Etlingera elatior

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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	UUID643ffa10009d8193899636
Scientific name	Etlingera elatior
Authority	(Jack) R.M.Sm.
First published in	Notes Roy. Bot. Gard. Edinburgh 43 (2):244. (1986)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Alpinia acrostachya	Steud.	Nomencl. bot. Ed. 2 62
Alpinia diracodes	Loes.	Nat. Pflanzenfam. Ed. 2 (A):614
Alpinia elatior	Jack	Descriptions of Malayan plants (7):2
Alpinia javanica	(Blume) D.Dietr.	Syn. pl. 13
Alpinia magnifica	Roscoe	Monandr. pl. Scitam. t75
Alpinia speciosa	(Blume) D.Dietr.	Syn. pl. 13; Lectotypified in: Edinburgh J. Bot. 60:192. (2003)
Amomum magnificum	(Roscoe) Benth. ex B.D.Jacks.	Index Kew. 108
Bojeria magnifica	(Roscoe) Raf.	Fl. Tellur. 4:50. (1838)
Cardamomum magnificum	(Roscoe) Kuntze	Revis. gen. pl. 687
Cardamomum speciosum	(Blume) Kuntze	Revis. gen. pl. 686
Diracodes javanica	Blume	Enum. pl. Javae 55
Elettaria speciosa	Blume	Enum. pl. Javae 51; Lectotypified in: Edinburgh J. Bot. 60:192. (2003)
Hornstedtia imperialis	(Lindl.) Ridl.	J. Straits Branch Roy. Asiat. Soc. 32:148. (1899)
Nicolaia elatior	(Jack) Horan.	Prodr. Monogr. Scitam. 32
Nicolaia imperialis	Horan.	Prodr. Monogr. Scitam. 32
Nicolaia intermedia	Valeton	Bull. Jard. Bot. Buitenzorg (series 3) 3:133. (1921)
Nicolaia magnifica	(Roscoe) K.Schum. ex Valeton	Bull. Inst. Bot. Buitenzorg 20:35. (1904)
Nicolaia speciosa	(Blume) Horan.	Prodr. Monogr. Scitam. 32; Lectotypified in: Edinburgh J. Bot. 60:192. (2003)
Phaeomeria imperialis	Lindl.	Intr. Nat. Syst. Bot. Ed. 2 446
Phaeomeria magnifica	(Roscoe) K.Schum.	Pflanzenr. IV (Heft 20):262
Phaeomeria speciosa	(Blume) Koord.	Exkurs.-Fl. Java 332; Lectotypified in: Edinburgh J. Bot. 60:192. (2003)

Common names Top

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Language	Common/alternative name
English	torch-ginger
ace	bungong kala
ace	kala
ban	kecicang
bjn	patikala
dtp	kombugu
French	rose de porcelaine
Indonesian	bunga kantan
Indonesian	asam cekala
Indonesian	kecombrang
Indonesian	sambuang
Indonesian	kumbang sekala
Indonesian	kincung
Indonesian	kecicang
Indonesian	kantan
Indonesian	honje
Indonesian	bungong kala
Indonesian	bunga rias
Indonesian	asam cikala
Japanese	トーチジンジャー
jv	kecombrang
Latvian	malajas laterningvers
min	kincuang
min	sambuang
min	kincong
Malay	bunga kantan
Malay	kecombrang
nia	silimo
Punjab	گلابی دیوا
Portuguese	rosa-de-porcelana
Portuguese	rosa de porcelana
su	honje
su	honjé
Thai	ต้นดาหลา
Thai	ดาหลา
ty	’ōpuhi ra’ura’a pa’ari
Chinese	火炬姜

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Etlingera elatior var. alba	S.Todam & C.K.Lim	Folia malaysiana 2:170. (2001)
Etlingera elatior var. elatior	R.M.Sm.	Notes Roy. Bot. Gard. Edinburgh 43:244. (1986)
Etlingera elatior var. pileng	Ongsakul & C.K.Lim	Folia malaysiana 2:169. (2001)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- West-central Tropical Africa
  - Gulf Of Guinea Islands
- Western Indian Ocean
  - Comoros
  - Mauritius

Asia-temperate click to expand
- China
  - China South-central

Asia-tropical click to expand
- Indo-China
  - Thailand
- Malesia
  - Borneo
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - New Guinea

Pacific click to expand
- Northwestern Pacific
  - Caroline Islands
- Southwestern Pacific
  - Vanuatu

Southern America click to expand
- Caribbean
  - Dominican Republic
  - Puerto Rico
  - Trinidad-Tobago
- Central America
  - Costa Rica
  - Honduras

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000415565
USDA Plants	ETEL
Tropicos	50068776
INPN	448304
KEW	urn:lsid:ipni.org:names:942355-1
The Plant List	kew-244696
Missouri Botanical Garden	291516
Open Tree Of Life	539421
NCBI Taxonomy	188493
IUCN Red List	117234456
IPNI	942355-1
iNaturalist	126577
GBIF	2759896
Freebase	/m/0b3p3t
EPPO	NCLEL
EOL	1119410
USDA GRIN	409477
Wikipedia	Etlingera_elatior
CMAUP	NPO5878

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

Worldwide forest surveys reveal forty-three new species in Phytophthora major Clade 2 with fundamental implications for the evolution and biogeography of the genus and global plant biosecurity

Jung T, Milenković I, Balci Y, Janoušek J, Kudláček T, Nagy ZÁ, Baharuddin B, Bakonyi J, Broders KD, Cacciola SO, Chang TT, Chi NM, Corcobado T, Cravador A, Đorđević B, Durán A, Ferreira M, Fu CH, Garcia L, Hieno A, Ho HH, Hong C, Junaid M, Kageyama K, Kuswinanti T, Maia C, Májek T, Masuya H, Magnano di San Lio G, Mendieta-Araica B, Nasri N, Oliveira LS, Pane A, Pérez-Sierra A, Rosmana A, Sanfuentes von Stowasser E, Scanu B, Singh R, Stanivuković Z, Tarigan M, Thu PQ, Tomić Z, Tomšovský M, Uematsu S, Webber JF, Zeng HC, Zheng FC, Brasier CM, Horta Jung M

Stud Mycol

27-Feb-2024

PMCID:	PMC11003442
doi:	10.3114/sim.2024.107.04
PMID:	38600961

Discovering Potential Compounds for Venous Disease Treatment through Virtual Screening and Network Pharmacology Approach

Barrera-Vázquez OS, Escobar-Ramírez JL, Santiago-Mejía J, Carrasco-Ortega OF, Magos-Guerrero GA

Molecules

05-Dec-2023

PMCID:	PMC10745828
doi:	10.3390/molecules28247937
PMID:	38138427

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

Analysis of the characterization of NaOH-treated natural cellulose fibre extracted from banyan aerial roots

Thandavamoorthy R, Devarajan Y, Thanappan S

Sci Rep

03-Aug-2023

PMCID:	PMC10400698
doi:	10.1038/s41598-023-39229-9
PMID:	37537228

Pseudanthia in angiosperms: a review

Baczyński J, Claßen-Bockhoff R

Ann Bot

21-Jul-2023

PMCID:	PMC10583202
doi:	10.1093/aob/mcad103
PMID:	37478306

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

Ethanolic extract of Etlingera elatior flower exhibits anthelmintic properties to Fasciola gigantica in vitro

Wulandari AR, Nurlaelasari A, Nugroho HA, Cahyadi M, Kurniawan W, Hamid PH

Open Vet J

11-May-2023

PMCID:	PMC10257460
doi:	10.5455/OVJ.2023.v13.i5.10
PMID:	37304615

A novel mushroom (Auricularia polytricha) glycoprotein protects against lead-induced hepatoxicity, promotes lead adsorption, inhibits organ accumulation of lead, upregulates detoxifying proteins, and enhances immunoregulation in rats

Zhao S, Gao Y, Wang H, Fan Y, Wang P, Zhao W, Wong JH, Wang D, Zhao X, Ng TB

Front Nutr

06-Apr-2023

PMCID:	PMC10116064
doi:	10.3389/fnut.2023.1144346
PMID:	37090774

Promising Application of Automated Liquid Culture System and Arbuscular Mycorrhizal Fungi for Large-Scale Micropropagation of Red Dragon Fruit

Dewir YH, Habib MM, Alaizari AA, Malik JA, Al-Ali AM, Al-Qarawi AA, Alwahibi MS

Plants (Basel)

24-Feb-2023

PMCID:	PMC10005386
doi:	10.3390/plants12051037
PMID:	36903898

A Review of Medicinal Plants with Renoprotective Activity in Diabetic Nephropathy Animal Models

Putra IM, Fakhrudin N, Nurrochmad A, Wahyuono S

Life (Basel)

16-Feb-2023

PMCID:	PMC9963806
doi:	10.3390/life13020560
PMID:	36836916

Therapeutic Potential of Extracts from Macaranga tanarius (MTE) in Diabetic Nephropathy

Hsu YC, Chang CC, Hsieh CC, Shih YH, Chang HC, Lin CL

Plants (Basel)

02-Feb-2023

PMCID:	PMC9920382
doi:	10.3390/plants12030656
PMID:	36771740

Functional bioactive compounds in ginger, turmeric, and garlic

Ajanaku CO, Ademosun OT, Atohengbe PO, Ajayi SO, Obafemi YD, Owolabi OA, Akinduti PA, Ajanaku KO

Front Nutr

08-Dec-2022

PMCID:	PMC9773837
doi:	10.3389/fnut.2022.1012023
PMID:	36570131

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

Novel Drug Design for Treatment of COVID-19: A Systematic Review of Preclinical Studies

Mousavi S, Zare S, Mirzaei M, Feizi A

Can J Infect Dis Med Microbiol

25-Sep-2022

PMCID:	PMC9527439
doi:	10.1155/2022/2044282
PMID:	36199815

Occurrence of Raoiella indica Hirst (Acari, Tenuipalpidae) in the Southeast region of the state of Pará, Brazil

da Cruz WP, Souza MC, Lacerda JD, Souza ÁI, Silva PA, dos Santos EC

J Plant Dis Prot (2006)

10-Aug-2022

PMCID:	PMC9364286
doi:	10.1007/s41348-022-00659-8
PMID:	35965942

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 / Anthracenes / Anthraquinones
Aloe emodin	10207	Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)CO	270.24	unknown	via CMAUP database
Pulmatin	442731	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)CO)O)O)O	416.40	unknown	via CMAUP database
Rheochrysin	168938	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)OC	446.40	unknown	via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 1-O-beta-D-glucoside	5319333	Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)O	432.40	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol	14529	Click to see CC1=CC=C(C=C1)C(C)(C)O	150.22	unknown	https://doi.org/10.1080/10412905.1993.9698191
> Benzenoids / Benzene and substituted derivatives / Toluenes
1-Allyl-2-methylbenzene	15317	Click to see CC1=CC=CC=C1CC=C	132.20	unknown	https://doi.org/10.1080/10412905.1993.9698191
Toluene	1140	Click to see CC1=CC=CC=C1	92.14	unknown	https://doi.org/10.1080/10412905.1993.9698191
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hexadecane	11006	Click to see CCCCCCCCCCCCCCCC	226.44	unknown	https://doi.org/10.1080/10412905.1993.9698191
Tetradecane	12389	Click to see CCCCCCCCCCCCCC	198.39	unknown	https://doi.org/10.1080/10412905.1993.9698191
Undecane	14257	Click to see CCCCCCCCCCC	156.31	unknown	https://doi.org/10.1080/10412905.1993.9698191
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristelaidic acid	5312402	Click to see CCCCC=CCCCCCCCC(=O)O	226.35	unknown	via CMAUP database
Myristic Acid	11005	Click to see CCCCCCCCCCCCCC(=O)O	228.37	unknown	https://doi.org/10.1080/10412905.1993.9698191
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid	2969	Click to see CCCCCCCCCC(=O)O	172.26	unknown	https://doi.org/10.1080/10412905.1993.9698191
Lauric Acid	3893	Click to see CCCCCCCCCCCC(=O)O	200.32	unknown	https://doi.org/10.1080/10412905.1993.9698191
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
7-Tetradecenyl acetate	86893	Click to see CCCCCCC=CCCCCCCOC(=O)C	254.41	unknown	https://doi.org/10.1080/10412905.1993.9698191
Decyl acetate	8167	Click to see CCCCCCCCCCOC(=O)C	200.32	unknown	https://doi.org/10.1080/10412905.1993.9698191
Dodecyl acetate	8205	Click to see CCCCCCCCCCCCOC(=O)C	228.37	unknown	https://doi.org/10.1080/10412905.1993.9698191
Oct-2-enyl acetate	102248	Click to see CCCCCC=CCOC(=O)C	170.25	unknown	https://doi.org/10.1080/10412905.1993.9698191
Tetradecyl acetate	12531	Click to see CCCCCCCCCCCCCCOC(=O)C	256.42	unknown	https://doi.org/10.1080/10412905.1993.9698191
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(Z)-7-Dodecen-1-ol	29925	Click to see CCCCC=CCCCCCCO	184.32	unknown	https://doi.org/10.1080/10412905.1993.9698191
1-Decanol	8174	Click to see CCCCCCCCCCO	158.28	unknown	https://doi.org/10.1080/10412905.1993.9698191
1-Dodecanol	8193	Click to see CCCCCCCCCCCCO	186.33	unknown	https://doi.org/10.1080/10412905.1993.9698191
1-Undecanol	8184	Click to see CCCCCCCCCCCO	172.31	unknown	https://doi.org/10.1080/10412905.1993.9698191
2-Nonanol	12367	Click to see CCCCCCCC(C)O	144.25	unknown	https://doi.org/10.1080/10412905.1993.9698191
9-Decen-1-OL	25612	Click to see C=CCCCCCCCCO	156.26	unknown	https://doi.org/10.1080/10412905.1993.9698191
9-Dodecen-1-ol	93181	Click to see CCC=CCCCCCCCCO	184.32	unknown	https://doi.org/10.1080/10412905.1993.9698191
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
1-Tetradecanol	8209	Click to see CCCCCCCCCCCCCCO	214.39	unknown	https://doi.org/10.1080/10412905.1993.9698191
Tetradec-10-en-1-ol	54009476	Click to see CCCC=CCCCCCCCCCO	212.37	unknown	https://doi.org/10.1080/10412905.1993.9698191
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
alpha-Tocopherolquinone	2734086	Click to see CC1=C(C(=O)C(=C(C1=O)C)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O)C	446.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698191
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698191
> 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/10.1080/10412905.1993.9698191
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one	6973628	Click to see CC1=CC(=O)C2CC1C2(C)C	150.22	unknown	https://doi.org/10.1080/10412905.1993.9698191
3-Carene	26049	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698191
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698191
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698191
trans-Borneol	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
Verbenone	29025	Click to see CC1=CC(=O)C2CC1C2(C)C	150.22	unknown	https://doi.org/10.1080/10412905.1993.9698191
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698191
Beta-Phellandrene	11142	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698191
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698191
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698191
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1Z,5E)-1,4,4-trimethyl-8-methylidenecycloundeca-1,5-diene	5879124	Click to see CC1=CCC(C=CCC(=C)CCC1)(C)C	204.35	unknown	via CMAUP database
(3R,6E)-nerolidol	11241545	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1080/10412905.1993.9698191
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698191
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698191
Nerolidol	8888	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1080/10412905.1993.9698191
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(2S)-3-[(E)-2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethenyl]-2-hydroxy-2H-furan-5-one	92466427	Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=CC(=O)OC3O)C)C	316.40	unknown	https://doi.org/10.1021/NP040098L
3-[2-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)ethenyl]-2-hydroxy-2H-furan-5-one	72756762	Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=CC(=O)OC3O)C)C	316.40	unknown	https://doi.org/10.1021/NP040098L
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,5R,8R,9S,10S,13R,14S,17R)-17-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,5,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	162888584	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2C=CC4C3(CCC(C4)O)C)C	398.70	unknown	https://doi.org/10.1021/NP040098L
17-(5,6-dimethylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	77708066	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2C=CC4C3(CCC(C4)O)C)C	398.70	unknown	https://doi.org/10.1021/NP040098L
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(6beta,24R)-6-Hydroxystigmast-4-en-3-one	14769504	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C	428.70	unknown	https://doi.org/10.1021/NP040098L
6beta-Hydroxystigmast-4-en-3-one	9823926	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C	428.70	unknown	https://doi.org/10.1021/NP040098L
Stigmast-4-ee-3,6-dione	14308881	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(=O)C4=CC(=O)CCC34C)C)C(C)C	426.70	unknown	https://doi.org/10.1021/NP040098L
Stigmast-4-en-3-one	5484202	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	412.70	unknown	https://doi.org/10.1021/NP040098L
Stigmast-4-ene-3,6-dione	5490007	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(=O)C4=CC(=O)CCC34C)C)C(C)C	426.70	unknown	https://doi.org/10.1021/NP040098L
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
Isoamyl alcohol	31260	Click to see CC(C)CCO	88.15	unknown	https://doi.org/10.1080/10412905.1993.9698191
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
10-Undecenal	8187	Click to see C=CCCCCCCCCC=O	168.28	unknown	https://doi.org/10.1080/10412905.1993.9698191
Decanal	8175	Click to see CCCCCCCCCC=O	156.26	unknown	https://doi.org/10.1080/10412905.1993.9698191
Dodecanal	8194	Click to see CCCCCCCCCCCC=O	184.32	unknown	https://doi.org/10.1080/10412905.1993.9698191
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Nonanone	13187	Click to see CCCCCCCC(=O)C	142.24	unknown	https://doi.org/10.1080/10412905.1993.9698191
2-Tridecanone	11622	Click to see CCCCCCCCCCCC(=O)C	198.34	unknown	https://doi.org/10.1080/10412905.1993.9698191
2-Undecanone	8163	Click to see CCCCCCCCCC(=O)C	170.29	unknown	https://doi.org/10.1080/10412905.1993.9698191
> Organoheterocyclic compounds / Benzodioxoles
Myristicin	4276	Click to see COC1=CC(=CC2=C1OCO2)CC=C	192.21	unknown	via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
Furfuryl alcohol	7361	Click to see C1=COC(=C1)CO	98.10	unknown	https://doi.org/10.1080/10412905.1993.9698191
> 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
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1E,4E,6E)-1,7-bis(4-hydroxyphenyl)hepta-1,4,6-trien-3-one	10447050	Click to see C1=CC(=CC=C1C=CC=CC(=O)C=CC2=CC=C(C=C2)O)O	292.30	unknown	https://doi.org/10.1021/NP040098L
(2E,4E,6E)-1,7-bis(4-hydroxyphenyl)hepta-2,4,6-trien-1-one	11277770	Click to see C1=CC(=CC=C1C=CC=CC=CC(=O)C2=CC=C(C=C2)O)O	292.30	unknown	https://doi.org/10.1021/NP040098L
1,7-Bis (4-hydroxyphenyl)-1,4,6-heptatrien-3-one	71346280	Click to see C1=CC(=CC=C1C=CC=CC(=O)C=CC2=CC=C(C=C2)O)O	292.30	unknown	https://doi.org/10.1021/NP040098L
1,7-Bis(4-hydroxyphenyl)hepta-2,4,6-trien-1-one	71406643	Click to see C1=CC(=CC=C1C=CC=CC=CC(=O)C2=CC=C(C=C2)O)O	292.30	unknown	https://doi.org/10.1021/NP040098L
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
1-(4-Hydroxy-3-methoxyphenyl)-7-(4-hydroxyphenyl)-1,6-heptadiene-3,5-dione	146723	Click to see COC1=C(C=CC(=C1)C=CC(=O)CC(=O)C=CC2=CC=C(C=C2)O)O	338.40	unknown	https://doi.org/10.1021/NP040098L
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	https://doi.org/10.1021/NP040098L
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
2,3-Dihydroamentoflavone 7,4'-dimethyl ether	11613892	Click to see COC1=C(C=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O	568.50	unknown	via CMAUP database
6-[5-(5,7-Dihydroxy-4-oxochromen-2-yl)-2-methoxyphenyl]-5,7-dihydroxy-2-(4-methoxyphenyl)chromen-4-one	11649838	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)OC)O	566.50	unknown	via CMAUP database
Amentoflavone	5281600	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O	538.50	unknown	via CMAUP database
Heveaflavone	15559724	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)OC)O)O	580.50	unknown	via CMAUP database
Robustaflavone-7,4'-dimethyl ether	10816812	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O)C4=C(C5=C(C=C4O)OC(=CC5=O)C6=CC=C(C=C6)O)O	566.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
Tsugafolin	21721822	Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(O2)C=C(C=C3OC)O	300.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Kavalactones
Demethoxyyangonin	5273621	Click to see COC1=CC(=O)OC(=C1)C=CC2=CC=CC=C2	228.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Cardamonin	641785	Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O	270.28	unknown	via CMAUP database

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Etlingera elatior

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