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Merck
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A0231

Sigma-Aldrich

AS 604850

≥98% (HPLC), solid

Sinonimo/i:

5-(2,2-Difluoro-benzo[1,3]dioxol-5-ylmethylene)-thiazolidine-2,4-dione, PI3Kγ inhibitor

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About This Item

Formula empirica (notazione di Hill):
C11H5F2NO4S
Numero CAS:
Peso molecolare:
285.22
Numero MDL:
Codice UNSPSC:
12352200
ID PubChem:
NACRES:
NA.77

Saggio

≥98% (HPLC)

Forma fisica

solid

Colore

off-white

Solubilità

DMSO: >10 mg/mL
H2O: <2 mg/mL

Condizioni di spedizione

wet ice

Temperatura di conservazione

2-8°C

Stringa SMILE

FC1(F)Oc2ccc(cc2O1)\C=C3/SC(=O)NC3=O

InChI

1S/C11H5F2NO4S/c12-11(13)17-6-2-1-5(3-7(6)18-11)4-8-9(15)14-10(16)19-8/h1-4H,(H,14,15,16)/b8-4-
SRLVNYDXMUGOFI-YWEYNIOJSA-N

Azioni biochim/fisiol

AS 604850 is a selective PI3Kγ inhibitor

Caratteristiche e vantaggi

This compound is a featured product for Kinase Phosphatase Biology research. Click here to discover more featured Kinase Phosphatase Biology products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
This compound is featured on the Phosphoinositide Kinases page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Montserrat Camps et al.
Nature medicine, 11(9), 936-943 (2005-08-30)
Phosphoinositide 3-kinases (PI3K) have long been considered promising drug targets for the treatment of inflammatory and autoimmune disorders as well as cancer and cardiovascular diseases. But the lack of specificity, isoform selectivity and poor biopharmaceutical profile of PI3K inhibitors have
Chatvadee Kornsuthisopon et al.
Scientific reports, 14(1), 6777-6777 (2024-03-22)
Extracellular matrix (ECM) is an intricate structure providing the microenvironment niche that influences stem cell differentiation. This study aimed to investigate the efficacy of decellularized ECM derived from human dental pulp stem cells (dECM_DPSCs) and gingival-derived mesenchymal stem cells (dECM_GSCs)
Hon Yan K Yip et al.
Molecular cell, 80(2), 279-295 (2020-10-17)
The PTEN tumor suppressor controls cell death and survival by regulating functions of various molecular targets. While the role of PTEN lipid-phosphatase activity on PtdIns(3,4,5)P3 and inhibition of PI3K pathway is well characterized, the biological relevance of PTEN protein-phosphatase activity

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