5(S),6(R),7-TRIHYDROXYHEPTANOIC ACID, METHYL ESTER
- Product Name
- 5(S),6(R),7-TRIHYDROXYHEPTANOIC ACID, METHYL ESTER
- CAS No.
- 78606-80-1
- Chemical Name
- 5(S),6(R),7-TRIHYDROXYHEPTANOIC ACID, METHYL ESTER
- Synonyms
- BML-111;BML111,BML 111;BML-111, Lipoxin A4 agonist;6(R)-7-trihydroxymethyl Heptanoate;1,3-Benzodioxole-9-sulfonylchloride;methyl (5R,6R)-5,6,7-trihydroxyheptanoate;(5S,6R)-METHYL 5,6,7-TRIHYDROXYHEPTANOATE;5(S),6(R),7-TRIHYDROXYHEPTANOIC ACID, METHYL ESTER;5(S),6(R)-trihydroxy-7-heptanoic acid, methyl ester;Heptanoic acid, 5,6,7-trihydroxy-, methyl ester, (5S,6R)-
- CBNumber
- CB2296632
- Molecular Formula
- C8H16O5
- Formula Weight
- 192.21
- MOL File
- Mol file
5(S),6(R),7-TRIHYDROXYHEPTANOIC ACID, METHYL ESTER Property
- Boiling point:
- 360.8±42.0 °C(Predicted)
- Density
- 1?+-.0.06 g/cm3(Predicted)
- storage temp.
- -20°C
- solubility
- H2O: ≥20mg/mL
- form
- powder
- pka
- 13.74±0.20(Predicted)
- color
- white to beige
- Stability:
- Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 3 months.
Safety
- WGK Germany
- 3
N-Bromosuccinimide Price
- Product number
- SML0215
- Product name
- 5(S),6(R),7-Trihydroxyheptanoic acid methyl ester
- Purity
- ≥98% (HPLC)
- Packaging
- 25mg
- Price
- $560
- Updated
- 2022/05/15
- Product number
- 10005032
- Product name
- 5(S),6(R)-7-trihydroxymethyl Heptanoate
- Purity
- ≥95%
- Packaging
- 1mg
- Price
- $57
- Updated
- 2024/03/01
- Product number
- 10005032
- Product name
- 5(S),6(R)-7-trihydroxymethyl Heptanoate
- Purity
- ≥95%
- Packaging
- 5mg
- Price
- $249
- Updated
- 2024/03/01
- Product number
- 10005032
- Product name
- 5(S),6(R)-7-trihydroxymethyl Heptanoate
- Purity
- ≥95%
- Packaging
- 10mg
- Price
- $437
- Updated
- 2024/03/01
- Product number
- 5488
- Product name
- BML111
- Packaging
- 10
- Price
- $182
- Updated
- 2021/12/16
5(S),6(R),7-TRIHYDROXYHEPTANOIC ACID, METHYL ESTER Chemical Properties,Usage,Production
Description
BML-111 (78606-80-1) novel truncated analog of lipoxin A4 which retains anti-inflammatory activity.1 Inhibits LTB4-induced leukocyte chemotaxis, IC50=5 nM).1 Attenuates hemorrhagic shock-induced acute lung injury in a rat model.2 Displays hepatoprotective effects in acetaminophen-induced liver injury in mice.3 Limits inflammatory damage in the cerebral cortex and helps maintain blood brain barrier integrity in a rat model of ischemic stroke.4 Attenuates renal ischemia/reperfusion injury via activation of p38 MAPK/PPARa/HO-1 pathway.5
Uses
5(S),6(R)-7-trihydroxymethyl Heptanoate is a potent lipoxin A4 agonist.
storage
Store at -20°C
References
1) Lee et al. (1991), Inhibition of leukotriene B4-induced neutrophil migration by lipoxin A4: structure-function relationships; Biochem. Biophys. Res. Commun., 180 1416 2) Li et al. (2013), BML-111 attenuates hemorrhagic shock-induced acute lung injury through inhibiting activation of mitogen-activated protein kinase pathway in rats; J. Surg. Res., 183 710 3) El-Agamy et al. (2014), Protective effects of BML-111 against acetaminophen-induced acute liver injury in mice; J. Physiol. Biochem., 70 141 4) Hawkins et al. (2014), Neurovascular protection by post-ischemic intravenous injections of the lipoxin A4 receptor agonist, BML-111, in a rat model of ischemic stroke; J. Neurochem., 129 130 5) Wu et al. (2016), BML-111-Attenuates renal Ischemia/Reperfusion Injury via Peroxisome Proliferator-Activates Receptor-α-Regulated Heme Oxygenase-1; Inflammation, 39 611
5(S),6(R),7-TRIHYDROXYHEPTANOIC ACID, METHYL ESTER Preparation Products And Raw materials
Raw materials
Preparation Products
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