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| Product | Description | |
|---|---|---|
| Moxifloxacin Impurity J | Moxifloxacin Impurity J. Uses: For analytical and research use. Alternative Names: 1-Cyclopropyl-6,7-difluoro-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic Acid. CAS No. 112811-72-0. Molecular formula: C14H11F2NO4. Mole weight: 295.24. Catalog: APB112811720. |  |
| Moxifloxacin Impurity K | Moxifloxacin Impurity K. Uses: For analytical and research use. CAS No. 2489671-14-7. Molecular formula: C17H18FNO5. Mole weight: 335.33. Catalog: APB2489671147. | |
| Moxifloxacin Impurity L | Moxifloxacin Impurity L. Uses: For analytical and research use. Alternative Names: 7-Amino-1-cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic Acid. CAS No. 172426-88-9. Molecular formula: C14H13FN2O4. Mole weight: 292.26. Catalog: APB172426889. | |
| Moxifloxacin Impurity M | Moxifloxacin Impurity M. Uses: For analytical and research use. Molecular formula: C21H24FN3O4. Mole weight: 401.44. Catalog: APB08572. | |
| Moxifloxacin Impurity N | Moxifloxacin Impurity N. Uses: For analytical and research use. Molecular formula: C35H34F2N4O8. Mole weight: 676.66. Catalog: APB08573. | |
| Moxifloxacin Impurity O | Moxifloxacin Impurity O. Uses: For analytical and research use. Molecular formula: C17H18FNO5. Mole weight: 335.33. Catalog: APB08574. | |
| Moxifloxacin Impurity P (Moxifloxacin hydrochloride EP impurity G) | Moxifloxacin Impurity P (Moxifloxacin hydrochloride EP impurity G). Uses: For analytical and research use. CAS No. 268545-13-7. Molecular formula: C21H24FN3O4. Mole weight: 401.44. Catalog: APB268545137. | |
| Moxifloxacin Impurity Q | Moxifloxacin Impurity Q. Uses: For analytical and research use. CAS No. 1329836-33-0. Molecular formula: C16H15F2NO4. Mole weight: 323.3. Catalog: APB1329836330. | |
| Moxifloxacin Impurity R | Moxifloxacin Impurity R. Uses: For analytical and research use. CAS No. 452092-31-8. Molecular formula: C15H13F2NO4. Mole weight: 309.27. Catalog: APB452092318. | |
| Moxifloxacin Impurity S | Moxifloxacin Impurity S. Uses: For analytical and research use. CAS No. 2205053-60-5. Molecular formula: C21H24FN3O4. Mole weight: 401.44. Catalog: APB2205053605. | |
| Moxifloxacin Impurity T | Moxifloxacin Impurity T. Uses: For analytical and research use. CAS No. 1797982-51-4. Molecular formula: C16H16FNO5. Mole weight: 321.3. Catalog: APB1797982514. | |
| Moxifloxacin Impurity U | Moxifloxacin Impurity U. Uses: For analytical and research use. CAS No. 172602-83-4. Molecular formula: C17H17F2NO4. Mole weight: 337.32. Catalog: APB172602834. | |
| Moxifloxacin Impurity V | Moxifloxacin Impurity V. Uses: For analytical and research use. CAS No. 112811-67-3. Molecular formula: C15H15F3O6. Mole weight: 348.27. Catalog: APB112811673. | |
| Moxifloxacin Impurity W | Moxifloxacin Impurity W. Uses: For analytical and research use. CAS No. 442882-27-1. Molecular formula: C15H12N2O3. Mole weight: 268.27. Catalog: APB442882271. | |
| Moxifloxacin Impurity Y | Moxifloxacin Impurity Y. Uses: For analytical and research use. CAS No. 2445515-66-0. Molecular formula: C21H25N3O5. Mole weight: 399.45. Catalog: APB2445515660. | |
| Moxifloxacin Impurity Z | Moxifloxacin Impurity Z. Uses: For analytical and research use. Alternative Names: 1-cyclopropyl-6,7-difluoro-8-hydroxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid. CAS No. 154093-72-8. Molecular formula: C13H9F2NO4. Mole weight: 281.21. Catalog: APB154093728. | |
| Moxifloxacin N-Sulfate Disodium Salt | A sulfometabolite of Moxifloxacin. Group: Biochemicals. Alternative Names: 1-Cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-[(4aS,7aS)-octahydro-1-sulfo-6H-pyrrolo[3,4-b]pyridin-6-yl]-4-oxo-3-quinolinecarboxylic Acid Disodium Salt. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| Moxifloxacin Related Compound A | Moxifloxacin Related Compound A. Uses: For analytical and research use. CAS No. 151213-15-9. Mole weight: 389.40. Catalog: AP151213159. | |
| Moxifloxacin Related Compound D | Moxifloxacin Related Compound D. Uses: For analytical and research use. CAS No. 1029364-77-9. Mole weight: 401.43. Catalog: AP1029364779. | |
| Moxifloxacin Related Compound E | Moxifloxacin Related Compound E. Uses: For analytical and research use. CAS No. 721970-36-1 (free base). Mole weight: 423.87. Catalog: ALP721970361. | |
| Moxifloxacin Related Compound F | Moxifloxacin Related Compound F. Uses: For analytical and research use. CAS No. 1179992-99-4. Catalog: AP1179992994. | |
| Moxifloxacin (Standard) | Moxifloxacin (Standard) is the analytical standard of Moxifloxacin. This product is intended for research and analytical applications. Moxifloxacin is an orally active 8-methoxyquinolone antimicrobial for use in the treatment of acute bacterial sinusitis, acute bacterial exacerbations of chronic bronchitis, and community-acquired pneumonia[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: BAY 12-8039 free base (Standard). CAS No. 151096-09-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-66011AR. |  |
| Moxilubant | Moxilubant (CGS 25019C free base) is an orally active BLT1 antagonist. Moxilubant inhibits LTB4 signaling with a potency of 2-4 nM. Moxilubant blocks LTB4-induced neutrophil functions. Moxilubant inhibits ear edema and neutrophil infiltration in mice. Moxilubant can be used in research related to chronic obstructive pulmonary disease[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CGS 25019C free base. CAS No. 146978-48-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg. Product ID: HY-106929. | |
| Moxonidine | Moxonidine is an antihypertensive agent. Group: Biochemicals. Alternative Names: 4-Chloro-N-(4,5-dihydro-1H-imidazol-2-yl)-6-methoxy-2-methyl-5-pyrimidinamine; 2-(6-Chloro-4-methoxy-2-methylpyrimidin-5-ylamino)-2-imidazoline; Lomox; Moxon; Norcynt; Normoxocin; Nucynt; Physiotens. Grades: Highly Purified. CAS No. 75438-57-2. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| Moxonidine-[d4] | Moxonidine-[d4] is the labelled analogue of Moxonidine. Moxonidine is a selective agonist at the imidazoline receptor subtype (I1). It binds with much greater affinity to the imidazoline I1-receptor than to the α2-receptor while clonidine binds to both receptors with equal affinity. Synonyms: Moxonidine D4; 4-Chloro-N-(4,5-dihydro-1H-imidazol-2-yl-d4)-6-methoxy-2-methyl-5-pyrimidinamine; 2-(6-Chloro-4-methoxy-2-methylpyrimidin-5-ylamino)-2-imidazoline-d4. Grade: 95% by HPLC; 95% atom D. CAS No. 1794811-52-1. Molecular formula: C9H8D4ClN5O. Mole weight: 245.7. |  |
| Moxonidine EP impurity B | Moxonidine EP impurity B. Uses: For analytical and research use. CAS No. 75439-01-9. Molecular formula: C10H15N5O2. Mole weight: 237.26. Catalog: APB75439019. | |
| Moxonidine EP impurity C | Moxonidine EP impurity C. Uses: For analytical and research use. CAS No. 352457-34-2. Molecular formula: C9H13N5O2. Mole weight: 223.24. Catalog: APB352457342. | |
| Moxonidine EP impurity D | Moxonidine EP impurity D. Uses: For analytical and research use. CAS No. 352457-33-1. Molecular formula: C8H10ClN5O. Mole weight: 227.65. Catalog: APB352457331. | |
| Moxonidine hydrochloride | Moxonidine (BDF5895) hydrochloride is an orally active imidazoline type 1 receptor (I1-R) agonist. Moxonidine hydrochloride activates imidazoline I1 receptors and α2 adrenoceptors, affecting oxidized low-density lipoprotein uptake. Moxonidine hydrochloride reduces atherosclerotic lesions and lowers blood pressure. Moxonidine hydrochloride can be used in the study of hypertension, heart failure, and atherosclerosis[1][2][3][4][5][6][7]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: BDF5895 hydrochloride. CAS No. 75536-04-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0374A. | |
| Moxonidine hydrochloride | Moxonidine hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 75536-04-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Moxonidine impurity 2 | Moxonidine impurity 2. Uses: For analytical and research use. Molecular formula: C9H10ClN7O3. Mole weight: 299.68. Catalog: APB08677. | |
| Moxonidine impurity 3 | Moxonidine impurity 3. Uses: For analytical and research use. Molecular formula: C9H11ClN6O2. Mole weight: 270.68. Catalog: APB08678. | |
| Moxonidine impurity 4 | Moxonidine impurity 4. Uses: For analytical and research use. Molecular formula: C9H10ClN7O3. Mole weight: 299.68. Catalog: APB08679. | |
| Mozavaptan | Mozavaptan (OPC-31260) is a benzazepine derivative and a potent, selective, competitive and orally active vasopressin V2 receptor antagonist with an IC50 of 14 nM. Mozavaptan shows ~85-fold selectivity for V2 receptor over V1 receptor (IC50 of 1.2 μM), and can antagonize the antidiuretic action of arginine vasopressin (AVP) in vivo. Mozavaptan has the potential for hyponatremia, syndrome of inappropriate antidiuretic hormone (SIADH), and congestive heart failure treatment[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: OPC-31260. CAS No. 137975-06-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-18346. | |
| Mozavaptan hydrochloride | Mozavaptan hydrochloride (OPC-31260 hydrochloride) is a benzazepine derivative and a potent, selective, competitive and orally active vasopressin V2 receptor antagonist with an IC50 of 14 nM. Mozavaptan hydrochloride shows ~85-fold selectivity for V2 receptor over V1 receptor (IC50 of 1.2 μM), and can antagonize the antidiuretic action of arginine vasopressin (AVP) in vivo. Mozavaptan hydrochloride has the potential for hyponatremia, syndrome of inappropriate antidiuretic hormone (SIADH), and congestive heart failure treatment[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: OPC-31260 hydrochloride. CAS No. 138470-70-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-123593. | |
| MP07-66 | MP07-66, a FTY720 analogue, is devoid of immunosuppressive effects and shows promising antitumor effects in chronic lymphocytic leukemia by disruption of the SET-PP2A complex leading to PP2A reactivation[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1938056-90-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-123794. | |
| MP7 | MP7 (PDK1 inhibitor) is a phosphoinositide-dependent kinase-1 (PDK1) inhibitor. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PDK1 inhibitor. CAS No. 1001409-50-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14440. | |
| MPC-3100 | MPC-3100 is a recently discovered fully synthetic purine-based Hsp90 Inhibitor exhibiting anticancer properties. Group: Biochemicals. Alternative Names: (2S)-1-[4-[2-[6-Amino-8-[(6-bromo-1,3-benzodioxol-5-yl)thio]-9H-purin-9-yl]ethyl]-1-piperidinyl]-2-hydroxy-1-propanone. Grades: Highly Purified. CAS No. 958025-66-6. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| MPC 6827 hydrochloride | MPC 6827 hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 917369-31-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| MPDC | MPDC. Group: Biochemicals. Grades: Purified. CAS No. 159262-32-5. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| MPDDA | MPDDA. Mole weight: 226. |  |
| m-PEG10000-NHS ester | m-PEG10000-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: mPEG10000-SC; mPEG10000-Succinimidyl ester. CAS No. 92451-01-9. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-140699. | |
| mPEG1000-amine | mPEG1000-amine (mPEG1000-NH2) is a class of functionalized polymers composed of a methoxy-terminated polyethylene glycol backbone and a terminal primary amine group. mPEG1000-amine serves as an important intermediate for constructing functionalized nanocarriers, modifying proteins or polypeptides, and developing novel drug delivery systems. Uses: Scientific research. Category: Signaling pathways. Alternative Names: mPEG1000-NH2. CAS No. 80506-64-5. Pack Sizes: 100 mg; 500 mg. Product ID: HY-140675. | |
| m-PEG10-CH2COOH | m-PEG10-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 908258-58-2. Pack Sizes: 100 mg; 250 mg; 1 g; 5 g. Product ID: HY-133285. | |
| mPEG10K-Propionaldehyde | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Alternative Names: mPEG-Propionaldehyde, mPEG-ALD, Methoxy-PEG-Propionaldehyde. Mole weight: average Mn 10000. | |
| mPEG10K-Succinimidyl Carboxymethyl Ester | Methoxy PEG NHS Ester (SCM PEG). Amine reactive PEG towards the amino groups of lysine(s) on proteins or other biologics; reaction occurs at room temperature in <1hr at pH 7-8. Stable linker between PEG and NHS ester. Alternative Names: mPEG-Succinimidyl Carboxymethyl Ester. Mole weight: average Mn 10000. | |
| m-PEG12-acid | m-PEG12-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2135793-73-4. Pack Sizes: 50 mg; 100 mg; 250 mg; 1 g; 5 g; 10 g. Product ID: HY-135820. | |
| mPEG12-Acrylate | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. | |
| mPEG12-Azide | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Mole weight: average Mn 12000. | |
| mPEG12-NH2 | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Molecular formula: C25H53NO12. Mole weight: 559.7g/mol. IUPAC Name: 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanamine. SMILES: COCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN. InChI: InChI=1S/C25H53NO12/c1-27-4-5-29-8-9-31-12-13-33-16-17-35-20-21-37-24-25-38-23-22-36-19-18-34-15-14-32-11-10-30-7-6-28-3-2-26/h2-26H2,1H3. | |
| m-PEG12-NHS ester | m-PEG12-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2207596-93-6. Pack Sizes: 100 mg; 500 mg. Product ID: HY-141106. | |
| mPEG12-OH | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Alternative Names: Methoxy-PEG12-Hydroxyl. Molecular formula: C25H52O13. Mole weight: 560.7g/mol. IUPAC Name: 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol. SMILES: [H]OCCOC. InChI: 1S/C3H8O2/c1-5-3-2-4/h4H,2-3H2,1H3. | |
| m-PEG12-OTs | m-PEG12-Ots is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2103241-71-8. Pack Sizes: 1 g; 5 g. Product ID: HY-161020. | |
| mPEG12-Propionic acid | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Alternative Names: mPEG12-PA, methoxy-PEG-Propionic acid. SMILES: OC(CCOCCOC)=O. InChI: 1S/C6H12O4/c1-9-4-5-10-3-2-6(7)8/h2-5H2,1H3,(H,7,8). | |
| mPEG12-SH | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Molecular formula: C25H52O12S. Mole weight: 576.7g/mol. IUPAC Name: 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanethiol. SMILES: COCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCS. InChI: InChI=1S/C25H52O12S/c1-26-2-3-27-4-5-28-6-7-29-8-9-30-10-11-31-12-13-32-14-15-33-16-17-34-18-19-35-20-21-36-22-23-37-24-25-38/h38H,2-25H2,1H3. | |
| mPEG16-NH2 | mPEG16-NH2. CAS No. 907577-50-8. Molecular formula: C33H69NO16. Mole weight: 735.9g/mol. IUPAC Name: 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanamine. SMILES: COCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN. InChI: InChI=1S/C33H69NO16/c1-35-4-5-37-8-9-39-12-13-41-16-17-43-20-21-45-24-25-47-28-29-49-32-33-50-31-30-48-27-26-46-23-22-44-19-18-42-15-14-40-11-10-38-7-6-36-3-2-34/h2-34H2,1H3. | |
| mPEG2000-amine | mPEG2000-amine (mPEG2000-NH2) is a class of functionalized polymers composed of a methoxy-terminated polyethylene glycol backbone and a terminal primary amine group. mPEG2000-amine serves as an important intermediate for constructing functionalized nanocarriers, modifying proteins or polypeptides, and developing novel drug delivery systems. Uses: Scientific research. Category: Signaling pathways. Alternative Names: mPEG2000-NH2. CAS No. 80506-64-5. Pack Sizes: 50 mg; 100 mg; 250 mg; 1 g; 5 g. Product ID: HY-140676. | |
| mPEG2000-DMG | DMG-PEG 2000 is used for the preparation of liposome for siRNA delivery with improved transfection efficiency in vitro. DMG-PEG 2000 is also used for the lipid nanoparticle for an oral plasmid DNA delivery approach in vivo through a facile surface modification to improve the mucus permeability and delivery efficiency of the nanoparticles[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 160743-62-4. Pack Sizes: 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-112764. | |
| MPEG-2000-DSPE | MPEG-2000-DSPE was used to study stability and biodistribution and toxicity of lung-specific liposomal antitubercular drugs. Group: Biochemicals. Grades: Highly Purified. CAS No. 147867-65-0. Pack Sizes: 100mg, 250mg. Molecular Formula: (C2H4O)nC43H84NO10P. US Biological Life Sciences. | Worldwide |
| m-PEG2000-NHS ester | m-PEG2000-NHS ester (mPEG2000-SC) is a reagent with both cell adhesion inhibition and peptide conjugation functions. The NHS ester group of m-PEG2000-NHS ester forms stable amide bonds with primary amine-containing molecules (e.g., the N-terminus of MMP-2-cleavable octapeptide) to generate mPEG-peptide intermediates for liposome surface modification. When m-PEG2000-NHS ester is immobilized on a cystamine-modified gold surface, it can construct an in vitro model for cell adhesion kinetic studies, and higher PEG density and thicker layers correlate with lower cell adhesion rates. m-PEG2000-NHS ester can synthesize MMP-2-responsive PEGylated lipid conjugates to achieve MMP-triggered dePEGylation in the tumor microenvironment. m-PEG2000-NHS ester can be used in studies related to colon cancer and other conditions[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: mPEG2000-SC; mPEG2000-Succinimidyl ester. CAS No. 92451-01-9. Pack Sizes: 100 mg; 250 mg; 500 mg. Product ID: HY-W591424. | |
| m-PEG2000-thiol | m-PEG2000-thiol is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: mPEG2000-SH. CAS No. 134874-49-0. Pack Sizes: 100 mg; 250 mg; 1 g; 5 g; 10 g. Product ID: HY-140706. | |
| mPEG20K-MAL | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Alternative Names: mPEG-MAL, Methoxy-PEG-Maleimide. Mole weight: average Mn 20000. | |
| mPEG20K-Silane | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Mole weight: average Mn 20000. | |
| mPEG20K-Succinimidyl Carboxymethyl Ester | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Alternative Names: mPEG-Succinimidyl Carboxymethyl Ester. Mole weight: average Mn 20000. | |
| m-PEG24-alcohol | m-PEG24-alcohol is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2376450-73-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-141225. | |
| m-PEG24-NH2 | m-PEG24-NH2 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2151823-08-2. Pack Sizes: 100 mg; 250 mg; 500 mg; 1 g; 5 g. Product ID: HY-140228. | |
| m-PEG24-NHS ester | m-PEG24-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2395839-96-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-130830. | |
| mPEG2K-MAL | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Alternative Names: mPEG-MAL, Methoxy-PEG-Maleimide. Mole weight: average Mn 2000. | |
| mPEG2k-PLA2k-PAE9k | mPEG2k-PLA2k-PAE9k. Synonyms: methoxy polyethylene glycol-Poly(D,L-lactide)-Poly(b-amino esters). Product ID: MSMN-057. Category: Raw Materials. |  |
| mPEG2K-Thioctic acid | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Mole weight: average Mn 2000. | |
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