About 10 results found for searched term "58-71-9" (0.054 seconds)
Cat.No. | Name | Target |
---|---|---|
M1801 | KU-55933 | ATM/ATR |
KU55933 | ||
KU-55933 is a cell-permeable ATP-competitive inhibitor of ATM (IC50 = 13 nM; Ki = 2.2 nM) with selectivity over other PIKK family kinases (IC50 = 2.5, 9.3, 16.6 μM for DNAPK, mTOR, PI 3-K, respectively; IC50 > 100 μM for PI 4-K and ATR). | ||
M5505 | Cephalothin sodium | Antibiotic |
Cefalotin sodium | ||
Cephalothin sodium is a first generation cephem antibiotic with a wide range antibacterial activity, is active against gram-positive and gram-negative bacteria. | ||
M7266 | SB 611812 | Others |
SB 611812 is a urotensin-II (UT) antagonist; attenuates cardiac dysfunction. | ||
M8677 | SB-258719 | Others |
SB-258719 is a selective and potent 5-HT7 antagonist. | ||
M10744 | V-9302 | Others |
V9302 | ||
V-9302 is a competitive antagonist of transmembrane glutamine flux. V-9302 selectively and potently targets the amino acid transporter ASCT2 (SLC1A5) not ASCT1. V-9302 inhibits ASCT2-mediated glutamine uptake (IC50=9.6 µM) in HEK-293 cells. | ||
M13893 | Labetalol | Adrenergic Receptor |
AH5158; Sch-15719W free base | ||
Labetalol (AH5158) is an orally active selective α1- and non-selective β-adrenergic receptors competitive antagonist. | ||
M20941 | Raloxifene | Estrogen Receptor |
Keoxifene, Pharoxifene, LY-139481, LY-156758, CCRIS-7129 | ||
Raloxifene is a second generation selective estrogen receptor modulator (SERM) used to prevent osteoporosis in postmenopausal women. | ||
M28627 | Atuzabrutinib | BTK |
SAR 444727; PRN473 | ||
Atuzabrutinib (SAR 444727) is a potent, selective reversible inhibitor of Btk (Bruton's tyrosine kinase) inhibitor. Atuzabrutinib inhibits neutrophil recruitment via inhibition of macrophage antigen-1 signalling. | ||
M50738 | Tripeptide-10 | Others |
Tripeptide-10 is a bioactive peptide withanti-wrinkleeffect and has been reported used as a cosmetic ingredient. | ||
M56081 | SB 258719 hydrochloride | 5-HT Receptor |
SB 258719 hydrochloride is a selective 5-HT7 receptor antagonist displayed high affnity (pKi=7.5) for the receptor. |
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