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Wurfbainia longiligularis

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

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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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
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
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
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
Comparative chloroplast genome analyses of Amomum: insights into evolutionary history and species identification Gong L, Ding X, Guan W, Zhang D, Zhang J, Bai J, Xu W, Huang J, Qiu X, Zheng X, Zhang D, Li S, Huang Z, Su H BMC Plant Biol 09-Nov-2022
PMCID:PMC9644571
doi:10.1186/s12870-022-03898-x
PMID:36352400
Chromosome-level genome assembly of Amomum tsao-ko provides insights into the biosynthesis of flavor compounds Li P, Bai G, He J, Liu B, Long J, Morcol T, Peng W, Quan F, Luan X, Wang Z, Zhao Y, Cha Y, Liu Y, He J, Wu L, Yang Y, Kennelly EJ, Yang Q, Sun L, Chen Z, Qian W, Hu J, Yan J Hortic Res 19-Sep-2022
PMCID:PMC9719038
doi:10.1093/hr/uhac211
PMID:36479578

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
(+)-Camphor 9543187 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 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,2S,4R)-Borneol 439568 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
(1S-endo)-1,7,7-trimethylbicyclo(2.2.1)heptan-2-ol 10049 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
(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
Borneo camphor 12242824 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
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-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
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
L-Born-2-yl acetate 44630108 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown via CMAUP database
Sumatra camphor 657014 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
trans-Borneol 44630107 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
(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)-caryophyllene 6429301 Click to see CC1=CCCC(=C)C2CC(C2CC1)(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
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-(2,3-dimethyltricyclo[2.2.1.0~2,6~]hept-3-yl)-2-methylpent-2-en-1-ol (alpha form) & 2-Methyl-5-(2-methyl-3-methylenebicyclo[2.2.1]hept-2-yl)pent-2-en-1-ol (beta form) 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
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
8-Isopropyl-1,3-dimethyltricyclo(4.4.0.02,7)dec-3-ene 12303902 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 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
alpha-Santalol 5281531 Click to see CC(=CCCC1(C2CC3C1(C3C2)C)C)CO 220.35 unknown via CMAUP database
beta-Sesquiphellandrene 519764 Click to see CC(CCC=C(C)C)C1CCC(=C)C=C1 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, (+)- 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
gamma-Elemene 94254 Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C 204.35 unknown via CMAUP database
Hedychiol A 10105633 Click to see CC(=CCC(C(=CCCC(C)(C=C)O)C)O)C 238.37 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)-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
1,6-Cyclodecadiene, 1-methyl-5-methylene-8-(1-methylethyl)-, [s-(E,E)]- 5373727 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
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 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
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
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
Genistein 7-O-beta-D-glucoside 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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