推荐产品
检测方案
≥94% (TLC)
≥94%
形式
liquid
折射率
n20/D 1.444
密度
0.966 g/mL at 20 °C (lit.)
SMILES字符串
CCCCCCC(OCC(COC(CCCCCC)=O)OC(CCCCCC)=O)=O
InChI
1S/C24H44O6/c1-4-7-10-13-16-22(25)28-19-21(30-24(27)18-15-12-9-6-3)20-29-23(26)17-14-11-8-5-2/h21H,4-20H2,1-3H3
InChI key
PJHKBYALYHRYSK-UHFFFAOYSA-N
WGK
WGK 1
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Juan M Pascual et al.
JAMA neurology, 71(10), 1255-1265 (2014-08-12)
Disorders of brain metabolism are multiform in their mechanisms and manifestations, many of which remain insufficiently understood and are thus similarly treated. Glucose transporter type I deficiency (G1D) is commonly associated with seizures and with electrographic spike-waves. The G1D syndrome
Keri J Fogle et al.
Molecular genetics and metabolism, 126(4), 439-447 (2019-01-27)
Seizures are a feature not only of the many forms of epilepsy, but also of global metabolic diseases such as mitochondrial encephalomyopathy (ME) and glycolytic enzymopathy (GE). Modern anti-epileptic drugs (AEDs) are successful in many cases, but some patients are
A pilot study of add-on oral triheptanoin treatment for children with medically refractory epilepsy.
Sophie Calvert et al.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 22(6), 1074-1080 (2018-08-22)
Despite antiepileptic medication and dietary treatment options available about 45% of children with epilepsy still suffer from uncontrolled seizures. Triheptanoin is an anaplerotic treatment designed to improve energy generation via the Krebs cycle. For the first time, we evaluated the
Mohan Gomathi et al.
Journal of autism and developmental disorders, 50(8), 2740-2764 (2020-02-06)
Drug studies on Rett syndrome (RTT) have drastically increased over the past few decades. This review aims to provide master data on bench-to-bedside drug studies involving RTT. A comprehensive literature review was performed by searching in PUBMED, MEDLINE and Google
Mahmoud Reza Ashrafi et al.
Brain & development, 39(5), 369-385 (2017-01-25)
Childhood leukodystrophies are a growing category of neurological disorders in pediatric neurology practice. With the help of new advanced genetic studies such as whole exome sequencing (WES) and whole genome sequencing (WGS), the list of childhood heritable white matter disorders
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