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 | |
|---|---|---|
| SU11652 | SU11652 is a potent receptor tyrosine kinase (RTK) inhibitor. SU11652 also inhibits several members of the split kinase family of RTKs, including VEGFR, FGFR, PDGFR, and Kit. SU11652 can be uesd for spontaneous cancers expressing Kit mutations research[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 326914-10-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112452. |  |
| SU1261 | SU1261 is an IKK inhibitor with Ki values of 10 nM and 680 nM for IKKα and IKKβ, respectively. SU1261 can inhibit non-canonical NF-κB signaling in U2OS osteosarcoma cells[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3061890-98-7. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-169053. | |
| SU14813 | SU14813 is a multi-targeted receptor tyrosine kinases inhibitor with IC50s of 50, 2, 4, 15 nM for VEGFR2, VEGFR1, PDGFRβ and KIT. Uses: Scientific research. Category: Signaling pathways. CAS No. 627908-92-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10501. | |
| SU1498 | SU1498 (AG 1498) is a selective inhibitor of the VEGFR2; inhibits Flk-1 with an IC50 of value of 700 nM[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AG 1498; Tyrphostin SU 1498. CAS No. 168835-82-3. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-19326. | |
| SU212 | SU212 is a podophyllotoxin-derived ENO1 inhibitor and AMPK activator. SU212 can selectively induce oxidative phosphorylation, reduce glycolysis activity and glucose uptake in tumor cells, and directly bind to ENO1 without affecting these pathways in normal cells. SU212 induces apoptosis and promotes ENO1 degradation via proteasomal and autophagic pathways without inhibiting the catalytic activity. SU212 leads to mitotic arrest and apoptosis in TNBC (triple-negative breast cancer) cells by activating AMPK, demonstrating potent anti-tumor activity in vitro. SU212 inhibits tumor growth and metastasis in syngeneic, xenograft, and diabetic mouse models, exhibiting an excellent safety profile. SU212 can be used in research on t TNBC, diabetes, and fatty liver disease[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1262219-89-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg. Product ID: HY-179578. | |
| SU 5402 | SU 5402 is a potent multi-targeted receptor tyrosine kinase inhibitor with IC50 of 20 nM, 30 nM, and 510 nM for VEGFR2, FGFR1, and PDGFRβ, respectively. Uses: Scientific research. Category: Signaling pathways. CAS No. 215543-92-3. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10407. | |
| SU6656 | SU6656 is a Src family kinases inhibitor with IC50s of 280, 20, 130, 170 nM for Src, Yes, Lyn, and Fyn, respectively. SU6656 inhibits FAK phosphorylation at Y576/577, Y925, Y861 sites. SU6656 also inhibits p-AKT. Uses: Scientific research. Category: Signaling pathways. CAS No. 330161-87-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0789. | |
| SU9516 | SU9516 is a potent CDK2 inhibitor, with an IC50 of 22 nM, and also shows inhibitory effects on CDK1 and CDK4, with IC50s of 40, 200 nM, respectively. Uses: Scientific research. Category: Signaling pathways. CAS No. 377090-84-1. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-18629. | |
| Subasumstat | Subasumstat (TAK-981) is a first in class and selective inhibitor of the SUMOylation enzymatic cascade, with potential immune-activating and antineoplastic activities[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: TAK-981. CAS No. 1858276-04-6. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-111789. | |
| Suberylglycine | Suberylglycine is an acyl glycine, which is a normally minor metabolite of fatty acid. Uses: Scientific research. Category: Signaling pathways. CAS No. 60317-54-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-113367. | |
| Submandibular mucin | Submandibular mucin is a high molecular weight glycoprotein that is used as a substrate for the viral enzyme neuraminidase[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 84195-52-8. Pack Sizes: 50 mg; 100 mg; 500 mg. Product ID: HY-P3008. | |
| Substance P | Substance P (Neurokinin P) is a CNS-penetrant neuropeptide, acting as a neurotransmitter and as a neuromodulator in the CNS. The endogenous receptor for substance P is neurokinin 1 receptor (NK1-receptor, NK1R). Uses: Scientific research. Category: Signaling pathways. Alternative Names: Neurokinin P. CAS No. 33507-63-0. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P0201. | |
| Substance P(1-7) TFA | Substance P(1-7) TFA is a fragment of the neuropeptide, substance P (SP). Substance P(1-7) TFA gives depressor and bradycardic effects when applied to the nucleus tractus solitarius[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2828433-22-1. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-P1485A. | |
| Substance P (1-9) | Substance P (1-9) is nonapeptide, which decreases the inactivation of substance P by the guinea-pig ileum and urinary bladder. Uses: Scientific research. Category: Signaling pathways. CAS No. 57468-17-4. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P1494. | |
| Subtilisin | Subtilisin (EC 3.4.21.14) is a bacterial serine protease. Subtilisin induces Apoptosis. Subtilisin stimulates the expression of pro-allergic cytokines (IL-1α, IL-33). Subtilisin induces prototypic allergic lung inflammation. Subtilisin exhibits anticancer activity against breast and colon cancer. Subtilisin shows antifouling activity. Subtilisin can be used as a detergent additive[1][2][3][4][5][6]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: EC 3.4.21.14. CAS No. 9014-1-1. Pack Sizes: 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-P2729. | |
| Suc-AAPF-AMC | Suc-AAPF-AMC is an α-chymotrypsin fluorogenic substrate for the quantitative determination of chymotrypsin activity[1]. Uses: Scientific research. Category: Peptides. Alternative Names: Suc-Ala-Ala-Pro-Phe-AMC. CAS No. 88467-45-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg. Product ID: HY-137811. | |
| Suc-AAPF-pNA | Suc-AAPF-pNA (Suc-Ala-Ala-Pro-Phe-pNA) is a chromogenic p-nitroanilide (pNA) substrate with the Km of 1.7 mM. Cleavage of Suc-AAPF-pNA releases 4-nitroaniline, which is yellow in colour and can be measured spectrophotometrically. Suc-AAPF-pNA can be used for the measurement of free and membrane-bound cathepsin G in human neutrophils[1][2][3]. Uses: Scientific research. Category: Peptides. Alternative Names: Suc-Ala-Ala-Pro-Phe-pNA. CAS No. 70967-97-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 100 mg. Product ID: HY-P2573. | |
| Suc-Ala-Leu-Pro-Phe-pNA | Suc-Ala-Leu-Pro-Phe-pNA (Suc-ALPF-pNA) is a synthetic polypeptide substrate that targets FK506-binding protein (FKBP). Suc-Ala-Leu-Pro-Phe-pNA can be used to determine peptidyl-prolyl cis-trans isomerase activity via the chymotrypsin-coupled assay. Suc-Ala-Leu-Pro-Phe-pNA serves as a substrate for human FK506-binding protein hFKBP-12 in the chymotrypsin-FKBP coupled PPIase assay. Suc-Ala-Leu-Pro-Phe-pNA is applicable for the detection and research of PPIase activity[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Suc-ALPF-pNA. CAS No. 128802-78-8. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P4581. | |
| Suc-Ala-Pro-pNA | Suc-Ala-Pro-pNA is a peptide that serves as a substrate to detect the activity and stability of prolyl endopeptidase (PEP)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 95632-46-5. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P4490. | |
| Succinaldehydic acid | Succinaldehydic acid is a catabolite of GABA. Uses: Scientific research. Category: Signaling pathways. CAS No. 692-29-5. Pack Sizes: 1 mg; 2.5 mg. Product ID: HY-104071. | |
| Succinate/succinate receptor antagonist 1 | Succinate/succinate receptor antagonist 1 is an antagonist of the succinate/succinate receptor. Succinate/succinate receptor antagonist 1 can inhibit the activation of succinate receptor 1 (SUCNR1). Succinate/succinate receptor antagonist 1 can block succinate signaling. Succinate/succinate receptor antagonist 1 can be used for the study of periodontal disease[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2361972-29-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-150205. | |
| Succinic acid | Succinic acid is an anti-anxiety agent with oral activity. Disodium succinate is the salt form of Succinic acid. Succinic acid is an intermediate product of the tricarboxylic acid cycle. Succinic acid is an important platform chemical. Succinic acid can be used as surfactant, additive, ion chelating agent, flavoring agent and other applications in chemical, pharmaceutical and food fields[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Wormwood acid. CAS No. 110-15-6. Pack Sizes: 10 mM * 1 mL in DMSO; 50 mg; 100 mg; 500 mg; 1 g; 5 g; 10 g; 25 g; 50 g; 100 g. Product ID: HY-N0420. | |
| Succinic acid-13C4 | Succinic acid-13C4 is the 13C labeled Succinic acid[1]. Succinic acid is a potent and orally active anxiolytic agent. Succinic acid is an intermediate product of the tricarboxylic acid cycle. Succinic acid can be used as a precursor of many industrially important chemicals in food, chemical and pharmaceutical industries[2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Wormwood acid-13C4. CAS No. 201595-67-7. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg. Product ID: HY-N0420S2. | |
| Succinic acid-d4 | Succinic-2,2,3,3-d4 acid is the deuterium labeled Succinic acid. Succinic acid is an intermediate product of the tricarboxylic acid cycle, as well as one of fermentation products of anaerobic metabolism. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Wormwood acid-d4. CAS No. 14493-42-6. Pack Sizes: 10 mM * 1 mL in DMSO; 50 mg; 100 mg. Product ID: HY-N0420S1. | |
| Succinic anhydride | Succinic anhydride is a cyclic anhydride and a nonclaevable ADC linker extracted from patent WO2009064913A1. Succinic anhydride can react with compound 4 of the patent to link the proagent to an amine or hydroxy 1 group of a targeting polypeptide[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 108-30-5. Pack Sizes: 25 g; 50 g; 100 g; 500 g; 1 k g. Product ID: HY-79369. | |
| Succinyladenosine | Succinyladenosine, the metabolic product of dephosphorylation of intracellular adenylosuccinic acid (S-AMP) by cytosolic 5-nucleotidase, is a biochemical marker of adenylosuccinase (ASL) deficiency[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: N6-Succinyl adenosine. CAS No. 4542-23-8. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg. Product ID: HY-113284. | |
| Succinyl-Coenzyme A sodium | Succinyl CoA (Succinyl-coenzyme A) sodium is a pivotal intermediate metabolite in the tricarboxylic acid cycle and a key coenzyme A metabolite. Succinyl CoA sodium is biosynthesized from α-ketoglutarate or propionyl-CoA. Succinyl CoA sodium acts as a critical precursor and substrate for heme biosynthesis and gluconeogenesis. Succinyl CoA sodium insufficiency caused by cobalamin deficiency is directly linked to growth retardation, impaired heme synthesis, tissue glycine accumulation and neurological abnormalities. Succinyl CoA sodium can be used in research on metabolic, neurological, and hematological abnormalities (such as porphyria) caused by nutritional vitamin B12 deficiency (leading to a lack of Succinyl-Coenzyme A synthesis)[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Succinyl-CoA sodium. CAS No. 108347-97-3. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-137808. | |
| Succinyl phosphonate trisodium salt | Succinyl phosphonate trisodium salt is a α-Ketoglutarate Dehydrogenase Complex (KGDHC) modulator with neuroprotective activity. Succinyl phosphonate trisodium salt protects this complex, reduces cellular succinyl-CoA concentration, downregulates protein succinylation levels, and inhibits the activity of the α-ketoglutarate dehydrogenase complex. Succinyl phosphonate trisodium salt corrects hypoxic or ethanol-induced behavioral impairments, modulates exploratory behavior and emotional stress responses, and improves hypoxia tolerance. Succinyl phosphonate trisodium salt reduces glutamate excitotoxicity, restores the activity of the α-ketoglutarate dehydrogenase complex, reverses the changes in glutamate dehydrogenase and glutamine synthetase activities induced by β-amyloid (Amyloid-β), modulates cognitive function, and prevents β-amyloid-induced neuronal damage. Succinyl phosphonate trisodium salt improves microglial senescence, alleviates neuroinflammation, reactive oxygen species (ROS) production, lipid peroxidation, and the expression of proinflammatory cytokines. Succinyl phosphonate trisodium salt can be used in the research of Alzheimer's disease, aging-related neuroinflammation, and Parkinson's disease[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 864167-45-3. Pack Sizes: 10 mM * 1 mL in Water; 5 mg; 10 mg. Product ID: HY-12688A. | |
| Suc-Gly-Pro-AMC | Suc-Gly-Pro-AMC is a fluorescent substrate. Suc-Gly-Pro-AMC is a fibroblast activation protein (FAP) specific substrate. Suc-Gly-Pro-AMC reacts with recombinant porcine prolyl oligopeptidase. Suc-Gly-Pro-AMC can be used to study the activity of FAP, prolyl endopeptidase (PREP). Suc-Gly-Pro-AMC is used in glioma research[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 80049-85-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-145983. | |
| Suc-Ile-Glu(γ-pip)-Gly-Arg-pNA hydrochloride | Suc-Ile-Glu(γ-pip)-Gly-Arg-pNA hydrochloride is a factor Xa specific chromogenic substrate[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1379822-04-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P3126. | |
| Suciraslimab | Suciraslimab (SM03) is an anti-human CD22 monoclonal antibody. Suciraslimab inhibits NLRP3 and ASC signaling. Suciraslimab suppresses cytokine (IL-1β, IL-12, IL-23) secretion and α4 integrin expression. Suciraslimab improves working memory and neuroinflammation[1]. Suciraslimab isotype control product: Human IgG1 kappa, Isotype Control (HY-P99001). Uses: Scientific research. Category: Signaling pathways. Alternative Names: SM03. CAS No. 2415439-63-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P990781. | |
| Suc-Leu-Leu-Val-Tyr-AMC | Suc-Leu-Leu-Val-Tyr-AMC is a membrane-permeable calpain-specific fluorogenic substrate (Ex/Em = 390/480 nm)[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Suc-LLVY-AMC. CAS No. 94367-21-2. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P1002. | |
| SUCNR1-IN-1 | SUCNR1-IN-1 is an orally active SUCNR1 inhibitor. SUCNR1-IN-1 exhibits inhibitory rates of 23% and 56% against rat and mouse SUCNR1 at 100 μM, respectively. SUCNR1-IN-1 can be used in the research of rheumatoid arthritis[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2711753-52-3. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-154946. | |
| SUCNR1-IN-2 | SUCNR1-IN-2 (Statement 35) is a SUCNR1 inhibitor. SUCNR1-IN-2 can be used for the study of neurodegenerative diseases such as neuroinflammation[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2988733-54-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-156955. | |
| Sucralfate | Sucralfate (Sucrose octasulfate-aluminum complex) is a potent and orally active gastroprotectant with no systemic effects. Sucralfate inhibits peptic activity and binds to negatively charged subepithelial proteins exposed during mucosal injury, forming a viscous layer that protects the vascular bed and proliferative zone. Sucralfate is used for prevention and research of several gastrointestinal diseases in vivo[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Sucrose octasulfate-aluminum complex. CAS No. 54182-58-0. Pack Sizes: 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-B0644. | |
| Sucralose (Standard) | Sucralose (Standard) is the analytical standard of Sucralose. This product is intended for research and analytical applications. Sucralose?(E955; Trichlorosucrose) is a?non-nutritive?artificial?sweetener and sugar substitute. Sucralose can activate a conserved neural fasting response and thereby exerts an appetite-stimulating effect in rodents[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: E955 (Standard); Trichlorosucrose (Standard). CAS No. 56038-13-2. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-N0614R. | |
| Sucrose | Sucrose (D-(+)-Saccharose) is a disaccharide which is composed of two monosaccharides, glucose and fructose. Sucrose can be applied in some animal models, including metabolic disease, obesity, diet on preference, and diabetes, et al[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: D-(+)-Saccharose. CAS No. 57-50-1. Pack Sizes: 5 g. Product ID: HY-B1779. | |
| Sucrose-13C6-1 | Sucrose-13C6-1 is 13C labeled Sucrose. Sucrose (D-(+)-Saccharose) is a disaccharide which is composed of two monosaccharides, glucose and fructose. Sucrose can be applied in some animal models, including metabolic disease, obesity, diet on preference, and diabetes, et al[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: D-(+)-Saccharose-13C6-1. CAS No. 1356354-37-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-W768340. | |
| Sucrose octasulfate sodium | Sucrose octasulfate sodium, a derivative of sulfated oligosaccharides, is a matrix metalloproteinase (MMP) inhibitor. Sucrose octasulfate sodium stimulates the release of somatostatin-like immunoreactivity (SLI) from the stomach by acting directly on D cells in the gastric mucosa. Sucrose octasulfate sodium exerts its ulcer-healing effect by releasing endogenous gastric somatostatin. Sucrose octasulfate sodium can be used as a pharmaceutical excipient and significantly improves wound closure in diabetic foot ulcers caused by nerve ischemia and venous leg ulcers. Sucrose octasulfate sodium can be used in the study of chronic wound healing[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 74135-10-7. Pack Sizes: 10 mM * 1 mL in Water; 100 mg; 500 mg; 1 g. Product ID: HY-137273. | |
| Sucrose (Standard) | Sucrose (Standard) is the analytical standard of Sucrose. This product is intended for research and analytical applications. Sucrose (D-(+)-Saccharose) is a disaccharide which is composed of two monosaccharides, glucose and fructose. Sucrose?can be applied in some animal models, including metabolic disease, obesity,?diet on preference,?and diabetes, et al[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: D-(+)-Saccharose (Standard). CAS No. 57-50-1. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-B1779R. | |
| Sudan Black B | Sudan Black B, a fat-soluble diazo dye, is a histochemical stain. Sudan Black B can be used for staining of neutral triglycerides and lipids[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 4197-25-5. Pack Sizes: 5 g. Product ID: HY-D0213. | |
| Sudan IV | Sudan IV is an agonist of the aryl hydrocarbon receptor (AhR) that activates downstream signaling pathways and induces CYP1A1 expression. Sudan IV promotes CYP1A1 gene transcription by activating AhR-ARNT heterodimers and binding to exogenous response elements (XREs) on DNA, thereby enhancing drug metabolizing enzyme activity. Sudan IV can be used to study the toxicity mechanisms of industrial dyes and the effects of interactions with serum proteins (such as bovine serum albumin (BSA)) on their distribution in vivo. Sudan IV is a fat-soluble diazo dye that can be used to stain lipids, triglycerides, and lipoproteins on frozen sections[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Solvent Red 24; C.I. 26105. CAS No. 85-83-6. Pack Sizes: 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-D0932. | |
| Sugammadex sodium | Sugammadex sodium is a synthetic γ-cyclodextrin derivative, and acts as a reversal agent for neuromuscular block. Sugammadex sodium shows nephroprotective effect in ischemia-reperfusion injury[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Org25969. CAS No. 343306-79-6. Pack Sizes: 10 mM * 1 mL in Water; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-B0079. | |
| Sugiol | Sugiol is an abietane diterpenoid, can be isolated from Calocedrus formosana bark. Sugiol has anti-inflammatory activity, could effectively reduce intracellular reactive oxygen species (ROS) production in lipopolysaccharide (LPS)-stimulated macrophages[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (+)-Sugiol; 10-Deoxoxanthoperol. CAS No. 511-05-7. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N1195. | |
| Sulanemadlin | Sulanemadlin (ALRN-6924) is a potent and cell-permeating p53-based peptidomimetic macrocycles. Sulanemadlin is a inhibitor of the p53-MDM2, p53-MDMX, or both p53 and MDM2 and MDMX protein-protein interactions. Sulanemadlin can be used for cancers research[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: ALRN-6924; MP-4897. CAS No. 1451199-98-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P4210. | |
| Sulbactam | Sulbactam (CP45899) is a competitive, irreversible beta-lactamase inhibitor. Sulbactam shows antimicrobial activity against multidrug-resistant (MDR) acinetobacter calcoaceticus--Acinetobacter baumannii (Acb) complex[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CP45899. CAS No. 68373-14-8. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg. Product ID: HY-B0334. | |
| Sulbactam sodium | Sulbactam (CP45899) sodium is a competitive, irreversible beta-lactamase inhibitor. Sulbactam sodium shows antimicrobial activity against multidrug-resistant (MDR) acinetobacter calcoaceticus--Acinetobacter baumannii (Acb) complex[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CP45899 sodium. CAS No. 69388-84-7. Pack Sizes: 100 mg. Product ID: HY-B0334A. | |
| Sulbactam sodium (Standard) | Sulbactam (sodium) (Standard) is the analytical standard of Sulbactam (sodium). This product is intended for research and analytical applications. Sulbactam (CP45899) sodium is a competitive, irreversible beta-lactamase inhibitor. Sulbactam sodium shows antimicrobial activity against multidrug-resistant (MDR) acinetobacter calcoaceticus--Acinetobacter baumannii (Acb) complex[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CP45899 sodium (Standard). CAS No. 69388-84-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0334AR. | |
| Sulbactam (Standard) | Sulbactam (Standard) is the analytical standard of Sulbactam. This product is intended for research and analytical applications. Sulbactam (CP45899) is a competitive, irreversible beta-lactamase inhibitor. Sulbactam shows antimicrobial activity against multidrug-resistant (MDR) acinetobacter calcoaceticus--Acinetobacter baumannii (Acb) complex[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CP45899 (Standard). CAS No. 68373-14-8. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0334R. | |
| Sulbutiamine | Sulbutiamine is a synthetic analogue of vitamin B1 used for the treatment of asthenia. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Bisibuthiamine. CAS No. 3286-46-2. Pack Sizes: 10 mM * 1 mL in DMSO; 500 mg; 1 g; 5 g; 10 g; 25 g. Product ID: HY-B2229. | |
| Sulconazole mononitrate | Sulconazole mononitrate ((±)-Sulconazole mononitrate), an imidazole derivative, is a broad-spectrum fungicide. Sulconazole mononitrate can be used for the research of dermatomycoses, pityriasis versicolor, and cutaneous candidiasis[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (±)-Sulconazole mononitrate. CAS No. 61318-91-0. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg. Product ID: HY-B1460. | |
| Sulfadiazine | Sulfadiazine is a sulfonamide antibiotic with antimalarial activity. Sulfadiazine can be used for toxoplasmosis research[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 68-35-9. Pack Sizes: 10 mM * 1 mL in DMSO; 500 mg; 1 g; 5 g; 10 g. Product ID: HY-B0273. | |
| Sulfadiazine sodium | Sulfadiazine sodium is a sulfonamide antibiotic with antimalarial activity. Sulfadiazine can be used for toxoplasmosis research[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 547-32-0. Pack Sizes: 10 mM * 1 mL in DMSO; 500 mg; 1 g; 5 g; 10 g. Product ID: HY-B0273A. | |
| Sulfadoxine | Sulfadoxine(Sulphadoxine) is a long acting sulfonamide that is used, usually in combination with other agents, for respiratory, urinary tract and malarial infections. Sulfadoxine inhibits HIV replication in peripheral blood mononuclear cells. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Sulphadoxine. CAS No. 2447-57-6. Pack Sizes: 10 mM * 1 mL in DMSO; 500 mg; 5 g; 10 g. Product ID: HY-B0439. | |
| Sulfamethoxazole | Sulfamethoxazole (Ro 4-2130) is a sulfonamide antibiotic with a widespread antibacterial activity. Sulfamethoxazole inhibits bacterial folate metabolism by competing with 4-Aminobenzoic acid (HY-B1008) (PABA) to act on dihydropteroate synthetase and dihydropteroate reductase. Sulfamethoxazole can be used for the study of urinary tract infections (UTIs), prostatitis, and bronchitis[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Ro 4-2130. CAS No. 723-46-6. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 500 mg; 1 g; 5 g; 10 g; 25 g. Product ID: HY-B0322. | |
| Sulfamethoxazole-13C6 | Sulfamethoxazole-13C6 (Ro 4-2130-13C6) is a 13C labeled Sulfamethoxazole (HY-B0322). Sulfamethoxazole (Ro 4-2130) is a sulfonamide antibiotic with a widespread antibacterial activity. Sulfamethoxazole inhibits bacterial folate metabolism by competing with 4-Aminobenzoic acid (HY-B1008) (PABA) to act on dihydropteroate synthetase and dihydropteroate reductase. Sulfamethoxazole can be used for the study of urinary tract infections (UTIs), prostatitis, and bronchitis[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Ro 4-2130-13C6. CAS No. 1196157-90-0. Pack Sizes: 1 mg; 5 mg. Product ID: HY-B0322S1. | |
| Sulfamethoxazole-d4 | Sulfamethoxazole-d4 (Ro 4-2130-d4) is a deuterium labeled Sulfamethoxazole (HY-B0322). Sulfamethoxazole (Ro 4-2130) is a sulfonamide antibiotic with a widespread antibacterial activity. Sulfamethoxazole inhibits bacterial folate metabolism by competing with 4-Aminobenzoic acid (HY-B1008) (PABA) to act on dihydropteroate synthetase and dihydropteroate reductase. Sulfamethoxazole can be used for the study of urinary tract infections (UTIs), prostatitis, and bronchitis[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Ro 4-2130-d4. CAS No. 1020719-86-1. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg. Product ID: HY-B0322S. | |
| Sulfamethoxazole sodium | Sulfamethoxazole (Ro 4-2130) sodium is a sulfonamide antibiotic with a widespread antibacterial activity. Sulfamethoxazole sodium inhibits bacterial folate metabolism by competing with 4-Aminobenzoic acid (HY-B1008) (PABA) to act on dihydropteroate synthetase and dihydropteroate reductase. Sulfamethoxazole sodium can be used for the study of urinary tract infections (UTIs), prostatitis, and bronchitis[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Ro 4-2130 sodium. CAS No. 4563-84-2. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 500 mg; 1 g; 5 g; 10 g; 25 g. Product ID: HY-B0322A. | |
| Sulfamethoxazole (Standard) | Sulfamethoxazole (Standard) (Ro 4-2130 (Standard)) is the analytical standard of Sulfamethoxazole (HY-B0322). This product is intended for research and analytical applications. Sulfamethoxazole (Ro 4-2130) is a sulfonamide antibiotic with a widespread antibacterial activity. Sulfamethoxazole inhibits bacterial folate metabolism by competing with 4-Aminobenzoic acid (HY-B1008) (PABA) to act on dihydropteroate synthetase and dihydropteroate reductase. Sulfamethoxazole can be used for the study of urinary tract infections (UTIs), prostatitis, and bronchitis. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Ro 4-2130 (Standard). CAS No. 723-46-6. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-B0322R. | |
| Sulfane sulfur probe 4 | Sulfane sulfur probe 4 (SSP4) is a fluorescent probe used to detect sulfane sulfur species (Ex/Em=494/515 nm). Sulfane sulfur probe 4 exhibits high sensitivity in detecting sulfane sulfur, even in the presence of other substances such as homocysteine, methionine, cysteine, glutathione, N-acetyl-L-cysteine, glycine, tyrosine, tryptophan, arginine, and metal ions (Fe2+, Fe3+, Mg2+, Ca2+, and Zn2+)[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: SSP4. CAS No. 1810731-98-6. Pack Sizes: 1 mg. Product ID: HY-158779. | |
| Sulfaphenazole | Sulfaphenazole is a selective inhibitor of human cytochrome P450 (CYP) 2C9 enzyme. Sulfaphenazole is a cytoprotective agent against light-induced death of photoreceptors. Sulfaphenazole inhibits light-induced necrosis and mitochondrial stress-initiated apoptosis. Sulfaphenazole is an off patent sulfonamide antibiotic and demonstrates bactericidal activity through enhanced M1 macrophage activity. Sulfaphenazole can significantly reduce infarct size and restore post-ischemic coronary flow following ischemia and reperfusion[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 526-08-9. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg. Product ID: HY-B1218. | |
| Sulfaphenazole (Standard) | Sulfaphenazole (Standard) is the analytical standard of Sulfaphenazole. This product is intended for research and analytical applications. Sulfaphenazole is a selective inhibitor of human cytochrome P450 (CYP) 2C9 enzyme. Sulfaphenazole is a cytoprotective agent against light-induced death of photoreceptors. Sulfaphenazole inhibits light-induced necrosis and mitochondrial stress-initiated apoptosis. Sulfaphenazole is an off patent sulfonamide antibiotic and demonstrates bactericidal activity through enhanced M1 macrophage activity. Sulfaphenazole can significantly reduce infarct size and restore post-ischemic coronary flow following ischemia and reperfusion[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 526-08-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B1218R. | |
| Sulfasalazine | Sulfasalazine (NSC 667219) is an anti-rheumatic agent for the research of rheumatoid arthritis and ulcerative colitis. Sulfasalazine can suppress NF-κB activity. Sulfasalazine is a type 1 ferroptosis inducer[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: NSC 667219. CAS No. 599-79-1. Pack Sizes: 10 mM * 1 mL in DMSO; 500 mg; 1 g; 5 g; 10 g. Product ID: HY-14655. | |
| Sulfasalazine-d4 | Sulfasalazine-d4 is the deuterium labeled Sulfasalazine. Sulfasalazine (NSC 667219) is an anti-rheumatic agent for the research of rheumatoid arthritis and ulcerative colitis. Sulfasalazine can suppress NF-κB activity. Sulfasalazine is a type 1 ferroptosis inducer[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1346606-50-5. Pack Sizes: 1 mg. Product ID: HY-14655S. | |
| Sulfatase, Helix pomatia | Sulfatase, Helix pomatia is an enzyme that catalyzes the hydrolysis of sulfate esters. Sulfatase, Helix pomatia participates in the metabolism of various substances[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 9068-67-1. Pack Sizes: 5 KU. Product ID: HY-P2972. | |
| Sulfatinib | Sulfatinib (Surufatinib) is a potent and highly selective tyrosine kinase inhibitor against VEGFR1/2/3, FGFR1 and CSF1R with IC50s of in a range of 1 to 24 nM. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Surufatinib; HMPL-012. CAS No. 1308672-74-3. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-12297. | |
| Sulfidefluor 7-AM | Sulfidefluor 7-AM is a stable hydrogen sulphide (H2S) fluorescent probe[1]. Sulfidefluor 7-AM is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. Uses: Scientific research. Category: Signaling pathways. Alternative Names: SF7-AM. CAS No. 1416872-50-8. Pack Sizes: 1 mg. Product ID: HY-110128. | |
| Sulfinpyrazone | Sulfinpyrazone (G-28315) is an orally active and potent uricosuric agent for chronic and intermittent gouty arthritis. Sulfinpyrazone has antithrombotic and platelet inhibitory effects[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: G-28315. CAS No. 57-96-5. Pack Sizes: 10 mM * 1 mL in DMSO; 500 mg; 1 g. Product ID: HY-B1271. | |
| Sulfisoxazole | Sulfisoxazole (Sulfafurazole) is an orally active endothelin receptor antagonist with IC50 values of 0.60 μM and 22 μM against endothelin receptor A and endothelin receptor B, respectively. Sulfisoxazole is a sulfonamide antibacterial agent with an oxazole substituent. Sulfisoxazole inhibits breast cancer exosome release by targeting endothelin receptor A[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Sulfafurazole. CAS No. 127-69-5. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 500 mg. Product ID: HY-B0323. | |
| Sulfo-ara-F-NMN | Sulfo-ara-F-NMN (CZ-48) is a mimetic of nicotinamide mononucleotide (NMN). Sulfo-ara-F-NMN acts selectively, activating SARM1 but inhibiting CD38 (IC50 around 10 μM). Sulfo-ara-F-NMN induces intracellular cyclic ADP-ribose (cADPR) production[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CZ-48. CAS No. 1374663-29-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-129522. | |
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