PI3K/Akt/mTOR Signaling
Research Areas
Products Related to PI3K/Akt/mTOR Signaling(719)
- GC107103-MethyladenineCAS: 5142-23-4Purity: >98.00%
3-Methyladenine is a PI3K inhibitor with IC 50 values of 25μM and 60μM for Vps34 and PtdIns3Kγ, respectively.
- GC10860Acalisib (GS-9820)CAS: 870281-34-8Purity: >99.50%
Acalisib (GS-9820) is a potent and selective PI3Kδ inhibitor with an IC50 of 12.7 nM.
- GC10918AT7867 dihydrochlorideCAS: 1431697-86-7Purity: >99.00%
A potent and orally bioavailable pan-Akt inhibitor
- GC11177GDC-0980 (RG7422)CAS: 1032754-93-0Purity: >98.00%
GDC-0980 (RG7422) (GDC-0980; GNE 390; RG 7422) is a selective, potent, orally bioavailable Class I PI3 kinase and mTOR kinase (TORC1/2) inhibitor with IC50s of 5 nM/27 nM/7 nM/14 nM for PI3Kα/PI3Kβ/PI3Kδ/PI3Kγ, and with aKiof 17 nM for mTOR.
- GC11190AMPK activatorCAS: 849727-81-7Purity: >98%
AMPK activator is a cell penetrant AMPK activator and partially inhibits the mitochondrial complex I. In multiple myeloma cells, AMPK activator inhibits cell growth.
- GC11214GDC-0068 (RG7440)CAS: 1001264-89-6Purity: >98.00%
GDC-0068 (RG7440) is an orally active, highly selective and ATP-competitive pan-Akt inhibitor with IC 50 values of 5, 18, 8nM for Akt1, Akt2, and Akt3, respectively.
- GC11325CX-4945 sodium saltCAS: 1309357-15-0Purity: >99.50%
CX-4945 sodium salt is an orally bioavailable, highly selective and potent CK2 inhibitor, with IC50 values of 1 nM against CK2α and CK2α'.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC10463 | SB 216763 | 280744-09-4 | >99.00% | |
SB 216763 stands out as a powerful, selective, and ATP-competitive inhibitor of GSK-3, effectively targeting both GSK-3α and GSK-3β with an impressive IC 50 of 34.3 nM [1-3] . | ||||
| GC10518 | AICAR | 2627-69-2 | >99.00% | |
AICAR (also called acadesine) is a purine nucleoside. | ||||
| GC10573 | L803-mts | 1043881-55-5 | >98% | |
Selective peptide inhibitor of glycogen synthase kinase-3 (GSK-3) | ||||
| GC10649 | TTP 22 | 329907-28-0 | >98.00% | |
A CK2 inhibitor | ||||
| GC10662 | WYE-354 | 1062169-56-5 | >98.00% | |
MTOR inhibitor,potent,ATP-competitive and cell-permeable | ||||
| GC10710 | 3-Methyladenine | 5142-23-4 | >98.00% | |
3-Methyladenine is a PI3K inhibitor with IC 50 values of 25μM and 60μM for Vps34 and PtdIns3Kγ, respectively. | ||||
| GC10752 | Bikinin | 188011-69-0 | >99.50% | |
Bikinin is a non-steroidal, ATP-competitive inhibitor of plant GSK-3 (glycogen synthase kinase 3)/Shaggy-like kinases. | ||||
| GC10812 | Compound 401 | 168425-64-7 | >99.50% | |
DNA-PK and mTOR inhibitor | ||||
| GC10857 | UCN-01 | 112953-11-4 | >98% | |
inhibitor of Akt, protein kinase C, PDK1 and cyclin-dependent kinases | ||||
| GC10860 | Acalisib (GS-9820) | 870281-34-8 | >99.50% | |
Acalisib (GS-9820) is a potent and selective PI3Kδ inhibitor with an IC50 of 12.7 nM. | ||||
| GC10900 | GDC-mTOR inhibitor | 1207358-59-5 | >99.00% | |
| GC10918 | AT7867 dihydrochloride | 1431697-86-7 | >99.00% | |
A potent and orally bioavailable pan-Akt inhibitor | ||||
| GC11003 | PP121 | 1092788-83-4 | >99.00% | |
Dual inhibitor of tyrosine and phosphoinositide kinases | ||||
| GC11018 | GSK1059615 | 958852-01-2 | >98.00% | |
PI3K and mTOR inhibitor,potent and reversible | ||||
| GC11135 | CAL-130 Hydrochloride | 1431697-78-7 | >99.50% | |
| GC11165 | PI-103 | 371935-74-9 | >98.00% | |
PI-103 is a potent cell-permeable multi-target inhibitor that primarily acts on the PI3K and mTOR signaling pathways. | ||||
| GC11177 | GDC-0980 (RG7422) | 1032754-93-0 | >98.00% | |
GDC-0980 (RG7422) (GDC-0980; GNE 390; RG 7422) is a selective, potent, orally bioavailable Class I PI3 kinase and mTOR kinase (TORC1/2) inhibitor with IC50s of 5 nM/27 nM/7 nM/14 nM for PI3Kα/PI3Kβ/PI3Kδ/PI3Kγ, and with aKiof 17 nM for mTOR. | ||||
| GC11190 | AMPK activator | 849727-81-7 | >98% | |
AMPK activator is a cell penetrant AMPK activator and partially inhibits the mitochondrial complex I. In multiple myeloma cells, AMPK activator inhibits cell growth. | ||||
| GC11214 | GDC-0068 (RG7440) | 1001264-89-6 | >98.00% | |
GDC-0068 (RG7440) is an orally active, highly selective and ATP-competitive pan-Akt inhibitor with IC 50 values of 5, 18, 8nM for Akt1, Akt2, and Akt3, respectively. | ||||
| GC11234 | A-769662 | 844499-71-4 | >98.50% | |
A-769662 is an activator of AMP-activated protein kinase, which has an EC 50 value of 0.8μM. | ||||
| GC11248 | AZD8835 | 1620576-64-8 | >98.50% | |
PI3Kα and PI3Kδ inhibitor | ||||
| GC11325 | CX-4945 sodium salt | 1309357-15-0 | >99.50% | |
CX-4945 sodium salt is an orally bioavailable, highly selective and potent CK2 inhibitor, with IC50 values of 1 nM against CK2α and CK2α'. | ||||
| GC11471 | SAR405 | 1523406-39-4 | >98.00% | |
SAR405 is a highly selective, ATP-competitive class III phosphoinositide 3-kinase (PIK3C3/Vps34) inhibitor with an IC 50 value of 1.2nM. | ||||
| GC11515 | TCS 184 | 1315378-71-2 | >98% | |
Scrambled control peptide for use with TCS 183 | ||||
