AZD2906

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AZD2906 Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354; +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:AZD2906
CAS:1034148-15-6
Purity:98.00% Package:1 mL * 10mM (in DMSO)；10 mg；100 mg；200 mg；25 mg；5 mg；50 mg；500 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: BOC Sciences
Tel: 16314854226; +8616314854226
Email: inquiry@bocsci.com
Products Intro: Product Name:AZD2906
CAS:1034148-15-6
Purity:>=95% Remarks:Please reach out to us for more information about custom solutions.
Company Name: InvivoChem
Tel: +1-708-310-1919 +1-13798911105
Email: sales@invivochem.cn
Products Intro: Product Name:AZD2906
CAS:1034148-15-6
Purity:98% Package:5mg Remarks:V4249
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354;
Email: support@targetmol.com
Products Intro: Product Name:AZD2906
CAS:1034148-15-6
Package:5mg;427USD|25mg;1400USD|50mg;1820USD
Company Name: TargetMol Chemicals Inc.
Tel: 13564774135
Email: marketing@targetmol.com
Products Intro: Product Name:AZD2906
CAS:1034148-15-6
Package:5mg;427USD|25mg;1400USD|50mg;1820USD

AZD2906 manufacturers

  • AZD2906
  • AZD2906 pictures
  • $427.00
  • 2026-04-22
  • CAS:1034148-15-6
  • Purity:
  • Supply Ability: 10g
  • AZD2906
  • AZD2906 pictures
  • $427.00
  • 2025-08-22
  • CAS:1034148-15-6
  • Purity:
  • Supply Ability: 10g
AZD2906 Basic information
Product Name:AZD2906
Synonyms:AZD2906;Cyclopropanecarboxamide, N-[(1R,2S)-2-[[1-(4-fluorophenyl)-1H-indazol-5-yl]oxy]-2-(6-methoxy-3-pyridinyl)-1-methylethyl]-, rel-;AZD2906,AZD-2906
CAS:1034148-15-6
MF:C26H25FN4O3
MW:460.5
EINECS:
Product Categories:
Mol File:1034148-15-6.mol
AZD2906 Structure
AZD2906 Chemical Properties
Boiling point 651.4±55.0 °C(Predicted)
density 1.33±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO : 125 mg/mL (271.44 mM)
form Solid
pka15.03±0.20(Predicted)
color Light yellow to yellow
Safety Information
MSDS Information
AZD2906 Usage And Synthesis
UsesAZD2906 is a selective glucocorticoid receptor (GR) agonist, increases micronucleated immature erythrocytes in the bone marrow of rats. AZD2906 shows IC50s of 2.2, 0.3, 41.6 and 7.5 nM at GR in human, rat PBMC and human, rat whole blood, respectively[1].
in vivo

AZD2906 (5, 25, 50 mg/kg, p.o.) increases micronucleated immature erythrocytes (MIE) in the bone marrow of rats after treatment for 2 days[1].
AZD2906 (5, 25 mg/kg, p.o.) induces an accumulation of glycogen in the liver of rats, and exhibits cortical lymphocytic atrophy of a moderate to marked degree in the thymus of rats[1].

Animal Model:Male Wistar Han rats (10 weeks old)[1]
Dosage:5, 25, 50 mg/kg
Administration:P.O. for 2 days
Result:Caused significant increase in micronucleated immature erythrocytes (MIE) at all doses after analysis of the standard 2000 IE.
References[1] Hayes JE, et al. Micronucleus induction in the bone marrow of rats by pharmacological mechanisms. I: glucocorticoid receptor agonism. Mutagenesis. 2013 Mar;28(2):227-32. DOI:10.1093/mutage/ges076
AZD2906 Preparation Products And Raw materials
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AZD2906