| 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 |
| M7310 | SMANT hydrochloride | SMANT hydrochloride is a inhibits Smoothened (Smo) accumulation. |
| M7309 | SM-21 maleate | SM-21 maleate is a presynaptic cholinergic modulator. |
| M7304 | SKF 97541 | SKF 97541 is a extremely potent GABA B agonist. |
| M7302 | SKF 83822 hydrobromide | SKF 83822 hydrobromide is a selective D 1-like agonist. |
| M7301 | SKF 81297 hydrobromide | SKF 81297 hydrobromide is a d 1 agonist. |
| M7300 | SKF 77434 hydrobromide | SKF 77434 hydrobromide is a selective D 1-like partial agonist. |
| M7298 | SJ 172550 | SJ 172550 is a mDMX inhibitor. Disrupts MDMX-p53 interaction. |
| M7295 | SID 26681509 | SID 26681509 is a cathepsin L inhibitor. |
| M7293 | SIB 1553A hydrochloride | SIB 1553A hydrochloride is a subunit selective nAChR agonist. |
| M7292 | SIB 1508Y maleate | SIB 1508Y maleate is a potent agonist of α4β2, α2β4, α4β4 and α3β4 nACh receptors. |
| M7291 | Shz 1 | Shz 1 is a activator of early cardiac genes in pluripotent stem cells; induces differentiation in M-PBMCs. |
| M7287 | SDZ SER 082 fumarate | SDZ SER 082 fumarate is a selective 5-HT 2B/2C antagonist. |
| M7286 | SDZ NKT 343 | SDZ NKT 343 is a highly selective, human NK 1 antagonist. |
| M7285 | SDZ 220-040 | SDZ 220-040 is a potent, competitive NMDA antagonist. |
| M7284 | SDZ 205-557 hydrochloride | SDZ 205-557 hydrochloride is a 5-HT 4/5-HT 3 receptor antagonist. |
| M7283 | SDM25N hydrochloride | SDM25N hydrochloride is a potent, selective non-peptide δ antagonist; also inhibits dengue virus replication. |
| M7280 | SCH 28080 | SCH 28080 is a h +,K +-ATPase inhibitor. |
| M7278 | SCH 221510 | SCH 221510 is a potent and selective NOP agonist. |
| M7277 | SCH 202676 hydrobromide | SCH 202676 hydrobromide is a inhibitor of ligand binding to G-protein-coupled receptors. |
| M7276 | SC 66 | SC 66 is a allosteric Akt inhibitor. |
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