11beta,17,21-Trihydroxy-pregn-4-ene-3,20-dione methyl ester 3-[(nitrooxy) methyl]-benzoic acid

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11beta,17,21-Trihydroxy-pregn-4-ene-3,20-dione methyl ester 3-[(nitrooxy) methyl]-benzoic acid manufacturers

  • NCX1022
  • NCX1022 pictures
  • $2500.00
  • 2026-05-11
  • CAS:571186-50-0
  • Purity:
  • Supply Ability: 10g
11beta,17,21-Trihydroxy-pregn-4-ene-3,20-dione methyl ester 3-[(nitrooxy) methyl]-benzoic acid Basic information
Product Name:11beta,17,21-Trihydroxy-pregn-4-ene-3,20-dione methyl ester 3-[(nitrooxy) methyl]-benzoic acid
Synonyms:NO-HYDROCORTISONE;Pregn-4-ene-3,20-dione, 11,17-dihydroxy-21-[[4-[(nitrooxy)methyl]benzoyl]oxy]-, (11β)-;NCX-1022,NCX1022;NCX 1022;11beta,17,21-Trihydroxy-pregn-4-ene-3,20-dione methyl ester 3-[(nitrooxy) methyl]-benzoic acid
CAS:571186-50-0
MF:C29H35NO9
MW:541.59
EINECS:
Product Categories:
Mol File:571186-50-0.mol
11beta,17,21-Trihydroxy-pregn-4-ene-3,20-dione methyl ester 3-[(nitrooxy) methyl]-benzoic acid Structure
11beta,17,21-Trihydroxy-pregn-4-ene-3,20-dione methyl ester 3-[(nitrooxy) methyl]-benzoic acid Chemical Properties
Boiling point 734.2±60.0 °C(Predicted)
density 1.37±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO
pka12.31±0.70(Predicted)
Safety Information
MSDS Information
11beta,17,21-Trihydroxy-pregn-4-ene-3,20-dione methyl ester 3-[(nitrooxy) methyl]-benzoic acid Usage And Synthesis
UsesNCX1022 is an NO-releasing derivative of Hydrocortisone, which is the most widely used anti-inflammatory agent for the treatment of skin inflammation.
in vivo

Topical pre- and post-treatment with NCX1022 (3 nmol) in C57BL6 mice not only reduces ear oedema formation in a dose-dependent manner, but also is significantly more effective than the parent compound during the initial stages of inflammation (from 1 to 5 h). NCX1022, but not Hydrocortisone, significantly inhibits granulocyte recruitment (tissue myeloperoxidase activity). Histological samples of mouse ears treated with NCX1022 show significant reduction in both the number of infiltrated cells and disruption of the tissue architecture compared to Hydrocortisone-treated tissues. Post-treatment with Hydrocortisone does not modify the increased granulocyte infiltration induced by benzalkonium application, but NCX1022 reduces by 63% the myeloperoxidase (MPO) activity, producing a maximum effect at the dose of 3 nmol per ear. NCX1022 is significantly more potent than Hydrocortisone in reducing contact dermatitis-induced leukocyte adhesion, particularly at the early time points (e.g., 30-60 min after dermatitis induction)[1].

References[1] Hyun E, et al. Anti-inflammatory effects of nitric oxide-releasing hydrocortisone NCX 1022, in a murine model of contact dermatitis. Br J Pharmacol. 2004 Nov;143(5):618-25. DOI:10.1038/sj.bjp.0705854
11beta,17,21-Trihydroxy-pregn-4-ene-3,20-dione methyl ester 3-[(nitrooxy) methyl]-benzoic acid Preparation Products And Raw materials
Tag:11beta,17,21-Trihydroxy-pregn-4-ene-3,20-dione methyl ester 3-[(nitrooxy) methyl]-benzoic acid(571186-50-0) Related Product Information
11beta,17,21-Trihydroxy-pregn-4-ene-3,20-dione methyl ester 3-[(nitrooxy) methyl]-benzoic acid Hydrocortisone acetate Deoxycorticosterone acetate Fucoxanthin Chondroitin sulfate NOC-18