| BN167535 |
118876-58-7 |
NBQX |
|
AMPA receptor antagonist |
BIO-X |
| BG166670 |
960539-70-2 |
GSK 1278863 |
|
Inhibitor of prolyl hydroxylases PHD1, PHD2 and PHD3 |
BIO-X |
| BP166583 |
1467057-23-3 |
PF 06409577 |
|
Activator of AMPK enzyme |
BIO-X |
| BR166508 |
339163-65-4 |
RCM 1 |
|
Inhibitor of FOXM1 transcriptional modulator |
BIO-X |
| BS166447 |
2088135-12-8 |
SR 16832 |
|
Antagonist of PPARγ receptor |
BIO-X |
| BP165815 |
315704-66-6 |
PTC 209 |
|
Inhibits polycomb complex protein BMI-1; antineoplastic in colorectal cancer |
BIO-X |
| BB165666 |
2101517-69-3 |
BL 918 |
|
Small-molecule activator of UNC-51-like kinase 1 |
BIO-X |
| BA165665 |
926023-82-7 |
AMTB |
|
TRPM8 channel blocker |
BIO-X |
| XM165579 |
51415-07-7 |
Momilactone A |
|
Diterpene phytoalexin from rice leaves (Oryza sativa) |
|
| XO165578 |
143437-61-0 |
Oryzalexin S |
|
Diterpene phytoalexin from rice leaves (Oryza sativa) |
|
| BR165563 |
199864-86-3 |
RS 127445 hydrochloride |
|
Serotonin receptor 5-HT2B antagonist |
BIO-X |
| BS165496 |
249889-64-3 |
SB 334867 hydrochloride |
|
Antagonist of orexin receptors; sedative; anorectic |
BIO-X |
| BJ165317 |
943540-75-8 |
JNJ 38877605 |
|
ATP-competitive inhibitor of c-Met |
BIO-X |
| BN165240 |
2089293-61-6 |
NAcM-OPT |
|
Inhibitor of DCN1, a component of E3 ubiquitin ligase complex |
BIO-X |
| BV165183 |
244133-31-1 |
VRT 043198 |
|
Caspase inhibitor; active metabolite of VX-765 |
BIO-X |
| BV165163 |
2165325-42-6 |
VU 6010608 |
|
Glutamate receptor mGlu7 negative allosteric inhibitor |
BIO-X |
| BP165159 |
1415637-72-7 |
PF 05085727 |
|
Brain-penetrant phosphodiesterase 2A Inhibitor |
BIO-X |
| BE165158 |
2083627-02-3 |
EED 226 monohydrate |
|
Inhibits histone methyltransferase activity of PRC2 |
BIO-X |
| BA165146 |
1268881-20-4 |
APD 371 |
|
Cannabinoid receptor CB2 agonist; analgesic |
BIO-X |
| BL165041 |
1698878-14-6 |
LSN 3154567 |
|
NAMPT competitive inhibitor with broad spectrum anti-cancer activity |
BIO-X |
| BC164191 |
300802-28-2 |
CA3 |
|
Inhibitor of YAP/Tead transcriptional activity |
BIO-X |
| BP164086 |
72882-78-1 |
PF 9366 |
|
Allosteric inhibitor of Mat2A, the catalytic subunit of extrahepatic MAT II |
BIO-X |
| BN164083 |
790702-57-7 |
NGI1 |
|
Inhibitor of OST, a type of glycosyltransferase |
BIO-X |
| BW164081 |
2012607-27-9 |
WNK463 monohydrate |
|
Pan-WNK kinase inhibitor |
BIO-X |
| BG163813 |
1346547-00-9 |
GSK 583 |
|
Inhibitor of RIP2 enzyme |
BIO-X |
| BA163812 |
566203-88-1 |
AZD 2098 |
|
Inhibitor of GSK3-β serine/threonine protein kinase |
BIO-X |
| BL163740 |
664969-54-4 |
LF3 |
|
Inhibitor of Wnt/β-catenin signal transduction pathway |
BIO-X |
| BT162782 |
436866-52-3 |
TD 114-2 |
|
Inhibitor of serine/threonine protein kinase GSK3-β |
BIO-X |
| BE162758 |
16470-02-3 |
Epiblastin A |
|
Inhibits serine-threonine protein kinases CK1: α, δ and ε isoforms |
BIO-X |
| BP162686 |
501925-31-1 |
PNU 120596 |
|
Type 2 positive allosteric modulator of α7 neuronal nAChR |
BIO-X |
| BW162077 |
634908-75-1 |
WAY 100635 maleate |
|
5-HT1A serotonin receptor antagonist |
BIO-X |
| BC161997 |
34233-69-7 |
Clozapine N-oxide dihydrochloride |
|
Major metabolite of clozapine; GPCR DREADD ligand; water soluble |
BIO-X |
| BF161243 |
1358575-02-6 |
FTBMT |
|
Agonist of GPR52 receptor, an orphan-A GPCR |
BIO-X |
| BU140504 |
546141-08-6 |
URB 597 |
|
Fatty acid amide hydrolase inhibitor; anti-inflammatory; anti-hypertensive |
BIO-X |
| FC139019 |
125941-87-9 |
SCH 23390 hydrochloride |
|
D1 and D5 dopamine receptor antagonist; 5-HT1C/2C serotonin receptor agonist |
BIO-X |
| FB52768 |
359860-27-8 |
(+)-Biotin-(PEO)4-amine |
|
Nucleophilic biotinylation reagent |
|
| BC165637 |
383432-38-0 |
CP 724714 |
|
ErbB2 tyrosine kinase inhibitor |
BIO-X |
| BK43330 |
587871-26-9 |
KU 55933 |
|
Inhibitor of ATM and AKT kinases |
BIO-X |
| BS43265 |
104104-50-9 |
SR 95531 hydrobromide |
|
GABA(A) receptor antagonist |
BIO-X |
| BA41291 |
1166227-08-2 |
A 66 |
|
Inhibitor of PI3K kinase; anti-cancer agent; arrhythmogenic |
BIO-X |
| BP34124 |
167869-21-8 |
PD 98059 |
|
MAP kinase kinase (MEK) inhibitor |
BIO-X |
| FA30834 |
289893-25-0 |
Arimoclomol |
|
Regulates expression of chaperonins Hsp70 and Hsp90 |
BIO-X |
| FV28720 |
139290-65-6 |
MDL 100907 |
|
Serotonin receptor 5-HT2A antagonist; anti-psychotic |
BIO-X |
| BA17338 |
183232-66-8 |
AM 251 |
|
CB1 cannabinoid receptor antagonist |
BIO-X |
| NC16650 |
124431-80-7 |
CGS 21680 HCl |
|
A2 adenosine receptor agonist |
BIO-X |
| MP05328 |
14937-32-7 |
1,2,3,4,6-Penta-O-galloyl-b-D-glucopyranose 1,2,3,4,6-O-五没食子酰葡萄糖 |
|
Pro-apoptotic; anti-cancer; anti-inflammatory; antioxidant |
|
| MG01912 |
15839-70-0 |
GDP-L-fucose disodium salt GDP-L-岩藻糖 |
|
Substrate for fucosyltransferase |
|