Cat. No. | Product name | CAS No. |
DC8342 |
EW-7197
Featured
EW-7197 is a potent ALK5 inhibitor. EW-7197 showed potent in vivo anti-metastatic activity, indicating its potential for use as an anti-cancer therapy. |
1352608-82-2 |
DCAPI1084 |
Ezetimibe (Zetia)
Featured
Ezetimibe (SCH 58235) is a potent cholesterol absorption inhibitor. Ezetimibe is a Niemann-Pick C1-like1 (NPC1L1) inhibitor, and is a potent Nrf2 activator. |
163222-33-1 |
DC9821 |
Ezutromid
Featured
Ezutromid is a novel Small utrophin's translation modulator with EC50 of 0.4 uM . |
945531-77-1 |
DC11329 |
Fadrozole (hydrochloride)
Featured
Fadrozole is a non-steroidal aromatase inhibitor (IC50s = 5 and 1.4 nM for human placental and rat ovarian microsomal aromatase, respectively). |
102676-31-3 |
DCAPI1011 |
Famciclovir (Famvir)
Famciclovir (Famvir) |
104227-87-4 |
DC9086 |
Fenofibrate
Fenofibrate is PPARα agonist with EC50 of 18 μM and 30 μM for mouse and human PPARα, respectively. |
49562-28-9 |
DC8912 |
Fesoterodine fumarate
Featured
Fesoterodine Fumarate is an antimuscarinic agent and is rapidly de-esterified to its active metabolite 5-hydroxymethyl tolterodine that is a muscarinic receptor antagonist. |
286930-03-8 |
DC11278 |
Fevipiprant
Featured
Fevipiprant(QAW039) is a selective, potent, reversible competitive CRTh2 antagonist with an in vitro dissociation constant KD value of 1.1nM at the CRTh2 receptor and an IC50 value of 0.44 nM for inhibition of PGD2-induced eosinophil shape change. |
872365-14-5 |
DC5193 |
Roxadustat(FG-4592)
Featured
FG-4592 is an HIF αprolyl hydroxylase inhibitor, stabilizes HIF-2 and induces EPO production. |
808118-40-3 |
DC10128 |
FGF401( Roblitinib)
Featured
FGF401 is an inhibitor of human fibroblast growth factor receptor 4 (FGFR4), with potential antineoplastic activity. |
1708971-55-4 |
DC1057 |
Fidaxomicin (Dificid)
Featured
Fidaxomicin, is an antibiotic that belongs to the class of macrocylic antibiotics. |
873857-62-6 |
DC8936 |
Fingolimod
Fingolimod(FTY720 free base) is a S1P antagonist with IC50 of 0.033 nM. |
162359-55-9 |
DC2014 |
Flavopiridol
Featured
Flavopiridol competes with ATP to inhibit CDKs including CDK1, CDK2, CDK4 and CDK6 with IC50 of ~ 40 nM, and CDK7 with IC50 of 300 nM. |
146426-40-6 |
DC8780 |
Flavopiridol Hydrochloride
Featured
Flavopiridol hydrochloride competes with ATP to inhibit CDKs including CDK1, CDK2, CDK4 and CDK6 with IC50 of ~ 40 nM. It is 7.5-fold more selective for CDK1/2/4/6 than CDK7. Flavopiridol is initially found to inhibit EGFR and PKA. |
131740-09-5 |
DC9623 |
Flecainide (acetate)
Featured
Flecainide(Tambocor) is a class 1C antiarrhythmic drug especially used for the management of supraventricular arrhythmia; works by blocking the Nav1.5 sodium channel in the heart, causing prolongation of the cardiac action potential. |
54143-56-5 |
DC8164 |
Gilteritinib(ASP2215)
Featured
FLT3/AXL inhibitor |
1254053-43-4 |
DC4239 |
Flupirtine maleate
Flupirtine maleateis a non-opioid, centrally acting analgesia, muscle relaxation and neuroprotection. Currently under a clinical trial (recruiting phase) as a treatment for Multiple Sclerosis and has been used as an analgesic. |
75507-68-5 |
DCAPI1206 |
Flurbiprofen (Ansaid)
Flurbiprofen (Ansaid) |
5104-49-4 |
DC11187 |
Fonadelpar
Fonadelpar (NPS-005,SJP-0035) is a potent, selective peroxisome proliferator activated receptor δ (PPARδ) agonist for the treatment of corneal disorders.. |
515138-06-4 |
DC7014 |
GPI-1046
For the detailed information of GPI-1046, the solubility of GPI-1046 in water, the solubility of GPI-1046 in DMSO, the solubility of GPI-1046 in PBS buffer, the animal experiment (test) of GPI-1046, the cell expriment (test) of GPI-1046, the in vivo, in vitro and clinical trial test of GPI-1046, the EC50, IC50,and Affinity of GPI-1046, Please contact DC Chemicals.. |
186452-09-5 |
DC7016 |
JNJ40411813
For the detailed information of JNJ40411813, the solubility of JNJ40411813 in water, the solubility of JNJ40411813 in DMSO, the solubility of JNJ40411813 in PBS buffer, the animal experiment (test) of JNJ40411813, the cell expriment (test) of JNJ40411813, the in vivo, in vitro and clinical trial test of JNJ40411813, the EC50, IC50,and Affinity of JNJ40411813, Please contact DC Chemicals.. |
1127498-03-6 |
DCAPI1596 |
Metroprolol succinate
For the detailed information of Metroprolol succinate, the solubility of Metroprolol succinate in water, the solubility of Metroprolol succinate in DMSO, the solubility of Metroprolol succinate in PBS buffer, the animal experiment (test) of Metroprolol succinate, the cell expriment (test) of Metroprolol succinate, the in vivo, in vitro and clinical trial test of Metroprolol succinate, the EC50, IC50,and Affinity of Metroprolol succinate, Please contact DC Chemicals.. |
98418-47-4 |