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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
M8429 CLEFMA CLEFMA is a curcumin analog that elevates ROS levels and induces oxidative stress and apoptosis in lung cancer cell lines.
M8427 MMB-4 MMB-4 is an oxime that can reactivate cholinesterases that have been inactivated by exposure to organophosphates such as sarin or soman.
M8426 3-AP-Me 3-AP-Me is a dimethyl derivative of the ribonucleotide reductase inhibitor 3-AP (SML0568).
M8425 SBI-0087702 SBI-0087702 promotes the cytoplasmic localization of ATF2 in melanoma cells.
M8423 MKC-733 MKC-733 is a 5-HT3 specific agonist.
M8418 L-742001 hydrochloride L-742,001 is an inhibitor of the influenza virus RNA polymerase PA subunit, implicated in several roles, including endonuclease and protease activities as well as viral RNA/complementary RNA promoter binding.
M8417 Geldanamycin-Biotin Geldanamycin-Biotin is a benzoquinone ansamycin antitumor antibiotic.
M8416 Darglitazone sodium salt Darglitazone is a highly potent and selective PPAR-γ (peroxisome proliferator-activated receptor-γ) agonist.
M8415 CID44216842 CID44216842 is a potent and selective non-competitive allosteric inhibitor of Cdc42 GTPase that does not inhabit Rho and Rac.
M8413 DAU-5884 DAU-5884 is a M3-selective muscarinic receptor antagonist.
M8412 Pivmecillinam Pivmecillinam is a gram negative antibiotic, and inhibitor of penicillin-binding protein 2 (PBP2).
M8411 Curvularin S - Curvularin is a macrocyclic lactone with cytotoxic activity.
M8410 Gossypin Gossypin is an anti-inflammatory pentahydroxyflavone glucoside isolated from Hibiscus vitifolius that is used as an herbal remedy for diabetes, jaundice, and inflammation.
M8407 W-13 W-13 has also been shown to inhibit the transcytosis of IgA, recycling of transferrin and overall alter the endocytic pathway in Madin-Darby canine kidney cells.
M8406 DDRI-18 DDRI-18 (DNA Damage Response Inhibitor-18) inhibits nonhomologous end-joining (NHEJ) DNA repair following double strand DNA breaks induced by ionizing radiation, and enhances the effects of DNA-damaging cancer drugs like etoposide, camptothecin and doxorubicin.
M8405 Febrifugine dihydrochloride Pyretin is an antimalarial compound and an active component of Changshan Chinese medicine. Recent studies have shown that its mechanism of action is as an inhibitor of proline transfer RNA synthase (ProRS).
M8403 VU0405601 VU0405601 is a hERG (the human Ether-à-go-go-Related Gene) agonist that increased the IC50 of dofetilide from 38.
M8402 LM11A-31 dihydrochloride LM11A-31 is a non-peptide ligand of the p75 neurotrophin receptor (p75NTR).
M8401 2-Methylserotonin maleate 2-Methylserotonin is a selective full agonist at the 5-HT3 receptor.
M8399 SDZ 220-581 hydrochloride SDZ 220-581 is a competitive NMDA receptor antagonist that penetrates the blood brain barrier.




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