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D-4476

D4476

CAS: 301836-43-1

Molecular Formula: C23H18N4O3

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D-4476 - Names and Identifiers

Name D4476
Synonyms D4476
D-4476
D 4476
4-(4-(2,3-DIHYDROBENZO[1,4]DIOXIN-6-YL)-5-PYRIDIN-2-YL-1H-IMIDAZOL-2-YL)BENZAMIDE
4-[4-(2,3-Dihydro-1,4-benzodioxin-6-yl)-5-(2-pyridinyl)-1H-imidazol-2-yl]benzamide
Benzamide,4-[4-(2,3-dihydro-1,4-benzodioxin-6-yl)-5-(2-pyridinyl)-1H-imidazol-2-yl]-
4-[4-(2,3-Dihydro-1,4-benzodioxin-6-yl)-5-(2-pyridinyl)-1H-imidazol-2-yl]benzamide D4476
CAS 301836-43-1

D-4476 - Physico-chemical Properties

Molecular FormulaC23H18N4O3
Molar Mass398.41
Density1.338±0.06 g/cm3(Predicted)
Boling Point675.0±55.0 °C(Predicted)
Solubility DMSO: ~20mg/mL
AppearanceSolid
Colorlight yellow
pKa10.16±0.10(Predicted)
Storage Condition2-8°C
In vitro study D4476 is a potent and rather selective inhibitor of CK1 in vitro and in cells. In H4IIE hepatoma cells, D4476 specifically inhibits the phosphorylation of endogenous forkhead box transcription factor O1a (FOXO1a) on Ser322 and Ser325 within its MPD, without affecting the phosphorylation of other sites. CK1δ assayed at 0.1 mM ATP using a phosphorylated peptide TFRPRTSpSNASTIS corresponding to residues 312–325 of FOXO1a is inhibited with an IC 50 value of 0.3 μM. The IC 50 value for CK1δ decreases progressively as the concentration of ATP is lowered, indicating that D4476 is an ATP-competitive inhibitor of CK1. CK1.

D-4476 - Risk and Safety

WGK Germany3

D-4476 - Reference Information

biological activity D4476 is a CK1 inhibitor with effectiveness, selectivity and cell permeability. Its IC50 value in vitro experiments is 0.3 μM.
target CK1 0.3 μM (IC 50 )
in vitro study d4476 is a potent and rather selective inhibitor of CK1 in vitro and in cells. in h4iie hepatoma cells, d4476 specifically inhibits the phosphorylation of endogenous forkhead box transcription factor O1a (FOXO1a) on ser322 and ser325 within its MPD, without affecting the phosphorylation of other sites. CK1δ assayed at 0.1 mM ATP using a phosphorylated peptide TFRPRTSpSNASTIS corresponding to residues 312-325 of FOXO1a is inhibited with an IC 50 value of 0.3 μ m. the IC 50 value for CK1δ decreases progressively as the concentration of ATP is lowered, indicating that D4476 is an ATP-competitive inhibitor of CK1.
Last Update:2024-04-09 02:00:00
D-4476
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Shanghai Macklin Biochemical Co., Ltd
Featured ProductsSpot supply
Product Name: D4476 Visit Supplier Webpage Request for quotation
CAS: 301836-43-1
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328 Click to send a QQ message
WhatsApp: +86-18821248368
Shanghai Amole Biotechnology Co., Ltd.
Spot supply
Product Name: D4476 Request for quotation
CAS: 301836-43-1
Tel: 400-968-2212
Email: 3623107365@qq.com
Mobile: 18916960931
QQ: 3623107365 Click to send a QQ message
Wechat: 18916960931
SHANGHAI ACMEC BIOCHEMICAL TECHNOLOGY CO., LTD.
Spot supply
Product Name: D4476 Visit Supplier Webpage Request for quotation
CAS: 301836-43-1
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922 Click to send a QQ message
Wechat: 18621343501
WhatsApp: +86-18621343501
MedChemExpress (MCE)
Spot supply
Product Name: Casein Kinase I Inhibitor Visit Supplier Webpage Request for quotation
CAS: 301836-43-1
Tel: 609-228-6898
Email: sales@medchemexpress.com
     tech@medchemexpress.com
Mobile: 609-228-6898
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