
BX795
CAS No. 702675-74-9
BX795( BX 795 | BX-795 )
Catalog No. M15696 CAS No. 702675-74-9
BX795 is a potent and relatively specific PDK1 inhibitor with IC50 of 6 nM; also inhibits TBK1 and IKKε with IC50 of 6 nM and 41 nM.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 49 | In Stock |
![]() ![]() |
10MG | 88 | In Stock |
![]() ![]() |
25MG | 198 | In Stock |
![]() ![]() |
50MG | 324 | In Stock |
![]() ![]() |
100MG | 486 | In Stock |
![]() ![]() |
200MG | 701 | In Stock |
![]() ![]() |
500MG | 1062 | In Stock |
![]() ![]() |
1G | Get Quote | In Stock |
![]() ![]() |
Biological Information
-
Product NameBX795
-
NoteResearch use only, not for human use.
-
Brief DescriptionBX795 is a potent and relatively specific PDK1 inhibitor with IC50 of 6 nM; also inhibits TBK1 and IKKε with IC50 of 6 nM and 41 nM.
-
DescriptionBX795 is a potent and relatively specific PDK1 inhibitor with IC50 of 6 nM; also inhibits TBK1 and IKKε with IC50 of 6 nM and 41 nM; shows no activity for PKA, PKC, c-Kit, GSK3β, IKKα, IKKβ, etc.; blocks the autophosphorylation of overexpressed TBK1 and IKKepsilon at Ser-172; has no effect on the canonical NFkappaB signaling pathway.
-
In Vitro——
-
In Vivo——
-
SynonymsBX 795 | BX-795
-
PathwayPI3K/Akt/mTOR signaling
-
TargetPDK
-
RecptorCDK2/CyclinE|Chk1|c-Kit|PDK1
-
Research AreaCancer
-
Indication——
Chemical Information
-
CAS Number702675-74-9
-
Formula Weight591.4677
-
Molecular FormulaC23H26IN7O2S
-
Purity>98% (HPLC)
-
Solubility10 mM in DMSO
-
SMILESO=C(N1CCCC1)NC2=CC=CC(NC3=NC=C(I)C(NCCCNC(C4=CC=CS4)=O)=N3)=C2
-
Chemical Name1-Pyrrolidinecarboxamide, N-[3-[[5-iodo-4-[[3-[(2-thienylcarbonyl)amino]propyl]amino]-2-pyrimidinyl]amino]phenyl]-
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Clark K, et al. J Biol Chem. 2009 May 22;284(21):14136-46.
2. Feldman RI, et al. J Biol Chem. 2005 May 20;280(20):19867-74.
3. Frémond ML, et al. Arthritis Rheumatol. 2017 Apr 20. doi: 10.1002/art.40122.
molnova catalog



related products
-
OSU-03012
OSU-03012 (AR-12) is a novel potent, orally active 3-phosphoinositide-dependent kinase-1 (PDK-1) with IC50 of 5 uM.
-
Clodronate Disodium
Clodronate Disodium, a bisphosphonate, is a potent antiosteolytic agent which inhibits bone resorption.
-
KPLH1130
KPLH1130 improves glucose tolerance in HFD-fed mice.?KPLH1130 is a specific pyruvate dehydrogenase kinase (PDK) inhibitor, blocks macrophage polarization and attenuates proinflammatory responses.