Cresols
Medchemexpress LLC Inx-P (glucocorticosteroid-target antibody-drug conjugate) | 2734878-02-3 | 99.6% | 866.79 g/mol | C43H52BrN3O11 | 10 MG
INX-P is an antibody-drug conjugate (ADC) linker that targets glucocorticosteroid pathways and is provided for laboratory research use only. It is intended for research applications and not for human or animal therapeutic use.
- Antibody-drug conjugate linker targeting glucocorticosteroid pathways.
- Research use only; not for human or animal therapeutic use.
- Available in multiple pack sizes, including 10 mg.
- CAS number 2734878-02-3 and molecular weight 866.79 g/mol.
- Reported purity 99.63% (supplier data).
Medchemexpress LLC Phenol, 4-amino-3-methyl- | 2835-99-6 | ≥98.0% | 123.16 | 50 G
4-Amino-m-cresol is recognized for its role as a soil urease inhibitor and is categorized as a biochemical assay reagent. This compound has been documented to actively suppress the activity of urease in soil environments.
- Inhibits soil urease activity.
- Intended for research applications.
- For research use only.
Medchemexpress LLC Mono-(6-p-toluenesulfonyl)-β-cyclodextrin | 67217-55-4 | MFCD05864975 | 95.0% | 1289.17 g/mol | C49H76O37S | 500 MG
Mono-(6-p-toluenesulfonyl)-β-cyclodextrin is a tosylated derivative of β-cyclodextrin supplied as a white to off-white solid. It is used as a biochemical reagent and intermediate for selective functionalization at the 6-position of β-cyclodextrin, and is commonly applied in host-guest chemistry, derivatization, and synthetic modification in life-science research.
- Purity 95.0%.
- Appearance white to off-white solid.
- Molecular formula C49H76O37S; molecular weight 1289.17 g/mol.
- Enables selective functionalization at the 6-position of β-cyclodextrin.
- Suitable for host-guest chemistry and derivatization studies.
- Available in small lab pack sizes for research use.
Medchemexpress LLC 5-fluorouridine 5'-phosphate | 796-66-7 | MFCD30532520 | 98.6% | 342.17 g·mol⁻¹ | C9H12FN2O9P | 100mg
5-Fluorouridine 5 -phosphate is an ODCase (orotidine-5 -monophosphate decarboxylase) inhibitor with a Ki value of 98 M for human ODCase and a Ki value of 645 M for Methanobacterium ODCase 5-Fluorouridine 5 -phosphate exhibits inhibitory activity against leukemia and lymphoma cell lines and can be used in cancer research [1]
![eMolecules 2-[(1H-1,2,3-Benzotriazol-1-ylmethyl)amino]benzonitrile | 298217-94-4 | MFCD00834821 | 100mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502150697.JPG-250.jpg)
eMolecules 2-[(1H-1,2,3-Benzotriazol-1-ylmethyl)amino]benzonitrile | 298217-94-4 | MFCD00834821 | 100mg
Oakwood Chemical | 2-[(1H-1,2,3-Benzotriazol-1-ylmethyl)amino]benzonitrile | 100mg | 537712912 | 181569 | | 298217-94-4 | MFCD00834821 | 249.277 | C14H11N5
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TARGETMOL CHEMICALS INC TNO155 5MG
Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. TNO155 is a protein tyrosine phosphatase (PTP) non-receptor type 11 (SHP2; src homology region 2 domain phosphatase; PTPN11) inhibitor(IC50 0.011 uM)with potential antineoplastic activity. purity: 99%
Cambridge Isotope Laboratories p-n-Nonylphenol monoethoxylate (unlabeled) 100 ug/mL in nonane 1 2 mL
p-n-Nonylphenol monoethoxylate (unlabeled) 100 ug/mL in nonane 1 2 mL
TARGETMOL CHEMICALS INC MRTX-1257 5MG
Also available in 1mg 2mg 10mg 25mg 50mg 100mg and bulk. Please contact Fisher for quotes. MRTX-1257 is a selective irreversible and covalent inhibitor of KRAS G12C. It has an IC50 of 900 pM for KRAS dependent ERK phosphorylation in H358 cells. MRTX1257 demonstrated 31% bioavailability in the mouse with free fraction exposures well above the cellular potency In a PK/PD experiment 77% target engagement. purity: 99%
FUJIFILM BIOSCIENCES INC p-Amidinophenylmethanesulf
p-APMSF is used as a serine protease activity inhibitor Since it specifically suppresses the activity of blood coagulation factor Xa it is used for the study of blood coagulation mechanism Compared to DFP diisopropylfluorophosphate it is easy to handle because it is powder and soluble to water In addition it is reported that serine protease inhibitory activity is several hundred times higher than DFP and PMSF It inhibits the activity of trypsin thrombin plasmin kallikrein and others It does not affect chymotrypsin or acetylcholinesterase For research use only RUO
Apexbio Technology LLC p-Cresyl sulfate potassium 91978-69-7 50mg
p-Cresyl sulfate potassium (CAS 91978-69-7) is the potassium salt form of p-cresyl sulfate a metabolite that accumulates as a protein-bound uremic toxin in patients with chronic kidney disease Biologically it exerts proinflammatory effects by activating cellular signaling pathways including c-Jun N-terminal kinase (JNK) and p38 mitogen-activated protein kinase (MAPK) which can enhance inflammatory responses Research indicates that p-cresyl sulfate potassium also contributes to cardiovascular risk by adversely impacting vascular and cardiac function This compound is utilized in experimental studies investigating the molecular mechanisms of uremic toxicity inflammation and cardiorenal syndromes
Medchemexpress LLC (S)-4-(2-(2-bromoacetamido)acetamido)-5-((3-(4-((6aR,6bS,7S,8aS,8bS)-7-hydroxy | 2734878-02-3 | 99.6% | 866.79 | C43H52BrN3O11 | 1 MG
INX-P is a glucocorticosteroid-target antibody drug conjugate (ADC) designed for research use. The compound targets the glucocorticoid receptor and is supplied as a solid with high reported purity and defined physicochemical properties.
- Intended use: research use only, not for human therapeutic use.
- Target: glucocorticoid receptor.
- Form: solid, white to off-white.
- Purity: 99.63% reported by certificate of analysis.
- Molecular weight: 866.79.
- Chemical formula: C43H52BrN3O11.
- CAS number: 2734878-02-3.
- Available pack sizes: 1 MG, 5 MG, 10 MG, larger sizes available by quote.
TARGETMOL CHEMICALS INC SELONSERTIB 25MG
Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 200 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Selonsertib (GS-4997) is an orally bioavailable inhibitor of apoptosis signal-regulating kinase 1 (ASK1) with potential anti-inflammatory antineoplastic and anti-fibrotic activities. purity: 98%