DH 97

DH 97 Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354; +17819995354
Email: marketing@targetmol.com
Products Intro: Product Name:DH97;DH 97
CAS:220339-00-4
Package:10 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: TargetMol Chemicals Inc.
Tel: +17819995354
Email: marketing@targetmol.com
Products Intro: Product Name:DH97
CAS:220339-00-4
Package:100mg;2500USD|50mg;1980USD|25mg;1520USD
Company Name: Amadis Chemical Company Limited
Tel: 571-89925085
Email: sales@amadischem.com
Products Intro: Product Name:DH 97
CAS:220339-00-4
Purity:0.97 Package:mgs,gs,kgs Remarks:A930677
Company Name: EMMX Biotechnology LLC  
Tel: 888-539-0666
Email: info@emmx.com
Products Intro: Product Name:DH 97
CAS:220339-00-4
Purity:98% HPLC Package:5mg;10mg;25mg;50mg;100mg;250mg;500mg;1g
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
Tel: 021-65675885 18964387627
Email: info@efebio.com
Products Intro: Product Name:DH 97
CAS:220339-00-4
Purity:99% Package:10mg;25mg;50mg

DH 97 manufacturers

  • DH97
  • DH97 pictures
  • $2500.00 / 100mg
  • 2025-10-27
  • CAS:220339-00-4
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  • Supply Ability: 10g
DH 97 Basic information
Product Name:DH 97
Synonyms:DH97,DH-97;Pentanamide, N-[2-[2-(phenylmethyl)-1H-indol-3-yl]ethyl]-
CAS:220339-00-4
MF:C22H26N2O
MW:334.45
EINECS:
Product Categories:
Mol File:220339-00-4.mol
DH 97 Structure
DH 97 Chemical Properties
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
pka16.36±0.46(Predicted)
Safety Information
MSDS Information
DH 97 Usage And Synthesis
DescriptionA 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.
UsesN-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].
DefinitionChEBI: N-[2-[2-(phenylmethyl)-1H-indol-3-yl]ethyl]pentanamide is a member of indoles.
IC 50MT2: 8.03 (pKi); MT1: 6.08 (pKi)
storageStore 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
DH 97 Preparation Products And Raw materials
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