Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN480792 JMS-17-2 hydrochloride 2341841-07-2
JMS-17-2 hydrochloride is a potent and selectiveCX3CR1antagonist with an IC50 of 0.32nM. JMS-17-2 hydrochloride impairs metastatic seeding and colonization of breast cancer cells.
YN484045 Lanreotide acetate 2378114-72-6
Lanreotide (Laromustine, Angiopeptin, BIM 23014, Dermopeptin, Ipstyl, ITM-014, Somatulina, Somatuline, Lanreotidum) acetate, an analog of the native somatostatin peptide, is a physiological inhibitor of growth hormone (GH...
YN320477 CCR1 antagonist 6 2436773-01-0
CCR1 antagonist 6 (compound 16q) is achemokine receptor 1 (CCR1)antagonist, with an IC50 of 3nM.
YN320458 CCR6 inhibitor 1 2437547-04-9
CCR6 inhibitor 1 is a potent and selectiveCCR6inhibitor, with IC50s of 0.45 and 6nM for monkey and human CCR6, much more selective at CCR6 over human CCR1 (IC50, > 30000nM), and CCR7 (IC50, 9400nM). CCR...
YN480609 T3-ATA (S-isomer) 2438721-48-1
T3-ATA S-isomer is the S-isomer of T3-ATA, which is the active form of the thyroid hormone.
YN320478 CCR1 antagonist 7 2446154-74-9
CCR1 antagonist 7 (compound 16r) is achemokine receptor 1 (CCR1)antagonist, with an IC50 of 4nM.
YN480610 T4-ATA (S-isomer) 2448470-97-9
T4-ATA S-isomer is the S-isomer of T4-ATA, which is the active form of the thyroid hormone.
BAY-899 is an orally active and selectiveluteinizing hormone receptor (LH-R)antagonist with IC50s of 185nM and 46nM for hLH (human LH) and rLH (rat LH), respectively. BAY-899 can reduce sex hormone levels.
BAY-298 is an orally active and selectiveluteinizing hormone receptor (LH-R)antagonist with IC50s of 96nM, 23nM and 78nM for hLH (human LH) and rLH (rat LH) and cLH (cynomolgus monkey LH), respectively. BAY...
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