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 |
M7543 | TP-808 | TP808 is a useful intermediate for the synthesis of diverse tetracycline antibiotics. |
M7525 | 6-Chloropurine | 6-Chloropurine is used in the preparation of 9-alkylpurines through alkylation with various substituted alkyl halides in dimethyl sulfoxide. |
M7495 | X-Gal | X-Gal is a used in cloning procedures with IPTG. |
M7489 | Wiskostatin | Wiskostatin is a n-WASP inhibitor; inhibits Arp2/3 activation. |
M7466 | VTP-27999 | VTP-27999 is a highly potent and selective renin inhibitor with IC50 of 0.47 nM. |
M7457 | UNC 3230 | UNC 3230 is a potent and selective PIP5K1C inhibitor; antinociceptive. |
M7439 | U-46619 | U-46619 is a pGH2 (TXA2) analog that is a potent and stable thromboxane A2 (TP) receptor agonist (EC50 = 0.035 μM). U-46619 potently stimulates TP receptor-mediated, but not other prostaglandin receptor-mediated responses in various in vitro preparations. |
M7432 | TRIS hydrochloride | TRIS hydrochloride is a commonly used laboratory reagent. |
M7402 | TES, free acid | TES, free acid is a buffering agent. |
M7381 | TCS 1105 | TCS 1105 is a gABA A α2 benzodiazepine receptor agonist. |
M7376 | TC-I 2014 | TC-I 2014 is a potent TRPM8 antagonist. |
M7343 | SZL P1-41 | SZL P1-41 is a selective Skp2 inhibitor; suppresses E3 ligase activity. |
M7342 | SYM 2081 | SYM 2081 is a highly selective kainate agonist. |
M7323 | SR 11302 | SR 11302 is an activator protein-1 (AP-1) transcription factor inhibitor. SR 11302 is a retinoid that specifically inhibits AP-1 activity without activating the transcription of retinoic acid response element (RARE). |
M7318 | Spermine NONOate | Spermine NONOate is a slow NO releasing agent. |
M7315 | Nitrosoglutathione | Nitrosoglutathione (GSNO; SNOG) is a exogenous NO donor and a substrate for rat alcohol dehydrogenase class III isoenzyme, inhibits cerebrovascular angiotensin II-dependent and -independent AT1 receptor responses. Breaks down to release NO. |
M7305 | SKPin C1 | SKPin C1 is a inhibitor of Skp2-mediated p27 degradation. SKPin C1 induces p27 accumulation in metastatic melanoma cell lines. SKPin C1 promotes G1/S cell cycle arrest in T47D cells and LNCaP cells. SKPin C1 induces G2/M cell cycle arrest in MCF-7 cells. |
M7246 | Sanguinarine chloride | Sanguinarine chloride is a inhibitor of protein phosphatase 2C (PP2C). |
M7234 | Ryanodine | Ryanodine is a ca2+ release inhibitor. |
M7152 | Potassium phosphate monobasic | Potassium phosphate monobasic is a commonly used in biological assay buffers. |
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