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A0233

AS605240

≥98% (HPLC)

Synonym(e):

5-(6-Quinoxalinylmethylene)-2,4-thiazolidinedione

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PackungsgrößeSKUVerfügbarkeitPreis
5 mg
Warenkorb auf Verfügbarkeit prüfen
€ 160,00
€ 136,00
25 mg
Warenkorb auf Verfügbarkeit prüfen
€ 579,00
€ 492,15

Über diesen Artikel

Empirische Formel (Hill-System):
C12H7N3O2S
CAS-Nummer:
Molekulargewicht:
257.27
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
Assay:
≥98% (HPLC)
Form:
powder
Quality level:

€ 136,00

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Quality Level

assay

≥98% (HPLC)

form

powder

color

, faint red to orange to dark brown

solubility

DMSO: 1 mg/mL, clear (warmed)

storage temp.

2-8°C

SMILES string

O=C1NC(=O)C(\S1)=C\c2ccc3nccnc3c2

InChI

1S/C12H7N3O2S/c16-11-10(18-12(17)15-11)6-7-1-2-8-9(5-7)14-4-3-13-8/h1-6H,(H,15,16,17)/b10-6-

InChI key

SQWZFLMPDUSYGV-POHAHGRESA-N

Application

AS605240 has been used:
  • as a phosphatidylinositol 3-kinase (PI3K) inhibitor to study its effect on Rab5-positive early endosome (EE) vesicles.[1]
  • as a (PI3K) inhibitor to treat splenocytes for graft-versus-host disease (GVHD) induction.[2]
  • as a class 1A PI3K inhibitor to treat CD4+ T cells.[3]

Biochem/physiol Actions

AS605240 inhibits human recombinant phosphatidylinositol 3-kinase (PI3K) γ, α, β, and δ by competing with adenosine triphosphate (ATP).[4] It plays a role in protecting injury following ischemic stroke. AS605240 also inhibits the activation of astrocytes under the influence of Interleukin-6 (IL-6) and its soluble receptor (sIL-6R).[5] It reduces collagen deposition and prevents lung inflammation. AS605240 also inhibits the increase of tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) expression instigated by bleomycin. It is effective in preventing pulmonary fibrosis by inhibiting the transforming growth factor β1 (TGF-β1) and T lymphocytes infiltration into lungs.[4]
AS605240 is a potent and selective PI3Kγ inhibitor.

Features and Benefits

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.

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Dieser Artikel
SML0569SML1268SML1884
form

powder

form

powder

form

powder

form

powder

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

−20°C

solubility

DMSO: 1 mg/mL, clear (warmed)

solubility

DMSO: 5 mg/mL, clear

solubility

DMSO: 25 mg/mL, clear

solubility

DMSO: 20 mg/mL, clear

color

, faint red to orange to dark brown

color

off-white to brown

color

white to beige

color

white to beige


Lagerklasse

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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Artikel

Discover Bioactive Small Molecules for Kinase Phosphatase Biology


Irene Filippi et al.
Journal of cellular physiology, 229(12), 2067-2076 (2014-05-14)
Hypoxia represents an inadequate oxygen supply to tissues, which can modulate cell functions, primarily through the hypoxia-inducible transcription factor HIF-1α. Dendritic cells (DC) are professional antigen-presenting cells and their migration maybe affected by hypoxia, since the local microenvironment in lymphoid
Cheng-Chang Chen et al.
Cell chemical biology, 24(7), 907-916 (2017-07-22)
To resolve the subcellular distribution of endolysosomal ion channels, we have established a novel experimental approach to selectively patch clamp Rab5 positive early endosomes (EE) versus Rab7/LAMP1-positive late endosomes/lysosomes (LE/LY). To functionally characterize ion channels in endolysosomal membranes with the patch-clamp
Xin Wei et al.
Biochemical and biophysical research communications, 397(2), 311-317 (2010-06-01)
Phosphoinositide 3-kinase-gamma (PI3Kgamma) has been identified to play the critical roles in inflammatory cells activation and recruitment in multiply inflammatory diseases and it promised to be a prospective target for relevant inflammatory diseases therapy. AS605240, a selective PI3Kgamma inhibitor, has



Global Trade Item Number

SKUGTIN
A0233-25MG04061832433714
A0233-5MG04061832433721

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