MedChemExpress MCE - Products
MedChemExpress (MCE) offers a wide range of high-quality research chemicals and biochemicals (novel life-science reagents, reference compounds and natural compounds) for scientific use.
| Product | Description | |
|---|---|---|
| Enfortumab vedotin-ejfv (solution) | Enfortumab vedotin-ejfv (solution) is an anti- Nectin-4 antibody-drug conjugate. Enfortumab vedotin-ejfv is a fully humanized IgG1 antibody conjugated to the microtubule disrupting agent MMAE (HY-15162) via a protease-cleavable maleimidocaproylvaline-citrulline linker (SGD-1006). Nectin-4 is an adhesion protein involved in cellular processes and tumorigenesis, and Enfortumab vedotin-ejfv is indicated for the inhibition of locally advanced or metastatic urothelial carcinoma [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 1346452-25-2. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P99016B. |  |
| Enfuvirtide | Enfuvirtide (T20;DP178) is an anti- HIV-1 fusion inhibitor peptide. Uses: Scientific research. Group: Peptides. Alternative Names: T20; DP178. CAS No. 159519-65-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-P0052. | |
| Enfuvirtide acetate | Enfuvirtide (T20; DP178) acetate is an anti- HIV-1 fusion inhibitor peptide. Uses: Scientific research. Group: Peptides. Alternative Names: T20 acetate; DP178 acetate. CAS No. 914454-00-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-P0052A. | |
| Engasertib | Engasertib is an orally active highly specific AKT inhibitor with IC50 values of 0.13 μM, 0.09 μM and 2.75 μM for AKT1, AKT2 and AKT3, respectively. Engasertib inhibits AKT phosphorylation and modulates downstream signalling in vitro. Engasertib can inhibit cancer cell proliferation and tumor growth[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ALM301. CAS No. 1313439-71-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-151504. | |
| Englerin A | Englerin A is a potent and selective activator of TRPC4 and TRPC5 channels, with EC50s of 11.2 and 7.6 nM, respectively. Englerin A can induce renal carcinoma cells death by elevated Ca2+ influx and Ca2+ cell overload[1][2][3]. Uses: Scientific research. Group: Natural products. CAS No. 1094250-15-3. Pack Sizes: 1 mg; 5 mg. Product ID: HY-133168. | |
| Enhanced Green Fluorescent Protein (EGFP) (200-208) | Enhanced Green Fluorescent Protein (EGFP) (200-208) is a marker gene product derived from the jellyfish Aequorea Victoria. Enhanced Green Fluorescent Protein (EGFP) (200-208) is a common reporter protein and is easy to detect[1]. Uses: Scientific research. Group: Peptides. CAS No. 323198-39-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P2528. | |
| Enibarcimab | Enibarcimab is a humanised murine monoclonal immunoglobulin G1 ( IgG1 ) antibody, could be used for acute heart failure, COVID-19 infections and septic shock research [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2305638-98-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99177. | |
| Eniluracil | Eniluracil (5-Ethynyluracil) is an orally active dihydropyrimidine dehydrogenase ( DPD ) inhibitor. Eniluracil irreversibly inhibits DPD , increases the oral bioavailability of 5-fluorouracil to 100%, and facilitates the uniform absorption and toxicity of 5-fluorouracil. Eniluracil can be used in cancer research of combination with fluoropyrimidines (including 5-fluorouracil) [1] [2]. Eniluracil is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 5-Ethynyluracil; GW776C85. CAS No. 59989-18-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10533. | |
| Eniporide hydrochloride | Eniporide hydrochloride (EMD-96785 hydrochloride) is a potent Na + /H + exchange inhibitor. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EMD-96785 hydrochloride. CAS No. 211813-86-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-106150B. | |
| (-)-Enitociclib | (-)-Enitociclib ((R)-Enitociclib) is an enanthiomer of BAY-1251152 with rotation (-). BAY-1251152 is a potent and highly selective PTEF/CDK9 inhibitor. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (R)-Enitociclib; (-)-BAY-1251152; (-)-VIP152. CAS No. 1610358-59-2. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 50 mg. Product ID: HY-103019B. | |
| (+)-Enitociclib | (+)-Enitociclib ((+)-BAY-1251152) is an enanthiomer of BAY-1251152 with rotation (+). Enitociclib is a potent and selective CDK9 inhibitor with an IC 50 of 3 nM. Enitociclib has anti-tumour activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (+)-BAY-1251152; (+)-VIP152; (S)-Enitociclib. CAS No. 1610358-56-9. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 50 mg. Product ID: HY-103019. | |
| (±)-Enitociclib | (±)-Enitociclib ((±)-BAY-1251152) is a racemic mixture of BAY-1251152. BAY-1251152 is a potent and highly selective PTEF/CDK9 inhibitor. BAY-1251152 can be used in the study of acute myelogenous leukemia and double-hit diffuse large B-cell lymphoma [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (±)-BAY-1251152; (±)-VIP152. CAS No. 1610358-53-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-103019A. | |
| Enlicitide chloride | Enlicitide chloride is an orally active inhibitor for PCSK9 that blocks the interaction between LPL receptor and PSCK9, with an IC 50 of 2.5 nM. Enlicitide chloride can be used in the study of cardiovascular diseases such as atherosclerosis, hypercholesterolemia, coronary heart disease, metabolic syndrome, acute coronary syndrome or related cardiovascular and cardiometabolic disorders [1] [2] [3]. Uses: Scientific research. Group: Peptides. Alternative Names: MK-0616 chloride. CAS No. 2407527-16-4. Pack Sizes: 500 μg; 1 mg; 5 mg; 10 mg. Product ID: HY-P4153. | |
| Enlimomab | Enlimomab (BI-RR 0001), a murine IgG2a monoclonal antibody to the human ICAM-1 , inhibits leukocyte adhesion to the vascular endothelium, thereby decreasing leukocyte extravasation and inflammatory tissue injury. Enlimomab has anti-inflammatory effects, and can be used for stroke research [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: BI-RR 0001; Anti-Human IL6 Recombinant Antibody. CAS No. 142864-19-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99336. | |
| Enmetazobactam | Enmetazobactam (AAI101) is an extended-spectrum β-lactamase inhibitor, against many resistant Gram-negative pathogens [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AAI101. CAS No. 1001404-83-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-103095. | |
| Enniatin B | Enniatin B is a Fusarium mycotoxin. Enniatin B inhibits acyl-CoA: cholesterol acyltransferase ( ACAT ) activity with an IC 50 of 113 μM in an enzyme assay using rat liver microsomes [1]. Enniatins B decreases the activation of ERK (p44/p42) [2]. Uses: Scientific research. Group: Natural products. CAS No. 917-13-5. Pack Sizes: 1 mg. Product ID: HY-N3806. | |
| Enoblituzumab | Enoblituzumab (MGA271) is a humanized IgG1κ monoclonal antibody recognizing human B7-H3 protein, a member of the B7 family of immune regulators [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: MGA271. CAS No. 1353485-38-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P9966. | |
| Enokizumab | Enokizumab (MEDI-528) is a monoclonal antibody targeting to interleukin (IL)-9. IL-9 regulates the development of airway inflammation, mucus production, airway hyperresponsiveness, and airway fibrosis largely by increasing mast cell numbers and activity in the airways [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: MEDI-528. CAS No. 909875-08-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99193. | |
| Enoticumab | Enoticumab (REGN421, SAR153192) is an IgG1κ antibody targeting human Dll4. DLL4 is a ligand of the Notch signaling pathway and regulates fatty acid uptake through non-transcriptional regulation of macropinocytosis-dependent long-chain fatty acid uptake. Specific in vivo activity of Enoticumab in an ovarian xenograft model. EGN421 (2.5 mg/kg once weekly) resulted in 86% and 83% tumor growth inhibition in mouse subcutaneous TOV-112D or intraperitoneal A2780 human tumor xenograft models, respectively [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: REGN421. CAS No. 1192578-27-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99925. | |
| Enoxacin hydrate | Enoxacin hydrate (Enoxacin sesquihydrate), a fluoroquinolone, interferes with DNA replication and inhibits bacterial DNA gyrase (IC 50 =126 μg/ml) and topoisomerase IV (IC 50 =26.5 μg/ml). Enoxacin hydrate is a miRNA processing activator and enhances siRNA-mediated mRNA degradation and promotes the biogenesis of endogenous miRNAs. Enoxacin hydrate has potent activities against gram-positive and -negative bacteria. Enoxacin hydrate is a cancer-specific growth inhibitor that acts by enhancing TAR RNA-binding protein 2 (TRBP)-mediated microRNA processing [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Enoxacin sesquihydrate; AT-2266 hydrate; CI-919 hydrate. CAS No. 84294-96-2. Pack Sizes: 100 mg; 500 mg. Product ID: HY-B0268A. | |
| Enoxaparin | Enoxaparin (PK 10169), a low-molecular-weight heparin (LMWH) derivative. Enoxaparin exerts anticoagulant activity through antithrombin III, an endogenous inhibitor of factor Xa and thrombin IIa. Enoxaparin protect the rat hippocampus against TBI (traumatic brain injury) via antioxidant and anti-inflammatory properties. Enoxaparin can be used for the research of deep vein thrombosis (DVT), pulmonary embolism, TBI and COVID-19 [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PK 10169; Enoxaparin sodium. CAS No. 679809-58-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109509. | |
| Enoximone | Enoximone is an inotropic vasodilating agent and a selective and orally active phosphodiesterase III (PDE3) inhibitor with an IC 50 of 5.9 μM. Enoximone induces vasodilatation and increases intracellular levels of cAMP by inhibiting cGMP-inhibited PDE. Enoximone also exhibits PDE4 inhibitory effect with an IC 50 of 21.1 μM for myocardial PDE4A. Enoximone has the potential for congestive heart failure research and has bronchodilatory, antiasthma and anti-inflammatory effects [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 77671-31-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-B1639. | |
| Enpatoran | Enpatoran (M5049) is a potent, orally active and dual TLR7/8 inhibitor with IC50s of 11.1 nM and 24.1 nM in HEK293 cells, respectively. Enpatoran is inactive against TLR3, TLR4 and TLR9. Enpatoran can block molecule synthetic ligands and natural endogenous RNA ligands. Enpatoran exhibits excellent pharmacokinetic properties in vivo. Enpatoran can be used for both innate and adaptive autoimmunity blocking research [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: M5049. CAS No. 2101938-42-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-134581. | |
| Enpp-1-IN-1 | Enpp-1-IN-1 is an effective selective enpp-1 (nucleotide pyrophosphatase-phosphodiesterase 1) inhibitor[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2289728-58-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-129490. | |
| Enprofylline | Enprofylline acts as a selective and competitive A2B receptor antagonist with the K i of 7 μM. Enprofylline also acts as a phosphodiesterase inhibitor. Enprofylline can be used for the research of asthma, chronic obstructive pulmonary disease [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 41078-02-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-14117. | |
| Enrofloxacin | Enrofloxacin (BAY Vp 2674) is an effective antibiotic with an MIC 90 of 0.312 μg/mL for Mycoplasma bovis. Uses: Scientific research. Group: Natural products. Alternative Names: BAY Vp 2674; PD160788. CAS No. 93106-60-6. Pack Sizes: 10 mM * 1 mL; 500 mg; 5 g; 10 g. Product ID: HY-B0502. | |
| Enrofloxacin-d5 | Enrofloxacin-d 5 is the deuterium labeled Enrofloxacin. Enrofloxacin (BAY Vp 2674) is an effective antibiotic with an MIC90 of 0.312 μg/mL for Mycoplasma bovis. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: BAY Vp 2674-d5; PD160788-d5. CAS No. 1173021-92-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-B0502S. | |
| Enrofloxacin (Standard) | Enrofloxacin (Standard) is the analytical standard of Enrofloxacin. This product is intended for research and analytical applications. Enrofloxacin (BAY Vp 2674) is an effective antibiotic with an MIC90 of 0.312 μg/mL for Mycoplasma bovis. Uses: Scientific research. Group: Natural products. CAS No. 93106-60-6. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-B0502R. | |
| Ensartinib | Ensartinib (X-396) is a potent and dual ALK / MET inhibitor with IC 50 s of <0.4 nM and 0.74 nM, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: X-396. CAS No. 1370651-20-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103714. | |
| Ensartinib dihydrochloride | Ensartinib dihydrochloride (X-396 dihydrochloride) is a potent and dual ALK / MET inhibitor with IC 50 s of <0.4 nM and 0.74 nM, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: X-396 dihydrochloride. CAS No. 2137030-98-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103714A. | |
| Ensifentrine | Ensifentrine (RPL-554) is an inhaled first-in-class dual inhibitor of phosphodiesterase 3 (PDE3) and PDE4 with IC 50 s of 0.4 nM and 1479 nM, respectively. Ensifentrine has bronchoprotective and anti-inflammatory activities. Ensifentrine can be used for chronic obstructive pulmonary disease (COPD) research [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: RPL-554. CAS No. 1884461-72-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-119708. | |
| Ensitrelvir | Ensitrelvir (S-217622) is the first orally active non-covalent, non-peptidic, SARS-CoV-2 3CL protease inhibitor ( IC 50 =13 nM) [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: S-217622. CAS No. 2647530-73-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-143216. | |
| Ensitrelvir fumarate | Ensitrelvir (S-217622) fumarate is the first orally active non-covalent, non-peptidic, SARS-CoV-2 3CL protease inhibitor ( IC 50 =13 nM) [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: S-217622 fumarate. CAS No. 2757470-18-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-143216A. | |
| Ensituximab | Ensituximab (NEO-102; NPC-1C) is a chimeric monoclonal IgG1 antibody targeting a variant of MUC5AC. Ensituximab shows specificity to colorectal and pancreatic cancer [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: Anti-MUC5AC Reference Antibody (ensituximab); NEO-102. CAS No. 1092658-06-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99362. | |
| Ensulizole | Ensulizole is a sulfonated UV absorber and can intense UVB and partial UVA absorption. Ensulizole can damage the DNA through the generation of reactive oxygen species ( ROS ) upon UV or sunlight irradiation [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 27503-81-7. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-109654. | |
| Entacapone | Entacapone is a potent, reversible, peripherally acting and orally active catechol-O-methyltransferase (COMT) inhibitor. Entacapone inhibits COMT from rat brain, erythrocytes and liver with IC 50 values of 10 nM, 20 nM, and 160 nM, respectively. Entacapone is selective for COMT over other catecholamine metabolizing enzymes, including MAO-A, MAO-B, phenolsulphotransferase M (PST-M) and PST-P (IC 50 s>50 μM). Entacapone can be used for the research of Parkinson's disease [1]. Entacapone serves as a inhibitor of FTO demethylation with an IC 50 of 3.5 μM, can be used for the research of metabolic disorders [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 130929-57-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14280. | |
| Entecavir | Entecavir (SQ 34676; BMS 200475) is a potent and selective inhibitor of HBV , with an EC 50 of 3.75 nM in HepG2 cell. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BMS200475; SQ34676. CAS No. 142217-69-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13623. | |
| Entecavir monohydrate | Entecavir monohydrate (BMS200475 monohydrate; SQ34676 monohydrate) is a potent and selective inhibitor of HBV , with an EC 50 of 3.75 nM in HepG2 cell. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BMS200475 monohydrate; SQ34676 monohydrate. CAS No. 209216-23-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-13623A. | |
| Enterobactin | Enterobactin is a siderophore produced by Gram-negative bacteria and has an extremely high affinity for iron. During the process of Salmonella typhimurium infecting macrophages, Enterobactin can not only help bacteria uptake iron but also reduce the antibacterial activity of macrophages. In addition, Enterobactin is also involved in the oxidative stress response of Escherichia coli. Enterobactin can be hydrolyzed by Fes in the cell and exert antioxidant effects by scavenging free radicals [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 28384-96-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-128525. | |
| Enterotoxin STp (E. coli) | Enterotoxin STp (E. coli) is a heat-stable enterotoxin that can be used in vaccine research [1]. Uses: Scientific research. Group: Peptides. CAS No. 115474-04-9. Pack Sizes: 1 mg. Product ID: HY-P5089. | |
| Entinostat | Entinostat is an oral and selective class I HDAC inhibitor, with IC 50 s of 243 nM, 453 nM, and 248 nM for HDAC1 , HDAC2 , and HDAC3 , respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MS-275; SNDX-275. CAS No. 209783-80-2. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-12163. | |
| Entospletinib | Entospletinib (GS-9973) is an orally bioavailable, selective Syk inhibitor with an IC 50 of 7.7 nM. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GS-9973. CAS No. 1229208-44-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-15968. | |
| Entrectinib | Entrectinib (NMS-E628) is an orally active, BBB-penetrated and centrally active inhibitor of TrkA/B/C , ROS1 and ALK , with IC 50 values of 1, 3, 5, 12 and 7 nM, respectively. Entrectinib induces apoptosis and cycle arrest in cancer cells, has antitumor activity, and attenuates bleomycin-induced lung fibrosis in mice [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NMS-E628; RXDX-101. CAS No. 1108743-60-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-12678. | |
| Envafolimab | Envafolimab (ASC 22; KN 035) is a recombinant protein of a humanized single-domain anti- PD-L1 antibody. Envafolimab is created by a fusion of the of anti-PD-L1 domain with Fc fragment of human IgG1 antibody. Envafolimab blocks interaction between PD-L1 and PD-1 with an IC 50 value of 5.25 nM. Envafolimab has the potential for the research of solid tumors [1] [2] [3]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: ASC 22; KN 035. CAS No. 2102192-68-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99115. | |
| Enzalutamide | Enzalutamide (MDV3100) is an androgen receptor (AR) antagonist with an IC 50 of 36 nM in LNCaP prostate cells. Enzalutamide is an autophagy activator [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MDV3100. CAS No. 915087-33-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg; 500 mg; 1 g; 2 g; 5 g. Product ID: HY-70002. | |
| Enzalutamide carboxylic acid | Enzalutamide carboxylic acid (MDV3100 carboxylic acid) is an inactive metabolite of Enzalutamide (MDV3100). Enzalutamide is an androgen receptor (AR) antagonist[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MDV3100 carboxylic acid. CAS No. 1242137-15-0. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-70002B. | |
| Enzastaurin | Enzastaurin (LY317615) is a potent and selective PKCβ inhibitor with an IC 50 of 6 nM, showing 6- to 20-fold selectivity over PKCα, PKCγ and PKCε [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY317615. CAS No. 170364-57-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10342. | |
| Enzomenib | Enzomenib is an inhibitor of the menin protein encoded by the multiple endocrine neoplasia (MEN) gene. Enzomenib can block the binding of the menin protein to mixed lineage leukemia (MLL) fusion proteins and can be used in the study of hematological malignancies[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: DSP-5336. CAS No. 2412555-70-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-156794. | |
| EOAI3402143 | EOAI3402143 is a deubiquitinase (DUB) inhibitor, which inhibits dose-dependently inhibits Usp9x/Usp24 and Usp5. Uses: Scientific research. Group: Signaling pathways. CAS No. 1699750-95-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-111408. | |
| (E)-Oct-2-enoic acid | (E)-Oct-2-enoic acid is an endogenous metabolite. Uses: Scientific research. Group: Natural products. CAS No. 1871-67-6. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-W046906. | |
| EOS-984 | EOS-984 is a highly potent and selective ENT1 (equilibrative nucleoside transporter 1) inhibitor. EOS-984 is designed to inhibit the immunosuppressive activity of adenosine and restore immune cell proliferation[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2724937-55-5. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-159650. | |
| Eosin 5-isothiocyanate | Eosin 5-isothiocyanate is a multifunctional dye. Dyes are important tools in biological experiments. They can help researchers observe and analyze cell structures, track biomolecules, evaluate cell functions, distinguish cell types, detect biomolecules, study tissue pathology and monitor microorganisms. Their applications range from basic scientific research to clinical A wide range of diagnostics. Dyes are also widely used in traditional fields such as textile dyeing, as well as in emerging fields such as functional textile processing, food pigments and dye-sensitized solar cells. Uses: Scientific research. Group: Fluorescent dye. CAS No. 60520-47-0. Pack Sizes: 5 mg; 10 mg. Product ID: HY-D0805. | |
| Eosin B | Eosin B (Acid Red 91) is a multifunctional dye. Dyes are important tools in biological experiments. They can help researchers observe and analyze cell structures, track biomolecules, evaluate cell functions, distinguish cell types, detect biomolecules, study tissue pathology and monitor microorganisms. Their applications range from basic scientific research to clinical A wide range of diagnostics. Dyes are also widely used in traditional fields such as textile dyeing, as well as in emerging fields such as functional textile processing, food pigments and dye-sensitized solar cells. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: Acid Red 91. CAS No. 548-24-3. Pack Sizes: 5 g; 25 g. Product ID: HY-D1198. | |
| Eosin Y | Eosin Y (Acid Red 87 free base) is a soluble acid red dye molecule. Eosin Y has a wide application in organic synthesis as a photoredox catalyst [1]. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: Acid Red 87 free base. CAS No. 15086-94-9. Pack Sizes: 5 g; 10 g; 25 g. Product ID: HY-D0505. | |
| EP4 receptor agonist 2 | EP4 receptor agonist 2 (compound 31) a potent EP4 receptor agonist with an EC 50 value of 0.8 nM; K i values of >100000, 38000, 3.1 nM for EP2, EP3, EP4 respectively [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 493035-81-7. Pack Sizes: 1 mg (21.28 mM * 100 μL in Ethanol). Product ID: HY-118609. | |
| EP4 receptor antagonist 1 | EP4 receptor antagonist 1 is a highly potent and selective competitive prostanoid EP4 receptor antagonist for cancer immunotherapy. EP4 receptor antagonist 1 inhibits human and mouse EP4 receptor with IC50s of 6.1 nM and 16.2 nM, respectively. IC50s >10 ?M for human EP1, EP2,and EP3 receptors[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2287259-07-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-133123. | |
| Epacadostat | Epacadostat (INCB 024360) is a potent and selective indoleamine 2,3-dioxigenase 1 (IDO1) inhibitor with an IC 50 of 71.8 nM [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: INCB 024360. CAS No. 1204669-58-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg; 500 mg; 1 g; 2 g. Product ID: HY-15689. | |
| Epacmarstobart | Epacmarstobart (FSI-189; GS-0189) is a chimeric humanized IgG1κ antibody targeting the mouse signal regulatory protein SIRPA. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: FSI-189; GS-0189. CAS No. 2518200-89-8. Pack Sizes: 1 mg. Product ID: HY-P990019. | |
| Epalrestat | Epalrestat is an orally active aldose reductase inhibitor that acts on diabetic neuropathy [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ONO2235. CAS No. 82159-09-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-66009. | |
| Epcoritamab | Epcoritamab (GEN3013) is an bispecific IgG1 antibody redirecting T-cells toward CD3×CD20 + tumor cells. Epcoritamab induces potent T-cell-mediated cytotoxicity towards B-cell NHL cell lines [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: GEN3013. CAS No. 2134641-34-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99931. | |
| Eperezolid | Eperezolid(PNU-100592) is a oxazolidinone antibacterial agent, Eperezolid demonstrated good in vitro inhibitory activity, regardless of methicillin susceptibility for staphylococci(MIC90= 1-4 mg/ml). Uses: Scientific research. Group: Signaling pathways. Alternative Names: PNU-100592. CAS No. 165800-04-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10393. | |
| Eperisone hydrochloride | Eperisone Hydrochloride ((±)-Eperisone hydrochloride) is an orally active antispastic agent with a vasodilator effect, used for the research of muscle stiffness and pain. Eperisone Hydrochloride is a potent and selectively P2X7 receptor antagonist, also shows antagonism for human P2X3. Eperisone Hydrochloride works by relaxing both skeletal muscles and vascularsmooth muscles, demonstrating a variety of effects such as reduction ofmyotonia, improvement of circulationand and suppression of the pain reflex [1] [2] [3] [4] [5] [6]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (±)-Eperisone hydrochloride. CAS No. 56839-43-1. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-B1901. | |
| Epetraborole hydrochloride | Epetraborole (GSK2251052) hydrochloride is a novel leucyl-tRNA synthetase ( LeuRS ) inhibitor ( IC 50 =0.31 μM), thereby inhibiting protein synthesis. Epetraborole hydrochloride can be used in multidrug-resistant gram-negative pathogens infection research [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GSK2251052 hydrochloride. CAS No. 1234563-16-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12479A. | |
| EphA2 antagonist 1 | EphA2 antagonist 1 (4b) is a bile acid conjugate and an ephrin type-A receptor 2 (EPHA2) inhibitor [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1428095-28-6. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-169849. | |
| EPI-001 | EPI-001, a selective inhibitor of Androgen Receptor (AR), targets transactivation unit 5 (Tau-5) of the AR. EPI-001 can inhibit transactivation of the AR amino-terminal domain (NTD), with an IC50 of ~6 ?M. EPI-001 is also a selective modulator of PPAR?. EPI-001 is active against castration-resistant prostate cancer[1][2][3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 227947-06-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-100348. | |
| EPI-589 | EPI-589, a quinone derivative, is a safe and well tolerated oxidoreductase enzyme inhibitor and a free radical scavenger, with blood-brain barrier permeable and orally available. EPI-589 is a redox-active neuroprotectant that effectively delays the symptoms of motor neuron disease in wobbler mice. EPI-589 can be used in amyotrophic lateral sclerosis (ALS) research [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1147883-03-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-125999. | |
| EPI-743 | EPI-743 (Vatiquinone; α-Tocotrienol quinone; PTC-743; NCT04378075) is a potent cellular oxidative stress protectant, inhibits ferroptosis in cells, which could be used for the study for mitochondrial diseases. EPI-743 is a synthetic analog of vitamin E with oral activity, targets repletion of reduced intracellular glutathione [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: α-Tocotrienol quinone; PTC-743; Vatiquinone; NCT04378075. CAS No. 1213269-98-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16772. | |
| (-)-Epiafzelechin | (-)-Epiafzelechin shows potent antioxidant activity with EC 50 20.9 μM (EC 50 =5.7 μg/mL) [1]. Uses: Scientific research. Group: Natural products. CAS No. 24808-04-6. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N0943. | |
| Epiandrosterone | Epiandrosterone is a steroid hormone with weak androgenic activity. Uses: Scientific research. Group: Natural products. Alternative Names: 3β-Androsterone; trans-Androsterone; iso-Androsterone. CAS No. 481-29-8. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-I0352. | |
| Epibrassinolide | Epibrassinolide (24-Epibrassinolide) is a ubiquitously occurring plant growth hormone which shows great potential to alleviate heavy metals and pesticide stress in plants [1]. Epibrassinolide is a potential apoptotic inducer in various cancer cells without affecting the non-tumor cell growth [2]. Uses: Scientific research. Group: Natural products. Alternative Names: 24-Epibrassinolide; B1105; BP55. CAS No. 78821-43-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-N0848. | |
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