Furans
Medchemexpress LLC 7-TFA-ap-7-Deaza-dA | 178420-75-2 | 98.8% | 399.32 | 100 MG
7-TFA-ap-7-Deaza-dA is a modified nucleoside and a click chemistry reagent. It is utilized in the synthesis of deoxyribonucleic acid or nucleic acid. Featuring an alkyne group, this compound is capable of undergoing copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide-containing molecules. It is intended for laboratory use and substance manufacturing, strictly for research purposes.
- Modified nucleoside
- Click chemistry reagent
- Contains an alkyne group for CuAAc reactions
- Supports DNA and nucleic acid synthesis
- For laboratory chemicals and substance manufacturing
- For research use only
Medchemexpress LLC Linperlisib | 1702816-75-8 | MFCD31544346 | 98.9% | 588.69 g·mol⁻¹ | C28H37FN6O5S | 25 MG
Linperlisib is a potent, orally bioavailable, and selective inhibitor of phosphoinositide 3-kinase delta (PI3Kδ) developed for research applications. It demonstrates an IC50 of approximately 6.4 nM against PI3Kδ and is supplied as a high-purity solid suitable for in vitro and preclinical studies.
- Potent, selective inhibitor of PI3Kδ (IC50 ≈ 6.4 nM).
- Orally bioavailable profile useful for in vivo studies.
- Supplied as a high-purity solid (≈98.9%).
- Suitable for in vitro and preclinical research applications.
- Available in multiple small-scale quantities for laboratory use.
- Recommended storage at low temperatures to preserve stability.
Apexbio Technology LLC Nitrofurazone 59-87-0 5g
Nitrofurazone (59-87-0) is a small-molecule antibacterial agent of the nitrofuran class It targets both Gram-positive and Gram-negative bacteria by generating DNA damage thereby impairing bacterial cellular replication and viability Nitrofurazone exerts its biological activity primarily through enzymatic reduction catalyzed by bacterial nitroreductases producing reactive intermediates that induce DNA strand breaks and oxidative lesions In microbiology research Nitrofurazone demonstrates inhibitory activity with reported IC50 values typically ranging from 5 30 M depending on bacterial strain and experimental conditions Based on these pharmacological properties Nitrofurazone holds research potential in bacterial susceptibility assays investigation of antibacterial mechanisms of action and studies on microbial DNA damage responses
Medchemexpress LLC Trotabresib | 1706738-98-8 | 99.7% | 383.46 | 100 MG
Trotabresib is a reversible and orally active BET inhibitor used in the study of advanced solid tumors. It inhibits the proliferation of diffuse midline glioma (DMG) cells and shows stronger antitumor activity against H3K27M mutant DMG cells than DMG wildtype.
- Reversible and orally active BET inhibitor
- Applied in studies for advanced solid tumors
- Inhibits proliferation of diffuse midline glioma (DMG) cells
- Shows stronger antitumor activity against H3K27M mutant DMG cells than DMG wildtype
Medchemexpress LLC Etiocholanolone (5β-androsterone) | 53-42-9 | MFCD00064133 | 99.5% | 290.44 g/mol | C19H30O2 | 5 MG
Etiocholanolone (5β-androsterone) is an endogenous metabolite of testosterone provided as a high-purity research standard. It demonstrates anticonvulsant activity and functions as a neurosteroid positive allosteric modulator (PAM) of GABAA receptors, making it useful for biochemical, pharmacological, and analytical applications.
Medchemexpress LLC DS08210767 | 2376334-75-5 | 99.4% | 513.67 | C31H39N5O2 | 5MG
DS08210767 is a small-molecule, orally bioavailable antagonist of the parathyroid hormone receptor 1 (PTHR1) with a reported IC50 of 90 nM. It is supplied for research use only and is provided as a light yellow solid intended for laboratory applications.
- Orally bioavailable PTHR1 antagonist with an IC50 of 90 nM.
- High chemical purity of 99.4%.
- Molecular weight 513.67 and chemical formula C31H39N5O2.
- Supplied as a light yellow solid suitable for laboratory research.
- Provided in a 5 mg quantity for experimental use.
Medchemexpress LLC Nitrofurantoin | 67-20-9 | C8H6N4O5 | 1 G
Nitrofurantoin is a potent and orally active broad-spectrum beta-lactamase antimicrobial agent. It acts as an antibiotic and can be used for the study of urinary tract infections (UTIs), including cystitis and kidney infections.
- Potent and orally active
- Broad-spectrum beta-lactamase antimicrobial agent
- Acts as an antibiotic
- Used for the study of urinary tract infections (UTIs), including cystitis and kidney infections
Medchemexpress LLC Sid7970631 | 868224-75-3 | MFCD04473864 | 98.3% | 452.46 g/mol | C24H24N2O7 | 5 MG
SID7970631 is an isoquinolinone analog reported as a potent and selective submicromolar inhibitor of Steroidogenic Factor-1 (SF-1) with an IC50 of 255 nM. Supplied as a solid research compound, it is intended for use in studies of SF-1 signaling and cancer-related cellular assays.
- Potent SF-1 inhibitor (IC50 255 nM).
- Submicromolar activity suitable for cell-based assays.
- Solid powder with high purity (98.3%).
- Molecular formula C24H24N2O7; molecular weight 452.46 g/mol.
- Storage recommendations: powder -20°C long term, 4°C short term; solutions -80°C for months.
- Available as small-scale solids and 10 mM solution in DMSO for research use.
Medchemexpress LLC Khasianine | 32449-98-2 | 5 MG
Khasianine is a steroidal glycoalkaloid obtained from black nightshade (Solanum Nigrum L.). It displays antitumor activity.
- Derived from black nightshade (Solanum Nigrum L.)
- Exhibits antitumor activity
- Steroidal glycoalkaloid