What is the catalog number for TGX-221?

The catalog number for TGX-221 is HY-10114.

What sizes are available for TGX-221?

TGX-221 is available in the following size(s): 5 mg, 10 mM - 1 mL, 10 mg, 25 mg, 50 mg, 100 mg.

How many pack sizes does TGX-221 come in?

TGX-221 is available in 6 different pack sizes.

TGX-221 is currently made to order / not held in immediate stock. Contact us for lead time.

Who manufactures TGX-221?

TGX-221 is manufactured by QuantiMol.

What is the estimated delivery time for TGX-221?

Estimated delivery time for TGX-221 is approximately 15 business day(s), depending on your location.

Where can I find the safety data sheet (SDS/MSDS) for TGX-221?

The safety data sheet for TGX-221 is available here: http://file.medchemexpress.com/batch_PDF/HY-10114/TGX-221-SDS-MedChemExpress.pdf.

TGX-221

TGX-221 is a potent, selective, and cell membrane permeable inhibitor of the PI3K p110β catalytic subunit, used for cancer treatment.

Product Specifications

CAS Number

663619-89-4

UNSPSC

12352005

Hazard Statement

H302

Target

PI3K

Type

Reference compound

Related Pathways

PI3K/Akt/mTOR

Applications

Cancer-Kinase/protease

Field of Research

Cancer

Assay Protocol

https://www.medchemexpress.com/TGX-221.html

Purity

99.74

Solubility

DMSO : 12.5 mg/mL (ultrasonic; warming; heat to 60°C)

Smiles

O=C1N2C(C(C(NC3=CC=CC=C3)C)=CC(C)=C2)=NC(N4CCOCC4)=C1

Molecular Formula

C21H24N4O2

Molecular Weight

364.44

Precautions

H302

References & Citations

[1]Zhao Y, et al. Prodrug strategy for PSMA-targeted delivery of TGX-221 to prostate cancer cells. Mol Pharm. 2012 Jun 4;9 (6) :1705-16.|[2]Ge Q, et al. The phosphoinositide 3'-kinase p110δ modulates contractile protein production and IL-6 release in human airway smooth muscle. J Cell Physiol. 2012 Aug;227 (8) :3044-52.|[3]Müller KM, et al. Role of protein kinase C and epidermal growth factor receptor signalling in growth stimulation by neurotensin in colon carcinoma cells. BMC Cancer. 2011 Oct 2;11:421.|[4]Sturgeon SA, et al. Advantages of a selective beta-isoform phosphoinositide 3-kinase antagonist, an anti-thrombotic agent devoid of other cardiovascular actions in the rat. Eur J Pharmacol. 2008 Jun 10;587 (1-3) :209-15.|[5]Chaussade C, et al. Evidence for functional redundancy of class IA PI3K isoforms in insulin signalling. Biochem J. 2007 Jun 15;404 (3) :449-58.