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Merck
CN

900120O

Avanti

PGB1

Avanti Polar Lipids 900120O

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别名:
Prostaglandin B1
经验公式(希尔记法):
C20H32O4
CAS号:
分子量:
336.47
UNSPSC代码:
12352211
NACRES:
NA.25

形式

liquid

包装

pkg of 1 × 1 mg (900120O-1mg)

制造商/商品名称

Avanti Polar Lipids 900120O

脂质类型

neutral glycerides
neutral lipids

运输

dry ice

储存温度

−20°C

SMILES字符串

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

一般描述

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.

生化/生理作用

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.

包装

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

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°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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