| 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 |
| M9002 | ML281 | ML-281 is a potent ans selective STK33 inhibitor with IC50 value of 14 nM. |
| M8965 | 2,6-Diaminopurine | 2, 6-diaminopurine is a compound used to study leukemia. |
| M8935 | EXP-3174 | EXP-3174 is a potent AT1 antagonist with Kis of 0.57 and 0.67 nM for rat and human forms, respectively. |
| M8929 | NAV-2729 | NAV-2729 is a selective ARF6 inhibitor with IC50 value of 1.0 μM. |
| M8907 | Acecainide HCl | Acecainide HCl, also known as N-acetylprocainamide and ASL 601, is the N-acetylated metabolite of procainamide. |
| M8905 | EBE-A22 | EBE-A22 is a derivative of PD 153035, has no effect on EGF-R TK but maintains a high cytotoxic profile. |
| M8894 | GJ-103 | GJ-103 is an active analog of the read-through compound GJ072. |
| M8878 | Inositol Nicotinate | Inositol Nicotinate is a formulation of niacin, which is also called vitamin B3, an essential human nutrient. |
| M8838 | UBP302 | UBP302 is a selective GluR5 antagonist. |
| M8821 | Triprolidine hydrochloride | H1 histamine receptor antagonist. |
| M8820 | Tyrphostin RG 14620 | Non-phenolic tyrphostin-class tyrosine kinase inhibitor. |
| M8819 | TOFA | TOFA is an allosteric inhibitor of acetyl-CoA carboxylase-α (ACCA). TOFA can inhibit the anorectic effect of subcutaneous tamoxifen (TMX) on food intake during refeeding experiments in rats. |
| M8811 | Triparanol | Triparanol (MER-29) is a potent cholesterol biosynthesis inhibitor blocking the 24-dehydrocholesterol reductase (24-DHCR). |
| M8806 | 6, 2′, 4′-trimethoxyflavone | 6, 2′, 4′-trimethoxyflavone is a selective aryl hydrocarbon receptor (AHR) antagonist with no partial agonist activity. |
| M8803 | Thiolutin | Thiolutin (Acetopyrrothin) is a disulfide-containing antibiotic and anti-angiogenic compound produced by Streptomyces. Thiolutin is a potent inhibitor of bacterial and yeast RNA polymerases. |
| M8789 | Biotinyl tyramide | Biotinyl tyramide is a reagent used for tyramide signal amplification for both immunohistochemistry (IHC) and in situ hybridiztion protocols and with either chromogenic or fluorescence detection. |
| M8777 | BPAM344 | BPAM344 is a potent positive allosteric modulator (PAM) on the three KAR subunits GluK1b, GluK2a, and GluK3a. |
| M8774 | CID 1375606 | CID 1375606 (N-[4-(Anilinocarbonyl)ph |
| M8755 | DIM-C-pPhCO2Me | DIM-C-pPhCO2Me is a NR4A1 (Nur77) antagonist that exhibit potent anticancer activity in pancreatic, colon, breast, kidney, and rhabdomyosarcoma cells. |
| M8729 | Syrosingopine | Syrosingopine is an antihypertensive agent related to reserpine that was found to potentiate the anticancer effects of the antidiabetic agent metformin and phenformin without harmful effects on normal cells. |
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