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经验公式（希尔记法）:
C20H32O4
化学文摘社编号:
分子量:
336.47
MDL number:
UNSPSC Code:
12352211
NACRES:
NA.25
产品名称
PGB1, Avanti Research™ - A Croda Brand 900120O
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
assay
>99% (TLC)
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
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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
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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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