| 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 |
| M7827 | HA-1077 dihydrochloride | Novel vasodilator agent which inhibits vascular smooth muscle contraction by acting as an intracellular Ca2+ antagonist. |
| M7824 | 6-Hydroxymelatonin | Melatonin metabolite with agonist activity. |
| M7823 | HT1171 | Selective inhibitor of mycobacterial proteosomes; 1000-fold selective for mycobacterial proteosomes over human proteosomes. |
| M7821 | GW833972A | GW833972A is a CB2 cannabinoid receptor agonist with 1000-fold selectivity relative to CB1. |
| M7819 | Proguanil hydrochloride | Chlorguanide (proguanil) is combined with atovaquone for malaria prophylaxis. |
| M7818 | GR 32191B | Selective TP prostanoid receptor antagonist. |
| M7817 | GYKI 52466 hydrochloride | Selective allosteric AMPA receptor antagonist; anticonvulsant; skeletal muscle relaxant. |
| M7815 | GW2974 | Potent and selective dual inhibitor of EGFR (IC50 = 0. |
| M7814 | Guvacine hydrochloride | GABA uptake inhibitor. |
| M7812 | Formoterol fumarate dihydrate | β2-Adrenoreceptor agonist. |
| M7809 | FM19G11 | FM19G11 is an inhibitor of Hypoxia Inducible Factors α (HIFα), reported to affect self-renewal and differentiation of stem cells. |
| M7808 | FR-900098 monosodium salt | 1-deoxy-D-xylulose 5-phosphate reductoisomerase (DXR) is an enzyme involved in the first step in the nonmevalonate pathway for isoprenoid biosynthesis in Gram-negative, Gram-positive bacteria, plants, and the parasite causing the most virulent form of malaria, Plasmodium falciparum (Mammals produce isoprenoids via the mevalonate pathway). |
| M7807 | Fusaric acid | Dopamine β-hydroxylase inhibitor. |
| M7806 | Fluorocurarine chloride | Short-acting selective sympathetic ganglioblocker with weak antagonist activity on the nicotinic receptor at the neuromuscular junction; hypotensive. |
| M7805 | Fasentin | Fasentin is a novel inhibitor of glucose uptake, GluT1 inhibitor. |
| M7803 | FAUC 213 | Highly selective D4 dopamine receptor full antagonist. |
| M7801 | 6-Fluoromevalonate | Mevalonate-pyrophosphate decarboxylase inhibitor. |
| M7800 | Fenvalerate | Type II pyrethroid. |
| M7799 | Norfluoxetine hydrochloride | Fluoxetine metabolite; more potent inhibitor of serotonin uptake than fluoxetine with a half-life in vivo of 5-7 days. |
| M7798 | FPL 64176 | Potent Ca2+ channel (L-type) activator. |
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