CRT0066101 dihydrochloride salt form · dihydrochloride · Parent CRT-0066101
CRT0066101 is a potent inhibitor of protein kinase D.
For research use only. Not for human or veterinary use.
Description
CRT0066101 is a potent inhibitor of protein kinase D (PKD). CRT0066101 inhibits all PKD isoforms.
Biological activity
In Vitro CRT0066101 (5 µM; 1 h) dihydrochloride blockS both the basal and NT-induced pS916-PKD1/2 (activated PKD1/2) in Panc-1 and Panc-28 cells. CRT0066101 dihydrochloride abrogates NT-induced phosphorylation of Hsp27 (pS82-Hsp27), attenuates PKD1-mediated NF-κB activation, and abrogates expression of NF-κB-dependent-dependent proliferative and pro-survival proteins. CRT0066101 dihydrochloride significantly inhibits Panc-1 cell proliferation, with an IC50 value of 1 µM. CRT0066101 dihydrochloride results in a 6-10 fold induction of apoptosis in Panc-1 cells. CRT0066101 dihydrochloride significantly reduces cell proliferation of Colo357, Panc-1, MiaPaCa-2, and AsPC-1 cells but had a modest effect in Capan-2 cells. In Vivo CRT0066101 dihydrochloride (80 mg/kg/day; oral gavage; once daily; for 21 days) dihydrochloride in Panc-1 orthotopic model potently blocks tumor growth in vivo. CRT0066101 dihydrochloride (10 mg/kg, i.p., every two days for 3 times) exhibits a protective effect against LPS-induced pneumonia and alleviates lung damage in C57BL/6J mice.
Identifiers
- SMILES
-
Cl.Cl.CC[C@@H](N)CNC1=NC(=NC=C1)C1=C(O)C=CC(=C1)C1=CN(C)N=C1 - InChIKey
-
CXYCRYGNFKDPRH-FMOMHUKBSA-N
Specifications
- MW (average)
- 411.3290
- Formula
- C18H24Cl2N6O
- CAS No.
- 1883545-60-5
- Physical state
- Solid
- Color
- Off-white to light yellow
- Shipping
- Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
- Storage
- Powder -20℃ 2 years; In solvent -20℃ 1 month;
Solubility
Soluble in DMSO
Documents
References
Same target
Search PKDSame research area
Search Inflammation/Immunology- BP-00006 SLF Exclusive free base · >98%
- BP-00008 NSC-339004 free base · >98%
- BP-00019 SLF-amido-C2-COOH free base · >98%
- BP-00022 Inolitazone free base · >98%
- BP-00030 EML4-ALK kinase inhibitor 1 free base · >98%
- BP-00037 SB 328437 free base · >98%
- BP-00041 Clobutinol free base · >98%
- BP-00044 Aloc-D-Ala-Phe-Lys(Aloc)-PAB-PNP free base · >98%