s38093

s38093 Suppliers list
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: Product Name:S38093
CAS:1222097-72-4
Purity:0.99 Package:5MG;10MG;50MG;100MG,1G,5G
Company Name: BOC Sciences
Tel: +1-631-485-4226
Email: inquiry@bocsci.com
Products Intro: Product Name:S38093 HCl
CAS:1222097-72-4
Package:25mg Remarks:BOC Sciences also provides custom synthesis services for S38093 HCl.
Company Name: career henan chemical co
Tel: +86-0371-86658258 +8613203830695
Email: factory@coreychem.com
Products Intro: Product Name: s38093
CAS:1222097-72-4
Purity:99% Package:1g;1USD
Company Name: SHANGHAI T&W PHARMACEUTICAL CO., LTD.
Tel: +86-021-61551413 +8618813727289
Email: contact@trustwe.com
Products Intro: Product Name:S38093
CAS:1222097-72-4
Purity:98% Package:Package as requetsed
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:S 38093 HCl
CAS:1222097-72-4
Purity:99.16% Package:1mg;47USD|2mg;65USD|5mg;98USD

s38093 manufacturers

  • S 38093 HCl
  • S 38093 HCl pictures
  • $47.00 / 1mg
  • 2024-11-19
  • CAS:1222097-72-4
  • Min. Order:
  • Purity: 99.16%
  • Supply Ability: 10g
  • s38093
  • 	s38093 pictures
  • $1.00 / 1g
  • 2019-12-24
  • CAS:1222097-72-4
  • Min. Order: 1g
  • Purity: 99%
  • Supply Ability: 20kg
s38093 Basic information
Product Name:s38093
Synonyms:s38093;S 38093; S38093; S-38093; S38093 HCL;S38093 HCl;S 38093 Hydrochloride;S 38093 HydrochL;4-(3-(Hexahydrocyclopenta[c]pyrrol-2(1H)-yl)propoxy)benzamide hydrochloride
CAS:1222097-72-4
MF:C17H25ClN2O2
MW:324.85
EINECS:
Product Categories:API
Mol File:1222097-72-4.mol
s38093 Structure
s38093 Chemical Properties
Safety Information
MSDS Information
s38093 Usage And Synthesis
DescriptionS38093 is an inverse agonist at histamine H3 receptors. S 38093 displays a moderate affinity for rat, mouse and human H3 receptors (Ki=8.8, 1.44 and 1.2μM, respectively) with no affinity for other histaminergic receptors. In cellular models, the compound was able to antagonize mice H3 receptors (KB=0.65μM) and to suppress cAMP decrease induced by an H3 agonist via human H3 receptors (KB=0.11μM).
s38093 Preparation Products And Raw materials
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