| 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 |
| M7208 | Ro 32-3555 | Ro 32-3555 is a potent, collagenase-selective MMP inhibitor. |
| M7207 | Ro 26-4550 trifluoroacetate | Ro 26-4550 trifluoroacetate is a competitive inhibitor of IL-2/ IL-2Rα receptor interaction. |
| M7206 | Ro 19-4603 | Ro 19-4603 is a benzodiazepine inverse agonist. |
| M7205 | Ro 15-4513 | Ro 15-4513 is a benzodiazepine partial inverse agonist. |
| M7204 | Ro 10-5824 dihydrochloride | Ro 10-5824 dihydrochloride is a selective D 4 receptor partial agonist. |
| M7203 | Ro 04-6790 | Ro 04-6790 is a potent and selective 5-HT 6 antagonist. |
| M7202 | Ro 04-5595 hydrochloride | Ro 04-5595 hydrochloride is a nR2B-selective NMDA antagonist. |
| M7200 | Ro 01-6128 | Ro 01-6128 is a positive allosteric modulator of mGlu 1. |
| M7198 | RN 1 dihydrochloride | RN 1 dihydrochloride is a lSD1 inhibitor. |
| M7197 | RMM 46 | RMM 46 is a mSK/RSK family kinase inhibitor. |
| M7196 | Ritanserin | Ritanserin is a potent 5-HT 2 antagonist. |
| M7195 | RHPS 4 methosulfate | RHPS 4 methosulfate is a telomerase inhibitor. |
| M7193 | RHC 80267 | RHC 80267 is a diacylglycerol lipase inhibitor. |
| M7192 | RG 102240 | RG 102240 is a gene switch ligand for use in inducible gene expression systems. |
| M7188 | Remacemide hydrochloride | Remacemide hydrochloride is a nMDA antagonist; blocks ion channel and allosteric modulatory site. |
| M7187 | Rec 15/2615 dihydrochloride | Rec 15/2615 dihydrochloride is a selective α 1B antagonist. |
| M7186 | RBC8 | RBC8 is a ralA and RalB GTPase inhibitor. |
| M7184 | Raclopride | Raclopride is a potent, selective D 2/D 3 antagonist. |
| M7183 | rac BHFF | rac BHFF is a potent, selective GABA B positive allosteric modulator. |
| M7181 | R 568 hydrochloride | R 568 hydrochloride is a positive allosteric modulator of the human calcium-sensing receptor. |
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