Home >> Research Area >>PI3K/Akt/mTOR Signaling>>PI3K>> CAL-130 Racemate

CAL-130 Racemate

PI3K inhibitor CAS# 474012-90-3

CAL-130 Racemate

Catalog No. BCC1442----Order now to get a substantial discount!

Product Name & Size Price Stock
CAL-130 Racemate: 5mg $311 In Stock
CAL-130 Racemate: 10mg Please Inquire In Stock
CAL-130 Racemate: 20mg Please Inquire Please Inquire
CAL-130 Racemate: 50mg Please Inquire Please Inquire
CAL-130 Racemate: 100mg Please Inquire Please Inquire
CAL-130 Racemate: 200mg Please Inquire Please Inquire
CAL-130 Racemate: 500mg Please Inquire Please Inquire
CAL-130 Racemate: 1000mg Please Inquire Please Inquire
Related Products
  • IPI-145 (INK1197)

    Catalog No.:BCC1104
    CAS No.:1201438-56-3
  • IC-87114

    Catalog No.:BCC1161
    CAS No.:371242-69-2
  • PI-103

    Catalog No.:BCC1162
    CAS No.:371935-74-9
  • PIK-75

    Catalog No.:BCC1163
    CAS No.:372196-77-5
  • TGX-221

    Catalog No.:BCC1244
    CAS No.:663619-89-4

Quality Control of CAL-130 Racemate

Number of papers citing our products

Chemical structure

CAL-130 Racemate

3D structure

Chemical Properties of CAL-130 Racemate

Cas No. 474012-90-3 SDF Download SDF
PubChem ID 10274049 Appearance Powder
Formula C23H22N8O M.Wt 426.47
Type of Compound N/A Storage Desiccate at -20°C
Solubility DMSO
Chemical Name 2-[1-[(2-amino-7H-purin-6-yl)amino]ethyl]-5-methyl-3-(2-methylphenyl)quinazolin-4-one
SMILES CC1=C2C(=CC=C1)N=C(N(C2=O)C3=CC=CC=C3C)C(C)NC4=NC(=NC5=C4NC=N5)N
Standard InChIKey PUYVJBBSBPUKBT-UHFFFAOYSA-N
Standard InChI InChI=1S/C23H22N8O/c1-12-7-4-5-10-16(12)31-21(28-15-9-6-8-13(2)17(15)22(31)32)14(3)27-20-18-19(26-11-25-18)29-23(24)30-20/h4-11,14H,1-3H3,(H4,24,25,26,27,29,30)
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Biological Activity of CAL-130 Racemate

DescriptionCAL-130 Racemate is the racemate of CAL-130. CAL-130 Racemate is a PI3Kδ inhibitor.In Vitro:CAL-130 Racemate (Compound D-081a) is a human phosphatidylinositol 3-kinase delta (PI3Kδ)[1].

References:
[1]. Sadhu, Chanchal, et al. Inhibitors of human phosphatidylinositol 3-kinase delta. US 20020161014 A1.

CAL-130 Racemate Dilution Calculator

Concentration (start)
x
Volume (start)
=
Concentration (final)
x
Volume (final)
 
 
 
C1
V1
C2
V2

calculate

CAL-130 Racemate Molarity Calculator

Mass
=
Concentration
x
Volume
x
MW*
 
 
 
g/mol

calculate

Preparing Stock Solutions of CAL-130 Racemate

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.3448 mL 11.7242 mL 23.4483 mL 46.8966 mL 58.6208 mL
5 mM 0.469 mL 2.3448 mL 4.6897 mL 9.3793 mL 11.7242 mL
10 mM 0.2345 mL 1.1724 mL 2.3448 mL 4.6897 mL 5.8621 mL
50 mM 0.0469 mL 0.2345 mL 0.469 mL 0.9379 mL 1.1724 mL
100 mM 0.0234 mL 0.1172 mL 0.2345 mL 0.469 mL 0.5862 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

Organizitions Citing Our Products recently

 
 
 

Calcutta University

University of Minnesota

University of Maryland School of Medicine

University of Illinois at Chicago

The Ohio State University

University of Zurich

Harvard University

Colorado State University

Auburn University

Yale University

Worcester Polytechnic Institute

Washington State University

Stanford University

University of Leipzig

Universidade da Beira Interior

The Institute of Cancer Research

Heidelberg University

University of Amsterdam

University of Auckland
TsingHua University
TsingHua University
The University of Michigan
The University of Michigan
Miami University
Miami University
DRURY University
DRURY University
Jilin University
Jilin University
Fudan University
Fudan University
Wuhan University
Wuhan University
Sun Yat-sen University
Sun Yat-sen University
Universite de Paris
Universite de Paris
Deemed University
Deemed University
Auckland University
Auckland University
The University of Tokyo
The University of Tokyo
Korea University
Korea University

Background on CAL-130 Racemate

CAL-130 is a novel phosphoinositide 3-kinase (PI3K) inhibitor. It is reported that combined inhibition of PI3Kγ/δ as therapy for T cell acute lymphoblastic leukemia (T-ALL). In the absence of PTEN phosphatase tumor suppressor function, PI3Kγ or PI3Kδ alone can support leukemogenesis, whereas inactivation of both isoforms suppressed tumor formation. The reliance of PTEN null T-ALL on the combined activities of PI3Kγ/δ was further demonstrated by the ability of a dual inhibitor to reduce disease burden and prolong survival in mice as well as prevent proliferation and promote activation of proapoptotic pathways in human tumors.

Featured Products
New Products
 

References on CAL-130 Racemate

Improved racemate resolution of pentan-2-ol and trans-(Z)-cyclooct-5-ene-1,2-diol by lipase catalysis.[Pubmed:27671695]

J Biotechnol. 2016 Nov 20;238:60-68.

Lipases are important catalysts in chiral synthesis due to their wide substrate recognition combined with a high stereoselectivity. We demonstrate here that the state, free or immobilized, of Candida antarctica lipase B (CaLB) affects enantioselectivity and also alters the temperature dependancy of the enzyme. This indicates that CaLB undergoes various conformations induced by its interaction with the different immobilization supports studied. Molecular imprinting experiments, using immobilized enzyme co-dried with mimic substrate molecules, enhanced the enantiomeric ratio two-fold or three-fold, depending on the immobilization support. The structure of the acyl donor has a pronounced effect on CaLB catalyzed resolution, due to the proximity of the acyl and alcohol moieties during catalysis. When the acylation of pentan-2-ol was examined, we found that the 3C methyl propanoate donor afforded the highest resolution. Trans-(Z)-cyclooct-5-en-1,2-diol was used as a model racemic substrate to study the ability of lipase to catalyze the resolution of difunctionalized compounds. There was a clear enhancement in the enantiomer selectivity of the biotransformation of the diol when vinyl butanoate is used as the acyl donor. The conversion and enantiomeric excess of (1R,2R)-monoacetates were enhanced, using immobilized CaLB, when the chain length of the donors increased from C2 to C4.

Analysis of metalaxyl racemate using high performance liquid chromatography coupled with four kinds of detectors.[Pubmed:27439358]

J Chromatogr A. 2016 Oct 7;1467:246-254.

Chiral stationary phase-high performance liquid chromatography coupled with various detectors has been one of most commonly used methods for analysis and separation of chiral compounds over the past decades. Various detectors exhibit different characteristics in qualitative and quantitative studies under different chromatographic conditions. Herein, a comparative evaluation of HPLC coupled with ultraviolet, optical rotation, refractive index, and evaporative light scattering detectors has been conducted for qualitative and quantitative analyses of metalaxyl racemate. Effects of separation conditions on the peak area ratio between two enantiomers, including sample concentration, column temperature, mobile phase composition, as well as flow rate, have been investigated in detail. In addition, the limits of detection, the limits of quantitation, quantitative range and precision for these two enantiomers by using four detectors have been also studied. As indicated, the chromatographic separation conditions have been slight effects on ultraviolet and refractive index detections and the peak area ratio between two enantiomers remains almost unchanged, but the evaporative light scattering detection has been significantly affected by the above-mentioned chromatographic conditions and the corresponding peak area ratios varied greatly. Moreover, the limits of detection, the limits of quantitation, and the quantitative ranges of two enantiomers with UV detection were remarkably lower by 1-2 magnitudes than the others.

A racemate-rules effect supramolecular polymer for ee determination of malic acid in the high ee region.[Pubmed:27722581]

Chem Commun (Camb). 2016 Oct 18;52(85):12669-12671.

A supramolecular polymeric system that shows an unusual "racemate-rules" chiroptical property, an effect opposite to the well-known "majority-rules", has been utilized for accurate determination of malic acid enantiopurity at high ee values.

A quantification method for determination of racemate praziquantel and R-enantiomer in rat plasma for comparison of their pharmacokinetics.[Pubmed:28222334]

J Chromatogr B Analyt Technol Biomed Life Sci. 2017 Mar 24;1048:64-69.

Praziquantel is the drug of first choice for the control and treatment of all forms of schistosomiasis. Praziquantel is administered as a racemate, including R-enantiomer and S-enantiomer. Among them, R-enantiomer has main contribution to schistosomicidal activity. In this study, a sensitive and rapid liquid chromatography with tandem mass spectrometry was established and validated to determine the concentration of racemate praziquantel and R-enantiomer in rat plasma after oral administration. Chromatographic separation was performed on an Agilent Zorbax SB-C18 column. An entire run time for chromatographic separation was no more than 5min. The present method for analytes manifested that high sensitivity (the lower limit of quantification was 3.0ng/mL), satisfactory accuracy (relative error

Description

CAL-130 Racemate is the racemate of CAL-130. CAL-130 Racemate is a PI3Kδ inhibitor.

Keywords:

CAL-130 Racemate,474012-90-3,Natural Products,PI3K, buy CAL-130 Racemate , CAL-130 Racemate supplier , purchase CAL-130 Racemate , CAL-130 Racemate cost , CAL-130 Racemate manufacturer , order CAL-130 Racemate , high purity CAL-130 Racemate

Online Inquiry for:

      Fill out the information below

      • Size:Qty: - +

      * Required Fields

                                      Result: