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Cat.No.  Name Information
M9451 Curcumin analog C1 Curcumin analog C1 is a potent, orally effective transcription factor EB (TFEB) activator and is a potential therapeutic agent for the treatment of neurodegenerative diseases.
M9450 N6-isopentenyladenosine N6-isopentenyladenosine is a plant hormone.
M9449 PFI-2 hydrochloride PFI-2 hydrochloride is a potent, highly selective and cell-active inhibitor of the methyltransferase activity of SETD7, with IC50 of 2 nM.
M9448 X-α-Gal X-α-Gal is suitable as a substrate for α-galactosidase.
M9447 RU320521 RU320521 (also known as RU521; RU.521) is a potent and selective inhibitor of cGAS, inhibiting cGAS-mediated interferon upregulation.
M9446 Dazoxiben hydrochloride Dazoxiben hydrochloride is a potent, orally active thromboxane (TX) synthase inhibitor that reduces the formation of blood clots.
M9445 YF2 YF2 is a selective HAT (histone acetyltransferase) activator, with EC50 values of 2.75 μM, 29.04 μM and 49.31 μM for CBP, PCAF and GCN5, respectively.
M9444 Cenicriviroc Mesylate Cenicriviroc Mesylate is a dual CCR2/CCR5 antagonist, and it also inhibits both HIV-1 and HIV-2.
M9443 Dextran sulfate sodium salt Dextran sulfate sodium salt is a polyanionic derivative of dextran produced by esterification of Dextran with chlorosulphonic acid.
M9442 CM-272 CM-272 is a first-in-class reversible dual small molecule inhibitor against G9a and DNMTs in hematological malignancies.
M9441 GSK656 HCl GSK656 is a potent Mtb LeuRS inhibitor, shows potent inhibition of Mtb LeuRS (IC50 = 0.20 μM) and in vitro antitubercular activity (Mtb H37Rv MIC = 0.08 μM).
M9440 3-Indoleacetic acid 3-Indoleacetic acid is a broad-spectrum plant growth regulator with indole auxin activity.
M9439 Paclobutrazol Paclobutrazol is a new, high-efficiency, low-toxicity plant growth regulator that can inhibit the production of gibberellin derivatives and reduce the division and elongation of plant cells.
M9438 Maleic hydrazide Maleic hydrazide is a plant growth regulator, which inhaled through the leaves or roots, conducted by the xylem and phloem, inhibiting cell division and inhibiting plant growth.
M9437 2,4-Dichlorophenoxyacetic acid 2,4-Dichlorophenoxyacetic acid is a plant growth hormone, used as a plant growth regulator.
M9436 Strigolactone Strigolactone is a type of signaling molecule that can regulate endogenous developmental processes in plants.
M9435 Methyl jasmonate Methyl jasmonate is a plant growth regulator isolated from Jasmine grandiflora.
M9434 N6-(delta 2-isopentenyl) adenine N6-(delta 2-isopentenyl) adenine is a bacteria-derived riboside cytokinin used to grow plant tissues such as tobacco and soybean callus.
M9433 trans-Zeatin-riboside trans-Zeatin-riboside is a type of cytokinin precursor, acts as a major long-distance signalling form in xylem vessels, regulates leaf size and meristem activity-related traits.
M9432 trans-Zeatin trans-Zeatin is a plant cytokinin, which plays an important role in cell growth, differentiation, and division.
M9431 Aureobasidin A Aureobasidin A (AbA) is a cyclic ester peptide antibiotics which derived from filamentous fungi, and it has strong antifungal ability.
M9430 Phleomycin Phleomycin is a glycopeptide antibiotic.
M9429 SU14813 SU14813 is a novel multiple receptor tyrosine kinase inhibitor with IC50s of 2, 50, 4, 15 nM for VEGFR-1, VEGFR-2, PDGFR-β and KIT.
M9428 MRTX849 MRTX849 is a potent, highly selective, oral available KRAS G12C inhibitor.
M9427 CU-CPT17e CU-CPT17e is a potent multi-Toll-like receptor (TLR) agonist, which activates TLR3, TLR8 and TLR9.
M9426 GSK2983559 free acid GSK2983559 free acid is a potent, specific and oral bioavailable receptor interacting protein 2 (RIP2) kinase inhibitor.
M9425 VU6015929 VU6015929 is a selective discoidin domain receptor 1/2 (DDR1/2) inhibitor with IC50s of 4.67 nM and 7.39 nM, respectively.
M9424 Adavivint Adavivint (SM04690) is a potent and specific inhibitor of canonical Wnt signaling with an EC50 of 19.5 nM for inhibiting the TCF/LEF reporter.
M9423 CLP290 CLP290 is a novel, orally available KCC2 modulator, highly selective for KCC2 over related Cl- transporters.
M9422 FB23-2 FB23-2 is a potent and selective FTO inhibitor with an IC50 of 2.6 μM, directly binds to FTO and selectively inhibit FTO's m6A demethylase activity.
M9421 Parsaclisib Parsaclisib (INCB050465) is a potent and selective PI3Kδ inhibitor, with an IC50 of 1 nM at 1 mM ATP.
M9420 GSK3326595 GSK3326595 is a potent, selective, reversible inhibitor of protein arginine methyltransferase 5 (PRMT5) with an IC50 of 6.2 nM.
M9419 Bax inhibitor peptide V5 Bax inhibitor peptide V5 is a Bax-mediated apoptosis inhibitor.
M9418 Apilimod mesylate Apilimod mesylate is a potent IL-12/IL-23 inhibitor, which inhibits the IL-12 production in cultures of IFN-γ/LPS–stimulated human PBMCs with an IC50 of 10 nM.
M9417 Gallocyanine Gallocyanine is a small molecule DKK1 inhibitor, which blocks DKK1 inhibitory activity on Wnt signaling.
M9416 Durvalumab Durvalumab (MEDI 4736) is an humanized anti-PD-L1 monoclonal antibody, it completely blocks the binding of PD-L1 to both PD-1 and CD80, with IC50s of 0.1 and 0.04 nM, respectively.
M9415 Recombinant Human EGF Recombinant Human EGF
M9414 OK432 OK432 is a freeze-dried vaccine.
M9413 Recombinant Human VEGF165 Recombinant Human VEGF165
M9412 IACS-10759 IACS-10759 is a potent inhibitor of complex I of oxidative phosphorylation (OXPHOS).
M9411 AZD-7325 AZD-7325 is a GABA-Aα2,3 -selective receptor modulator.
M9410 Remodelin hydrobromide Remodelin hydrobromide is a novel potent and selective inhibitor of the acetyl-transferase protein NAT10.
M9409 Glycoursodeoxycholic acid Glycoursodeoxycholic acid, a acyl glycine and a bile acid-glycine conjugate, is a metabolite of ursodeoxycholic acid.
M9408 Glycochenodeoxycholic acid Glycochenodeoxycholic acid (Chenodeoxycholylglycine) is a bile acid formed in the liver from chenodeoxycholate and glycine.
M9407 Ercalcidiol Ercalcidiol is a metabolite of vitamin D2, is regarded as an indicator of vitamin D nutritional status.
M9406 Recombinant Human bFGF Recombinant Human bFGF
M9405 NBD-F NBD-F is a fluorescent derivatization reagent for amino acid analysis.
M9404 UAMC-3203 hydrochloride UAMC-3203 hydrochloride is a potent and selective Ferroptosis inhibitor, with an IC50 of 12 nM.
M9403 TPI-1 TPI-1 is a SHP-1 inhibitor, inhibits recombinant SHP-1 with an IC50 of 40 nM.
M9402 Recombinant Human PDGF-BB Recombinant Human PDGF-BB
M9401 Dicyandiamide Dicyandiamide is a nitrification inhibitor that is said to be capable of reducing nitrate (NO3-) leaching and nitrous oxide (N2O) emissions from grazed pasture soils.
M9400 AST2818 mesylate AST2818 mesylate is a third generation EGFR inhibitor that targets both EGFR activating mutations and T790M thus leading to tumor growth inhibition.
M9399 PNPP
M9398 Recombinant Human IL-1β Recombinant Human IL-1β
M9397 MS4078 MS4078 is a PROTAC degrader of ALK which potently decreases cellular levels of oncogenic active ALK fusion proteins in SU-DHL-1 lymphoma and NCI-H2228 lung cancer cells.
M9396 A1874 A1874 is a BRD4-degrading PROTAC which inhibits many cancer cell lines proliferation, with DC50 of 32 nM (induce BRD4 degradation in cells).
M9395 HG-9-91-01 HG-9-91-01 is a potent and highly selective salt-inducible kinase (SIK) inhibitor with IC50s of 0.92 nM, 6.6 nM and 9.6 nM for SIK1, SIK2 and SIK3 respectively.
M9394 BMS-191011 BMS-191011 is a potent BKCa channel opener (large-conductance Ca2+-activated potassium channel, KCa1.1).
M9393 PTZ-343 PTZ-343 is a water-soluble enhancer of luminol chemiluminescent peroxidation catalyzed by horseradish peroxidase (HRP).
M9392 Tetraxetan Bifunctional DOTA aconjugates to peptides and has become an established strategy for constructing target-specific metal containing agents including targeted MRI contrast agents and diagnostic and ther apeutic radiopharmaceuticals.
M9391 Recombinant Human TGF-β1 Recombinant Human TGF-β1
M9390 FITC-Dextran FITC-Dextran is a marker consisting of coupling fluorescein-isothiocyanate to dextran.
M9389 740 Y-P 740 Y-P is a potent and cell permeable PI3K activator.
M9388 Tanzisertib Tanzisertib (CC-930) is a potent JNK1/2/3 inhibitor with IC50s of 61/7/6 nM, respectively.
M9387 Spermine Spermine is a biogenic polyamine formed from spermidine, which binds to and activates NMDA and has been shown to potentiate NMDA-induced currents in a concentration-dependent manner.
M9386 Verubecestat (MK-8931) Verubecestat (MK-8931) is a beta-secretase 1 (BACE1) inhibitor.
M9385 RU-301 RU-301 is a pan-TAM receptor inhibitor, with Kd and IC50 values of 12 μM and 10 μM, respectively.
M9384 WST-8 WST-8 is a water-soluble tetrazolium dye, WST-8 enhances sensitivity of the WST-8-based assay over the conventional MTS-based assay.
M9383 Opaganib (ABC294640) Opaganib (ABC294640) is an orally bioavailable and selective sphingosine kinase-2 (SphK2) inhibitor with IC50 of approximately 60 μM.
M9382 D-Lin-MC3-DMA D-Lin-MC3-DMA is the most potent cationic lipid that has been synthesized for lipid nanoparticles (LNPs) to deliver the siRNA.
M9381 Recombinant Human IGF-1 Recombinant Human IGF-1
M9380 Solutol HS-15 Solutol HS-15 is a permeability enhancer.
M9379 DiD Perchlorate DiD perchlorate is a lipophilic cyanine dye.
M9378 NHS-Biotin NHS-Biotin is an amine reactive biotinylation reagent, used in the biotinylation of proteins and peptides.
M9377 Polycaprolactone
M9376 Dapansutrile Dapansutrile is a potent, selective and orally active inhibitor of NLRP3 inflammasome.
M9375 QC6352 QC6352 is a potent KDM4C inhibitor.
M9374 Fmoc-Trp(1-Me)-OH Fmoc-Trp(1-Me)-OH is synthesized by N-(9-Fluorenylmethoxycarbonyloxy)succinimide (Fmoc-ONSu) and 1-Methyl-Ltrypthophan.
M9373 T-5224 T-5224 is a transcription factor c-Fos/activator protein (AP)-1 inhibitor with anti-inflammatory effects.
M9372 Yoda1 Yoda1 is an agonist of the mechanotransduction channel Piezo1.
M9371 Recombinant Human Fibronectin Recombinant Human Fibronectin
M9370 Recombinant Human TNF α Recombinant Human TNF α
M9369 Recombinant Human IL-21 (CHO-expressed) Recombinant Human IL-21
M9368 Recombinant Human IL-18 Recombinant Human IL-18 (also known as γ-interferon-inducible factor) is an inflammatory cytokine belonging to the interleukin-1 family and can be produced by macrophages and other cells.
M9367 Recombinant Human IL-15 (CHO-expressed) Recombinant Human IL-15
M9366 Recombinant Human IL-12 Recombinant Human IL-12 is also known as p70, and is an interleukin that is naturally produced by dendritic cells, macrophages and human B-lymphoblastoid cells (NC-37) in response to antigenic stimulation.
M9365 Recombinant Human IL-7 (CHO-expressed) Recombinant Human IL-7 (CHO-expressed)
M9364 Recombinant Human IL-6 Recombinant Human IL-6
M9363 Recombinant Human IL-4 (CHO-expressed) Recombinant Human IL-4 (CHO-expressed)
M9362 Recombinant Human IL-2 (CHO-expressed) Recombinant Human IL-2 (CHO-expressed)
M9361 Recombinant Human IL-1α Recombinant Human IL-1α
M9360 Dicoumarol Dicoumarol is an inhibitor of both NAD(P)H:quinone oxidoreductase 1 (NQO1) and PDK1 with IC50s of 0.37 and 19.42 μM, respectively.
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.

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