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| Product | Description | |
|---|---|---|
| 5-Bromo-4-chloro-3-indolyl Acetate | A histochemical substrate for esterase. Synonyms: acetic acid (5-bromo-4-chloro-1H-indol-3-yl) ester; (5-bromo-4-chloro-1H-indol-3-yl) acetate. CAS No. 3252-36-6. Molecular formula: C10H7BrClNO2. Mole weight: 288.53. |  |
| 5-Bromo-6-chloro-3-indolyl acetate | 5-Bromo-6-chloro-3-indolyl acetate, a chemical compound widely utilized in the biomedical sector, assumes a paramount role in enzymatic assays within academic and scientific circles. Its primary function involves the detection and quantification of β-galactosidase, an indispensable enzyme intrinsic to numerous pharmaceuticals, malignancies, pathogens, and hereditary abnormalities. In research and diagnostic domains, this highly efficacious substrate guarantees dependable and precise outcomes, thereby exemplifying its quintessential significance. Synonyms: 5-Bromo-6-chloro-3-indoxyl 3-acetate. CAS No. 102185-48-8. Molecular formula: C10H7BrClNO2. Mole weight: 288.52. | |
| 6-Chloro-3-indolyl 1,3-diacetate | 6-Chloro-3-indolyl 1,3-diacetate. Group: Biochemicals. Alternative Names: Salmon-acetate. Grades: Highly Purified. CAS No. 108761-33-7. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C12H10ClNO3. US Biological Life Sciences. |  Worldwide |
| 1H-Indol-3-ol,6-chloro-,3-acetate | Heterocyclic Organic Compound. Alternative Names: 6-CHLORO-3-INDOLYL ACETATE, 114305-99-6, 1H-Indol-3-ol,6-chloro-, 3-acetate, ACMC-20mk1u, SureCN1614860, CTK4A8669, BIC1358, ZINC02562314, AKOS015914574, AG-D-34517, KB-248358, I14-42460, 1H-Indol-3-ol,6-chloro-, acetate (ester) (9CI); Indoxyl, 6-chloro-, acetate (6CI);3-Acetoxy-6-chloroindole; 6-Chloro-3-indoxyl acetate. CAS No. 114305-99-6. Molecular formula: C10H8ClNO2. Mole weight: 209.63. Purity: 0.96. IUPACName: (6-chloro-1H-indol-3-yl) acetate. Canonical SMILES: CC(=O)OC1=CNC2=C1C=CC(=C2)Cl. Catalog: ACM114305996. |  |
| Indomethacin-d4 Methyl Ester | Labeled selective COX-2 inhibitor. Group: Biochemicals. Alternative Names: 1-(4-(Chlorobenzoyl-d4))-5-methoxy-2-methyl-1H-indole-3-acetic Acid Methyl Ester; Methyl N-(p-Chlorobenzoyl-d4)-2-methyl-5-methoxy-3-indolylacetate; L 588983-d4. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Indomethacin Methyl Ester | Selective COX-2 inhibitor. Group: Biochemicals. Alternative Names: 1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetic Acid Methyl Ester; Methyl N-(p-Chlorobenzoyl)-2-methyl-5-methoxy-3-indolylacetate; L 588983. Grades: Highly Purified. CAS No. 1601-18-9. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| 5-Bromo-4-chloro-3-indolyl 2-acetamido-2-deoxy-a-D-galactopyranoside | 5-Bromo-4-chloro-3-indolyl 2-acetamido-2-deoxy-a-D-galactopyranoside is a compound extensively used in biomedicine for its role as a chromogenic substrate. It is specifically utilized in enzymatic assays to detect the presence and activity of β-galactosidase, an enzyme associated with various diseases and cellular processes. This product assists in the diagnosis, research, and treatment of conditions related to β-galactosidase, contributing to advancements in the biomedical industry. Synonyms: 5-Bromo-4-chloro-3-(2-acetamido-2-deoxy-a-D-galactopyranosyloxy)indole X-alpha-GalNAc. CAS No. 210110-89-7. Molecular formula: C16H18BrClN2O6. Mole weight: 449.68. | |
| 5-Bromo-4-chloro-3-indolyl 2-acetamido-2-deoxy-a-D-glucopyranoside | 5-Bromo-4-chloro-3-indolyl 2-acetamido-2-deoxy-a-D-glucopyranoside is a highly esteemed substrate, finding extensive employment in the realm of biomedical studies. Its indispensability lies in its remarkable aptitude for discerning and appraising the activity of β-galactosidase. Demonstrating its versatility, this compound functions as a chromogenic substrate within enzyme-linked immunosorbent assays (ELISAs) and histochemical staining methodologies. Molecular formula: C16H18BrClN2O6. Mole weight: 449.68. | |
| 5-Bromo-4-chloro-3-indolyl 2-Acetamido-2-deoxy-α-D-glucopyranoside | Nutrient medium for yeast culture. Synonyms: 5-Bromo-4-chloro-1H-indol-3-yl 2-(Acetylamino)-2-deoxy-α-D-glucopyranoside. Molecular formula: C16H18BrClN2O6. Mole weight: 449.68. | |
| 5-Bromo-4-chloro-3-indolyl 2-acetamido-2-deoxy-b-D-galactopyranoside | 5-Bromo-4-chloro-3-indolyl 2-acetamido-2-deoxy-b-D-galactopyranoside, an indispensable compound employed extensively in the biomedical domain, plays a pivotal role in appraising the activity of β-galactosidase during biochemical investigations. Synonyms: 5-Bromo-4-chloro-3-indolyl N-acetyl-b-D-galactosaminide X-GalNAc. CAS No. 129572-48-1. Molecular formula: C16H18BrClN2O6. Mole weight: 449.68. | |
| 5-Bromo-4-chloro-3-indolyl 2-acetamido-2-deoxy-b-D-glucopyranoside | 5-Bromo-4-chloro-3-indolyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a key biochemical recompound used in the detection of β-galactosidase activity. It acts as a chromogenic substrate, producing an intense blue compound upon enzymatic hydrolysis. This compound plays a crucial role in studying gene expression, protein labeling and drug discovery for the research of various diseases, including lysosomal storage disorders and cancers. Synonyms: 5-Bromo-4-chloro-3-indolyl N-acetyl-b-D-glucosaminide; X-GlcNAc; β-D-Glucopyranoside, 5-bromo-4-chloro-1H-indol-3-yl 2-(acetylamino)-2-deoxy-; 5-Bromo-4-chloro-1H-indol-3-yl 2-(acetylamino)-2-deoxy-β-D-glucopyranoside; Indole, 3-[(2-acetamido-2-deoxy-β-D-glucopyranosyl)oxy]-5-bromo-4-chloro-; 5-Bromo-4-chloro-3-indolyl N-acetyl-beta-D-glucosaminide. Grades: ≥95%. CAS No. 4264-82-8. Molecular formula: C16H18BrClN2O6. Mole weight: 449.68. | |
| 5-Bromo-4-chloro-3-indolyl-α-D-N-acetylneuraminic Acid, Methyl Ester | Used as a substrate for the detection of sialidase-like enzyme in screening of enzymes, studying physiological activities of gangliosides, and recombinant technologies. Grades: 95%. Molecular formula: C20H24BrClN2O9. Mole weight: 551.77. | |
| 5-Bromo-4-chloro-3-indolyl N-acetyl-a-D-neuraminic acid ammonium salt | 5-Bromo-4-chloro-3-indolyl N-acetyl-α-D-neuraminic acid ammonium salt is a compelling biochemical recompound, unequivocally facilitates the scrutiny, identification and optical rendering of the existence of sialic acid residues on heterogeneous carbohydrates, glycoconjugates and glycoproteins. Its utilization extends to the exploration of cellular mechanisms, molecular interplays and the involvement of sialic acids in afflictions encompassing cancer, viral infections and autoimmune disorders. Synonyms: X-Sialic acid X-Nana 5-Bromo-4-chloro-3-indolyl a-D-N-acetylneuraminic acid. Molecular formula: C19H22BrClN2O9.NH3.2H2O. Mole weight: 590.80. | |
| 5-Bromo-4-chloro-3-indolyl N-acetyl-a-D-neuraminic acid methyl ester | 5-Bromo-4-chloro-3-indolyl N-acetyl-α-D-neuraminic acid methyl ester is a highly sophisticated compound, serving as a cardinal tool in unraveling the intricate and enigmatic world of sialoglycoconjugate glycosylation. Bestowing with the exquisite ability to discern and evaluate glycosylation patterns, this remarkable compound propels the research of complex ailments, encompassing cancer and neurodegenerative disorders. Molecular formula: C20H24BrClN2O9. Mole weight: 551.77. | |
| 5-Bromo-4-chloro-3-indolyl-N-acetyl-b-D-glucosaminide 99+% (HPLC) | 5-Bromo-4-chloro-3-indolyl-N-acetyl-b-D-glucosaminide 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
| 5-Bromo-4-chloro-3-indolyl-N-acetyl-beta-D-galactosaminide | Heterocyclic Organic Compound. Alternative Names: N-Acetyl-5-bromo-4-chloro-3-indolyl-beta-D-galactosaminide. CAS No. 129572-48-1. Molecular formula: C16H18BrClN2O6. Mole weight: 449.68. Appearance: Pale grey to light grey powder. Purity: 0.98. IUPACName: N-[(2S,3R,4R,5R,6R)-2-[(5-bromo-4-chloro-1H-indol-3-yl)oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide. Canonical SMILES: CC (=O)N[C@@H]1[C@H] ([C@H] ([C@H] (O[C@H]1OC2=CNC3=C2C (=C (C=C3)Br)Cl)CO)O)O. Catalog: ACM129572481. | |
| 5-Bromo-6-chloro-3-indolyl-2-acetamido-2-deoxy-a-D-glucopyranoside | 5-Bromo-6-chloro-3-indolyl-2-acetamido-2-deoxy-a-D-glucopyranoside is a highly intricate and multifaceted substrate analog, finding widespread application in the realm of biomedical research. Its paramount utility lies in the profound detection and meticulous localization of β-galactosidase activity is an intricate nexus with diverse afflictions, notably cancer. | |
| 5-Bromo-6-chloro-3-indolyl 2-acetamido-2-deoxy-b-D-glucopyranoside | 5-Bromo-6-chloro-3-indolyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a compound used in the research and development of drugs targeting specific diseases acting as a substrate for certain enzymes. It is a valuable tool for studying enzyme kinetics and activities. It is commonly employed in assays to detect and measure enzyme activity linked to various drug researchs and disease pathways. Synonyms: Magenta-b-D-GlcNAc. CAS No. 5609-91-6. Molecular formula: C16H18BrClN2O6. Mole weight: 449.68. | |
| 6-Chloro-3-indolyl 2-acetamido-2-deoxy-b-D-galactopyranoside | 6-Chloro-3-indolyl 2-acetamido-2-deoxy-b-D-galactopyranoside, a potent biomedicine compound, serves as a crucial tool in scientific research. Its utility lies in precisely detecting and localizing targeted enzymes, making it indispensable in biomedicine exploration. Researchers harness its potential to unravel the intricacies of drug resistance, microbial infections, and various diseases, which expedites the progress of drug discovery and development. Synonyms: 6-Chloro-3-indolyl-N-acetyl-b-D-galactosaminide Salmon-b-D-GalNAc 6-Chloro-3-(2-acetamido-2-deoxy-b-D-galactopyranosyloxy)indole. CAS No. 501432-61-7. Molecular formula: C16H19ClN2O6. Mole weight: 370.78. | |
| 6-Chloro-3-indolyl 2-acetamido-2-deoxy-b-D-glucopyranoside | 6-Chloro-3-indolyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a highly potent and invaluable instrument within the realm of biomedicine, exhibiting its prominence in the context of cellular analysis. With its proficient utility in cell staining, it showcasing a profound ability to monitor and gauge the functionality of β-glucosidases. Additionally, this remarkable compound's inherent capabilities render it conducive to the comprehensive investigation of various afflictions, encompassing lysosomal storage disorders, cancer is and neurological maladies. Synonyms: 6-Chloro-3-indolyl N-acetyl-b-D-glucosaminide Salmon-b-D-GlcNAc 6-Chloro-3-(2-acetamido-2-deoxy-b-D-glucopyranosyloxy)indole. CAS No. 156117-44-1. Molecular formula: C16H19ClN2O6. Mole weight: 370.78. | |
| Diethyl (6-Chloro-2-indolylmethyl) acetamidomalonate | Diethyl (6-Chloro-2-indolylmethyl) acetamidomalonate. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| MDM2/MDMX Dual Inhibitor, RO-5963 ((Z)-2-(4-((6-Chloro-7-methyl-1H-indol-3-yl)methylene)-2,5-dioxoimidazolidin-1-yl)-2-(3,4-difluorophenyl)-N-(1,3-dihydroxypropan-2-yl)acetamide, MDM2 Inhibitor VII, MDMX Inhibitor III) | A cell-permeable indolyl-hydantoin compound that simultaneously inhibits the interaction of both, MDM2 and MDMX with p53 (IC50 = 17.3 and 24.7nM, respectively, in vitro). Releases p53 from MDMX inhibition, stabilizes it, and fully restores its function. Shown to be far more superior to Nutlin-3a in blocking p53 interaction with MDMX. Binds to Phe, Trp, and Leu sub-pockets on the surface of MDMX and MDM2, and promotes MDMX and MDM2 dimer formation. Shown to induce cell cycle arrest in G1 and G2 phases. Also reported to induce apoptosis in several tumor cell lines expressing wild-type p53/MDMX (~10-20uM). Its actions are not believed to be due to any genotoxic stress. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| N-Deschlorobenzoyl Indomethacin | A metabolite of Indomethacin. Group: Biochemicals. Alternative Names: 5-Methoxy-2-methyl-1H-indole-3-acetic Acid; 2-Methyl-5-methoxy-3-indolylacetic Acid; De (chlorobenzoyl) indomethacin; N-Des (4-chlorobenzoyl) indomethacin; NSC 97026;DBI. Grades: Highly Purified. CAS No. 2882-15-7. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| N-Deschlorobenzoyl Indomethacin | N-Deschlorobenzoyl Indomethacin. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 5-Methoxy-2-methyl-1H-Indole-3-acetic acid, De(chlorobenzoyl)indomethacin, 2-(5-Methoxy-2-methylindol-3-yl)acetic acid, 2-(5-Methoxy-2-methyl-1H-indol-3-yl)acetic acid, 5-Methoxy-2-methyl-3-indolylacetic acid,(5-Methoxy-2-methyl-1H-indol-3-yl)acetic acid, N-Des(4-chlorobenzoyl)indomethacin, 2-Methyl-5-methoxy-3-indolylacetic acid, 5-Methoxy-2-methylindol-3-acetic acid, 5-Methoxy-2-methylindole-3-acetic acid, 2-Methyl-5-methoxyindole-3-acetic acid, NSC 97026. CAS No. 2882-15-7. Pack Sizes: 10MG. IUPAC Name: 2-(5-methoxy-2-methyl-1H-indol-3-yl)acetic acid. Molecular Formula: C12H13NO3. Mole Weight: 219.24. Catalog: APS2882157. SMILES: COc1ccc2[nH]c(C)c(CC(=O)O)c2c1. Format: Neat. Shipping: Room Temperature. |  |
| X-NeuNAc | Used as a substrate for the detection of sialidase-like enzyme in screening of enzymes, studying physiological activities of gangliosides, and recombinant technologies. Synonyms: N-Acetyl-2-O-(5-bromo-4-chloro-1H-indol-3-yl)-α-neuraminic Acid Monosodium Salt; 5-bromo-4-chloro-1H-indol-3-yl 5-(Acetylamino)-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosidonic Acid Monosodium Salt; 5-Bromo-4-chloro-3-indolyl-α-D-N-acetylneuraminic acid sodium salt. Grades: ≥98.0%. CAS No. 160369-85-7. Molecular formula: C19H25N2NaO3S. Mole weight: 559.73. | |
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