编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
---|---|---|---|---|
110220 | SB-3CT | 292605-14-2 | 98% | ![]() |
SB-3CT is a potent matrix metalloproteinase MMP-2 and MMP-9 inhibitor, which is a 2-[ | ||||
102622 | Spautin-1 | 1262888-28-7 | 98% | ![]() |
Spautin-1 is a novel autophagy inhibitor, IM inhibited the growth of K562 cells with | ||||
102605 | STF-118804 | 894187-61-2 | 98% | ![]() |
STF-118804 is a highly specific NAMPT inhibitor; reduces the viability of most B-ALL | ||||
102205 | SB 525334 | 356559-20-1 | 98% | ![]() |
SB 525334 is a potent and selective inhibitor of TGF_beta_ receptor I (ALK5) with IC5 | ||||
101917 | SAR191801 | 1234708-04-3 | 98% | ![]() |
Coming soon! | ||||
101913 | SEP-0372814 | 1516895-53-6 | 98% | ![]() |
Coming soon! | ||||
101909 | SP-2509 | 1423715-09-6 | 98% | ![]() |
SP-2509 is a novel histone demethylase LSD1 inhibitor, which showed high actitivity o | ||||
101908 | SB239063 | 193551-21-2 | 98% | ![]() |
SB 239063 is a potent p38MAPK inhibitor, which had an IC(50) of 44 nM for inhibition | ||||
101901 | SCR-1481B1 | 1174161-69-3 | 98% | ![]() |
SCR-1481B1 is a potent and selective MET inhibitor. SCR-1481B1 inhibited MET kinase w | ||||
101208 | SB-590885 | 405554-55-4 | 98% | ![]() |
SB590885 is a potent B-Raf inhibitor with Ki of 0.16 nM, 11-fold greater selectivity | ||||
101002 | SBC-115076 | 489415-96-5 | 98% | ![]() |
SBC-115076 is an anti-proprotein convertase subtilisin kexin type 9 (anti-PCSK9) comp | ||||
100503 | Selonsertib(GS-4997) | 1448428-04-3 | 98% by HPLC/HNMR | ![]() |
Selonsertib is a apoptosis signal-regulating kinase inhibitor (ASK1). Selonsertib may | ||||
92802 | SAG | 912545-86-9 | 99.03% | ![]() |
SAG is a potent Smoothened (Smo) receptor agonist (Kd = 59 nM); antagonizes Cyclopami | ||||
91813 | (1S,3r,5R)-8-(5,6,7,8-tetrahydro-6-(5-isopropyl-2-methylphenyl)-2-(3,5-dimethyl-1H-indazol-4-yl) | 1421249-72-0 | 98% | ![]() |
Coming soon! | ||||
91811 | (S)-2-phenyl-1-(thiazol-2-yl)ethanaMine hydrochloride | 135383-60-7 | 98% | ![]() |
Coming soon! | ||||
91414 | SA-4503.HCl (Cutamesine.HCl) | 165377-44-6 | 98% by HPLC | ![]() |
SA4503 (1-(3,4-dimethoxyphenethyl)-4-(3-phenylpropyl)piperazine dihydrochloride) is a | ||||
91128 | (S)-1-(2-chlorophenyl)ethanaMine | 68285-26-7 | 98% | ![]() |
Coming soon! | ||||
91127 | (S)-1-(3-Chlorophenyl)ethanamine | 68297-62-1 | 98% | ![]() |
Coming soon! | ||||
91125 | (S)-1-(4-Chlorophenyl)ethylamine | 4187-56-8 | 98% | ![]() |
Coming soon! | ||||
91122 | (S)-1-(4-Fluorophenyl)propan-1-amine hydrochloride | 1145786-74-8 | 98% | ![]() |
Coming soon! | ||||
91119 | (S)-1-(2-Methoxyphenyl)ethanamine | 68285-24-5 | 98% | ![]() |
Coming soon! | ||||
91117 | (S)-1-(3-Methoxyphenyl)ethanamine | 82796-69-8 | 98% | ![]() |
Coming soon! | ||||
91115 | (S)-4-Fluoro-2,3-dihydro-1H-inden-1-amine | 946053-90-3 | 98% | ![]() |
Coming soon! | ||||
91112 | (S)-5-Fluoro-2,3-dihydro-1H-inden-1-amine hydrochloride | 1114333-11-7 | 98% | ![]() |
Coming soon! | ||||
91109 | (1S)-1-(2,6-dimethylphenyl)ethanamine,hydrochloride | 1213479-78-7 | 98% | ![]() |
Coming soon! | ||||
91107 | (1S)-1-(2,5-dimethylphenyl)ethanamine | 4187-33-1 | 98% | ![]() |
Coming soon! | ||||
91105 | (S)-1-P-TOLYLPROPAN-1-AMINE-HCl | 623143-32-8 | 98% | ![]() |
Coming soon! | ||||
91104 | (S)-2-Methyl-1-phenylpropan-1-amine | 68906-26-3 | 98% | ![]() |
Coming soon! | ||||
91004 | SYM2206 | 173952-44-8 | 98% | ![]() |
SYM 2206 is a potent, novel, non-competitive AMPA receptor antagonist (IC50 = 2.8 M ). | ||||
91002 | SLx-2119 | 911417-87-3 | 98% | ![]() |
SLx-2119(KD-025) is a small molecule and selective inhibitor of ROCK2 with IC50 of 10 |