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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
Molecular Weight:
368.46
MDL Number:
MFCD00036971
MOL File:
51982-36-6.mol
Last updated:2023-05-04 17:34:39

PROSTAGLANDIN G2 Properties

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)
FDA UNII AZ87DUD2Y8

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS02,GHS07
Signal word  Danger
Hazard statements  H225-H319-H336
Precautionary statements  P210-P305+P351+P338
Hazard Codes  F,Xi
Risk Statements  11-36-66-67
Safety Statements  9-16-26
RIDADR  UN 1090 3/PG 2
WGK Germany  1

PROSTAGLANDIN G2 price More Price(6)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich P7742 Prostaglandin G2 ≥95% (HPLC), acetone solution 51982-36-6 500μg $1750 2023-01-07 Buy
Cayman Chemical 17010 Prostaglandin G2 ≥95% 51982-36-6 25μg $89 2024-03-01 Buy
Cayman Chemical 17010 Prostaglandin G2 ≥95% 51982-36-6 50μg $168 2024-03-01 Buy
Cayman Chemical 17010 Prostaglandin G2 ≥95% 51982-36-6 100μg $315 2024-03-01 Buy
Cayman Chemical 17010 Prostaglandin G2 ≥95% 51982-36-6 500μg $1398 2024-03-01 Buy
Product number Packaging Price Buy
P7742 500μg $1750 Buy
17010 25μg $89 Buy
17010 50μg $168 Buy
17010 100μg $315 Buy
17010 500μg $1398 Buy

PROSTAGLANDIN G2 Chemical Properties,Uses,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-).

506-32-1
51982-36-6
Synthesis of PROSTAGLANDIN G2 from Arachidonic acid

PROSTAGLANDIN G2 Preparation Products And Raw materials

Raw materials

Preparation Products

PROSTAGLANDIN G2 Suppliers

Global( 24)Suppliers
Supplier Tel Email Country ProdList Advantage
Aladdin Scientific
+1-+1(833)-552-7181 sales@aladdinsci.com United States 57505 58
3B Pharmachem (Wuhan) International Co.,Ltd. 821-50328103-801 18930552037 3bsc@sina.com China 15839 69
Shanghai Aladdin Bio-Chem Technology Co.,LTD 400-400-6206333 18521732826 market@aladdin-e.com China 25003 65
Hangzhou Synstar pharmaceutical Technology CO.,Ltd 0571-85361029 synstar518@163.com China 1990 58
ChemeGen(Shanghai) Biotechnology Co.,Ltd. 18818260767 sales@chemegen.com China 11217 58
Energy Chemical 021-58432009 400-005-6266 marketing@energy-chemical.com China 44918 58
Shanghai Yifei Biotechnology Co. , Ltd. 021-65675885 18964387627 customer_service@efebio.com China 11974 58
TargetMol Chemicals Inc. 15002134094 marketing@targetmol.cn China 19711 58
(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