Lutexin (BioDeep_00000270254)

PANOMIX_OTCML-2023

代谢物信息卡片

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]chromen-4-one

化学式: C21H20O11 (448.1006)
中文名称: 荭草苷
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C(C(O)1)(c(c(O)4)c(O2)c(c(O)c4)C(=O)C=C2c(c3)cc(c(O)c3)O)OC(CO)C(O)C1O
InChI: InChI=1S/C21H20O11/c22-6-14-17(28)18(29)19(30)21(32-14)16-11(26)4-10(25)15-12(27)5-13(31-20(15)16)7-1-2-8(23)9(24)3-7/h1-5,14,17-19,21-26,28-30H,6H2/t14-,17+,18-,19+,21-/m0/s1

描述信息

Orientin is a naturally occurring bioactive flavonoid that possesses diverse biological properties, including anti-inflammation, anti-oxidative, anti-tumor, and cardio protection. Orientin is a promising neuroprotective agent suitable for therapy for neuropathic pain[1][2].
Orientin is a naturally occurring bioactive flavonoid that possesses diverse biological properties, including anti-inflammation, anti-oxidative, anti-tumor, and cardio protection. Orientin is a promising neuroprotective agent suitable for therapy for neuropathic pain[1][2].

同义名列表

23 个代谢物同义名

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]-4-chromenone; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-methylol-tetrahydropyran-2-yl]chromone; 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-8-.beta.-D-glucopyranosyl-5,7-dihydroxy-; 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-8-beta-D-glucopyranosyl-5,7-dihydroxy-; 2-(3,4-Dihydroxyphenyl)-8-beta-D-glucopyranosyl-5,7-dihydroxy-4H-1-benzopyran-4-one; 2-(3,4-dihydroxyphenyl)-8-beta-D-glucopyranosyl-5,7-dihydroxy-4H-chromen-4-one; 8-beta-D-glucosylluteolin; Luteolin 8-C-glucoside; Luteolin 8-glucoside; Orientin (Flavone); AIDS-026706; 28608-75-5; CHEBI:7781; AIDS026706; Orientin; Lutexin; C10114; 2- (3,4-Dihydroxyphenyl) -8-beta-D-glucopyranosyl-5,7-dihydroxy-4H-1-benzopyran-4-one; 8-beta-D-Glucopyranosyl-3,4,5,7-tetrahydroxyflavone; luteolin 8-C-beta-D-glucopyranoside; Orientin

数据库引用编号

14 个数据库交叉引用编号

ChEBI: CHEBI:7781
KEGG: C10114
PubChem: 5281675
ChEMBL: CHEMBL520866
KNApSAcK: C00001078
CAS: 28608-75-5
Flavonoid: FL3FACCS0002
PubChem: 12300
LipidMAPS: LMPK12110470
PDB-CCD: USE
3DMET: B03552
NIKKAJI: J17.734B
medchemexpress: HY-N0405
KNApSAcK: 7781

分类词条

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

169 个相关的物种来源信息

3816 - Abrus Precatorius L.: -
282753 - Achillea nobilis: 10.1515/ZNC-2003-1-202
175392 - Adenocarpus anagyrifolius: 10.1016/J.BSE.2011.12.023
692153 - Adenocarpus artemisiifolius: 10.1016/J.BSE.2011.12.023
175393 - Adenocarpus bacquei: 10.1016/J.BSE.2011.12.023
692157 - Adenocarpus cincinnatus: 10.1016/J.BSE.2011.12.023
175395 - Adenocarpus decorticans: 10.1016/J.BSE.2011.12.023
49790 - Adenocarpus telonensis: 10.1016/J.BSE.2011.12.023
293749 - Aeluropus lagopoides: 10.1021/NP50031A032
7461 - Apis cerana: 10.1371/JOURNAL.PONE.0175573
4458 - Arum maculatum: 10.1016/0031-9422(75)85315-5
130721 - Ascarina lucida: 10.1021/NP50022A009
155124 - Aspalathus linearis: 10.1021/JF0347721
3821 - Cajanus cajan: 10.3390/MOLECULES14031032
49799 - Calicotome villosa: 10.1016/S0367-326X(03)00061-3
3449 - Caltha palustris: 10.1515/ZNC-2002-5-606
3483 - Cannabis sativa:
3483 - Cannabis Sativa L.: -
61141 - Carallia brachiata: 10.1016/J.FITOTE.2004.09.019
538481 - Carlina corymbosa: 10.1016/0031-9422(79)83089-7
143183 - Carlina gummifera: 10.1016/0031-9422(79)83089-7
143185 - Carlina macrocephala: 10.1016/0031-9422(79)83089-7
1824952 - Cecropia glaziovii: 10.1016/J.PHYMED.2008.02.006
1958848 - Cecropia hololeuca: 10.1078/0944-7113-00003
1472306 - Cecropia pachystachya:
668807 - Centaurea horrida: 10.1016/S0305-1978(02)00055-8
1486575 - Centaurea pseudomaculosa: 10.1007/BF00630667
49807 - Chamaecytisus supinus: 10.1021/NP50050A058
128608 - Cinnamomum verum: 10.1007/SPRINGERREFERENCE_68291
578542 - Combretum micranthum: 10.1007/BF00579081
298648 - Crataegus curvisepala: 10.1007/BF00598320
140997 - Crataegus monogyna: 10.1007/BF00598320
510738 - Crataegus rhipidophylla: 10.1007/BF00598320
32127 - Crepidomanes minutum: 10.1002/J.1537-2197.1996.TB13914.X
170354 - Crossopteryx febrifuga: 10.1055/S-2006-962425
1237663 - Crotalaria sessiliflora: 10.1271/BBB.67.410
3659 - Cucumis sativus: 10.1021/NP030150Y
869827 - Cucumis sativus var. sativus: 10.1021/NP030150Y
66014 - Cymbopogon citratus: 10.1021/JF0479766
1234173 - Cyperus alopecuroides: 10.1016/S0031-9422(02)00060-2
4509 - Dactylis glomerata: 10.1016/0305-1978(84)90034-6
224034 - Daphne gnidium:
223749 - Daphne laureola: 10.1016/S0031-9422(96)00800-X
419419 - Davallia heterophylla: 10.1002/J.1537-2197.1996.TB13914.X
159298 - Deschampsia antarctica: 10.1016/S0031-9422(00)89660-0
932098 - Desmodium canadense: 10.1007/BF00563474
1217287 - Dianthus arenarius: 10.1007/BF00579784
746759 - Dianthus crinitus: 10.1007/BF00579784
58832 - Didymoglossum krausii: 10.1002/J.1537-2197.1996.TB13914.X
58833 - Didymoglossum membranaceum: 10.1002/J.1537-2197.1996.TB13914.X
381256 - Didymoglossum reptans: 10.1002/J.1537-2197.1996.TB13914.X
4373 - Drosophyllum lusitanicum: 10.1016/S0031-9422(02)00258-3
2291122 - Eleutherococcus brachypus: 10.1248/CPB.59.135
866555 - Eremochloa ophiuroides: 10.3390/MOLECULES15118251
3617 - Fagopyrum esculentum: 10.1515/ZNC-1985-3-402
62330 - Fagopyrum tataricum: -
79245 - Ficaria verna: 10.1515/ZNC-2002-5-606
55624 - Gaillardia aristata: 10.1016/0031-9422(83)83059-3
128738 - Gaillardia pulchella: 10.1016/0031-9422(72)80069-4
50748 - Gentiana algida: 10.1016/0031-9422(95)00599-4
648866 - Grona styracifolia: 10.1007/S10600-010-9746-7
235358 - Gypsophila paniculata:
40000 - Heterotis rotundifolia: 10.1007/BF02688048
42079 - Hyparrhenia hirta: 10.1016/S0305-1978(01)00028-X
34213 - Iris ensata: 10.1007/BF00574811
1009483 - Itea chinensis: 10.1016/0031-9422(88)87036-5
96938 - Itea ilicifolia: 10.1016/0031-9422(88)87036-5
108596 - Itea japonica: 10.1016/0031-9422(88)87036-5
1679360 - Itea macrophylla: 10.1016/0031-9422(88)87036-5
2338903 - Itea oldhamii: 10.1016/0031-9422(88)87036-5
1008918 - Itea omeiensis: 10.1016/0031-9422(88)87036-5
1609873 - Itea parviflora: 10.1016/0031-9422(88)87036-5
210359 - Itea yunnanensis: 10.1016/0031-9422(88)87036-5
179731 - Itoa orientalis: 10.1021/NP800014S
313527 - Lamyropsis cynaroides: 10.1016/S0305-1978(99)00121-0
699700 - Lepisorus ussuriensis: 10.1016/S0031-9422(96)00417-7
556514 - Lespedeza bicolor:
688281 - Lespedeza davurica: 10.1007/BF02491247
688283 - Lespedeza juncea:
3874 - Lupinus polyphyllus: 10.1007/BF00565265
28959 - Lupinus texensis: 10.1016/0305-1978(87)90107-4
13129 - Lythrum salicaria:
111923 - Melanargia galathea: 10.1016/S0031-9422(00)82535-2
200951 - Melilotus indicus: 10.1016/J.FITOTE.2006.04.007
306395 - Micromeria juliana: 10.1021/ACS.JNATPROD.6B00839
76306 - Mimosa pudica: 10.1016/S0305-1978(01)00086-2
148530 - Moraea sisyrinchium: 10.1055/S-0033-1352160
1317686 - Musanga cecropioides: 10.1078/0944-7113-00003
4432 - Nelumbo nucifera: 10.1371/JOURNAL.PONE.0108860
204149 - Ocimum tenuiflorum:
238283 - Oenothera canescens: 10.1002/J.1537-2197.1988.TB13465.X
260701 - Oenothera macrocarpa: 10.1016/0305-1978(91)90116-H
22694 - Papaver orientale: 10.1002/ARDP.19142520309
58886 - Parkinsonia aculeata: 10.1016/0031-9422(91)83679-F
159422 - Passiflora alata:
237836 - Passiflora allantophylla: 10.1076/PHBI.40.2.81.5844
196576 - Passiflora ambigua: 10.1076/PHBI.40.2.81.5844
1822410 - Passiflora colinvauxii: 10.1076/PHBI.40.2.81.5844
78168 - Passiflora edulis: 10.1076/PHBI.40.2.81.5844
159425 - Passiflora incarnata:
196581 - Passiflora menispermifolia: 10.1021/NP50015A025
159432 - Passiflora misera: 10.1076/PHBI.40.2.81.5844
196582 - Passiflora oerstedii: 10.1076/PHBI.40.2.81.5844
1510925 - Passiflora pinnatistipula: 10.1076/PHBI.40.2.81.5844
231188 - Passiflora serratifolia:
231183 - Passiflora sexflora: 10.1021/NP50024A029
59871 - Pelargonium reniforme: 10.1016/S0031-9422(01)00403-4
446123 - Phoenix loureiroi: 10.1248/CPB.39.1455
446188 - Phoenix loureiroi var. loureiroi: 10.1016/J.PHYTOCHEM.2009.06.006
538350 - Piper solmsianum: 10.1248/BPB.28.1527
4477 - Pistia stratiotes: 10.1016/0304-3770(77)90003-1
33090 - Plants: -
93036 - Poa annua: 10.1016/S0031-9422(00)84808-6
289064 - Poa supina: 10.1016/S0031-9422(00)84808-6
120625 - Podocarpus nivalis: 10.1016/S0031-9422(00)84968-7
100812 - Pseudarrhenatherum longifolium: 10.1016/0031-9422(89)80274-2
286917 - Ranunculus illyricus: 10.1007/BF00636015
49837 - Retama raetam: 10.1021/NP50029A031
49838 - Retama sphaerocarpa:
1378005 - Rhynchosia beddomei: 10.1007/BF02002621
2059504 - Rhynchosia capitata: 10.1007/BF02002621
132461 - Rhynchosia minima: 10.1007/BF02002621
41241 - Rumex acetosa: 10.1248/CPB.38.2277
291102 - Rumex cyprius: 10.1016/0305-1978(93)90049-W
1786036 - Rumex pictus: 10.1016/0305-1978(93)90049-W
317192 - Rumex vesicarius: 10.1016/0305-1978(93)90049-W
4547 - Saccharum officinarum:
35974 - Santalum Album L\uff0e: -
1907919 - Scutellaria albida: 10.1055/S-2007-987153
4555 - Setaria italica:
185191 - Sigesbeckia orientalis: 10.1007/BF00567822
1137874 - Silene banksia: 10.1007/BF00564824
1390722 - Silene saxatilis: 10.1007/BF00566811
1850527 - Silene wilfordii: 10.1007/BF00564824
581250 - Stellaria holostea: 10.1007/BF00574225
13274 - Stellaria media: 10.1080/14786410701642532
128002 - Tanacetum vulgare: 10.1007/S10600-011-9906-4
578549 - Terminalia brachystemma: 10.1016/J.FITOTE.2009.05.006
578554 - Terminalia myriocarpa: 10.1055/S-2002-32549
476039 - Thalictrum minus: 10.1016/S0031-9422(00)89915-X
285591 - Tinospora crispa: 10.1016/J.BMC.2015.04.053
261649 - Tragopogon orientalis: 10.5586/ASBP.1988.009
41653 - Tragopogon pratensis: 10.5586/ASBP.1988.009
221314 - Trichomanes crispum: 10.1002/J.1537-2197.1996.TB13914.X
1631473 - Trichomanes cupressoides: 10.1002/J.1537-2197.1996.TB13914.X
381238 - Trichomanes holopterum: 10.1002/J.1537-2197.1996.TB13914.X
221323 - Trichomanes lucens: 10.1002/J.1537-2197.1996.TB13914.X
221328 - Trichomanes polypodioides: 10.1002/J.1537-2197.1996.TB13914.X
1210110 - Trigonella grandiflora: 10.1007/BF00579155
78479 - Trollius chinensis:
78479 - Trollius Chinensis: -
46346 - Trollius ledebouri: 10.1016/J.PHYTOCHEM.2005.03.021
1051480 - Vellozia epidendroides: 10.1016/0031-9422(92)90037-Q
54477 - Vitex agnus-castus: 10.1080/14786410701592612
361442 - Vitex negundo: 10.1002/PS.1278
223431 - Vitex negundo var. cannabifolia: 10.1002/PS.1278
3605 - Vitis aestivalis: 10.1016/0305-1978(87)90085-8
226012 - Vitis cinerea: 10.1016/0305-1978(87)90085-8
703182 - Wilbrandia ebracteata:
33090 - 山楂叶: -
33090 - 檀香: -
33090 - 水红花子: -
33090 - 浮萍: -
33090 - 火麻仁: -
33090 - 相思子: -
33090 - 豨莶草: -
33090 - 金莲花: -
33090 - 骨碎补: -
33090 - 鸭跖草: -

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。

亚细胞结构定位		关联基因列表
Cytoplasm	12	AKT1, AXIN2, BCL2, CA1, CASP3, CAT, EP300, MAPK8, PIK3CA, PRKAA2, PTGS2, SLC6A3
Peripheral membrane protein	1	PTGS2
Endoplasmic reticulum membrane	4	BCL2, HMOX1, PTGS2, RTN4
Nucleus	9	AKT1, AXIN2, BCL2, CASP3, EP300, GABPA, HMOX1, MAPK8, PRKAA2
cytosol	12	AKT1, AXIN2, BCL2, CA1, CASP3, CAT, COMT, EP300, HMOX1, MAPK8, PIK3CA, PRKAA2
dendrite	2	COMT, PRKAA2
centrosome	1	AXIN2
nucleoplasm	7	AKT1, CASP3, EP300, GABPA, HMOX1, MAPK8, PRKAA2
Cell membrane	5	AKT1, COMT, RTN4, SLC6A3, TNF
Cytoplasmic side	2	HMOX1, RTN4
lamellipodium	2	AKT1, PIK3CA
Cell projection, axon	1	SLC6A3
Multi-pass membrane protein	2	RTN4, SLC6A3
Synapse	3	COMT, MAPK8, RTN4
cell cortex	1	AKT1
cell junction	1	RTN4
cell surface	2	SLC6A3, TNF
glutamatergic synapse	3	AKT1, CASP3, RTN4
Golgi apparatus	2	ATRN, PRKAA2
Golgi membrane	1	INS
neuronal cell body	5	CASP3, PRKAA2, RTN4, SLC6A3, TNF
postsynapse	1	AKT1
presynaptic membrane	1	SLC6A3
plasma membrane	8	AKT1, ATRN, AXIN2, COMT, PIK3CA, RTN4, SLC6A3, TNF
Membrane	7	AKT1, BCL2, CAT, COMT, HMOX1, PRKAA2, SLC6A3
axon	4	COMT, MAPK8, PRKAA2, SLC6A3
caveola	1	PTGS2
extracellular exosome	4	ATRN, CA1, CAT, COMT
endoplasmic reticulum	4	BCL2, HMOX1, PTGS2, RTN4
extracellular space	5	ATRN, HMOX1, IL6, INS, TNF
perinuclear region of cytoplasm	2	HMOX1, PIK3CA
intercalated disc	1	PIK3CA
mitochondrion	2	BCL2, CAT
protein-containing complex	4	AKT1, BCL2, CAT, PTGS2
intracellular membrane-bounded organelle	2	CAT, COMT
Microsome membrane	1	PTGS2
postsynaptic density	2	CASP3, RTN4
Single-pass type I membrane protein	1	ATRN
Secreted	2	IL6, INS
extracellular region	4	CAT, IL6, INS, TNF
Mitochondrion outer membrane	1	BCL2
Single-pass membrane protein	1	BCL2
mitochondrial outer membrane	2	BCL2, HMOX1
neuronal cell body membrane	1	SLC6A3
[Isoform 2]: Secreted	1	ATRN
mitochondrial matrix	1	CAT
Extracellular side	2	COMT, RTN4
anchoring junction	1	RTN4
transcription regulator complex	1	EP300
Nucleus membrane	1	BCL2
Bcl-2 family protein complex	1	BCL2
nuclear membrane	1	BCL2
external side of plasma membrane	1	TNF
beta-catenin destruction complex	1	AXIN2
microtubule cytoskeleton	1	AKT1
cell-cell junction	1	AKT1
recycling endosome	1	TNF
Single-pass type II membrane protein	2	COMT, TNF
vesicle	1	AKT1
postsynaptic membrane	1	SLC6A3
Membrane raft	2	SLC6A3, TNF
pore complex	1	BCL2
focal adhesion	1	CAT
spindle	1	AKT1
flotillin complex	1	SLC6A3
Peroxisome	1	CAT
Peroxisome matrix	1	CAT
peroxisomal matrix	1	CAT
peroxisomal membrane	1	CAT
Mitochondrion intermembrane space	1	AKT1
mitochondrial intermembrane space	1	AKT1
nuclear speck	1	PRKAA2
Nucleus inner membrane	1	PTGS2
Nucleus outer membrane	1	PTGS2
nuclear inner membrane	1	PTGS2
nuclear outer membrane	1	PTGS2
Cell projection, neuron projection	1	SLC6A3
neuron projection	3	PTGS2, RTN4, SLC6A3
ciliary basal body	1	AKT1
chromatin	2	EP300, GABPA
phagocytic cup	1	TNF
Chromosome	1	EP300
[Isoform 3]: Secreted	1	ATRN
nuclear envelope	1	RTN4
endosome lumen	1	INS
cytoplasmic stress granule	1	PRKAA2
myelin sheath	1	BCL2
ficolin-1-rich granule lumen	1	CAT
secretory granule lumen	2	CAT, INS
Golgi lumen	1	INS
endoplasmic reticulum lumen	3	IL6, INS, PTGS2
axon terminus	1	SLC6A3
phosphatidylinositol 3-kinase complex	1	PIK3CA
phosphatidylinositol 3-kinase complex, class IA	1	PIK3CA
transport vesicle	1	INS
Endoplasmic reticulum-Golgi intermediate compartment membrane	1	INS
Single-pass type IV membrane protein	1	HMOX1
histone acetyltransferase complex	1	EP300
protein-DNA complex	1	EP300
basal dendrite	1	MAPK8
death-inducing signaling complex	1	CASP3
[Isoform 1]: Cell membrane	1	ATRN
dopaminergic synapse	1	SLC6A3
nucleotide-activated protein kinase complex	1	PRKAA2
[Tumor necrosis factor, soluble form]: Secreted	1	TNF
catalase complex	1	CAT
interleukin-6 receptor complex	1	IL6
BAD-BCL-2 complex	1	BCL2
[Isoform Soluble]: Cytoplasm	1	COMT
[Isoform Membrane-bound]: Cell membrane	1	COMT
phosphatidylinositol 3-kinase complex, class IB	1	PIK3CA
endoplasmic reticulum tubular network	1	RTN4
[C-domain 2]: Secreted	1	TNF
[Tumor necrosis factor, membrane form]: Membrane	1	TNF
[C-domain 1]: Secreted	1	TNF
endoplasmic reticulum tubular network membrane	1	RTN4
[Isoform a]: Endoplasmic reticulum membrane	1	RTN4
[Isoform b]: Endoplasmic reticulum membrane	1	RTN4
[Isoform C]: Endoplasmic reticulum membrane	1	RTN4

文献列表

Lucia Camelia Pirvu, Lucia Pintilie, Adrian Albulescu, Amalia Stefaniu, Georgeta Neagu. Anti-Proliferative Potential of Cynaroside and Orientin-In Silico (DYRK2) and In Vitro (U87 and Caco-2) Studies. International journal of molecular sciences. 2023 Nov; 24(23):. doi: 10.3390/ijms242316555. [PMID: 38068880]
Jia-Yi Tao, Jing Li, Lu Wan, Bi-Zhen Dong, Yong-Jie Yu, Ye-Mao Liu, Mao-Lin Yi, Li-Peng Wan. Orientin regulates the proliferation and migration of hepatocellular carcinoma cells. Naunyn-Schmiedeberg's archives of pharmacology. 2023 May; ?(?):. doi: 10.1007/s00210-023-02472-y. [PMID: 37178274]
Dong-Dong Guo, Hai-Yan Huang, Hai-E Liu, Kun Liu, Xing-Jing Luo. Orientin Reduces the Effects of Repeated Procedural Neonatal Pain in Adulthood: Network Pharmacology Analysis, Molecular Docking Analysis, and Experimental Validation. Pain research & management. 2023; 2023(?):8893932. doi: 10.1155/2023/8893932. [PMID: 38047157]
Qingfei Xiao, Ying Zhao, Lei Ma, Rongli Piao. Orientin reverses acetaminophen-induced acute liver failure by inhibiting oxidative stress and mitochondrial dysfunction. Journal of pharmacological sciences. 2022 May; 149(1):11-19. doi: 10.1016/j.jphs.2022.01.012. [PMID: 35369900]
Weiqin Ji, Wei Xu. Orientin inhibits the progression of fibroblast-like synovial cells in rheumatoid arthritis by regulating MAPK-signaling pathway. Allergologia et immunopathologia. 2022; 50(6):154-162. doi: 10.15586/aei.v50i6.742. [PMID: 36335459]
Yuan Qu, Lin Shi, Yu Liu, Lv Huang, Huai-Rong Luo, Gui-Sheng Wu. Orientin Prolongs the Longevity of Caenorhabditis elegans and Postpones the Development of Neurodegenerative Diseases via Nutrition Sensing and Cellular Protective Pathways. Oxidative medicine and cellular longevity. 2022; 2022(?):8878923. doi: 10.1155/2022/8878923. [PMID: 35237385]
Aboli Girme, Prajkta Bhoj, Ganesh Saste, Sandeep Pawar, Amit Mirgal, Dipak Raut, Machindra Chavan, Lal Hingorani. Development and Validation of RP-HPLC Method for Vicenin-2, Orientin, Cynaroside, Betulinic Acid, Genistein, and Major Eight Bioactive Constituents with LC-ESI-MS/MS Profiling in Ocimum Genus. Journal of AOAC International. 2021 Dec; 104(6):1634-1651. doi: 10.1093/jaoacint/qsab067. [PMID: 33930142]
Sithandiwe E Mazibuko-Mbeje, Sinenhlanhla X H Mthembu, Andani Tshiitamune, Ndivhuwo Muvhulawa, Fikile T Mthiyane, Khanyisani Ziqubu, Christo J F Muller, Phiwayinkosi V Dludla. Orientin Improves Substrate Utilization and the Expression of Major Genes Involved in Insulin Signaling and Energy Regulation in Cultured Insulin-Resistant Liver Cells. Molecules (Basel, Switzerland). 2021 Oct; 26(20):. doi: 10.3390/molecules26206154. [PMID: 34684734]
Clara Azalea Berenguer-Rivas, Julio César Escalona-Arranz, Gabriel Llauradó-Maury, Anastasia Van der Auwera, Stefano Piazza, Daniel Méndez-Rodríguez, Kenn Foubert, Paul Cos, Luc Pieters. Anti-inflammatory effect of Adelia ricinella L. aerial parts. The Journal of pharmacy and pharmacology. 2021 Mar; 73(4):553-559. doi: 10.1093/jpp/rgaa057. [PMID: 33793832]
Md Nurul Huda, Shuai Lu, Tanzim Jahan, Mengqi Ding, Rintu Jha, Kaixuan Zhang, Wei Zhang, Milen I Georgiev, Sang Un Park, Meiliang Zhou. Treasure from garden: Bioactive compounds of buckwheat. Food chemistry. 2021 Jan; 335(?):127653. doi: 10.1016/j.foodchem.2020.127653. [PMID: 32739818]
Mariane B Chagas, Daniel O B Pontes, Allan V D Albino, Emanuel J Ferreira, Jovelina S F Alves, Anallicy S Paiva, Daniel L Pontes, Silvana M Z Langansser, Leandro S Ferreira. Bioinspired oxidation in cytochrome P450 of isomers orientin and isoorientin using Salen complexes. Rapid communications in mass spectrometry : RCM. 2020 Sep; 34 Suppl 3(?):e8757. doi: 10.1002/rcm.8757. [PMID: 32061191]
Tiejun Chen, Meizi Piao, Syed Md Ehsanur Rahman, Lehong Zhang, Yang Deng. Influence of fermentation on antioxidant and hypolipidemic properties of maifanite mineral water-cultured common buckwheat sprouts. Food chemistry. 2020 Aug; 321(?):126741. doi: 10.1016/j.foodchem.2020.126741. [PMID: 32276146]
Eui Jeong Nam, Gyhye Yoo, Joo Young Lee, Myungsuk Kim, Changho Jhin, Yang-Ju Son, Sun Young Kim, Sang Hoon Jung, Chu Won Nho. Glycosyl flavones from Humulus japonicus suppress MMP-1 production via decreasing oxidative stress in UVB irradiated human dermal fibroblasts. BMB reports. 2020 Jul; 53(7):379-384. doi: . [PMID: 32317077]
Amsha Viraragavan, Nokulunga Hlengwa, Dalene de Beer, Sylvia Riedel, Neil Miller, Sandra Bowles, Beata Walczak, Christo Muller, Elizabeth Joubert. Model development for predicting in vitro bio-capacity of green rooibos extract based on composition for application as screening tool in quality control. Food & function. 2020 Apr; 11(4):3084-3094. doi: 10.1039/c9fo02480h. [PMID: 32195502]
Chunmeng Li, Chanchun Cai, Xiangjian Zheng, Jun Sun, Liou Ye. Orientin suppresses oxidized low-density lipoproteins induced inflammation and oxidative stress of macrophages in atherosclerosis. Bioscience, biotechnology, and biochemistry. 2020 Apr; 84(4):774-779. doi: 10.1080/09168451.2019.1702871. [PMID: 31829093]
Luciana Arantes Dantas, Márcio Rosa, Erika Crispim Resende, Fabiano Guimarães Silva, Paulo Sérgio Pereira, Ana Cristina Lourenço Souza, Fernando Higino de Lima E Silva, Aurélio Rubio Neto. Spectral quality as an elicitor of bioactive compound production in Solanum aculeatissimum JACQ cell suspension. Journal of photochemistry and photobiology. B, Biology. 2020 Mar; 204(?):111819. doi: 10.1016/j.jphotobiol.2020.111819. [PMID: 32062388]
Eun Mi Choi, Kwang Sik Suh, So Young Park, Soojin Yun, Sang Ouk Chin, Sang Youl Rhee, Suk Chon. Orientin reduces the inhibitory effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin on adipogenic differentiation and insulin signaling pathway in murine 3T3-L1 adipocytes. Chemico-biological interactions. 2020 Feb; 318(?):108978. doi: 10.1016/j.cbi.2020.108978. [PMID: 32044341]
Francisco Oiram Filho, Ebenézer de Oliveira Silva, Mônica Maria de Almeida Lopes, Paulo Riceli Vasconselos Ribeiro, Andréia Hansen Oster, Jhonyson Arruda Carvalho Guedes, Dávila de Souza Zampieri, Patrícia do Nascimento Bordallo, Guilherme Julião Zocolo. Effect of pulsed light on postharvest disease control-related metabolomic variation in melon (Cucumis melo) artificially inoculated with Fusarium pallidoroseum. PloS one. 2020; 15(4):e0220097. doi: 10.1371/journal.pone.0220097. [PMID: 32310943]
Fenghao Tian, Ming Tong, Zizhi Li, Weichao Huang, Yanyang Jin, Qingfei Cao, Xiaoli Zhou, Guangquan Tong. The Effects of Orientin on Proliferation and Apoptosis of T24 Human Bladder Carcinoma Cells Occurs Through the Inhibition of Nuclear Factor-kappaB and the Hedgehog Signaling Pathway. Medical science monitor : international medical journal of experimental and clinical research. 2019 Dec; 25(?):9547-9554. doi: 10.12659/msm.919203. [PMID: 31837261]
Aleksandra Maria Juszczak, Marijana Zovko-Končić, Michał Tomczyk. Recent Trends in the Application of Chromatographic Techniques in the Analysis of Luteolin and Its Derivatives. Biomolecules. 2019 11; 9(11):. doi: 10.3390/biom9110731. [PMID: 31726801]
Michael McCullagh, Cintia Alessandra Matiucci Pereira, Janete Harumi Yariwake. Use of ion mobility mass spectrometry to enhance cumulative analytical specificity and separation to profile 6-C/8-C-glycosylflavone critical isomer pairs and known-unknowns in medicinal plants. Phytochemical analysis : PCA. 2019 Jul; 30(4):424-436. doi: 10.1002/pca.2825. [PMID: 30891865]
Akeem O Lawal, Lester M Davids, Jeanine L Marnewick. Rooibos (Aspalathus linearis) and honeybush (Cyclopia species) modulate the oxidative stress associated injury of diesel exhaust particles in human umbilical vein endothelial cells. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2019 Jun; 59(?):152898. doi: 10.1016/j.phymed.2019.152898. [PMID: 30986715]
Shiqi Zheng, Di Geng, Shuangyue Liu, Qingqing Wang, Siqi Liu, Rufeng Wang. A newly isolated human intestinal bacterium strain capable of deglycosylating flavone C-glycosides and its functional properties. Microbial cell factories. 2019 May; 18(1):94. doi: 10.1186/s12934-019-1144-7. [PMID: 31138294]
Kalaiyarasu Thangaraj, Karthi Natesan, Kandakumar Settu, Mariyappan Palani, Mydhili Govindarasu, Vanitha Subborayan, Manju Vaiyapuri. Orientin mitigates 1, 2-dimethylhydrazine induced lipid peroxidation, antioxidant and biotransforming bacterial enzyme alterations in experimental rats. Journal of cancer research and therapeutics. 2018 Oct; 14(6):1379-1388. doi: 10.4103/jcrt.jcrt_1363_16. [PMID: 30488860]
Li-Jia Liu, Xiu-Hua Hu, Li-Na Guo, Ru-Feng Wang, Qi-Tao Zhao. Anti-inflammatory effect of the compounds from the flowers of Trollius chinensis. Pakistan journal of pharmaceutical sciences. 2018 Sep; 31(5):1951-1957. doi: ". [PMID: 30150194]
Dongdong Guo, Xinyi Hu, Haojie Zhang, Chenghua Lu, Guangwei Cui, Xingjing Luo. Orientin and neuropathic pain in rats with spinal nerve ligation. International immunopharmacology. 2018 May; 58(?):72-79. doi: 10.1016/j.intimp.2018.03.013. [PMID: 29558662]
Nan Zhao, Qi Sun, Yang Song, Lin Wang, Tingjian Zhang, Fanhao Meng. Comparative pharmacokinetics study of orientin in rat plasma by UHPLC-MS/MS after intravenous administration of single orientin and Trollius chinensis Bunge extract. Biomedical chromatography : BMC. 2018 Apr; 32(4):. doi: 10.1002/bmc.4142. [PMID: 29148582]
Izabel Lucena Gadioli, Marcela de Sá Barreto da Cunha, Mariana Veras Oliveira de Carvalho, Ana Maria Costa, Lívia de Lacerda de Oliveira Pineli. A systematic review on phenolic compounds in Passiflora plants: Exploring biodiversity for food, nutrition, and popular medicine. Critical reviews in food science and nutrition. 2018 Mar; 58(5):785-807. doi: 10.1080/10408398.2016.1224805. [PMID: 27645583]
Shiori Nagai, Chihiro Matsumoto, Makio Shibano, Ko Fujimori. Suppression of Fatty Acid and Triglyceride Synthesis by the Flavonoid Orientin through Decrease of C/EBPδ Expression and Inhibition of PI3K/Akt-FOXO1 Signaling in Adipocytes. Nutrients. 2018 Jan; 10(2):. doi: 10.3390/nu10020130. [PMID: 29373533]
Jiwon Baek, Dahae Lee, Tae Kyoung Lee, Ji Hoon Song, Ju Sung Lee, Seong Lee, Sang-Woo Yoo, Ki Sung Kang, Eunjung Moon, Sanghyun Lee, Ki Hyun Kim. (-)-9'-O-(α-l-Rhamnopyranosyl)lyoniresinol from Lespedeza cuneata suppresses ovarian cancer cell proliferation through induction of apoptosis. Bioorganic & medicinal chemistry letters. 2018 01; 28(2):122-128. doi: 10.1016/j.bmcl.2017.11.045. [PMID: 29223588]
Mengxia Wei, Lei Yang. Determination of orientin in Trollius chinensis using ultrasound-assisted extraction and high performance liquid chromatography: Several often-overlooked sample preparation parameters in an ultrasonic bath. Journal of chromatography. A. 2017 Dec; 1530(?):68-79. doi: 10.1016/j.chroma.2017.11.034. [PMID: 29153914]
Man Liao, Xiaoye Cheng, Xinpeng Diao, Yupeng Sun, Lantong Zhang. Metabolites identificaion of two bioactive constituents in Trollius ledebourii in rats using ultra-high-performance liquid chromatography coupled to quadrupole time-of-flight mass spectrometry. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2017 Nov; 1068-1069(?):297-312. doi: 10.1016/j.jchromb.2017.10.061. [PMID: 29127056]
Yinnan Sun, Kui Yang, Qin Cao, Jinde Sun, Yu Xia, Yinhang Wang, Wei Li, Chunhui Ma, Shouxin Liu. Homogenate-assisted Vacuum-powered Bubble Extraction of Moso Bamboo Flavonoids for On-line Scavenging Free Radical Capacity Analysis. Molecules (Basel, Switzerland). 2017 Jul; 22(7):. doi: 10.3390/molecules22071156. [PMID: 28696360]
Fengli Chen, Qiang Zhang, Junling Liu, Huiyan Gu, Lei Yang. An efficient approach for the extraction of orientin and vitexin from Trollius chinensis flowers using ultrasonic circulating technique. Ultrasonics sonochemistry. 2017 Jul; 37(?):267-278. doi: 10.1016/j.ultsonch.2017.01.012. [PMID: 28427633]
Petra Terpinc, Blaž Cigić, Tomaž Polak, Janez Hribar, Tomaž Požrl. LC-MS analysis of phenolic compounds and antioxidant activity of buckwheat at different stages of malting. Food chemistry. 2016 Nov; 210(?):9-17. doi: 10.1016/j.foodchem.2016.04.030. [PMID: 27211614]
Roswitha Schuster, Wolfgang Holzer, Hannes Doerfler, Wolfram Weckwerth, Helmut Viernstein, Siriporn Okonogi, Monika Mueller. Cajanus cajan- a source of PPARγ activators leading to anti-inflammatory and cytotoxic effects. Food & function. 2016 Sep; 7(9):3798-806. doi: 10.1039/c6fo00689b. [PMID: 27603115]
Yang Xie, Qiu-Shi Guo, Guang-Shu Wang. Preparative Separation and Purification of the Total Flavonoids in Scorzonera austriaca with Macroporous Resins. Molecules (Basel, Switzerland). 2016 Jun; 21(6):. doi: 10.3390/molecules21060768. [PMID: 27304948]
Liya Liu, Youxi Wu, Xiulan Huang. Orientin protects myocardial cells against hypoxia-reoxygenation injury through induction of autophagy. European journal of pharmacology. 2016 Apr; 776(?):90-8. doi: 10.1016/j.ejphar.2016.02.037. [PMID: 26875637]
Shuting Wang, Yinghua Yu, Yan Feng, Fang Zou, Xiaofei Zhang, Jie Huang, Yuyun Zhang, Xian Zheng, Xu-Feng Huang, Yufu Zhu, Yi Liu. Protective effect of the orientin on noise-induced cognitive impairments in mice. Behavioural brain research. 2016 Jan; 296(?):290-300. doi: 10.1016/j.bbr.2015.09.024. [PMID: 26392065]
Pooja Sharma, Om Prakash, Aparna Shukla, Chetan Singh Rajpurohit, Prema G Vasudev, Suaib Luqman, Santosh Kumar Srivastava, Aditya Bhushan Pant, Feroz Khan. Structure-Activity Relationship Studies on Holy Basil (Ocimum sanctum L.) Based Flavonoid Orientin and its Analogue for Cytotoxic Activity in Liver Cancer Cell Line HepG2. Combinatorial chemistry & high throughput screening. 2016; 19(8):656-666. doi: 10.2174/1386207319666160709192801. [PMID: 27396915]
Ana Paula do Nascimento Duque, Nícolas de Castro Campos Pinto, Renata de Freitas Mendes, Josiane Mello da Silva, Danielle Maria de Oliveira Aragão, Maria Christina Marques Nogueira Castañon, Elita Scio. In vivo wound healing activity of gels containing Cecropia pachystachya leaves. The Journal of pharmacy and pharmacology. 2016 Jan; 68(1):128-38. doi: 10.1111/jphp.12496. [PMID: 26727296]
Roshan R Kulkarni, Wonhwa Lee, Tae Su Jang, JungIn Lee, Soyoung Kwak, Mi Seon Park, Hyun-Shik Lee, Jong-Sup Bae, MinKyun Na. Caffeoyl glucosides from Nandina domestica inhibit LPS-induced endothelial inflammatory responses. Bioorganic & medicinal chemistry letters. 2015 Nov; 25(22):5367-71. doi: 10.1016/j.bmcl.2015.09.031. [PMID: 26410076]
Yuan-zhi Yao, Sheng-hua Li. [Chemical Constituents from Angelica keiskei]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2015 Aug; 38(8):1656-60. doi: . [PMID: 26983239]
Chi-Chih Chang, Sheau Ling Ho, Shoei-Sheng Lee. Acylated glucosylflavones as α-glucosidase inhibitors from Tinospora crispa leaf. Bioorganic & medicinal chemistry. 2015 Jul; 23(13):3388-96. doi: 10.1016/j.bmc.2015.04.053. [PMID: 25999202]
Dalene de Beer, Christiaan J Malherbe, Theresa Beelders, Elize L Willenburg, D Jacobus Brand, Elizabeth Joubert. Isolation of aspalathin and nothofagin from rooibos (Aspalathus linearis) using high-performance countercurrent chromatography: sample loading and compound stability considerations. Journal of chromatography. A. 2015 Feb; 1381(?):29-36. doi: 10.1016/j.chroma.2014.12.078. [PMID: 25614190]
Linjie Yu, Sulei Wang, Xiang Chen, Hui Yang, Xiaoxi Li, Yun Xu, Xiaolei Zhu. Orientin alleviates cognitive deficits and oxidative stress in Aβ1-42-induced mouse model of Alzheimer's disease. Life sciences. 2015 Jan; 121(?):104-9. doi: 10.1016/j.lfs.2014.11.021. [PMID: 25497709]
Xiang Ma, Erpei Wang, Yuyun Lu, Yong Wang, Shiyi Ou, Rian Yan. Acylation of Antioxidant of Bamboo Leaves with Fatty Acids by Lipase and the Acylated Derivatives' Efficiency in the Inhibition of Acrylamide Formation in Fried Potato Crisps. PloS one. 2015; 10(6):e0130680. doi: 10.1371/journal.pone.0130680. [PMID: 26098744]
Mahmut Toprak, Mustafa Arık. The investigation of the interaction between orientin and bovine serum albumin by spectroscopic analysis. Luminescence : the journal of biological and chemical luminescence. 2014 Nov; 29(7):805-9. doi: 10.1002/bio.2624. [PMID: 24376141]
Chun-Juan Zhang, Zhi-Fen Meng, Xue-Feng Guo, Yong-De Yue, Feng Tang, Jin Yu, Chao Chen. [Simultaneous determination of four flavone C-glycosides in Phyllostachys edulis leaves by high-performance liquid chromatography with ultraviolet spectrometry]. Guang pu xue yu guang pu fen xi = Guang pu. 2014 Sep; 34(9):2568-72. doi: . [PMID: 25532365]
Mahmoud Nawwar, Amani El-Mousallami, Sahar Hussein, Amani Hashem, Mona Mousa, Ulrike Lindequist, Michael Linscheid. Three new di-O-glycosyl-C-glucosyl flavones from the leaves of Caesalpinia ferrea Mart.. Zeitschrift fur Naturforschung. C, Journal of biosciences. 2014 Sep; 69(9-10):357-62. doi: 10.5560/znc.2014-0113. [PMID: 25711035]
Jun-Peng Yang, Hao He, Yan-Hua Lu. Four flavonoid compounds from Phyllostachys edulis leaf extract retard the digestion of starch and its working mechanisms. Journal of agricultural and food chemistry. 2014 Aug; 62(31):7760-70. doi: 10.1021/jf501931m. [PMID: 25019533]
Kilani-Jaziri Soumaya, Ghedira Zied, Nasr Nouha, Krifa Mounira, Ghedira Kamel, Franca Dijoux Marie Genviève, Ghedira Chekir Leila. Evaluation of in vitro antioxidant and apoptotic activities of Cyperus rotundus. Asian Pacific journal of tropical medicine. 2014 Feb; 7(2):105-12. doi: 10.1016/s1995-7645(14)60004-3. [PMID: 24461522]
June Lee Chelyn, Maizatul Hasyima Omar, Nor Syaidatul Akmal Mohd Yousof, Ramesh Ranggasamy, Mohd Isa Wasiman, Zakiah Ismail. Analysis of flavone C-glycosides in the leaves of Clinacanthus nutans (Burm. f.) Lindau by HPTLC and HPLC-UV/DAD. TheScientificWorldJournal. 2014; 2014(?):724267. doi: 10.1155/2014/724267. [PMID: 25405231]
Jun Xu, Dawei Qian, Shu Jiang, Jianming Guo, Er-xin Shang, Jin-ao Duan, Jing Yang. Application of ultra-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry to determine the metabolites of orientin produced by human intestinal bacteria. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2014 Jan; 944(?):123-7. doi: 10.1016/j.jchromb.2013.11.002. [PMID: 24316522]
Ming Yuan, Ru-Feng Wang, Li-Jia Liu, Xin Yang, Yu-Shuai Peng, Zhen-Xiao Sun. Contribution evaluation of the floral parts to orientin and vitexin concentrations in the flowers of Trollius chinensis. Chinese journal of natural medicines. 2013 Nov; 11(6):699-704. doi: 10.1016/s1875-5364(13)60082-5. [PMID: 24345513]
I Stanimirova, M Kazura, D de Beer, E Joubert, A E Schulze, T Beelders, A de Villiers, B Walczak. High-dimensional nested analysis of variance to assess the effect of production season, quality grade and steam pasteurization on the phenolic composition of fermented rooibos herbal tea. Talanta. 2013 Oct; 115(?):590-9. doi: 10.1016/j.talanta.2013.06.023. [PMID: 24054637]
Madeline J Simpson, Daisy Hjelmqvist, Camilo López-Alarcón, Nadja Karamehmedovic, Thomas G Minehan, Akop Yepremyan, Baback Salehani, Eduardo Lissi, Elizabeth Joubert, Klas I Udekwu, Emilio I Alarcon. Anti-peroxyl radical quality and antibacterial properties of rooibos infusions and their pure glycosylated polyphenolic constituents. Molecules (Basel, Switzerland). 2013 Sep; 18(9):11264-80. doi: 10.3390/molecules180911264. [PMID: 24036515]
Alan Cesar Pilon, R L Carneiro, F Carnevale Neto, Vanderlan da S Bolzani, I Castro-Gamboa. Interval multivariate curve resolution in the dereplication of HPLC-DAD data from Jatropha gossypifolia. Phytochemical analysis : PCA. 2013 Jul; 24(4):401-6. doi: 10.1002/pca.2423. [PMID: 23483597]
Ebenézer de Mello Cruz, Edson Roberto da Silva, Claudia do Carmo Maquiaveli, Eliomara Sousa Sobral Alves, João Francisco Lucon, Matheus Balduino Gonçalves dos Reis, Cleyton Eduardo Mendes de Toledo, Frederico Guaré Cruz, Marcos André Vannier-Santos. Leishmanicidal activity of Cecropia pachystachya flavonoids: arginase inhibition and altered mitochondrial DNA arrangement. Phytochemistry. 2013 May; 89(?):71-7. doi: 10.1016/j.phytochem.2013.01.014. [PMID: 23453911]
Qinxue Ni, Zhiqiang Wang, Guangzhi Xu, Qianxin Gao, Dongdong Yang, Fumiki Morimatsu, Youzuo Zhang. Altitudinal variation of antioxidant components and capability in Indocalamus latifolius (Keng) McClure leaf. Journal of nutritional science and vitaminology. 2013; 59(4):336-42. doi: 10.3177/jnsv.59.336. [PMID: 24064734]
Hong Yao, Yan Chen, Peiying Shi, Juan Hu, Shaoguang Li, Liying Huang, Jianhua Lin, Xinhua Lin. Screening and quantitative analysis of antioxidants in the fruits of Livistona chinensis R. Br using HPLC-DAD-ESI/MS coupled with pre-column DPPH assay. Food chemistry. 2012 Dec; 135(4):2802-7. doi: 10.1016/j.foodchem.2012.07.076. [PMID: 22980875]
Jeong-Ho Lim, Kee-Jai Park, Bum-Keun Kim, Jin-Woong Jeong, Hyun-Jin Kim. Effect of salinity stress on phenolic compounds and carotenoids in buckwheat (Fagopyrum esculentum M.) sprout. Food chemistry. 2012 Dec; 135(3):1065-70. doi: 10.1016/j.foodchem.2012.05.068. [PMID: 22953825]
Vishal R Mali, V Mohan, Subhash L Bodhankar. Antihypertensive and cardioprotective effects of the Lagenaria siceraria fruit in NG-nitro-L-arginine methyl ester (L-NAME) induced hypertensive rats. Pharmaceutical biology. 2012 Nov; 50(11):1428-35. doi: 10.3109/13880209.2012.684064. [PMID: 22994444]
Bharathi Avula, Yan-Hong Wang, Chidananda Swamy Rumalla, Troy J Smillie, Ikhlas A Khan. Simultaneous determination of alkaloids and flavonoids from aerial parts of Passiflora species and dietary supplements using UPLC-UV-MS and HPTLC. Natural product communications. 2012 Sep; 7(9):1177-80. doi: . [PMID: 23074901]
Xiaohua Li, Aye Aye Thwe, Nam Il Park, Tatsuro Suzuki, Sun Ju Kim, Sang Un Park. Accumulation of phenylpropanoids and correlated gene expression during the development of tartary buckwheat sprouts. Journal of agricultural and food chemistry. 2012 Jun; 60(22):5629-35. doi: 10.1021/jf301449a. [PMID: 22587625]
Rahmat Ali Khan, Muhammad Rashid Khan, Sumaira Sahreen, Mushtaq Ahmed. Assessment of flavonoids contents and in vitro antioxidant activity of Launaea procumbens. Chemistry Central journal. 2012 May; 6(1):43. doi: 10.1186/1752-153x-6-43. [PMID: 22616896]
Urmila M Aswar, V Mohan, Subhash L Bodhankar. Antiosteoporotic activity of phytoestrogen-rich fraction separated from ethanol extract of aerial parts of Cissus quadrangularis in ovariectomized rats. Indian journal of pharmacology. 2012 May; 44(3):345-50. doi: 10.4103/0253-7613.96310. [PMID: 22701244]
Silvana Maria Zucolotto, Carize Fagundes, Flávio Henrique Reginatto, Freddy A Ramos, Leonardo Castellanos, Carmenza Duque, Eloir Paulo Schenkel. Analysis of C-glycosyl flavonoids from South American Passiflora species by HPLC-DAD and HPLC-MS. Phytochemical analysis : PCA. 2012 May; 23(3):232-9. doi: 10.1002/pca.1348. [PMID: 21858882]
Sung Hee Ryou, Min Sook Kang, Kyu Il Kim, Young Hee Kang, Jung Sook Kang. Effects of green tea or Sasa quelpaertensis bamboo leaves on plasma and liver lipids, erythrocyte Na efflux, and platelet aggregation in ovariectomized rats. Nutrition research and practice. 2012 Apr; 6(2):106-12. doi: 10.4162/nrp.2012.6.2.106. [PMID: 22586498]
Rahul V Takawale, Vishal R Mali, Chinmay U Kapase, Subhash L Bodhankar. Effect of Lagenaria siceraria fruit powder on sodium oxalate induced urolithiasis in Wistar rats. Journal of Ayurveda and integrative medicine. 2012 Apr; 3(2):75-9. doi: 10.4103/0975-9476.96522. [PMID: 22707863]
Nicoleta G Hădărugă. Ficaria verna Huds. extracts and their β-cyclodextrin supramolecular systems. Chemistry Central journal. 2012 Mar; 6(1):16. doi: 10.1186/1752-153x-6-16. [PMID: 22390207]
Dalene de Beer, Elizabeth Joubert, Melvi Viljoen, Marena Manley. Enhancing aspalathin stability in rooibos (Aspalathus linearis) ready-to-drink iced teas during storage: the role of nano-emulsification and beverage ingredients, citric and ascorbic acids. Journal of the science of food and agriculture. 2012 Jan; 92(2):274-82. doi: 10.1002/jsfa.4571. [PMID: 21780136]
Leon I C Tang, Anna P K Ling, Rhun Y Koh, Soi M Chye, Kenny G L Voon. Screening of anti-dengue activity in methanolic extracts of medicinal plants. BMC complementary and alternative medicine. 2012 Jan; 12(?):3. doi: 10.1186/1472-6882-12-3. [PMID: 22244370]
Theresa Beelders, Gunnar O Sigge, Elizabeth Joubert, Dalene de Beer, André de Villiers. Kinetic optimisation of the reversed phase liquid chromatographic separation of rooibos tea (Aspalathus linearis) phenolics on conventional high performance liquid chromatographic instrumentation. Journal of chromatography. A. 2012 Jan; 1219(?):128-39. doi: 10.1016/j.chroma.2011.11.012. [PMID: 22153205]
Qinxue Ni, Guangzhi Xu, Zhiqiang Wang, Qianxin Gao, Shu Wang, Youzuo Zhang. Seasonal variations of the antioxidant composition in ground bamboo Sasa argenteastriatus leaves. International journal of molecular sciences. 2012; 13(2):2249-2262. doi: 10.3390/ijms13022249. [PMID: 22408451]
Chong Yan, Li Lin, Hongju Liu, Zhixin Lin, Panyu Chen, Cong Cai, Laian Zheng. [Study of flavonoids from leaves of Santalum album]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2011 Nov; 36(22):3130-3. doi: 10.4268/cjcmm20112214. [PMID: 22375392]
Taha S El-Alfy, Hamida M A El-Gohary, Nadia M Sokkar, Mohammed Hosny, Dalia A Al-Mahdy. A New Flavonoid C-Glycoside from Celtis australis L. and Celtis occidentalis L. Leaves and Potential Antioxidant and Cytotoxic Activities. Scientia pharmaceutica. 2011 Oct; 79(4):963-75. doi: 10.3797/scipharm.1108-19. [PMID: 22145118]
Sura Baykan Erel, Canan Karaalp, Erdal Bedir, Hanspeter Kaehlig, Sabine Glasl, Shabana Khan, Liselotte Krenn. Secondary metabolites of Centaurea calolepis and evaluation of cnicin for anti-inflammatory, antioxidant, and cytotoxic activities. Pharmaceutical biology. 2011 Aug; 49(8):840-9. doi: 10.3109/13880209.2010.551538. [PMID: 21612369]
Sumaira Sahreen, Muhammad R Khan, Rahmat A Khan. Hepatoprotective effects of methanol extract of Carissa opaca leaves on CCl4-induced damage in rat. BMC complementary and alternative medicine. 2011 Jun; 11(?):48. doi: 10.1186/1472-6882-11-48. [PMID: 21699742]
Hyun-Jin Kim, Kee-Jai Park, Jeong-Ho Lim. Metabolomic analysis of phenolic compounds in buckwheat (Fagopyrum esculentum M.) sprouts treated with methyl jasmonate. Journal of agricultural and food chemistry. 2011 May; 59(10):5707-13. doi: 10.1021/jf200396k. [PMID: 21417394]
Qiuping Zhang, Binfeng Zhang, Guixin Chou, Zhengtao Wang. [Chemical constituents of aerial parts of Gelsemium elegans]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2011 May; 36(10):1305-10. doi: 10.4268/cjcmm20111012. [PMID: 21837971]
Li-Zhen Wu, Hai-Feng Wu, Xu-Dong Xu, Jun-Shan Yang. Two new flavone C-glycosides from Trollius ledebourii. Chemical & pharmaceutical bulletin. 2011; 59(11):1393-5. doi: 10.1248/cpb.59.1393. [PMID: 22041076]
Jing Zhang, Ke Yuan, Wen-Long Zhou, Jian Zhou, Ping Yang. Studies on the active components and antioxidant activities of the extracts of Mimosa pudica Linn. from southern China. Pharmacognosy magazine. 2011 Jan; 7(25):35-9. doi: 10.4103/0973-1296.75899. [PMID: 21472077]
Ana Catarina Rezende Leite, Tiago Gomes Araújo, Bruno de Melo Carvalho, Maria Bernadete Souza Maia, Vera Lúcia de Menezes Lima. Characterization of the Antidiabetic Role of Parkinsonia aculeata (Caesalpineaceae). Evidence-based complementary and alternative medicine : eCAM. 2011; 2011(?):. doi: 10.1155/2011/692378. [PMID: 20953386]
Pankaj Chaudhary, Sandeep Kumar Shukla, Rakesh Kumar Sharma. REC-2006-A Fractionated Extract of Podophyllum hexandrum Protects Cellular DNA from Radiation-Induced Damage by Reducing the Initial Damage and Enhancing Its Repair In Vivo. Evidence-based complementary and alternative medicine : eCAM. 2011; 2011(?):473953. doi: 10.1093/ecam/nep212. [PMID: 20008078]
François Muanda, Donatien Koné, Amadou Dicko, Rachid Soulimani, Chafique Younos. Phytochemical composition and antioxidant capacity of three malian medicinal plant parts. Evidence-based complementary and alternative medicine : eCAM. 2011; 2011(?):674320. doi: 10.1093/ecam/nep109. [PMID: 19736222]
François Nsemi Muanda, Jaouad Bouayed, Abdelouaheb Djilani, Chunyan Yao, Rachid Soulimani, Amadou Dicko. Chemical Composition and, Cellular Evaluation of the Antioxidant Activity of Desmodium adscendens Leaves. Evidence-based complementary and alternative medicine : eCAM. 2011; 2011(?):620862. doi: 10.1155/2011/620862. [PMID: 20976084]
Yuan-gang Zu, Xiao-lei Liu, Yu-jie Fu, Nan Wu, Yu Kong, Michael Wink. Chemical composition of the SFE-CO extracts from Cajanus cajan (L.) Huth and their antimicrobial activity in vitro and in vivo. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2010 Dec; 17(14):1095-101. doi: 10.1016/j.phymed.2010.04.005. [PMID: 20576412]
Atef A El-Hela, Hussein A Al-Amier, Taghreed A Ibrahim. Comparative study of the flavonoids of some Verbena species cultivated in Egypt by using high-performance liquid chromatography coupled with ultraviolet spectroscopy and atmospheric pressure chemical ionization mass spectrometry. Journal of chromatography. A. 2010 Oct; 1217(41):6388-93. doi: 10.1016/j.chroma.2010.08.025. [PMID: 20817165]
JinPyo Kim, IkSoo Lee, JeongJu Seo, MunyHung Jung, YoungHee Kim, NamHui Yim, KiHwan Bae. Vitexin, orientin and other flavonoids from Spirodela polyrhiza inhibit adipogenesis in 3T3-L1 cells. Phytotherapy research : PTR. 2010 Oct; 24(10):1543-8. doi: 10.1002/ptr.3186. [PMID: 20878708]
Rosi Zanoni Da Silva, Rosendo Augusto Yunes, Márcia Maria de Souza, Franco Delle Monache, Valdir Cechinel-Filho. Antinociceptive properties of conocarpan and orientin obtained from Piper solmsianum C. DC. var. solmsianum (Piperaceae). Journal of natural medicines. 2010 Oct; 64(4):402-8. doi: 10.1007/s11418-010-0421-x. [PMID: 20473574]
Jin Wang, Feng Tang, Yongde Yue, Xuefeng Guo, Xi Yao. Development and validation of an HPTLC method for simultaneous quantitation of isoorientin, isovitexin, orientin, and vitexin in bamboo-leaf flavonoids. Journal of AOAC International. 2010 Sep; 93(5):1376-83. doi: . [PMID: 21140646]
P Tripathi, R Kumar, A K Sharma, A Mishra, R Gupta. Pistia stratiotes (Jalkumbhi). Pharmacognosy reviews. 2010 Jul; 4(8):153-60. doi: 10.4103/0973-7847.70909. [PMID: 22228955]
Hee Ju Lee, Kyung-A Kim, Kui Dong Kang, Eun Ha Lee, Chul Young Kim, Byung Hun Um, Sang Hoon Jung. The compound isolated from the leaves of Phyllostachys nigra protects oxidative stress-induced retinal ganglion cells death. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2010 Jun; 48(6):1721-7. doi: 10.1016/j.fct.2010.03.052. [PMID: 20381571]
Danielle M O Aragão, Lyvia Guarize, Juliana Lanini, Juliana C da Costa, Raúl M G Garcia, Elita Scio. Hypoglycemic effects of Cecropia pachystachya in normal and alloxan-induced diabetic rats. Journal of ethnopharmacology. 2010 Apr; 128(3):629-33. doi: 10.1016/j.jep.2010.01.008. [PMID: 20064597]
Yegang Du, Hung Chu, Mingfu Wang, Ivan K Chu, Clive Lo. Identification of flavone phytoalexins and a pathogen-inducible flavone synthase II gene (SbFNSII) in sorghum. Journal of experimental botany. 2010 Feb; 61(4):983-94. doi: 10.1093/jxb/erp364. [PMID: 20007684]
Thamolwan Suanarunsawat, Watcharaporn Devakul Na Ayutthaya, Thanapat Songsak, Suwan Thirawarapan, Somlak Poungshompoo. Antioxidant Activity and Lipid-Lowering Effect of Essential Oils Extracted from Ocimum sanctum L. Leaves in Rats Fed with a High Cholesterol Diet. Journal of clinical biochemistry and nutrition. 2010 Jan; 46(1):52-9. doi: 10.3164/jcbn.09-52. [PMID: 20104265]
Priyabrata Pattanayak, Pritishova Behera, Debajyoti Das, Sangram K Panda. Ocimum sanctum Linn. A reservoir plant for therapeutic applications: An overview. Pharmacognosy reviews. 2010 Jan; 4(7):95-105. doi: 10.4103/0973-7847.65323. [PMID: 22228948]
Manjuan Liu, David R Katerere, Alexander I Gray, Véronique Seidel. Phytochemical and antifungal studies on Terminalia mollis and Terminalia brachystemma. Fitoterapia. 2009 Sep; 80(6):369-73. doi: 10.1016/j.fitote.2009.05.006. [PMID: 19446614]