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| Product | Description | |
|---|---|---|
| Atropine sulfate EP Impurity G | Atropine sulfate EP Impurity G. Uses: For analytical and research use. Alternative Names: (R)-(1R,3r,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl 2-hydroxy-3-phenylpropanoate. CAS No. 21956-47-8. Molecular formula: C17H23NO3. Mole weight: 289.37. Catalog: APB21956478. |  |
| Atropine sulfate hydrate (2:1:1) | Atropine is a medication used to treat certain types of nerve agent and pesticide poisonings, some types of slow heart rate, and to decrease saliva production during surgery. Uses: Adjuvants, anesthesia. Alternative Names: Atropine sulfate monohydrate; Atropini sulfas; Isopto Atropine; Atropinum sulphuricum; Atropine sulfate. Grades: >98%. CAS No. 5908-99-6. Molecular formula: 2C17H23NO3.H2O4S.H2O. Mole weight: 694.837. |  |
| Atropine sulfate Impurity 11 | Atropine sulfate Impurity 11. Uses: For analytical and research use. Alternative Names: (1R,3r,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-oxo-2-phenylpropanoate. CAS No. 22226-37-5. Molecular formula: C17H21NO3. Mole weight: 287.35. Catalog: APB22226375. | |
| Atropine sulfate Impurity 13 | Atropine sulfate Impurity 13. Uses: For analytical and research use. Alternative Names: (1R,3r,5S)-3-((3-hydroxy-2-phenylpropanoyl)oxy)-8-methyl-8-azabicyclo[3.2.1]octane 8-oxide. CAS No. 4438-22-6. Molecular formula: C17H23NO4. Mole weight: 305.37. Catalog: APB4438226. | |
| Atropine sulfate monohydrate | Atropine sulfate monohydrate. Alternative Names: 8-Methyl-8-azabicyclo[3.2.1]oct-3-yl 3-hydroxy-2-phenylpropanoate sulfate (2:1) hydrate (salt). CAS No. 5908-99-6. Purity: >99.0%. Product ID: FFC-AR-5908996. Molecular formula: C17H25NO7S. Mole weight: 387.45. IUPAC Name: bis([(1S,5R)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] 3-hydroxy-2-phenylpropanoate);sulfuric acid;hydrate. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Atropine sulfate monohydrate | 25g Pack Size. Group: Bioactive Small Molecules, Biochemicals, Research Organics & Inorganics. Formula: C34H46N2O6 · H2O4S · H2O. CAS No. 5908-99-6. Prepack ID 40811084-25g. Molecular Weight 694.83. See USA prepack pricing. |  |
| Atropine Sulfate Monohydrate | Mydriatic; antispasmodic; used in preanesthetic medication. Group: Biochemicals. Alternative Names: α - (Hydroxymethyl) benzeneacetic Acid (3-endo)-8-Methyl-8-azabicyclo[3.2.1]oct-3-yl Ester Sulfate Hydrate; Atropine Sulfate Hydrate; Atropisol; Atropt. Grades: Highly Purified. CAS No. 5908-99-6. Pack Sizes: 10g. US Biological Life Sciences. |  Worldwide |
| ATROPINE SULFATE(RG) | ATROPINE SULFATE(RG). Product ID: ACMA00004923. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Atropine Sulphate USP | Atropine Sulphate USP. |  CA, FL & NJ |
| Atrosab | Atrosab is a humanized IgG1 antagonistic anti-TNFR1 antibody. Atrosab inhibits TNF-mediated Apoptosis induction and IL-6 and IL-8 production. Atrosab reduces neurological deficits. Atrosab can be used for research of inflammatory disease. The recommend isotype control is Human IgG1 kappa, Isotype Control (HY-P99001)[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1365659-05-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P990008. |  |
| Atrovastatin-PEG3-FITC | Atrovastatin-PEG3-FITC (compound S31) is a KRAS-PDEδ interaction inhibitor. Atrovastatin-PEG3-FITC acts as a ligand in fluorescence anisotropy assay[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1440755-31-6. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-134977. | |
| Atrovenetin | Atrovenetin is an antibiotic produced by Penicillum herquei PRL 1838 and Pen. atrovenetum SM 683. Molecular formula: C19H18O6. Mole weight: 342.34. | |
| atroxase | A nonhemorrhagic endopeptidase from the venom of the western diamondback rattlesnake (Crotalus atrox) that cleaves fibrinogen. In peptidase family M12 (astacin family). Group: Enzymes. Enzyme Commission Number: EC 3.4.24.43. CAS No. 181186-94-7. 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-4325; atroxase; EC 3.4.24.43; 181186-94-7. Cat No: EXWM-4325. |  |
| Attacin-C | Attacin-C is an antimicrobial peptide produced by Drosophila melanogaster (Fruit fly). It has antibacterial and antifungal activity. Alternative Names: AttC; Gln-Arg-Pro-Tyr-Thr-Gln-Pro-Leu-Ile-Tyr-Tyr-Pro-Pro-Pro-Pro-Thr-Pro-Pro-Arg-Ile-Tyr-Arg-Ala. Grades: >98%. Molecular formula: C133H198N34O32. Mole weight: 2785.24. | |
| Attapulgite | Attapulgite is widely used as an adsorbent for solid dosage forms. Alternative Names: Actapulgite; Attaclay; Attacote; Attagel; attapulgus; palygorscite; palygorskite; Pharmsorb Regular. Grades: 95%. CAS No. 12174-11-7. Molecular formula: Al.Fe.4H2O.HO.Mg.Si2O5. Mole weight: 332.37. | |
| ATTO 390 NHS ester | ATTO 390 NHS ester is a new fluorescent marker based on the Rhodamine structure. It has strong absorption, high fluorescence quantum yield, high thermal stability and photochemical stability, and is suitable for single molecule detection and high-resolution microscopy. ATTO 390 NHS ester is an NHS ester derivative of ATTO 390 that can be used to label proteins or antibodies. Uses: Scientific research. Category: Signaling pathways. CAS No. 914203-48-8. Pack Sizes: 5 mg; 10 mg. Product ID: HY-D1917. | |
| Atto 425-NHS ester | Atto 425-NHS Ester is a fluorescent label useful in monitoring three-component protein-protein interactions in vitro and in living cells. Furthermore, it is utilized to identify and measure the concentration of specific proteins in biological specimens. Alternative Names: Atto 425-N-hydroxysuccinimide ester; ATTO 425-3; Atto 425-N-hydroxysuccinimide ester. CAS No. 892156-28-4. Molecular formula: C26H30N2O8. Mole weight: 498.53. | |
| ATTO 488 | ATTO 488 is a hydrophilic rhodamine-based fluorescent dye with strong absorption and high fluorescence quantum yield. ATTO 488 is suitable for flow cytometry (FACS), fluorescence in situ hybridization (FISH) and most other labeling uses (Ex/Em: 500/520 nm)[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 923585-42-6. Pack Sizes: 1 mg. Product ID: HY-D2000. | |
| ATTO 488 carboxylic acid | ATTO 488 carboxylic acid is a new fluorescent label based on the Rhodamine structure. It has strong absorption, high fluorescence quantum yield, high thermal stability and photochemical stability, and is suitable for single molecule detection and high-resolution microscopy. ATTO 488 carboxylic acid is a carboxylic acid derivative of ATTO 488, which can be used to label proteins or antibodies. Uses: Scientific research. Category: Signaling pathways. CAS No. 1443553-08-9. Pack Sizes: 5 mg; 10 mg. Product ID: HY-D1305. | |
| ATTO 488 carboxylic acid | ATTO 488 is a rhodamine-based fluorescent label. ATTO 488 carboxylic acid is a carboxylic acid derivative of ATTO 488, which can be used to label proteins or antibodies. Molecular formula: C25H23N3O10S2. Mole weight: 589.59. | |
| ATTO 488 maleimide | ATTO 488 maleimide is a new fluorescent marker based on the Rhodamine structure. It has strong absorption, high fluorescence quantum yield, high thermal stability and photochemical stability, and is suitable for single molecule detection and high-resolution microscopy. ATTO 488 maleimide is a maleimide derivative of ATTO 488, which can be used to label proteins or antibodies. Uses: Scientific research. Category: Signaling pathways. CAS No. 1219127-42-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-D2002. | |
| ATTO 488 NHS ester | ATTO 488 NHS ester is a new fluorescent marker based on the Rhodamine structure. It has strong absorption, high fluorescence quantum yield, high thermal stability and photochemical stability, and is suitable for single molecule detection and high-resolution microscopy. ATTO 488 NHS ester is an NHS ester derivative of ATTO 488 that can be used to label proteins or antibodies. Uses: Scientific research. Category: Signaling pathways. CAS No. 863772-22-9. Pack Sizes: 1 mg. Product ID: HY-D2001. | |
| ATTO 514 NHS ester | ATTO 514 is a new hydrophilic fluorescent label with excellent water solubility. The dye exhibits strong absorption, high fluorescence quantum yield and exceptional thermal and photo-stability. Thus ATTO 514 is highly suitable for single-molecule detection applications and high-resolution microscopy such as PALM, dSTORM, STED etc. Additionally the dye highly qualifies to be applied in flow cytometry (FACS), fluorescence in-situ hybridization (FISH) and many more. The fluorescence is excited most efficiently in the range 510-535 nm. A suitable source of excitation is the 514 nm line of the Argon-Ion laser.find more information here. | |
| ATTO 532 NHS ester | ATTO 532 NHS ester. CAS No. 924660-19-5. | |
| ATTO 550 NHS ester | ATTO 550 NHS ester. CAS No. 1005770-00-2. | |
| ATTO 565 NHS ester | ATTO 565 NHS ester is a commonly used amine-reactive reagent, provided by ATTO-TEC. It is widely used in protein labeling and readily reacts with compounds containing amino groups, forming a chemically stable amide bond between the dye, e.g., a protein. The optimum pH-range for NHS-ester coupling is pH 8.0-9.0. At this pH amino groups of proteins, i.e., the ε-amino groups of lysines are unprotonated to a degree sufficiently high for fast coupling. Grades: ≥90% (HPLC). Molecular formula: C35H34ClN3O11. Mole weight: 708.11. | |
| Atto 590 nhs ester | ATTO 590 is a novel fluorescent label belonging to the class of Rhodamine dyes. The dye is designed for application in the area of life science, e.g. labeling of DNA, RNA or proteins. The ATTO dyes are a series of fluorescent dyes that provide all the crucial properties required for modern fluorescent technologies, such as fluorescence microscopy, flow-cytometry, fluorescence in situ hybridization (FISH), receptor binding assays or enzyme assays. The dye is highly suitable for single-molecule detection applications and high-resolution microscopy. The NHS-esters are used in common conjugation protocols.ATTO 590 is a novel fluorescent label belonging to the class of Rhodamine dyes, which has an absorption maximum of 594 nm and an emission maximum of 624 nm. ATTO 590-N-hydroxysuccinimide (NHS) is membrane permeable. Uses: Molar absorption 120,000 1/m cm, abs: 593 nm, em: 620 nm, qy=0.93, tfl 4.0 ns (unpublished data)atto 590 nhs ester may be suitable for use in site-specific labeling of human embryonic kidney (hek293t) cell lysates for western blotting, fluorescence, and widefield microscopy studies. Alternative Names: 2-(6,20-diethyl-7,7,9,17,19,19-hexamethyl-2-oxa-20-aza-6-azoniapentacyclo[12.8.0.03,12.05,10.016,21; docosa-1(14),3,5,8,10,12,15,17,21-nonaen-13-yl)-4-(2,5-dioxopyrrolidin-1-yl)oxycarbonylbenzoic acid;perchlorate; 6-(2-Carboxy-5-{[(2,5-dioxopyrrolidin-1-yl)oxy]carbonyl}phenyl)-1,11-diethyl-2,2,4,8,10,10-hex | |
| ATTO 633 NHS ester | ATTO 633 NHS ester. Uses: The active ester of atto 633 fluorescence dye reacts with amino groups under mild conditions. atto 633 is a red-emitting fluorescence label with strong absorption, high quantum yield (64%), high photostability, good water solubility, and very little triplet formation. Grades: ≥90% (HPLC). | |
| ATTO 647 | ATTO 647 is a zwitterionic dye with a net electrical charge of zero. It is a pH sensitive product. While practically stable up to pH 8.5, it slowly degrades at higher pH. ATTO 647 is a new label with high molecular absorption (120,000) and quantum yield (0.20) as well as enough Stokes shift between excitation and emission maximum. ATTO 647 is characterized by a high photostability and brightness. In addition, this label has good water solubility and low triplet formation ability. Uses: Atto fluorescent labels are designed for high sensitivity applications, including single molecule detection. atto labels have rigid structures that do not show any cis-trans-isomerization. thus these labels display exceptional intensity with minimal spectral shift on conjugation. Grades: ≥90% (HPCE). | |
| ATTO 647N | ATTO 647N. Uses: Atto 647n is a superior red-emitting fluorescence dye with a strong absorption, excellent fluorescence quantum yield (65%), high photostability, excellent ozone resistance, good solubility, and very little triplet formation. Grades: ≥98.0% (HPCE). | |
| ATTO 647N Chloride | ATTO 647N Chloride. | |
| ATTO 647N DOPE | ATTO 647N belongs to a new generation of fluorescent labels for the red spectral region. The dye is designed for application in the area of life science, e.g. labeling of DNA, RNA or proteins. Characteristic features of the label are strong absorption, excellent fluorescence quantum yield, high photostability, excellent ozone resistance, good solubility, and very little triplet formation. ATTO 647N is a cationic dye. After coupling to a substrate the dye carries a net electrical charge of +1. In common with most ATTO-labels, absorption and fluorescence are independent of pH in the range of 2 to 11, used in typical applications. As supplied ATTO 647N consists of a mixture of two isomers with practically identical absorption and fluorescence properties.ATTO-Dye Labeled Phospholipids Sigma-Aldrich offers a variety of glycero-phospholipids carrying one or two fatty acid groups (lipophilic groups) and a phosphate ester residue (hydrophilic group). They are labeled at the hydrophilic head group. After incorporation of the phospholipid into a membrane the fluorophore is located at the water / lipid interface of the membrane. We currently provide 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine (DPPE), 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE), palmitoyl-sn-glycero-phosphoethanolamine (PPE), and 1,2-dimyristoyl-sn-glycero-3-phospho-ethanolamine (DMPE) labeled with ATTO-dyes.find more information here. Grades: ≥80.0% | |
| ATTO 647N NHS ester | ATTO 647N is a superior red-emitting fluorescence dye with a strong absorption, excellent fluorescence quantum yield (65%), high photostability, excellent ozone resistance, good solubility, and very little triplet formation. Uses: Atto 647n belongs to a new generation of fluorescent labels for the red spectral region. the dye is designed for application in the area of life science, e.g. labeling of dna, rna or proteins. characteristic features of the label are strong absorption, excellent fluorescence quantum yield, high photostability, excellent ozone resistance, good solubility, and very little triplet formation. atto 647n is a cationic dye. the active ester of atto 647n fluorescence dye reacts with amino groups under mild conditions. after coupling to a substrate the dye carries a net electrical charge of +1. in common with most atto-labels, absorption and fluorescence are independent of ph in the range of 2 to 11, used in typical applications. as supplied atto 647n consists of a mixture of two isomers with practically identical absorption and fluorescence properties. Grades: ≥90% (HPLC). | |
| ATTO 647N PPE | ATTO 647N belongs to a new generation of fluorescent labels for the red spectral region. The dye is designed for application in the area of life science, e.g. labeling of DNA, RNA or proteins. Characteristic features of the label are strong absorption, excellent fluorescence quantum yield, high photostability, excellent ozone resistance, good solubility, and very little triplet formation. ATTO 647N is a cationic dye. After coupling to a substrate the dye carries a net electrical charge of +1. In common with most ATTO-labels, absorption and fluorescence are independent of pH in the range of 2 to 11, used in typical applications. As supplied ATTO 647N consists of a mixture of two isomers with practically identical absorption and fluorescence properties.ATTO-Dye Labeled Phospholipids Sigma-Aldrich offers a variety of glycero-phospholipids carrying one or two fatty acid groups (lipophilic groups) and a phosphate ester residue (hydrophilic group). They are labeled at the hydrophilic head group. After incorporation of the phospholipid into a membrane the fluorophore is located at the water / lipid interface of the membrane. We currently provide 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine (DPPE), 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE), palmitoyl-sn-glycero-phosphoethanolamine (PPE), and 1,2-dimyristoyl-sn-glycero-3-phospho-ethanolamine (DMPE) labeled with ATTO-dyes.find more information here. Grades: ≥80.0% ( | |
| ATTO MB2 | ATTO MB2 is a derivative of the well-known redox dye Methylene Blue. The dye can be reversibly reduced to the Colorless leuko form. Upon oxidation (e.g. with oxygen) the dye recovers, and the absorption is fully restored.The dye is suitable for labeling of DNA, RNA, proteins etc. In common with most ATTO-labels the dye shows a high extinction coefficient.ATTO MB2 is moderately hydrophilic.find more information here. | |
| ATTO MB2 maleimide | ATTO MB2 maleimide. Uses: Atto mb2 is a derivative of the well-known redox dye methylene blue. the dye can be reversibly reduced to the colorless leuko form. upon oxidation the dye recovers and the absorption is fully restored. in common with most atto-labels the dye shows a high extinction coefficient. the dye is moderately hydrophilic. atto mb2 is a cationic dye. after coupling to a substrate the dye carries a net electrical charge of +1. maleimides are well suited for coupling to thiol groups. this is similar to iodacetamides, but maleimides react more selectively with thiols. they do not show significant reaction with histidine or methionine. hydrolysis of maleimides to a mixture of isomeric nonreactive maleamic acids can compete significantly with thiol modification, particularly above ph 8. maleimides may be used for labeling of amines, which usually requires a higher ph than reaction of maleimides with thiols. Grades: ≥90% (HPLC). | |
| AtuFECT01 | AtuFect01 is part of the lipid system AtuPLEX and shows more effective siRNA binding activity and delivery to vascular endothelial cells. Alternative Names: β-Alaninamide, L-arginyl-2-amino-N-hexadecyl-N-(9Z)-9-octadecenyl-, trihydrochloride, (2S)-; β-Alaninamide, L-arginyl-2-amino-N-hexadecyl-N-(9Z)-9-octadecen-1-yl-, hydrochloride (1:3), (2S)-; (S)-2-amino-N-((S)-2-amino-3-(hexadecyl((Z)-octadec-9-en-1-yl)amino)-3-oxopropyl)-5-guanidinopentanamide trihydrochloride. Grades: ≥95%. CAS No. 869094-19-9. Molecular formula: C43H87N7O2.3HCl. Mole weight: 843.58. | |
| Atuliflapon | Atuliflapon (AZD5718) is an orally active inhibitor of FLAP (5?Lipoxygenase activating protein), with an IC50 of 2 nM. Atuliflapon is used in the study for coronary artery disease[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AZD5718. CAS No. 2041075-86-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-122908. | |
| Atuveciclib | Atuveciclib (BAY-1143572) is a potent and highly selective, oral PTEFb/CDK9 inhibitor. Atuveciclib (BAY-1143572) inhibits CDK9/CycT1 with an IC50 of 13 nM[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: BAY-1143572. CAS No. 2923012-24-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12871B. | |
| ATUX-1215 | ATUX-1215 is an activator of protein phosphatase 2A (PP2A). ATUX-1215 reduced the phosphorylation of ERK, p38, JNK, and Akt and the secretion of IL-12p70, GM-CSF, and IL1α in Bleomycin hydrochloride (HY-17565A)-treated animals. ATUX-1215 can slow the progression of lung fibrosis[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2910929-53-0. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-156420. | |
| ATWLPPR Peptide | ATWLPPR Peptide is a biological active peptide. (This peptide is a specific VEGFR2/KDR heptapeptide antagonist, it binds VEGFR2 (KDR/flk), completely inhibiting VEGF binding to KDR and preventing VEGF-induced angiogenesis in-vivo. It specifically inhibits human endothelial cell proliferation in-vitro and totally abolishes VEGF-induced angiogenesis in-vivo.). Uses: Scientific research. Category: Signaling pathways. CAS No. 272121-15-0. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P1663. | |
| ATX-100 | ATX-100 is an ionizable cationic lipid that has been used in the generation of lipid nanoparticles (LNPs) for the delivery of siRNA. Alternative Names: ATX100; ATX 100; 4,4'-[[[[3-(dimethylamino)propyl]thio]carbonyl]imino]bis-butanoic acid, 1,1'-bis(1-heptyloctyl) ester. CAS No. 2230647-37-5. Molecular formula: C44H86N2O5S. Mole weight: 755.23. | |
| ATX-II | ATX-II is a selective sodium channel modulator toxin. ATX-II enhances late sodium current, prevents full sodium channel inactivation, and generates persistent current fractions. ATX-II has pro-arrhythmic effect. ATX-II slows intrinsic heart rate, prolongs QT interval and sinus node recovery time, and causes sinus pauses and arrests. ATX-II can be used for the research of atrial fibrillation, long QT syndrome, and long QT3 syndrome[1][2][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 60748-45-0. Pack Sizes: 100 μg; 500 μg; 1 mg; 5 mg; 10 mg. Product ID: HY-P1604. | |
| AU1235 | AU1235, an adamantyl urea, is a potent MmpL3 inhibitor. The Mycobacterium tuberculosis protein MmpL3 performs an essential role in cell wall synthesis, since it effects the transport of trehalose monomycolates across the inner membrane[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1338780-86-1. Pack Sizes: 10 mM * 1 mL in DMSO; 2 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101867. | |
| AU-15330 | AU-15330 is a proteolysis-targeting chimera (PROTAC) degrader of the SWI/SNF ATPase subunits, SMARCA2 and SMARCA4. AU-15330 induces potent inhibition of tumour growth in xenograft models of prostate cancer and synergizes with the AR antagonist enzalutamide. AU-15330 induces disease remission in castration-resistant prostate cancer (CRPC) models without toxicity[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2380274-50-8. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-145388. | |
| AU-16235 | AU-16235 is an inactive epimer of AU-15330. AU-16235 has no effect on cancer cell survival and growth[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2380275-40-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-145388B. | |
| AU-24118 | AU-24118 is a selective and orally bioavailable PROTAC degrader of mSWI-SNF ATPases (SMARCA2 and SMARCA4) and PBRM1. AU-24118 integrates a bait moiety binding to the bromodomains of SMARCA2 and SMARCA4, along with a ligand moiety for CRBN ligase. AU-24118 demonstrates tumor regression in prostate cancer model. AU-24118 can be studied to combat prostate cancer. (Pink: PBRM1/SMARCA2,4 ligand (HY-171774); Blue: CRBN ligand (HY-171775))[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3084244-26-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-163410. | |
| Au/ CdS Core-Shell Nanoparticles | Au/ CdS Core-Shell Nanoparticles. Purity: 99.9%. |  |
| Aucubin | Aucubin is an iridoid glycoside with a wide range of biological activities, including anti-inflammatory, anti-microbial, anti-algesic as well as anti-tumor activities. It may be a potential therapeutic choice in the treatment of OA due to its anti-inflammatory and chondroprotective features. Administration of Aucubin improved nerve regeneration in the rat model of sciatic nerve injury, suggesting that Aucubin may be a useful therapeutic compound for the human peripheral nervous system after various nerve injuries. Besides, Aucubin may improve obesity-induced atherosclerosis by attenuating TNF-α-induced inflammatory responses. Uses: Anti-inflammatory / chondroprotective. Alternative Names: (1S,4aR,5S,7aS)-1-4a,5,7a-Tetrahydro-5-hydroxy-7-(hydroxymethyl)cyclopenta[c]pyran-1-yl b-D-glucopyranoside. Grades: >98%. CAS No. 479-98-1. Molecular formula: C15H22O9. Mole weight: 346.33. | |
| Aucubin | Aucubin. Group: Biochemicals. Alternative Names: Aucuboside; Rhinanthin; Rhimantin. Grades: Plant Grade. CAS No. 479-98-1. Pack Sizes: 20mg. Molecular Formula: C15H22O9, Molecular Weight: 346.33. US Biological Life Sciences. | Worldwide |
| Aucubin | Aucubin Inhibitor. Uses: Scientific use. Product Category: T3416. CAS No. 479-98-1. |  |
| Augeo Clean Multi | Augeo Clean Multi. CAS No. 100-79-8. VIGON Item # 505110. Categories: Speciality Ingredients Suppliers, Fragrances, Perfumers. |  America & Internationally |
| Auglurant | Auglurant (VU0424238) is a novel and selective mGlu5 antagonist with an IC50 value of 11 nM (rat) and an IC50 value of 14 nM (human). Auglurant (VU0424238) has an acceptable CNS penetration[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: VU0424238. CAS No. 1396337-04-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-16617. | |
| Au Nanoparticles(D: 100 nm ) | Gold-coloured powder or tiny sheets;Soft yellow metal; gold-colored powder or tiny sheets. CAS No. 7440-57-5. Molecular formula: Au;Au. Mole weight: 196.96657g/mol. IUPAC Name: gold. SMILES: [Au]. InChI: InChI=1S/Au. | |
| Au Nanoparticles(D: 12 nm ) | Gold-coloured powder or tiny sheets;Soft yellow metal; gold-colored powder or tiny sheets. CAS No. 7440-57-5. Molecular formula: Au;Au. Mole weight: 196.96657g/mol. IUPAC Name: gold. SMILES: [Au]. InChI: InChI=1S/Au. | |
| Au Nanoparticles(D: 140 nm ) | Gold-coloured powder or tiny sheets;Soft yellow metal; gold-colored powder or tiny sheets. CAS No. 7440-57-5. Molecular formula: Au;Au. Mole weight: 196.96657g/mol. IUPAC Name: gold. SMILES: [Au]. InChI: InChI=1S/Au. | |
| Au Nanoparticles(D: 15 nm ) | Gold-coloured powder or tiny sheets;Soft yellow metal; gold-colored powder or tiny sheets. CAS No. 7440-57-5. Molecular formula: Au;Au. Mole weight: 196.96657g/mol. IUPAC Name: gold. SMILES: [Au]. InChI: InChI=1S/Au. | |
| Au Nanoparticles(D: 160 nm ) | Gold-coloured powder or tiny sheets;Soft yellow metal; gold-colored powder or tiny sheets. CAS No. 7440-57-5. Molecular formula: Au;Au. Mole weight: 196.96657g/mol. IUPAC Name: gold. SMILES: [Au]. InChI: InChI=1S/Au. | |
| Au Nanoparticles(D: 180 nm ) | Gold-coloured powder or tiny sheets;Soft yellow metal; gold-colored powder or tiny sheets. CAS No. 7440-57-5. Molecular formula: Au;Au. Mole weight: 196.96657g/mol. IUPAC Name: gold. SMILES: [Au]. InChI: InChI=1S/Au. | |
| Au Nanoparticles(D: 200 nm ) | Gold-coloured powder or tiny sheets;Soft yellow metal; gold-colored powder or tiny sheets. CAS No. 7440-57-5. Molecular formula: Au;Au. Mole weight: 196.96657g/mol. IUPAC Name: gold. SMILES: [Au]. InChI: InChI=1S/Au. | |
| Au Nanoparticles(D: 80 nm ) | Gold-coloured powder or tiny sheets;Soft yellow metal; gold-colored powder or tiny sheets. CAS No. 7440-57-5. Molecular formula: Au;Au. Mole weight: 196.96657g/mol. IUPAC Name: gold. SMILES: [Au]. InChI: InChI=1S/Au. | |
| AUR1545 | AUR1545 is a selective KAT2A/KAT2B ((GCN5/PCAF)) PROTAC degrader that induces monocyte differentiation and inhibits the growth of acute myeloid leukemia cells. AUR1545 inhibits cell growth, induces epithelial differentiation and suppresses tumor growth in small cell lung cancer models. AUR1545 inhibits cell growth and induces differentiation in neuroendocrine prostate cancer cells and primary patient-derived organoids. AUR1545 is applicable to research related to acute myeloid leukemia, small cell lung cancer and neuroendocrine prostate cancer[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3031593-79-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg. Product ID: HY-173158. | |
| aurachin B dehydrogenase | The enzyme from the bacterium Stigmatella aurantiaca catalyses the final step in the conversion of aurachin C to aurachin B. In vivo the enzyme catalyses the reduction of 4-hydroxy-2-methyl-3-oxo-4-[(2E,6E)-farnesyl]-3,4-dihydroquinoline-1-oxide to form 2-methyl-1-oxo-4-[(2E,6E)-farnesyl]-3,4-dihydroquinoline-3,4-diol (note that the reactions written above proceed from right to left), which then undergoes a spontaneous dehydration to form aurachin B. Group: Enzymes. Synonyms: AuaH. Enzyme Commission Number: EC 1.1.1.394. 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-0314; aurachin B dehydrogenase; EC 1.1.1.394; AuaH. Cat No: EXWM-0314. | |
| Aurachin C | Aurachin C is a quinoline compound produced by Stigmatella aurantiaca Sg al5. It has the activity of inhibiting gram-positive bacteria and a few yeasts and filamentous fungi, and can block the NADH oxidation of bovine heart microsomal particles. CAS No. 108354-14-9. Molecular formula: C25H33NO2. Mole weight: 379.53. | |
| aurachin C monooxygenase/isomerase | The aurachin C monooxygenase from the bacterium Stigmatella aurantiaca accepts both NADH and NADPH as cofactor, but has a preference for NADH. It catalyses the initial steps in the conversion of aurachin C to aurachin B. The FAD-dependent monooxygenase catalyses the epoxidation of the C2-C3 double bond of aurachin C, which is followed by a semipinacol rearrangement, causing migration of the farnesyl group from C3 to C4. Group: Enzymes. Synonyms: auaG (gene name); aurachin C monooxygenase. Enzyme Commission Number: EC 1.14.13.222. 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-0825; aurachin C monooxygenase/isomerase; EC 1.14.13.222; auaG (gene name); aurachin C monooxygenase. Cat No: EXWM-0825. | |
| Aurachin D | Aurachin D is a quinoline compound produced by Stigmatella aurantiaca Sg al5. It has the activity of inhibiting gram-positive bacteria and a few yeasts and filamentous fungi, and can block the NADH oxidation of bovine heart microsomal particles. CAS No. 108354-13-8. Molecular formula: C25H33NO. Mole weight: 363.53. | |
| Aurachin D | Aurachin D is an antibiotic. Aurachin D inhibits Gram-positive bacteria and a few funguses. Aurachin D blocks NADH oxidation in beef heart submitochondrial particles[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 108354-13-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N7151. | |
| Auramine O (For Biological Stains and Dyes) | Auramine O (For Biological Stains and Dyes). Uses: For analytical and research use. Alternative Names: Auramine hydrochloride; Basic yellow 2; Pyocatanium aureum; Aizen auramine; Pyoktanin yellow. CAS No. 2465-27-2. Molecular formula: C17H22ClN3. Mole weight: 303.8. IUPAC Name: 4-[4-(dimethylamino)benzenecarboximidoyl]-N,N-dimethylaniline;hydrochloride. Catalog: APB2465272. | |
| Auramine O, technicaL grade | Auramine O, technicaL grade. Group: Biochemicals. Grades: Purified. CAS No. 2465-27-2. Pack Sizes: 100g, 250g, 500g, 1kg, 2kg. US Biological Life Sciences. | Worldwide |
| Auramycin A | It is produced by the strain of Streptomyces galilaeus. Auramycin has the ability of anti gram-positive bacteria and tumor, with the LD50 100mg/kg (Mouse, abdominal cavity). Alternative Names: methyl (1R,2R,4S)-4-[(2S,4S,5S,6S)-4-dimethylamino-5-[(2S,4S,5R,6S)-4- hydroxy-6-methyl-5-[(2S,6S)-6-methyl-5-oxo-oxan-2-yl]oxy-oxan-2-yl]oxy -6-methyl-oxan-2-yl]oxy-2,5,7-trihydroxy-2-methyl-6,11-dioxo-3,4-dihyd ro-1H-tetracene-1-carboxylate; auramycin A. Grades: 95%. CAS No. 78173-92-9. Molecular formula: C41H51NO15. Mole weight: 797.84. | |
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