[CAS NO. 638156-11-3]  CID2011756

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PRODUCTS SPECIFICATIONS [638156-11-3]

Catalog
HY-13454
Brand
MCE
CAS
638156-11-3

DESCRIPTION [638156-11-3]

Overview

MDLMFCD04094273
Molecular Weight396.87
Molecular FormulaC22H21ClN2O3
SMILESO=C(C1=CC=C(C2=CC=CC(Cl)=C2)O1)NC3=CC=C(CN4CCOCC4)C=C3

For research use only. We do not sell to patients.

Summary

CID 2011756 is an ATP competitive PKD inhibitor, with an IC 50 of 3.2 µM for PKD1 in cell free assay, and also shows cellular pan-PKD inhibitory activity against PKD2 and PKD3 ( IC 50 , 0.6 and 0.7 µM, respectively). CID 2011756 also has antitumor activity.


IC50 & Target

IC50: 3.2 µM (PKD1), 0.6 µM (Cellular PKD2), 0.7 µM (Cellular PKD3) [1]


In Vitro

CID 2011756 is an ATP-competitive PKD1 inhibitor, with an IC 50 of 3.2 µM. CID 2011756 decreases the phosphorylation of endogenous PKD1 Ser 916 in LNCaP cancer cells with an EC 50 of 10±0.7 µM. CID 2011756 also has cellular pan-PKD inhibitory effects, with IC 50 s of 0.6±0.1 µM and 0.7±0.2 µM for PKD2 and PKD3, respectively [1] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.


Appearance

Solid


Shipping

Room temperature in continental US; may vary elsewhere.


Storage

Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month

Solvent & Solubility

In Vitro:

DMSO : 20 mg/mL ( 50.39 mM ; Need ultrasonic)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.5197 mL 12.5986 mL 25.1972 mL
5 mM 0.5039 mL 2.5197 mL 5.0394 mL
10 mM 0.2520 mL 1.2599 mL 2.5197 mL
* Please refer to the solubility information to select the appropriate solvent.
In Vivo:
  • 1.

    Add each solvent one by one: 10% DMSO >> 40% PEG300 >> 5% Tween-80 >> 45% saline

    Solubility: ≥ 2 mg/mL (5.04 mM); Clear solution

  • 2.

    Add each solvent one by one: 10% DMSO >> 90% corn oil

    Solubility: ≥ 2 mg/mL (5.04 mM); Clear solution

* All of the co-solvents are available by MCE.