1. GPCR/G Protein
  2. Adenosine Receptor
  3. KI-7

KI-7 

目录号: HY-131032
产品使用指南

KI-7 是一种 A2B 腺苷受体阳性变构调节剂。KI-7 增强非选择性 A2B 腺苷受体激动剂 NECA 诱导的 cAMP 积累 (EC50=445.8 nM)。KI-7 还增强了选择性 A2B 腺苷受体激动剂 BAY 60-6583 和 adenosine 诱导的 cAMP 积累,EC50 分别为 2390 nM 和 2550 nM。

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KI-7 Chemical Structure

KI-7 Chemical Structure

CAS No. : 1489263-00-4

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Description

KI-7 is an A2B adenosine receptor positive allosteric modulator. KI-7 potentiates the cAMP accumulation induced by the non-selective A2B adenosine receptor agonist NECA (EC50=445.8 nM). KI-7 also potentiates the cAMP accumulation induced by the selective A2B adenosine receptor agonist BAY 60-6583 as well as by adenosine with EC50s of 2390 nM and 2550 nM, respectively[1][2].

In Vitro

KI-7 (1 μM; 5-21 days; mesenchymal stem cells) induces a significant increase in mRNA expression of Runx2 and Osterix[1].
KI-7 (1 μM; 15-21 days) induced a significant increase in cell viability in both differentiation stages[1].
KI-7, as A2B adenosine receptor positive allosteric modulator in MSCs, demonstrating it is able to potentiate the effects of either adenosine and synthetic orthosteric A2B adenosine receptor agonists in mediating osteoblast differentiation in vitro. NECA, BAY 60-6583 and KI-7 induce a strong increase in IL-6 production. KI-7 is able to potentiate the effects of orthosteric agonists in both differentiation stages, even if the effect became significant only at 21 days[1].

Molecular Weight

354.40

Formula

C₂₃H₁₈N₂O₂

CAS No.

1489263-00-4

SMILES

O=C(NC1=CC=CC=C1)C(C2=CN(CC3=CC=CC=C3)C4=C2C=CC=C4)=O

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

References
  • 摩尔计算器

  • 稀释计算器

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Keywords:

KI-7KI7KI 7Adenosine ReceptorP1 receptorRunx2OsterixorthostericallostericMSCpotentiatecAMPaccumulationInhibitorinhibitorinhibit

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KI-7
目录号:
HY-131032
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