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P7617

Sigma-Aldrich

Prostaglandin G1

>95% (HPLC), acetone solution

Synonym(s):

15-Hydroperoxyprostaglandin R1, 8,11-Epidioxy-15-hydroperoxy-(9α,11α, 13E,15)-prost-13-ene-1-oic acid, PGG1

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About This Item

Empirical Formula (Hill Notation):
C20H34O6
CAS Number:
52162-11-5
Molecular Weight:
370.48
EC Number:
200-662-2
MDL number:
MFCD04974503
UNSPSC Code:
12352202
PubChem Substance ID:
329820312

Assay

>95% (HPLC)

form

acetone solution

shipped in

dry ice

storage temp.

−70°C

SMILES string

CCCCC[C@H](OO)\C=C\[C@H]1[C@H]2C[C@H](OO2)[C@@H]1CCCCCCC(O)=O

InChI

1S/C20H34O6/c1-2-3-6-9-15(24-23)12-13-17-16(18-14-19(17)26-25-18)10-7-4-5-8-11-20(21)22/h12-13,15-19,23H,2-11,14H2,1H3,(H,21,22)/b13-12+/t15-,16+,17+,18-,19+/m0/s1

InChI key

QXCRWNZYEVOQMB-CDIPTNKSSA-N

Application

Used in studies of prostacylcin synthetase

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Statements

H225,H319,H336

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

Target Organs

Central nervous system

Supplementary Hazards

EUH066

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

1.4 °F - closed cup

Flash Point(C)

-17 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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E A Ham et al.
The Journal of biological chemistry, 254(7), 2191-2194 (1979-04-10)
A study of the enzymes of the arachidonic acid cascade revealed a high sensitivity of prostacyclin synthetase and a complete resistance of thromboxane A2 synthetase to time-dependent destruction by an oxidant [Ox] released during the peroxidase-catalyzed reduction of hydroperoxy fatty

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