ChemicalBook--->CAS DataBase List--->37786-06-4

37786-06-4

37786-06-4 Structure

37786-06-4 Structure
IdentificationBack Directory
[Name]

11-DEOXY PROSTAGLANDIN F2ALPHA
[CAS]

37786-06-4
[Synonyms]

11-deoxyPGF2a
11-deoxy-PGF2a
11-deoxy PGF2a
11-Deoxyprostaglandin F2α
11-deoxy-Prostaglandin F2a
11-deoxy Prostaglandin F2α
YRFLKMLJQWGIIZ-APRRXLQMSA-N
1-deoxy Prostaglandin F2alpha
11-DEOXY PROSTAGLANDIN F2ALPHA
1-deoxy Prostaglandin F
11deoxyPGF2a,11-deoxy-PGF-2a,11 deoxy PGF2a
9ALPHA,15S-DIHYDROXY-PROSTA-5Z,13E-DIEN-1-OIC ACID
[Molecular Formula]

C20H34O4
[MDL Number]

MFCD00797656
[MOL File]

37786-06-4.mol
[Molecular Weight]

338.48
Chemical PropertiesBack Directory
[Boiling point ]

511.4±45.0 °C(Predicted)
[density ]

1.090±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

10 mM Na2CO3: >6.5 mg/ml (from PGF2a); DMF: >100 mg/ml (from PGF2a); DMSO: >100 mg/ml (from PGF2a); Ethanol: >100 mg/ml (from PGF2a); PBS pH 7.2: >10 mg/ml (from PGF2a)
[pka]

4.76±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Flame (GHS02)Exclamation Mark (GHS07)Health Hazard (GHS08)
GHS02,GHS07,GHS08
[Signal word ]

Danger
[Hazard statements ]

H225-H319-H360-H336
[Precautionary statements ]

P201-P202-P210-P240-P241-P242-P243-P261-P264-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P308+P313-P312-P337+P313-P370+P378-P403+P233-P403+P235-P405-P501
Hazard InformationBack Directory
[Description]

11-deoxy PGF is a synthetic analog of PGF. It is a more potent agonist than PGF at inducing smooth muscle contractions of rabbit aorta, dog saphenous vein, and guinea pig trachea. It is approximately 20% less potent than U-46619.
[Uses]

11-Deoxyprostaglandin F2α is an activator for TREK-2 channels with EC50 of 0.294 μM. 11-Deoxyprostaglandin F2α inhibits the K2P channel TREK-1[1].
[storage]

Store at -20°C
[References]

[1] Dadi PK,et al., Selective Small Molecule Activators of TREK-2 Channels Stimulate Dorsal Root Ganglion c-Fiber Nociceptor Two-Pore-Domain Potassium Channel Currents and Limit Calcium Influx. ACS Chem Neurosci. 2017 Mar 15;8(3):558-568. DOI:10.1021/acschemneuro.6b00301
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