Gonane
Stereo, skeletal formula of gonane ((1R,2S,10S,11R,15S)-heptadecane) with all chiral centres hydrogenised
Carbon numbering in gonane
Names
IUPAC name
5ξ-Gonane
Systematic IUPAC name
(3aR,3bS,5aΞ,9aS,9bR,11aS)-Hexadecahydro-1H-cyclopenta[a]phenanthrene
Identifiers
  • 4732-76-7 (1R,2S,10S,11R,15S)- heptadecane ☒N
3D model (JSmol)
ChEBI
ChemSpider
  • 5256859 (1R,2S,10S,11R,15S)- heptadecane checkY
  • 5256861 (1R,2S,7R,10S,11R,15S)- heptadecane checkY
  • 5256860 (1R,2S,7S,10S,11R,15S)- heptadecane checkY
  • 1077 checkY
KEGG
  • 1108
  • 6857523 (1R,2S,10S,11R,15S)- heptadecane
  • 6857525 (1R,2S,7R,10S,11R,15S)- heptadecane
  • 6857524 (1R,2S,7S,10S,11R,15S)- heptadecane
  • InChI=1S/C17H28/c1-2-6-14-12(4-1)8-10-17-15-7-3-5-13(15)9-11-16(14)17/h12-17H,1-11H2/t12?,13-,14-,15+,16+,17-/m0/s1 checkY
    Key: UACIBCPNAKBWHX-CTBOZYAPSA-N checkY
  • C2C1[C@H](CCCC1)[C@H]3CC[C@H]4[C@H]([C@@H]3C2)CCC4
Properties
C17H28
Molar mass 232.411 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Infobox references

Gonane (cyclopentanoperhydrophenanthrene) is a chemical compound with formula C
17H
28, whose structure consists of four hydrocarbon rings fused together: three cyclohexane units and one cyclopentane. It can also be viewed as the result of fusing a cyclopentane molecule with a fully hydrogenated molecule of phenanthrene, hence the more descriptive name perhydrocyclopenta[a]phenanthrene. The non-systematic version of the above name is cyclopentanoperhydrophenanthrene.

It has no double bonds and is considered the main structure of steroids, sometimes referred to as a steroid nucleus. There are many forms of gonane, but only a few occur naturally in living organisms. Some common forms include 5α-gonane and 5β-gonane. Estrane, androstane, and pregnane are variants of gonane with additional methyl or ethyl groups attached to certain carbon positions. The term gonane is also used to describe a group of progestins that are similar to levonorgestrel but have a slightly different structure than other hormones like estranes.

Significance

Gonane is a significant chemical compound in the field of steroids because its structure comprises four hydrocarbon rings fused together, consisting of three cyclohexane units and one cyclopentane, which is often referred to as the "steroid nucleus" and serves as the parent compound for steroids.

The discovery of gonane and its role as a steroid nucleus has been fundamental in understanding the structure and function of various steroid hormones. The numbering of steroid rings is determined based on the skeletal structure of gonane, providing a framework for the classification and identification of different steroids.

Structure

Gonane is a tetracyclic hydrocarbon with no double bonds. It is formally the parent compound of the steroids; its carbon skeleton is called the "steroid nucleus".[1][2][3] Some important gonane derivatives are the steroid hormones, characterized by methyl groups at the C10 and C13 positions and a side chain at the C17 position.[3]

Because gonane has six centers of chirality, it has 64 (26) theoretically possible stereoisomers,[2] that differ on the position of the lone hydrogens at carbons 5, 8, 9, 10, 13 and 14 in the direction perpendicular to the mean plane of the carbons. However, only a few of these stereoisomers occur in living organisms.[2] The most common are 5α-gonane and 5β-gonane.

Variants

Estrane (C18) is the 13β-methyl variant of gonane, androstane (C19) is the 10β,13β-dimethyl variant of gonane, and pregnane (C21) is the 10β,13β-dimethyl, 17β-ethyl variant of gonane.[4][5]

Term

The term gonane is also used to refer to a group of progestins[6] that are carbon 18-homologated 19-nortestosterone derivatives including levonorgestrel and its analogues.[7] The term is used to distinguish them from the estranes (19-nortestosterone derivatives).[7]

References

  1. ↑ Yang, Yanqing; Krin, Anna; Cai, Xiaoli; Poopari, Mohammad Reza; Zhang, Yuefei; Cheeseman, James R.; Xu, Yunjie (2023-01-12). "Conformations of Steroid Hormones: Infrared and Vibrational Circular Dichroism Spectroscopy". Molecules (Basel, Switzerland). 28 (2): 771. doi:10.3390/molecules28020771. ISSN 1420-3049. PMC 9864676. PMID 36677830.
  2. 1 2 3 Burkhard Fugmann; Susanne Lang-Fugmann; Wolfgang Steglich (28 May 2014). RÖMPP Encyclopedia Natural Products, 1st Edition, 2000. Thieme. pp. 1918–. ISBN 978-3-13-179551-9.
  3. 1 2 James G. Speight (24 December 2010). Handbook of Industrial Hydrocarbon Processes. Gulf Professional Publishing. pp. 474–. ISBN 978-0-08-094271-1.
  4. ↑ D. Sriram (1 September 2010). Medicinal Chemistry. Pearson Education India. pp. 594–. ISBN 978-81-317-3144-4.
  5. ↑ Etienne-Emile Baulieu; Paul A. Kelly (30 November 1990). Hormones: From Molecules to Disease. Springer Science & Business Media. pp. 391–. ISBN 978-0-412-02791-8.
  6. ↑ Loiseau C, Cayetanot F, Joubert F, Perrin-Terrin AS, Cardot P, Fiamma MN, Frugiere A, Straus C, Bodineau L (2018). "Current Perspectives for the use of Gonane Progesteronergic Drugs in the Treatment of Central Hypoventilation Syndromes". Curr Neuropharmacol. 16 (10): 1433–1454. doi:10.2174/1570159X15666170719104605. PMC 6295933. PMID 28721821.
  7. 1 2 Edgren RA, Stanczyk FZ (December 1999). "Nomenclature of the gonane progestins". Contraception. 60 (6): 313. doi:10.1016/s0010-7824(99)00101-8. PMID 10715364.
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