| R11375 |
Rapastinel;GLYX-13 |
Rapastinel (GLYX-13) is an N-methyl-D-aspartate receptor (NMDAR) modulator that
|
| R11376 |
GDC0152 |
GDC-0152 is a potent IAPs inhibitor, and binds to the BIR3 domains of XIAP, cIAP
|
| R11377 |
Raltegravir intermediates |
N/A
|
| R11378 |
Donepezil Hydrochloride;E2020 |
Donepezil (Hydrochloride) (E-2020) is a noncompetitive acetylcholinesterase inhi
|
| R11379 |
PLX7904 |
PLX7904 is a potent and selective BRAF inhibitor, with IC50 of appr 5 nM against
|
| R11380 |
ACP196;acalabrutinib |
Acalabrutinib is an orally active, irreversible, and highly selective BTK inhibi
|
| R11381 |
Ap26113; brigatinib |
Brigatinib is a highly potent and selective ALK inhibitor, with an IC50 of 0.6 n
|
| R11382 |
EAI-045;EAI045 |
EAI045 is an allosteric and the fourth-generation inhibitor of mutant EGFR&
|
| R11383 |
Olmutinib (Synonyms: HM61713, BI 1482694) |
Olmutinib (HM61713; BI-1482694) is an orally bioavailab and irreversible third E
|
| R11386 |
Cladribine |
N/A
|
| R11389 |
Mivebresib (Synonyms: ABBV-075) |
Mivebresib is a potent and orally available bromodomain and extraterminal domain
|
| R11390 |
Madrasin (DDD00107587) |
Madrasin (DDD00107587) is a splicing inhibitor that prevents formation of both s
|
| R11391 |
MK-571;MK571 |
MK-571 is a selective, orally active leukotriene D4 receptor antagonist, with Ki
|
| R11392 |
(E)-SIS3 |
(E)-SIS3 is a specific, cell-permeable, and selective Smad3 inhibitor, which inh
|
| R11393 |
Odanacatib;MK-0822 |
Odanacatib (MK-0822) is a potent and selective inhibitor of cathepsin K, with an
|
| R11395 |
WIN35428 |
(–)-2-β-Carbomethoxy-3-β-(4-fluorophenyl)tropane (β-CFT, WIN 35,428) is a stimul
|
| R11397 |
BM212 |
BM212 exerts bactericidal activity against intracellular bacilli residing, compl
|
| R11398 |
SKF96365 HCl |
SKF-96365 hydrochloride is a non-selective TRP Channel blocker.
|
| R11400 |
MK-5172 intermediates 1 |
N/A
|
| R11401 |
MK-5172 intermediates 2 |
N/A
|
| R11402 |
GANT 61 (Synonyms: NSC 136476) |
GANT 61 is an inhibitor of Gli1 and Gli2 targeting the Hedgehog/GLI pathway.&nbs
|
| R11403 |
SB216763 |
SB 216763 is potent, selective and ATP-competitive GSK-3 inhibitor with IC50s of
|
| R11406 |
Fluticasone propionate |
N/A
|
| R11425 |
Sugammadex sodium (Synonyms: Org25969) |
Sugammadex (Org 25969, tradename Bridion) is an agent for reversal of neuromuscu
|
| R11448 |
Fostamatinib Disodium (Synonyms: R788(Disodium)) |
R788 (Fostamatinib) disodium, a prodrug of the active metabolite R406, is a Syk
|