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Home > Products
| Cat.No. | Product name | Product Description |
| R2033130 | A-381393 | A-381393 is a potent, selective, brain penetrate dopamine D4 receptor antagonist |
| R2033131 | DJ-V-159 | DJ-V-159 is an agonist for G protein-coupled receptor family C group 6 member A |
| R2033132 | EZM2302 | EZM 2302 is an inhibitor of coactivator-associated arginine methyltransferase 1 |
| R2033133 | Gboxin | Gboxin is an oxidative phosphorylation inhibitor that targets glioblastoma.Gboxi |
| R2033134 | KHS101 | KHS101 could selectively induce a neuronal differentiation phenotype and interac |
| R2033135 | KHS101 hydrochloride | KHS101 hydrochloride could selectively induce a neuronal differentiation phenoty |
| R2033136 | LJ570 | LJ570 is a PPARα/PPARγ dual agonist with EC50s of 1.05 and 0.12 μM, respectively |
| R2033137 | LX-2343 | LX2343 is a BACE1 enzyme inhibitor with an IC50 value of 11.43±0.36 μM.LX2343 ac |
| R2033138 | MHP | MHP (Methyl caprooyl tyrosinate) is an activator of sphingosine kinase (SPHK1), |
| R2033139 | MK-3903 | MK-3903 is a potent and selective AMP-activated protein kinase (AMPK) activator |
| R2033140 | NMS-1286937 | NMS-1286937 is a potent, selective and orally available PLK1 inhibitor, with an |
| R2033141 | Risdiplam | Risdiplam (RG7916; RO7034067) is an orally administered, centrally and periphera |
| R2033142 | TAK931 | Simurosertib (TAK-931) is a selective cycle 7 (CDC7) kinase inhibitor, with an I |
| R2033143 | VL285 | VL285 is a potent VHL ligand with an IC50 of 0.34 μM. |
| R2033144 | WHI-P97 | WHI-P97 is a rationally designed potent inhibitor of JAK-3.IC50 value: Target: J |
| R2033145 | RN1747 | RN-1747 is a selective transient receptor potential cation channel subfamily V m |
| R2033146 | D-Lin-MC3-DMA | D-Lin-MC3-DMA, an ionizable cationic lipid, is a potent siRNA delivery vehicle. |
| R2033147 | ERK5-IN-1 | ERK5-IN-1 is a potent ERK5 inhibitor with an IC50 of 87±7 nM.ERK5-IN-1 also inhi |
| R2033148 | Cl-amidine trifluoroacetate salt | Cl-amidine is a peptidylarginine deminase (PAD) inhibitor, with an IC50 5.9 μM f |
| R2033149 | Cl-amidine | Cl-amidine is a peptidylarginine deminase (PAD) inhibitor, with an IC50 5.9 μM f |
| R2033150 | Cl-amidine hydrochloride | Cl-amidine (hydrochloride) is a peptidylarginine deminase (PAD) inhibitor, with |
| R2033151 | GW788388 | GW788388 is a potent and selective inhibitor of ALK5 with IC50 of 18 nM, and als |
| R2033152 | MDK7526 | (S,R,S)-AHPC (MDK7526) is the VH032-based VHL ligand used in the recruitment of |
| R2033153 | Acrizanib | Acrizanib is a VEGFR-2 inhibitor, with an IC50 of 17.4 nM for BaF3-KDR. |
| R2033154 | TC13172 | TC13172 is a mixed lineage kinase domain-like protein (MLKL) inhibitor with an E |
