Lanostane

Lanostane
Names

Other names 4,4,14-Trimethylcholestane
Identifiers
CAS Number	474-20-4 (5α)^Y 57496-02-3 (5β)^Y
3D model (Jmol)	(5α): Interactive image (5β): Interactive image
ChEBI	CHEBI:20265 (5α)^N
ChemSpider	7827588 (5α)^N
PubChem	9548665 (5α)
InChI (5α): InChI=1S/C30H54/c1-21(2)11-9-12-22(3)23-15-19-30(8)25-13-14-26-27(4,5)17-10-18-28(26,6)24(25)16-20-29(23,30)7/h21-26H,9-20H2,1-8H3/t22-,23-,24+,25-,26+,28-,29-,30+/m1/s1^N Key: ZQIOPEXWVBIZAV-ZKYCIREVSA-N^N (5α): InChI=1/C30H54/c1-21(2)11-9-12-22(3)23-15-19-30(8)25-13-14-26-27(4,5)17-10-18-28(26,6)24(25)16-20-29(23,30)7/h21-26H,9-20H2,1-8H3/t22-,23-,24+,25-,26+,28-,29-,30+/m1/s1 Key: ZQIOPEXWVBIZAV-ZKYCIREVBA
SMILES (5α): C[C@H](CCCC(C)C)[C@@]1([H])CC[C@@]2(C)[C@]3([H])CC[C@@]4([H])C(C)(C)CCC[C@]4(C)[C@@]3([H])CC[C@@]21C (5β): C[C@H](CCCC(C)C)[C@@]1([H])CC[C@@]2(C)[C@]3([H])CC[C@]4([H])C(C)(C)CCC[C@]4(C)[C@@]3([H])CC[C@@]21C
Properties
Chemical formula	C₃₀H₅₄
Molar mass	414.76 g·mol⁻¹
Melting point	98 to 99 °C (208 to 210 °F; 371 to 372 K)^[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 ^YN ?)
Infobox references

Lanostane or 4,4,14-trimethylcholestane is a chemical compound with formula C
30H
54. It is a polycyclic hydrocarbon, specifically a triterpene. It is an isomer of cucurbitane.

The name is applied to two stereoisomers, distinguished by the prefixes 5α- and 5β-, which differ by the handedness of the bonds at a particular carbon atom (number 5 in the standard steroid numbering scheme).^[2]

5α-Lanostane
5β-Lanostane

Replacement of a hydrogen atom attached to carbon number 3 in the 5α isomer with a hydroxyl group results in lanosterol, the biogenetic precursor of the steroids in animals.^[2]

References

↑ Voser, W.; Montavon, M.; Günthard, Hs. H.; Jeger, O.; Ruzicka, L. (1950). "Zur Kenntnis der Triterpene. 156. Mitteilung. Zur Konstitution des Lanostadienols". Helvetica Chimica Acta. 33: 1893–1910. doi:10.1002/hlca.19500330658.
1 2 IUPAC Commission on the Nomenclature of Organic Chemistry and IUPAC-IUB Commission on Biochemical Nomenclature (1969), The Nomenclature of Steroids - Revised Tentative Rules. European J. of Biochemistry, volume 10, 1-19

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