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5-氯-3-乙基N-[2-(4-哌啶-1-基)苯基乙基]-1H-吲哚-2-甲酰胺

Org 27569

CAS: 868273-06-7

Molecular Formula: C24H28ClN3O

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  5. 5-氯-3-乙基N-[2-(4-哌啶-1-基)苯基乙基]-1H-吲哚-2-甲酰胺

5-氯-3-乙基N-[2-(4-哌啶-1-基)苯基乙基]-1H-吲哚-2-甲酰胺 - Names and Identifiers

Name Org 27569
Synonyms CS-412
Org 27569
Org 27569
N-(4-(piperidin-1-yl)phenethyl)-5-chloro-3-ethyl-1H-indole-2-carboxamide
5-Chloro-3-ethyl-N-(4-(piperidin-1-yl)phenethyl)-1H-indole-2-carboxamide
5-Chloro-3-ethyl-N-[2-[4-(1-piperidinyl)phenyl]ethyl-1H-indole-2-carboxamide
1H-Indole-2-carboxamide,5-chloro-3-ethyl-N-[2-[4-(1-piperidinyl)phenyl]ethyl]-
Org27569 5-Chloro-3-ethyl-N-[2-[4-(1-piperidinyl)phenyl]ethyl-1H -indole-2-carboxamide
5-chloro-3-ethyl-1H-indole-2-carboxylic acid [2-(4-piperidin-1-yl-phenyl)-ethyl]-amide
CAS 868273-06-7
EINECS 278-169-7

5-氯-3-乙基N-[2-(4-哌啶-1-基)苯基乙基]-1H-吲哚-2-甲酰胺 - Physico-chemical Properties

Molecular FormulaC24H28ClN3O
Molar Mass409.95
Density1.218±0.06 g/cm3(Predicted)
Boling Point660.3±55.0 °C(Predicted)
Solubility H2O: <2mg/mL
Appearancepowder
Colorwhite
pKa14.87±0.30(Predicted)
Storage Condition2-8°C
MDLMFCD11045300
UseOrg 27569 is an allosteric modulator of cannabinoid CB1 receptor, which induces changes in CB1 receptor state by enhancing the affinity of agonists and reduces the affinity of inverse agonists.
In vitro studyOrg 27569 is an allosteric modulator of the CB1 cannabinoid receptor. It significantly increases the binding of the CB1 receptor to the agonist and significantly reduces the specific binding of the CB1 receptor to the inverse agonist. Org 27569 induces CB1 to bind agonists with high affinity, receptor internalization, and downstream ERK phosphorylation. Allosteric ligand Org 27569 promotes the binding of agonists to CB1, but blocks conformational changes in tm6. The Org 27569 decoy receptors bind to different agonists, but do not signal a conformational state.
Org 27569 is an allosteric modulator of the CB1 cannabinoid receptor. It significantly increases the binding of the CB1 receptor to the agonist and significantly reduces the specific binding of the CB1 receptor to the inverse agonist. Org 27569 induces CB1 to bind agonists with high affinity, receptor internalization, and downstream ERK phosphorylation. Allosteric ligand Org 27569 promotes the binding of agonists to CB1, but blocks conformational changes in tm6. The Org 27569 decoy receptors bind to different agonists, but do not signal a conformational state.

5-氯-3-乙基N-[2-(4-哌啶-1-基)苯基乙基]-1H-吲哚-2-甲酰胺 - Risk and Safety

Hazard SymbolsXn - Harmful
Harmful
Risk Codes22 - Harmful if swallowed
WGK Germany3

5-氯-3-乙基N-[2-(4-哌啶-1-基)苯基乙基]-1H-吲哚-2-甲酰胺 - Preparation solution concentration reference

 1mg5mg10mg
1 mM2.439 ml12.197 ml24.393 ml
5 mM0.488 ml2.439 ml4.879 ml
10 mM0.244 ml1.22 ml2.439 ml
5 mM0.049 ml0.244 ml0.488 ml
Last Update:2024-01-02 23:10:35

5-氯-3-乙基N-[2-(4-哌啶-1-基)苯基乙基]-1H-吲哚-2-甲酰胺 - Reference Information

Biological activity Org 27569 is an allosteric modulator of cannabinoid CB1 receptor, which induces changes in CB1 receptor state by enhancing the affinity of agonists and reduces the affinity of reverse agonists.
Org 27569 is an allosteric modulator of cannabinoid CB1 receptor, which induces changes in CB1 receptor state by enhancing the affinity of agonists and reduces the affinity of inverse agonists.
In vitro study Org 27569 is an allosteric modulator of CB1 cannabinoid receptor. It significantly increases the binding of CB1 receptors to agonists and significantly reduces the specific binding of CB1 receptors to inverse agonists. Org 27569 induces CB1 to bind agonists with high affinity, receptor internalization, and downstream ERK phosphorylation. The allosteric ligand Org 27569 promotes the binding of the agonist to CB1, but blocks the conformational change in TM6. Org 27569 trapping receptors bind to different agonists, but there is no signal of conformational state.
Org 27569 is an allosteric modulator of CB1 cannabinoid receptor. It significantly increases the binding of CB1 receptors to agonists and significantly reduces the specific binding of CB1 receptors to inverse agonists. Org 27569 induces CB1 to bind agonists with high affinity, receptor internalization, and downstream ERK phosphorylation. The allosteric ligand Org 27569 promotes the binding of the agonist to CB1, but blocks the conformational change in TM6. Org 27569 trapping receptors bind to different agonists, but there is no signal of conformational state.
Features The trap receptor binds to different agonists, but there is no signal of conformational state.
target TargetValue CB1
TargetValue
Last Update:2024-04-09 21:31:59
5-氯-3-乙基N-[2-(4-哌啶-1-基)苯基乙基]-1H-吲哚-2-甲酰胺
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MedChemExpress (MCE)
Spot supply
Product Name: Org 27569 Visit Supplier Webpage Request for quotation
CAS: 868273-06-7
Tel: 609-228-6898
Email: sales@medchemexpress.com
     tech@medchemexpress.com
Mobile: 609-228-6898
BOC Sciences
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Product Name: ORG-27569 Visit Supplier Webpage Request for quotation
CAS: 868273-06-7
Tel: +16314854226
Email: info@bocsci.com
Mobile: +16314854226
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Product List: View Catalog
SHANGHAI ACMEC BIOCHEMICAL TECHNOLOGY CO., LTD.
Spot supply
Product Name: Org 27569 Visit Supplier Webpage Request for quotation
CAS: 868273-06-7
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
Shanghai Macklin Biochemical Co., Ltd
Spot supply
Product Name: Org 27569 Visit Supplier Webpage Request for quotation
CAS: 868273-06-7
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.
Product Name: Org 27569 Visit Supplier Webpage Request for quotation
CAS: 868273-06-7
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409 Click to send a QQ message
View History
5-氯-3-乙基N-[2-(4-哌啶-1-基)苯基乙基]-1H-吲哚-2-甲酰胺
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