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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T7015 | Vps34-IN-1 | VPS34-IN1 | PI3K , Autophagy |
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 as well as class II PI3Ks. | |||
T6945 | Vps34-PIK-III | PIK-III,VPS34-IN2 | PI3K , Autophagy |
Vps34-PIK-III (VPS34-IN2), a selective inhibitor of VPS34 enzymatic activity, inhibits autophagy and results in the stabilization of autophagy substrates. | |||
T7944 | VPS34 inhibitor 1 (Compound 19, PIK-III analogue) | PIK-III analogue | PI3K |
VPS34 inhibitor 1 (Compound 19, PIK-III analogue) (PIK-III analogue) is a potent and selective inhibitor of VPS34( IC50 : 15 nM) | |||
T13311 | Vps34-IN-2 | PI3K | |
Vps34-IN-2 is a potent and selective Vps34 inhibitor (IC50s: 2 and 82 nM on the Vps34 enzymatic assay and the GFP-FYVE cellular assay, respectively). | |||
T60506 | Vps34-IN-3 | ||
Vps34-IN-3 is a potent, selective, and orally bioavailable inhibitor of VPS34 kinase . | |||
T1879 | 3-Methyladenine | 3-MA,NSC 66389 | Mitophagy , PI3K , Endogenous Metabolite , Autophagy |
3-Methyladenine (3-MA) is a PI3K inhibitor that selectively inhibits class IB PI3Kγ (IC50=60 μM) and class III VPS34 (IC50=25 μM). 3-Methyladenine inhibits autophagy. | |||
T12831L | SAR405 | PI3K , Autophagy | |
SAR-405 is a potent and selective PIK3C3/Vps34 inhibitor (IC50:1.2 nM; Kd:1.5 nM) that prevents autophagy and synergizes with MTOR inhibition in tumor cells. SAR405 treatment also inhibits autophagy induced either by sta... | |||
T6938 | PF-4989216 | PF 4989216 | Apoptosis , PI3K |
PF-4989216 is a potent and selective PI3K inhibitor with IC50 of 2 nM, 142 nM, 65 nM, 1 nM, and 110 nM for p110α, p110β, p110γ, p110δ, and VPS34, respectively. | |||
T12831 | SAR405 R enantiomer | Others | |
SAR405 R enantiomer is the less active enantiomer of SAR405. SAR405 is an inhibitor of PIK3C3/Vps34. | |||
T4219 | Autophinib | PI3K , Autophagy | |
Autophinib is a potent autophagy inhibitor with a novel chemotype with IC50 values of 90 and 40 nM for autophagy in starvation induced autophagy assay and rapamycin induced autophagy assay. | |||
T10804 | CHMFL-PI3KD-317 | PI3K , PI4K | |
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 class I, II and III PIKK family isoforms, such as PI3Kα (IC50, ... | |||
T9533 | BC-LI-0186 | 4-(2,3-dimethyl-5-oxo-4-propan-2-ylpyrazol-1-yl)-N-(2-phenoxyethyl)benzenesulfonamide | Others |
BC-LI-0186 (4-(2,3-dimethyl-5-oxo-4-propan-2-ylpyrazol-1-yl)-N-(2-phenoxyethyl)benzenesulfonamide) is a potent and selective inhibitor of the interaction of Leucyl-tRNA synthetase (LRS) and Ras-related GTP-binding protei... | |||
T28413 | PI3KD/V-IN-01 | PI3KD/V IN 01,PI3KD/VIN01 | |
PI3KD/V-IN-01 is a potent ATP-competitive PI3Kδ/Vps34 dual inhibitor. | |||
T69888 | SB02024 | ||
SB02024 is a VPS34 inhibitor. SB02024 activates cGAS-STING signaling and sensitizes tumors to STING agonist. SB02024 blocked autophagy in vitro and reduced xenograft growth of two breast cancer cell lines, MDA-MB-231 a... | |||
T79756 | Beclin1-ATG14L interaction inhibitor 1 | Autophagy | |
Beclin1-ATG14L Interaction Inhibitor 1 (COM 19) is a selective inhibitor targeting the specific interaction between Beclin1 and ATG14L. It impedes the formation of complex I in the lipid kinase VPS34, thus inhibiting aut... | |||
T1827 | Buparlisib | BKM120,NVP-BKM120 | Apoptosis , PI3K |
Buparlisib (BKM120) is an orally bioavailable specific oral inhibitor of the pan-class I PI3K (IC50s: 52/166/116/nM for p110α, p110β, and p110δ). | |||
T16841 | SAR-260301 | PI3K | |
SAR-260301 is an orally available and selective inhibitor of PI3Kβ (IC50: 23 nM). | |||
T16365 | Buparlisib Hydrochloride | NVP-BKM120 Hydrochloride,BKM120 Hydrochloride | Others |
Buparlisib Hydrochloride is an inhibitor of pan-class I PI3K (IC50: 52 nM/166 nM/116 nM/262 nM for p110α/p110β/p110δ/p110γ, respectively). |