CID755673, >=98% (HPLC), powder

CID755673, >=98% (HPLC), powder

Application

CID755673 was used to study the role of PKD in dendrite retraction in mouse Purkinje cells.

Biochem/physiol Actions

CID755673 is a cell-permeable, potent and selective inhibitor of all three protein kinase D (PKD) isoforms PKD1 (PKCµ), PKD2, and PKD3 (PKCΝ). CID755673 is not competitive with ATP.

CID755673 was not suitable to inhibit PKD in Swiss 3T3 cells as it utilizes PKD-dependent pathway to enhance the mitogenic signaling triggered by EGF, phorbol esters and bombesin. It should, therefore, be used with caution.

Features and Benefits

This compound is featured on the PKC page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Packaging

5, 25 mg in glass bottle

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Code Description Colour Quality Level InChI key InChI Manufacturer Solubility Form Assay Price Quantity
3573966 CID755673, >=98% (HPLC), powder white to tan 100 AACFPJSJOWQNBN-UHFFFAOYSA-N 1S/C12H11NO3/c14-7-3-4-10-9(6-7)8-2-1-5-13-12(15)11(8)16-10/h3-4,6,14H,1-2,5H2,(H,13,15) SIGMA-ALDRICH DMSO: ≥15 mg/mL powder ≥98% (HPLC)
£557.14 (exc VAT) per 25MG
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3573967 CID755673, >=98% (HPLC), powder white to tan 100 AACFPJSJOWQNBN-UHFFFAOYSA-N 1S/C12H11NO3/c14-7-3-4-10-9(6-7)8-2-1-5-13-12(15)11(8)16-10/h3-4,6,14H,1-2,5H2,(H,13,15) SIGMA-ALDRICH DMSO: ≥15 mg/mL powder ≥98% (HPLC)
£186.64 (exc VAT) per 5MG
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