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| Product | Description | |
|---|---|---|
| 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. | |
| GeA-69 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Gear Clamps | Gear Clamps. Group: Polymers. |  |
| Gebapentine USP | (3-Methacryoyloxypropyl)-trimethoxysilane; 1-(Aminomethyl)cyclohexaneacetic acid; gabapentin; Neurontin. antidepressant. Grades: USP. CAS No. 60142-96-3. Product ID: 8-01590. Molecular formula: C9H17NO2. Mole weight: 171.23. Purity: ³98%. Reference: J. Clin. Psychiatry 63,:331, 2002. |  |
| 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 | 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 |
| 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. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. CAS No. 2753-30-2. Molecular formula: C28H34O7. Mole weight: 482.57. Purity: 0.98. Product ID: ACM2753302. Alfa Chemistry ISO 9001:2015 Certified. |  |
| 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 | 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. | |
| 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 | 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 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. | |
| 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. | |
| 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. | |
| Gefitinib | Gefitinib. CAS No. 184475-35-2. Product ID: 8-04227. Molecular formula: C30H35N7O4S. Mole weight: 589.71. | |
| Gefitinib | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopyapi standardseuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: N-(3-Chloro-4-fluorophenyl)-7-methoxy-6-[3-(4-morpholinyl)propoxy]-4-quinazolinamine, (3-Chloro-4-fluorophenyl)[7-methoxy-6-[3-(morpholin-4-yl)propoxy]quinazolin-4-yl]amine, ZD1839, Gefonib, Iressa, ZD 1839, Gefitinib, 4-(3'-Chloro-4'-fluoroanilino)-7-methoxy-6-(3-morpholinopropoxy)quinazoline, 4-(3-Chloro-4-fluorophenylamino)-7-methoxy-6-[3-(4-morpholinyl)propoxy]quinazoline. | |
| 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 | Gefitinib. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 4-Chloro-6-[3-(4-morpholinyl)propoxy]-4-quinazoline;4-Chloro-7-methoxy-6-(3-morpholinopropoxy)quinazoline;4-Chloro-7-methoxy-6-[3-(morpholin-4-yl)propoxy]quinazoline. Product Category: Heterocyclic Organic Compound. CAS No. 199327-59-8. Molecular formula: C16H20ClN3O3. Mole weight: 0. Product ID: ACM199327598. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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 | 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 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-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, 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 Impurity | Cas No. 13794-72-4. | |
| 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 2 | Cas No. 675126-26-8. | |
| Gefitinib Impurity 3 | Grades: > 95%. Molecular formula: C15H22N2O5. Mole weight: 310.35. | |
| Gefitinib Impurity 34 | Gefitinib Impurity 34. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 3-(3-chloropropoxy)-4-methoxybenzonitrile. CAS No. 1315512-60-7. Molecular formula: C11H12ClNO2. Mole weight: 225.67. Catalog: APB1315512607. | |
| Gefitinib Impurity 35 | Gefitinib Impurity 35. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 5-(3-bromopropoxy)-4-methoxy-2-nitrobenzonitrile. CAS No. 1325726-60-0. Molecular formula: C11H11BrN2O4. Mole weight: 315.12. Catalog: APB1325726600. | |
| Gefitinib Impurity 43 | Gefitinib Impurity 43. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 5-(3-chloropropoxy)-4-methoxy-2-nitrobenzaldehyde. CAS No. 1072107-50-6. Molecular formula: C11H12ClNO5. Mole weight: 273.67. Catalog: APB1072107506. | |
| Gefitinib impurity F | Gefitinib impurity F. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: N-(3-chloro-4-fluorophenyl)-6,7-dimethoxyquinazolin-4-amine. CAS No. 153437-78-6. Molecular formula: C16H13ClFN3O2. Mole weight: 333.74. Catalog: APB153437786. | |
| Gefitinib Impurity HCl | Synonyms: 3-Deschloro-4-Desfluoro-4-Chloro-3-Fluoro Gefitinib HCl. Grades: > 95%. Molecular formula: C22H25Cl2FN4O3. Mole weight: 483.37. | |
| Gefitinib Impurity I | Grades: > 95%. Molecular formula: C29H37ClFN5O4. Mole weight: 574.10. | |
| Gefitinib Impurity II | Synonyms: N-(3-chloro-4-fluorophenyl)-6 ,7-dimethoxyquinazolin-4-amine. Grades: > 95%. CAS No. 153437-78-6. Molecular formula: C16H13ClFN3O2. Mole weight: 333.75. | |
| Gefitinib Impurity IV | Grades: > 95%. Molecular formula: C22H24Cl2N4O3. Mole weight: 463.37. | |
| Gefitinib impurity K | Gefitinib impurity K. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 4-methoxy-3-(3-morpholinopropoxy)-2-nitrobenzonitrile. CAS No. 1006378-06-8. Molecular formula: C15H19N3O5. Mole weight: 321.33. Catalog: APB1006378068. | |
| Gefitinib Impurity VI | Gefitinib Impurity VI is Gefitinib intermediate. Synonyms: 4-(3-Chloropropyl)morpholine; 1-Chloro-3-morpholinopropane; 3-(Morpholin-4-yl)propyl Chloride; 3-Chloro-1-(morpholin-4-yl)propane; 3-Morpholinopropyl Chloride; NSC 28831; NSC 38889; N-(3-Chloropropyl)morpholine. Grades: > 95%. CAS No. 7357-67-7. Molecular formula: C7H14ClNO. Mole weight: 163.65. | |
| Gefitinib Impurity VII | An impurity of Gefitinib. Gefitinib is an EGFR inhibitor. It is used for the treatment of certain breast, lung and other cancers. Synonyms: 3,4-Dihydro-4-oxo-6-acetoxy-7-methoxyquinazoline; 6-(Acetyloxy)-7-methoxy-4(3H)-quinazolinone; 3,4-Dihydro-7-methoxy-4-oxoquinazolin-6-yl acetate; Gefitinib interMidiate IV; 7-Methoxy-4-oxo-3,4-dihydroquinazolin-6-yl acetate. Grades: > 95%. CAS No. 179688-53-0. Molecular formula: C11H10N2O4. Mole weight: 234.21. | |
| Gefitinib Impurity VIII | Synonyms: 4-[(3-Chloro-4-fluorophenyl)amino]-7-methoxy-6-quinazolinol 6-acetate; 4-(3-Chloro-4-fluorophenylamino)-7-methoxyquinazolin-6-yl acetate; 6-Quinazolinol,4-[(3-chloro-4-fluorophenyl)amino]-7-methoxy-, 6-acetate; Gefitinib intermediate VI. Grades: > 95%. CAS No. 788136-89-0. Molecular formula: C17H13ClFN3O3. Mole weight: 361.76. | |
| Gefitinib Impurity X | Synonyms: 6-Acetoxy-4-chloro-7-methoxyquinazoline; 4-Chloro-6-acetoxy-7-methoxyquinazoline; 4-Chloro-7-methoxy-6-quinazolinol 6-acetate; Gefitinib interMediate V; 6-Quinazolinol, 4-chloro-7-Methoxy-, 6-acetate; N-(3-chloro-4-fluorophenyl)-7-methoxy-6-(3-morpholinopropox. Grades: > 95%. CAS No. 230955-75-6. Molecular formula: C11H9ClN2O3. Mole weight: 252.66. | |
| Gefitinib (Iressa) | Gefitinib (Iressa). Group: Biochemicals. Alternative Names: Iressa. Grades: Highly Purified. CAS No. 184475-35-2. Pack Sizes: 500mg. US Biological Life Sciences. | Worldwide |
| Gefitinib N-Oxide | Gefitinib N-oxide is the N-oxide derivative of Gefitinib. Synonyms: Gefitinib Morpholine N-oxide; N-(3-Chloro-4-fluorophenyl)-7-methoxy-6-[3-(4-oxido-4-morpholinyl)propoxy]-4-quinazolinamine; 4-(3-((4-((3-chloro-4-fluorophenyl)amino)-7-methoxyquinazolin-6-yl)oxy)propyl)morpholine 4-oxide. Grades: > 95%. CAS No. 847949-51-3. Molecular formula: C22H24ClFN4O4. Mole weight: 462.91. | |
| Gefurulimab | Gefurulimab (ALXN-1720) is a human-derived bispecific antibody against complement C5 and albumin that binds C5 and blocks its activation [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: ALXN-1720. CAS No. 2456407-94-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99638. | |
| geissoschizine dehydrogenase | Involved in the interconversion of heteroyohimbine alkaloids in Catharanthus roseus. Group: Enzymes. Enzyme Commission Number: EC 1.3.1.36. CAS No. 84399-94-0. 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-1308; geissoschizine dehydrogenase; EC 1.3.1.36; 84399-94-0. Cat No: EXWM-1308. | |
| Gelastatin A | It is produced by the strain of Westerdykella multispora F50733. It can inhibit the activity of leucinase A and the IC50 of leucinase A is 0.63 μmol/L. Synonyms: (all-E)-5-(2,4-Hexadienylidene)-5,6-dihydro-2-oxo-2H-pyran-3-propanoic acid. Grades: ≥98%. Molecular formula: C14H16O4. Mole weight: 248.27. | |
| Gelatin | Gelatin. CAS No. 9000-70-8. Product ID: PE-0255. Category: Drop Pill Base. Product Keywords: Pharmaceutical Excipients; Semi-solid Dosage Form; Drop Pill Base; Gelatin; PE-0255; 9000-70-8; 9000-70-8. EC Number: 232-554-6. |  |
| Gelatin | Gelatin. CAS No. 9000-70-8. Product ID: PE-0167. Category: Filler. Product Keywords: Pharmaceutical Excipients; Solid Dosage Form; Capsule Excipients; Filler; Gelatin; PE-0167; 9000-70-8; 9000-70-8. EC Number: 232-554-6. | |
| Gelatin | Gelatin. CAS No. 9000-70-8. Product ID: PE-0140. Category: Binder Excipients. Product Keywords: Pharmaceutical Excipients; Solid Dosage Form; Binder Excipients; Gelatin; PE-0140; 9000-70-8; 9000-70-8. EC Number: 232-554-6. | |
| Gelatin | Gelatin occurs as a light-amber to faintly yellow-colored, vitreous, brittle solid. It is practically odorless and tasteless, and is available as translucent sheets, flakes, and granules, or as a coarse powder. Synonyms: Byco; Cryogel; E441; gelatina; gelatine; Instagel; Kolatin; Solugel; Vitagel. CAS No. 9000-70-8. Product ID: PE-0070. Category: Coating Agents; Film-forming Agents; Gelling Agents; Suspending Agents; Tablet Binder; Viscosity-increasing Agents. Product Keywords: Binder Excipients; Suspending Agents; PE-0070; Gelatin; Coating Agents; Film-forming Agents; Gelling Agents; Suspending Agents; Tablet Binder; Viscosity-increasing Agents; ; 9000-70-8. UNII: 2G86QN327L. Chemical Name: Gelatin. Grade: Pharmceutical Excipients. Administration route: Dental; inhalations; injections; oral; topical and vaginal. Dosage Form: Dental preparations; inhalations; injections; oral capsules, pastilles, solutions, syrups and tablets; topical and vaginal preparations. Stability and Storage Conditions: Dry gelatin is stable in air. Aqueous gelatin solutions are also stable for long periods if stored under cool conditions but they are subject to bacterial degradation. At temperatures above about 50°C, aqueous gelatin solutions may undergo slow depolymerization and a reduction in gel strength may occur on resetting. Depolymerization becomes more rapid at temperatures above 65°C, and gel strength may be reduced by half when a solution i | |
| Gelatin | Gelatin. CAS No. 9000-70-8. Product ID: PE-0022. Category: Emulsifier Excipients. Product Keywords: Pharmaceutical Excipients; Liquid Dosage Form; Semi-solid Dosage Form; Suppository Bases;Micro-drug Delivery Systems; Emulsifier Excipients; Gelatin; PE-0022; 9000-70-8; 9000-70-8. EC Number: 232-554-6. | |
| Gelatin | Gelatin. Uses: Designed for use in research and industrial production. Product Category: 3D Printing Materials for Research and Development. CAS No. 9000-70-8. Purity: PURIFIED. Product ID: ACM9000708-3. Alfa Chemistry ISO 9001:2015 Certified. | |
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