PI3Kα-IN-9
Modify Date: 2024-01-11 17:21:38
PI3Kα-IN-9 structure
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Common Name | PI3Kα-IN-9 | ||
|---|---|---|---|---|
| CAS Number | 2715287-67-3 | Molecular Weight | 383.40 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C18H21N7O3 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of PI3Kα-IN-9PI3Kα-IN-9 (compound 27) is a selective, long-acting and oral active PI3Kα inhibitor with IC50 values of 4.4, 128, 146 and 153 nM for PI3Kα, PI3Kγ, PI3Kδ and PI3Kβ, respectively. PI3Kα-IN-9 has antiproliferative activity and induces apoptosis. PI3Kα-IN-9 can be used for cancer research[1]. |
| Name | PI3Kα-IN-9 |
|---|
| Description | PI3Kα-IN-9 (compound 27) is a selective, long-acting and oral active PI3Kα inhibitor with IC50 values of 4.4, 128, 146 and 153 nM for PI3Kα, PI3Kγ, PI3Kδ and PI3Kβ, respectively. PI3Kα-IN-9 has antiproliferative activity and induces apoptosis. PI3Kα-IN-9 can be used for cancer research[1]. |
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| Related Catalog | |
| Target |
PI3Kα:4.4 nM (IC50) PI3Kβ:153 nM (IC50) PI3Kδ:146 nM (IC50) PI3Kγ:128 nM (IC50) |
| In Vitro | PI3Kα-IN-9 (compound 27) (0-8 μM; 72 hours; cancer cell lines) has antiproliferative activity and induces apoptosis[1]. PI3Kα-IN-9 (compound 27) (0-8 μM; MGC-803 cells) down-regulates the expression of PI3Kα protein, the proteins of PI3K downstream, p-AKT and p-P70S6 K[1]. Cell Viability Assay[1] Cell Line: MGC-803 (gastric cancer), SKOV-3 (ovarian cancer), PC-3(prostate cancer), MCF-7 (breast cancer), MDA-MB-231 (triple-negative breast cancer), HepG2 (liver cancer), RPMI8226 (multiple myeloma), K562 (chronic myeloid leukemia), U251 (glioma) and MOLT-4 (acute lymphoblastic leukemia) cell lines Concentration: 0-2 μM Incubation Time: 72 hours Result: Inhibited the growth of a variety of cancer cells with IC50 values ranging from 0.43 to 1.33 μM. Apoptosis Analysis[1] Cell Line: MGC-803 cells Concentration: 0, 2, 4 and 8 μM Incubation Time: 36 hours Result: Increased the percentage of apoptotic cells from 12.07 to 61.69% in a dose-dependent manner. |
| In Vivo | PI3Kα-IN-9 (compound 27) (1-10 mg/kg; p.o. and i.v.; for 24 hours; male Sprague-Dawley rat) has favorable stability (T1/2>10 h) and high bioavailability (130%)[1]. PI3Kα-IN-9 (compound 27) (30 mg/kg; p.o.; daily, for 3 weeks; male BALB/c nude mice) has antitumor activity and low cytotoxicity[1]. Animal Model: Male Sprague-Dawley rat[1] Dosage: 1 and 10 mg/kg Administration: Oral administration and intravenous injection; for 24 hours (Pharmacokinetic Analysis) Result: 1.19 parameters IV PO dose (mg/kg) 1 10 T1/2 (h) 6.29 ﹥10 Tmax (h) 0.003 9.33 Cmax (ng/mL) 454.7 2256.7 AUC0-t (ng·h/mL) 2237 36697 AUC0-∞ (ng·h/mL) 2922.4 38114.3 CL (mL/h/kg) 343 F % 130.4 Animal Model: Male BALB/c nude mice[1] Dosage: 30 mg/kg Administration: Oral administration; daily, for 3 weeks Result: Inhibited tumor growth with a tumor growth inhibition (TGI) rate of 41.5%. |
| References |
| Molecular Formula | C18H21N7O3 |
|---|---|
| Molecular Weight | 383.40 |