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Merck
CN

870855A

Avanti

3-Me-Glutaryl Carnitine

Avanti Polar Lipids 870855A, paste

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别名:
3-methylglutaryl L-carnitine
经验公式(希尔记法):
C13H23NO6
分子量:
289.32
UNSPSC代码:
12352211
NACRES:
NA.25

形式

paste

包装

pkg of 1 × 5 mg (870855A-5mg)

制造商/商品名称

Avanti Polar Lipids 870855A

脂质类型

bioactive lipids

运输

dry ice

储存温度

−20°C

SMILES字符串

C[N+](C)(C)C[C@H](OC(CC(C)CC(O)=O)=O)CC([O-])=O

InChI

1S/C13H23NO6/c1-9(5-11(15)16)6-13(19)20-10(7-12(17)18)8-14(2,3)4/h9-10H,5-8H2,1-4H3,(H-,15,16,17,18)

InChI key

HFCPFJNSBPQJDP-UHFFFAOYSA-N

生化/生理作用

3-Me-Glutaryl Carnitine metabolite may be found in urine samples. The detection of 3-methylglutarylcarnitine and other metabolites may play a role in a treatment strategy for carnitine deficiency.

包装

5 mL Clear Glass Sealed Ampule (870855A-5mg)

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S Jooste et al.
Clinica chimica acta; international journal of clinical chemistry, 230(1), 1-8 (1994-10-14)
Two patients, diagnosed with 3-methylglutaconic aciduria, who presented with diverse clinical and metabolic manifestations, were studied. Glycine conjugation as a possible detoxification mechanism in these two patients yielded negative results. Carnitine conjugates were however detected. 3-Methylglutarylcarnitine was observed in the
C R Roe et al.
The Journal of clinical investigation, 77(4), 1391-1394 (1986-04-01)
Deficiency of 3-hydroxy-3-methylglutaryl-coenzyme A (CoA) lyase affects the metabolism of leucine as well as ketogenesis. This disorder is one of an increasing list of inborn errors of metabolism that presents clinically like Reye's Syndrome or nonketotic hypoglycemia. Four patients with

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