T37379 |
Protectin D1
|
660430-03-5
|
99.72%
|
|
Protectin D1 (Neuroprotectin D1) is a neuroprotectin produced by neuronal cells and is a potential cardioprotective agent.Protectin D1 attenuates myocardial isch...
|
TN1153 |
Polyporenic acid C
|
465-18-9
|
99.71%
|
|
Polyporenic acid C shows inhibitory activity against human collagenase.
|
T13119 |
Tenalisib
|
1639417-53-0
|
99.71%
|
|
Tenalisib (RP6530) (RP6530) is a potent and selective inhibitor of PI3Kδ and PI3Kγ(IC50 values of 25 and 33 nM, respectively.)
|
T2235 |
Dactolisib
|
915019-65-7
|
99.71%
|
|
Dactolisib (BEZ235) is an orally bioavailable inhibitor of PI3K and mTOR (IC50s: 4 nM/5 nM/7 nM/75 nM, and 20.7 nM for p110α/p110γ/p110δ/p110β and mTOR).
|
T3533 |
Apilimod mesylate
|
870087-36-8
|
99.7%
|
|
Apilimod mesylate (STA 5326 mesylate) is a potent IL-12/IL-23 inhibitor.
|
T1994 |
Pictilisib
|
957054-30-7
|
99.69%
|
|
Pictilisib (GDC-0941) (GDC-0941) is a potent pan inhibitor of class I catalytic subunits of PI3K (IC50s: 3/33/3/75 nM for p110α/β/δ/γ).
|
T11381 |
Pictilisib dimethanesulfonate
|
957054-33-0
|
99.69%
|
|
Pictilisib dimethanesulfonate (GDC-0941 2 MeSO3H salt) is a potent inhibitor of PI3Kα/δ with IC50 of 3 nM, with modest selectivity against p110β (11-fold) and p1...
|
T60196 |
IHMT-PI3Kδ-372 S-isomer
|
2429889-61-0
|
99.68%
|
|
IHMT-PI3Kδ-372 S-isomer is a potent and selective PI3Kδ inhibitor with an IC50 of 14 nM. IHMT-PI3Kδ-372 S-isomer shows high selectivity over other class I PI3Ks ...
|
T2078 |
Fimepinostat
|
1339928-25-4
|
99.66%
|
|
Fimepinostat (CUDC 907) is an orally bioavailable inhibitor of both phosphoinositide 3-kinase (PI3K) class I and pan-histone deacetylase (HDAC) enzymes, with pot...
|
TN4673 |
(+)-Nortrachelogenin
|
61521-74-2
|
99.64%
|
|
(+)-Nortrachelogenin is a lignan isolated from Wikstroemia indica C.A. Meyer (Thymelaeaceae). (+)-Nortrachelogenin possesses antileukemic activity.
|
T6730 |
WAY-600
|
1062159-35-6
|
99.63%
|
|
WAY-600 is a potent, ATP-competitive and selective inhibitor of mTOR with IC50 of 9 nM; blocks mTORC1/P-S6K(T389) and mTORC2/P-AKT(S473) but not P-AKT(T308); sel...
|
T14944 |
CGS 15943
|
104615-18-1
|
99.63%
|
|
CGS 15943 is an orally bioavailable non-xanthine antagonist of Adenosine Receptor. In transfected CHO cells, its Ki for human A1, A2A, A2B, and A3 Adenosine Rec...
|
T8461 |
SKI V
|
24418-86-8
|
99.62%
|
|
SKI V is a potent and noncompetitive non-lipid sphingosine kinase (SPHK; SK) inhibitor (GST-hSK,IC50 : 2 μM), and is a PI3K inhibitor(hPI3k,IC50 : 6 μM), induces...
|
T6883 |
Samotolisib
|
1386874-06-1
|
99.61%
|
|
Samotolisib (LY3023414) is an oral ATP competitive inhibitor of the class I PI3K isoforms, DNA-PK, and mTOR. Samotolisib (LY3023414) has been used in trials stud...
|
T3410 |
Momordin Ic
|
96990-18-0
|
99.61%
|
|
Momordin Ic (Momordin 1c) might represent a potential anticancer activity, by inducing apoptosis through oxidative stress-regulated mitochondrial dysfunction inv...
|
T60564 |
PI3K/Akt/mTOR-IN-2
|
2757804-89-8
|
99.61%
|
|
PI3K/Akt/mTOR-IN-2 is a potent PI3K/AKT/mTOR inhibitor.PI3K/Akt/mTOR-IN-2 has anticancer effects and is selective for MDA-MB-231 cells with an IC50 of 2.29 μM.PI...
|
T12365 |
PARP/PI3K-IN-1
|
2337386-47-5
|
99.59%
|
|
PARP/PI3K-IN-1 is a novel dual poly (ADP-ribose) polymerase (PARP) and phosphatidylinositol 3-kinase (PI3K) dual inhibitor with anticancer, antitumour and antipr...
|
T21938 |
AS-041164
|
6318-41-8
|
99.59%
|
|
AS-041164 is a selective and orally active PI3Kγ isoform inhibitor(IC50 of 70 nM), and shows less activity against PI3Kα, PI3Kβ, and PI3Kδ (IC50s of 240 nM, 1.45...
|
TN2259 |
Taurocholic acid
|
81-24-3
|
99.59%
|
|
Taurocholic acid (N-Choloyltaurine) is a bile acid involved in the emulsification of fats.Taurocholic acid is cytoprotective, preventing tumor necrosis factor-al...
|
T4S0498 |
Glaucocalyxin A
|
79498-31-0
|
99.56%
|
|
1. Glaucocalyxin A (Leukamenin F)-SBE-β-CD could be useful with a better solubility and sustained function in drug delivery. 2. Glaucocalyxin A activates caspase...
|