D-Citronellol (BioDeep_00000000679)
Secondary id: BioDeep_00000014724, BioDeep_00000397389, BioDeep_00000620010, BioDeep_00001892742
human metabolite PANOMIX_OTCML-2023 Endogenous
代谢物信息卡片
化学式: C10H20O (156.1514)
中文名称: D-香茅醇, (R)-3,7-二甲基-6-辛烯醇, (+)-β-Citronellol
谱图信息:
最多检出来源 Homo sapiens(lipidomics) 36.4%
分子结构信息
SMILES: C/C(C)=C\CC[C@@H](C)CCO
InChI: InChI=1S/C10H20O/c1-9(2)5-4-6-10(3)7-8-11/h5,10-11H,4,6-8H2,1-3H3/t10-/m1/s1
描述信息
Citronellol is formally classified as alkylalcohol although it is biochemically a monoterpenoid as it is synthesized from isoprene units. Citronellol is a neutral compound. It is a naturally occurring organic compound found in cannabis plants (PMID:6991645 ). Citronellol occurs in many essential oils as either – or + enantiomers. -Citronellol is found in the oils of rose (18-55\\\\\\%) and Pelargonium geraniums while + citronellol is found in citronella oils extracted from the leaves and stems of Cymbopogon nardus or citronella grass. Citronellol has a citrus, floral, and geranium taste with a floral leathery waxy rose citrus odor ( Ref:DOI ). It is used in perfumery to add scents to soaps and incense. It is an insect repellent that repels mosquitos at short distances (PMID:2862274 ). Citronellol is found in highest concentrations in gingers, sweet basils, and winter savories and in lower concentrations in highbush blueberries, bilberries, and cardamoms. Citronellol has also been detected in blackcurrants, fennels, evergreen blackberries, herbs and spices, and nutmegs making citronellol a potential biomarker for the consumption of these foods. Citronellol has promising pharmacological activities (PMID:30453001 ) against human lung cancer (PMID:31280209 ), against induced rat breast cancer (PMID:31313341 ), has antifungal activity against Candida species (PMID:32150884 ) and has anti-hypertensive properties (PMID:26872991 ).
(R)-(+)-citronellol is a citronellol that is oct-6-ene substituted by a hydroxy group at position 1 and methyl groups at positions 3 and 7 (the 3R-enantiomer). It is an enantiomer of a (S)-(-)-citronellol.
D-Citronellol is a natural product found in Azadirachta indica, Saxifraga stolonifera, and other organisms with data available.
See also: beta-CITRONELLOL, (R)-; GERANIOL (component of); beta-CITRONELLOL, (R)-; GERANIOL; LINALOOL, (+/-)- (component of) ... View More ...
Constituent of black cumin (Nigella sativa) seeds. A common constituent of plant oils, especies in the Rutaceae. D-Citronellol is found in herbs and spices.
(R)-Citronellol (D-Citronellol) is an alcoholic monoterpene found in geranium essential oil. (R)-Citronellol inhibits degranulation of mast cells and does not affect caffeine bitterness perception. (R)-Citronellol can be used in decorative cosmetics, toiletries as well as in non-cosmetic products[1][2][3].
(R)-Citronellol (D-Citronellol) is an alcoholic monoterpene found in geranium essential oil. (R)-Citronellol inhibits degranulation of mast cells and does not affect caffeine bitterness perception. (R)-Citronellol can be used in decorative cosmetics, toiletries as well as in non-cosmetic products[1][2][3].
Citronellol ((±)-Citronellol) is a monoterpene Pelargonium graveolens. Citronellol ((±)-Citronellol) induces necroptosis of cancer cell via up-regulating TNF-α, RIP1/RIP3 activities, down-regulating caspase-3/caspase-8 activities and increasing ROS (reactive oxygen species) accumulation[1].
Citronellol ((±)-Citronellol) is a monoterpene Pelargonium graveolens. Citronellol ((±)-Citronellol) induces necroptosis of cancer cell via up-regulating TNF-α, RIP1/RIP3 activities, down-regulating caspase-3/caspase-8 activities and increasing ROS (reactive oxygen species) accumulation[1].
同义名列表
64 个代谢物同义名
Purifying relief soothing gel essence; 6-Octen-1-ol, 3,7-dimethyl-, (theta)-; D-Citronellol;(R)-(+)--Citronellol; (R)-(+)-3,7-dimethyl-oct-6-en-1-ol; 6-Octen-1-ol, 3,7-dimethyl-, (3R)-; 6-Octen-1-ol, 3,7-dimethyl-, (R)-; (R)-(+)-3,7-Dimethyl-6-octen-1-ol; Hydrating extra concentrate serum; 6-Octen-1-ol,3,7-dimethyl-,(3R)-; citronellol, titanium (+4) salt; (3R)-3,7-dimethyloct-6-en-1-ol; 3,7-Dimethyl-(3R)-6-Octen-1-ol; (R)-(+)-beta-Citronellol, 98\\%; (3R)-3,7-Dimethyl-6-octen-1-ol; 3,7-Dimethyl-(R)-6-Octen-1-ol; (R)-3,7-Dimethyl-6-octen-1-ol; (R)-3,7-Dimethyloct-6-en-1-ol; 3,7-Dimethyl-6-octen-1-ol #; (R)-(+)-.beta.-Citronellol; (R)-(+)- beta -Citronellol; (R)-3,7-dimethyl-6-octenol; .BETA.-CITRONELLOL, R-(+)-; Hydrating Treatment Toner; (3R)-(+)-beta-Citronellol; (R)-(+)-beta -Citronellol; (R)-(+)-beta-Citronellol; .BETA.-CITRONELLOL, (R)-; citronellol, (+-)-isomer; R-(+)-.BETA.-CITRONELLOL; citronellol, (R)-isomer; citronellol, (S)-isomer; beta-CITRONELLOL, (R)-; (3R)-(+)-β-Citronellol; (R)-(+)-ss-Citronellol; (R)-(+)-b-Citronellol; (R)-(+)-β-Citronellol; (+)-beta-Citronellol; (R)-beta-Citronellol; (R)-(+)-Citronellol; (+)-(R)-Citronellol; CITRONELLOL [FHFI]; CITRONELLOL [INCI]; CITRONELLOL [FCC]; (+)-A-Citronellol; (+)-R-Citronellol; (R)-β-Citronellol; (+)-β-Citronellol; beta-citronellol; (R)-Citronellol; CITRONELLOL, D-; UNII-P01OUT964K; (+)-citronellol; b-citronellol; Β-citronellol; D-Citronellol; citronellol; P01OUT964K; AI3-00204; β-Citronellol; (±)-Citronellol; (±)-β-Citronellol; beta-Citronellol; D-Citronellol; Citronellol
数据库引用编号
29 个数据库交叉引用编号
- ChEBI: CHEBI:10360
- KEGG: C09849
- PubChem: 101977
- PubChem: 8842
- HMDB: HMDB0035093
- Metlin: METLIN41101
- ChEMBL: CHEMBL1907993
- Wikipedia: Citronellol
- LipidMAPS: LMPR0102010008
- MeSH: citronellol
- ChemIDplus: 0001117619
- KNApSAcK: C00003038
- foodb: FDB013722
- chemspider: 92127
- CAS: 1117-61-9
- medchemexpress: HY-124257
- PMhub: MS000016252
- PubChem: 12036
- KNApSAcK: C00000844
- CAS: 106-22-9
- PDB-CCD: ODM
- 3DMET: B03321
- NIKKAJI: J3.238G
- NIKKAJI: J67.959C
- RefMet: beta-Citronellol
- medchemexpress: HY-W010201
- KNApSAcK: 10360
- LOTUS: LTS0271008
- wikidata: Q418813
分类词条
相关代谢途径
Reactome(0)
PlantCyc(0)
代谢反应
1 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(1)
- citronellol degradation:
ATP + citronellate + coenzyme A ⟶ AMP + citronellyll-CoA + diphosphate
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
148 个相关的物种来源信息
- 97169 - Abies sibirica: 10.1007/BF00600860
- 654 - Aeromonas veronii: 10.3389/FCIMB.2020.00044
- 501610 - Agathosma betulina: 10.1021/JF60201A021
- 925377 - Aloysia citrodora: 10.1016/S0367-326X(98)00016-1
- 542672 - Aloysia triphylla: 10.1016/S0367-326X(98)00016-1
- 125259 - Alpinia hainanensis: 10.1080/10412905.1990.9697877
- 299928 - Alpinia latilabris:
- 43982 - Ambrosiozyma monospora: 10.1055/S-2007-969476
- 7461 - Apis cerana: 10.1371/JOURNAL.PONE.0175573
- 259893 - Artemisia argyi: 10.1016/0031-9422(83)80141-1
- 259893 - Artemisia argyi Lévl.et Vant.: -
- 265783 - Artemisia capillaris: 10.1016/0031-9422(83)80141-1
- 1473222 - Artemisia cina: 10.1016/0031-9422(83)80141-1
- 401898 - Artemisia gmelinii: 10.1016/0031-9422(83)80141-1
- 205369 - Artemisia judaica: 10.1080/10412905.1990.9697881
- 669134 - Artemisia montana: 10.1016/0031-9422(83)80141-1
- 223870 - Artemisia princeps: 10.1016/0031-9422(83)80141-1
- 72351 - Artemisia scoparia: 10.1016/0031-9422(83)80141-1
- 4458 - Arum maculatum: 10.1016/0305-1978(95)00026-Q
- 385370 - Aster scaber: 10.1021/JF00034A033
- 124943 - Azadirachta indica: 10.1246/CL.1979.1137
- 72900 - Baccharis dracunculifolia: 10.1002/(SICI)1099-1026(199601)11:1<15::AID-FFJ541>3.0.CO;2-H
- 375214 - Blepharocalyx salicifolius: 10.1021/NP50035A036
- 260124 - Blepharocalyx tweediei: 10.1021/NP50035A036
- 3483 - Cannabis sativa: 10.1021/NP50008A001
- 119266 - Cinnamomum sieboldii: 10.1248/YAKUSHI1947.106.1_17
- 2706 - Citrus: 10.1080/10412905.1993.9698179
- 558547 - Citrus deliciosa:
- 170989 - Citrus hystrix: 10.1021/NP100531X
- 200542 - Citrus limettioides: 10.3390/MOLECULES21060814
- 37334 - Citrus maxima: 10.1271/BBB1961.55.2571
- 85571 - Citrus reticulata:
- 55188 - Citrus unshiu: 10.1007/BF00580068
- 332445 - Clinopodium gilliesii: 10.1080/10412905.1993.9698276
- 450191 - Conopeum seurati: 10.1515/ZNC-1987-9-1001
- 4047 - Coriandrum sativum: 10.1080/10412905.1996.9700565
- 34329 - Corymbia citriodora:
- 87660 - Corymbia maculata: 10.1300/J044V07N04_10
- 3369 - Cryptomeria japonica: 10.1080/10412905.1991.9697930
- 66014 - Cymbopogon citratus:
- 79835 - Cymbopogon flexuosus:
- 79840 - Cymbopogon nardus: 10.5897/JMPR10.078
- 1414754 - Cymbopogon winterianus:
- 329675 - Daphne odora: 10.1271/BBB1961.47.483
- 2715869 - Daphne papyracea: 10.1271/BBB1961.47.483
- 239547 - Dryopteris affinis: 10.1080/10412905.1990.9697863
- 3289 - Dryopteris filix-mas: 10.1080/10412905.1990.9697863
- 377494 - Elwendia persica: 10.1007/BF00630023
- 1580845 - Endoconidiophora coerulescens: 10.1515/ZNC-1987-1-227
- 33169 - Eremothecium gossypii: 10.1007/BF00630334
- 1711162 - Eucalyptus astringens: 10.1080/10412905.1992.9698059
- 338533 - Eucalyptus blakelyi: 10.1080/10412905.1992.9698059
- 33130 - Eucalyptus botryoides: 10.1080/10412905.1992.9698059
- 183814 - Eucalyptus brassiana: 10.1080/10412905.1991.9697906
- 34316 - Eucalyptus camaldulensis: 10.1080/10412905.1991.9697921
- 452569 - Eucalyptus cladocalyx: 10.1080/10412905.1992.9698059
- 468242 - Eucalyptus moluccana: 10.1080/10412905.1992.9698059
- 627157 - Eucalyptus paniculata: 10.1080/10412905.1992.9698059
- 338543 - Eucalyptus punctata: 10.1080/10412905.1992.9698059
- 102770 - Eupatorium cannabinum: 10.1055/S-2007-969599
- 371376 - Ferula ovina: 10.1080/10412905.2005.9698829
- 4028 - Geranium:
- 3635 - Gossypium hirsutum: 10.1021/JF60200A011
- 630287 - Helichrysum amorginum: 10.1055/S-2006-957914
- 261786 - Helichrysum italicum: 10.1055/S-2006-957914
- 9606 - Homo sapiens: -
- 124778 - Illicium verum: 10.1007/BF02860485
- 58039 - Juniperus communis: 10.1080/10412905.1997.9700711
- 633661 - Juniperus monticola: 10.1021/NP50009A015
- 61308 - Juniperus phoenicea: 10.1016/S0021-9673(01)84593-3
- 884047 - Juniperus taxifolia: 10.1016/0305-1978(85)90081-X
- 106032 - Kunzea salina: 10.1080/10412905.1994.9698327
- 3326 - Larix laricina: 10.1021/NP50050A051
- 71405 - Larix lyallii: 10.1021/NP50050A051
- 3327 - Larix occidentalis: 10.1021/NP50050A051
- 63011 - Laser trilobum:
- 39329 - Lavandula angustifolia: 10.1080/10412905.1997.9700727
- 268881 - Lepechinia chamaedryoides: 10.1055/S-2006-961452
- 295139 - Leptospermum scoparium: 10.1016/J.PHYTOCHEM.2004.03.019
- 151069 - Litchi chinensis: 10.1021/JF60230A021
- 105884 - Lonicera japonica: 10.1021/JF950275B
- 105884 - Lonicera japonica Thunb.: -
- 29686 - Melica uniflora: 10.1080/10412905.1990.9697863
- 1898872 - Micromeria biflora: 10.1080/10412905.1997.9700709
- 242164 - Morina persica: 10.1080/10412905.1998.9700856
- 2901850 - Murraya exotica L.: -
- 43711 - Murraya paniculata (L.)Jack: -
- 119949 - Myrtus communis: 10.1080/10412905.1992.9698084
- 39350 - Ocimum basilicum: 10.1007/BF02860485
- 145953 - Ophrys sphegodes: 10.1016/S0031-9422(00)81276-5
- 268884 - Origanum majorana: 10.1055/S-2006-960024
- 1082757 - Origanum syriacum: 10.1080/10412905.1991.9697923
- 35924 - Paeonia lactiflora: 10.1016/S0031-9422(00)94541-2
- 73200 - Pelargonium graveolens:
- 73200 - Pelargonium graveolens: 10.1016/0031-9422(83)80140-X
- 1167265 - Pelargonium odoratissimum: 10.1016/0031-9422(83)80140-X
- 253082 - Pelargonium quercifolium: 10.1080/10412905.1991.9697953
- 163050 - Pelargonium ternifolium:
- 253086 - Pelargonium vitifolium: 10.1080/10412905.1992.9698083
- 260139 - Pimenta racemosa: 10.1080/10412905.1991.9697952
- 58041 - Pinus cembra: 10.1016/S0021-9673(01)84593-3
- 71633 - Pinus halepensis: 10.1016/S0021-9673(01)84593-3
- 13216 - Piper nigrum: 10.1021/JF60071A008
- 33090 - Plants: -
- 1643381 - Pteris preussii: 10.1246/CL.1979.831
- 170716 - Pteris quadriaurita: 10.1246/CL.1979.831
- 313948 - Rhanterium epapposum: 10.1002/FFJ.2730020106
- 242839 - Rhodiola crenulata: 10.1515/ZNC-2003-3-402
- 35938 - Robinia pseudoacacia: 10.1039/AN9285300411
- 74632 - Rosa gallica:
- 74645 - Rosa rugosa: 10.1002/FFJ.2730050406
- 74645 - Rosa rugosa Thunb.: -
- 77063 - Salix fragilis: 10.1080/10412905.1990.9697863
- 933131 - Salvia dorisiana:
- 268878 - Salvia dorystaechas: 10.1055/S-2007-969275
- 39367 - Salvia rosmarinus: 10.1080/10412905.1998.9700854
- 35974 - Santalum album: 10.1021/NP050386X
- 35974 - Santalum album: 10.3390/MOLECULES22071139
- 546409 - Satureja cuneifolia: 10.1016/S0031-9422(00)90514-4
- 49988 - Satureja montana: 10.1080/10412905.1991.9700495
- 182070 - Saxifraga stolonifera: 10.1016/0031-9422(83)85064-X
- 50507 - Schisandra chinensis (Turcz.) Baill.: -
- 2816102 - Seriphium plumosum: 10.1076/PHBI.35.1.66.13267
- 155267 - Sideritis tragoriganum: 10.1016/B978-0-444-88558-6.50020-9
- 4081 - Solanum lycopersicum: 10.1021/JF00014A016
- 4113 - Solanum tuberosum: 10.1007/BF02853856
- 1735431 - Stoebe plumosa: 10.1076/PHBI.35.1.66.13267
- 1237821 - Stoebe vulgaris: 10.1076/PHBI.35.1.66.13267
- 547782 - Symphyotrichum undulatum: 10.1021/JF00034A033
- 334483 - Syzygium jambos: 10.1080/10412905.1991.9697916
- 25629 - Taxus baccata: 10.1080/10412905.1990.9697863
- 99806 - Taxus cuspidata: 10.1080/10412905.1990.9697863
- 2878273 - Thymus carnosus: 10.1016/S0021-9673(00)94572-2
- 1885666 - Thymus cilicicus: 10.1055/S-2007-969176
- 1718167 - Thymus sibthorpii: 10.1055/S-2007-969172
- 1132411 - Thymus sipyleus: 10.1055/S-2007-969176
- 3438 - Umbellularia californica: 10.1016/0031-9422(74)85146-0
- 54477 - Vitex agnus-castus:
- 361442 - Vitex negundo: 10.1055/S-2006-959580
- 29760 - Vitis vinifera:
- 552636 - Xanthium strumarium var. canadense: 10.1021/NP50041A038
- 462584 - Xenophyllum poposum: 10.1076/1388-0209(200007)3831-SFT197
- 1005655 - Xylopia aromatica: 10.1080/10412905.1993.9698250
- 1291627 - Zanthoxylum gilletii: 10.1002/FFJ.2730040411
- 4577 - Zea mays: 10.1016/J.PHYTOCHEM.2004.03.019
- 94328 - Zingiber officinale:
- 94328 - Zingiber officinale Rosc.: -
- 94328 - Zingiber Officinale Roscoe: -
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:
- PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。
文献列表
- Stoja Milovanovic, Darka Markovic, Ivona Jankovic-Castvan, Ivana Lukic. Cornstarch aerogels with thymol, citronellol, carvacrol, and eugenol prepared by supercritical CO2- assisted techniques for potential biomedical applications.
Carbohydrate polymers.
2024 May; 331(?):121874. doi:
10.1016/j.carbpol.2024.121874
. [PMID: 38388060] - Yimeng Li, Runyang Sun, Yajing Kong, Xiaolin Cai, Tongyu Jiang, Shuai Cheng, Hui Yang, Luyi Song, Xin Lü, Xin Wang, Chao Shi. Antibacterial effect of ultrasound and β-citronellol against Listeria monocytogenes and its application in carrot preservation.
Ultrasonics sonochemistry.
2024 Jan; 102(?):106752. doi:
10.1016/j.ultsonch.2023.106752
. [PMID: 38211495] - Maryam Jadidi, Hasan Mumivand, Abdollah Ehtesham Nia, Alireza Shayganfar, Filippo Maggi. UV-A and UV-B combined with photosynthetically active radiation change plant growth, antioxidant capacity and essential oil composition of Pelargonium graveolens.
BMC plant biology.
2023 Nov; 23(1):555. doi:
10.1186/s12870-023-04556-6
. [PMID: 37946108] - Laure Martinelli, Camille Bihanic, Aurélie Bony, Florence Gros, Corentin Conart, Sébastien Fiorucci, Hervé Casabianca, Frédéric Schiets, Giorgiana Chietera, Benoît Boachon, Bernard Blerot, Sylvie Baudino, Frédéric Jullien, Denis Saint-Marcoux. Citronellol biosynthesis in pelargonium is a multi-step pathway involving PRISE enzymes.
Plant physiology.
2023 Oct; ?(?):. doi:
10.1093/plphys/kiad550
. [PMID: 37831417] - Praveen Thangaraj, Krishnamoorthy Akkanna Subbiah, Nakkeeran Sevugapperumal, Sivakumar Uthandi, Amirtham Damodarasamy, Haripriya Shanmugam. Activity of volatiles induced by microbes and natural plants stifled the growth of Pythium aphanidermatum - the damping off in Tomato.
BMC plant biology.
2023 Aug; 23(1):384. doi:
10.1186/s12870-023-04351-3
. [PMID: 37563742] - Taotao Li, Wenfei Wang, Qiuting Guo, Jia Li, Tiantian Tang, Yujiao Wang, Ding Liu, Kai Yang, Jiayi Li, Kaixue Deng, Fang Wang, Huiting Li, Zhenfeng Wu, Jianbo Guo, Dongyan Guo, Yajun Shi, Junbo Zou, Jing Sun, Xiaofei Zhang, Ming Yang. Rosemary (Rosmarinus officinalis L.) hydrosol based on serotonergic synapse for insomnia.
Journal of ethnopharmacology.
2023 Jul; ?(?):116984. doi:
10.1016/j.jep.2023.116984
. [PMID: 37532071] - Yasameen Shakir Mahmood, Sarmed Hashim Kathem. Protective effect of citronellol in rhabdomyolysis-induced acute kidney injury in mice.
Journal of medicine and life.
2023 Jul; 16(7):1057-1061. doi:
10.25122/jml-2023-0102
. [PMID: 37900084] - Ajay Kumar, Rahul Dev Gautam, Satbeer Singh, Ramesh Chauhan, Manish Kumar, Dinesh Kumar, Ashok Kumar, Sanatsujat Singh. Phenotyping floral traits and essential oil profiling revealed considerable variations in clonal selections of damask rose (Rosa damascena Mill.).
Scientific reports.
2023 May; 13(1):8101. doi:
10.1038/s41598-023-34972-5
. [PMID: 37208367] - Xiao Liu, Chunji Zhu, Yong Yin. Anti-ischemic effect of monoterpene citronellol on experimental stroke models mediated by proinflammatroy cytokines.
Combinatorial chemistry & high throughput screening.
2022 Nov; ?(?):. doi:
10.2174/1386207326666221110092715
. [PMID: 36372917] - Valtcho D Zheljazkov, Giuseppe Micalizzi, Solomon Yilma, Charles L Cantrell, Amber Reichley, Luigi Mondello, Ivanka Semerdjieva, Tzenka Radoukova. Melissa officinalis L. as a Sprout Suppressor in Solanum tuberosum L. and an Alternative to Synthetic Pesticides.
Journal of agricultural and food chemistry.
2022 Nov; 70(44):14205-14219. doi:
10.1021/acs.jafc.2c05942
. [PMID: 36306427] - Amanda Staudt, Patrícia Fonseca Duarte, Bruna Paes do Amaral, Bárbara Carolina de Oliveira Peixoto Andrade, Naomi Kato Simas, Ivana Correa Ramos Leal, Leandro Stefano Sangenito, André Luis Souza Dos Santos, Débora de Oliveira, Alexander Junges, Rogério Luis Cansian, Natalia Paroul. Biological properties of functional flavoring produced by enzymatic esterification of citronellol and geraniol present in Cymbopogon winterianus essential oil.
Natural product research.
2021 Dec; 35(24):5981-5987. doi:
10.1080/14786419.2020.1810032
. [PMID: 32840398] - Zhenghui Jiang, Chen Xu, Limin Wang, Kai Hong, Changwei Ma, Chenyan Lv. Potential enzymes involved in beer monoterpenoids transformation: structures, functions and challenges.
Critical reviews in food science and nutrition.
2021 Aug; ?(?):1-11. doi:
10.1080/10408398.2021.1970510
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