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| Product | Description | |
|---|---|---|
| Molybdic Acid | Molybdic Acid. Grade: ACS. CAS: 7782-91-4. Packing: Metal Drums. |  New Jersey NJ |
| Molybdic Acid | DryPowder. Group: Glass additives. Product ID: dihydroxy(dioxo)molybdenum. Molecular formula: 162g/mol. Mole weight: H2MoO4;H2MoO4. O[Mo](=O)(=O)O. InChI=1S/Mo.2H2O.2O/h; 2*1H2; ; /q+2; ; ; ; /p-2. VLAPMBHFAWRUQP-UHFFFAOYSA-L. |  |
| Molybdic acid ≥85.0% ACS | Molybdic acid ≥85.0% ACS. Group: Biochemicals. Grades: ACS Grade. CAS No. 7782-91-4. Pack Sizes: 25g, 100g, 250g, 1Kg, 2.5Kg. US Biological Life Sciences. |  Worldwide |
| molybdopterin adenylyltransferase | Catalyses the activation of molybdopterin for molybdenum insertion. In eukaryotes, this reaction is catalysed by the C-terminal domain of a fusion protein that also includes molybdopterin molybdotransferase (EC 2.10.1.1). The reaction requires a divalent cation such as Mg2+ or Mn2+. Group: Enzymes. Synonyms: MogA; Cnx1 (ambiguous). Enzyme Commission Number: EC 2.7.7.75. 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-3287; molybdopterin adenylyltransferase; EC 2.7.7.75; MogA; Cnx1 (ambiguous). Cat No: EXWM-3287. |  |
| molybdopterin molybdotransferase | Catalyses the insertion of molybdenum into the ene-dithiol group of molybdopterin. In eukaryotes this reaction is catalysed by the N-terminal domain of a fusion protein whose C-terminal domain catalyses EC 2.7.7.75, molybdopterin adenylyltransferase. Requires divalent cations such as Mg2+ or Zn2+ for activity. Group: Enzymes. Synonyms: MoeA; Cnx1 (ambiguous). Enzyme Commission Number: EC 2.10.1.1. 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-2024; molybdopterin molybdotransferase; EC 2.10.1.1; MoeA; Cnx1 (ambiguous). Cat No: EXWM-2024. | |
| molybdopterin synthase | Catalyses the synthesis of molybdopterin from cyclic pyranopterin monophosphate. Two sulfur atoms are transferred to cyclic pyranopterin monophosphate in order to form the characteristic ene-dithiol group found in the molybdenum cofactor. Molybdopterin synthase consists of two large subunits forming a central dimer and two small subunits (molybdopterin-synthase sulfur-carrier proteins) that are thiocarboxylated at the C-terminus by EC 2.8.1.11, molybdopterin synthase sulfurtransferase. The reaction occurs in prokaryotes and eukaryotes. Group: Enzymes. Synonyms: MPT synthase. Enzyme Commission Number: EC 2.8.1.12. 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-3357; molybdopterin synthase; EC 2.8.1.12; MPT synthase. Cat No: EXWM-3357. | |
| molybdopterin-synthase adenylyltransferase | Adenylates the C-terminus of the small subunit of the molybdopterin synthase. This activation is required to form the thiocarboxylated C-terminus of the active molybdopterin synthase small subunit. The reaction occurs in prokaryotes and eukaryotes. In the human, the reaction is catalysed by the N-terminal domain of the protein MOCS3, which also includes a molybdopterin-synthase sulfurtransferase (EC 2.8.1.11) C-terminal domain. Group: Enzymes. Synonyms: MoeB; adenylyltransferase and sulfurtransferase MOCS3. Enzyme Commission Number: EC 2.7.7.80. 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-3293; molybdopterin-synthase adenylyltransferase; EC 2.7.7.80; MoeB; adenylyltransferase and sulfurtransferase MOCS3. Cat No: EXWM-3293. | |
| molybdopterin synthase sulfurtransferase | The enzyme transfers sulfur to form a thiocarboxylate moiety on the C-terminal glycine of the small subunit of EC 2.8.1.12, molybdopterin synthase. In the human, the reaction is catalysed by the rhodanese-like C-terminal domain (cf. EC 2.8.1.1) of the MOCS3 protein, a bifunctional protein that also contains EC 2.7.7.80, molybdopterin-synthase adenylyltransferase, at the N-terminal domain. Group: Enzymes. Synonyms: adenylyltransferase and sulfurtransferase MOCS3; Cnx5 (gene name); molybdopterin synthase sulfurylase. Enzyme Commission Number: EC 2.8.1.11. 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-3356; molybdopterin synthase sulfurtransferase; EC 2.8.1.11; adenylyltransferase and sulfurtransferase MOCS3; Cnx5 (gene name); molybdopterin synthase sulfurylase. Cat No: EXWM-3356. | |
| Molyorange 10190-55-3 | Molyorange 10190-55-3. SUPPLIERS TO BUSINESS CUSTOMERS ONLY. |  North America & APAC |
| MOMBA | MOMBA is a selective FFA2 ( Free Fatty Acid Receptor 2 ) orthosteric agonist that activates receptor signaling pathways by binding to the orthosteric site of FFA2 with high specificity. MOMBA holds potential for research on metabolic and inflammatory diseases [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 6880-4-2. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-59384. |  |
| Momelotinib | Momelotinib (CYT387) is an ATP-competitive inhibitor of JAK1/JAK2 with IC 50 a of 11 nM and 18 nM,respectively. CYT387 shows much less activity against JAK3. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CYT387. CAS No. 1056634-68-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10961. | |
| Momelotinib sulfate | Momelotinib sulfate (CYT387 sulfate salt) is an ATP-competitive inhibitor of JAK1/JAK2 with IC 50 of 11 nM/18 nM, 10-fold selectivity versus JAK3 (IC 50 =155 nM). Uses: Scientific research. Group: Signaling pathways. Alternative Names: CYT387 sulfate salt. CAS No. 1056636-06-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-10962. | |
| Mometasone | Mometasone is an inhaled glucocorticoid. Mometasone can be used in mild asthma with a low sputum eosinophil level. Mometasone has the potential for the research of chronic hand eczema and rhinosinusitis [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 105102-22-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-B0629. | |
| Mometasone-d5 | Mometasone-d5. Group: Biochemicals. Alternative Names: (11 β,16α)-9,21-Dichloro-11,17-dihydroxy-16-methylpregna-1,4-diene-3,20-dione-d5; (+)-Mometasone-d5. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C22H23D5Cl2O4, Molecular Weight: 432.39. US Biological Life Sciences. | Worldwide |
| Mometasone furoate | Mometasone furoate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Mometasone Furoate; [(8S,9R,10S,11S,13S,14S,16R,17R)-9-chloro-17-(2-chloroacetyl)-11-hydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl] furan-2-carboxylate. Product Category: Steroidal Compounds. Appearance: Distributed as 0.1% ointment with a petrolatum base. CAS No. 83919-23-7. Molecular formula: C27H30Cl2O6. Mole weight: 521.44. Purity: 0.99. IUPACName: [(8S,9R,10S,11S,13S,14S,16R,17R)-9-chloro-17-(2-chloroacetyl)-11-hydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl]furan-2-carboxylate. Canonical SMILES: CC1CC2C3CCC4=CC(=O)C=CC4(C3(C(CC2(C1(C(=O)CCl)OC(=O)C5=CC=CO5)C)O)Cl)C. Density: 1.37 g/cm³. ECNumber: 617-501-0. Product ID: ACM83919237. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Mometasone furoate | Mometasone furoate (Sch32088) is a glucocorticoid receptor agonist with anti-inflammatory and anti-allergic activity. Mometasone furoate acts as a corticosteroid agent and used for topical applications in chronic skin eczema and airway inflammation management of asthma in vivo [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Sch32088. CAS No. 83919-23-7. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-13693. | |
| Mometasone furoate | Mometasone furoate. Group: Biochemicals. Grades: Purified. CAS No. 83919-23-7. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
| Mometasone Furoate | Mometasone furoate is a half-synthetic glucocorticoid, which has anti-inflammatory, anti-allergic, vasoconstriction, reduced vascular permeability, inhibition of cell division and antipruritus effects. It is characterized by increased intensity of action and disproportionate increase in side effects, and is used only once a day. Mometasone furoate is effective for corticosteroid treatment of skin diseases, such as neurodermatitis, eczema, atopic dermatitis, seborrheic dermatitis and seborrheic dermatitis. CAS No. 83919-23-7. Product ID: PAP-0082. Molecular formula: C27H30Cl2O6. Category: Hormone drug. Product Keywords: Hormone Series; Mometasone Furoate; PAP-0082; Hormone drug; C27H30Cl2O6; 83919-23-7. Appearance: Powder. Standard: USP. Color: White to Off-White. Physical State: neat. Solubility: DMSO: ≥20mg/mL. Storage: 2-8°C. Applications: Mometasone furoate is used for skin diseases effective in the treatment of corticosteroids, such as neurodermatitis, eczema, atopic dermatitis caused by skin inflammation and skin itching symptoms, local use of medium effect corticosteroids, anti-inflammatory, anti-itch and vasoconstriction effects. Boiling Point: 655.5±55.0 °C(Predicted). Melting Point: 218-220°C. Density: 1.37±0.1 g/cm3(Predicted). |  |
| Mometasone Furoate | Mometasone Furoate. CAS No: 149-64-4 |  Sarchem Laboratories New Jersey NJ |
| Mometasone Furoate | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardspesticides & metabolitespharma & vet compounds & metabolitespharma & vet compounds & metabolitesapi standardsbritish pharmacopoeiaeuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: Asmanex, Twisthaler, Monovo, Ecural, Elocom, Elomet, Mometasone furoate, Ovixan, (11beta,16alpha)-9,21-Dichloro-17-[(2-furanylcarbonyl)oxy]-11-hydroxy-16-methylpregna-1,4-diene-3,20-dione, Elocon, Nasonex, Mometasone 17-(2-furoate), Asmanex Twisthaler, Sch 32088. |  |
| Mometasone Furoate-[13C,d6] | Mometasone Furoate-[13C,d6] is the labelled analogue of Mometasone furoate, which is an antiallergic drug with a high affinity for glucocorticoid receptors. It can be used to treat asthma and allergic rhinitis. Synonyms: Mometasone Furoate 13CD6; (11β,16α)-9,21-Dichloro-17-[(2-furanylcarbonyl)oxy]-11-hydroxy-16-methyl-pregna-1,4-diene-3,20-dione-13C,d6; Elocon-13C,d6; Nasonex-13C,d6; Asmanex-13C,d6. Grade: 95% by HPLC; 98% atom D; 98% atom 13C. Molecular formula: C26[13C]H24D6Cl2O6. Mole weight: 528.46. |  |
| Mometasone Furoate-d3 | A deuterated topical corticosteroid used as an anti-inflammatory. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Mometasone Furoate-[d3] | Mometasone Furoate-[d3] is the labelled analogue of Mometasone furoate, which is an antiallergic drug with a high affinity for glucocorticoid receptors. It can be used to treat asthma and allergic rhinitis. Synonyms: Mometasone furoate D3; (11β,16α)-9,21-Dichloro-17-[(2-furanylcarbonyl)oxy]-11-hydroxy-16-methyl-pregna-1,4-diene-3,20-dione-d3. Grade: > 95%. Molecular formula: C27H27D3Cl2O6. Mole weight: 524.46. | |
| Mometasone Furoate Impurity A | Impurity of Mometasone Furoate, a topical corticosteroid used as an anti-inflammatory. Group: Biochemicals. Alternative Names: (16α)-21-Chloro-17-[(2-furanylcarbonyl)oxy]-16-methylpregna-1,4,9(11)-triene-3,20-dione. Grades: Highly Purified. CAS No. 83880-65-3. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Mometasone Furoate Impurity A | Mometasone Furoate Impurity A. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: Mometasone Furoate Imp. A (EP), 21-Chloro-16?-methyl-3,20-dioxopregna-1,4,9(11)-trien-17-yl Furan-2-carboxylate,Pregna-1,4,9(11)-triene-3,20-dione, 21-chloro-17-[(2-furanylcarbonyl)oxy]-16-methyl-, (16?)-. CAS No. 83880-65-3. IUPAC Name: [(8S,10S,13S,14S,16R,17R)-17-(2-chloroacetyl)-10,13,16-trimethyl-3-oxo-7,8,12,14,15,16-hexahydro-6H-cyclopenta[a]phenanthren-17-yl] furan-2-carboxylate. Molecular formula: C27H29ClO5. Mole weight: 468.97. Catalog: APS83880653. SMILES: C[C@@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)C3=CC[C@]2(C)[C@@]1(OC(=O)c5occc5)C(=O)CCl. Format: Neat. | |
| Mometasone Furoate Impurity F | Mometasone Furoate Impurity F. Uses: Designed for use in research and industrial production. CAS No. 1305334-30-8. Purity: 0.95. Product ID: APB1305334308. Alfa Chemistry ISO 9001:2015 Certified. | |
| Mometasone Furoate Impurity G | Mometasone Furoate Impurity G. Uses: For analytical and research use. Group: Impurity standards. CAS No. 105102-22-5. Molecular formula: C22H28Cl2O4. Mole weight: 427.36. Catalog: APB105102225. | |
| Mometasone Furoate Impurity V | Mometasone Furoate Impurity V. Uses: For analytical and research use. Group: Impurity standards. CAS No. 109183-56-4. Molecular formula: C29H32O8. Mole weight: 508.57. Catalog: APB109183564. | |
| Mometasone Furoate (Sch-32088, Elocon, Nasonex) | A topical corticosteroid used as an anti-inflammatory. Group: Biochemicals. Alternative Names: Sch-32088, Elocon, Nasonex. Grades: Highly Purified. CAS No. 83919-23-7. Pack Sizes: 10mg, 50mg, 100mg, 1g. US Biological Life Sciences. | Worldwide |
| Mometasone furoate (Standard) | Mometasone furoate (Standard) is the analytical standard of Mometasone furoate. This product is intended for research and analytical applications. Mometasone furoate (Sch32088) is a glucocorticoid receptor agonist with anti-inflammatory and anti-allergic activity. Mometasone furoate acts as a corticosteroid agent and used for topical applications in chronic skin eczema and airway inflammation management of asthma in vivo [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Sch32088 (Standard). CAS No. 83919-23-7. Pack Sizes: 10 mg; 25 mg; 50 mg. Product ID: HY-13693R. | |
| momilactone-A synthase | The rice phytoalexin momilactone A is a diterpenoid secondary metabolite that is involved in the defense mechanism of the plant. Momilactone A is produced in response to attack by a pathogen through the perception of elicitor signal molecules such as chitin oligosaccharide, or after exposure to UV irradiation. The enzyme, which catalyses the last step in the biosynthesis of momilactone A, can use both NAD+ and NADP+ but activity is higher with NAD+. Group: Enzymes. Synonyms: momilactone A synthase; OsMAS. Enzyme Commission Number: EC 1.1.1.295. 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-0204; momilactone-A synthase; EC 1.1.1.295; momilactone A synthase; OsMAS. Cat No: EXWM-0204. | |
| Momordicine I | Momordicine I, a triterpenoid compound extracted from momordica charantia L. Momordicine I alleviates isoproterenol-induced cardiomyocyte hypertrophy through suppression of PLA2G6 and DGK-ζ [1]. Uses: Scientific research. Group: Natural products. CAS No. 91590-76-0. Pack Sizes: 1 mg; 5 mg. Product ID: HY-122949. | |
| Momordicoside G | Momordicoside G is isolated from the herbs of Mormodica charantia L. Synonyms: (1R,4S,5S,8R,9R,12S,13S,16S)-8-[(2R,4E)-6-Methoxy-6-methyl-4-hepten-2-yl]-5,9,17,17-tetramethyl-18-oxapentacyclo[10.5.2.01,13.04,12.05,9]nonadec-2-en-16-yl β-D-allopyranoside. Grade: 96%. CAS No. 81371-54-2. Molecular formula: C37H60O8. Mole weight: 632.9. | |
| Momordicoside K | Momordicoside K is a cucurbitacin found in Momordica charantia (bitter melon). Synonyms: 19-Norlanosta-5,23-diene-9-carboxaldehyde, 7-(β-D-glucopyranosyloxy)-3-hydroxy-25-methoxy-, (3β,7β,9β,10α,23E)-; (1S,4R,7S,9β,23E)-9-Formyl-1-hydroxy-25-methoxy-10,14-dimethyl-4,9-cyclo-9,10-secocholesta-5,23-dien-7-yl β-D-glucopyranoside. Grade: ≥95%. CAS No. 81348-84-7. Molecular formula: C37H60O9. Mole weight: 648.88. | |
| Momordicoside L | Momordicoside L is a cucurbitacin found in Momordica charantia (bitter melon). Synonyms: 19-Norlanosta-5,23-diene-9-carboxaldehyde, 7-(β-D-glucopyranosyloxy)-3,25-dihydroxy-, (3β,7β,9β,10α,23E)-; (1S,4R,7S,9β,23E)-9-Formyl-1,25-dihydroxy-10,14-dimethyl-4,9-cyclo-9,10-secocholesta-5,23-dien-7-yl β-D-glucopyranoside; (3β,7β,9β,10α,17β)-7-(β-D-glucopyranosyloxy)-3-hydroxy-17-[(3E)-5-hydroxy-1,5-dimethylhex-3-en-1-yl]-4,4,14-trimethylestr-5-ene-9-carboxaldehyde. Grade: ≥95%. CAS No. 81348-83-6. Molecular formula: C36H58O9. Mole weight: 634.85. | |
| Momordin Ic | Momordin Ic is an orally active triterpenoid saponin that can be isolated from Kochia scoparia. It is also a SUMO specific protease 1 (SENP1) inhibitor, SENP1/c-MYC signaling pathway inhibitor, and apoptosis inducer. Momordin Ic induces autophagy and apoptosis in liver cancer cells through the PI3K/Akt and MAPK signaling pathways mediated by reactive oxygen species. Momordin Ic has the ability to control glucose induced blood glucose elevation, inhibit gastric emptying, resist rheumatoid arthritis, reduce CCl4 (HY-Y0298) induced hepatotoxicity and anti-tumor activity[1][2].. Uses: Scientific research. Group: Natural products. CAS No. 96990-18-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0330. | |
| Momordin Ic | Momordin Ic. Group: Biochemicals. Grades: Plant Grade. CAS No. 96990-18-0. Pack Sizes: 20mg. Molecular Formula: C41H64O13, Molecular Weight: 764.94. US Biological Life Sciences. | Worldwide |
| monacolin J acid methylbutanoate transferase | The enzyme catalyses the ultimate reaction in the lovastatin biosynthesis pathway of the filamentous fungus Aspergillus terreus. Group: Enzymes. Synonyms: LovD. Enzyme Commission Number: EC 2.3.1.238. 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-2186; monacolin J acid methylbutanoate transferase; EC 2.3.1.238; LovD. Cat No: EXWM-2186. | |
| monacolin L hydroxylase | A heme-thiolate protein (cytochrome P-450). The enzyme from fungi also catalyses the reaction of EC 1.14.13.197, dihydromonacolin L hydroxylase. Group: Enzymes. Synonyms: LovA (ambiguous). Enzyme Commission Number: EC 1.14.13.198. 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-0798; monacolin L hydroxylase; EC 1.14.13.198; LovA (ambiguous). Cat No: EXWM-0798. | |
| Monactin | A member of the macrotetrolide complex produced by a range of streptomyces species; a monovalent cation ionophore with high selectivity for ammonium and potassium; inhibits T-cell proliferation induced by IL-2 and cytokine production at nanomolar levels for IL-2, IL-4, IL-5 and IFN-γ. It is also resistant to gram-positive bacteria and mycobacteria. Synonyms: 4,13,22,31,37,38,39,40-Octaoxapentacyclo[32.2.1.17,10.116,19.125,28]tetracontane-3,12,21,30-tetrone,5-ethyl-2,11,14,20,23,29,32-heptamethyl-, (1R,2R,5R,7R,10S,11S,14S,16S,19R,20R,23R,25R,28S,29S,32S,34S)-; Akd-1B. Grade: >95% by HPLC. CAS No. 7182-54-9. Molecular formula: C41H66O12. Mole weight: 750.95. | |
| Monactin (5-demethyl-5-ethylnonactin, Antibiotic AKD 1B) | Monactin is a member of the macrotetrolide complex produced by a range of Streptomyces species. Unlike nonactin, monactin has not previously been available for intensive investigation. Early literature reported that the related dinactin is a monovalent cation ionophore with high selectivity for ammonium and potassium. Monactin inhibits T-cell proliferation induced by IL-2 and cytokine production at nanomolar levels for IL-2, IL-4, IL-5 and interferon-gamma. Group: Biochemicals. Alternative Names: 5-demethyl-5-ethylnonactin, Antibiotic AKD 1B. Grades: Highly Purified. CAS No. 7182-54-9. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Monalizumab | Monalizumab (IPH2201) is an immune checkpoint inhibitor targeting Natural Killer Group 2A ( NKG2A ). Monalizumab, a humanized anti-NKG2A blocking mAb, increases IFN-γ production, thereby promoting NK cell effector functions. Monalizumab can be used for the research of head and neck squamous cell carcinoma (HNSCC) [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: IPH2201. CAS No. 1228763-95-8. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P99032. | |
| Monamycin C | Monamycin C is an ester peptide antibiotic produced by Str. jamaicensis A-154. Activity against gram-positive bacteria. CAS No. 31764-92-8. Molecular formula: C34H57N7O8. Mole weight: 691.86. | |
| Monamycin E | Monamycin E is an ester peptide antibiotic produced by Str. jamaicensis A-154. Activity against gram-positive bacteria. CAS No. 31871-62-2. Molecular formula: C35H59N7O8. Mole weight: 705.88. | |
| Monascin | Monascin is a kind of azaphilonoid pigments extracted from Monascus pilosus -fermented rice (red-mold rice). Monascin also exhibits anti-tumor-initiating activity and anti-inflammatory activity with oral administration. Monascin inhibits the activation of NOR 1 (an NO donor). Monascin is a Nrf2 activator and PPARγ agonist [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 21516-68-7. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N6641. | |
| Monascuspiloin | Monascuspiloin is a fungal metabolite isolated from M. pilosus M93-fermented rice. It induces endoplasmic reticulum stress and autophagy in PC3 prostate cancer cells. It is a moderately potent inhibitor of HMG-CoA reductase and has potent anti-androgen activity. Synonyms: Monascinol; (3S,3aR,9aR)-3-(1-hydroxyhexyl)-9a-methyl-6-((E)-prop-1-en-1-yl)-3a,4,8,9a-tetrahydro-2H-furo[3,2-g]isochromene-2,9(3H)-dione. Grade: ≥95% by HPLC. CAS No. 1011244-19-1. Molecular formula: C21H28O5. Mole weight: 360.44. | |
| Monastrol | Monastrol is a potent and cell-permeable inhibitor of the mitotic kinesin Eg5 with an IC50 value of 14 ?M. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (±)-Monastrol. CAS No. 329689-23-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101071A. | |
| Monastrol | ?98% (HPLC), solid. Group: Fluorescence/luminescence spectroscopy. | |
| Monastrol (6-Methyl-4-(3-hydroxyphenyl)-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate) | A cell-permeablesmall molecule inhibitor of the mitotic kinesin, Eg5, arrests cells in mitosis with monoastral spindles. Group: Biochemicals. Alternative Names: 6-Methyl-4-(3-hydroxyphenyl)-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Monazomycin | It is a macrocylic polyol lactone antibiotic isolated from several species of streptoverticillium. It has the activity against gram-positive bacteria and has weak activity against gram-negative bacteria. It is an important bioprobe for understanding membrane channels. Synonyms: Takacidin; U-0142; 48-(7-amino-1-methylheptyl)-8,10,16,20,24,26,28,32,36,38,40,42,44,46-tetradecahydroxy-23-(α-D-mannopyranosyloxy)-9,15,17,19,21,25,31,33,39,41,47-undecamethyl-oxacyclooctatetraconta-13,17,21,29-tetraen-2-one. Grade: >95% by HPLC. CAS No. 11006-31-8. Molecular formula: C72H133NO22. Mole weight: 1364.82. | |
| Monensin A | Monensin A is an oxygen-containing heterocyclic polyether antibiotic produced by Str. cinnamonensis. It has antibacterial, mycobacterial, fungal and protozoan activity, but it has a weaker effect on gram-negative bacteria and has an inhibitory effect on HeLa cells. Synonyms: Monensic acid; monensin; Monensina; Monensinum. Grade: >95% by HPLC. CAS No. 17090-79-8. Molecular formula: C36H62O11. Mole weight: 670.87. | |
| Monensin A | Monensin A is a polyether antibiotic first isolated from Streptomyces cinnamonensis in 1967. Monensin is a broad- spectrum anticoccicidial antibiotic also exhibiting antifungal and antiviral activity. Monensin A forms complexes with monovalent cations such as Li+, Na+, K+, Rb+, Ag+ and Tl+ and is thus able to transport these cations across lipid membranes of cells, playing an important role as an Na+/H+ antiporter. It blocks intracellular protein transport and is used in the treatment of animals to prevent coccidiosis, promote growth and prevent bloat. Derivatives of monensin, monensin methyl ester and particularly monensin decyl ester, are used in ion selective electrodes. Group: Biochemicals. Grades: Highly Purified. CAS No. 17090-79-8. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Monensin B | Monensin B is an oxygen-containing heterocyclic polyether antibiotic produced by Str. cinnamonensis. It has antibacterial, mycobacterial, fungal and protozoan activity, but it has a weaker effect on gram-negative bacteria and has an inhibitory effect on HeLa cells. Synonyms: 16-Deethyl-16-methylmonensin. CAS No. 30485-16-6. Molecular formula: C35H60O11. Mole weight: 656.84. | |
| Monensin C | Monensin C is an oxygen-containing heterocyclic polyether antibiotic produced by Str. cinnamonensis. It has antibacterial, mycobacterial, fungal and protozoan activity, but it has a weaker effect on gram-negative bacteria and has an inhibitory effect on HeLa cells. CAS No. 31980-87-7. Molecular formula: C37H64O11. Mole weight: 684.89. | |
| Monensin D | Monensin D is an oxygen-containing heterocyclic polyether antibiotic produced by Str. cinnamonensis. It has antibacterial, mycobacterial, fungal and protozoan activity, but it has a weaker effect on gram-negative bacteria and has an inhibitory effect on HeLa cells. Molecular formula: C37H64O11. Mole weight: 684.89. | |
| Monensin (HRP) | Monensin (HRP). Group: Biochemicals. Grades: Purified. Pack Sizes: 500ul. US Biological Life Sciences. | Worldwide |
| Monensin methyl ester | ?97.0% (TLC). Group: Ionophores potentiometric for ise. | |
| Monensin Methyl Ester | A polyether ionophore antibiotic. Widely used in ion selective electrodes. Group: Biochemicals. Alternative Names: Methyl Monensin. Grades: Highly Purified. CAS No. 28636-21-7. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
| Monensin sodium | Monensin (Monensin A) sodium, an orally active antibiotic , is an ionophore that mediates Na + /H + exchange. Monensin sodium is a potent Wnt signaling inhibitor. Monensin sodium causes a marked enlargement of the multivesicular bodies (MVBs) and regulates exosome secretion. Monensin sodium can be used for bacterial, fungal, and parasitic infections research, and shows anticancer effects [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. Alternative Names: Monensin A sodium. CAS No. 22373-78-0. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-N0150. | |
| Monensin sodium | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Monensin sodium salt | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C36H61NaO11. CAS No. 22373-78-0. Prepack ID 85518862-1g. Molecular Weight 692.85. See USA prepack pricing. |  |
| Monensin sodium salt | Sodium Monensin, isolated from Streptomyces cinnamonensis, is a well-known representative of naturally polyether ionophore antibiotics. It is widely used in ruminant animal feeds. Synonyms: Monensin A sodium salt; 2-[5-ethyltetrahydro-5-[tetrahydro-3-methyl-5-[tetrahydro-6-hydroxy-6-hydroxymethyl-3,5-dimethyl-2H-pyran-2-yl]-2-furyl]-2-furyl]-9-hydroxy-β-methoxy-α,γ,2,8-tetramethyl-1,6-dioxaspiro[4.5]decane-7-butyric acid, monosodium salt; A 3823A; Coban; Rumensin; NSC 343257. Grade: >98%. CAS No. 22373-78-0. Molecular formula: C36H61NaO11. Mole weight: 692.85. | |
| Monensin Sodium Salt | Poliether antibiotic. Coccidiostat. Group: Biochemicals. Alternative Names: 2-[5-Ethyltetrahydro-5-[tetrahydro-3-methyl-5-[tetrahydro-6-hydroxy-6-(hydroxymethyl)-3,5-dimethyl-2H-pyran-2-yl]-2-furyl]-2-furyl]-9-hydroxy- β-methoxy-α,γ,2,8-tetramethyl-. Grades: Highly Purified. CAS No. 22373-78-0. Pack Sizes: 10mg, 100mg, 250mg, 500mg. Molecular Formula: C36H61NaO11, Form: Off-White. US Biological Life Sciences. | Worldwide |
| Monensin Sodium Salt | 90-95% (TLC). Group: Fluorescence/luminescence spectroscopypharma & vet compounds & metabolitesenvironmental food contaminantspharma & vet compounds & metaboliteschiral molecules. Alternative Names: Coban, Monensin sodium, Sodium monensin, CRC Rumensin, Monensin A sodium salt, 1,6-Dioxaspiro[4.5]decane-7-butyric acid, 2-[5-ethyltetrahydro-5-[tetrahydro-3-methyl-5-[tetrahydro-6-hydroxy-6-(hydroxymethyl)-3,5-dimethyl-2H-pyran-2-yl]-2-furyl]-2-furyl]-9-hydroxy-β-methoxy-α,γ,2,8-tetramethyl-, monosodium salt (8CI),Monensin, sodium salt (1:1), Monensin, monosodium salt (9CI), Monensin sodium salt, Rumensin, Coban 45, NSC 343257. | |
| Monensin Sodium salt, 90- ≥95% (TLC) | Monensin Sodium salt, 90- ≥95% (TLC). Group: Biochemicals. Grades: Reagent Grade. CAS No. 22373-78-0. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| Monepantel | Monepantel is organic anthelmintic, and acts as a positive allosteric modulator of a nematode-specific clade of nicotinic acetylcholine receptor ( nAChR ) subunits. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AAD1566. CAS No. 887148-69-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14774. | |
| Monepantel-[d5] | Monepantel-[d5] is the labelled analogue of Monepantel, which is a new anthelmintic agent used in the treatment of parasitic nematodes via stun or kill without damaging the host entity. Synonyms: Monepantel-D5; N-[(1S)-1-Cyano-2-(5-cyano-2-trifluoromethylphenoxy)-1-methylethyl-D5]-4-trifluoromethylsulfanyl benzamide; N-[(1S)-1-Cyano-2-[5-cyano-2-(trifluoromethyl)phenoxy]-1-methylethyl]-4-[(trifluoromethyl)thio]benzamide-d5. Grade: > 95%. Molecular formula: C20H8D5F6N3O2S. Mole weight: 478.43. | |
| Mongersen sodium | Mongersen sodium is a specific and orally active SMAD7 antisense oligonucleotide. Mongersen sodium restores TGF-?1 activity leading to inhibition of inflammatory signals. Mongersen sodium can attenuate Crohn's disease-like experimental colitis in mice[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GED-0301 sodium. CAS No. 1443994-98-6. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-145721A. | |
| Monic Acid A | Monic Acid A is the major metabolite of the antibiotic Mupirocin. Monic Acid A is also used in the preparation of cereal herbicide and mycoplasma inhibitors. Group: Biochemicals. Alternative Names: (2E) -5, 9-Anhydro-2, 3, 4, 8-tetradeoxy-8- [ [ (2S, 3S) -3- [ (1S, 2S) -2-hydroxy-1-methylpropyl] oxiranyl] methyl] -3-methyl-L-talo-non-2-enonic Acid; [2E, 8[2S, 3S (1S, 2S) ]]-5, 9-anhydro-2, 3, 4, 8-tetradeoxy-8-[[3- (2-hydroxy-1-methylpropyl) oxiranyl]methyl]-3-methyl-L-talo-non-2-enonic Acid; Monic Acid. Grades: Highly Purified. CAS No. 66262-68-8. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Moniliformin | Moniliformin is a potent, water-soluble mycotoxin produced by several species of Fusarium. Comparative studies of the toxicity of moniliformin to chicken cell lines revealed no toxicity to chondrocytes and macrophages, but toxicity to splenocytes, cardiac and skeletal myocytes. Moniliformin selectively inhibits mitochondrial oxidization of pyruvate and a-ketoglutarate, however the mode of action is not yet completely resolved. Group: Biochemicals. Grades: Highly Purified. CAS No. 52591-22-7. Pack Sizes: 500ug. Molecular Formula: C4HNO3Na, Molecular Weight: ~120. US Biological Life Sciences. | Worldwide |
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