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Filtered Search Results
Chem Service Inc Acetamiprid, 135410-20-7, MFCD06201842, 100 mg
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Molecular Formula: C10-H11-Cl-N4, MW: 222.7, 99.5%, Alternate Name(s): Mospilan, Saniprid, Acer, Aspilan.
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Medchemexpress LLC Thienopyridone | 1018454-97-1 | 95.1% | 10 MG
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Thienopyridone is a potent and selective phosphatase of regenerating liver (PRL) phosphatase inhibitor with IC50s of 173 nM, 277 nM and 128 nM for PRL-1, PRL-2, and PRL-3, respectively. It shows minimal effects on other phosphatases. Thienopyridone induces p130Cas cleavage and apoptosis and has anticancer effects. It is intended for research use only.
- Potent and selective PRL phosphatase inhibitor
- Minimal effects on other phosphatases
- Induces p130Cas cleavage and apoptosis
- Exhibits anticancer effects
- Significantly inhibits tumor cell anchorage-independent growth
- Suppresses HUVEC migration
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Medchemexpress LLC 2-methylbutyryl-L-carnitine-d3 (chloride) | 00-00-0 | MFCD34676379 | 99.2% | 284.79 g/mol | C12H21D3ClNO4 | 5 MG
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2-Methylbutyryl-L-carnitine-d3 (chloride) is the deuterium-labeled form of 2-methylbutyryl-L-carnitine supplied as the chloride salt. It is intended for use as a stable isotope internal standard or tracer in analytical chemistry and biochemical assays, particularly for LC-MS quantitation.
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Medchemexpress LLC Crisaborole (standard) | 906673-24-3 | 98.3% | 251.05 | 50 MG
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Crisaborole (Standard) serves as an analytical standard for Crisaborole, a potent inhibitor of PDE4 and cytokine release with an IC50 of 0.49 μM. This reference standard is suitable for research and analytical applications.
- Analytical standard for Crisaborole
- Potent inhibitor of PDE4 and cytokine release
- Used in qualitative, quantitative, and methodological research experiments
- Applications include HPLC, GC, and MS
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Cayman Chemical FenpropImorph 50mg
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A fungicide that inhibits the sterol pathway
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Medchemexpress LLC Metronidazole | 443-48-1 | 99.9% | 1 ML
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Metronidazole is an orally active nitroimidazole antibiotic with broad activity against anaerobic bacteria and protozoa, known for its ability to cross the blood-brain barrier. It is effective in inhibiting various anaerobic protozoa and exhibits bactericidal activity against anaerobic bacteria. It also induces apoptosis in Blastocystis sp. cells. This product is provided as a 10 mM solution in 1 mL of DMSO for research into anaerobic infections.
- Orally active nitroimidazole antibiotic.
- Can cross the blood-brain barrier.
- Effective against anaerobic protozoa, including Trichomonas vaginalis, Entamoeba histolytica, Giardia lamblia, and Balantidium coli.
- Demonstrates bactericidal activity against anaerobic bacteria.
- Induces apoptosis in Blastocystis sp. cells.
- Provided as a 10 mM solution in DMSO.
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![eMolecules Ambeed / 2-Hydroxybenzoic acid / 10g / 490527872 / A187633 / / 69-72-7 / [null] / 138.122 / C7H6O3](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502424839.PNG-250.jpg)
eMolecules Ambeed / 2-Hydroxybenzoic acid / 10g / 490527872 / A187633 / / 69-72-7 / [null] / 138.122 / C7H6O3
Ambeed / 2-Hydroxybenzoic acid / 10g / 490527872 / A187633 / / 69-72-7 / [null] / 138.122 / C7H6O3
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eMolecules Ambeed / 4-(4-Methoxyphenyl)butyric acid / 1g / 552565960 / A132991 / / 4521-28-2 / MFCD00004404 / 194.230 / C11H14O3
Ambeed / 4-(4-Methoxyphenyl)butyric acid / 1g / 552565960 / A132991 / / 4521-28-2 / MFCD00004404 / 194.230 / C11H14O3
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Medchemexpress LLC Olodaterol (BI1744) | 868049-49-4 | 99.9% | C21H26N2O5 | 50 MG
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Olodaterol (BI1744) is a selective, long-acting β2-adrenoceptor (β2-AR) agonist with an EC50 of 0.1 nM and a pKi of 9.14 for human β2-adrenoceptor. It is used for chronic obstructive pulmonary disease (COPD) and pulmonary fibrosis. Olodaterol exhibits subnanomolar affinity for the β2-AR and is selective compared to β1-AR and β3-AR subtypes.
- Attenuates growth factor-induced motility and proliferation in fibroblasts.
- Interferes with FGF-induced phosphorylation of signaling cascades.
- Increases intracellular cAMP in a concentration-dependent manner.
- Inhibits PICP increase with maximal efficacy of 70% at 10 nM.
- Accelerates body weight recovery and attenuates TGF-β-induced lung fibrosis in C57BL/6 mice.
- Induces a dose-dependent bronchoprotection in guinea pigs and dogs.
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eMolecules AstaTech / TERT-BUTYL 4-(3-CHLOROPHENYL)PIPERAZINE-1-CARBOXYLATE / 0.25g / 387752404 / A10043 / 95.000 / 186790-11-4 / MFCD11872670 / 296.800 / C15H21ClN2O2
AstaTech / TERT-BUTYL 4-(3-CHLOROPHENYL)PIPERAZINE-1-CARBOXYLATE / 0.25g / 387752404 / A10043 / 95.000 / 186790-11-4 / MFCD11872670 / 296.800 / C15H21ClN2O2
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eMolecules Ambeed / 4-Biphenylacetic acid / 5g / 552726410 / A410938 / / 5728-52-9 / MFCD00004351 / 212.248 / C14H12O2
Ambeed / 4-Biphenylacetic acid / 5g / 552726410 / A410938 / / 5728-52-9 / MFCD00004351 / 212.248 / C14H12O2
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eMolecules Ambeed / 34-Dihydroxybenzoic acid / 25g / 552642376 / A202277 / / 99-50-3 / MFCD00002509 / 154.121 / C7H6O4
Ambeed / 34-Dihydroxybenzoic acid / 25g / 552642376 / A202277 / / 99-50-3 / MFCD00002509 / 154.121 / C7H6O4
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Medchemexpress LLC Acifluorfen | 50594-66-6 | 98.95% | 100 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Acifluorfen is a protoporphyrinogen oxidase (PROTOX) inhibitor herbicide that promotes the accumulation of protoporphyrin IX (PPIX) and induces tumors in the rodent liver. It also causes strong photooxidative destruction of pigments and lipids in sensitive plant species.
- Promotes accumulation of protoporphyrin IX (PPIX)
- Induces tumors in rodent liver
- Causes strong photooxidative destruction of pigments and lipids in sensitive plant species
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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STA PHARMACEUTICAL US LLC Dde-L-Dapa(Fmoc)-OH | 5 g | CAS 1263046-98-5 | MDL MFCD05663745
Dde-L-Dapa(Fmoc)-OH is a Amino Acid reagent (Subcategory: Lys) sold by WuXi TIDES. Offered in 5 g. Store at 4 °C. SDS available for reference.
Specifications
- CAS: 1263046-98-5
- MDL: MFCD05663745
- InChIKey: IRGLZXIDGOBCJV-QFIPXVFZSA-N
- Molecular Weight: 490.556
- Molecular Formula: C28H30N2O6
- Purity: ≥95%
- Container Type: 30 mL HDPE
- Pack Size: 5 g
- Net Weight: 5 g
- Gross Weight: 16.5 g
- Commodity Code: 29242970
- Country Of Origin: China
- IUPAC: (S)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-((1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl)amino)propanoic acid
- SMILES: O=C(NC[C@H](N/C(C)=C1C(CC(C)(C)CC\1=O)=O)C(O)=O)OCC2C(C=CC=C3)=C3C4=C2C=CC=C4
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC JAB-3068 (hydrochloride) | 2169223-49-6 | 98.9% | 100 MG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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JAB-3068 hydrochloride is a potent SHP2 inhibitor with an IC50 of 25.8 nM. It inhibits the proliferation of KYSE-520 cells with an IC50 of 2.17 μM.
- Potent SHP2 inhibitor
- Inhibits proliferation of KYSE-520 cells
- Solid appearance
- Light yellow to yellow color
- Molecular weight of 513.00
- Chemical formula C22H27ClF2N6O2S
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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