Benzenesulfonamides
Medchemexpress LLC N-Benzyl-N-Cbz-glycine | 76315-01-0 | MFCD02094473 | 265.31 | 5 G
2-(Benzyl(tert-butoxycarbonyl)amino)acetic acid, also known as N-Benzyl-N-Cbz-glycine, is a derivative of Glycine. It is intended for research use only and is not sold to patients. Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances.
- Amino acid derivative
- Purity: 98.0%
- Physical appearance: solid, ranging from white to off-white
- Molecular weight: 265.31
- Formula: C14H19NO4
- Cas no.: 76315-01-0
- Storage conditions:
- Powder: -20°c for 3 years, 4°c for 2 years
- In solvent: -80°c for 6 months, -20°c for 1 month
Enzo Life Sciences NBQX . disodium salt (25mg). CAS: 118876-58-7 (non-salt)
Water soluble, potent and selective AMPA/kainate receptor antagonist. For literature references, see NBQX (ALX-550-044). Alternative name: 2,3-Dihydroxy-6-nitro-7-sulphamoylbenzo(f)-quinoxaline . 2Na, 6-Nitro-7-sulphamoylbenzo(f)-quinoxaline-2,3-dione . 2Na. Purity: ≥98% (HPLC). Solubility: Soluble in water (5mg/ml) or DMSO. Long Term Storage: -20°C.
Medchemexpress LLC XMU-MP-3 | 2031152-08-4 | 95.8% | 536.55 | 50 MG
XMU-MP-3 is a potent non-covalent BTK inhibitor with IC50s of 10.7 nM for BTK WT and 17.0 nM for BTK C481S mutation in the presence of 10 μM ATP. It also induces apoptosis and inhibits the auto- and trans-phosphorylation of BTK at Y223 and Y551.
- Potent non-covalent BTK inhibitor
- Induces apoptosis
- Inhibits BTK-transformed Ba/F3 cell proliferation
- Maintains inhibitory potency against BTK(C481S)-Ba/F3 cells
- Substantially suppresses tumor growth in mouse xenograft models
Medchemexpress LLC HY-10799 5mg Medchemexpress, EG00229 CAS:1210945-69-9 Purity:>98%
Medchemexpress, HY-10799 5mg EG00229 CAS:1210945-69-9 EG00229 is a neuropilin 1 (NRP1) receptor antagonist. EG00229 selectively inhibits VEGF-A binding to NRP1 b1 domain with an IC50 of 3 μM, but has no effect on VEGFA binding to VEGFR-1 and VEGFR-2. 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.
Sigma Aldrich Fine Chemicals Biosciences Clopamide for system suitability European Pharmacopoeia (EP) Reference Standard | 636-54-4 | MFCD00941495 |
Clopamide for system suitability European Pharmacopoeia (EP) Reference Standard | Mol Wt: 345.84 | 636-54-4 | MFCD00941495 |
Cayman Chemical Sildenafil Inhibitors
A PDE5 inhibitor (IC50s = 3.6 and 3 nM for PDE5 activity in isolated rabbit platelets and human corpus cavernosum, respectively); selective for PDE5 over PDE1 and PDE3 (IC50s = 0.26 and 65 μM, respectively); reverses glucose-induced decreases in ANG1 expression and reduction of capillary-like tube formation by mouse dermal endothelial cells in vitro; increases the number of functional blood vessels and regional blood flow in the sciatic nerve in a db/db mouse model of diabetic peripheral neuropathy; increases ICP/MAP ratio in castrated rats at 20 mg/kg per day; reduces cardiac arrest and resuscitation-induced increases in angiotensin II ACE, ACE2, and various angiotensin receptors and increases survival in a porcine model of ischemia/reperfusion injury
eMolecules N,N-Diethyl-p-toluenesulfonamide | Combi-Blocks | 649-15-0 | MFCD00059369 | 227.320 | C11H17NO2S | 98.000 | CCN(CC)S(=O)(=O)c1ccc(C)cc1 | 25g | 267191703
N,N-Diethyl-p-toluenesulfonamide | Combi-Blocks | 649-15-0 | MFCD00059369 | 227.320 | C11H17NO2S | 98.000 | CCN(CC)S(=O)(=O)c1ccc(C)cc1 | 25g | 267191703
Medchemexpress LLC HY-12149 10mg Medchemexpress, A-867744 CAS:1000279-69-5 Purity:>98%
Medchemexpress, HY-12149 10mg A-867744 CAS:1000279-69-5 A-867744 is a highly potent and selective type II positive allosteric modulator (PAM) of the alpha7 nicotinic acetylcholine receptors (nAChR) with an EC50 of 1.0 μM. 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 HY-19320 5mg Medchemexpress, Orexin 2 Receptor Agonist CAS:1796565-52-0 Purity:>98%
Medchemexpress, HY-19320 5mg Orexin 2 Receptor Agonist CAS:1796565-52-0 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.
eMolecules 4-Bromo-1-phenylsulfonyl-7-azaindole-2-carboxyaldehyde | Combi-Blocks, Inc. | 942920-59-4 | MFCD15529514 | 365.200 | C14H9BrN2O3S | 95.000 | Brc1ccnc2n(c(C=O)cc12)S(=O)(=O)c1ccccc1 | 5g | 603147831
4-Bromo-1-phenylsulfonyl-7-azaindole-2-carboxyaldehyde | Combi-Blocks, Inc. | 942920-59-4 | MFCD15529514 | 365.200 | C14H9BrN2O3S | 95.000 | Brc1ccnc2n(c(C=O)cc12)S(=O)(=O)c1ccccc1 | 5g | 603147831
eMolecules 1681056-61-0 | Medchem Express | OSMI-1 | 5mg | 599150495 | HY-119738 | MFCD30187585 | 563.64 | C28H25N3O6S2
Ambeed | (4S5R)-45-Diphenyl-2-(quinolin-2-yl)-45-dihydrooxazole | 100mg | 549151969 | A1258477 | 2411386-00-8 | 350.421 | C24H18N2O
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eMolecules N,N-Diethyl 3-boronobenzenesulfonamide | 871329-58-7 | 5G | Purity: 98%
Combi-Blocks | N,N-Diethyl 3-boronobenzenesulfonamide | 5G | 871329-58-7 | MFCD07363746
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Medchemexpress LLC HY-108339 5mg Medchemexpress, PF-06471553 CAS:1808094-07-6 Purity:>98%
Medchemexpress, HY-108339 5mg PF-06471553 CAS:1808094-07-6 PF-06471553 is a potent, selective and orally available monoacylglycerol acyltransferase 3 (MGAT3) inhibitor, with an IC50 of 92 nM. 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.
Apexbio Technology LLC Benzenesulfonamide 98-10-2 100mg
Benzenesulfonamide (CAS 98-10-2) is an amide derivative of benzenesulfonic acid widely utilized as a synthetic intermediate for pharmaceuticals and other chemicals Mechanistically benzenesulfonamide derivatives have been investigated for their inhibitory activity against various human carbonic anhydrases (CAs) with certain 4-substituted diazo derivatives exhibiting strong binding affinity particularly for CA I and II isoforms as demonstrated by isothermal titration calorimetry and fluorescence-based thermal shift assays In in vivo models indole-based benzenesulfonamide derivatives show oral activity in rat and sheep models of airway inflammation attenuating physiological responses to antigenic or cholinergic challenge Benzenesulfonamide remains in preclinical evaluation
eMolecules 173529-10-7 | Medchem Express | HMN-176 | 5mg | 446263262 | HY-13647 | 382.43 | C20H18N2O4S
Ambeed | 5-Iodo-123-trimethoxybenzene | 1g | 570567928 | A155143 | 25245-29-8 | MFCD01318153 | 294.088 | C9H11IO3
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