10 Results for "

p4EBP1

" in MedChemExpress (MCE) Product Catalog:
Products (10)

10 Results for "p4EBP1" in MCE Product Catalog:

8
8 Cited Publications
Cat. No.: HY-132168
CAS No.: 2382768-62-7
Pureté:  99.94%
Target:  

mTOR

Domaines de recherche:  

Cancer

RMC-5552 is a potent and selective mTORC1 inhibitor. RMC-5552 inhibits phosphorylation of mTORC1 pS6K and p4EBP1 with IC50s of 0.14 nM and 0.48 nM, respectively. RMC-5552 shows much lower pAKT inhibition (IC50 of 19 nM), resulting in mTORC1/mTORC2 selectivity approaching 40-fold. RMC-5552 has anti-cancer activity .
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Cat. No.: HY-W348485
CAS No.: 899937-47-4
Target:  

mTOR

Domaines de recherche:  

Cancer

WRX606 is an orally active nonrapalog inhibitor for mTOR complex 1 (mTORC1M). WRX606 inhibits the phosphorylation of mTORC1 substrate S6 kinase 1 (S6K1) (IC50 = 10 nM) and eukaryotic translation initiation factor 4E binding protein (p-4E-BP1) (IC50 = 0.27 μM) in MCF-7 cells. WRX606 suppresses tumor growth in mice without promotion of metastasis. WRX606 can be studied in research as an antitumor agent .
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Cat. No.: HY-115590
CAS No.: 1902983-63-4
Domaines de recherche:  

Cancer

JP-11646 is a pan-PIM inhibitor with increased potency against PIM2 (IC50 = 0.5 nM). JP11646 is freely reversible and ATP non-competitive. JP-11646 results in a decrease of PIM1, 2, and 3 mRNA. JP-11646 can effectively inhibit cell viability in small cell lung cancer (SCLC) and large cell neuroendocrine carcinomas of the lung (LCNEC). JP-11646 can cause a decrease in p-4EBP-1 protein, increasing the cleavage of caspases while decreasing caspase-3. JP-11646 induces apoptosis or necroptosis in cells. JP-11646 leads to reductions in MYC paralogs. JP-11646 can be used for the study of SCLC, LCNEC, human acute leukemia (AML), multiple myeloma (MM), and triple-negative breast cancer (TNBC) .
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Cat. No.: HY-134903
CAS No.: 2382768-55-8
Pureté:  95.41%
Target:  

mTOR

Domaines de recherche:  

Cancer

(32-Carbonyl)-RMC-5552 is a potent mTOR inhibitor. (32-Carbonyl)-RMC-5552 inhibits mTORC1 and mTORC2 substrate (p-P70S6K-(T389), p-4E-BP1-(T37/36), AND p-AKT1/2/3-(S473)) phosphorylation with pIC50s of > 9, >9 and between 8 and 9, respectively (patent WO2019212990A1, example 2) .
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Cat. No.: HY-124348
CAS No.: 701947-53-7
Synonyms: 3,5-Dimethyl PIT-1
Target:  

PI3K

Domaines de recherche:  

Cancer

DM-PIT-1 is a PIP3/PH (phosphatidylinositol-3,4,5-triphosphate/Pleckstrin) interaction inhibitor. DM-PIT-1 decreases he expression of P-Akt, P-GSK-3-β, P-p70S6K, P-S6, P-4E-BP1. DM-PIT-1 induces apoptosis and shows anticancer activity. DM-PIT-1 has the potential for the research of ovarian cancer .
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Cat. No.: HY-111370
CAS No.: 2219323-96-1
Target:  

mTOR

Domaines de recherche:  

Cancer

mTOR inhibitor-2 is a highlt potent, selective and oral mTOR inhibitor with an IC50 of 7 nM. mTOR inhibitor-2 inhibits cellular phosphorylation of mTORC1 (pS6 and p4E-BP1) and mTORC2 (pAKT (S473)) substrates .
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Cat. No.: HY-115869
CAS No.: 2250059-27-7
Target:  

mTOR

Domaines de recherche:  

Cancer

RMC-4529 has an IC50 value of 1.0 nM against p-4E-BP1-(T37/46) in mTOR kinase cellular assay.
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Cat. No.: HY-189376
CAS No.: 3105699-76-8
Target:  

mTOR Autophagy

Domaines de recherche:  

Cancer

IMHDPA-4-OH is an mTORC1 inhibitor and autophagy inducer. IMHDPA-4-OH inhibits mTORC1 signaling and reduces p70S6K and p4EBP1 phosphorylation, thereby relieving the autophagy blockade. IMHDPA-4-OH interferes with cholesterol metabolism and induces cell cycle arrest at G0. IMHDPA-4-OH can be used for research on cervical cancer .
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Cat. No.: HY-176948
CAS No.: 1887095-86-4
Target:  

mTOR

Domaines de recherche:  

Cancer

M-1111 is a Rapa-Link inhibitor. M-1111 is covalently linked by Rapamycin (HY-10219) and an inhibitor of the active site mTOR. M-1111 has strong inhibitory activity on the mTORC1 signaling pathway (pS6 and p4E-BP1). M-1111 has nanomolar-level inhibitory activity against various cancer cells. M-1111 completely inhibits p4E-BP1 without inhibiting pAkt S473. M-1111 can be used for research on liver cancer, kidney cancer, and colorectal cancer .
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Cat. No.: HY-182957
CAS No.: 3081482-46-1
Domaines de recherche:  

Cancer

MNK/PIM-IN-2 is a Mnk/Pim kinase inhibitor with an IC50 of 32 nM for Mnk1, 3 nM for Mnk2, and 37 nM for Pim1. MNK/PIM-IN-2 reduces the levels of p-eIF4E and p-4EBP1. MNK/PIM-IN-2 induces cell cycle arrest, apoptosis (apoptosis) and exerts antiproliferative effects in leukemia cells. MNK/PIM-IN-2 can be used in studies related to leukemia .
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