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Cat.No.  Name Information
M9359 BAY-293 BAY-293 is a potent inhibitor of Son of Sevenless 1 (SOS1), blocks RAS activation via disruption of the KRAS-SOS1 interaction with an IC50 of 21 nM.
M9358 ITE ITE is a potent endogenous agonist of aryl hydrocarbon receptor (AhR), which directly binding to AHR with a Ki of 3 nM.
M9357 AMG-510 racemate AMG-510 racemate is a racemic of AMG-510, which is a potent KRAS G12C covalent inhibitor.
M9356 AMG-510 AMG-510 is a potent KRAS G12C covalent inhibitor.
M9355 UNC2541 UNC2541 is a potent and MerTK-specific inhibitor, which binds in the MerTK ATP pocket with an IC50 of 4.4 nM.
M9354 SR9238 SR9238 is a liver X receptor (LXR) inverse agonist with IC50s of 214 nM and 43 nM for LXRα and LXRβ, respectively.
M9353 N-Ethylmaleimide N-Ethylmaleimide (NEM) is a cysteine protease inhibitor.
M9352 Gramicidin Gramicidin is an antimicrobial peptide assembling as channels in membranes and increasing their permeability towards cations.
M9351 Verinurad Verinurad, also known as RDEA3170, is an organic anion transporter URAT1 inhibitor with an IC50 of 25 nM.
M9350 URMC-099 URMC-099 is an orally bioavailable, potent mixed lineage kinase type 3 (MLK3) inhibitor with IC50 of 14 nM, which has excellent blood-brain barrier penetration properties.
M9349 Adenosine Dialdehyde Adenosine Dialdehyde (ADOX) is an adenosine analog and S-adenosylmethionine-dependent methyltransferase inhibitor with an IC50 of 40 nM.
M9348 Amarogentin Amarogentin is a secoiridoid glycoside that exhibits many biological effects, including anti-oxidative, anti-tumour, and anti-diabetic activities.
M9347 ITI-214 phosphate ITI-214 phosphate is an orally active, potent and selective inhibitors of PDE1, exhibits potent PDE1 inhibitory activity (Ki = 58 pM).
M9346 Pralsetinib Pralsetinib (BLU-667) is a next generation highly potent, selective RET inhibitor with IC50 of 0.3-0.4 nM for WT RET, RET mutants V804L, V804M, M918T and CCDC6-RET fusion.
M9345 Preladenant Preladenant is a potent and competitive antagonist of the human adenosine A2A receptor with a Ki of 1.1 nM.
M9344 Recombinant Human GM-CSF (CHO-expressed) Recombinant Human Granulocyte-Macrophage Colony Stimulating Factor (CHO-expressed) is a hematopoietic growth factor and immune modulator.
M9343 Glutathione Oxidized Glutathione oxidized is produced by the oxidation of glutathione.
M9342 NG25 NG25 is a potent dual TAK1 and MAP4K2 inhibitor with IC50s of 149 nM and 21.7 nM, respectively.
M9341 AZD-7648 AZD-7648 is a potent and selective DNA-PK inhibitor.
M9340 IRAK-1-4 Inhibitor I IRAK-1-4 Inhibitor I is an inhibitor of interleukin-1 receptor-associated kinase 1/4 (IRAK 1/4) with IC50s of 0.3 μM and 0.2 μM, respectively.
M9339 Methyl arachidonate Methyl arachidonate is the keystone essential fatty acid at the origin of the arachidonic acid cascade.
M9338 JNJ-47117096 JNJ-47117096 is potent and selective MELK inhibitor with IC50 of 23 nM.
M9337 Sodium iodoacetate
M9335 Cefazolin Cefazolin is a semisynthetic cephalosporin analog with broad-spectrum antibiotic action due to inhibition of bacterial cell wall synthesis.
M9334 Vancomycin Vancomycin is an antibiotic for the treatment of bacterial infections.
M9333 Phytohemagglutinin Phytohemagglutinin is a lectin obtained from the red kidney bean that binds to the membranes of T-cells, stimulates metabolic activity and involves inflammatory pathways.
M9332 Apilimod Apilimod is a potent IL-12/IL-23 inhibitor, and it is also a cell permeable small molecule which specifically inhibits PIKfyve with an IC50 of 14 nM in an in vitro kinase assay.
M9331 10-Hydroxy-trans-2-decenoic acid 10-Hydroxy-trans-2-decenoic acid is the principal lipid component in royal jelly which is the food for queen and larvae honeybees.
M9330 Brij-35 Brij-35 (Polidocanol) is a high HLB, ethoxylated, nonionic ether of lauryl alcohol with broad pH stability.
M9329 Fenoterol Fenoterol is a β2 adrenoreceptor agonist with bronchodilator activity.
M9328 Hyaluronic Acid Hyaluronic acid (HA) is an anionic, nonsulfated glycosaminoglycan distributed widely throughout connective, epithelial, and neural tissues.
M9327 L-Isoleucine L-isoleucine is a nonpolar hydrophobic amino acid.
M9326 Methyl cellulose Methyl cellulose
M9325 EGTA EGTA is a chelating agent selective for Ca2+.
M9324 TD139 TD-139 is a potent, synthetic inhibitor of galectin-3.
M9323 Succimer Succimer is a widely used chelating agent for the treatment of Pb poisoning.
M9322 2-Nitrophenyl β-D-galactopyranoside 2-Nitrophenyl β-D-galactopyranoside is a colorimetric and spectrophotometric substrate for detection of β-galactosidase activity.
M9321 Nourseothricin sulfate Nourseothricin is a broad-spectrum antibiotic derived from Streptomyces noursei.
M9320 Gastrin-I (human) Gastrin-I (human) is the endogenous peptide produced in the stomach, which increases gastric acid secretion via cholecystokinin 2 (CCK2) receptor.
M9319 Dimethyl anthranilate Dimethyl anthranilate is widely used in the preparation of flavours.
M9318 Chymostatin Chymostatin is a chymotryptase-like serine proteases inhibitor, with Ki values of 9.36 and 13.1 nM for chymotrypsin and chymase, respectively.
M9317 Carboxymethyl cellulose sodium Carboxymethyl cellulose sodium is frequently used as viscous agent, paste and barrier agent.
M9316 Ceruletide Ceruletide is a biologically active decapeptide isolated from the skin of the Australian frog Hyla caerulea, acts as a cholecystokinin receptor agonist.
M9315 Gibberellin Gibberellic acid (Gibberellin) is a plant hormone stimulating plant growth and development.
M9314 Brassinolide Brassinolide is a plant steroid that promotes cell elongation and cell devision and thus regulates plant growth and development.
M9313 25-Hydroxycholesterol 25-Hydroxycholesterol (a metabolite of cholesterol) is a potent and selective suppressor of IgA production by B cells (EC50≈65 nM).
M9312 Glucagon Glucagon is a peptide hormone that helps regulate the blood sugar (glucose) levels in the body.
M9311 Liraglutide Liraglutide is a glucagon-like peptide-1 (GLP-1) receptor agonist.
M9310 4-Methylumbelliferone 4-Methylumbelliferone is a hyaluronic acid (HA) synthesis inhibitor with IC50 value of 0.4 mM.
M9309 ML327 ML327 is a blocker of MYC, which mediated transcriptional de-repression of E-cadherin and inhibition of epithelial-to-mesenchymal transition.
M9308 LY344864 LY344864 is a selective 5-HT1F receptor agonist with an affinity of 6 nM (Ki).
M9307 TC-S 7005 TC-S 7005 is a potent and selective polo-like kinase 2 (PLK2) inhibitor (IC50 = 4 nM).
M9305 Targocil Targocil is a bacteriostatic inhibitor of wall teichoic acid (WTA) biosynthesis, with MIC90s of 2 μg/ mL for both MRSA and MSSA.
M9304 KNK437 KNK437 is a novel inhibitor of acquisition of thermotolerance and heat shock protein.
M9303 Amenamevir Amenamevir is a herpes virus helicase-primase inhibitor, with an EC50 of 14 ng/mL against HSVs.
M9302 CBL0137 CBL0137 is a metabolically stable curaxin that activates p53 with an EC50 value of 0.37 µM and inhibits NF-κB with an EC50 of 0.47 µM.
M9301 Telithromycin Telithromycin is a semi-synthetic erythromycin derivative used for mild to moderate respiratory infections.
M9300 AG 126 AG 126 is a cell-permeable inhibitor of lipopolysaccharide (LPS)-induced synthesis of tumor necrosis factor-α and nitric oxide in murine peritoneal macrophages.
M9299 HSF1A HSF1A is an activator of Heat shock transcription factor 1 (HSF1).
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.


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