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Home > Products
| Cat.No. | Product name | Product Description |
| R11939 | 2-amino-4,5,6,7-tetrahydrobenzothiophene-3-carboxamide | N/A |
| R11940 | (1S,2R,3S,5R)-2-(Benzyloxymethyl)-6-oxabicyclo[3.1.0]hexan-3-ol | N/A |
| R11941 | 3-Methoxy-4-morpholinoaniline Dihydrochloride | N/A |
| R11928 | RSV604 | RSV604 is a novel inhibitor of respiratory syncytial virus replication(EC50=0.86 |
| R11943 | 612829-88-6 | N/A |
| R11944 | 1H-CINNOLIN-4-ONE | N/A |
| R11942 | RIPA-56 | RIPA-56 is a highly potent, selective, and metabolically stable inhibitor of rec |
| R11945 | 4-(4-(4-bromophenyl)thiazol-2-yl)-2-propylpyridine | N/A |
| R11946 | LAZABEMIDE | N/A |
| R11948 | SHP-627 | FT011 is an anti-fibrotic agent, reduces mRNA expression of collagens I and III |
| R11947 | 4-(3-Methyl-5-oxo-2-pyrazolin-1-yl)benzoic acid | N/A |
| R11950 | TCS401 | TCS 401 is a selective inhibitor of protein tyrosine phosphatase 1B (PTP1B).&nbs |
| R11951 | AT-9283 L-lactate | AT9283 is a potent JAK2/3 inhibitor with IC50 of 1.2 nM/1.1 |
| R11952 | C188-9 | C188-9 is a Stat3 inhibitor, with a Kd of 4.7 nM. |
| R11953 | HG-9-91-01 (Synonyms: SIK inhibitor 1) | HG-9-91-01 is a potent and highly selective salt-inducible kinase (SIK) inhibito |
| R11954 | BD1063 dihydrochloride | BD1063 or 1-[2-(3,4-dichlorophenyl)ethyl]-4-methylpiperazine is a selective sigm |
| R11955 | JNJ-7706621 | JNJ-7706621 is a potent aurora kinase inhibitor, and also inhibits CDK1 and CDK2 |
| R11956 | GSK3326595 | N/A |
| R11957 | RESATORVID;TAK-242 | N/A |
| R11958 | Blu-285;Avapritinib | Avapritinib (BLU-285) is a highly potent, selective, and orally bioavailable KIT |
| R11959 | THZ2 | THZ2 is a potent and selective CDK7 inhibitor with an IC50 o |
| R11960 | THZ531 | THZ531 is a covalent inhibitor of both CDK12 and CDK13 with& |
| R11961 | KO-947 | KO-947 is a potent and selective inhibitor of ERK1/2 kinases with pote |
| R11963 | Lyn-IN-1 (Bafetinib analog) | Lyn-IN-1 (Bafetinib analog) is a potent and selective dual Bcr-Abl/Lyn inhibitor |
| R11964 | JNK-IN-8 | JNK-IN-8 is a potent JNK inhibitor with IC50s of 4.7 nM, 18.7 nM, |
