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 | |
|---|---|---|
| Cenderitide | Cenderitide is a potent agonist of particulate guanylyl cyclase receptor (pGC). Cenderitide is a natriuretic peptide (NP) composed of C-type natriuretic peptide (CNP) fused to the C-terminus of Dendroaspis natriuretic peptide (DNP). Cenderitide activates both pGC-A and pGC-B , activates the second messenger cGMP , suppresses aldosterone , and preserves GFR without reducing blood pressure. Cenderitide can be used for heart failure research [1] [2] [3]. Uses: Scientific research. Group: Peptides. CAS No. 507289-11-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P3624. |  |
| Cenerimod | Cenerimod (ACT-334441) is a potent, selective and orally active S1P1 receptor modulator, with an EC 50 of 1 nM. Cenerimod shows more than 36 fold selctivity for hS1P1 over hS1P2, hS1P3, hS1P4, and hS1P5 receptor subtypes (EC 50 s=>10000, 228, 2134, and 36 nM, respectively). Cenerimod can attenuate murine experimental autoimmune encephalomyelitis (EAE) and murine sclerodermatous [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ACT-334441. CAS No. 1262414-04-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-17606. | |
| Cenicriviroc | Cenicriviroc (TAK-652) is an orally active, dual CCR2/CCR5 antagonist, also inhibits both HIV-1 and HIV-2, and displays potent anti-inflammatory and antiinfective activity [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TAK-652; TBR-652. CAS No. 497223-25-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14882. | |
| Cenicriviroc Mesylate | Cenicriviroc Mesylate (TAK-652 Mesylate) is a dual CCR2/CCR5 antagonist, also inhibits both HIV-1 and HIV-2, and displays potent anti-inflammatory and antiinfective activity. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TAK-652 Mesylate; TBR-652 Mesylate. CAS No. 497223-28-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-14882A. | |
| Centanafadine | Centanafadine is dual norepinephrine (NE)/dopamine (DA) transporter inhibitor, also inhibits serotonin transporter, with IC 50 s of 6 nM, 38 nM and 83 nM for human NE, DA and serotonin transporter , respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EB-1020. CAS No. 924012-43-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16736. | |
| Centanafadine hydrochloride | Centanafadine (hydrochloride) is dual norepinephrine (NE)/dopamine (DA) transporter inhibitor, also inhibits serotonin transporter, with IC 50 s of 6 nM, 38 nM and 83 nM for human NE, DA and serotonin transporter , respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EB-1020 hydrochloride. CAS No. 923981-14-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16736A. | |
| Centhaquin | Centhaquine (Centhaquin; PMZ-2010) is a novel agent has the potential for treatment of haemorrhagic shock. Centhaquine (Centhaquin; PMZ-2010) can augment cardiac output, reduce systemic vascular resistance in haemorrhagic models [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Centhaquine; PMZ-2010. CAS No. 57961-90-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-106690. | |
| CEP-1347 | CEP-1347 is an inhibitor of the JNK/SAPK pathway with neuroprotective effects. CEP-1347 blocks JNK1 activation induced by members of the mixed lineage kinase (MLK) family (MLK3, MLK2, MLK1, dual leucine zipper kinase, and leucine zipper kinase). As an inhibitor of MDM4 , CEP-1347 can more effectively inhibit the growth of glioma cells expressing wild-type p53 [1] [2] [3] [4] [5] [6]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: KT7515. CAS No. 156177-65-0. Pack Sizes: 1 mg. Product ID: HY-10412. | |
| Ceperognastat | Ceperognastat (LY3372689) is an orally active O-GlcNAcase (OGA) enzyme inhibitor. Ceperognastat can be used for tauopathies research, including Alzheimers disease [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY3372689. CAS No. 2241514-56-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-144681. | |
| Cephalexin | Cephalexin (Cefalexin) is a potent, orally active semisynthetic cephalosporin antibiotic with a broad antibacterial spectrum. Cephalexin has antibacterial activity against a wide variety of gram-positive and gram-negative bacteria. Cephalexin targets penicillin-binding proteins (PBPs) to inhibit bacterial cell wall assembly. Cephalexin is used for the research of pneumonia, strep throat, and bacterial endocarditis, et al [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefalexin; Cephacillin. CAS No. 15686-71-2. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g; 10 g. Product ID: HY-B0200. | |
| Cephalexin hydrochloride | Cephalexin (Cefalexin) hydrochloride is a potent, orally active new semisynthetic cephalosporin antibiotic with a broad antibacterial spectrum. Cephalexin (Cefalexin) hydrochloride has antibacterial activity against a wide variety of gram-positive and gram-negative bacteria. Cephalexin (Cefalexin) hydrochloride targets penicillin-binding proteins (PBPs) to inhibit bacterial cell wall assembly. Cephalexin (Cefalexin) hydrochloride is used for the research of pneumonia, strep throat, and bacterial endocarditis, et al [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefalexin hydrochloride; Cephacillin hydrochloride. CAS No. 59695-59-9. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-B0200A. | |
| Cephalexin monohydrate | Cephalexin (Cefalexin) monohydrate is a potent, orally active new semisynthetic cephalosporin antibiotic with a broad antibacterial spectrum. Cephalexin (Cefalexin) monohydrate has antibacterial activity against a wide variety of gram-positive and gram-negative bacteria. Cephalexin (Cefalexin) monohydrate targets penicillin-binding proteins (PBPs) to inhibit bacterial cell wall assembly. Cephalexin (Cefalexin) monohydrate is used for the research of pneumonia, strep throat, and bacterial endocarditis, et al [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefalexin hydrate; Cephacillin hydrate. CAS No. 23325-78-2. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B0200B. | |
| Cephalexin (Standard) | Cephalexin (Standard) is the analytical standard of Cephalexin. This product is intended for research and analytical applications. Cephalexin (Cefalexin) is a potent, orally active semisynthetic cephalosporin antibiotic with a broad antibacterial spectrum. Cephalexin has antibacterial activity against a wide variety of gram-positive and gram-negative bacteria. Cephalexin targets penicillin-binding proteins (PBPs) to inhibit bacterial cell wall assembly. Cephalexin is used for the research of pneumonia, strep throat, and bacterial endocarditis, et al [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefalexin (Standard); Cephacillin (Standard). CAS No. 15686-71-2. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0200R. | |
| Cephaloridine hydrate | Cephaloridine hydrate is a broad-spectrum antibacterial antibiotic. Cephaloridine has certain dose-related nephrotoxicity [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 102039-86-1. Pack Sizes: 5 mg; 10 mg. Product ID: HY-B2072A. | |
| Cephalotaxine | Cephalotaxlen ((-)-Cephalotaxine) is an alkaloid that can be isolated from Cephalotaxus fortunei , with antileukemic and antiviral activities. Cephalotaxlen has anti-ZIKV (Zika virus) activity [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: (-)-Cephalotaxine; ZINC19795976. CAS No. 24316-19-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-N0838. | |
| Cephalothin | Cephalotin (Cephalotin) is a beta-lactam antibiotic , inhibits class C β-lactamase AmpC , with an K i of 0.32 μM [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cephalotin. CAS No. 153-61-7. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B1275A. | |
| Cephalothin sodium | Cephalothin sodium is a first-generation cephalosporin antibiotic with broad antibacterial activity and is effective against Gram-positive and Gram-negative bacteria. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefalotin sodium. CAS No. 58-71-9. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B1275. | |
| Cephapirin | Cephapirin (Cefapirin) is an ephalosporin antibiotic with broad-spectrum antimicrobial activity [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefapirin. CAS No. 21593-23-7. Pack Sizes: 5 mg. Product ID: HY-A0153. | |
| Cephapirin Benzathine | Cephapirin Benzathine is the benzathine salt form of cephapirin. Cephapirin Benzathine is the first generation cephalosporin with broad spectrum antibiotic activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 97468-37-6. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-113735. | |
| Cephapirin sodium | Cephapirin sodium (Cefapirin sodium) is an ephalosporin antibiotic with broad-spectrum antimicrobial activity [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefapirin sodium. CAS No. 24356-60-3. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg. Product ID: HY-A0153A. | |
| Cepharanthine | Cepharanthine is a natural product that can be isolated from the plant Stephania?cephalantha?Hayata. Cepharanthine has anti-severe acute respiratory syndrome coronavirus 2 (anti-SARS-CoV-2) activities. Cepharanthine has good effective in suppressing viral proliferation (half maximal (50%) inhibitory concentration ( IC 50 ) and 90% inhibitory concentration ( IC 90 ) values of 1.90 and 4.46?μM [1]. Cepharanthine can also effectively reverses P-gp-mediated multidrug resistance in K562 cells and increase enhances the sensitivity of anticancer agents in xenograft mice model [2] [3]. Cepharanthine shows inhibitory effects of human liver cytochrome P450 enzymes CYP3A4, CYP2E1 and CYP2C9. Cepharanthine has antitumor, anti-inflammatory and antinociceptive effects [4] [5] [6] [7] [8]. Uses: Scientific research. Group: Natural products. CAS No. 481-49-2. Pack Sizes: 10 mM * 1 mL; 50 mg. Product ID: HY-N6972. | |
| Cephradine | Cephradine (Cefradine) is a broad-spectrum and orally active cephalosporin. Cephradine is active against both gram-positive and gram-negative pathogens. Cephradine is effective in eradicating most penicillinase-producing organisms. Cephradine has been used in the research of genitourinary, gastrointestinal and respiratory tract infections, and in infections of the skin and soft tissues. Cephradine blocks solar-ultraviolet induced skin inflammation through direct inhibition of TOPK [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefradine; SQ-11436. CAS No. 38821-53-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g. Product ID: HY-B1156. | |
| Cephradine monohydrate | Cephradine (Cefradine) monohydrate is a broad-spectrum and orally active cephalosporin. Cephradine monohydrate is active against both grampositive and gram-negative pathogens and effective in eradicating most penicillinase-producing organisms known to be resistant to penicillin G, penicillin V, and ampicillin. Cephradine monohydrate has been used in the research of genitourinary, gastrointestinal and respiratory tract infections, and in infections of the skin and soft tissues. Cephradine monohydrate blocks solar-ultraviolet induced skin inflammation through direct inhibition of TOPK [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefradine monohydrate. CAS No. 75975-70-1. Pack Sizes: 100 mg; 500 mg. Product ID: HY-128449. | |
| CER3-d9 | CER3-d 9 is deuterium labeled CER3. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 2260669-53-0. Pack Sizes: 1 mg; 5 mg. Product ID: HY-146831S. | |
| CER5-2R-d9 | CER5-2R-d 9 is deuterium labeled CER5-2R. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 2260670-31-1. Pack Sizes: 1 mg. Product ID: HY-146909S. | |
| Ceralasertib | Ceralasertib (AZD6738) is an orally active and bioavailable inhibitor of ATR kinase with an IC 50 of 1 nM. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AZD6738. CAS No. 1352226-88-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-19323. | |
| Ceramide 1-phosphate | Ceramide 1-phosphate is a bioactive lipid and one of the key components of sphingolipids. Ceramide 1-phosphate playing diverse roles in cellular behaviors such as cell differentiation, migration, proliferation and death [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 128543-23-7. Pack Sizes: 1 mg. Product ID: HY-P2982. | |
| Ceramide 3 | C18 Phytoceramide (t18:0/18:0) (Cer(t18:0/18:0)) is a bioactive sphingolipid found in the stratum corneum of Saccharomyces cerevisiae, wheat grain, and mammalian epidermis. Cer(t18:0/18:0) consists of a phytosphingosine backbone amine linked to a C18 fatty acid chain. Cer(t18:0/18:0) has the function of regulating apoptosis, cell differentiation, proliferation of smooth muscle cells and inhibition of mitochondrial respiratory chain. It also suppresses the expression of allergic cytokines IL-4, TNF-α, and transcription factors c-Jun and NF-κB in histone-stimulated mouse skin tissue. Formulations containing cer(t18:0/18:0) have been used as skin protectants in cosmetics as they reduce water loss and prevent epidermal dehydration and irritation. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: N-Stearoyl phytosphingosine. CAS No. 34354-88-6. Pack Sizes: 1 mg; 5 mg. Product ID: HY-141582. | |
| Cercosporin | Cercosporin is produced by a plant pathogen, Pseudocercosporella capsellae. Cercosporin is a potent photosensitizer with a short activation wavelength, mostly suitable for superficial photodynamic therapy ( PDT ) treatments, especially when it is necessary to avoid perforations [1]. Cercosporin contains the perylenequinone structural features necessary to PKC activity with an IC 50 of 0.6-1.3 μM [2]. Uses: Scientific research. Group: Natural products. Alternative Names: CGP049090. CAS No. 35082-49-6. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N6743. | |
| Cerdulatinib | Cerdulatinib (PRT062070) is a selective Tyk2 inhibitor with an IC 50 of 0.5 nM. Cerdulatinib (PRT062070) also is a dual JAK and SYK inhibitor with IC 50 s of 12, 6, 8 and 32 for JAK1, 2, 3 and SYK, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PRT062070; PRT2070. CAS No. 1198300-79-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-15999. | |
| Cerdulatinib hydrochloride | Cerdulatinib hydrochloride (PRT062070) is a selective, oral active and reversible ATP-competitive inhibitor of dual SYK and JAK , with IC 50 s of 32 nM, 0.5 nM, 12 nM, 6 nM and 8 nM for SYK and Tyk2 , JAK1 , 2 , 3 , respectively. Cerdulatinib hydrochloride could be used to research autoimmune disease and B-cell malignancies [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PRT062070 hydrochloride; PRT2070 hydrochloride. CAS No. 1369761-01-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15999A. | |
| Cereulide-13C6 | Cereulide-13C6 is the 13C6 labeled Cereulide. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 1487375-69-8. Pack Sizes: 20 μg (17.25 μM * 1 mL in Acetonitrile). Product ID: HY-P3003S. | |
| Ceritinib | Ceritinib (LDK378) is a selective, orally bioavailable, and ATP-competitive ALK tyrosine kinase inhibitor with an IC 50 of 200 pM. Ceritinib (LDK378) also inhibits IGF-1R , InsR , and STK22D with IC 50 values of 8, 7, and 23 nM, respectively. Ceritinib (LDK378) shows great antitumor potency [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LDK378. CAS No. 1032900-25-6. 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-15656. | |
| Ceritinib dihydrochloride | Ceritinib dihydrochloride (LDK378 dihydrochloride) is a selective, orally bioavailable and ATP-competitive ALK tyrosine kinase inhibitor with an IC 50 of 200 pM. Ceritinib dihydrochloride (LDK378 dihydrochloride) also inhibits IGF-1R , InsR , and STK22D with IC 50 values of 8, 7, and 23 nM, respectively. Ceritinib dihydrochloride (LDK378 dihydrochloride) shows great antitumor potency [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LDK378 dihydrochloride. CAS No. 1380575-43-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15656A. | |
| Cerivastatin sodium | Cerivastatin sodium is a synthetic lipid-lowering agent and a highly potent, well-tolerated and orally active HMG-CoA reductase inhibitor, with a K i of 1.3 nM/L. Cerivastatin sodium reduces low-density lipoprotein cholesterol levels. Cerivastatin sodium also inhibits proliferation and invasiveness of MDA-MB-231 cells, mainly by RhoA inhibition, and has anti-cancer effect [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 143201-11-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109523. | |
| Certolizumab pegol | Certolizumab pegol (Certolizumab) is a recombinant, polyethylene glycolylated, antigen-binding fragment of a humanized monoclonal antibody that selectively targets and neutralizes tumour necrosis factor-α ( TNF-α ). Certolizumab pegol can be used for rheumatoid arthritis and Crohn disease research [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: Certolizumab; CDP870. CAS No. 428863-50-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P9953. | |
| Ceruletide | Ceruletide is a decapeptide and a potent cholecystokinin receptor agonist. Ceruletide is a safe and effective cholecystokinetic agent with a direct spasmogenic effect on the gallbladder muscle and bile ducts [1]. Uses: Scientific research. Group: Peptides. Alternative Names: Caerulein; Cerulein; FI-6934. CAS No. 17650-98-5. Pack Sizes: 100 μg; 500 μg; 1 mg; 5 mg. Product ID: HY-A0190. | |
| Ceruloplasmin | Ceruloplasmin is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Signaling pathways. CAS No. 9031-37-2. Pack Sizes: 100 U. Product ID: HY-P2777. | |
| Cesium chloride | Cesium chloride is a blocker of potassium channel. Cesium chloride prevents the decrease of Na + transport produced by Alloxan [1] [2]. Cesium chloride has induced cardiac arrhythmias, including torsade de pointes in animal models [3]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 7647-17-8. Pack Sizes: 5 g; 10 g. Product ID: HY-107754. | |
| Cesiumiodide | Cesiumiodide (Cesiumiodidewhitextl) is a biological material or organic compound that can be used in life science research [1]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Cesiumiodidewhitextl. CAS No. 7789-17-5. Pack Sizes: 10 mM * 1 mL; 10 g; 25 g. Product ID: HY-W040160. | |
| Cetalkonium chloride | Cetalkonium chloride is an ammonium antiseptic agent used in many topical agents for infections of mouth, throat and eye. Cetalkonium chloride acts as anti-inflammatory amphiphilic agent. Cetalkonium chloride is a cationic surfactant, that improves the precorneal residence time and bioavailability of drugs. Cetalkonium chloride interacts with the negative charges on the bacterial cell membrane, disrupts the integrity of the cell membrane, causes leakage of cell contents and ultimately leading to bacterial death [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Benzyldimethylhexadecylammonium chloride. CAS No. 122-18-9. Pack Sizes: 10 mM * 1 mL; 1 g. Product ID: HY-B1597. | |
| Cethromycin | Cethromycin (ABT-773) is a ketolide antibiotic [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ABT-773; Abbott-195773; A-195773. CAS No. 205110-48-1. Pack Sizes: 1 mg; 5 mg. Product ID: HY-19655. | |
| Cetilistat | Cetilistat (ATL-962), an inhibitor of pancreatic lipase , acts as an effective anti-obesity agent. Cetilistat inhibits rat and human pancreatic lipase activity with IC 50 s of 54.8 nM, and 5.95 nM, respectively [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ATL-962. CAS No. 282526-98-1. Pack Sizes: 200 mg; 500 mg; 1 g; 5 g. Product ID: HY-14471. | |
| Cetirizine | Cetirizine, a second-generation antihistamine and the carboxylated metabolite of hydroxyzine, is a specific, orally active and long-acting histamine H1-receptor antagonist. Cetirizine marks antiallergic properties and inhibits eosinophil chemotaxis during the allergic response [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 83881-51-0. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-17042. | |
| Cetirizine-d4 | Cetirizine-d 4 is a deuterium labeled Cetirizine. Cetirizine, a second-generation antihistamine and the carboxylated metabolite of hydroxyzine, is a specific, orally active and long-acting histamine H1-receptor antagonist. Cetirizine marks antiallergic properties and inhibits eosinophil chemotaxis during the allergic response[1][2][3]. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 1219803-84-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-17042S. | |
| Cetirizine dihydrochloride | Cetirizine dihydrochloride, a second-generation antihistamine and the carboxylated metabolite of hydroxyzine, is a specific, orally active and long-acting histamine H1-receptor antagonist. Cetirizine dihydrochloride marks antiallergic properties and inhibits eosinophil chemotaxis during the allergic response [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: P071. CAS No. 83881-52-1. Pack Sizes: 10 mM * 1 mL; 100 mg; 200 mg; 500 mg. Product ID: HY-17042A. | |
| Cetirizine Impurity C dihydrochloride | Cetirizine Impurity C dihydrochloride is an impurity of Cetirizine. Cetirizine, a second-generation antihistamine and the carboxylated metabolite of hydroxyzine, is a specific, orally active and long-acting histamine H1-receptor antagonist [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2702511-37-1. Pack Sizes: 5 mg; 10 mg. Product ID: HY-131256A. | |
| Cetraxate hydrochloride | Cetraxate hydrochloride (DV-1006), an orally active anti-ulcer agent with mucosal protective effects, can be used for gastric ulcers research [1]. Cetraxate hydrochloride is a potent acrosomal proteinase acrosin inhibitor with a K i and an IC 50 of 0.94 μM and 3.3 μM, respectively [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: DV-1006. CAS No. 27724-96-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-122762. | |
| Cetrelimab | Cetrelimab (JNJ 63723283; JNJ 3283) is a human IgG4κ mAb targeting PD-1. Cetrelimab binds PD-1 (K d =1.72 nM, HEK293) to block the interaction of PD-1 with PD-L1 and PD-L2 ( IC 50 s=111.7 ng/mL and 138.6 ng/mL, respectively). Cetrelimab stimulates peripheral T cells, increases IFN-γ , IL-2 , TNF-α level and inhibits tumor growth in vivo [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: JNJ 63723283; JNJ 3283. CAS No. 2050478-92-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99499. | |
| Cetrimonium bromide | Cetrimonium bromide (CTAB), a quaternary ammonium, is an orally active cationic surfaetant. Cetrimonium bromide has toxicity and anticancer effect. Cetrimonium bromide inhibits cell migration and invasion through modulating the canonical and non-canonical TGF-β signaling pathways. Cetrimonium bromide can be used for DNA extraction [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CTAB; Cetyltrimethylammonium bromide; Hexadecyltrimethylammonium bromide. CAS No. 57-09-0. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B1260. | |
| Cetrorelix | Cetrorelix is a potent gonadotrophin-releasing hormone (GnRH) antagonist. Cetrorelix inhibits the endogenous luteinizing hormone surge during ovarian stimulation. Cetrorelix reduces cyclophosphamide induced ovarian follicular destruction in mice [1] [2]. Uses: Scientific research. Group: Peptides. Alternative Names: SB-75. CAS No. 120287-85-6. Pack Sizes: 1 mg. Product ID: HY-P0009. | |
| Cetrorelix Acetate | Cetrorelix Acetate (SB-75 acetate) is a potent gonadotropin-releasing hormone (GnRH) receptor antagonist with an IC 50 of 1.21 nM [1]. Uses: Scientific research. Group: Peptides. Alternative Names: SB-75 acetate. CAS No. 145672-81-7. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P0009A. | |
| Cetuximab | Cetuximab (C225) is a human IgG1 monoclonal antibody that inhibits epidermal growth factor receptor ( EGFR ), with a K d of 0.201 nM for EGFR by SPR. Cetuximab has potent antitumor activity [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: C225. CAS No. 205923-56-4. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-P9905. | |
| Cetylamine | Cetylamine (Hexadecylamine) denatures proteins faster and prevents flocculation. Cetylamine can cap zinc sulfide nanoparticles and is used in cancer research [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Hexadecylamine. CAS No. 143-27-1. Pack Sizes: 1 g. Product ID: HY-W110707. | |
| Cetylpyridinium chloride | Cetylpyridinium chloride, a cationic quaternary ammonium compound, is an anti-bacterial agent with broad-spectrum activity. Cetylpyridinium chloride is an effective anti- HBV capsid assembly inhibitor with an IC 50 of 2.5 μM. Cetylpyridinium chloride is used in pesticides and various types of mouthwashes, and other personal care products [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 123-03-5. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-B1464. | |
| Cetylpyridinium chloride monohydrate | Cetylpyridinium chloride monohydrate is a cationic quaternary ammonium compound used in some types of mouthwashes, toothpastes, and throat and nasal sprays as an antiseptic that kills bacteria and other microorganisms. Effectively prevents plaque and reduces gingivitis. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Hexadecylpyridinium chloride monohydrate. CAS No. 6004-24-6. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-B1289. | |
| Cevadine | Cevadine is a voltage-sensitive sodium channel agonist. Cevadine has insecticidal activity [1]. Uses: Scientific research. Group: Natural products. CAS No. 62-59-9. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N12093. | |
| Cevidoplenib | Cevidoplenib (SKI-O-703) is an orally available inhibitor of spleen tyrosine kinase (Syk) , with potential anti-inflammatory and immunomodulating activities. Cevidoplenib is also the mesylate form of SKI-O-592. Cevidoplenib and SKI-O-592 inhibits BCR-mediated survival, proliferation, and differentiation of B cells. And SKI-O-592 potently inhibits multiple kinases with IC 50 s of 6.2 nM (Syk), 1.859 μM (Jak2), 5.807 μM (Jak3), 0.412 μM (RET), 0.687 μM (KOR), 1.783 μM (FLT3), 16.96 μM (FGFR1), 5.662 μM (FGFR3), and 0.709 μM (Pyk2), respectively [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SKI-O-703. CAS No. 1703788-21-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109082. | |
| Cevimeline hydrochloride | Cevimeline hydrochloride (AF102B hydrochloride) is a quinuclidine derivative of acetylcholine and a selective and orally active muscarinic M1 and M3 receptor agonist. Cevimeline hydrochloride stimulates secretion by the salivary glands and can be used as a sialogogue for xerostomia [1] [2] [3] [4]. Cevimeline hydrochloride can cross the blood-brain barrier (BBB) [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AF102B hydrochloride. CAS No. 107220-28-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-70020B. | |
| Cevipabulin | Cevipabulin (TTI-237) is an oral, microtubule-active antitumor compound and inhibits the binding of [ 3 H] vinblastine to tubulin, with an IC 50 of 18-40 nM for cytotoxicity in human tumor cell line [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TTI-237. CAS No. 849550-05-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14949. | |
| Cevipabulin fumarate | Cevipabulin fumarate (TTI-237 fumarate) is an oral, microtubule-active, antitumor compound and inhibits the binding of [ 3 H]NSC 49842 to tubulin, with an IC 50 of 18-40 nM for cytotoxicity in human tumor cell line [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TTI-237 fumarate. CAS No. 849550-67-0. Pack Sizes: 10 mM * 1ML; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14949C. | |
| Cevostamab | Cevostamab (BFCR4350A; RG6160; RO7187797) is a humanized IgG1-based BsAb that targets membrane-proximal extracellular domain of FcRH5 on multiple myeloma (MM) cells as well as CD3 on T cells. Moreover, Cevostamab facilitates efficient synapse formation, improves killing activity of T cells against MM tumor cells [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: BFCR 4350A; RG 6160; RO 7187797. CAS No. 2249888-53-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99601. | |
| CF53 | CF53 is a highly potent, selective and orally active inhibitor of BET protein, with a K i of <1 nM, K d of 2.2 nM and an IC 50 of 2 nM for BRD4 BD1. CF53 binds to both the BD1 and BD2 domains of BRD2, BRD3, BRD4, and BRDT BET proteins with high affinities, very selective over non-BET bromodomain-containing proteins. CF53 shows potent anti-tumor activity both in vitro and in vivo [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1808160-52-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-112610. | |
| CFDA-SE | CFDA-SE is a fluorescent dye that can penetrate the cell membrane. It can react with the free amine group in the cytoskeleton protein inside the cell, and finally form a protein complex with fluorescence. After entering the cell, CFDA-SE locates in the cell membrane, cytoplasm and nucleus, and the fluorescence staining is strongest in the nucleus [1]. CFDA-SE dye can be uniformly inherited by the cells with cell division and proliferation, and its attenuation is proportional to the number of cell divisions. This phenomenon can be detected and analyzed by flow cytometry under the excitation light of 488 nm, and can be used to detect the proliferation of cells [1]. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: CFSE; 5(6)-Carboxyfluorescein diacetate succinimidyl ester; 5(6)-CFDA N-succinmidyl ester. CAS No. 150347-59-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-D0938. | |
| CFM-2 | CFM-2 is a potent and selective non-competitive AMPAR antagonist [1]. CFM-2 possesses anticonvulsant activity in various models of seizures [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 178616-26-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-12503. | |
| CFM-4 | CFM-4 is a potent small molecular antagonist of CARP-1/APC-2 binding. CFM-4 prevents CARP-1 binding with APC-2, causes G 2 M cell cycle arrest, and induces apoptosis with an IC 50 range of 10-15 μM. CFM-4 also suppresses growth of drug-resistant human breast cancer cells [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 331458-02-7. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-103255. | |
| CFTR activator 2 | CFTR activator 2 (WAY-326769) is an activator of mutant cystic fibrosis transmembrane conductance regulator (mutant-CFTR) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: WAY-326769. CAS No. 871700-29-7. Pack Sizes: 5 mg; 10 mg. Product ID: HY-169536. | |
| CFTR corrector 15 | CFTR corrector 15 (Compound 4172) is a corrector for cystic fibrosis transmembrane conductance regulator ( CFTR ), that repairs the F508del-CFTR folding defect when used with VX-809 (HY-13262). CFTR corrector 15 can be used in research of cystic fibrosis disease [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1170387-92-4. Pack Sizes: 1 mg. Product ID: HY-164000. | |
| CFTR corrector 17 | CFTR corrector 17 (example 17) is a cystic fibrosis transmembrane conductance regulator (CFTR) modulator. CFTR corrector 17 can be used for the study of CFTR-mediated diseases [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 912790-04-6. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-W984122. | |
| CFTR corrector 2 | CFTR corrector 2 is a cystic fibrosis transmembrane conductance corrector (CFTR) , extracted from patent US20140274933 [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1628416-28-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-125381. | |
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