ChemicalBook > CAS DataBase List > 15D-PGJ2

15D-PGJ2

Product Name
15D-PGJ2
CAS No.
87893-55-8
Chemical Name
15D-PGJ2
Synonyms
15D-PGJ2;15d-PGJ?;15-deoxy-Δ-12;15-deoxy-Δdelta12,14-Pgj 2;15-Deoxy-Delta12;14-Prostaglandin J2;15-Deoxy-Δ12,14-PGJ2;12,14-prostaglandin J2;15-DEOXY-DELTA12,14-PGJ2
CBNumber
CB5206904
Molecular Formula
C20H28O3
Formula Weight
316.43
MOL File
87893-55-8.mol
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15D-PGJ2 Property

Flash point:
-9℃
storage temp. 
-20°C
solubility 
Soluble in Methyl acetate (supplied pre-dissolved - 1mg/ml)
form 
methyl acetate solution
color 
Colorless to light yellow
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Safety

Hazard Codes 
F,Xi
Risk Statements 
11-36/38-66-67-36
Safety Statements 
16-26-29-33-36/37/39
RIDADR 
UN 1231 3/PG 2
WGK Germany 
1
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H225Highly Flammable liquid and vapour

H319Causes serious eye irritation

H336May cause drowsiness or dizziness

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
D8440
Product name
15-Deoxy-Δ12,14-prostaglandin J2
Purity
≥95%(HPLC),1?mg/mLinmethylacetate
Packaging
100μg
Price
$47.4
Updated
2024/03/01
Sigma-Aldrich
Product number
538927
Product name
15d-PGJ?
Packaging
1mg
Price
$196
Updated
2024/03/01
Alfa Aesar
Product number
J67427
Product name
15-Deoxy-delta12,14-prostaglandin J2, 97%
Packaging
1mg
Price
$196
Updated
2021/12/16
Cayman Chemical
Product number
18570
Product name
15-deoxy-Δ12,14-Prostaglandin J2
Purity
≥95%
Packaging
100μg
Price
$32
Updated
2024/03/01
Cayman Chemical
Product number
10007235
Product name
15-deoxy-Δ12,14-Prostaglandin J2 MaxSpec? Standard
Purity
≥95%
Packaging
100μg
Price
$66
Updated
2023/06/20
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15D-PGJ2 Chemical Properties,Usage,Production

Uses

15-Deoxy-Δ12,14-prostaglandin J2 has been used:

  • to study its effect on lipid accumulation, viability/mitochondrial activity, and amount of vasculature in vascularized adipose tissue model
  • as a peroxisome proliferator-activated receptor (PPARγ) agonist to activate intestinal fatty acid binding protein (I-FABP)-PPARγ pathway
  • as a supplement in culture medium for induced neural stem/progenitor cells (NSPCs) differentiation

Definition

ChEBI: 15-deoxy-Delta(12,14)-prostaglandin J2 is a prostaglandin J derivative comprising prostaglandin J2 lacking the 15-hydroxy group and having C=C double bonds at the 12- and 14-positions. It has a role as a metabolite, an electrophilic reagent and an insulin-sensitizing drug. It is functionally related to a prostaglandin J2. It is a conjugate acid of a 15-deoxy-Delta(12,14)-prostaglandin J2(1-).

General Description

A metabolite of PGD2 that has recently been identified as a natural ligand for PPARγ-dependent adipogenesis in transfected 3T3 cells and for PPARγ response element (PPRE) in CV-1 cells. Competes with thiazolidinediones for PPARγ binding.

Biological Activity

Selective PPAR γ agonist that induces adipocyte differentiation in C3H10Y1/2 fibroblasts (EC 50 = 7 μ M).

Biochem/physiol Actions

15-Deoxy-Δ12,14-prostaglandin J2 (15d-PGJ2) regulates inflammatory response in vivo. 15d-PGJ2 also elicits PPARγ-independent inhibition of nuclear factor (NF)-κB dependent transcription. It acts as an anti-angiogenic factor and triggers endothelial cell apoptosis.

15D-PGJ2 Preparation Products And Raw materials

Raw materials

Preparation Products

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15D-PGJ2 Suppliers

3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Fax
86-21-50328109
Email
3bsc@sina.com
Country
China
ProdList
15839
Advantage
69
NCE Biomedical Co.,Ltd.
Tel
4000-027-021 |24 +86-13986109188 | +86-15623472865 | +81-08033611988
Fax
+86-27-87599188
Country
China
ProdList
1493
Advantage
55
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51456
Advantage
80
SPIRO PHARMA
Tel
Fax
-
Email
eric_feng1954@126.com
Country
China
ProdList
9248
Advantage
55
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
ProdList
9806
Advantage
58
Hangzhou Synstar pharmaceutical Technology CO.,Ltd
Tel
0571-85361029
Fax
0571-85361029
Email
synstar518@163.com
Country
China
ProdList
1990
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32161
Advantage
58
DC Chemicals
Tel
021-58447131 13564518121
Email
sales@dcchemicals.com
Country
China
ProdList
9409
Advantage
58
MedBioPharmaceutical Technology Inc
Tel
021-69568360 18916172912
Email
order@med-bio.cn
Country
China
ProdList
8140
Advantage
58
Energy Chemical
Tel
021-58432009 400-005-6266
Fax
021-58436166
Email
marketing@energy-chemical.com
Country
China
ProdList
44918
Advantage
58

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