PI3K/Akt/mTOR Signaling
Research Areas
Products Related to PI3K/Akt/mTOR Signaling(719)
- GC80871IsopsoralidinCAS: 3564-61-2Purity: >98.00%
Isopsoralidin is a phosphatidylinositol 3-kinase ( PI3K ) inhibitor with potential hepatotoxicity and CYP2D6 inhibitory activity [1] .
- GC80872PDKtide TFAPurity: >98.50%
PDKtide TFA, a biological active peptide, is a substrate for phosphatidylinositide-dependent kinase 1 ( PDK1 ) [1] .
- GC80873Tovophyllin ACAS: 40738-44-1Purity: >98%
Tovophyllin A is an orally active xanthonoid compound.
- GC81027PROTAC HIF-1α degrader-2CAS: 3095636-64-6Purity: >98%
PROTAC HIF-1α degrader-2 is a highly efficient and selective PROTAC degrader targeting HIF-1α. PROTAC HIF-1α degrader-2 promotes HIF-1α degradation via the ubiquitin-proteasome pathway by facilitating the formation of a HIF-1α/VHL ternary complex.
- GC81042PI3K/mTOR ligand-1CAS: 1197160-66-9Purity: >97.00%
PI3K/mTOR ligand-1 is a ligand for the target protein of PROTAC ( PI3K / mTOR ).
- GC81323PDGFRA/CAIX/XII-IN-1Purity: >98.00%
PDGFRA/CAIX/XII-IN-1 is an inhibitor of PDGFRA, CA IX and CA XII, with an IC 50 of 20 nM against PDGFRA, a K i of 93.3 nM against CA IX, and a K i of 80.0 nM against CA XII.
- GC81325VEGFR2-IN-84CAS: 861877-12-5Purity: >98%
VEGFR2-IN-84 is an orally active, multi-targeted tyrosine kinase inhibitor based on a naphthalene ring scaffold.
- GC81556FZ1 peptidePurity: >99.50%
FZ1 peptide is a cyclic heptapeptide and also an integrin αvβ3 agonist.
- GC81606DX-8951 Hydroxy-acid sodiumPurity: >98.50%
DX-8951 Hydroxy-acid sodium is a prodrug of phosphoramide.
- GC81682Sialorphin TFAPurity: >97.00%
Sialorphin TFA is a neutral endopeptidase ( NEP ) and aminopeptidase N ( APN ) inhibitor that responds to androgen signals.
- GC81862YJ1206 TFAPurity: >98.00%
YJ1206 TFA is an orally active selective CDK12 / CDK13 PROTAC degrader.
- GC81873Ciprofloxacin hydrochlorideCAS: 86483-48-9Purity: >98.00%
Ciprofloxacin hydrochloride (Bay-09867 hydrochloride) is an orally active, blood-brain barrier permeable fluoroquinolone antibacterial agent.
- GC81892Vevorisertib tetrahydrochloridePurity: >98.00%
Vevorisertib tetrahydrochloride (ARQ 751 tetrahydrochloride) is an orally active allosteric AKT inhibitor that blocks AKT phosphorylation.
- GC903765-Bromopentanoic Acid-d4CAS: 42932-62-7Purity: >99.00%
An internal standard for the quantification of 5-bromopentanoic acid
- GC90702Triciribine PhosphateCAS: 61966-08-3Purity: >95.00%
An Akt activation inhibitor and active metabolite of triciribine
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC80871 | Isopsoralidin | 3564-61-2 | >98.00% | |
Isopsoralidin is a phosphatidylinositol 3-kinase ( PI3K ) inhibitor with potential hepatotoxicity and CYP2D6 inhibitory activity [1] . | ||||
| GC80872 | PDKtide TFA | - | >98.50% | |
PDKtide TFA, a biological active peptide, is a substrate for phosphatidylinositide-dependent kinase 1 ( PDK1 ) [1] . | ||||
| GC80873 | Tovophyllin A | 40738-44-1 | >98% | |
Tovophyllin A is an orally active xanthonoid compound. | ||||
| GC80874 | ARN25699 | - | >98% | |
ARN25699 is a kinase inhibitor with an IC 50 of 5.5 nM against GSK-3β, 2.2 nM against FYN-α, and 242.3 nM against DYRK1A, and it exhibits oral bioavailability. | ||||
| GC81027 | PROTAC HIF-1α degrader-2 | 3095636-64-6 | >98% | |
PROTAC HIF-1α degrader-2 is a highly efficient and selective PROTAC degrader targeting HIF-1α. PROTAC HIF-1α degrader-2 promotes HIF-1α degradation via the ubiquitin-proteasome pathway by facilitating the formation of a HIF-1α/VHL ternary complex. | ||||
| GC81041 | GP262 | 3107761-81-6 | >98.50% | |
GP262 is a PI3K/mTOR PROTAC degrader targeting PI3Kγ, PI3Kα and mTOR with DC 50 values of 42.23 nM, 227.4 nM and 45.4 nM, respectively in MDA-MB-231 cells. | ||||
| GC81042 | PI3K/mTOR ligand-1 | 1197160-66-9 | >97.00% | |
PI3K/mTOR ligand-1 is a ligand for the target protein of PROTAC ( PI3K / mTOR ). | ||||
| GC81323 | PDGFRA/CAIX/XII-IN-1 | - | >98.00% | |
PDGFRA/CAIX/XII-IN-1 is an inhibitor of PDGFRA, CA IX and CA XII, with an IC 50 of 20 nM against PDGFRA, a K i of 93.3 nM against CA IX, and a K i of 80.0 nM against CA XII. | ||||
| GC81324 | FGF7p | 2758194-43-1 | >99.00% | |
FGF7p is a small molecule peptide and a potential bladder protector. | ||||
| GC81325 | VEGFR2-IN-84 | 861877-12-5 | >98% | |
VEGFR2-IN-84 is an orally active, multi-targeted tyrosine kinase inhibitor based on a naphthalene ring scaffold. | ||||
| GC81443 | E8431 | 2419580-01-9 | >97.00% | |
E8431 is a DCSTAMP antagonist with an IC 50 value of 775.8 nM for osteoclastogenesis. | ||||
| GC81453 | FOXM1-IN-3 | - | >98% | |
FOXM1-IN-3 is a potent FOXM1 inhibitor. | ||||
| GC81556 | FZ1 peptide | - | >99.50% | |
FZ1 peptide is a cyclic heptapeptide and also an integrin αvβ3 agonist. | ||||
| GC81606 | DX-8951 Hydroxy-acid sodium | - | >98.50% | |
DX-8951 Hydroxy-acid sodium is a prodrug of phosphoramide. | ||||
| GC81609 | YHV98-4 | 132858-26-5 | >98.00% | |
YHV98-4 is a selective, blood-brain barrier-permeable Hv1 inhibitor with an IC 50 of 0.7 μM. | ||||
| GC81682 | Sialorphin TFA | - | >97.00% | |
Sialorphin TFA is a neutral endopeptidase ( NEP ) and aminopeptidase N ( APN ) inhibitor that responds to androgen signals. | ||||
| GC81684 | CK37 | 1001478-90-5 | >98% | |
CK37 is a competitive choline kinase-α inhibitor. | ||||
| GC81846 | Nivitol | 869743-37-3 | >98.00% | |
Nivitol (UP302) is a natural phenolic compound discovered from Dianella ensifolia and also acts as a Tyrosinase inhibitor. | ||||
| GC81862 | YJ1206 TFA | - | >98.00% | |
YJ1206 TFA is an orally active selective CDK12 / CDK13 PROTAC degrader. | ||||
| GC81873 | Ciprofloxacin hydrochloride | 86483-48-9 | >98.00% | |
Ciprofloxacin hydrochloride (Bay-09867 hydrochloride) is an orally active, blood-brain barrier permeable fluoroquinolone antibacterial agent. | ||||
| GC81892 | Vevorisertib tetrahydrochloride | - | >98.00% | |
Vevorisertib tetrahydrochloride (ARQ 751 tetrahydrochloride) is an orally active allosteric AKT inhibitor that blocks AKT phosphorylation. | ||||
| GC90376 | 5-Bromopentanoic Acid-d4 | 42932-62-7 | >99.00% | |
An internal standard for the quantification of 5-bromopentanoic acid | ||||
| GC90702 | Triciribine Phosphate | 61966-08-3 | >95.00% | |
An Akt activation inhibitor and active metabolite of triciribine | ||||
| GC91100 | UCL-TRO-1938 | 2919575-27-0 | >98.00% | |
An allosteric PI3Kα activator | ||||
