Alternate Text DC Chemicals' products qualify for U.S. tariff exemptions. We guarantee no price increases due to customs duties and maintain stable supply, continuing to deliver reliable research solutions to our American clients.

BPKDi

  Cat. No.:  DC71294   Featured
Chemical Structure
1201673-28-0
For research use only. We do not sell to patients.
We match the best price and quality on market.
Email:order@dcchemicals.com  sales@dcchemicals.com
Tel:+86-021-58447131
We are official vendor of:
  • 20
  • 19
  • 18
  • 17
  • 16
  • 15
  • 14
  • 12
  • 11
  • 10
  • 9
  • 8
  • 13
  • 6
  • 5
  • 4
  • 3
  • 2
  • 1
More than 5000 active chemicals with high quality for research!
Field of application
BPKDi is a potent bipyridyl PKD inhibitor with IC50s of 1 nM, 9 nM and 1 nM for PKD1, PKD2 and PKD3, respectively. BPKDi blocks signal-dependent phosphorylation and nuclear export of class IIa HDACs in cardiomyocytes.
Cas No.: 1201673-28-0
Chemical Name: Bpkdi
Synonyms: bpkdi;bipyridyl PKD inhibitor;GTPL9370;BDBM50324323;6-Piperazino-2'-(cyclohexylamino)-2,4'-bipyridine-4-carboxamide;2'-(Cyclohexylamino)-6-(1-piperazinyl)-[2,4'-bipyridine]-4-carboxamide;2'-(Cyclohexylamino)-6-(piperazin-1-yl)-2,4'-bipyridine-4-carboxamide;2-[2-(cyclohexylamino)pyridin-4-yl]-6-piperazin-1-ylpyridine-4-carboxamide;2''-Cyclohexylamino-6-piperazin-1-yl[2,4'']bipyridinyl-4-carboxylicAcid Amide
SMILES: O=C(C1C=C(C2C=CN=C(C=2)NC2CCCCC2)N=C(C=1)N1CCNCC1)N
Formula: C21H28N6O
M.Wt: 380.486623764038
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
MSDS
TITLE DOWNLOAD
MSDS_35529_DC71294_1201673-28-0
COA
LOT NO. DOWNLOAD
Cat. No. Product name Field of application
DC71294 BPKDi BPKDi is a potent bipyridyl PKD inhibitor with IC50s of 1 nM, 9 nM and 1 nM for PKD1, PKD2 and PKD3, respectively. BPKDi blocks signal-dependent phosphorylation and nuclear export of class IIa HDACs in cardiomyocytes.
DC7385 CID-755673 CID755673 is a potent and selective cell-active small molecule inhibitor for PKD with an IC50 of 182 nM; exhibits selective PKD1 inhibition when compared with AKT, PLK1, CAK, CAMKIIα, and PKC isoforms.
X