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Cat.No.  Name Information
M10430 Recombinant Human TGF-α (E. coli) Recombinant Human TGF-α, also known as sarcoma growth factor, TGF-type I and ETGF, is a member of the EGF family of cytokines. TGF-α signals through EGFR and acts synergistically with TGF-beta to promote the proliferation of a wide range of epidermal and epithelial cells.
M10429 Ciprofloxacin hydrochloride Ciprofloxacin hydrochloride is a β-diketone antibiotic with a broad spectrum antibacterial activity.
M10428 N-Acetyl-D-galactosamine (D-N-Acetylgalactosamine) N-Acetyl-D-galactosamine (D-N-Acetylgalactosamine) is an endogenous metabolite, it is the important constituent of brain heteropolysaccharides (glycoproteins).
M10427 OVA Peptide (257-264) TFA OVA Peptide (257-264) TFA is a class I (Kb)-restricted peptide epitope of OVA, an octameric peptide from ovalbumin presented by the class I MHC molecule, H-2Kb.
M10426 1,3-Benzoxazole-6-carboxylic acid 1,3-Benzoxazole-6-carboxylic acid
M10425 Dimethyl succinate (Standard for GC) Dimethyl succinate is a biodegradable ester with low odor and low volatility and commonly serves as a flavoring agent that can be used in perfumery and personal are products, including skin-conditioning agents and emollient.
M10424 Deoxyartemisinin Deoxyartemisinin
M10423 DT2216 DT2216 is a selective B-cell lymphoma extra large (BCL-XL) proteolysis-targeting chimera (PROTAC).
M10422 Sodium bicarbonate Sodium bicarbonate is an inorganic salt used as a buffering agent and a pH adjuster, it also serves as a neutralizer.
M10421 Sodium citrate (dihydrate) Sodium citrate dehydrate is an anticoagulant and also used as a buffer and food preservatives.
M10420 Proglumide Proglumide is a nonpeptide and orally active cholecystokinin (CCK)-A/B receptors antagonist.
M10419 Fmoc-Asn(Trt)-OPfp Fmoc-Asn(Trt)-OPfp is a non-essential amino acid.
M10418 Malvidin chloride Malvidin (chloride) is a bioactive compound demonstrates antioxidant capacity with free radical scavenging properties in vitro.
M10417 Delphinidin chloride Delphinidin (chloride) is an anthocyanidin, a natural plant pigment which can modulate JAK/STAT3 and MAPKinase signaling to induce apoptosis in HCT116 cells.
M10416 Ac4ManNAz Ac4ManNAz is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
M10415 Curdlan Curdlan is a polysaccharide produced by bacteria and a homopolymer of glucose with β-1,3-glucosidic linkage.
M10404 Tosufloxacin tosylate hydrate Tosufloxacin tosylate hydrate is a fluoroquinolone antibacterial agent used to treat susceptible infections.
M10395 MKC-3946 MKC-3946 is a potent IRE1α inhibitor which triggered modest growth inhibition in multiple myeloma cell lines.
M10394 FL118 FL118 is an inhibitor of human survivin expression, activating tumor suppressor p53 as a novel MOA in p53 wild-type cancer cells.
M10393 Eribulin mesylate Eribulin mesylate (E7389 mesylate) is a microtubule targeting agent that is used for the research of metastatic breast cancer.
M10392 Corticotropin Corticotropin (ACTH) is a polypeptide hormone extracted from the anterior lobe of the pituitary gland of mammals, acts on the adrenal cortex, and has the effect of promoting the proliferation of adrenal cortex tissue and the production and secretion of corticosteroids.
M10391 Osthole Osthole (Osthol) is a natural antihistamine alternative with potential inhibition of histamine H1 receptor activity.
M10390 Aminooxy-acetic acid (AOA) Aminooxy-acetic acid (AOA) is a GABA transaminase (GABA-T) inhibitor (Ki = 9.16 μM) that induces GABA accumulation in the brain. It also inhibits cystathionine β synthase (CBS) and cystathionine γ lyase (CSE) with IC50 values of 8.5 and 1.1 μM, respectively.
M10389 Aminoethoxyvinyl glycine hydrochloride Aminoethoxyvinyl glycine hydrochloride is an ethylene synthesis inhibitor. It is used to study the roles of ethylene in plant processes such as gravitropism and fasciation/cresting.
M10382 PROTAC SGK3 degrader-1 PROTAC SGK3 degrader-1 (SGK3-PROTAC1) is a potent SGK3 degrader, it is a PROTAC conjugate of the 308-R SGK inhibitor with the VH032 VHL binding ligand, targeting SGK3.
M10381 TD-165 TD-165 is a PROTAC-based cereblon (CRBN) degrader.
M10380 dBET57 dBET57 is a novel BRD4 heterobifunctional small-molecule ligand (PROTAC) which exhibits significant and selective degradation of BRD4 BD1 but is inactive on BRD4 BD2.
M10379 BSJ-03-123 BSJ-03-123 is a novel, potent CDK6-selective small-molecule degrader (PROTAC).
M10378 Cycloleucine Cycloleucine is antagonist of NMDA receptor associated glycine receptor, with a Ki of 600 μM. Cycloleucine is a specific inhibitor of S-adenosyl-methionine mediated methylation.
M10377 AZD4205 AZD4205 is a novel potent and selective janus kinase 1 (JAK1) inhibitor, with IC50 value of 73 nM.
M10376 Atranorin Atranorin is a lichen secondary metabolite which shows significant antinociceptive and antiinflammatory activities, it has a relevant redox-active action, acting as a pro-oxidant or antioxidant agent depending on the radical.
M10375 AD80 AD80 is a multikinase inhibitor, it potently targets human RET, BRAF, S6K, and SRC.
M10374 AMG 232 AMG 232 is an extremely potent MDM2 inhibitor (SPR KD = 0.045 nM, SJSA-1 EdU IC50 = 9.1 nM), with remarkable pharmacokinetic properties and in vivo antitumor activity in the SJSA-1 osteosarcoma xenograft model (ED50 = 9.1 mg/kg). *The compound is unstable in solutions, freshly prepared is recommended
M10373 CB-103 CB-103 is a first-in-class, orally active γ-secretase inhibitor, CB-103 inhibits Notch signaling in primary human T cell acute lymphoblastic leukemia and other Notch-dependent human tumor cell lines, and concomitantly induces cell cycle arrest and apoptosis.
M10372 Vazegepant hydrochloride Vazegepant (BHV-3500) hydrochloride is a highly affinity CGRP receptor antagonist (hCGRP Ki= 0.023 nM).
M10371 Cabotegravir Cabotegravir, also known as S/GSK1265744 or GSK744, is potent HIV integrase inhibitor.
M10370 Larazotide acetate Larazotide acetate also known as AT-1001, is a tight junction regulator and reverses leaky junctions to their normally closed state.
M10369 RO5126766 (VS-6766) RO5126766 (CH5126766, VS 6766) is a first-in-class dual MEK/RAF inhibitor with IC50 values of 8.2 nM, 19 nM, 56 nM and 160 nM for BRAF V600E, BRAF, CRAF and MEK1, respectively.
M10368 Gelatin (from porcine skin) Gelatin is a heterogeneous mixture of water-soluble proteins of high average molecular masses, present in collagen. Gelatin has been used in many applications. It has use in coating cell culture to improve attachment of cells, being added to PCR to stabilize Taq DNA, as a blocking reagent in Western blotting, ELISA, and immunochemistry, and as a component of media for species differentiation in bacteriology.
M10367 Ruthenium red Ruthenium red (Ammoniated ruthenium oxychloride) is a polycationic dye widely used for electron microscopy (EM) of cells, tissues and vegetative bacteria. Ruthenium red is also a L-type calcium current (ICa) blocker, blocks Ca2+ uptake and release, and voltage-sensitive Ca2+ channels.
M10366 Carbutamide Carbutamide (BZ-55) is the first-generation orally active sulfonylurea with hypoglycemic activity.
M10365 L-JNKI-1 L-JNKI-1 is a cell-permeable peptide inhibitor specific for JNK.
M10364 Tenofovir hydrate Tenofovir hydrate is a nucleotide reverse transcriptase inhibitor to treat HIV and chronic Hepatitis B.
M10363 Cyclic ADP-​ribose ammonium Cyclic ADP-ribose is a cyclic purine nucleotide that is synthesised from NAD+ by ADP-ribosyl cyclase; acts as an agonist at ryanodine receptors.
M10362 Beaucage reagent Beaucage reagent is a potent DNA cleavage agent. Beaucage reagent can be used for preparing phosphorothioate oligomers.
M10361 Albumin, Fatty Acid Free
M10360 Arteannuin B Arteannuin B co-occurs with artemisinin, Arteannuin B shows anti-SARS-CoV-2 potential with an EC50 of 10.28 μM.
M10359 Dihydroartemisinic acid Dihydroartemisinic acid is a natural product from Artemisia annua and the main direct precursor of artemisinin, which is a medicinal herb that is widely used to treat Malaria.
M10358 C-Type Natriuretic Peptide (CNP) (1-22), human C-Type Natriuretic Peptide (CNP) (1-22), human is the 1-22 fragment of C-Type Natriuretic Peptide.
M10357 Rhod-2 AM Rhod-2 AM is a fluorescent, mitochondrial probe (λex=552 nm, λem=581 nm).
M10356 Calcein Red, AM Calcein AM is one of the most popular fluorescent probes used for labeling and monitoring cellular functions of live cells. Non-fluorescent Calcein Red AM can easily get into live cells and hydrolyzes to generate strongly fluorescent Calcein Red dye. Calcein Red dye can be monitored with the common TRITC/Cy3 filter set.
M10355 Uric acid sodium Uric acid sodium is a scavenger of oxygen radical, it is a very important antioxidant that help maintains the stability of blood pressure and antioxidant stress.
M10354 Recombinant Human EGF (E. coli) Epidermal Growth Factor (EGF) is a potent growth factor that stimulates the proliferation of various epidermal and epithelial cells.
M10353 Recombinant Human FGF-10/KGF-2 (E. coli) Recombinant Human Fibroblast Growth Factor-10 (FGF-10) is a mitogen mainly produced by mesenchymal stem cells in the lung. FGF-10 belongs to the heparin binding FGF family, and is also known as Keratinocyte Growth Factor-2 (KGF-2). It shares homology with KGF and receptor binding to FGFR2-IIIb.
M10352 Recombinant Human HGF (CHO-expressed) Recombinant human Hepatocyte Growth Factor (rhHGF) , also known as hepatopoietin-A and scatter factor, is a pleiotropic mitogen belonging to the peptidase S1 family (plasminogen subfamily). It is produced by mesenchymal cells and acts on epithelial cells, endothelial cells and haemopoietic progenitor cells.
M10351 IKarisoside A IKarisoside A is a natural compound isolated from Epimedium koreanum (Berberidaceae) with anti-inflammatory properties.
M10350 Resazurin sodium Resazurin sodium salt is a blue non-fluorescent dye,is widely used as a metabolic indicator for living cells.
M10349 Dihydrocytochalasin B Dihydrocytochalasin B is a Cytokinesis inhibitor and changes the morphology of the cells, similar to that of cytochalasin B.
M10348 27-Hydroxycholesterol 27-Hydroxycholesterol is a selective estrogen receptor modulator, and it is also an agonist of the liver X receptor.
M10347 Abemaciclib (LY2835219) Abemaciclib (LY2835219) is a potent and selective inhibitor for CDK4 and CDK6 with IC50 values of 2 nM and 10 nM, respectively.
M10346 Glutamic acid (L-Glutamic acid) L-Glutamic acid acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA).
M10345 Eucalyptol Eucalyptol is an inhibitor of 5-HT3 receptor, potassium channel, with anti-inflammatory and antioxidant activities.
M10344 Recombinant Human Glial Cell Line-derived Neurotrophic Factor Glial cell-derived neurotrophic factor is a neurotrophic factor that enhances survival and morphological differentiation of dopaminergic neurons and increases their high-affinity dopamine uptake.
M10342 [Leu31,Pro34]-NPY TFA (human,rat) [Leu31,Pro34]-NPY TFA (human,rat) is a specific neuropeptide Y1 receptor agonist.
M10341 Lauric acid Lauric acid is a middle chain-free fatty acid with strong bactericidal properties.
M10340 Ghrelin (human) Acetate Ghrelin (human) Acetate is an endogenous agonist peptide for the ghrelin (GHS) receptor. Ghrelin (human) Acetate stimulates release of growth hormone from the pituitary gland and regulates feeding, appetite, growth and energy homeostasis.
M10339 Fexinidazole Fexinidazole (also known as Hoe-239) is an orally active, potent antiparasitic agent.
M10338 Azophloxine Azophloxine, also known as acid red 1 (AR 1), is a member of synthetic red azo dye family.
M10337 Avitinib (AC0010) Avitinib (Abivertinib; AC0010) is a third-generation irreversible EGFR tyrosine kinase inhibitor, with potential antineoplastic activity.
M10336 KL1333 KL1333 is an orally available, small organic molecule that reacts with NAD(P)H:quinone oxidoreductase 1 (NQO1) as a substrate, resulting in increases in intracellular NAD+ levels via NADH oxidation.
M10335 IDH-305 IDH-305 is an orally available, mutant-selective and brain-penetrant IDH1 inhibitor that targets IDH1(R132) mutation with IC50 values of 27 nM, 28 nM and 6.14 μM for IDH1R132H, IDH1R132C and IDH1WT, respectively.
M10334 FF-10101 FF-10101 is a novel irreversible FLT3 inhibitor.
M10333 CRF (bovine) TFA CRF (bovine) TFA is a potent agonist of CRF receptor, and displaces [125I-Tyr]ovine CRF with a Ki of 3.52 nM.
M10332 Vapreotide acetate Vapreotide acetate (BMY-41606 acetate; RC160 acetate) is a neurokinin-1 (NK1) receptor antagonist with IC50 value of 330 nM.
M10331 CRX-527 CRX-527 is a highly specific and potent TLR4 agonist, which displays significantly less toxicity when compared to LPS.
M10330 Teriparatide acetate Teriparatide acetate is a PHT agonist, with an IC50 of 2 nM in HEK293 cells.
M10329 Ningetinib Ningetinib is a potent, orally bioavailable tyrosine kinase inhibitor for Axl, VEGFR2 and c-Met with IC50 values of <1.0, 1.9 and 6.7 nM, respectively.
M10328 MRX-2843 MRX-2843 (UNC2371) is a potent and orally active inhibitor of MERTK and FLT3 with IC50 values of 1.3 nM and 0.64 nM, respectively.
M10327 Zotiraciclib Zotiraciclib (TG02, SB1317) is an orally bioavailable, brain penetrant multi-kinase inhibitor of CDK2, JAK2, and FLT3 with IC50 values of 13, 73, and 56 nM, respectively.
M10326 Zuranolone Zuranolone also known as SAGE-217, is a potent GABAA receptor agonist with EC50 values of 296 nM and 163 nM for α1β2γ2 and α4β3δ GABAA receptors.
M10325 Diphyllin Diphyllin is an arylnaphthalene lignan isolated from Justicia procumbens and is a potent HIV-1 inhibitor with an IC50 of 0.38 μM.
M10324 Cynaropicrin Cynaropicrin is a sesquiterpene lactone which can inhibit tumor necrosis factor (TNF-α) release and the increase of cartilage degradation factor (MMP13) and suppresses NF-κB signaling.
M10323 ULK-101 ULK-101 is a potent and selective ULK1 inhibitor with in vitro IC50 of 8.3 nM.
M10322 GSK-2330672 (Linerixibat) GSK-2330672, also known as linerixibat, is a highly potent, nonabsorbable apical sodium-dependent bile acid transporter inhibitor for the research of type 2 diabetes.
M10321 XTT sodium salt XTT sodium salt is a tetrazolium salt, which forms water-soluble formazan on bioreduction.
M10320 Chondroitin sulfate Chondroitin sulfate is a class of sulfated glycosaminoglycans that are linear polysaccharides consisting of repeating disaccharide units composed of uronic acid and N-acetylhexosamine, which has been widely used in the treatment of osteoarthritis.
M10319 Parathyroid Hormone (1-34), bovine Acetate Parathyroid Hormone (1-34), bovine Acetate is a potent parathyroid hormone (PTH) receptor agonist.
M10318 AC1903 AC1903 is a specific inhibitor of TRPC5 channel.
M10317 LNP023 hydrochloride (Iptacopan HCl) Iptacopan (LNP023) hydrochloride is a first-in-class orally bioavailable, highly potent and selective complement factor B inhibitor with an IC50 value of 10 nM.
M10316 Stearic acid Stearic acid is a long chain dietary saturated fatty acid which exists in many animal and vegetable fats and oils.
M10315 MK6-83 MK6-83 is an agonist of the transient receptor potential channel ML3 (TRPML3).
M10314 Lariciresinol Lariciresinol can inhibit the proliferation of human dendritic cells in vitro, and enhance the ability of human dendritic cells to secrete interleukin 10.
M10313 Recombinant Human Granulocyte Colony Stimulating Factor (CHO-expressed) Human Granulocyte Colony Stimulating Factor (G-CSF) is a pleiotropic cytokine, mainly produced by monocytes and macrophages upon activation by endotoxin, TNF-α and IFN-γ.
M10312 Vasopressin Acetate Vasopressin acetate (AVP) is a peptide hormone with antidiuretic and vasoconstrictive activities, and plays an important part in circulatory and water homoeostasis.
M10311 PF-06882961 PF-06882961 is a potent, orally bioavailable agonist of the glucagon-like peptide-1 receptor (GLP-1R) agonist.
M10310 Miglustat hydrochloride Miglustat hydrochloride also known as OGT 918 and NB-DNJ, inhibits glucosylceramide synthase, and is used primarily to treat Type I Gaucher disease (GD1).
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.


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