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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
M5002 4'-Chloropropiophenone 4-pyridazinecarboxamides and esters as interleukin-1beta converting enzyme inhibitors .
M4967 Gap 27 Gap 27 is a peptide(Ser-Arg-Pro-Thr-Glu-Lys-Thr-Ile-Phe-Ile-Ile) derived from connexin 43 that is a selective gap junction blocker.
M4963 2,3-Dichloro-5-(trifluoromethyl)pyridine In the crystal structure, centrosymmetric dimers arise from pairs of N-H⋯N hydrogen bonds.
M4952 Avenasterol Avenasterol is a natural, non-cholesterol sterol.
M4951 d-Alaninol Coenzyme B(12)-dependent ethanolamine ammonia-lyase acts on both enantiomers of the substrate 2-amino-1-propanol.
M4921 Chlorhexidine digluconate Chlorhexidine is an antiseptic effective against a wide variety of gram-negative and gram-positive organisms.
M4911 Isoxazole 9 Isoxazole 9 (Isx-9) is a synthetic promotor of adult neurogenesis by triggering neuronal differentiation of adult neural stem/precursor cells (NSPCs).
M4888 AC-6111
M4883 RO 48-8071 fumarate Ro 48-8071 fumarate is an inhibitor of OSC(Oxidosqualene cyclase; IC50=6.5 nM) that has low-density lipoprotein (LDL) cholesterol lowering activity.
M4873 Salicyl alcohol Salicyl alcohol is an intermediate for medicine, perfume, pesticide.
M4812 Genz-123346 Genz-123346 is an inhibitor of GL1 synthase that blocks the conversion of ceramide to GL1.
M4796 Veratramine Veratramine(NSC17821; NSC23880) is a signal transduction inhibitor that acts on tumors.
M4787 Euphorbia-factor-L1 Euphorbia Factor L1, a diterpenoid compound, can reduce the protein and mRNA levels of Bcl-2, PI3K, AKT and mTOR, and up-regulate the protein levels of Caspase-9 and Caspase-3. There was no effect on caspase-9 and caspase-3 protease. Euphorbia Factor L1 can induce autophagy and has anti-cancer, anti-adipogenesis, anti-osteoclast formation and multiple drug resistance regulation effects.
M4782 Bilirubin Bilirubin is a yellow breakdown product of heme catabolism.
M4773 Jatropholone-B Jatropholone-B
M4771 Dihydroberberine Dihydroberberine inhibited the human Ether-related gene (hERG) channel and significantly reduced the expression of heat shock protein 90 (Hsp90) and its interaction with hERG. Dihydroberberine has anti-inflammatory, antiatherosclerotic, hylipidemic and antitumor activities.
M4766 Adynerin Adynerin is a natural steroid found in the oleander plant.
M4764 taraxasteryl-acetate Taraxasteryl acetate was isolated from sagittal plasmodium and showed a broad spectrum of anti-inflammatory activity. Taraxasteryl acetate can reduce posterior claw edema induced by dextran, yeast glycan and arachidonic acid in rats. Taraxasteryl acetate can be used to study local inflammation.
M4763 15-hydroxy-dehydroabietic-acid 15-hydroxy-dehydroabietic-acid
M4759 Tiliroside Tiliroside is a glycoside flavonoid with antidiabetic properties. Tiliroside is a noncompetitive inhibitor of α-amylase with a Ki value of 84.2 μM. Tiliroside inhibits carbohydrate digestion and glucose absorption in the gastrointestinal tract.




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