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Filtered Search Results
CHEMSCENE
5000579936 2 2 6 2-TERPYRIDINE -4-CA 100G
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CHEMSCENE
5000579937 2-BROMO-1H-IMIDAZOLE 1G
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MEDCHEMEXPRESS LLC 2-aminobenzimidazole | 934-32-7 | MFCD00005596 | 100.0% | 133.15 g/mol | C7H7N3 | 25g
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2-Aminobenzimidazole (2-Iminobenzimidazoline 1H-Benzimidazol-2-ylamine 2-Benzimidazolamine) is a heterocyclic aromatic compound 2-Aminobenzimidazole is a kind of biological materials or organic compounds that are widely used in life science research[1]
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MEDCHEMEXPRESS LLC Hdhodh-in-1 | 1173715-42-8 | MFCD32671346 | >98.0% | C17H14N2O2 | 10MG
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hDHODH-IN-1 is a small-molecule inhibitor of human dihydroorotate dehydrogenase (hDHODH) used in research to probe DHODH-dependent pyrimidine biosynthesis and inflammation-related pathways. It is supplied as a research reagent and has documented activity in biochemical and cellular assays.
- Inhibits human dihydroorotate dehydrogenase.
- Useful for studying pyrimidine biosynthesis and inflammatory responses.
- Applicable in biochemical and cellular assay formats.
- High purity confirmed by LCMS (>99.9%).
- Molecular formula C17H14N2O2 and molecular weight 278.31 g/mol.
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![MEDCHEMEXPRESS LLC N-[5-[[3-cyano-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidin-5-yl]amino]-2-methylphenyl]propanamide | 2470424-39-4 | 99.7% | C20H21N7O | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000259288.png-250.jpg)
MEDCHEMEXPRESS LLC N-[5-[[3-cyano-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidin-5-yl]amino]-2-methylphenyl]propanamide | 2470424-39-4 | 99.7% | C20H21N7O | 10MG
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SGC-CK2-1 is a selective, cell-active ATP-competitive chemical probe for casein kinase 2 (CK2) used in research to investigate CK2 signaling and neurodegenerative disease-related pathways. It shows low-nanomolar potency in cellular assays and is suitable for mechanistic and cell-based studies.
- Low-nanomolar cellular potency against CK2 isoforms.
- High selectivity for CK2 over other kinases.
- Cell-permeable and active in cell-based assays.
- Suitable for mechanistic studies of CK2 signaling and neurodegeneration.
- Stable solid form with recommended cold storage for long-term retention.
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MEDCHEMEXPRESS LLC B7-H6 protein, rat (HEK293, His tag) | ≥95.0% | 5 UG
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Recombinant rat B7-H6 (NCR3LG1) extracellular domain expressed in HEK293 cells with a C-terminal His tag. Supplied as a lyophilized powder from PBS, the protein is suitable for binding and functional assays with NCR3/NKp30 and shows an ED50 of 14.43 ng/mL in ELISA.
- Species: Rat
- Expression system: HEK293 cells
- Tag: His tag
- Amino acid length: 308 (M1-S308)
- Molecular weight: ~35-46 kDa (glycosylated)
- Purity: ≥95.0%
- Endotoxin level: <1 EU/μg
- Formulation: Lyophilized from PBS, pH 7.0
- Storage recommendation: Store at -20°C; after reconstitution 4°C short-term or -20°C/-80°C long-term with carrier protein
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MEDCHEMEXPRESS LLC DiABZI-C2-NH2 | 2137975-93-8 | 96.1% | C36H43N13O4 | 10MG
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diABZI-C2-NH2 is a synthetic small-molecule STING agonist for research use. It is an active analogue containing a primary amine functionality and is supplied with supporting documentation (data sheet, COA, SDS) for experimental reproducibility.
- Acts as a STING agonist in immuno-oncology research
- Contains a primary amine functionality
- High purity: 96.1%
- Available as solid and as a 10 mM solution in DMSO
- Soluble in DMSO (100 mg/mL) for in vitro use
- Recommended storage: solid at -20°C under nitrogen; in solution store at -80°C
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![MEDCHEMEXPRESS LLC N-[(2R)-4-amino-3,4-dioxo-1-phenylbutan-2-yl]-4-(2-fluorophenyl)-2-methyl-1,3-oxazole-5-carboxamide | 2221010-42-8 | 98.0% | C21H18FN3O4 | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000261493.png-250.jpg)
MEDCHEMEXPRESS LLC N-[(2R)-4-amino-3,4-dioxo-1-phenylbutan-2-yl]-4-(2-fluorophenyl)-2-methyl-1,3-oxazole-5-carboxamide | 2221010-42-8 | 98.0% | C21H18FN3O4 | 10MG
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Dazcapistat is a small-molecule calpain inhibitor with reported IC50s of <3 μM for calpain 1, calpain 2, and calpain 9. It is provided as a high-purity research reagent in both powder and solution formats for biochemical and cell-based studies, with recommended storage conditions to maintain stability.
- Potent calpain inhibition with IC50s <3 μM for calpain 1, 2, and 9.
- High purity (98.0%) suitable for research applications.
- Available as powder and pre-made solution formats for flexible use.
- Defined storage recommendations to preserve compound integrity.
- Appropriate for biochemical assays and cellular studies of protease activity.
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![MEDCHEMEXPRESS LLC N-[(2R)-4-amino-3,4-dioxo-1-phenylbutan-2-yl]-4-(2-fluorophenyl)-2-methyl-1,3-oxazole-5-carboxamide | 2221010-42-8 | 98.0% | 395.38 | C21H18FN3O4 | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000262950.png-250.jpg)
MEDCHEMEXPRESS LLC N-[(2R)-4-amino-3,4-dioxo-1-phenylbutan-2-yl]-4-(2-fluorophenyl)-2-methyl-1,3-oxazole-5-carboxamide | 2221010-42-8 | 98.0% | 395.38 | C21H18FN3O4 | 5 MG
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Dazcapistat is a research-grade calpain inhibitor with reported IC50s of <3 μM for calpain 1, calpain 2, and calpain 9. Supplied as a white to off-white solid with a stated purity of 98.0%, it is intended for in vitro and in vivo research; follow supplier protocols for solubility, formulation, and storage.
- Molecular formula C21H18FN3O4; molecular weight 395.38
- Purity 98.0%
- Appearance white to off-white solid
- In vitro solubility: DMSO 100 mg/mL (ultrasonic recommended)
- In vivo formulation: ≥2.5 mg/mL in recommended vehicle protocols (10% DMSO/40% PEG300/5% Tween-80/45% saline; alternatives available)
- Storage: powder -20°C (3 years) or 4°C (2 years); in solvent -80°C (6 months) or -20°C (1 month)
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![MEDCHEMEXPRESS LLC Benzaldehyde, 4-[(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)oxy]- | 31873-42-4 | 98.0% | 452.41 g/mol | C21H24O11 | 100mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000270320.png-250.jpg)
MEDCHEMEXPRESS LLC Benzaldehyde, 4-[(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)oxy]- | 31873-42-4 | 98.0% | 452.41 g/mol | C21H24O11 | 100mg
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4-Formylphenyl 2 3 4 6-tetra-O-acetyl -D-glucopyranoside (compound 2a) is a helicid analogue[1]
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MEDCHEMEXPRESS LLC Mesosulfuron-methyl | 208465-21-8 | 98.0% | 10 G
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Mesosulfuron-methyl is a sulfonylurea herbicide that inhibits acetolactate synthase (ALS) and is used in research for post-emergence control of ryegrass and *Avena spp.* (wild oat) in wheat fields.
- Inhibits acetolactate synthase (ALS)
- Used for post-emergence control of ryegrass and *Avena spp.* (wild oat) in wheat fields
- Molecular weight: 503.51
- Appearance: White to off-white powder
- For research use only
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MEDCHEMEXPRESS LLC 1-Dodecylimidazole | 4303-67-7 | MFCD00278859 | 99.8% | 236.40 | 1 G
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1-Dodecylimidazole is a lysosomotropic detergent and a cytotoxic agent. It induces cell death by accumulating in lysosomes in an acid-dependent manner, disrupting the lysosomal membrane and releasing cysteine proteases into the cytoplasm. The compound also exhibits hypocholesterolaemic activity and broad-spectrum antifungal activity, partly by inhibiting cholesterol biosynthesis.
- Lysosomotropic detergent and cytotoxic agent
- Induces cell death through acid-dependent lysosomal accumulation
- Disrupts lysosomal membranes, releasing cysteine proteases
- Exhibits hypocholesterolaemic activity
- Possesses broad-spectrum antifungal activity
- Shows extracellular pH-dependent cytotoxicity
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MEDCHEMEXPRESS LLC Losartan Carboxylic Acid | 124750-92-1 | 99.5% | 10 MG
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Losartan Carboxylic Acid (E-3174) is an active carboxylic acid metabolite of Losartan, functioning as an angiotensin II receptor type 1 (AT1) antagonist. It blocks angiotensin II-induced responses in vascular smooth muscle cells and elevates plasma renin activities while reducing mean arterial pressure.
- Blocks angiotensin II-induced responses in vascular smooth muscle cells.
- Elevates plasma renin activities.
- Reduces mean arterial pressure.
- Inhibits specific binding of angiotensin II to vascular smooth muscle cells with an IC50 of 1.1 nM.
- Abolishes angiotensin II-induced formation of inositolphosphates in vascular smooth muscle cells.
- Inhibits angiotensin II-induced elevation of intracellular cytosolic Ca2+ concentration with an IC50 of 5 nM.
- Inhibits angiotensin II-induced cell protein synthesis with an IC50 of 3 nM.
- Induces an 87±4% inhibition of pressor responses to angiotensin I in mongrel dogs at 0.1 mg/kg.
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BOSTON BIOPRODUCTS INC Krebs-Henseleit Solution (without Calcium) - 500ml
Krebs-Henseleit Solution (without Calcium) - 500ml (For Research Use and Further Manufacturing Only)
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MEDCHEMEXPRESS LLC Tenofovir amibufenamide | 1571076-26-0 | 99.7% | 490.49 | 50 MG
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Tenofovir amibufenamide (HS-10234) is an orally active Tenofovir prodrug and antiviral agent. It is designed to inhibit HBV and is suitable for studies related to chronic hepatitis B (CHB).
- Inhibits HBV DNA replication
- Corrects metabolic disorders of host liver cells caused by HBV infection
- Regulates hepatocyte metabolism and exhibits antiviral effects
- Decreases HBV DNA levels in serum
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