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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