J. Org. Chem.

2000, 65, 445-449 445

Peloruside A: A Potent Cytotoxic Macrolide Isolated from the

New Zealand Marine Sponge Mycale sp.

Lyndon M. West and Peter T. Northcote*

School of Chemical and Physical Sciences, Victoria, University of Wellington, P.O. Box 600,
Wellington, New Zealand

Chris N. Battershill
National Institute of Water and Atmospheric Research (NIWA), Wellington, New Zealand

Received August 16, 1999

A novel, polyoxygenated, pyranose ring containing 16-membered macrolide peloruside A (1)

exhibiting cytotoxic activity in the nanomolar range was isolated from the New Zealand marine
sponge Mycale sp. The structure of 1 and relative stereochemistry of the 10 stereogenic centers
were determined on a 3 mg sample using a variety of spectroscopic methods. Compound 1 was
isolated along with the previously reported cytotoxins mycalamide A (2) and pateamine (3) from a
single specimen of this sponge.

Marine sponges of the genus Mycale (Carmia) are a

rich source of bioactive secondary metabolites of diverse
structures. The mycalisines1 and mycalolides2-4 are
examples isolated from members of this genus. In par-
ticular a Mycale species occurring in Otago Harbor on
the southeast coast of the South Island of New Zealand
was found to produce the antiviral and antitumor agents
mycalamides A (2) and B (4).5,6 In a subsequent study of
a population of the same species collected in Thompson
Sound, on the southwest coast of the South Island, the
cytotoxic macrolide pateamine (3) was isolated.7 The total
synthesis of pateamine has been recently reported along
with its interesting immunosuppressive properties.8 No
mycalamides were detected in the specimens collected
from Thompson Sound. Recently we have examined
specimens of the same species of Mycale collected from
Pelorus Sound on the north coast of the South Island.
NMR-guided isolation yielded the novel cytotoxic mac-
rolide peloruside A (1) together with mycalamide A (2)
and pateamine (3). Methanolic extracts of the sponge
were fractionated on polymeric reversed-phase chromato-
graphic material to yield 3.0 mg of peloruside A (1), 10.6
mg of mycalamide A (2), and 11.7 mg of pateamine (3).
The previously reported compounds were identified by
comparison of 1H and 13C NMR data to those published. presence of three oxymethyl groups (δH 3.48, δC 59.1; δH
The molecular formula of peloruside A was established 3.38, δC 55.7; δH 3.31, δC 56.1), a saturated ester or
as C27H48O11 from the observation of a parent ion in the lactone (δC 174.0; IR 1738 cm-1), and a trisubstituted
HRFABMS (571.308 26, [M + Na]+ ∆ -2.11 ppm) con- C-C double bond (δH 5.05, δC 131.1, δC 136.1) were
sistent with both the 13C and 1H NMR spectra. The evident from the IR and NMR spectra, suggesting the
possibility of a highly oxygenated macrolide.
(1) Kato, Y.; Fusetani, N.; Matsunaga, S.; Hashimoto, K. Tetrahe- Cross-peaks in a COSY spectrum established the
dron Lett. 1985, 26, 3483-3486.
(2) Fusetani, N.; Yasumuro, K.; Matsunaga, S.; Hashimoto, K.
connectivity between two oxygenated methines, C-2 (δH
Tetrahedron Lett. 1989, 30, 2809-2812. 4.53, δC 70.3), C-3 (δH 4.22, δC 78.3), and a methylene,
(3) Matsunaga, S.; Nogata, Y.; Fusetani, N. J. Nat. Prod. 1998, 61, C-4 (δH 2.13, 1.78; δC 32.6). Similarly, COSY cross-peaks
663-666.
(4) Matsunaga, S.; Sugawara, T.; Fusetani, N. J. Nat. Prod. 1998, revealed a linear system comprised of an oxymethine, C-5
61, 1164-1167. (δH 4.25, δC 63.5), a methylene, C-6 (δH 1.78, 1.53; δC
(5) Perry, N. B.; Blunt, J. W.; Munro, H. G. J. Am. Chem. Soc. 1988, 31.7), and two oxymethines, C-7 (δH 3.82, δC 75.9) and
110, 4850-4851.
(6) Perry, N. B.; Blunt, J. W.; Munro, H. G.; Thompson, A. M. J. C-8 (δH 4.02, δC 66.8). Three oxymethines, C-11 (δH 4.89,
Org. Chem. 1990, 55, 223-227. δC 73.9), C-13 (δH 3.99, δC 77.9), and C-15 (δH 5.68, δC
(7) Northcote, P. T.; Blunt, J. W.; Munro, H. G. Tetrahedron Lett. 70.9), together with two methylenes, C-12 (δH 2.07, 1.40;
1991, 32, 6411-6414.
(8) Romo, D.; Rzasa, R. M.; Shea, H. A.; Park, K.; Langenhan, S. δC 33.9) and C-14 (δH 2.15, 2.02, δC 35.7), were assigned
L.; Akhiezer, A.; Liu, J. O. J. Am. Chem. Soc. 1998, 120, 12237-12254. to a linear subunit from interpretation of COSY cross-
10.1021/jo991296y CCC: $19.00 © 2000 American Chemical Society
Published on Web 12/29/1999
446 J. Org. Chem., Vol. 65, No. 2, 2000 West et al.

peaks and a series of 1D TOCSY experiments. Con- correlation from H-15 to the carbonyl carbon C-1 estab-
nectivity between C-11 and C-12, and between C-14 and lished 1 as a 16-membered macrolide, leaving a single
C-15, was evident from COSY cross-peaks, but spectral ether linkage to be accounted for. Addition of H2O/D2O,
overlap of the C-12 and C-14 proton resonances made it 1:1 (50 µL), to a sample of 1 dissolved in CDCl3 (600 µL)
difficult to establish connectivity at C-13. Selective ir- caused observable splitting or broadening of the 13C
radiation of H-11 in a series of 1D TOCSY experiments resonances of C-8, C-9, and C-11, indicating hydroxyl
sequentially revealed proton resonances assigned to the attachment at these centers.9 A COSY correlation was
C-12 methylene, C-13 methine, and C-15 methine as the observed at -10 °C from the oxygenated methine proton
mixing time was increased from 20 to 80 ms. Similarly, at C-2 to a proton resonance at δ 6.75 that lacked a
selective irradiation of H-15 sequentially revealed the correlation to carbon in the HSQC experiment, establish-
H-14 methylene pair, H-13, the upfield C-12 methylene ing the R-hydroxyester functionality at C-1 and C-2.
resonance (δH 1.40), and H-11, clearly establishing the Oxygens at C-5, C-9, and C-24 remained as possible sites
linear sequence of this subunit. for an ether linkage. Chemical reasoning suggested a link
The remaining proton couplings evident in the COSY between C-5 and C-9 to form a stable six-membered cyclic
spectrum of 1 were assigned to a branched seven-carbon hemiketal ring. An analysis of 1H-1H coupling constants
subunit. A linear arrangement of an oxymethylene, C-24 and NOE enhancements observed for protons attached
(δH 3.64, 3.36; δC 66.9), methine, C-18 (δH 2.61, δC 43.3), to carbons C-5 through C-8 provided strong evidence for
methylene C-19 (δH 1.44, 1.17; δC 24.6) and a primary a six-membered ring in a chair conformation. An HMBC
methyl group, C-20 (δH 0.85, δC 12.2), was evident from correlation from H-5 to C-9 through the ether linkage
vicinal couplings. The H-18 methine resonance also was not observed in three separate experiments opti-
showed coupling to an olefinic proton resonance at C-17 mized for nJCH coupling constants of 4, 6, and 9 Hz. The
(δH 5.05, δC 131.1) of the trisubstituted C-C double bond. lack of HMBC correlations across a pyran(ose) ring has
Allylic coupling between this olefinic proton and the C-23 been reported and rationalized as caused by an unfavor-
methyl proton resonance evident in the COSY spectrum able dihedral angle.9
and a ROESY correlation established a cis relationship Chemical shift differences of methylene protons and
across the double bond of these two substituents. the presence of both large and small 1H-1H coupling
Long-range proton-carbon correlations from the oxy- constants at centers throughout the molecule which did
methyl protons to oxygenated methines at C-3, C-7, and not change with temperature provided evidence of a
C-13 observed in an HMBC experiment revealed the single predominant conformer.10 This suggested that a
attachment points of the three oxymethyl groups (OCH3- spectroscopic assignment of relative stereochemistry
3, δH 3.31; OCH3-7, δH 3.38; OCH3-13, δH 3.48). Further would be possible from a combination of NOE and vicinal
HMBC correlations provided supportive evidence for the coupling.11 NOE correlations were detected with ROESY
four subunits, and revealed their connectivity, along with and selective 1D GOESY12 experiments. Approximate
the remaining carbonyl, ketal, or hemiketal carbon, two 1H-1H coupling constants were determined for all but

tertiary methyl groups, and a quaternary carbon, in a five of the nonexchangeable proton resonances from an
contiguous carbon chain (C-1 to C-20). Correlations were analysis of 1H and HOMO2DJ experiments at 500 and
observed from the oxymethine protons at C-2 and C-3 to 300 MHz, and 1D TOCSY, 1D GOESY, and homonuclear
the carbonyl carbon C-1 (δC 174.0), establishing the decoupling at 300 MHz.
unusual R,β-dioxyester moiety. Connection between C-4 The resonance of one of the methylene protons attached
and C-5 was revealed by correlations from the upfield to C-6 appeared as a quartet of 12 Hz attributed to one
H-6 methylene resonance (δH 1.53) to C-5 and C-4, and geminal and two large vicinal couplings. H-5, H-6a, and
the downfield H-4 resonance (δH 2.13) to C-5 and C-6. H-7 could be assigned as axial on the basis of these H-6a
Selective excitation of H-7 (δH 3.81) in a series of 1D vicinal couplings of greater than 10 Hz, placing H-5 and
TOCSY experiments with increasing mixing times se- H-7 on the β side of the six-membered ring. NOEs
quentially revealed both C-6 methylene protons, H-5, and observed between H-5 and H-7 confirmed their 1-3
the downfield C-4 methylene proton (δH 2.13). diaxial arrangement. The oxygenated methine proton (H-
An HMBC correlation from the olefinic methyl protons 8) was assigned as equatorial on the basis of its small
of C-23 to the oxygenated methine C-15 established a link coupling to H-7 (3 Hz) and the observation of a W
between C-15 and the substituted olefinic carbon (C-16). coupling to the equatorial methylene proton at C-6 (δH
Weak COSY and 1D TOCSY correlations between H-17 1.78) in a COSY experiment optimized for long-range
and H-15 confirmed the allylic relationship of these two coupling.
protons. Both aliphatic tertiary methyl groups (C-21, δH An analysis of coupling constants and NOE enhance-
1.08, δC 15.8; C-22 δH 1.12, δC 20.8) showed proton ments revealed that C-3 and C-4 form an extended zigzag
correlations to the remaining quaternary carbon (C-10, chain with carbons C-5 to C-7 of the six-membered ring
δC 43.6) and to each other’s carbon resonance, which (Figure 1). A large vicinal coupling (11.5 Hz) between H-5
revealed the presence a gem-dimethyl moiety. Both gem- and H-4b established an antiperiplanar arrangement of
dimethyl proton resonances also correlated in the HMBC these two protons consistent with the observation of an
experiment to the C-9 ketal or hemiketal and the oxy- NOE enhancement observed between H-6a and H-4b. A
methine carbon at C-11 (δC 73.9), establishing the C-9 smaller coupling (4.5 Hz) and the presence of an NOE
to C-10 and C-10 to C-11 linkages. The final carbon-
carbon connectivity between C-8 and C-9 was supported
(9) Bauer, I.; Maranda, L.; Young, K. A.; Shimizu, Y. J. Org. Chem.
by an HMBC correlation observed between the H-8 and 1995, 60, 1084-1086.
C-9 resonances. (10) Kessler, H. Angew. Chem., Int. Ed. Engl. 1982, 21, 512-523.
With all carbon connectivities accounted for, the re- (11) Eberstadt, M.; Gemmecker, G.; Mierke, D. F.; Kessler, H.
Angew. Chem., Int. Ed. Engl. 1995, 34, 1671-1695.
maining two degrees of unsaturation of the molecular (12) Stonehouse, J.; Adell, P.; Keeler, J.; Shaka, A. J. J. Am. Chem.
formula required a bioxycyclic structure. An HMBC Soc. 1994, 116, 6037-6038.
Peloruside A from Marine Sponge Mycale sp. J. Org. Chem., Vol. 65, No. 2, 2000 447

of the macrolide ring from C-9 to C-13 with H-12b above

and H-12a below the plane and extending away from the
center. Small vicinal couplings (4.5 Hz, <1 Hz) and strong
NOE enhancements observed from H-13 to H-12a and
H-12b indicate a turn in the macrolide skeleton at C-13,
with H-13 bisecting H-12a and H-12b. The oxymethyl
group at C-13 could be assigned syn to the C-11 hydroxyl
on the β side of the macrolide ring on the basis of an NOE
observed from this oxymethyl group to H-12b. Once again
an analysis of vicinal couplings and NOE correlations
revealed that H-13 bisects H-14a and H-14b. A large
coupling to H-14b (9.5 Hz) and a small coupling to H-14a
(<1 Hz) from H-13 and an NOE observed to H-14b
indicate a near 90° angle between H-13 and H-14a and
a near 0° angle between H-13 and H-14b, assigning the
slightly downfield resonance (H-14b, δ 2.15) to the β side
of the macrocycle. This assignment was confirmed by the
observation of an NOE between H-14a and H-12a on the
R side of the macrocycle. A large vicinal coupling between
H-14a and H-15 and an NOE observed between OCH3-
13 and H-15 place the C-16 to C-20 side chain R with
H-15 trans diaxial to H-14a.
The relative stereochemistry of C-2 could not be
determined directly from correlations to C-3 or C-4. A
small coupling constant of less than 1 Hz between H-2
Figure 1. Relative stereochemistry of C-3 to C-7 of peloruside and H-3 together with NOE correlations (H-2 to H-3, H-2
A (1). Important NOEs are illustrated with dashed arrows and to H-5, and H2 to H11) indicates that H-2 is on the inside
vicinal couplings with solid arrows. Coupling constants are of the macrocycle. These observations are consistent with
given in hertz. both possible epimers at C-2. An NOE observed between
CH3-23 and H-3, however, is only consistent with the
enhancement between H-5 and H-4a established a syn13 relative stereochemistry at C-2 as drawn. The other
relationship between them. Similarly, a large vicinal possible isomer would place the C-2 hydroxyl directly
coupling (10.5 Hz) between H-3 and H-4a, a smaller between CH3-23 and H-3.
coupling (5.5 Hz) between H-3 and H-4b, and NOE
An examination of proton couplings and NOE enhance-
enhancements (H-3 to H-4b, H-4a to C-3OCH3, H-4b to
ments observed on the C-16 to C-20 side revealed that
C-3OCH3) established antiperiplanar relationships of H-3
rotation is restricted in solution. In particular, the bonds
and H-4a, and H-4b and C-2. These correlations assign
C-17-C-18 and C-18-C-24 appear to be fixed. A large
the relative stereochemistry of C-5 to C-3 as drawn in
coupling (10 Hz) between H-18 and H-17 and an NOE
Figure 1 (1-3 syn oxygen substitution at C-5 and C-3
enhancement (H-24a to H-18) clearly place H-17 and
with the C-2 to C-6 chain in an extended zigzag confor-
H-18 antiperiplanar. Similarly the pattern of large (H-
mation).
24b-H-18, 10.5 Hz) and small (H-24a-H-18, 4 Hz)
The hydroxyl group attached to C-9 (Figure 2) can be couplings indicates restricted rotation. Observation of
assigned as axial above the six-membered ring on the NOE enhacements between H-18 and H-19a, H-19b, and
basis of an NOE correlation from H-3 to CH3-22 on the CH3-20, however, indicates some flexibility of the ethyl
underside of both rings as drawn in Figure 3. The moiety.
placement of C-10 is consistent with the anomeric effect,
the placement of the bulky gem-dimethyl group equato- Observations of NOE enhancements (H-18 to H-15,
rial upon ring closure and the observation of NOE CH3-23 to H-3) establish the coplanarity of H-15, H-18,
enhancements from the equatorial H-8 to both CH3-21 and CH3-23. An NOE correlation observed between CH3-
and CH3-22. These NOE correlations also assign CH3-22 20 and H-14a indicates that the ethyl side chain sits
above and CH3-21 below the macrocyclic ring. An NOE below the plane of the macrolide ring. These observations
correlation between CH3-22 and H-11 places H-11 on the lead to the assignment of the stereochemistry at C-18 as
underside of the macrocycle with the C-11 hydroxyl group S*. On the basis of the above arguements, we propose
syn to the hydroxyl on C-9. This stereochemical assign- the relative stereochemistry of peloruside (1) as 2R*,-
ment is confirmed by an NOE correlation observed 3S*,5S*,7S*,8S*,9S*,11R*,13R*,15R*,16Z, 18S*. All NOE
between H-3 and H-11 across the underside of the correlations observed in the ROESY spectrum and a
macrocyclic ring. Large (11 Hz) and small (<1 Hz) vicinal series of GOESY spectra are consistent with this con-
couplings were observed between H-11 and the downfield figurational assignment in a single conformation.
(H-12b, δ 2.07) and upfield (H-12a, δ 1.40) resonances, Peloruside A (1) was found to be cytotoxic to P388
respectively, assigned to the C-12 methylene. These murine leukemia cells at approximately 10 ng/mL (18
couplings, along with NOE correlations observed from the nM). Although it bears some structural features of both
geminal methyls to these protons (CH3-21 to H-12b, CH3- mycalamides (gem-dimethyls and polyhydroxylation) and
22 to H-12a), revealed an extended zigzag conformation pateamine (macrolide ring), it does not appear to be
closely related biochemically. Interestingly, while all
(13) Masamune, S.; Ali, Sk. A.; Snitman, D. L.; Garvey, D. S. Angew. sponge individuals tested revealed consistent levels of
Chem., Int. Ed., Engl. 1980, 19, 557. mycalamide A, and varying amounts of pateamine, only
448 J. Org. Chem., Vol. 65, No. 2, 2000 West et al.

Figure 2. Relative stereochemistry of C-8 to C-15 of peloruside A (1). Important NOEs are illustrated with dashed arrows and
vicinal couplings with solid arrows. Coupling constants are given in hertz.

specimens collected at the deeper range of the population

contained detectable amounts of peloruside A.

Experimental Section
NMR Experiments. 1H and 13C NMR spectra were mea-
sured with 300 and 500 MHz spectrometers. All chemical shifts
(δ) are referenced to the solvent peak (CDCl3: 1H, δ 7.25 ppm;
13C, δ 77.0 ppm).14 Short- and long-range 1H-13C correlations

were determined with gradient-enhanced inverse-detected

HSQC and HMBC experiments. 1D TOCSY experiments were
performed with shaped pulse-selective excitation and spin lock
mixing times of 15-80 ms. NOE enhancements were detected
with a GOESY experiment with Gaussian-selective excitation
and a 0.5 s mixing time.
Collection, Extraction, and Isolation. Sponge specimens
were collected by SCUBA in Pelorus Sound, South Island, New
Zealand, at depths of 7-15 m. A single frozen specimen (170
g wet weight, NIWA no. 95DBMYC 2-6) was cut into small
segments and extracted with methanol (2 × 600 mL) for 24 h.
The second and first methanolic extracts were passed through
a glass column packed with 75 mL of Diaion HP20 poly-
Figure 3. Probable conformation of the carbon skeleton of
(14) Gottieb, H. E.; Kotlar, V.; Nudelman, A. J. Org. Chem. 1997, peloruside A (1). Selected NOEs are illustrated with dashed
62, 7512. arrows.
Peloruside A from Marine Sponge Mycale sp. J. Org. Chem., Vol. 65, No. 2, 2000 449
1H 13C
Table 1. and NMR Assignments of 1 in CDCl3 was diluted with water (2.8 L) and passed back through the
13C 1H same column. The column was then washed with water (100
mL) and eluted with 150 mL fractions of (1) 20% acetone/
position δ (ppm) mult δ (ppm) mult, J (Hz) water, (2) 55% acetone/water, (3) 55% acetone/0.2 M NH4OH,
1 174.0 s and (4) 55% acetone/0.2 M NH4OH adjusted to pH 4.0 with
2 70.3 d 4.53 s AcOH. Fraction 2 was diluted with water (250 mL) and passed
3 78.3 d 4.22 dd (10.5, 5.5) through a glass column packed with 35 mL of HP20 preequili-
4a 32.6 t 1.78 m brated with water. The column was washed with water (50
4b 2.13 m mL) and eluted with 100 mL of acetone. The acetone eluent
5 63.5 d 4.25 tdd (11, 4.5, 2.5) was concentrated to dryness to yield 78.8 mg of a viscous
6a 31.7 t 1.53 q (12) brown oil. The resulting oil was dissolved in methanol (25 mL)
6b 1.78 ddd (12.5, 5.5, 2.5) and passed through a small glass column containing 250 mg
7 75.9 d 3.82 ddd (11.5, 5, 3) of TosoHass Amberchrom. The column eluent was diluted with
8 66.8 d 4.02 d (3) water (100 mL) and passed back through the column. The
9 101.9 s column was washed with water (20 mL), and the Amberchrom
10 43.6 s was transferred on top of a 20 × 1.5 cm Amberchrom column
11 73.9 d 4.89 br d (10) preequilibrated with water. The column was eluted with
12a 33.9 t 1.40 d (14.5)
increasing concentrations of acetone in water in a stepped
12b 2.07 ddd (15, 11.5, 4.5)
13 77.9 d 3.99 br d (9.5)
gradient fashion. The 32-34% acetone/water fractions were
14a 35.7 t 2.02 ddd (15.5, 11.5, 1) concentrated to dryness to yield 1 as a colorless oil (3.0 mg).
14b 2.15 ddd (15.5, 10, 1.5) The 38-40% acetone/water fractions were concentrated to
15 70.9 d 5.68 d (10.5) dryness to yield 10.6 mg of mycalamide A (2). The fourth
16 136.1 s fraction eluted from the original HP20 column at pH 4.0 was
17 131.1 d 5.05 d (10) diluted with 150 mL of water, adjusted to pH 7.0 with aqueous
18 43.3 d 2.61 m NH3, and passed through a glass column packed with 30 mL
19a 24.6 t 1.17 m of HP20 preequilibrated with water. The column was washed
19b 1.44 m with water (50 mL) and eluted with 100 mL of acetone. The
20 12.2 q 0.85a t (7.5) acetone eluent was concentrated to dryness to yield 38 mg of
21 15.8 q 1.08a s a yellow oil. The oil was dissolved in methanol (10 mL) and
22 20.8 q 1.12a s passed through 2.5 mL of amino-bonded phase packing mate-
23 17.5 q 1.67a d (1) rial. The eluent was concentrated to dryness to yield 11.7 mg
24a 66.9 t 3.36 t (10.5) of pateamine (3).
24b 3.64 dd (10.5, 4)
Peloruside A (1): a colorless oil; [R]20D +16°(c 0.30 CH2-
3OCH3 56.1 q 3.31a s
7OCH3 55.7 q 3.38a s Cl2); IR (KBr) νmax 3336, 2919, 2849, 1738, 1667, 1462, 1385,
13OCH3 59.1 q 3.48a s 1225, 1155, 1082 cm-1; 1H and 13C NMR (Table 1); HRFABMS
2OH 6.75 s m/z 571.308 26 (calcd for C27H48O11 (M + Na)+, 571.309 46).
a 3H.
Supporting Information Available: NMR spectra of 1
including 1H, 13C, DEPT, COSY, ROESY, HSQC, HMBC, and
(styrene-divinylbenzene) beads preequilibrated with meth- selected 1D TOCSY and GOESY. This material is available
anol. The eluents were combined and passed through the same free of charge via the Internet at http://pubs.acs.org.
column. The resulting eluent was diluted with water (100 mL)
and passed through the column. Finally the resulting eluent JO991296Y