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| Cat.No. | Product name | Product Description |
| R21082330 | SB21664 hydrochloride | SB 216641 has been reported as a selective SR-1B antagonist with approximately 2 |
| R21082331 | Talnetant | Talnetant (SB 223412) is a highly active NK3 receptor selective antagonist with |
| R21082332 | Tepoxalin | Tepoxalin is a 5-lipoxygenase inhibitor potentially for the treatment of asthma, |
| R21082333 | Pagoclone | Pagoclone is an active (+)-RP59037, A local activator of GABA(A) receptor, which |
| R21082334 | Trovafloxacin | Trovafloxacin is a broad-spectrum quinolone antibiotic with potent activity agai |
| R21082335 | PRE 084 | PRE-084 hydrochloride is a high affinity, selective σ1 agonist (Ki values are 2. |
| R21082336 | GSK8573 | GSK8573 is an inactive control compound of GSK2801. GSK8573 had binding activit |
| R21082337 | NCH 51 | PTACH (NCH-51) is a novel HDAC inhibitor. PTACH is effective in inhibiting the g |
| R21082338 | MK0812 | Mk-0812 is an effective and selective CCR2 antagonist that acts on human mononuc |
| R21082339 | FUB359 | Ciproxifan(FUB-359) maleate is a highly active H3 receptor antagonist with IC50 |
| R21082340 | Verteporfin | Verteporfin is a photosensitizer used in photodynamic therapy to eliminate abnor |
| R21082341 | AZ876 | AZ876 is a novel LXR stimulant, which is 25 and 2.5 times stronger than GW3965 ( |
| R21082342 | CA-074(OMe) | Ca-074 Methyl ester is a specific Cathepsin B inhibitor with neuroprotective, an |
| R21082343 | CAY10505 | CAY10505 is a potent and selective PI3Kγ inhibitor targeting neurons with IC50 o |
| R21082344 | K-Ras-IN-1 | K-ras-in -1 is an inhibitor of K-RAS. |
| R21082345 | Mozavaptan | Mozavaptan (OPC31260) is an oral active non-peptide vasopressin V2 receptor anta |
| R21082346 | Conivaptan hydrochloride | Conivaptan hydrochloride is a non-peptide vasopressin receptor antagonist, which |
| R21082347 | Benzarone | Benzarone (NSC 82134) is a small molecule inhibitor of Eyes Absen (EYA) protein |
| R21082348 | CID5721353 BDL6 inhribitor | CID5721353 is a BCL6 inhibitor with IC50 of 212 μM and Ki of 147 μM. |
| R21082349 | IDE-1 | IDE1 is a formalized endoderm inducer (IDE) that may be used in organ transplant |
| R21082350 | GSK9311 | GSK9311 is a potent BRPF bromine domain inhibitor with pIC50 values of 6.0 and 4 |
| R21082351 | CUDC-908 | PI3Kα inhibitor 1 is a selective PI3Kα inhibitor with IC50<0.1 μM and also in |
| R21082352 | GSK3008348 hydrochloride | GSK3008348 is an Integrin alphaV inhibitor. |
| 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 |