| 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 |
| M7758 | 1,7-Dimethylxanthine | Adenosine receptor ligand; major metabolite of caffeine. |
| M7757 | Dilazep dihydrochloride | Adenosine uptake inhibitor; coronary and cerebral vasodilator; suppresses effects of ischemia; antiplatelet agent. |
| M7756 | Dihydroeponemycin | Dihydroeponemycin is an active derivative of eponemycin an antitumor antibiotic isolated from Streptomyces hygroscopicus. |
| M7753 | DAPH | DAPH is an inhibitor of Aβ fibril formation; Protein tyrosine kinase inhibitor, specific for EGFR. |
| M7751 | DPPE hydrochloride | DPPE is a potent, selective ligand of the microsomal anti-estrogen binding site. |
| M7750 | Desvenlafaxine hydrochloride | Desvenlafaxine hydrochloride is a dual SERT/NET reuptake inhibitor. |
| M7748 | DAF-FM | DAF-FM is a highly sensitive, photo-stable fluorescent probe for the detection of nitric oxide (NO). |
| M7745 | DCB | Neutral allosteric modulator of the metabotropic glutamate receptor mGluR5. |
| M7740 | DS1 | δ-GABAA receptors are emerging as an important pharmacological target. |
| M7739 | (+)-Butaclamol hydrochloride | (+)-Butaclamol is a dopamine receptor antagonist; active enantiomer. |
| M7731 | CHIC-35 | CHIC-35 is cell-permeable, metabolically stable, and very potent inhibitor of SIRT1; IC50 of S-isomer is 60 nM; IC50 of mixed isomers is 124 nM. |
| M7725 | CK-548 | CK-548 inhibits the activity of actin-related protein (Arp)2/3 complex by inserting into the hydrophobic core of Arp3 and altering its conformation: inhibits. |
| M7724 | CAY10397 | Potent and selective inhibitor of 15-hydroxyprostaglandin dehydrogenase (15-hydroxy-PGDH). |
| M7723 | CBIQ | CBIQ is an activator of the cystic fibrosis transmembrane conductance regulator (CFTR) and the intermediate-conductance calcium-sensitive K+ channel (KCNN4). |
| M7722 | Ciproxifan hydrochloride | Ciproxifan belongs to a novel chemical series of histamine H3-receptor antagonists. |
| M7721 | Chrysomycin B | Antibiotic from Streptomyces sp. |
| M7717 | CGP 52608 | CGP 52608 is a specific activator of retinoic acid receptor-related orphan receptor α (RORA). |
| M7716 | CIL-102 | CIL-102 is a tubulin polymerization inhibitor: apoptosis inducer. |
| M7714 | Cinnarizine | Ca2+ channel blocker; central and peripheral vasodilator. |
| M7712 | Cisapride monohydrate | 5-HT4 serotonin receptor agonist. |
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