levocabastine
chemical compound
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levocabastine
Summary
levocabastine is a type of chemical entity[1]. levocabastine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (42 views/month).[2]
Key Facts
- levocabastine's instance of is recorded as type of chemical entity[3].
- levocabastine's chemical structure is recorded as Levocabastine.svg[4].
- levocabastine's CAS Registry Number is recorded as 79516-68-0[5].
- levocabastine's canonical SMILES is recorded as N#CC1(CCC(CC1)N2CCC(C(C2)C)(C(=O)O)C3=CC=CC=C3)C4=CC=C(C=C4)F[6].
- levocabastine's InChI is recorded as InChI=1S/C26H29FN2O2/c1-19-17-29(16-15-26(19,24(30)31)21-5-3-2-4-6-21)23-11-13-25(18-28,14-12-23)20-7-9-22(27)10-8-20/h2-10,19,23H,11-17H2,1H3,(H,30,31)/t19-,23-,25-,26-/m1/s1[7].
- levocabastine's InChIKey is recorded as ZCGOMHNNNFPNMX-KYTRFIICSA-N[8].
- levocabastine's ATC code is recorded as R01AC02[9].
- levocabastine's ATC code is recorded as S01GX02[10].
- levocabastine's chemical formula is recorded as C₂₆H₂₉FN₂O₂[11].
- levocabastine's subclass of is recorded as cabastine[12].
- levocabastine's has use is recorded as medication[13].
- levocabastine's Commons category is recorded as Levocabastine[14].
- levocabastine's MeSH descriptor ID is recorded as C047340[15].
- levocabastine's ChEMBL ID is recorded as CHEMBL1615438[16].
- levocabastine's Guide to Pharmacology Ligand ID is recorded as 1586[17].
- levocabastine's Freebase ID is recorded as /m/087vby[18].
- levocabastine's UNII is recorded as H68BP06S81[19].
- levocabastine's UNII is recorded as COU3RRH769[20].
- levocabastine's ChemSpider ID is recorded as 16736421[21].
- levocabastine's KEGG ID is recorded as D01717[22].
- levocabastine's ChEBI ID is recorded as 135679[23].
- levocabastine's DrugBank ID is recorded as DB01106[24].
- levocabastine's NCI Thesaurus ID is recorded as C61806[25].
- levocabastine's different from is recorded as (3S,4R)-1-[4-cyano-4-(4-fluorophenyl)cyclohexyl]-3-methyl-4-phenyl-4-piperidinecarboxylic acid[26].
- levocabastine's isomeric SMILES is recorded as C[C@@H]1CN(CC[C@]1(C(O)=O)C2=CC=CC=C2)[C@H]3CCC@(C#N)C4=CC=C(F)C=C4C@(C#N)C4=CC=C(F)C=C4">[27].
Why It Matters
levocabastine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (42 views/month).[2] levocabastine has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[28]