Phenylcarbamic acid esters
Medchemexpress LLC 2-Iodoaniline | 615-43-0 | 219.03 | 500 MG
2-Iodoaniline (2-Iodophenylamine) is an aniline derivative with potential hepatotoxic and nephrotoxic activity. This compound is for research use only and not sold to patients. Studies have shown that 2-Iodoaniline can induce oliguria, diminish kidney weight, cause tubular casts, and decrease renal cortical slice accumulation of organic anions. It also elevates plasma ALT/GPT activity and alters morphology in the centrilobular region.
- Induces oliguria
- Diminishes kidney weight
- Causes tubular casts
- Decreases renal cortical slice accumulation of organic anions
- Elevates plasma ALT/GPT activity
- Alters morphology in the centrilobular region
- Soluble in DMSO: 100 mg/mL (456.57 mM), requires ultrasonic
- Solid storage: 4°C, protect from light
- In solvent storage: -80°C for 6 months; -20°C for 1 month, protect from light
Medchemexpress LLC 4,7,10,14-tetraoxahexadecanoic acid, 15,15-dimethyl-13-oxo- | 1807539-06-5 | >=97.0% | 250 MG
Acid-PEG3-C2-Boc is a PEG- and Alkyl/ether-based PROTAC linker, with a molecular weight of 306.35 and chemical formula C14H26O7. It appears as a colorless to light yellow liquid and is for research use only. The pure form should be stored at -20°C for 3 years or 4°C for 2 years, while in solvent, it should be stored at -80°C for 6 months or -20°C for 1 month. It is soluble in DMSO at concentrations of 175 mg/mL (571.24 mM) or greater. This product is utilized in the synthesis of PROTACs.
- Can be used in the synthesis of PROTACs for the degradation of EGFR.
- Inhibits mTOR.
- Utilizes the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- Contains two different ligands connected by a linker; one for an E3 ubiquitin ligase and the other for the target protein.
Medchemexpress LLC S100P Human N-His 100ug
Recombinant human S100P protein with an N-terminal 6xHis tag, expressed in E. coli and supplied as a lyophilized powder. Purified to >95% by reducing SDS-PAGE and supplied in a 100 μg package with formulation designed for stability. The product is intended for in vitro research applications and is accompanied by a datasheet, COA, and SDS for batch-specific information.
- High purity (>95%) for reliable assay performance.
- N-terminal 6xHis tag for straightforward purification and detection.
- Lyophilized formulation with trehalose for extended shelf life.
- Low endotoxin (<1 EU/μg) suitable for sensitive assays.
- Supplied with datasheet, COA, and SDS for batch-specific validation.
- Recommended storage and reconstitution guidance to preserve activity.
eMolecules 127828-22-2 | Amino-PEG2-NH-Boc | Ambeed | MFCD12031501 | 204.270 | C9H20N2O3 | 97.000 | CC(C)(C)OC(=O)NCCOCCN | 5g | 490492220
Amino-PEG2-NH-Boc | Ambeed | 127828-22-2 | MFCD12031501 | 204.270 | C9H20N2O3 | 97.000 | CC(C)(C)OC(=O)NCCOCCN | 5g | 490492220
Medchemexpress LLC Ald-Ph-PEG4-Boc | 1807518-64-4 | C23H35NO8 | 100 MG
Ald-Ph-PEG4-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. They exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- Used in the synthesis of PROTACs.
- Facilitates the selective degradation of target proteins.
- Utilizes the intracellular ubiquitin-proteasome system.
- Available in various quantities for research needs.
eMolecules 111721-74-5 | 2-Bromo-5-iodoaniline | Apollo Scientific | MFCD16038675 | 297.921 | C6H5BrIN | 0.000 | Nc1cc(I)ccc1Br | 250mg | 562453786
2-Bromo-5-iodoaniline | Apollo Scientific | 111721-74-5 | MFCD16038675 | 297.921 | C6H5BrIN | 0.000 | Nc1cc(I)ccc1Br | 250mg | 562453786
Medchemexpress LLC Amino-PEG24-Boc | 2170987-96-7 | 99.81% | C55H111NO26 | 25 MG
Amino-PEG24-Boc is a PEG-based PROTAC linker designed for the synthesis of PROTACs. PROTACs are compounds that utilize the intracellular ubiquitin-proteasome system to selectively degrade target proteins. They consist of two different ligands connected by a linker; one ligand binds to an E3 ubiquitin ligase and the other to the target protein.
- Utilizes the ubiquitin-proteasome system
- Selectively degrades target proteins
- PEG-based linker
- Intended for research use only
Medchemexpress LLC (3S,4R)-3-(1,3-benzodioxol-5-yloxymethyl)-4-(4-fluorophenyl)-1-methylpiperidine | 110429-36-2 | MFCD03788781 | 10g
N-Methylparoxetine is a derivative of Paroxetine that induces Apoptosis NSCLC cells by activating mitogen-activated protein kinase ( MAPK) N-Methylparoxetine has antitumor activity[1]
Medchemexpress LLC Neuritin Human N-H 50ug
Recombinant human Neuritin (partial length) with an N-terminal His tag, expressed in E. coli. This ~11 kDa protein promotes neurite outgrowth and synaptic plasticity and is supplied as a lyophilized powder formulated in Tris-NaCl buffer. It is intended for in vitro assays, biochemical characterization, and protein interaction studies; store frozen and follow recommended reconstitution and stabilizer guidelines for best results.
- Expressed in E. coli and supplied with an N-terminal His tag.
- Approximately 11 kDa partial-length protein that promotes neurite growth.
- Purity greater than 95% as determined by reducing SDS-PAGE.
- Lyophilized formulation in 50 mM Tris-HCl, 300 mM NaCl, pH 7.4.
- Stable when stored at -20°C; aliquot and freeze for long-term storage.
- Recommended reconstitution at ≥100 μg/mL with carrier protein for stability.