Identification | Back Directory | [Name]
PROFOXYDIM-LITHIUM | [CAS]
139001-49-3 | [Synonyms]
AIK ARK1 AURA STK7 BTAK STK6 AURKA AIRK1 STK15 TETRIS BAS625H MGC34538 Aurora-A CLEFOXYDIM PROFOXYDIM PROFOXYDIM-LITHIUM Aurora-family kinase 1 Aurora-related kinase 1 PROFOXYDIM LITHIUM SALT CLEFOXYDIM LITHIUM SALT Aurora Kinase A active human GRK2, active, GST tagged human AURORA A, active, GST tagged human Anti-Serine/threonine protein kinase 15 AURORA A, active, GST tagged from mouse Anti-Aurora Kinase antibody produced in rabbit AntiSTK15 (Serine/threonine protein kinase 15) ANTI-AIK(N-TERMINAL) antibody produced in rabbit Monoclonal Anti-AURKA antibody produced in mouse Anti-AURA, C-Terminal antibody produced in rabbit ANTI-AURORA-A(C-TERMINAL) antibody produced in rabbit 2-Cyclohexen-1-one, 2-[1-[[2-(4-chlorophenoxy)propoxy]imino]butyl]-3-hydroxy-5-(tetrahydro-2H-thiopyran-3-yl)- (5RS)-2-{(EZ)-1-[(2RS)-2-(4-chlorophenoxy)propoxyimino]butyl}-3-hydroxy-5-[(3RS)-thian-3-yl]cyclohex-2-en-1-one | [Molecular Formula]
C24H32ClNO4S | [MDL Number]
MFCD04112607 | [MOL File]
139001-49-3.mol | [Molecular Weight]
466.03 |
Chemical Properties | Back Directory | [Melting point ]
<25 °C | [Boiling point ]
597.2±60.0 °C(Predicted) | [density ]
1.26±0.1 g/cm3(Predicted) | [storage temp. ]
-70°C | [solubility ]
DMSO (Slightly), Methanol (Slightly), Water (Slightly) | [form ]
neat | [pka]
4.25±0.25(Predicted) | [color ]
White to Off-White | [Stability:]
Hygroscopic, Unstable in Solution | [EPA Substance Registry System]
Profoxydim (139001-49-3) |
Hazard Information | Back Directory | [Uses]
Profoxydim Lithium Salt is a salt of Profoxydim (139001-49-3) and an herbicide. | [Definition]
ChEBI: Profoxydim is a cyclic ketone that is 3-hydroxycyclohex-2-en-1-one substituted by a N-[2-(4-chlorophenoxy)propoxy]butanimidoyl group at position 2 and by a thian-3-yl group at position 5. It is a herbicide used for the control of grass weeds in rice. It has a role as a herbicide and an EC 6.4.1.2 (acetyl-CoA carboxylase) inhibitor. It is an oxime O-ether, a member of monochlorobenzenes, an aromatic ether, an enol, an organosulfur heterocyclic compound and a cyclic ketone. | [General Description]
G-protein-coupled receptor kinase 2 (GRK2), which is officially known as adrenergic, beta, receptor kinase 1 (ADRBK1), gene codes for a 689 amino acid protein, that is of 79.573kDa. This gene has 12 catalytic region subdomains. GRK2 is expressed in the vascular endothelium, arterial smooth muscle, myocardium, kidney and in the renal proximal tubule. It is mapped to human chromosome 11q13. | [Biochem/physiol Actions]
G-protein-coupled receptor kinase 2 (GRK2) or ADRBK1 is a ubiquitous cytosolic enzyme that specifically phosphorylates the activated form of the beta-adrenergic and related G protein-coupled receptors. GRK2 phosphorylates the beta-2-adrenergic receptor and appears to mediate agonist-specific desensitization. Abnormal coupling of beta-adrenergic receptor to G protein is involved in the pathogenesis of the failing heart. RAF kinase inhibitor protein RKIP is a physiologic inhibitor of GRK2. After stimulation of G protein-coupled receptors, RKIP dissociates from its known target, RAF1 to associate with GRK2 and block its activity. G-protein-coupled receptor kinase 2 (GRK2) controls several intracellular mechanisms. It helps to maintain the structure and activities of the heart. Hence it participates in several cardiovascular diseases. GRK2 also modulates ion and fluid transport and eventually, blood pressure. It increases the synthesis of mitochondrial superoxide and reduces oxygen utilization and ATP synthesis. This protein serves as a major onco-modulator. |
|
|