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Structure Cat No. Product Name CAS No. Product Description
BMS 433771 V4498 BMS 433771 543700-68-1 BMS 433771 is a novel and potent inhibitor of RSV (respiratory syncytial virus) replication in vitro.
Fosdagrocorat V4492 Fosdagrocorat 1044535-58-1 Fosdagrocorat (formerly known as PF-04171327) is a phosphate ester prodrug of PF-00251802 (dagrocorat), a selective high-affinity partial agonist of the glucocorticoid receptor, which is further metabolized to PF-04015475.
Lanraplenib (GS-9876) V5310 Lanraplenib (GS-9876) 1800046-95-0 Lanraplenib (also known as GS-9876; GS-SYK) is a highly selective and orally bioavailable Spleen Tyrosine Kinase (SYK) inhibitor with IC50of 9.5 nM).
NE10790 (3-PEHPC) V5289 NE10790 (3-PEHPC) 152831-36-2 NE10790, an analog of risedronate, is a poor farnesyl pyrophosphate synthase inhibitor and a weak antiresorptive agent.
PF-06795071 V4479 PF-06795071 2075629-81-9 PF-06795071 is a novel, potent, selective and covalentMAGL (Monoacylglycerol lipase)inhibitor with anIC50of 3 nM and with en excellent CNS exposure.
seco-雷帕霉素钠 V5204 Seco Rapamycin sodium (Secorapamycin A monosodium) 148554-65-8 Seco Rapamycin sodium (Secorapamycin A monosodium), the sodium salt of the ring-opened product of Rapamycin, is reported not to affect the mTOR function.
THZ1-R V5013 THZ1-R 1621523-07-6 THZ1-R is a novel and non-cysteine reactive analog of THZ1 which shows lower activity for CDK7 inhibition with a Kdof 142 nM for binding to CDK7.
UNC4976 V5201 UNC4976 UNC4976 is a significantly improved cellularly efficacious chemical probe of CBX7.
来他替尼 V5213 Lesraurtinib (CEP701; KT5555) 111358-88-4 Lestaurtinib (CEP-701; KT-5555; SP-924) is a novel,orally bioavailable and potent multi-kinase inhibitor with anticancer and anti-inflammatory activity.
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