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| Product | Description | |
|---|---|---|
| Mometasone Furoate Impurity 4 | Mometasone Furoate Impurity 4. Uses: For analytical and research use. Molecular formula: C27H29Cl3O5. Mole weight: 539.87. Catalog: APB08571. |  |
| Mometasone Furoate Impurity 5 | Mometasone Furoate Impurity 5. Uses: For analytical and research use. Molecular formula: C37H34Cl2O10. Mole weight: 709.57. Catalog: APB08570. | |
| 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 B | Mometasone Furoate Impurity B. Uses: For analytical and research use. CAS No. 223776-49-6. Molecular formula: C28H31ClO8S. Mole weight: 563.06. Catalog: APB223776496. | |
| Mometasone Furoate Impurity C | Mometasone Furoate Impurity C. Uses: For analytical and research use. CAS No. 1305334-31-9. Molecular formula: C27H29ClO6. Mole weight: 484.97. Catalog: APB1305334319. | |
| Mometasone Furoate Impurity D | Mometasone Furoate Impurity D. Uses: For analytical and research use. CAS No. 83881-09-8. Molecular formula: C27H31ClO6. Mole weight: 486.99. Catalog: APB83881098. | |
| Mometasone Furoate Impurity E | Mometasone Furoate Impurity E. Uses: For analytical and research use. CAS No. 1370190-33-2. Molecular formula: C32H32Cl2O8. Mole weight: 615.5. Catalog: APB1370190332. | |
| Mometasone Furoate Impurity F | Mometasone Furoate Impurity F. Uses: For analytical and research use. Alternative Names: Pregna-1,4-diene-3,6,20-trione, 9,21-dichloro-17-[(2-furanylcarbonyl)oxy]-11- hydroxy-16-methyl. CAS No. 1305334-30-8. Molecular formula: C27H28Cl2O7. Mole weight: 535.41 g/mol. Catalog: APB1305334308. | |
| Mometasone Furoate Impurity H | Mometasone Furoate Impurity H. Uses: For analytical and research use. CAS No. 148596-90-1. Molecular formula: C27H31ClO7. Mole weight: 502.99. Catalog: APB148596901. | |
| Mometasone Furoate Impurity I | Mometasone Furoate Impurity I. Uses: For analytical and research use. Molecular formula: C29H34Cl2O8. Mole weight: 581.48. Catalog: APB08565. | |
| Mometasone Furoate Impurity J | Mometasone Furoate Impurity J. Uses: For analytical and research use. CAS No. 1370190-55-8. Molecular formula: C28H32Cl2O6. Mole weight: 535.46. Catalog: APB1370190558. | |
| Mometasone Furoate Impurity K | Mometasone Furoate Impurity K. Uses: For analytical and research use. CAS No. 4647-20-5. Molecular formula: C22H29ClO5. Mole weight: 408.92. Catalog: APB4647205. | |
| Mometasone Furoate Impurity M | Mometasone Furoate Impurity M. Uses: For analytical and research use. CAS No. 57780-86-6. Molecular formula: C22H29ClO4. Mole weight: 392.92. Catalog: APB57780866. | |
| Mometasone Furoate Impurity N | Mometasone Furoate Impurity N. Uses: For analytical and research use. CAS No. 352315-75-4. Molecular formula: C23H31ClO7S. Mole weight: 487.01. Catalog: APB352315754. | |
| Mometasone Furoate Impurity O | Mometasone Furoate Impurity O. Uses: For analytical and research use. CAS No. 24916-91-4. Molecular formula: C24H31ClO6. Mole weight: 450.96. Catalog: APB24916914. | |
| Mometasone Furoate Impurity P | Mometasone Furoate Impurity P. Uses: For analytical and research use. Molecular formula: C27H31ClO7. Mole weight: 502.99. Catalog: APB08566. | |
| Mometasone Furoate Impurity R | Mometasone Furoate Impurity R. Uses: For analytical and research use. CAS No. 1370190-08-1. Molecular formula: C28H33ClO9S. Mole weight: 581.07. Catalog: APB1370190081. | |
| Mometasone Furoate Impurity S | Mometasone Furoate Impurity S. Uses: For analytical and research use. CAS No. 2231764-75-1. Molecular formula: C27H30Cl2O6. Mole weight: 521.43. Catalog: APB2231764751. | |
| Mometasone Furoate Impurity T | Mometasone Furoate Impurity T. Uses: For analytical and research use. Molecular formula: C27H29Cl3O6. Mole weight: 555.87. Catalog: APB08567. | |
| Mometasone Furoate Impurity U | Mometasone Furoate Impurity U. Uses: For analytical and research use. CAS No. 134429-33-7. Molecular formula: C27H30Cl2O7. Mole weight: 537.43. Catalog: APB134429337. | |
| Mometasone Furoate Impurity V | Mometasone Furoate Impurity V. Uses: For analytical and research use. 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 (Standard) | Mometasone (Standard) is the analytical standard of Mometasone. This product is intended for research and analytical applications. 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. Category: Signaling pathways. CAS No. 105102-22-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-B0629R. |  |
| 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. |  |
| MOMIPP | MOMIPP, a macropinocytosis inducer, is a PIKfyve inhibitor. MOMIPP penetrates the blood-brain barrier (BBB)[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1363421-46-8. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-119624. | |
| Momordicin IV | Momordicin IV is a natural product found in Momordica charantia (bitter melon). Alternative Names: 19-Norlanosta-5,24-diene-9-carboxaldehyde, 7-(β-D-glucopyranosyloxy)-3,23-dihydroxy-, (3β,7β,9β,10α,24R)-; (3S,7S,8S,9R,10R,13R,14S,17R)-3-hydroxy-17-((2R,4R)-4-hydroxy-6-methylhept-5-en-2-yl)-4,4,13,14-tetramethyl-7-(((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-1,2,3,4,7,8,10,11,12,13,14,15,16,17-tetradecahydro-9H-cyclopenta[a]phenanthrene-9-carbaldehyde; (3β,7β,9β,10α,24R)-7-(β-D-Glucopyranosyloxy)-3,23-dihydroxy-19-norlanosta-5,24-diene-9-carboxaldehyde; Momordicine IV. Grades: ≥95%. CAS No. 894412-35-2. Molecular formula: C36H58O9. Mole weight: 634.85. |  |
| Momordicoside G | Momordicoside G is isolated from the herbs of Mormodica charantia L. Alternative Names: (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. Grades: 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). Alternative Names: 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. Grades: ≥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). Alternative Names: 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. Grades: ≥95%. CAS No. 81348-83-6. Molecular formula: C36H58O9. Mole weight: 634.85. | |
| Momordin 1e | Momordin 1e is a potent bioactive compound derived from the Chinese medicinal herb, Momordica charantia. It exhibits remarkable anticancer activity by inhibiting cell proliferation and inducing apoptosis in various cancer cells. Alternative Names: Momordin Ie; (3β)-17-Carboxy-28-norolean-12-en-3-yl O-α-L-arabinopyranosyl-(1→3)-O-[β-D-xylopyranosyl-(1→2)]-β-D-glucopyranosiduronic acid. CAS No. 96158-13-3. Molecular formula: C46H72O17. Mole weight: 897.05. | |
| Momordin 2e | Momordin 2e is a remarkable compound, holding immense application for cancer research. Carefully extracted from the renowned Chinese herb, Momordica grosvenori, it showcases extraordinary inhibition against diverse cancer cell lines, such as breast, lung and colon. Alternative Names: (3β)-28-(β-D-Glucopyranosyloxy)-28-oxoolean-12-en-3-yl O-α-L-arabinopyranosyl-(1→3)-O-[β-D-xylopyranosyl-(1→2)]-β-D-glucopyranosiduronic acid; Hemsloside Ma 2; Momordin IIe. CAS No. 96158-12-2. Molecular formula: C52H82O22. Mole weight: 1059.19. | |
| 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. Category: Signaling pathways. CAS No. 96990-18-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0330. | |
| Momordin Ic | Momordin Ic, isolated from the fruits of Kochia scoparia (L.) Schrad, induced apoptosis through oxidative stress-regulated mitochondrial dysfunction involving the MAPK and PI3K-mediated iNOS and HO-1 pathways. Thus, Momordin Ic might represent a potential source of anticancer candidate. Momordin Ic and oleanolic acid obtained from KF appear to contribute to alleviating the adverse effects of CCl4 treatment by enhancing the hepatic antioxidant defense system. What's more, Momordin Ic accelerates gastrointestinal transit partially by stimulating synthesis of 5-HT to act through 5-HT(2), possibly 5-HT(2C) and/or 5-HT(2B) receptors, which, in turn, increases synthesis of prostaglandins. Uses: Antibacterial. Alternative Names: (3b)-17-Carboxy-28-norolean-12-en-3-yl 3-O-(b-D-xylopyranosyl)-b-D-glucuronide; (3β)-17-Carboxy-28-norolean-12-en-3-yl 3-O-β-D-xylopyranosyl-β-D-glucopyranosiduronic acid; Mormordin Ic. Grades: >98%. CAS No. 96990-18-0. Molecular formula: C41H64O13. Mole weight: 764.94. | |
| 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. Alternative Names: 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. Grades: >95% by HPLC. CAS No. 7182-54-9. Molecular formula: C41H66O12. Mole weight: 750.95. | |
| 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. Category: Signaling pathways. Alternative Names: IPH2201. CAS No. 1228763-95-8. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-P99032. | |
| Monalizumab | Monalizumab is a first-in-class immune checkpoint inhibitor that targets Natural Killer Group 2A (NKG2A). Monalizumab increased degranulation and IFN-γ production by NKG2A+ NK cell against HLA-E+ target cells, thereby promoting NK cell effector functions. Alternative Names: IPH2201. CAS No. 1228763-95-8. | |
| 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 pigment that displays more anti-atherosclerosis effect and less side effect involving increasing creatinine phosphokinase activity. Alternative Names: Monascoflavin; 2H-Furo[3,2-g][2]benzopyran-2,9(3H)-dione, 3a,4,8,9a-tetrahydro-9a-methyl-3-(1-oxohexyl)-6-(1E)-1-propen-1-yl-, (3S,3aR,9aR)-. Grades: >95%. CAS No. 21516-68-7. Molecular formula: C21H26O5. Mole weight: 358.44. | |
| 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. Category: Signaling pathways. CAS No. 21516-68-7. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N6641. | |
| Monascorubramine | Monascorubramine is a microbial colorant. Monascorubramine is capable of producing by the Monascus, which is from the bacteria Talaromyces. Under the condition of different pH value, the hue and chromaticity value of the colorant are also different[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3627-51-8. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N11071. | |
| Monascuspiloin | Monascuspiloin (Monascinol) exhibits anti-androgenic activity with an IC50 of 7 μM. Monascuspiloin inhibits viability of PC-3 and LNCaP with IC50 of 45 and 47 μM. Monascuspiloin induces apoptosis in LNCaP through inhibition of Akt/mTOR signaling pathway, induces autophagy through activation AMPK signaling pathway and arrest cell cycle at G2/M phase in PC-3. Monascuspiloin exhibits antitumor efficacy in mice[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Monascinol. CAS No. 1011244-19-1. Pack Sizes: 500 μg; 1 mg. Product ID: HY-N12124. | |
| 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. Alternative Names: 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. Grades: ≥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 μM. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (±)-Monastrol. CAS No. 329689-23-8. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101071A. | |
| 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. Alternative Names: 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. Grades: >95% by HPLC. CAS No. 11006-31-8. Molecular formula: C72H133NO22. Mole weight: 1364.82. | |
| Monensin | Monensin (Monensin A), an orally active antibiotic, is an ionophore that mediates Na+/H+ exchange. Monensin is a potent Wnt signaling inhibitor. Monensin causes a marked enlargement of the multivesicular bodies (MVBs) and regulates exosome secretion. Monensin can be used for bacterial, fungal, and parasitic infections research, and shows anticancer effects[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Monensin A. CAS No. 17090-79-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N4302. | |
| 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. Alternative Names: Monensic acid; monensin; Monensina; Monensinum. Grades: >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. Alternative Names: 16-Deethyl-16-methylmonensin. CAS No. 30485-16-6. Molecular formula: C35H60O11. Mole weight: 656.84. | |
| Monensin B | Monensin B is a polyketide produced by Streptomyces cinnamonensis. Fermentations of Streptomyces cinnamonensis produce a mixture of Monensin A and Monensin B in a ratio dependent upon the relative concentrations of ethylmalonyl-CoA and methylmalonyl-CoA[1]. Uses: Scientific research. Category: Natural products. CAS No. 30485-16-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N4301. | |
| 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 decyl ester | Monensin decyl ester. CAS No. 164231-69-6. Purity: 96%. Product ID: ACM164231696. Molecular formula: C46H82O11. Mole weight: 811.14. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Monensin decyl ester | Monensin decyl ester. Alternative Names: Monensin decyl ester, 164066-23-3. CAS No. 164066-23-3. Purity: 96%. Product ID: ACM164066233. Molecular formula: C46H82O11. Mole weight: 811.14. IUPAC Name: decyl (2S,3R,4S)-4-[(2S,7S,8R,9S)-2-[(2R,5S)-5-ethyl-5-[(2R,3S,5R)-5-[(2S,3S,5R,6R)-6-hydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]-3-methyloxolan-2-yl]oxolan-2-yl]-7-hydroxy-2,8-dimethyl-1,10-dioxaspiro[4.5]decan-9-yl]-3-methoxy-2-methylpentanoate. Alfa Chemistry - ISO 9001:32057 Certified. | |
| 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 Methyl Ester | Monensin Methyl Ester. CAS No. 28636-21-7. Molecular formula: C37H64O11. Mole weight: 684.9. | |
| 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. Category: Signaling pathways. Alternative Names: Monensin A sodium. CAS No. 22373-78-0. Pack Sizes: 10 mM * 1 mL in Ethanol; 100 mg. Product ID: HY-N0150. | |
| 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. Alternative Names: 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. Grades: >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) | 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, also known as AAD 1566, is a new anthelmintic agent used in the treatment of parasitic nematodes via stun or kill without damaging the host entity. Alternative Names: AAD1566; AAD 1566; N-(2-Cyano-1-((2S)-5-cyano-2-(trifluoromethyl)phenoxy)propan-2-yl)-4-(trifluoromethylsulfanyl)benzamide. Grades: 98%. CAS No. 887148-69-8. Molecular formula: C20H13F6N3O2S. Mole weight: 473.39. | |
| Monepantel | Monepantel (AAD1566, NUZ-001), an antiparasitic agent, is an orally active mTOR inhibitor. Monepantel triggers autophagy through the deactivation of mTOR/p70S6K signalling pathway. Monepantel is a positive allosteric modulator of a nematode-specific clade of nAChR subunits. Monepantel can be used for the study of amyotrophic lateral sclerosis (ALS) and ovarian cancer[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AAD1566; NUZ-001. CAS No. 887148-69-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14774. | |
| Mongersen sodium | Mongersen sodium is a specific and orally active SMAD7 antisense oligonucleotide. Mongersen sodium restores TGF-β1 activity leading to inhibition of inflammatory signals. Mongersen sodium can attenuate Crohn's disease-like experimental colitis in mice[1][2]. Uses: Scientific research. Category: 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, a kind of water-soluble mycotoxin, could be obtained from sorts of Fusarium and has been found to exhibit toxicity to splenocytes, cardiac and skeletal myocytes. Alternative Names: 1-Hydroxycyclobut-1-ene-3,4-dione. Grades: >98%. CAS No. 71376-34-6. Molecular formula: C4HO3Na. Mole weight: 120.00. | |
| 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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