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| Cat.No. | Product name | Product Description |
| R2032898 | AS1842856 | AS1842856, a specific Foxo1 inhibitor (IC50=30 nM), potently suppresses autophag |
| R2032899 | BIBS39 | BIBS 39 is a new nonpeptide angiotensin II (AII) receptor antagonist.Target: Ang |
| R2032900 | CCT245737 | CCT245737 is an orally active and seletive Chk1 inhibitor, with an IC50 of 1.3 n |
| R2032901 | Grapiprant | Grapiprant (CJ-023423) is a selective EP4 receptor antagonist whose physiologica |
| R2032902 | HG-14-10-04 | HG-14-10-04 is a potent and specific ALK inhibitor with IC50 of 20 nM.IC50 value |
| R2032903 | WNK463 | WNK463 is an orally bioavailable pan-With-No-Lysine (K) (WNK)-kinase inhibitor w |
| R2032904 | AZD5153 | AZD5153 6-Hydroxy-2-naphthoic acid is the 6-Hydroxy-2-naphthoic acid of AZD5153. |
| R2032905 | GGTI298 Trifluoroacetate | GGTI298 Trifluoroacetate is a CAAZ peptidomimetic geranylgeranyltransferase I (G |
| R2032906 | INF39 | INF39 is an irreversible and noncytotoxic NLRP3 inhibitor. |
| R2032907 | ML213 | ML213 is a selective activator of Kv7.2 and Kv7.4 channels, enhances Kv7.2 and K |
| R2032908 | NCB-0846 | NCB-0846 is an orally available TNIK inhibitor with an IC50 of 21 nM. |
| R2032909 | Sapacitabine | Sapacitabine is an orally available nucleoside analog prodrug that is structural |
| R2032910 | STAT5 | STAT5-IN-1 is a STAT5 inhibitor with an IC50 of 47 μM for STAT5β isoform. |
| R2032911 | TM5441 | TM5441 is an orally bioavailable inhibitor of plasminogen activator inhibitor-1 |
| R2032912 | A-1331852 | A-1331852 is an orally available BCL-XL selective inhibitor with a Ki of less th |
| R2032913 | AMG-3969 | AMG-3969 is a potent glucokinase-glucokinase regulatory protein interaction (GK- |
| R2032914 | Belizatinib(TSR011) | Belizatinib is an oral, dual, potent inhibitor of ALK and TRKA, TRKB, and TRKC, |
| R2032915 | BI605906 | BI605906 is a novel IKKβ inhibitor with an IC50 value of 380 nM when assayed at |
| R2032916 | BMS378806 | BMS-378806 is a potent HIV-1 attachment inhibitor that interferes with CD4-gp120 |
| R2032917 | BMS-986020 | BMS-986020 is a high-affinity and selective lysophosphatidic acid receptor 1 (LP |
| R2032918 | Cenerimod(ACT-334441) | Cenerimod (ACT-334441) is a potent and orally available sphingosine 1-phosphate |
| R2032919 | CZC25146 | CZC-25146 is a potent, selective and metabolically stable LRRK2 inhibitor with I |
| R2032920 | ETP-46321 | ETP-46321 is a potent and orally bioavailable PI3Kα and PI3Kδ inhibitor with Kia |
| R2032921 | JPH203 | JPH203 is a potent and selective L-type amino acid transporter 1 (LAT-1) inhibit |
| R2032922 | Q203 | Q203 (IAP6) is a midazopyridine amide compound.Q203 is active against Mycobacter |
