methylphenidate
central nervous system stimulant of the phenethylamine and piperidine classes that is used in the treatment of attention deficit hyperactivity disorder and narcolepsy
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methylphenidate
Summary
methylphenidate is a group of stereoisomers[1]. methylphenidate ranks in the top 0.38% of group_of_stereoisomers entities by monthly Wikipedia readership (4,123 views/month, #4 of 1,063).[2]
Key Facts
- methylphenidate's instance of is recorded as group of stereoisomers[3].
- methylphenidate's chemical structure is recorded as Methyl 2-phenyl-2-(piperidin-2-yl)acetate 200.svg[4].
- methylphenidate's chemical structure is recorded as Methylphenidate-2D-skeletal.svg[5].
- methylphenidate's physically interacts with is recorded as solute carrier family 6 member 3[6].
- methylphenidate's physically interacts with is recorded as Solute carrier family 6 member 2[7].
- methylphenidate's GND ID is recorded as 4467327-9[8].
- methylphenidate's CAS Registry Number is recorded as 113-45-1[9].
- methylphenidate's EC number is recorded as 204-028-6[10].
- methylphenidate's canonical SMILES is recorded as COC(=O)C(C1CCCCN1)C2=CC=CC=C2[11].
- methylphenidate's InChI is recorded as InChI=1S/C14H19NO2/c1-17-14(16)13(11-7-3-2-4-8-11)12-9-5-6-10-15-12/h2-4,7-8,12-13,15H,5-6,9-10H2,1H3[12].
- methylphenidate's InChIKey is recorded as DUGOZIWVEXMGBE-UHFFFAOYSA-N[13].
- methylphenidate's Library of Congress authority ID is recorded as sh91001552[14].
- methylphenidate's ATC code is recorded as N06BA04[15].
- methylphenidate's chemical formula is recorded as C₁₄H₁₉NO₂[16].
- methylphenidate's subclass of is recorded as carboxylate ester[17].
- methylphenidate's subclass of is recorded as substituted benzene[18].
- methylphenidate's subclass of is recorded as piperidine[19].
- methylphenidate's part of is recorded as response to methylphenidate[20].
- methylphenidate's has use is recorded as medication[21].
- methylphenidate's Commons category is recorded as Methylphenidate[22].
- methylphenidate's MeSH descriptor ID is recorded as D008774[23].
- methylphenidate's has part is recorded as nitrogen[24].
- methylphenidate's has part is recorded as carbon[25].
- methylphenidate's has part is recorded as hydrogen[26].
- methylphenidate's has part is recorded as oxygen[27].
Why It Matters
methylphenidate ranks in the top 0.38% of group_of_stereoisomers entities by monthly Wikipedia readership (4,123 views/month, #4 of 1,063).[2] methylphenidate has Wikipedia articles in 27 language editions, a strong signal of global cultural recognition.[28] methylphenidate is known by 37 alternative names across languages and contexts.[29]