Piperidines
Matrix Scientific PAROXETINE HYDROCHLORIDE HE-1G
Paroxetine hydrochloride hemihydrate, >95%; 1g,C38H42F2N2O7, MFCD03658863, mw 676.76, [110429-35-1]
eMolecules 626-58-4 | 4-Methylpiperidine | Oakwood Chemicals | MFCD00006005 | 99.177 | C6H13N | 98.000 | CC1CCNCC1 | 1g | 480104223
4-Methylpiperidine | Oakwood Chemicals | 626-58-4 | MFCD00006005 | 99.177 | C6H13N | 98.000 | CC1CCNCC1 | 1g | 480104223
Medchemexpress LLC Avibactam free acid | 1192500-31-4 | 99.27% | 265.24 | 50 MG
Avibactam free acid is a covalent and reversible non-β-lactam β-lactamase inhibitor. It effectively inhibits β-lactamase TEM-1 and CTX-M-15.
- Inhibits class A and C β-lactamases
- Has little antibacterial activity
- Does not inhibit metallo-type β-lactamases or Acinetobacter OXA carbapenemases
Matrix Scientific 4-PHENYLPIPERIDINE MF C11H15N MW 161.25 CAS 771-99-3 MDL MFCD00006002 QTY 5 UOM G
4-PHENYLPIPERIDINE MF C11H15N MW 161.25 CAS 771-99-3 MDL MFCD00006002 QTY 5 UOM G
Apexbio Technology LLC Avibactam sodium 1192491-61-4 5mg
Avibactam sodium (1192491-61-4) is a small-molecule inhibitor targeting bacterial -lactamase enzymes including CTX-M-15 and TEM-1 It is designed to inhibit -lactamase activity thereby preventing the hydrolysis of -lactam antibiotics Avibactam sodium exerts its biological activity primarily through reversible covalent non- -lactam inhibition of its targets In in vitro studies avibactam sodium demonstrates inhibitory activity with IC50 values of 5 nM for CTX-M-15 and 8 nM for TEM-1 Based on these pharmacological properties avibactam sodium holds research potential in studies of combination therapy for bacterial infections involving -lactamase-producing Gram-negative pathogens
Apexbio Technology LLC Quisinostat dihydrochloride 875320-31-3 10mg
Quisinostat dihydrochloride (CAS 875320-31-3) also known as JNJ-26481585 dihydrochloride is an orally bioavailable pan-histone deacetylase (HDAC) inhibitor It potently suppresses the enzymatic activity of several HDAC isoforms including HDAC1 (IC50 0 11 nM) HDAC2 (IC50 0 33 nM) HDAC4 (IC50 0 64 nM) HDAC10 (IC50 0 46 nM) and HDAC11 (IC50 0 37 nM) By interfering with histone deacetylation Quisinostat dihydrochloride induces apoptosis and cell cycle arrest in tumor cells This compound is widely utilized in studies addressing tumor biology and epigenetic regulation
Accela Chembio Inc 1-boc-3-piperidone | 25g | 98977-36-7 | MFCD01631193 | 97+% | Shelf Life: 1080 Days | Moisture Sensitive/+4
1-boc-3-piperidone | 25g | 98977-36-7 | MFCD01631193 | 97+% | Shelf Life: 1080 Days | Moisture Sensitive/+4
Accela Chembio Inc 1-boc-3-piperidone | 100g | 98977-36-7 | MFCD01631193 | 97+% | Shelf Life: 1080 Days | Moisture Sensitive/+4
1-boc-3-piperidone | 100g | 98977-36-7 | MFCD01631193 | 97+% | Shelf Life: 1080 Days | Moisture Sensitive/+4
Apexbio Technology LLC Octenidine (dihydrochloride) 70775-75-6 200mg
Octenidine dihydrochloride (CAS 70775-75-6) is a small-molecule inhibitor designed to disrupt microbial membrane integrity thereby inhibiting bacterial proliferation Octenidine dihydrochloride exerts its biological activity primarily through disruption of microbial membrane integrity In in vitro studies Octenidine dihydrochloride demonstrates inhibitory activity against diverse Gram-positive and Gram-negative bacterial strains with reported IC50 values typically ranging from 1 to 10 g/mL depending on test organisms and experimental conditions Based on these pharmacological properties Octenidine dihydrochloride holds research potential in infection control wound management and microbiological assay applications
Apexbio Technology LLC Octenidine (dihydrochloride) 70775-75-6 1g
Octenidine dihydrochloride (CAS 70775-75-6) is a small-molecule inhibitor designed to disrupt microbial membrane integrity thereby inhibiting bacterial proliferation Octenidine dihydrochloride exerts its biological activity primarily through disruption of microbial membrane integrity In in vitro studies Octenidine dihydrochloride demonstrates inhibitory activity against diverse Gram-positive and Gram-negative bacterial strains with reported IC50 values typically ranging from 1 to 10 g/mL depending on test organisms and experimental conditions Based on these pharmacological properties Octenidine dihydrochloride holds research potential in infection control wound management and microbiological assay applications
Sigma Aldrich Fine Chemicals Biosciences Donepezil hydrochloride United States Pharmacopeia (USP) Reference Standard | 120011-70-3 | 200MG
Donepezil hydrochloride United States Pharmacopeia (USP) Reference Standard | Mol Wt: 415.95 | 120011-70-3 | 200MG
Medchemexpress LLC Piperine | 94-62-2 | 98.99% | 285.34 | 100 G
Piperine is an alkaloid isolated from pepper. It can inhibit the activity of P-glycoprotein and CYP3A4, and inhibits HeLa cells with an IC50 of 61.94±0.054 μg/mL.
- Alkaloid isolated from pepper.
- Inhibits the activity of P-glycoprotein and CYP3A4.
- Inhibits HeLa cells with an IC50 of 61.94±0.054 μg/mL.
- Shown to possess in vitro cytotoxic activity.
- Immunomodulatory, anti-oxidant, anti-asthmatic, anti-carcinogenic, anti-inflammatory, anti-ulcer, and anti-amoebic properties.
- Enhances the bioavailabilities of other drugs, including rosuvastatin, puerarin, and docetaxel (DOX) by inhibiting CYP3A and P-glycoprotein activity.
- Inhibits the phosphorylation of I-κB, p65, p38, ERK, and JNK in a dose-dependent manner, suggesting potential as an anti-inflammatory drug.
Medchemexpress LLC Avibactam free acid | 1192500-31-4 | 99.3% | 265.24 | 5 MG
Avibactam free acid is a covalent and reversible non-β-lactam β-lactamase inhibitor. It effectively inhibits β-lactamase TEM-1 and CTX-M-15, with IC50s of 8 nM and 5 nM respectively. This product exhibits minimal antibacterial activity but targets class A and C β-lactamases, excluding metallo types and Acinetobacter OXA carbapenemases. It is intended for research use only.
- Covalent and reversible non-β-lactam β-lactamase inhibitor
- Inhibits β-lactamase TEM-1 and CTX-M-15
- Targets class A and C β-lactamases
- Minimal antibacterial activity
- Suitable for research applications
Medchemexpress LLC Avibactam free acid | 1192500-31-4 | 99.3% | 265.24 | 100 MG
Avibactam free acid is a covalent and reversible non-β-lactam β-lactamase inhibitor that inhibits β-lactamase TEM-1 and CTX-M-15.
- Covalent and reversible non-β-lactam β-lactamase inhibitor.
- Inhibits β-lactamase TEM-1 and CTX-M-15 with IC50s of 8 nM and 5 nM, respectively.
- Exhibits little antibacterial activity.
- Inhibits class A and C β-lactamases, but not metallo types and Acinetobacter OXA carbapenemases.