Norerythromycin

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

What is the Norerythromycin?

The molecule Norerythromycin presents a molecular formula of C35H63NO13 and its IUPAC name is (3R,4R,5S,6S,7S,9S,11R,12S,13R,14S)-6-[(2R,3S,4R,6S)-4-amino-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-7,12,13-trihydroxy-4-[(2S,4S,5R,6R)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-3,5,7,9,11,13-hexamethyl-oxacyclotetradecane-2,10-dione.

Norethindrone, also known as norethisterone, is a synthetic progestin medication which is used in a wide variety of hormonal birth control and hormonal therapy for women. It is also used in the treatment of menopausal symptoms and endometriosis. Norethindrone is a prodrug of norethisterone, and both drugs are active progestogens. Norethindrone is used as a birth control pill, either alone or in combination with an estrogen..

3D structure

Cartesian coordinates

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

2D drawing

 

Norerythromycin NAZBWJMUFFNFTC-RDEJFGNWSA-N chemical compound 2D structure molecule svg
Norerythromycin

 

Molecule descriptors

 
IUPAC name(3R,4R,5S,6S,7S,9S,11R,12S,13R,14S)-6-[(2R,3S,4R,6S)-4-amino-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-7,12,13-trihydroxy-4-[(2S,4S,5R,6R)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-3,5,7,9,11,13-hexamethyl-oxacyclotetradecane-2,10-dione
InChI codeInChI=1S/C35H63NO13/c1-12-23-35(10,43)28(39)18(4)25(37)16(2)14-33(8,42)30(49-32-26(38)22(36)13-17(3)45-32)19(5)27(20(6)31(41)47-23)48-24-15-34(9,44-11)29(40)21(7)46-24/h16-24,26-30,32,38-40,42-43H,12-15,36H2,1-11H3/t16-,17-,18-,19-,20+,21+,22+,23-,24+,26-,27+,28-,29+,30-,32+,33-,34-,35-/m0/s1
InChI KeyNAZBWJMUFFNFTC-RDEJFGNWSA-N
SMILESCC[C@@H]1OC(=O)[C@H](C)[C@H](O[C@@H]2C[C@](C)(OC)[C@H](O)[C@@H](C)O2)[C@H](C)[C@H](O[C@H]2O[C@@H](C)C[C@@H](N)[C@@H]2O)[C@@](C)(O)C[C@H](C)C(=O)[C@H](C)[C@H](O)[C@@]1(C)O

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.

  • (3R,4R,5S,6S,7S,9S,11R,12S,13R,14S)-6-[(2R,3S,4R,6S)-4-amino-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-7,12,13-trihydroxy-4-[(2S,4S,5R,6R)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-3,5,7,9,11,13-hexamethyl-oxacyclotetradecane-2,10-dione
  • Norerythromycin
  • norerythromycin

Reference codes for other databases

There exist several different chemical codes commonly used in orded to identify molecules:
  • CHEBI:156150

Physico-Chemical properties

IUPAC name(3R,4R,5S,6S,7S,9S,11R,12S,13R,14S)-6-[(2R,3S,4R,6S)-4-amino-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-7,12,13-trihydroxy-4-[(2S,4S,5R,6R)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-3,5,7,9,11,13-hexamethyl-oxacyclotetradecane-2,10-dione
Molecular formulaC35H63NO13
Molecular weight705.874
Melting point (ºC)
Boiling point (ºC)
Density (g/cm3)
Molar refractivity179.56
LogP1.9
Topological polar surface area216.7

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.