| 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 |
| M7002 | MRS 2279 | MRS 2279 is a selective, high affinity P2Y 1 antagonist. |
| M7001 | MRS 2219 | MRS 2219 is a potentiates P2X 1-mediated responses. |
| M6997 | MRS 1220 | MRS 1220 is a highly potent, selective hA 3 antagonist. |
| M6996 | MRK 560 | MRK 560 is a γ-secretase inhibitor; attenuates amyloid plaque deposition. |
| M6994 | MR 16728 hydrochloride | MR 16728 hydrochloride is a stimulates ACh release. |
| M6993 | Mps BAY 2a | Mps BAY 2a is a potent and selective Mps1 kinase inhibitor. |
| M6990 | MNI-caged-NMDA | MNI-caged-NMDA is a caged NMDA. |
| M6989 | MNI-caged-D-aspartate | MNI-caged-D-aspartate is a caged D-aspartate; NMDA agonist. |
| M6988 | MNI caged kainic acid | MNI caged kainic acid is a caged kainic acid. |
| M6987 | MNI 137 | MNI 137 is a selective negative allosteric modulator of group II mGlu receptors. |
| M6986 | MN 64 | MN 64 is a potent and selective tankyrase inhibitor. |
| M6982 | ML 786 dihydrochloride | ML 786 dihydrochloride is a potent Raf kinase inhibitor; orally bioavailable. |
| M6977 | ML 337 | ML 337 is a selective negative allosteric modulator of mGlu 3. |
| M6974 | ML 289 | ML 289 is a selective negative allosteric modulator of mGlu 3. |
| M6973 | ML 240 | ML 240 is a aTP-competitive inhibitor of p97 ATPase. |
| M6971 | ML 218 hydrochloride | ML 218 hydrochloride is a ca 2+ channel blocker (T-type). |
| M6969 | ML 154 | ML 154 is a potent Neuropeptide S receptor antagonist. |
| M6967 | ML 10302 hydrochloride | ML 10302 hydrochloride is a potent and selective 5-HT 4 partial agonist. |
| M6964 | MK 217 | MK 217 is a inhibitor of farnesyl diphosphate synthase (FPPS) and osteoclast-mediated bone resorption. |
| M6963 | MK 212 hydrochloride | MK 212 hydrochloride is a 5-HT 2C agonist. |
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