计算溶液所需的质量、体积或浓度。
活性类型 | 活性值-log(M) | 作用机制 | 期刊 | 参考文献(PubMed IDs) |
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货号 (SKU) | 包装规格 | 是否现货 | 价格 | 数量 |
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C127776-5mg |
5mg |
现货 ![]() |
| |
C127776-10mg |
10mg |
现货 ![]() |
| |
C127776-25mg |
25mg |
现货 ![]() |
| |
C127776-50mg |
50mg |
现货 ![]() |
| |
C127776-100mg |
100mg |
期货 ![]() |
|
别名 | [1-[2-[5-(3-甲基氧杂环丁烷-3-基甲氧基)苯并咪唑-1-基]喹啉-8-基]哌啶-4-基]胺 |
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英文别名 | ETHYL .ALPHA.-AMINOPHENYLACETATE | AKOS026750597 | Crenolanib [USAN] | 6T2 | AS-57698 | CP-868596 (Crenolanib) | CRENOLANIB [INN] | DYNHJHQFHQTFTP-UHFFFAOYSA-N | 2-morpholino-1-ethanamine | CP868596 | CP-868596 | Crenolanib | D10102 | MLS006010956 | NCGC0 |
规格或纯度 | Moligand™, ≥98% |
英文名称 | Crenolanib (CP-868596) |
生化机理 | PDGFR(α Kd = 2.1 nM;β Kd = 3.2 nM)和 FLT3(Kd = 0.74 nM)的强效抑制剂。 I 型抑制剂,只与活性激酶构象结合。对伊马替尼耐药性相关的 PDGFR-α 突变(D842I、D842V、D842Y、DI842-843M 和缺失 I843)具有活性。对 FLT3/ITD 和 FLY3/D835 突变体有活性。相对于 c-Kit、VEGFR-2、TIE-2、FGFR-2、EGFR、erbB2 和 Src,对 PDGFR 的选择性超过 100 倍。 |
储存温度 | -20°C储存 |
运输条件 | 超低温冰袋运输 |
作用类型 | 抑制剂 |
作用机制 | 酪氨酸蛋白激酶受体 FLT3 抑制剂 |
备注 | 如果有可能,您尽量在使用的当天配置溶液,并在当天使用完它。但是,如果您需要预先配制储备溶液,我们建议您将溶液等份保存在-20°C的密封小瓶中。通常,它们最多可以使用一个月。在使用前和打开样品瓶之前,我们建议您让您的产品在室温下平衡至少1小时。有关更多信息,请参阅SDS。有关溶解度,用法和处理的更多建议?请访问我们的常见问题(FAQ)页面以获取更多详细信息。 |
产品介绍 |
Crenolanib (CP-868596, ARO 002)是一种有效的,选择性PDGFRα/β抑制剂,在CHO细胞中Kd为2.1 nM/3.2 nM,也能有效抑制FLT3,对D842V突变型敏感对V561D突变型不敏感,作用于PDGFR比作用于c-Kit,VEGFR-2,TIE-2,FGFR-2,EGFR,erbB2,和Src的选择性高100倍以上。Crenolanib可辅助诱导线粒体自噬。 Crenolanib (CP-868596, ARO 002) is a potent and selective PDGFRα/β inhibitor with a Kd of 2.1 nM/3.2 nM in CHO cells. It can also effectively inhibit FLT3. It is sensitive to the D842V mutant and sensitive to the V561D mutant. It is not sensitive, and the selectivity for PDGFR is more than 100 times higher than that for c-Kit, VEGFR-2, TIE-2, FGFR-2, EGFR, erbB2, and Src. Crenolanib can help induce mitochondrial autophagy. |
ALogP | 3.7 |
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作用机制 | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | 参考文献 |
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PubChem SID | 504765417 |
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分子类型 | 小分子 |
IUPAC Name | 1-[2-[5-[(3-methyloxetan-3-yl)methoxy]benzimidazol-1-yl]quinolin-8-yl]piperidin-4-amine |
INCHI | InChI=1S/C26H29N5O2/c1-26(14-32-15-26)16-33-20-6-7-22-21(13-20)28-17-31(22)24-8-5-18-3-2-4-23(25(18)29-24)30-11-9-19(27)10-12-30/h2-8,13,17,19H,9-12,14-16,27H2,1H3 |
InChi Key | DYNHJHQFHQTFTP-UHFFFAOYSA-N |
Canonical SMILES | CC1(COC1)COC2=CC3=C(C=C2)N(C=N3)C4=NC5=C(C=CC=C5N6CCC(CC6)N)C=C4 |
Isomeric SMILES | CC1(COC1)COC2=CC3=C(C=C2)N(C=N3)C4=NC5=C(C=CC=C5N6CCC(CC6)N)C=C4 |
PubChem CID | 10366136 |
分子量 | 443.54 |
溶解性 | ≥22.2mg/mL in DMSO, ≥2.5 mg/mL in EtOH with ultrasonic,insoluble in H2O |
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分子量 | 443.500 g/mol |
XLogP3 | 3.700 |
氢键供体数Hydrogen Bond Donor Count | 1 |
氢键受体数Hydrogen Bond Acceptor Count | 6 |
可旋转键计数Rotatable Bond Count | 5 |
精确质量Exact Mass | 443.232 Da |
单同位素质量Monoisotopic Mass | 443.232 Da |
拓扑极表面积Topological Polar Surface Area | 78.400 Ų |
重原子数Heavy Atom Count | 33 |
形式电荷Formal Charge | 0 |
复杂度Complexity | 667.000 |
同位素原子数Isotope Atom Count | 0 |
定义的原子立体中心计数Defined Atom Stereocenter Count | 0 |
未定义的原子立体中心计数Undefined Atom Stereocenter Count | 0 |
定义的键立体中心计数Defined Bond Stereocenter Count | 0 |
未定义的键立体中心计数Undefined Bond Stereocenter Count | 0 |
所有立体化学键的总数The total count of all stereochemical bonds | 0 |
共价键合单元计数Covalently-Bonded Unit Count | 1 |
1. Heinrich MC, Griffith D, McKinley A, Patterson J, Presnell A, Ramachandran A, Debiec-Rychter M. (2012) Crenolanib inhibits the drug-resistant PDGFRA D842V mutation associated with imatinib-resistant gastrointestinal stromal tumors.. Clin Cancer Res, 18 (16): (4375-84). [PMID:22745105] [10.1021/op500134e] |
2. Zimmerman EI, Turner DC, Buaboonnam J, Hu S, Orwick S, Roberts MS, Janke LJ, Ramachandran A, Stewart CF, Inaba H et al.. (2013) Crenolanib is active against models of drug-resistant FLT3-ITD-positive acute myeloid leukemia.. Blood, 122 (22): (3607-15). [PMID:24046014] [10.1021/op500134e] |
3. Smith CC, Lasater EA, Lin KC, Wang Q, McCreery MQ, Stewart WK, Damon LE, Perl AE, Jeschke GR, Sugita M et al.. (2014) Crenolanib is a selective type I pan-FLT3 inhibitor.. Proc Natl Acad Sci USA, 111 (14): (5319-24). [PMID:24623852] [10.1021/op500134e] |