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PROSTAGLANDIN J2

Product Name
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, PGD2 analog;9-deoxy-delta-9-prostaglandind2;Prostaglandin J2 Lipid Maps MS Standard;PROSTAGLANDIN J2, 5MG/ML IN METHYL ACETA
CBNumber
CB4477024
Molecular Formula
C20H30O4
Formula Weight
334.45
MOL File
60203-57-8.mol
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PROSTAGLANDIN J2 Property

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
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Safety

Hazard Codes 
Xn,Xi,F
Risk Statements 
20/21/22-36/37/38-67-66-36-11
Safety Statements 
26-36-33-29-16
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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.

P240Ground/bond container and receiving equipment.

P241Use explosion-proof electrical/ventilating/lighting/…/equipment.

P242Use only non-sparking tools.

P243Take precautionary measures against static discharge.

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

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

P312Call a POISON CENTER or doctor/physician if you feel unwell.

P337+P313IF eye irritation persists: Get medical advice/attention.

P370+P378In case of fire: Use … for extinction.

P403+P233Store in a well-ventilated place. Keep container tightly closed.

P403+P235Store in a well-ventilated place. Keep cool.

P405Store locked up.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Cayman Chemical
Product number
18500
Product name
Prostaglandin J2
Purity
≥95%
Packaging
500μg
Price
$86
Updated
2024/03/01
Cayman Chemical
Product number
18500
Product name
Prostaglandin J2
Purity
≥95%
Packaging
1mg
Price
$161
Updated
2024/03/01
Cayman Chemical
Product number
18500
Product name
Prostaglandin J2
Purity
≥95%
Packaging
5mg
Price
$671
Updated
2024/03/01
Cayman Chemical
Product number
18500
Product name
Prostaglandin J2
Purity
≥95%
Packaging
10mg
Price
$1172
Updated
2024/03/01
TRC
Product number
P294203
Product name
PGJ2(ProstaglandinJ2)
Packaging
1mg
Price
$180
Updated
2021/12/16
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PROSTAGLANDIN J2 Chemical Properties,Usage,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

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PROSTAGLANDIN J2 Suppliers

Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
400-6206333 13167063860
Fax
021-50323701
Email
anhua.mao@aladdin-e.com
Country
China
ProdList
25003
Advantage
65
Shanghai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847; 18021002903
Fax
QQ:3008007432
Email
3008007409@qq.com
Country
China
ProdList
71826
Advantage
60
Aikon International Limited
Tel
025-58851090 15955137747
Fax
(6)02557626880
Email
sales01@aikonchem.com
Country
China
ProdList
15949
Advantage
58
Career Henan Chemica Co
Tel
+86-0371-86658258 +8613203830695
Fax
0371-86658258
Email
laboratory@coreychem.com
Country
China
ProdList
30229
Advantage
58
ChemeGen(Shanghai) Biotechnology Co.,Ltd.
Tel
18818260767
Fax
QQ 3610331285
Email
sales@chemegen.com
Country
China
ProdList
11218
Advantage
58
Energy Chemical
Tel
021-58432009 400-005-6266
Fax
021-58436166
Email
marketing@energy-chemical.com
Country
China
ProdList
44918
Advantage
58
Shanghai Universal Biotech Co.,Ltd
Tel
15921930842 15921930842
Email
yh-wang@univ-bio.com
Country
China
ProdList
25004
Advantage
58
amyjetsci
Tel
027-59626688 18771149750
Email
sales@amyjet.com
Country
China
ProdList
2917
Advantage
58
TargetMol Chemicals Inc.
Tel
4008200310
Email
marketing@tsbiochem.com
Country
China
ProdList
24961
Advantage
58
Hubei Aiputi Bioengineering Co., Ltd.
Tel
17762444226
Email
d17762444226@163.com
Country
China
ProdList
2402
Advantage
58

60203-57-8, PROSTAGLANDIN J2Related Search:


  • 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
  • PGJ2
  • 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
  • 60203-57-8