A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
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| Product | Description | |
|---|---|---|
| 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 (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 | 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 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 Inhibitor. Uses: Scientific use. Product Category: T19850. CAS No. 910463-68-2. |  |
| Semaglutide | Semaglutide is used to manage type 2 diabetes along with lifestyle changes, such as dietary restrictions and increased physical activity. It also works by slowing the movement of food through the stomach and may decrease appetite and cause weight loss. Alternative Names: Semaglutide impurity;semaglutide. CAS No. 910463-68-2. Product ID: PIPB-0170. Molecular formula: C187H291N45O59. Mole weight: 4113.57754. EINECS: 203-405-2. SMILES: CC[C@H](C)[C@@H](C(=O)N[C@@H](C)C(=O)N[C@@H](CC1=CNC2=CC=CC=C21)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)NCC(=O)N[C@@H](CCCNC(=N)N)C(=O)NCC(=O)O)NC(=O)[C@H](CC3=CC=CC=C3)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCNC(=O)COCCOCCNC(=O)COCCOCCNC(=O)CC[C@H](C(=O)O)NC(=O)CCCCCCCCCCCCCCCCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(=O)N)NC(=O)CNC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC4=CC=C(C=C4)O)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CO)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CC5=CC=CC=C5)NC(=O)[C@H]([C@@H](C)O)NC(=O)CNC(=O)[C@H](CCC(=O)O)NC(=O)C(C)(C)NC(=O)[C@H](CC6=CN=CN6)N. Standard: US DMF/EDMF/CN CDE. Category: Peptide. |  |
| 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 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 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. | |
| 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. | |
| 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. | |
| Semaxinib | Semaxinib Inhibitor. Uses: Scientific use. Product Category: T2064. CAS No. 204005-46-9. | |
| Semaxinib | Semaxinib Inhibitor. Uses: Scientific use. Product Category: T2496. CAS No. 194413-58-6. | |
| 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. | |
| 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. | |
| Semen Cassiae Extract | Semen Cassiae Extract. Applications: Used for health care products, dietary supplements, good for eyesight. Group: Others. Synonyms: Semen Cassiae Extract; Cassia obtusifolia L. Purity: 5:1, 10?1 By TLC. Appearance: Brown fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Seed. Species: Cassia obtusifolia L. Semen Cassiae Extract; Cassia obtusifolia L.; plant extract. Pack: 20KG-25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-108. |  |
| semenogelase | A peptidase of family S1 (trypsin family) from seminal plasma. Slowly inhibited by α1-antichymotrypsin. Group: Enzymes. Synonyms: prostate-specific antigen; α-seminoprotein; seminin; P-30 antigen; antigen (human clone HPSA-1 prostate-specific protein moiety reduced); γ-seminoglycoprotein (human protein moiety reduced); γ-SM; antigen PSA (human prostate-specific); human glandular kallikrein; antigen PSA (human clone 5P1 protein moiety reduced). Enzyme Commission Number: EC 3.4.21.77. CAS No. 110157-83-0, 95829-41-7. 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-4169; semenogelase; EC 3.4.21.77; 110157-83-0, 95829-41-7; prostate-specific antigen; α-seminoprotein; seminin; P-30 antigen; antigen (human clone HPSA-1 prostate-specific protein moiety reduced); γ-seminoglycoprotein (human protein moiety reduced); γ-SM; antigen PSA (human prostate-specific); human glandular kallikrein; antigen PSA (human clone 5P1 protein moiety reduced). Cat No: EXWM-4169. | |
| Se-Methyl-L-Selenocysteine | Se-Methyl-L-Selenocysteine. Categories: se-methylselenocysteine; 26046-90-2. | CA, FL & NJ |
| Se-Methylselenocysteine | Se-Methylselenocysteine, a precursor of Methylselenol, has potent cancer chemopreventive activity and anti-oxidant activity. Se-Methylselenocysteine is orally bioavailable, and induces apoptosis [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Methylselenocysteine; Se-Methylseleno-L-cysteine. CAS No. 26046-90-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-114245. | |
| Se-(Methyl)selenocysteine (free base) | Se-(Methyl)selenocysteine (free base) |  Sarchem Laboratories New Jersey NJ |
| Se-(Methyl)selenocysteine hydrochloride | ?95% (TLC). Group: Fluorescence/luminescence spectroscopy. | |
| Se-methyl-seleno-L-cysteine | Se-methyl-seleno-L-cysteine. CAS No: 26046-90-2 | Sarchem Laboratories New Jersey NJ |
| Semialactone | Semialactone isolated from the barks of Rhus javanica L. Synonyms: (2S,3R,4S)-4-(2-{[(2E)-3-(3,4-Dihydroxyphenyl)-2-propenoyl]oxy}et hyl)-2-(β-D-glucopyranosyloxy)-3-vinyl-3,4-dihydro-2H-pyran-5-car boxylic acid. Grade: 95%. CAS No. 366450-46-6. Molecular formula: C30H44O4. Mole weight: 468.7. | |
| Semicarbazide | 6 wt. % (on silica gel). Group: Derivatization reagents hplc. | |
| Semicarbazide hydrochloride | 100g Pack Size. Group: Building Blocks, Organics. Formula: CH5N3O · HCl. CAS No. 563-41-7. Prepack ID 12845490-100g. Molecular Weight 111.53. See USA prepack pricing. |  |
| Semicarbazide hydrochloride | 500g Pack Size. Group: Building Blocks, Organics. Formula: CH5N3O · HCl. CAS No. 563-41-7. Prepack ID 12845490-500g. Molecular Weight 111.53. See USA prepack pricing. | |
| Semicarbazide hydrochloride | analytical standard. Group: Application areaspharma & vet compounds & metabolitesstandards for environmental regulatory methodspharma & vet compounds & metabolites. | |
| Semicarbazide hydrochloride | Semicarbazide hydrochloride is an orally active urea derivative. Semicarbazide hydrochloride binds to copper or iron in cells. Semicarbazide hydrochloride inhibits the activity of soluble semicarbazide sensitive amine oxidase ( SSAO ). Semicarbazide hydrochloride damages cartilage, blood vessels, ovaries, testicles, and thyroid follicles [1] [2] [3] [4] [5] [6] [7] [8] [9]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Aminourea hydrochloride; Hydrazinecarboxamide hydrochloride. CAS No. 563-41-7. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g. Product ID: HY-Y0470. | |
| Semicarbazide hydrochloride | Semicarbazide hydrochloride. Group: Biochemicals. Alternative Names: Hydrazinecarboxamide monohydrochloride; Aminourea hydrochloride. Grades: Highly Purified. CAS No. 563-41-7. Pack Sizes: 2g, 5g, 10g, 25g, 50g. Molecular Formula: CH6ClN3O. US Biological Life Sciences. | Worldwide |
| Semilicoisoflavone B | Semilicoisoflavone B. Group: Biochemicals. CAS No. 129280-33-7. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Semilicoisoflavone B | Semilicoisoflavone B is a compound of the flavonoid class found in the roots of Glycyrrhiza uralensis Fisch. Study shows that Semilicoisoflavone B inhibits sorbitol formation of rat lens incubated with a high concentration of glucose. Synonyms: 5,7,8'-Trihydroxy-2',2'-dimethyl-2'H-(3,6')bi(1-benzopyranyl)-4-one; 4H-1-Benzopyran-4-one,5,7-dihydroxy-3-(8-hydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl)-. Grade: >98%. CAS No. 129280-33-7. Molecular formula: C20H16O6. Mole weight: 352.342. | |
| Seminalplasmin | Seminalplasmin is an antibacterial peptide isolated from Bovine Bos taurus. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. Synonyms: Ser-Asp-Glu-Lys-Ala-Ser-Pro-Asp-Lys-His-His-Arg-Phe-Ser-Leu-Ser-Arg-Tyr-Ala-Lys-Leu-Ala-Asn-Arg-Leu-Ala-Asn-Pro-Lys-Leu-Leu-Glu-Thr-Phe-Leu-Ser-Lys-Trp-Ile-Gly-Asp-Arg-Gly-Asn-Arg-Ser-Val. CAS No. 147958-06-3. Molecular formula: C76H123N17O16. Mole weight: 1530.9. | |
| Seminal Vesicles, Ram, Frozen HisTek | Application: Group: Biologicals. Pack Sizes: 250g. US Biological Life Sciences. | Worldwide |
| Seminal Vesicles, Ram, Microsomal Fraction HisTek | Microsomal fraction of ram seminal vesicles. Group: Biologicals. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Semivolatiles on PUF | Proficiency Testing Material. Group: Atomic absorption spectroscopy (aas). | |
| Semorinemab | Semorinemab (RG 6100) is an anti- Tau humanized IgG4 monoclonal antibody, targets the N-terminal portion of the Tau protein (amino acid residues 6-23). Semorinemab binds with human Tau with a K d value of 3.8 nM. Semorinemab can be used for the research of Alzheimer's Disease [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: RG 6100; RO7105705; MTAU-9937A. CAS No. 2159141-27-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99399. | |
| Sempervirin | Sempervirine is an indole alkaloid isolated from Gelsemium elegans. It exhibits a selective inhibitory effect on in vitro synthesis of cancer DNA. Synonyms: 1,2,3,4-tetrahydroindolo[2',3':3,4]pyrido[1,2-b]isoquinoline. Grade: 98.0%. CAS No. 6882-99-1. Molecular formula: C19H16N2. Mole weight: 272.4. | |
| Sempervirine | Sempervirine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2,3,4,13-tetrahydro-1h-benz[g]indolo[2,3-a]quinolizin-6-ium; 2,3,4,13-Tetrahydro-1H-benz(g)indolo(2,3)quinolizin-6-ium; 3,4,5,6,14,15,20,21-octadehydroyohimban-4-ium. Product Category: Heterocyclic Organic Compound. CAS No. 6882-99-1. Molecular formula: C19H16N2. Mole weight: 273.3511. Purity: 0.96. IUPACName: 16,17,18,19-tetrahydro-3H-yohimban-13-ium. Canonical SMILES: C1CCC2=C[N+]3=C(C=C2C1)C4=C(C=C3)C5=CC=CC=C5N4. Density: g/cm³. Product ID: ACM6882991. Alfa Chemistry ISO 9001:2015 Certified. | |
| Semustine | Semustine is a DNA alkylator , binds to DNA, and acts as a cancer chemotherapeutic agent [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 13909-09-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13747. | |
| Semustine | Semustine is an alkylating agent and interstrand DNA cross linker. Anti-cancer chemotherapeutic agents, which are used in the treatment of different types of cancer such as brain tumors, resistant HodgkinÂs disease, lung cancer and malignant melanoma. Group: Biochemicals. Grades: Highly Purified. CAS No. 13909-09-6. Pack Sizes: 100mg, 250mg. Molecular Formula: C10H18ClN3O2, Molecular Weight: 247.72. US Biological Life Sciences. | Worldwide |
| SEN 12333 | SEN 12333. Group: Biochemicals. Grades: Purified. CAS No. 874450-44-9. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| SEN 1269 | SEN 1269. Group: Biochemicals. Grades: Purified. CAS No. 956128-01-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| SEN177 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Senaparib | Senaparib (IMP4297) is a highly potent, selective and orally active PARP1/2 inhibitor. Senaparib (IMP4297) exhibits strong antitumor activity in animal models [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: IMP4297; JS109. CAS No. 1401682-78-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-137450. | |
| Senecionine | Senecionine (Senecionan-11,16-dione, 12-hydroxy-) is a pyrrolizidine alkaloid could be isolated from Senecio vulgaris. Senecionine decreases the activities of glutathione S-transferase, aminopyrine demethylase and arylhydrocarbon hydroxylase (AHH) [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Senecionan-11,16-dione, 12-hydroxy-; Aureine; Senecionin. CAS No. 130-01-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N2560. | |
| Senecionine | Senecionine. Group: Biochemicals. Alternative Names: (-)-Senecionine; Aureine; NSC 89935; Senecionin; [5R- (3Z, 5R*, 6R*, 14aR*, 14bR*) ]-3-Ethylidene-3, 4, 5, 6, 9, 11, 13, 14, 14a, 14b-decahydro-6-hydroxy-5, 6-dimethyl- [1, 6]dioxacyclododecino [2, 3, 4-gh]pyrrolizine-2, 7-dione. Grades: Highly Purified. CAS No. 130-01-8. Pack Sizes: 2.5mg. Molecular Formula: C18H25NO5, Molecular Weight: 335.39. US Biological Life Sciences. | Worldwide |
| SENECIONINE | Senecionine is a pyrrolizidine alkaloid isolated from Senecio scandens. Study shows that senecionine exhibits activity against hepatic drug metabolizing enzymes in rat cells. Synonyms: Aureine; Senecionin; 12-Hydroxysenecionan-11,16-dione. Grade: 97.5%. CAS No. 130-01-8. Molecular formula: C18H25NO5. Mole weight: 335.4. | |
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