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PROSTAGLANDIN J2

CAS No.
60203-57-8
Chemical Name:
PROSTAGLANDIN J2
Synonyms
PGJ2;Aids058772;Aids-058772;PROSTAGLANDIN J2;PGJ2 (Prostaglandin J2);Prostaglandin J2 (PGJ2);Prostaglandin J2 (Standard);Prostaglandin J2, PGD2 analog;9-deoxy-delta-9-prostaglandind2;Prostaglandin J2 Lipid Maps MS Standard
CBNumber:
CB4477024
Molecular Formula:
C20H30O4
Molecular Weight:
334.45
MDL Number:
MFCD00065804
MOL File:
60203-57-8.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 02:55:27

PROSTAGLANDIN J2 Properties

Boiling point 521.7±50.0 °C(Predicted)
Density 1.103±0.06 g/cm3(Predicted)
storage temp. −20°C
solubility DMF: >100 mg/ml (from PGD2); DMSO: >50 mg/ml (from PGD2); Ethanol: >75 mg/ml (from PGD2); PBS pH 7.2: >2.7 mg/ml (from 15-deoxy-.DEL
pka 4.75±0.10(Predicted)
form Liquid
color Colorless to light yellow
EWG's Food Scores 1

SAFETY

Risk and Safety Statements

Symbol(GHS)  Flame (GHS02)Exclamation Mark (GHS07)
GHS02,GHS07
Signal word  Danger
Hazard statements  H225-H319-H336
Precautionary statements  P210-P240-P241-P242-P243-P261-P264-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P312-P337+P313-P370+P378-P403+P233-P403+P235-P405-P501
Hazard Codes  Xn,Xi,F
Risk Statements  20/21/22-36/37/38-67-66-36-11
Safety Statements  26-36-33-29-16
NFPA 704
3
2 0

PROSTAGLANDIN J2 price More Price(16)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 18500 Prostaglandin J2 ≥95% 60203-57-8 500μg $97 2026-04-30 Buy
Cayman Chemical 18500 Prostaglandin J2 ≥95% 60203-57-8 1mg $184 2026-04-30 Buy
Cayman Chemical 18500 Prostaglandin J2 ≥95% 60203-57-8 5mg $775 2026-04-30 Buy
Cayman Chemical 18500 Prostaglandin J2 ≥95% 60203-57-8 10mg $1356 2026-04-30 Buy
Usbiological 462340 PGJ2 (Prostaglandin J2) 60203-57-8 1mg $489 2026-06-03 Buy
Product number Packaging Price Buy
18500 500μg $97 Buy
18500 1mg $184 Buy
18500 5mg $775 Buy
18500 10mg $1356 Buy
462340 1mg $489 Buy

PROSTAGLANDIN J2 Chemical Properties, Uses, Production

Description

Prostaglandin J2 (PGJ2) is formed from PGD2 by the elimination of the C-9 hydroxyl group, a process which is accelerated by the presence of albumin. PGJ2 inhibits platelet aggregation with an IC50 of about 5-10 nM. PGJ2 has antimitotic and antiproliferative effects on a variety of cultured normal cells and tumor cell lines. However, this activity has been attributed to further metabolites of PGJ2 and not the parent compound itself.

Uses

PGJ2 (Prostaglandin J2) is a Prostaglandin D2 metabolite that has shown potent anti-neoplastic and antiviral activity.

Definition

ChEBI: A member of the class of prostaglandins J that consists of prosta-5,9,13-trien-1-oic acid substituted by an oxo group at position 11 and a hydroxy group at position 15 (the 5Z,13E,15S stereoisomer).

in vivo

Prostaglandin J2 (PGJ2; 33.4 μg/injection; unilateral injection to the SNpc; once per week for 2 or 4 weeks) induces progressive PD-like pathology and exhibites microglia and astrocyte activation and motor deficits in the rats[4].

Animal Model:Sixteen-week-old Sprague Dawley male rats[4]
Dosage:33.4 μg/injection
Administration:Unilateral (right side) injections to the SNpc; once per week for 2 or 4 weeks
Result:Induced progressive dopaminergic neuronal loss in the rat substantia nigra pars compacta (SNpc).
Developed parkinsonian-like motor deficits in a progressive manner.

IC 50

hDP: 0.9 nM (Ki); hCRTH2: 6.6 nM (Ki); hEP1: 15.678 μM (Ki); hEP2: 989 nM (Ki); hEP3: 319 nM (Ki); hEP4: 1065 nM (Ki); hFP: 553 nM (Ki); hIP: >25 μM (Ki); hTP: 6426 nM (Ki); Human Endogenous Metabolite

References

[1] D. HAMISH WRIGHT. Characterization of the recombinant human prostanoid DP receptor and identification of L-644,698, a novel selective DP agonist[J]. British Journal of Pharmacology, 2009, 123 7: 1317-1324. DOI: 10.1038/sj.bjp.0701708
[2] NICOLE SAWYER. Molecular pharmacology of the human prostaglandin D2 receptor, CRTH2[J]. British Journal of Pharmacology, 2009, 137 8: 1163-1172. DOI: 10.1038/sj.bjp.0704973
[3] TENEKA JEAN-LOUIS  Maria E F P  Patricia Rockwell. Prostaglandin J2 promotes O-GlcNAcylation raising APP processing by α- and β-secretases: relevance to Alzheimer’s disease[J]. Neurobiology of Aging, 2018, 62: Pages 130-145. DOI: 10.1016/j.neurobiolaging.2017.10.009
[4] MARIA E. FIGUEIREDO-PEREIRA  John B  Chuhyon Corwin. Prostaglandin J2: a potential target for halting inflammation-induced neurodegeneration[J]. Annals of the New York Academy of Sciences, 2016, 1363 1: 125-137. DOI: 10.1111/nyas.12987
[5] CHUHYON CORWIN. Prostaglandin D2/J2 signaling pathway in a rat model of neuroinflammation displaying progressive parkinsonian-like pathology: potential novel therapeutic targets.[J]. Journal of Neuroinflammation, 2018: 272. DOI: 10.1186/s12974-018-1305-3
[6] ABHITA MALAVIYA  Paul W S. Synergistic Antiproliferative Effects of Combined γ -Tocotrienol and PPAR γ Antagonist Treatment Are Mediated through PPAR γ -Independent Mechanisms in Breast Cancer Cells.[J]. PPAR Research, 2014: 439146. DOI: 10.1155/2014/439146

PROSTAGLANDIN J2 Preparation Products And Raw materials

Raw materials

Preparation Products

PROSTAGLANDIN J2 Suppliers

Global Suppliers ( 48)
Supplier Tel Email Country ProdList Advantage
Shanghai Aladdin Bio-Chem Technology Co.,LTD 400-6206333 13167063860 anhua.mao@aladdin-e.com China 29985 65
Shanghai YuanYe Biotechnology Co., Ltd. 15026964105 2881489226@qq.com China 89667 60
Aikon International Limited 025-58851090 13913916777 sales01@aikonchem.com China 15947 58
Career Henan Chemica Co +86-0371-86658258 +86-13203830695 laboratory@coreychem.com China 30203 58
ChemeGen(Shanghai) Biotechnology Co.,Ltd. 18818260767 sales@chemegen.com China 11123 58
Energy Chemical 021-58432009 400-005-6266 marketing@energy-chemical.com China 44871 58
Shanghai Universal Biotech Co.,Ltd 15921930842 15921930842 yh-wang@univ-bio.com China 25030 58
amyjet 4006800868;027-59626688 18771149750 sales@amyjet.com China 2909 58
TargetMol Chemicals Inc. 4008200310 15002144251 marketing@tsbiochem.com China 24951 58
Hubei Aiputi Bioengineering Co., Ltd. 17762444226 d17762444226@163.com China 2400 58
11-OXO-15S-HYDROXY-PROSTA-5Z,9,13E-TRIEN-1-OIC ACID (5Z,13E,15S)-15-HYDROXY-11-OXOPROSTA-5,9,13-TRIEN-1-OIC ACID PROSTAGLANDIN J2 9-deoxy-delta-9-prostaglandind2 PROSTAGLANDIN J2, 5MG/ML IN METHYL ACETA (Z)-7-[(1S,5R)-5-[(E,3S)-3-hydroxyoct-1-enyl]-4-oxo-1-cyclopent-2-enyl]hept-5-enoic acid (5Z,13E,15S)-15-Hydroxy-11-oxoprosta-5,9,13-triene-1-oic acid Aids058772 Aids-058772 Prosta-5,9,13-trien-1-oic acid, 15-hydroxy-11-oxo-, (5Z,13E,15S)- Prostaglandin J2 Lipid Maps MS Standard PGJ2 (Prostaglandin J2) Prostaglandin J2 (PGJ2) Prostaglandin J2, PGD2 analog Prostaglandin J2 (Standard) PGJ2 60203-57-8