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 |
M6716 | ER 819762 | ER 819762 is a potent EP 4 receptor antagonist; orally bioavailable. |
M6715 | ER 27319 maleate | ER 27319 maleate is a selective Syk kinase inhibitor. |
M6713 | Eplivanserin hemifumarate | Eplivanserin hemifumarate is a potent and selective 5-HT 2A antagonist. |
M6712 | EO 1428 | EO 1428 is a selective inhibitor of p38α and p38β 2. |
M6711 | Enoximone | Enoximone is a pDE3 inhibitor. |
M6709 | EMD 66684 | EMD 66684 is a potent, selective non-peptide AT 1 antagonist. |
M6708 | EMD 386088 hydrochloride | EMD 386088 hydrochloride is a potent 5-HT 6 agonist. |
M6707 | EMD 281014 hydrochloride | EMD 281014 hydrochloride is a selective 5-HT 2A antagonist. |
M6702 | EGLU | EGLU is a highly selective group II mGlu antagonist. |
M6701 | Eggmanone | Eggmanone is a potent and selective PDE4 inhibitor; suppresses hedgehog signaling. |
M6698 | Edelfosine | Edelfosine is a selective PI-PLC inhibitor, also PAF receptor agonist. |
M6697 | EC 144 | EC 144 is a high affinity, potent and selective Hsp90 inhibitor. |
M6696 | EB 47 | EB 47 is a potent PARP-1 inhibitor. |
M6694 | E4CPG | E4CPG is a group I/group II mGlu antagonist. |
M6684 | DMP 543 | DMP 543 is a potent, orally active ACh release enhancer. |
M6683 | DMH4 | DMH4 is a selective VEGFR-2 inhibitor. |
M6682 | DMeOB | DMeOB is a negative allosteric modulator at mGlu 5. |
M6679 | DL-AP4 Sodium salt | DL-AP4 Sodium salt is a broad spectrum EAA antagonist. Sodium salt of DL-AP4. |
M6678 | DL-AP4 | DL-AP4 is a broad spectrum EAA antagonist. |
M6677 | DL-AP3 | DL-AP3 is a group I mGlu antagonist. |
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