Acetone (BioDeep_00000004334)
Secondary id: BioDeep_00000405460, BioDeep_00000863193
human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite
代谢物信息卡片
Dimethylformaldehyde
化学式: C3H6O (58.0419)
中文名称: 丙酮
谱图信息:
最多检出来源 Homo sapiens(blood) 26.37%
分子结构信息
SMILES: CC(=O)C
InChI: InChI=1S/C3H6O/c1-3(2)4/h1-2H3
描述信息
Acetone, or propanone, is an organic compound with the formula (CH3)2CO. It is the simplest and smallest ketone. It is a colourless, highly volatile and flammable liquid with a characteristic pungent odour. Acetone is miscible with water and serves as an important organic solvent in its own right, in industry, home, and laboratory. Acetone is produced and disposed of in the human body through normal metabolic processes. It is normally present in blood and urine. People with diabetic ketoacidosis produce it in larger amounts. Acetone is not regarded as a waste product of metabolism. However, its physiological role in biochemical machinery is not clear. A model for the role of acetone metabolism is presented that orders the events occurring in acetonemia in sequence: in diabetic ketosis or starvation, ketone body production (b-hydroxy-butyrate, acetoacetate) provides fuel for vital organs (heart, brain, among others) raising the chance of survival of the metabolic catastrophe. However, when ketone body production exceeds the degrading capacity, the accumulating acetoacetic acid presents a new challenge to the pH regulatory system. Acetone production and its further degradation to C3 fragments fulfill two purposes: the maintenance of pH buffering capacity and provision of fuel for peripheral tissues. Since ketosis develops under serious metabolic circumstances, all the mechanisms that balance or moderate the effects of ketosis enhance the chance for survival. From this point of view, the theory that transportable C3 fragments can serve as additional nutrients is a novel view of acetone metabolism which introduces a new approach to the study of acetone degradation, especially in understanding its physiological function and the interrelationship between liver and peripheral tissues. (PMID 10580530). Acetone is typically derived from acetoacetate through the action of microbial acetoacetate decarboxylases found in gut microflora. In chemistry, acetone is the simplest representative of the ketones. Acetone is a colorless, mobile, flammable liquid readily soluble in water, ethanol, ether, etc., and itself serves as an important solvent. It is an irritant and inhalation may lead to hepatotoxic effects (causing liver damage). Acetone can be found in Clostridium (PMID:685531).
Solvent used in food processing as a colour diluent, flavour ingredient, etc.
D012997 - Solvents
同义名列表
数据库引用编号
22 个数据库交叉引用编号
- ChEBI: CHEBI:15347
- KEGG: C00207
- KEGGdrug: D02311
- PubChem: 180
- HMDB: HMDB0001659
- Metlin: METLIN3745
- ChEMBL: CHEMBL14253
- Wikipedia: Acetone
- MeSH: Acetone
- MetaCyc: ACETONE
- KNApSAcK: C00048304
- foodb: FDB008301
- chemspider: 175
- CAS: 67-64-1
- PMhub: MS000016587
- PubChem: 3507
- LipidMAPS: LMFA12000057
- PDB-CCD: ACN
- 3DMET: B00058
- NIKKAJI: J2.365E
- RefMet: Acetone
- KNApSAcK: 15347
分类词条
相关代谢途径
Reactome(0)
BioCyc(15)
- propane degradation II
- isopropanol biosynthesis (engineered)
- acetone degradation III (to propane-1,2-diol)
- acetone degradation I (to methylglyoxal)
- acetone degradation II (to acetoacetate)
- linear furanocoumarin biosynthesis
- atrazine degradation II
- superpathway of Clostridium acetobutylicum acidogenic and solventogenic fermentation
- pyruvate fermentation to acetone
- geosmin biosynthesis
- superpathway of Clostridium acetobutylicum solventogenic fermentation
- propane degradation I
- linamarin degradation
- linustatin bioactivation
- ketogenesis
PlantCyc(5)
代谢反应
145 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(21)
- ketogenesis:
H+ + acetoacetate ⟶ CO2 + acetone - acetone degradation I (to methylglyoxal):
H+ + acetoacetate ⟶ CO2 + acetone - isopropanol biosynthesis (engineered):
NADP+ + propan-2-ol ⟶ H+ + NADPH + acetone - acetone degradation III (to propane-1,2-diol):
NADP+ + propan-2-ol ⟶ H+ + NADPH + acetone - acetone degradation I (to methylglyoxal):
NADP+ + propan-2-ol ⟶ H+ + NADPH + acetone - acetone degradation II (to acetoacetate):
NADP+ + propan-2-ol ⟶ H+ + NADPH + acetone - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - atrazine degradation II:
A(H2) + O2 + atrazine ⟶ A + H2O + acetone + deethylsimazine - superpathway of Clostridium acetobutylicum acidogenic and solventogenic fermentation:
H+ + acetoacetate ⟶ CO2 + acetone - pyruvate fermentation to acetone:
H+ + acetoacetate ⟶ CO2 + acetone - geosmin biosynthesis:
(1E,4S,5E,7R)-germacra-1(10),5-dien-11-ol ⟶ (8S,9S,10S)-8,10-dimethyl-1-octalin + acetone - superpathway of Clostridium acetobutylicum solventogenic fermentation:
H+ + acetoacetate ⟶ CO2 + acetone - propane degradation I:
NAD+ + propan-2-ol ⟶ H+ + NADH + acetone - propane degradation II:
NAD+ + propan-2-ol ⟶ H+ + NADH + acetone - linamarin degradation:
2-hydroxy-2-methylpropanenitrile ⟶ acetone + hydrogen cyanide - linustatin bioactivation:
2-hydroxy-2-methylpropanenitrile ⟶ acetone + hydrogen cyanide - ketogenesis:
H+ + acetoacetate ⟶ CO2 + acetone - ketogenesis:
H+ + acetoacetate ⟶ CO2 + acetone - ketogenesis:
H+ + acetoacetate ⟶ CO2 + acetone - linamarin degradation:
H2O + linamarin ⟶ β-D-glucose + acetone cyanohydrin - pyruvate fermentation to acetone:
acetoacetate + acetyl-CoA ⟶ acetate + acetoacetyl-CoA
WikiPathways(3)
- Metabolism overview:
NH3 ⟶ Glutamic acid - Ketogenesis and ketolysis:
ACA ⟶ BHB - Disorders in ketone body synthesis:
acetoacetate ⟶ acetone
Plant Reactome(3)
- Metabolism and regulation:
ATP + CoA + propionate ⟶ AMP + PPi + PROP-CoA - Secondary metabolism:
GPP + H2O ⟶ PPi + geraniol - Linear furanocoumarin biosynthesis:
H+ + H2O + TPNH + psoralen ⟶ TPN + bergaptol
INOH(0)
PlantCyc(111)
- linear furanocoumarin biosynthesis:
H+ + NADPH + O2 + psoralen ⟶ H2O + NADP+ + bergaptol - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + H+ + NADPH + O2 ⟶ H2O + NADP+ + acetone + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linamarin degradation:
H2O + linamarin ⟶ 2-hydroxy-2-methylpropanenitrile + D-glucopyranose - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + H+ + NADPH + O2 ⟶ H2O + NADP+ + acetone + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linustatin bioactivation:
H2O + linamarin ⟶ 2-hydroxy-2-methylpropanenitrile + D-glucopyranose - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - geosmin biosynthesis:
(1E,4S,5E,7R)-germacra-1(10),5-dien-11-ol ⟶ (8S,9S,10S)-8,10-dimethyl-1-octalin + acetone - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + H+ + NADPH + O2 ⟶ H2O + NADP+ + acetone + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linustatin bioactivation:
2-hydroxy-2-methylpropanenitrile ⟶ acetone + hydrogen cyanide - linamarin degradation:
2-hydroxy-2-methylpropanenitrile ⟶ acetone + hydrogen cyanide - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linustatin bioactivation:
H2O + linustatin ⟶ D-glucopyranose + linamarin - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linamarin degradation:
H2O + linamarin ⟶ 2-hydroxy-2-methylpropanenitrile + D-glucopyranose - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen - linear furanocoumarin biosynthesis:
H+ + NADPH + O2 + psoralen ⟶ H2O + NADP+ + bergaptol - ketogenesis:
(R)-3-hydroxybutanoate + NAD+ ⟶ H+ + NADH + acetoacetate - linear furanocoumarin biosynthesis:
H+ + NADPH + O2 + psoralen ⟶ H2O + NADP+ + bergaptol - ketogenesis:
(R)-3-hydroxybutanoate + NAD+ ⟶ H+ + NADH + acetoacetate
COVID-19 Disease Map(0)
PathBank(7)
- Ketone Body Metabolism:
(R)-3-Hydroxybutyric acid + NAD ⟶ Acetoacetic acid + NADH - Succinyl CoA: 3-Ketoacid CoA Transferase Deficiency:
(R)-3-Hydroxybutyric acid + NAD ⟶ Acetoacetic acid + NADH - Ketone Body Metabolism:
(R)-3-Hydroxybutyric acid + NAD ⟶ Acetoacetic acid + NADH - Succinyl CoA: 3-Ketoacid CoA Transferase Deficiency:
(R)-3-Hydroxybutyric acid + NAD ⟶ Acetoacetic acid + NADH - Ketone Body Metabolism:
(R)-3-Hydroxybutyric acid + NAD ⟶ Acetoacetic acid + NADH - Ketone Body Metabolism:
(R)-3-Hydroxybutyric acid + NAD ⟶ Acetoacetic acid + NADH - Succinyl CoA: 3-Ketoacid CoA Transferase Deficiency:
(R)-3-Hydroxybutyric acid + NAD ⟶ Acetoacetic acid + NADH
PharmGKB(0)
36 个相关的物种来源信息
- 97173 - Abies concolor: 10.1016/S0031-9422(00)90700-3
- 34340 - Abies lasiocarpa: 10.1016/S0031-9422(00)90700-3
- 75745 - Acer saccharinum: 10.1016/S0031-9422(00)90700-3
- 68299 - Ageratum conyzoides: 10.1080/10412905.1993.9698184
- 714446 - Angelica dahurica var. formosana: 10.1007/BF02975883
- 205369 - Artemisia judaica: 10.1080/10412905.1990.9697881
- 3589 - Basella alba: 10.1016/0889-1575(91)90017-Z
- 3483 - Cannabis sativa: 10.1021/NP50008A001
- 119266 - Cinnamomum sieboldii: 10.1248/YAKUSHI1947.106.1_17
- 558547 - Citrus deliciosa: 10.1016/J.PHYTOCHEM.2009.07.031
- 170989 - Citrus hystrix: 10.1016/J.PHYTOCHEM.2009.07.031
- 37334 - Citrus maxima: 10.1016/J.PHYTOCHEM.2009.07.031
- 85571 - Citrus reticulata: 10.1016/J.PHYTOCHEM.2009.07.031
- 13443 - Coffea arabica: 10.1021/JF60160A010
- 58228 - Garcinia mangostana: 10.1016/0031-9422(82)80025-3
- 3635 - Gossypium hirsutum: 10.1021/JF60200A011
- 9606 - Homo sapiens:
- 9606 - Homo sapiens: -
- 3750 - Malus domestica: 10.1002/FOOD.19810250610
- 283210 - Malus pumila: 10.1002/FOOD.19810250610
- 29780 - Mangifera indica: 10.1016/0031-9422(88)80124-9
- 1970105 - Micromeria myrtifolia: 10.1080/10412905.1992.9698015
- 54731 - Nepeta racemosa: 10.1080/10412905.1993.9698205
- 4146 - Olea europaea: 10.1016/S0031-9422(97)00730-9
- 371859 - Opuntia ficus-indica: 10.1021/JF60218A053
- 1132404 - Origanum sipyleum: 10.1080/10412905.1992.9698035
- 3334 - Picea engelmannii: 10.1016/S0031-9422(00)90700-3
- 3330 - Picea glauca: 10.1016/S0031-9422(00)90700-3
- 3331 - Picea pungens: 10.1016/S0031-9422(00)90700-3
- 3339 - Pinus contorta: 10.1016/S0031-9422(00)90700-3
- 3357 - Pseudotsuga menziesii: 10.1016/S0031-9422(00)90700-3
- 120290 - Psidium guajava: 10.1016/0031-9422(82)80138-6
- 3893 - Pueraria montana var. lobata: 10.1271/BBB1961.52.1053
- 1194133 - Thymus longicaulis: 10.1080/10412905.1992.9698070
- 39416 - Tuber melanosporum: 10.1021/JF00077A031
- 94328 - Zingiber officinale: 10.1016/S0031-9422(00)86412-2
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
- Rajasree Shanmuganathan, Sandhanasamy Devanesan, Goldie Oza, Ashutosh Sharma. Assessment of antimicrobial, antidiabetic, and anti-inflammatory properties of acetone extract of Aerva lanata (L.) by in-vitro approach and bioactive compounds characterization.
Environmental research.
2024 May; 248(?):118348. doi:
10.1016/j.envres.2024.118348. [PMID: 38295976] - Nikhil Mehta, Rhea Ahuja, Neetu Bhari, Kaushal Verma. A comparison of parthenium 15\% in Indian Standard Series versus acetone extract 2\% of parthenium plant in diagnosing contact allergy to parthenium.
Contact dermatitis.
2024 May; 90(5):538-540. doi:
10.1111/cod.14517. [PMID: 38316109] - Minna K Karjalainen, Savita Karthikeyan, Clare Oliver-Williams, Eeva Sliz, Elias Allara, Wing Tung Fung, Praveen Surendran, Weihua Zhang, Pekka Jousilahti, Kati Kristiansson, Veikko Salomaa, Matt Goodwin, David A Hughes, Michael Boehnke, Lilian Fernandes Silva, Xianyong Yin, Anubha Mahajan, Matt J Neville, Natalie R van Zuydam, Renée de Mutsert, Ruifang Li-Gao, Dennis O Mook-Kanamori, Ayse Demirkan, Jun Liu, Raymond Noordam, Stella Trompet, Zhengming Chen, Christiana Kartsonaki, Liming Li, Kuang Lin, Fiona A Hagenbeek, Jouke Jan Hottenga, René Pool, M Arfan Ikram, Joyce van Meurs, Toomas Haller, Yuri Milaneschi, Mika Kähönen, Pashupati P Mishra, Peter K Joshi, Erin Macdonald-Dunlop, Massimo Mangino, Jonas Zierer, Ilhan E Acar, Carel B Hoyng, Yara T E Lechanteur, Lude Franke, Alexander Kurilshikov, Alexandra Zhernakova, Marian Beekman, Erik B van den Akker, Ivana Kolcic, Ozren Polasek, Igor Rudan, Christian Gieger, Melanie Waldenberger, Folkert W Asselbergs, Caroline Hayward, Jingyuan Fu, Anneke I den Hollander, Cristina Menni, Tim D Spector, James F Wilson, Terho Lehtimäki, Olli T Raitakari, Brenda W J H Penninx, Tonu Esko, Robin G Walters, J Wouter Jukema, Naveed Sattar, Mohsen Ghanbari, Ko Willems van Dijk, Fredrik Karpe, Mark I McCarthy, Markku Laakso, Marjo-Riitta Järvelin, Nicholas J Timpson, Markus Perola, Jaspal S Kooner, John C Chambers, Cornelia van Duijn, P Eline Slagboom, Dorret I Boomsma, John Danesh, Mika Ala-Korpela, Adam S Butterworth, Johannes Kettunen. Genome-wide characterization of circulating metabolic biomarkers.
Nature.
2024 Apr; 628(8006):130-138. doi:
10.1038/s41586-024-07148-y. [PMID: 38448586] - Özge Üst, Emine Yalçin, Kültiğin Çavuşoğlu, Burak Özkan. LC-MS/MS, GC-MS and molecular docking analysis for phytochemical fingerprint and bioactivity of Beta vulgaris L.
Scientific reports.
2024 03; 14(1):7491. doi:
10.1038/s41598-024-58338-7. [PMID: 38553576] - Gatluak Goanar, Geremew Tafesse, Workineh Mengesha Fereja. In vitro antibacterial activity of fruit pulp extracts of Tamarindus indica against Staphylococcus aureus and Klebsiella pneumoniae.
BMC complementary medicine and therapies.
2024 Mar; 24(1):127. doi:
10.1186/s12906-024-04404-6. [PMID: 38504277] - Jolanta Flieger, Natalia Żuk, Sylwia Pasieczna-Patkowska, Marcin Kuśmierz, Rafał Panek, Wojciech Franus, Jacek Baj, Grzegorz Buszewicz, Grzegorz Teresiński, Wojciech Płaziński. Selective Removal of Chlorophyll and Isolation of Lutein from Plant Extracts Using Magnetic Solid Phase Extraction with Iron Oxide Nanoparticles.
International journal of molecular sciences.
2024 Mar; 25(6):. doi:
10.3390/ijms25063152. [PMID: 38542125] - İnan Dursun, İkranur Felek, Duygu Nur Çobanoğlu. Analyzing the Antioxidant Activity and Fatty Acid Composition of Monofloral Mullein (Verbascum sp.) Pollen Oil obtained via Various Extraction Techniques.
Chemistry & biodiversity.
2024 Mar; 21(3):e202400117. doi:
10.1002/cbdv.202400117. [PMID: 38366982] - Rizwan Ahmad, Muhammad Riaz, Mohammed Aldholmi, Ahad Alsulays, Wala Alsulais, Deema Alaswad, Alhassan Ibrahim Almutawah, Hasan Zaki Al Nahab. Solanum pseudocapsicum vs Capsicum annum; comparative phenolics profiling using green ultrasonic extraction and UHPLC analysis.
Ultrasonics sonochemistry.
2024 Feb; 103(?):106789. doi:
10.1016/j.ultsonch.2024.106789. [PMID: 38309047] - Supachai Changphuek, Thaneeya Chetiyanukornkul, Yaowatat Boongla. Simulation analysis of hazardous chemicals released from the furniture plant using ALOHA software.
Environmental monitoring and assessment.
2024 Jan; 196(2):207. doi:
10.1007/s10661-024-12322-w. [PMID: 38280056] - Li Jiang, Chenxing Wang, Tingting Fan, Siyuan Lv, Si Pan, Peng Sun, Jie Zheng, Chuan Zhang, Fangmeng Liu, Geyu Lu. Mixed Potential Type Acetone Sensor with Ultralow Detection Limit for Diabetic Ketosis Breath Analysis.
ACS sensors.
2024 Jan; 9(1):464-473. doi:
10.1021/acssensors.3c02253. [PMID: 38153408] - Giulia Coradello, Chiara Setti, Roberto Donno, Matilde Ghibaudi, Federico Catalano, Nicola Tirelli. A Quantitative Re-Assessment of Microencapsulation in (Pre-Treated) Yeast.
Molecules (Basel, Switzerland).
2024 Jan; 29(2):. doi:
10.3390/molecules29020539. [PMID: 38276617] - Eirini Stini, Dimitrios Tsimogiannis, Vassiliki Oreopoulou. The Valorisation of Melissa officinalis Distillation By-Products for the Production of Polyphenol-Rich Formulations.
Molecules (Basel, Switzerland).
2024 Jan; 29(2):. doi:
10.3390/molecules29020377. [PMID: 38257290] - Priyanka Mandal, Goutam Chandra. Casearia tomentosa fruit extracts exposed larvicidal activity and morphological alterations in Culex quinquefasciatus and Aedes albopictus under in vitro and semi field conditions.
BMC research notes.
2024 Jan; 17(1):6. doi:
10.1186/s13104-023-06663-x. [PMID: 38167220] - Felipe Carlos de Macêdo Oliveira, Tatiana Moura Vasconcelos Holanda, Cristiane Fernandes de Assis, Francisco Humberto Xavier Júnior, Francisco Canindé de Sousa Júnior. Flours from Spondias mombin and Spondias tuberosa seeds: Physicochemical characterization, technological properties, and antioxidant, antibacterial, and antidiabetic activities.
Journal of food science.
2024 Jan; 89(1):342-355. doi:
10.1111/1750-3841.16882. [PMID: 38126119] - Jazia Sriti, Wissem Aidi Wannes, Olfa Bachrouch, Jihed Aouini, Emna Boushih, Ferid Limam, Jouda Mediouni Ben Jemaa. Phenolic constitutents, antioxidant and repellent activities of coriander (Coriandrum sativum L.) fruits using different solvent extracts.
International journal of environmental health research.
2024 Jan; 34(1):225-237. doi:
10.1080/09603123.2022.2143483. [PMID: 36369804] - Marijana Kosanić, Nevena Petrovic, Dragana Šeklić, Marko Živanović, Mihajlo Kokanović. Bioactivities and Medicinal Value of the Fruiting Body Extracts of Laetiporus sulphureus and Meripilus giganteus Polypore Mushrooms (Agaricomycetes).
International journal of medicinal mushrooms.
2024; 26(1):17-26. doi:
10.1615/intjmedmushrooms.2023051297. [PMID: 38305259] - Zhijie Zheng, Mei Tian, Guozhou Liao, Guanghui Chen, Yanru Zhong, Yuan Yang, Guiying Wang. Evaluation of the effects of compound curing agents on the lipid profiles and volatile flavors in Nuodeng ham based on lipidomics and GC-IMS analysis.
Food research international (Ottawa, Ont.).
2024 Jan; 176(?):113810. doi:
10.1016/j.foodres.2023.113810. [PMID: 38163715] - Godfrey O Mauti. Extracts of Jamun seeds inhibited the growth of human (Hep-2) cancer cells.
Journal of cancer research and therapeutics.
2024 Jan; 20(1):189-192. doi:
10.4103/jcrt.jcrt_638_22. [PMID: 38554319] - Usama Mohammed Abu El-Ghiet, Abdullah Mohammed Salman Alhuraysi, Tarek Mohamed Yousry Elsheikh, Mohamed Abdel-Monem El-Sakhawy. Oviposition Deterrent Activity of Some Wild Plants for Adult Females of Chrysomya albiceps with Medical and Veterinary Importance.
Pakistan journal of biological sciences : PJBS.
2024 Jan; 27(1):8-17. doi:
10.3923/pjbs.2024.8.17. [PMID: 38413393] - Mari Ogawa-Ohnishi, Yoshikatsu Matsubayashi. Extraction of Apoplastic Peptides for the Structural Elucidation of Mature Peptide Hormones in Arabidopsis.
Methods in molecular biology (Clifton, N.J.).
2024; 2731(?):81-87. doi:
10.1007/978-1-0716-3511-7_6. [PMID: 38019427] - Mysoon Al-Ansari, Nora Dahmash Al-Dahmash, Paola Isabel Angulo-Bejarano, Hai-Anh Ha, Thai-Hang Nguyen-Thi. Phytochemical, bactericidal, antioxidant and anti-inflammatory properties of various extracts from Pongamia pinnata and functional groups characterization by FTIR and HPLC analyses.
Environmental research.
2023 Dec; 245(?):118044. doi:
10.1016/j.envres.2023.118044. [PMID: 38157963] - Wanda Shekwa, Tsolanku Sidney Maliehe, Peter Masoko. Antimicrobial, antioxidant and cytotoxic activities of the leaf and stem extracts of Carissa bispinosa used for dental health care.
BMC complementary medicine and therapies.
2023 Dec; 23(1):462. doi:
10.1186/s12906-023-04308-x. [PMID: 38102607] - Jelena Šuran, Božo Radić, Dilza Trevisan-Silva, Mario Cindrić, Amela Hozić. First Proteome Analysis of Poplar-Type Propolis.
Plant foods for human nutrition (Dordrecht, Netherlands).
2023 Dec; ?(?):. doi:
10.1007/s11130-023-01127-w. [PMID: 38048032] - Hudson V V Tomé, Stephen L Clark, Brant C Jorgenson, Stefan Kimmel, Bettina Wenzel, Carmen Gimeno, John Porch, Michael R Patnaude, Kristin Schmidt, Line Deslandes, Daniel R Schmehl. Chronic larval and adult honey bee laboratory testing: Which dietary additive should be considered when a test substance is not solubilized in acetone?.
Ecotoxicology and environmental safety.
2023 Dec; 268(?):115718. doi:
10.1016/j.ecoenv.2023.115718. [PMID: 38000305] - Tatapudi Kiran Kumar, Bandi Siva, Basani Kiranmai, Vidya Jyothi Alli, Surender Singh Jadav, Araveeti Madhusudana Reddy, Joël Boustie, Françoise Le Devehat, Ashok Kumar Tiwari, Katragadda Suresh Babu. Salazinic Acid and Norlobaridone from the Lichen Hypotrachyna cirrhata: Antioxidant Activity, α-Glucosidase Inhibitory and Molecular Docking Studies.
Molecules (Basel, Switzerland).
2023 Nov; 28(23):. doi:
10.3390/molecules28237840. [PMID: 38067568] - Kalaivani Madhavaram Kuppusamy, Sivakumar Selvaraj, Pujithaa Singaravelu, Cordelia Mano John, Kalaiselvan Racheal, Keziaann Varghese, Dinesh Kaliyamoorthy, Elumalai Perumal, Krishnamoorthy Gunasekaran. Anti-microbial and anti-cancer efficacy of acetone extract of Rosa chinensis against resistant strain and lung cancer cell line.
BMC complementary medicine and therapies.
2023 Nov; 23(1):406. doi:
10.1186/s12906-023-04222-2. [PMID: 37950173] - Altevir Rossato Viana, Isadora Nicola, Camila Franco, Patrícia Acosta Caetano, Eduardo Jacob-Lopes, Leila Queiroz Zepka, Daniel Santos, Erico Marlon Moraes Flores, Bruno Stefanello Vizzotto, Katianne Wolf, Aline Ferreira Ourique, Sergio Roberto Mortari, Cristiano Rodrigo Bohn Rhoden, Luciana Maria Fontanari Krause. Phytochemical characterization and toxicological activity attributed to the acetonic extract of South American Vassobia breviflora.
Journal of toxicology and environmental health. Part A.
2023 Nov; 86(21):816-832. doi:
10.1080/15287394.2023.2254316. [PMID: 37667472] - Elena V Emelyanova. Micromycete Responses to Acetone: Electrochemical Express Evaluation of Acetone Metabolism.
Applied biochemistry and biotechnology.
2023 Oct; 195(10):6359-6368. doi:
10.1007/s12010-023-04408-x. [PMID: 36867387] - Maryam Koopaie, Hanieh Karimi, Mohammad Sohrabi, Hooman Norouzi. Cytotoxic, anti-proliferative, and apoptotic evaluation of Ramalina sinensis (Ascomycota, Lecanoromycetes), lichenized fungus on oral squamous cell carcinoma cell line; in-vitro study.
BMC complementary medicine and therapies.
2023 Aug; 23(1):296. doi:
10.1186/s12906-023-04118-1. [PMID: 37608377] - Alfredi A Moyo, Kishor S Jagadhane, Sneha R Bhosale, Devashree N Patil, Vinod B Shimpale, Prashant V Anbhule. Phytochemical Profiling, Antimicrobial, Antiproliferative and Apoptotic Effects of Stemodia viscosa Roxb. of Western Ghats Region, India.
Chemistry & biodiversity.
2023 Aug; 20(8):e202300332. doi:
10.1002/cbdv.202300332. [PMID: 37461844] - Dimitri Wendgida Wangrawa, Félix Yaméogo, Aboubacar Sombié, Edward Esalimba, Eric Ochomo, Dov Borovsky, Athanase Badolo, Antoine Sanon. Methanol and acetone extracts from the leaves of selected aromatic plants affect survival of field collected Anopheles arabiensis (Diptera: Culicidae) from Kisumu, Kenya.
Journal of medical entomology.
2023 Jul; ?(?):. doi:
10.1093/jme/tjad066. [PMID: 37478413] - Magdalena Kulinowska, Sławomir Dresler, Agnieszka Skalska-Kamińska, Agnieszka Hanaka, Maciej Strzemski. Methodological Aspects of Green Extraction of Usnic Acid Using Natural Deep Eutectic Solvents.
Molecules (Basel, Switzerland).
2023 Jul; 28(14):. doi:
10.3390/molecules28145321. [PMID: 37513195] - Ting Li, Yifan Wang, Nannan Liu. Mosquito Adult Bioassays.
Cold Spring Harbor protocols.
2023 07; 2023(7):.pdb.prot108041. doi:
10.1101/pdb.prot108041. [PMID: 36882289] - Yue Sun, Jia-Xin Feng, Zhong-Bao Wei, Hui Sun, Li Li, Jun-Yi Zhu, Guang-Qing Xia, Hao Zang. Phytochemical Analysis, Antioxidant Activities In Vitro and In Vivo, and Theoretical Calculation of Different Extracts of Euphorbia fischeriana.
Molecules (Basel, Switzerland).
2023 Jul; 28(13):. doi:
10.3390/molecules28135172. [PMID: 37446834] - Hosakatte Niranjana Murthy, Guggalada Govardhana Yadav, Sathish Shekhappa Kadapatti, M Sandhya. Phytochemical Analysis, GC-MS Identification of Bioactive Compounds, and In Vitro Antioxidant Activities of Resin of Garcinia indica (Thouars) Choisy.
Applied biochemistry and biotechnology.
2023 Jul; 195(7):4570-4582. doi:
10.1007/s12010-023-04343-x. [PMID: 36705843] - Yu Zhang, Xiaosan Wang, Xingguo Wang. Acyl migration of 2-monoacylglycerols rich in DHA: Effect of temperature and solvent medium.
Food chemistry.
2023 Jun; 412(?):135501. doi:
10.1016/j.foodchem.2023.135501. [PMID: 36716621] - Xuehui Xu, Wei Han. Analysis of tetrabromobisphenol A and bisphenol A in plant sample-method optimization and identification of the derivatives.
Environmental science and pollution research international.
2023 Jun; ?(?):. doi:
10.1007/s11356-023-28241-1. [PMID: 37335514] - Raghavakumari R Sunagar, Yadahally N Sreerama. Implication of solvent polarities on browntop millet (Urochloa ramosa) phenolic antioxidants and their ability to protect oxidative DNA damage and inhibit α-amylase and α-glucosidase enzymes.
Food chemistry.
2023 Jun; 411(?):135474. doi:
10.1016/j.foodchem.2023.135474. [PMID: 36681026] - Ivana D Radojević, Mirjana Ž Grujović, Olivera Milošević-Djordjević, Jovana Tubić Vukajlović, Aleksandra Marković, Darko Grujičić, Andrija Ćirić, Gorica Djelić, Marina Topuzović, Ljiljana R Čomić. Putative application of Najas marina L. extracts as a source of bioactive compounds and their antioxidant, antimicrobial, antibiofilm, and genotoxic properties.
Letters in applied microbiology.
2023 May; 76(5):. doi:
10.1093/lambio/ovad055. [PMID: 37158292] - Elisabetta Lambertini, Letizia Penolazzi, Maria Pina Notarangelo, Serena Fiorito, Francesco Epifano, Assunta Pandolfi, Roberta Piva. Pro‑differentiating compounds for human intervertebral disc cells are present in Violina pumpkin leaf extracts.
International journal of molecular medicine.
2023 May; 51(5):. doi:
10.3892/ijmm.2023.5242. [PMID: 37026516] - Veysel Çomaklı, Rüya Sağlamtaş, Müslüm Kuzu, Yalçın Karagöz, Tuba Aydın, Ramazan Demirdağ. Enzyme Inhibition and Antioxidant Activities of Asparagus officinalis L. and Analysis of Its Phytochemical Content by LC/MS/MS.
Chemistry & biodiversity.
2023 Apr; ?(?):e202201231. doi:
10.1002/cbdv.202201231. [PMID: 37096958] - Nadjet Mostefa, Noureddine Djebli, Pham Ngoc Khanh, Nguyen Xuan Ha, Hoang Thi Ngoc Anh, Vu Thi Ha, Tran Thu Huong, Dang Viet Anh, Nguyen Manh Cuong. Anti-Alzheimer's Activity of Polyphenolic Stilbene-Rich Acetone Fraction of the Oil-Removed Seeds of Passiflora edulis: in Vivo and in Silico Studies.
Chemistry & biodiversity.
2023 Apr; ?(?):e202201051. doi:
10.1002/cbdv.202201051. [PMID: 37032441] - Buket Askin, Gulce Bedis Kaynarca. VALUE-ADDED PROCESSING OF SEEDS FROM TOMATO SAUCE INDUSTRY AND COMPARISON OF EXTRACTION SOLVENTS ON ITS CHEMICAL PROPERTIES.
Journal of the science of food and agriculture.
2023 Mar; ?(?):. doi:
10.1002/jsfa.12584. [PMID: 36988948] - Segun A Aderibigbe, Sunday O Idowu, Ajibola A Olaniyi. Isotonic, aqueous-based media as simple and suitable test media for short-term Haemonchus placei adult worm motility assay.
Experimental parasitology.
2023 Mar; 249(?):108516. doi:
10.1016/j.exppara.2023.108516. [PMID: 36967034] - Yangyang Liao, Xinjie Zhang, Dongyi Cao, Fei Wang, Hulan Chen, Rui Li. Separation and identification of terpene-conjugated curcuminoids based on liquid chromatography-tandem mass spectrometry and their in vitro anti-inflammatory activities.
Journal of separation science.
2023 Mar; ?(?):e2200789. doi:
10.1002/jssc.202200789. [PMID: 36892097] - Daniel Augustynowicz, Marta Kinga Lemieszek, Jakub Władysław Strawa, Adrian Wiater, Michał Tomczyk. Phytochemical Profiling of Extracts from Rare Potentilla Species and Evaluation of Their Anticancer Potential.
International journal of molecular sciences.
2023 Mar; 24(5):. doi:
10.3390/ijms24054836. [PMID: 36902263] - Xin Li, Jingying Pan, Yue Wu, Huan Xing, Zijian An, Zhenghan Shi, Jingjiang Lv, Fenni Zhang, Jing Jiang, Di Wang, Ray P S Han, Bin Su, Yanli Lu, Qingjun Liu. MXene-based wireless facemask enabled wearable breath acetone detection for lipid metabolic monitoring.
Biosensors & bioelectronics.
2023 Feb; 222(?):114945. doi:
10.1016/j.bios.2022.114945. [PMID: 36462428] - Wengang Zhang, Yongli Lan, Bin Dang, Jie Zhang, Wancai Zheng, Yan Du, Xijuan Yang, Zhonghong Li. Polyphenol Profile and In Vitro Antioxidant and Enzyme Inhibitory Activities of Different Solvent Extracts of Highland Barley Bran.
Molecules (Basel, Switzerland).
2023 Feb; 28(4):. doi:
10.3390/molecules28041665. [PMID: 36838651] - Mariana Leal, María Alejandra Moreno, Patricia Liliana Albornoz, María Inés Mercado, Iris Catiana Zampini, María Inés Isla. Nicotiana tabacum Leaf Waste: Morphological Characterization and Chemical-Functional Analysis of Extracts Obtained from Powder Leaves by Using Green Solvents.
Molecules (Basel, Switzerland).
2023 Feb; 28(3):. doi:
10.3390/molecules28031396. [PMID: 36771071] - Ayesha Sani, Ali Murad, Dilawar Hassan, Ghulam Mustafa Channa, Ahmed El-Mallul, Dora Iliana Medina. Photo-catalytic and biomedical applications of one-step, plant extract-mediated green-synthesized cobalt oxide nanoparticles.
Environmental science and pollution research international.
2023 Feb; 30(8):20736-20745. doi:
10.1007/s11356-022-23645-x. [PMID: 36255577] - Zhiming Shi, Mei Wen, Yonghua Zhao, Congying Wang. Vermitoxicity of aged biochar and exploring potential damage factors.
Environment international.
2023 02; 172(?):107787. doi:
10.1016/j.envint.2023.107787. [PMID: 36738583] - Sujosh Nandi, Proshanta Guha. Technique for order preference by similarity to ideal solution (TOPSIS): a MCDM approach for selecting suitable solvent considering biochemical profiles and in vitro antibacterial efficacy of petioles of betel leaf (Piper betle L.).
Environmental science and pollution research international.
2023 Jan; ?(?):. doi:
10.1007/s11356-023-25485-9. [PMID: 36715795] - Subrata Das, Ashikur Rahaman, Rajat Nath, Anupam Das Talukdar, Deepa Nath, Shamee Bhattacharjee, Deba Prasad Mandal, Manabendra Dutta Choudhury, Dipika Das, Gitishree Das, Jayanta Kumar Patra. Effect of acetone fraction of Ottelia alismoides on the G2/M cell cycle arrest and apoptosis in the human carcinoma cell lines.
Journal of ethnopharmacology.
2023 Jan; 300(?):115729. doi:
10.1016/j.jep.2022.115729. [PMID: 36162544] - P Jambwa, S M Nkadimeng, T N Mudimba, G Matope, L J McGaw. Antibacterial and anti-inflammatory activity of plant species used in traditional poultry ethnomedicine in Zimbabwe: A first step to developing alternatives to antibiotic poultry feed additives.
Journal of ethnopharmacology.
2023 Jan; 300(?):115687. doi:
10.1016/j.jep.2022.115687. [PMID: 36084819] - Yunchang Li, Israel Emiezi Agarry, Desheng Ding, Zsolt Zalán, Pimiao Huang, Tian Cai, Kewei Chen. Screening of dephytinization reaction of chlorophyll pigments with citrus acetone powder by UPLC-DAD-MS.
Journal of food science.
2023 Jan; 88(1):147-160. doi:
10.1111/1750-3841.16411. [PMID: 36517982] - Elif Meltem İşçimen, Serap Berktaş, Mustafa Çam, Mehmet Hayta. Optimization of ultrasound-assisted aqueous two-phase system (ATPS) of phenolics from apple pulp and peel.
Preparative biochemistry & biotechnology.
2023; 53(2):207-214. doi:
10.1080/10826068.2022.2062774. [PMID: 35436177] - Mahantesh Banni, M Jayaraj. Identification of Bioactive Compounds of Leaf Extracts of Sida cordata (Burm.f.) Borss.Waalk. by GC/MS Analysis.
Applied biochemistry and biotechnology.
2023 Jan; 195(1):556-572. doi:
10.1007/s12010-022-04115-z. [PMID: 36107388] - Ravin Bhandari, Dhakaraj Pant, Kamal Singh Kathayat, Ramesh Bhattarai, Himal Barakoti, Jitendra Pandey, Nirmala Jamarkatel-Pandit. Preliminary Study on the Antibacterial Activities and Antibacterial Guided Fractionation of Some Common Medicinal Plants Practices in Itum Bahal, Kathmandu Valley of Nepal.
TheScientificWorldJournal.
2023; 2023(?):7398866. doi:
10.1155/2023/7398866. [PMID: 37780640] - Basile Konmy, Pascal Abiodoun Olounladé, Tomabu Adjobimey, Christian Cocou Dansou, Akouavi Carine Chimène Adoho, Esaïe Tchetan, Georcelin Goué Alowanou, Erick Virgile Bertrand Azando, Adolphe Adjanohoun, Sanni-Yo Doko Allou, Lamine Baba-Moussa. In vivo anticoccidial activity and immune response of Moringa oleifera and Vernonia amygdalina leaves against Eimeria magna and Eimeria media in rabbits.
Frontiers in cellular and infection microbiology.
2023; 13(?):1173138. doi:
10.3389/fcimb.2023.1173138. [PMID: 37274317] - Yasaman Yazdi, Mohammad Reza Rezaei, Hamid R Pourianfar. Antibacterial Activity of Culinary-Medicinal Polypore Mushroom Lentinus tigrinus (Agaricomycetes).
International journal of medicinal mushrooms.
2023; 25(6):21-30. doi:
10.1615/intjmedmushrooms.2023048172. [PMID: 37522530] - Fuat Yetişsin. Exogenous acetone O-(2-naphthylsulfonyl)oxime improves the adverse effects of excess copper by copper detoxification systems in maize.
International journal of phytoremediation.
2023; 25(14):2001-2013. doi:
10.1080/15226514.2023.2234489. [PMID: 37434299] - Dziyana Shymialevich, Michał Wójcicki, Artur Wardaszka, Olga Świder, Barbara Sokołowska, Stanisław Błażejak. Application of Lytic Bacteriophages and Their Enzymes to Reduce Saprophytic Bacteria Isolated from Minimally Processed Plant-Based Food Products-In Vitro Studies.
Viruses.
2022 12; 15(1):. doi:
10.3390/v15010009. [PMID: 36680050] - Mohamed R Habib, Ahmed A Hamed, Rasha E M Ali, Khaled M Zayed, Rasha M Gad El-Karim, Rehab Sabour, Hanaa M Abu El-Einin, Mosad A Ghareeb. Thais savignyi tissue extract: bioactivity, chemical composition, and molecular docking.
Pharmaceutical biology.
2022 Dec; 60(1):1899-1914. doi:
10.1080/13880209.2022.2123940. [PMID: 36200747] - Jawad Khan, Gowhar Ali, Asma Khurshid, Aamer Saeed, Sajjad Ahmad, Najeeb Ullah, Ashrafullah Khan, Robert D Sewell, Muhammad Zakria. Mechanistic efficacy assessment of selected novel methanimine derivatives against vincristine induced Neuropathy: In-vivo, Ex-vivo and In-silico correlates.
International immunopharmacology.
2022 Nov; 112(?):109246. doi:
10.1016/j.intimp.2022.109246. [PMID: 36116153] - Sunil B Yarazari, M Jayaraj. GC-MS Analysis of Bioactive Compounds of Flower Extracts of Calycopteris floribunda Lam.: A Multi Potent Medicinal Plant.
Applied biochemistry and biotechnology.
2022 Nov; 194(11):5083-5099. doi:
10.1007/s12010-022-03993-7. [PMID: 35689756] - Blassan P George, Naresh K Rajendran, Nicolette N Houreld, Heidi Abrahamse. Rubus Capped Zinc Oxide Nanoparticles Induce Apoptosis in MCF-7 Breast Cancer Cells.
Molecules (Basel, Switzerland).
2022 Oct; 27(20):. doi:
10.3390/molecules27206862. [PMID: 36296460] - Tatapudi Kiran Kumar, Bandi Siva, Ajay Anand, Komati Anusha, Satish Mohabe, Araveeti Madhusudana Reddy, Françoise Le Devehat, Ashok Kumar Tiwari, Joël Boustie, Katragadda Suresh Babu. Comprehensive Lichenometabolomic Exploration of Ramalina conduplicans Vain Using UPLC-Q-ToF-MS/MS: An Identification of Free Radical Scavenging and Anti-Hyperglycemic Constituents.
Molecules (Basel, Switzerland).
2022 Oct; 27(19):. doi:
10.3390/molecules27196720. [PMID: 36235256] - Hannah M Hynds, Kelly M Hines. Ion Mobility Shift Reagents for Lipid Double Bonds Based on Paternò-Büchi Photoderivatization with Halogenated Acetophenones.
Journal of the American Society for Mass Spectrometry.
2022 Oct; 33(10):1982-1989. doi:
10.1021/jasms.2c00211. [PMID: 36126229] - Jiahong Sun, Wenqing Ding, Xue Liu, Min Zhao, Bo Xi. Serum metabolites of hypertension among Chinese adolescents aged 12-17 years.
Journal of human hypertension.
2022 10; 36(10):925-932. doi:
10.1038/s41371-021-00602-8. [PMID: 34480101] - M Meischner, S Haberstroh, L E Daber, J Kreuzwieser, M C Caldeira, J-P Schnitzler, C Werner. Soil VOC emissions of a Mediterranean woodland are sensitive to shrub invasion.
Plant biology (Stuttgart, Germany).
2022 Oct; 24(6):967-978. doi:
10.1111/plb.13445. [PMID: 35661369] - Alexey A Zabelin, Vyacheslav B Kovalev, Anatoly Ya Shkuropatov. On the Mechanism of Selective Chemical Exchange of Bacteriopheophytins in the Reaction Centers of Rhodobacter sphaeroides R-26.
Biochemistry. Biokhimiia.
2022 Oct; 87(10):1119-1129. doi:
10.1134/s0006297922100054. [PMID: 36273880] - Kamal Y Thajudeen, Yahya I Asiri, Shahana Salam, Shabeer Ali Thorakkattil, Mohamed Rahamathulla, Ilyas Uoorakkottil. A Box-Behnken Extraction Design and Hepatoprotective Effect of Isolated Eupalitin-3-O-β-D-Galactopyranoside from Boerhavia diffusa Linn.
Molecules (Basel, Switzerland).
2022 Sep; 27(19):. doi:
10.3390/molecules27196444. [PMID: 36234981] - Vandana Thotathil, Hanan Hosni Rizk, Ameena Fakrooh, Lakshmaiah Sreerama. Phytochemical Analysis of Acaciaehrenbergiana (Hayne) Grown in Qatar: Identification of Active Ingredients and Their Biological Activities.
Molecules (Basel, Switzerland).
2022 Sep; 27(19):. doi:
10.3390/molecules27196400. [PMID: 36234937] - Andrea Cerrato, Anna Laura Capriotti, Chiara Cavaliere, Carmela Maria Montone, Susy Piovesana, Aldo Laganà. Novel Aza-Paternò-Büchi Reaction Allows Pinpointing Carbon-Carbon Double Bonds in Unsaturated Lipids by Higher Collisional Dissociation.
Analytical chemistry.
2022 09; 94(38):13117-13125. doi:
10.1021/acs.analchem.2c02549. [PMID: 36121000] - Jorge R Virués-Segovia, Fernando Reyes, Sandra Ruíz, Jesús Martín, Ignacio Fernández-Pastor, Carlos Justicia, Mercedes de la Cruz, Caridad Díaz, Thomas A Mackenzie, Olga Genilloud, Ignacio González, José R Tormo. Kribbellichelins A and B, Two New Antibiotics from Kribbella sp. CA-293567 with Activity against Several Human Pathogens.
Molecules (Basel, Switzerland).
2022 Sep; 27(19):. doi:
10.3390/molecules27196355. [PMID: 36234892] - Rabia Nisar, Sanjay Adhikary, Saeed Ahmad, Mohammad Abrar Alam. In Vitro Antimelanoma Properties of Verbena officinalis Fractions.
Molecules (Basel, Switzerland).
2022 Sep; 27(19):. doi:
10.3390/molecules27196329. [PMID: 36234866] - Saima Muzammil, Yunsheng Wang, Muhammad Hussnain Siddique, Errum Zubair, Sumreen Hayat, Muhammad Zubair, Arpita Roy, Rabia Mumtaz, Muhammad Azeem, Talha Bin Emran, Muhammad Qasim Shahid. Polyphenolic Composition, Antioxidant, Antiproliferative and Antidiabetic Activities of Coronopus didymus Leaf Extracts.
Molecules (Basel, Switzerland).
2022 Sep; 27(19):. doi:
10.3390/molecules27196263. [PMID: 36234800] - Brandon Alexis López-Romero, Gabriel Luna-Bárcenas, María de Lourdes García-Magaña, Luis Miguel Anaya-Esparza, Luis Gerardo Zepeda-Vallejo, Ulises Miguel López-García, Rosa Isela Ortiz-Basurto, Gabriela Aguilar-Hernández, Alejandro Pérez-Larios, Efigenia Montalvo-González. Extraction of Acetogenins Using Thermosonication-Assisted Extraction from Annona muricata Seeds and Their Antifungal Activity.
Molecules (Basel, Switzerland).
2022 Sep; 27(18):. doi:
10.3390/molecules27186045. [PMID: 36144779] - Kokoette Bassey, Malebelo Mabowe, Mmamosheledi Mothibe, Bwalya A Witika. Chemical Characterization and Nutritional Markers of South African Moringa oleifera Seed Oils.
Molecules (Basel, Switzerland).
2022 Sep; 27(18):. doi:
10.3390/molecules27185749. [PMID: 36144484] - Mareena Daus, Suda Chakthong, Krittima Dumjun, Supakit Paosen, Supayang P Voravuthikunchai, Preeyaporn Poldorn, Siriporn Jungsuttiwong, Natharika Chomlamay, Kanyaluck Yangok, Ramida Watanapokasin. New acylphloroglucinols from a crude acetone extract of Eucalyptus camaldulensis Dehnh. leaf.
Natural product research.
2022 Sep; ?(?):1-8. doi:
10.1080/14786419.2022.2118742. [PMID: 36054811] - Ge Zhang, Chao Zhang, Zheng Wang, Qinhong Wang, Jens Nielsen, Zongjie Dai. Dual β-oxidation pathway and transcription factor engineering for methyl ketones production in Saccharomyces cerevisiae.
Metabolic engineering.
2022 09; 73(?):225-234. doi:
10.1016/j.ymben.2022.08.004. [PMID: 35987431] - Pati Kemala, Rinaldi Idroes, Khairan Khairan, Muliadi Ramli, Zulkarnain Jalil, Ghazi Mauer Idroes, Trina Ekawati Tallei, Zuchra Helwani, Eka Safitri, Muhammad Iqhrammullah, Rosnani Nasution. Green Synthesis and Antimicrobial Activities of Silver Nanoparticles Using Calotropis gigantea from Ie Seu-Um Geothermal Area, Aceh Province, Indonesia.
Molecules (Basel, Switzerland).
2022 Aug; 27(16):. doi:
10.3390/molecules27165310. [PMID: 36014547] - Sonda Samet, Amani Ayachi, Mariam Fourati, Lotfi Mallouli, Noureddine Allouche, Michel Treilhou, Nathan Téné, Raoudha Mezghani-Jarraya. Antioxidant and Antimicrobial Activities of Erodium arborescens Aerial Part Extracts and Characterization by LC-HESI-MS2 of Its Acetone Extract.
Molecules (Basel, Switzerland).
2022 Jul; 27(14):. doi:
10.3390/molecules27144399. [PMID: 35889269] - Luis Fernando Plenge-Tellechea, Sergio Acosta-Lara, Joaquín Rodrigo-García, Emilio Álvarez-Parrilla, David Meléndez-Martínez, Ana Gatica-Colima, Jorge A Sierra-Fonseca. Cytoprotective effects of creosote bush (Larrea tridentata) and Southern live oak (Quercus virginiana) extracts against toxicity induced by venom of the black-tailed rattlesnake (Crotalus ornatus).
Drug and chemical toxicology.
2022 Jul; 45(4):1698-1706. doi:
10.1080/01480545.2020.1856864. [PMID: 33297789] - Marina Radović Jakovljević, Milan Stanković, Nenad Vuković, Milena Vukić, Darko Grujičić, Olivera Milošević-Djordjević. Comparative study of the genotoxic activity of Artemisia vulgaris L. and Artemisia alba Turra extracts in vitro.
Drug and chemical toxicology.
2022 Jul; 45(4):1915-1922. doi:
10.1080/01480545.2021.2007025. [PMID: 34844486] - Omnia Hamdy Abdel-Karim, Atef Mohamed Abo-Shady, Gehan Ahmed Ismail, Saly Farouk Gheda. Potential effect of Turbinaria decurrens acetone extract on the biochemical and histological parameters of alloxan-induced diabetic rats.
International journal of environmental health research.
2022 Jul; 32(7):1447-1468. doi:
10.1080/09603123.2021.1888895. [PMID: 33678072] - R T Akande, G Fouche, I M Famuyide, F N Makhubu, S M Nkadimeng, A O Aro, P N Kayoka-Kabongo, L J McGaw. Anthelmintic and antimycobacterial activity of fractions and compounds isolated from Cissampelos mucronata.
Journal of ethnopharmacology.
2022 Jun; 292(?):115130. doi:
10.1016/j.jep.2022.115130. [PMID: 35292375] - Yongqin Yan, Jianuo Chen, Qian Liang, Hong Zheng, Yiru Ye, Wengang Nan, Xi Zhang, Hongchang Gao, Yuping Li. Metabolomics profile in acute respiratory distress syndrome by nuclear magnetic resonance spectroscopy in patients with community-acquired pneumonia.
Respiratory research.
2022 Jun; 23(1):172. doi:
10.1186/s12931-022-02075-w. [PMID: 35761396] - Annalisa Romani, Giulia Marrone, Roberto Celotto, Margherita Campo, Chiara Vita, Carlo Chiaramonte, Andrea Carretta, Nicola Di Daniele, Annalisa Noce. Utility of SIFT-MS to evaluate volatile organic compounds in nephropathic patients' breath.
Scientific reports.
2022 06; 12(1):10413. doi:
10.1038/s41598-022-14152-7. [PMID: 35729207] - Xi Zhang, Binbin Xia, Hong Zheng, Jie Ning, Yinjie Zhu, Xiaoguang Shao, Binrui Liu, Baijun Dong, Hongchang Gao. Identification of characteristic metabolic panels for different stages of prostate cancer by 1H NMR-based metabolomics analysis.
Journal of translational medicine.
2022 06; 20(1):275. doi:
10.1186/s12967-022-03478-5. [PMID: 35715864] - R Krebbers, N Liu, K E Jahromi, M Nematollahi, O Bang, G Woyessa, C R Petersen, G van Rooij, F J M Harren, A Khodabakhsh, S M Cristescu. Mid-infrared supercontinuum-based Fourier transform spectroscopy for plasma analysis.
Scientific reports.
2022 Jun; 12(1):9642. doi:
10.1038/s41598-022-13787-w. [PMID: 35688925] - Vijay Singh, Rupinderpal Kaur, Yumnam Devashree, Damanjeet Kaur, Saurabh Gupta. In vitro Antimicrobial Activity of Cucumis L. and Momordica L. against Human Pathogens.
Doklady biological sciences : proceedings of the Academy of Sciences of the USSR, Biological sciences sections.
2022 Jun; 504(1):85-93. doi:
10.1134/s0012496622030048. [PMID: 35821301] - Sowmya Sankaranarayanan, Inbarajan Kathiravan, Janarthanan Balasundaram, Mohd Shkir, Salem AlFaify. An analysis of the dye-sensitized solar cells fabricated with the dyes extracted from the leaves and flowers of Amaranthus cruentus.
Environmental science and pollution research international.
2022 Jun; 29(29):44271-44281. doi:
10.1007/s11356-022-19004-5. [PMID: 35129747] - Damian Feldman-Kiss, Dailin Li, Richard Cleve, Graham Sinclair, Joshua A Dubland, Li Wang. Interference of ketone bodies on laboratory creatinine measurement in children with DKA: a call for change in testing practices.
Pediatric nephrology (Berlin, Germany).
2022 06; 37(6):1347-1353. doi:
10.1007/s00467-021-05324-0. [PMID: 34757480] - Marzieh Sadat Shojaee, Marzieh Moeenfard, Reza Farhoosh. Kinetics and stoichiometry of gallic acid and methyl gallate in scavenging DPPH radical as affected by the reaction solvent.
Scientific reports.
2022 05; 12(1):8765. doi:
10.1038/s41598-022-12803-3. [PMID: 35610331] - Priyanka Sheladiya, Chintan Kapadia, Vimal Prajapati, Hesham Ali El Enshasy, Roslinda Abd Malek, Najat Marraiki, Nouf S S Zaghloul, R Z Sayyed. Production, statistical optimization, and functional characterization of alkali stable pectate lyase of Paenibacillus lactis PKC5 for use in juice clarification.
Scientific reports.
2022 05; 12(1):7564. doi:
10.1038/s41598-022-11022-0. [PMID: 35534597] - Varsha S Honmore, Arun D Natu, Vijay M Khedkar, Manisha A Arkile, Dhiman Sarkar, Supada R Rojatkar. Two antibacterial spiro compounds from the roots of Artemisia pallens wall: evidence from molecular docking.
Natural product research.
2022 May; 36(10):2465-2472. doi:
10.1080/14786419.2021.1902325. [PMID: 33749414] - Shahnaz Akhtar, Abdul Razaq, Khalid Sajjad Faras, Muhammad Irfan Ashiq, Mohammad Ashraf Tahir. Identification of the polymer-bounded drugs on the fabric surface: A challenge to the forensic drug analysts.
Journal of forensic sciences.
2022 May; 67(3):1267-1273. doi:
10.1111/1556-4029.14980. [PMID: 35005790] - Carolina Pascual-Silva, Ailén Alemán, M Pilar Montero, M Carmen Gómez-Guillén. Extraction and characterization of Argentine red shrimp (Pleoticus muelleri) phospholipids as raw material for liposome production.
Food chemistry.
2022 Apr; 374(?):131766. doi:
10.1016/j.foodchem.2021.131766. [PMID: 34883425]
