R21082315 |
L-778123HCL |
L-778123 hydrochloride is a dual inhibitor of FPTase and GGptase-I with IC50 val
|
R21082316 |
TP434 |
Eravacycline is an effective broad-spectrum antimicrobial.
|
R21082317 |
CYC-116 |
Cyc-116 is A potent inhibitor of aurora A and B with Ki values of 8 and 9 nM, re
|
R21082318 |
AV-412 Tosylate |
Av-412 (MP412) is an EGFR inhibitor with IC50 values of 0.75, 0.5, 0.79, 2.3, 19
|
R21082319 |
JNJ5207852 |
Jnj-5207852 is an effective and selective antagonist of histamine H3 receptor wi
|
R21082320 |
SQ109 |
SQ109 effectively inhibited the adult stage of the parasite, killing cells with
|
R21082321 |
WAY181187 hydrochloride |
|
R21082322 |
MK7622 |
Mk-7622 is a positive allosteric regulator of muscarine M1 receptor.
|
R21082323 |
LU AE58054 |
Idalopirdine (Lu AE58054) is a potent, selective 5-HT6 receptor antagonist with
|
R21082324 |
Pardoprunox hydrochloride |
Pardoprunox hydrochloride is an agonist of dopamine receptors D2, D3, and 5-HT1A
|
R21082325 |
AL 082D06 |
AL 082D06 is a selective nonsteroidal glucocorticoid receptor (GR) antagonist wi
|
R21082326 |
eliprodil |
|
R21082327 |
Sertindole |
Sertindole is a 5-HT2A, 5-HT2C, D2 and α L receptor antagonist.
|
R21082328 |
Carbazeran |
Carbazeran is a PDE-II and PDE-III inhibitor that produces concentration-depende
|
R21082329 |
Deracoxib |
Deracoxib is a non-narcotic, non-steroidal anti-inflammatory compound that is a
|
R21082330 |
SB21664 hydrochloride |
SB 216641 has been reported as a selective SR-1B antagonist with approximately 2
|
R21082331 |
Talnetant |
Talnetant (SB 223412) is a highly active NK3 receptor selective antagonist with
|
R21082332 |
Tepoxalin |
Tepoxalin is a 5-lipoxygenase inhibitor potentially for the treatment of asthma,
|
R21082333 |
Pagoclone |
Pagoclone is an active (+)-RP59037, A local activator of GABA(A) receptor, which
|
R21082334 |
Trovafloxacin |
Trovafloxacin is a broad-spectrum quinolone antibiotic with potent activity agai
|
R21082335 |
PRE 084 |
PRE-084 hydrochloride is a high affinity, selective σ1 agonist (Ki values are 2.
|
R21082336 |
GSK8573 |
GSK8573 is an inactive control compound of GSK2801. GSK8573 had binding activit
|
R21082337 |
NCH 51 |
PTACH (NCH-51) is a novel HDAC inhibitor. PTACH is effective in inhibiting the g
|
R21082338 |
MK0812 |
Mk-0812 is an effective and selective CCR2 antagonist that acts on human mononuc
|
R21082339 |
FUB359 |
Ciproxifan(FUB-359) maleate is a highly active H3 receptor antagonist with IC50
|