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Cat.No.  Name Information
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.
M9193 Carbetocin Carbetocin is an agonist at peripheral oxytocin receptors.
M9192 Cholic acid Cholic acid is a major primary bile acid produced in the liver and usually conjugated with glycine or taurine. It facilitates fat absorption and cholesterol excretion.
M9191 Sodium pyrophosphate Sodium pyrophosphate is a colorless transparent crystalline chemical compound with the formula Na4P2O7.
M9190 β-Glycerol phosphate disodium salt pentahydrate β-Glycerol phosphate disodium salt pentahydrate is a potent protein phosphatase and tensin homolog (PTEN) inhibitor.
M9189 Eldecalcitol Eldecalcitol is an analog of 1,25-dihydroxyvitamin D3 that improves bone mineral density.
M9188 Clomethiazole Clomethiazole is a positive allosteric modulator at the barbiturate/picrotoxin site of the GABAA receptor.
M9187 p-Nitrophenol p-Nitrophenol (4-NP) can be used to prepare 4-aminophenol.
M9186 Bedaquiline Bedaquiline, a diarylquinoline antibiotic that targets ATP synthase, is effective for the treatment of Mycobacterium tuberculosis infections.
M9185 Serlopitant Serlopitant is a selective Neurokinin-1 (NK-1) receptor antagonist.
M9184 RO8994 RO8994 is a potent and selective spiroindolinone MDM2 inhibitor, with IC50 of 5 nM (HTRF binding assays) and 20 nM (MTT proliferation assays).
M9182 Gefapixant Gefapixant, also known as AF-219 or MK-7264, is a P2X3 receptor antagonist.
M9181 8-OH-DPAT 8-OH-DPAT (8-Hydroxy-DPAT) is a potent and selective 5-HT agonist, with a pIC50 of 8.19 for 5-HT1A.
M9180 Pyridostatin Trifluoroacetate Salt Pyridostatin Trifluoroacetate Salt is a G-quadruplexe stabilizer, with a Kd of 490 nM.
M9179 Nolatrexed HCl Nolatrexed HCl, also known as AG337, is a thymidylate synthase inhibitor.
M9178 GSK2292767 GSK2292767 is a potent and selective PI3Kδ inhibitor.
M9177 SirReal2 SirReal2 is a potent and selective Sirt2 inhibitor with IC50 of 140 nM.
M9176 DTP3 DTP3 is a selective GADD45β/MKK7 inhibitor, which inhibits cancer-selective NF-κB survival pathway.
M9175 Vacquinol-1 Vacquinol-1 is an MKK4 activator, which rapidly and selectively induces glioma cell death.
M9174 ARQ 621 ARQ 621 is an allosteric, and selective Eg5 mitotic motor protein inhibitor.
M9173 Cilengitide trifluoroacetate Cilengitide is a potent integrin inhibitor for αvβ3 and αvβ5 receptor with IC50 of 4.1 nM, 79 nM in cell-free assays respectively.
M9172 Emedastine Difumarate Emedastine Difumarate is a second generation, selective histamine H1 receptor antagonist with anti-allergic activity.
M9171 Sodium succinate Sodium succinate is an important metabolite at the cross-road of several metabolic pathways.
M9170 Sodium Houttuyfonate Sodium Houttuyfonate is the active compound of the Houttuynia plant.
M9169 Thimerosal Thimerosal inhibits a wide range of thiol-dependent enzymes and proteins, such as PI3-kinase-dependent methionine synthetase, glutamate transport receptor, and Na++K+ dependence ATPase.
M9168 Berberine Berberine is an alkaloid in several plants with various biological functions, including insulin-sensitizing, anti-inflammatory, and anti-oxidant activity.
M9166 BMS-986142 BMS-986142 is a potent, selective, reversible BTK inhibitor, shows BTK IC50 = 0.5nM; human WB IC50 = 90 nM.
M9165 Rimegepant Rimegepant, also known as BMS-927711, is a potent, selective, competitive, and orally active calcitonin gene-related peptide (CGRP) antagonist with a Ki value of 0.027 nM.
M9164 Insulin(cattle) Insulin is a peptide hormone produced by beta cells of the pancreatic islets. The compound is unstable in solutions, freshly prepared is recommended.
M9163 Blasticidin S hydrochloride Blasticidin S HCl is a potent inhibitor of protein synthesis in both prokaryotic and eukaryotic cells. Blasticidin S hydrochloride is a nucleoside antibiotic isolated from Streptomyces griseochromogenes.
M9162 Triton x-100 Triton x-100 is a nonionic, non-denaturing detergent suitable for solubilization, isolation and purification of membrane protein complexes.It is chemically indistinguishable from Nonidet P-40.
M9161 NVP-ACC789 NVP-ACC789 is an inhibitor of human VEGFR-1, VEGFR-2 (mouse VEGFR-2), VEGFR-3 and PDGFR-β with IC50s of 0.38, 0.02 (0.23), 0.18, 1.4 μM, respectively.
M9160 BMS-582949 BMS-582949 is a potent and selective P38 mitogen-activated protein kinase (P38 MAPK) inhibitor with IC50 of 13nM.


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