Benzenesulfonamides
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.
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 HY-19970 10mg Medchemexpress, KM11060 CAS:774549-97-2 Purity:>98%
Medchemexpress, HY-19970 10mg KM11060 CAS:774549-97-2 KM11060 is a corrector of the F508 deletion (F508del)-cystic fibrosis transmembrane conductance regulator (CFTR) trafficking defect. KM11060 can be used for the research of F508del-CFTR processing defect and development of cystic fibrosis therapeutics. 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-B0261 100mg Medchemexpress, Meloxicam CAS:71125-38-7 Purity:>98%
Medchemexpress, HY-B0261 100mg Meloxicam CAS:71125-38-7 Meloxicam is a non-steroidal antiinflammatory agent, inhibits COX activity, with IC50s of 0.49 µM and 36.6 µM for COX-2 and COX-1, respectively. 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-12045 5mg Medchemexpress, HMN-214 CAS:173529-46-9 Purity:>98%
Medchemexpress, HY-12045 5mg HMN-214 CAS:173529-46-9 HMN-214, an orally bioavailable prodrug of HMN-176, is an inhibitor of polo-like kinase-1 (plk1), with antitumor activity. 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-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-13255 50mg Medchemexpress, TAME CAS:901-47-3 Purity:>98%
Medchemexpress, HY-13255 50mg TAME CAS:901-47-3 TAME is an inhibitor of anaphase-promoting complex/cyclosome (APC/C or APC), which binds to APC/C and prevents its activation by Cdc20 and Cdh1, produces mitotic arrest. 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.
Matrix Scientific 4-CYANOBENZENESULFONAMIDE-1G
4-Cyanobenzenesulfonamide, 97%; 1g,C7H6N2O2S, MFCD00178767, mw 182.20, [3119-02-6]
Apexbio Technology LLC Glibenclamide 10238-21-8 10mM (in 1mL DMSO)
Glibenclamide (CAS 10238-21-8) is a sulfonylurea-class small molecule widely utilized in biomedical research for its ability to modulate insulin release It acts primarily by binding to ATP-sensitive potassium channels (K ATP channels) in pancreatic beta cells This interaction results in channel closure leading to cellular depolarization calcium ion influx and subsequent insulin secretion Due to its well-characterized mechanism glibenclamide is particularly relevant in diabetes-related research focusing on insulin regulation and beta-cell physiology
Selleck Chemical LLC CA3
CA3 (CIL56) has potent inhibitory effects on YAP1/Tead transcriptional activity and primarily targets YAP1 high and therapy-resistant esophageal adenocarcinoma cells endowed with CSC properties CA3(CIL56) induces ferroptosis and iron-dependent reactive oxygen species (ROS)
Selleck Chemical LLC Pilaralisib
Pilaralisib (XL147) is a selective and reversible class I PI3K inhibitor for PI3K / / with IC50 of 39 nM/36 nM/23 nM in cell-free assays less potent to PI3K Phase 1/2
Sigma Aldrich Fine Chemicals Biosciences (+/-)-Sulpiride | 15676-16-1 | MFCD00055061 | 25G
(+/-)-Sulpiride | Mol Wt: 341.43 | 15676-16-1 | MFCD00055061 | 25G
Sigma Aldrich Fine Chemicals Biosciences Tolbutamide United States Pharmacopeia (USP) Reference Standard | 64-77-7 | MFCD00027169 | 200MG
Tolbutamide United States Pharmacopeia (USP) Reference Standard | Mol Wt: 270.35 | 64-77-7 | MFCD00027169 | 200MG