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| Cat.No. | Product name | Product Description |
| R2032948 | GSK561679A;Verucerfont | Verucerfont is a corticotropin-releasing factor receptor 1 (CRF1) antagonist wit |
| R2032949 | KIRA6 | KIRA6 is an advanced small-molecule IRE1α RNase kinase inhibitor with an IC50 of |
| R2032950 | LTURM34 | LTURM34 is a specific DNA-PK inhibitor (IC50=34 nM).LTURM34 exhibits 170-fold se |
| R2032951 | LY2955303 | LY2955303 is a potent and selective retinoic acid receptor gamma (RARγ) antagoni |
| R2032952 | MK-7655(Relebactam) | Relebactam is a diazabicyclooctane inhibitor with activity against a wide spectr |
| R2032953 | PD128907 | PD 128907 is a selective dopamine D2/D3 receptor agonist, with Kis of 1.7, 0.84 |
| R2032954 | Rotigotine hydrochloride | Rotigotine (N-0437; N-0923) is a full agonist of dopamine receptor, a partial ag |
| R2032955 | Sitravatinib;MGCD516 | Sitravatinib (MGCD516) is an orally bioavailable receptor tyrosine kinase (RTK) |
| R2032956 | VO-Ohpic trihydrate | VO-Ohpic trihydrate is a highly potent inhibitor of PTEN with an IC50 of 46±10 n |
| R2032957 | 3-TYP | 3-TYP is a selective SIRT3 inhibitor, with an IC50 of 16 nM, more potent over SI |
| R2032958 | AG-494 | AG-494, a member of the tyrphostin family of tyrosine kinase inhibitors, is a po |
| R2032959 | Anavex2-73 | AVex-73 hydrochloride is a Sigma-1 Receptor agonist with an IC50 of 860 nM. |
| R2032960 | HTL-1071 | AZD4635 is a potent and selective, orally available adenosine A2A receptor (A2AR |
| R2032961 | BPTU;BMS-646786 | BPTU is a novel P2Y1 allosteric antagonist. |
| R2032962 | CY-09 | CY-09 is a selective and direct NLRP3 inhibitor.CY-09 directly binds to the ATP- |
| R2032963 | Danirixin | Danirixin is a selective, and reversible CXCR2 antagonist, with IC50 of 12.5 nM |
| R2032964 | Esaxerenone | Esaxerenone is a novel, highly potent and selective non-steroidal mineralocortic |
| R2032965 | Fmoc-Val-ala-PAB | Fmoc-Val-Ala-PAB, also known as Fmoc-Val-Ala-PAB-OH, is a useful linker for maki |
| R2032966 | GSK-j5 | GSK-J5 is a cell-permeable, inactive control for histone demethylase JMJD3/UTX i |
| R2032967 | NCT-503 | NCT-503 is a phosphoglycerate dehydrogenase (PHGDH) inhibitor with an IC50 of 2. |
| R2032968 | PF-06409577 | PF-06409577 is a potent and selective allosteric activator of AMPK α1β1γ1 isofor |
| R2032969 | TAK659 | TAK-659 hydrochloride is a potent, selective and orally available spleen tyrosin |
| R2032970 | TLR7-IN-1 | TLR7 agonist 2 is a potent and selective Toll-like Receptor 7 (TLR7) agonist wit |
| R2032971 | UCPH-101 | UCPH-101 is an excitatory amino acid transporter subtype 1 (EAAT1) inhibitor wit |
| R2032972 | ASK1-IN-1 | GS-444217 is a potent, orally available and selective ATP-competitive inhibitor |
