T7166 |
GNE-493
|
1033735-94-2
|
98%
|
|
GNE-493 is potent, selective, and orally available PI3K and mTOR inhibitor with potential anticancer activity.IC50s of 3.4 nM, 12 nM, 16 nM, 16 nM and 32 nM for ...
|
T2P2919 |
(2S,3R,4S)-4-Hydroxyisoleucine
|
55399-93-4
|
98%
|
|
(2S,3R,4S)-4-Hydroxyisoleucine (Hydroxyisoleucine) from fenugreek (Trigonella foenum-graecum) seeds is a potential insulinotropic (anti-diabetic) and anti-obesit...
|
T6319 |
OSI-027
|
936890-98-1
|
98%
|
|
OSI-027 (ASP4786) is a selective and potent dual inhibitor of mTORC1 and mTORC2 with IC50 of 22 nM and 65 nM, and more than 100-fold selectivity observed for mTO...
|
T1961 |
Vistusertib
|
1009298-59-2
|
97.94%
|
|
Vistusertib (AZD2014) is an orally bioavailable inhibitor of the mammalian target of rapamycin (mTOR) with potential antineoplastic activity.
|
T24642 |
YH-306
|
1373764-75-0
|
97.87%
|
|
YH-306 (TRV055 acetate ) is a modulator of the FAK signaling pathway that acts by suppressing colorectal tumor growth and metastasis.
|
T4867 |
Erucic acid
|
112-86-7
|
97.85%
|
|
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...
|
T10804 |
CHMFL-PI3KD-317
|
2244992-76-3
|
97.8%
|
|
CHMFL-PI3KD-317 is a highly potent, selective and orally active PI3Kδ inhibitor, with an IC50 of 6 nM, and exhibits over 10-1500 fold selectivity over other clas...
|
T22377 |
NIBR-17
|
944396-88-7
|
97.67%
|
|
NIBR-17 is a pan class I PI3K inhibitor. NIBR-17 inhibits PI3KKα, PI3KKβ, PI3KKγ, and PI3KKδ with IC50 of 1 nM, 9.2 nM, 9 nM, and 20 nM respectively.
|
T64392 |
PI3K-IN-46
|
304645-61-2
|
97.51%
|
|
PI3K-IN-46 is a specific inhibitor of PI3Kγ.
|
TMA2474 |
δ-Tocotrienol
|
25612-59-3
|
97.38%
|
|
δ-Tocotrienol (Delta-Tocotrienol) is a potential angiogenic inhibitor. δ-Tocotrienol is also a nontoxic activator of mir-34a which can inhibit nonsmall cell lung...
|
T16750 |
Rigosertib
|
592542-59-1
|
97.33%
|
|
Rigosertib (ON-01910) is a selective and non-ATP-competitive inhibitor of PLK1 (IC50: 9 nM). Rigosertib is a multi-kinase inhibitor and a selective anti-cancer a...
|
T3208 |
Brevianamide F
|
38136-70-8
|
97.30%
|
|
Brevianamide F (Cyclo(L-Pro-L-Trp)), also known as cyclo-(L-Trp-L-Pro), belongs to a class of naturally occurring 2,5-diketopiperazines. Brevianamide F possess i...
|
T1826 |
PI3K-IN-1
|
1349796-36-6
|
97.07%
|
|
PI3K-IN-1 (Voxtalisib Analogue) is a dual inhibitor of mTOR/PI3K, mostly for p110γ , also inhibits DNA-PK and mTOR.
|
T7015 |
Vps34-IN-1
|
1383716-33-3
|
97.04%
|
|
Vps34-IN-1 (VPS34-IN1) is a potent and highly selective Vps34 inhibitor with IC50 of 25 nM in vitro, which does not significantly inhibit the isoforms of class I...
|
T6630 |
Quercetin Dihydrate
|
6151-25-3
|
97.03%
|
|
Quercetin Dihydrate (Sophoretin) is a polyphenolic flavonoid that was found in a wide variety of plant-based foods, such as apples, onions, berries, and red wine...
|
T3190 |
PIK-inhibitors
|
371934-59-7
|
96.98%
|
|
PIK-inhibitors (MDK34597) is a pan PI3K inhibitors, an analog of PI-103.
|
TN1405 |
Arnicolide D
|
34532-68-8
|
96.66%
|
|
Arnicolide D is a sesquiterpene lactone. Arnicolide D isolates from Centipeda minima. Arnicolide D modulates the cell cycle, activates the caspase signaling path...
|
T11593 |
I-OMe-Tyrphostin AG 538
|
1094048-77-7
|
96.66%
|
|
I-OMe-Tyrphostin AG 538 is a specific IGF-1R inhibitor and ATP-competitive inhibitor of PI5P4Kα (IC50: 1 µM).I-OMe-Tyrphostin AG 538 inhibits IGF-1R-mediated sig...
|
T6072L |
BGT226
|
915020-55-2
|
95.74%
|
|
BGT226 (NVP-BGT226) is a novel dual PI3K / mTOR inhibitor, it acts on PI3K α/β/γ with IC50 of 4 nM / 63 nM / 38 nM, respectively.
|
T13140 |
Umbralisib R-enantiomer
|
1532533-69-9
|
95.61%
|
|
Umbralisib R-enantiomer (RP5264 R-enantiomer) is a delta inhibitor of PI3K and a less active enantiomer of TGR-1202. The IC50 of Umbralisib R-enantiomers against...
|