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Cat.No.  Name Information
M10309 CYN 154806 TFA CYN 154806 TFA is a cyclic octapeptide and an effective selective somatostatin sst2 receptor antagonist.
M10308 Vorasidenib Vorasidenib (AG-881) is a potent and selective orally available inhibitor of mutated forms of both isocitrate dehydrogenase type 1 (IDH1, IDH1 [NADP+] soluble) in the cytoplasm and type 2 (IDH2, isocitrate dehydrogenase [NADP+], mitochondrial) in the mitochondria.
M10307 Benzolamide Benzolamide is a carbonic anhydrase inhibitor.
M10306 ARV-110 ARV-110 is an oral, specific androgen receptor (AR) PROTAC degrader.
M10305 AZD1656 AZD1656 is a potent, selective and orally active glucokinase (GK) activator, with an EC50 of 60 nM.
M10304 MYLS22 MYLS22 is a first-in-class and selective optic atrophy 1 (OPA1) inhibitor with anti-angiogenesis and anti-cancer activity.
M10303 D(+)-Xylose D(+)-Xylose is a natural product, mainly used to produce xylitol, as a non-calorie sweetener in foods and beverages.
M10302 1-Methyl-L-tryptophan 1-Methyl-L-tryptophan is an inhibitor of indoleamine 2,3-dioxygenase (IDO).
M10301 Fucoxanthin Fucoxanthin is a carotenoid that occurs naturally in certain algae with anti-obesity, anti-oxidant, anti-diabetic, anticancer and anti-inflammatory activities.
M10300 Thymosin alpha 1 Thymosin alpha 1 (Thymalfasin) is an immunomodulating agent able to enhance the Thl immune response.
M10299 c-di-AMP c-di-AMP (Cyclic diadenylate) is a STING agonist, it binds to the transmembrane protein STING thereby activating the TBK3-IRF3 signaling pathway.
M10298 AZD5305 AZD5305 is a potent and oral active, second-generation PARP (highly selective PARP1) inhibitor.
M10297 Recombinant Rat Interferon-gamma (CHO-expressed) Recombinant Rat Interferon-gamma (IFN-γ, Rat) also known as Type II interferon or immune interferon, is a cytokine produced primarily by T-lymphocytes and natural killer cells.
M10296 Recombinant Murine Interleukin-2 IL-2 is a powerful immunoregulatory lymphokine produced by T-cells in response to antigenic or mitogenic stimulation.
M10295 CAY10602 CAY10602 is a SIRT1 activator, which suppresses the NF-κB-dependent induction of TNF-α by lipopolysaccharide in THP-1 cells dose-dependently.
M10294 Scopolamine hydrobromide trihydrate Scopolamine hydrobromide trihydrate is a competitive muscarinic acetylcholine receptor with an IC50 of 55.3 ± 4.3 nM.
M10293 Mca-Tyr-Val-Ala-Asp-Ala-Pro-Lys(Dnp)-OH TFA Mca-Tyr-Val-Ala-Asp-Ala-Pro-Lys(Dnp)-OH TFA is a substrate for caspase-1 and angiotensin-converting enzyme 2 (ACE2).
M10292 Salicylhydroxamic acid
M10291 Ethyl 4-hydroxy-3-methoxycinnamate Ethyl ferulate is the alkyl ester derivative of ferulic acid which is a naturally occurring plant product with anti-oxidative, anti-inflammatory, neuroprotective, and antiproliferative activities.
M10290 BMS-1166 BMS-1166 is a potent PD-1/PD-L1 interaction inhibitor, which binds to human PD-L1 and blocks its interaction with PD-1.
M10289 Cucurbitacin D Cucurbitacin D induces apoptosis through caspase-3 and phosphorylation of JNK in hepatocellular carcinoma cells.
M10288 BMS-1001 BMS-1001 is a potent PD-1/PD-L1 interaction inhibitor.
M10287 GSK547 GSK547 is a potent and highly selective receptor-interacting serine/threonine protein kinase 1 (RIPK1) inhibitor.
M10286 Recombinant Murine Midkine Midkine is a heparin-binding growth factor, which contains 121 amino acid residues with 5 disulfide bonds.
M10285 MID-1 MID-1 is an inhibitor of MG53-IRS-1 (Mitsugumin 53-Insulin Receptor Substrate-1) interaction.
M10284 7-Fluorobenzofurazan-4-sulfonic acid ammonium salt 7-Fluorobenzofurazan-4-sulfonic acid ammonium salt is a fluorescent probe for thiols and pre-column labeling of biological thiols for HPLC.
M10283 AZD-5991 Racemate AZD-5991 Racemate is a Mcl-1 inhibitor with an IC50 of <3 nM in FRET assay.
M10282 (Thr4,Gly7)-Oxytocin (Thr4,Gly7)-Oxytocin is a peptide.
M10281 Somatostatin Somatostatin is a tetradecapeptide which can suppress the growth hormone (GH) secretion, and regulate the endocrine system to control the pituitary hormone secretion in human CNS.
M10280 L006235 L006235 (L235) is a potent, reversible cathepsin K inhibitor (IC50 = 0.25 nM) that displays > 4000-fold selectivity over cathepsins B, L and S.
M10279 Ibiglustat Ibiglustat (Venglustat) is a potent and selective Glucosylceramide synthase inhibitor and ceramide glucosyltransferase inhibitor.
M10278 Raphin1 Raphin1 is an orally bioavailable, selective R15B (PPP1R15B, a regulatory subunit of protein phosphatase 1) inhibitor, strongly binding to the R15B-PP1c holophosphatase with Kd of 33 nM.
M10277 EN6 EN6 is a small-molecule in vivo activator of autophagy that covalently targets cysteine 277 in the ATP6V1A subunit of the lysosomal the vacuolar H+ ATPase (v-ATPase).
M10276 Elastase (from porcine pancreas) Elastase from porcine pancreas is a serine protease that can hydrolyze proteins and polypeptide.
M10275 Bobcat339 Bobcat339 is a novel cytosine-based TET enzyme inhibitor with IC50s of 33 and 73 uM for TET1/2, it does not inhibit the DNA methyltransferase DNMT3a.
M10274 Tolebrutinib Tolebrutinib, also known as SAR442168, is a Bruton tyrosine kinase (BTK) inhibitor, with IC50 values of 0.4 nM and 0.7 nM in Ramos B cells and HMC microglia cells, respectively.
M10273 AVE 0991 AVE 0991 is an orally active agonist of angiotensin-(1-7) receptor with IC50 of 21 nM.
M10272 Fluorescein Sodium Fluorescein Sodium is a phthalic indicator dye used as a diagnostic aid in corneal injuries and corneal trauma.
M10271 mTOR inhibitor-1 mTOR inhibitor-1 is a potential ATP-competitive inhibitor of mTOR which could inhibit cell growth and proliferation.
M10270 Agnuside Agnuside is a compound isolated from Vitex negundo with anti-arthritic activity.
M10269 N-Acetyl-β-Asp-Glu N-Acetyl-β-Asp-Glu (βNAAG) is used as a substrate/inhibitor to identify and characterize glutamate carboxypeptidase(s).
M10268 CID-1067700 (ML282) CID-1067700 (ML282) is a competitive inhibitors of nucleotide binding by Ras-related GTPases with a Ki of 13 nM for Rab7.
M10267 Sodium thiocyanate Sodium thiocyanate is used in printing and dyeing and pharmaceutical industries, as well as reagents and solvents for polyacrylonitrile.
M10266 Sodium cyclamate Cyclamate is a commonly used non-nutritive synthetic sweetener.
M10265 Albumin Low endotoxin
M10264 4-Methylumbelliferyl α-D-galactopyranoside 4-Methylumbelliferyl α-D-galactopyranoside
M10263 Sodium hyaluronate Sodium Hyaluronic is is an anionic, nonsulfated glycosaminoglycan distributed widely throughout connective, epithelial, and neural tissues, it is used as a humectant to increase moisture in the skin, it may also serve as an emulsifier.
M10262 Mavacamten (MYK-461) Mavacamten, also known as SAR-439152 and MYK-461, is a myosin inhibitor potentially for the treatment of hypertrophic cardiomyopathy.
M10261 Gboxin Gboxin is an inhibitor of oxidative phosphorylation that targets glioblastoma, inhibits the activity of F0F1 ATP synthase, with antitumour activity.
M10260 γ-Cyclodextrin Cyclodextrins may be used to form inclusion complexes with a variety of drug molecules, resulting primarily in improvements to dissolution and bioavailability owing to enhanced solubility and improved chemical and physical stability.
M10259 Spastazoline Spastazoline is a potent and selective, cell permeable inhibitor for aaa+ (atpases associated with diverse cellular activities) proteins, inhibiting the microtubule-severing aaa+ protein spastin, with IC50 of 99 nM for human spastin.
M10258 SR-4835 SR-4835 is a highly selective, dual inhibitor of CDK12 with IC50 values of 99 nM, Kd of 98 nM and CDK13 with Kd of 4.9 nM, respectively.
M10257 Glycycoumarin Glycycoumarin is a bioactive coumarin of licorice, it inhibits hepatocyte lipoapoptosis through activation of autophagy and inhibition of ER stress-mediated JNK and GSK-3-mediated mitochondrial pathway.
M10256 Neoliquiritin Neoliquiritin is isolated from Glycyrrhiza uralensis with an anti-inflammatory activity.
M10255 Phosphatidylserine
M10254 SAR439859 SAR439859 is an orally active, nonsteroidal and selective degrader of estrogen receptor, it is also a potent antagonist of ER with EC50 of 0.2 nM for ERα degradation.
M10253 Ralinepag Ralinepag (APD811) is a potent, orally bioavailable and non-prostanoid prostacyclin (IP) receptor agonist with EC50 of 8.5 nM, 530 nM and 850 nM for human IP receptor, rat IP receptor and human DP1 receptor, respectively.
M10252 4-Hydroxytamoxifen 4-Hydroxytamoxifen is a selective estrogen receptor modulator.
M10251 Gly-β-MCA Gly-β-MCA is a potent, stable, intestine-selective and oral bioactive farnesoid X receptor (FXR) inhibitor.
M10250 Degarelix Degarelix is a competitive and reversible gonadotropin-releasing hormone receptor (GnRHR) antagonist.
M10249 Teduglutide Teduglutide is a glucagon-like peptide-2 (GLP- 2) receptor agonist used for the treatment of short-bowel syndrome.
M10248 Lanreotide Lanreotide is a somatostatin analogue, acts as an inhibitor of growth hormone (GH).
M10247 Nesiritide acetate Nesiritide acetate is an agonist of natriuretic peptide receptors (NPRs), with Kd values of 7.3 and 13 pM for NPR-A and NPR-C, respectively.
M10246 Bulevirtide Bulevirtide is a first-in-class entry inhibitor for the treatment of chronic Hepatitis D infection.
M10245 Pemafibrate Pemafibrate is a potent and highly specific PPARα agonist, with EC50s of 1 nM, 1.10 μM and 1.58 μM for h-PPARα, h-PPARγ and h-PPARδ, respectively.
M10244 Imidazole ketone erastin Imidazole ketone erastin (IKE) is an inducer of ferroptosis, and it is also a potent, selective, and metabolically stable inhibitor of the cystine-glutamate antiporter, system Xc-.
M10243 D-Kynurenine D-kynurenine is a metabolite of D-tryptophan, which can be used as a biological precursor of KYNA and 3-hydroxykynurenine.
M10242 Antagonist G Antagonist G is an anticancer peptide and it is also a potent vasopressin antagonist.
M10241 Polymyxin B nonapeptide TFA Polymyxin B nonapeptide TFA is a cyclic peptide from the naturally occurring peptide polymyxin B, it can increase the permeability of the outer membrane of Gram-negative bacteria toward hydrophobic antibiotics.
M10240 CTOP TFA CTOP TFA is a peptide that acts as a potent and selective μ opioid receptor antagonist, with Ki values of 0.96 and >10,000 nM for μ and δ receptors, respectively.
M10239 H-gamma-Glu-Phe-OH γ-Glu-Phe (γ-Glutamylphenylalanine) is a γ-3 glutamyl dipeptide synthesized by Bacillus amyloliquefaciens (GBA) and Aspergillus oryzae (GAO).
M10238 PAR-2 (6-1) amide (human) VKGILS-NH2 is a reversed amino acid sequence control peptide for SLIGKV-NH2.
M10237 Protease-Activated Receptor-2, amide Protease-Activated Receptor-2, amide (SLIGKV-NH2) is a highly potent agonist of PAR2 with IC50 of 10.4 uM.
M10236 PAR-2 (1-6) (mouse, rat) PAR-2 (1-6) (mouse, rat) is a PAR2 activator, it can be used to explore signaling through PAR2 in cells.
M10235 SLIGRL-NH2 SLIGRL-NH2 (Protease-Activated Receptor-2 Activating Peptide) is an agonist of Protease-Activated Receptor-2 (PAR-2).
M10234 Bradykinin Acetate Bradykinin Acetate is an active peptide that is generated by the kallikrein-kinin system, it is also recognized as a neuromediator and regulator of several vascular and renal functions.
M10233 ((Cys31,Nva34)-Neuropeptide Y (27-36))2 ((Cys31,Nva34)-Neuropeptide Y (27-36))2, also called BWX 46, is a neuropeptide Y (NPY) Y5 receptor selective agonist.
M10232 Cefotaxime Cefotaxime is an inhibitor of penicillin binding protein.
M10231 Neutral Protease (from Bacillus polymyxa) Neutral Protease is a type of protease that acts on the peptide bond of protein under neutral pH conditions, it can hydrolyze protein into amino acids, peptides and free amino acids.
M10230 LY2510924 LY2510924 is a potent and selective CXCR4 antagonist, which blocks SDF-1 binding to CXCR4 with IC50 of 0.079 nM.
M10229 Porcine dynorphin A (1-13) Porcine dynorphin A (1-13) is a potent, endogenous κ opioid receptor agonist.
M10228 Caspase-9 Inhibitor III Caspase-9 Inhibitor III is a potent and irreversible inhibitor of caspase-9.
M10227 Pim1/AKK1-IN-1 Pim1/AKK1-IN-1 is a potent multi-kinase inhibitor with Kd values of 35 nM/53 nM/75 nM/380 nM for Pim1/AKK1/MST2/LKB1 respectively.
M10226 Etrasimod (APD334) Etrasimod (APD334) is a specific and orally available antagonist of the sphingosine-1-phosphate-1 (S1P1) receptor, with IC50 of 1.88 nM in CHO cells.
M10225 Tat-NR2B9c Tat-NR2B9c is a 20-aa peptide, it acts as a postsynaptic density-95 (PSD-95) inhibitor with EC50 of 6.7 nM for PSD-95d2.
M10224 YAP-TEAD-IN-1 TFA YAP-TEAD-IN-1 TFA is a competitive inhibitor of YAP-TEAD interaction with IC50 of 25 nM.
M10223 Okanin Okanin attenuates LPS-induced microglial activation through inhibition of the TLR4/NF-κB signaling pathways, it is the effective constituent of the flower tea Coreopsis tinctoria.
M10222 COG 133 COG 133 is a fragment of Apolipoprotein E (APOE) peptide with potent anti-inflammatory and neuroprotective effects.
M10221 Gly-Gly-Tyr-Arg Gly-Gly-Tyr-Arg
M10220 PHM-27 (human) PHM-27 (human) is a human prepro-vasoactive intestinal polypeptide (27 amino acid).
M10219 D-Glucuronic acid D-Glucuronic acid is a carboxylic acid with structural similarity to glucose with detoxifying activity.
M10218 (+)-Gallocatechin (+)-Gallocatechin is found notably in green tea, it has moderate affinity to the human cannabinoid receptor and acts as an antioxidant.
M10217 Diethyldithiocarbamate sodium Sodium diethyldithiocarbamate is an accelerator of the rate of copper cementation. Sodium diethyldithiocarbamate reduces the incidence of HIV infection.
M10216 11C,14C-Eicosadienoic Acid 11C,14C-Eicosadienoic Acid is a rare, naturally occurring n-6 polyunsaturated fatty acid found mainly in animal tissues.
M10215 Motixafortide (BL-8040) Motixafortide (BL-8040) is an antagonist of CXCR4 with IC50 value of 1 nM.
M10214 Agouti-related Protein (AGRP) (25-82), human Agouti-related protein (AgRP) is a neuropeptide produced in the brain by the AgRP/NPY neuron.
M10213 L-Tryptophan L-tryptophan is an amino acid. it is necessary for normal growth in infants and for nitrogen balance in adults, which cannot be synthesized from more basic substances in humans and other animals.
M10212 L-Threonine L-threonine could adjust the balance of amino acid in feed, promote growth, improve meat quality and improve ncrease the value of feed raw materials of lower amino acid digestibility and produce the low protein feed, save protein resources, reduce the cost of feed ingredients, reduce the nitrogen content of manure and urine and decrease the concentration and release rate of animal building ammonia.
M10211 Obtustatin Obtustatin is a potent integrin α1β1 inhibitor with IC50 of 0.8 nM for α1β1 binding to type IV collagen.
M10210 Amylin, amide, human Amylin, amide, human is a 37-amino acid polypeptide, it is a pancreatic hormone cosecreted with insulin that exerts unique roles in metabolism and glucose homeostasis.

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