{
"METABOLOMICS WORKBENCH":{"STUDY_ID":"ST002102","ANALYSIS_ID":"AN003436","VERSION":"1","CREATED_ON":"March 12, 2022, 3:54 pm"},

"PROJECT":{"PROJECT_TITLE":"Volatilomic compound identification in several Indonesian underutilized Zingiberaceae spices using SPME-GC/MS","PROJECT_TYPE":"Research","PROJECT_SUMMARY":"to identify compounds in Zingiberaceae spices grown in Indonesia using SPME-GC/MS","INSTITUTE":"IPB University","DEPARTMENT":"Departement of Food Science and Technology","LABORATORY":"Food Chemistry","LAST_NAME":"Yuliana","FIRST_NAME":"Nancy Dewi","ADDRESS":"Fakultas Teknologi Pertanian (FATETA) Institut Pertanian Bogor. Kampus IPB Darmaga Jl. Lingkar Akademik, Jawa Barat 16680, Telp./faksimili : (0251) 8626725","EMAIL":"nancy_dewi@apps.ipb.ac.id","PHONE":"+6282236024900","FUNDING_SOURCE":"Ministry of Research and Technology/National Research and Innovation Agency through the scheme of World Class Research (WCR) Financial Year 2021 Number: 2355 /IT3.L1/PN/2021","PUBLICATIONS":"Food Chemistry:X","CONTRIBUTORS":"Fitra Tunnisa, Didah Nur Faridah, Ani Afriyanti, Dian Rosalina, Mohamad Ana Syabana, Noviyan Darmawan, Nancy Dewi Yuliana"},

"STUDY":{"STUDY_TITLE":"Volatilomic compound identification in several Indonesian underutilized Zingiberaceae spices using SPME-GC/MS","STUDY_SUMMARY":"To identify compounds in 12 minor Zingiberaceae spices grown in Indonesia using SPME-GC/MS","INSTITUTE":"IPB University","DEPARTMENT":"Departement of Food Science and Technology","LABORATORY":"Food Chemistry","LAST_NAME":"Yuliana","FIRST_NAME":"Nancy Dewi","ADDRESS":"Fakultas Teknologi Pertanian (FATETA) Institut Pertanian Bogor. Kampus IPB Darmaga Jl. Lingkar Akademik, Jawa Barat 16680, Telp./faksimili : (0251) 8626725","EMAIL":"nancy_dewi@apps.ipb.ac.id","STUDY_TYPE":"Research","PHONE":"+6282236024900"},

"SUBJECT":{"SUBJECT_TYPE":"Plant","SUBJECT_SPECIES":"Zingiberaceae","TAXONOMY_ID":"4642"},
"SUBJECT_SAMPLE_FACTORS":[
{
"Subject ID":"-",
"Sample ID":"AC U1",
"Factors":{"Species":"Amomum compactum Sol. ex Maton"},
"Additional sample data":{"RAW_FILE_NAME":"AC U1.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"AC U2",
"Factors":{"Species":"Amomum compactum Sol. ex Maton"},
"Additional sample data":{"RAW_FILE_NAME":"AC U2.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"AC U3",
"Factors":{"Species":"Amomum compactum Sol. ex Maton"},
"Additional sample data":{"RAW_FILE_NAME":"AC U3.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"AM U1",
"Factors":{"Species":"Alpinia malaccensis (Burm.f.) Roscoe"},
"Additional sample data":{"RAW_FILE_NAME":"AM U1.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"AM U2",
"Factors":{"Species":"Alpinia malaccensis (Burm.f.) Roscoe"},
"Additional sample data":{"RAW_FILE_NAME":"AM U2.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"AM U3",
"Factors":{"Species":"Alpinia malaccensis (Burm.f.) Roscoe"},
"Additional sample data":{"RAW_FILE_NAME":"AM U3.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"BR U1",
"Factors":{"Species":"Boesenbergia rotunda L. Mansf."},
"Additional sample data":{"RAW_FILE_NAME":"BR U1.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"BR U2",
"Factors":{"Species":"Boesenbergia rotunda L. Mansf."},
"Additional sample data":{"RAW_FILE_NAME":"BR U2.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"BR U3",
"Factors":{"Species":"Boesenbergia rotunda L. Mansf."},
"Additional sample data":{"RAW_FILE_NAME":"BR U3.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"CA U1",
"Factors":{"Species":"Curcuma aeruginosa Roxb"},
"Additional sample data":{"RAW_FILE_NAME":"CA U1.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"CA U2",
"Factors":{"Species":"Curcuma aeruginosa Roxb"},
"Additional sample data":{"RAW_FILE_NAME":"CA U2.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"CA U3",
"Factors":{"Species":"Curcuma aeruginosa Roxb"},
"Additional sample data":{"RAW_FILE_NAME":"CA U3.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"CH U1",
"Factors":{"Species":"Curcuma heyneana Val. & Zijp"},
"Additional sample data":{"RAW_FILE_NAME":"CH U1.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"CH U2",
"Factors":{"Species":"Curcuma heyneana Val. & Zijp"},
"Additional sample data":{"RAW_FILE_NAME":"CH U2.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"CH U3",
"Factors":{"Species":"Curcuma heyneana Val. & Zijp"},
"Additional sample data":{"RAW_FILE_NAME":"CH U3.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"CP U1",
"Factors":{"Species":"Curcuma purpurascens Blume"},
"Additional sample data":{"RAW_FILE_NAME":"CP U1.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"CP U2",
"Factors":{"Species":"Curcuma purpurascens Blume"},
"Additional sample data":{"RAW_FILE_NAME":"CP U2.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"CP U3",
"Factors":{"Species":"Curcuma purpurascens Blume"},
"Additional sample data":{"RAW_FILE_NAME":"CP U3.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"CT U1",
"Factors":{"Species":"Curcuma petiolata Roxb"},
"Additional sample data":{"RAW_FILE_NAME":"CT U1.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"CT U2",
"Factors":{"Species":"Curcuma petiolata Roxb"},
"Additional sample data":{"RAW_FILE_NAME":"CT U2.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"CT U3",
"Factors":{"Species":"Curcuma petiolata Roxb"},
"Additional sample data":{"RAW_FILE_NAME":"CT U3.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"CZ U1",
"Factors":{"Species":"Curcuma zedoria Roscoe"},
"Additional sample data":{"RAW_FILE_NAME":"CZ U1.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"CZ U2",
"Factors":{"Species":"Curcuma zedoria Roscoe"},
"Additional sample data":{"RAW_FILE_NAME":"CZ U2.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"CZ U3",
"Factors":{"Species":"Curcuma zedoria Roscoe"},
"Additional sample data":{"RAW_FILE_NAME":"CZ U3.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"ZA U1",
"Factors":{"Species":"Zingiber aromaticum Val."},
"Additional sample data":{"RAW_FILE_NAME":"ZA U1.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"ZA U2",
"Factors":{"Species":"Zingiber aromaticum Val."},
"Additional sample data":{"RAW_FILE_NAME":"ZA U2.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"ZA U3",
"Factors":{"Species":"Zingiber aromaticum Val."},
"Additional sample data":{"RAW_FILE_NAME":"ZA U3.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"ZC U1",
"Factors":{"Species":"Zingiber purpureum Roscoe"},
"Additional sample data":{"RAW_FILE_NAME":"ZC U1.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"ZC U2",
"Factors":{"Species":"Zingiber purpureum Roscoe"},
"Additional sample data":{"RAW_FILE_NAME":"ZC U2.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"ZC U3",
"Factors":{"Species":"Zingiber purpureum Roscoe"},
"Additional sample data":{"RAW_FILE_NAME":"ZC U3.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"ZO U1",
"Factors":{"Species":"Zingiber ottensii Val."},
"Additional sample data":{"RAW_FILE_NAME":"ZO U1.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"ZO U2",
"Factors":{"Species":"Zingiber ottensii Val."},
"Additional sample data":{"RAW_FILE_NAME":"ZO U2.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"ZO U3",
"Factors":{"Species":"Zingiber ottensii Val."},
"Additional sample data":{"RAW_FILE_NAME":"ZO U3.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"ZZ U1",
"Factors":{"Species":"Zingiber zerumpet L. Roscoe ex Sm."},
"Additional sample data":{"RAW_FILE_NAME":"ZZ U1.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"ZZ U2",
"Factors":{"Species":"Zingiber zerumpet L. Roscoe ex Sm."},
"Additional sample data":{"RAW_FILE_NAME":"ZZ U2.qgd"}
},
{
"Subject ID":"-",
"Sample ID":"ZZ U3",
"Factors":{"Species":"Zingiber zerumpet L. Roscoe ex Sm."},
"Additional sample data":{"RAW_FILE_NAME":"ZZ U3.qgd"}
}
],
"COLLECTION":{"COLLECTION_SUMMARY":"Volatilomic compound using SPME-GC/MS from 12 minor Zingiberaceae spices","SAMPLE_TYPE":"Rhizome","COLLECTION_METHOD":"The thawed spice samples","COLLECTION_LOCATION":"Indonesia","STORAGE_CONDITIONS":"-20℃"},

"TREATMENT":{"TREATMENT_SUMMARY":"The twelve of spice samples were cut, sliced thinly into a uniform size, and put in a headspace vial.","TREATMENT_PROTOCOL_ID":"method of SPME/GC-MS"},

"SAMPLEPREP":{"SAMPLEPREP_SUMMARY":"The samples was heated, and the SPME was then inserted into the headspace vial and was exposed to the sample without touching it, and then inject to GC-MS"},

"CHROMATOGRAPHY":{"CHROMATOGRAPHY_SUMMARY":"Samples injected to GC-MS","CHROMATOGRAPHY_TYPE":"GC","INSTRUMENT_NAME":"Shimadzu Nexis GC-2030","COLUMN_NAME":"Stabilwax column (60 m, 0.25 mm ID, film thickness 0.25 m","FLOW_RATE":"1 mL/min","COLUMN_TEMPERATURE":"40- 250","METHODS_FILENAME":"GC-MS Analysis","SOLVENT_A":"Helium","INJECTION_TEMPERATURE":"80","TIME_PROGRAM":"40 minutes"},

"ANALYSIS":{"ANALYSIS_TYPE":"MS"},

"MS":{"INSTRUMENT_NAME":"Shimadzu GCMS-QP2020 NX","INSTRUMENT_TYPE":"Single quadrupole","MS_TYPE":"EI","ION_MODE":"UNSPECIFIED","MS_COMMENTS":"GCMSsolution"},

"MS_METABOLITE_DATA":{
"Units":"Percent peak area (%)",

"Data":[{"Metabolite":"Tricyclo[2.2.1.0(2,6)]heptane, 1,7,7-trimethyl-","ZC U1":"0","ZC U2":"0","ZC U3":"0","ZA U1":"0.603031964","ZA U2":"0.481831123","ZA U3":"0.469420371","AM U1":"0","AM U2":"0","AM U3":"0","CP U1":"0","CP U2":"0","CP U3":"0","AC U1":"0","AC U2":"0","AC U3":"0","CA U1":"0","CA U2":"0","CA U3":"0","BR U1":"0.451880897","BR U2":"0.451892105","BR U3":"0.381187167","ZZ U1":"0.182021387","ZZ U2":"0.178875346","ZZ U3":"0.112447549","CT U1":"0.224192907","CT U2":"0.327577216","CT U3":"0.279579501","CZ U1":"0.160983996","CZ U2":"0.124127177","CZ U3":"0.14200675","CH U1":"0","CH U2":"0.128187159","CH U3":"0","ZO U1":"0","ZO U2":"0","ZO U3":"0"},{"Metabolite":"α-Pinene","ZC U1":"2.46448252","ZC U2":"2.735150965","ZC U3":"2.711015136","ZA U1":"5.93084379","ZA U2":"5.038169915","ZA U3":"6.333570018","AM U1":"11.31097296","AM U2":"11.53813566","AM U3":"10.3057997","CP U1":"5.332196099","CP U2":"5.532141187","CP U3":"4.106169521","AC U1":"3.335303428","AC U2":"1.356397566","AC U3":"2.745088219","CA U1":"2.737398916","CA U2":"2.021686846","CA U3":"1.758509806","BR U1":"1.426946678","BR U2":"1.435790894","BR U3":"1.389866008","ZZ U1":"2.809454716","ZZ U2":"3.051820026","ZZ U3":"2.442763219","CT U1":"1.112255213","CT U2":"1.924130517","CT U3":"1.378578409","CZ U1":"0.865063636","CZ U2":"0.768472124","CZ U3":"0.819201549","CH U1":"3.506253977","CH U2":"6.296680665","CH U3":"3.746934465","ZO U1":"3.999421851","ZO U2":"3.265728899","ZO U3":"3.664473688"},{"Metabolite":"α-Phellandrene","ZC U1":"1.109235929","ZC U2":"1.25104341","ZC U3":"1.072971681","ZA U1":"0.044915762","ZA U2":"0.172574723","ZA U3":"0.172549496","AM U1":"11.03512502","AM U2":"7.660831584","AM U3":"9.286668686","CP U1":"1.15193829","CP U2":"1.529197617","CP U3":"0.871176337","AC U1":"0.143470729","AC U2":"0.124802975","AC U3":"0.247196124","CA U1":"0.24511362","CA U2":"0.181992375","CA U3":"0.115354321","BR U1":"0","BR U2":"0","BR U3":"0","ZZ U1":"0.665223129","ZZ U2":"0.950811419","ZZ U3":"1.588581006","CT U1":"0.039070479","CT U2":"0.080186466","CT U3":"0.052705434","CZ U1":"0","CZ U2":"0","CZ U3":"0","CH U1":"0","CH U2":"1.869635724","CH U3":"0.855611481","ZO U1":"0.823867188","ZO U2":"0.76674341","ZO U3":"1.008048158"},{"Metabolite":"Bicyclo[2.2.1]heptane, 7,7-dimethyl-2-methylene","ZC U1":"0","ZC U2":"0","ZC U3":"0","ZA U1":"0","ZA U2":"0","ZA U3":"0.065033408","AM U1":"0.067158827","AM U2":"0.060369584","AM U3":"0.080708578","CP U1":"0","CP U2":"0","CP U3":"0","AC U1":"0.173666134","AC U2":"0.050899448","AC U3":"0.19288506","CA U1":"0","CA U2":"0.062904099","CA U3":"0.297667799","BR U1":"0.06033023","BR U2":"0.056684826","BR U3":"0.0469118","ZZ U1":"0.094986105","ZZ U2":"0.073448058","ZZ U3":"0.04208152","CT U1":"0","CT U2":"0","CT U3":"0","CZ U1":"0","CZ U2":"0","CZ U3":"0","CH U1":"0","CH U2":"0","CH U3":"0","ZO U1":"0","ZO U2":"0","ZO U3":"0"},{"Metabolite":"Camphene","ZC U1":"0.076253805","ZC U2":"0.058366859","ZC U3":"0.076624676","ZA U1":"19.96981599","ZA U2":"17.72460712","ZA U3":"14.83908678","AM U1":"0.86387839","AM U2":"0.89993269","AM U3":"1.15864608","CP U1":"2.212279221","CP U2":"3.362736512","CP U3":"1.765413831","AC U1":"0.409029553","AC U2":"0.128761859","AC U3":"0.443116836","CA U1":"5.364350446","CA U2":"0.159130386","CA U3":"0.683835302","BR U1":"7.801182044","BR U2":"8.013248018","BR U3":"6.797673999","ZZ U1":"6.498779545","ZZ U2":"5.323132166","ZZ U3":"2.662788911","CT U1":"6.067634351","CT U2":"8.755533112","CT U3":"7.470644749","CZ U1":"3.60807122","CZ U2":"3.084400488","CZ U3":"3.125451253","CH U1":"1.768652956","CH U2":"2.794081037","CH U3":"2.895406022","ZO U1":"0.345051144","ZO U2":"0.267249345","ZO U3":"0.319944821"},{"Metabolite":"β-Pinene","ZC U1":"4.873013547","ZC U2":"5.371269981","ZC U3":"5.098579511","ZA U1":"0.198131808","ZA U2":"0.19189438","ZA U3":"0.325489777","AM U1":"16.16843605","AM U2":"17.7983055","AM U3":"13.35016561","CP U1":"10.46730983","CP U2":"11.2986042","CP U3":"7.126892739","AC U1":"2.975529668","AC U2":"5.614490878","AC U3":"5.547966026","CA U1":"3.787169434","CA U2":"2.929800974","CA U3":"3.193433841","BR U1":"0.021663263","BR U2":"0.030028173","BR U3":"0.039718946","ZZ U1":"0.397152721","ZZ U2":"0.700070466","ZZ U3":"0.643911956","CT U1":"1.339743288","CT U2":"7.300410153","CT U3":"5.05935776","CZ U1":"0","CZ U2":"0","CZ U3":"0","CH U1":"9.290943865","CH U2":"14.74155945","CH U3":"8.088326176","ZO U1":"12.55729572","ZO U2":"11.59843115","ZO U3":"12.15853977"},{"Metabolite":"β-Phellandrene","ZC U1":"35.84447768","ZC U2":"30.06449606","ZC U3":"40.03770141","ZA U1":"0","ZA U2":"0.034888227","ZA U3":"0","AM U1":"0.441118996","AM U2":"0.536187106","AM U3":"0.321054846","CP U1":"3.019290621","CP U2":"0.161132114","CP U3":"0.249229925","AC U1":"1.110004399","AC U2":"0.94745348","AC U3":"1.349922998","CA U1":"0.789290456","CA U2":"0.345274801","CA U3":"1.208632844","BR U1":"0.02280275","BR U2":"0.051318483","BR U3":"0.014364225","ZZ U1":"0","ZZ U2":"0.391739228","ZZ U3":"2.426119371","CT U1":"0","CT U2":"0.155069522","CT U3":"0.058505086","CZ U1":"0","CZ U2":"0","CZ U3":"0","CH U1":"0.570622237","CH U2":"0.764056367","CH U3":"0.385928673","ZO U1":"28.00360339","ZO U2":"27.10031395","ZO U3":"27.01164161"},{"Metabolite":"3-Carene","ZC U1":"0.009941914","ZC U2":"0","ZC U3":"0","ZA U1":"0.743134673","ZA U2":"2.779510626","ZA U3":"4.256081244","AM U1":"0.066376441","AM U2":"0.101142455","AM U3":"0.084955783","CP U1":"0","CP U2":"0","CP U3":"0","AC U1":"0.612533455","AC U2":"0.068853575","AC U3":"0.637450659","CA U1":"0.022508873","CA U2":"0","CA U3":"0","BR U1":"0","BR U2":"0.017167339","BR U3":"0","ZZ U1":"4.220528971","ZZ U2":"5.676431753","ZZ U3":"8.091587051","CT U1":"0","CT U2":"0","CT U3":"0","CZ U1":"0","CZ U2":"0","CZ U3":"0","CH U1":"0","CH U2":"0","CH U3":"0.075479712","ZO U1":"0.070493277","ZO U2":"0.059118378","ZO U3":"0.075587339"},{"Metabolite":"(+)-3-Carene","ZC U1":"0","ZC U2":"0","ZC U3":"0","ZA U1":"1.495075929","ZA U2":"0.480891346","ZA U3":"3.99228972","AM U1":"0","AM U2":"0","AM U3":"0","CP U1":"0.094710586","CP U2":"0.160700144","CP U3":"0.0734197","AC U1":"0","AC U2":"0","AC U3":"0","CA U1":"0","CA U2":"0","CA U3":"0","BR U1":"0","BR U2":"0","BR U3":"0","ZZ U1":"0","ZZ U2":"0","ZZ U3":"0","CT U1":"0","CT U2":"0","CT U3":"0","CZ U1":"0","CZ U2":"0","CZ U3":"0","CH U1":"0.063078119","CH U2":"0","CH U3":"0.130984156","ZO U1":"0.019382395","ZO U2":"0.013241238","ZO U3":"0.020637672"},{"Metabolite":"β-Myrcene","ZC U1":"3.219586154","ZC U2":"2.890742317","ZC U3":"2.953182231","ZA U1":"2.057772951","ZA U2":"1.468102577","ZA U3":"1.809357129","AM U1":"1.879649734","AM U2":"3.222041823","AM U3":"1.940168528","CP U1":"2.160339103","CP U2":"2.238316437","CP U3":"1.480686722","AC U1":"0","AC U2":"0","AC U3":"1.642459194","CA U1":"1.018102753","CA U2":"0.664803625","CA U3":"0.661474395","BR U1":"1.093548996","BR U2":"1.18072888","BR U3":"1.25635403","ZZ U1":"1.929990467","ZZ 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"Metabolites":[{"metabolite_name":"Tricyclo[2.2.1.0(2,6)]heptane, 1,7,7-trimethyl-"},{"metabolite_name":"α-Pinene"},{"metabolite_name":"α-Phellandrene"},{"metabolite_name":"Bicyclo[2.2.1]heptane, 7,7-dimethyl-2-methylene"},{"metabolite_name":"Camphene"},{"metabolite_name":"β-Pinene"},{"metabolite_name":"β-Phellandrene"},{"metabolite_name":"3-Carene"},{"metabolite_name":"(+)-3-Carene"},{"metabolite_name":"β-Myrcene"},{"metabolite_name":"(+)-4-Carene"},{"metabolite_name":"D-Limonene"},{"metabolite_name":"Eucalyptol"},{"metabolite_name":"trans β-Ocimene"},{"metabolite_name":"γ-Terpinene"},{"metabolite_name":"β-Ocimene"},{"metabolite_name":"1,3,6-Octatriene, 3,7-dimethyl-, (Z)-"},{"metabolite_name":"o-Cymene"},{"metabolite_name":"Cyclohexene, 1-methyl-4-(1-methylethylidene)-"},{"metabolite_name":"2-Heptanol"},{"metabolite_name":"2-Nonanone"},{"metabolite_name":"Fenchone"},{"metabolite_name":"2-Octanol"},{"metabolite_name":"Thujone"},{"metabolite_name":"alpha.-Cubebene"},{"metabolite_name":"2-Nonanol, acetate"},{"metabolite_name":"5-Isopropyl-2-methylbicyclo[3.1.0]hexan-2-ol"},{"metabolite_name":"gamma.-Muurolene"},{"metabolite_name":"Copaene"},{"metabolite_name":"2-Decanone"},{"metabolite_name":"Hexadecane"},{"metabolite_name":"(+)-2-Bornanone"},{"metabolite_name":"(-)-Aristolene"},{"metabolite_name":"Linalool"},{"metabolite_name":"α-Guaiene"},{"metabolite_name":"Azulene, 1,2,3,5,6,7,8,8a-octahydro-1,4-dimethyl-7-(1-methylethenyl)-, [1S-(1.alpha.,7.alpha.,8a.beta.)]-"},{"metabolite_name":"4-Isopropyl-1-methylcyclohex-2-enol"},{"metabolite_name":"Pinocarvone"},{"metabolite_name":"(1R,2R,4R)-2,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol"},{"metabolite_name":"gamma.-Elemene"},{"metabolite_name":"Bornyl acetate"},{"metabolite_name":"Isobornyl acetate"},{"metabolite_name":"Fenchol"},{"metabolite_name":"trans-.alpha.-Bergamotene"},{"metabolite_name":"Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, [1S-(1.alpha.,2.beta.,4.beta.)]-"},{"metabolite_name":"Caryophyllene"},{"metabolite_name":"Terpinen-4-ol"},{"metabolite_name":".alpha.-Muurolene"},{"metabolite_name":"2-Decanol"},{"metabolite_name":"Alloaromadendrene"},{"metabolite_name":"beta.-Guaiene"},{"metabolite_name":"trans-p-Mentha-2,8-dienol"},{"metabolite_name":"isoledene"},{"metabolite_name":"alpha.-Campholenal"},{"metabolite_name":"(E)-.beta.-Famesene"},{"metabolite_name":"Isoborneol"},{"metabolite_name":"Humulene"},{"metabolite_name":"4a,8-Dimethyl-2-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,7-octahydronaphthalene"},{"metabolite_name":"Neral"},{"metabolite_name":"Naphthalene, 2,3,4,4a,5,6-hexahydro-1,4a-dimethyl-7-(1-methylethyl)-"},{"metabolite_name":"α-Terpineol"},{"metabolite_name":"endo-Borneol"},{"metabolite_name":"Germacrene D"},{"metabolite_name":"Dodecanal"},{"metabolite_name":"2-Tridecanol"},{"metabolite_name":"Naphthalene, 1,2,3,5,6,7,8,8a-octahydro-1,8a-dimethyl-7-(1-methylethenyl)-, [1R-(1.alpha.,7.beta.,8a.alpha.)]-"},{"metabolite_name":"β-Bisabolene"},{"metabolite_name":"Naphthalene, 1,2,3,5,6,8a-hexahydro-4,7-dimethyl-1-(1-methylethyl)-, (1S-cis)-"},{"metabolite_name":"Selina-3,7(11)-diene"}]
}

}