T2P2806 |
Hederacolchiside A1
|
106577-39-3
|
99.92%
|
|
Hederacolchiside A1 (Raddeanoside R13) shows anti-leishmanial activity, it exhibits a strong antiproliferative activity on all stages of development of the paras...
|
T4398 |
LX2343
|
333745-53-2
|
99.92%
|
|
LX2343 is a BACE1 enzyme inhibitor with an IC50 value of 11.43±0.36 μM. LX2343 acts as a non-ATP competitive PI3K inhibitor with an IC50 of 15.99±3.23 μM. LX2343...
|
T33467 |
MOMIPP
|
1363421-46-8
|
99.92%
|
|
MOMIPP is a PIKfyve inhibitor and a macropinocytosis inducer. MOMIPP readily penetrates the blood-brain barrier and is moderately effective in suppressing progre...
|
T2248 |
AS-605240
|
648450-29-7
|
99.91%
|
|
AS-605240 is an effective and specific inhibitor of PI3Kγ (IC50/Ki: 87.8 nM).
|
T15789 |
LTURM34
|
1879887-96-3
|
99.91%
|
|
LTURM34 is an inhibitor of DNA-PK with IC50 of 34 nM. LTURM34 displays effective antiproliferative activity in a wide range of tumor cell lines. LTURM34 shows 17...
|
T15431 |
Nemiralisib
|
1254036-71-9
|
99.91%
|
|
Nemiralisib(GSK-2269557 free base) is an orally available, potent and specific PI3Kδ inhibitor with a pKi of 9.9.Nemiralisib is used for the treatment of respira...
|
T12310 |
ON 146040
|
1404231-34-0
|
99.89%
|
|
ON 146040 is an effective inhibitor of PI3K isoforms with IC50s of 14 and 20 nM for PI3Kα and PI3Kδ, respectively.
|
T2667 |
PIK-75
|
372196-67-3
|
99.88%
|
|
PIK-75, a DNA-PK and PI3K inhibitor, suppresses DNA-PK(IC50=2 nM), p110α(IC50=5.8 nM) and p110γ(IC50=76 nM).
|
T2265 |
Bimiralisib
|
1225037-39-7
|
99.88%
|
|
Bimiralisib (PI3K-IN-2) is an orally bioavailable pan inhibitor of PI3K and inhibitor of the mTOR, with potential antineoplastic activity. PI3K-IN-2 inhibits the...
|
T2619 |
CH5132799
|
1007207-67-1
|
99.87%
|
|
CH5132799 has been used in trials studying the treatment of Solid Tumors.
|
T2682 |
Acalisib
|
870281-34-8
|
99.87%
|
|
Acalisib (CAL-120) (GS-9820) is a potent and selective inhibitor of PI3Kδ.
|
T11129L |
Duvelisib (R enantiomer) hydrochloride
|
|
99.87%
|
|
Duvelisib (R enantiomer) hydrochloride (INK1197 R enantiomer HCl) is a PI3K inhibitor. Duvelisib (R enantiomer) hydrochloride is the less active enantiomer of Du...
|
T67845 |
ARUK2001607
|
|
99.86%
|
|
ARUK2001607 is a selective inhibitor of phosphatidylinositol 5-phosphate 4-kinase γ (PI5P4Kγ, Kd= 7.1 nM). ARUK2001607 exhibits high selectivity over other >150 ...
|
T12468 |
PI4KIIIbeta-IN-10
|
1881233-39-1
|
99.85%
|
|
PI4KIIIbeta-IN-10 is a potent inhibitor of PI4KIIIβ (IC50 of 3.6 nM).
|
T14552 |
Dactolisib Tosylate
|
1028385-32-1
|
99.85%
|
|
Dactolisib Tosylate (BEZ235 Tosylate) is a dual kinase inhibitor that targets PI3K and mTOR. dactolisib Tosylate exhibits IC50 values of 4, 75, 7, and 5 nM for P...
|
T6394 |
AS-604850
|
648449-76-7
|
99.84%
|
|
AS-604850 is a specific and ATP-competitive PI3Kγ inhibitor (IC50: 250 nM), 18-fold more selective for PI3Kγ than PI3Kα, and over 80-fold selectivity for PI3Kγ t...
|
T3556 |
NIH-12848
|
959551-10-1
|
99.84%
|
|
NIH-12848 is a putative inhibitor of phosphatidylinositol 5-phosphate 4-kinase γ (PI5P4Kγ) with an IC50 of 1 μM.
|
T5S0896 |
Loureirin A
|
119425-89-7
|
99.84%
|
|
Loureirin A has an inhibitory effect on platelet activation, perhaps through an impairment of PI3K/Akt signaling.Loureirin A negatively affects agonist-induced p...
|
T2616 |
PIK-93
|
593960-11-3
|
99.83%
|
|
PIK-93 is the first potent, synthetic PI4K inhibitor with IC50 of 19 nM; inhibits PI3Kα with IC50 of 39 nM.
|
T4976 |
Umbralisib
|
1532533-67-7
|
99.83%
|
|
Umbralisib (TGR 1202) is a PI3Kδ inhibitor.
|