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| Product | Description | |
|---|---|---|
| MS 245 oxalate | MS 245 oxalate. Group: Biochemicals. Grades: Purified. CAS No. 275363-58-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| MS-275 | HDAC 1 inhibitor. Antitumor compound. Antiproliferative. TGF-beta type II receptor inducer. Apoptosis inducer. Anti-inflammatory. Angiogenesis inhibitor. Group: Biochemicals. Grades: Highly Purified. CAS No. 209783-80-2. Pack Sizes: 1mg, 5mg, 25mg. Molecular Formula: C21H20N4O3. US Biological Life Sciences. | Worldwide |
| MS-275 (Entinostat, SNDX-275) | Preferentially inhibits HDAC1 (IC50=300 nM) over HDAC3 (IC50=8uM). Has no inhibitory activity towards HDAC8 (IC50>100uM). Group: Biochemicals. Grades: Highly Purified. CAS No. 209783-80-2. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| MS-282a | MS-282a is produced by the strain of Streptomyces tauricus. It inhibits calmodulin-dependent MLCK with an IC50 of 3.8 μmol/L. It has anti-gram-positive bacteria activity. Synonyms: MS-282-A. CAS No. 152158-04-8. Molecular formula: C37H65NO7. Mole weight: 635.91. |  |
| MS-282b | MS-282b is produced by the strain of Streptomyces tauricus. It inhibits calmodulin-dependent MLCK with an IC50 of 5.2 μmol/L. It has anti-gram-positive bacteria activity. Synonyms: MS-282-B. CAS No. 152759-50-7. Molecular formula: C37H65NO7. Mole weight: 635.91. | |
| MS39 | MS39 (compound 6) is a PROTAC targeting EGFR. MS39 reduces the expression of EGFR and downstream signaling in HCC-827 and H3255 cells. MS39 inhibits the proliferation of H3255 cells[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2675490-92-1. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-157581. |  |
| MS402 | MS402 is a BD1-selective BET BrD inhibitor with Kis of 77 nM, 718 nM, 110 nM, 200 nM, 83 nM, and 240 nM for BRD4(BD1), BRD4(BD2), BRD3(BD1), BRD3(BD2), BRD2(BD1) and BRD2(BD2), respectively. MS402 blocks Th17 cell differentiation and ameliorates colitis in mice[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1672684-68-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-120000. | |
| MS4077 | MS4077 is an anaplastic lymphoma kinase (ALK) PROTAC (degrader) based on Cereblon ligand, with a Kd of 37 nM for binding affinity to ALK[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2230077-10-6. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg. Product ID: HY-112156. | |
| MS4078 | MS4078 is an anaplastic lymphoma kinase (ALK) PROTAC (degrader) based on Cereblon ligand, with a Kd of 19?nM for binding affinity to ALK[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2229036-62-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-112155. | |
| MS41 | MS41 is a selective eleven-nineteen leukemia (ENL) PROTAC degrader, with DC50s of 3.50 nM (MV4;11), 2.84 nM (SEMK2), 3.03 nM (Jurkat), and 26.58 nM (KASUMI1), respectively. MS41 effectively inhibits the growth of ENL-dependent leukemia cells, induces G1 cell cycle arrest and increases apoptosis. MS41 reduces the chromatin occupancy of ENL-associated transcription elongation machinery, and suppresses oncogenic gene expression and leukemia progression. Red: ENL ligand (HY-169094). Black: linker (HY-W105744). Blue: VHL ligand (HY-112078)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2768610-97-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg. Product ID: HY-169093. | |
| MS417 | MS417 is a selective BET-specific BRD4 inhibitor, binds to BRD4-BD1 and BRD4-BD2 with IC50s of 30, 46 nM and Kds of 36.1, 25.4 nM, respectively, with weak selectivity at CBP BRD (IC50, 32.7 μM). Uses: Scientific research. Category: Signaling pathways. Alternative Names: GTPL7512. CAS No. 916489-36-6. Pack Sizes: 10 mM * 1 mL in Ethanol; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-111139. | |
| MS432 | MS432 is a first-in-class and highly selective PD0325901-based von Hippel-Lindau-recruiting PROTAC degrader for MEK1 and MEK2. MS432 displays good plasma exposure in mice, exhibiting DC50 values of 31 nM and 17 nM for MEK1, MEK2 in HT29 cells respectively[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2672512-44-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-130602. | |
| MS4322 | MS4322 (YS43-22) is a specific PRMT5 PROTAC degrader. MS4322 reduces the PRMT5 protein level with a DC50 of 1.1 μM in MCF-7 cells. MS4322 inhibits the methyltransferase activity of PRMT5 with an IC50 of 18 nM. MS4322 promotes ubiquitination and degradation of PRMT5. MS4322 can be used for the research of breast cancer, lung cancer, and hepatocellular cancer. (Pink: PRMT5 ligand (HY-173092); Blue: E3 ligase ligand HY-112078); Black: linker (HY-124780); E3+linker (HY-173093 ))[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: YS43-22. CAS No. 2375432-47-4. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-141877. | |
| MS436 | MS436 is a new class of bromodomain inhibitor, exhibits potent affinity of an estimated Ki=30-50 nM for the BRD4 BrD1 and a 10-fold selectivity over the BrD2. Uses: Scientific research. Category: Signaling pathways. CAS No. 1395084-25-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13959. | |
| MS437 | MS437 is a potent TSH receptor (TSHR) stimulator with an EC50 value of 13x10-8 M. MS437 shows potent activation of Gsα, Gαq and Gα12 and up-regulation of thyroglobulin (Tg), sodium iodine symporter (NIS) and TSHR gene expressions[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 541535-31-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-114994. | |
| MS438 | MS438 is a potent thyrotropin receptor (TSHR) agonist with an EC50 of 53 nM. MS438 binds to the serpentine portion of the TSHR. MS438 induces T4 secretion in mice[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 512840-45-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg. Product ID: HY-114918. | |
| MS-444 | MS-444 (BE-34776) is a HuR (ELAVL1) inhibitor that blocks the cytoplasmic translocation of HuR and inhibits its dimerization. MS-444 reduces cytoplasmic HuR levels by preventing the binding of HuR to ARE-mRNA, without altering the total expression of HuR. MS-444 induces apoptosis, inhibits cell growth, angiogenesis and invasion, and also regulates immune function and microbiota. MS-444 effectively alters the number, size and invasiveness of tumors in various cancer models. MS-444 is tolerable to intraperitoneal injection in vivo and can be applied to research related to colorectal cancer, familial adenomatous polyposis, colitis-associated cancer and glioblastoma[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: BE-34776. CAS No. 150045-18-4. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100685. | |
| MS-444 | MS-444, originally isolated from Micromonospora sp. KY7123, is a myosin light chain kinase (MLCK) inhibitor. Synonyms: 5,8-Dihydroxy-3-methyl-4-(9H)-naphtho(2,3-c)furanone; MS 444; 5,8-dihydroxy-3-methyl-9H-benzo[f][2]benzofuran-4-one. CAS No. 150045-18-4. Molecular formula: C13H10O4. Mole weight: 230.22. | |
| MS48107 | MS48107 is a potent and selective positive allosteric modulator of G protein-coupled receptor 68 (GPR68). MS48107 is selective for GPR68 over the closely related proton GPCRs, neurotransmitter transporters, and hERG ion channels. MS48107 can readily cross the blood-brain barrier (BBB) in mice[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2375070-79-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-134494. | |
| MS-553 | MS-553 is a potent, ATP-competitive and reversible inhibitor of conventional PKC enzymes with Kis of 5.3 and 10.4 nM for human PKCβ and PKCα, and IC50s of 2.3, 8.1, 7.6, 25.6, 57.5, 314, 808 nM for PKCα, PKCβI, PKCβII, PKCθ, PKCγ, PKC mu and PKCε, respectively. Uses: Scientific research. Category: Signaling pathways. CAS No. 1046787-18-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-16903. | |
| MS6105 | MS6105 is an LDH protein hydrolysis-targeted chimera (PROTAC) that effectively degrades LDHA and LDHB in a time- and ubiquitin-proteasome system-dependent manner and has anticancer activity[1]. MS6105 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. Category: Signaling pathways. CAS No. 2891709-58-1. Pack Sizes: 5 mg; 10 mg. Product ID: HY-152261. | |
| MS67 | MS67 is a potent and selective WD40 repeat domain protein 5 (WDR5) degrader with a Kd of 63 nM. MS67 is inactive against other protein methyltransferases, kinases, GPCRs, ion channels, and transporters. MS67 shows potent acticancer effects[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2407452-77-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-141796. | |
| MS-681a | MS-681a, originally isolated from Myrothecium sp. KY6568, is a myosin light chain kinase (MLCK) inhibitor (IC50=0.11 μmol/L). CAS No. 173485-72-8. Molecular formula: C61H91N13O9. Mole weight: 1150.45. | |
| MS7710 | MS7710 is a hyperpolarization-activated cyclic nucleotide-gated (HCN) channel inhibitor with blood-brain barrier permeability and an excellent brain/plasma concentration ratio. MS7710 inhibits HCN channel-mediated Ih current, and reduces the firing frequency and burst activity of dopaminergic neurons in the ventral tegmental area. MS7710 ameliorates chronic social defeat stress-induced deficits in social interaction and impairments in reward-related cognitive flexibility in mice. MS7710 exerts only limited effects on ventral tegmental area dopaminergic neuron activity, social interaction, exploratory behavior, locomotor activity or sucrose preference in control mice. MS7710 is applicable to the research of major depressive disorder[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3095336-10-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-172550. | |
| MS7-H550-Pro LCD Digital Magnetic Hotplate Stirrer With 7 Inch Ceramic Plate | LCD displays actual temperature & speed. Built-in PID controller ensures safe heating of the medium with overheating protection. Maximum heating plate temperature up to 550°C. Glass ceramic work plate is resistant to corrosion and is easy to clean. External temperature control is possible by connecting temperature sensor(PT1000) with an accuracy of ±0. 2°C. Digital speed control with maximum range of 1500rpm. Outstanding brushless DC motor offers more stirring power. Two knobs enable easy adjustment of speed and temperature. HOT warning flashes when work plate temperature is above 50°C even when hotplate is turned off. Remote function provides PC control and data transmission. Uses: Equipment for sample preparation. Group: Laboratory equipment. Product ID: 8030122111. Categories: Magnetic Hotplate Stirrer. |  |
| MS7-H550-S LED Magnetic Hotplate Stirrer With 7 Inch Ceramic Plate | LED displays actual temperature. Built-in PID controller ensures safe heating of the medium with overheating protection. Maximum heating plate temperature up to 550°C. Glass ceramic work plate is resistant to corrosion and is easy to clean. External temperature control is possible by connecting temperature sensor(PT1000) with an accuracy of ±0. 2°C. Digital speed control with maximum range of 1500rpm. Outstanding brushless DC motor offers more stirring power. Two knobs enable easy adjustment of speed and temperature. HOT warning flashes when work plate temperature is above 50°C even when hotplate is turned off. Remote function provides PC control and data transmission. Uses: Equipment for sample preparation. Group: Laboratory equipment. Product ID: 8030122211. Categories: Magnetic Hotplate Stirrer. | |
| MS8709 | MS8709 (compound 10), a potential anticancer therapeutic, is a first-in-class G9a/GLP PROTAC degrader. MS8709 is based on G9a/GLP inhibitor UNC0642 and recruits the von Hippel Lindau (VHL) E3 ligase (Red: G9a/GLP inhibitor UNC0642; Blue: VHL ligand; Black: linker)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3060730-06-2. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-162362. | |
| MS8815 | MS8815 is a selective enhancer of zeste homolog 2 (EZH2) PROTAC degrader. MS8815 has inhibition activity for EZH2 with an IC50 value of 8.6 nM. MS8815 can be used for the research of triple-negative breast cancer (TNBC)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2855085-25-3. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148334. | |
| MS8847 | MS8847 is a PROTAC degrader and antiproliferative agent targeting EZH2 (DC50=34.4 nM in EOL-1 MLL-rAML cells). MS8847 recruits the E3 ligase von Hippel-Lindau (VHL) to mediate the degradation of EZH2 via the ubiquitin-proteasome system. MS8847 induces antiproliferative effects in MLL-rearranged acute myeloid leukemia cells and inhibits the growth of triple-negative breast cancer cell lines or 3D triple-negative breast cancer models. MS8847 is applicable to research related to MLL-rearranged acute myeloid leukemia and triple-negative breast cancer[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3050872-59-5. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-162250. | |
| MS934 | MS934 is a novel improved VHL-recruiting MEK 1/2 PROTAC degrader. MS934 also degrades CRAF. MS934 can be used for the research of variety of human cancers, such as melanoma, nonsmall cell lung cancer (NSCLC), colorectal cancer, primary brain tumors, and hepatocellular carcinoma (Pink: Target protein ligand (HY-168288); Black: linker (HY-168289); Blue: E3 ligase ligand (HY-112078))[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2756323-15-4. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-153863. | |
| MSA-2 | MSA-2, a potent and orally available non-nucleotide STING agonist, is bound to STING as a noncovalent dimer with nanomolar affinity. MSA-2 shows EC50s of 8.3 and 24 μM for human STING isoforms WT and HAQ, respectively. MSA-2 stimulates interferon-β secretion in tumors, induces tumor regression with durable antitumor immunity, and synergizes with anti-PD-1 in syngeneic mouse tumor models[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 129425-81-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg; 500 mg; 1 g. Product ID: HY-136927. | |
| MSA-2 | MSA-2 Inhibitor. Uses: Scientific use. Product Category: T8798. CAS No. 129425-81-6. |  |
| MSAB | MSAB is a potent and selective inhibitor of Wnt/β-catenin signaling. MSAB binds to β-catenin and promotes its degradation, and specifically downregulates Wnt/β-catenin target genes. MSAB exhibits potent anti-tumor effects selectively on Wnt-dependent cancer cells[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 173436-66-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-120697. | |
| m-Salicylic Acid | m-Salicylic Acid is widely used in organic synthesis. It is also an important active metabolite of aspirin (A187780). Group: Biochemicals. Alternative Names: 3-Hydroxybenzoic Acid; 3-Carboxyphenol; NSC 55746; m-Carboxyphenol; m-Hydroxybenzoic Acid. Grades: Highly Purified. CAS No. 99-06-9. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
| MSC1094308 | MSC1094308 is a non-competitive and reversible VPS4B/p97 (VCP) (I/II type AAA ATPase) allosteric inhibitor, with IC50 values of 0.71 μM and 7.2 μM for VPS4B and p97, respectively[1]. MSC1094308 inhibits the D2 ATPase activity by binding to a agentable hotspot of p97. MSC1094308 can be used in study of cancer[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2219320-08-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-123872. | |
| MSC-1186 | MSC-1186, a chemical probe, is a highly selective pan-SRPK inhibitor. MSC-1186 has activity for SRPK1, SRPK2 and SRPK3 with IC50 values of 2.7 nM, 81 nM and 0.6 nM, respectively. MSC-1186 can be used for the research of cancer[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2871698-23-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148518. | |
| MSC2504877 | MSC2504877 (M2912) is a potent and orally active tankyrase inhibitor with IC50s of 0.0007, 0.0008, 0.54 μM for TNKS, TNKS2, PARP1, respectively. MSC2504877 increases the expression of AXIN2 and TNKS protein levels and decreases β-catenin levels. MSC2504877 shows anti-tumor activity[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: M2912. CAS No. 1460286-21-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-123851. | |
| MSC2530818 | MSC2530818 is a potent, selective and orally available CDK8 inhibitor with an IC50 of 2.6 nM for CDK8. Uses: Scientific research. Category: Signaling pathways. CAS No. 1883423-59-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101611. | |
| MSC-4106 | MSC-4106 is an orally active and potent inhibitor of YAP/TAZ-TEAD. MSC-4106 inhibits TEAD1 or TEAD3 auto-palmitoylation and shows inhibitory effect on NCI-H226 tumor xenograft model[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2738542-58-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-147208. | |
| MSC-4381 | MSC-4381 (MCT4-IN-1), a chemical probe, is an orally active and selective monocarboxylate transporter 4 (MCT4/SLC16A3) inhibitor with an IC50 of 77 nM and a Ki of 11 nM. MSC-4381 targets to the cytosolic domain of MCT4. MSC-4381 results in lactate efflux inhibition and reduction of cellular viability in MCT4 high expressing cells. MSC-4381 has the potential for MCT4 transporter inhibition research[1]. MSC-4381 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. Category: Signaling pathways. Alternative Names: MCT4-IN-1. CAS No. 2445185-57-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-132301. | |
| m-Scrobiculin | m-Scrobiculin. Synonyms: Scrobiculin. CAS No. 15081-04-6. Molecular formula: C22H26O8. Mole weight: 418.44. | |
| MSD-819 | MSD-819 is extracted from Streptomycess ambofaciens. It has anti-gram-positive and anti-gram-negative bacteria activity. Synonyms: 2-Quinoxalinecarboxylicacid, 6-chloro-, 1,4-dioxide; 3-Carboxy-7-chloro-1-oxoquinoxalin-1-ium-4(1H)-olate. CAS No. 22587-15-1. Molecular formula: C9H5ClN2O4. Mole weight: 240.60. | |
| MSD-92 | It is originally isolated from Actinomyces sp. MSD-92 has anti-gram-positive and anti-gram-negative activity, and the MIC of it against Escherichia coli was 2 μg/mL. Synonyms: 2-Methylfervenulone; BRN 0540815; 2,8-Dihydro-2,6,8-trimethylpyrimido(5,4-e)-as-triazine-3,5,7-trione. CAS No. 22712-32-9. Molecular formula: C8H9N5O3. Mole weight: 223.19. | |
| MSDC 0160 | MSDC 0160 (Mitoglitazone) is a mitochondrial target of thiazolidinediones (mTOT)-modulating insulin sensitizer and a modulator of mitochondrial pyruvate carrier (MPC). MSDC 0160 is a thiazolidinedione (TZD) with antidiabetic and neuroprotective activities. MSDC 0160 has the potential for Alzheimers disease[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Mitoglitazone; CAY10415. CAS No. 146062-49-9. Pack Sizes: 10 mM * 1 mL in DMSO; 2 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-100550. | |
| MSG606 | MSG606 is a selective melanocortin 1 receptor (MC1R) antagonist. MSG606 can abolish the neuroprotective effects of BMS-470539 (HY-15616) (MC1R agonist). MSG606 can inhibit cancer cell proliferation and transition from the G1 to the S phase. MSG606 can delay pain hypersensitivity and reduce cholesterol levels. MSG606 can be used for the researches of cancer, inflammation, neurological and metabolic disease, such as breast cancer and subarachnoid hemorrhage (SAH)[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1416983-77-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P1726. | |
| MSG 606 | MSG 606 is a potent human MC1 receptor antagonist (IC50 = 17 nM), and also partial agonist at human MC3 and MC5 receptors (EC50= 59 and 1300 nM, respectively). Synonyms: MSG 606; MSG606; MSG-606. CAS No. 1416983-77-1. Molecular formula: C62H82N20O13S. Mole weight: 1347.51. | |
| MS-H220-V3 LCD Digital Heating Magnetic Stirring Bath | High borosilicate glass liner, resistant to sudden changes from hot to cold without breaking, transparent glass window for monitoring reaction product changes; stainless steel base, rust-resistant, easy to clean; high-temperature. resistant protective outer shell to prevent direct contact with hot glass and burns. Dual-use stirring bath for water and oil, with secondary stirring in the bath pot. The stirring of the bath liquid simultaneously stirs the liquid sample in the flask, ensuring uniform heating of both bath liquid and sample. Safety lock to prevent accidental changes in operational status. Buzzer: A beep beep beep alert sounds when the countdown timer function ends. Button tone. Features a timer function with a range of 1 min to 99h59min. It stops heating when the countdown ends but continues stirring to prevent heat damage to the sample. Touch buttons with audible prompts. Working status indicator light: Green during operation, flashing green before reaching set temperature; alarm red. Reversible function. Protection features: dry burning protection, overcurrent protection, ground fault protection, and over temperature protection. Residual heat warning function. When the plate temperature is above 50°C , heating is turned off, and the screen flashes HOT as a reminder of the high temperature even after the power is off. Two independent safety circuits continuously monitor | |
| MS-H220-V5 LCD Digital Heating Magnetic Stirring Bath | High borosilicate glass liner, resistant to sudden changes from hot to cold without breaking, transparent glass window for monitoring reaction product changes; stainless steel base, rust-resistant, easy to clean; high-temperature. resistant protective outer shell to prevent direct contact with hot glass and burns. Dual-use stirring bath for water and oil, with secondary stirring in the bath pot. The stirring of the bath liquid simultaneously stirs the liquid sample in the flask, ensuring uniform heating of both bath liquid and sample. Safety lock to prevent accidental changes in operational status. Buzzer: A beep beep beep alert sounds when the countdown timer function ends. Button tone. Features a timer function with a range of 1 min to 99h59min. It stops heating when the countdown ends but continues stirring to prevent heat damage to the sample. Touch buttons with audible prompts. Working status indicator light: Green during operation, flashing green before reaching set temperature; alarm red. Reversible function. Protection features: dry burning protection, overcurrent protection, ground fault protection, and over temperature protection. Residual heat warning function. When the plate temperature is above 50°C , heating is turned off, and the screen flashes HOT as a reminder of the high temperature even after the power is off. Two independent safety circuits continuously monitor | |
| MS-H280-Pro LED Digital Magnetic Hotplate Stirrer | Digital temperature control with maximum temperature up to 280°C. Digital speed control with maximum speed up to 1500rpm. Stainless steel with ceramic coating work plate provides high chemical resistant performance. External temperature control is possible by connecting temperature sensor(PT1000) with an accuracy at ±0.2°C. LED display shows temperature and stirring speed. "HOT" warning flashes if work plate temperature is above 50°C. Uses: Equipment for sample preparation. Group: Laboratory equipment. Product ID: 8030101212. Categories: Magnetic Hotplate Stirrer. | |
| MS-H340-S4 | Independent heating and stirring control for each position. LCD display shows real-time temperature and speed. PID controller ensures a precise and stable heating process (maximum temperature up to 340°C). Brushless DC motor is quiet, reliable & maintenance free, and provides more powerful speed control. External temperature sensor (PT1000) with accuracy 0.2°C. Overheating protection temperature at 420°C. Stainless steel work plate with ceramic coating provides good chemical resistance. Wide variety of accessories available to choose from. Categories: Labooratory Mixers, Shakers & Stirrers. | |
| MSH, N(alpha)-chlorotriazinylaminofluorescein-1-Ser-4-Nle-7-Phe-alpha- | MSH, N(alpha)-chlorotriazinylaminofluorescein-1-Ser-4-Nle-7-Phe-alpha-. CAS No. 97475-26-8. Product ID: ACM97475268. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| MS-H-ProA LCD Digital Magnetic Hotplate Stirrer | DC brushless motor free of maintenance and spark, and with long service life. Digital temperature control up to 340°C. Digital speed control up to 1500rpm. Maximum stirring quantity of H2O is 20L. Safety circuits provide overheating protection. "HOT" warning flashes if plate temperature is above 50°C even when hotplate is turned off. External temperature control is possible by connecting the temperature sensor(PT 1000)with accuracy at ±0.2°C. Work plate with ceramic coating provides good chemical-resistantperformance. Remote function provides PC control and data transmission. Wide variety of accessories available to choose. Uses: Equipment for sample preparation. Group: Laboratory equipment. Product ID: 8060221110. Categories: Magnetic Hotplate Stirrer. | |
| MS-H-S | Brushless DC motor is maintenance free and explosion-proof. Digital temperature control up to 340°C. Digital speed control up to 1500rpm. Maximum stirring quantity of H2O is 20L. Safety circuits provide overheating protection. "HOT" warning flashes if plate temperature is above 50°C even when hotplate is turned off. Work plate with ceramic coating provides good chemical-resistantperformance. Wide variety of accessories available to choose. Categories: Labooratory Mixers, Shakers & Stirrers. | |
| MSI-1436 lactate | MSI-1436 lactate is a selective, non-competitive inhibitor of the enzyme protein-tyrosine phosphatase 1B (PTP1B), with an IC50 of 1 μM, 200-fold preference over TCPTP (IC50 of 224 μM). Uses: Scientific research. Category: Signaling pathways. Alternative Names: Trodusquemine lactate; Aminosterol-1436 lactate. CAS No. 1309370-86-2. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12219A. | |
| MSI-594 | MSI-594 is a highly active AMP with a broad-spectrum of activities against bacteria, fungi, and virus. | |
| MS-L6 | MS-L6 is a potent inhibitor of oxidative phosphorylation (OXPHOS) that can acts as electron transport chain complexes I (ETC-I) combining inhibition of NADH oxidation and uncoupling effect[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 63498-32-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-158421. | |
| MSM - Methyl Sulfonyl Methane | MSM - Methyl Sulfonyl Methane. |  CA, FL & NJ |
| MSN-125 | MSN-125 is a potent Bax and Bak oligomerization inhibitor. MSN-125 prevents mitochondrial outer membrane permeabilization (MOMP) with an IC50 of 4 μM. MSN-125 potently inhibits Bax/Bak-mediated apoptosis in HCT-116, BMK Cells, and primary cortical neurons, protects primary neurons against glutamate excitotoxicity[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1592908-16-1. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-120079. | |
| MSN-50 | MSN-50 is a Bax and Bak oligomerization inhibitor. MSN-50 efficiently inhibits liposome permeabilization, prevents genotoxic cell death and promotes neuroprotection[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1592908-75-2. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-118948. | |
| MSNBA | MSNBA is a potent and selective GLUT5 fructose transport inhibitor with an IC50 of 0.10?mM. MSNBA does not affect the transport activity of human GLUT1, GLUT2, GLUT3, GLUT4 or bacterial GlcPSe. MSNBA competitively inhibits GLUT5 fructose uptake with a Ki of 3.2 μM in MCF7 cells. MSNBA can be used for the study of cancer or diabetes[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 852702-51-3. Pack Sizes: 10 mM * 1 mL in DMSO; 25 mg; 50 mg; 100 mg. Product ID: HY-W179181. | |
| MSOP | MSOP. Group: Biochemicals. Grades: Purified. CAS No. 66515-29-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| MSOP | MSOP is a selective group III metabotropic glutamate receptor antagonist with apparent KD of 51 μM for the L-AP4-sensitive presynaptic mGluR. Uses: Scientific research. Category: Signaling pathways. CAS No. 66515-29-5. Pack Sizes: 10 mM * 1 mL in Water; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101226. | |
| MS-PA | Digital speed control within the range of 0-1500rpm. Maximum stirring quantity of H2O at 3L. LED display shows stirring speed. Categories: Labooratory Mixers, Shakers & Stirrers. | |
| MspA1 I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA in 1 hour at 37°C in a total reaction volume of 50 μl. Applications: After 10-fold overdigestion with enzyme 90% of the dna fragments can be ligated and recut. Group: Restriction Enzymes. Purity: 500 U; 2500U. CMG↑CKG GKC↓GMC. Activity: 5000u.a./ml. Appearance: 10 X SE-buffer Y, BSA. Storage: -20°C. Storage at -70°C is recommended for periods longer than 30 days. Form: Liquid. Source: Moraxella species A1. Pack: 20 mM Tris-HCl (pH 7.6); 300 mM NaCl; 0,1 mM EDTA; 7 mM 2-mercaptoethanol; 10 mM MgCl2, 200 μg/ml BSA, 50% glycerol. Cat No: ET-1140RE. |  |
| MS-PB | Digital speed control within the range of 0-1500rpm. Maximum stirring quantity of H2O at 3L. Categories: Labooratory Mixers, Shakers & Stirrers. | |
| MS-PEG3-t-butyl ester | MS-PEG3-t-butyl ester. CAS No. 1312309-62-8. Purity: 95%+. Product ID: ACM1312309628. Molecular formula: C12H24O7S. Mole weight: 312.38. Alfa Chemistry - ISO 9001:32057 Certified. | |
| MSPG | MSPG. Group: Biochemicals. Grades: Purified. CAS No. 169209-64-7. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Msp I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA in 1 hour at 37°C in a total reaction volume of 50 μl. Applications: After 20-fold overdigestion with enzyme more than 95% of the dna fragments can be ligated and recut. Group: Restriction Enzymes. Purity: 1000U; 5000U. C↑CGG GGC↓C. Activity: 20000u.a./ml. Appearance: 10 X SE-buffer B. Storage: -20°C. Form: Liquid. Source: Moraxella species. Pack: 10 mM Tris-HCl (pH 7.5); 50 mM KCl; 0,1 mM EDTA; 7 mM 2-mercaptoethanol; 200 μg/ml BSA; 50% glycerol. Cat No: ET-1139RE. | |
| MspR9 I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA (dcm-) in 1 hour at 37°C in a total reaction volume of 50 μl. Applications: After 2-fold mspr9 i overdigestion >5% of the dna fragments can be ligated and recut. Group: Restriction Enzymes. Purity: 1000U; 5000U. CC↑NGG GGN↓CC. Activity: 20000u.a./ml. Appearance: 10 X SE-buffer O. Storage: -20°C. Form: Liquid. Source: Micrococcus species R9. Pack: 10 mM Tris-HCl (pH 7.5); 100 mM NaCl; 0,1 mM EDTA; 7 mM 2-mercaptoetyanol; 100 μg/ml BSA; and 50% glycerol. Cat No: ET-1141RE. | |
| MST-312 | MST-312 is a telomerase inhibitor. MST-312 is a chemically modified derivative of green tea epigallocatechin gallate (EGCG). MST-312 can be used for the research of cancer, such as multiple myeloma (MM)[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Telomerase Inhibitor IX. CAS No. 368449-04-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-120145. | |
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