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 |
M21735 | Abafungin | Abafungin |
M21734 | Arprinocid | Arprinocid |
M21733 | Atorvastatin Lactone | Atorvastatin Lactone |
M21732 | Amineptine | Amineptine |
M21731 | Alexamorelin | Alexamorelin |
M21730 | 3-Amino-2-chlorobenzoic acid | 3-Amino-2-chlorobenzoic acid |
M21729 | 3-Aminophenylacetic acid | 3-Aminophenylacetic acid |
M21728 | Allitol | Allitol |
M21660 | MMI-0100 | MMI-0100 is a novel cell permeant peptide inhibitor of Mitogen Activated Protein Kinase Activated Protein Kinase II (MK2), MMI-0100 suppresses IL-6 expression without effect on IL-8 expression. MMI-0100 suppresses fibrotic processes such as vein graft disease. |
M21622 | Bepirovirsen | Bepirovirsen is an antisense oligonucleotide targeting all HBV messenger RNAs. Bepirovirsen leads to reductions in HBV-derived RNAs, HBV DNA and viral proteins. |
M21594 | Aeroplysinin 1 | Aeroplysinin 1 is a metabolite isolated from sponge V. aerophoba and has anti-inflammatory, antiangiogenic and antitumor activities. It's a tertiary alcohol. Aeroplysinin 1 induced endothelial cell Apoptosis. |
M21587 | OBI-3424 | OBI-3424 is a highly selective precursor compound that can be converted into an effective dna alkylating agent by AKR1C3(aldokeone reductase 1C3). It can be used in studies of hepatocellular carcinoma, castration-resistant prostate cancer and acute lymphoblastic leukemia (ALL). |
M21579 | TDI-11861 | sAC inhibitors such as DI-11861 can be used effectively as a compound for on-demand, non-hormonal male contraception. |
M21578 | ENT-01 | ENT-01 is an antibiotic. |
M21577 | Sirpiglenastat | Sirpiglenastat (DRP-104) is a broad acting glutamine (glutamine) antagonist. Sirpiglenastat has anticancer effects by directly targeting tumor metabolism and simultaneously inducing an effective antitumor immune response. |
M21576 | PTC258 | PTC258 is an oral, brain-penetrating splicing modulator targeting ELP1. |
M21559 | ART615 | ART615 is a related isomer of ART558. ART615 is an inactive form of ART558, causing <10% Polθ inhibition at 12 μM, so it can be used as a control for ART558 (IC50=7.9 nM). |
M21536 | BAY-069 | BAY-069 is a branched-chain amino acid transaminase (BCAT) 1/2 inhibitor. Involved in the synthesis and catabolism of branched-chain amino acids. |
M21535 | UCB7362 | UCB7362 is an oral plasma protease X (PMX) inhibitor that is being developed as an anti-malarial compound. |
M21534 | AN15368 | AN15368 is an oral cleavage and polyadenylate specific factor (CPSF3) inhibitor being developed for use in Chagas disease (also known as American trypanosomiasis). |
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