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Home > Products
| Cat.No. | Product name | Product Description |
| R21082353 | M2698 | M2698 (MSC2363318A) is an oral active, ATP-competing, selective dual inhibitor o |
| R21082354 | ARM390 Hydrochloride | Ar-m 1000390 is a selective δ opioid receptor agonist with an EC50 of 7.2±0.9 nM |
| R21082355 | nicainoprol | Nicainoprol is a fast sodium-channel blocker and an effective antiarrhythmic age |
| R21082356 | DAA1106 | DAA1106 is a peripheral benzodiazepine receptor (PBR) agonist, but has no affini |
| R21082357 | eptapirone | F11440 is a potent, selective, and highly effective 5HT1A receptor agonist with |
| R21082358 | piperoxan hydrochloride | Piperoxan hydrochloride (Piperoxan) is one of the α2 adrenergic receptor antagon |
| R21082359 | pipequaline | Pipequaline (PK 8165) is a non-selective partial agonist of GABAA receptors with |
| R21082360 | nifenalol hydrochloride | Nifenalol is a beta-adrenoceptor antagonist. |
| R21082361 | Src kinase inhibitor I | Src Inhibitor 1 is a highly selective two-site Src tyrosine kinase Inhibitor wit |
| R21082362 | TB5 | TB5 is an effective, selective and reversible HMAO-B inhibitor with a Ki value o |
| R21082363 | NSC303580;Pifithrin-μ | Pifithrin-μ is an inhibitor of p53 and HSP70, and has antitumor and neuroprotect |
| R21082364 | NQ301 | NQ301 is an antiblood suppository; It could inhibit collagen-induced platelet a |
| 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 |
