| Cat.No. | Name | Information |
|---|---|---|
| M6098 | Baicalein | Baicalein is a CYP2C9 and prolyl endopeptidase inhibitor, IC50 value of 3.12 mM. |
| M9325 | EGTA | EGTA is a specific calcium chelator with a Kd of 60.5 nM at physiological pH (7.4) and a high specificity for Ca2+ than for Mg2+.EGTA significantly inhibits the substrate adhesion capacity of inflammatory macrophages. |
| M9330 | Brij-35 | Brij-35 (Polidocanol) is a high HLB, ethoxylated, nonionic ether of lauryl alcohol with broad pH stability. |
| M6154 | 2-PMPA tetrasodium | 2-PMPA (PMPA tetrasodium salt) is a potent and selective inhibitor of glutamate carboxypeptidase II (GCPII) with an IC50 of 300 pM. |
| M2250 | Pamidronate disodium | Pamidronate disodium is a nitrogen containing bisphosphonate, used to the research of preventing osteoporosis. |
| M9916 | DPPH | DPPH (2,2-Diphenyl-1-picrylhydrazyl) is a stable free radical that measures the free radical scavenging activity of antioxidants. |
| M9194 | Insulin (human) | Insulin (human) is a polypeptide hormone that regulates the level of sugar (glucose) in the blood and is produced by beta cells of islets. |
| M3409 | Formestane | Formestane is a second generation selective aromatase inhibitor with an IC50 of 80 nM. |
| M9665 | N-(2-amino-2-oxoethyl)acrylamide | N-(2-Amino-2-oxoethyl)acrylamide |
| M7791 | Exo-1 | Exo1 is a reversible inhibitor of exocytosis, also a Golgi ARF 1 (ADP-Ribosylation Factor) GTPase activator. |
| M7158 | Pregnanolone | Pregnanolone is a gABA A receptor positive allosteric modulator. |
| M7157 | PQ 69 | PQ 69 is a potent and selective A 1 inverse agonist. |
| M7156 | PPY A | PPY A is a potent inhibitor of Abl T315l mutant and wild-type Abl kinases. |
| M7155 | PPPA | PPPA is a competitive NR2A antagonist. |
| M7154 | PPDA | PPDA is a subtype-selective NR2C/NR2D antagonist. |
| M7153 | PP 3 | PP 3 is a negative control for PP 2. |
| M7151 | Polygodial | Polygodial is a tRPA1 channel activator; analgesic and antifungal. |
| M7150 | PNU 96415E | PNU 96415E is a d 4 and 5-HT 2A Antagonists. Antipsychotic compounds. |
| M7149 | PNU 37883 hydrochloride | PNU 37883 hydrochloride is a vascular K ir6 (K ATP) channel blocker. |
| M7148 | PNU 22394 hydrochloride | PNU 22394 hydrochloride is a 5-HT 2C agonist and 5-HT 2A/2B partial agonist. |
| M7147 | PMPA (NMDA antagonist) | PMPA (NMDA antagonist) is a competitive NMDA antagonist. |
| M7146 | PLX 647 dihydrochloride | PLX 647 dihydrochloride is a potent dual Fms/KIT inhibitor. |
| M7144 | PK-THPP | PK-THPP is a potent K 2P9.1 (TASK-3) channel blocker. |
| M7143 | PK 44 phosphate | PK 44 phosphate is a potent and selective dipeptidyl peptidase IV (DPP-IV) inhibitor. |
| M7142 | PIT 1 | PIT 1 is a pIP 3 antagonist. Blocks PIP 3-PH interaction; inhibits Akt signaling. |
| M7140 | PIM-1 Inhibitor 2 | PIM-1 Inhibitor 2 is a pim-1 kinase inhibitor. |
| M7138 | PHP 501 trifluoroacetate | PHP 501 trifluoroacetate is a potent GABA A antagonist. |
| M7134 | Phenserine | Phenserine is a cholinesterase inhibitor. |
| M7129 | PG 01037 dihydrochloride | PG 01037 dihydrochloride is a d 3 receptor selective antagonist. |
| M7127 | PFM 01 | PFM 01 is a mRE11 endonuclease inhibitor. |
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