Benzenesulfonamides
STA PHARMACEUTICAL US LLC 4-(Fmoc-amino)-1-methyl-1H-imidazole-2-carboxylic acid | 5 g | CAS 252206-28-3 | MDL MFCD02259498
4-(Fmoc-amino)-1-methyl-1H-imidazole-2-carboxylic acid is a Amino Acid reagent (Subcategory: Aryl AA) sold by WuXi TIDES. Offered in 5 g. Store at 4 °C. SDS available for reference.
Specifications
- CAS: 252206-28-3
- MDL: MFCD02259498
- InChIKey: AFUJLUWSTBUALR-UHFFFAOYSA-N
- Molecular Weight: 363.373
- Molecular Formula: C20H17N3O4
- Purity: ≥95%
- Container Type: 30 mL HDPE
- Pack Size: 5 g
- Net Weight: 5 g
- Gross Weight: 16.5 g
- Commodity Code: 29332990
- Country Of Origin: China
- IUPAC: 4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-1-methyl-1H-imidazole-2-carboxylic acid
- SMILES: CN1C=C(N=C1C(O)=O)NC(OCC2C3=CC=CC=C3C4=CC=CC=C42)=O
Medchemexpress LLC Sildenafil impurity 3 | 1357931-55-5 | MFCD22683782 | 10mg
Sildenafil Impurity 3 is an impurity of Sildenafil (HY-15025)
eMolecules 43189-50-0 | 3-(4-Methyl-2,5-dioxo-imidazolidin-4-yl)-propionic acid | J&W PharmLab LLC | MFCD08445781 | 186.167 | C7H10N2O4 | 96.000 | CC1(CCC(O)=O)NC(=O)NC1=O | 50mg | 716241727
3-(4-Methyl-2,5-dioxo-imidazolidin-4-yl)-propionic acid | J&W PharmLab LLC | 43189-50-0 | MFCD08445781 | 186.167 | C7H10N2O4 | 96.000 | CC1(CCC(O)=O)NC(=O)NC1=O | 50mg | 716241727
eMolecules 2132396-40-6 | Medchem Express | CD73-IN-1 | 1mg | 446258343 | HY-103695 | 371.41 | C18H17N3O4S
Ambeed | Benzo[c][125]oxadiazol-5-ylboronic acid | 100mg | 490552947 | A311681 | 426268-09-9 | MFCD07186239 | 163.930 | C6H5BN2O3
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Cayman Chemical SIldenafIl Chlorosulfonyl 1g
An intermediate in the synthesis of sildenafil; a potential impurity found in commercial preparations of sildenafil
Medchemexpress LLC Sildenafil citrate | 171599-83-0 | C28H38N6O11S | 1 G
Sildenafil citrate is a potent phosphodiesterase type 5 (PDE5) inhibitor with an IC50 of 5.22 nM. It is for research use only.
- Potent phosphodiesterase type 5 (PDE5) inhibitor.
- Potentiates phosphorylation of ERK1/ERK2 in vitro.
- Increases percentage of cells in S phase and enhances cell proliferation in vitro.
- Significantly increases intracavernosal pressure (ICP) in a dog model of erection in vivo.
- Reduces the number of TL+-cells in vivo.
- Decreases flap necrosis in preclinical animal models by increasing secretion of growth factors (FGF and VEGF).
Medchemexpress LLC Bosentan | 147536-97-8 | 99.9% | C27H29N5O6S | 1 ML
Bosentan is a competitive and dual antagonist of endothelin-1 (ET) for the ETA and ETB receptors, with Ki values of 4.7 nM and 95 nM in human SMC, respectively. It is for research use only.
- Competitive and dual antagonist of endothelin-1 (ET)
- Acts on ETA and ETB receptors
- Research use only
eMolecules 873-41-6 | 3,5,6-trichloro-1,2,4-triazine | Pharmablock | MFCD09033774 | 184.400 | C3Cl3N3 | 97.000 | Clc1nnc(Cl)c(Cl)n1 | 5g | 551253161
3,5,6-trichloro-1,2,4-triazine | Pharmablock | 873-41-6 | MFCD09033774 | 184.400 | C3Cl3N3 | 97.000 | Clc1nnc(Cl)c(Cl)n1 | 5g | 551253161
eMolecules 835619-41-5 | Medchem Express | Indeglitazar | 5mg | 446264614 | HY-14817 | MFCD18633304 | 389.42 | C19H19NO6S
Medchem Express | Indeglitazar | 5mg | 446264614 | HY-14817 | 835619-41-5 | MFCD18633304 | 389.420 | C19H19NO6S
Medchemexpress LLC HY-19977 5mg Medchemexpress, YU238259 CAS:1943733-16-1 Purity:>98%
Medchemexpress, HY-19977 5mg YU238259 CAS:1943733-16-1 YU238259 is an inhibitor of homology-dependent DNA repair (HDR), used for cancer research. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC MF-766 5mg | 1050656-06-8 | 5 MG
MF-766 is a potent, selective, orally active EP4 receptor antagonist used in preclinical research on cancer and inflammatory pathways. The compound is supplied as a white to off-white solid with documented purity, molecular weight, and solubility data to support experimental use.
- Potent EP4 antagonist with low nanomolar activity in functional assays.
- High purity suitable for research-grade applications.
- White to off-white solid for easy handling and storage.
- High solubility in DMSO for stock solution preparation.
- Stable when stored under recommended conditions.
Apexbio Technology LLC RQ-00203078 1254205-52-1 10mg
RQ-00203078 (CAS 1254205-52-1) is a selective antagonist of the transient receptor potential melastatin 8 (TRPM8) ion channel a member of the TRP melastatin subfamily implicated in cold-induced pain hypersensitivity and neuropathic pain including chemotherapy-induced peripheral neuropathy diabetic neuropathy migraine and overactive bladder In in vitro assays RQ-00203078 inhibits menthol-induced TRPM8-mediated calcium influx with IC50 values of 8 3 nM in human and 5 8 nM in rat models demonstrating high selectivity over other TRP channels In vivo oral administration suppresses icilin-evoked tremors in rats in a dose-dependent manner (ED50 0 65 mg/kg) The compound remains in preclinical development and serves as a valuable tool for investigating TRPM8-related pathophysiology and potential therapeutic interventions
Medchemexpress LLC 7-Methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene | 84030-20-6 | MFCD00043004 | 99.2% | C8H15N3 | 500 MG
7-Methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene is a drug intermediate used for the synthesis of various active compounds. This product is intended for research use only.
- Purity: 99.2%
- Molecular weight: 153.23
- Chemical formula: C8H15N3
- CAS number: 84030-20-6
- Appearance: Liquid
- Color: Colorless to light yellow
- Storage conditions:
- Pure form: -20°C for 3 years, 4°C for 2 years
- In solvent: -80°C for 6 months, -20°C for 1 month
Apexbio Technology LLC Sildenafil mesylate 1308285-21-3 500mg
Sildenafil mesylate (CAS 1308285-21-3) is a potent and selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type 5 (PDE5) exhibiting an IC50 of 3 5 nM By inhibiting PDE5-mediated cGMP hydrolysis it enhances endogenous cGMP levels particularly within corpus cavernosum tissue In vitro sildenafil mesylate reversibly potentiates relaxation responses in precontracted corpus cavernosum strips following sodium nitroprusside exposure or electrical stimulation and increases intracellular cGMP in treated smooth muscle cells In vivo it augments erectile responses in anesthetized canine models This compound is widely used for studying PDE5-related signaling pathways and pharmacological modulation in erectile and vascular function research