11 Results for "

PI3Kδ-IN-1

" in MedChemExpress (MCE) Product Catalog:
Products (11)

11 Results for "PI3Kδ-IN-1" in MCE Product Catalog:

Cat. No.: HY-101921
CAS No.: 1911564-39-0
Purity:  99.60%
Target:  

PI3K

Research Areas:  

Inflammation/Immunology

PI3Kδ-IN-1 is a potent, selective, and efficacious PI3Kδ inhibitor with an IC50 of 1.7 nM.
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3
3 Cited Publications
Cat. No.: HY-143404
CAS No.: 2281803-22-1
Purity:  98.19%
Target:  

PI3K

Research Areas:  

Cancer

PI3K-IN-30 (compound 6d) is a potent PI3K inhibitor with IC50s of 5.1, 136, 30.7 and 8.9 nM for PI3Kα, PI3Kβ, PI3Kγ and PI3Kδ, respectively .
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Cat. No.: HY-112443
CAS No.: 2132961-46-5
Purity:  99.71%
Target:  

PI3K

AZD3458 is a potent and remarkably selective PI3Kγ inhibitor with pIC50s of 9.1, 5.1, <4.5, and 6.5 for PI3Kγ, PI3Kα, PI3Kβ, and PI3Kδ, respectively .
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Cat. No.: HY-176239
Research Areas:  

Cancer

PROTAC PI3Kδ degrader-1 is a Lysine-targeted covalent PI3Kδ PROTAC degrader with a DC50 of 3.98 nM. PROTAC PI3Kδ degrader-1 has a potent antiproliferative activity and selective PI3Kδ inhibition (IC50: 8 nM). PROTAC PI3Kδ degrader-1 also significantly degrades p-AKT, induces cell cycle arrest in G1 phase and prompts cell apoptosis and autophagy. PROTAC PI3Kδ degrader-1 effectively inhibits the tumor growth in SU-DHL-6 xenograft mice model .
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Cat. No.: HY-101921R
CAS No.: 1911564-39-0
Research Areas:  

Inflammation/Immunology

PI3Kδ-IN-1 (Standard) is the analytical standard of PI3Kδ-IN-1 (HY-101921). This product is intended for research and analytical applications. PI3Kδ-IN-1 is a potent, selective, and efficacious PI3Kδ inhibitor with an IC50 of 1.7 nM.
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Cat. No.: HY-W040417
CAS No.: 155905-77-4
Target:  

PI3K

Research Areas:  

Others

Boc-L-cyclobutylglycine is a Boc-protected L-cyclic amino acid and synthetic intermediate in the preparation of purinyl quinazolinone PI3Kδ inhibitors .
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Cat. No.: HY-40029
CAS No.: 625471-18-3
Synonyms: (S)-(+)-3-AmINo-1-boc-PIperidINe
(S)-1-Boc-3-aminopiperidine is a key intermediate for the synthesis of various novel inhibitors, such as CHK1 inhibitors and PI3Kδ inhibitors .
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Cat. No.: HY-15288
CAS No.: 1332075-63-4
Target:  

PI3K

Research Areas:  

Cancer

PI3kδ inhibitor 1 is a potent and selective PI3Kδ inhibitor with an IC50 of 3.8 nM.
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Cat. No.: HY-113572
CAS No.: 1012327-63-7
Target:  

PI3K

Research Areas:  

Cancer

PX-866-17OH is the metabolite of PX-866 (Sonolisib, HY-N6775) and a pan-isoform inhibitor of PI3K with IC50s of 14, 57, 131, and 148 nM against PI3Kα, PI3Kβ, PI3K , and PI3Kδ, respectively .
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Cat. No.: HY-147285
CAS No.: 1392421-71-4
Target:  

mTOR PI3K

Research Areas:  

Neurological Disease

PI3K/mTOR Inhibitor-9 (Compound 1) is a potent mTOR and PI3K inhibitor with IC50 values of 38 nM, 6.6 μM, 6.6 μM and 0.8 μM against mTOR (phospho-S6 cellular assay), PI3Kα, PI3Kγ and PI3Kδ, respectively .
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Cat. No.: HY-W937057
CAS No.: 2638512-56-6
Research Areas:  

Cancer

(S,R,S)-AHPC-Me-10-bromodecanoic acid is an E3 ligase ligand-linker conjugate that incorporates a VHL ligand 2 (HY-112078) and linker 10-bromoheptanoic acid. (S,R,S)-AHPC-Me-10-bromodecanoic acid can be used for synthesis of PROTAC PI3Kδ degrader-1 (HY-176239) .
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