PI3K/Akt/mTOR Signaling
Research Areas
Products Related to PI3K/Akt/mTOR Signaling(719)
- GC467246-Hydroxypyridin-3-ylboronic AcidCAS: 903899-13-8Purity: >98.00%
A heterocyclic building block
- GC467387-Methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-amineCAS: 1032570-74-3Purity: >95.00%
A building block
- GC47328Everolimus-d4CAS: 1338452-54-2Purity: >99.00%
An internal standard for the quantification of everolimus
- GC48012PtdIns-(4,5)-P2-fluorescein (triethylammonium salt)Purity: >95.00%
A neuropeptide with diverse biological activities
- GC48027Rapamycin-d3CAS: 392711-19-2Purity: >≥98% deuterated forms (d1-d3)
An internal standard for the quantification of rapamycin
- GC48256VS-5584 analogCAS: 1246535-95-4Purity: >98.00%
VS-5584 analog is a dimethyl analog of VS-5584 which is an potent and selective mTOR/PI3K dual inhibitor with pyrido [2,3-d] pyrimidine structure.
- GC48507Kaempferol 3-O-galactosideCAS: 23627-87-4Purity: >98.00%
Kaempferol 3-O-galactoside (Trifolin) is a derivative of flavonoid, which is isolated from the aerial part of Consolida oliveriana.
- GC50009LY 294002 hydrochlorideCAS: 934389-88-5Purity: >98.00%
Prototypical PI 3-kinase inhibitor; also inhibits other kinases
- GC50332TC KHNS 11CAS: 1431540-99-6Purity: >98%
Potent and selective PI 3-kinase δ inhibitor; orally bioavailable
- GC60258MT 63-78CAS: 1179347-65-9Purity: >98.00%
MT 63-78 is a specific and potent direct AMPK activator with an EC50 of 25 μM. MT 63–78 also induces cell mitotic arrest and apoptosis. MT 63-78 blocks prostate cancer growth by inhibiting the lipogenesis and mTORC1 pathways. MT 63-78 has antitumor effects.
- GC60262N-FeruloyloctopamineCAS: 66648-44-0Purity: >98.50%
N-Feruloyloctopamine is an antioxidant constituent. N-Feruloyloctopamine significantly decreases thephosphorylationlevels of Akt and p38MAPK.
- GC60339SKI VCAS: 24418-86-8Purity: >98.00%
SKI V is a noncompetitive and potent non-lipid sphingosine kinase (SPHK; SK) inhibitor with an IC50 of 2 μM for GST-hSK. SKI V potently inhibits PI3K with an IC50 of 6 μM for hPI3k. SKI V decreases formation of the mitogenic second messenger sphingosine-1-phosphate (S1P). SKI V induces apoptosis and has antitumor activity.
- GC60782Disitertide TFAPurity: >96.00%
Disitertide TFA is a specific inhibitor of transforming growth factor β1 (TGF-β1) receptor type I.
- GC61045Metformin D6 hydrochlorideCAS: 1185166-01-1Purity: >98.00%
An internal standard for the quantification of metformin
- GC61227Quercetin D5CAS: 263711-78-0Purity: >99.00%
Quercetin D5 is a deuterated internal standard for the natural compound quercetin, its chemical structure is essentially the same as quercetin, except that five deuterium (D) atoms replace five hydrogen (H) atoms in the A ring.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC46531 | 2-Amino-5-bromo-6-chloropyrazine | 173253-42-4 | >98.00% | |
A heterocyclic building block | ||||
| GC46724 | 6-Hydroxypyridin-3-ylboronic Acid | 903899-13-8 | >98.00% | |
A heterocyclic building block | ||||
| GC46738 | 7-Methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-amine | 1032570-74-3 | >95.00% | |
A building block | ||||
| GC47328 | Everolimus-d4 | 1338452-54-2 | >99.00% | |
An internal standard for the quantification of everolimus | ||||
| GC48012 | PtdIns-(4,5)-P2-fluorescein (triethylammonium salt) | - | >95.00% | |
A neuropeptide with diverse biological activities | ||||
| GC48027 | Rapamycin-d3 | 392711-19-2 | >≥98% deuterated forms (d1-d3) | |
An internal standard for the quantification of rapamycin | ||||
| GC48256 | VS-5584 analog | 1246535-95-4 | >98.00% | |
VS-5584 analog is a dimethyl analog of VS-5584 which is an potent and selective mTOR/PI3K dual inhibitor with pyrido [2,3-d] pyrimidine structure. | ||||
| GC48507 | Kaempferol 3-O-galactoside | 23627-87-4 | >98.00% | |
Kaempferol 3-O-galactoside (Trifolin) is a derivative of flavonoid, which is isolated from the aerial part of Consolida oliveriana. | ||||
| GC48707 | MDK34597 | 371934-59-7 | >98.00% | |
MDK34597 (compound 35) is a potent PI3K p110α inhibitor with an pIC50 of 6.85. | ||||
| GC49392 | CHIR98024 | 556813-39-9 | >95.00% | |
A GSK3 inhibitor | ||||
| GC50009 | LY 294002 hydrochloride | 934389-88-5 | >98.00% | |
Prototypical PI 3-kinase inhibitor; also inhibits other kinases | ||||
| GC50072 | ETP 45658 | 1198357-79-7 | >98% | |
Potent PI 3-kinase inhibitor; also inhibits DNA-PK and mTOR | ||||
| GC50276 | LTURM 36 | 1879887-94-1 | >98% | |
PI 3-kinase δ inhibitor | ||||
| GC50332 | TC KHNS 11 | 1431540-99-6 | >98% | |
Potent and selective PI 3-kinase δ inhibitor; orally bioavailable | ||||
| GC52091 | 5,7-Dichlorothiazolo[5,4-d]pyrimidine | 13479-88-4 | >95.00% | |
A building block | ||||
| GC52387 | Crosstide (trifluoroacetate salt) | - | >95.00% | |
A peptide substrate for Akt | ||||
| GC52443 | Akt Substrate (trifluoroacetate salt) | - | >98.00% | |
An Akt peptide substrate | ||||
| GC60258 | MT 63-78 | 1179347-65-9 | >98.00% | |
MT 63-78 is a specific and potent direct AMPK activator with an EC50 of 25 μM. MT 63–78 also induces cell mitotic arrest and apoptosis. MT 63-78 blocks prostate cancer growth by inhibiting the lipogenesis and mTORC1 pathways. MT 63-78 has antitumor effects. | ||||
| GC60262 | N-Feruloyloctopamine | 66648-44-0 | >98.50% | |
N-Feruloyloctopamine is an antioxidant constituent. N-Feruloyloctopamine significantly decreases thephosphorylationlevels of Akt and p38MAPK. | ||||
| GC60339 | SKI V | 24418-86-8 | >98.00% | |
SKI V is a noncompetitive and potent non-lipid sphingosine kinase (SPHK; SK) inhibitor with an IC50 of 2 μM for GST-hSK. SKI V potently inhibits PI3K with an IC50 of 6 μM for hPI3k. SKI V decreases formation of the mitogenic second messenger sphingosine-1-phosphate (S1P). SKI V induces apoptosis and has antitumor activity. | ||||
| GC60782 | Disitertide TFA | - | >96.00% | |
Disitertide TFA is a specific inhibitor of transforming growth factor β1 (TGF-β1) receptor type I. | ||||
| GC61029 | Marein | 535-96-6 | >99.00% | |
A glucoside chalcone with diverse biological activities | ||||
| GC61045 | Metformin D6 hydrochloride | 1185166-01-1 | >98.00% | |
An internal standard for the quantification of metformin | ||||
| GC61227 | Quercetin D5 | 263711-78-0 | >99.00% | |
Quercetin D5 is a deuterated internal standard for the natural compound quercetin, its chemical structure is essentially the same as quercetin, except that five deuterium (D) atoms replace five hydrogen (H) atoms in the A ring. | ||||
