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 | |
|---|---|---|
| Panitumumab | Panitumumab (ABX-EGF) is a fully human IgG2 anti- EGFR monoclonal antibody with anti-tumor activity. Panitumumab inhibits tumor cell proliferation, survival and angiogenesis. Panitumumab can be used in the research of cancers, such as colon cancer [1] [2] [4]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: ABX-EGF. CAS No. 339177-26-3. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P99041. |  |
| Panitumumab | Panitumumab is a humanized monoclonal antibody that binds to epidermal growth factor receptor (EGFR), which is often overexpressed in colorectal cancers. Combination of Panitumumab and EGFR reduces cell proliferation therefore inhibits colorectal cancers. It was approved for the treatment of EGFR-expressing metastatic colorectal cancer. Uses: The treatment of egfr-expressing metastatic colorectal cancer. Synonyms: Abenix; Abx-egf; Vectibix; Abx-egf mab; Unii-6A901E312a; Immunoglobulin, anti-(human epidermal growth factor receptor) (human monoclonal abx-egf heavy chain), disulfide with human monoclonal abx-egf light chain, dimer. CAS No. 339177-26-3. Molecular formula: C6398H9878N1694O2016S48. Mole weight: 144324.12. |  |
| Pannaric acid | Synonyms: 3,9-dihydroxy-1,7-dimethyldibenzo[b,d]furan-2,6-dicarboxylic acid; 2,6-Dibenzofurandicarboxylic acid, 3,9-dihydroxy-1,7-dimethyl-; Pannarsaeure. CAS No. 479-46-9. Molecular formula: C16H12O7. Mole weight: 316.26. | |
| Pannaric acid 6-methyl ester | Pannaric acid 6-methyl ester is a metabolite from the lichen leproloma diffusum. Molecular formula: C17H14O7. Mole weight: 330.29. | |
| Pannarin | It is a lichen metabolite isolated from several Psoroma species. Synonyms: 8-chloro-9-hydroxy-3-methoxy-1,4,7-trimethyl-6-oxobenzo[b][1,4]benzodioxepine-10-carbaldehyde; Pannarine; NSC 646008; 11H-Dibenzo(b,e)(1,4)dioxepin-4-carboxaldehyde, 2-chloro-3-hydroxy-8-methoxy-1,6,9-trimethyl-11-oxo-. CAS No. 55609-84-2. Molecular formula: C18H15ClO6. Mole weight: 362.76. | |
| Pannorin | Pannorin. Uses: Designed for use in research and industrial production. Additional or Alternative Names: pannorin;4,8,10-Trihydroxy-5-methyl-2H-naphtho[1,2-b]pyran-2-one. Product Category: Heterocyclic Organic Compound. CAS No. 137023-81-5. Molecular formula: C14H10O5. Product ID: ACM137023815. Alfa Chemistry ISO 9001:2015 Certified. Categories: Pandorina kutija. |  |
| Panobacumab | Panobacumab is a human monoclonal antibody with antibacterial activity against Pseudomonas aeruginosa. Synonyms: KBPA101. CAS No. 885053-97-4. | |
| Panobacumab | Panobacumab (KBPA101) is a fully human IgM/κ monoclonal antibody generated by immortalizing human B lymphocytes against the LPS O polysaccharide of serotype O11 of P. aeruginosa [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: KBPA101. CAS No. 885053-97-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99214. | |
| Panobinostat | Panobinostat is a cinnamic hydroxamic acid analogue with potential antineoplastic activity. Panobinostat selectively inhibits histone deacetylase (HDAC), inducing hyperacetylation of core histone proteins, which may result in modulation of cell cycle protein expression, cell cycle arrest in the G2/M phase and apoptosis. In addition, this agent appears to modulate the expression of angiogenesis-related genes, such as hypoxia-inducible factor-1alpha (HIF-1a) and vascular endothelial growth factor (VEGF), thus impairing endothelial cell chemotaxis and invasion. HDAC is an enzyme that deacetylates chromatin histone proteins. Uses: Antineoplastic agents. Synonyms: LBH589; LBH 589; LBH-589; NVP-LBH589; NVP-LBH 589; Panobinostat; trade name Farydak. Grades: >98%. CAS No. 404950-80-7. Molecular formula: C21H23N3O2. Mole weight: 349.434. | |
| Panobinostat | Panobinostat. Group: Biochemicals. Alternative Names: (2E) -N-Hydroxy-3- [4- [ [ [2- (2-methyl-1H-indol-3-yl) ethyl] amino] methyl] phenyl] -2-propenamide. Grades: Highly Purified. CAS No. 404950-80-7. Pack Sizes: 25mg, 50mg, 100mg, 250mg, 500mg. Molecular Formula: C21H23N3O2. US Biological Life Sciences. |  Worldwide |
| Panobinostat | Panobinostat (LBH589; NVP-LBH589) is a potent and orally active non-selective HDAC inhibitor, and has antineoplastic activities [1] [2]. Panobinostat induces HIV-1 virus production even at low concentration range 8-31 nM, stimulates HIV-1 expression in latently infected cells [4]. Panobinostat induces cell apoptosis and autophagy. Panobinostat can be used for the study of refractory or relapsed multiple myeloma [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LBH589; NVP-LBH589. CAS No. 404950-80-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-10224. | |
| Panobinostat Carboxylic Acid Methyl Ester Hydrochloride | Intermediate in the preparation of Panobinostat. Group: Biochemicals. Alternative Names: (2E) -3- [4- [ [ [2- (2-Methyl-1H-indol-3-yl) ethyl] amino] methyl] phenyl] -2-propenoic Acid Methyl Ester, Hydrochloride. Grades: Highly Purified. CAS No. 441741-66-8. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Panobinostat lactate | Panobinostat lactate is a potent and orally active non-selective HDAC inhibitor. Panobinostat lactate has antineoplastic activities. Panobinostat lactate effectively disrupts HIV latency. Panobinostat lactate induces cell apoptosis and autophagy. Panobinostat lactate can be used for the study of refractory or relapsed multiple myeloma [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LBH589 lactate; NVP-LBH589 lactate. CAS No. 960055-56-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10224A. | |
| Panobinostat (LBH-589, LBH589, LBN-589, NVP-LBH589) | Panobinostat (LBH589) is a highly potent inhibitor of both histone deacetylase 1 (HDAC1) activity and tumor cell proliferation in vitro. The IC50 values of HDAC isozymes HDAC1-IP Ac-H4, HDAC8, MALunselective, B61HDAC1 and B12HDAC6 are 0.23±0.06, 283±29, 75±4, 47±5 and 89±12nm, respectively. And to A2780 proliferation, IC50 value is 4.6±1.8nm. Group: Biochemicals. Grades: Highly Purified. CAS No. 404950-80-7. Pack Sizes: 1mg, 5mg. US Biological Life Sciences. | Worldwide |
| Panomifene | Panomifene is an Estrogen receptor antagonist under the development of Egis Pharmaceuticals. Phase II clinical trials for the treatment of breast cancer was discontinued. Uses: Breast cancer. Synonyms: GYKI-13504; GYKI 13504; GYKI13504; EGIS-5650; EGIS5650; EGIS 5650; PAN; Panomifene; 2-[[2-[4-[(1E)-3,3,3-Trifluoro-1,2-diphenyl-1-propen-1-yl]phenoxy]ethyl]amino]-ethanol; (E)-2-[[2-[4-(3,3,3-Trifluoro-1,2-diphenyl-1-propenyl)phenoxy]ethyl]amino]-ethanol; 2-[[2-[4-[(1E)-3,3,3-Trifluoro-1,2-diphenyl-1-propenyl]phenoxy]ethyl]amino]-ethanol; EGIS 5660; GYKI 13504. Grades: 95%. CAS No. 77599-17-8. Molecular formula: C25H24F3NO2. Mole weight: 427.46. | |
| Panose | a-D-glucopyranosyl-1,6-a-D-glucopyranosyl-1,4-D-glucose, 4-a-Isomaltosylglucose. CAS No. 33401-87-5. Product ID: 3-00042. Molecular formula: C18H32O16. Mole weight: 504.44. Purity: 0.98. |  |
| Panosialin A | It is produced by the strain of Str. sp OH-5186. It can inhibit α,β-glucosidase and mannose glycosidase. It can inhibit the influenza virus and has weak anti-microbial effect. Synonyms: Panosialin I; 1,3-Benzenediol, 5-(13-methyltetradecyl)-, bis(hydrogen sulfate). Molecular formula: C21H36O8S2. Mole weight: 480.63. | |
| Panosialin B | It is produced by the strain of Str. sp OH-5186. It can inhibit α,β-glucosidase and mannose glycosidase. It does not inhibit the influenza virus, but it has weak anti-microbial effect. Synonyms: 5-Pentadecylresorcinol 1,3-bissulfuric acid; Panosialin II; Panosialin-IA; Resorcinol, 5-pentadecyl-, disulfate (ester); 5-Pentadecyl-1,3-phenylenbis(hydrogensulfat). Molecular formula: C21H36O8S2. Mole weight: 480.63. | |
| Panosialin C | It is produced by the strain of Str. sp OH-5186. It can inhibit α,β-glucosidase and mannose glycosidase. It does not inhibit the influenza virus, but it has weak anti-microbial effect. Synonyms: 5-(14-Methylpentadecyl)resorcinol 1,3-bissulfuric acid; Panosialin III. Molecular formula: C22H38O8S2. Mole weight: 494.66. | |
| Panosialin D | It is produced by the strain of Str. sp OH-5186. It can inhibit α,β-glucosidase and mannose glycosidase. It does not inhibit the influenza virus, but it has weak anti-microbial effect. Synonyms: 5-(13-methylpentadecyl)-1,3-phenylene bis(hydrogen sulfate); 1,3-Benzenediol, 5-(13-methylpentadecyl)-, bis(hydrogen sulfate); Panosialin ?. Molecular formula: C22H38O8S2. Mole weight: 494.66. | |
| Panosialin wA | It is produced by the strain of Str. sp OH-5186. It can inhibit α,β-glucosidase and mannose glycosidase. It does not inhibit the influenza virus, it has weak anti-microbial effect. Molecular formula: C21H36O5S. Mole weight: 400.57. | |
| Panosialin wB | It is produced by the strain of Str. sp OH-5186. It can inhibit α,β-glucosidase and mannose glycosidase. It does not inhibit the influenza virus, it has weak anti-microbial effect. Molecular formula: C21H36O5S. Mole weight: 400.57. | |
| Panosialin wC | It is produced by the strain of Str. sp OH-5186. It can inhibit α,β-glucosidase and mannose glycosidase. It does not inhibit the influenza virus, it has weak anti-microbial effect. Molecular formula: C22H38O5S. Mole weight: 414.60. | |
| Panosialin wD | It is produced by the strain of Str. sp OH-5186. It can inhibit α,β-glucosidase and mannose glycosidase. It does not inhibit the influenza virus, it has weak anti-microbial effect. Molecular formula: C22H38O5S. Mole weight: 414.60. | |
| Panowamycin A | Panowamycins A is a new antitrypanosomal isochromans produced by the strain of Streptomyces sp. K07-0010. CAS No. 1375224-55-7. Molecular formula: C17H24O3. Mole weight: 276.37. | |
| Panowamycin B | Panowamycins B is a new antitrypanosomal isochromans produced by the strain of Streptomyces sp. K07-0010. CAS No. 1375224-56-8. Molecular formula: C17H26O3. Mole weight: 278.39. | |
| Pan-RAS-IN-1 | Pan-RAS-IN-1 is a pan-Ras inhibitor and exhibits lethality in cells partially dependent on expression of Ras proteins. Synonyms: RasIN3144; Ras IN-3144; Ras-IN 3144; Ras-IN-3144; 3144; pan-RAS inhibitor-3144; 4-amino-N-[3-[5-[[4-[(2,6-dichlorophenyl)methyl]piperazin-1-yl]methyl]-3-[4-(trifluoromethoxy)phenyl]indol-1-yl]propyl]piperidine-4-carboxamide. CAS No. 1835283-94-7. Molecular formula: C36H41Cl2F3N6O2. Mole weight: 717.65. | |
| pantetheine hydrolase | The enzyme hydrolyses only one of the amide bonds of pantetheine. The substrate analogues phosphopantetheine and CoA are not substrates. The enzyme recycles pantothenate (vitamin B5) and produces 2-aminoethanethiol (cysteamine), a potent anti-oxidant. Group: Enzymes. Synonyms: pantetheinase; vanin; vanin-1. Enzyme Commission Number: EC 3.5.1.92. CAS No. 56093-18-6. 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-4484; pantetheine hydrolase; EC 3.5.1.92; 56093-18-6; pantetheinase; vanin; vanin-1. Cat No: EXWM-4484. |  |
| pantetheine kinase | This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing groups (phosphotransferases) with an alcohol group as acceptor. The systematic name of this enzyme class is ATP:pantetheine 4'-phosphotransferase. This enzyme is also called pantetheine kinase (phosphorylating). This enzyme participates in pantothenate and coa biosynthesis. Group: Enzymes. Synonyms: pantetheine kinase (phosphorylating). Enzyme Commission Number: EC 2.7.1.34. CAS No. 9026-49-7. 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-3065; pantetheine kinase; EC 2.7.1.34; 9026-49-7; pantetheine kinase (phosphorylating). Cat No: EXWM-3065. | |
| pantetheine-phosphate adenylyltransferase | The enzyme from several bacteria (e.g. Escherichia coli, Bacillus subtilis and Haemophilus influenzae) has been shown to be bifunctional and also to possess the activity of EC 2.3.1.157, glucosamine-1-phosphate N-acetyltransferase. Group: Enzymes. Synonyms: dephospho-CoA pyrophosphorylase; pantetheine phosphate adenylyltransferase; dephospho-coenzyme A pyrophosphorylase; 3'-dephospho-CoA pyrophosphorylase. Enzyme Commission Number: EC 2.7.7.3. CAS No. 9026-99-7. PPAT. 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-3240; pantetheine-phosphate adenylyltransferase; EC 2.7.7.3; 9026-99-7; dephospho-CoA pyrophosphorylase; pantetheine phosphate adenylyltransferase; dephospho-coenzyme A pyrophosphorylase; 3'-dephospho-CoA pyrophosphorylase. Cat No: EXWM-3240. | |
| Pantethine | Pantethine is an orally active lipid-lowering agent. Pantethine has anti-tumor, anti-inflammatory and anti-SARS-COV virus activities. Pantethine is also a neuroprotective agent. Pantethine can be used in the study of Alzheimer's disease, Parkinson's disease, major depression, systemic sclerosis and pantothenate kinase-related neurodegeneration [1] [2] [3] [4] [5] [6]. Uses: Scientific research. Group: Natural products. Alternative Names: D-Pantethine; LBF disulfide. CAS No. 16816-67-4. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g. Product ID: HY-B1028. | |
| Pantethine 55% Granular Powder | Pantethine 55% Granular Powder. |  CA, FL & NJ |
| Panthenol | Panthenol is an analogue of vitamin B5, and it would be oxidized to vitamin B5 in organisms. Panthenol is used as moisturizer and humectant in ointments, lotions and other pharmaceutic preparations for the treatment of sunburns. Synonyms: DL-Panthenol; DL-Pantothenol; DL-Pantothenyl alcohol. CAS No. 62507-76-0. Molecular formula: C9H19NO4. Mole weight: 205.254. | |
| Panthenol, racemic | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. |  |
| Panthenol, racemic | Pharmacopeia & Metrological Institutes Standards. Uses: For analytical and research use. Group: Reagents. CAS No. 16485-10-2. Pack Sizes: 200MG. | |
| pantoate 4-dehydrogenase | This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is (R)-pantoate:NAD+ 4-oxidoreductase. Other names in common use include pantoate dehydrogenase, pantothenase, and D-pantoate:NAD+ 4-oxidoreductase. This enzyme participates in pantothenate and coa biosynthesis. Group: Enzymes. Synonyms: pantoate dehydrogenase; pantothenase; D-pantoate:NAD+ 4-oxidoreductase. Enzyme Commission Number: EC 1.1.1.106. CAS No. 37250-38-7. 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-0009; pantoate 4-dehydrogenase; EC 1.1.1.106; 37250-38-7; pantoate dehydrogenase; pantothenase; D-pantoate:NAD+ 4-oxidoreductase. Cat No: EXWM-0009. | |
| pantoate-β-alanine ligase (ADP-forming) | The enzyme, characterized from the archaeon Methanosarcina mazei, is involved in the biosynthesis of pantothenate. It is different from EC 6.3.2.1, the AMP-forming pantoate-β-alanine ligase found in bacteria and eukaryota. Group: Enzymes. Synonyms: pantothenate synthetase (ambiguous); pantoate-β-alanine ligase (ambiguous). Enzyme Commission Number: EC 6.3.2.44. 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-5762; pantoate-β-alanine ligase (ADP-forming); EC 6.3.2.44; pantothenate synthetase (ambiguous); pantoate-β-alanine ligase (ambiguous). Cat No: EXWM-5762. | |
| pantoate-β-alanine ligase (AMP-forming) | This enzyme belongs to the family of ligases, specifically those forming carbon-nitrogen bonds as acid-D-amino-acid ligases (peptide synthases). This enzyme participates in beta-alanine metabolism and pantothenate and CoA biosynthesis. Group: Enzymes. Synonyms: pantothenate synthetase; pantoate activating enzyme; pantoic-activating enzyme; D-pantoate:β-alanine ligase (AMP-forming); pantoate-β-alanine ligase (ambiguous). Enzyme Commission Number: EC 6.3.2.1. CAS No. 9023-49-8. 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-5730; pantoate-β-alanine ligase (AMP-forming); EC 6.3.2.1; 9023-49-8; pantothenate synthetase; pantoate activating enzyme; pantoic-activating enzyme; D-pantoate:β-alanine ligase (AMP-forming); pantoate-β-alanine ligase (ambiguous). Cat No: EXWM-5730. | |
| pantoate kinase | The conversion of (R)-pantoate to (R)-4'-phosphopantothenate is part of the pathway leading to biosynthesis of 4'-phosphopantetheine, an essential cofactor of coenzyme A and acyl-carrier protein. In bacteria and eukaryotes this conversion is performed by condensation with β-alanine, followed by phosphorylation (EC 6.3.2.1 and EC 2.7.1.33, respectively). In archaea the order of these two steps is reversed, and phosphorylation precedes condensation with β-alanine. Group: Enzymes. Synonyms: PoK; TK2141 protein. Enzyme Commission Number: EC 2.7.1.169. 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-2999; pantoate kinase; EC 2.7.1.169; PoK; TK2141 protein. Cat No: EXWM-2999. | |
| Pantolactone | Pantolactone is an endogenous metabolite. Uses: Scientific research. Group: Natural products. CAS No. 599-04-2. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-W010396. | |
| Pantolactone | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardseuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: D-(-)-Pantolactone. | |
| Pantolactone | Pharmacopeia & Metrological Institutes Standards; European Pharmacopoeia (Ph. Eur.); Pharmacopoeial Standards. Uses: For analytical and research use. Group: Reagents. Alternative Names: D-(-)-Pantolactone. CAS No. 599-04-2. Pack Sizes: 500MG. IUPAC Name: (3R)-3-hydroxy-4,4-dimethyloxolan-2-one. | |
| Pantoonen | Pantoonen. Group: Elements nanoparticles. 99,9999%. |  |
| Pantoprazole | Pantoprazole, sold under the brand name Protonix among others, is used for short-term treatment of erosive esophagitis associated with gastroesophageal reflux disease (GERD), maintenance of healing of erosive esophagitis, and pathological hypersecretory conditions including Zollinger-Ellison Syndrome.Some common side effects of pantoprazole use in adults include: headache, diarrhea, nausea, abdominal pain, vomiting, flatulence, dizziness, and joint pain (>2%). Use of pantoprazole for a long period of time may lead to chronic inflammation of stomach lining or atrophic gastritis, vitamin B-12 deficiency, and low magnesium.Pantoprazole is a proton pump inhibitor drug that inhibits gastric acid secretion. It works on gastric parietal cells to irreversibly inhibit (H+/K+)-ATPase function and suppress the production of gastric acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Pantoprazole acid. Product Category: Inhibitors. Appearance: Solid. CAS No. 102625-70-7. Molecular formula: C16H15F2N3O4S. Mole weight: 383.37. Purity: 0.98. IUPACName: 6-(Difluoromethoxy)-2-[(3,4-dimethoxypyridin-2-yl)methylsulfinyl]-1H-benzimidazole. Canonical SMILES: COC1=C(C(=NC=C1)CS(=O)C2=NC3=C(N2)C=C(C=C3)OC(F)F)OC. Density: 1.51±0.1 g/cm³. Product ID: ACM102625707. Alfa Chemistry ISO 9001:2015 Certified. | |
| Pantoprazole | Pantoprazole, an irreversible protonpump inhibitor, inhibits the final step of the production ofgastric acid by binding to the sites of H+/K+ ATPase system in gastric parietal cells. Uses: Pantoprazole, an irreversible protonpump inhibitor, inhibits the final step of the production ofgastric acid by binding to the sites of h+/k+ atpase system in gastric parietal cells. Synonyms: Pantoprazole; BY 1023; BY-1023; SK&F 96022; SK&F-96022; Protonix; 102625-70-7; Pantozol; PantoprazoleSodium; Pantoprazolum. Grades: 95%. CAS No. 102625-70-7. Molecular formula: C16H15F2N3O4S. Mole weight: 383.37. | |
| Pantoprazole | Pantoprazole (BY10232) is an orally active and potent proton pump inhibitor (PPI) [1]. Pantoprazole, a substituted benzimidazole, is a potent H + /K + -ATPase inhibitor with an IC 50 of 6.8 μM. Pantoprazole improves pH stability and has anti-secretory, anti-ulcer activities. Pantoprazole significantly increased tumor growth delay combined with Doxorubicin (HY-15142) [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BY1023; SKF96022. CAS No. 102625-70-7. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-17507. | |
| Pantoprazole Deuterated, Sodium Salt | Deuterated Pantoprazole, an antiulcerative, gastric pump inhibitor.A representative current lot contains: 19% d95.5% d83.5 d756% d616% d52% d4no d0. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Pantoprazole EP Impurity B | Pantoprazole EP Impurity B. Uses: For analytical and research use. Group: Impurity standards. CAS No. 102625-64-9. Molecular formula: C16H15F2N3O3S. Mole weight: 367.37. Catalog: APB102625649. | |
| Pantoprazole EP Impurity E | Pantoprazole EP Impurity E is an impurity of Pantoprazole, a first-generation proton pump inhibitor (PPI) used as a drug for the treatment of gastroesophageal reflux disease (GERD). Synonyms: 6,6'-Bis(difluoromethoxy)-2,2'-bis(((3,4-dimethoxypyridin-2-yl)methyl)sulfinyl)-3H,3'H-5,5'-bibenzo[d]imidazolel; USP Pantoprazole Related Compound E; Pantoprazole Related Compound E. Grades: > 95%. CAS No. 2115779-15-0. Molecular formula: C32H28F4N6O8S2. Mole weight: 764.72. | |
| Pantoprazole Impurity 1 | An impurity of Pantoprazole which is a proton pump inhibitor used to treat erosive esophagitis (damage to the esophagus from stomach acid), and other conditions involving excess stomach acid such as Zollinger-Ellison syndrome. Synonyms: 2-[[Chloro(3,4-dimethoxy-2-pyridinyl)methyl]sulfinyl]-5-(difluoromethoxy)-1H-benzimidazole; 2-[[Chloro(3,4-dimethoxy-2-pyridinyl)methyl]sulfinyl]-6-(difluoromethoxy)-1H-benzimidazole; Pantoprazole Impurity 1. Grades: > 95%. CAS No. 812664-93-0. Molecular formula: C16H14ClF2N3O4S. Mole weight: 417.82. | |
| Pantoprazole Impurity D | Cas No. 624742-53-6. | |
| Pantoprazole Impurity (Mixture of Impurity D and F) | | |
| Pantoprazole Magnesium | An impurity of Pantoprazole which is a proton pump inhibitor drug that inhibits gastric acid secretion. Synonyms: 6-(difluoromethoxy)-2-(((3,4-dimethoxypyridin-2-yl)methyl)sulfinyl)-1H-benzo[d]imidazole magnesium. Grades: > 95%. CAS No. 1022083-88-0. Molecular formula: C32H28F4N6O8S2.Mg. Mole weight: 789.05. | |
| Pantoprazole N-Oxide | An impurity of Pantoprazole which is used to treat erosive esophagitis (damage to the esophagus from stomach acid), and other conditions involving excess stomach acid such as Zollinger-Ellison syndrome. Synonyms: 6-(Difluoromethoxy)-2-[[(3,4-dimethoxy-1-oxido-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole. Grades: > 95%. CAS No. 953787-60-5. Molecular formula: C16H15F2N3O5S. Mole weight: 399.38. | |
| Pantoprazole N-Oxide | An impurity in the synthesis of Pantoprazole, an antiulcerative, gastric pump inhibitor. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Pantoprazole Related Compound A | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Pantoprazole Related Compound B | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Pantoprazole Related Compound C | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Pantoprazole Related Compound E | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Pantoprazole Related Compounds D and F Mixture | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Pantoprazole sodium | 100mg Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C16H15F2N3O4S. CAS No. 102625-70-7. Prepack ID 16568378-100mg. Molecular Weight 383.4. See USA prepack pricing. |  |
| Pantoprazole sodium | Pantoprazole sodium (BY10232 sodium) is an orally active and potent proton pump inhibitor (PPI) [1]. Pantoprazole sodium, a substituted benzimidazole, is a potent H + /K + -ATPase inhibitor with an IC 50 of 6.8 μM. Pantoprazole sodium improves pH stability and has anti-secretory, anti-ulcer activities. Pantoprazole sodium significantly increased tumor growth delay combined with Doxorubicin (HY-15142) [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BY1023 sodium; SKF96022 sodium. CAS No. 138786-67-1. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-17507A. | |
| Pantoprazole sodium | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Pantoprazole sodium hydrate | Pantoprazole sodium hydrate is a proton pump inhibitor which acts as selective inhibiton of H+/K+-ATPase. With antiulcerative effects in vivo, it treats or ameliorates peptic ulcer or irritation of the gastrointestinal tract. Synonyms: sodium;5-(difluoromethoxy)-2-[(3,4-dimethoxypyridin-2-yl)methylsulfinyl]benzimidazol-1-ide;hydrate BY 1023 BY-1023 pantoprazole pantoprazole sodium Protonix SK and F 96022 SK and F-96022 SKF-96022. Grades: >98%. CAS No. 164579-32-2. Molecular formula: C16H14F2N3NaO4S. Mole weight: 405.35. | |
| Pantoprazole sodium hydrate | Pantoprazole sodium hydrate (BY10232 sodium hydrate) is an orally active and potent proton pump inhibitor (PPI) [1]. Pantoprazole sodium hydrate, a substituted benzimidazole, is a potent H + /K + -ATPase inhibitor with an IC 50 of 6.8 μM. Pantoprazole sodium hydrate improves pH stability and has anti-secretory, anti-ulcer activities. Pantoprazole sodium hydrate significantly increased tumor growth delay combined with Doxorubicin (HY-15142) [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BY1023 sodium hydrate; SKF96022 sodium hydrate. CAS No. 164579-32-2. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 500 mg. Product ID: HY-17507B. | |
| Pantoprazole sodium hydrate | ?98% (HPLC). Group: Pharmacology standards. | |
| Pantoprazole Sodium Monohydrate | The sodium salt form of Pantoprazole, a gastic proton pump inhibitor, could be used in the treatment of ulceration and some diseases induced by gastroesophageal reflux through influencing gastric acid secretion. Uses: The sodium salt form of pantoprazole is a gastic proton pump inhibitor that could be used in the treatment of ulceration and some diseases induced by gastroesophageal reflux through influencing gastric acid secretion. Synonyms: Pantoloc; Pantoprazole (sodium); Pantoprazole Sodium; Protonix IV; Protonix delayed-release; Pantoprazole Sodium [USAN]. Grades: ≥98%. CAS No. 138786-67-1. Molecular formula: C16H35F2N3NaO4S. Mole weight: 426.52. | |
| Pantoprazole sodium salt | 1g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C16H14F2N3NaO4S. CAS No. 138786-67-1. Prepack ID 29296273-1g. Molecular Weight 405.35. See USA prepack pricing. | |
| Pantoprazole, Sodium Salt (Eupantol, Pantecta, Pantozol, 5- (Difluoromethoxy) -2-[[ (3, 4-dimethoxy-2-pyridinyl) methyl]sulfinyl]-1H-benzimidazole) | An antiulcerative. Gastric pump inhibitor. Group: Biochemicals. Alternative Names: Eupantol, Pantecta, Pantozol, 5- (Difluoromethoxy) -2-[[ (3, 4-dimethoxy-2-pyridinyl) methyl]sulfinyl]-1H-benzimidazole. Grades: Highly Purified. CAS No. 138786-67-1. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Pantoprazole Sulfide | Pantoprazole Sulfide. Uses: For analytical and research use. Group: Impurity standards. CAS No. 102625-64-9. Pack Sizes: 100MG. IUPAC Name: 5-(difluoromethoxy)-2-[(3,4-dimethoxypyridin-2-yl)methylsulfanyl]-1H-benzimidazole. Molecular formula: C16H15F2N3O3S. Mole weight: 367.37. Catalog: APS102625649A. SMILES: COc1ccnc(CSc2nc3cc(OC(F)F)ccc3[nH]2)c1OC. Format: Neat. Shipping: Room Temperature. | |
Our database is helping our users find suppliers everyday.
