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900120O

Avanti

PGB1

Avanti Research™ - A Croda Brand 900120O

Synonym(s):

Prostaglandin B1

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About This Item

Empirical Formula (Hill Notation):
C20H32O4
CAS Number:
13345-51-2
Molecular Weight:
336.47
UNSPSC Code:
12352211
NACRES:
NA.25

form

liquid

packaging

pkg of 1 × 1 mg (900120O-1mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand 900120O

lipid type

neutral glycerides
neutral lipids

shipped in

dry ice

storage temp.

−20°C

SMILES string

O=C1C(CCCCCCC(O)=O)=C(/C=C/[C@H](CCCCC)O)CC1

InChI

1S/C20H32O4/c1-2-3-6-9-17(21)14-12-16-13-15-19(22)18(16)10-7-4-5-8-11-20(23)24/h12,14,17,21H,2-11,13,15H2,1H3,(H,23,24)/b14-12+/t17-/m0/s1

InChI key

YBHMPNRDOVPQIN-VSOYFRJCSA-N

General description

Prostaglandins are hormones present in many tissues and organs.Prostaglandin B1 (PGB1) is a ketone molecule with a five carbon ring structure. It also contains two side chains linked to its unsaturated region.

Biochem/physiol Actions

Prostaglandin B1 (PGB1) is a metabolic product of PGE1 dehydration. It is known to specifically bind to peroxisome proliferator-activated receptor-γ. By this, PGB1 mediates fat accumulation and metabolism. Oligomerization of PGB1 potentiates its anti-oxidative property.

Packaging

5 mL Clear Glass Sealed Ampule (900120O-1mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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General Approach to Prostanes B1 by Intermolecular Pauson-Khand Reaction: Syntheses of Methyl Esters of Prostaglandin B1 and Phytoprostanes 16-B1-PhytoP and 9-L1-PhytoP
Vazquez RA, et al.
European Journal of Organic Chemistry, 2013(9), 1716-1725 (2013)
Synthesis of Prostaglandin and Phytoprostane B1 Via Regioselective Intermolecular Pauson- Khand Reactions
Vazquez RA, et al.
Organic Letters, 11(14), 3104-3107 (2009)

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