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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
M7861 H-7 Inhibitor of cyclic nucleotide dependent protein kinase (PKA) and protein kinase C.
M7860 ISCK03 ISCK03 inhibits in vitro phosphorylation of c-Kit in a dose dependent manner.
M7859 Idazoxan hydrochloride α2-adrenoceptor antagonist; I2 imidazoline receptor agonist; I1 imidazoline receptor antagonist.
M7858 Ibandronate sodium salt Ibandronate sodium inhibits farnesyl diphosphate synthase (IC50 = 20 nM).
M7856 Immepip dihydrobromide Immepip is a H3 and H4 histamine receptor agonist.
M7855 ICI 192605 ICI 192605 is a potent thromboxane A2 receptor antagonist.
M7854 Ilmofosine Protein Kinase C (PKC) inhibitor; an ether lipid derivative of lysophosphatidylcholine has antineoplastic activity in vitro and in vivo.
M7852 I-AB-MECA Reference standard for radioiodinated I-AB-MECA, a widely used, high affinity radioligand for the A3 adenosine receptor.
M7851 ITX3 ITX3 is a specific inhibitor of endogenous TrioN activity acting on the GEF domain and selective cell active inhibitor of the Trio/RhoG/Rac1 pathway.
M7850 1,5-Isoquinolinediol DiQ is a potent inhibitor of Poly(ADP-ribose) synthetase which is activated by nitric oxide; neuroprotective agent.
M7849 Imetit dihydrobromide Potent and selective H3 histamine receptor agonist.
M7847 Indatraline hydrochloride Potent inhibitor of dopamine, norepinephrine and serotonin uptake.
M7844 Hyp9 Hyperforin is the active ingredient in St.
M7843 5HPP-33 5HPP-33 is a thalidomide derivative which was reported to be active as anticancer agent through stabilization of the microtubules.
M7842 Halofantrine hydrochloride Halofantrine is a blocker of delayed rectifier potassium current via the inhibition of hERG channel.
M7840 6β-Hydroxycortisol 6β-Hydroxycortisol is a metabolite of cortisol.
M7834 HMBA HMBA is an Inhibitor of microtubule polymerization; apoptosis inducer.
M7833 Serotonin hydrogen maleate Neurotransmitter.
M7830 Halopemide Halopemide is a dopamine receptor antagonist and a phospholipase D2 inhibitor.
M7828 Hypothemycin Hypothemycin, one of the highly oxygenated analogues in the group of 14-membered resorcylic acid lactones (RAL), has minor antifungal and cytotoxic activity and exhibits an in vitro anti-malarial activity with an IC50 of 2.




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