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Compound 1 (FTY720, Fingolimod) represents a new generation of immunosuppressant that modulates lymphocyte trafficking by interacting with the S1P1 receptor. Compound 1 also provides a template molecule for studying the molecular biology of S1P receptors and related enzymes (kinases and phosphatases). In this study, two conformationally constrained analogues of 1 (3a and 3c) were asymmetrically synthesized in high optical purity. In vitro assessment documented that both analogues are Sphk2 substrates, their phosphorylated species are potent S1P1 receptor agonists, and 3a-P is a potent S1P3 antagonist. After oral administration in mice, both compounds evoked lymphopenia, but their duration of action differed markedly.
Drug-induced modulation of the immune system is a cornerstone of the treatment of autoimmune diseases and allows organ allografting. In addition to biological (e.g., monoclonal antibody) immunosuppressants, the small-molecule drugs used commonly are cytotoxins (e.g., cyclophosphamide), corticosteroids, purine synthesis inhibitors, and immunophilin-binding compounds [cyclosporine A (CsA), rapamycin,1 and tacrolimus (FK506)2].3 All of these chemical agents function by either depleting lymphocytes or preventing lymphocyte activation. Although these small-molecule drugs have enabled widespread organ transplantation, they also have significant adverse effects as consequences of both the therapeutic target and often alternative, “off” targets. Thus, additional drugs are needed to modulate the immune system.
A new modality for the treatment of immunological disorders arose from the discovery of 1 (FTY720, Fingolimod).4 This compound, which is a sphingosine (2) analogue, modulates the immune system by a unique mechanism, i.e., disruption of normal lymphocyte trafficking. Specifically, 1 inhibits egress of lymphocytes from secondary lymphoid tissues, such as lymph nodes;5 the biomarker of 1 is thus lymphopenia (abnormally low numbers of circulating lymphocytes). Preventing effector lymphocytes from traveling to sites of inflammation might underlie the efficacy of 1 in prolonging allograft survival and in autoimmune disease models. Compound 1 has completed a phase-III human renal transplantation trial, and phase-III trials for relapsing-remitting multiple sclerosis (MS) are underway currently.
Compound 1 is a prodrug; it enters cells and invades the sphingolipid catabolic pathway, proceeding through cycles of phosphorylation and dephosphorylation.6 In vivo phosphorylation of 1 by Sphk2a produces the S-phosphate species 1-P specifically,7 which mimics much of S1P’s (2-P in Chart 1 is an important extracellular lipid mediator) biological behavior. Compound 2-P signals cells via five GPCRs: S1P1–5 (formerly, EDG1, EDG5, EDG3, EDG6, and EDG8).8 Compound 1-P is an agonist at four of the five receptors: S1P1, S1P3, S1P4, and S1P5. The physiological activities of the S1P family of receptors are currently under intense investigation through both genetic and chemical biological approaches. Current evidence documents that in vivo activation of the S1P1 receptor by agonists (e.g., 2-P and 1-P) induces lymphopenia, but the precise mechanism is disputed.9–11 Thus, 1 occupies an interesting chemical space; it is a substrate for phosphorylation by Sphk2, avoids the phosphatase activities relative to 2-P, and interacts with a subset of S1P receptors, including those necessary for lymphopenia.
An adverse event associated with 1-P administration is bradycardia; in rodents and perhaps other mammalian species, this response is mapped to the S1P3 receptor.12 Activation of the S1P3 receptor is also suspected to cause pulmonary leakage.13 Thus, S1P3 receptor activity may limit the usefulness of 1 as a therapeutic agent.
The study reported herein was undertaken in efforts to define further the molecular pharmacology of the S1P receptor family and 2-P’s activating (Sphks) and inactivating (phosphatases) enzymes. Using 1 as a template, we sought to restrict the conformations of the three bonds that “link” the (hydroxymethyl)amino-substituted carbon “head group” and the octylphenyl “tail group” (see 1 in Chart 1). Our initial efforts focused on two-dimensional or planar “linker” groups to restrict conformations.14 Subsequent studies have restricted the sp3 hybridized “linker” backbone of the parent molecule through ring formation. These studies led to the identification of 3 (VPC0109115), which evokes a profound, long lasting lymphopenia in rodents without a reduction in heart rate (data not shown). However, our lead compound 3 was a mixture of four stereoisomers. To elucidate the structure–activity relationships (SARs) of the stereoisomers, it was necessary to isolate and identify the active isomer(s) from the 4-component mixture (3a–3d). This work presents the activities of each of the four stereoisomers and selective asymmetric syntheses of the isomers active in vivo.
Asymmetric synthesis (Scheme 1) began with a modified Kumada cross-coupling of 2-chloropropenol 4 to (p-octyl)phenyl magnesium bromide to produce hydroxymethyl styrene 5,16 which was subsequently transformed into the corresponding iodide 6 in two steps. The C-1 chiral center was generated by alkylation of 4-pentenoic oxazolidinone using the Evans’ chiral auxiliary technology.17 Cyclization using a second-generation Grubbs’ catalyst furnished the cyclopentene ring with the retention of stereochemistry at the hydroxymethyl-bearing carbon, and reductive removal of the chiral auxiliary gave the first key intermediate, 1-(4′-Octyl)phenyl-4(S)-hydromethyl cyclopent-1-ene (9).
We intended to use the hydroxymethyl group to direct reduction selectively to each face of the cyclopentene, thereby inducing chirality at the phenyl-bearing carbon. The Crabtree catalyst efficiently hydrogenated the alkene from the same face of alcohol, producing the S stereochemistry of the octylphenyl group (see 10). However, generation of the R stereochemistry was more challenging. Little stereoselectivity was obtained with most common heterogeneous catalysts, and many homogeneous catalysts were unreactive, for example, Pfaltz’s catalyst.18 Only after installation of the bulky TIPS group on the alcohol could hydrogenation on the opposite face of the hydroxymethyl group be effective with acceptable selectivity (see 9–12).
The critical transformation in the syntheses was the rhodium-catalyzed C–H bond amination developed by Du Bois (Scheme 2).19 After transforming the 1(S)-hydroxymethyl-3-octylphenyl alcohol 13 (13 represents either 10 or 12) to carbamate 14, the carbamate amine inserted into the tertiary C–H bond on the cyclopentyl ring via a rhodium-mediated nitrene mechanism with retained stereochemistry to give oxazolidinone 15. Introduction of the Boc group on the oxazolidinone nitrogen facilitated the hydrolysis of carbamate to the N-Boc diastereomers 16.20 After removal of the N-Boc group with triflouroacetic acid, the final products 3a and 3c could be obtained as their hydrochloride salts. For in vitro receptor assays, we treated 3 with PPA to transform the alcohol into phosphates 3-P. Ultimately, this was found to work equally well on both diastereomers 10 and 12.
To confirm the validity of this synthesis, we compared the stereoselectively synthetic isomers with racemic 3 by chiral chromatography (Figure 1) and nuclear magnetic resonance (NMR). The asymmetrically synthesized 3a and 3c proved to be the first and third eluent, respectively.
We phosphorylated the four isomers of 3 obtained either by chiral chromatography or by our asymmetric synthetic routes. Because of the greater degree of purity of the synthetic material, we present the data obtained from that set of phosphorylated compounds. In a broken-cell assay of ligand efficacy and potency, both 3a-P and 3c-P proved to be partial agonists at the S1P1 receptor, with potency comparable to 2-P (Figure 2a). Interestingly, their respective enantiomers, 3d-P and 3b-P exhibited minimal, if any, agonist activity at the S1P1 receptor. Conversely, all four isomers lack agonist activity at the S1P3 receptor. Because 3a-P (derived from the parent alcohol-isolated chiral chromatography) showed inverse agonism (i.e., negative efficacy) at the S1P3 receptor (not shown), we collided each of the phosphorylated synthetic isomers with 2-P at the S1P3 receptor. As documented in Figure 2b, 3a-P, 3b-P, and 3d-P but not 3c-P behaved as surmountable antagonists at the S1P3 receptor. We did not test the individual phosphorylated synthetic isomers at the S1P2, S1P4, or S1P5 receptors, but the racemate, 3-P, is inactive at S1P2, a full agonist at S1P4, and a partial agonist at S1P5 (not shown).
Compounds 3a and 3c but not 3b or 3d were substrates of recombinant Sphk2 (Figure 3). None of the isomers is either a substrate for or an inhibitor of Sphk1.
From reference to 1, we expect that 3 is also a prodrug, i.e., requiring phosphorylation to achieve activity (indeed, 3 is not active in a Sphk2 null mouse22). To test the hypothesis that only the Sphk2 substrates 3a and 3c evoke lymphopenia, each of the isomers was introduced into mice by oral gavage. After a single dose (1 mg/kg body weight), both 3a and 3c evoked lymphopenia and maintained a low level of circulating lymphocytes for at least 48 h after dosing (Figure 4). Interestingly, 8 days after dosing, the mice receiving 3c remained lymphopenic, while the blood lymphocyte counts in the 3a-treated mice had returned to normal. As expected from the in vitro activity profiles at both the kinase and the S1P1 receptor, neither 3b nor 3d evoked lymphopenia (not shown).
Understanding the molecular pharmacology of the S1P receptors is evolving rapidly. Although an increasing number of compounds have been developed to study these receptors,14,23 additional molecules of varying behavior will be necessary to fully elucidate the pharmacology of these new targets. Here, we report the asymmetric syntheses of two compounds that are S1P1 agonists, but one is an S1P3 antagonist; a profile heretofore unreported. Although both diastereomers are prodrugs, are analogous to 1, and have similar kinase and receptor profiles, they exhibit very different duration in vivo. Thus, these compounds may have significant utility in further parsing out the roles that these receptors play in normal and pathologic physiology.
These compounds (3a and 3c) were designed as conformationally restricted analogues of 1, and analysis of the limited conformational space of each diastereomer is facilitating the definition of the binding site for the S1P1 and S1P3 receptors. The compounds also have three preferred properties of 1-like prodrugs: first, the potency and efficacy at S1P1 is retained; second, the new analogues are substrates for either Sphk1 or Sphk2 (or possibly other lipid kinases); and third, the activity at the S1P3 receptor is minimized.
Because of their highly hydrophobic structures, it was challenging to isolate the four isomers in quantities sufficient for broad biological evaluation. Milligram scale pure isomers could be isolated through high-performance liquid chromatography (HPLC) on chiral columns, and a preliminary assay of these four isomers suggested that 3a and 3c are the two active species in vivo (named in order of the chiral HPLC eluting sequence). These two compounds proved to be diastereomers (at the C-3 position) instead of enantiomers (as assessed by optical rotation and NMR spectroscopy).
To establish definitively the stereochemistry of 3a and 3c, we chemically synthesized the two isomers through a short sequence involving an intramolecular nitrene C–H insertion. It was suspected that the active species would have the R stereocenter at the quaternary amino-bearing carbon,7,14a,24 and thus, our synthesis was designed with that stereochemical outcome anticipated. The stereochemical configuration of the benzylic carbon remained undefined until this work was done. Using several established asymmetric synthesis methods, we constructed the two stereocenters predicted for 3a with high selectivity and 3c with > 85% optical purity (with ~15% 3a).
The pharmacological profiles of the isomers are different in important ways, particularly in vivo. As determined using the GTP[γ-35S] binding assay, compound 3c was slightly more efficacious than 3a. The greater efficacy of 3c is perhaps reflected in the lower lymphocyte counts in 3c- versus 3a-treated mice at 24 and 48 h. However, 3c is also a somewhat better substrate at mouse Sphk2; this may further enhance the lymphopenic effect of 3c. In contrast, there was no indication from in vitro analysis that the 3a/3c enantiomers would differ greatly in their duration of action. It will be interesting to learn whether the pharmacokinetic profile of these compounds parallels this pharmacodynamic property.
Perhaps the most salient property of compound 3a-P is the antagonism at the S1P3 receptor. The lead compound in this class, 1, is a potent S1P3 agonist. In rodents, agonist activity at the S1P3 receptor is associated with toxicities.12,13 If this is true in humans also, the more selective 3-type compounds might be superior because of reduced toxicity. Finally, 3a-P is 1 log order more potent than previously reported S1P3 antagonists.25 However, we do not know at present whether antagonism at the S1P3 receptor would have any therapeutic benefit.
We asymmetrically synthesized all of the four stereoisomers of a 4-component immunomodulatory S1P prodrug. Two of the isomers, 3a and 3c, are substrates for Sphk2 and, following phosphorylation, are potent partial agonists at the S1P1 receptor. Further, one isomer is the most potent S1P3 antagonist reported to date. The unique biological properties of 3 make it a useful chemical tool for the study of S1P signaling.
All chemicals and solvents were purchased from Aldrich or Fisher unless specified; anhydrous solvents and amine bases were used without further distillation. All reactions were performed under inert gas protection in oven-dried reaction vessels unless specified. Analytical thin-layer chromatography (TLC) was carried out on a Merck silica gel 60F254 aluminum-based plate, and preparative TLC separation was performed on Analtech 02013 (1000 μm) or a similar plate with a varied thickness of coating. UV absorption was detected at 254 nm. All NMR raw data were collected on a Varian Mercury Plus or Unity Inova 300 MHz (75 MHz carbon) and processed by MestReC 126.96.36.199 with the default setting. Optical rotation was obtained on a Perkin-Elmer 343 plus polarimeter. Low-resolution mass spectrometry (MS) [electrospray ionization (ESI)] were recorded on ThermoFinnigan LCQ, and high-resolution MS (ESI-TOF) analysis was performed by the University of Illinois MS laboratory. Elemental analysis was performed by the Atlantic Micro Laboratory. Chiral HPLC separations were obtained from a Chiralpak AD 4.6 mm i.d. × 250 mm column using isocratic conditions with 95% A and 5% B at a flow rate of 0.8 mL/min and monitoring at a wavelength of 254 nm or with an evaporative light scattering detector (ELSD). The column was maintained at 35 °C using a column heater. Mobile phase A was heptane with a 0.2% diethylamine modifier. Mobile phase B was 50:50 methanol/ethanol with a 0.2% diethylamine modifier.
In a 250 mL round-bottom flask, 24 mmol (0.576 g) of magnesium turnings and 20 mmol (5.36 g) of p-octylbromobenzene (TCI Chemicals) in 80 mL of dry tetrahydrofuran (THF) were refluxed for 1 h. In another 100 mL flask, 16 mmol (1.472 g) of 2-chloro-2-propen-1-ol (4, 90% tech grade) in 40 mL of dry THF was cooled to 0 °C and 17 mmol (6.8 mL) of 2.5 M n-butyl lithium (in hexane) was added dropwise. After 10 min, the deprotonated chloride was syringed into the flask containing the Grignard reagent. After the addition of 1 mmol (0.542 g) NiDPPPCl2, the reaction mixture was refluxed for 3 h. After removal of the solvent, the mixture was partitioned between half-saturated NH4Cl solution (25 mL) and CH2Cl2 (25 mL × 2). The combined organic solution was dried over NaSO4, concentrated, and columned with CH2Cl2 (Rf = 0.25). A total of 2.51 g (10.2 mmol, 71%) of white solid was collected. 1H NMR (300 MHz, CDCl3) δ: 7.50–7.08 (m, 4H), 5.46 (s, 1H), 5.31 (m, 1H), 4.54 (d, J = 5.66 Hz, 1H), 2.62 (app t, J = 8.00 Hz 2H), 1.61 (m, 1H), 1.31 (m, 10H), 0.90 (t, J = 6.69 Hz, 3H). 13C NMR (75 MHz, CDCl3) δ: 147.3, 143.2, 135.9, 128.8, 126.1, 112.1, 65.3, 35.9, 32.2, 31.7, 29.8, 29.6, 29.5, 22.9, 14.4.
A total of 9.55 mmol (2.35 g) of 5 in 40 mL of dry CH2Cl2 was reacted with 10 mmol (1.34 g) of MsCl and 11 mmol (1.11 g) of TEA at 0 °C for 1 h. After removal of the solvent and excess reagents, the mixture was suspended in 30 mL of acetone and filtered through a Celite pad. After another two washes, 10 mmol (1.50 g) of NaI was added to the combined filtrate and stirred overnight. Removal of the solvent was followed by hexane washes (30 mL × 3). When the filtrate was concentrated, 3.00 g (85%) of light brown oil was collected and used for the next step without further purification. 1H NMR (300 MHz, CDCl3) δ: 7.52–7.20 (m, 4H), 5.50 (s, 1H), 5.48 (s, 1H), 4.33 (s, 2H), 2.63 (app t, J = 7.52 Hz 2H), 1.64 (m, 2H), 1.36 (m, 10H), 0.90 (t, J = 6.71 Hz, 3H). 13C NMR (75 MHz, CDCl3) δ: 145.5, 143.5, 135.2, 128.8, 126.1, 115.1, 35.9, 32.1, 31.6, 29.7, 29.6, 29.5, 22.9, 14.4, 7.6.
A total of 9 mmol (2.33 g) of (R)-4-benzyl-3-pent-4-enoyloxazolidin-2-one in 60 mL of dry THF was cooled to −78°C, and 9 mmol (9 mL) of 1 N NaHMDS (in THF) was added slowly. After 30 min, 9 mmol (3.18 g) of 6 was added dropwisely through a synringe. The reaction was maintained at −78°C for 1.5 h, then warmed up to 0 °C, and quenched with half-saturated NH4Cl solution. After removal of THF, the residue was patitioned between NH4Cl solution (25 mL) and CH2Cl2 (25 mL × 2). The combined organic layer was dried over NaSO4 and concentrated. Flash column eluting with 10% EtOAc in hexanes (Rf = 0.35) gave 3.5 g (7.2 mmol, 80%) of clear oil. 1H NMR (300 MHz, CDCl3) δ: 7.50–6.97 (m, 9H), 5.91–5.62 (m, 1H), 5.33 (d, J = 1.04 Hz, 1H), 5.20–4.92 (m, 3H), 4.61 (m, 1H), 4.13 (m, 3H), 3.25–2.90 (m, 2H), 2.73 (m, 1H), 2.57 (m, 3H), 2.41 (m, 1H), 2.33 (m, 1H), 1.58 (m, 1H), 1.27 (s, 10H), 0.89 (t, J = 6.69 Hz, 3H). 13C NMR (75 MHz, CDCl3) δ: 175.6, 153.2, 145.9, 142.7, 138.2, 135.7, 135.4, 129.6, 129.1, 128.6, 127.5, 126.4, 117.5, 114.0, 66.1, 55.6, 41.7, 38.1, 37.2, 37.0, 35.8, 32.1, 31.6, 29.7, 29.6, 29.5, 22.9, 14.3.
A total of 3.5 g (11.2 mmol) of 7 was refluxed in 40 mL of CH2Cl2 with 20 mg of second-generation Grubbs catalyst for 2 h. Flash column with 10% EtOAc in hexanes (Rf = 0.3) gave 2.70 g (9.5 mmol, 85%) of clear oil. 1H NMR (300 MHz, CDCl3) δ: 7.55–6.93 (m, 9H), 6.08 (m, 1H), 4.72 (m, 1H), 4.41 (m, 1H), 4.33–4.10 (m, 2H), 3.32 (dd, J = 13.35, 3.12 Hz, 1H), 3.23 (m, 1H), 3.16–3.03 (m, 1H), 2.98–2.89 (m, 2H), 2.82 (dd, J = 13.34, 9.61 Hz, 1H), 2.62 (t, J = 7.66 Hz, 2H), 1.62 (m, 2H), 1.32 (m, 10H), 0.91 (t, J = 6.67 Hz, 3H). 13C NMR (75 MHz, CDCl3) δ: 175.7, 153.4, 142.4, 140.4, 135.6, 133.5, 129.7, 129.2, 128.6, 127.6, 125.8, 122.8, 66.4, 55.7, 41.8, 38.1, 37.3, 36.6, 35.9, 32.2, 31.7, 29.8, 29.6, 29.5, 22.9, 14.4.
A total of 3.4 mmol (1.55 g) of 8 and 3.5 mmol (0.11 g) of MeOH were dissolved in 40 mL of THF, and 7 mmol (3.5 mL) of 2 M LiBH4 in THF was added at 0°C. After 1 h of the reaction at 0°C, the mixture was concentrated and partitioned between water and CH2Cl2 (25 mL/25 mL × 2). The combined organic layer was dried over NaSO4 and concentrated. Flash column eluting with CH2Cl2 (Rf = 0.2) gave 0.61 g (2.1 mmol, 63%) of white flakes (recrystallized from hexanes). 1H NMR (300 MHz, CDCl3) δ: 7.36 (d, J = 8.13 Hz, 2H), 7.14 (d, J = 8.13 Hz, 2H), 6.17–5.99 (m, 1H), 3.64 (d, J = 6.63 Hz, 2H), 2.96–2.81 (m, 1H), 2.69 (m, 2H), 2.63–2.57 (m, 2H), 2.52 (m, 1H), 2.32 (m, 1H), 1.62 (m, 3H), 1.43–1.17 (m, 10H), 0.90 (t, J = 6.71 Hz, 3H). 13C NMR (75 MHz, CDCl3) δ: 142.1, 141.3, 134.1, 128.6, 125.6, 123.8, 67.5, 39.9, 36.5, 35.9, 32.1, 31.7, 29.7, 29.6, 29.5, 22.9, 14.4.
A total of 0.20 g of 9 and 5 mg of Crabtree catalyst (Strem) were dissolved in 50 mL of dry CH2Cl2 in an oven-dried 100 mL flask under nitrogen protection. The mixture reacted under a hydrogen balloon for 1 day. After removal of the solvent, the product was used for the next step without purification. 1H NMR (300 MHz, CDCl3) δ: 7.15 (q, J = 8.17 Hz, 4H), 3.58 (d, J = 7.02 Hz, 2H), 3.17–2.98 (m, 1H), 2.66–2.52 (app t, J = 7.55 Hz, 2H), 2.48–2.30 (m, 1H), 2.21–1.54 (m, 8H), 1.47–1.19 (m, 10H), 0.91 (t, J = 6.66 Hz, 3H). 13C NMR (75 MHz, CDCl3) δ: 143.2, 140.7, 128.5, 127.1, 67.7, 44.5, 41.5, 37.1, 35.8, 35.0, 32.2, 31.9, 29.8, 29.7, 29.6, 29.6, 23.0, 14.4.
A total of 1.33 mmol (0.380 g) of 9, 1.6 mmol (0.307 g) of TIPSCl, and 2.0 mmol (0.136 g) of imidazole were dissolved in 15 mL of CH2Cl2 and reacted overnight. Upon removal of the solvent, the mixture was suspended in 20 mL of hexane and filtered through a Celite pad. The filtrate was concentrated and redissolved in 50 mL of EtOAc; this solution was hydrogenated under a H2 balloon overnight with Pd/C (10%, wt). When strong UV absorption disappeared on TLC, the Pd/C was filtered off followed by removal of EtOAc. The mixture was deprotected with 4 mmol (1.046 g) of TBAF in 40 mL of THF overnight. After removal of most of the solvent, the mixture was separated on a 1000 μm preparative TLC (or a small column) with CH2Cl2 (Rf = 0.2). A total of 0.285 g (9.9 mmol, 75%) of clear oil was collected. 1H NMR (300 MHz, CDCl3) δ: 7.24–7.08 (m, 4H), 3.61 (dd, J = 6.58, 1.51 Hz, 2H), 3.06 (m, 1H), 2.59 (app t, J = 7.58 Hz, 3H), 2.41–1.81 (m, 6H), 1.75–1.51 (m, 4H), 1.45–1.21 (m, 10H), 0.91 (t, J = 6.85 Hz, 3H). 13C NMR (75 MHz, CDCl3) δ: 142.8, 140.7, 128.5, 127.1, 67.7, 45.8, 42.2, 38.5, 35.8, 33.6, 32.2, 31.9, 29.8, 29.7, 29.6, 28.6, 23.0, 14.4.
A total of 0.42 mmol (0.120 g) of 10 was dissolved in 15 mL of dry CH2Cl2, and 0.50 mmol (0.094 g) of Cl3CC(O)NCO was added at 0°C. After about 0.5–1 h (track by TLC in CH2Cl2), the solvent was removed and the mixture was redissolved in 10 mL of MeOH and 1 mL of H2O. A total of 0.5 g of K2CO3 was added and reacted for 5 h. Upon removal of most solvents, the residue was loaded on preparative TLC and developed in CH2Cl2 (just above the starting point, weak UV absorption). A total of 0.130 g (3.9 mmol, 93%) of white solid was collected. 1H NMR (300 MHz, CDCl3) δ: 7.22–7.04 (m, 4H), 5.05 (b, 2 H), 4.08–3.96 (m, 2H), 3.18–3.00 (m, 1H), 2.59 (app t, J = 7.76 Hz, 2H), 2.54–2.42 (m, 1H), 2.19–1.54 (m, 8H), 1.48–1.16 (m, 10H), 0.91 (t, J = 7.47 Hz, 3H). 13C NMR (75 MHz, CDCl3) δ: 157.8, 143.0, 140.7, 128.6, 127.1, 69.4, 44.3, 38.2, 37.3, 35.8, 34.9, 32.2, 31.9, 29.8, 29.7, 29.6, 23.0, 14.4.
This compound was prepared in a manner similar to 14a (88%). 1H NMR (300 MHz, CDCl3) δ: 7.13 (q, J = 8.20 Hz, 4H), 4.87 (b, 1H), 4.03 (m, 2H), 3.14–2.96 (m, 1H), 2.58 (app t, J = 7.75 Hz, 2H), 2.40 (m, 1H), 2.24 (m, 1H), 2.15–2.02 (m, 1H), 1.98–1.51 (m, 6H), 1.46–1.15 (m, 10H), 0.89 (t, J = 6.63 Hz, 3H). 13C NMR (75 MHz, CDCl3) δ: 157.6, 142.6, 140.8, 128.5, 127.1, 69.5, 45.7, 38.8, 38.6, 35.8, 33.5, 32.2, 31.9, 29.8, 29.7, 29.5, 28.7, 22.9, 14.4.
15a. A total of 0.78 mmol (0.26 g) of 14a, 1.10 mmol (0.354 g) of BAIB, 1.79 mmol (0.072 g) of MgO, and 0.039 mmol (0.017 g) of [Rh(CH3COO)2]2 · 2H2O were refluxed in 10 mL of CH2Cl2 for 14 h. The reaction mixture was TLC-separated in acetone/CHCl3 (5:95, v/v, Rf = 0.3, weak UV). A total of 0.14 g (0.44 mmol, 57%) of white solid was collected. 1H NMR (300 MHz, CDCl3) δ: 7.13 (m, 1H), 6.64 (s, 1H), 4.29 (dd, J = 17.60, 8.40 Hz, 2H), 3.01 (m, 1H), 2.62–2.47 (app t, J = 7.75 Hz, 2H), 2.29 (dd, J = 13.23, 6.98 Hz, 1H), 2.20–2.03 (m, 3H), 2.03–1.73 (m, 3H), 1.59 (m, 2H), 1.40–1.16 (m, 10H), 0.88 (t, J = 6.70 Hz, 3H). 13C NMR (75 MHz, CDCl3) δ: 159.6, 141.4, 140.8, 128.8, 126., 65.0, 47.2, 43.3, 38.7, 35.8, 32.4, 32.1, 31.8, 29.7, 29.6, 29.5, 22.9, 14.4.
15c. This compound was prepared in a manner similar to 15a (66%). 1H NMR (300 MHz, CDCl3) δ: 7.19–7.06 (m, 4H), 4.32 (q, J = 8.50 Hz, 2H), 3.38–3.15 (m, 0.86H), 3.11–2.92 (m, 0.14H), 2.63–2.50 (app t, J = 7.75 Hz, 2H), 2.38 (dd, J = 13.51, 7.49 Hz, 1H), 2.31–1.94 (m, 4H), 1.88–1.65 (m, 2H), 1.59 (m, 2H), 1.28 (m, 10H), 0.88 (t, J = 6.62 Hz, 3H). 13C NMR (75 MHz, CDCl3) δ: 159.9, 141.3, 141.2, 128.7, 126.9, 65.4, 47.3, 43.5, 39.7, 35.8, 32.6, 32.1, 31.8, 29.7, 29.6, 29.5, 22.9, 14.4.
A total of 0.14 mmol (46 mg) of 15a, 0.2 mmol (44 mg) of Boc2O, 0.3 mmol (30 mg) of triethylamine, and a catalytic amount of DMAP were reacted in 5 mL of CH2Cl2 for 4 h. After removal of the solvent, the mixture was redissolved in 5 mL of MeOH and 2 drops of water and 0.1 g of K2CO3 was added and reacted overnight. The reaction mixture was then TLC-purified in acetone/CHCl3 (5:95, v/v, Rf = 0.3, weak UV). A total of 42 mg (0.1 mmol, 74%) of product was collected. 1H NMR (300 MHz, CDCl3) δ: 7.18–7.07 (m, 4H), 4.93 (s, 1H), 3.72 (q, J = 11.27 Hz, 1H), 3.08 (m, 1H), 2.57 (app t, J = 7.75 Hz, 1H), 2.46 (dd, J = 13.29, 7.55 Hz, 1H), 2.16–2.03 (m, 1H), 2.00–1.80 (m, 3H), 1.73 (dd, J = 13.16, 11.13 Hz, 1H), 1.59 (m, 2H), 1.45 (s, 9H), 1.38–1.18 (m, 10H), 0.88 (t, J = 6.74 Hz, 3H). 13C NMR (75 MHz, CDCl3) δ: 156.6, 141.8, 141.0, 128.6, 127.1, 80.2, 69.4, 65.0, 44.4, 44.0, 43.3, 35.9, 35.8, 32.9, 32.1, 31.8, 29.7, 29.6, 29.5, 22.9, 14.4.
This compound was prepared in a manner similar to 16a (78%). 1H NMR (300 MHz, CDCl3) δ: 7.13 (m, 4H), 4.89 (s, 1H), 3.73 (dd, J = 23.07, 11.08 Hz, 2H), 3.30 (m, 0.86H), 3.13–3.01 (m, trace amount), 2.57 (app t, J = 7.77 Hz, 1H), 2.29 (m, 1H), 2.23–2.03 (m, 2H), 1.78 m, 3H), 1.58 (m, 2H), 1.53–1.38 (m, 9H), 1.28 (m, 10H), 0.88 (t, J = 6.69 Hz, 3H). 13C NMR (75 MHz, CDCl3) δ: 156.5, 141.7, 141.0, 128.6, 127.1, 80.1, 69.9, 65.1, 43.8, 39.7, 36.4, 35.8, 33.3, 32.1, 31.8, 29.7, 29.6, 29.5, 28.7, 22.9, 14.4.
A total of 100 mg (0.25mmol) of 16a was stirred in 5 mL of CH2Cl2 and 1.5 mL of TFA at 0°C for 1 h; after quenching with 5 mL of methanol and evaporation of excess reagents, the product was partitioned between CH2Cl2 and 1 N NaOH (10 mL/10 mL × 3). The combined organic layer was dried over Na2SO4 and concentrated to 15 mL; this solution was treated with 1 drop of concentrated hydrochloric acid, and a fine needle product precipitated within minutes. A total of 73 mg (0.22 mmol, 88%) of HCl salt was collected. NMR, elemental analysis, and rotation was performed on the free amine form of the product. 1H NMR (300 MHz, CDCl3) δ: 7.14 (dd, J = 17.60, 8.04 Hz, 4H), 3.46 (m, 2H), 3.06 (m, 1H), 2.65–2.49 (m, 2H), 2.28 (m, 4H), 2.14–2.00 (m, 1H), 1.90 (m, 1H), 1.70 (m, 2H), 1.65–1.55 (m, 2H), 1.50 (m, 1H), 1.29 (m, 10H), 0.88 (t, J = 6.33 Hz, 3H). 13C NMR (75 MHz, CDCl3) δ: 142.2, 140.9, 128.6, 127.0, 70.2, 62.3, 46.5, 44.8, 38.6, 35.8, 33.3, 32.1, 31.8, 29.7, 29.7, 29.5, 22.9, 14.4. HRMS (ESI+) (m/z): calcd for C20H34NO (MH+), 304.2640; found, 304.2641. Anal. Calcd for C20H33NO: C, 79.15; H, 10.96; N, 4.62. Found: C, 78.86; H, 11.01; N, 4.60. (c 1.05, CHCl3).
This compound was prepared in a manner similar to 3a (67%). 1H NMR (300 MHz, CDCl3) δ: 7.13 (m, 4H), 3.46 (s, 2H), 3.40–3.21 (m, 0.85H), 3.09–2.97 (m, 0.15H), 2.54 (m, 2H), 2.11 (m, 4H), 2.04–1.83 (m, 2H), 1.78–1.64 (m, 2H), 1.58 (m, 4H), 1.27 (m, 10H), 0.88 (t, J = 8.27 Hz, 3H). 13C NMR (75 MHz, CDCl3) δ: 142.2, 141.0, 128.6, 127.0, 70.9, 62.4, 46.9, 43.8, 37.9, 35.8, 33.7, 32.1, 31.8, 29.7, 29.6, 29.5, 22.9, 14.4. HRMS (ESI+) (m/z): calcd for C20H34NO (MH+), 304.2640; found, 304.2641.
A total of 10.0 mg (0.03 mmol) of 3a was vigorously stirred in ~2 mL of freshly prepared pyrophosphoric acid (PPA) at 100 °C for 2 h. Upon cooling, ~9 mL of ice was added to the reaction mixture and the product precipitated as a white solid. The product was collected on a Buchner funnel, further washed by water (8 mL × 2), and then vaccuum-dried. A total of 6.3 mg (0.016 mmol, 56%) of white solid was collected. 1H NMR (300 MHz, CD3OD) δ: 7.27–7.12 (m, 4H), 4.04–3.86 (app q, J = 5.62 Hz, 1H), 2.94–2.72 (b, 2H), 2.66–2.57 (m, 2H), 2.57–2.48 (m, 1H), 2.23–2.13 (m, 1H), 2.13–1.89 (m, 2H), 1.82–1.69 (m, 1H), 1.68–1.55 (m, 2H), 1.33 (m, 10H), 0.93 (t, J = 6.60 Hz, 1H). HRMS (ESI+) (m/z): calcd for C20H35NO4P (MH+), 384.2304; found, 384.2305.
A total of 10.0 mg (0.03 mmol) of 3c was treated similarly to PPA as 3a. After hydrolysis, the gummy product was briefly centrifuged; after removal of phosphoric acid, the product was further washed and centrifuged in water (8 mL × 2). A total of 5.5 mg (0.014 mmol, 50%) of white solid was collected. 1H NMR (300 MHz, CD3OD) δ: 7.18 (m, 4H), 4.21–4.07 (m, 1H), 4.05–3.92 (m, 1H), 2.60 (app t, J = 7.65 Hz, 2H), 2.39–2.14 (m, 3H), 2.07–1.75 (m, 3H), 1.62 (m, 2H), 1.43–1.26 (m, 10H), 0.93 (t, J = 6.65 Hz, 3H). HRMS (ESI+) (m/z): calcd for C20H35NO4P (MH+), 384.2304; found, 384.2311.
A plasmid encoding the human S1P1 receptor was introduced into CHO K1 cells by DNA-mediated transfection, and a clonal line expressing high levels of the receptor was isolated. Crude membrane fractions from these cells containing ca. 5 μg of protein were incubated in 0.1 mL of binding buffer [50 mM N-2-hydroxyethylpiperazine-N′-2-ethane-sulfonic acid (HEPES), 100 mM NaCl, and 10 mM MgCl2 at pH 7.5] containing 5 μg of saponin, 0.10 mM GDP, 0.1 nM [γ-35S]GTP (1200 Ci/mmol), and the indicated compounds for 30 min at 30°C. Membranes were collected on GF/C filters using a Brandel Cell Harvester (Gaithersburg, MD), and samples were analyzed for bound radionuclide using a TopCount β scintillation counter. Each of the eight points on a concentration effect curve were determined in triplicate and are presented as standard errors of the mean.
A plasmid encoding the human S1P3 receptor containing an amino-terminal HA epitope tag was introduced into CHO K1 cells by DNA-mediated transfection, and a clonal line expressing high levels of the receptor was isolated using a fluorescence-activated cell sorter. Cells were plated on a clear bottom, black wall 96-well plate; the cell monolayers were grown to confluence, washed, and loaded with a calcium-sensitive fluorescent dye; and calcium transients in response to compound addition were monitored using a Molecular Devices FLEXStation. Each of the eight points on a concentration effect curve were determined in triplicate and are presented as standard errors of the mean.
Mouse Sphk2 was expressed by the introduction of plasmid DNA into HEK293T cells. Sphk2 activity was measured in a solution that consisted of 20 mM Tris-Cl (pH 7.4), 1 mM 2-mercaptoethanol, 1 mM ethylenediaminetetraacetic acid (EDTA), 5 mM sodium orthovanadate, 40 mM β-glycerophosphate, 15 mM NaF, 1 mM phenylmethylsulfonyl fluoride, 10 mM MgCl2, 0.5 mM 4-deoxypyridoxine, 10% glycerol, and 0.01 mg/mL each of leupeptin, aprotinin, and soybean trypsin inhibitor. To determine the fractional activity of Sphk1 versus Sphk2, the buffer was supplemented with either 0.5% Triton X-100 or 1 M KCl, respectively. The buffer was supplemented with substrate (D-erythro-sphingosine, 15 μM; 3a–3d, 50 μM), [γ32P]ATP (10 μM, specific activity = 8.3 Ci/mmol), and cell extract (0.02–0.03 mg of total protein). After 30 min at 37°C, the reaction mixture was extracted with 2 volumes of chloroform/methanol/HCl (100:200: 1), and the components in the organic phase were separated by normal-phase TLC using a 1-butanol/acetic acid/water (3:1:1) solvent system. Radiolabeled enzyme products were detected by autoradiography and identified by migration, relative to authentic standards. For quantification, the silica gel containing radiolabeled lipid was scraped into a scintillation vial and counted.
Mice were dosed by oral gavage with isomers of 3 (1 mg/kg), dissolved in 2% hydroxypropyl β-cyclo-dextrin. Peripheral blood was collected from the orbital sinus of lightly anesthetized mice, and total lymphocytes were counted using a Hemavet 950 blood analyzer (Drew Scientific, Oxford, CT).
This work was supported in part by a research grant from the NIH (R01 GM067958). We also thank the UIUC mass spec lab for HRMS (NSF DBI-0100085) and the Atlantic Micro Lab for elemental analysis.
aAbbreviations: S1P, sphingosine 1-phosphate; Sphk1, sphingosine 1-phosphate kinase type I; Sphk2, sphingosine 1-phosphate kinase type II; S1Pn, sphingosine 1-phosphate receptor subtype n (n = 1–5); GPCR, G-protein coupled receptor; EDG, endothelial differentiation gene; SAR, structure–activity relationship; PPA, pyrophosphoric acid.
Supporting Information Available: Proton and carbon NMR of new compounds. This material is available free of charge via the Internet at http://pubs.acs.org.