R2032126 |
Retigabine |
Retigabine(free base) is a novel anticonvulsant with activity in a broad range o
|
R2032127 |
Batimastat;BB94 |
Batimastat is a potent broad spectrum MMP inhibitor with IC50 of 3, 4, 4, 6, and
|
R2032128 |
Marimastat;BB2516;TA2516 |
Marimastat (BB2516) is a broad spectrum and orally bioavailable inhibitor of MMP
|
R2032129 |
Epoxomicin |
Epoxomicin is a cell-permeable and irreversible proteasome inhibitor, primarily
|
R2032130 |
Tipiracil hydrochloride |
Tipiracil (hydrochloride) is a thymidine phosphorylase inhibitor (TPI), used for
|
R2032131 |
Valrubicin |
Valrubicin is a chemotherapy agent, inhibits TPA- and PDBu-induced PKC activatio
|
R2032132 |
PP1;AGL 1872;EI 275 |
PP1 is a potent, and Src family-selective tyrosine kinase inhibitor with IC50 of
|
R2032133 |
Elagolix sodium;NBI-56418 sodium |
Elagolix sodium is a human GnRH receptor (GnRHR) antagonist with an IC50 and Ki
|
R2032134 |
Coelenterazine |
Coelenterazine is a luminescent enzyme substrate for apoaequorin and Renilla luc
|
R2032135 |
Anidulafungin;LY303366 |
Anidulafungin is a new semisynthetic echinocandin with antifungal potency.
|
R2032136 |
Setipiprant;ACT-129968;KYTH-105 |
Setipiprant is an orally available, selective CRTH2 antagonist.CRTH2 is a G prot
|
R2032137 |
Tosedostat;CHR-2797 |
Tosedostat is an aminopeptidase inhibitor.
|
R2032138 |
Azeliragon;TTP488;PF-04494700 |
Azeliragon (TTP488) is an orally bioavailable inhibitor of the receptor for adva
|
R2032139 |
(-)-Huperzine A(HupA) |
(-)-Huperzine A (Huperzine A), an active Lycopodium alkaloid extracted from trad
|
R2032140 |
Crisaborole;AN-2728;PF-06930164 |
Crisaborole (AN-2728) is a potent inhibitor of PDE4 and cytokine release; inhibi
|
R2032141 |
Ascomycin;Immunomycin;FR-900520;FK520) |
Ascomycin(Immunomycin, FR-900520, FK520) is an ethyl analog of tacrolimus (FK506
|
R2032142 |
Balicatib(AAE-581) |
Balicatib(AAE-581) is a potent and selective inhibitor of cathepsin K; 10-100 fo
|
R2032143 |
Dovitinib(TKI-258, CHIR-258) |
Dovitinib (TKI258; CHIR-258) is a multi-targeted tyrosine kinase inhibitor with
|
R2032144 |
E-3810(Lucitanib) |
Lucitanib (E-3810) is a novel dual inhibitor of VEGFR and FGFR, potently and sel
|
R2032145 |
Ellipticine(NSC71795) |
Ellipticine (NSC 71795) is a potent antineoplastic agent; inhibits DNA topoisome
|
R2032146 |
Enocitabine |
Enocitabine is a nucleoside analog, and is a potent DNA replication inhibitor, a
|
R2032147 |
Entinostat(MS-275, SNDX-275) |
Entinostat is an oral and selective class I HDAC inhibitor, with IC50s of 243 nM
|
R2032148 |
Epothilone A |
Epothilone A is a competitive inhibitor of the binding of [3H] paclitaxel to tub
|
R2032149 |
FK866 |
(E)-Daporinad (FK866) is an effective inhibitor of nicotinamide phosphoribosyltr
|
R2032150 |
Flavopiridol Hydrochloride;Alvocidib Hydrochloride;L86-8275 Hydrochloride;HMR-1275 Hydrochloride) |
Flavopiridol Hydrochloride (Alvocidib Hydrochloride) is a broad inhibitor of CDK
|