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NVS-PAK1-1 ceclofenac specific [3H]5-CT binding sites from

SKU: 47355946888

4.9
USD119.00 USD142.00

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Description

specific [3H]5-CT binding sites from rat and human 5-HT7 receptor express in HEK293 cells (pKi=8

Smiles: CCOC1=CC(=CC=C1NC1=NC=C2C(=N1)N(C1CCCC1)C1=CC=CC=C1C(=O)N2C)C(=O)N1CCC(CC1)N1CCN(C)CC1

Molecular Weight: 465

TC-A 2317 hydrochloride exhibits excellent selectivity to Aurora B kinase (Ki=101 nM) and other 60 kinases

such as tumor necrosis factor-alpha (TNF-alpha) and interleukin-1 beta (IL-1 beta)

NVS-PAK1-1 ceclofenac specific [3H]5-CT binding sites fromNVS PAK1 1 is a potent and selective allosteric PAK1 inhibitor with an IC50 of 5 nM. Product information CAS Number: 1783816 74 9 Molecular Weight: 479. 93 Formula: C23H25ClF3N5O Chemical Name: (3S) 3 {[13 chloro 2 (2,2 difluoroethyl) 6 fluoro 2,9 diazatricyclo[9. 4. 0. 0,]pentadeca 1(11),3(8),4,6,9,12,14 heptaen 10 yl]amino} N (propan 2 yl)pyrrolidine 1 carboxamide Smiles: CC(C)NC(=O)N1CC[C@@H](C1)NC1=NC2C=C(F)C=CC=2N(CC(F)F)C2C=CC(Cl)=CC=21

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