SB-435495 ditartrate

Catalog No.: A77193
Lp-PLA2 Inhibitor
SB-435495 ditartrate is a potent and selective inhibitor of lipoprotein-associated phospholipase A2 (Lp-PLA2), demonstrating a remarkable IC50 of 0.06 nM. This compound functions as a reversible, non-covalent inhibitor and is suitable for oral administration. Its inhibition of Lp-PLA2 has significant implications for research in cardiovascular diseases and inflammatory processes, making it a valuable tool for investigating pathophysiological roles and therapeutic interventions in related conditions.
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5mg
10mg
50mg
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Free Delivery on orders over $500
Research use only. We do not sell to patients.

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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
DescriptionSB-435495 ditartrate is a potent and selective inhibitor of lipoprotein-associated phospholipase A2 (Lp-PLA2), demonstrating a remarkable IC50 of 0.06 nM. This compound functions as a reversible, non-covalent inhibitor and is suitable for oral administration. Its inhibition of Lp-PLA2 has significant implications for research in cardiovascular diseases and inflammatory processes, making it a valuable tool for investigating pathophysiological roles and therapeutic interventions in related conditions.
Product Information
Catalog NumA77193
FormulaC46H52F4N6O14S
Molecular Weight1021.00
CAS Number304694-43-7
SMILESO=C(N(CCN(CC)CC)CC1=CC=C(C2=CC=C(C(F)(F)F)C=C2)C=C1)CN(C(SCC3=CC=C(F)C=C3)=N4)C=C(CC5=CN(C)N=C5)C4=O.OC([C@H](O)[C@@H](O)C(O)=O)=O.OC([C@H](O)[C@@H](O)C(O)=O)=O
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