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AZD7547

AZD7545

CAS: 252017-04-2

Molecular Formula: C19H18ClF3N2O5S

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AZD7547 - Names and Identifiers

Name AZD7545
Synonyms AZD7545
AZD4575
AZD7547
CS-1842
AZD 7547
AZD-7547
4-[[3-Chloro-4-[[(2R)-3,3,3-trifluoro-2-hydroxy-2-methyl-1-oxopropyl]amino]phenyl]sulfonyl]-N,N-dimethylbenzamide
CAS 252017-04-2

AZD7547 - Physico-chemical Properties

Molecular FormulaC19H18ClF3N2O5S
Molar Mass478.87
Density1.473±0.06 g/cm3(Predicted)
Boling Point683.1±55.0 °C(Predicted)
Solubility DMSO: ≥ 46 mg/mL
pKa10.39±0.29(Predicted)
Storage Condition2-8°C
In vitro studyAZD7545 increases PDH activity in the presence of recombinant human PDHK2 with an EC50 of 5.2 nM. AZD7545 increases PDH activity in primary rat hepatocytes with an EC50 of 105 nM. AZD7545 inhibits PDHK activity by disrupting the interaction of PDHK2 with the internal thiooctanoyl domain (L2) of the dihydrolipoic acid acetyltransferase component (E2) of PDC.
In vivo studyIn Wistar rats, AZD7545 increases the percentage of active PDH in liver and skeletal muscle. In obese, insulin-resistant Zuker rats, AZD7545 abolished the rise in postprandial blood glucose.

AZD7547 - Preparation solution concentration reference

 1mg5mg10mg
1 mM2.088 ml10.441 ml20.883 ml
5 mM0.418 ml2.088 ml4.177 ml
10 mM0.209 ml1.044 ml2.088 ml
5 mM0.042 ml0.209 ml0.418 ml
Last Update:2024-01-02 23:10:35

AZD7547 - Reference Information

biological activity AZD7545 is a potent PDHK inhibitor with an IC50 of 36.8 nM and 6.4 nM for PDHK1 and PDHK2, respectively. PDHK4 cannot be inhibited at high concentrations, which can stimulate PDHK4 activity.
Target TargetValue PDHK2 6.4 nM PDHK1 36.8 nM
TargetValue
PDHK2 6.4 nM
PDHK1 36.8 nM
in vitro study in the presence of recombinant human PDHK2, AZD7545 increased PDH activity with an EC50 of 5.2 nM. AZD7545 increases PDH activity in primary rat hepatocytes with an EC50 of 105 nM. AZD7545 inhibits PDHK activity by disrupting the interaction of PDHK2 with the internal thiooctanoyl domain (L2) of the dihydrolipoic acid acetyltransferase component (E2) of PDC.
in vivo study in Wistar rats, AZD7545 increased the percentage of active PDH in liver and skeletal muscle. In obese, insulin-resistant Zuker rats, AZD7545 abolished the rise in postprandial blood glucose.
Last Update:2024-04-10 22:29:15
AZD7547
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Product Name: AZD7545 Visit Supplier Webpage Request for quotation
CAS: 252017-04-2
Tel: 609-228-6898
Email: sales@medchemexpress.com
     tech@medchemexpress.com
Mobile: 609-228-6898
SHANGHAI ACMEC BIOCHEMICAL TECHNOLOGY CO., LTD.
Spot supply
Product Name: AZD7545 Visit Supplier Webpage Request for quotation
CAS: 252017-04-2
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922 Click to send a QQ message
Wechat: 18621343501
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Shanghai Macklin Biochemical Co., Ltd
Spot supply
Product Name: (2,4-Dihydroxy-5-isopropylphenyl){5-[(4-methyl-1-piperazinyl)meth yl]-1,3-dihydro-2H-isoindol-2-yl}methanone Visit Supplier Webpage Request for quotation
CAS: 252017-04-2
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328 Click to send a QQ message
WhatsApp: +86-18821248368
Shanghai Yuanye Bio-Technology Co., Ltd.
Spot supply
Product Name: AZD7545 Visit Supplier Webpage Request for quotation
CAS: 252017-04-2
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409 Click to send a QQ message
View History
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