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| Cat.No. | Product name | Product Description |
| R0012027 | 辅降血脂素(HSK7653)(化合物2) | Cofrogliptin (HSK7653) (compound 2), a tetrahydropyran derivative, is a potent o |
| R0012028 | N-(3-(4-氟苯基磺酰氨基)-4-甲氧基苯基)-[1,1"-联苯]-4-甲酰胺 | SN-001 is a STING inhibitor with an IC50 of 3.82 μM. |
| R0012029 | MB-07344 | MB-07344 has additive cholesterol lowering activity in combination with Atorvast |
| R0012030 | (4R)-(-)-2-硫酮基-4-噻唑烷羧酸 | |
| R0012031 | 2-硫氧代噻唑烷-4-羧酸 | |
| R0012032 | STING激动剂-1 | STING agonist-1 (G10) is human-specific STING agonist that elicits antiviral act |
| R0012033 | E3连接酶配体5 | PROTAC ERRα ligand 1 is an estrogen-related receptor α (ERRα) antagonist with IC |
| R0012034 | CRBN modulator-1 | CRBN modulator-1, a Thalidomide analog and a CRBN modulator extracted from WO202 |
| R0012036 | EG1 | EG1, a specific Pax2 inhibitor, directly binds the paired domain of Pax2 (Kd=1.3 |
| R0012037 | BC1618 | BC1618, an orally active Fbxo48 inhibitory compound, stimulates Ampk-dependent s |
| R0012038 | Bemnifosbuvir(AT-511) | Bemnifosbuvir (AT-511) is a potent and orally active HCV viral replication inhib |
| R0012039 | Bemnifosbuvir hemisulfate(AT-527) | Bemnifosbuvir hemisulfate (AT-527), a hemisulfate salt of AT-511, a guanosine nu |
| R0012040 | 苜蓿素 | Tricin is a natural flavonoid found in large amounts in wheat. Tricin inhibits H |
| R0012041 | STING agonist-12 | STING agonist-12 (Compound 53) is a potent, orally active human STING activator |
| R0012042 | RBN013209 | RBN013209 is a potent CD38 inhibitor with an IC50 of 0.01-0.1 μM for human CD38. |
| R0012043 | PF-07202954 | PF-07202954 is a weakly basic DGAT2 inhibitor with an IC50 of 10 nM for human DG |
| R0012044 | AZD1656 | AZD1656 is a potent, selective and orally active glucokinase activator with an E |
| R0012045 | 反式-4-[4-(4-氨基-7,7-二甲基-7H-嘧啶并[4,5-B][1,4]噁唑-6-基)苯基]-环己基乙酰胺 | T863 is an orally active, selective and potent DGAT1 (acyl-CoA:diacylglycerol ac |
| R0012046 | 反式-4-[4-(4-氨基-7,8-二氢-5-氧代嘧啶并[5,4-f][1,4]氧氮杂卓-6(5H)-基)苯基]环己烷乙酸 | PF-04620110 is a potent, selective and orally bioavailable diglyceride acyltrans |
| R0012047 | Pradigastat(LCQ-908) | Pradigastat (LCQ-908) is a potent, selective and orally active diacylglycerol ac |
| R0012049 | (R)-CR8(CR8, (R)-Isomer) | (R)-CR8 (CR8), a second-generation analog of Roscovitine, is a potent CDK1/2/5 |
| R0012050 | N5-(6-氨基己基)-N7-苄基-3-异丙基吡唑并[1,5-a]嘧啶-5,7-二胺 | BS-181 is a potent and selective CDK7 inhibitor (IC50=21 nM) than Seliciclib (HY |
| R0012051 | CT7001盐酸盐 | Samuraciclib hydrochloride (CT7001 hydrochloride) is a potent, selective, ATP-co |
| R0012053 | TVB-3166 | TVB-3166 is an orally-available, reversible, and selective fatty acid synthase ( |
| R0012054 | Denifanstat(TVB-2640) | Denifanstat (TVB-2640) is an orally active and potent Fatty Acid Synthase (FASN) |
