| 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 |
| M7386 | TCS 46b | TCS 46b is a orally active, subtype-selective NR1A/NR2B antagonist. |
| M7383 | TCS 2002 | TCS 2002 is a potent GSK-3β inhibitor. |
| M7382 | TCS 1205 | TCS 1205 is a subtype-selective GABA A receptor agonist. |
| M7379 | TCN 237 dihydrochloride | TCN 237 dihydrochloride is a highly potent and selective NR2B antagonist. |
| M7378 | TC-N 22A | TC-N 22A is a potent, selective mGlu 4 positive allosteric modulator. |
| M7377 | TC-MCH 7c | TC-MCH 7c is a selective melanin-concentrating hormone receptor 1 (MCH 1R) antagonist. |
| M7373 | TC-G 1004 | TC-G 1004 is a potent and selective A 2A antagonist. |
| M7371 | TC-G 1001 | TC-G 1001 is a gPR35 agonist; more potent than zaprinast. |
| M7369 | TC-F 2 | TC-F 2 is a potent, reversible and selective FAAH inhibitor. |
| M7368 | TC-E 5008 | TC-E 5008 is a selective mutant isocitrate dehydrogenase 1 (mIDH1) inhibitor; phenotypically lethal. |
| M7367 | TC-E 5006 | TC-E 5006 is a γ-secretase modulator; reduces Aβ42 levels. |
| M7366 | TC-E 5005 | TC-E 5005 is a potent and selective PDE10A inhibitor. |
| M7363 | TC-A 2317 hydrochloride | TC-A 2317 hydrochloride is a potent, selective Aurora kinase A inhibitor. |
| M7362 | TC NTR1 17 | TC NTR1 17 is a selective NTS 1 partial agonist. |
| M7361 | TC Mps1 12 | TC Mps1 12 is a potent and selective Mps1 kinase inhibitor. |
| M7359 | TC AC 28 | TC AC 28 is a high affinity BET bromodomain ligand. |
| M7358 | TC 1 | TC 1 is a high affinity σ 1 ligand. |
| M7357 | TB 21007 | TB 21007 is a α5-selective GABA A inverse agonist. |
| M7355 | TAS 301 | TAS 301 is a inhibitor of smooth muscle cell migration and proliferation. |
| M7354 | Tandospirone hydrochloride | Tandospirone hydrochloride is a selective 5-HT 1A partial agonist. |
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