C=C1CCC3C2CCC4(C3CCC4=O)C	286.40	unknown	via CMAUP database
Testosterone	6013	Click to see CC12CCC3C(C1CCC2O)CCC4=CC(=O)CCC34C	288.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Spirosolanes and derivatives
(2S,4S,5'R,6R,9S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol	45114619	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1	413.60	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
Aurantiamide	185904	Click to see C1=CC=C(C=C1)CC(CO)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3	402.50	unknown	https://doi.org/10.1016/J.FITOTE.2009.05.004
Benzenepropanamide, alpha-(benzoylamino)-N-[1-(hydroxymethyl)-2-phenylethyl]-, [S-(R,R)]-; (alphaS)-alpha-(Benzoylamino)-N-[(1S)-1-(hydroxymethyl)-2-phenylethyl]benzenepropanamide	53463263	Click to see C1=CC=C(C=C1)CC(CO)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3	402.50	unknown	https://doi.org/10.1016/J.FITOTE.2009.05.004
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(1S,2R,5S,6R)-2,5,6-triacetyloxy-1-hydroxycyclohex-3-en-1-yl]methyl benzoate	163056874	Click to see CC(=O)OC1C=CC(C(C1OC(=O)C)(COC(=O)C2=CC=CC=C2)O)OC(=O)C	406.40	unknown	https://doi.org/10.1016/J.FITOTE.2009.05.004
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
Cibarin	322363	Click to see C(C[N+](=O)[O-])C(=O)OCC1C(C(C(C(O1)OC(=O)CC[N+](=O)[O-])O)O)O	382.28	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Benzofuran	9223	Click to see C1=CC=C2C(=C1)C=CO2	118.13	unknown	https://doi.org/10.1016/J.ACA.2011.11.010
> 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	https://doi.org/10.1016/J.BSE.2009.09.008
Hydron;2,3,5,6-tetramethylpyrazine;chloride	45108167	Click to see [H+].CC1=C(N=C(C(=N1)C)C)C.[Cl-]	172.65	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3S,5S,6S,9S)-6-methyl-3-propan-2-yl-9-prop-1-en-2-yl-1-oxaspiro[4.4]nonan-2-one	101618788	Click to see CC1CCC(C12CC(C(=O)O2)C(C)C)C(=C)C	236.35	unknown	https://doi.org/10.1248/CPB.33.2179
> Organoheterocyclic compounds / Oxanes
Eucalyptol	2758	Click to see CC1(C2CCC(O1)(CC2)C)C	154.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1E,6e)-1-(4-hydroxy-3-methoxyphenyl)-7-(3-methoxy-4-methylphenyl)-1,6-heptadiene-3,5-dione	44629981	Click to see CC1=C(C=C(C=C1)C=CC(=O)CC(=O)C=CC2=CC(=C(C=C2)O)OC)OC	366.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
(1E,4Z,6E)-5-hydroxy-1,7-bis(4-hydroxy-3-methoxyphenyl)hepta-1,4,6-trien-3-one	5281767	Click to see COC1=C(C=CC(=C1)C=CC(=CC(=O)C=CC2=CC(=C(C=C2)O)OC)O)O	368.40	unknown	via CMAUP database
(1E,4Z,6E)-5-hydroxy-1,7-bis(4-hydroxyphenyl)hepta-1,4,6-trien-3-one	5324473	Click to see C1=CC(=CC=C1C=CC(=CC(=O)C=CC2=CC=C(C=C2)O)O)O	308.30	unknown	via CMAUP database
(1Z,6E)-1,7-bis(4-hydroxy-3-methoxyphenyl)-4-[1-hydroxy-2-(4-methylphenyl)ethyl]hepta-1,6-diene-3,5-dione	5321967	Click to see CC1=CC=C(C=C1)CC(C(C(=O)C=CC2=CC(=C(C=C2)O)OC)C(=O)C=CC3=CC(=C(C=C3)O)OC)O	502.60	unknown	via CMAUP database
Curcumin	969516	Click to see COC1=C(C=CC(=C1)C=CC(=O)CC(=O)C=CC2=CC(=C(C=C2)O)OC)O	368.40	unknown	via CMAUP database
Demethoxycurcumin	5469424	Click to see COC1=C(C=CC(=C1)C=CC(=O)CC(=O)C=CC2=CC=C(C=C2)O)O	338.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Phellatin	44258781	Click to see CC(C)(CCC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	534.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
7-Epi-Zeaenol	53355130	Click to see CC1CC=CC(C(C(CC=CC2=C(C(=CC(=C2)OC)O)C(=O)O1)O)O)O	364.40	unknown	via CMAUP database
Cochliomycin A, (rel)-	52952745	Click to see CC1CC=CC2C(C(CC=CC3=C(C(=CC(=C3)OC)O)C(=O)O1)O)OC(O2)(C)C	404.50	unknown	via CMAUP database
Cochliomycin B	52952746	Click to see CC1CC=CC(C2C(CC=CC3=C(C(=CC(=C3)OC)O)C(=O)O1)OC(O2)(C)C)O	404.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues / Zearalenones
5E-7-oxozeaenol	9799061	Click to see CC1CC=CC(=O)C(C(CC=CC2=C(C(=CC(=C2)OC)O)C(=O)O1)O)O	362.40	unknown	via CMAUP database
5Z-7-Oxozeaenol	9863776	Click to see CC1CC=CC(=O)C(C(CC=CC2=C(C(=CC(=C2)OC)O)C(=O)O1)O)O	362.40	unknown	via CMAUP database

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Curcuma aromatica

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