Haloperidol Glucuronide

A summary of the most common chemical descriptors (InChI Key and SMILES codes) for Haloperidol Glucuronide are summarized together with 3D and 2D structures and relevant physico-chemical properties.

What is the Haloperidol Glucuronide?

The molecule Haloperidol Glucuronide presents a molecular formula of C27H31ClFNO8 and its IUPAC name is (2S,3S,4S,5R,6S)-6-[4-(4-chlorophenyl)-1-[4-(4-fluorophenyl)-4-oxobutyl]piperidin-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid.

Haloperidol Glucuronide is a molecule that is used as a medication. It is a derivative of haloperidol, and is used to treat schizophrenia and other mental disorders. It is also used as an antipsychotic medication..

3D structure

Cartesian coordinates

Geometry of Haloperidol Glucuronide in x, y and z coordinates (Å units) to copy/paste elsewhere. Generated with Open Babel software.

2D drawing


Haloperidol Glucuronide ZFNLYKVTHNLKNZ-AMWBNRJOSA-N chemical compound 2D structure molecule svg
Haloperidol Glucuronide


Molecule descriptors

IUPAC name(2S,3S,4S,5R,6S)-6-[4-(4-chlorophenyl)-1-[4-(4-fluorophenyl)-4-oxobutyl]piperidin-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid
InChI codeInChI=1S/C27H31ClFNO8/c28-18-7-5-17(6-8-18)27(38-26-23(34)21(32)22(33)24(37-26)25(35)36)11-14-30(15-12-27)13-1-2-20(31)16-3-9-19(29)10-4-16/h3-10,21-24,26,32-34H,1-2,11-15H2,(H,35,36)/t21-,22-,23+,24-,26-/m0/s1

Other names (synonyms)

IUPAC nomenclature provides a standardized method for naming chemical compounds. Although this system is widely used in chemistry, many chemical compounds have also other names commonly used in different contexts. These synonyms can come from a variety of sources and are used for a variety of purposes.

One common source of synonyms for chemical compounds is the common or trivial names, assigned on the basis of appearance, properties, or origin of the molecule.

Another source of synonyms are historical or obsolete names employed in the past, however replaced nowadays by more modern or standardized names.

In addition to common and historical names, chemical compounds may also have synonyms that are specific to a particular field or industry.

  • (2R,3S,4R,5S,6R)-6-(4-(4-Chlorophenyl)-1-(4-(4-fluorophenyl)-4-oxidanylidene-butyl)piperidin-4-yl)oxy-3,4,5-tris(oxidanyl)oxane-2-carboxylic acid
  • (2S,3S,4S,5R,6S)-6-[4-(4-chlorophenyl)-1-[4-(4-fluorophenyl)-4-oxobutyl]piperidin-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid
  • (2S,3S,4S,5R,6S)-6-[4-(4-chlorophenyl)-1-[4-(4-luorophenyl)-4-oxobutyl]piperidin-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid
  • 100442-88-4
  • 4-(4-Chlorophenyl)-1-(4-(4-fluorophenyl)-4-oxobutyl)-4-piperidinyl beta-D-glucopyranosiduronic acid
  • 4-(4-Chlorophenyl)-1-[4-(4-fluorophenyl)-4-oxobutyl]piperidin-4-yl beta-D-glucopyranosiduronic acid
  • 4W53FP2YJV
  • A-D-Glucuronide
  • Discontinued. Please see H103755.
  • Haloperidol
  • Haloperidol ?-D-Glucuronide
  • Haloperidol Glucuronide
  • Haloperidol beta-D-Glucuronide
  • HaloperidolGlucuronide
  • beta-D-Glucopyranosiduronic acid, 4-(4-chlorophenyl)-1-(4-(4-fluorophenyl)-4-oxobutyl)-4-piperidinyl

Reference codes for other databases

There exist several different chemical codes commonly used in orded to identify molecules:
  • ZINC77293241
  • DTXSID70747874
  • CHEMBL3527395
  • CHEBI:185622

Physico-Chemical properties

IUPAC name(2S,3S,4S,5R,6S)-6-[4-(4-chlorophenyl)-1-[4-(4-fluorophenyl)-4-oxobutyl]piperidin-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid
Molecular formulaC27H31ClFNO8
Molecular weight551.988
Melting point (ºC)
Boiling point (ºC)
Density (g/cm3)
Molar refractivity138.48
Topological polar surface area136.8

LogP and topological polar surface area (TPSA) values were estimated using Open Babel software.

The n-octanol/water partition coeficient (Kow) data is applied in toxicology and drug research. Kow values are used, to guess the environmental fate of persistent organic pollutants. High partition coefficients values, tend to accumulate in the fatty tissue of organisms. Molecules with a log(Kow) (or LogP) greater than 5 are considered to bioaccumulate.

TPSA values are the sum of the surface area over all polar atoms or molecules, mainly oxygen and nitrogen, also including hydrogen atoms.

In medicinal chemistry, TPSA is used to assess the ability of a drug to permeabilise cells.

For molecules to penetrate the blood-brain barrier (and act on receptors in the central nervous system), TPSA values below 90 Å2 are required. Thus, molecules with a polar surface area greater than 140 Å2 tend to be poorly permeable to cell membranes.