Vanillin (BioDeep_00000000091)

Secondary id: BioDeep_00000269025, BioDeep_00000859823

natural product human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite

代谢物信息卡片

Vanillin melting point standard, Pharmaceutical Secondary Standard; Certified Reference Material

化学式: C8H8O3 (152.0473418)
中文名称: 4-羟基-3-甲氧基-13C-苯甲醛, 香草醛, 香兰素, 香兰素
谱图信息: 最多检出来源 Viridiplantae(plant) 0.27%

分子结构信息

SMILES: COC1=C(C=CC(=C1)C=O)O
InChI: InChI=1/C8H8O3/c1-11-8-4-6(5-9)2-3-7(8)10/h2-5,10H,1H3

描述信息

Vanillin, also known as vanillaldehyde or lioxin, belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety. It is used by the food industry as well as ethylvanillin. Vanillin exists in all living species, ranging from bacteria to humans. Vanillin is a sweet, chocolate, and creamy tasting compound. Vanillin is found, on average, in the highest concentration within a few different foods, such as corns, ryes, and sherries and in a lower concentration in beers, rums, and oats. Vanillin has also been detected, but not quantified, in several different foods, such as gooseberries, other bread, brazil nuts, shea tree, and ohelo berries. This could make vanillin a potential biomarker for the consumption of these foods. Vanillin is a potentially toxic compound. Synthetic vanillin, instead of natural Vanillin extract, is sometimes used as a flavouring agent in foods, beverages, and pharmaceuticals. Vanillin is the primary component of the extract of the Vanillin bean. Because of the scarcity and expense of natural Vanillin extract, there has long been interest in the synthetic preparation of its predominant component. Artificial Vanillin flavoring is a solution of pure vanillin, usually of synthetic origin. Today, artificial vanillin is made from either guaiacol or from lignin, a constituent of wood which is a byproduct of the paper industry. The first commercial synthesis of vanillin began with the more readily available natural compound eugenol.
Vanillin appears as white or very slightly yellow needles.
Vanillin is a member of the class of benzaldehydes carrying methoxy and hydroxy substituents at positions 3 and 4 respectively. It has a role as a plant metabolite, an anti-inflammatory agent, a flavouring agent, an antioxidant and an anticonvulsant. It is a member of phenols, a monomethoxybenzene and a member of benzaldehydes.
Vanillin is a natural product found in Ficus erecta var. beecheyana, Pandanus utilis, and other organisms with data available.
Vanillin is the primary component of the extract of the vanilla bean. Synthetic vanillin, instead of natural vanilla extract, is sometimes used as a flavouring agent in foods, beverages, and pharmaceuticals. It is used by the food industry as well as ethylvanillin.Artificial vanilla flavoring is a solution of pure vanillin, usually of synthetic origin. Because of the scarcity and expense of natural vanilla extract, there has long been interest in the synthetic preparation of its predominant component. The first commercial synthesis of vanillin began with the more readily available natural compound eugenol. Today, artificial vanillin is made from either guaiacol or from lignin, a constituent of wood which is a byproduct of the paper industry. (Wiki).
Vanillin is a metabolite found in or produced by Saccharomyces cerevisiae.
Constituent of vanilla (Vanilla subspecies) and many other plants, e.g. Peru balsam, clove bud oil. Widely used flavouring agent especies in cocoa products. obtained from spent wood-pulp liquors. Vanillin is found in many foods, some of which are pomes, elderberry, common cabbage, and dock.
A member of the class of benzaldehydes carrying methoxy and hydroxy substituents at positions 3 and 4 respectively.
D002491 - Central Nervous System Agents > D000927 - Anticonvulsants
D020011 - Protective Agents > D016587 - Antimutagenic Agents
D020011 - Protective Agents > D000975 - Antioxidants
CONFIDENCE standard compound; ML_ID 59
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

105 个代谢物同义名

Vanillin melting point standard, Pharmaceutical Secondary Standard; Certified Reference Material; Vanillin Melting Point Standard, United States Pharmacopeia (USP) Reference Standard; Vanillin, Pharmaceutical Secondary Standard; Certified Reference Material; Vanillin, United States Pharmacopeia (USP) Reference Standard; Vanillin, European Pharmacopoeia (EP) Reference Standard; InChI=1/C8H8O3/c1-11-8-4-6(5-9)2-3-7(8)10/h2-5,10H,1H; Vanillin, TraceCERT(R), certified reference material; 1-(AMINOMETHYL)-CYCLOPROPANECARBOXYLICACIDETHYLESTER; 4-hydroxy-3-methoxy-Benzaldehyde-5-chlorovanillin; 4-hydroxy-3-methoxybenzaldehyde (ACD/Name 4.0); Vanillin (83 degrees C) Melting Point Standard; vanillin (3-methoxy-4-hydroxy- benzaldehyde); 4-08-00-01763 (Beilstein Handbook Reference); 4-Hydroxy-3-methoxybenzaldehyde(Vanilline); 3-Methoxy-4-hydroxybenzaldehyde (vanillin); 4-hydroxy-3-methoxybenzaldehyde (vanillin); Vanillin, Vetec(TM) reagent grade, 98\\%; Vanillin, tested according to Ph.Eur.; Vanillin, JIS special grade, >=98.0\\%; Protocatechualdehyde 3-methyl ether; trans-2-Ethoxy-5-(1-propenyl)phenol; 4-hydoxy-3-(methyloxy)benz aldehyde; Benzaldehyde, 4-hydroxy-3-methoxy-; Vanillin, natural, >=97\\%, FCC, FG; 4-hydoxy-3-(methyloxy)benzaldehyde; 4-hydroxy-3-(methoxy)benzaldehyde; 3-methoxy-4-hydroxy benzoaldehyde; 4-hydroxy-3-methoxy benzaldehyde; 3-methoxy-4-hydroxy-benzaldehyde; 4-Hydroxy-3-methoxy-benzaldehyde; 3-methoxy-4-hydroxy benzaldehyde; 4-HYDROXY,3-METHOXY-BENZALDEHYDE; 4-hydroxy-3-methoxy-benzyldehyde; p-Hydroxy-m-methoxybenzaldehyde; 4-hydroxy-3-methoxybenzaldehyde; 4-Hydroxy-5-methoxybenzaldehyde; Vanillin Melting Point Standard; Vanilla oleoresin (vanilla SPP); 4-hydroxy 3-methoxybenzaldehyde; 3-Methoxy-4-hydroxybenzaldehyde; m-Methoxy-p-hydroxybenzaldehyde; Vanillin, ReagentPlus(R), 99\\%; Methylprotocatechuic aldehyde; Protocatechualdehyde, methyl-; Methylprotcatechuic aldehyde; methyl-Protocatechualdehyde; m-Anisaldehyde, 4-hydroxy-; METHYLPROTOCATECHUALDEHYDE; Vanillin, puriss., 99.5\\%; Vanillin, >=97\\%, FCC, FG; oleo-Resins vanilla-bean; 2-Methoxy-4-formylphenol; VANILLIN, NATURAL [FHFI]; 4-Formyl-2-methoxyphenol; 4-Hydroxy-m-anisaldehyde; VANILLIN (EP MONOGRAPH); VANILLIN [EP MONOGRAPH]; VANILLIN (METHOXY-13C); vanillin, sodium salt; Vanillin sodium salt; Vanillin (Standard); oleo-Resins vanilla; Vanillin (natural); VANILLIN [USP-RS]; VANILLIN [WHO-DD]; Vanilla oleoresin; Vanillic aldehyde; Oleoresin vanilla; Vanillin, natural; VANILLIN [VANDF]; 5-chlorovanillin; Propenylguaethol; VANILLIN (MART.); VANILLIN [MART.]; 5-bromovanillin; VANILLIN [INCI]; WLN: VHR DQ CO1; VANILLIN [FHFI]; VANILLIN [HSDB]; Vanillin [USAN]; VANILLIN [FCC]; vanillaldehyde; Tox21_113534_1; VANILLIN [II]; Vanillin [NF]; Vanillin (NF); VANILLIN (II); VANILLIN [MI]; Tox21_113534; Tox21_300352; NCI60_001085; Tox21_201925; p-Vanillin; Vanilline; AI3-00093; Vanillin; Rhovanil; vaniline; Vanillum; Vanilin; Vanilla; Lioxin; Zimco; V55; Vanillin

数据库引用编号

28 个数据库交叉引用编号

ChEBI: CHEBI:18346
KEGG: C00755
KEGGdrug: D00091
PubChem: 1183
HMDB: HMDB0012308
Metlin: METLIN62927
ChEMBL: CHEMBL13883
Wikipedia: Vanillin
MeSH: vanillin
ChemIDplus: 0000121335
MetaCyc: VANILLIN
KNApSAcK: C00002683
foodb: FDB000838
chemspider: 13860434
CAS: 86884-84-6
CAS: 121-33-5
MoNA: PS073503
MoNA: PS073501
MoNA: ML005951
MoNA: PS073502
medchemexpress: HY-N0098
PMhub: MS000001893
MetaboLights: MTBLC18346
PubChem: 4017
PDB-CCD: V55
3DMET: B00167
NIKKAJI: J2.923H
RefMet: Vanillin

分类词条

代谢反应

15 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(12)

vanillin biosynthesis I: 4-hydroxybenzaldehyde + O₂ + a reduced [NADPH-hemoprotein reductase] ⟶ 3,4-dihydroxybenzaldehyde + H₂O + an oxidized [NADPH-hemoprotein reductase]
vanillin and vanillate degradation II: H⁺ + NADH + O₂ + vanillate ⟶ H₂O + NAD⁺ + formaldehyde + protocatechuate
vanillin and vanillate degradation I: H₂O + NAD⁺ + vanillin ⟶ H⁺ + NADH + vanillate
ferulate degradation: 4-hydroxy-3-methoxyphenyl-β-hydroxypropanoyl-CoA ⟶ acetyl-CoA + vanillin
pinoresinol degradation: (+)-pinoresinol + A + H₂O ⟶ (+)-6-hydroxypinoresinol + A(H2)
(-)-dehydrodiconiferyl alcohol degradation: (-)-dehydrodiconiferyl acid aldehyde gem-diol + an electron-transfer quinone ⟶ (-)-dehydrodiconiferyl acid carboxylate + H⁺ + an electron-transfer quinol
superpathway of vanillin and vanillate degradation: H₂O + NAD⁺ + vanillin ⟶ H⁺ + NADH + vanillate
ferulate degradation: 4-hydroxy-3-methoxyphenyl-β-hydroxypropionyl-CoA ⟶ acetyl-CoA + vanillin
vanillin and vanillate degradation I: tetrahydrofolate + vanillate ⟶ 5-methyl-tetrahydrofolate + protocatechuate
vanillin and vanillate degradation II: H⁺ + NADH + O₂ + vanillate ⟶ H₂O + NAD⁺ + formaldehyde + protocatechuate
superpathway of aromatic compound degradation: O₂ + protocatechuate ⟶ 3-carboxy-cis,cis-muconate + H⁺
vanillin and vanillate degradation II: H⁺ + NADH + O₂ + vanillate ⟶ H₂O + NAD⁺ + formaldehyde + protocatechuate

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(3)

vanillin biosynthesis I: 4-hydroxybenzaldehyde + O₂ + a reduced [NADPH-hemoprotein reductase] ⟶ 3,4-dihydroxybenzaldehyde + H₂O + an oxidized [NADPH-hemoprotein reductase]
capsaicin biosynthesis: H⁺ + NADPH + a malonyl-[acp] + isobutanoyl-CoA ⟶ 8-methyl-6-nonenoate + H₂O + NADP⁺ + a holo-[acyl-carrier protein] + coenzyme A
capsaicin biosynthesis: 8-methyl-6-nonenoate + vanillylamine ⟶ H₂O + capsaicin

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

417 个相关的物种来源信息

33090 香草兰: -
52153 Festuca rubra: 10.1016/0031-9422(91)84185-U
4606 Lolium arundinaceum: 10.1016/0031-9422(91)84185-U
375857 Scolochloa festucacea: 10.1016/0031-9422(91)84185-U
29760 Vitis vinifera:
65409 Scutellaria baicalensis: 10.1271/BBB1961.51.1449
3760 Prunus persica: 10.1021/JF00004A032
36596 Prunus armeniaca: 10.1021/JF00004A032
3758 Prunus domestica: 10.1021/JF00004A032
3750 Malus domestica: 10.1021/JF00025A025
283210 Malus pumila: 10.1021/JF00025A025
128608 Cinnamomum verum: 10.1021/JF60218A031
3589 Basella alba: 10.1016/0889-1575(91)90017-Z
3635 Gossypium hirsutum:
158550 Aristolochia kaempferi:
977953 Cinnamomum subavenium:
415155 Aster indicus: 10.1016/J.PHYTOCHEM.2007.05.027
159071 Zanthoxylum ailanthoides:
354522 Tetradium glabrifolium: 10.1016/0031-9422(95)00248-6
256638 Euchresta formosana:
4498 Avena sativa:
1094085 Colchicum kotschyi: 10.1016/0031-9422(90)87143-I
13445 Colchicum speciosum: 10.1016/0031-9422(90)87143-I
1208297 Colchicum bornmuelleri: 10.1016/0031-9422(90)87143-I
4146 Olea europaea:
90037 Taraxacum mongolicum: 10.1248/CPB.53.853
170733 Taraxacum formosanum: 10.1248/CPB.53.853
49314 Annona cherimola:
23224 Spiraea: 10.1248/CPB.52.1227
139927 Carya cathayensis: 10.1016/J.BMCL.2012.01.062
16752 Houttuynia cordata: 10.1248/CPB.57.1227
1815962 Petasites formosanus: 10.1248/CPB.47.375
265783 Artemisia capillaris: 10.1016/S0968-0896(00)00225-X
55489 Posidonia oceanica: 10.1016/S0031-9422(97)01118-7
82096 Eleutherococcus senticosus: 10.1007/BF00629948
4111 Solanum melongena:
1132458 Cinnamomum kotoense:
72645 Molineria capitulata:
175969 Aeschynanthus bracteatus: 10.1016/J.PHYTOCHEM.2008.05.012
697043 Zanthoxylum wutaiense:
1123437 Annona purpurea:
35899 Galium odoratum: 10.1039/J39680000854
3330 Picea glauca: 10.1016/S0031-9422(96)00388-3
4550 Secale cereale: 10.1016/J.FOODCHEM.2005.07.053
51239 Vanilla planifolia:
1056465 Zanthoxylum beecheyanum: 10.1002/JCCS.200400159
4232 Helianthus annuus: 10.1021/JF00123A021
447671 Lonicera microphylla: 10.1007/BF00565263
289753 Rhus chinensis: 10.1248/CPB.55.804
210348 Brucea javanica:
78253 Begonia nantoensis:
210369 Tribulus terrestris: 10.1016/S0031-9422(97)01086-8
50172 Viscum articulatum:
159976 Viscum coloratum:
429701 Handroanthus impetiginosus: 10.1002/HLCA.19890720406
1898877 Hibiscus taiwanensis:
117957 Vanilla pompona: 10.1080/10412905.1997.9700743
79022 Thapsia garganica: 10.1055/S-2006-960216
3696 Populus deltoides: 10.1515/ZNC-1990-0604
97171 Abies nephrolepis:
313931 Duhaldea cappa: 10.1007/S10600-010-9595-4
223102 Orobanche crenata: 10.1055/S-2006-958118
36748 Orobanche minor: 10.1055/S-2006-958118
41511 Centaurea calcitrapa: 10.1007/S10600-007-0232-9
2072395 Centaurea scoparia:
38724 Haplopteris anguste-elongata: 10.1021/NP050060O
4081 Solanum lycopersicum:
663965 Anastatica hierochuntica:
75702 Populus euphratica:
40321 Capsicum annuum var. annuum: 10.1007/BF00048188
165789 Capsicum annuum var. glabriusculum: 10.1007/BF00048188
38942 Quercus robur: 10.1021/JF9502461
453298 Quercus pyrenaica: 10.1021/JF9502461
501392 Quercus faginea: 10.1021/JF9502461
38865 Quercus petraea: 10.1021/JF9502461
161934 Beta vulgaris: 10.1271/BBB1961.44.205
2803928 Neolitsea acuminatissima: 10.1021/NP010236W
128638 Licaria triandra: 10.1021/NP010236W
88853 Litsea glaucescens: 10.1021/NP010236W
244352 Mondia whitei: 10.1016/J.PHYTOCHEM.2004.11.012
121073 Cassytha filiformis: 10.1021/NP970348G
1008913 Ficus erecta var. beecheyana: 10.1002/JCCS.200400067
3708 Brassica napus: 10.1016/J.FOODCHEM.2006.08.014
139932 Engelhardia roxburghiana: 10.1016/J.PHYTOCHEM.2007.01.018
43522 Morinda citrifolia:
58331 Quercus suber:
318068 Xanthium strumarium: 10.1055/S-2008-1081295
492000 Decalepis hamiltonii: 10.1002/1099-1026(200101/02)16:1<27::AID-FFJ937>3.0.CO;2-F
2306982 Antidesma pentandrum var. barbatum: 10.1002/JCCS.200700187
1053410 Xanthium spinosum: 10.1016/0031-9422(91)83230-I
204149 Ocimum tenuiflorum: 10.1248/CPB.57.245
97169 Abies sibirica: 10.1007/BF00564181
44685 Panax japonicus:
91201 Gastrodia elata:
586100 Phyllanthus oligospermus: 10.1248/CPB.54.1223
1548370 Rolandra fruticosa: 10.1016/S0031-9422(00)97890-7
363212 Pisonia aculeata: 10.1021/NP1008575
147275 Taxus wallichiana var. wallichiana:
3641 Theobroma cacao: 10.1007/S00217-006-0252-X
109101 Chaerophyllum hirsutum: 10.1021/NP040046W
128742 Psilostrophe cooperi: 10.1016/S0031-9422(00)81432-6
72351 Artemisia scoparia: 10.1016/0031-9422(73)80524-2
482945 Populus grandidentata: 10.1515/ZNC-1987-9-1004
2039844 Lagochilus leiacanthus: 10.1248/CPB.59.1535
1165086 Pandanus odorifer: 10.1016/S0031-9422(98)00390-2
4726 Pandanus tectorius: 10.1016/S0031-9422(98)00390-2
240453 Pandanus odoratissimus: 10.1016/S0031-9422(98)00390-2
56992 Araucaria angustifolia: 10.1016/S0031-9422(00)00239-9
431268 Aristolochia heterophylla:
35927 Aristolochia tomentosa: 10.1016/S0031-9422(99)00176-4
1604314 Gynura japonica:
210888 Gynura segetum: 10.1016/S0031-9422(99)00599-3
592600 Chamaecrista flexuosa: 10.1016/S0040-4020(01)81569-6
642575 Pedalium murex: 10.1016/0031-9422(83)85033-X
75727 Zizania aquatica: 10.1021/JF940651C
78264 Abies sachalinensis:
308680 Picea koraiensis: 10.1007/BF00563906
331118 Picea obovata: 10.1007/BF00563906
155640 Melia azedarach:
229543 Hibiscus cannabinus: 10.1016/S0031-9422(00)00473-8
463862 Ficus nervosa: 10.1002/CBDV.200900227
137934 Aralia bipinnata:
2831626 Angelica pachycarpa: 10.1055/S-0028-1097274
1609853 Beilschmiedia erythrophloia: 10.1021/NP800504W
1224803 Vernonanthura chamaedrys:
3702 Arabidopsis thaliana: 10.1016/J.PHYTOCHEM.2003.12.009
72955 Myriactis humilis: 10.1055/S-2005-864107
1172173 Magnolia crassipes: 10.4268/CJCMM20141019
52471 Ferula assa-foetida: 10.1021/NP900158F
48042 Levisticum officinale:
3349 Pinus sylvestris: 10.1021/JF048948Q
4577 Zea mays: 10.1248/CPB.55.153
143780 Aristolochia elegans: 10.1016/J.BMC.2003.10.031
325095 Aristolochia littoralis: 10.1016/J.BMC.2003.10.031
461588 Fibraurea tinctoria: 10.1016/J.BMC.2008.09.023
551215 Euploea sylvester: 10.1515/ZNC-1988-1-219
2689076 Ligusticum chuanxiong:
1508160 Ligusticum striatum:
1310066 Lagotis yunnanensis:
429256 Carissa spinarum: 10.1016/S0031-9422(00)86976-9
992661 Carissa edulis: 10.1016/S0031-9422(00)86976-9
58039 Juniperus communis: 10.1248/CPB.58.742
884034 Juniperus communis var. depressa: 10.1248/CPB.58.742
375272 Pimenta dioica: 10.1016/S0031-9422(99)00406-9
1603837 Strobilanthes dimorphotricha: 10.1055/S-2005-873125
35608 Artemisia annua: 10.1016/S0031-9422(98)00607-4
1089418 Microtropis japonica: 10.1021/NP800097T
165353 Angelica sinensis:
1603694 Beilschmiedia tsangii:
223868 Artemisia japonica: 10.1007/BF02978255
128687 Phoebe formosana: 10.1021/NP970147C
285591 Tinospora crispa: 10.1055/S-2006-957466
145508 Centaurea ornata: 10.1021/NP50069A006
904463 Pojarkovia pojarkovae:
189220 Ligularia stenocephala:
217501 Ligularia dentata:
40705 Paeonia clusii: 10.1515/ZNC-2002-3-406
557622 Allagopappus canariensis: 10.1021/NP50117A014
56513 Allagopappus dichotomus: 10.1021/NP50117A014
4234 Helianthus petiolaris:
68527 Aegle marmelos: 10.1016/J.PHYTOCHEM.2009.10.013
697038 Melicope semecarpifolia: 10.1055/S-2005-871295
13715 Tetracentron sinense: 10.1016/S0031-9422(99)00457-4
199633 Curcuma comosa: 10.1248/CPB.56.1604
4079 Hyoscyamus niger:
224738 Lepidothamnus intermedius: 10.1071/CH9851631
461553 Arcangelisia flava: 10.1016/J.PHYTOL.2011.07.002
1609885 Neolitsea hiiranensis: 10.1016/J.PHYTOCHEM.2011.01.006
73292 Helianthus heterophyllus: 10.1016/S0031-9422(00)81173-5
1826902 Stellaria dichotoma:
53751 Echinacea purpurea: 10.1016/0031-9422(83)80215-5
409890 Robinsonia thurifera: 10.1016/0031-9422(88)83126-1
358659 Isatis quadrialata:
185543 Ilex pubescens: 10.1002/HLCA.200890135
1354278 Radermachera sinica: 10.1039/P19810002764
1094094 Colchicum manissadjianii: 10.1016/0031-9422(89)80310-3
337466 Machilus zuihoensis: 10.1080/14786410802401432
1924212 Nectandra oppositifolia: 10.1021/NP50009A006
180097 Sporobolus cynosuroides: 10.1021/NP50028A035
1261582 Vertebrata lanosa: 10.1021/NP0305268
1462929 Marsypopetalum modestum: 10.1080/14786419.2022.2097229
136217 Curcuma longa: 10.1016/0021-9673(96)00103-3
311405 Zingiber zerumbet: 10.1007/BF02980078
761071 Tabernaemontana glandulosa: 10.1016/S0031-9422(00)89602-8
187461 Chamaecyparis formosensis: 10.1016/J.PHYMED.2006.11.029
1582456 Chuquiraga atacamensis: 10.4067/S0366-16442000000100007
1234283 Aristolochia asclepiadifolia: 10.1002/FFJ.2730080104
682177 Tolpis webbii: 10.1016/J.FITOTE.2009.06.001
1911 Streptomyces griseus:
4097 Nicotiana tabacum: 10.1080/10826079308019709
872941 Onobrychis meschetica: 10.1007/BF00563835
637488 Artemisia stolonifera: 10.1007/BF02975098
259893 Artemisia argyi: 10.1007/BF02975098
51238 Vanilla:
123165 Leptotes bicolor: 10.1016/J.MOLP.2014.11.008
88731 Pinus tabuliformis: 10.1016/J.MOLP.2014.11.008
4896 Schizosaccharomyces pombe: 10.1128/AEM.02681-08
1087767 Euphorbia hirsuta: 10.1021/NP0400048
52153 Festuca rubra: 10.1016/0031-9422(91)84185-U
4606 Lolium arundinaceum: 10.1016/0031-9422(91)84185-U
375857 Scolochloa festucacea: 10.1016/0031-9422(91)84185-U
29760 Vitis vinifera:
65409 Scutellaria baicalensis: 10.1271/BBB1961.51.1449
3760 Prunus persica: 10.1021/JF00004A032
36596 Prunus armeniaca: 10.1021/JF00004A032
3758 Prunus domestica: 10.1021/JF00004A032
3750 Malus domestica: 10.1021/JF00025A025
283210 Malus pumila: 10.1021/JF00025A025
128608 Cinnamomum verum: 10.1021/JF60218A031
3589 Basella alba: 10.1016/0889-1575(91)90017-Z
3635 Gossypium hirsutum:
158550 Aristolochia kaempferi:
977953 Cinnamomum subavenium:
415155 Aster indicus: 10.1016/J.PHYTOCHEM.2007.05.027
159071 Zanthoxylum ailanthoides:
354522 Tetradium glabrifolium: 10.1016/0031-9422(95)00248-6
256638 Euchresta formosana:
4498 Avena sativa:
1094085 Colchicum kotschyi: 10.1016/0031-9422(90)87143-I
13445 Colchicum speciosum: 10.1016/0031-9422(90)87143-I
1208297 Colchicum bornmuelleri: 10.1016/0031-9422(90)87143-I
4146 Olea europaea:
90037 Taraxacum mongolicum: 10.1248/CPB.53.853
170733 Taraxacum formosanum: 10.1248/CPB.53.853
49314 Annona cherimola:
23224 Spiraea: 10.1248/CPB.52.1227
139927 Carya cathayensis: 10.1016/J.BMCL.2012.01.062
16752 Houttuynia cordata: 10.1248/CPB.57.1227
1815962 Petasites formosanus: 10.1248/CPB.47.375
265783 Artemisia capillaris: 10.1016/S0968-0896(00)00225-X
55489 Posidonia oceanica: 10.1016/S0031-9422(97)01118-7
82096 Eleutherococcus senticosus: 10.1007/BF00629948
4111 Solanum melongena:
1132458 Cinnamomum kotoense:
72645 Molineria capitulata:
175969 Aeschynanthus bracteatus: 10.1016/J.PHYTOCHEM.2008.05.012
697043 Zanthoxylum wutaiense:
1123437 Annona purpurea:
35899 Galium odoratum: 10.1039/J39680000854
3330 Picea glauca: 10.1016/S0031-9422(96)00388-3
4550 Secale cereale: 10.1016/J.FOODCHEM.2005.07.053
51239 Vanilla planifolia:
1056465 Zanthoxylum beecheyanum: 10.1002/JCCS.200400159
4232 Helianthus annuus: 10.1021/JF00123A021
447671 Lonicera microphylla: 10.1007/BF00565263
289753 Rhus chinensis: 10.1248/CPB.55.804
210348 Brucea javanica:
78253 Begonia nantoensis:
210369 Tribulus terrestris: 10.1016/S0031-9422(97)01086-8
50172 Viscum articulatum:
159976 Viscum coloratum:
429701 Handroanthus impetiginosus: 10.1002/HLCA.19890720406
1898877 Hibiscus taiwanensis:
117957 Vanilla pompona: 10.1080/10412905.1997.9700743
79022 Thapsia garganica: 10.1055/S-2006-960216
3696 Populus deltoides: 10.1515/ZNC-1990-0604
97171 Abies nephrolepis:
313931 Duhaldea cappa: 10.1007/S10600-010-9595-4
223102 Orobanche crenata: 10.1055/S-2006-958118
36748 Orobanche minor: 10.1055/S-2006-958118
41511 Centaurea calcitrapa: 10.1007/S10600-007-0232-9
2072395 Centaurea scoparia:
38724 Haplopteris anguste-elongata: 10.1021/NP050060O
4081 Solanum lycopersicum:
663965 Anastatica hierochuntica:
75702 Populus euphratica:
40321 Capsicum annuum var. annuum: 10.1007/BF00048188
165789 Capsicum annuum var. glabriusculum: 10.1007/BF00048188
38942 Quercus robur: 10.1021/JF9502461
453298 Quercus pyrenaica: 10.1021/JF9502461
501392 Quercus faginea: 10.1021/JF9502461
38865 Quercus petraea: 10.1021/JF9502461
161934 Beta vulgaris: 10.1271/BBB1961.44.205
2803928 Neolitsea acuminatissima: 10.1021/NP010236W
128638 Licaria triandra: 10.1021/NP010236W
88853 Litsea glaucescens: 10.1021/NP010236W
244352 Mondia whitei: 10.1016/J.PHYTOCHEM.2004.11.012
121073 Cassytha filiformis: 10.1021/NP970348G
1008913 Ficus erecta var. beecheyana: 10.1002/JCCS.200400067
3708 Brassica napus: 10.1016/J.FOODCHEM.2006.08.014
139932 Engelhardia roxburghiana: 10.1016/J.PHYTOCHEM.2007.01.018
43522 Morinda citrifolia:
58331 Quercus suber:
318068 Xanthium strumarium: 10.1055/S-2008-1081295
492000 Decalepis hamiltonii: 10.1002/1099-1026(200101/02)16:1<27::AID-FFJ937>3.0.CO;2-F
2306982 Antidesma pentandrum var. barbatum: 10.1002/JCCS.200700187
1053410 Xanthium spinosum: 10.1016/0031-9422(91)83230-I
204149 Ocimum tenuiflorum: 10.1248/CPB.57.245
97169 Abies sibirica: 10.1007/BF00564181
44685 Panax japonicus:
91201 Gastrodia elata:
586100 Phyllanthus oligospermus: 10.1248/CPB.54.1223
1548370 Rolandra fruticosa: 10.1016/S0031-9422(00)97890-7
363212 Pisonia aculeata: 10.1021/NP1008575
147275 Taxus wallichiana var. wallichiana:
3641 Theobroma cacao: 10.1007/S00217-006-0252-X
109101 Chaerophyllum hirsutum: 10.1021/NP040046W
128742 Psilostrophe cooperi: 10.1016/S0031-9422(00)81432-6
72351 Artemisia scoparia: 10.1016/0031-9422(73)80524-2
482945 Populus grandidentata: 10.1515/ZNC-1987-9-1004
2039844 Lagochilus leiacanthus: 10.1248/CPB.59.1535
1165086 Pandanus odorifer: 10.1016/S0031-9422(98)00390-2
4726 Pandanus tectorius: 10.1016/S0031-9422(98)00390-2
240453 Pandanus odoratissimus: 10.1016/S0031-9422(98)00390-2
56992 Araucaria angustifolia: 10.1016/S0031-9422(00)00239-9
431268 Aristolochia heterophylla:
35927 Aristolochia tomentosa: 10.1016/S0031-9422(99)00176-4
1604314 Gynura japonica:
210888 Gynura segetum: 10.1016/S0031-9422(99)00599-3
592600 Chamaecrista flexuosa: 10.1016/S0040-4020(01)81569-6
642575 Pedalium murex: 10.1016/0031-9422(83)85033-X
75727 Zizania aquatica: 10.1021/JF940651C
78264 Abies sachalinensis:
308680 Picea koraiensis: 10.1007/BF00563906
331118 Picea obovata: 10.1007/BF00563906
155640 Melia azedarach:
229543 Hibiscus cannabinus: 10.1016/S0031-9422(00)00473-8
463862 Ficus nervosa: 10.1002/CBDV.200900227
137934 Aralia bipinnata:
2831626 Angelica pachycarpa: 10.1055/S-0028-1097274
1609853 Beilschmiedia erythrophloia: 10.1021/NP800504W
1224803 Vernonanthura chamaedrys:
3702 Arabidopsis thaliana: 10.1016/J.PHYTOCHEM.2003.12.009
72955 Myriactis humilis: 10.1055/S-2005-864107
1172173 Magnolia crassipes: 10.4268/CJCMM20141019
52471 Ferula assa-foetida: 10.1021/NP900158F
48042 Levisticum officinale:
3349 Pinus sylvestris: 10.1021/JF048948Q
4577 Zea mays: 10.1248/CPB.55.153
143780 Aristolochia elegans: 10.1016/J.BMC.2003.10.031
325095 Aristolochia littoralis: 10.1016/J.BMC.2003.10.031
461588 Fibraurea tinctoria: 10.1016/J.BMC.2008.09.023
551215 Euploea sylvester: 10.1515/ZNC-1988-1-219
2689076 Ligusticum chuanxiong:
1508160 Ligusticum striatum:
1310066 Lagotis yunnanensis:
429256 Carissa spinarum: 10.1016/S0031-9422(00)86976-9
992661 Carissa edulis: 10.1016/S0031-9422(00)86976-9
58039 Juniperus communis: 10.1248/CPB.58.742
884034 Juniperus communis var. depressa: 10.1248/CPB.58.742
375272 Pimenta dioica: 10.1016/S0031-9422(99)00406-9
1603837 Strobilanthes dimorphotricha: 10.1055/S-2005-873125
35608 Artemisia annua: 10.1016/S0031-9422(98)00607-4
1089418 Microtropis japonica: 10.1021/NP800097T
165353 Angelica sinensis:
1603694 Beilschmiedia tsangii:
223868 Artemisia japonica: 10.1007/BF02978255
128687 Phoebe formosana: 10.1021/NP970147C
285591 Tinospora crispa: 10.1055/S-2006-957466
145508 Centaurea ornata: 10.1021/NP50069A006
904463 Pojarkovia pojarkovae:
189220 Ligularia stenocephala:
217501 Ligularia dentata:
40705 Paeonia clusii: 10.1515/ZNC-2002-3-406
557622 Allagopappus canariensis: 10.1021/NP50117A014
56513 Allagopappus dichotomus: 10.1021/NP50117A014
4234 Helianthus petiolaris:
68527 Aegle marmelos: 10.1016/J.PHYTOCHEM.2009.10.013
697038 Melicope semecarpifolia: 10.1055/S-2005-871295
13715 Tetracentron sinense: 10.1016/S0031-9422(99)00457-4
199633 Curcuma comosa: 10.1248/CPB.56.1604
4079 Hyoscyamus niger:
224738 Lepidothamnus intermedius: 10.1071/CH9851631
461553 Arcangelisia flava: 10.1016/J.PHYTOL.2011.07.002
1609885 Neolitsea hiiranensis: 10.1016/J.PHYTOCHEM.2011.01.006
73292 Helianthus heterophyllus: 10.1016/S0031-9422(00)81173-5
1826902 Stellaria dichotoma:
53751 Echinacea purpurea: 10.1016/0031-9422(83)80215-5
409890 Robinsonia thurifera: 10.1016/0031-9422(88)83126-1
358659 Isatis quadrialata:
185543 Ilex pubescens: 10.1002/HLCA.200890135
1354278 Radermachera sinica: 10.1039/P19810002764
1094094 Colchicum manissadjianii: 10.1016/0031-9422(89)80310-3
337466 Machilus zuihoensis: 10.1080/14786410802401432
1924212 Nectandra oppositifolia: 10.1021/NP50009A006
180097 Sporobolus cynosuroides: 10.1021/NP50028A035
1261582 Vertebrata lanosa: 10.1021/NP0305268
1462929 Marsypopetalum modestum: 10.1080/14786419.2022.2097229
136217 Curcuma longa: 10.1016/0021-9673(96)00103-3
311405 Zingiber zerumbet: 10.1007/BF02980078
761071 Tabernaemontana glandulosa: 10.1016/S0031-9422(00)89602-8
187461 Chamaecyparis formosensis: 10.1016/J.PHYMED.2006.11.029
1582456 Chuquiraga atacamensis: 10.4067/S0366-16442000000100007
1234283 Aristolochia asclepiadifolia: 10.1002/FFJ.2730080104
682177 Tolpis webbii: 10.1016/J.FITOTE.2009.06.001
1911 Streptomyces griseus:
4097 Nicotiana tabacum: 10.1080/10826079308019709
872941 Onobrychis meschetica: 10.1007/BF00563835
637488 Artemisia stolonifera: 10.1007/BF02975098
259893 Artemisia argyi: 10.1007/BF02975098
51238 Vanilla:
123165 Leptotes bicolor: 10.1016/J.MOLP.2014.11.008
88731 Pinus tabuliformis: 10.1016/J.MOLP.2014.11.008
4896 Schizosaccharomyces pombe: 10.1128/AEM.02681-08
1087767 Euphorbia hirsuta: 10.1021/NP0400048
9606 Homo sapiens: -
569774 金线莲: -
85571 Citrus Reticulata: -
3677 Trichosanthes Kirilowii Maxim: -
3483 Cannabis Sativa L.: -
4111 Solanum Melongena L: -
16906 Cornus Officinalis Sieb. Et Zucc.: -
94328 Zingiber Officinale Roscoe: -
13699 Styrax: -
35974 Santalum Album L\uff0e: -
2764646 Gypsophila Licentiana Hand.-Mazz.: -
153559 Styrax tonkinensis (Pierre) Craib ex Hart.: -
2689076 Ligusticum chuanxiong Hort.: -
165353 Angelica sinensis (Oliv.)Diels: -
204215 Vitex trifolia l.var.simplicifolia Cham.: -
204215 Vitex trifolia L.: -
3262 Equisetum hyemale L.: -
63360 Liquidambar orientalis Mill.: -
91201 Gastrodia elata Bl.: -
72351 Artemisia scoparia Waldst.et Kit.: -
265783 Artemisia capillaris Thunb.: -
33090 Plants: -

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]
Muhammad Abu Taher, Xiaolin Wang, K M Faridul Hasan, Mohammad Raza Miah, Jin Zhu, Jing Chen. Lignin Modification for Enhanced Performance of Polymer Composites. ACS applied bio materials. 2023 Dec; 6(12):5169-5192. doi: 10.1021/acsabm.3c00783. [PMID: 38036466]
Mohamed A El Hamd, Mahmoud El-Maghrabey, Saud Almawash, Rania El-Shaheny, Galal Magdy. Self-ratiometric fluorescence approach based on plant extract-assisted synthesized silver nanoparticles for the determination of vanillin. Mikrochimica acta. 2023 12; 191(1):16. doi: 10.1007/s00604-023-06093-3. [PMID: 38086991]
Mahdi Aalikhani, Ensie Taheri, Masoumeh Khalili. Vanillin serves as a potential substitute for chemical chelator desferal in iron-overloaded mice. European journal of pharmacology. 2023 Dec; 960(?):176153. doi: 10.1016/j.ejphar.2023.176153. [PMID: 38059446]
Gang Xiang, Wensi Xu, Wenfeng Zhuge, Qing Huang, Cuizhong Zhang, Jinyun Peng. Conductive phthalocyanine-based porous organic polymer as sensing platform for rapid determination of vanillin. The Analyst. 2023 Dec; 148(24):6274-6281. doi: 10.1039/d3an01758c. [PMID: 37969078]
Zhi-Qiang Wei, Ji-Xiang Wang, Jin-Meng Guo, Xiao-Long Liu, Qi Yan, Jin Zhang, Shuang-Lin Dong. An odorant receptor tuned to an attractive plant volatile vanillin in Spodoptera litura. Pesticide biochemistry and physiology. 2023 Nov; 196(?):105619. doi: 10.1016/j.pestbp.2023.105619. [PMID: 37945255]
Fangyi Mei, Hongling Wang, Yuquan Zhang, Mei Zhang, Shuai Zhou, Haiming Shi, Yuanrong Jiang. Development and Validation of a Stable Isotope Dilution Headspace-SPME-GC/MS Method for the Determination of Vanillin in Fragrant Vegetable Oils. Molecules (Basel, Switzerland). 2023 Oct; 28(21):. doi: 10.3390/molecules28217288. [PMID: 37959708]
Evamaria Hofmann, Pierre Degot, Didier Touraud, Burkhard König, Werner Kunz. Novel green production of natural-like vanilla extract from curcuminoids. Food chemistry. 2023 Aug; 417(?):135944. doi: 10.1016/j.foodchem.2023.135944. [PMID: 36934704]
Ying Liu, Lichao Sun, Yi-Xin Huo, Shuyuan Guo. Strategies for improving the production of bio-based vanillin. Microbial cell factories. 2023 Aug; 22(1):147. doi: 10.1186/s12934-023-02144-9. [PMID: 37543600]
Qiaofang Lu, Kunguang Wang, Zhechao Dou, Lina Zhong, Yuanyuan Yao, Yuanmei Zuo. Vanillin in Resistant Tomato Plant Root Exudate Suppresses Meloidogyne incognita Parasitism. Journal of agricultural and food chemistry. 2023 Jun; ?(?):. doi: 10.1021/acs.jafc.3c00661. [PMID: 37386871]
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]
Jieren Liao, Veronika Lederer, Alba Bardhi, Zhiwei Zou, Timothy D Hoffmann, Guangxin Sun, Chuankui Song, Thomas Hoffmann, Wilfried Schwab. Acceptors and Effectors Alter Substrate Inhibition Kinetics of a Plant Glucosyltransferase NbUGT72AY1 and Its Mutants. International journal of molecular sciences. 2023 May; 24(11):. doi: 10.3390/ijms24119542. [PMID: 37298492]
Camila S Freitas, Samira S Santiago, Daniela P Lage, Luciana M R Antinarelli, Fabrício M Oliveira, Danniele L Vale, Vívian T Martins, Lícia N D Magalhaes, Raquel S Bandeira, Fernanda F Ramos, Isabela A G Pereira, Marcelo M de Jesus, Fernanda Ludolf, Grasiele S V Tavares, Adilson V Costa, Rafaela S Ferreira, Elaine S Coimbra, Róbson R Teixeira, Eduardo A F Coelho. In vitro evaluation of antileishmanial activity, mode of action and cellular response induced by vanillin synthetic derivatives against Leishmania species able to cause cutaneous and visceral leishmaniasis. Experimental parasitology. 2023 May; 251(?):108555. doi: 10.1016/j.exppara.2023.108555. [PMID: 37247802]
Nicholas J Day, Juan Wang, Carl J Johnston, So-Young Kim, Heather M Olson, Emma L House, Isaac Kwame Attah, Geremy C Clair, Wei-Jun Qian, Matthew D McGraw. Rat bronchoalveolar lavage proteome changes following e-cigarette aerosol exposures. American journal of physiology. Lung cellular and molecular physiology. 2023 05; 324(5):L571-L583. doi: 10.1152/ajplung.00016.2023. [PMID: 36881561]
Kandrakonda Yelamanda Rao, Shaik Jeelan Basha, Kallubai Monika, Navya Naidu Gajula, Irla Sivakumar, Sandeep Kumar, Ramakrishna Vadde, Bindu Madhava Reddy Aramati, Rajagopal Subramanyam, Amooru Gangaiah Damu. Development of quinazolinone and vanillin acrylamide hybrids as multi-target directed ligands against Alzheimer's disease and mechanistic insights into their binding with acetylcholinesterase. Journal of biomolecular structure & dynamics. 2023 Apr; ?(?):1-18. doi: 10.1080/07391102.2023.2203255. [PMID: 37098803]
Visessakseth So, Philip Poul, Sokunvary Oeung, Pich Srey, Kimchhay Mao, Huykhim Ung, Poliny Eng, Mengkhim Heim, Marnick Srun, Chantha Chheng, Sin Chea, Tarapong Srisongkram, Natthida Weerapreeyakul. Bioactive Compounds, Antioxidant Activities, and HPLC Analysis of Nine Edible Sprouts in Cambodia. Molecules (Basel, Switzerland). 2023 Mar; 28(6):. doi: 10.3390/molecules28062874. [PMID: 36985845]
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]
Ronivaldo Rodrigues da Silva, Mohammed Anas Zaiter, Maurício Boscolo, Roberto da Silva, Eleni Gomes. Xylose consumption and ethanol production by Pichia guilliermondii and Candida oleophila in the presence of furans, phenolic compounds, and organic acids commonly produced during the pre-treatment of plant biomass. Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]. 2023 Feb; ?(?):. doi: 10.1007/s42770-023-00937-z. [PMID: 36826705]
A Diamond, S Barnabé, I Desgagné-Penix. Is a spice missing from the recipe? The intra-cellular localization of vanillin biosynthesis needs further investigations. Plant biology (Stuttgart, Germany). 2023 Jan; 25(1):3-7. doi: 10.1111/plb.13465. [PMID: 36066305]
Sooyeon Choi, Chae Eun Haam, Eun-Yi Oh, Seonhee Byeon, Soo-Kyoung Choi, Young-Ho Lee. Vanillin Induces Relaxation in Rat Mesenteric Resistance Arteries by Inhibiting Extracellular Ca2+ Influx. Molecules (Basel, Switzerland). 2022 Dec; 28(1):. doi: 10.3390/molecules28010288. [PMID: 36615485]
Laura S Bailey, Dilip V Prajapati, Kari B Basso. Optimization of the Sulfo-Phospho-Vanillin Assay for Total Lipid Normalization in Untargeted Quantitative Lipidomic LC-MS/MS Applications. Analytical chemistry. 2022 12; 94(51):17810-17818. doi: 10.1021/acs.analchem.2c03488. [PMID: 36520113]
David L Avetyan, Andrey Shatskiy, Markus D Kärkäs, Elena V Stepanova. Scalable total synthesis of natural vanillin-derived glucoside ω-esters. Carbohydrate research. 2022 Dec; 522(?):108683. doi: 10.1016/j.carres.2022.108683. [PMID: 36179617]
Siyao Shao, Sufen Zhang, Zhiyang Yu, Qingfu Ye. Accumulation and biotransformation of the novel vanillin-derived pesticide, vanisulfane, in laying hens after dietary exposure. Journal of hazardous materials. 2022 10; 439(?):129677. doi: 10.1016/j.jhazmat.2022.129677. [PMID: 36104905]
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]
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