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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
M6562 Cardiogenol C hydrochloride Cardiogenol C hydrochloride is a diaminopyrimidine compound that induces the differentiation of MHC- (myosin heavy chain) positive cardiomyocytes from embryonic stem cells with an EC50 value of 0.1 µM.
M6544 BW 723C86 hydrochloride BW 723C86 hydrochloride is a 5-HT 2B agonist.
M6533 BRL 50481 BRL 50481 is a selective PDE7 inhibitor.
M6518 BMS 453 BMS 453 is a synthetic retinoid and RARβ agonist; also RARα and RARγ antagonist.
M6511 BIS-TRIS BIS-TRIS is a commonly used buffering agent.
M6506 Bicine Bicine is a general purpose buffer.
M6501 BHQ BHQ is a inhibitor of SERCA ATPase.
M6474 AY 9944 AY 9944 is a specific cholesterol biosynthesis inhibitor. AY 9944 inhibits the 7-dehydro cholesterol Δ7-reductase (DHCR7) enzyme with an IC50 of 13 nM.
M6462 ARN272 ARN272 is a fAAH-like anandamide transporter (FLAT) inhibitor.
M6444 Andrographolide Andrographolide is a NF-κB inhibitor that inhibits NF-κB activation by covalently modifying the cysteine residue of P50 in endothelial cells without affecting IκBα degradation or p50/ P65 nuclear translocation. Andrographolide has antiviral effects.
M6420 AIM-100 AIM-100 is a potent and selective Ack1 (TNK2) inhibitor (IC50 = 22 nM).
M6407 AdipoRon hydrochloride AdipoRon hydrochloride is a orally active AdipoR1 and AdipoR2 agonist; antidiabetic.
M6406 Adaptaquin Adaptaquin is a hIF-prolyl hydroxylase-2 (PHD2) inhibitor. Adaptaquin blocks glutamate induced ROS production in HT-22 cells, independent of MnSOD. Adaptaquin exhibits neuroprotective effects and enhances functional recovery in rodent intracerebral hemorrhage models, via inhibition of ATF4 dependent genes. Brain penetrant. Also antioxidant.
M6395 Emapunil Emapunil is a selective TSPO ligand.
M6353 6bK 6bK is a insulin degrading enzyme (IDE) inhibitor.
M6311 GO-203 GO-203 is a D-amino acid cell-penetrating peptide inhibitor of MUC1-C dimerization and thereby its oncogenic function.
M6298 Sodium tartrate Sodium tartrate has been used in organic synthesis to break up emulsions in aqueous workups. The compound is an ingredient of Fehling's solution and of the reagent Biuret (sc-239384).
M6265 BMS 309403 BMS-309403 is a potent, selective and cell-permeable inhibitor of fatty acid binding protein 4 (FABP4) with a Ki of less than 2 nM.
M6252 Sulbutiamine Sulbutiamine is a highly lipid soluble synthetic analogue of vitamin B1, used for the treatment of asthenia.
M6228 Wilforine Wilforine is a sesquiterpene pyridine alkaloid; important bioactive compound in T. wilfordii plants, and is effective in idiopathic pulmonary fibrosis.




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