R2032151 |
甲磺酸氟马替尼/氟马替尼;FluMatinib Mesylate |
Flumatinib mesylate (HH-GV-678 mesylate), a derivative of imatinib, is a multi-k
|
R2032152 |
Fulvestrant(ICI182780;ZD9238;ZM182780) |
Fulvestrant (ICI 182780; ZD 9238; ZM 182780) is a potent estrogen receptor antag
|
R2032153 |
Icotinib(Hydrochloride) |
Icotinib Hydrochloride (BPI-2009) is a potent and specific EGFR inhibitor with a
|
R2032154 |
Ispinesib(SB-715992) |
Ispinesib is a specific inhibitor of kinesin spindle protein (KSP), with a Ki ap
|
R2032155 |
MK-0524;Laropiprant |
Laropiprant is a potent, selective DP receptor antagonist with Ki values of 0.57
|
R2032156 |
Mubritinib(TAK 165) |
Mubritinib (TAK-165) is a potent and selective EGFR2/HER2 inhibitor with an IC50
|
R2032157 |
Nolatrexed dihydrochloride(AG-337 dihydrochloride) |
Nolatrexed dihydrochloride (AG 337) is a non-competitive lipophilic inhibitor of
|
R2032158 |
GS9620;Vesatolimod(GS-9620) |
Vesatolimod (GS-9620) is a potent, selective and orally active agonist of Toll-L
|
R2032159 |
Ribociclib;LEE011 |
Ribociclib (LEE01) is a highly specific CDK4/6 inhibitor with IC50 values of 10
|
R2032160 |
Everolimus;RAD001;SDZ-RAD |
Everolimus (RAD001) is a potent mTOR inhibitor that binds to FKBP-12 to generate
|
R2032162 |
PF-04971729(Ertugliflozin) |
Ertugliflozin (PF-04971729) is a potent, selective and orally active inhibitor o
|
R2032163 |
OligoMycin A |
Oligomycin A, created by Streptomyces, acts as a mitochondrial F0F1-ATPase inhib
|
R2032164 |
吡美莫司;匹美克莫司;PiMecroliMus |
Pimecrolimus is an immunophilin ligand, which binds specifically to the cytosoli
|
R2032165 |
pirodavir |
Pirodavir is a potent, broad-spectrum picornavirus inhibitor, and is highly acti
|
R2032166 |
Raltegravir(MK0518) |
Raltegravir is a potent integrase (IN) inhibitor, used to treat HIV infection.
|
R2032167 |
Regadenoson |
Regadenoson is an A2A adenosine receptor agonist that is a coronary vasodilator
|
R2032168 |
Apabetalone;RVX-208 |
Apabetalone (RVX-208) is an inhibitor of BET transcriptional regulators with sel
|
R2032169 |
Saracatinib(AZD0530) |
Saracatinib (AZD0530) is a potent Src family inhibitor with IC50s of 2.7 to 11 n
|
R2032170 |
Preladenant |
Preladenant is a potent and competitive antagonist of the human adenosine A2A re
|
R2032171 |
Telatinib |
Telatinib (Bay 57-9352) is an orally active, small molecule inhibitor of VEGFR2,
|
R2032172 |
Triciribine |
Triciribine is a DNA synthesis inhibitor, also inhibits Akt and HIV-1/2 with IC5
|
R2032173 |
Vilanterol(GW642444 |
Vilanterol (GW642444) is a long-acting β2-adrenoceptor (β2-AR) agonist with 24 h
|
R2032174 |
VisModegib(GDC0449) |
Vismodegib (GDC-0449) is an orally active hedgehog pathway inhibitor with an IC5
|
R2032175 |
Zosuquidar(LY3359793HCl |
Zosuquidar trihydrochloride is an inhibitor of P-glycoprotein with a Ki value of
|
R2032176 |
BAF312(SiponiMod) |
Siponimod (BAF-312) is a potent and selective sphingosine-1-phosphate (S1P) rece
|