| 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 |
| 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. |
| M7352 | Talsupram hydrochloride | Talsupram hydrochloride is a selective inhibitor of noradrenalin transporters. |
| M7349 | TAK 21d | TAK 21d is a potent FAAH inhibitor. |
| M7348 | TACA | TACA is a gABA A agonist. Also GABA-T substrate and GABA uptake inhibitor. |
| M7347 | Tabimorelin hemifumarate | Tabimorelin hemifumarate is a potent, orally active ghrelin receptor agonist. |
| M7345 | T 98475 | T 98475 is a gnRH receptor antagonist. |
| M7344 | T 5601640 | T 5601640 is a selective LIMK2 inhibitor; antitumor. |
| M7338 | Sulfidefluor 7 AM | Sulfidefluor 7 AM is a h 2S fluorescent probe. |
| M7337 | STOCK2S 26016 | STOCK2S 26016 is a lysine deficient protein kinase (WNK) signaling inhibitor. |
| M7335 | STEARDA | STEARDA is a endogenous lipid, active in vivo. Enhances effects of endovanilloids at TRPV1 receptors. |
| M7334 | ST 1936 oxalate | ST 1936 oxalate is a selective, high affinity 5-HT 6 agonist. |
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