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  • Product Name: A-841720
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  • Purity: 98.0%
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  • Contact: Tony Cao

869802-58-4

869802-58-4 structure
869802-58-4 structure
  • Name: A 841720
  • Chemical Name: 3-(azepan-1-yl)-9-(dimethylamino)pyrido[1,2]thieno[3,4-d]pyrimidin-4-one
  • CAS Number: 869802-58-4
  • Molecular Formula: C17H21N5OS
  • Molecular Weight: 343.44700
  • Catalog: Signaling Pathways GPCR/G Protein mGluR
  • Create Date: 2017-01-09 19:26:59
  • Modify Date: 2024-01-14 18:47:00
  • A-841720 is a potent, non-competitive and selective mGlu1 receptor antagonist with an IC50 of 10 nM for human mGlu1 receptor. A-841720 displays 34-fold selectivity over mGlu5 (IC50 of 342 nM), and no significant activity at a range of other neurotransmitter receptors, ion channels, and transporters. A-841720 has the potential for chronic pain research[1][2].

Name 3-(azepan-1-yl)-9-(dimethylamino)pyrido[1,2]thieno[3,4-d]pyrimidin-4-one
Synonyms BU 224 hydrochloride
Description A-841720 is a potent, non-competitive and selective mGlu1 receptor antagonist with an IC50 of 10 nM for human mGlu1 receptor. A-841720 displays 34-fold selectivity over mGlu5 (IC50 of 342 nM), and no significant activity at a range of other neurotransmitter receptors, ion channels, and transporters. A-841720 has the potential for chronic pain research[1][2].
Related Catalog
Target

Human mGluR1:10 nM (IC50)

human mGluR5:342 nM (IC50)

References

[1]. O El-Kouhen, et al. Blockade of mGluR1 receptor results in analgesia and disruption of motor and cognitive performances: effects of A-841720, a novel non-competitive mGluR1 receptor antagonist. Br J Pharmacol. 2006 Nov;149(6):761-74.

[2]. Lorenzo Morè, et al. Comparison of the mGluR1 antagonist A-841720 in rat models of pain and cognition. Behav Pharmacol. 2007 Jul;18(4):273-81.

Molecular Formula C17H21N5OS
Molecular Weight 343.44700
Exact Mass 343.14700
PSA 82.50000
LogP 2.64920
RIDADR NONH for all modes of transport

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869802-58-4 structure

869802-58-4

Literature: Zheng, Guo Zhu; Bhatia, Pramila; Kolasa, Teodozyj; Patel, Meena; El Kouhen, Odile F.; Chang, Renjie; Uchic, Marie E.; Miller, Loan; Baker, Scott; Lehto, Sonya G.; Honore, Prisca; Wetter, Jill M.; Marsh, Kennan C.; Moreland, Robert B.; Brioni, Jorge D.; Stewart, Andrew O. Bioorganic and Medicinal Chemistry Letters, 2006 , vol. 16, # 18 p. 4936 - 4940

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869802-58-4 structure

869802-58-4

Literature: Zheng, Guo Zhu; Bhatia, Pramila; Daanen, Jerome; Kolasa, Teodozyj; Patel, Meena; Latshaw, Steven; El Kouhen, Odile F.; Chang, Renjie; Uchic, Marie E.; Miller, Loan; Nakane, Masaki; Lehto, Sonya G.; Honore, Marie P.; Moreland, Robert B.; Brioni, Jorge D.; Stewart, Andrew O. Journal of Medicinal Chemistry, 2005 , vol. 48, # 23 p. 7374 - 7388

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869802-58-4 structure

869802-58-4

Literature: Zheng, Guo Zhu; Bhatia, Pramila; Daanen, Jerome; Kolasa, Teodozyj; Patel, Meena; Latshaw, Steven; El Kouhen, Odile F.; Chang, Renjie; Uchic, Marie E.; Miller, Loan; Nakane, Masaki; Lehto, Sonya G.; Honore, Marie P.; Moreland, Robert B.; Brioni, Jorge D.; Stewart, Andrew O. Journal of Medicinal Chemistry, 2005 , vol. 48, # 23 p. 7374 - 7388

~%

869802-58-4 structure

869802-58-4

Literature: Zheng, Guo Zhu; Bhatia, Pramila; Daanen, Jerome; Kolasa, Teodozyj; Patel, Meena; Latshaw, Steven; El Kouhen, Odile F.; Chang, Renjie; Uchic, Marie E.; Miller, Loan; Nakane, Masaki; Lehto, Sonya G.; Honore, Marie P.; Moreland, Robert B.; Brioni, Jorge D.; Stewart, Andrew O. Journal of Medicinal Chemistry, 2005 , vol. 48, # 23 p. 7374 - 7388