| Cat.No. | Name | Information |
|---|---|---|
| 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 |
| M7791 | Exo-1 | Exo1 is a reversible inhibitor of exocytosis, also a Golgi ARF 1 (ADP-Ribosylation Factor) GTPase activator. |
| M7777 | Donitriptan monohydrochloride | Donitriptan is a potent, selective 5-HT1B/1D agonist. |
| M7776 | N-Desmethyltamoxifen HCl | N-Desmethyltamoxifen HCl is the primary metabolite of tamoxifen. |
| M7774 | DBO-83 | Novel nicotinic acetylcholine receptor agonist, structurally related to epibatidine, with antinociceptive properties in rodents. |
| M7772 | Diethylumbelliferyl phosphate | Diethylumbelliferyl phosphate is a selective, potent cholesterol esterase inhibitor. |
| M7770 | DPO-1 | DPO-1 is an inhibitor of human Kv1. |
| M7769 | Daltroban | Selective thromboxane A2 receptor antagonist. |
| M7766 | Domoic acid | Potent agonist at receptors for excitatory amino acids glutamate and kainate; has highest affinity for AMPA/kainate receptor of any kainate agonist; causes excessive excitation of neurons leading to depletion of energy stores. |
| M7765 | Diphenylacetohydroxamic acid | Diphenylacetohydroxamic acid is a class IIa selective histone deacetylase inhibitor. |
| M7762 | DS2 | DS2 is a selective positive allosteric modulator of δ-GABAA receptors. |
| M7759 | DCHC | DCHC is a SIRT1 activator. |
| 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. |
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