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| Cat.No. | Product name | Product Description |
| R2033074 | BI-409306 | BI-409306 is a potent and selective PDE9A inhibitor, with an IC50 of 52 nM, and |
| R2033075 | B-Raf inhibitor 1 dihydrochloride | B-Raf inhibitor 1 is a potent Raf kinase inhibitor with Kis of 1 nM, 1 nM, and 0 |
| R2033076 | BV6 | BV6 is an antagonist of cIAP1 and XIAP, members of the inhibitors of apoptosis ( |
| R2033077 | GSK2807 Trifluoroacetate | GSK2807 Trifluoroacetate is a potent, selective and SAM-competitive inhibitor of |
| R2033078 | LY2828360 | LY2828360 is a slowly acting but efficacious G protein-biased cannabinoid (CB2) |
| R2033079 | NCGC00244536 | NCGC00244536 is a potent KDM4B inhibitor with an IC50 of 10 nM. |
| R2033080 | INCB053914 phosphate | INCB053914 phosphate is an inhibitor of Pim extracted from patent WO 2017044730 |
| R2033081 | SB297006 | SB297006 is a CCR3 antagonist, which significantly inhibits proliferation and ne |
| R2033082 | AMG176 | AMG-176 is a potent, selective and orally bioavailable MCL-1 inhibitor, with a K |
| R2033083 | AZD7507 | AZD7507 is a potent and orally active CSF-1R inhibitor, with antitumor activity. |
| R2033084 | BB-Cl-Amidine | BB-Cl-Amidine is a peptidylarginine deminase (PAD) inhibitor. |
| R2033085 | BTSA1 | BTSA1 is a potent, high affinity and orally active BAX activator with an IC50 of |
| R2033086 | CVT-12012 | CVT-12012 is a potent and orally bioavailable stearoyl-coA desaturase (SCD) inhi |
| R2033087 | Edicotinib(JNJ-40346527;JNJ-527) | Edicotinib (JNJ-40346527; JNJ-527) is a potent, selective, brain penetrant and o |
| R2033088 | Gilteritinib | Gilteritinib is a potent FLT3/AXL inhibitor with IC50s of 0.29 nM/0.73 nM, respe |
| R2033089 | JNJ42165279 | JNJ-42165279 is a FAAH inhibitor with IC50 of 70 ± 8 nM and 313 ± 28 nM for hFAA |
| R2033090 | JNJ64619178 | JNJ-64619178 is a selective, orally active and pseudo-irreversible PRMT5 inhibit |
| R2033091 | LKB1 | Pim1/AKK1-IN-1 is a potent multi-kinase inhibitor with Kd values of 35 nM/53 nM/ |
| R2033092 | LY2562175 | LY2562175 is a potent and selective FXR agonist with an EC50 of 193 nM. |
| R2033093 | ML221 | ML221 is a potent apelin (APJ) functional antagonist, inhibiting apelin-13-media |
| R2033094 | MRT67307 | MRT67307 is a dual inhibitor of the IKKε and TBK-1 with IC50s of 160 and 19 nM, |
| R2033095 | PF-04418948 | PF-04418948 is an orally active, potent and selective prostaglandin EP2 receptor |
| R2033096 | Pibrentasvir | Pibrentasvir is a novel and pan-genotypic hepatitis C virus (HCV) NS5A inhibitor |
| R2033097 | RGX-104 | RGX-104 is a small-molecule LXR agonist that modulates innate immunity via trans |
| R2033098 | SBI-0640756 | SBI-0640756 (SBI-756) is a water soluble inhibitor of eIF4G1 and disrupts the eI |
