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Product details
名称
EMD534085
分子类型
小分子
英文别名
NSC763564 | NSC-763564 | Q27273980 | EMD 534085 | EX-A2369 | BCP9000643 | BDBM50313428 | BCP0726000144 | EMD534085 | EMD-534085 | 1-(2-(dimethylamino)ethyl)-3-(((2R,4aS,5R,10bS)-5-phenyl-9-(trifluoromethyl)-3,4,4a,5,6,10b-hexahydro-2H-pyrano[3,2-c]quinoli
英文名称
EMD534085
货号
E646285-5mg
包装规格
5mg
浓度
≥99%
储存温度
-20°C储存
运输条件
超低温冰袋运输
产品介绍
EMD534085 is a potent and selective inhibitor of the mitotic kinesin-5 with an IC 50 of 8 nM. In Vitro EMD 534085 does not inhibit any other tested kinesins (BimC, CEN-PE, Chromokinesin, KHC, KIF3C, KIFC3, MKLP-1, and MCAK) at 1 μM or 10 μM concentration, showing selectively over kinesin-5. EMD 534085 binds to the allosteric pocket of kinesin-5. EMD534085 induces rapid cell death in HL60 during mitotic arrest. Caspase-8, −9, −3, −7 are activated; Parp1 is cleaved; Mcl1 and XIAP are degraded in EMD534085-treated HL60 cells. EMD534085 treated HL60 cells also shows significantly accumulated phospho-Histone H3 level starting at 6 hrs post thymidine release. MCE has not independently confirmed the accuracy of these methods. They are for reference only. In Vivo In a low dose PK of EMD 534085 in mice the clearance is 1.8 L/h/kg on average, the volume of distribution is 7.4 L/kg and the half life around 2.5 h. The bioavailability in high dose experiments (>10 mg/kg) is always above 50% in mice. Intraperitonal administration of EMD 534085 enables significant systemic exposure in mice leading to a significant tumor growth\nreduction without toxic side effects . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Assay Epithelial cell lines HeLa and MCF7 are synchronized in G2-phase using RO-3306. Cells are treated with 10 µM RO-3306 for 16 hrs, and then are ished and released to either warm growth medium or medium supplemented with 500 nM EMD534085. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid IC50& Target:Kinesin-5 8 nM (IC 50 )
生化机理
EMD534085 是有丝分裂驱动蛋白-5 的强效选择性抑制剂,其 IC 50 为 8 nM。
CAS号
858668-07-2
分子式
C25H31F3N4O2
分子量
476.53 g/mol
PubChem编号
23634407
Isomeric SMILES
CN(C)CCNC(=O)NC[C@H]1CC[C@H]2[C@@H](NC3=C([C@H]2O1)C=C(C=C3)C(F)(F)F)C4=CC=CC=C4
IIUPAC Name
1-[[(2R,4aS,5R,10bS)-5-phenyl-9-(trifluoromethyl)-3,4,4a,5,6,10b-hexahydro-2H-pyrano[3,2-c]quinolin-2-yl]methyl]-3-[2-(dimethylamino)ethyl]urea
INCHI
1S/C25H31F3N4O2/c1-32(2)13-12-29-24(33)30-15-18-9-10-19-22(16-6-4-3-5-7-16)31-21-11-8-17(25(26,27)28)14-20(21)23(19)34-18/h3-8,11,14,18-19,22-23,31H,9-10,12-13,15H2,1-2H3,(H2,29,30,33)/t18-,19+,22+,23+/m1/s1
InChi Key
MARIUIDCPUZLKZ-FUKQBSRTSA-N
Smiles
CN(C)CCNC(=O)NCC1CCC2C(NC3=C(C2O1)C=C(C=C3)C(F)(F)F)C4=CC=CC=C4
PubChem CID
23634407
关联CAS
1035647-06-3,858668-07-2
MeSH Entry Terms
EMD 534085;EMD-534085;EMD534085
溶解性
DMSO : ≥ 26 mg/mL (54.56 mM)
氢键供体数Hydrogen Bond Donor Count
3
氢键受体数Hydrogen Bond Acceptor Count
7
可旋转键计数Rotatable Bond Count
6
精确质量Exact Mass
476.24 Da
单同位素质量Monoisotopic Mass
476.24 Da
拓扑极表面积Topological Polar Surface Area
65.600 Ų
重原子数Heavy Atom Count
34
形式电荷Formal Charge
0
复杂度Complexity
671.000
同位素原子数Isotope Atom Count
0
共价键合单元计数Covalently-Bonded Unit Count
1
XLogP3
3.800
Safety
「No Dangerous Attributes」
Related
「No upstream and downstream information yet」
Technical Documents
「No technical documents」
Articles
「No related articles yet」
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EMD534085 5mg

EMD534085 5mg; supplied for laboratory research, analysis, inspection, and scientific procurement use; specifications: 5mg; ≥99%.

item number:E646285-5mg
Product model:5mg
level: 5mg; ≥99%
Lead Time:30days
sold 220 Items
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5mg

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