740 Y-P (trifluoroacetate salt) |
A PI3K activator; increases phosphorylation of PI3K, mTOR, and GSK3β… |
500 µg |
22598-500 |
More Info
|
YQ-128 |
An NLRP3 inflammasome inhibitor (IC50 = 0.3 µM); inhibits LPS- and A… |
1 mg |
36451-1 |
More Info
|
YQ-128 |
An NLRP3 inflammasome inhibitor (IC50 = 0.3 µM); inhibits LPS- and A… |
10 mg |
36451-10 |
More Info
|
YQ-128 |
An NLRP3 inflammasome inhibitor (IC50 = 0.3 µM); inhibits LPS- and A… |
25 mg |
36451-25 |
More Info
|
YQ-128 |
An NLRP3 inflammasome inhibitor (IC50 = 0.3 µM); inhibits LPS- and A… |
5 mg |
36451-5 |
More Info
|
YS-121 |
A dual inhibitor of mPGES-1 (IC50 = 3.9 µM ) and 5-LO (IC50 = 4.1 &m… |
1 mg |
13665-1 |
More Info
|
YS-121 |
A dual inhibitor of mPGES-1 (IC50 = 3.9 µM ) and 5-LO (IC50 = 4.1 &m… |
10 mg |
13665-10 |
More Info
|
YS-121 |
A dual inhibitor of mPGES-1 (IC50 = 3.9 µM ) and 5-LO (IC50 = 4.1 &m… |
25 mg |
13665-25 |
More Info
|
YS-121 |
A dual inhibitor of mPGES-1 (IC50 = 3.9 µM ) and 5-LO (IC50 = 4.1 &m… |
5 mg |
13665-5 |
More Info
|
YS-49 |
A platelet aggregation inhibitor; inhibits ADP-, collagen-, or epinephrine… |
1 mg |
30970-1 |
More Info
|
YS-49 |
A platelet aggregation inhibitor; inhibits ADP-, collagen-, or epinephrine… |
10 mg |
30970-10 |
More Info
|
YS-49 |
A platelet aggregation inhibitor; inhibits ADP-, collagen-, or epinephrine… |
25 mg |
30970-25 |
More Info
|
YS-49 |
A platelet aggregation inhibitor; inhibits ADP-, collagen-, or epinephrine… |
5 mg |
30970-5 |
More Info
|
YS-035 (hydrochloride) |
A verapamil derivative that dose-dependently blocks calcium uptake via Na+… |
10 mg |
17705-10 |
More Info
|
YS-035 (hydrochloride) |
A verapamil derivative that dose-dependently blocks calcium uptake via Na+… |
50 mg |
17705-50 |
More Info
|
YSK05 |
An ionizable cationic amino lipid (apparent pKa = ~6.5); has been used in… |
10 mg |
35786-10 |
More Info
|
YSK05 |
An ionizable cationic amino lipid (apparent pKa = ~6.5); has been used in… |
25 mg |
35786-25 |
More Info
|
YSK05 |
An ionizable cationic amino lipid (apparent pKa = ~6.5); has been used in… |
5 mg |
35786-5 |
More Info
|
YTHDC2 (human, recombinant) |
Source: Recombinant N-terminal GST-tagged YTHDC2 purified from E. coli &bu… |
100 µg |
26344-100 |
More Info
|
YTHDF2 (human recombinant) |
Source: Recombinant N-terminal GST-tagged YTHDF2 purified from E. coli &bu… |
100 µg |
26345-100 |
More Info
|
YU238259 |
An inhibitor of homology-dependent DNA repair; lethal to BRCA2-/- but not… |
1 mg |
25452-1 |
More Info
|
YU238259 |
An inhibitor of homology-dependent DNA repair; lethal to BRCA2-/- but not… |
10 mg |
25452-10 |
More Info
|
YU238259 |
An inhibitor of homology-dependent DNA repair; lethal to BRCA2-/- but not… |
25 mg |
25452-25 |
More Info
|
YU238259 |
An inhibitor of homology-dependent DNA repair; lethal to BRCA2-/- but not… |
5 mg |
25452-5 |
More Info
|
Yunaconitine |
A diterpenoid alkaloid with diverse biological activities; active against… |
1 mg |
34127-1 |
More Info
|
Yunaconitine |
A diterpenoid alkaloid with diverse biological activities; active against… |
10 mg |
34127-10 |
More Info
|
Yunaconitine |
A diterpenoid alkaloid with diverse biological activities; active against… |
25 mg |
34127-25 |
More Info
|
Yunaconitine |
A diterpenoid alkaloid with diverse biological activities; active against… |
5 mg |
34127-5 |
More Info
|
YVAD-CHO (trifluoroacetate salt) |
A caspase-1 / ICE inhibitor; prevents ICE-like and CPP32-like proteinase a… |
1 mg |
27420-1 |
More Info
|
YVAD-CHO (trifluoroacetate salt) |
A caspase-1 / ICE inhibitor; prevents ICE-like and CPP32-like proteinase a… |
5 mg |
27420-5 |
More Info
|
YW1128 |
An inhibitor of Wnt signaling (IC50 = 4.1 nM); decreases lipid accumulatio… |
1 mg |
27450-1 |
More Info
|
YW1128 |
An inhibitor of Wnt signaling (IC50 = 4.1 nM); decreases lipid accumulatio… |
10 mg |
27450-10 |
More Info
|
YW1128 |
An inhibitor of Wnt signaling (IC50 = 4.1 nM); decreases lipid accumulatio… |
5 mg |
27450-5 |
More Info
|
YW1159 |
An inhibitor of Wnt signaling (IC50 = 1.2 nM); not cytotoxic to HEK293 cel… |
1 mg |
27451-1 |
More Info
|
YW1159 |
An inhibitor of Wnt signaling (IC50 = 1.2 nM); not cytotoxic to HEK293 cel… |
10 mg |
27451-10 |
More Info
|
YW1159 |
An inhibitor of Wnt signaling (IC50 = 1.2 nM); not cytotoxic to HEK293 cel… |
5 mg |
27451-5 |
More Info
|
YYA-021 |
A small molecule CD4 mimetic; inhibits gp120 and CD4 interaction, preventi… |
1 mg |
22915-1 |
More Info
|
YYA-021 |
A small molecule CD4 mimetic; inhibits gp120 and CD4 interaction, preventi… |
10 mg |
22915-10 |
More Info
|
YYA-021 |
A small molecule CD4 mimetic; inhibits gp120 and CD4 interaction, preventi… |
25 mg |
22915-25 |
More Info
|
YYA-021 |
A small molecule CD4 mimetic; inhibits gp120 and CD4 interaction, preventi… |
5 mg |
22915-5 |
More Info
|
YZ9 |
A potent inhibitor of the glycolysis enzyme PFKFB3, with an IC50 value of… |
10 mg |
15352-10 |
More Info
|
YZ9 |
A potent inhibitor of the glycolysis enzyme PFKFB3, with an IC50 value of… |
100 mg |
15352-100 |
More Info
|
YZ9 |
A potent inhibitor of the glycolysis enzyme PFKFB3, with an IC50 value of… |
5 mg |
15352-5 |
More Info
|
YZ9 |
A potent inhibitor of the glycolysis enzyme PFKFB3, with an IC50 value of… |
50 mg |
15352-50 |
More Info
|
Z944 |
A T-type calcium channel inhibitor (IC50s = 0.050-0.160 µM for human… |
1 mg |
27679-1 |
More Info
|
Z944 |
A T-type calcium channel inhibitor (IC50s = 0.050-0.160 µM for human… |
10 mg |
27679-10 |
More Info
|
Z944 |
A T-type calcium channel inhibitor (IC50s = 0.050-0.160 µM for human… |
25 mg |
27679-25 |
More Info
|
Z944 |
A T-type calcium channel inhibitor (IC50s = 0.050-0.160 µM for human… |
5 mg |
27679-5 |
More Info
|
Z-AEVD-FMK |
An irreversible inhibitor of caspase-10 and related caspases that at 10 &m… |
1 mg |
14987-1 |
More Info
|
Z-AEVD-FMK |
An irreversible inhibitor of caspase-10 and related caspases that at 10 &m… |
5 mg |
14987-5 |
More Info
|