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CH5424802 (Synonyms: Alectinib, RO5424802)

Catalog No.GC16025

CH5424802 (CH5424802) est un inhibiteur ALK puissant, sélectif et disponible par voie orale avec une IC50 de 1,9 nM et une valeur Kd de 2,4 nM (de manière compétitive avec l'ATP), et inhibe également ALK F1174L et ALK R1275Q avec des IC50 de 1 nM et 3,5 nM, respectivement. CH5424802 démontre une pénétration efficace du système nerveux central (SNC).

Products are for research use only. Not for human use. We do not sell to patients.

CH5424802 Chemical Structure

Cas No.: 1256580-46-7

Taille Prix Stock Qté
5mg
62,00 $US
En stock
50mg
172,00 $US
En stock

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Sample solution is provided at 25 µL, 10mM.

Description of CH5424802

CH5424802 is a potent and selective ALK inhibitor.

Anaplastic lymphoma kinase (ALK) is a tyrosine kinase that is constitutively activated in certain cancers. .

In vitro: In cell free assays the IC50 of CH5424802 for enzyme activity of ALK was 1.9 nM; the dissociation constant (KD) value for ALK in an ATP-competitive manner was 2.4 nM. The inhibitory activity for two hot spot-activating mutations (F1174L and R1275Q) in neuroblastoma was comparable to that for wildtype ALK [1].

In vivo: In the NCI-H2228 model, oral administration of CH5424802 resulted in dose-dependent tumor growth inhibition (ED50 = 0.46 mg/kg) and tumor regression. Moreover, treatment of 20 mg/kg CH5424802 showed rapid tumor regression and tumor regrowth did not occur throughout the 4-week drug-free period [2].

Clinical trial: No clinical data are available currently.

Reference:
[1] Sakamoto H, Tsukaguchi T, Hiroshima S, Kodama T, Kobayashi T, Fukami TA, Oikawa N, Tsukuda T, Ishii N, Aoki Y.  CH5424802, a selective ALK inhibitor capable of blocking the resistant gatekeeper mutant. Cancer Cell. 2011 May 17;19(5):679-90.

Chemical Properties of CH5424802

Cas No. 1256580-46-7 SDF
Synonymes Alectinib, RO5424802
Chemical Name 9-ethyl-6,6-dimethyl-8-(4-morpholin-4-ylpiperidin-1-yl)-11-oxo-5H-benzo[b]carbazole-3-carbonitrile
Canonical SMILES CCC1=C(C=C2C(=C1)C(=O)C3=C(C2(C)C)NC4=C3C=CC(=C4)C#N)N5CCC(CC5)N6CCOCC6
Formula C30H34N4O2 M.Wt 482.62
Solubility ≥ 4.83mg/mL in DMSO with ultrasonic and warming Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of CH5424802

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1 mg 5 mg 10 mg
1 mM 2.072 mL 10.3601 mL 20.7202 mL
5 mM 0.4144 mL 2.072 mL 4.144 mL
10 mM 0.2072 mL 1.036 mL 2.072 mL
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Average Rating: 5 ★★★★★ (Based on Reviews and 13 reference(s) in Google Scholar.)

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