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| Product | Description | |
|---|---|---|
| Selenium XRF Standard - 0.47 wt% | certified reference material. Group: Certified reference materials (crms). |  |
| Selenium Yeast 0.2% Powder | Selenium Yeast 0.2% Powder . |  CA, FL & NJ |
| Selenocyanatoacetic acid | Selenocyanatoacetic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: SELENOCYANATOACETIC ACID. Product Category: Heterocyclic Organic Compound. CAS No. 19188-17-1. Molecular formula: C3H3NO2Se. Mole weight: 164.02. Product ID: ACM19188171. Alfa Chemistry ISO 9001:2015 Certified. |  |
| selenocysteine lyase | A pyridoxal-phosphate protein. Dithiothreitol or 2-mercaptoethanol can act as the reducing agent in the reaction. The enzyme from animals does not act on cysteine, serine or chloroalanine, while the enzyme from bacteria shows activity with cysteine (cf. EC 2.8.1.7, cysteine desulfurase). Group: Enzymes. Synonyms: selenocysteine reductase; selenocysteine β-lyase. Enzyme Commission Number: EC 4.4.1.16. CAS No. 82047-76-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5318; selenocysteine lyase; EC 4.4.1.16; 82047-76-5; selenocysteine reductase; selenocysteine β-lyase. Cat No: EXWM-5318. |  |
| selenocysteine Se-methyltransferase | The enzyme uses S-adenosyl-L-methionine as methyl donor less actively than S-methyl-L-methionine. The enzyme from broccoli (Brassica oleracea var. italica) also has the activity of EC 2.1.1.10, homocysteine S-methyltransferase. Group: Enzymes. Synonyms: SMT. Enzyme Commission Number: EC 2.1.1.280. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1887; selenocysteine Se-methyltransferase; EC 2.1.1.280; SMT. Cat No: EXWM-1887. | |
| Selenocystine | Selenocystine is a broad-spectrum anti-cancer agent. Selenocystine induces DNA damage in HepG2 cells, particularly in the form of DNA double strand breaks (DSBs). Selenocystine exhibits great promise as a therapeutic or adjuvant agent targeting DNA repair for cancer treatment [1]. Uses: Scientific research. Group: Peptides. CAS No. 2897-21-4. Pack Sizes: 10 mg; 25 mg. Product ID: HY-113064. |  |
| Seleno-D,L-ethionine | Used as a substrate for methionine adenosyltransferase from rat liver. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 50mg. US Biological Life Sciences. |  Worldwide |
| Seleno-DL-ethionine | Seleno-DL-ethionine. CAS No: 2578-27-0 |  Sarchem Laboratories New Jersey NJ |
| Seleno-L-cysteine | Seleno-L-cysteine is an amino acid used as a nutritional supplement, dietary supplement, health food additive, sport nutrition, sport supplement, bodybuilding supplement, pharmaceutical raw material and a building block of selenoproteins. Uses: Nutritional supplement; dietary supplements; health food additives; sport nutrition; sport supplements; bodybuilding supplement; pharmaceutical raw material; as a building block of selenoproteins. Synonyms: Seleno-L-cysteine; 3-Selenyll-alanine. Grade: ≥ 97.0 %. CAS No. 10236-58-5. Molecular formula: C3H7NO2Se. Mole weight: 168.05. |  |
| Seleno-L-methionine | Seleno-L-methionine. CAS No: 3211-76-5 | Sarchem Laboratories New Jersey NJ |
| Seleno-L-methionine | ?98% (TLC), powder. Group: Fluorescence/luminescence spectroscopy. | |
| Seleno L Methionine 5,000 MCG/G | Seleno L Methionine 5,000 MCG/G. | CA, FL & NJ |
| Selenomethionine | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Selenomethionine | Selenomethionine is a naturally occurring amino acid containing selenium that has oral activity and is a common natural food source. Selenomethionine has antitumor activity [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Seleno-DL-methionine; DL-Selenomethionine. CAS No. 1464-42-2. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 500 mg. Product ID: HY-B1000. | |
| Selenomethionine | Selenomethionine is used in the anticancer/antitumor drug combinations in an effort to minimize tumor sizes and improve survivability of breast cancer patients. Also used in the treatment of autoimmune thyroiditis, acting through eurothyroidism it reduces thyroid stimulating hormone levels (TSH). Group: Biochemicals. Grades: Highly Purified. CAS No. 1464-42-2. Pack Sizes: 25mg, 100mg. Molecular Formula: C5H11NO2Se. US Biological Life Sciences. | Worldwide |
| Selenomethionine USP | Selenomethionine USP. CAS No. 3211-76-5. Molecular formula: C5H11NO2Se. |  |
| Selenophene | 1g Pack Size. Group: Building Blocks, Research Organics & Inorganics. Formula: C4H4Se. CAS No. 288-05-1. Prepack ID 76723073-1g. Molecular Weight 131.03. See USA prepack pricing. |  |
| Selenophene-2-boronic acid | Selenophene-2-boronic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: RARECHEM AH PB 0118;selenophen-2-ylboronic acid;SELENOPHENE-2-BORONIC ACID. Product Category: Boronic Acids. CAS No. 35133-86-9. Molecular formula: C4H5BO2Se. Mole weight: 174.85. Purity: 0.98. Density: g/cm³. Product ID: ACM35133869. Alfa Chemistry ISO 9001:2015 Certified. | |
| Selenosulfuric Acid Dipotassium Salt | Selenosulfuric Acid Dipotassium Salt is used in the synthesis of CdSe photocatalysts with enhanced photocatalytic ativitys. Possible application towards industrial wastewater treatment and pollutant removal. Group: Biochemicals. Alternative Names: Dipotassium Selenosulfate; potassium selenosulfate; potassium selenosulfate (K2SeSO3). Grades: Purified. CAS No. 15571-89-8. Pack Sizes: 50mg. Molecular Formula: K2O3SSe, Molecular Weight: 237.22. US Biological Life Sciences. | Worldwide |
| Selenous Acid | SELENOUS ACID, 65% SOLUTION, 99% pure, 39.8% Se, Formula: H2SeO3. CAS No. 7783-00-8. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| Selenous Acid | SELENOUS ACID, 99% pure, -4 mesh, Formula: H2SeO3. CAS No. 7783-00-8. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
| Selenous (Selenous) Acid | Selenous (Selenous) Acid. Group: Biochemicals. Alternative Names: Selenious Acid; Selenium dioxide, hydrated. Grades: Molecular Biology Grade. CAS No. 7783-00-8. Pack Sizes: 25g. Molecular Formula: H2SeO3, Molecular Weight: 128.97. US Biological Life Sciences. | Worldwide |
| Selepag impurity 5 | Selepag impurity 5. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1693685-49-2. Molecular formula: C7H16ClN. Mole weight: 149.66. Catalog: APB1693685492. | |
| Selepressin | Selepressin (FE 202158) is a selective vasopressin V 1A receptor agonist. Selepressin is a potent vasopressor. Selepressin can be used in the research of septic shock [1] [2] [4]. Uses: Scientific research. Group: Peptides. Alternative Names: FE 202158. CAS No. 876296-47-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-105239. | |
| Selepressin | Selepressinis is an agonist of the vasopressin 1A receptor and can be used to treat vasodilatory hypotension in septic shock. Synonyms: Cbz-Phe-Ala-CH2F; Z-FA-fluoromethyl ketone; Zfa-fmk; Z-Phe-Ala-fluoromethyl ketone; benzyloxycarbonyl-Phe-Ala-fluormethylketone; Cathepsin B inhibitor. Grade: ≥95%. CAS No. 876296-47-8. Molecular formula: C21H23FN2O4. Mole weight: 386.42. | |
| Seletracetam | Seletracetam (Ucb 44212), as an analog of the antiepileptic agent Levetiracetam, is a SV2A modulator for the research of epilepsy [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ucb 44212. CAS No. 357336-74-4. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-119810. | |
| Selexipag | Selexipag (NS-304) is an orally available and potent agonist for the Prostacyclin ( PGI 2 ) receptor (IP receptor). Uses: Scientific research. Group: Signaling pathways. Alternative Names: NS-304; ACT-293987. CAS No. 475086-01-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14870. | |
| Selfotel | Selfotel (CGS 19755) is a selective and competitive antagonist at N-methyl-D-aspartate (NMDA) -preferring receptor. CGS 19755 inhibits the binding of [3H]-3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid to NMDA-type receptors with an IC 50 of 50 nM [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CGS 19755. CAS No. 110347-85-8. Pack Sizes: 5 mg; 10 mg. Product ID: HY-15086. | |
| Selgantolimod | Selgantolimod (GS-9688) is an orally active, potent and selective toll-like receptor 8 (TLR8) agonist for the treatment of hepatitis B virus (HBV) and human immunodeficiency virus (HIV) infection[1][2][3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GS-9688. CAS No. 2004677-13-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-109137. | |
| Selicrelumab | Selicrelumab is an agonist CD40 antibody, induces changes in the tumor microenvironment. Selicrelumab can be used for the research of pancreatic cance and neoadjuvant study [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 1622140-49-1. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P99046. | |
| Seliforant | Seliforant (SENS-111) is a selective and orally histamine H4 receptor antagonist. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SENS-111. CAS No. 1164115-89-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109074. | |
| Selinexor | Selinexor (KPT-330), analog of KPT-185, is an orally bioavailable and selective CRM1 inhibitor [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: KPT-330. CAS No. 1393477-72-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-17536. | |
| Selinexor | Selinexor Inhibitor. Uses: Scientific use. Product Category: T6106. CAS No. 1393477-72-9. |  |
| Selinidin | Selinidin is a natural compound found in several plants. Synonyms: (Z)-2-Methyl-2-butenoic acid [(S)-9,10-dihydro-8,8-dimethyl-2-oxo-2H,8H-benzo[1,2-b:3,4-b']dipyran-9-yl] ester; Jatamansin; Secryptotaenin A. Grade: >97%. CAS No. 19427-82-8. Molecular formula: C19H20O5. Mole weight: 328.36. | |
| Selisistat | Selisistat (EX-527) is a potent and selective SirT1 (Sir2 in Drosophila melanogaster) inhibitor with an IC 50 of 123 nM for SirT1. Selisistat alleviates pathology in multiple animal and cell models of Huntington's disease [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EX-527. CAS No. 49843-98-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15452. | |
| Selitrectinib | Selitrectinib (LOXO-195) is a next-generation TRK kinase inhibitor, with IC 50 s of 0.6 nM and <2.5 nM for TRKA and TRKC , respectively [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LOXO-195. CAS No. 2097002-61-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101977. | |
| Seliwanoff Reagent, Laboratory Grade, 100 mL | Storage Code: White; corrosive. Grades: chem-grade laboratory. Product ID: 887365. -- SOLD FOR EDUCATIONAL USE ONLY -- |  |
| Selnoflast | Selnoflast (RO7486967), formerly somalix/RG6418/IZD334, is an orally active, potent, selective and reversible small molecule NLRP3 inflammasome inhibitor. Selnoflast is a potent inhibitor of IL-1? release stimulated by NLRP3 activation in human Alzheimer's disease (AD) monocyte-derived macrophages. Selnoflast is promising for research of AD and systemic inflammatory diseases, such as ulcerative colitis and chronic obstructive pulmonary disease[1][2][3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Somalix; RO-7486967; IZD334. CAS No. 2260969-36-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-132831. | |
| Selonsertib | Selonsertib (GS-4997), an orally bioavailable, selective apoptosis signal-regulating kinase 1 ( ASK1 ) inhibitor with a pIC 50 of 8.3, has been evaluated as an experimental treatment for diabetic nephropathy and kidney fibrosis. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GS-4997. CAS No. 1448428-04-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-18938. | |
| Selpercatinib | Selpercatinib (LOXO-292) is a potent, selective RET kinase inhibitor with IC 50 values of 14.0 nM, 24.1 nM, and 530.7 nM for RET (WT), RET (V804M), and RET (G810R), respectively. Selpercatinib has anticancer activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LOXO-292. CAS No. 2152628-33-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-114370. | |
| SelSA | SelSA is a selective, orally active inhibitor for histone deacetylase 6 ( HDAC6 ) with IC 50 of 56.9 nM. SelSA inhibits the phosphorylation of ERK1/2. SelSA inhibits the proliferation of breast cancer cells and hepatocellular carcinoma cells with IC 50 of 0.58-2.6 μM, inhibits cell migration and invasion of Huh7, and induces apoptosis. SelSA exhibits antitumor activity in mouse model [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1225038-92-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-162616. | |
| Seltorexant | Seltorexant (JNJ-42847922) is an orally active, high-affinity, and selective orexin-2 receptor (OX2R) antagonist ( pK i values of 8.0 and 8.1 for human and rat OX2R). Seltorexant (JNJ-42847922) crosses the blood-brain barrier and quickly occupies OX2R binding sites in the rat brain [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: JNJ-42847922. CAS No. 1293281-49-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109012. | |
| Seltorexant hydrochloride | Seltorexant hydrochloride (JNJ-42847922 hydrochloride) is an orally active, high-affinity, and selective OX2R antagonist ( pK i values of 8.0 and 8.1 for human and rat OX2R). Seltorexant hydrochloride crosses the blood-brain barrier and quickly occupies OX2R binding sites in the rat brain [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: JNJ-42847922 hydrochloride. CAS No. 1293284-49-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109012A. | |
| Selumetinib | Selumetinib. Group: Biochemicals. Alternative Names: 5-[(4-Bromo-2-chlorophenyl)amino]-4-fluoro-N-(2-hydroxyethoxy)-1-methyl-1H-benzimidazole-6-carboxamide; ARRY 142886; AZD 6244. Grades: Highly Purified. CAS No. 606143-52-6. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C17H15BrClFN4O3. US Biological Life Sciences. | Worldwide |
| Selumetinib | Selumetinib (AZD6244) is selective, non-ATP-competitive oral MEK1/2 inhibitor, with an IC 50 of 14 nM for MEK1. Selumetinib (AZD6244) inhibits ERK1/2 phosphorylation. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AZD6244; ARRY-142886. CAS No. 606143-52-6. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 200 mg; 500 mg; 1 g. Product ID: HY-50706. | |
| Selumetinib sulfate | Selumetinib (AZD6244) is selective, non-ATP-competitive oral MEK1/2 inhibitor, with an IC 50 of 14 nM for MEK1. Selumetinib (AZD6244) inhibits ERK1/2 phosphorylation. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AZD6244 sulfate; ARRY-142886 sulfate. CAS No. 943332-08-9. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 200 mg; 500 mg; 1 g. Product ID: HY-50706A. | |
| Selurampanel | Selurampanel (BGG 492) is an orally active and competitive AMPA receptor antagonist with an IC 50 of 190 nM. Selurampanel has reasonable blood-brain barrier penetration. Selurampanel can be used for epilepsy research [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BGG 492. CAS No. 912574-69-7. Pack Sizes: 1 mg; 5 mg. Product ID: HY-105860. | |
| Selvigaltin | Selvigaltin (GB1211) is an orally active galectin-3 small molecule inhibitor with an IC 50 value of 12 nM in rabbits, showing anti-tumor activity. Selvigaltin decreases galectin-3 levels in the liver and reduces biomarkers of liver function (AST, ALT, bilirubin), inflammation (cells foci) and fibrosis (PSR, SHG), as well as decreasing the mRNA and protein expression of several key inflammation and fibrosis biomarkers (IL6, TGFβ3, SNAI2, collagen). Selvigaltin restores T-cell activity and induces less tumors and metastasis [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GB1211. CAS No. 1978336-95-6. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-147041. | |
| SEMA4D/CD100 human | recombinant, expressed in HEK 293 cells, ?95% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| Semagacestat | Semagacestat is a γ-secretase inhibitor, inhibits β-amyloid ( Aβ42 ), Aβ38 and Aβ40 with IC 50 s of 10.9, 12 and 12.1 nM, respectively; also inhibits Notch signaling with IC 50 of 14.1 nM. Semagacestat can be used for the research of alzheimer's disease [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY450139. CAS No. 425386-60-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-10009. | |
| Semagacestat | Semagacestat is an inhibitor of the γ-secretase enzyme. γ-Secretase enzyme is pivotal in the generation of β-amyloid (A β), a neurotoxic endogenous peptide believed to be involved in the pathogenesis of Alzheimer's disease (AD). Group: Biochemicals. Alternative Names: (2S) -2-Hydroxy-3-methyl-N- [ (1S) -1-methyl-2-oxo-2- [ [ (1S) -2, 3, 4, 5-tetrahydro-3-methyl-2-oxo-1H-3-benzazepin-1-yl] amino] ethyl] butanamide; LY 450139. Grades: Highly Purified. CAS No. 425386-60-3. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Semaglutide | Semaglutide. Categories: semaglutide; ozempic. | CA, FL & NJ |
| Semaglutide | Semaglutide, a long-acting GLP-1 analogue, is a glucagon-like peptide-1 (GLP-1) receptor agonist. Semaglutide has the potential for type 2 diabetes treatment. Uses: Scientific research. Group: Peptides. CAS No. 910463-68-2. Pack Sizes: 500 μg; 1 mg; 5 mg; 10 mg. Product ID: HY-114118. | |
| Semaglutide | Semaglutide Inhibitor. Uses: Scientific use. Product Category: T19850. CAS No. 910463-68-2. | |
| Semaglutide acetate | Semaglutide acetate, a long-acting GLP-1 analogue, is a glucagon-like peptide-1 (GLP-1) receptor agonist. Semaglutide acetate has the potential for type 2 diabetes treatment. Uses: Scientific research. Group: Peptides. CAS No. 1997361-85-9. Pack Sizes: 500 μg; 1 mg; 5 mg; 10 mg. Product ID: HY-114118B. | |
| Semaglutide, FITC labeled | Semaglutide, FITC labeled is a long-acting, selective, competitive GLP-1R agonist that can penetrate the blood-brain barrier. After activating GLP-1R, Semaglutide, FITC labeled promotes insulin secretion, inhibits gastric emptying and appetite, and at the same time enhances autophagy, inhibits oxidative stress and apoptosis. Semaglutide, FITC labeled also regulates mitochondrial function and lipid metabolism (such as reducing de novo lipogenesis in the liver). Semaglutide, FITC labeled has activities such as lowering blood sugar, reducing weight, neuroprotection (such as improving motor function in Parkinson's disease models, reducing ?-synuclein aggregation) and improving hepatic steatosis. Semaglutide, FITC labeled can be used for the study of neurodegenerative diseases and liver diseases such as type 2 diabetes, obesity, Parkinson's disease, metabolic associated fatty liver disease (MASLD), and cancer[1][2][3][4][5]. Uses: Scientific research. Group: Peptides. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-114118F. | |
| Semaglutide intermediate P29 | An intermediate of Semaglutide, an agonist of glucagon-like peptide-1 (GLP-1) receptor that is developed to treat type 2 diabetes. Synonyms: Semaglutide [sequence (9-37)]; L-α-Glutamylglycyl-L-threonyl-L-phenylalanyl-L-threonyl-L-seryl-L-α-aspartyl-L-valyl-L-seryl-L-seryl-L-tyrosyl-L-leucyl-L-α-glutamylglycyl-L-glutaminyl-L-alanyl-L-alanyl-L-lysyl-L-α-glutamyl-L-phenylalanyl-L-isoleucyl-L-alanyl-L-tryptophyl-L-leucyl-L-valyl-L-arginylglycyl-L-arginylglycine; H-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Gly-Gln-Ala-Ala-Lys-Glu-Phe-Ile-Ala-Trp-Leu-Val-Arg-Gly-Arg-Gly-OH. Grade: ≥95%. CAS No. 1169630-82-3. Molecular formula: C142H216N38O45. Mole weight: 3175.47. | |
| Semaglutide sodium salt | Semaglutide is an agonist of glucagon-like peptide-1 (GLP-1) receptor that is developed to treat type 2 diabetes. It reduces blood sugar via increasing the production of insulin. On Oct 18, 2017, Novo Nordisk received positive 16-0 vote from FDA Advisory Committee in favor of approval for Semaglutide. Uses: Semaglutide, a glucagon-like peptide-1 (glp-1) receptor agonist, has shown promising applications in drug discovery due to its unique pharmacological properties. originally developed for the treatment of type 2 diabetes, semaglutide has recently gained attention for its potential in various therapeutic areas beyond diabetes management. this peptide-based drug has demonstrated efficacy in controlli. Synonyms: His-Aib-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Gly-Gln-Ala-Ala-Lys(PEG2-PEG2-γ-Glu-17-carboxyheptadecanoyl)-Glu-Phe-Ile-Ala-Trp-Leu-Val-Arg-Gly-Arg-Gly; L-Histidyl-2-methylalanyl-L-α-glutamylglycyl-L-threonyl-L-phenylalanyl-L-threonyl-L-seryl-L-α-aspartyl-L-valyl-L-seryl-L-seryl-L-tyrosyl-L-leucyl-L-α-glutamylglycyl-L-glutaminyl-L-alanyl-L-alanyl-N6-[N-(17-carboxy-1-oxoheptadecyl)-L-γ. Molecular formula: C187H291N45O59 (free base). Mole weight: 4113.64 (free base). | |
| Semaglutide TFA | Semaglutide TFA is a long-acting, selective, competitive GLP-1R agonist that can penetrate the blood-brain barrier. After activating GLP-1R, Semaglutide TFA promotes insulin secretion, inhibits gastric emptying and appetite, and at the same time enhances autophagy, inhibits oxidative stress and apoptosis. Semaglutide TFA also regulates mitochondrial function and lipid metabolism (such as reducing de novo lipogenesis in the liver). Semaglutide TFA has activities such as lowering blood sugar, reducing weight, neuroprotection (such as improving motor function in Parkinson's disease models, reducing ?-synuclein aggregation) and improving hepatic steatosis. Semaglutide TFA can be used for the study of neurodegenerative diseases and liver diseases such as type 2 diabetes, obesity, Parkinson's disease, metabolic associated fatty liver disease (MASLD), and cancer[1][2][3][4][5]. Uses: Scientific research. Group: Peptides. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-114118A. | |
| Sematilide hydrochloride | Sematilide, also known as CK-1752, is a class III antiarrhythmic. It is a selective delayed rectifier K+ current (IKr) channel blocker. It inhibits rapidly activating Ik in guinea pig atrial myocytes, resulting in the prolongation of action potential duration and refractoriness. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Sematilide hydrochloride; Sematilide HCl; Sematilide hydrochloride; Sematilide; CK-1752A; CK1752A; CK 1752A; CK-1752; CK1752; CK 1752. Product Category: Others. Appearance: Solid powder. CAS No. 101526-62-9. Molecular formula: C14H24ClN3O3S. Mole weight: 349.87. Purity: >98%. IUPACName: Benzamide, N-(2-(diethylamino)ethyl)-4-((methylsulfonyl)amino)-, monohydrochloride. Canonical SMILES: O=C(NCCN(CC)CC)C1=CC=C(NS(=O)(C)=O)C=C1.[H]Cl. Product ID: ACM101526629-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Sematilide monohydrochloride monohydrate | ?98% (HPLC), powder. Group: Fluorescence/luminescence spectroscopy. | |
| Semax | Semax is a peptide analog of adrenocorticotropic hormone (ACTH) (4-10). ACTH is a tropic hormone produced by the anterior pituitary. Uses: Enzyme inhibitors. Synonyms: H-Met-Glu-His-Phe-Pro-Gly-Pro-OH; L-Proline, L-methionyl-L-α-glutamyl-L-histidyl-L-phenylalanyl-L-prolylglycyl-; L-Methionyl-L-α-glutamyl-L-histidyl-L-phenylalanyl-L-prolylglycyl-L-proline; L-Proline, 1-[N-[1-[N-[N-(N-L-methionyl-L-α-glutamyl)-L-histidyl]-L-phenylalanyl]-L-prolyl]glycyl]-; ACTH (4-7), Pro-Gly-Pro-; Pro-gly-pro-ACTH (4-7). Grade: 98%. CAS No. 80714-61-0. Molecular formula: C37H51N9O10S. Mole weight: 813.92. | |
| Semax acetate | Semax acetate is a nootropic neuroprotective peptide. Semax acetate can be used in the research of brain stroke [1]. Uses: Scientific research. Group: Peptides. CAS No. 2828433-33-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P1146A. | |
| Semax acetate | Semax acetate is a synthetic adrenocorticotropic hormone (ACTH) (4-10) peptide analog with neuroprotective, analgesic, and anti-anxiety properties. Synonyms: L-Proline, L-methionyl-L-α-glutamyl-L-histidyl-L-phenylalanyl-L-prolylglycyl-, acetate (1:1); H-Met-Glu-His-Phe-Pro-Gly-Pro-OH acetate; L-Methionyl-L-α-glutamyl-L-histidyl-L-phenylalanyl-L-prolylglycyl-L-proline acetate; L-Proline, 1-[N-[1-[N-[N-(N-L-methionyl-L-α-glutamyl)-L-histidyl]-L-phenylalanyl]-L-prolyl]glycyl]-, acetate. Grade: ≥95%. CAS No. 2828433-33-4. Molecular formula: C39H55N9O12S. Mole weight: 873.98. | |
| Semaxinib | Semaxinib Inhibitor. Uses: Scientific use. Product Category: T2496. CAS No. 194413-58-6. | |
| Semaxinib | Semaxinib Inhibitor. Uses: Scientific use. Product Category: T2064. CAS No. 204005-46-9. | |
| Semaxinib | Semaxinib is a quinolone derivative with potential antineoplastic activity. Semaxinib reversibly inhibits ATP binding to the tyrosine kinase domain of vascular endothelial growth factor receptor 2 (VEGFR2), which may inhibit VEGF-stimulated endothelial cell migration and proliferation and reduce the tumor microvasculature. This agent also inhibits the phosphorylation of the stem cell factor receptor tyrosine kinase c-kit, often expressed in acute myelogenous leukemia cells. Uses: Angiogenesis inhibitors. Synonyms: SU5416; SU-5416; SU 5416; Sugen 5416; semoxind. Grade: 98%. CAS No. 204005-46-9. Molecular formula: C15H14N2O. Mole weight: 238.28. | |
| Semaxinib | Semaxinib (SU5416) is a potent and selective inhibitor of VEGFR (Flk-1/KDR) with an IC50 of 1.23 ?M[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SU5416. CAS No. 204005-46-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-10374. | |
| SEMBL | SEMBL is a potent NF-κB inhibitor. SEMBL can inhibit NF-κB-DNA binding, and also inhibits NF-κB-dependent inflammatory cytokine secretions. SEMBL inhibits cancer cell migration and invasion via decreasing MMP expression. SEMBL can be used for researching anticancer [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1443448-82-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-124651. | |
| Semduramicin | Semduramicin. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Semduramicin;Semduramycin;2H-Pyran-2-acetic acid, tetrahydro-2,4-dihydroxy-6-(1R)-1-(2S,5R,7S,8R,9S)-9-hydroxy-2,8-dimethyl-2-(2S,2R,3S,5R,5R)-octahydro-2-methyl-5-(2S,3S,5R,6S)-tetrahydro-6-hydroxy-3,5,6-trimethyl-2H-pyran-2-yl-3-(2S,5S,6R)-tetrahydro-5-methoxy-6-methyl-2H-pyran-;UK-61689. CAS No. 113378-31-7. Molecular formula: C45H76O16. Mole weight: 873.079. Purity: 0.95. IUPACName: Semduramicin. Density: 1.27g/cm³. Product ID: ACM113378317. Alfa Chemistry ISO 9001:2015 Certified. | |
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