TN2259 |
Taurocholic acid
|
81-24-3
|
98%
|
|
Taurocholic acid is a bile acid involved in the emulsification of fats.Taurocholic acid is cytoprotective, preventing tumor necrosis factor-alpha-induced cholang...
|
T3P2904 |
α-Linolenic acid
|
463-40-1
|
98%
|
|
Linolenic Acid is an essential fatty acid belonging to the omega-3 fatty acids group. It is highly concentrated in certain plant oils and has been reported to in...
|
TN2019 |
Orobol
|
480-23-9
|
98%
|
|
Orobol is an inhibitor of tyrosine-specific protein kinase and phosphatidylinositol turnover. Orobol inhibits PI3K isoforms with IC50s of 3.46-5.27 μM for PI3K α...
|
T2S1040 |
Jolkinolide B
|
37905-08-1
|
98%
|
|
Jolkinolide B is a bioactive diterpene isolated from the roots of Euphorbia fischeriana Steud. Jolkinolide B induces apoptosis in cancer cells. Jolkinolide B can...
|
T2265 |
Bimiralisib
|
1225037-39-7
|
98%
|
|
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 PI3K kinase i...
|
T36083 |
DS-7423
|
1222104-37-1
|
98%
|
|
DS-7423 is a dual PI3K and mTOR inhibitor, with IC50 values of 15.6 nM, 34.9 nM for PI3Kα and mTOR, respectively. DS-7423 possesses anti-tumor activity[1][2].
DS...
|
T39573 |
GSK251
|
2125968-05-8
|
98%
|
|
GSK251 is a novel, orally bioavailable inhibitor of PI3Kδ, exhibiting high potency and selectivity, with a unique binding mode.
|
TN1134 |
Euscaphic acid
|
53155-25-2
|
98%
|
|
Euscaphic acid has anti-diabetic, and anti-inflammatory activities, it inhibits LPS-induced inflammatory responses by interference with the clustering of TRAF6 w...
|
T8651 |
CAL-101
|
1146702-54-6
|
98%
|
|
CAL-101 is a selective inhibitor of p110δ(IC50 : 2.5 nM; in cell-free assays); shown to have 40- to 300-fold greater selectivity for p110δ than p110α/β/γ, and 40...
|
T5818 |
Rigosertib sodium
|
592542-60-4
|
98%
|
|
Rigosertib, a non-ATP-competitive inhibitor of PLK1(IC50=9 nM), exhibits 30-fold higher specificity activity over Plk2 and no effect on Plk3.
|
T61618 |
PI3K-IN-38
|
1382979-64-7
|
98%
|
|
PI3K-IN-38 is an orally available and potent PI3K inhibitor with an IC50 value of 0.541 µM for PI3K-α. PI3K-IN-38 exhibits anticancer and anti-inflammatory activ...
|
T11129 |
Duvelisib (R enantiomer)
|
1261590-48-0
|
98%
|
|
Duvelisib R enantiomer is an enantiomer with low activity of Duvelisib and is an inhibitor of PI3K.
|
T4867 |
Erucic acid
|
112-86-7
|
98%
|
|
Increased levels of erucic acid (22:1n9) have been found in the red blood cell membranes of autistic subjects with developmental regression (PMID: 16581239 ). Er...
|
T9788 |
SN32976
|
1246202-11-8
|
98%
|
|
SN32976 is a pan PI3K inhibitor. SN32976 potently inhibited PI3K isoforms and mTOR, displaying preferential activity for PI3Kα and sparing of PI3Kδ.
|
T13386 |
Zandelisib
|
1401436-95-0
|
98%
|
|
Zandelisib is an inhibitor of phosphatidylinositol 3-kinase (PI3K)(p110δ, IC50 of 3.5 nM), and with antineoplastic activity.
|
T26252 |
PI3Kδ-IN-3
|
1431540-99-6
|
98%
|
|
PI3Kδ-IN-3 is a PI3Kδ inhibitor with an IC50 value of 9 nM.PI3Kδ-IN-3 has a favorable pharmacokinetic profile and inhibits B cell function.
|
TQ0003L1 |
740 Y-P acetate
|
TQ0003L1
|
98%
|
|
740 Y-P acetate is a potent and cell-permeable PI3K activator.740 Y-P acetate tends to bind to GST fusion proteins containing the N- and C-terminal SH2 structura...
|
T2083 |
PI-3065
|
955977-50-1
|
98%
|
|
PI-3065 is a novel potent and selective PI3K p110δ inhibitor.
|
T1827 |
Buparlisib
|
944396-07-0
|
98%
|
|
Buparlisib is an orally bioavailable specific oral inhibitor of the pan-class I PI3K (IC50s: 52/166/116/nM for p110α, p110β, and p110δ).
|
TN2063 |
Physalin B
|
23133-56-4
|
98%
|
|
Physalin B is one of the major active compounds from the Solanaceae family of plants and has a wide range of biological activities for the treatment of inflammat...
|