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Cat.No.  Name Information
M9298 AX-024 hydrochloride AX-024 hydrochloride is a potent cytokine release inhibitor, inhibits the production of interferon-γ (IFN-γ), interleukin-6 (IL-6), tumor necrosis factor-α (TNFα), IL-10 and IL-17A.
M9297 Chlorin E6 Chlorin E6 is a natural molecule and a promising photosensitizer, isolated from renewable natural sources.
M9295 Calf thymus DNA Calf thymus DNA is high quality double-stranded template DNA isolated from the thymus of male and female calves.
M9293 Z-Asp-CH2-DCB Z-Asp-CH2-DCB is an irreversible, cell permeable broad-spectrum caspase inhibitor, with IC50 values of 1.1 and 4.1 μM for caspase-3 and caspase-6 respectively.
M9292 PEG300 PEG300 is a neutral and biocompatible hydrophilic polymer.
M9291 MnTMPyP Pentachloride MnTMPyP Pentachloride is a superoxide dismutase (SOD) mimetic and peroxynitrite scavenger.
M9290 S 38093 S 38093 is an inverse agonist at histamine H3 receptors, displays a moderate affinity for rat, mouse and human H3 receptors with Ki of 8.8, 1.44 and 1.2µM, respectively.
M9289 E6446 dihydrochloride E6446 dihydrochloride is a synthetic antagonist of TLR7 and TLR9.
M9288 MSX-130 MSX-130 is CXCR4 Antagonist.
M9286 MSX-127 MSX-127 (NSC-23026) is a CXCR4 receptor modulator.
M9285 SU 5205 SU 5205 is a VEGFR2 inhibitor.
M9284 SU-5408 SU-5408 is a potent, cell-permeable inhibitor of mouse VEGFR2 kinase with IC50 of 70 nM.
M9283 SU 5214 SU 5214 is a modulator of tyrosine kinase signal transduction.
M9282 D-Glucose 6-Phosphate D-Glucose 6-Phosphate is a glucose sugar phosphorylated at the hydroxy group on carbon 6.
M9281 KIN1148 KIN1148 is a IRF3 agonist, it is also a novel influenza vaccine adjuvant found to enhance flu vaccine efficacy.
M9280 HMN-154 HMN-154 is a benzenesulfonamide anticancer agent.
M9279 LW6 LW6 is a novel HIF-1alpha inhibitor, with an IC50 of 4.4 μM.
M9278 P7C3-A20 P7C3-A20 is an analogue of P7C3, and is a proneurogenic, neuroprotective agent.
M9277 TG4-155 TG4-155 is a brain penetrant prostaglandin EP2 specific antagonist, with a Ki of 9.9 nM.
M9276 6-Methoxyflavanone 6-Methoxyflavanone is an inhibitors of bitter taste receptor.
M9275 AZD-5069 AZD-5069 is a potent CXCR2 chemokine receptor antagonist, and is claimed to be useful in the treatment of inflammatory diseases.
M9274 SMI-16a SMI-16a is a potent, cell-permeable, ATP-competitive inhibitor of Pim-1/2 kinases with IC50s of 150 nM and 20 nM against Pim-1 and Pim-2, respectively.
M9273 HSP70-IN-1 HSP70-IN-1 is a heat shock protein (HSP) inhibitor with an IC50 of 2.3 μM inhibiting the growth of Kasumi-1 cells.
M9272 S107 S107 is a Type 1 ryanodine receptor (RyR1) stabilizer.
M9271 BIA 10-2474 BIA 10-2474 is a long-acting reversible inhibitor of fatty acid amide hydrolase (FAAH).
M9270 COH29 COH29 is an orally available, aromatically substituted thiazole and inhibitor of the human ribonucleotide reductase (RNR), with potential antineoplastic activity.
M9269 TMB 3,3’,5,5’-Tetramethylbenzidine(TMB) is a chromogenic substrate used in staining procedures in immunohistochemistry as well as being a visualising reagent used in enzyme-linked immunosorbent assays (ELISA).
M9268 Met-Enkephalin Met-Enkephalin (H-Tyr-Gly-Gly-Phe-Met-OH) inhibits tumor growth via binding to the opioid receptor.
M9267 Coelenterazine Coelenterazine is the luciferin, the light-emitting molecule, used for monitoring reporter genes in BRET, ELISA and HTS techniques.
M9266 STO-609 acetate STO-609 acetate is a cell-permeable inhibitor of calcium/calmodulin-dependent kinase kinases (CaMKK) isoforms CaMKKα and CaMKKβ with Ki of 80 and 15 ng/ml, respectively.
M9265 Vimirogant Vimirogant (also known as AGN-242428 and VTP-43742) is a potent, selective and orally active RORγt inhibitor.
M9264 Norepinephrine Norepinephrine is generally considered to be a β1-selective adrenergic receptor agonist with EC50 of 5.37 μM.
M9263 CY-09 CY-09 is a selective and direct NLRP3 inhibitor.
M9262 Plicamycin Plicamycin, also known as mithramycin or Mithramycin A is a n antibiotic isolated from the bacterium Streptomyces plicatus with antineoplastic activity.
M9261 Fluorescein Fluorescein is a synthetic organic compound and dye.
M9260 SBI-0640756 SBI-0640756 is a first-in-class inhibitor that targets eIF4G1 and disrupts the eIF4F complex.
M9259 Asciminib Asciminib, also known as ABL001, is a potent allosteric inhibitor of BCR-ABL, with a Kd value of 0.5-0.8 nM.
M9258 HS-1371 HS-1371 is a potent RIP3 kinase inhibitor with an IC50 of 20.8 nM.
M9257 Evobrutinib Evobrutinib is a selective BTK inhibitor with an IC50 of 37.9 nM.
M9256 Solanesol Solanesol (Nonaisoprenol) is a long-chain polyisoprenoid alcohol compound with inhibitory activities toward FAK.
M9255 UKI-1 UKI-1 is a novel synthetic inhibitor of the urokinase-type plasminogen activator, which inhibits the invasive capacity of carcinoma cells with a Ki of 0.41 μM.
M9254 KN-92 phosphate KN-92 is an inactive analog of the CaM kinase II inhibitor KN-93.
M9253 BGP-15 2HCl BGP-15 is a novel poly(ADP-ribose) polymerase inhibitor with an IC50 and a Ki of 120 μM and 57 μM, respectively.
M9252 YL-0919 YL-0919 is a novel 5-HT1A receptor agonist and selective serotonin reuptake inhibitor.
M9251 HTHQ HTHQ is a lipid peroxidation inhibitor potentially for the treatment of hepatic fibrosis.
M9250 HMN-176 HMN-176 inhibits mitosis, interfering with polo-like kinase-1 (plk1), without significant effect on tubulin polymerization.
M9249 BFH772 BFH772 is a potent and selective VEGFR2 inhibitor with an IC50 value of 3 nM.
M9248 CID5721353 CID5721353 is a B-Cell Lymphoma 6 inhibitor with IC50 of 212 μM.
M9247 YM-90709 YM-90709 is an interleukin-5 receptor antagonist.
M9246 HUHS015 HUHS015 is a potent PCA-1/ALKBH3 inhibitor, which continuously administering HUHS015 significantly suppressed the growth of DU145 cells.
M9245 GTPL5846 GTPL5846 (6-OAU) is a surrogate agonist of GPR84; activates human GPR84 in the presence of Gqi5 chimera in HEK293 cells with an EC50 of 105 nM in the PI assay.
M9244 1-methoxy PMS 1-methoxy PMS is stable electron-transport mediator between NAD(P)H and tetrazolium dyes.
M9243 ITD-1 ITD-1 is a selective inhibitor of TGF-β signaling (IC50 ~ 0.4-0.8 μM).
M9242 ISRIB ISRIB is a potent and selective PERK inhibitor with IC50 of 5 nM.
M9241 EPO Erythropoietin (EPO) is a glycoprotein cytokine secreted by the kidney in response to cellular hypoxia.
M9240 IFNγ, Human(CHO-expressed) Human Interferon gamma (hIFN-γ) is a dimerized soluble cytokine that is the only member of the type II class of interferons.
M9239 BSJ-03-123 BSJ-03-123 is a potent and novel CDK6-selective small-molecule degrader.
M9238 dBET6 dBET6 is a highly potent, selective and cell-permeable degrader of BET with an IC50 of 14 nM.
M9237 dBET1 dBET1 is a potent BRD4 protein degrader with an EC50 of 430 nM.
M9236 Ranibizumab Ranibizumab is a monoclonal antibody that inhibits angiogenesis by inhibiting Vascular endothelial growth factor A.
M9235 ARS-853 ARS-853 is a selective, covalent KRASG12C inhibitor with an IC50 of 2.5 μM.
M9234 Hecogenin Hecogenin is a potent and highly selective inhibitor of UGT1A4 with an IC50 value of 1.5 μM.
M9232 PF-04418948 PF-04418948 is a novel, potent and selective prostaglandin EP2 receptor antagonist with IC50 of 16 nM.
M9231 RMC-4550 RMC-4550 is a potent and selective SHP2 inhibitor, with an IC50 of 0.583 nM.
M9230 Indole-3-acetamide Indole-3-acetamide is an auxin precursor.
M9229 GS-444217 GS-444217 is a potent and selective inhibitor of apoptosis signal-regulating kinase 1 (ASK1) with an IC50 of 2.87±0.85 nM.
M9228 D-Gluconic acid copper(II) salt D-gluconic acid copper (II) salt is the copper salt of D-gluconic acid that is an organic acid.
M9227 Arachidonic acid Arachidonic acid (AA) is an unsaturated ω6 fatty acid constituent of the phospholipids of cell membranes.
M9226 D-Mannose D-Mannose is a carbohydrate, which plays an important role in human metabolism, especially in the glycosylation of specific proteins.
M9225 4-Octyl Itaconate 4-Octyl Itaconate is a cell-permeable anti-inflammatory metabolite that activates Nrf2 via alkylation of KEAP1.
M9223 R-268712 R-268712 is a potent and selective inhibitor of ALK5 with an IC50 of 2.5nM, an approximately 5000-fold more selectivity for ALK5 than p38 mitogen-activated protein kinase (MAPK).
M9222 LY3200882 LY3200882 is a novel, highly selective TGFβRI small molecule inhibitor.
M9221 GSK805 GSK805 is a potent, orally bioavailable RORγγ Inhibitor, with pIC50 of 8.4 and >8.2 for RORγ FRET assay and Th17 assay.
M9220 SR2211 SR2211 is a synthetic RORγ-selective modulator, functions as an inverse agonist, with a Ki of 105 nM and an IC50 of ~320 nM.
M9219 all-trans 4-Keto Retinoic Acid all-trans 4-Keto Retinoic Acid is an active metabolite of vitamin A, induces gene transcription via binding to nuclear retinoic acid receptors (RARs).
M9218 ABBV-744 ABBV-744 is a BDII-selective BET bromodomain inhibitor that is used in the research of AML and metastic castration-resistant prostate cancer.
M9217 Givinostat Givinostat is an HDAC inhibitor with IC50s of 198 and 157 nM for HDAC1 and HDAC3, respectively.
M9216 VcMMAE VcMMAE is a anti-mitotic agent, monomethyl auristatin E (MMAE), linked via the lysosomally cleavable dipeptide, valine-citrulline (vc).
M9215 GK921 GK921 is a transglutaminase 2 (TGase 2) inhibitor.
M9214 GC7 Sulfate GC7 Sulfate is a deoxyhypusine synthase (DHPS) inhibitor.
M9213 Miridesap Miridesap is a ligand for serum amyloid P component (SAP) and intends to inhibit and dissociate SAP binding to amyloid fibrils and tangles.
M9212 Aramchol Aramchol is a cholesterol solubilizer that prevents gallstone formation in inbred mice.
M9211 BDP5290 BDP5290 is a potent inhibitor of both ROCK and MRCK with IC50s of 5 nM, 50 nM, 10 nM and 100 nM for ROCK1, ROCK2, MRCKα and MRCKβ, respectively.
M9210 Ampicillin Ampicillin is an antibiotic against a variety of gram-positive and gram-negative bacteria.
M9209 SLx-2119 SLx-2119, also known as KD-025, is an orally bioavailable inhibitor of ROCK-II with IC50 of 105 nM.
M9208 PD0166285 PD0166285 is a potent Wee1 inhibitor and Chk1 inhibitor with IC50s of 24 nM and 72 nM, respectively.
M9207 Tributylammonium pyrophosphate Tributylammonium pyrophosphate
M9206 Biphenyl-4-sulfonyl chloride Biphenyl-4-sulfonyl chloride is a HDAC inhibitor with synthetic applications in palladium-catalyzed desulfitative C-arylation.
M9205 Glasdegib Glasdegib (PF-04449913) is a potent, orally bioavailable Smoothened (Smo) inhibitor with an IC50 of 4 nM.
M9204 Pam3CSK4 Pam3CSK4 is a Toll-like receptor 1/2 (TLR1/2) agonist.
M9203 Cytochalasin B Cytochalasin B is a cell-permeable mycotoxin binding to the barbed end of actin filaments, disrupting the formation of actin polymers, with Kd value of 1.4-2.2 nM for F-actin.
M9202 α-cyano-4-hydroxy-cinnamic acid α-CHCA is a classic monocarboxylate transporters (MCT) inhibitor.
M9201 Vibegron Vibegron is a potent and selective beta 3 adrenergic receptor agonist.
M9200 Ibodutant Ibodutant (MEN15596) is a potent and selective tachykinin NK2 receptor antagonist with a pKi of 10.1.
M9199 Avacopan Avacopan (CCX168) is a potent, selective and orally available complement 5a receptor inhibitor with an IC50 of 0.1 nM.
M9198 JTZ-951 Enarodustat (JTZ-951) is a potent and orally active factor prolyl hydroxylase inhibitor, with an EC50 of 0.22 μM.
M9197 Relugolix Relugolix, also known as TAK-385, is a luteinizing hormone-releasing hormone (LH-RH) receptor antagonist with an IC50 of 0.12 nM.
M9196 Elagolix sodium Elagolix Soidum is a potent, selective, orally active, non-peptide antagonist of the gonadotropin-releasing hormone receptor (GnRHR) with Kd value of 54 pM.
M9195 Saroglitazar Saroglitazar is a novel peroxisome proliferator-activated receptor (PPAR) agonist with predominant PPARα and moderate PPARγ activity, with EC50 values of 0.65 pM and 3 nM in HepG2 cells, respectively.
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.


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