Date published: 2026-2-2

1-800-457-3801

SCBT Portrait Logo
Seach Input

ATC 0065 (CAS 510732-84-0)

0.0(0)
Write a reviewAsk a question

Alternate Names:
N2-[cis-4-[[2-[4-Bromo-2-(trifluoromethoxy)phenyl]ethyl]amino]cyclohexyl]-N4,N4-dimethyl-2,4-quinazolinediamine dihydrochloride
Application:
ATC 0065 is A selective and potent antagonist of the MCH-1R
CAS Number:
510732-84-0
Molecular Weight:
625.35
Molecular Formula:
C25H29BrF3N5O•2HCl
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

ATC 0065 emerges as a highly selective and potent antagonist targeting the melanin-concentrating hormone receptor 1 (MCH-1R), a pivotal receptor implicated in the regulation of energy balance and feeding behavior among other physiological processes. Its mechanism of action is distinguished by its ability to selectively inhibit MCH-1R, thereby modulating the signaling pathways that MCH-1R influences. This specificity is further underscored by its remarkable 96-fold selectivity for MCH-1R over its counterpart, MCH2, highlighting its targeted approach in research applications that necessitate precise modulation of the MCH signaling pathway. Beyond its primary target, ATC 0065 also exhibits affinity towards the serotonin receptors 5-HT1A and 5-HT2B, suggesting a broader scope of interaction with neurotransmitter systems. This multifaceted receptor affinity positions ATC 0065 as useful in neuroscientific research, particularly in studies exploring the complex interplay between neurotransmitters and their impact on behavior and physiological functions. Its unique profile not only facilitates the exploration of the MCH-1R′s role in various biological processes but also aids in dissecting the nuanced contributions of serotonin receptors in the broader neural communication network.


ATC 0065 (CAS 510732-84-0) References

  1. Anxiolytic- and antidepressant-like profile of ATC0065 and ATC0175: nonpeptidic and orally active melanin-concentrating hormone receptor 1 antagonists.  |  Chaki, S., et al. 2005. J Pharmacol Exp Ther. 313: 831-9. PMID: 15677346
  2. Identification of 4-amino-2-cyclohexylaminoquinazolines as metabolically stable melanin-concentrating hormone receptor 1 antagonists.  |  Kanuma, K., et al. 2006. Bioorg Med Chem. 14: 3307-19. PMID: 16434202
  3. MCH-R1 antagonists: what is keeping most research programs away from the clinic?  |  Méndez-Andino, JL. and Wos, JA. 2007. Drug Discov Today. 12: 972-9. PMID: 17993417
  4. Design, synthesis and evaluation of MCH receptor 1 antagonists--Part II: Optimization of pyridazines toward reduced phospholipidosis and hERG inhibition.  |  Roth, GJ., et al. 2015. Bioorg Med Chem Lett. 25: 3270-4. PMID: 26077492

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

ATC 0065, 10 mg

sc-358785
10 mg
$350.00

ATC 0065, 50 mg

sc-358785A
50 mg
$1200.00