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ChemicalBook--->CAS DataBase List--->220339-00-4

220339-00-4

220339-00-4 Structure

220339-00-4 Structure
IdentificationBack Directory
[Name]

DH 97
[CAS]

220339-00-4
[Synonyms]

DH97,DH-97
[Molecular Formula]

C22H26N2O
[MOL File]

220339-00-4.mol
[Molecular Weight]

334.45
Chemical PropertiesBack Directory
[Boiling point ]

580.1±38.0 °C(Predicted)
[density ]

1.105±0.06 g/cm3(Predicted)
[storage temp. ]

Store at RT
[solubility ]

Soluble to 100 mM in DMSO
[form ]

Powder
[pka]

16.36±0.46(Predicted)
Hazard InformationBack Directory
[Description]

A relatively potent MT2 melatonin receptor antagonist (pKi value = 8.03), displaying 89- and 229-fold selectivity over MT1 and GPR50 (melatonin-related orphan receptor) respectively.
[Uses]

N-Pentanoyl 2-benzyltryptamine is a potent and selective antagonist of MT2 melatonin receptor, with a pKi of 8.03 for human MT2. N-Pentanoyl 2-benzyltryptamine shows 89- and 229-fold selectivity for human MT2 over human mt1 and Xenopus mel1c receptor subtypes. N-Pentanoyl 2-benzyltryptamine can inhibit melatonin-induced enhancement of electrically-evoked responses[1][2].
[Definition]

ChEBI: N-[2-[2-(phenylmethyl)-1H-indol-3-yl]ethyl]pentanamide is a member of indoles.
[IC 50]

MT2: 8.03 (pKi); MT1: 6.08 (pKi)
[storage]

Store at RT
[References]

[1] Teh MT, et, al. Comparison of the structure-activity relationships of melatonin receptor agonists and antagonists: lengthening the N-acyl side-chain has differing effects on potency on Xenopus melanophores. Naunyn Schmiedebergs Arch Pharmacol. 1998 Nov;358(5):522-8. DOI:10.1007/pl00005288
[2] Ting KN, et, al. Molecular and pharmacological evidence for MT1 melatonin receptor subtype in the tail artery of juvenile Wistar rats. Br J Pharmacol. 1999 Jun;127(4):987-95. DOI:10.1038/sj.bjp.0702612
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