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Catalog	name	Description	price
R-R-2427	SRX3177 CAS No.2241237-51-2	SRX3177/CAS No.2241237-51-2 is a triple inhibitor of CDK4/6, PI3K, and BRD4, with IC50s of 33 nM (BRD4 BD1), 89 nM (BRD4 BD2), 79 nM (PI3Kα), 83 nM (PI3Kδ), 3.18 μM (PI3Kγ), <2.5 nM (CDK4), 3.3 nM (CDK6), respectively. SRX3177 exerts broad cytotoxic activity against cancer cells, but acts friendly with normal epithelial cells.	price>
R-C-728	CP673451 CAS No. 924416-43-3	CP-673451 is a selective inhibitor of PDGFRα/βwith IC50 of 10 nM/1 nM in cell-free assays,exhibits >450-fold selectivity over other angiogenic receptors,has antiangiogenic and antitumor activity.	price>
R-R-2428	SMD-3040	SMD-3040 is a potent and selective of SMARCA2 PROTAC degrader (DC50: 12 nM). SMD-3040 contains SMARCA2/4 ligand, linker and VHL ligand. SMD-3040 demonstrates excellent degradation selectivity for SMARCA2 protein over SMARCA4 protein.SMD-3040 achieves strong tumor growth inhibition in xenograft models.	price>
R-C-729	Capivasertib (AZD5363) CAS No. 1143532-39-1	AZD5363 is a potent inhibitor of AKT with pharmacodynamic activity in vivo,has potential to treat a range of solid and hematologic tumors as monotherapy or a combinatorial agent.	price>
R-R-2429	Inobrodib CAS No.2222941-37-7	Inobrodib (CCS1477)/CAS No.2222941-37-7 is an orally active, potent, and selective inhibitor of the p300/CBP bromodomain. Inobrodib binds to p300 and CBP with Kd values of 1.3 and 1.7 nM, respectively, and with 170/130-fold selectivity compared with BRD4 with a Kd of 222 nM. CCS1477 inhibits cell proliferation in prostate cancer cell lines and decreases androgen receptor (AR)- and C-MYC-regulated gene expression.	price>
R-C-730	UPF-1069 CAS NO. 1048371-03-4	UPF 1069 is a selective poly(ADP-ribose)polymerase (PARP)2 inhibitor(IC50 values are 0.3 and 8.0 μM for PARP-2 and PARP-1 respectively).	price>
R-R-2430	BRM/BRG1 ATP Inhibitor-1 CAS No.2270879-17-7	BRM/BRG1 ATP Inhibitor-1 (compound 14)/CAS No.2270879-17-7 is an orally active allosteric dual brahma homolog (BRM)/SWI/SNF related matrix associated actin dependent regulator of chromatin subfamily A member 2 (SMARCA2) and brahma related gene 1 (BRG1)/SMARCA4 ATPase activity inhibitor, both IC50s are below 0.005 µM. BRM/BRG1 ATP Inhibitor-1 has anticancer activity.	price>
R-C-731	VS-5584 (SB2343) CAS No. 1246560-33-7	VS-5584 is a pan-PI3K/mTOR kinase inhibitor with IC50s of 16 nM,68 nM,42 nM,25 nM,and 37 nM for PI3Kα,PI3Kβ,PI3Kδ,PI3Kγ and mTOR,respectively.VS-5584 simultaneously blocks mTORC2 as well as mTORC1.	price>
R-R-2431	dBET6 CAS No.1950634-92-0	dBET6/CAS No.1950634-92-0 is a highly potent, selective and cell-permeable PROTAC connected by ligands for Cereblon and BET, with an IC50 of 14 nM, and has antitumor activity.	price>
R-C-732	Wnt-C59 (C59) CAS No. 1243243-89-1	Wnt-C59 is a very potent and highly selective Wnt signaling antagonist with an IC50 ~ 74 pM in the Wnt signaling reporter assay.	price>
R-R-2432	MZ 1 CAS No.1797406-69-9	MZ 1/CAS No.1797406-69-9 is a PROTAC connected by ligands for von Hippel-Lindau and BRD4. MZ 1 potently and rapidly induces reversible, long-lasting, and selective removal of BRD4 over BRD2 and BRD3. Kds of 382/120, 119/115, and 307/228 nM for BRD4 BD1/2, BRD3 BD1/2, and BRD2 BD1/2, respectively.	price>
R-C-733	MK4827 CAS No. 1038915-60-4	Niraparib(MK-4827)is a highly potent and orally bioavailable PARP1 and PARP2 inhibitor with IC50s of 3.8 and 2.1 nM,respectively.Niraparib leads to inhibition of repair of DNA damage, activates apoptosis and shows anti-tumor activity.	price>
R-R-2433	ARV-825 CAS No.1818885-28-7	ARV-825/CAS No.1818885-28-7 is a PROTAC connected by ligands for Cereblon and BRD4. ARV-825 binds to BD1 and BD2 of BRD4 with Kds of 90 and 28 nM, respectively.	price>
R-C-734	SB216763 CAS No. 280744-09-4	SB 216763 is a potent and selective cell permeable ATP-competitive inhibitor of GSK3α with an IC50 value of 34 nM(similar potency for GSK3β).	price>
R-R-2434	666-15 CAS No.1433286-70-4	666-15/CAS No.1433286-70-4 is a potent and selective CREB inhibitor with an IC50 of 81 nM. 666-15 suppresses tumor growth in a breast cancer xenograft model.	price>
R-C-735	Plinabulin (NPI-2358) CAS NO. 714272-27-2	NPI-2358 is a synthetic analog of NPI-2350,a natural product isolated from Aspergillus sp.,which depolymerizes microtubules in A549 human lung carcinoma cells.	price>
R-R-2435	SGC-CBP30 CAS No.1613695-14-9	SGC-CBP30/CAS No.1613695-14-9 is a potent and highly selective CBP/p300 bromodomain (Kds of 21 nM and 32 nM for CBP and p300, respectively) inhibitor, displaying 40-fold selectivity over the first bromodomain of BRD4 [BRD4(1)] bound. SGC-CBP30 strongly reduces secretion of IL-17A in Th17 cells and has anti-inflammatory effects.	price>
R-C-736	Atglistatin CAS No. 1469924-27-3	Atglistatin is a highly potent,selective and competitive inhibitor of adipose triglyceride lipase(ATGL)with an IC50 of ~0.7 μM for inhibition of lipolysis in vitro,but no toxicity up to a concentration of 50 μM.	price>
R-R-2436	AU-15330 CAS No.2380274-50-8	AU-15330/CAS No.2380274-50-8 is a proteolysis-targeting chimera (PROTAC) degrader of the SWI/SNF ATPase subunits, SMARCA2 and SMARCA4. AU-15330 induces potent inhibition of tumour growth in xenograft models of prostate cancer and synergizes with the AR antagonist enzalutamide. AU-15330 induces disease remission in castration-resistant prostate cancer (CRPC) models without toxicity.	price>
R-C-737	FLI-06 CAS No. 313967-18-9	FLI-06 is a Notch inhibitor and the early secretory pathway inhibitor.FLI-06 disrupts the Golgi apparatus in a manner distinct from that of brefeldin A and golgicide A.	price>

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