YM-254890
0.01 EURAsk for quotation
On request
quantity
Produktdetaljer
Katalognummer: 931 - T17273-5mg
Produktkategori: Företag och industri > Vetenskap och laboratorium
Gentaur
Storlek: 5mg
Parameters
| Additional information | SMILES: [C@@H](OC([C@H]([C@@H](C(C)C)O)NC(C)=O)=O)(C(C)C)[C@]1(C(=O)N(C)[C@@]([C@H](OC)C)(C(=O)O[C@H](C)[C@H](NC(C)=O)C(=O)O[C@H](CC2=CC=CC=C2)C(=O)N(C)C(=C)C(=O)N[C@@H](C)C(=O)N(C)[C@@H](C)C(=O)N1)[H])[H]; Formula: C46H69N7O15 |
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HY-111557
YM-254890
YM-254890 is a selective Gαq/11 protein inhibitor isolated from Chromobacterium sp. YM-254890 shows no inhibition of other G protein subtypes. YM-254890 inhibits platelet aggregation induced by ADP by blocking the P2Y1 signal transduction pathway, with an IC50 value below 0.6 μM[1][2].
1078 €
HY-100313A
YM-53601
YM-53601, a squalene synthase inhibitor, reduces plasma cholesterol and triglyceride levels in vivo[1]. YM-53601 inhibits squalene synthase derived from human hepatoma cells with an IC50 of 79 nM. Lipid-lowering agent[2]. YM-53601 is also an inhibitor of farnesyl-diphosphate farnesyltransferase 1 (FDFT1) enzyme activity and abrogates HCV propagation[3].
1818.27 €
HY-100831
YM-58483
YM-58483 (BTP2) is the first selective and potent inhibitor of CRAC channels and subsequent Ca2+ signals[1]. YM-584832 is a blocker of store-operated Ca2+ entry (SOCE)[2].
772.81 €
HY-101679
YM-58790
YM-58790 is a potent antagonist of mAChR. YM-58790 binds M1, M2, M3 with Ki values of 28 nM, 260 nM, and 15 nM. YM-58790 exhibits potent inhibitory activity on bladder pressuer in reflexly-evoked rhythmic contraction in rats[1].
2688.42 €
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