Wurfbainia longiligularis

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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	UUID644069c72a35b598018115
Scientific name	Wurfbainia longiligularis
Authority	(T.L.Wu) Škorničk. & A.D.Poulsen
First published in	Taxon 67:30. (2018)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Amomum longiligulare	T.L.Wu	Fl. Hainan. 533

Common names Top

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Language	Common/alternative name
Japanese	カイナンシャジン
Chinese	海南砂仁

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 Southeast
  - Hainan

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

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0001426461
KEW	urn:lsid:ipni.org:names:77178281-1
Open Tree Of Life	424823
NCBI Taxonomy	648859
IUCN Red List	202212
IPNI	77178281-1
GBIF	10748345
CMAUP	NPO1479

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

Effects of intercropping teak with Alpinia katsumadai Hayata and Amomum longiligulare T.L. Wu on rhizosphere soil nutrients and bacterial community diversity, structure, and network

Xianbang W, Mingping L, Kunliang L, Qiang H, Dongkang P, Haibin M, Guihua H

Front Microbiol

19-Feb-2024

PMCID:	PMC10910098
doi:	10.3389/fmicb.2024.1328772
PMID:	38440142

Zishen Yutai Pills Promote Angiogenesis at the Maternal-Fetal Interface in Recurrent Spontaneous Abortion Mice by Regulating miR-187/VEGF Axis

Wang X, Hu H, Yu X, Liang C, Han Y, Chen H, Chu J

Drug Des Devel Ther

12-Feb-2024

PMCID:	PMC10871043
doi:	10.2147/DDDT.S436718
PMID:	38370565

Integrated transcriptomics and metabolomics analysis provides insights into aromatic volatiles formation in Cinnamomum cassia bark at different harvesting times

Yao S, Tan X, Huang D, Li L, Chen J, Ming R, Huang R, Yao C

BMC Plant Biol

02-Feb-2024

PMCID:	PMC10835945
doi:	10.1186/s12870-024-04754-w
PMID:	38308239

Efficacy and safety of the integration of traditional Chinese medicine and western medicine in the treatment of diabetes-associated cognitive decline: a systematic review and meta-analysis

Su J, Sun G, An J, Ao Y, Li J, Shen Z, Zhang L, Zhang S, Yang Y, Shi Y

Front Pharmacol

22-Nov-2023

PMCID:	PMC10703163
doi:	10.3389/fphar.2023.1280736
PMID:	38074157

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

Li MF, Xiao T, Zhang YH

Mitochondrial DNA B Resour

15-Nov-2023

PMCID:	PMC10653761
doi:	10.1080/23802359.2023.2281029
PMID:	38026495

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

Multiomics comparison among populations of three plant sources of Amomi Fructus

Chen X, Sun S, Han X, Li C, Wang F, Nie B, Hou Z, Yang S, Ji J, Li G, Wang Y, Han X, Yue J, Li C, Li W, Zhang L, Yang D, Wang L

Hortic Res

01-Aug-2023

PMCID:	PMC10407604
doi:	10.1093/hr/uhad128
PMID:	37560015

Development of a variety and quality evaluation method for Amomi fructus using GC, electronic tongue, and electronic nose

Hou F, Fan X, Gui X, Li H, Li H, Wang Y, Shi J, Zhang L, Yao J, Li X, Liu R

Front Chem

15-Jun-2023

PMCID:	PMC10310405
doi:	10.3389/fchem.2023.1188219
PMID:	37398979

Pharmacological targeting of gastric mucosal barrier with traditional Chinese medications for repairing gastric mucosal injury

Jia X, He Y, Li L, Xu D

Front Pharmacol

08-Jun-2023

PMCID:	PMC10285076
doi:	10.3389/fphar.2023.1091530
PMID:	37361204

Insight into the phytochemical profile and antimicrobial activities of Amomum subulatum and Amomum xanthioides: an in vitro and in silico study

Alruhaili MH, Almuhayawi MS, Gattan HS, Alharbi MT, Nagshabandi MK, Jaouni SK, Selim S, AbdElgawad H

Front Plant Sci

20-Apr-2023

PMCID:	PMC10157186
doi:	10.3389/fpls.2023.1136961
PMID:	37152127

Chemopreventive effects of Xiang Sha Liu Jun Zi Tang on paclitaxel-induced leucopenia and neuropathy in animals

Shiah HS, Lee CJ, Lee FY, Tseng SH, Chen SH, Wang CC

Front Pharmacol

02-Mar-2023

PMCID:	PMC10032344
doi:	10.3389/fphar.2023.1106030
PMID:	36969850

Salt processing: A unique and classic technology for Chinese medicine processing

Hou A, Lv J, Zhang S, Zhang J, Yang L, Jiang H, Kuang H

Front Pharmacol

30-Jan-2023

PMCID:	PMC9922854
doi:	10.3389/fphar.2023.1116047
PMID:	36794272

‘Food and medicine continuum’ in the East and West: Old tradition and current regulation

Yao R, He C, Xiao P

Chin Herb Med

17-Dec-2022

PMCID:	PMC9975626
doi:	10.1016/j.chmed.2022.12.002
PMID:	36875443

Progress of Studies on Plant-Derived Polysaccharides Affecting Intestinal Barrier Function in Poultry

Guo S, Xing Y, Xu Y, Jin X, Yan S, Shi B

Animals (Basel)

18-Nov-2022

PMCID:	PMC9686483
doi:	10.3390/ani12223205
PMID:	36428432

Chinese herbal medicine for migraine management: A hospital-based retrospective analysis of electronic medical records

Lyu S, Zhang CS, Sun J, Weng H, Xue CC, Guo X, Zhang AL

Front Med (Lausanne)

10-Nov-2022

PMCID:	PMC9684313
doi:	10.3389/fmed.2022.936234
PMID:	36438031

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 / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
p-Anisic acid	7478	Click to see COC1=CC=C(C=C1)C(=O)O	152.15	unknown	via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-(4-Hydroxyphenyl)-2-butanone	21648	Click to see CC(=O)CCC1=CC=C(C=C1)O	164.20	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Cycloalkanes
Cycloeicosane	520444	Click to see C1CCCCCCCCCCCCCCCCCCC1	280.50	unknown	via CMAUP database
Cyclotetracosane	520449	Click to see C1CCCCCCCCCCCCCCCCCCCCCCC1	336.60	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Hexadecene	12395	Click to see CCCCCCCCCCCCCCC=C	224.42	unknown	via CMAUP database
1-Nonadecene	29075	Click to see CCCCCCCCCCCCCCCCCC=C	266.50	unknown	via CMAUP database
1-Octadecene	8217	Click to see CCCCCCCCCCCCCCCCC=C	252.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	via CMAUP database
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(Z)-Santalol	91753183	Click to see CC=CC=CC=CC=CCCCCCCO	220.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
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	via CMAUP database
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-(1S,4S)-Borneol	6850744	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
(-)-Camphene	440966	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	via CMAUP database
(-)-Camphor	444294	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
(-)-Fenchone	82229	Click to see CC1(C2CCC(C2)(C1=O)C)C	152.23	unknown	via CMAUP database
(+)-4-Carene	71351627	Click to see CC1CC2C(C2(C)C)C=C1	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
(+)-Fenchone	1201521	Click to see CC1(C2CCC(C2)(C1=O)C)C	152.23	unknown	via CMAUP database
(+)-Isoborneol	6973640	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
(1R,2R)-1,7,7-trimethylnorbornan-2-ol	512289	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	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
(1R,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-OL	12242824	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	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,2S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol	12242815	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
(1S)-1,3,3-Trimethylbicyclo[2.2.1]heptan-2-one	12049113	Click to see CC1(C2CCC(C2)(C1=O)C)C	152.23	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
(2S,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl acetate	44630108	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
(4R)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-one	16213045	Click to see CC1(C2CCC(C2)(C1=O)C)C	152.23	unknown	via CMAUP database
(R)-Fenchone; L-(-)-Fenchone; L-Fenchone; l-Fenchone	2794921	Click to see CC1(C2CCC(C2)(C1=O)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	via CMAUP database
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	via CMAUP database
Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, exo-	439569	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
Borneol	6552009	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
Borneol, (-)-	1201518	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
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	via CMAUP database
Camphor	2537	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
Camphor (synthetic)	159055	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
Camphor, (1S,4S)-(-)-	10050	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
d-2-Bornanone	9543187	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
d-Borneol	61060	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
d-Camphor	230921	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
DL-2-Bornanol	10049	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
DL-Borneol	10492	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
DL-Isoborneol	230920	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
endo-2-Bornanol	439568	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
Fenchone	14525	Click to see CC1(C2CCC(C2)(C1=O)C)C	152.23	unknown	via CMAUP database
Isoborneol	6321405	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
Sumatra camphor	657014	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
> 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
(+) Menthol	12285346	Click to see CC1CCC(C(C1)O)C(C)C	156.26	unknown	via CMAUP database
(+)-alpha-Phellandrene	443160	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	via CMAUP database
(+)-Menthol	165675	Click to see CC1CCC(C(C1)O)C(C)C	156.26	unknown	via CMAUP database
(+)-Neomenthol	439263	Click to see CC1CCC(C(C1)O)C(C)C	156.26	unknown	via CMAUP database
(+)-Terpinen-4-ol	2724161	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	via CMAUP database
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	via CMAUP database
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	via CMAUP database
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	via CMAUP database
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	via CMAUP database
beta-Terpineol	8748	Click to see CC(=C)C1CCC(CC1)(C)O	154.25	unknown	via CMAUP database
l-Menthol	16666	Click to see CC1CCC(C(C1)O)C(C)C	156.26	unknown	via CMAUP database
l-Menthyl propionate	221455	Click to see CCC(=O)OC1CC(CCC1C(C)C)C	212.33	unknown	via CMAUP database
Limonene, (-)-	439250	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Menthol	1254	Click to see CC1CCC(C(C1)O)C(C)C	156.26	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Copaene	442355	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
(-)-alpha-Cubebene	86609	Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	via CMAUP database
(+)-beta-Caryophyllene	20831623	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
(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	via CMAUP database
(3S,6E,8S)-3,7,11-trimethyldodeca-1,6,10-triene-3,8-diol	10105633	Click to see CC(=CCC(C(=CCCC(C)(C=C)O)C)O)C	238.37	unknown	via CMAUP database
(4Z)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene	5322111	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
(E)-5-(2,3-dimethyl-3-tricyclo[2.2.1.02,6]heptanyl)-2-methylpent-2-en-1-ol;(E)-2-methyl-5-(2-methyl-3-methylidene-2-bicyclo[2.2.1]heptanyl)pent-2-en-1-ol	6537105	Click to see CC(=CCCC1(C2CCC(C2)C1=C)C)CO.CC(=CCCC1(C2CC3C1(C3C2)C)C)CO	440.70	unknown	via CMAUP database
(Z)-2-methyl-6-(2-methyl-3-tricyclo[2.2.1.02,6]heptanyl)hept-2-en-1-ol	5352146	Click to see CC(CCC=C(C)CO)C1C2CC3C1(C3C2)C	234.38	unknown	via CMAUP database
(Z)-5-(2,3-dimethyl-3-tricyclo[2.2.1.02,6]heptanyl)-2-methylpent-2-en-1-ol;(Z)-2-methyl-5-(2-methyl-3-methylidene-2-bicyclo[2.2.1]heptanyl)pent-2-en-1-ol	5351571	Click to see CC(=CCCC1(C2CCC(C2)C1=C)C)CO.CC(=CCCC1(C2CC3C1(C3C2)C)C)CO	440.70	unknown	via CMAUP database
(Z)-alpha-Santalol	5281531	Click to see CC(=CCCC1(C2CC3C1(C3C2)C)C)CO	220.35	unknown	via CMAUP database
(Z)-caryophyllene	6429301	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
1-Methyl-4-(1-methylethylidene)-2-(1-methylvinyl)-1-vinylcyclohexane	94254	Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C	204.35	unknown	via CMAUP database
1,3-Dimethyl-8-(1-methylethyl)-tricyclo[4.4.0.02,7]dec-3-ene	25245021	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane	6432312	Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C	204.35	unknown	via CMAUP database
3-((1S)-1,5-Dimethyl-4-hexenyl)-6-methylene-1-cyclohexene, (3R)-	91746521	Click to see CC(CCC=C(C)C)C1CCC(=C)C=C1	204.35	unknown	via CMAUP database
3-(1,5-Dimethyl-4-hexenyl)-6-methylene-1-cyclohexene	519764	Click to see CC(CCC=C(C)C)C1CCC(=C)C=C1	204.35	unknown	via CMAUP database
4-Isopropyl-1,6-dimethyl-1,2,3,4,4a,7,8,8a-octahydro-1-naphthalenol	519662	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
5-(2,3-Dimethyl-3-tricyclo[2.2.1.02,6]heptanyl)-2-methylpent-2-en-1-ol;2-methyl-5-(2-methyl-3-methylidene-2-bicyclo[2.2.1]heptanyl)pent-2-en-1-ol	61530	Click to see CC(=CCCC1(C2CCC(C2)C1=C)C)CO.CC(=CCCC1(C2CC3C1(C3C2)C)C)CO	440.70	unknown	via CMAUP database
5-[(1R,3R)-2,3-dimethyl-3-tricyclo[2.2.1.02,6]heptanyl]-2-methylpent-2-en-1-ol;2-methyl-5-[(1R,2S,4S)-2-methyl-3-methylidene-2-bicyclo[2.2.1]heptanyl]pent-2-en-1-ol	53488169	Click to see CC(=CCCC1(C2CCC(C2)C1=C)C)CO.CC(=CCCC1(C2CC3C1(C3C2)C)C)CO	440.70	unknown	via CMAUP database
5-[(1S,3R)-2,3-dimethyl-3-tricyclo[2.2.1.02,6]heptanyl]-2-methylpent-2-en-1-ol;2-methyl-5-[(1S,2R,4R)-2-methyl-3-methylidene-2-bicyclo[2.2.1]heptanyl]pent-2-en-1-ol	16072318	Click to see CC(=CCCC1(C2CCC(C2)C1=C)C)CO.CC(=CCCC1(C2CC3C1(C3C2)C)C)CO	440.70	unknown	via CMAUP database
alpha-Cadinol #1	6431302	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
alpha-Copaene	70678558	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
Alpha-Farnesene	5281516	Click to see CC(=CCCC(=CCC=C(C)C=C)C)C	204.35	unknown	via CMAUP database
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
Caryophyllene,alpha + beta mixt.	5354499	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
cis-Nerolidol	5320128	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	via CMAUP database
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
Copaene	12303902	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
Copaene, (+)-	636457	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
d-alpha-Santalol	5368797	Click to see CC(=CCCC1(C2CC3C1(C3C2)C)C)CO	220.35	unknown	via CMAUP database
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	via CMAUP database
Isocaryophyllene	5281522	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
Santalol (alpha and beta)	24832101	Click to see CC(=CCCC1(C2CCC(C2)C1=C)C)CO.CC(=CCCC1(C2CC3C1(C3C2)C)C)CO	440.70	unknown	via CMAUP database
tau-Muurolol	6432221	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
trans-Nerolidol	5284507	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)-	9859094	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Pygmol	14167388	Click to see CC12CCCC(C1C(C(CC2)C(C)(C)O)O)(C)O	256.38	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(+)-Germacrene D	24771782	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
(1E)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene	74764030	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
(1Z,6Z)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene	5373727	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
(1Z)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene	92003564	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
(2E,6E)-Hedycaryol	10998630	Click to see CC1=CCCC(=CCC(CC1)C(C)(C)O)C	222.37	unknown	via CMAUP database
(6E,8S)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene	49796490	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
1-Hydroxy-1,7-dimethyl-4-isopropyl-2,7-cyclodecadiene	5367550	Click to see CC1=CCCC(C=CC(CC1)C(C)C)(C)O	222.37	unknown	via CMAUP database
1-Methyl-5-methylene-8-(1-methylethyl)-1,6-cyclodecadiene	6436582	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
Hedycaryol	6432240	Click to see CC1=CCCC(=CCC(CC1)C(C)(C)O)C	222.37	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 oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
5-(3,3-Dimethyloxiran-2-yl)-3-methylpent-1-en-3-ol	529304	Click to see CC1(C(O1)CCC(C)(C=C)O)C	170.25	unknown	via CMAUP database
> 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
Dihydroyashabushiketol	10265808	Click to see C1=CC=C(C=C1)CCC(CC(=O)CCC2=CC=CC=C2)O	282.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(1R,2R,3S,4R,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexoxy]chromen-4-one	15959354	Click to see C1C(C(C(C(C1OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O)CO	462.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5-Dihydroxy-7-methoxy-2-(4-methoxyphenyl)-4H-chromen-4-one	5378823	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)O	314.29	unknown	via CMAUP database
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	via CMAUP database
Ombuin	5320287	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)O)O	330.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin	5280804	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database
Quercetin 3-O-rhamnoside	5353915	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	via CMAUP database
Quercitrin	5280459	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Genistoside	5284639	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	via CMAUP database

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Wurfbainia longiligularis

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