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| Cat.No. | Product name | Product Description |
| R10529 | Perifosine(KRX-0401; NSC 639966; D21266) | Perifosine (KRX-0401) is a novel Akt inhibitor with IC50 of 4.7 μM in MM.1S cell |
| R10554 | Ipatasertib;GDC-0068; RG7440 | Ipatasertib (GDC-0068) is a highly selective pan-Akt inhibitor targeting Akt1/2/ |
| R10601 | CGK733 | CGK 733 is a potent and selective inhibitor of ATM/ATR with IC50 of ~200 nM. |
| R10602 | AR-A014418 | AR-A014418 is an ATP-competitive, and selective GSK3β inhibitor with IC50 and Ki |
| R10607 | CAL-101;GS-1101 | CAL-101 (Idelalisib, GS-1101) is a selective p110δ inhibitor with IC50 of 2.5 nM |
| R10622 | Buparlisib Hydrochloride (BKM120 Hydrochloride) | NVP-BKM120 Hydrochloride is a selective PI3K inhibitor of p110 with IC50 of 52 n |
| R10626 | xL019; SAR245409 | Voxtalisib (SAR245409, XL765) is a dual inhibitor of mTOR/PI3K, mostly for p110γ |
| R10768 | KU-60019 | KU-60019 is an improved analogue of KU-55933, with IC50 of 6.3 nM for ATM in cel |
| R10871 | Dorsomorphin (Synonyms: BML-275; Compound C) | Dorsomorphin (Compound C) 2HCl is a potent, reversible, selective AMPK inhibitor |
| R10872 | Dorsomorphin dihydrochloride (Synonyms: BML-275 dihydrochloride; Compound C dihydrochloride) | Dorsomorphin (Compound C) 2HCl is a potent, reversible, selective AMPK inhibitor |
| R10868 | MK-2206 dihydrochloride | MK-2206 2HCl is a highly selective inhibitor of Akt1/2/3 with IC50 of 8 nM/12 nM |
| R10859 | Tacrolimus; FK506 | Tacrolimus (FK506) is a 23-membered macrolide lactone, it reduces peptidyl-proly |
| R10905 | XL147; SAR245408 | XL147 analogue is a selective and reversible class I PI3K inhibitor for PI3Kα/δ/ |
| R10907 | AMG319 | AMG319 is a potent and selective PI3Kδ inhibitor with IC50 of 18 nM, >47-fold |
| R10920 | HTH-01-015 | HTH-01-015 is a potent and selective NUAK1 inhibitor with IC50 of 100 nM, >10 |
| R10927 | Pilaralisib;SAR245408;XL147 | Pilaralisib (XL147) is a selective and reversible class I PI3K inhibitor for PI3 |
| R10957 | PI103 | PI-103 is a multi-targeted PI3K inhibitor for p110α/β/δ/γ with IC50 of 2 nM/3 nM |
| R10958 | AS605240 | AS-605240 selectively inhibits PI3Kγ with IC50 of 8 nM, over 30-fold and 7.5-fol |
| R10969 | HS-173 | HS-173 is a potent PI3Kα inhibitor with IC50 of 0.8 nM. |
| R10977 | PIK-294 | PIK-294 is a highly selective p110δ inhibitor with IC50 of 10 nM, 1000-, 49- and |
| R11026 | CT98014 | CHIR-98014 is a potent GSK-3α/β inhibitor with IC50 of 0.65 nM/0.58 nM in cell-f |
| R11555 | Ly2584702 | LY2584702 is a selective, ATP-competitive p70S6K inhibitor with IC50 of 4 nM. Ph |
| R11565 | NU7026 | NU7026 is a potent DNA-PK inhibitor with IC50 of 0.23 μM in |
| R11608 | Mirin | Mirin is a potent Mre11–Rad50–Nbs1 (MRN) complex inhibitor, and inhibits Mre11-a |
| R11896 | deguelin | Deguelin, a naturally occurring rotenoid, is a potent PI3K/AKT inhibit |
