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Cat.No.  Name Information
M2206 TH-302 (Evofosfamide) TH-302 is a highly potent and selective hypoxia-activated procompound targeting hypoxic regions of solid tumors with IC50 of 19 nM.
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
M7161 Proglumide sodium salt Proglumide sodium salt is a non-selective CCK antagonist; orally active.
M7159 Pregnenolone sulfate sodium salt Pregnenolone sulfate sodium salt is a nMDA Potentiator.
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.




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