Chiral analytical method development and application to pre-clinical pharmacokinetics of pinocembrin.Bioassay-guided isolation of constituents of Piper sarmentosum using a mitochondrial transmembrane potential assay.Pinocembrin, a major flavonoid in propolis, improves the biological functions of EPCs derived from rat bone marrow through the PI3K-eNOS-NO signaling pathway.Alkylated flavanones from the bark of Cryptocarya chartacea as dengue virus NS5 polymerase inhibitors.Pinocembrin protects brain against ischemia/reperfusion injury by attenuating endoplasmic reticulum stress induced apoptosis.Protection of mice against lipopolysaccharide-induced endotoxic shock by pinocembrin is correlated with regulation of cytokine secretion.Pinocembrin inhibits angiotensin II-induced vasoconstriction via suppression of the increase of [Ca2+]i and ERK1/2 activation through blocking AT(1)R in the rat aorta.Subinhibitory concentrations of pinocembrin exert anti-Staphylococcus aureus activity by reducing α-toxin expression.Phytotoxicity of secondary metabolites isolated from Flourensia oolepis S.F.Blake.Evaluation of the In Vitro Wound-Healing Activity of Calabrian HoneysPinocembrin protects rats against cerebral ischemic damage through soluble epoxide hydrolase and epoxyeicosatrienoic acidsRho kinase inhibition activity of pinocembrin in rat aortic rings contracted by angiotensin II
P921
Q34501465-44BAF699-ACC4-4557-8E77-F1E4021A90BAQ35506565-8ED2D38B-F225-44A8-A683-14A0F9C2AEBFQ37039329-F57E424C-4CED-4B81-B2DD-6A99E259C897Q40306969-56F95367-5795-4893-84DA-AE2C9DF97790Q45267868-4EC0783F-0513-4C63-9224-45211693EC14Q47755591-F9D38E7D-1044-443C-A0F5-CC180385479FQ51048940-E5B77967-B77F-4254-9708-F466756543EFQ51063911-0D586ECA-D2C2-4D05-83DB-F895B396984CQ53098676-9CC05187-7261-4ECE-9A50-38B95B194BFFQ64245726-FA2F5B18-754A-4907-9AD0-CE3958D73DCBQ86880912-DD587D2B-8CBC-46A3-8FA8-97739CAC5FEFQ86880935-566FC0DC-0E91-4FB4-8303-C8D2A60EB982
P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
Pinocembrin
@es
Pinocembrin
@nl
Pinocembrin
@sh
Pinocembrin
@sr
Pinocembrina
@it
pinocembrin
@en
pinocembrine
@fr
پینوکمبرین
@azb
پینوکمبرین
@fa
ピノセムブリン
@ja
type
label
Pinocembrin
@es
Pinocembrin
@nl
Pinocembrin
@sh
Pinocembrin
@sr
Pinocembrina
@it
pinocembrin
@en
pinocembrine
@fr
پینوکمبرین
@azb
پینوکمبرین
@fa
ピノセムブリン
@ja
altLabel
5,7-dihydroxyflavanone
@en
dihydrochrysin
@en
galangin flavanone
@en
prefLabel
Pinocembrin
@es
Pinocembrin
@nl
Pinocembrin
@sh
Pinocembrin
@sr
Pinocembrina
@it
pinocembrin
@en
pinocembrine
@fr
پینوکمبرین
@azb
پینوکمبرین
@fa
ピノセムブリン
@ja
P4964
P6689
P592
P6366
P646
P661
P662
P665
P683
P2057
HMDB0030808
P2063
LMPK12140214
P2064
P231
P233
O=C2c3c(OC(c1ccccc1)C2)cc(O)cc3O
P234
1S/C15H12O4/c16-10-6-11(17)15-12(18)8-13(19-14(15)7-10)9-4-2-1-3-5-9/h1-7,13,16-17H,8H2
P235
URFCJEUYXNAHFI-UHFFFAOYSA-N
P274
P2840
P3117
DTXSID80285959
P373
Pinocembrin
P4964
splash10-004i-0890000000-123a4c1e576644198225
splash10-03di-0590000000-694b7335d1677c72efb9
splash10-0a4i-0090000000-7c3a74cf7e01436ee64a
splash10-0a4i-0090000000-84235fc0e6a9b64a53ff
splash10-0a4i-0090000000-de17696c7369872e0a2a
splash10-0a4i-0090000000-e7a2d42e43fa0b871d58
splash10-0a4i-0490000000-db48745a3d543c14c6fc
splash10-0a4i-0490000000-e3e0fd288f81b7d8a9f6
splash10-0pi0-0900000000-31c7469fd05b2dfa0d26
splash10-0sra-0990000000-2ff19c1dd1db18d885d7
P592
CHEMBL399910