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 | |
|---|---|---|
| CFTR(inh)-172 | CFTR(inh)-172 is a potent and selective blocker of the CFTR chloride channel; reversibly inhibits CFTR short-circuit current in less than 2 minutes with a K i of 300 nM. Uses: Scientific research. Group: Signaling pathways. CAS No. 307510-92-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-16671. |  |
| cGAMP | cGAMP (Cyclic GMP-AMPP) functions as an endogenous second messenger in metazoans and triggers interferon production in response to cytosolic DNA. cGAMP activates stimulator of interferon genes (STING), which activates a signaling cascade leading to the production of type I interferons and other immune mediators [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cyclic GMP-AMP; 3',3'-cGAMP. CAS No. 849214-04-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-12512. | |
| cGAS-IN-2 | cGAS-IN-2 (compound 109) is a potent inhibitor of Cyclic GMP-AMP Synthase (cGAS), with IC 50 of 0.01512 μM for h-cGAS [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2765273-11-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-160546. | |
| CGP 12177 hydrochloride | CGP 12177 ((±)-CGP 12177) hydrochloride is a β Adrenergic Receptor Ligand. CGP 12177 hydrochloride is a high affinity antagonist of β1- and β2-AR. CGP 12177 hydrochloride is also shown to interact, with a lower affinity, with the β3-AR and to exhibit a partial agonist activity on rodent and human β3-AR. CGP 12177 hydrochloride exhibits partial agonist properties for α1-AR in rat pulmonary artery [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (±)-CGP 12177 hydrochloride. CAS No. 64208-32-8. Pack Sizes: 5 mg; 10 mg. Product ID: HY-101393A. | |
| CGP 20712 dihydrochloride | CGP 20712 dihydrochloride is a highly selective β1-adrenoceptor antagonist with an IC 50 of 0.7 nM. CGP 20712 dihydrochloride exhibits ~10,000-fold selectivity over β2-adrenoceptors [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1216905-73-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-101355A. | |
| CGP35348 | CGP 35348 is a selective, brain penetrant, centrally active GABAB receptor antagonist with an EC 50 of 34 μM. CGP 35348 shows affinity for the GABAB receptor only [1]. CGP 35348 has a potential to improve neuromuscular coordination and spatial learning in albino mouse following neonatal brain damage [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 123690-79-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103530. | |
| CGP 37849 | CGP 37849 is a potent, competitive and orally active N-methyl-D-aspartate (NMDA) receptor antagonist. CGP 37849 is an anticonvulsant in rodents and has antidepressant and anxiolytic-like effects [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 127910-31-0. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-107702. | |
| CGP52432 | CGP52432 is a GABA B receptor antagonist, with an IC 50 of 85 nM. Uses: Scientific research. Group: Signaling pathways. CAS No. 139667-74-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103531. | |
| CGP 54626 hydrochloride | CGP 54626 (hydrochloride) is a selective antagonist of GABA B receptor with an IC 50 value of 4 nM. CGP 54626 (hydrochloride) can be used to investigate the role of GABA B receptors in neurological signaling [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 149184-21-4. Pack Sizes: 1 mg. Product ID: HY-101378. | |
| CGP55845 hydrochloride | CGP55845 hydrochloride is a potent and selective GABAB receptor antagonist with an IC 50 of 6 nM. CGP55845 hydrochloride can be used for neurological research [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 149184-22-5. Pack Sizes: 5 mg; 10 mg. Product ID: HY-103516. | |
| CGP 57380 | CGP 57380 is a cell-permeable pyrazolo-pyrimidine compound that acts as a selective inhibitor of Mnk1 with IC 50 of 2.2 μM, but has no inhibitory activity against p38, JNK1, ERK1/2, PKC, or Src-like kinases. Uses: Scientific research. Group: Signaling pathways. CAS No. 522629-08-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10520. | |
| CGP71683 hydrochloride | CGP71683 hydrochloride is a competitive neuropeptide Y5 receptor antagonist with a K i of 1.3 nM, and shows no obvious activity at Y1 receptor ( K i , >4000 nM) and Y2 receptor ( K i , 200 nM) in cell membranes. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CGP71683A. CAS No. 192322-50-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-107723. | |
| CGP77675 | CGP77675 is an orally active and potent inhibitor of Src family kinases. CGP77675 inhibits phosphorylation of peptide substrates and autophosphorylation of purified Src ( IC 50 s of 5-20 and 40 nM, respectively), and also inhibits Src, EGFR, KDR, v-Abl, and Lck with IC 50 s of 5-20, 40, 20, 150, 1000, 310, and 290 nM, respectively. Anticancer activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 234772-64-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W062835. | |
| CGP 78608 hydrochloride | CGP 78608 hydrochloride is a highly potent and selective antagonist at the glycine-binding site of the NMDA receptor , with an IC 50 of 6 nM. CGP 78608 hydrochloride acts as a potentiator of GluN1/GluN3A-mediated glycine currents, with an estimated EC 50 in the low nM range (26.3 nM). Anticonvulsant activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1135278-54-4. Pack Sizes: 1 mg. Product ID: HY-107701. | |
| CGP7930 | CGP7930 (3-(3,5-Di-tert-butyl-4-hydroxy) phenyl-2, 2-dimethylpropanol) is a positive metabotropic GABAB receptor allosteric modulator. CGP7930 enhances the inhibitory effect of l-baclofen on the oscillatory activity of cultured cortical neurons [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 57717-80-3. Pack Sizes: 1 mg. Product ID: HY-103502. | |
| CGS 21680 Hydrochloride | CGS 21680 Hydrochloride is a selective adenosine A2A receptor agonist with a K i of 27 nM. Uses: Scientific research. Group: Signaling pathways. CAS No. 124431-80-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-13201A. | |
| CGS 8216 | CGS 8216, a benzodiazepine receptor antagonist, inhibits 3 H-flunitrazepam ( 3 H-FLU) binding to rat synaptosomal membranes in vitro at subnanomolar concentrations [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 77779-60-3. Pack Sizes: 1 mg; 5 mg. Product ID: HY-121116. | |
| CH-223191 | CH-223191 is a potent and specific antagonist of aryl hydrocarbon receptor ( AhR ). CH-223191 inhibits TCDD-mediated nuclear translocation and DNA binding of AhR, and inhibits TCDD-induced luciferase activity with an IC 50 of 0.03 μM [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 301326-22-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12684. | |
| CH7057288 | CH7057288 is a potent and selective TRK inhibitor. CH7057288 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. CAS No. 2095616-82-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-107362. | |
| Chaetocin | Chaetocin is a specific inhibitor of the histone methyltransferase ( HMT ) SU(VAR)3-9 with an IC 50 of 0.6 μM for SU(VAR)3-9. It also inhibits thioredoxin reductase ( TrxR ) with an IC 50 of 4 μM. Uses: Scientific research. Group: Natural products. CAS No. 28097-03-2. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N2019. | |
| Chaetoglobosin A | Chaetoglobosin A, the active principle within the extract of Penicillium aquamarinium , is a member of the cytochalasan family. Chaetoglobosin A preferentially induces apoptosis. Chaetoglobosin A targets filamentous actin in CLL cells and thereby induces cell-cycle arrest and inhibits membrane ruffling and cell migration [1]. Uses: Scientific research. Group: Natural products. CAS No. 50335-03-0. Pack Sizes: 1 mg. Product ID: HY-N6744. | |
| Chalcone | Chalcone is isolated from Glycyrrhiza uralensis and used to synthesize chalcone derivatives. Chalcone derivatives possess varied biological and pharmacological activity, including anti-inflammatory, antioxidative, antibacterial, anticancer, and anti-parasitic activities [1]. Uses: Scientific research. Group: Natural products. CAS No. 94-41-7. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-121054. | |
| CHAPS | CHAPS, a derivative of Cholic acid, is a zwitterionic detergent for solubilizing membrane proteins. CHAPS is used for stabilization of various protein-DNA complexes and can retain biochemical activity of proteins in solution [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 75621-03-3. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-15435. | |
| CHAPS hydrate | CHAPS hydrate, a derivative of Cholic acid, is a zwitterionic detergent for solubilizing membrane proteins. CHAPS hydrate is used for stabilization of various protein-DNA complexes and can retain biochemical activity of proteins in solution [1] [2]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 331717-45-4. Pack Sizes: 500 mg; 1 g. Product ID: HY-15435A. | |
| CHAPSO | CHAPSO is a zwitterionic detergent that is thermally stable. CHAPSO is able to broaden the particle orientation distribution, enabling single-particle cryo-electron microscopy (cryo-EM) to produce isotropically uniform maps. CHAPSO can eliminate the directional bias of bacterial transcription complexes and help determine the structure of bacterial transcription complexes under cryo-electron microscopy [1] [2]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: 3-[3- (Cholamidopropyl)dimethylammonio]-2-hydroxy-1-propanesulfonate. CAS No. 82473-24-3. Pack Sizes: 100 mg; 500 mg. Product ID: HY-W040201. | |
| Chavicol | Chavicol (p-Hydroxyallylbenzene, compound 6) can inhibit acetylcholinesterase ( Cholinesterase (ChE) ), with an IC 50 of 7.42 μM. Chavicol has anti-cancer activity and can suppress the growth, survival, migration, and invasion of cancer cells. Chavicol cytotoxic effect is significant, approximately 31 μg/mL in A-549 cells [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: p-Hydroxyallylbenzene. CAS No. 501-92-8. Pack Sizes: 10 mM * 1 mL; 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-W159754. | |
| CHD-5 | CHD-5 is a potent AhR (aryl hydrocarbon receptor) antagonist [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 289494-16-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-118780. | |
| Chebulagic acid | Chebulagic acid is a COX-LOX dual inhibitor isolated from the fruits of Terminalia chebula Retz, on angiogenesis. Chebulagic acid is a M2 serine to asparagine 31 mutation (S31N) inhibitor and influenza antiviral. Chebulagic acid also against SARS-CoV-2 viral replication with an EC 50 of 9.76 μM. Uses: Scientific research. Group: Natural products. CAS No. 23094-71-5. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg. Product ID: HY-N1996. | |
| Chebulic acid | Chebulic acid is a phenolic acid compound isolated from Terminalia chebula with strong antioxidant activity, which breaks protein cross-links induced by advanced glycation end products ( AGEs ) and inhibits the formation of AGEs. Chebulic acid is effective in controlling elevated metabolic parameters, oxidative stress, and liver damage, supporting its beneficial role in asthma, diabetes, and liver protection [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Natural products. CAS No. 23725-05-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N4170. | |
| Chebulinic acid | Chebulinic acid is a potent natural inhibitor of M. tuberculosis DNA gyrase, also can inhibit SMAD-3 phosphorylation, inhibit H+ K+-ATPase activity. Uses: Scientific research. Group: Natural products. CAS No. 18942-26-2. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N2033. | |
| Chelerythrine chloride | Chelerythrine chloride is a potent, cell-permeable inhibitor of protein kinase C , with an IC 50 of 660 nM. Chelerythrine chloride inhibits the Bcl-XL-Bak BH3 peptide binding with IC 50 of 1.5 μM and displaces Bax from Bcl-XL. Chelerythrine chloride induces apoptosis and autophagy. Uses: Scientific research. Group: Natural products. CAS No. 3895-92-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12048. | |
| Chelidamic acid | Chelidamic acid is a heterocyclic organic acid with a pyran skeleton. Chelidamic acid has good coordination ability with noble metal ions. Chelidamic acid is also one of the most potent inhibitors of glutamate decarboxylase, with a K i of 33 μM. Uses: Scientific research. Group: Signaling pathways. CAS No. 138-60-3. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-W016349. | |
| Chelidonic acid | Chelidonic acid is a component of Chelidonium majus L., used as an antimicrobial. Chelidonic acid also shows anti-inflammatory activity. Chelidonic acid has potential to inhibit IL-6 production by blocking NF-κB and caspase-1 [1]. Chelidonic acid is a glutamate decarboxylase inhibitor, with a K i of 1.2 μM [2]. Uses: Scientific research. Group: Natural products. CAS No. 99-32-1. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-W041489. | |
| Chelidonine | Chelidonine, an isoquinoline alkaloid, can be isolated from Chelidonium majus L. Chelidonine causes G 2/M arrest and induces caspase-dependent and caspase-independent apoptosis , and prevents cell cycle progression of stem cells in Dugesia japonica. Chelidonine has cytotoxic activity against melanoma cell lines. with anticancer and antiviral activity [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 476-32-4. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N2369. | |
| Chenodeoxycholic Acid | Chenodeoxycholic Acid is a hydrophobic primary bile acid that activates nuclear receptors ( FXR ) involved in cholesterol metabolism. Uses: Scientific research. Group: Natural products. Alternative Names: CDCA. CAS No. 474-25-9. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g; 5 g; 10 g. Product ID: HY-76847. | |
| Chenodeoxycholic acid sodium | Chenodeoxycholic acid sodium is a hydrophobic primary bile acid that activates nuclear receptors ( FXR ) involved in cholesterol metabolism. Uses: Scientific research. Group: Natural products. Alternative Names: CDCA sodium. CAS No. 2646-38-0. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g; 5 g; 10 g. Product ID: HY-76847A. | |
| CHES | CHES (N-Cyclohexyltaurine) is a zwitterionic buffer. CHES can bind to hemagglutinin (HA) emulating with sialic acid (SA) and receptor binding site (RBS)-targeting broadly neutralizing antibodies [1]. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: N-Cyclohexyltaurine. CAS No. 103-47-9. Pack Sizes: 25 g; 50 g. Product ID: HY-D0871. | |
| CHI3L1-IN-1 | CHI3L1-IN-1 (Compound 30) is an inhibitor for Chitinase-3-like protein 1 ( CHI3L1 ) (YKL-40) with IC 50 of 50 nM. CHI3L1-IN-1 inhibits hERG channel with an IC 50 of 2.3 μM [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2982256-78-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-163387. | |
| Chiauranib | Chiauranib (CS2164) is an orally active multi-target inhibitor against tumor angiogenesis. Chiauranib potently inhibits the angiogenesis-related kinases ( VEGFR1 , VEGFR2 , VEGFR3 , PDGFRα and c-Kit ), mitosis-related kinase Aurora B , and chronic inflammation-related kinase CSF-1R , with IC 50 values ranging from 1-9 nM. Chiauranib has strongly anticancer effects [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ibcasertib; CS2164. CAS No. 1256349-48-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-124526. | |
| Chicoric acid | Chicoric acid (Cichoric acid), an orally active dicaffeyltartaric acid, induces reactive oxygen species (ROS) generation. Chicoric acid inhibits cell viability and induces mitochondria-dependent apoptosis in 3T3-L1 preadipocytes through ROS-mediated PI3K/Akt and MAPK signaling pathways. Chicoric acid increases glucose uptake, improves insulin resistance, and attenuates glucosamine-induced inflammation. Chicoric acid has antidiabetic properties and antioxidant, anti-inflammatory effects [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Cichoric acid; Dicaffeoyltartaric acid. CAS No. 6537-80-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-N0457. | |
| Chiglitazar | Chiglitazar (Carfloglitazar) is a PPARα/γ dual agonist, with EC 50 s of 1.2, 0.08, 1.7 μM for PPARα, PPARγ and PPARδ, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Carfloglitazar. CAS No. 743438-45-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-106266. | |
| Chitinase, Serratia marcescens | Chitinase, Serratia marcescens (EC 3.2.1.14) has partial lysozyme activity and is widely found in bacteria, fungi, animals and some plants. Chitinase belongs to the glycosyl hydrolase family. Chitinase catalyzes chito-oligosaccharide hydrolysis. Chitinases also can serve as prognostic biomarkers of disease progression. Chitinase can be used in the research of pathogenesis of various human fibrotic and inflammatory disorders, particularly those of the lung (idiopathic pulmonary fibrosis, chronic obstructive pulmonary disease, sarcoidosis, and asthma) and the gastrointestinal tract (inflammatory bowel diseases (IBDs) and colon cancer) [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AMCase, Serratia marcescens. CAS No. 9001-6-3. Pack Sizes: 5 U. Product ID: HY-P2797. | |
| Chitinase, Streptomyces griseus | Chitinase, Streptomyces griseus is a chitinase mainly found in Bacillus species and uses colloidal chitin as a substrate. The Km and Vmax of Chitinase are 4.28 mg/mL and 14.29 μg/(Min·mL) respectively. The final enzymatic hydrolysis product is N-acetylglucosamine, and the monomer and dimer contents are 14.33% and 85.67% respectively [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AMCase, Streptomyces griseus. CAS No. 9001-6-3. Pack Sizes: 1 g; 5 g. Product ID: HY-P2797A. | |
| Chitobiose dihydrochloride | Chitobiose dihydrochloride, a chitosan oligosaccharide, is a dimer of β-1,4-linked glucosamine units [1]. Uses: Scientific research. Group: Natural products. CAS No. 115350-24-8. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N7697B. | |
| Chitosan oligosaccharide | Chitosan oligosaccharide (COS) is an oligomer of β-(1→4)-linked D-glucosamine. Chitosan oligosaccharide (COS) activates AMPK and inhibits inflammatory signaling pathways including NF-κB and MAPK pathways. Uses: Scientific research. Group: Natural products. Alternative Names: COS. CAS No. 148411-57-8. Pack Sizes: 500 mg; 1 g; 5 g. Product ID: HY-112108. | |
| Chk1-IN-6 | Chk1-IN-6 is a potent, selective, and orally bioavailable CHK1 inhibitor candidate. Uses: Scientific research. Group: Signaling pathways. CAS No. 2428423-77-0. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139901. | |
| Chlophedianol hydrochloride | Chlophedianol (Clofedanol) hydrochloride is an orally active and potent antitussive agent. Chlophedianol hydrochloride can be used for the research of acute cough due to upper respiratory tract infections (URIs) [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Clofedanol hydrochloride; Calmotusin hydrochloride; NSC 113595 hydrochloride. CAS No. 511-13-7. Pack Sizes: 5 mg; 10 mg. Product ID: HY-A0161A. | |
| Chloramben | Chloramben (3-Amino-2,5-dichlorobenzoic acid) is a pre-emergence herbicide used to control the seedlings of annual grasses and broadleaf weeds [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 133-90-4. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g. Product ID: HY-119417. | |
| Chloramine-T | Chloramine-T is a titrimetric reagent, and an oxidizing agent. Chloramine-T is an oxidizing biocide [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 127-65-1. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g; 10 g. Product ID: HY-B0959. | |
| Chloramphenicol | Chloramphenicol is an orally active, potent and broad-spectrum antibiotic. Chloramphenicol shows antibacterial activity. Chloramphenicol represses the oxygen-labile transcription factor and hypoxia inducible factor-1 alpha ( HIF-1α ) in hypoxic A549 and H1299 cells. Chloramphenicol suppresses the mRNA levels of vascular endothelial growth factor ( VEGF ) and glucose transporter 1 , eventually decreasing VEGF release. Chloramphenicol can be used for anaerobic infections and lung cancer research [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 56-75-7. Pack Sizes: 500 mg; 1 g; 5 g. Product ID: HY-B0239. | |
| Chloramphenicol palmitate | Chloramphenicol palmitate is an orally active broad spectrum antibiotic and has a broad spectrum of activity against gram positive and gram negative bacteria. Chloramphenicol palmitate inhibits bacterial protein synthesis by blocking the peptidyl transferase step. Chloramphenicol palmitate can be used as bacterial selection agent in transformed cells containing chloramphenicol resistance genes [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 530-43-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-B1599. | |
| Chloramphenicol (Standard) | Chloramphenicol (Standard) is the analytical standard of Chloramphenicol. This product is intended for research and analytical applications. Chloramphenicol is an orally active, potent and broad-spectrum antibiotic. Chloramphenicol shows antibacterial activity. Chloramphenicol represses the oxygen-labile transcription factor and hypoxia inducible factor-1 alpha (HIF-1α) in hypoxic A549 and H1299 cells. Chloramphenicol suppresses the mRNA levels of vascular endothelial growth factor (VEGF) and glucose transporter 1, eventually decreasing VEGF release. Chloramphenicol can be used for anaerobic infections and lung cancer research [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 56-75-7. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-B0239R. | |
| Chloramphenicol succinate sodium | Chloramphenicol succinate sodium is a proagent of Chloramphenicol, with Haemotoxicity. Chloramphenicol succinate is a competitive substrate and inhibitor of succinate dehydrogenase (SDH) that is the possible reason for its toxicity [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 982-57-0. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-N7114A. | |
| Chloranil | Chloranil (Tetrachloro-p-benzoquinone), an orally active metabolite of pentachlorophenol and hexachlorobenzene, is a widely used fungicide. Chloranil can induce ROS production. Chloranil induces neutrophil extracellular traps through the ROS-JNK-NOX2 pathway. Chloranil induces ferroptosis and neuroinflammation. Chloranil induces apoptosis of mouse embryonic stem cells [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Tetrachloro-p-benzoquinone; TCBQ. CAS No. 118-75-2. Pack Sizes: 10 mM * 1 mL; 25 g; 100 g. Product ID: HY-Y0278. | |
| Chlorantraniliprole | Chlorantraniliprole is an insecticide that potently and selectively activates insect ryanodine receptor , with EC 50 s of 40 nM and 50 nM for Drosophila melanogaster and H. virescens ryanodine receptor, and ~300-fold more potent than that in the mouse myoblast cell line, C2C12 ( EC 50 , 14 μM). Uses: Scientific research. Group: Signaling pathways. CAS No. 500008-45-7. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-112820. | |
| Chlorazanil | Chlorazanil is a triazine derivative and also a new nonmercurial diuretic agent. Uses: Scientific research. Group: Signaling pathways. CAS No. 500-42-5. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-B1045A. | |
| Chlorcyclizine hydrochloride | Chlorcyclizine hydrochloride is a histamine H1 antagonist. Uses: Scientific research. Group: Signaling pathways. CAS No. 14362-31-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 200 mg; 500 mg. Product ID: HY-112067A. | |
| Chlorfenapyr | Chlorfenapyr is a pyrrole insecticide. Chlorfenapyr has a mode of action: the mixed function oxidase oxidizes and removes the Nethoxymethyl group to form the active metabolite, CL 303268. Chlorfenapyr is used for termite control and crop protection against a variety of insect and mite pests [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 122453-73-0. Pack Sizes: 10 mM * 1 mL; 100 mg; 250 mg; 500 mg. Product ID: HY-B0840. | |
| Chlorfluazuron | Chlorfluazuron (IKI-7899) is a benzoylurea insecticide. Chlorfluazuron inhibts insect chitin and disrupts normal exuviation by inducing malformations, thereby preventing and controlling lepidopteran pests [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: IKI-7899. CAS No. 71422-67-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-133204. | |
| Chlorhexidine | Chlorhexidine is an antibacterial used as an antiseptic and for other applications. Chlorhexidine is used to clean the skin after an injury, before surgery, or before an injection. Chlorhexidine is also used to clean the hands before a procedure [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 55-56-1. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B1248. | |
| Chlorhexidine diacetate | Chlorhexidine diacetate is a biguanide disinfectant with rapid bactericidal activity against both Gram-positive and Gram-negative organism. The antibacterial effect of chlorhexidine diacetate is related to its action on the bacterial cell membrane and to precipitation of intracellular contents [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 56-95-1. Pack Sizes: 100 mg; 500 mg. Product ID: HY-W013699. | |
| Chlorhexidine (digluconate) (20% in water) | Chlorhexidine digluconate is a chlorophenyl biguanide with broad antibacterial action against both Gram (+) and (-) bacteria and fungi. Chlorhexidine digluconate is a broad-spectrum antiseptic and disinfectant. Chlorhexidine digluconate is effective to prevent and control infectious diseases of the mouth by killing bacteria in saliva and tongue. Chlorhexidine digluconate is a cytotoxic agent and induces cell necrosis and apoptosis [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 18472-51-0. Pack Sizes: 5 g (222.8 mM * 25 mL in Water); 20 g (222.8 mM * 100 mL in Water). Product ID: HY-B0608. | |
| Chlorhexidine dihydrochloride | Chlorhexidine dihydrochloride is an orally active antimicrobial agent. Chlorhexidine dihydrochloride can damage the bacteria cell wall, inhibit proliferation of S. sobrinus and induce DNA damage [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 3697-42-5. Pack Sizes: 10 mM * 1 mL; 5 g; 10 g. Product ID: HY-B1145. | |
| Chlorimuron-ethyl | Chlorimuron-ethyl induces oxidative stress. Chlorimuron-ethyl is an important herbicide that has been widely used in soybean production [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 90982-32-4. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-W040262. | |
| Chlorin e6 | Chlorin e6 is a photosensitizer and has strong absorption peaks at wavelength of 402 and 662 nm, as well as exhibiting intense fluorescence at 668 nm. Chlorin e6 has antimicrobial efficacy and anticancer activity. Chlorin e6 induces cell apoptosis via caspase-3 activation and can be used for the research of cancer [1] [2] [3]. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: Ce6. CAS No. 19660-77-6. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-13594. | |
| Chlormadinone acetate | Chlormadinone acetate is a steroidal progestin, with antiandrogen and antiestrogenic effects. Uses: Scientific research. Group: Signaling pathways. CAS No. 302-22-7. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g. Product ID: HY-B1095. | |
| Chlormethiazole hydrochloride | Clomethiazole hydrochloride is a anticonvulsant. Clomethiazole hydrochloride is neuroprotective and prevents the degeneration of serotonergic nerve terminals induced by 3,4-methylenedioxymethamphetamine (MDMA) [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Clomethiazole hydrochloride. CAS No. 6001-74-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-A0296. | |
| Chlormezanone | Chlormezanone resembles benzodiazepine. The action of Chlormezanone is similar to benzodiazepine-type agents. Chlormezanone is used as an anxiolytic and a muscle relaxant. Uses: Scientific research. Group: Signaling pathways. CAS No. 80-77-3. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-B0353. | |
| Chlormidazole hydrochloride | Chlormidazole hydrochloride is an antifungal agent and has inhibitory activity against many fungi and some gram-positive cocci. Chlormidazole hydrochloride can be applied in fungal and bacterial infections of nails and skin, including interdigital and periungual mycoses [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Clomidazole hydrochloride. CAS No. 74298-63-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-B1144A. | |
| Chlorobutanol | Chlorobutanol is an orally active and potent inhibitor of platelet aggregation and release and a pharmaceutical preservative with antibacterial activity. Chlorobutanol inhibits thromboxane B2 formation, ATP release, and elevation of cytosolic free calcium caused by collagen, ADP, epinephrine, arachidonic acid and thrombin. Chlorobutanol is active against a wide variety of Gram-positive and Gram-negative bacteria , and several mold spores and fungi. Chlorobutanol is widely used in food and cosmetic industry [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 57-15-8. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-B1263. | |
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