| 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 |
| M7403 | Tetrindole mesylate | Tetrindole mesylate is a mAO-A inhibitor. |
| M7401 | Telenzepine dihydrochloride | Telenzepine dihydrochloride is a potent, selective M 1 antagonist. |
| M7400 | Teijin compound 1 | Teijin compound 1 is a potent CCR2b antagonist. |
| M7399 | TC-T 6000 | TC-T 6000 is a potent equilibrative nucleoside transporter 4 (ENT4) inhibitor. |
| M7397 | TCS PrP Inhibitor 13 | TCS PrP Inhibitor 13 is a antiprion agent; inhibits PrP Sc accumulation. |
| M7394 | TCS HDAC6 20b | TCS HDAC6 20b is a selective HDAC6 inhibitor. |
| M7393 | TC-S 7010 | TC-S 7010 is a potent and selective Aurora kinase A inhibitor. |
| M7392 | TC-S 7009 | TC-S 7009 is a high affinity and selective HIF-2α inhibitor. |
| M7390 | TC-S 7004 | TC-S 7004 is a potent and selective DYRK1A/B inhibitor. |
| M7389 | TC-S 7003 | TC-S 7003 is a potent Lck inhibitor. |
| 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. |
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