23 Results for "

pKi

" in MedChemExpress (MCE) Product Catalog:
Products (23)

23 Results for "pKi" in MCE Product Catalog:

11
11 Publications Verification
Cat. No.: HY-10683
CAS No.: 1173204-81-3
Purity:  99.17%
Target:  

PI3K mTOR

Research Areas:  

Cancer

PKI-402 is a selective, reversible, ATP-competitive inhibitor of PI3K, including PI3K-α mutants, and mTOR (IC50=2, 3, 7,14 and 16 nM for PI3Kα, mTOR, PI3Kβ, PI3Kδ and PI3Kγ).
loading...
    loading...
8
8 Cited Publications
Cat. No.: HY-12014
CAS No.: 658084-23-2
Purity:  98.82%
Synonyms: pKi-SU11274
Research Areas:  

Cancer

SU11274 is a selective Met inhibitor with IC50 of 10 nM, but has no effects on PGDFRβ, EGFR or Tie2.
loading...
    loading...
6
6 Cited Publications
Cat. No.: HY-10681
CAS No.: 1197160-78-3
Purity:  99.68%
Synonyms: pKi-587; PF-05212384
Target:  

PI3K mTOR

Research Areas:  

Cancer

Gedatolisib (PKI-587) is a highly potent dual inhibitor of PI3Kα, PI3Kγ, and mTOR with IC50s of 0.4 nM, 5.4 nM and 1.6 nM, respectively . Gedatolisib is equally effective in both complexes of mTOR, mTORC1 and mTORC2 .
loading...
    loading...
5
5 Cited Publications
Cat. No.: HY-P1290
CAS No.: 121932-06-7
Synonyms: pKi-(6-22)-amide
Target:  

PKA

Research Areas:  

Neurological Disease

PKA Inhibitor Fragment (6-22) amide is a highly potent and specific competitive inhibitor of PKA, with Ki values of 1.7 nM and 1.6 nM against human and bovine PKA catalytic subunits, respectively. The IC50 of PKA Inhibitor Fragment (6-22) amide targeting bovine PKA is 8.6 nM. PKA Inhibitor Fragment (6-22) amide effectively abolishes PKA activity in mouse brain and spinal cord, and exerts in vivo efficacy via intracerebroventricular administration. PKA Inhibitor Fragment (6-22) amide significantly reverses low-dose morphine analgesic tolerance in mice and blocks photoaffinity labeling of cAMP-dependent protein kinase. PKA Inhibitor Fragment (6-22) amide can be applied to research in fields related to the mechanism of morphine analgesic tolerance and skin wound healing .
loading...
    loading...
5
5 Cited Publications
Cat. No.: HY-P1290A
Synonyms: pKi-(6-22)-amide TFA
Target:  

PKA

Research Areas:  

Neurological Disease

PKA Inhibitor Fragment (6-22) amide TFA is an inhibitor of cAMP-dependent protein kinase A (PKA), with a Ki of 2.8 nM. PKA Inhibitor Fragment (6-22) amide TFA can significantly reverse antinociceptive tolerance in mice .
loading...
    loading...
3
3 Cited Publications
Cat. No.: HY-P1291
CAS No.: 201422-03-9
PKI 14-22 amide, myristoylated is a selective, cAMP-dependent, competitive PKA inhibitor with Ki=~36 nM. The myristoylation modification of PKI 14-22 amide, myristoylated makes it more permeable to cell membranes and blood-brain barriers than the precursor molecule. PKI 14-22 amide, myristoylated can block the phosphorylation of cAMP-dependent downstream targets (such as CREB). PKI 14-22 amide, myristoylated can prevent the development of morphine analgesic tolerance in mice, and also inhibits protein translation and negative-strand RNA synthesis of Zika virus. PKI 14-22 amide, myristoylated can be used in research fields such as opioid tolerance mechanisms and antiviral drugs .
loading...
    loading...
3
3 Cited Publications
Cat. No.: HY-P0222
CAS No.: 99534-03-9
Target:  

PKA

Research Areas:  

Others

PKI(5-24) is a potent, competitive, and synthetic peptide inhibitor of PKA (cAMP-dependent protein kinase), with a Ki of 2.3 nM. PKI(5-24) corresponds to residues 5-24 in the naturally occurring heat-stable protein kinase inhibitor .
loading...
    loading...
3
3 Cited Publications
Cat. No.: HY-P1291A
PKI 14-22 amide, myristoylated TFA is a selective, cAMP-dependent, competitive PKA inhibitor with Ki=~36 nM. The myristoylation modification of PKI 14-22 amide, myristoylated TFA makes it more permeable to cell membranes and blood-brain barriers than the precursor molecule. PKI 14-22 amide, myristoylated TFA can block the phosphorylation of cAMP-dependent downstream targets (such as CREB). PKI 14-22 amide, myristoylated TFA can prevent the development of analgesic tolerance in mice, and also inhibits protein translation and negative-strand RNA synthesis of Zika virus. PKI 14-22 amide, myristoylated TFA can be used in research fields such as opioid tolerance mechanisms and antiviral drugs .
loading...
    loading...
1
1 Cited Publications
Cat. No.: HY-117155
CAS No.: 187724-61-4
Purity:  99.58%
Target:  

EGFR

Research Areas:  

Cancer

PKI-166 is a potent, selective and orally bioavailable EGFR tyrosine kinase inhibitor, with an IC50 of 0.7 nM .
loading...
    loading...
1
1 Cited Publications
Cat. No.: HY-11080
CAS No.: 1197160-28-3
Purity:  ≥98.0%
Target:  

PI3K mTOR

Research Areas:  

Cancer

PKI-179 is a potent and orally active dual PI3K/mTOR inhibitor, with IC50s of 8 nM, 24 nM, 74 nM, 77 nM, and 0.42 nM for PI3K-α, PI3K-β, PI3K-γ, PI3K-δ and mTOR, respectively. PKI-179 also exhibits activity over E545K and H1047R, with IC50s of 14 nM and 11 nM, respectively. PKI-179 shows anti-tumor activity in vivo .
loading...
    loading...
1
1 Cited Publications
Cat. No.: HY-P3929A
CAS No.: 1293946-39-0
Target:  

PKA

Research Areas:  

Cancer

PKI (14-24)amide TFA is a potent PKA inhibitor. PKI (14-24)amide strongly inhibited cyclic AMP-dependent protein kinase activity in the cell homogenate .
loading...
    loading...
1
1 Cited Publications
Cat. No.: HY-11080A
CAS No.: 1463510-35-1
Purity:  99.66%
Target:  

PI3K mTOR

Research Areas:  

Cancer

PKI-179 hydrochloride is a potent and orally active dual PI3K/mTOR inhibitor, with IC50s of 8 nM, 24 nM, 74 nM, 77 nM, and 0.42 nM for PI3K-α, PI3K-β, PI3K-γ, PI3K-δ and mTOR, respectively. PKI-179 hydrochloride also exhibits activity over E545K and H1047R, with IC50s of 14 nM and 11 nM, respectively. PKI-179 hydrochloride shows anti-tumor activity in vivo .
loading...
    loading...
Cat. No.: HY-107642
CAS No.: 287206-61-5
Purity:  99.79%
Target:  

Motilin Receptor

Research Areas:  

Metabolic Disease

MA-2029 is a selective, orally active, and competitive motilin receptor antagonist (IC50=4.9 nM). MA-2029 is selective for the motilin receptor over various other receptors and ion channels. MA-2029 may be useful for gastrointestinal disorders associated with disturbed gastrointestinal motility .
loading...
    loading...
Cat. No.: HY-P3930
CAS No.: 100891-36-9
Synonyms: IP20-amide
Target:  

PKA

Research Areas:  

Neurological Disease

PKI (5-24),amide (IP20-amide) is a 20-residue peptide that corresponds to the active portion of the heat-stable inhibitor protein of cAMP-dependent protein kinase. PKI (5-24),amide is a potent cAMP-dependent protein kinase (PKA) (PKA) inhibitor with a Ki of 2.3 nM .
loading...
    loading...
Cat. No.: HY-110328
CAS No.: 2230253-82-2
Target:  

EGFR

Research Areas:  

Cancer

PKI-166 hydrochloride is a potent, selective and orally active EGFR tyrosine kinase inhibitor, with an IC50 of 0.7 nM .
loading...
    loading...
Cat. No.: HY-P3785
CAS No.: 100853-58-5
Target:  

PKA

Research Areas:  

Neurological Disease

PKI(5-22)amide is the active inhibitory fragment of the inhibitor of the cyclic AMP-dependent protein kinase (PKA). PKI(5-22)amide inhibits PKA activation, but fails to attenuate homologous desensitization of CRF1 receptors .
loading...
    loading...
Cat. No.: HY-P0222A
Target:  

PKA

Research Areas:  

Others

PKI(5-24) TFA is a potent, competitive, and synthetic peptide inhibitor of PKA (cAMP-dependent protein kinase), with a Ki of 2.3 nM. PKI(5-24) TFA corresponds to residues 5-24 in the naturally occurring heat-stable protein kinase inhibitor .
loading...
    loading...
Cat. No.: HY-P3929
CAS No.: 100853-61-0
Target:  

PKA

Research Areas:  

Cancer

PKI (14-24)amide is a potent PKA inhibitor. PKI (14-24)amide strongly inhibited cyclic AMP-dependent protein kinase activity in the cell homogenate .
loading...
    loading...
Cat. No.: HY-136219
CAS No.: 2098621-90-8
Target:  

Fluorescent Dye

Research Areas:  

Others

Protein kinase affinity probe 1 is a novel protein kinase affinity probe for the functional identification of protein kinases (PKs). Protein kinase affinity probe 1 is a modified Purvalanol B (HY-18299) probe with 50% beads loading (Compound S3) .
loading...
    loading...
Cat. No.: HY-P2629
CAS No.: 128022-93-5
Target:  

PKA

Research Areas:  

Infection

PKI (5-22) is a specific inhibitory peptide targeting the catalytic subunit of protein kinase A (PKA) and contains the active region of PKI. PKI (5-22) inhibits the enzymatic activity of the PKA catalytic subunit-like protein in Trypanosoma equiperdum. PKI (5-22) can be used in the research of trypanosomiasis .
loading...
    loading...