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Cat.No. | Product name | Product Description |
R21082365 | TPEN | TPEN is a specific heavy metal chelating agent that is permeable to cells. |
R21082366 | Idelalisib | CAL-101 is a selective inhibitor of p110δ(IC50 : 2.5 nM; in cell-free assays); s |
R21082367 | Radezolid | Radezolid is an oxazolidone antibiotic. |
R21082368 | ITE | ITE is a potent endogenous aromatic hydrocarbon receptor (AhR) agonist that bind |
R21082369 | IRAK-1/4 INHIBITOR I | Irak-1 -4 Inhibitor I is AN IRAK1/4 Inhibitor with IC50 of 0.2 μM and 0.3 μM, re |
R21082370 | GSK-189254 | GSK 189254A is a histamine H3 receptor antagonist for the treatment of narcoleps |
R21082371 | E7449 | E7449 is an effective inhibitor of PARP1 and PARP2, and can inhibit the activity |
R21082372 | AZD-9362 | AZD-9362 is dual IGF-IR/InsR inhibitor. |
R21082373 | Debio 0617B | Debio 0617B has been developed as a first-in-class kinase inhibitor with a uniqu |
R21082374 | SH5-07 | Sh5-07 is a Stat3 inhibitor based on hydroxamic acid with an IC50 value of 3.9 μ |
R21082375 | BP-1-102 | Bp-1-102 is a small molecule inhibitor of the orally active transcription factor |
R21082376 | Prucalopride | Prucalopride (R093877) is a high-affinity 5-HT4 receptor agonist with a pKi of 8 |
R21082377 | GK921 | GK921 is an inhibitor of transglutaminase 2 (TGase2). The IC50 value of recombin |
R21082378 | SB408124 | SB408124 was a non-peptide OX1 receptor antagonist with Ki of 57 nM and 27 nM in |
R21082379 | R112 | |
R21082380 | CP-544326 | Cp-544326 is a potent, selective prostaglandin E2 receptor agonist with an EC50 |
R21082381 | broxaldine | Broxaldine (Brobenzoxaldine) is an antigenitor drug. |
R21082382 | PE859 | PE859 is an effective inhibitor of Tau and Aβ accumulation with IC50 values of 0 |
R21082383 | A419259 trihydrochloride | A 419259 trihydrochloride is A Src family kinase inhibitor with IC50 values of 9 |
R21082384 | AN-2718 | AN2718 inhibits fungal growth by inhibiting protein synthesis through OBORT mech |
R21082385 | Pleconaril;VP 63843;Win 63843 | Pleconaril is a capsid inhibitor that can be used to treat enteroviruses. Plecon |
R21082386 | TCS OX2 29 | Cts-ox2-29 is a strong and selective OX2 receptor antagonist with an IC50 of 40 |
R21082387 | PLX8394 | PLX8394 is a potent, selective Raf inhibitor that inhibits BRAFV600E activity wi |
R21082388 | AG 555 | AG 555 is an EGFR tyrosine kinase inhibitor. |
R21082389 | BIX02189 | BIX02189 is a potent and selective MEK5 inhibitor with IC50 of 1.5 nM. BIX02189 |