Vanillin (BioDeep_00000269025)

natural product PANOMIX_OTCML-2023

代谢物信息卡片

4-hydroxy-3-methoxybenzaldehyde

化学式: C8H8O3 (152.0473418)
中文名称: 香草醛
谱图信息: 最多检出来源 Homo sapiens(blood) 0.79%

Reviewed

Last reviewed on 2024-08-20.

Cite this Page

Vanillin. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/vanillin (retrieved 2024-11-08) (BioDeep RN: BioDeep_00000269025). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: c1(ccc(cc1OC)C=O)O
InChI: InChI=1S/C8H8O3/c1-11-8-4-6(5-9)2-3-7(8)10/h2-5,10H,1H3

描述信息

CONFIDENCE standard compound; INTERNAL_ID 952; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3579; ORIGINAL_PRECURSOR_SCAN_NO 3578
D002491 - Central Nervous System Agents > D000927 - Anticonvulsants
D020011 - Protective Agents > D016587 - Antimutagenic Agents
D020011 - Protective Agents > D000975 - Antioxidants
CONFIDENCE standard compound; INTERNAL_ID 952; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3566; ORIGINAL_PRECURSOR_SCAN_NO 3561
CONFIDENCE standard compound; INTERNAL_ID 952; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3549; ORIGINAL_PRECURSOR_SCAN_NO 3546
CONFIDENCE standard compound; INTERNAL_ID 952; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3560; ORIGINAL_PRECURSOR_SCAN_NO 3556
CONFIDENCE standard compound; INTERNAL_ID 952; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3573; ORIGINAL_PRECURSOR_SCAN_NO 3570
CONFIDENCE standard compound; INTERNAL_ID 952; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3577; ORIGINAL_PRECURSOR_SCAN_NO 3575
relative retention time with respect to 9-anthracene Carboxylic Acid is 0.504
relative retention time with respect to 9-anthracene Carboxylic Acid is 0.503
relative retention time with respect to 9-anthracene Carboxylic Acid is 0.500
Vanillin (p-Vanillin) is a single molecule extracted from vanilla beans and also a popular odor used widely in perfume, food and medicine.
Vanillin (p-Vanillin) is a single molecule extracted from vanilla beans and also a popular odor used widely in perfume, food and medicine.

同义名列表

6 个代谢物同义名

Vanillin; 4-hydroxy-3-methoxybenzaldehyde; Vanillic aldehyde; p-Vanillin; m-Methoxy-p-hydroxybenzaldehyde; p-Hydroxy-m-methoxybenzaldehyde

数据库引用编号

44 个数据库交叉引用编号

ChEBI: CHEBI:18346
KEGG: C00755
KEGGdrug: D00091
PubChem: 1183
ChEMBL: CHEMBL13883
KNApSAcK: C00029531
CAS: 121-33-5
MoNA: CCMSLIB00000424792
MoNA: CCMSLIB00000424793
MoNA: MoNA038813
MoNA: MoNA038661
MoNA: MoNA038308
MoNA: MoNA038047
MoNA: MoNA036779
MoNA: MoNA036773
MoNA: MoNA036772
MoNA: MoNA035399
MoNA: MoNA035396
MoNA: MoNA035394
MoNA: MoNA034534
MoNA: MoNA034533
MoNA: MoNA034532
MoNA: LU095256
MoNA: LU095255
MoNA: LU095254
MoNA: LU095253
MoNA: LU095252
MoNA: LU095251
MoNA: FiehnHILIC003048
MoNA: FiehnHILIC002408
MoNA: FiehnHILIC001573
MoNA: FiehnHILIC000845
MoNA: CCMSLIB00003142440
MoNA: PM005204
MoNA: BML82328
MoNA: BML82327
MoNA: BML82326
MoNA: BML82325
KNApSAcK: C00002683
PDB-CCD: V55
3DMET: B00167
NIKKAJI: J2.923H
RefMet: Vanillin
medchemexpress: HY-N0098

分类词条

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

218 个相关的物种来源信息

97171 - Abies nephrolepis:
78264 - Abies sachalinensis:
97169 - Abies sibirica: 10.1007/BF00564181
68527 - Aegle marmelos: 10.1016/J.PHYTOCHEM.2009.10.013
175969 - Aeschynanthus bracteatus: 10.1016/J.PHYTOCHEM.2008.05.012
557622 - Allagopappus canariensis: 10.1021/NP50117A014
56513 - Allagopappus dichotomus: 10.1021/NP50117A014
663965 - Anastatica hierochuntica:
2831626 - Angelica pachycarpa: 10.1055/S-0028-1097274
165353 - Angelica sinensis:
165353 - Angelica sinensis (Oliv.)Diels: -
49314 - Annona cherimola:
1123437 - Annona purpurea:
2306982 - Antidesma pentandrum var. barbatum: 10.1002/JCCS.200700187
3702 - Arabidopsis thaliana: 10.1016/J.PHYTOCHEM.2003.12.009
137934 - Aralia bipinnata:
56992 - Araucaria angustifolia: 10.1016/S0031-9422(00)00239-9
461553 - Arcangelisia flava: 10.1016/J.PHYTOL.2011.07.002
1234283 - Aristolochia asclepiadifolia: 10.1002/FFJ.2730080104
143780 - Aristolochia elegans: 10.1016/J.BMC.2003.10.031
431268 - Aristolochia heterophylla:
158550 - Aristolochia kaempferi:
325095 - Aristolochia littoralis: 10.1016/J.BMC.2003.10.031
35927 - Aristolochia tomentosa: 10.1016/S0031-9422(99)00176-4
35608 - Artemisia annua: 10.1016/S0031-9422(98)00607-4
259893 - Artemisia argyi: 10.1007/BF02975098
265783 - Artemisia capillaris: 10.1016/S0968-0896(00)00225-X
265783 - Artemisia capillaris Thunb.: -
223868 - Artemisia japonica: 10.1007/BF02978255
72351 - Artemisia scoparia: 10.1016/0031-9422(73)80524-2
72351 - Artemisia scoparia Waldst.et Kit.: -
637488 - Artemisia stolonifera: 10.1007/BF02975098
415155 - Aster indicus: 10.1016/J.PHYTOCHEM.2007.05.027
4498 - Avena sativa:
3589 - Basella alba: 10.1016/0889-1575(91)90017-Z
78253 - Begonia nantoensis:
1609853 - Beilschmiedia erythrophloia: 10.1021/NP800504W
1603694 - Beilschmiedia tsangii:
161934 - Beta vulgaris: 10.1271/BBB1961.44.205
3708 - Brassica napus: 10.1016/J.FOODCHEM.2006.08.014
210348 - Brucea javanica:
3483 - Cannabis Sativa L.: -
40321 - Capsicum annuum var. annuum: 10.1007/BF00048188
165789 - Capsicum annuum var. glabriusculum: 10.1007/BF00048188
992661 - Carissa edulis: 10.1016/S0031-9422(00)86976-9
429256 - Carissa spinarum: 10.1016/S0031-9422(00)86976-9
139927 - Carya cathayensis: 10.1016/J.BMCL.2012.01.062
121073 - Cassytha filiformis: 10.1021/NP970348G
41511 - Centaurea calcitrapa: 10.1007/S10600-007-0232-9
145508 - Centaurea ornata: 10.1021/NP50069A006
2072395 - Centaurea scoparia:
109101 - Chaerophyllum hirsutum: 10.1021/NP040046W
592600 - Chamaecrista flexuosa: 10.1016/S0040-4020(01)81569-6
187461 - Chamaecyparis formosensis: 10.1016/J.PHYMED.2006.11.029
1582456 - Chuquiraga atacamensis: 10.4067/S0366-16442000000100007
1132458 - Cinnamomum kotoense:
977953 - Cinnamomum subavenium:
128608 - Cinnamomum verum: 10.1021/JF60218A031
85571 - Citrus Reticulata: -
1208297 - Colchicum bornmuelleri: 10.1016/0031-9422(90)87143-I
1094085 - Colchicum kotschyi: 10.1016/0031-9422(90)87143-I
1094094 - Colchicum manissadjianii: 10.1016/0031-9422(89)80310-3
13445 - Colchicum speciosum: 10.1016/0031-9422(90)87143-I
16906 - Cornus Officinalis Sieb. Et Zucc.: -
199633 - Curcuma comosa: 10.1248/CPB.56.1604
136217 - Curcuma longa: 10.1016/0021-9673(96)00103-3
492000 - Decalepis hamiltonii: 10.1002/1099-1026(200101/02)16:1<27::AID-FFJ937>3.0.CO;2-F
313931 - Duhaldea cappa: 10.1007/S10600-010-9595-4
53751 - Echinacea purpurea: 10.1016/0031-9422(83)80215-5
82096 - Eleutherococcus senticosus: 10.1007/BF00629948
139932 - Engelhardia roxburghiana: 10.1016/J.PHYTOCHEM.2007.01.018
3262 - Equisetum hyemale L.: -
256638 - Euchresta formosana:
1087767 - Euphorbia hirsuta: 10.1021/NP0400048
551215 - Euploea sylvester: 10.1515/ZNC-1988-1-219
52471 - Ferula assa-foetida: 10.1021/NP900158F
52153 - Festuca rubra: 10.1016/0031-9422(91)84185-U
461588 - Fibraurea tinctoria: 10.1016/J.BMC.2008.09.023
1008913 - Ficus erecta var. beecheyana: 10.1002/JCCS.200400067
463862 - Ficus nervosa: 10.1002/CBDV.200900227
35899 - Galium odoratum: 10.1039/J39680000854
91201 - Gastrodia elata:
91201 - Gastrodia elata Bl.: -
3635 - Gossypium hirsutum:
1604314 - Gynura japonica:
210888 - Gynura segetum: 10.1016/S0031-9422(99)00599-3
2764646 - Gypsophila Licentiana Hand.-Mazz.: -
429701 - Handroanthus impetiginosus: 10.1002/HLCA.19890720406
38724 - Haplopteris anguste-elongata: 10.1021/NP050060O
4232 - Helianthus annuus: 10.1021/JF00123A021
73292 - Helianthus heterophyllus: 10.1016/S0031-9422(00)81173-5
4234 - Helianthus petiolaris:
229543 - Hibiscus cannabinus: 10.1016/S0031-9422(00)00473-8
1898877 - Hibiscus taiwanensis:
16752 - Houttuynia cordata: 10.1248/CPB.57.1227
4079 - Hyoscyamus niger:
185543 - Ilex pubescens: 10.1002/HLCA.200890135
358659 - Isatis quadrialata:
58039 - Juniperus communis: 10.1248/CPB.58.742
884034 - Juniperus communis var. depressa: 10.1248/CPB.58.742
2039844 - Lagochilus leiacanthus: 10.1248/CPB.59.1535
1310066 - Lagotis yunnanensis:
224738 - Lepidothamnus intermedius: 10.1071/CH9851631
123165 - Leptotes bicolor: 10.1016/J.MOLP.2014.11.008
48042 - Levisticum officinale:
128638 - Licaria triandra: 10.1021/NP010236W
217501 - Ligularia dentata:
189220 - Ligularia stenocephala:
2689076 - Ligusticum chuanxiong:
2689076 - Ligusticum chuanxiong Hort.: -
1508160 - Ligusticum striatum:
63360 - Liquidambar orientalis Mill.: -
88853 - Litsea glaucescens: 10.1021/NP010236W
4606 - Lolium arundinaceum: 10.1016/0031-9422(91)84185-U
447671 - Lonicera microphylla: 10.1007/BF00565263
337466 - Machilus zuihoensis: 10.1080/14786410802401432
1172173 - Magnolia crassipes: 10.4268/CJCMM20141019
3750 - Malus domestica: 10.1021/JF00025A025
283210 - Malus pumila: 10.1021/JF00025A025
1462929 - Marsypopetalum modestum: 10.1080/14786419.2022.2097229
155640 - Melia azedarach:
697038 - Melicope semecarpifolia: 10.1055/S-2005-871295
1089418 - Microtropis japonica: 10.1021/NP800097T
72645 - Molineria capitulata:
244352 - Mondia whitei: 10.1016/J.PHYTOCHEM.2004.11.012
43522 - Morinda citrifolia:
72955 - Myriactis humilis: 10.1055/S-2005-864107
1924212 - Nectandra oppositifolia: 10.1021/NP50009A006
2803928 - Neolitsea acuminatissima: 10.1021/NP010236W
1609885 - Neolitsea hiiranensis: 10.1016/J.PHYTOCHEM.2011.01.006
4097 - Nicotiana tabacum: 10.1080/10826079308019709
204149 - Ocimum tenuiflorum: 10.1248/CPB.57.245
4146 - Olea europaea:
872941 - Onobrychis meschetica: 10.1007/BF00563835
223102 - Orobanche crenata: 10.1055/S-2006-958118
36748 - Orobanche minor: 10.1055/S-2006-958118
40705 - Paeonia clusii: 10.1515/ZNC-2002-3-406
44685 - Panax japonicus:
240453 - Pandanus odoratissimus: 10.1016/S0031-9422(98)00390-2
1165086 - Pandanus odorifer: 10.1016/S0031-9422(98)00390-2
4726 - Pandanus tectorius: 10.1016/S0031-9422(98)00390-2
642575 - Pedalium murex: 10.1016/0031-9422(83)85033-X
1815962 - Petasites formosanus: 10.1248/CPB.47.375
128687 - Phoebe formosana: 10.1021/NP970147C
586100 - Phyllanthus oligospermus: 10.1248/CPB.54.1223
3330 - Picea glauca: 10.1016/S0031-9422(96)00388-3
308680 - Picea koraiensis: 10.1007/BF00563906
331118 - Picea obovata: 10.1007/BF00563906
375272 - Pimenta dioica: 10.1016/S0031-9422(99)00406-9
3349 - Pinus sylvestris: 10.1021/JF048948Q
88731 - Pinus tabuliformis: 10.1016/J.MOLP.2014.11.008
363212 - Pisonia aculeata: 10.1021/NP1008575
33090 - Plants: -
904463 - Pojarkovia pojarkovae:
3696 - Populus deltoides: 10.1515/ZNC-1990-0604
75702 - Populus euphratica:
482945 - Populus grandidentata: 10.1515/ZNC-1987-9-1004
55489 - Posidonia oceanica: 10.1016/S0031-9422(97)01118-7
36596 - Prunus armeniaca: 10.1021/JF00004A032
3758 - Prunus domestica: 10.1021/JF00004A032
3760 - Prunus persica: 10.1021/JF00004A032
128742 - Psilostrophe cooperi: 10.1016/S0031-9422(00)81432-6
501392 - Quercus faginea: 10.1021/JF9502461
38865 - Quercus petraea: 10.1021/JF9502461
453298 - Quercus pyrenaica: 10.1021/JF9502461
38942 - Quercus robur: 10.1021/JF9502461
58331 - Quercus suber:
1354278 - Radermachera sinica: 10.1039/P19810002764
289753 - Rhus chinensis: 10.1248/CPB.55.804
409890 - Robinsonia thurifera: 10.1016/0031-9422(88)83126-1
1548370 - Rolandra fruticosa: 10.1016/S0031-9422(00)97890-7
35974 - Santalum Album L\uff0e: -
4896 - Schizosaccharomyces pombe: 10.1128/AEM.02681-08
375857 - Scolochloa festucacea: 10.1016/0031-9422(91)84185-U
65409 - Scutellaria baicalensis: 10.1271/BBB1961.51.1449
4550 - Secale cereale: 10.1016/J.FOODCHEM.2005.07.053
4081 - Solanum lycopersicum:
4111 - Solanum melongena:
4111 - Solanum Melongena L: -
23224 - Spiraea: 10.1248/CPB.52.1227
180097 - Sporobolus cynosuroides: 10.1021/NP50028A035
1826902 - Stellaria dichotoma:
1911 - Streptomyces griseus:
1603837 - Strobilanthes dimorphotricha: 10.1055/S-2005-873125
13699 - Styrax: -
153559 - Styrax tonkinensis (Pierre) Craib ex Hart.: -
761071 - Tabernaemontana glandulosa: 10.1016/S0031-9422(00)89602-8
170733 - Taraxacum formosanum: 10.1248/CPB.53.853
90037 - Taraxacum mongolicum: 10.1248/CPB.53.853
147275 - Taxus wallichiana var. wallichiana:
13715 - Tetracentron sinense: 10.1016/S0031-9422(99)00457-4
354522 - Tetradium glabrifolium: 10.1016/0031-9422(95)00248-6
79022 - Thapsia garganica: 10.1055/S-2006-960216
3641 - Theobroma cacao: 10.1007/S00217-006-0252-X
285591 - Tinospora crispa: 10.1055/S-2006-957466
682177 - Tolpis webbii: 10.1016/J.FITOTE.2009.06.001
210369 - Tribulus terrestris: 10.1016/S0031-9422(97)01086-8
3677 - Trichosanthes Kirilowii Maxim: -
51238 - Vanilla:
51239 - Vanilla planifolia:
117957 - Vanilla pompona: 10.1080/10412905.1997.9700743
1224803 - Vernonanthura chamaedrys:
1261582 - Vertebrata lanosa: 10.1021/NP0305268
50172 - Viscum articulatum:
159976 - Viscum coloratum:
204215 - Vitex trifolia L.: -
204215 - Vitex trifolia l.var.simplicifolia Cham.: -
29760 - Vitis vinifera:
1053410 - Xanthium spinosum: 10.1016/0031-9422(91)83230-I
318068 - Xanthium strumarium: 10.1055/S-2008-1081295
159071 - Zanthoxylum ailanthoides:
1056465 - Zanthoxylum beecheyanum: 10.1002/JCCS.200400159
697043 - Zanthoxylum wutaiense:
4577 - Zea mays: 10.1248/CPB.55.153
94328 - Zingiber Officinale Roscoe: -
311405 - Zingiber zerumbet: 10.1007/BF02980078
75727 - Zizania aquatica: 10.1021/JF940651C
569774 - 金线莲: -

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

Abeer S Elsherbiny, Alyaa Galal, Khalid M Ghoneem, Nehal A Salahuddin. Graphene oxide-based nanocomposites for outstanding eco-friendly antifungal potential against tomato phytopathogens. Biomaterials advances. 2024 Jun; 160(?):213863. doi: 10.1016/j.bioadv.2024.213863. [PMID: 38642516]
Bijoy Biswas, Manish Sakhakarmy, Tawsif Rahman, Hossein Jahromi, Sushil Adhikari, Bhavya B Krishna, Thallada Bhaskar, Jonas Baltrusaitis, Mohamed Eisa, Seyed Morteza Taghavi Kouzehkanan, Tae-Sik Oh. Selective production of phenolic monomer via catalytic depolymerization of lignin over cobalt-nickel-zirconium dioxide catalyst. Bioresource technology. 2024 Apr; 398(?):130517. doi: 10.1016/j.biortech.2024.130517. [PMID: 38437961]
Natalia Saudade de Aguiar, Fabricio Augusto Hansel, Cristiane Aparecida Fioravante Reis, Marcelo Lazzarotto, Ivar Wendling. Optimizing the Vanillin-Acid Sulfuric Method to Total Saponin Content in Leaves of Yerba Mate Clones. Chemistry & biodiversity. 2024 Apr; 21(4):e202301883. doi: 10.1002/cbdv.202301883. [PMID: 38358959]
Xiaochong Zhu, Jieyuan Wu, Shizhong Li, La Xiang, Jian-Ming Jin, Chaoning Liang, Shuang-Yan Tang. Artificial Biosynthetic Pathway for Efficient Synthesis of Vanillin, a Feruloyl-CoA-Derived Natural Product from Eugenol. Journal of agricultural and food chemistry. 2024 Mar; 72(12):6463-6470. doi: 10.1021/acs.jafc.3c08723. [PMID: 38501643]
Mervt M Almostafa, Maged E Mohamed, Nancy S Younis. Ameliorative effects of vanillin against pentylenetetrazole-induced epilepsy and associated memory loss in mice: The role of Nrf2/HO-1/NQO1 and HMGB1/RAGE/TLR4/NFκB pathways. International immunopharmacology. 2024 Mar; 129(?):111657. doi: 10.1016/j.intimp.2024.111657. [PMID: 38335655]
Yang Yang, Justin Flaven-Pouchon, Jerôme Cortot, Jean-François Ferveur, Bernard Moussian. Colorimetric surface lipid quantification in Drosophila. Archives of insect biochemistry and physiology. 2024 Feb; 115(2):e22091. doi: 10.1002/arch.22091. [PMID: 38385805]
Yanfei Huang, Yuhua Yang, Jinghua Xue, Yinyin Liao, Xiumin Fu, Chen Zhu, Jianlong Li, Lanting Zeng, Ziyin Yang. Biosynthetic Pathway and Bioactivity of Vanillin, a Highly Abundant Metabolite Distributed in the Root Cortex of Tea Plants (Camellia sinensis). Journal of agricultural and food chemistry. 2024 Jan; 72(3):1660-1673. doi: 10.1021/acs.jafc.3c07206. [PMID: 38193455]
Ryota Nakaniwa, Yuki Misawa, Saika Nakasato, Kaori Sano, Yoshiyuki Tanaka, Sachie Nakatani, Kenji Kobata. Biochemical Aspects of Putative Aminotransferase Responsible for Converting Vanillin to Vanillylamine in the Capsaicinoid Biosynthesis Pathway in Capsicum Plants. Journal of agricultural and food chemistry. 2024 Jan; 72(1):559-565. doi: 10.1021/acs.jafc.3c07369. [PMID: 38134368]
Yuan Gao, Jiang Liu, Xiaoyan Wang, Qiang Meng. Vanillin attenuates oxidative stress and neurochemical balance in MPTP-induced Parkinson's disease mice by regulating the TLR-4 inflammatory pathway. Folia neuropathologica. 2024 Jan; ?(?):. doi: 10.5114/fn.2023.131191. [PMID: 38174675]
Luis Chel-Guerrero, David Betancur-Ancona, Manuel Aguilar-Vega, Wilbert Rodríguez-Canto. Films properties of QPM corn starch with Delonix regia seed galactomannan as an edible coating material. International journal of biological macromolecules. 2024 Jan; 255(?):128408. doi: 10.1016/j.ijbiomac.2023.128408. [PMID: 38016603]
Marco A Ramírez-Mosqueda, Marco Vinicio Rodríguez-Deméneghi, Heidi P Medorio-García, Rubén H Andueza-Noh. Large-Scale Micropropagation of Vanilla (Vanilla planifolia Jacks.) in a Temporary Immersion Bioreactor (TIB). Methods in molecular biology (Clifton, N.J.). 2024; 2759(?):45-52. doi: 10.1007/978-1-0716-3654-1_4. [PMID: 38285137]
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Zarmin Iqbal, Ruhul Quds, Riaz Mahmood. Vanillin attenuates CdCl2-induced cytotoxicity in isolated human erythrocytes. Toxicology in vitro : an international journal published in association with BIBRA. 2023 Jun; ?(?):105633. doi: 10.1016/j.tiv.2023.105633. [PMID: 37336463]
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Xiao Han, Jiayan Huang, Jia Lu, Feng He, Fang Wang, Shuangfeng Li, Hao Zhong, Haiyang Yu, Weiling Pu. Active compounds and potential targets of Shuganning injection in the treatment of hepatocellular carcinoma by network pharmacology and in vitro validation. Naunyn-Schmiedeberg's archives of pharmacology. 2023 Mar; ?(?):. doi: 10.1007/s00210-023-02432-6. [PMID: 36869905]
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Jingyu Gou, Yuxi Guo, Huan Liu, Yanni Zhao, Rongjing Zhu, Yue Dang, Nannan Liu, Mengyin Chen, Xuefeng Chen. Process optimization of vanillin production by conversion of ferulic acid by Bacillus megaterium. Journal of the science of food and agriculture. 2022 Oct; 102(13):6047-6061. doi: 10.1002/jsfa.11957. [PMID: 35462414]
Dengyue Liu, Runjiang Song, Zengxue Wu, Zhifu Xing, Deyu Hu. Pyrido [1,2-a] Pyrimidinone Mesoionic Compounds Containing Vanillin Moiety: Design, Synthesis, Antibacterial Activity, and Mechanism. Journal of agricultural and food chemistry. 2022 Aug; 70(34):10443-10452. doi: 10.1021/acs.jafc.2c01838. [PMID: 35972464]
Hong-Wei He, Fei-Yu Wang, Danyang Zhang, Cai-Yun Chen, Dan Xu, Huan Zhou, Xili Liu, Gong Xu. Discovery of Novel α-Methylene-γ-Butyrolactone Derivatives Containing Vanillin Moieties as Antiviral and Antifungal Agents. Journal of agricultural and food chemistry. 2022 Aug; 70(33):10316-10325. doi: 10.1021/acs.jafc.2c03632. [PMID: 35960686]
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Cody Pinger, Louise Copeman, Michelle Stowell, Bryan Cormack, Corey Fugate, Matthew Rogers. Rapid measurement of total lipids in zooplankton using the sulfo-phospho-vanillin reaction. Analytical methods : advancing methods and applications. 2022 07; 14(27):2665-2672. doi: 10.1039/d2ay00665k. [PMID: 35748590]
Abeer S Elsherbiny, Alyaa Galal, Khalid M Ghoneem, Nehal A Salahuddin. Novel chitosan-based nanocomposites as ecofriendly pesticide carriers: Synthesis, root rot inhibition and growth management of tomato plants. Carbohydrate polymers. 2022 Apr; 282(?):119111. doi: 10.1016/j.carbpol.2022.119111. [PMID: 35123746]
Siyao Shao, Xi Cheng, Ruonan Zheng, Sufen Zhang, Zhiyang Yu, Haiyan Wang, Wei Wang, Qingfu Ye. Sex-related deposition and metabolism of vanisulfane, a novel vanillin-derived pesticide, in rats and its hepatotoxic and gonadal effects. The Science of the total environment. 2022 Mar; 813(?):152545. doi: 10.1016/j.scitotenv.2021.152545. [PMID: 34952065]
Heba A Metwaly, Abdulrahman M El-Eraky, Eman E Ibrahim, Khaled K Kandil, Mohamed A El-Sayed, Nayra M El-Tabakh, Amr M Motawea, Helmi A Ali, Maher Z Jabban, Mona E Mahmoud, Walaa H Abdelfattah, Mohammad A Elmorsy, Amal M H Ghanim. Vanillin attenuates thioacetamide-induced renal assault by direct and indirect mediation of the TGFβ, ERK and Smad signalling pathways in rats. Cell biochemistry and function. 2022 Mar; 40(2):175-188. doi: 10.1002/cbf.3686. [PMID: 35092082]
Sabeeha Ali, Manzar Alam, Fatima Khatoon, Urooj Fatima, Abdelbaset Mohamed Elasbali, Mohd Adnan, Asimul Islam, Md Imtaiyaz Hassan, Mejdi Snoussi, Vincenzo De Feo. Natural products can be used in therapeutic management of COVID-19: Probable mechanistic insights. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2022 Mar; 147(?):112658. doi: 10.1016/j.biopha.2022.112658. [PMID: 35066300]
Andrej Minich, Zdenko Levarski, Mária Mikulášová, Marek Straka, Adriána Liptáková, Stanislav Stuchlík. Complex Analysis of Vanillin and Syringic Acid as Natural Antimicrobial Agents against Staphylococcus epidermidis Biofilms. International journal of molecular sciences. 2022 Feb; 23(3):. doi: 10.3390/ijms23031816. [PMID: 35163738]
Hyungjoo Kim, Seungdo Yang, Yong Hyun Lim, Jeong-Myeong Ha, Do Heui Kim. Upgrading bio-oil model compound over bifunctional Ru/HZSM-5 catalysts in biphasic system: Complete hydrodeoxygenation of vanillin. Journal of hazardous materials. 2022 02; 423(Pt A):126525. doi: 10.1016/j.jhazmat.2021.126525. [PMID: 34246521]
Camila Mottin, Mariana Garcia Ornaghi, Venício Macêdo Carvalho, Ana Guerrero, Ana Carolina Pelaes Vital, Tatiane Rogelio Ramos, Edinéia Bonin, Fabiana Lana de Araújo, Ricardo de Araújo Castilho, Ivanor Nunes do Prado. Carcass characteristics and meat evaluation of cattle finished in temperate pasture and supplemented with natural additive containing clove, cashew oil, castor oils, and a microencapsulated blend of eugenol, thymol, and vanillin. Journal of the science of food and agriculture. 2022 Feb; 102(3):1271-1280. doi: 10.1002/jsfa.11465. [PMID: 34358347]
Atsushi Mitsumoto, Tohru Yamazaki. [Repellent Activity of Vanillin Derivatives and Monoterpenes to Olive Weevil]. Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan. 2022; 142(9):1005-1014. doi: 10.1248/yakushi.22-00086. [PMID: 36047212]
Guzel Ziyatdinova, Anastasiya Zhupanova, Rustam Davletshin. Simultaneous Determination of Ferulic Acid and Vanillin in Vanilla Extracts Using Voltammetric Sensor Based on Electropolymerized Bromocresol Purple. Sensors (Basel, Switzerland). 2021 Dec; 22(1):. doi: 10.3390/s22010288. [PMID: 35009830]
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Deepa Priya Ramadoss, Nageswaran Sivalingam. Vanillin extracted from proso and barnyard millets induces cell cycle inhibition and apoptotic cell death in MCF-7 cell line. Journal of cancer research and therapeutics. 2021 Oct; 17(6):1425-1433. doi: 10.4103/jcrt.jcrt_1128_19. [PMID: 34916373]
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Daniel Ribeiro Grijó, José Eduardo Olivo, Oswaldo Curty da Motta Lima. Simple chemical tests to identify Cannabis derivatives: Redefinition of parameters and analysis of concepts. Journal of forensic sciences. 2021 Sep; 66(5):1647-1657. doi: 10.1111/1556-4029.14777. [PMID: 34142715]
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Chih-Hsin Yeh, Kai-Yi Chen, Chia-Yi Chou, Hsin-Yi Liao, Hsin-Chun Chen. New Insights on Volatile Components of Vanilla planifolia Cultivated in Taiwan. Molecules (Basel, Switzerland). 2021 Jun; 26(12):. doi: 10.3390/molecules26123608. [PMID: 34204654]
Guoli Li, Beibei Kong, Qingchao Tong, Yejia Li, Lifen Chen, Jin Zeng, Haitao Yu, Xinyou Xie, Jun Zhang. Vanillin downregulates NNMT and attenuates NNMT‑related resistance to 5‑fluorouracil via ROS‑induced cell apoptosis in colorectal cancer cells. Oncology reports. 2021 Jun; 45(6):. doi: 10.3892/or.2021.8061. [PMID: 33907844]
Jing Yang, Yun-Ze Chen, Wu Yu-Xuan, Li Tao, Yun-Di Zhang, Shu-Ren Wang, Guo-Cai Zhang, Jie Zhang. Inhibitory effects and mechanisms of vanillin on gray mold and black rot of cherry tomatoes. Pesticide biochemistry and physiology. 2021 Jun; 175(?):104859. doi: 10.1016/j.pestbp.2021.104859. [PMID: 33993955]
Xiaxia Wang, Dinglei Xiang, Ziyi Wang, Zhaoguo Wang, Xue Yang, Shuai Yu, Qiuxia Pang, Sheng Liu, Li Yan. Label-free quantitative proteomics analysis of Humulus scandens (Lour.) Merr. leaves treated by an odor compound of Periploca sepium Bunge. Ecotoxicology and environmental safety. 2021 Jun; 215(?):112131. doi: 10.1016/j.ecoenv.2021.112131. [PMID: 33752163]
Veronica F Salau, Ochuko L Erukainure, Kolawole A Olofinsan, Md Shahidul Islam. Vanillin exerts therapeutic effects against hyperglycemia-altered glucose metabolism and purinergic activities in testicular tissues of diabetic rats. Reproductive toxicology (Elmsford, N.Y.). 2021 06; 102(?):24-34. doi: 10.1016/j.reprotox.2021.03.007. [PMID: 33823243]
InWha Park, Hee Sun Byun, Gang Min Hur, MinKyun Na. Tulipiferamide A, an Alkamide from Liriodendron tulipifera, Exhibits an Anti-Inflammatory Effect via Targeting IKKβ Phosphorylation. Journal of natural products. 2021 05; 84(5):1598-1606. doi: 10.1021/acs.jnatprod.1c00146. [PMID: 33939429]
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Xuanxuan Zhang, Yang He, Zhe Wu, Guoxia Liu, Yong Tao, Jian-Ming Jin, Wei Chen, Shuang-Yan Tang. Whole-Cell Biosensors Aid Exploration of Vanillin Transmembrane Transport. Journal of agricultural and food chemistry. 2021 Mar; 69(10):3114-3123. doi: 10.1021/acs.jafc.0c07886. [PMID: 33666081]
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Thae Thae San, Yue-Hu Wang, Dong-Bao Hu, Jun Yang, Dong-Dong Zhang, Meng-Yuan Xia, Xue-Fei Yang, Yong-Ping Yang. A new sesquineolignan and four new neolignans isolated from the leaves of Piper betle, a traditional medicinal plant in Myanmar. Bioorganic & medicinal chemistry letters. 2021 01; 31(?):127682. doi: 10.1016/j.bmcl.2020.127682. [PMID: 33207281]
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Mohammed Omar Faruque, Muhammad Ilyas, Mohammad Mozahar Hossain, Shaikh Abdur Razzak. Influence of Nitrogen to Phosphorus Ratio and CO2 Concentration on Lipids Accumulation of Scenedesmus dimorphus for Bioenergy Production and CO2 Biofixation. Chemistry, an Asian journal. 2020 Dec; 15(24):4307-4320. doi: 10.1002/asia.202001063. [PMID: 33108039]
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Naoki Kitaoka, Taiji Nomura, Shinjiro Ogita, Yasuo Kato. Bioproduction of glucose conjugates of 4-hydroxybenzoic and vanillic acids using bamboo cells transformed to express bacterial 4-hydroxycinnamoyl-CoA hydratase/lyase. Journal of bioscience and bioengineering. 2020 Jul; 130(1):89-97. doi: 10.1016/j.jbiosc.2020.02.010. [PMID: 32192841]
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