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| Product | Description | |
|---|---|---|
| Maprotiline hydrochloride | Maprotiline hydrochloride is a highly selective noradrenergic reuptake inhibitor that has strong antidepressant, antitumor and neuropathic pain-relieving effects with oral activity. Maprotiline hydrochloride induces cancer cell apoptosis by targeting the ERK signaling pathway and CRABP1 [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 10347-81-6. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0444. |  |
| Maprotiline Hydrochloride | Antidepressant. Group: Biochemicals. Alternative Names: N-Methyl-. Grades: Highly Purified. CAS No. 10347-81-6. Pack Sizes: 1g. US Biological Life Sciences. |  Worldwide |
| Maprotiline Related Compound D | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. |  |
| Maqui Berry Extract | Maqui Berry Extract. Applications: Can lower blood pressure, improve white blood cell count, but also has the effect of treatment of children with anorexia. Group: Others. Synonyms: Maqui Berry Extract; Lonicera caerulea L.var.enulis Turcz et Herd. Purity: 5%-10%Anthocyanidins, 5%-20% Proanthocyanidins, 4-50:1. Appearance: Yellow brown fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Fruit. Species: Lonicera caerulea L.var.enulis Turcz et Herd. Maqui Berry Extract; Lonicera caerulea L.var.enulis Turcz et Herd; plant extract. Pack: 25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-192. |  |
| Maralixibat chloride | Maralixibat (SHP625) chloride is an orally active ileal bile acid transporter (IBAT) inhibitor. Maralixibat chloride can be used for the research of rare cholestatic liver diseases including Alagille syndrome (ALGS), progressive familial intrahepatic cholestasis (PFIC) and biliary atresia [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SHP625 chloride; LUM001 chloride; Lopixibat chloride. CAS No. 228113-66-4. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16747. | |
| Marasmic acid | It is produced by the strain of Marasmius conigenus 6890. It's a terpene antibiotic. It has anti-gram-positive bacteria effect. It also has anti-gram-negative bacteria, mycobacteria and fungi effect, but the effect is weak. Synonyms: 3H,6H-3a,8b-Methano-1H-indeno[4,5-c]furan-4-carboxaldehyde,5a,7,8,8a-tetrahydro-3-hydroxy-7,7-dimethyl-1-oxo-, [3S-(3a,3ab,5ab,8ab,8bb)]-; NSC 318506; (3S,3aR,5aR,8aS,8bS)-3-hydroxy-7,7-dimethyl-1-oxo-5a,7,8,8a-tetrahydro-1H,3H,6H-3a,8b-methanoindeno[4,5-c]furan-4-carbaldehyde. CAS No. 2212-99-9. Molecular formula: C15H18O4. Mole weight: 262.30. |  |
| Maraviroc | Maraviroc (UK-427857) is a selective CCR5 antagonist with activity against human HIV. Uses: Scientific research. Group: Signaling pathways. Alternative Names: UK-427857. CAS No. 376348-65-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-13004. | |
| Maraviroc | Maraviroc. Group: Biochemicals. Alternative Names: 4, 4-Difluoro-N- [ (1S) -3- [ (3-exo) -3- [3- methyl -5- (1- methyl ethyl-d6) -4H-1, 2, 4-triazol-4-yl] -8-azabicyclo [3. 2. 1] oct-8-yl] -1-phenylpropyl ] cyclohexane carboxamide; UK 427857-d6. Grades: Highly Purified. CAS No. 376348-65-1. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C29H41F2N5O. US Biological Life Sciences. | Worldwide |
| Maraviroc | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopychiral moleculesenzyme activators, inhibitors & substrates. Alternative Names: Cyclohexanecarboxamide, 4,4-difluoro-N-[(1S)-3-[(3-exo)-3-[3-methyl-5-(1-methylethyl)-4H-1,2,4-triazol-4-yl]-8-azabicyclo[3.2.1]oct-8-yl]-1-phenylpropyl]-, Celsentri, Maraviroc, 4,4-Difluoro-N-[(1S)-3-[(3-exo)-3-[3-methyl-5-(1-methylethyl)-4H-1,2,4-triazol-4-yl]-8-azabicyclo[3.2.1]oct-8-yl]-1-phenylpropyl]cyclohexanecarboxamide, 4,4-Difluoro-N[(1S)-3-[(1R,5S)-3-(3-methyl-5-propan-2-yl-1,2,4-triazol-4-yl)-8-azabicyclo[3.2.1]octan-8-yl]-1-phenylpropyl]cyclohexane-1-carboxamide, Selzentry, UK 427857. | |
| Maraviroc-d6 | Potent, non-competitive CCR5 receptor antagonist; inhibits binding of HIV viral coat protein gp120. Antiviral. Group: Biochemicals. Alternative Names: 4, 4-Difluoro-N- [ (1S) -3- [ (3-exo) -3- [3- methyl -5- (1- methyl ethyl-d6) -4H-1, 2, 4-triazol-4-yl] -8-azabicyclo [3. 2. 1] oct-8-yl] -1-phenylpropyl ] cyclohexane carboxamide; UK 427857-d6. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Maraviroc-[d6] | Maraviroc-[d6] is the labelled analogue of Maraviroc. Maraviroc is an antiretroviral medicine developed for the treatment of HIV infecions. Synonyms: Maraviroc D6; 4,4-Difluoro-N-[(1S)-3-[(3-exo)-3-[3-methyl-5-(1-methylethyl-d6)-4H-1,2,4-triazol-4-yl]-8-azabicyclo[3.2.1]oct-8-yl]-1-phenylpropyl]cyclohexanecarboxamide. Grade: 95% by HPLC; 95% atom D. CAS No. 1033699-22-7. Molecular formula: C29H35D6F2N5O. Mole weight: 519.7. | |
| Marble Chips, Laboratory Grade, 2 kg | Characteristic: Gray/white. Storage Code: Green; general chemical storage. Alternative Names: Limestone, calcium carbonate. Grades: chem-grade laboratory. CAS No. 471-34-1. Product ID: 874052. -- SOLD FOR EDUCATIONAL USE ONLY -- |  |
| Marble Chips, Laboratory Grade, 500 g | Storage Code: Green; general chemical storage. Alternative Names: Limestone, calcium carbonate. Grades: chem-grade laboratory. CAS No. 471-34-1. Product ID: 874050. -- SOLD FOR EDUCATIONAL USE ONLY -- | |
| Marble's Reagent | For etching Ni, Ni-Cu and Ni-Fe alloys and superalloys. Add a few drops of H2SO4 to increase activity. Group: Etchants. |  |
| Marboflooxacin | Marbofloxacin is a Fluoroquinolone antibacterial agent specially used for veterinary use. Synonyms: 7h-pyrido(3, 2, 1-ij)(4, 1, 2)benzoxadiazine-6-carboxylicacid, 2, 3-dihydro-9-fluor; o-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-; MARBOFLOXACIN; Marbofloxacin, >=99%; MarbofloxacinChemicalbookSolution, 1000ppm; MarbofloxacinSolution, 100ppm; CS-939; 9-FLUORO-2, 3-DIHYDRO-3-METHYL-10-(4-METHYL-PIPERAZINO)-7-OXO-7H-PYRIDO[1, 2, 3-IJ][1, 2, 4]BENZOXADIAZINE-6-CARBOXYLICACID. CAS No. 115550-35-1. Product ID: PAP-0057. Molecular formula: C17H19FN4O4. Category: Anti-Infectives. Product Keywords: Antibacterial, Anti-inflammatory and Antiviral Series; Marboflooxacin; PAP-0057; Anti-Infectives; C17H19FN4O4; 115550-35-1. Appearance: Light Yellow. Standard: EP 10.0. Chemical Name: 7h-pyrido(3,2,1-ij)(4,1,2)benzoxadiazine-6-carboxylicacid,2,3-dihydro-9-fluor. Grade: Veterinary Grade. Solubility: Chloroform (Slightly, Heated). Storage: Inert atmosphere,2-8°C. Applications: antibacterial drug. Boiling Point: 571°C. Melting Point: 268-269°C (dec.). Density: 1.55±0.1 g/cm3(Predicted). Product Description: a Fluoroquinolone antibacterial agent specially used for veterinary use. |  |
| Marbofloxacin | analytical standard. Group: Application areaspharma & vet compounds & metabolitesstandards for environmental regulatory methodspharma & vet compounds & metabolitesapi standardseuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: Aurizon, Zeniquin, Marbofloxacin, Marbocyl,9-Fluoro-3-methyl-10-(4-methylpiperazin-1-yl)-7-oxo-2,3-dihydro-7H-pyrido[3,2,1-ij][4,1,2]benzoxadiazine-6-carboxylic acid. | |
| Marbofloxacin | Marbofloxacin is a third generation fluoroquinolone and orally active antimicrobial agent, which has a broad spectrum bactericidal activity and good efficacy. Marbofloxacin can be used for the research of infections by Gram-positive and Gram-negative bacteria and Mycoplasma [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 115550-35-1. Pack Sizes: 100 mg; 500 mg. Product ID: HY-B0126. | |
| Marbofloxacin | 100mg Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C17H19N4O4F. CAS No. 115550-35-1. Prepack ID 73817541-100mg. Molecular Weight 362.36. See USA prepack pricing. |  |
| Marbofloxacin | Fluorinated quinolone antibacterial. Group: Biochemicals. Alternative Names: 9-Fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-. Grades: Highly Purified. CAS No. 115550-35-1. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| Marbofloxacin | Marbofloxacin is a third generation fluoroquinolone antibiotic. Marbofloxacin exhibits high bactericidal activity against a broad spectrum of aerobic Gram-negative and some Gram-positive bacteria, as well as Mycoplasma spp. Uses: Anti-bacterial agents. Synonyms: 9-Fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyrido[3,2,1-ij][4,1,2]benzoxadiazine-6-carboxylic Acid; Marbocyl; Zeniquin; Marbofloxacinum. Grade: >98%. CAS No. 115550-35-1. Molecular formula: C17H19FN4O4. Mole weight: 362.36. | |
| Marbofloxacin EP Impurity D | Marbofloxacin EP Impurity D. Uses: For analytical and research use. Group: Impurity standards. CAS No. 100276-37-7. Molecular formula: C16H18F2N4O3. Mole weight: 352.34. Catalog: APB100276377. | |
| Marbon CNB 23010. | Halogenated norbornene-methanonaphthalene derivative. Group: Biochemicals. Alternative Names: 1, 2, 3, 4, 9, 9-Hexachloro-6-(1, 4, 5, 6, 7, 7-hexachlorobicyclo[2. 2. 1]hept-5-en-2-yl)-1, 4, 4a, 5, 6, 7, 8, 8a-octahydro-1, 4-methanonaphthalene. Grades: Highly Purified. CAS No. 26595-57-3. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Marcellomycin | Marcellomycin is produced by the strain of Actinosporangium bohemicum sp. nov. C-36145. It is a glycoside and quinone antibiotic. It has anti-gram-positive bacteria effect, especially has strong effect on streptococcus. It also has effect on individual gram-negative bacteria, but the activity is not strong. Marcellomycin was 4 times stronger than Musettamycin in the treatment of leukemia L-1210. Synonyms: Morcellomycin; Pyrromycin; Mar; Rhodirubin E; Antibiotic MA 144U2; 1-Naphthacenecarboxylic acid, 4-((O-2,6-dideoxy-alpha-L-lyxo-hexopyranosyl-(1-4)-O-2,6-dideoxy-alpha-L-lyxo-hexopyranosyl-(1-4)-2,3,6-trideoxy-3-(dimethylamino)-alpha-L-lyxo-hexopyranosyl)oxy)-2-ethyl-1,2,3,4,6,11-hexahydro-2,5,7,10-tetrahydroxy-6,11-dioxo-, methyl ester, (1R-(1-alpha,2-beta,4-beta))-. CAS No. 63710-10-1. Molecular formula: C42H55NO17. Mole weight: 845.89. | |
| Marcfortine A | It is an indole alkaloid isolated from Aspergillus and Penicillium species. It has strong nematicidal activity. It is structurally related to paracetamol and can act by preventing cholinergic neuromuscular transmission. Synonyms: UK 111866. Grade: >99% by HPLC. CAS No. 75731-43-0. Molecular formula: C28H35N3O4. Mole weight: 477.59. | |
| Marcfortine A (Antibiotic UK 111866) | Marcfortine A is an indole alkaloid isolated from Aspergillus and Pencillium species with potent nematocidal activity. The marcfortines are structurally related to paraherquamides and thought to act by blockade of cholinergic neuromuscular transmission. Group: Biochemicals. Alternative Names: Antibiotic UK 111866. Grades: Highly Purified. CAS No. 75731-43-0. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| MARCKS Peptide (151-175), Phosphorylated | MARCKS Peptide (151-175), Phosphorylated is a phosphorylated peptide corresponding to the basic effector domain of myristoylated alanine-rich protein kinase C substrate protein (MARCKS). Phosphorylation of MARCKS Peptide (151-175) reverses its inhibition of phosphatidylinositol 4,5-diphosphate (PIP2) catalyzed hydrolysis by phospholipase C (PLC). Synonyms: Lys-Lys-Lys-Lys-Lys-Arg-Phe-pSer-Phe-Lys-Lys-pSer-Phe-Lys-Leu-Ser-Gly-Phe-pSer-Phe-Lys-Lys-Asn-Lys-Lys. Grade: ≥95%. Molecular formula: C147H246N41O40P3. Mole weight: 3320.69. | |
| Mardepodect | Mardepodect (PF-2545920) is a potent, orally active and selective PDE10A inhibitor with an IC 50 of 0.37 nM, with >1000-fold selectivity over other PDEs. Mardepodect can cross the blood-brain barrier [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PF-2545920. CAS No. 898562-94-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-50098. | |
| Mardepodect free base | Mardepodect, also known as PF-2545920, is a phosphodiesterase inhibitor selective for the PDE10A subtype, which is potentially useful for the treatment of schizophrenia. Phosphodiesterase 10A (PDE10A) is highly expressed in striatal medium spiny neurons of both the direct and indirect output pathways. PDE10A inhibitors have shown behavioral effects in rodent models that predict antipsychotic efficacy. PF-2545920 is active in a range of antipsychotic models, antagonizing apomorphine-induced climbing in mice, inhibiting conditioned avoidance responding in both rats and mice, and blocking N-methyl-D-aspartate antagonist-induced deficits in prepulse inhibition of acoustic startle response in rats, while improving baseline sensory gating in mice. Uses: Designed for use in research and industrial production. Additional or Alternative Names: PF-2545920; PF 2545920; PF2545920; MP-10; MP10; MP 10, Mardepodect. Product Category: Inhibitors. Appearance: Solid powder. CAS No. 898562-94-2. Molecular formula: C25H20N4O. Mole weight: 392. Purity: >98%. IUPACName: 2-(4-(1-methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)phenoxymethyl)quinoline. Canonical SMILES: CN1N=C(C2=CC=C(OCC3=NC4=CC=CC=C4C=C3)C=C2)C(C5=CC=NC=C5)=C1. Product ID: ACM898562942. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Mardepodect hydrochloride | Mardepodect hydrochloride (PF-2545920 hydrochloride) is a potent, orally active and selective PDE10A inhibitor with an IC 50 of 0.37 nM, with >1000-fold selectivity over other PDEs. Mardepodect hydrochloride can cross the blood-brain barrier [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PF-2545920 hydrochloride. CAS No. 2070014-78-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-50098A. | |
| Marein | Marein has the neuroprotective effect due to a reduction of damage to mitochondria function and activation of the AMPK signal pathway. Marein improves insulin resistance induced by high glucose in HepG2 cells through CaMKK/AMPK/GLUT1 to promote glucose uptake, through IRS/Akt/GSK-3β to increase glycogen synthesis, and through Akt/FoxO1 to decrease gluconeogenesis. Marein is a HDAC inhibitor with an IC50 of 100 μM. Marein has beneficial antioxidative, antihypertensive, antihyperlipidemic and antidiabetic effects. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: Solid. CAS No. 535-96-6. Molecular formula: C21H22O11. Mole weight: 450.39. Purity: 0.99. Canonical SMILES: O=C(C1=CC=C(O[C@H]2[C@@H]([C@H]([C@@H]([C@@H](CO)O2)O)O)O)C(O)=C1O)/C=C/C3=CC=C(O)C(O)=C3. Product ID: ACM535966. Alfa Chemistry ISO 9001:2015 Certified. | |
| Maresin 1 | Maresin 1, produced by human Mφs from endogenous docosahexaenoic acid (DHA) and a specialized proresolving mediator, stimulates intracellular [Ca 2+ ] and secretion. Maresin 1 possesses anti-inflammatory activity [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1268720-28-0. Pack Sizes: 10 μg (277.4 μM * 100 μL in Ethanol); 25 μg (277.4 μM * 250 μL in Ethanol). Product ID: HY-116429. | |
| Marfey's Reagent | Used for chiral amino acid analysis. Group: Biochemicals. Alternative Names: Nα-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide; 1-Fluoro-2,4-dinitrophenyl-5-L-alanine Amide; FDAA; Marfeys Reagent. Grades: Highly Purified. CAS No. 95713-52-3. Pack Sizes: 250mg, 500mg, 1g. Molecular Formula: C?H?FN?O?, Molecular Weight: 272.19. US Biological Life Sciences. | Worldwide |
| Margarine (vitamins) | certified Reference Material. Group: Certified reference materials (crms). | |
| Margatoxin | ?99%, recombinant, expressed in E. coli. Group: Fluorescence/luminescence spectroscopy. | |
| Margatoxin | Potent KV1.3 channel blocker (IC50 = 36 pM). Displays no effect at calcium-activated channels. Reduces VEGF-induced transmembrane calcium influxes and nitric oxide production in human endothelial cells. Group: Biochemicals. Grades: Purified. CAS No. 145808-47-5. Pack Sizes: 100ug. Molecular Formula: C178H286N52O50S7, Sequence: TIINVKCTSPKQCLPPCKAQFG QSAGAKCMNGKCKCYPH. US Biological Life Sciences. | Worldwide |
| Margatoxin | ?90% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Margatoxin | Margatoxin (MgTx) is a component of the venom of Scorpio Centruroides margaritatus. Margatoxin preferentially inhibits voltage-dependent potassium channels Kv1.3 with an IC50 value around 50 pM (20 fold more potent than Charybdotoxin) and irreversibly inhibits the proliferation response of human T-cells at 20 μM concentration. Uses: Potassium channel blockers. Synonyms: MgTX. Grade: >98%. CAS No. 145808-47-5. Molecular formula: C178H286N52O50S7. Mole weight: 4178.96. | |
| Margetuximab | Margetuximab (MGAH22) is a chimeric anti- HER2 monoclonal antibody optimized Fc domain, with an EC 50 value of 39.33 ng/mL. Margetuximab can be used for researching metastatic HER2-positive breast cancer [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 1350624-75-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99030. | |
| Maribavir | Maribavir is a potent inhibitor of histone phosphorylation catalyzed by wild-type pUL97 in vitro, with an IC 50 of 3 nM. Maribavir has potent antiviral activity against HCMV and Epstein-Barr virus ( EBV ). Uses: Scientific research. Group: Signaling pathways. Alternative Names: 1263W94; BW1263W94; GW257406X. CAS No. 176161-24-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16305. | |
| Maridebart | Maridebart is a human immunoglobulin G1-kappa, anti-GIPR (gastric inhibitory polypeptide receptor) monoclonal antibody [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: AMG133 antibody. CAS No. 2761478-99-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P990047. | |
| Maridebart cafraglutide | Maridebart cafraglutide (AMG 133) is an antibody-peptide conjugate acting as a GLP-1 receptor agonist and an antagonist of the GIP receptor. Maridebart cafraglutide reduces body weight and improve metabolic markers in male obese mice and cynomolgus monkeys. Maridebart cafraglutide is promising for research of obesity [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AMG 133. CAS No. 2887445-76-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-164535. | |
| Maridomycin II | It is produced by the strain of Str. hygroscopicus B-5050. It's a macrolide antibiotic. It has the activity against gram-positive bacteria and mycoplasma. It has anti-mycobacterial effect but the effect is not strong. Serum dose not affect its antibacterial activity. It has the effect of protecting gram-positive bacterial infection mice, and the therapeutic dose is similar to styloleomycin. Synonyms: 9-Dihydrocarbomycin A; Antibiotic B 5050B; B 5050B; Antibiotic YL 704C4; Leucomycin V, 12,13-dihydro-12,13-epoxy-, 3-acetate 4B-(3-methylbutanoate), (12S,13S)-. Grade: ≥95%. CAS No. 35908-45-3. Molecular formula: C42H69NO16. Mole weight: 843.99. | |
| Maridomycin III | It is produced by the strain of Str. hygroscopicus B-5050. It's a macrolide antibiotic. It has the activity against gram-positive bacteria and mycoplasma. Serum dose not affect its antibacterial activity. It has the effect of protecting gram-positive bacterial infection mice, and the therapeutic dose is similar to styloleomycin. Synonyms: Platenomycin C1; Leucomycin V, 12,13-epoxy-12,13-dihydro-, 3,4B-dipropanoate, (12S,13S)-; Antibiotic B 5050C; Antibiotic YL 704C1; Turimycin EP3; Maridomycine; Maridomycinum. Grade: ≥95%. CAS No. 35775-82-7. Molecular formula: C41H67NO16. Mole weight: 829.97. | |
| Maridomycin IV | It is produced by the strain of Str. hygroscopicus B-5050. It's a macrolide antibiotic. It has the activity against gram-positive bacteria and mycoplasma. Serum dose not affect its antibacterial activity. It has the effect of protecting gram-positive bacterial infection mice, and the therapeutic dose is similar to styloleomycin. Synonyms: Antibiotic B 5050D; Turimycin EA3; Leucomycin V, 12,13-dihydro-12,13-epoxy-, 3-acetate 4B-propanoate, (12S,13S)-. Grade: ≥95%. CAS No. 35942-56-4. Molecular formula: C40H65NO16. Mole weight: 815.94. | |
| Maridomycin V | It is produced by the strain of Str. hygroscopicus B-5050. It's a macrolide antibiotic. It has the activity against gram-positive bacteria and mycoplasma. Serum dose not affect its antibacterial activity. It has the effect of protecting gram-positive bacterial infection mice, and the therapeutic dose is similar to styloleomycin. Synonyms: Antibiotic B 5050E; Turimycin EP2; Leucomycin V, 12,13-dihydro-12,13-epoxy-, 4B-acetate 3-propanoate, (12S,13S)-. Grade: ≥95%. CAS No. 35942-57-5. Molecular formula: C40H65NO16. Mole weight: 815.94. | |
| Maridomycin VI | It is produced by the strain of Str. hygroscopicus B-5050. It's a macrolide antibiotic. It has the activity against gram-positive bacteria and mycoplasma. Serum dose not affect its antibacterial activity. It has the effect of protecting gram-positive bacterial infection mice, and the therapeutic dose is similar to styloleomycin. Synonyms: Antibiotic B 5050F; B 5050F; Leucomycin V, 12,13-dihydro-12,13-epoxy-, 3,4B-diacetate, (12S,13S)-. Grade: ≥95%. CAS No. 35775-66-7. Molecular formula: C39H63NO16. Mole weight: 801.92. | |
| Marigold Extract | Marigold flower extract is prepared from calendula marigold flower tagetes plant, which is a pigment widely used in food additives, also used as a medicinal pigment. Marigold extract lutein is an excellent anti-oxidant in food, marigold extract can prevent cellular senescence and aging body organs, but can also prevent age-related macular degeneration eye due to decreased vision and blindness. Group: Others. Mole weight: 568.88. Marigold Extract; Calendula Officinalis L. Cat No: EXTC-047. | |
| Marigold Flower Extract (Ratio) | Marigold Flower Extract (Ratio). Group: Others. Purity: 4:1~20:1. Marigold Flower Extract (Ratio). Cat No: EXTW-044. | |
| Marigold Flower P.E. Zeaxanthin 5% HPLC | Marigold Flower P.E. Zeaxanthin 5% HPLC. |  CA, FL & NJ |
| Marigold Flower Powder (Calendula Officinalis) | Marigold Flower Powder (Calendula Officinalis). | CA, FL & NJ |
| Marilactone | Marilactone is produced from the fungus Stachylidium sp. Synonyms: 2H-Pyran-2-one, 6-ethyl-4-hydroxy-3-methyl-; 3-Methyl-4-hydroxy-6-ethyl-2-pyron. Grade: ≥98%. CAS No. 34818-17-2. Molecular formula: C8H10O3. Mole weight: 154.16. | |
| Marimastat | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Marimastat | Marimastat (BB2516) is a broad spectrum and orally bioavailable inhibitor of MMPs , with potent activity against MMP-9 ( IC 50 =3 nM), MMP-1 ( IC 50 =5 nM), MMP-2 ( IC 50 =6 nM), MMP-14 ( IC 50 =9 nM) and MMP-7 ( IC 50 =13 nM), used in the treatment of cancer. Marimastat (BB2516) is an angiogenesis and metastasis inhibitor, which limits the growth and production of blood vessels. As an antimetatstatic agent it prevents malignant cells from breaching the basement membranes [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BB2516; TA2516. CAS No. 154039-60-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg. Product ID: HY-12169. | |
| Marimastat | Marimastat. Group: Biochemicals. Alternative Names: [2S-[N4 (R*) , 2R*, 3S*]]-N4-[2, 2-Dimethyl-1-[ (methylamino) carbonyl]propyl]-N1, 2-dihydroxy-3- (2-methylpropyl) butanediamide; BB 2516; GI 5712; KB-R 8898; TA 2516; (2S, 3R) -N4-[ (1S) -2, 2-Dimethyl-1-[ (methylamino) carbonyl]propyl]-N1, 2-dihydroxy-3- (2-methylpropyl) butanediamide. Grades: Highly Purified. CAS No. 154039-60-8. Pack Sizes: 5mg. Molecular Formula: C15H29N3O5, Molecular Weight: 331.41. US Biological Life Sciences. | Worldwide |
| Marimastat ( (2S, 3R) -N4-[ (1S) -2, 2-Dimethyl-1-[ (-[ (methylamino) carbonyl]propyl]-N1, 2-dihydroxy-3- (2-methylpropyl) butanediamide, BB-2516, TA-2516) | A broad spectrum matrix metalloprotease (MMP) inhibitor with IC50 values of 3, 5, 6, 9 and 13 nM for MMP-9, MMP-1, MMP-2, MMP-14 and MMP-7 respectively. It covalently binds to the zinc(II) ion in the active site of MMPs, thereby inhibiting the action of MMPs, inducing extracellular matrix degradation, and inhibiting angiogenesis, tumor growth and invasion, and metastasis. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 5mg. US Biological Life Sciences. | Worldwide |
| Marimastat - CAS 154039-60-8 | An orally active peptidyl hydroxamate-based broad-spectrum MMP inhibitor that targets both the substrate binding site and the active-site Zn2+. Group: Fluorescence/luminescence spectroscopy. | |
| Marine Costus Powder | Marine Costus Powder. | CA, FL & NJ |
| Marine venom from Chrysaora quinquecirrha (Sea Nettle) | lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| Maritimein | Maritimein. Uses: Designed for use in research and industrial production. Additional or Alternative Names: MARITIMEIN;MARITIMETIN-6-GLUCOSIDE;MARITIMETIN-6-O-GLUCOSIDE;(Z)-2-[(3,4-dihydroxyphenyl)methylene]-6-(beta-D-glucopyranosyloxy)-7-hydroxybenzofuran-3(2H)-one;MARITIMEIN WITH HPLC;MARITIMEIN hplc;2-[(Z)-3,4-Dihydroxyphenylmethylene]-6-(β-D-glucopyranosyl. Product Category: Heterocyclic Organic Compound. Appearance: Powder. CAS No. 490-54-0. Molecular formula: C21H20O11. Mole weight: 448.4. Purity: 0.98. IUPACName: (2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-7-hydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1-benzofuran-3-one. Canonical SMILES: C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O)O. Product ID: ACM490540. Alfa Chemistry ISO 9001:2015 Certified. | |
| Maritime pine extract | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Marizomib | ?95% (HPLC), (Salinospora tropica). Group: Fluorescence/luminescence spectroscopy. | |
| Marizomib | Marizomib (Salinosporamide A) is a second-generation, irreversible, brain-penetrant, pan-proteasome inhibitor. Marizomib inhibits the CT-L (β5), CT-T-laspase-like (C-L, β1) and trypsin-like (T-L, β2) activities of the 20S proteasome (IC 50 =3.5, 28, and 430 nM, respectively) [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Salinosporamide A; NPI-0052. CAS No. 437742-34-2. Pack Sizes: 100 μg; 500 μg; 1 mg; 5 mg. Product ID: HY-10985. | |
| Marizomib | Marizomib is a naturally-occurring salinosporamide, isolated from the marine actinomycete Salinospora tropica, with potential antineoplastic activity. Marizomib irreversibly binds to and inhibits the 20S catalytic core subunit of the proteasome by covalently modifying its active site threonine residues. Synonyms: (-)-Salinosporamide A; ML 858; ML858; ML-858; Marizomib; NPI 0052; NPI0052; NPI-0052; Salinosporamide A. Grade: ≥95%. CAS No. 437742-34-2. Molecular formula: C15H20ClNO4. Mole weight: 313.78. | |
| Marjoram Essential Oil | Marjoram Essential Oil. | CA, FL & NJ |
| MARK1, active, GST tagged human | recombinant, expressed in baculovirus infected Sf9 cells, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| MARK2, active, GST tagged human | recombinant, expressed in baculovirus infected Sf9 cells, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| MARK4, active, GST tagged human | recombinant, expressed in baculovirus infected Sf9 cells, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| MARK4 inhibitor 1 | MARK4 inhibitor 1 is a potent and selective microtubule affinity-regulating kinase 4 (MARK4) inhibitor, with an IC50 of 1.54 ?M. MARK4 inhibitor 1 inhibits cancer cell proliferation, metastasis and induces apoptosis[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2271081-58-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-114317. | |
| MARK-IN-1 | MARK-IN-1 is a potent microtubule affinity regulating kinase ( MARK ) inhibitor with an IC 50 of <0.25 nM. Uses: Scientific research. Group: Signaling pathways. CAS No. 1109283-93-3. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-101933. | |
| MARK-IN-2 | MARK-IN-2 is a potent microtubule affinity regulating kinase ( MARK ) inhibitor with an IC 50 of 5 nM. Uses: Scientific research. Group: Signaling pathways. CAS No. 1314893-26-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101934. | |
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