Benzenesulfonamides
Sigma Aldrich Fine Chemicals Biosciences Oxamflatin >=98% (HPLC), solid | 151720-43-3 | MFCD00949087 | 1MG
Oxamflatin >=98% (HPLC), solid | Purity: >=98% (HPLC) | Mol Wt: 342.37 | 151720-43-3 | MFCD00949087 | 1MG
![Aobchem 6-Chloro-8-fluoro-[1 2 4]triazolo[4 3-a]pyridine | ≥97% | CAS 1020253-21-7 | C6H3ClFN3 | 5g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000952295.png-250.jpg)
Aobchem 6-Chloro-8-fluoro-[1 2 4]triazolo[4 3-a]pyridine | ≥97% | CAS 1020253-21-7 | C6H3ClFN3 | 5g
6-Chloro-8-fluoro-[1 2 4]triazolo[4 3-a]pyridine | ≥97% | CAS 1020253-21-7 | C6H3ClFN3 | 5g
eMolecules 873-41-6 | 3,5,6-Trichloro-1,2,4-triazine | Ambeed | MFCD09033774 | 184.400 | C3Cl3N3 | 98.000 | Clc1nnc(Cl)c(Cl)n1 | 5g | 586033905
3,5,6-Trichloro-1,2,4-triazine | Ambeed | 873-41-6 | MFCD09033774 | 184.400 | C3Cl3N3 | 98.000 | Clc1nnc(Cl)c(Cl)n1 | 5g | 586033905
Medchemexpress LLC Azido PEG-linked naphthyl propanoic acid, TFA salt | 2320477-41-4 | 899.91 | C43H52F3N7O11 | 10mg
(S)-3-(4-(4-((14-Azido-3 6 9 12-tetraoxatetradecyl)oxy)naphthalen-1-yl)phenyl)-3-(2-(4-((4-methylpyridin-2-yl)amino)butanamido)acetamido)propanoic acid compound trifluoroacetate is a drug intermediate for synthesis of various active compounds
eMolecules 1314594-23-4 | Medchem Express | PKR-IN-C51 | 5mg | 719835740 | HY-118131 | 367.456 | C23H21N5
Ambeed | 5-Chloro-2-cyano-3-methylpyridine | 1g | 525233235 | A681695 | 156072-84-3 | MFCD17214209 | 152.580 | C7H5ClN2
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Aobchem 6-Chloro-1-(phenylsulfonyl)-1H-indole | ≥95% | CAS 231295-53-7 | C14H10ClNO2S | 500mg
6-Chloro-1-(phenylsulfonyl)-1H-indole | ≥95% | CAS 231295-53-7 | C14H10ClNO2S | 500mg
Medchemexpress LLC Furosemide-d5 | 1189482-35-6 | 99.9% | 1 MG
Furosemide-d5 is the deuterium labeled Furosemide. Furosemide is a potent and orally active inhibitor of Na+/K+/2Cl- (NKCC) cotransporter, specifically NKCC1 and NKCC2. It also acts as a GABAA receptors antagonist, showing 100-fold selectivity for α6-containing receptors over α1-containing receptors. Furosemide is a loop diuretic used in the study of congestive heart failure, hypertension, and edema. Deuterium substitution in drug molecules is explored for its potential impact on pharmacokinetic and metabolic profiles.
- Can be used as a tracer
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
- Potent and orally active inhibitor of Na+/K+/2Cl- (NKCC) cotransporter
- Acts as a GABAA receptors antagonist
- Used in the study of congestive heart failure, hypertension, and edema
Medchemexpress LLC HY-50907 200mg , ABT-737 CAS:852808-04-9 Purity:98%
Medchemexpress, HY-50907 200mg ABT-737 CAS:852808-04-9 Formula:C42H45ClN6O5S2 EC50: 78.7 nM (Bcl-xL), 30.3 nM (Bcl-2), 197.8 nM (Bcl-w) Purity:98% ABT-737 is a BH3 mimetic inhibitor of Bcl-xL , Bcl-2 and Bcl-w with EC 50 of 78.7 nM, 30.3 nM and 197.8 nM in cell-free assays, respectively, and shows no inhibition against Mcl-1, Bcl-B or Bfl-1. 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 Seclidemstat mesylate | 2044953-70-8 | 99.8% | 547.04 g/mol | C20H23ClN4O4S·CH4O3S | 100 MG
Seclidemstat mesylate is the mesylate salt of seclidemstat (SP-2577), a reversible, noncompetitive inhibitor of lysine-specific demethylase 1 (KDM1A/LSD1) used in preclinical research. It exhibits potent biochemical activity and is investigated for antitumor immunity and cancer research applications, including studies of Ewing sarcoma and SWI/SNF-mutated ovarian cancer.
- Reversible, noncompetitive KDM1A (LSD1) inhibitor.
- Demonstrates potent biochemical activity (Ki ≈ 31 nM; IC50 ≈ 13 nM).
- High purity suitable for research (99.8%).
- Provided as a mesylate salt to improve handling and stability.
- Supplied as a powder; store at 4°C away from moisture and light.
- Used in oncology and virology research applications.
Medchemexpress LLC HY-111777 5mg Medchemexpress, FASN-IN-1 CAS:1808260-84-5 Purity:>98%
Medchemexpress, HY-111777 5mg FASN-IN-1 CAS:1808260-84-5 FASN-IN-1 is a fatty acid synthase (FASN) inhibitor extracted from patent WO2015134790A1, compound 56 [1] . 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.
Aobchem 3-Methylbenzenesulfonamide | 95% | CAS 1899-94-1 | C7H9NO2S | 500mg
3-Methylbenzenesulfonamide | 95% | CAS 1899-94-1 | C7H9NO2S | 500mg
Medchemexpress LLC Pci-27483 | 871266-63-6 | 99.10% | 596.57 | 100 MG
Pci-27483 | 871266-63-6 | 99.10% | 596.57 | 100 MG
Medchemexpress LLC Sultiame | 61-56-3 | MFCD00865304 | 290.36 | C10H14N2O4S2 | 50 MG
Sultiame is a sulfonamide carbonic anhydrase inhibitor used as an antiepileptic agent and supplied as an analytical standard for laboratory research. It is intended for use in method development, qualitative and quantitative analyses, and other research applications.
- Carbonic anhydrase inhibitor with antiepileptic activity.
- Provided as an analytical standard for research and method development.
- Suitable for HPLC, GC, and MS qualitative and quantitative analyses.
- Supplied as a solid compatible with common laboratory preparation methods.
- Molecular formula C10H14N2O4S2; molecular weight 290.36.
- Available in small scales appropriate for analytical use (for example, 5-500 mg).
Medchemexpress LLC HY-112292 5mg Medchemexpress, GW806742X CAS:579515-63-2 Purity:>98%
Medchemexpress, HY-112292 5mg GW806742X CAS:579515-63-2 GW806742X is a Mixed Lineage Kinase Domain-Like protein (MLKL) inhibitor which binds the MLKL pseudokinase domain with a K d value of 9.3 μM and has anti-necroptosis activity. GW806742X has activity against VEGFR2 [1] [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.