Benzenesulfonamides
Medchemexpress LLC HY-112929B 5mg Medchemexpress, (1S,2S,3R)-DT-061 CAS:1809427-20-0 Purity:>98%
Medchemexpress, HY-112929B 5mg (1S,2S,3R)-DT-061 CAS:1809427-20-0 (1S,2S,3R)-DT-061 is an enantiomer of DT-061. DT-061 is an orally bioavailable activator of protein phosphatase 2A (PP2A) and could be applied in the therapy of KRAS-mutant and MYC-driven tumorigenesis [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.
Medchemexpress LLC HY-17443 10mg Medchemexpress, Sivelestat CAS:127373-66-4 Purity:>98%
Medchemexpress, HY-17443 10mg Sivelestat CAS:127373-66-4 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.
Selleck Chemical LLC Furosemide sodium S5194-25mg
Furosemide (Frusemide) sodium is a potent and orally active inhibitor of Na-K-Cl cotransporter (NKCC) Furosemide sodium is a subtype-selective antagonist of gamma-aminobutyric acid type A (GABAA) receptor
Medchemexpress LLC Pkr-in-c51 | 1314594-23-4 | 99.8% | 367.45 g/mol | C23H21N5 | 5 MG
PKR-IN-C51 is an ATP-competitive inhibitor of double-stranded RNA-activated protein kinase (PKR) for research use in cellular and biochemical studies. It has a reported IC50 of 9 μM against PKR, a molecular weight of 367.45 g/mol, and is supplied at high purity for laboratory applications.
- ATP-competitive inhibitor of PKR for cellular and biochemical studies.
- Reported IC50 of 9 μM against PKR.
- High supplied purity (≈99.8%).
- Available in small research quantities, including 5 mg.
- Storage: in solvent, -80°C for 6 months or -20°C for 1 month; protect from light.
Selleck Chemical LLC Furosemide S1603-50mg
Furosemide is a potent NKCC2 (Na-K-2Cl symporter) inhibitor used in the treatment of congestive heart failure and edema
Medchemexpress LLC HY-10409 10mg Medchemexpress, Fedratinib CAS:936091-26-8 Purity:>98%
Medchemexpress, HY-10409 10mg Fedratinib CAS:936091-26-8 Fedratinib (TG-101348) is a potent, selective, ATP-competitive and orally active JAK2 inhibitor with IC50s of 3 nM for both JAK2 and JAK2V617F kinase. Fedratinib shows 35- and 334-fold selectivity over JAK1 and JAK3, respectively. Fedratinib induces cancer cell apoptosis and has the potential for myeloproliferative disorders research[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.
eMolecules AstaTech / ETHYL 2-METHYL-4-NITROPHENYLACETATE / 1g / 458234177 / 97488 / 95.000 / 50712-66-8 / MFCD18396753 / 223.228 / C11H13NO4
AstaTech / ETHYL 2-METHYL-4-NITROPHENYLACETATE / 1g / 458234177 / 97488 / 95.000 / 50712-66-8 / MFCD18396753 / 223.228 / C11H13NO4
Medchemexpress LLC Sildenafil N-oxide | 1094598-75-0 | MFCD22683784 | 10mg
Sildenafil Impurity 1 is an impurity of Sildenafil (HY-15025)
eMolecules 1276110-06-5 | Medchem Express | HS-173 | 5mg | 446266809 | HY-15868 | MFCD28023584 | 422.46 | C21H18N4O4S
Medchem Express | MKT-077 | 5mg | 437899410 | HY-15096 | 147366-41-4 | MFCD27665468 | 432.000 | C21H22ClN3OS2
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eMolecules 326886-05-9 | Medchem Express | Shz-1 | 5mg | 785215131 | HY-108440 | MFCD00853265 | 355.21 | C13H11BrN2O3S
Ambeed | (R)-33-Bis[4-(trifluoromethyl)phenyl]-[11-binaphthalene]-22-diol | 100mg | 624120823 | A276989 | 791616-58-5 | 574.522 | C34H20F6O2
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eMolecules 2271358-65-5 | Medchem Express | UAMC-3203 hydrochloride | 5mg | 455326080 | HY-112909A | 508.12 | C25H38ClN5O2S
Ambeed | 14-Bis(2-methyl-1H-imidazol-1-yl)butane | 100mg | 602852056 | A443716 | 52550-63-7 | 218.304 | C12H18N4
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Medchemexpress LLC FASN-IN-3 | 2097262-60-5 | 384.47 | 10 MG
FASN-IN-3 is a fatty acid synthase (FASN) inhibitor. It was extracted from patent US20170119786A1, compound 242A. In vitro studies showed that FASN-IN-3 treatment of PBMC reduces IL-1 beta secretion from LPS or LTA stimulation. For monocytes, it reduces IL-1 beta from LTA stimulation, with a slight reduction after LPS stimulation.
- Inhibits fatty acid synthase (FASN)
- Reduces IL-1 beta secretion from PBMC stimulated with LPS or LTA
- Reduces IL-1 beta from monocyte LTA stimulation
- Solid appearance, off-white to yellow color