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KT 5720

SIGMA/K3761 - ≥98% (HPLC), powder

Synonym: (9S,10S,12R)-2,3,9,10,11,12-Hexahydro-10-hydroxy-9-methyl-1-oxo-9,12-epoxy-1H-diindolo[1,2,3-fg:3′,2′,1′-kl]pyrrolo[3,4-i][1,6]benzodiazocine-10-carboxylic acid hexyl ester

CAS Number: 108068-98-0
Empirical Formula (Hill Notation): C32H31N3O5
Molecular Weight: 537.61
MDL Number: MFCD00132118
Linear Formula: C32H31N3O5
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-K3761-.1MG 0.1 mg
$285.00
1/EA
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assay ≥98% (HPLC)
biological source microbial
color white to faint yellow
form powder
InChI 1S/C32H31N3O5/c1-3-4-5-10-15-39-30(37)32(38)16-23-34-21-13-8-6-11-18(21)25-26-20(17-33-29(26)36)24-19-12-7-9-14-22(19)35(28(24)27(25)34)31(32,2)40-23/h6-9,11-14,23,38H,3-5,10,15-17H2,1-2H3,(H,33,36)/t23-,31+,32-/m0/s1
InChI key ZHEHVZXPFVXKEY-IKZDWWSZSA-N
Quality Level 200 
shipped in wet ice
SMILES string CCCCCCOC([C@@]1(O)C[C@@]2([H])N3C(C=CC=C4)=C4C5=C3C6=C(C(C=CC=C7)=C7N6[C@]1(C)O2)C8=C5C(NC8)=O)=O
solubility methanol: 5 mg/mL
storage temp. −20°C
Application: KT 5720 has been used as a chemical inhibitor of cell signaling pathway. It has also been used as a protein kinase A (PKA) inhibitor to study its effect on the nuclear import of CRTC1 in α-MSH-activated B16-F0 cells and on COX-2 stimulation of tumor-associated Vascular endothelial growth factor (VEGF) expression.
Biochem/physiol Actions: Specific, cell-permeable inhibitor of protein kinase A (PKA). No significant effect on protein kinase C (PKC), protein kinase G (PKG) or myosin light chain kinase (MLCK).
Features and Benefits: This compound is featured on the PKA & PKG  page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here .
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥98% (HPLC)
Storage Temp. −20°C
UNSPSC 51111800

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