MedChemExpress MCE - Products
MedChemExpress (MCE) offers a wide range of high-quality research chemicals and biochemicals (novel life-science reagents, reference compounds and natural compounds) for scientific use.
| Product | Description | |
|---|---|---|
| Meticrane | Meticrane is a diuretic. Meticrane inhibits the reabsorption of sodium and chloride ions in the distal convoluted tubule. Meticrane is used to treat essential hypertension. Uses: Scientific research. Group: Signaling pathways. CAS No. 1084-65-7. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B0908. |  |
| Metipranolol | Metipranolol is a nonselective and orally active β-adrenergic receptor antagonist. Metipranolol can be used for hypertension and glaucoma research [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 22664-55-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-121567. | |
| Metipranolol hydrochloride | Metipranolol hydrochloride is a non-selective β adrenergic receptor blocking agent. Uses: Scientific research. Group: Signaling pathways. CAS No. 36592-77-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16316. | |
| Metixene hydrochloride hydrate | Metixene (Piperidine) hydrochloride hydrate is an anticholinergic and antiparkinsonian agent. Metixene hydrochloride hydrate potently inhibits binding of quinuclidinyl benzilate (QNB) with the muscarinic receptor, IC 50 and K i values of 55 nM and 15 nM, respectively. Metixene hydrochloride hydrate can be used for the research of parkinsonian [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 7081-40-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-120081A. | |
| Metoclopramide | Metoclopramide is a potent antagonist of 5-HT 3 and dopamine D2 receptor , with IC 50 s of 308 nM and 483 nM, respectively. Metoclopramide can be used for the research of nausea and vomiting, gastro-oesophageal reflux, and gastroparesis [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 364-62-5. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-17382. | |
| Metoclopramide hydrochloride hydrate | Metoclopramide hydrochloride hydrate is a potent antagonist of 5-HT 3 and dopamine D2 receptor , with IC 50 s of 308 nM and 483 nM, respectively. Metoclopramide hydrochloride hydrate can be used for the research of nausea and vomiting, gastro-oesophageal reflux, and gastroparesis [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 54143-57-6. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-17382A. | |
| Metolachlor | Metolachlor is a pre-emergent selective, chloroacetanilide herbicide for the control of a variety of annual grass and broad leaf weeds in corn and other crops. Metolachlor is a chiral herbicide consisting of four stereoisomers [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 51218-45-2. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-B1871. | |
| Metolazone | Metolazone (SR-720-22) is primarily used to treat congestive heart failure and high blood pressure. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SR-720-22. CAS No. 17560-51-9. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-B0209. | |
| Metopimazine | Metopimazine (EXP999) is a phenothiazine derivative used to prevent emesis during chemotherapy. Metopimazine belongs to the anti-dopaminergic anti-emetics (ADA) class. Metopimazine can be used for the research of gastroenteritis (GE) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EXP999; RP9965. CAS No. 14008-44-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-116578. | |
| Metoprine | Metoprine (BW 197U) is a potent histamine N-methyltransferase (HMT) inhibitor. Metoprine, a diaminopyrimidine derivative, can cross the blood-brain barrier and increase brain histamine levels by inhibiting HMT [1] [2]. Metoprine is an antifolate and antitumor agent [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BW 197U. CAS No. 7761-45-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-129441. | |
| Metoprolol | Metoprolol is an orally active, selective β1-adrenoceptor antagonist. Metoprolol shows anti-inflammation, antitumor and anti-angiogenic properties [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 51384-51-1. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-17503. | |
| Metoprolol (Standard) | Metoprolol (Standard) is the analytical standard of Metoprolol. This product is intended for research and analytical applications. Metoprolol is an orally active, selective β1-adrenoceptor antagonist. Metoprolol shows anti-inflammation, antitumor and anti-angiogenic properties [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 51384-51-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-17503R. | |
| Metoprolol succinate | Metoprolol succinate is an orally active, selective β1-adrenoceptor antagonist. Metoprolol succinate shows anti-inflammation, antitumor and anti-angiogenic properties [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 98418-47-4. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-17503A. | |
| Metoprolol tartrate | Metoprolol tartrate is an orally active, selective β1-adrenoceptor antagonist. Metoprolol tartrate shows anti-inflammation, antitumor and anti-angiogenic properties [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 56392-17-7. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-17503B. | |
| Metrizamide | Metrizamide (Amipaque) is used as the contrast medium for angiography in neuroradiological investigations [1]. Metrizamide inhibits human brain hexokinase [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Amipaque. CAS No. 31112-62-6. Pack Sizes: 1 mg. Product ID: HY-W000133. | |
| Metronidazole | Metronidazole is an orally active nitroimidazole antibiotic. Metronidazole can cross blood brain barrier. Metronidazole can be used for the research of anaerobic infections [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. CAS No. 443-48-1. Pack Sizes: 10 mM * 1 mL; 500 mg; 5 g; 10 g. Product ID: HY-B0318. | |
| Metronidazole Benzoate | Metronidazole Benzoate, derives from a metronidazole and a benzoic acid, has a role as an antibacterial, antimicrobial, antiparasitic, and antitrichomonal agent [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Benzoyl metronidazole. CAS No. 13182-89-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-122975. | |
| Metronidazole (Standard) | Metronidazole (Standard) is the analytical standard of Metronidazole. This product is intended for research and analytical applications. Metronidazole is an orally active nitroimidazole antibiotic. Metronidazole can cross blood brain barrier. Metronidazole can be used for the research of anaerobic infections [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. CAS No. 443-48-1. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-B0318R. | |
| Metsulfuron-methyl | Metsulfuron-methyl is a systemic sulfonylurea herbicide that has been widely used to control broadleaf weeds and annual grasses in rice, corn, wheat, and barley. Metsulfuron-methyl exhibits high herbicidal activity and low mammalian toxicity, with an LD 50 for rats exceeding 5000 mg/kg [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 74223-64-6. Pack Sizes: 50 mg; 100 mg. Product ID: HY-B1869. | |
| METTL16-IN-1 | METTL16-IN-1 is a potent METTL16 inhibitor with an IC50 value of 1.7 ?M and a Kd value of 1.35 ?M. Mettl16-in-1 inhibits the binding interaction of U6 snRNA deletion and METTL16 MTD with an IC50 value of 2.5 ?M. METTL16-IN-1 has antitumor activity[1]. Uses: Scientific research. Group: Signaling pathways. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-161402. | |
| METTL3 activator-1 | METTL3 activator-1 (2-Piperazinecarboxylic acid methyl ester dihydrochloride) is a Mettl3 activator that can promote the expression of Mettl3. METTL3 activator-1 can be used for the study of liver fibrosis[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 122323-88-0. Pack Sizes: 10 mM * 1 mL; 100 mg; 250 mg; 500 mg. Product ID: HY-W037893. | |
| Metyrapone | Metyrapone (Su-4885) is a potent and orally active 11β-hydroxylase inhibitor and an autophagy activator, also inhibits the production of aldosterone. Metyrapone inhibits synthesis of endogenous adrenal corticosteroid, decreases glucocorticoid levels, and also affects behavior and emotion. In addition, Metyrapone increases the efficiency of autophagic process via downregulation of mTOR pathway, and interacts with Pseudomonas putida cytochrome P-450. Metyrapone can be used for researching Cushing's syndrome and depression [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Natural products. Alternative Names: Su-4885. CAS No. 54-36-4. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B1232. | |
| Metyrosine | Metyrosine is a selective tyrosine hydroxylase enzyme inhibitor. Metyrosine exerts anti-inflammatory and anti-ulcerative effects. Metyrosine significantly inhibits high COX-2 activity [1]. Metyrosine is a very effective agent for blood pressure control [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 672-87-7. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-W015007. | |
| Mevalonic acid lithium salt | Mevalonic acid (MVA) lithium salt is a precursor substance of the mevalonate pathway, which is essential for cell growth and proliferation. Mevalonic acid lithium salt is effective in inhibiting Simvastatin (HY-17502)-induced decrease in C2C12 cell viability in vitro. Mevalonic acid lithium salt can be used in studies of myopathy and heart failure[1][2]. Uses: Scientific research. Group: Natural products. Alternative Names: MVA lithium salt. CAS No. 2618458-93-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 250 mg; 500 mg. Product ID: HY-113071A. | |
| Mevastatin | Mevastatin (Compactin) is a first HMG-CoA reductase inhibitor that belongs to the statins class. Mevastatin is a lipid-lowering agent, and induces apoptosis , arrests cancer cells in G 0 /G 1 phase. Mevastatin also increases endothelial nitric oxide synthase (eNOS) mRNA and protein levels. Mevastatin has antitumor activity and has the potential for cardiovascular diseases treatment [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Compactin; ML236B. CAS No. 73573-88-3. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 500 mg. Product ID: HY-17408. | |
| Mevociclib | Mevociclib (SY-1365) is a potent and first-in-class selective CDK7 inhibitor, with a Ki of 17.4 nM. Mevociclib exhibits anti-proliferative and apoptotic effects in solid tumor cell lines. Mevociclib possesses anti-tumor activity in hematological and multiple aggressive solid tumors[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SY-1365. CAS No. 1816989-16-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-128587. | |
| Mexiletine hydrochloride | Mexiletine is an orally effective antiarrhythmic agent which has also been found to be effective for myotonia and neuropathic pain. Mexiletine exerts its efficacy through blocking sodium channels ( IC 50 : 75±8 μM for tonic block, 23.6±2.8 μM for use-dependent block), therefore can be used for cardiovascular and neurological research [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: KOE-1173 hydrochloride. CAS No. 5370-1-4. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-A0093. | |
| Mezagitamab | Mezagitamab (TAK-079) is a IgG1λ anti- CD38 monoclonal antibody. Mezagitamab depletes tumor cells expressing CD38 through antibody and complement dependent cytotoxicity. Mezagitamab has potential application in relapsed/refractory multiple myeloma (RRMM) and idiopathic thrombocytopenic purpura (ITP) [1] [2] [3]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: TAK-079. CAS No. 2227490-52-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99730. | |
| Mezigdomide | Mezigdomide (CC-92480), a cereblon E3 ubiquitin ligase modulating agent (CELMoD), acts as a molecular glue. Mezigdomide shows high affinity to cereblon, resulting in potent antimyeloma activity [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CC-92480. CAS No. 2259648-80-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-129395. | |
| Mezlocillin sodium | Mezlocillin (BAY-f 1353) sodium is a β-lactam antibiotic, a semisynthetic and extended-spectrum antibiotic. Mezlocillin sodium is active against both gram-negative and gram-positive bacteria. Mezlocillin sodium can be used in bacterial infection research [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAY-f 1353 sodium. CAS No. 42057-22-7. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-B1466. | |
| MF-094 | MF-094 is a potent and selective USP30 inhibitor with an IC50 of 120 nM. MF-094 increases protein ubiquitination and accelerates mitophagy[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2241025-68-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112438. | |
| MFI8 | MFI8 is a small molecule inhibitor of mitochondrial[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 694488-83-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-150031. | |
| MFZ 10-7 | MFZ 10-7 is a highly potent and selective mGluR5 NAM (negative allosteric modulator), with a K i of 0.67 nM for rat mGluR5 [1]. MFZ 10-7 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Uses: Scientific research. Group: Signaling pathways. CAS No. 1224431-15-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103575. | |
| MG-101 | MG-101 (ALLN) is an inhibitor of cysteine proteases which inhibits calpain I, calpain II, cathepsin B and cathepsin L with K i s of 190, 220, 150 and 500 pM, respectively. MG-101 induces apoptosis and inhibits tumor growth, it can be used for the research of colon cancer [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Calpain inhibitor I; Ac-LLnL-CHO; ALLN. CAS No. 110044-82-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-18964. | |
| MG-132 | MG-132 (Z-Leu-Leu-Leu-al) is a potent proteasome and calpain inhibitor with IC 50 s of 100 nM and 1.2 μM, respectively. MG-132 effectively blocks the proteolytic activity of the 26S proteasome complex. MG-132, a peptide aldehyde, also is an autophagy activator. MG-132 also induces apoptosis [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Z-Leu-Leu-Leu-al; MG132. CAS No. 133407-82-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-13259. | |
| MG-132 (negative control) | MG-132 negative control is the negative control form of MG-132 (HY-13259). MG-132 is a potent proteasome and calpain inhibitor[1]. Uses: Scientific research. Group: Signaling pathways. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13259D. | |
| MG 149 | MG149 (Tip60 HAT inhibitor) is a selective and potent Tip60 inhibitor with IC50 of 74 uM, similar potentcy for MOF (IC50= 47 uM); little potent for PCAF and p300 (IC50 >200 uM)[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Tip60 HAT inhibitor. CAS No. 1243583-85-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-15887. | |
| MG-262 | MG-262 (Z-Leu-Leu-LeuB(OH)2; ZL3B) is a reversible proteasome inhibitor. MG-262 down-regulates VEGF receptor Flt-1. MG-262 inhibits cell growth and induces apoptosis in malignant cells. MG-262 induces reactive oxygen species (ROS). MG-262 can be used for anti-cancer study[1][2][3][4][5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Z-Leu-Leu-LeuB(OH)2; ZL3B. CAS No. 179324-22-2. Pack Sizes: 1 mg. Product ID: HY-108551. | |
| MGB-BP-3 | MGB-BP-3 is an antibiotic that has been shown to be active against a broad range of important multi-resistant Gram-positive pathogens. Uses: Scientific research. Group: Signaling pathways. CAS No. 1000277-08-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-U00035. | |
| MGCD-265 analog | MGCD-265 analog is a potent and oral active inhibitor of c-Met and VEGFR2 tyrosine kinases, with IC 50 s of 29 nM and 10 nM, respectively. MGCD-265 analog has significant antitumor activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 875337-44-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-10991. | |
| MGH-CP1 | MGH-CP1 is a potent and orally active TEAD2 and TEAD4 auto-palmitoylation inhibitor with IC50s of 710 nM and 672 nM, respectively. MGH-CP1 can decrease the palmitoylation levels of endogenous or ectopically expressed TEAD proteins in cells. MGH-CP1 can suppress Myc expression, inhibit epithelial over-proliferation, and induce apoptosis when together with Lats1/2 deletion[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 896657-58-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139330. | |
| MGK-264 | MgK-264 (N-octylbicycloheptenedicarboximide) is a synergist enhancing the potency of pyrethroid ingredients. MgK-264 has no intrinsic pesticidal qualities itself [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: N-Octylbicycloheptenedicarboximide; ENT 8184. CAS No. 113-48-4. Pack Sizes: 50 mg; 100 mg. Product ID: HY-W013170. | |
| MHP | MHP (Methyl caprooyl tyrosinate) is an activator of sphingosine kinase ( SPHK1 ), and significantly stimulates CAMP mRNA and protein production. MHP (Methyl caprooyl tyrosinate) enhances antimicrobial defense and innate immunity [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Methyl caprooyl tyrosinate. CAS No. 1104874-94-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101572. | |
| MHY1485 | MHY1485 is a potent cell-permeable mTOR activator that targets the ATP domain of mTOR. MHY1485 inhibits autophagy by suppression of fusion between autophagosomes and lysosomes[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 326914-06-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg; 500 mg; 1 g. Product ID: HY-B0795. | |
| MI-1061 | MI-1061 is a potent, orally bioavailable, and chemically stable MDM2 (MDM2-p53 interaction) inhibitor (IC50=4.4 nM; Ki=0.16 nM). MI-1061 potently activates p53 and induces apoptosis in the SJSA-1 xenograft tumor tissue in mice. Anti-tumor activity[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1410737-34-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-125858. | |
| MI 14 | MI 14 is a selective PI4KIIIβ inhibitor with IC 50 s of 54 nM, >100 μM, >100 μM for PI4KIIIβ, PI4KIIIα, PI4KIIα, respectively. MI 14 has antiviral activity against HCV 1b, CVB3, HRVM, HVC 2a [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1715934-43-2. Pack Sizes: 5 mg; 10 mg. Product ID: HY-110248. | |
| MI-3 | MI-3 (Menin-MLL inhibitor 3) is a potent and high affinity menin-MLL inhibitor with an IC 50 of 648 nM and a K d of 201 nM [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Menin-MLL inhibitor 3. CAS No. 1271738-59-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15223. | |
| MI-3454 | MI-3454 is an orally active, highly potent and selective menin-MLL1 interaction inhibitor with an IC50 of 0.51 nM. MI-3454 inhibits proliferation, induces differentiation and complete remission or regression of leukemia in mouse models of MLL1-rearranged or NPM1-mutated leukemia through downregulation of key genes involved in leukemogenesis[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2134169-43-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-136360. | |
| MI-463 | MI-463 is a highly potent and orally bioavailable small molecule inhibitor of the menin-mLL interaction. Uses: Scientific research. Group: Signaling pathways. CAS No. 1628317-18-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-19809. | |
| MI-503 | MI-503 is a highly potent and orally bioavailable small molecule inhibitor of the menin-mLL interaction. Uses: Scientific research. Group: Signaling pathways. CAS No. 1857417-13-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16925. | |
| Mianserin hydrochloride | Mianserin hydrochloride (Org GB 94) is a H1 receptor inverse agonist and is a psychoactive agent of the tetracyclic antidepressant. Uses: Scientific research. Group: Natural products. Alternative Names: Org GB 94. CAS No. 21535-47-7. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-B0188A. | |
| Mibavademab | Mibavademab is a CHO-expressed humanized antibody that targets LEPR/CD295. Mibavademab is equipped with a huIgG4SP heavy chain and a huκ light chain, with a predicted molecular weight (MW) of 145.58 kDa. The isotype control for Mibavademab can be referenced as Human IgG4 kappa, Isotype Control (HY-P99003). Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2305770-44-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P990631. | |
| Mibefradil dihydrochloride | Mibefradil dihydrochloride (Ro 40-5967 dihydrochloride) is a calcium channel blocker with moderate selectivity for T-type Ca 2+ channels ( IC 50 s of 2.7 μM and 18.6 μM for T-type and L-type currents, respectively) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ro 40-5967 dihydrochloride. CAS No. 116666-63-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-15553A. | |
| Micafungin sodium | Micafungin sodium (FK 463 sodium) is an antifungal agent which inhibits 1, 3-beta-D-glucan synthesis. Uses: Scientific research. Group: Signaling pathways. Alternative Names: FK 463 sodium. CAS No. 208538-73-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-16321. | |
| Micheliolide | Micheliolide is a sesquiterpene lactone with anti-cancer and anti-inflammatory effects, which is derived from Michelia compressa and Michelia champaca. Micheliolide can attenuate high glucose-stimulated NF-κB activation, IκBα degradation, and the expression of MCP-1, TGF-β1, and FN in mouse mesangial cells. Micheliolide inhibits LPS (HY-D1056)-induced activation of NF-κB and PI3K/Akt/p70S6K pathways to play an anti-inflammatory role. Micheliolide inhibits dextran sodium sulphate (DSS) (HY-116282)-induced inflammatory intestinal disease, colitis-associated cancer and rheumatic arthritis [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. CAS No. 68370-47-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N0847. | |
| Miconazole | Miconazole (R18134) is an imidazole antifungal agent. Miconazole also has antibacterial effects [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: R18134. CAS No. 22916-47-8. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-B0454. | |
| Miconazole nitrate | Miconazole nitrate (R18134 nitrate) is an imidazole antifungal agent. Miconazole nitrate also has antibacterial effects [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: R18134 nitrate. CAS No. 22832-87-7. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B0454A. | |
| Micrococcal nuclease | Micrococcal nuclease is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Signaling pathways. CAS No. 9013-53-0. Pack Sizes: 5 KU. Product ID: HY-P2754. | |
| Micrococcin P1 | Micrococcin P1 is a macrocyclic peptide antibiotic and is a potent hepatitis C virus (HCV) inhibitor with an EC 50 range of 0.1-0.5 μM [1]. Micrococcin P1 has in vitro antibacterial activity against Gram-positive bacterial strains. The MIC values of Micrococcin P1 against S. aureus 1974149, E. faecalis 1674621 and S. pyogenes 1744264 are 2 μg/mL, 1 μg/mL and 1 μg/mL, respectively [2]. Micrococcin P1 is also a potent inhibitor of the malaria parasite Plasmodium falciparum [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 67401-56-3. Pack Sizes: 500 μg; 1 mg. Product ID: HY-125728. | |
| Micronomicin | Micronomicin (Gentamicin C2b) is an aminoglycoside antibiotic, with antibacterial and bactericidal activities [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Gentamicin C2b; Antibiotic XK-62-2; Sagamicin. CAS No. 52093-21-7. Pack Sizes: 100 mg. Product ID: HY-B1915. | |
| Micronomicin sulfate | Micronomicin sulfate (Gentamicin C2b sulfate) is an aminoglycoside antibiotic isolated from Micromonospora. Micronomicin sulfate is a broad-spectrum antibiotic close to the gentamicin-type antibiotics, exhibits a high activity against Pseudomonas , Proteus , Klebsiella pneumoniae , Serratia , etc ( MIC =0.001-8.3 μg/ml) [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Gentamicin C2b sulfate; Antibiotic XK-62-2 sulfate; Sagamicin sulfate. CAS No. 66803-19-8. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-108307. | |
| microRNA-21-IN-1 | microRNA-21-IN-1 (compound A7) is an efficient microRNA inhibitor. microRNA-21-IN-1 has antiproliferative activity against Hela and HCT-116 cells with IC 50 s of 5.5 μM and 2.8 μM respectively, as well as promotes apoptosis of Hela cells. microRNA-21-IN-1 upregulates the expression of microRNA-21 downstream functional targets (PTEN, EGR1 and SLIT2). microRNA-21-IN-1 can be used for researching anticancer [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2848720-31-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-146411. | |
| microRNA-21-IN-3 | microRNA-21-IN-3 (compound 45) can specifically bind to the precursor of oncogenic and pro-inflammatory microRNA-21 with medium nanomolar affinity, reduce cancer cell proliferation and miR-21 levels, and can be used in antitumor research [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2766106-83-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-153534. | |
| MID-1 | MID-1 is a disruptor of MG53-IRS-1 (Mitsugumin 53-insulin receptor substrate-1) interaction. MID-1 disrupts molecular association of MG53 with IRS-1 and abolishes MG53-induced IRS-1 ubiquitination and degradation in skeletal muscle, leading to elevated IRS-1 expression level and increased insulin signaling and glucose uptake [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 312608-54-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-115461. | |
| Midecamycin | Midecamycin, an acetoxy-substituted macrolide antibiotic, is tested against gram-positive and gram-negative bacteria. Uses: Scientific research. Group: Natural products. Alternative Names: SF-837; Antibiotic SF-837. CAS No. 35457-80-8. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-B1908. | |
| Midodrine | Midodrine is an α1-receptor agonist, for the treatment of dysautonomia and orthostatic hypotension. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (±)-Midodrin. CAS No. 42794-76-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-12749. | |
| Midodrine hydrochloride | Midodrine hydrochloride ((±)-Midodrine hydrochloride) is an α1-receptor agonist, for the treatment of dysautonomia and orthostatic hypotension. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (±)-Midodrine hydrochloride. CAS No. 43218-56-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-12749A. | |
| Midostaurin | Midostaurin (PKC412; CGP 41251) is an orally active, reversible multi-targeted protein kinase inhibitor. Midostaurin inhibits PKCα/β/γ , Syk , Flk-1 , Akt , PKA , c-Kit , c-Fgr , c-Src , FLT3 , PDFRβ and VEGFR1/2 with IC 50 s ranging from 22-500 nM [1] [2]. Midostaurin also upregulates endothelial nitric oxide synthase (eNOS) gene expression. Midostaurin shows powerful anticancer effects [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PKC412; CGP 41251. CAS No. 120685-11-2. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-10230. | |
| MIF098 | MIF098 is a macrophage migration inhibitory factor (MIF) antagonist. MIF098 inhibits proliferation, migration and fibrosis of pulmonary smooth muscle cells. MIF098 can be used for immunoinflammation-related disease research[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1208448-95-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-147390. | |
| Mifamurtide | Mifamurtide (MTP-PE), an analog of the muramyl dipeptide (MDP), is a nonspecific immunomodulator by stimulating the immune response activating macrophages and monocytes. Mifamurtide is a specific ligand for NOD2 and acts as an insulin sensitizer. Mifamurtide has potential for use in rare disease and osteosarcoma research [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MTP-PE; L-MTP-PE; CGP 19835. CAS No. 83461-56-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-13682. | |
Would you like to list your products on USA Chemical Suppliers?
Our database is helping our users find suppliers everyday.