| 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 |
| M8147 | RX 821002 hydrochloride | Selective α2-adrenoceptor antagonist. |
| M8145 | Ro4368554 | Ro4368554 is a 5-HT6 receptor antagonist. |
| M8143 | Razoxane | Razoxane is clinically active against angiogenesis and metastasis. |
| M8142 | RRD-251 hydrochloride | RRD-251 hydrochloride is a reversible, potent, and selective disruptor of Rb/Raf-1 interaction. |
| M8140 | REV 5901 | Leukotriene D4 receptor antagonist. |
| M8139 | Ridaifen-B | Ridaifen-B (RID-B) is a novel tamoxifen (TAM) analog that significantly augments apoptosis-inducing effect of TAM in estrogen receptor (ER)-negatives cells. |
| M8138 | RU 26752 | RU 26752 is a mineralocorticoid receptor antagonist. |
| M8137 | RK-682 | RK-682 is a specific and noncompetitive inhibitor of protein tyrosine phosphatase; It inhibited dephosphorylation activity of CD45 and VHR with IC50 54 and 2. |
| M8135 | Rhodblock 1a | Rhodblock 1a is an inhibitor of the Rho Kinase pathway. |
| M8134 | RU7 | RU7 is a selective inhibitor of bacterial β-clamp interaction with DNA polymerase POL III, and an inhibitor of a DNA polymerase sliding clamp. |
| M8133 | Ro 31-0432 | Protein kinase C (PKC) inhibitor; membrane-derived PKC inhibitor. |
| M8132 | Rilmenidine hemifumarate salt | Selective I1 imidazoline receptor agonist. |
| M8131 | Rhodblock 6 | Rhodblock 6 is an inhibitor of the Rho Kinase pathway. |
| M8127 | Ro 90-7501 | Inhibitor of Aß42 fibril formation. |
| M8126 | Ro 23-9358 | Diacylglycerol lipase inhibitor. |
| M8121 | PD-85639 | PD-85639 (PD85,639) is a voltage-gated sodium (Na+) channel blocker (75% in 10 min & >95% in 25 min blockage of Na+ current by 25 μM PD85,639; whole-cell patch clamp using primary rat brain neurons) that is shown to target rat brain Nav1. |
| M8120 | PF-04217329 | PF-04217329 is a selective and potent prostaglandin EP2 receptor agonist. |
| M8117 | CP-376395 hydrochloride | CP-376395 is a potent and selective antagonist of the CRF1 receptor, which has been shown to play an important role in mediating behavioral and endocrine responses to fear and stress. |
| M8115 | PF-4191834 | PF-4191834 a selective, non-redox, non-iron chelating competitive inhibitor of 5-lipoxygenase effective in inflammation and pain. |
| M8112 | PF-05085727 | PF-05085727 is a potent inhibitor against cGMP-dependent phosphodiesterase PDE2 (PDE2A; IC50 = 2. |
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