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19
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or product name starting with:
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H406366
WYE-125132
featured
WYE-125132, also known as WYE-132, is a highly potent, ATP-competitive, and specific mTOR kinase inh…
H406447
Wortmannin
featured
Wortmannin, a steroid metabolite of the fungi Penicillium funiculosum, Talaromyces (Penicillium) wor…
H406190
TG101209
featured
TG101209 is a novel and potent JAK2 inhibitor, which induced dose- and time-dependent cytotoxicity i…
H403010
TG100713
featured
TG100713 is an inhibitor of PI3-kinase that inhibits endothelial cell proliferation.
H406324
PKI-402
featured
PKI-402 is a selective, reversible, ATP-competitive, equipotent inhibitor of class I phosphatidylino…
H406322
PIK-124
PIK-124 is a potent PI3K inhibitor.
H406325
PIK-93
new
featured
PIK-93 is a potent PI3K inhibitor. PIK93 selectively inhibits the type III PI 4-kinase beta enzyme,…
H406326
PIK-90
new
featured
PIK-90 is a potent PI3K inhibitor with potential anticancer activity.
H406327
PIK-39
PIK-39 is a potent PI3K inhibitor.
H406267
PF-4989216
featured
PF-4989216 is a novel potent and selective PI3K inhibitor. PF-4989216 inhibits the phosphorylation o…
H406321
PF-376304
PF-376304 is a nonspecific PI3K inhibitor under development for anti-inflammatory indications. Phosp…
H406355
HS-173
new
featured
HS-173 is a potent PI3Kα inhibitor with potential anticancer activity. HS-173 inhibited the PI3K sig…
H406145
ETP-46321
featured
ETP-46321 is a potent and orally bioavailable PI3K α, δ inhibitor with potent biochemical and cellul…
H406335
Deguelin
featured
Deguelin is a naturally occurring rotenoid, is known to be an Akt inhibitor and to have an anti-tumo…
H406246
CNX-1351
featured
CNX-1351 is a selective covalent Inhibitor of PI3Kα. In an end point assay, CNX-1351 potently inhibi…
H406316
CAY10505
featured
CAY10505 is a phosphatidylinositol 3-kinase-γ inhibitor , was found to significantly improve acetylc…
H406318
AS-604850
featured
AS-604850 is a selective PI3Kγ inhibitor, which significantly reduced the number of infiltrated leuk…
H401010
A-443654
A-443654 is a potent and selective AKT inhibitor. A-443654 induces rapid Akt Ser-473 phosphorylation…
H205795
ZSTK474
featured
ZSTK474 is a novel orally applicable phosphoinositide 3-kinase-specific inhibitor that strongly inhi…
H203187
Voxtalisib
featured
Voxtalisib, also known as XL-765 and SAR245409, is a PI3K/mTOR dual kinase inhibitor XL765 is an ora…
H206015
XL-418
XL-418 is a selective, orally active small molecule, targeting protein kinase B (PKB or AKT) and rib…
H203181
Pilaralisib
featured
Pilaralisib, also known as XL147, is a Class 1 PI3K kinase family inhibitor with potential antineopl…
H206048
WX-037
WX-037 is a potent phosphatidylinositol-3-kinase/proteine-kinase (PI3K) inhibitor with potential ant…
H206109
VS-5584
featured
VS-5584, also known as SB2343, is a potent and selective inhibitor of both phosphatidylinositol 3 ki…
H205931
Tyroserleutide
Tyroserleutide is a tripeptide consisting of tyrosine, serine, and leucine with potential antineopla…
H205938
Umbralisib
featured
Umbralisib, also known as TGR1202 and RP5264 , is a highly specific, orally available, PI3K delta i…
H202892
TG100-115
new
featured
TG100-115, inhibited PI3K γ and -δ(IC50 values of 83 and 235 nM, respectively), whereas both PI3Kα …
H205672
SR13668
SR13668 is an Akt inhibitor, is also a n orally bioavailable indole-3-carbinol (I3C) analogue inhibi…
H205736
SNX-2112
featured
SNX-2112, also known as PF 04928473, is an Hsp90 inhibitor which is currently undergoing multiple p…
H202601
SF1126
SF1126 is a water soluble, small-molecule prodrug containing the pan-PI3K/mTOR inhibitor LY294002/SF…
H206110
SAR260301
featured
SAR260301 is potent and selective Class I phosphatidylinositol-3-kinase (PI3K)β specific inhibitor w…
H206093
Tenalisib
new
featured
Tenalisib, also known as RP6530, is a potent and selective dual PI3Kδ/γ inhibitor that inhibited gro…
H200860
Ridaforolimus
featured
Ridaforolimus, also known as AP23573, is an investigational small-molecule inhibitor of mTOR, a prot…
H202360
Sonolisib (PX-866)
featured
Sonolisib, also known as PX-866, is a small-molecule wortmannin analogue inhibitor of the alpha, gam…
H205745
PWT33597 mesylate
PWT33597, also known as VDC-597, is an orally bioavailable dual inhibitor of phosphatidylinositide …
H206146
Bimiralisib free base
new
featured
Bimiralisib, also known as PQR309, is an orally bioavailable pan inhibitor of phosphoinositide-3-ki…
H202324
Torkinib (PP242)
featured
Torkinib, also known as PP242 is a selective mTOR inhibitor with IC50 of 8 nM. PP242 suppresses blad…
H205989
PKI-179
featured
PKI-179 is a second generation, small-molecule mimetic of ATP that targets the mammalian target of r…
H202235
PI-103
new
featured
PI-103 is a potent, cell-permeable, ATP-competitive inhibitor of phosphatidylinositol 3-kinase (PI3K…
H202226
PF-04691502
new
featured
PF-04691502 is a PI3K/mTOR kinase inhibitor , is also an agent targeting the phosphatidylinositol 3 …
H206131
Panulisib
Panulisib, also known as P7170 and AK151761, is a small molecule inhibitor of PI3K (IC50 = 2.2 nM) …
H206164
M2698 HCl
MSC2363318A, also known as M2698, is an orally available inhibitor of the serine/threonine protein …
H205885
MRK003
MRK003 is a γ-secretase inhibitor exhibits promising in vitro pre-clinical activity in multiple myel…
H205743
MLN-1117
featured
Serabelisib (also known as MLN1117, INK1117, and TAK-117) is an orally bioavailable inhibitor of the…
H205495
Sapanisertib (MLN0128)
featured
Sapanisertib, also known as TAK-228, MLN0128 and INK128, is a TORC1/2 inhibitor, is an orally bioava…
H206214
Samotolisib
featured
Samotolisib, also known as LY3023414, is a small molecule that has been shown in vitro to be a selec…
H201795
LY294002
featured
LY294002 is a morpholine derivative of quercetin. It is a potent inhibitor of phosphoinositide 3-kin…
H205525
LY2780301
LY2780301 is an orally bioavailable inhibitor of the serine/threonine protein kinase Akt (protein ki…
H406418
LB42708
featured
LB42708 is a potent, orally active and selective nonpeptidic farnesyltransferase inhibitor (FTase in…
H203060
KRX-0601
featured
KRX-0601, also known as UCN-01, is a synthetic derivative of staurosporine with antineoplastic activ…
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