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Spirorenone
Clinical data
Routes of; administration	Oral
ATC code	None;
Identifiers
	IUPAC name (1aR,5aR,5bS,7aS,8S,8aS,9aS,9bS,9cR,9dR)-5a,7a-Dimethyl-1,1a,5b,6,7,7a,8a,9,9a,9b,9c,9d-dodecahydro-3'H-spiro[cyclopropa[4,5]cyclopenta[1,2-a]cyclopropa[l]phenanthrene-8,2'-furan]-3,5'(4'H,5aH)-dione;
CAS Number	74220-07-8;
PubChem CID	68923;
ChemSpider	62150;
UNII	B8TEV07170;
ChEMBL	ChEMBL2107584;
CompTox Dashboard (EPA)	DTXSID501024537 ;
ECHA InfoCard	100.070.679
Chemical and physical data
Formula	C24H28O3
Molar mass	364.485 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CC12CCC3C(C1C4CC4C25CCC(=O)O5)C6CC6C7=CC(=O)C=CC37C;
	InChI InChI=InChI=1S/C24H28O3/c1-22-6-3-12(25)9-17(22)13-10-14(13)20-16(22)4-7-23(2)21(20)15-11-18(15)24(23)8-5-19(26)27-24/h3,6,9,13-16,18,20-21H,4-5,7-8,10-11H2,1-2H3/t13-,14+,15-,16+,18+,20-,21+,22-,23+,24+/m1/s1; Key:NZUIUYWHFPQZBH-HXCATZOESA-N;

Spirorenone (INN) (developmental code name ZK-35973) is a steroidal antimineralocorticoid of the spirolactone group that was never marketed.^[1]^[2] Spirorenone possesses 5–8 times the antimineralocorticoid activity of spironolactone in animal studies.^[3] The initial discovery of spirorenone was deemed a great success, as no compound with greater antimineralocorticoid activity had been developed since spironolactone in 1957.^[4] Moreover, spirorenone itself has virtually no affinity for the androgen receptor while its progestogenic activity shows species differences, being somewhat greater than that of spironolactone in rabbits but absent in mice and rats.^[3] As such, it was characterized as a highly potent antimineralocorticoid with far fewer hormonal side effects relative to spironolactone.^[4]

In clinical trials, spirorenone was found to be 4- to 10-fold as potent as spironolactone as an antimineralocorticoid, and is said to be the most active antimineralocorticoid identified to date.^[3] However, it was serendipitously and unexpectedly found that low doses of spirorenone lowered testosterone levels in men during clinical studies.^[4]^[5] This was determined to be due to metabolic conversion of spirorenone into drospirenone (1,2-dihydrospirorenone) by the enzyme Δ¹-hydrase, a transformation that occurs only in monkeys and humans.^[4]^[5] Unlike spirorenone, drospirenone was found to be a highly potent progestin and antiandrogen in addition to antimineralocorticoid,^[5] with 8-fold the potency of spironolactone as an antimineralocorticoid and 0.3 times the potency of cyproterone acetate as an antiandrogen.^[6] Subsequently, investigation of spirorenone was discontinued and drospirenone was developed and eventually introduced instead as a contraceptive.^[4]^[5]

Synthesis

The 7-hydroxylation of 15,16β-cyclopropan-Androstenolone PC13075949 (1). Though this transformation has also been accomplished by chemical means, microbiological oxidation by Botryodiplodia malorum apparently proves superior to give PC44520204 (2). Acylation with pivalic anhydride proceeds selectively at the 3 hydroxyl group [82543-09-7] (). Epoxidation by means of tertiary butylhydroperoxide (tbhp) and Vanadyl acetylacetonate gives affords exclusively the β-epoxide [82544-13-6] (3). The remaining hydroxyl is then displaced by chlorine by means of triphenylphosphine and carbon tetrachloride, PC13075960 (4). Sequential reductive elimination followed by saponification gives the allylic alcohol [82543-15-5] (5). Reaction with the Simmons-Smith reagent affords the corresponding cyclopropane [82543-16-6] (6) the stereochemistry being determined by the adjacent hydroxyl group. Addition of the dianion from propargyl alcohol to the carbonyl group at position 17 adds the required carbon atoms for the future lactone [82543-17-7] (7). The alkyne bond is doubly reduced by catalytic hydrogenation [82543-18-8] (8). Pyridinium chlorochromate (PCC) mediated oxidation converts the primary alcohol to an acid while the secondary C3 alcohol is oxidized to a oxidized to a β-hydroxyketone (9). The carboxylic acid lactonizes to the gbl ring, while dehydration of the 5β-hydroxyl group leads to the conjugated enone (10). Dehydrogenation by means of DDQ introduces the C1=C2 olefin to afford spirorenone.

References

^ Elks J (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 1112–. ISBN 978-1-4757-2085-3.
^ Morton IK, Hall JM (6 December 2012). Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer Science & Business Media. pp. 106–. ISBN 978-94-011-4439-1.
^ ^a ^b ^c James VH, Pasqualini JR (22 October 2013). Hormonal Steroids: Proceedings of the Sixth International Congress on Hormonal Steroids. Elsevier Science. pp. 776–. ISBN 978-1-4831-9067-9.
^ ^a ^b ^c ^d ^e Fischer J, Ganellin CR (13 December 2006). Analogue-based Drug Discovery. John Wiley & Sons. pp. 396–. ISBN 978-3-527-60749-5.
^ ^a ^b ^c ^d Fischer J, Rotella DP (4 May 2015). Successful Drug Discovery. John Wiley & Sons. pp. 8–. ISBN 978-3-527-33685-2.
^ Pollow K, Juchem M, Elger W, Jacobi N, Hoffmann G, Möbus V (December 1992). "Dihydrospirorenone (ZK30595): a novel synthetic progestagen--characterization of binding to different receptor proteins". Contraception. 46 (6): 561–74. doi:10.1016/0010-7824(92)90121-9. PMID 1493716.
^ Serradell, MN; Robinson, CP; Castaer, J.; Spirorenone. Drugs Fut 1985, 10, 6, 478.
^ Bittler, Dieter; Hofmeister, Helmut; Laurent, Henry; Nickisch, Klaus; Nickolson, Robert; Petzoldt, Karl; Wiechert, Rudolf (1982). "Synthesis of Spirorenone?A Novel Highly Active Aldosterone Antagonist". Angewandte Chemie International Edition in English. 21 (9): 696–697. doi:10.1002/anie.198206961.
^ Bittler, Dieter; Hofmeister, Helmut; Laurent, Henry; Nickisch, Klaus; Petzoldt, Karl; et al. Angewandte Chemie, 1982 , vol. 94, # 9 p. 718 – 719.
^ , DE2922500 (1980); CA, 95, 25402g (synth, uu)
^ Rudolf Wiechert, et al. US4291029 (1981 to Bayer Pharma AG).
^ Romano, Andrea; Romano, Diego; Ragg, Enzio; Costantino, Francesca; Lenna, Roberto; Gandolfi, Raffaella; Molinari, Francesco (2006). "Steroid hydroxylations with Botryodiplodia malorum and Colletotrichum lini". Steroids. 71 (6): 429–434. doi:10.1016/j.steroids.2006.01.014.
^ Krause, W. eta/, J. Chromatogr., 1982,230,37 (hplc)