A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the suppliers website for prices or more information.
| Product | Description | |
|---|---|---|
| GDP-Man:Man1GlcNAc2-PP-dolichol α-1,3-mannosyltransferase | The biosynthesis of asparagine-linked glycoproteins utilizes a dolichyl diphosphate-linked glycosyl donor, which is assembled by the series of membrane-bound glycosyltransferases that comprise the dolichol pathway. Alg2 mannosyltransferase from Saccharomyces cerevisiae carries out an α1,3-mannosylation of D-Man-β-(1?4)-D-GlcNAc-β-(1?4)-D-GlcNAc-diphosphodolichol, followed by an α1,6-mannosylation (cf. EC 2.4.1.257), to form the first branched pentasaccharide intermediate of the dolichol pathway. Group: Enzymes. Synonyms: Alg2 mannosyltransferase (ambiguous); ALG2 (gene name, ambiguous); glycolipid 3-α-mannosyltransferase; GDP-mannose:glycolipid 3-&alph. Enzyme Commission Number: EC 2.4.1.132. CAS No. 81181-76-2. 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-2357; GDP-Man:Man1GlcNAc2-PP-dolichol α-1,3-mannosyltransferase; EC 2.4.1.132; 81181-76-2; Alg2 mannosyltransferase (ambiguous); ALG2 (gene name, ambiguous); glycolipid 3-α-mannosyltransferase; GDP-mannose:glycolipid 3-α-D-mannosyltransferase; GDP-Man:Man1GlcNAc2-PP-Dol α-1,3-mannosyltransferase; GDP-D-mannose:D-Man-β-(1?4)-D-GlcNAc-β-(1?4)-D-GlcNAc-diphosphodolichol 3-α-mannosyltransferase. Cat No: EXWM-2357. |  |
| GDP-Man:Man2GlcNAc2-PP-dolichol α-1,6-mannosyltransferase | The biosynthesis of asparagine-linked glycoproteins utilizes a dolichyl diphosphate-linked glycosyl donor, which is assembled by the series of membrane-bound glycosyltransferases that comprise the dolichol pathway. Alg2 mannosyltransferase from Saccharomyces cerevisiae carries out an α1,3-mannosylation (cf. EC 2.4.1.132) of β-D-Man-(1?4)-β-D-GlcNAc-(1?4)-α-D-GlcNAc-diphosphodolichol, followed by an α1,6-mannosylation, to form the first branched pentasaccharide intermediate of the dolichol pathway. Group: Enzymes. Synonyms: GDP-Man:Man2GlcNAc2-PP-Dol α-1,6-mannosyltransferase; Alg2 mannosyltransferase (ambiguous); ALG2 (gene name, ambiguous); GDP-Man:Man1GlcNAc2-PP-dolichol mannosyltransfera. Enzyme Commission Number: EC 2.4.1.257. 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-2487; GDP-Man:Man2GlcNAc2-PP-dolichol α-1,6-mannosyltransferase; EC 2.4.1.257; GDP-Man:Man2GlcNAc2-PP-Dol α-1,6-mannosyltransferase; Alg2 mannosyltransferase (ambiguous); ALG2 (gene name, ambiguous); GDP-Man:Man1GlcNAc2-PP-dolichol mannosyltransferase (ambiguous); GDP-D-mannose:D-Man-α-(1?3)-D-Man-β-(1?4)-D-GlcNAc-β-(1?4)-D-GlcNAc-diphosphodolichol α-6-mannosyltransferase. Cat No: EXWM-2487. | |
| GDP-Man:Man3GlcNAc2-PP-dolichol α-1,2-mannosyltransferase | The biosynthesis of asparagine-linked glycoproteins (N-linked protein glycosylation) utilizes a dolichyl diphosphate-linked glycosyl donor, which is assembled by the series of membrane-bound glycosyltransferases that comprise the dolichol pathway. ALG11 mannosyltransferase from Saccharomyces cerevisiae carries out two sequential steps in the formation of the lipid-linked core oligosaccharide, adding two mannose residues in α(1?2) linkages to the nascent oligosaccharide. Group: Enzymes. Synonyms: ALG11; AL. Enzyme Commission Number: EC 2.4.1.131. CAS No. 74506-43-7. 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-2356; GDP-Man:Man3GlcNAc2-PP-dolichol α-1,2-mannosyltransferase; EC 2.4.1.131; 74506-43-7; ALG11; ALG11 mannosyltransferase; LEW3 (gene name); At2G40190 (gene name); gmd3 (gene name); galactomannan deficiency protein 3; GDP-mannose:glycolipid 1,2-α-D-mannosyltransferase; glycolipid 2-α-mannosyltransferase; GDP-mannose:glycolipid 2-α-D-mannosyltransferase; GDP-Man:Man3GlcNAc2-PP-Dol α-1,2-mannosyltransferase; GDP-α-D-mannose:D-Man-α-(1?3)-[D-Man-α-(1?6)]-D-Man-β-(1?4)-D-GlcNAc-β-(1?4)-D-GlcNAc-diphosphodolichol 2-α-D-mannosyltransferase. Cat No: EXWM-2356. | |
| GDP-mannose 3,5-epimerase | This enzyme belongs to the family of isomerases, specifically those racemases and epimerases acting on carbohydrates and derivatives. This enzyme participates in ascorbate and aldarate metabolism. Group: Enzymes. Synonyms: GDP-D-mannose:GDP-L-galactose epimerase; guanosine 5'-diphosphate D-mannose:guanosine 5'-diphosphate L-galactose epimerase. Enzyme Commission Number: EC 5.1.3.18. CAS No. 72162-82-4. 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-5403; GDP-mannose 3,5-epimerase; EC 5.1.3.18; 72162-82-4; GDP-D-mannose:GDP-L-galactose epimerase; guanosine 5'-diphosphate D-mannose:guanosine 5'-diphosphate L-galactose epimerase. Cat No: EXWM-5403. | |
| GDP-mannose 4,6-dehydratase | The bacterial enzyme requires bound NAD+. This enzyme forms the first step in the biosynthesis of GDP-α-D-rhamnose and GDP-β-L-fucose. In Aneurinibacillus thermoaerophilus L420-91T, this enzyme acts as a bifunctional enzyme, catalysing the above reaction as well as the reaction catalysed by EC 1.1.1.281, GDP-4-dehydro-6-deoxy-D-mannose reductase. Belongs to the short-chain dehydrogenase/reductase enzyme family, having homologous structures and a conserved catalytic triad of Lys, Tyr and Ser/Thr residues. Group: Enzymes. Synonyms: guanosine 5'-diphosphate-D-mannose oxidoreductase; guanosine diphosphomannose oxidoreductase; guanosine diphosphomannose 4,6-dehydratase; GDP-D-mannose dehydratase; GDP-D-mannose 4,6-dehydratase; Gmd; GDP-mannose 4,6-hydro-lyase; GDP-mannose 4,6-hydro-. Enzyme Commission Number: EC 4.2.1.47. CAS No. 37211-59-9. 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-5036; GDP-mannose 4,6-dehydratase; EC 4.2.1.47; 37211-59-9; guanosine 5'-diphosphate-D-mannose oxidoreductase; guanosine diphosphomannose oxidoreductase; guanosine diphosphomannose 4,6-dehydratase; GDP-D-mannose dehydratase; GDP-D-mannose 4,6-dehydratase; Gmd; GDP-mannose 4,6-hydro-lyase; GDP-mannose 4,6-hydro-lyase (GDP-4-dehydro-6-deoxy-D-mannose-forming). Cat No: EXWM-5036. | |
| GDP-mannose 6-dehydrogenase | Also acts on the corresponding deoxynucleoside diphosphate derivative as a substrate. Group: Enzymes. Synonyms: guanosine diphosphomannose dehydrogenase; GDP-mannose dehydrogenase; guanosine diphosphomannose dehydrogenase; guanosine diphospho-D-mannose dehydrogenase. Enzyme Commission Number: EC 1.1.1.132. CAS No. 37250-63-8. 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-0036; GDP-mannose 6-dehydrogenase; EC 1.1.1.132; 37250-63-8; guanosine diphosphomannose dehydrogenase; GDP-mannose dehydrogenase; guanosine diphosphomannose dehydrogenase; guanosine diphospho-D-mannose dehydrogenase. Cat No: EXWM-0036. | |
| GDP-mannose:cellobiosyl-diphosphopolyprenol α-mannosyltransferase | In the bacterium Gluconacetobacter xylinus (previously known as Acetobacter xylinum) the enzyme is involved in the biosynthesis of the exopolysaccharide acetan. In Xanthomonas campestris the enzyme is involved in the biosynthesis of the exopolysaccharide xanthan. Group: Enzymes. Synonyms: GumH; AceA; α1,3-mannosyltransferase AceA. Enzyme Commission Number: EC 2.4.1.252. 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-2482; GDP-mannose:cellobiosyl-diphosphopolyprenol α-mannosyltransferase; EC 2.4.1.252; GumH; AceA; α1,3-mannosyltransferase AceA. Cat No: EXWM-2482. | |
| GDP-Mannose pyrophosphorylase from Pyrococcus furiosus, Recombinant | In enzymology, a mannose-1-phosphate guanylyltransferase (EC 2.7.7.13) is an enzyme that catalyzes the chemical reaction: GTP + alpha-D-mannose 1-phosphate ? diphosphate + GDP-mannose. Thus, the two substrates of this enzyme are GTP and alpha-D-mannose 1-phosphate, whereas its two products are diphosphate and GDP-mannose. Group: Enzymes. Synonyms: GTP-mannose-1-phosphate guanylyltransferase; PIM-GMP; GDP-mannose pyrophosphorylase; guanosine 5'-diphospho-D-mannose pyrophosphorylase; guanosine diphosphomannose pyrophosphorylase; guanosine triphosphate-mannose 1-phosphate guanylyltransferase; mannose 1-phosphate guanylyltransferase (guanosine triphosphate); mannose-1-phosphate guanylyltransferase; EC 2.7.7.13. Enzyme Commission Number: EC 2.7.7.13. CAS No. 37278-24-3. Purity: min 95% by SDS-PAGE. GDP-Mannose pyrophosphorylase. Source: E. coli. Species: Pyrococcus furiosus. GTP-mannose-1-phosphate guanylyltransferase; PIM-GMP; GDP-mannose pyrophosphorylase; guanosine 5'-diphospho-D-mannose pyrophosphorylase; guanosine diphosphomannose pyrophosphorylase; guanosine triphosphate-mannose 1-phosphate guanylyltransferase; mannose 1-phosphate guanylyltransferase (guanosine triphosphate); mannose-1-phosphate guanylyltransferase; EC 2.7.7.13. Cat No: NATE-1504. | |
| GDP-perosamine N-acetyltransferase | D-Perosamine is one of several dideoxy sugars found in the O-antigen component of the outer membrane lipopolysaccharides of Gram-negative bacteria. Group: Enzymes. Synonyms: perB (gene name); GDP-α-D-perosamine N-acetyltransferase. Enzyme Commission Number: EC 2.3.1.227. 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-2174; GDP-perosamine N-acetyltransferase; EC 2.3.1.227; perB (gene name); GDP-α-D-perosamine N-acetyltransferase. Cat No: EXWM-2174. | |
| GDP-perosamine synthase | A pyridoxal 5'-phosphate enzyme. D-Perosamine is one of several dideoxy sugars found in the O-specific polysaccharide of the lipopolysaccharide component of the outer membrane of Gram-negative bacteria. The enzyme catalyses the final step in GDP-α-D-perosamine synthesis. Group: Enzymes. Synonyms: RfbE; GDP-4-keto-6-deoxy-D-mannose-4-aminotransferase; GDP-perosamine synthetase; PerA; GDP-4-amino-4,6-dideoxy-α-D-mannose:2-oxoglutarate aminotransferase. Enzyme Commission Number: EC 2.6.1.102. 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-2842; GDP-perosamine synthase; EC 2.6.1.102; RfbE; GDP-4-keto-6-deoxy-D-mannose-4-aminotransferase; GDP-perosamine synthetase; PerA; GDP-4-amino-4,6-dideoxy-α-D-mannose:2-oxoglutarate aminotransferase. Cat No: EXWM-2842. | |
| GDP polyribonucleotidyltransferase | The enzyme from rhabdoviruses transfers 5'-monophosphorylated (p-)mRNA from 5'-triphosphorylated (ppp-)mRNA to GDP to form 5'-capped mRNA (GpppmRNA) in a viral mRNA-start sequence-dependent manner. The (p-)mRNA transfer reaction proceeds through a covalent enzyme-pmRNA intermediate. Group: Enzymes. Enzyme Commission Number: EC 2.7.7.88. 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-3301; GDP polyribonucleotidyltransferase; EC 2.7.7.88. Cat No: EXWM-3301. | |
| GE20372 A | GE20372 A, a tetrapeptide, is produced by the strain of Streptomyces sp. It is used as a human immunodeficiency virus (HIV-L) protease inhibitor. Synonyms: GE20372 Factor A; GE-20372A; (1(S),2(S))-N2-(((1-Carboxy-2-(4-hydroxyphenyl)ethyl)amino)carbonyl)-L-arginyl-N-(1-formyl-2-phenylethyl)-L-valinamide. CAS No. 163565-75-1. Molecular formula: C30H41N7O7. Mole weight: 611.69. |  |
| GE20372 B | GE20372 B is a tetrapeptide produced by the strain of Streptomyces sp. It is used as a human immunodeficiency virus (HIV-L) protease inhibitor. Molecular formula: C30H41N7O7. Mole weight: 611.69. | |
| GE 2270A | GE 2270A is a thiopeptide antibiotic produced by the strain of Planobispora rosea. It inhibits bacterial protein synthesis and has anti-Gram-positive aerobic and anaerobic bacteria (MIC = 0.03-0.25 μg/mL) and Mycobacterium tuberculosis (MIC = 1 μg/mL) activities. Synonyms: Antibiotic GE 2270A; MDL 62879; Antibiotic MDL 62879; GE-2270A; GE-2270. CAS No. 134861-34-0. Molecular formula: C56H55N15O10S6. Mole weight: 1290.52. | |
| GE 23077A1 | A cyclic peptide antibiotic isolated from actinomadura sp. strain GE23077. It inhibits bacterial RNA polymerase. Synonyms: Antibiotic GE 23077A1; GE-23077-A1. CAS No. 435344-49-3. Molecular formula: C31H49N9O16. Mole weight: 803.77. | |
| Gear Clamps | Gear Clamps. Group: Polymers. |  |
| Gedatolisib | Gedatolisib (PKI-587) is a highly potent dual inhibitor of PI3Kα , PI3Kγ , and mTOR with IC 50 s of 0.4 nM, 5.4 nM and 1.6 nM, respectively [1]. Gedatolisib is equally effective in both complexes of mTOR, mTORC1 and mTORC2 [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PKI-587; PF-05212384. CAS No. 1197160-78-3. Pack Sizes: 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-10681. |  |
| Gedatolisib (PF-05212384, PKI-587) | Gedatolisib (PF-05212384, PKI-587) is a highly potent dual inhibitor of PI3Kα, PI3Kγ and mTOR with IC50 of 0.4 nM, 5.4 nM and 1.6 nM, respectively. Phase 2. Synonyms: PKI587; PKI-587; PKI 587; PF05212384; PF-05212384; PF 05212384; PF5212384; PF-5212384; PF 5212384; Gedatolisib. Grades: >98%. CAS No. 1197160-78-3. Molecular formula: C32H41N9O4. Mole weight: 615.73. | |
| Gedunin | Gedunin is a limonoid with anti-cancer, anti-viral, anti-inflammatory and insecticidal activities. Gedunin acts as a potent Hsp90 inhibitor and induces the degradation of Hsp90-dependent client proteins. Geduni may obstructs the entry of SARS-CoV-2 virus into human host cells and can be used for COVID-19 research [3]. Uses: Scientific research. Group: Natural products. CAS No. 2753-30-2. Pack Sizes: 1 mg; 5 mg. Product ID: HY-107577. | |
| Gedunin | Gedunin is a limonoid with anti-cancer, anti-viral, anti-inflammatory and insecticidal activities. Gedunin acts as a potent Hsp90 inhibitor and induces the degradation of Hsp90-dependent client proteins. Geduni may obstructs the entry of SARS-CoV-2 virus into human host cells and can be used for COVID-19 research. Group: Inhibitors. CAS No. 2753-30-2. Molecular formula: C28H34O7. Mole weight: 482.57. Purity: 0.98. Catalog: ACM2753302. |  |
| Gedunin | Gedunin Inhibitor. Uses: Scientific use. Product Category: T21883. CAS No. 2753-30-2. |  |
| Gedunin | Gedunin is a naturally occurring Hsp90 inhibitor. Induces Hsp90-dependent client protein degradation and displays antiproliferative activity in vitro (IC50 values are 3.22, 8.84 and 16.8 μM in SKBr3, MCF-7 and CaCo-2 cancer cell lines respectively). It also exhibits antimalarial activity against P. falciparum (IC50 values are 0.14 and 3.1 μM in parasite development and [3H]-hypoxanthine uptake assays respectively). Grades: >98%. CAS No. 2753-30-2. Molecular formula: C28H34O7. Mole weight: 482.57. | |
| Gedunin | Method for Determining Identity: Group: Biochemicals. Alternative Names: (1S, 3aS, 4aR, 4bS, 5R, 6aR, 10aR, 10bR, 12aS) -5- (Acetyloxy) -1- (3-furanyl) -1, 5, 6, 6a, 7, 10a, 10b, 11, 12, 12a, decahydro-4b, 7, 7, 10a, 12a, -pentamethyloxireno [c]phenanthro [1, 2-d]pyran-3, 8 (3aH, 4bH) -dione. Grades: Purified. CAS No. 2753-30-2. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| Gefapixant | Gefapixant is an orally active and potent purinergic P2X3 receptor ( P2X3R ) antagonist, with IC 50 values of ~30 nM versus recombinant hP2X3 homotrimers and 100-250 nM at hP2X2/3 heterotrimeric receptors. Gefapixant can be used for the research of chronic cough and knee osteoarthritis [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MK-7264; AF-219. CAS No. 1015787-98-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101588. | |
| Gefapixant | Gefapixant is a P2X3 receptor (P2X3R) antagonist with IC50s of ~30 nM versus recombinant hP2X3 homotrimers and 100-250 nM at hP2X2/3 heterotrimeric receptors. It is under a clinical trial for the treatment of chronic cough. Synonyms: AF-219; MK-7264. CAS No. 1015787-98-0. Molecular formula: C14H19N5O4S. Mole weight: 353.4. | |
| Gefapixant | Gefapixant. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1015787-98-0. Molecular Formula: C14H19N5O4S. Mole Weight: 353.4. Catalog: APB1015787980. |  |
| Gefapixant citrate | Gefapixant citrate is an orally active and potent purinergic P2X3 receptor ( P2X3R ) antagonist, with IC 50 values of ~30 nM versus recombinant hP2X3 homotrimers and 100-250 nM at hP2X2/3 heterotrimeric receptors. Gefapixant citrate can be used for the research of chronic cough and knee osteoarthritis [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MK-7264 citrate; AF-219 citrate. CAS No. 2310299-91-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101588A. | |
| Gefapixant Impurity 1 | Gefapixant Impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 865304-71-8. Molecular Formula: C14H18N4O2. Mole Weight: 274.32. Catalog: APB865304718. | |
| Gefapixant Impurity 2 | Gefapixant Impurity 2. Uses: For analytical and research use. Group: Impurity standards. CAS No. 2413718-92-8. Molecular Formula: C14H18N4O4S. Mole Weight: 338.38. Catalog: APB2413718928. | |
| Gefapixant Impurity 7 | Gefapixant Impurity 7. Uses: For analytical and research use. Group: Impurity standards. CAS No. 2527107-23-7. Molecular Formula: C20H25N5O3. Mole Weight: 383.45. Catalog: APB2527107237. | |
| Gefapixant Impurity 8 | Gefapixant Impurity 8. Uses: For analytical and research use. Group: Impurity standards. CAS No. 2527107-24-8. Molecular Formula: C20H25N5O3. Mole Weight: 383.45. Catalog: APB2527107248. | |
| Gefarnate | Gefarnate. Group: Biochemicals. Alternative Names: Geranyl farnesylacetate. Grades: Highly Purified. CAS No. 51-77-4. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C27H44O2. US Biological Life Sciences. | Worldwide |
| Gefarnate | Gefarnate is a drug used for the treatment of gastritis and gastric ulcer, in vivo, the instillation of gefarnate reduced corneal epithelial damage from desiccation in a dose-dependent fashion. Besides Gefarnate has been proposed for use in the treatment of dry eye syndrome. Synonyms: [(2E)-3,7-dimethylocta-2,6-dienyl] (4E,8E)-5,9,13-trimethyltetradeca-4,8,12-trienoate; Farnesylacetate, Geranyl; Gefarnate; Gefarnil; Gepharnate; Geranyl Farnesylacetate; Ulco. CAS No. 51-77-4. Molecular formula: C27H44O2. Mole weight: 400.64. | |
| Gefarnate | Gefarnate is a agent used for the treatment of gastritis and gastric ulcer, and has been proposed for use in the treatment of dry eye syndrome. Uses: Scientific research. Group: Signaling pathways. CAS No. 51-77-4. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-B2206. | |
| Gefitinib | Gefitinib (ZD1839) is a potent, selective and orally active EGFR tyrosine kinase inhibitor with an IC 50 of 33 nM. Gefitinib selectively inhibits EGF-stimulated tumor cell growth (IC 50 of 54 nM) and that blocks EGF-stimulated EGFR autophosphorylation in tumor cells. Gefitinib also induces autophagy and cell apoptosis , which can be used for cancer related research, such as Lung cancer and breast cancer [1] [2] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ZD1839. CAS No. 184475-35-2. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-50895. | |
| Gefitinib | 100mg Pack Size. Group: Bioactive Small Molecules, Biochemicals, Research Organics & Inorganics. Formula: C22H24ClFN4O3. CAS No. 184475-35-2. Prepack ID 57220562-100mg. Molecular Weight 446.9. See USA prepack pricing. |  |
| Gefitinib | Gefitinib. Group: Biochemicals. Grades: Highly Purified. CAS No. 184475-35-2. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C22H24ClFN4O3. US Biological Life Sciences. | Worldwide |
| Gefitinib 3,4-Difluoro Impurity HCl | Grades: > 95%. CAS No. 184475-68-1. Molecular formula: C22H25F2N4O3Cl. Mole weight: 466.92. | |
| Gefitinib 4-Desfluoro Impurity HCl | Grades: > 95%. Molecular formula: C22H26Cl2N4O3. Mole weight: 465.38. | |
| Gefitinib Chloro Impurity | Grades: > 95%. Molecular formula: C16H21Cl2N3O3. Mole weight: 374.27. | |
| Gefitinib-d3 | Labeled Gefitinib. Gefitinib is an antineoplastic. Group: Biochemicals. Alternative Names: N-(3-Chloro-4-fluorophenyl)-7-(methoxy-d3)-6-[3-(4-morpholinyl)propoxy]-4-quinazolinamine; Iressa-d3; ZD 1839-d3. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Gefitinib-d3 | 2H Labeled Compounds. CAS No. 1173976-40-3. Molecular formula: C22H21D3ClFN4O3. Mole weight: 449.92. Catalog: ACM1173976403. | |
| Gefitinib-D6 | Gefitinib-D6. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1228664-49-0. Molecular Formula: C22H18D6ClFN4O3. Mole Weight: 452.94. Catalog: APB1228664490. | |
| Gefitinib-D8 | Gefitinib-D8. Uses: For analytical and research use. Group: Impurity standards. CAS No. 857091-32-8. Molecular Formula: 22H16D8ClFN4O3. Mole Weight: 454.96. Catalog: APB857091328. | |
| Gefitinib Difluoro Impurity | Gefitinib Difluoro Impurity. Uses: For analytical and research use. Group: Impurity standards. CAS No. 184475-50-1. Molecular Formula: C22H24F2N4O3. Mole Weight: 430.46. Catalog: APB184475501. | |
| Gefitinib Dihydrochloride | Gefitinib Dihydrochloride. Uses: For analytical and research use. Group: Impurity standards. CAS No. 184475-56-7. Molecular Formula: C22H26Cl3FN4O3. Mole Weight: 519.82. Catalog: APB184475567. | |
| Gefitinib EP Impurity B | Gefitinib EP Impurity B. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1603814-04-5. Molecular Formula: C22H24ClFN4O3. Mole Weight: 446.91. Catalog: APB1603814045. | |
| Gefitinib, Free Base (Iressa) | EGFR tyrosine kinase inhibitor that binds to the ATP-binding site of the enzyme. The functions of the EGFR tyrosine kinase in activating the Ras signal transduction cascade and malignant cell growth are thus inhibited. It has been shown that a mutation in the EGFR tyrosine kinase domain is responsible for activating anti-apoptotic pathways in gefitinib-sensitive non-small cell lung cancers. These mutations tend to increase sensitivity to tyrosine kinase inhibitors including gefitinib and erlotinib. The adenocarcinoma subset of non-small cell lung cancer histologies often have these mutations, which are commonly found in Asians, women, and non-smokers. Group: Biochemicals. Grades: Highly Purified. CAS No. 184475-35-2. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Gefitinib hydrochloride | Gefitinib hydrochloride (ZD1839 hydrochloride) is a potent, selective and orally active EGFR tyrosine kinase inhibitor with an IC 50 of 33 nM. Gefitinib hydrochloride selectively inhibits EGF-stimulated tumor cell growth (IC 50 of 54 nM) and that blocks EGF-stimulated EGFR autophosphorylation in tumor cells. Gefitinib hydrochloride also induces autophagy. Gefitinib hydrochloride has antitumour activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ZD-1839 hydrochloride. CAS No. 184475-55-6. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-50895A. | |
| Gefitinib hydrochloride | Gefitinib Hcl(ZD-1839 Hcl) is an EGFR inhibitor, which interrupts signaling through the epidermal growth factor receptor (EGFR) in target cells. Synonyms: Iressa hydrochloride; ZD 1839 hydrochloride; ZD-1839 hydrochloride; ZD1839 hydrochloride. Grades: >98%. CAS No. 184475-55-6. Molecular formula: C22H25Cl2FN4O3. Mole weight: 483.36. | |
| Gefitinib Hydrochloride | Gefitinib Hydrochloride. Uses: For analytical and research use. Group: Impurity standards. CAS No. 184475-55-6. Molecular Formula: C22H25Cl2FN4O3. Mole Weight: 483.37. Catalog: APB184475556. | |
| Gefitinib Hydrolysate Precursor (HCl) | Gefitinib Hydrolysate Precursor (HCl). Uses: For analytical and research use. Group: Impurity standards. CAS No. 184475-70-5. Molecular Formula: C17H14Cl2FN3O3. Mole Weight: 398.22. Catalog: APB184475705. | |
| Gefitinib Impurity | Cas No. 13794-72-4. | |
| Gefitinib impurity 1 | Gefitinib impurity 1. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 4-chloro-7-methoxyquinazolin-6-ol. CAS No. 574745-95-4. Molecular Formula: C9H7ClN2O2. Mole Weight: 210.62. Catalog: APB574745954. | |
| Gefitinib Impurity 1 | Gefitinib Impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1561173-24-7. Molecular Formula: C15H22ClN3O3. Mole Weight: 327.81. Catalog: APB1561173247. | |
| Gefitinib Impurity 1 | Synonyms: 2-Amino-4-methoxy-5-(3-morpholin-4-ylpropoxy)-benzamide. Grades: > 95%. CAS No. 246512-44-7. Molecular formula: C15H23N3O4. Mole weight: 309.37. | |
| Gefitinib Impurity 10 | Gefitinib Impurity 10. Uses: For analytical and research use. Group: Impurity standards. CAS No. 690206-97-4. Molecular Formula: C16H13ClFN3O2. Mole Weight: 333.75. Catalog: APB690206974. | |
| Gefitinib Impurity 11 | Gefitinib Impurity 11. Uses: For analytical and research use. Group: Impurity standards. CAS No. 16064-25-8. Molecular Formula: C8H6N2O2. Mole Weight: 162.15. Catalog: APB16064258. | |
| Gefitinib Impurity 12 | Gefitinib Impurity 12. Uses: For analytical and research use. Group: Impurity standards. CAS No. 385784-71-4. Molecular Formula: C15H19N3O5. Mole Weight: 321.33. Catalog: APB385784714. | |
| Gefitinib Impurity 13 | Gefitinib Impurity 13. Uses: For analytical and research use. Group: Impurity standards. CAS No. 215659-03-3. Molecular Formula: C9H9NO6. Mole Weight: 227.17. Catalog: APB215659033. | |
| Gefitinib Impurity 15 | Gefitinib Impurity 15. Uses: For analytical and research use. Group: Impurity standards. CAS No. 847949-50-2. Molecular Formula: C22H25ClN4O4. Mole Weight: 444.92. Catalog: APB847949502. | |
| Gefitinib Impurity 19 | Gefitinib Impurity 19. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1803045-02-4. Molecular Formula: C22H24ClFN4O4. Mole Weight: 462.91. Catalog: APB1803045024. | |
| Gefitinib Impurity 2 | Cas No. 675126-26-8. | |
| Gefitinib Impurity 23 | Gefitinib Impurity 23. Uses: For analytical and research use. Group: Impurity standards. CAS No. 675126-28-0. Molecular Formula: C15H20N2O3. Mole Weight: 276.34. Catalog: APB675126280. | |
| Gefitinib Impurity 24 | Gefitinib Impurity 24. Uses: For analytical and research use. Group: Impurity standards. CAS No. 194423-17-1. Molecular Formula: C10H12N4. Mole Weight: 188.23. Catalog: APB194423171. | |
| Gefitinib Impurity 25 | Gefitinib Impurity 25. Uses: For analytical and research use. Group: Impurity standards. CAS No. 214472-41-0. Molecular Formula: C16H24N2O5. Mole Weight: 324.38. Catalog: APB214472410. | |
| Gefitinib Impurity 26 | Gefitinib Impurity 26. Uses: For analytical and research use. Group: Impurity standards. CAS No. 193552-54-4. Molecular Formula: C18H16O6. Mole Weight: 328.32. Catalog: APB193552544. | |
| Gefitinib Impurity 28 | Gefitinib Impurity 28. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1379208-77-1. Molecular Formula: C8H6N2O4. Mole Weight: 194.15. Catalog: APB1379208771. | |
| Gefitinib impurity 29 | Gefitinib impurity 29. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: N-(3-chloro-4-fluorophenyl)-7-methoxy-6-(3-morpholinopropoxy)quinazolin-4-amine. CAS No. 184475-35-2. Molecular Formula: C22H24ClFN4O3. Mole Weight: 446.9. Catalog: APB184475352. | |
| Gefitinib Impurity 3 | Grades: > 95%. Molecular formula: C15H22N2O5. Mole weight: 310.35. | |
Our database is helping our users find suppliers everyday.
