| Cat.No. | Name | Information |
|---|---|---|
| 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 |
| M7791 | Exo-1 | Exo1 is a reversible inhibitor of exocytosis, also a Golgi ARF 1 (ADP-Ribosylation Factor) GTPase activator. |
| M31270 | N1-Glutathionyl-spermidine disulfide | N1-Glutathionyl-spermidine disulfide is a substrate of trypanothione reductase. |
| M31269 | Insulin icodec | Insulin icodec is a basal insulin analog. Insulin icodec can be used for the research of type 2 diabetes. |
| M31266 | Chitopentaose pentahydrochloride | Chitopentaose pentahydrochloride is a chitosan oligosaccharide with anti-inflammatory effect. Chitopentaose pentahydrochloride is a substrate of gene encoding chitinase B (FjchiB). |
| M31260 | Nordefrin | Nordefrin ((±)-Cobefri), a Norepinephrine derivative, is a vasoconstrictor agent. |
| M31259 | ART615 | ART615 is the related isomer of ART558. ART615, the inactive of ART558, elicits <10% Polθ inhibition at 12 µM, thus serving as a control for ART558 (IC50=7.9 nM). |
| M31255 | W140 TFA | W140 (TFA) is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
| M31253 | Chitoheptaose | Chitoheptaose is a chitosan oligosaccharide. Chitoheptaose has cardioprotective effects and improves cardiac parameters (left ventricular internal size, end-systolic and end-diastolic, ejection fraction and shortening fraction), inflammatory cytokines (IL-1β) in vanishing models. |
| M31252 | 8,11,14-Eicosatriynoic acid | 8,11,14-Eicosatriynoic Acid, as an inhibitor of prostaglandin, leukotriene biosynthesis, and arachidonic acid-induced platelet aggregation, blocks human 12-lipoxygenase (12-LO), cyclooxygenase (COX)and 5-lipoxygenase (5-LO) with IC50 values of 0.46 μM, 14 μMand 25 μM, respectively. |
| M31186 | 1,3-Dichloro-1,1,3,3-tetraisopropyldisiloxane | 1,3-Dichloro-1,1,3,3-tetraisopropyldisiloxane (TIPDSiCl2,) is a silylation reagent that can be used to protect the 3'- and 5'-hydroxyl functions of ribonucleosides, to analyze Watson-Crick and Hoogstein base pairing in nucleotides, and to form ribavirin chemical delivery system. In addition, 1,3-Dichloro-1,1,3,3-tetraisopropyldisiloxane is also a protecting group reagent for open-chain polyhydroxy compounds, which can be used to prepare cyclic bridging peptides. |
| M31185 | Tributyltin Hydride | Tributyltin Hydride (Bu3SnH) is an important pharmaceutical intermediate and reducing agent for reductive cleavage reactions, dehalogenation reactions, and intramolecular group ring-forming reactions. |
| M31182 | N,N-DiMethylMethyleneaMMoniuM Iodide | N,N-DiMethylMethyleneaMMoniuM Iodide is an imide salt produced by formaldehyde and dimethylamine, as well as a dimethylamine methylation reagent. |
| M31180 | Benzyl bromide | Benzyl bromide is an organobromide. It is used in organic synthesis to introduce benzyl protecting groups to alcohols and carboxylic acids. |
| M31159 | Ammuxetine HCl | Ammuxetine HCl is the hydrochloride form of Ammuxetine, a chiral compound that is also a 5-HT and norepinephrine reuptake inhibitor (SSRI) with antidepressant activity and can be used in studies related to depression. |
| M31156 | Glucoiberin | Glucoiberin, a thioglucoside present in kale, has anticancer activity. |
| M31096 | Olpasiran | Olpasiran (AMG890) is a small interfering RNA (siRNA) molecule that significantly reduces the production of Lp(a) in hepatocytes and can be used in studies related to atherosclerotic cardiovascular disease (ASCVD). |
| M31069 | DB772 hydrate | DB772 hydrate is a bovine viral diarrhoea virus (BVDV) inhibitor. DB772 also has anti-prion activity. |
| M31068 | Lafadofensine (D-(-)-Mandelic acid) | Lafadofensine D-(-)-Mandelic acid is the monoamines reuptake inhibitor. Lafadofensine D-(-)-Mandelic acid has sufficient effects after short-term administration. |
| M31055 | Gln-AMS TFA | Gln-AMS (TFA) is a type Ia aminoacyl-tRNA synthetase (AARS) inhibitor. Gln-AMS inhibits glutaminyl-tRNA synthetase (GlnRS) with a Ki of 1.32 µM. |
| M30994 | Tos-Gly-Pro-Arg-ANBA-IPA | Tos-Gly-Pro-Arg-ANBA-IPA is a chromogenic peptide substrate. Tos-Gly-Pro-Arg-ANBA-IPA can be used for luminescence measurement. |
| M30981 | Diphenidol | Diphenidol is an orally active antiemetic. Diphenidol reduces abnormal neuropathic pain and TNF-α overexpression in rats following chronic compression injury. Diphenidol also has local anaesthetic activity and inhibits sodium currents. Diphenidol can be used in studies of meniere′s disease, anti-vertigo, antiemetic and analgesia. |
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