PI3K/Akt/mTOR Signaling
Research Areas
Products Related to PI3K/Akt/mTOR Signaling(719)
- GC15392TriciribineCAS: 35943-35-2Purity: >98.50%
Triciribine is an adenosine analog that targets protein kinase B (Akt) with an IC 50 value of 130nM and has antitumor activity.
- GC15615BX517(PDK1 inhibitor2)CAS: 850717-64-5Purity: >98.00%
BX517(PDK1 inhibitor2) is a potent and selective inhibitor of PDK1 with IC50 of 6 nM.
- GC15642CHIR 99021 trihydrochlorideCAS: 1782235-14-6Purity: >99.00%
Laduviglusib (CHIR-99021) trihydrochloride is a potent and selective GSK-3α/β inhibitor with IC50s of 10 nM and 6.7 nM. CHIR 99021 trihydrochloride shows >500-fold selectivity for GSK-3 over CDC2, ERK2 and other protein kinases. CHIR 99021 trihydrochloride is also a potent Wnt/β-catenin signaling pathway activator. CHIR 99021 trihydrochloride enhances mouse and human embryonic stem cells self-renewal. CHIR 99021 trihydrochloride induces autophagy.
- GC15653PF-05212384 (PKI-587)CAS: 1197160-78-3Purity: >98.00%
PF-05212384 (PKI-587) is a potent dual PI3K/mTOR inhibitor, exhibiting inhibitory effects against PI3Kα (IC₅₀=0.4nM), PI3Kβ (IC₅₀=6nM), PI3Kγ (IC₅₀=8nM), PI3Kδ (IC₅₀=6nM), and mTOR (IC₅₀=1.4nM).
- GC15665Quercetin dihydrateCAS: 6151-25-3Purity: >98%
Quercetin dihydrate is the dihydrate form of the flavonoid quercetin, which possesses various biological activities.
- GC16154GDC-0941 dimethanesulfonateCAS: 957054-33-0Purity: >99.00%
A pan inhibitor of class I PI3K isoforms
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC15167 | KU-0063794 | 938440-64-3 | >99.00% | |
MTORC1 and mTORC2 inhibitor | ||||
| GC15310 | PI-3065 | 955977-50-1 | >99.50% | |
P110δkinase inhibitor | ||||
| GC15392 | Triciribine | 35943-35-2 | >98.50% | |
Triciribine is an adenosine analog that targets protein kinase B (Akt) with an IC 50 value of 130nM and has antitumor activity. | ||||
| GC15423 | GNE-493 | 1033735-94-2 | >98.00% | |
Pan-PI3K/mTOR inhibitor | ||||
| GC15425 | AR-A014418 | 487021-52-3 | >99.00% | |
A selective inhibitor of GSK3β | ||||
| GC15484 | Deguelin | 522-17-8 | >99.00% | |
Deguelin is one of four major naturally occurring rotenoids isolated from root extracts and is best recognized as a NADH: ubiquinone oxidoreductase (complex I) inhibitor, resulting in significant alterations in mitochondrial function. | ||||
| GC15508 | PI4KIII beta inhibitor 3 | 1245319-54-3 | >99.00% | |
| GC15540 | IC-87114 | 371242-69-2 | >98.50% | |
PI3Kδ inhibitor | ||||
| GC15553 | KP372-1 | 1374996-60-7 | >99.50% | |
specific Akt inhibitor | ||||
| GC15595 | GSK2269557 | 1254036-77-5 | >98% | |
inhibitor of PI3Kδ | ||||
| GC15615 | BX517(PDK1 inhibitor2) | 850717-64-5 | >98.00% | |
BX517(PDK1 inhibitor2) is a potent and selective inhibitor of PDK1 with IC50 of 6 nM. | ||||
| GC15642 | CHIR 99021 trihydrochloride | 1782235-14-6 | >99.00% | |
Laduviglusib (CHIR-99021) trihydrochloride is a potent and selective GSK-3α/β inhibitor with IC50s of 10 nM and 6.7 nM. CHIR 99021 trihydrochloride shows >500-fold selectivity for GSK-3 over CDC2, ERK2 and other protein kinases. CHIR 99021 trihydrochloride is also a potent Wnt/β-catenin signaling pathway activator. CHIR 99021 trihydrochloride enhances mouse and human embryonic stem cells self-renewal. CHIR 99021 trihydrochloride induces autophagy. | ||||
| GC15653 | PF-05212384 (PKI-587) | 1197160-78-3 | >98.00% | |
PF-05212384 (PKI-587) is a potent dual PI3K/mTOR inhibitor, exhibiting inhibitory effects against PI3Kα (IC₅₀=0.4nM), PI3Kβ (IC₅₀=6nM), PI3Kγ (IC₅₀=8nM), PI3Kδ (IC₅₀=6nM), and mTOR (IC₅₀=1.4nM). | ||||
| GC15665 | Quercetin dihydrate | 6151-25-3 | >98% | |
Quercetin dihydrate is the dihydrate form of the flavonoid quercetin, which possesses various biological activities. | ||||
| GC15679 | GSK2292767 | 1254036-66-2 | >98% | |
PI3Kδ inhibitor,potent and selective | ||||
| GC15680 | Perifosine | 157716-52-4 | >98.00% | |
Perifosine is an inhibitor of Akt . | ||||
| GC15740 | OXA-01 | 936889-68-8 | >98% | |
mTORC1 and mTORC2 inhibitor | ||||
| GC15841 | Alsterpaullone | 237430-03-4 | >98.00% | |
CDKs and GSK3β inhibitor | ||||
| GC15904 | PP242 | 1092351-67-1 | >98.50% | |
PP242 (PP 242) is a selective and ATP-competitive mTOR inhibitor with an IC50 of 8 nM. PP242 inhibits both mTORC1 and mTORC2 with IC50s of 30 nM and 58 nM, respectively. | ||||
| GC15935 | TGX-221 | 663619-89-4 | >99.50% | |
PI3Kβ inhibitor,potent,selective and ATP competitive | ||||
| GC16039 | LJH685 | 1627710-50-2 | >98.00% | |
RSK (p90 ribosomal S6 kinase) inhibitor | ||||
| GC16154 | GDC-0941 dimethanesulfonate | 957054-33-0 | >99.00% | |
A pan inhibitor of class I PI3K isoforms | ||||
| GC16157 | 740 Y-P | 1236188-16-1 | >98.00% | |
740 Y-P is a potent, cell-permeable activator of phosphoinositide 3-kinase (PI3K). | ||||
| GC16187 | GSK-3β Inhibitor II | 478482-75-6 | >98% | |
GSK-3β inhibitor | ||||
