| 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 prevent 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. |
| M9331 | 10-Hydroxy-trans-2-decenoic acid | 10-hydroxy-2-decenoic acid (10-H2DA) is the principal lipid component in royal jelly which is the food for queen and larvae honeybees. |
| M7805 | Fasentin | Fasentin is a novel inhibitor of glucose uptake, GluT1 inhibitor. |
| M7804 | 5-Fluoro-2′-deoxycytidine | 5-Fluoro-2′-deoxycytidine is a mechanism based DNMT (DNA cytosine-5 methyltransferase) inhibitor, that forms a covalent link with the cysteine residue in the active site of DNMT. |
| M7803 | FAUC 213 | Highly selective D4 dopamine receptor full antagonist. |
| M7802 | Fadrozole hydrochloride | Fadrozole is a nonsteroidal aromatase inhibitor. |
| M7801 | 6-Fluoromevalonate | Mevalonate-pyrophosphate decarboxylase inhibitor. |
| M7800 | Fenvalerate | Type II pyrethroid. |
| M7799 | Norfluoxetine hydrochloride | Fluoxetine metabolite; more potent inhibitor of serotonin uptake than fluoxetine with a half-life in vivo of 5-7 days. |
| M7798 | FPL 64176 | Potent Ca2+ channel (L-type) activator. |
| M7797 | FPL-55712 | CysLT1 leukotriene receptor antagonist. |
| M7794 | Encainide hydrochloride | Encanide hydrochloride is a sodium channel blocker and Ic antiarrhythmic compound. |
| M7792 | EF-24 | EF-24 is a IKK inhibitor and curcumin analog. |
| M7789 | Exo2 | Exo2 acts as a chemical probe of intracellular transport. |
| M7788 | Ethopropazine hydrochloride | Ethoproprazine hydrochloride is an inhibitor of butyrylcholinesterase; antiparkinsonian. |
| M7787 | Eupatorin | Eupatorin acts as an antiproliferative in cells expressing the CYP1A- family. |
| M7786 | 17-Epiestriol | 17-epiestriol is an estradiol metabolite and a selective estrogen receptor (ER) beta agonist. |
| M7784 | 16-Epiestriol | 16-Epiestriol is an estradiol metabolite that exhibits significant anti-inflammatory activity without glycogenic activity. |
| M7783 | Efaroxan hydrochloride | (+)-Isomer is a selective α-adrenoceptor antagonist; (−)-isomer is an imidazoline ligand that induces insulin secretion, mediated by the blockade of ATP-sensitive potassium channels in pancreatic β cells; I1 imidazoline binding site antagonist. |
| M7781 | 7-Ethoxycoumarin | Substrate for CYP2B6. |
| M7780 | 116-9e | 116-9e is a blocker of Hsp40-Hsp70 binding thereby inhibiting the chaperone activity of Hsp70-Hsp40. |
| M7777 | Donitriptan monohydrochloride | Donitriptan is a potent, selective 5-HT1B/1D agonist. |
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