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| Cat.No. | Product name | Product Description |
| R2304206 | LDC7559 | LDC7559 is a gasdermin D (GSDMD) inhibitor via blocking neutrophil extracellular |
| R2304207 | NCATS-SM1441 | |
| R2304208 | ZN-c3 | ZN-c3 is a potent and selective Wee1 inhibitor with balanced potency, ADME, and |
| R2304209 | GMB-475 | GMB-475 is a degrader of BCR-ABL1 tyrosine kinase based on PROTAC, overcoming BC |
| R2304210 | Gefitinib hydrochloride | Gefitinib hydrochloride (ZD1839 hydrochloride) is a potent, selective and orally |
| R2304211 | AZM475271 | AZM475271 is a potent and selective Src kinase inhibitor with IC50 of 5 nM; no i |
| R2304212 | Taraxasterol | Taraxasterol is a pentacyclic triterpenoid isolated from Taraxacum mongolicum. T |
| R2304213 | Bicyclol | Bicyclol(SY 801) is a anti-hepatitis drug. Target: HBV Oral administration of bi |
| R2304214 | HQ461 | HQ461 is a molecular glue that promotes CDK12-DDB1 interaction to trigger cyclin |
| R2304215 | JNJ-5207852 dihydrochloride | JNJ-5207852 dihydrochloride is a selective and potent histamine H3 receptor (H3R |
| R2304216 | Melperone hydrochloride | |
| R2304217 | MRK 560 | MRK-560 is an orally active, brain barrier-penetrating γ-Secretase inhibitor, ca |
| R2304218 | Bifemelane hydrochloride | Bifemelane hydrochloride (MCI-2016) is a potent, selective and competitive inhib |
| R2304219 | MK1903 | MK-1903 is a potent and selective hydroxycarboxylic acid receptor 2 (HCA2, GPR10 |
| R2304220 | Compound 10 | GPR35 agonist 3 is a synthetic GPR35 agonist with an EC50value of 1.4 μM. GPR35 |
| R2304221 | Zolmitriptan | Zolmitriptan (BW-311C90; 311C90) is a 5-HT1B/1D receptor partial agonist with Ki |
| R2304222 | SR11237 (BMS-649) | SR11237 (BMS-649) is a potent retinoid X receptor (RXR)-selective agonist that i |
| R2304223 | R-10015 | R-10015, a broad-spectrum antiviral compound for HIV infection, acts as a potent |
| R2304224 | Dxd | Dxd (Exatecan derivative for ADC) is a potent DNA topoisomerase I inhibitor, wit |
| R2304225 | inS3-54A18 | inS3-54A18 is a potent STAT3 inhibitor, with anti-cancer properties. |
| R2304226 | CC-90009 | Eragidomide (CC-90009) is a first-in-class GSPT1-selective cereblon (CRBN) E3 li |
| R2304227 | AZD9574 | AZD-9574 is a potent and brain penetrant PARP1 inhibitor and shows >8000-fold |
| R2304228 | TES-1025 | TES-1025 is a potent and selective human α-amino-β-carboxymuconate-ε-semialdehyd |
| R2304229 | BMX-IN-1 | BMX-IN-1 is a selective, irreversible inhibitor of bone marrow tyrosine kinase o |
| R2304230 | AGI-25696 | AGI-25696 is a methionine adenosyltransferase 2A (MATA2 ) inhibitors useful for |
