| 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 |
| M7468 | VU 0155041 sodium salt | VU 0155041 sodium salt is a potent, positive allosteric mGlu 4 agonist. |
| M7467 | VU 0155041 | VU 0155041 is a potent, positive allosteric mGlu 4 agonist. |
| M7464 | VO-OHpic | VO-OHpic is a potent PTEN inhibitor. |
| M7462 | VDM 11 | VDM 11 is a potent, selective anandamide transport inhibitor. |
| M7461 | Vatalanib succinate | Vatalanib succinate is a potent VEGFR inhibitor; also aromatase inhibitor. |
| M7459 | UNC 926 hydrochloride | UNC 926 hydrochloride is a l3MBTL1 domain inhibitor. |
| M7451 | UCPH 101 | UCPH 101 is a selective non-substrate EAAT1 inhibitor. |
| M7450 | UCL 2077 | UCL 2077 is a slow afterhyperpolarization (sAHP) channel blocker; sub-type selective Kv channel effects. |
| M7449 | UCL 1684 | UCL 1684 is a highly potent blocker of K Ca2. |
| M7448 | UBP1112 | UBP1112 is a group III mGlu antagonist. |
| M7447 | UBP 310 | UBP 310 is a gLU K5 antagonist. |
| M7446 | UBP 301 | UBP 301 is a kainate receptor antagonist. |
| M7445 | UBP 282 | UBP 282 is a aMPA/kainate antagonist; distinguishes between motoneuron and dorsal root kainate receptors. |
| M7444 | UAMC 00039 dihydrochloride | UAMC 00039 dihydrochloride is a dipeptidyl peptidase II (DPP-II) inhibitor. |
| M7443 | U 99194 maleate | U 99194 maleate is a potent, selective D 3 antagonist. |
| M7441 | U 90042 | U 90042 is a gABA A receptor ligand. |
| M7437 | TWS 119 Trifluoroacetate | TWS 119 Trifluoroacetate is a gSK-3β inhibitor; induces neuronal differentiation in ESCs. |
| M7436 | Trovafloxacin mesylate | Trovafloxacin mesylate is a antibiotic; inhibits bacterial DNA synthesis. |
| M7435 | Tropanyl-3,5-dimethylbenzoate | Tropanyl-3,5-dimethylbenzoate is a 5-HT 3 antagonist. |
| M7433 | TRO 19622 | TRO 19622 is a binds voltage-dependent anion channel (VDAC). |
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