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PROSTAGLANDIN G2

Product Name
PROSTAGLANDIN G2
CAS No.
51982-36-6
Chemical Name
PROSTAGLANDIN G2
Synonyms
PGG2;PROSTAGLANDIN G2;Prostaglandin?G2?(PGG2);Prostaglandin G2 Solution;SGUKUZOVHSFKPH-KOOCKTTBSA-N;Prostaglandin G2 DISCONTINUED, UNSTABLE;9ALPHA,11ALPHA-EPIDIOXY-15S-HYDROPEROXY-PROSTA-5Z,13E-DIEN-1-OIC ACID;(5Z,13E,15S)-9α,11α-Epidioxy-15-hydroperoxyprosta-5,13-dien-1-oic acid;Prosta-5,13-dien-1-oic acid, 9,11-epidioxy-15-hydroperoxy-, (5Z,9α,11α,13E,15S)-;(E)-7-[(1S,2R,3S,4R)-3-[(E,3S)-3-hydroperoxyoct-1-enyl]-5,6-dioxabicyclo[2.2.1]hept-2-yl]hept-5-enoic acid
CBNumber
CB1329896
Molecular Formula
C20H32O6
Formula Weight
368.46
MOL File
51982-36-6.mol
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PROSTAGLANDIN G2 Property

Boiling point:
517.3±50.0 °C(Predicted)
Density 
1.157±0.06 g/cm3(Predicted)
Flash point:
-17 °C
storage temp. 
−70°C
solubility 
Ethanol: >100 mg/ml; PBS pH 7.2: >2 mg/ml
form 
acetone solution
pka
4.76±0.10(Predicted)
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Safety

Hazard Codes 
F,Xi
Risk Statements 
11-36-66-67
Safety Statements 
9-16-26
RIDADR 
UN 1090 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
P7742
Product name
Prostaglandin G2
Purity
≥95% (HPLC), acetone solution
Packaging
500μg
Price
$1750
Updated
2023/01/07
Cayman Chemical
Product number
17010
Product name
Prostaglandin G2
Purity
≥95%
Packaging
25μg
Price
$89
Updated
2024/03/01
Cayman Chemical
Product number
17010
Product name
Prostaglandin G2
Purity
≥95%
Packaging
50μg
Price
$168
Updated
2024/03/01
Cayman Chemical
Product number
17010
Product name
Prostaglandin G2
Purity
≥95%
Packaging
100μg
Price
$315
Updated
2024/03/01
Cayman Chemical
Product number
17010
Product name
Prostaglandin G2
Purity
≥95%
Packaging
500μg
Price
$1398
Updated
2024/03/01
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PROSTAGLANDIN G2 Chemical Properties,Usage,Production

Uses

Prostaglandin G2 is the first intermediary in the COX pathway which is stable enough to be isolated and characterized. It maintains the ability to inhibit indoleamine 2,3-dioxygenase activity and affect immune suppression and tumor induce tolerance.

Definition

ChEBI: Prostaglandin G2 is a prostaglandins G. It has a role as a mouse metabolite and a human metabolite. It is a conjugate acid of a prostaglandin G2(1-).

PROSTAGLANDIN G2 Preparation Products And Raw materials

Raw materials

Preparation Products

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PROSTAGLANDIN G2 Suppliers

China 14 Germany 1 Japan 1 Switzerland 1 United Kingdom 1 United States 6 Global 24
Service Chemical Inc.
Tel
--
Fax
--
Email
sales@chemos-group.com
Country
Germany
ProdList
6350
Advantage
71

51982-36-6, PROSTAGLANDIN G2Related Search:

TRANS-5-DECEN-1-OL 1,3-CYCLOPENTANEDIOL PROSTAGLANDIN G2 ethyl hydroperoxide Dinoprost tromethamine PROSTAGLANDIN H2 ALLYLCYCLOPENTANE 2,7-OCTADIENOL VINYLCYCLOPENTANE CIS-5-DODECENOIC ACID Latanoprost Lactol Fluprostenol Prostaglandin E1 PROSTAGLANDIN B1 Carboprost PROSTAGLANDIN A1 Latanoprost Lactone Diol Latanoprost

  • (5Z,13E,15S)-9α,11α-Epidioxy-15-hydroperoxyprosta-5,13-dien-1-oic acid
  • Prostaglandin G2 Solution
  • PROSTAGLANDIN G2
  • PGG2
  • 9ALPHA,11ALPHA-EPIDIOXY-15S-HYDROPEROXY-PROSTA-5Z,13E-DIEN-1-OIC ACID
  • Prostaglandin?G2?(PGG2)
  • (E)-7-[(1S,2R,3S,4R)-3-[(E,3S)-3-hydroperoxyoct-1-enyl]-5,6-dioxabicyclo[2.2.1]hept-2-yl]hept-5-enoic acid
  • SGUKUZOVHSFKPH-KOOCKTTBSA-N
  • Prosta-5,13-dien-1-oic acid, 9,11-epidioxy-15-hydroperoxy-, (5Z,9α,11α,13E,15S)-
  • Prostaglandin G2 DISCONTINUED, UNSTABLE
  • 51982-36-6
  • Biochemicals and Reagents
  • BioChemical
  • Prostaglandins
  • Lipids
  • Fatty Acids
  • Prostaglandins
  • ProstaglandinsLipids
  • Arachidonic Acid Cascade
  • Fatty Acids
  • Lipids in Cell Signaling