carnitine
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carnitine
Summary
carnitine is a group of stereoisomers[1]. carnitine ranks in the top 5% of group_of_stereoisomers entities by monthly Wikipedia readership (466 views/month).[2]
Key Facts
- carnitine's instance of is recorded as group of stereoisomers[3].
- carnitine's chemical structure is recorded as Carnitine.svg[4].
- carnitine's CAS Registry Number is recorded as 406-76-8[5].
- carnitine's EC number is recorded as 206-976-6[6].
- carnitine's canonical SMILES is recorded as CN+(C)CC(CC(=O)[O-])ON+(C)CC(CC(=O)[O-])O">[7].
- carnitine's InChI is recorded as InChI=1S/C7H15NO3/c1-8(2,3)5-6(9)4-7(10)11/h6,9H,4-5H2,1-3H3/t6-/m1/s1[8].
- carnitine's InChIKey is recorded as PHIQHXFUZVPYII-UHFFFAOYSA-N[9].
- carnitine's Library of Congress authority ID is recorded as sh85143975[10].
- carnitine's ATC code is recorded as A16AA01[11].
- carnitine's Bibliothèque nationale de France ID is recorded as 120496452[12].
- carnitine's chemical formula is recorded as C₇H₁₅NO₃[13].
- carnitine's subclass of is recorded as zwitterion[14].
- carnitine's NDL Authority ID is recorded as 00565066[15].
- carnitine's part of is recorded as carnitine metabolic process[16].
- carnitine's part of is recorded as carnitine biosynthetic process[17].
- carnitine's part of is recorded as carnitine transmembrane transport[18].
- carnitine's part of is recorded as carnitine transmembrane transporter activity[19].
- carnitine's part of is recorded as carnitine transport[20].
- carnitine's part of is recorded as carnitine:acyl carnitine antiporter activity[21].
- carnitine's part of is recorded as carnitine catabolic process[22].
- carnitine's part of is recorded as gamma-butyrobetaine dioxygenase activity[23].
- carnitine's part of is recorded as carnitine 3-dehydrogenase activity[24].
- carnitine's part of is recorded as carnitine decarboxylase activity[25].
- carnitine's Commons category is recorded as Carnitine[26].
- carnitine's MeSH descriptor ID is recorded as D002331[27].
Why It Matters
carnitine ranks in the top 5% of group_of_stereoisomers entities by monthly Wikipedia readership (466 views/month).[2] carnitine has Wikipedia articles in 26 language editions, a strong signal of global cultural recognition.[28] carnitine is known by 41 alternative names across languages and contexts.[29]