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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
M6921 LUF 6283 LUF 6283 is a hCA 2 (GPR109A) partial agonist.
M6920 Lu AA 47070 Lu AA 47070 is a potent and selective precursor compound of adenosine A2A receptor antagonists with Ki values of 5.9, 260, 410 and <10,000 nM for A2A, A2B, A1 and A3 receptors, respectively.
M6918 L-Quisqualic acid L-Quisqualic acid is a aMPA/group I mGlu agonist.
M6917 LP 20 hydrochloride LP 20 hydrochloride is a selective 5-HT 7 ligand.
M6916 LP 12 hydrochloride LP 12 hydrochloride is a 5-HT 7 agonist.
M6915 Loreclezole hydrochloride Loreclezole hydrochloride is a subtype-selective GABA A receptor modulator.
M6913 LOE 908 hydrochloride LOE 908 hydrochloride is a broad spectrum cation channel blocker; neuroprotective.
M6912 L-NIL hydrochloride L-NIL hydrochloride is a selective iNOS inhibitor.
M6911 LM11A 31 dihydrochloride LM11A 31 dihydrochloride is a nonpeptide p75 NTR ligand; neuroprotective.
M6909 Lisuride maleate Lisuride maleate is a dA receptor agonist; antiparkinson's agent.
M6904 Lestaurtinib Lestaurtinib is a jAK2, FLT3 and TrkA inhibitor; also inhibits AurA and AurB.
M6902 Leelamine hydrochloride Leelamine hydrochloride is a cB 1 agonist.
M6901 LE 300 LE 300 is a potent and selective dopamine D 1 antagonist.
M6898 L-CCG-l L-CCG-l is a potent group II mGlu agonist.
M6897 L-Canavanine sulfate L-Canavanine sulfate is a nOS inhibitor.
M6893 L-AP4 L-AP4 is a selective group III mGlu agonist.
M6889 L-798,106 L-798,106 is a potent and highly selective EP 3 antagonist.
M6888 L-759,633 L-759,633 is a high affinity, selective CB 2 agonist.
M6886 L-748,337 L-748,337 is a selective β 3 antagonist.
M6885 L-733,060 hydrochloride L-733,060 hydrochloride is a potent NK 1 antagonist.




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