AU2003270999A8 - Anti-mitotic agents which inhibit tubulin polymerization - Google Patents

Description

AUSTRALIA

PATENTS ACT 1990 DIVISIONAL APPLICATION NAME OF APPLICANTS: Baylor University AND Arizona Disease Control Research Commission ADDRESS FOR SERVICE: DAVIES COLLISON CAVE Patent Attorneys 1 Nicholson Street Melbourne, 3000.

INVENTION TITLE: "Anti-mitotic agents which inhibit tubulin polymerization" The following statement is a full description of this invention, including the best method of performing it known to us: Q:\OPER\MKR\GENERAL\12384700-div filc.doc 18/12/03 P:OPER\MKRSPECI\765418-div.doc- 1/12/03 -1- ANTI-MITOTIC AGENTS WHICH INHIBIT TUBULIN POLYMERIZATION BACKGROUND OF THE INVENTION This is a divisional of application No. 24860/01 (765,418), the disclosure of which is included herein in its entirety by way of reference.

1. Field of the Invention The present invention relates generally to the field of tubulin polymerization inhibitors. More particularly, it concerns the use of 3-aroyl-2-aryl-benzo[b]thiophenes and analogues thereof as anti-tumor agents.

2. Description of Related Art An aggressive chemotherapeutic strategy toward the treatment and maintenance of solid-tumor cancers continues to rely on the development of architecturally new and biologically more potent anti-tumor, anti-mitotic agents. A variety of clinically-promising compounds which demonstrate potent cytotoxic and anti-tumor activity are known to effect their primary mode of action through an efficient inhibition of tubulin polymerization (Gerwick et al). This class of compounds undergoes an initial binding interaction to the ubiquitous protein tubulin which in turn arrests the ability of tubulin to polymerize into microtubules which are essential components for cell maintenance and cell division (Owellen et al).

Currently the most recognized and clinically useful tubulin polymerization inhibitors for the treatment of cancer are vinblastine and vincristine (Lavielle, et al.).

Additionally, the natural products rhizoxin (Nakada, et al., 1993a and 1993b; Boger et al.; Rao et al., 1992 and 1993; Kobayashi et al., 1992 and 1993) combretastin A-4 and A-2 (Lin et al.; Petit, et al., 1982, 1985, and 1987) and taxol (Kingston et al.; Schiff et al.; Swindell, et al., 1991; Parness, et al.) as well as certain synthetic analogues including the 2-styrylquinazolin-4(3H)-ones (SQO) (Jiang et al.) and highly oxygenated derivatives of cis- and trans-stilbene (Cushman et al) and dihydrostilbene are all known to mediate their cytotoxic activity through a binding interaction with tubulin. The exact nature of this interaction remains unknown and most likely varies somewhat between the series of compounds.

P:\OPER\MKR\SPECI\765418-div.doc-18/12/03 1A- Tubulin is a heterodimer of the globular a and 0 tubulin subunits. A number of photoaffinity labeling reagents for tubulin have been developed and evaluated (Rao et al., 1992 and 1994; Chavan et al.; Sawada et al., 1991, 1993a and 1993b; Staretz et al.; Hahn et al.; Wolff et al.; Floyd et al.; Safa et al; Williams et These reagents have identified three distinct small molecule binding sites on tubulin: the colchicine site, the vinblastine site and the maytansine/rhizoxin site. Additionally, a first generation rhizoxin-based photoaffinity labeling reagent has suggested binding to the Met-363-Lys-379 site on p-tubulin (Sawada et al., 1993a), and a taxol-based reagent has been found to label the N-terminal 31 amino acid residues of 3tubulin (Swindell et al, 1991 and 1994; Rao et al., 1994). Taxol itself is known to bind to polymerized microtubules, but not at distinct sites on the monomer subunits of tubulin (Kingston et al.; Schiffet al.; Swindell et al., 1991; Pamess et al.).

The discovery of new antimitotic agents may result from the judicious combination of a molecular template which in appropriately substituted form phenolic moieties, etc..) interacts with the estrogen receptor suitably modified with structural features deemed imperative for binding to the colchicine site on p-tubulin (arylalkoxy groups, certain halogen substitutions, pseudo aryl ring stacking, etc.). The methoxy aryl functionality seems especially important for increased interaction at the colchicine binding site in certain analogs. (Shirai et al.. D'Amato et al.. Hamel, 1996). Recent studies have shown that certain estrogen receptor (ER) binding compounds as structurally modified congeners (2-methoxyestradiol, for example) interact with tubulin and inhibit tubulin polymerization. (D'Amato et al., Cushman et al., 1995, Hamel, et al..

1996, Cushman et al., 1997). Estradiol is. of course, perhaps the most important estrogen in humans, and it is intriguing and instructive that the addition of the methoxy aryl motif to this compound makes it interactive with tubulin. As a steroid, however, the use of 2methoxyestradiol as an anti-cancer agent may lead to unwanted side effects.

Even before the discovery and realization that molecular templates (of traditionally estrogen receptor active compounds) suitably modified with alkoxyaryl or other groups deemed necessary for tubulin binding often result in the formation of new classes of inhibitors of tubulin polymerization, antiestrogens were developed to treat hormone-dependent cancers and a number of nonsteroidal agents were developed. Tamoxifcn, for instance, has been widely used to treat estrogen-dependent metastatic mammary carcinoma (Mouridsen. ct The structure of trioxifene mesylate. a tetralin based compound which exhibits anti-tumor effects at the same or higher level as tamoxifen (Jones et al., 1979), includes a ketone moiety as part of its triarylethylene core, thereby overcoming the isomerization tendencies of the ethylene double bond of this class of compounds, assuring the stability of the molecule's three-dimensional structure. Unfortunately, despite their antiestrogen properties, tamoxifen and the related triarylethylene derivatives retain some intrinsic estrogen agonist properties, reducing their ability to fully inhibit biological responses to exogenous or endogenous estrogens (Jones et al., 1984).

P:OPER\M KR\SPECI\765418-div.doc 18/12/03 -3- The benzo[b]thiophenes are another example of a class of compounds which often exhibit very high affinity for the estrogen receptor (Kym et al.; Pinney et al., 1991a and 1991b; WO 95/10513). The 2,3-diaryl substituted benzo[b]thiophenes greatly resemble the triarylethylene-based core structure of tamoxifen. The estrogenicity of the triarylethylene compounds has been shown to be substantially overcome in 3-aroyl-2arylbenzo[b]thiophene compounds substituted at the 3-aroyl group with basic amine moieties (Jones et al., 1984). A prime example of this type of compound is LY117018 Patent No. 4,656,187). 3-aroyl-2-arylbenzo[b]thiophenes have also been found to be useful antifertility agents Patent No. 4,133,814) and as inhibitors for Patent No. 5,532,382).

SUMMARY OF THE INVENTION The present invention provides benzo[b]thiophene-based inhibitors of tubulin polymerization, thereby providing novel anti-tumor compounds of increased cytotoxicity and fewer side effects. This is accomplished through the introduction of small alkoxy aryl substituents to the estrogenic benzo[b]thiophene skeleton or the skeleton of compounds similar to benzo[b]thiophene, such as indene, benzofuran, and indole. The tubulin polymerization inhibitors of this invention are illustrated below.

According to one embodiment of the present invention there is provided a compound of the structure:

R,

Z-Y-Ar' Ar R3 R4 wherein X is chosen from the group consisting of O, NH, and CH 2

R

1

-R

4 are independently chosen from the group consisting of H, OH and CI-C alkoxy, Z is chosen from the group consisting of C=O, CH 2

C

2

H

2 CHOH, and CHOCH 3 Y is chosen from the group consisting of a covalent bond, CH 2 and CH 2

CH

2 P:OPER\MKR\SPECI\765418-div.doc-18/12/03 -4and Ar and Ar' are aryl moieties chosen from the group consisting of phenyl and napthyl, further substituted with at least one C 1

-C

5 alkoxy group, at least one of which has at least two Ci-C 5 alkoxy groups, wherein Ar' is 3,4,5-trimethoxyphenyl, Z is C=O, Y is a covalent bond, R 3 is methoxy, R 1

R

2 and R 4 are H, and Ar is substituted with a methoxy group.

Preferably, the tubulin polymerization inhibitors of this invention will be of the above formula wherein X is S. The most preferred R group substitution pattern will be wherein R 3 is OCH 3 and R 1

R

2 and R 4 are H. Z will preferably be C=O, Y will preferably be a covalent bond, and Ar will preferably be 4-methoxyphenyl. The most preferred Ar' groups will be singly and multiply substituted phenyl groups containing para ethoxy or methoxy substituents. The most preferred tubulin polymerization inhitibor of this invention is 3-(3',4',5'-trimethoxybenzoyl)-2-(4'-methoxyphenyl)-6-methoxybenzo[b]thiophene.

The term "Ci-C 5 alkoxy" as used herein contemplates both straight chain and branched chain alkyl radicals and therefore defines groups such as, for example, methoxy, ethoxy, n-propoxy, isopropoxy, n-butyloxy, isobutyloxy, tert-butyloxy, sec-butyloxy, pentyloxy, isopentyloxy, t-pentyloxy, neopentyloxy, and the like. The preferred alkoxy groups are methoxy and ethoxy.

According to another embodiment of the present invention there is provided a method for inhibiting tubulin polymerization by contacting a tubulin-containing system with an effective amount of a compound having the structure:

R,

Z-Y-Ar' R2 A r R3 R4 wherein X is chosen from the group consisting of S, NH, CH 2 and 0, P:\OPER\MKR\SPECI\765418 divdoc-18/1203 -4A-

RI-R

4 are independently chosen from the group consisting of H, OH and C 1

-C

alkoxy, Z is chosen from the group consisting of C=O, CH 2

C

2

H

2 CHOH, and CHOCH 3 Y is chosen from the group consisting of a covalent bond, CH 2 and CH 2

CH

2 and Ar and Ar' are aryl substituents chosen from the group consisting of phenyl and napthyl, further substituted with at least one Ci-C 5 alkoxy group.

According to a further embodiment of the present invention there is provided a method for inhibiting the growth of tumor cells comprising contacting the tumor cells with an effective amount of a tubulin polymerization inhibitor, said inhibitor having the structure:

R,

Z-Y-Ar' A r R3 R4 wherein X is chosen from the group consisting of S, NH, CH 2 and 0,

R

1

-R

4 are independently chosen from the group consisting of H, OH and C 1 -Cs alkoxy, Z is chosen from the group consisting of C=O, CH 2

C

2

H

2 CHOH, and CHOCH 3 Y is chosen from the group consisting of a covalent bond, CH 2 and CH 2

CH

2 and Ar and Ar' are aryl substituents chosen from the group consisting of phenyl and napthyl, further substituted with at least one CI-C 5 alkoxy group.

In another embodiment of the invention there is provided a method of inhibiting tumor cell growth comprising administering a therapeutically effective amount of the structure P:OPERMMRSPECX7654 I 8.di.dmc. 112/03 4B

CH

3 0

GH

3O&

CH

3 0

X

CH

3

O

where X is CHOH or C=0.

The preferred novel compounds of this invention will be those wherein X is S, Z is C=O. R 3 is methoxy and Ar is 4-methoxyphenyl. The preferred novel compounds of this invention include: 3-(2 ','-dimethoxybenzoyl)-2-(4 '-methoxyphenyl)-6-methoxybenzo[b]thiophene, 3-.(3',5P-dimethoxybenzoyl)-2-(4 '-methoxyphenyl)-6-methoxybenzo[b]thiophene, 3 ,4 '-dimethoxybenzoyl)-2-(4' -methoxyphenyl)-6-methoxybenzo[b]thiophene, 3 -ethoxybenzoyl)-2-(4' -methoxyphenyl)-6-methoxybenzo[b]thiophene, 3-(3 ,5 '-trimethoxybenzoyl)-2-(4 '-methoxyphenyl)-6methoxybenzo[b]thiophene, and 3-[3'-(3",4",5"-trimethoxyphenyl)propanoyl]-2-(4'methoxyphenyl)-6methoxybenzo[b]thiophene.

The most preferred novel compounds of this invention will be those wherein X is S, Z is C=O, Ar is 4-methoxyphenyl,

R

3 is methoxy, and Ar' is a phenyl group substituted with an alkoxy group at the para position. The most preferred novel compounds of this invention include: 3-( 3 4 '-dimethoxybenzoyl)-2-(4methoxyphenyl)-6-methoxybenzo[b]thiophene, 3-( 4 '-ethoxybenzoyl)-2-(4'-methoxyphenyl)-6-methoxybenzo[b]thiophene, 3 3 ',4,5'-triethoxybenzoyl)-2-(4'-methoxyphenyl)-6-methoxybenzo[b]-thiophene, and 3 3 4",4"5"-trimethoxyphenyl)propanoyl]-2(4'-methoxyphenyl)-6methoxybenzo[b]thiophene.

As a preferred embodiment of the invention, the tubulin polymerization inhibitors will be used as part of pharmacologically active compositions for treating leukemias. melanomas, and colon, lung, ovarian, CNS, and renal cancers, as well as other cancers. In the most preferred embodiment of this aspect of the invention, the tubulin polymerization inhibitors will be used to treat colon cancers.

As a further preferred embodiment, the tubulin polymerization inhibitors of this invention may be used to treat any disease for which tubulin polymerization plays a crucial role. In addition to anti-tumor activity, caused by lack of mitosis in cells in which tubulin polymerization is absent, the tubulin polymerization inhibitors of this invention would also be useful in treating diseases caused by flagellated parasites, for whom tubulin polymerization is crucial to movement. In particular, the tubulin polymerization inhibitors of this invention will be useful in treating Chagas' disease or diseases caused by the parasite Lcishmania.

The present invention also includes a compound of the structure

R

6 R7 RS Rg R4 RI H H H j 1 P:\OPER\MKRSPECI\7654 I 8.div~dc.l S 1/03 -6where R, is H or CH 3 O; R 2 is H, CH 3 0 or C 2

H

5 0; R 3 is CH 3 0 or C 2

H

5 0; R 4

R

5

R

7 and R 8 are independently H, CH 3 O, C 2

H

5 0, or F; R 6 is H, CH 3 O, C 2

H

5 0, OH, F or N(CH 3 2 wherein at least one of R 4

R

5

R

6

R

7 of R 8 is F or N(CH 3 2 and X is 0 0 0 0 11 11 11 or 11 C CCH 2

CC

2

H

4

CC

2

H

2 The present invention also includes a compound of the structure where X is S or S=0.

Also included is a compound of the structure

-OCH,

as well as a compound of the structure where X is CHOH or C=O. A compound of the following structure is also included in the present invention

R,

C

2 H I-R 2

CH

3 where R, and R 2 are independently CH30, NO 2 NH, or N 3 and CH 3 O; and C 2 H, is in the E or Z configuration; with the proviso that one of R, and R, is CH 3 0 and the other is NO,, NH, or N 3 One preferred embodiment is where CH 2 1- is E Cz,, R, is CH 3 0 and R, is NH, in the immediately prior structure. Another embodiment is where C2H, is E C 2 R, is NH, and R, is CHO3 in the immediately prior structure. Yet another embodiment is where C 2

H

2 is Z C:Hs. R, is CH30 and R, is NH 2 in the immediately prior structure. Another embodiment is where C2H, is Z CzH.1- R, is NHI and R, is CH30 in the immediately prior structure. Another embodiment is where C 2 H, is E CH,, R, is CH30 and R, is NO, in the immediately prior structure. In another embodiment CH 2 is E C 2

H

2 R, is NO, and R, is CH 3 0 in the immediately prior structure.

One preferred embodiment of the present invention is where C 2 H, is Z CZH 5 RI is CH 3

O

and R 2 is NO, in the immediately prior structure.

One embodiment is where CH, is Z R, is NO, and R, is CH 3 0 in the immediately prior structure.

Yet another embodiment is where C1H: is E C 2 11,. R, is CHO and R, is N3 in the immediately prior structure. A preferred embodiment also is where C 2 ll, is E C,i 2 R, is N, and R, is CH 3 0 in the immediately prior structure. Also preferred is the compound where CH., is Z

C.H

5 R, is CH 3 0 and R: is N3 in the immediately prior structure. Another embodiment described is where CH, is Z C,H 2 R, is N 3 and R 2 is CH30 in the immediately prior structure.

BRIEF DESCRIPTION OF THE DRAWINGS The following drawings form part of the present specification and are included to further demonstrate certain aspects of the present invention. The invention may be better understood by reference to one or more of these drawings in combination with the detailed description of specific embodiments presented herein.

FIG. I shows the general structure of certain tubulin polymerization inhibitor compounds.

FIG. 2 shows the pseudo-cis (FIG. 2A) and pseudo-trans (FIG 2B) orientations of 3aroyl-benzo[b]thiophefle compounds and the structure of Combretastatin A-4 (FIG. 2C).

FIG. 3 shows the X-ray crystal structure of 3-(3',4',5'-trimethoxybenzoyl)-2-( 4 methoxypheflyl)-6-mfethoxybeflzo[b~thiophene (FIG. 3A) and the energy minimized (MM2) structure of Combretastatin A-4 (FIG. 313).

FIG. 4 shows a general scheme for the synthesis of the 3-aroyl-2phenybcnzo~b]thiophene compounds.

FIG. 5 shows compound 2A, 6'-dimethoxybe1zoyl)-2-(4'-methoxyphenyl)- 6 methoxybenzo[b]thiophene FIG. 6 shows compound 3A, 5' dimethoxybenzoyl)-2-(4'-methoxyphcflY 6 methoxybenzo~jb~thiophefle FIG. 7 shows compound 4A, 3 4'-dimethoxybenzoyl)-2-(4'-methoxyphenyI)- 6 methoxybenzo[b]thiophene FIG. 8 shows compound 5A, 3')(4'-methoxybenzoyl)-2-(4'-methoxypheflyl)- 6 methoxybertzo[b]thiophefle FIG. 9 shows compound 6A, 3-4-toyezy)2-4-ehxpey)6 methoxybenzo[bjthiophefle FIG. 10 shows compound 7A, 5'-triethoxybcnzoyl)-2-(4'-methoxyphefl)- 6 methoxybcnzo[hthiophene FIG. 11 shows compound 8A, 5'-trimethoxyphenyl)propioflyl- 2 4 mcthoxyphenyl ).6-methoxybcnzo[b]thiophene FIG. 12 shows compound 9A. 3',4'.5'-triethoxylbcnzoyl)-2-(4'-CthoxYphel)-6ethoxybenzo[bllthiophene FIG. 13 shows compound 10A, 3-(4'-ethoxy-3', 5'-dimethoxybenzoyl)- 2 49 methoxyphenyl)-6-methoxybenzollb]thiophene FIG. 14 shows compound 1 IA, _3 .(4'-N,N-dimethylaminobeflzoy) 2 4 methoxyphenyl)-6-methoxybeflzo[b~thiophene FIG. 15 shows compound 12A, 5t-trifluorobenzoy1)-2-(4'-methoxyphenyl)- 4 methoxybenzo~b]thiophene FIG. 16 shows compound 1 3A, 5'-trimethoxybenzoyl)-2-(4' -methoxyphenyl)- 4-methoxybenzo [b]thiophene FIG. 17 shows compound 14A, 5'-trifluorobenzoy1)-2-(4'-methoxyph el)- 6 methoxybenzolthiophefle FIG. 18 shows compound 15A, 6'-pentafluorobenzoyl)-2-( 4 methoxypheny)-6-methoxybenzo[blthiophene FIG. 19 shows compound 16A, 5'-trimethoxybenzoyl)-2-(4'-methoxyphel)benzo[hlthiophene FIG. 20 shows compound 17A, 5'-trimethoxyphenvl)cinlamloyllj- 2 4 methoxyphenyl)-6-methoxybeflzo[blthiophene FIG. 21 shows compound 18A, 5'-trimethoxvbenzoyl)-2-(4'-tho~yphenfl)- 6 ethoxvbenzo[hllthiophefle FIG. 22 shows compound 19A, 3-(4'-hydroxy -3'.5'-dimethoxybenzoyl)-2-(4'methoxvphenyl)-6-methoxybenzo~ib]thiophene FIG. 23 shows compound 20A, 3-(phenylacetyI)-2-(4'-methoxYphenfl)-6methoxNybenzo (hlthiophene FIG. 24 shows compound 21A, 5'-trimethoxy)phenylacetyl)- 2 4 methoxyphenyI)-6-methoxybelzo[b]thiophene FIG. 25 shows compound 22B, 3)-(3',4',5'-trimethoxypheloxy)-2-(4'-methoxyphenyO- 6 methoxvlbenzo[blthiophefle S-oxide FIG. 26 shows compound 23B. 3-3.'5-rmto~peox)2('mto~pev)6 mcthox,.benzofh]thiophene FIG. 27 shows compound 24C. 3-(3.4'.5'timchoxbclezoY1-)-2-(4-mthoxYphenY.I 6 mcthoxy bcnzo [blfuran FIG. 28 shows compound -15D. I -(hydroxvmcthyI.-3',45'trimhoxY.pheflI) 6 -mcthoxv- 3 .4-dihvdronaphthalene FIG. 29 shows compound 26D, I -(3',4',5'-trimethoxybenzoy1)-6-methoxy- 3 4 dihydronaphthalene FIG. 30 shows -compound 27E, 1-(3'-methoxy-4'-nitrophelyl)- 2 3 trimethoxyphenyl) ethene FIG. 31 shows compound 28E, (E)-1-(3'-methoxy-4'-nitropheny)- 2 3 't, 4 trimethoxyphenyl) ethene FIG. 32 shows trimethoxyphenyl)ethefle FIG. 33 shows trimethoxyphenyl)ethefle FIG. 34 shows trimethoxyphenyl)ethefle FIG. 35 shows trimethoxyphenyl)ethefle FIG. 36 shows trimethoxyphenyl)ethefle FIG. 37 shows compound 29E, 1-(4'amino-3'-methoxypheflyl)- 2 3 compound 30E, -(4'azido-3'-methoxypheflyl)- 2 3 compound 31 E, -(4"-methoxy-3 "-nitrophenyl)-2-(3',4',5'compound 32E, I-(4"-methoxy-3 "-nitrophenyl)-2-( 3 4 compound 3 3E, -(3'-amino-4'-methoxypheflyl)- 2 3 compound 34E, -(3'azido-4'-methoxyphenyl)- 2 3 trimcthoxyphenyl )cthene DESCRIPTION OF ILLUSTRATIVE

EMBODIMENTS

The present example relates to the inventors' discovery that certain compounds described herein, including 3-(3'4'5'-trimethoxybenzoyl)-2-(4'-methoxyphelyl)- 6 mcthoxybenzo[hlthiophene, inhibit tubulin polymerization and inhibit tumor cell population to nearly the same extent as Combretastatin A-4, one of the most potent inhibitors known. The tubulin polymerization

IC

50 of the methoxyaroyl -substituted benzo[b]thiophene, for example, was 1.5 2.5 [Ni while that of Combretastatin A-4 was 0.75 1 iM. 3-(3'4'5'-trimethoxybenZoyl)- 2-(4'-mcthoxyphenyl)-6-mfethoxvbeflzo[blthiophene and other examples also showed significant cell growth inhibitory activity against the growth of several tumor cell lines. The compounds were particularly effective against the colon KM20L2 cell line, exhibiting a GIS 0 of 4.9 x 1 0,2 pg/ml or less.

The molecular structure of certain tubulin polymerization inhibitors of the present invention are based on the structure of ben~zo[hlthiophene and the similar structures of indole.

benzofuran and indene (FIG. The six-membered ring of these fused systems is substituted by one or more hydroxy or alkoxy groups, in any substitution pattern. C-2 of the benzo[blthiophene, benzofuran or indole or C-3 of the indene is substituted with an aromatic moiety, preferably phenyl. This aromatic substituent will also contain one or more alkoxy substituents. Although it is unlikely that this group will interact at the colchicine binding site of tubulin, elaboration of the molecules at this site may provide interactions with other small molecule binding sites on tubulin. C-3 of the benzo[b]thiophene, indole, or benzofuran and C-2 of the indene is also substituted with an alkoxy-substituted aryl moiety, and will contain a linker group connecting the parent benzo[b]thiophene, benzofuran, indole, or indene structure and the aromatic substituent. The linker group is of between one and three carbons, and may or may not contain a carbonyl functionality or another oxygen-containing group, such as alpoxy such as methoxy or ethoxy, e.g. Possible linker groups include C=O, CH 2

C

2

H

2

C

2 4

C

3

H

6

CHOH,

CHOCH

3

C(=O)CH

2

CH(OCH

3

)CH

2 CH(OH)CH2,

C(=O)CH

2

CH

2

C(OCH

3

)CH

2

CH

2 and

C(OH)CHCH

2 The design of this new class of benzo[b]thiophene-based and related molecules takes advantage of the known estrogenicity of the benzo[b]thiophenes (Jones et al., 1984) and combines this trait with alkoxy substitution of the aryl rings, a factor recently discovered to be important in tubulin binding (Shirai. et al., D'Amato et al.) The 3-aroyl substituent of many of these new compounds is particularly useful because the carbonyl moiety, by forcing the adjoining atoms into or nearly into planarity, serves to reduce the number of three-dimensional configurations available to the substituted benzothiophene. Recent studies have shown that less flexible ligands. although they may bind to fewer molecules, generally have higher binding affinities. More flexible molecules, on the other hand, are less discriminatory in finding a binding partner, but usually bind with lower affinity (Eaton et al.).

The most likely configurations for the 3-aroylbenzo[b]thiophenes is either the pseudo-cis configuration (FIG 2A) or the pseudo-trans configuration (FIG 2B). It is well know that the cis or Z form of the stilbenoid Combretastatin A-4 (FIG. 2C) has a much higher binding affinity for tubulin as compared to its trans or E counterpart (Cushman ct As shown in FIG. 2. both the pseudo-cis and pseudo-trans configurations of the aroyl benzo[b]thiophenes retain a great deal of structural overlap with the cis conformation of Combrctastatin A-4. Recently. the X-ray crystal structures of 3-(3'.4'.5'-trimethoxybenzoyl)-2-(4'-mcthoxyphcnyl)-6-methoxybenz7o b hthiophen e and other 3-aroyl-2-phenylbenzolh]thiophenes were solved and show that the preferred conformation of the 3-aroylbenzo[b]thiophene compounds is indeed the pseudo-trans configuration (Mullica et The X-ray crystal structure of3-(3',4'.5'-trimethoxybenzoyl)- 2 4 methoxyphenyl)-6-methoxybenzo[b]thiophene and the computationally minimized (MM2) structure of Combretastatin A-4 are shown for comparison in FIG. 3.

A typical synthesis of the benzo[b]thiophene compounds is shown in FIG. 4 for 3- (3',4',5'-trimethoxybenzoyl)-2-(4'- methoxyphenyl)methoxybenzo[b]thiophene 1. Intermediate 6-methoxy--(4'-methoxyphenyl)-benzo[b]thiophene, was prepared from 3-methoxybenzene thiol 2 and bromoacetotophenone 3 according to the method of Kost et al. The polyphosphoric acid (PPA) catalyzed cyclization of the substituted thiol 4 produced regioisomers 5 and 6 in a 3:1 ratio separable due to differences in the molecules' solubility in acetone). The use of other thiols and acyl halides can allow for alternative substitution patterns on the benzene ring of the benzo[b]thiophene and the C-2 substituent aryl group. Alternatively, phenols or anilines may be.

used in place of the thiol to produce benzofurans or indoles. Friedel-Crafts aroylation of results in functionalization at C-3 of the benzo[b]thiophene skeleton, giving the 3-aroyl-2phenylbenzo[b]thiophene 1. By a similar scheme, Friedel-Crafts alkylation of 6-methoxy-2-(4'methoxyphenyl)benzo[b]thiophene provides a route to the benzyl and phenylethyl substituted benzo[b]thiophenes, while reduction of the aroyl carbonyl can lead to the hydroxybenzyl compounds. Suitable reduction agents include lithium aluminum hydride and sodium borohydride. The hydroxy compounds can be further elaborated with the addition of alkoxy substituents through a variety of nucleophilic substitution reactions. For example, deprotonation of the benzylic alcohol formed from reduction of compound 1, followed by reaction with an alkyl halide could be used to form a benzylic ether. In addition, dehydration of a CH(OH)CH 2 or a CH(OH)CH 2 CH-, linker group would lead to linker groups containing double bonds. The indenes of this invention could be made by a different route, involving treatment of the proper 1indanone with tosyl hydrazine followed by a modified Shapiro reaction with the resulting hydrazone to complete attachment of the alkoxy-substituted benzoyl moiety. An organocuprate 1.4 addition to the resultant xa,3-unsaturated ketone will effect suitable attachment of the additional aryl group. while treatment with phcnylsclcnium chloride, followed by oxidation and elimination would regenerate the indene double bond, completing the synthesis.

The ability of the various above described compounds to inhibit tubulin polymerization can be determined by in vitro assay. A suitable assay system is that described by Bai et al. A method for purifying tubulin from bovine brain cells is described by Hamel and Lin. The IC, 0 values for tubulin polymerization determined for some of the compounds of this invention demonstrate the importance of the alkoxy substituent at the para position of the 3-aroyl phenyl group. As described above, the IC 50 of 3-(3',4',5'-trimethoxybenzoyl)-2-(4'-methoxyphenyl)- 6 methoxybenzo[b]thiophene is comparable to that of Combretastatin A-4. Otherwise identical 3,5-dimethoxybenzoyl, 2,6-dimethoxybenzoyl and 3,5-dimethoxy-4-hydroxybenzoyl compounds showed no observable tubulin polymerization inhibition activity. It is contemplated, however, that any novel. benzo[b]thiophene compounds of this invention that do not inhibit tubulin polymerization may still be useful based upon their inherent estrogenicity, for example, as antifertility theraputics.

A measurement of each compound's tubulin affinity may also be determined through the compound's ability to inhibit colchichine-tubulin binding. A suitable assay is that described by Kang el al., involving the use of commercially available tritiated colchicine. Decreases in the amount of 3 H]colchicine-tubulin interaction due to the competitive binding of one of the novel inhibitors of this invention may be measured by autoradiography or scintillation counting.

The tubulin polymerization compounds can also be tested for their ability to inhibit tumor cell growth. Initially, cytotoxicity of the various compounds may be measured against the leukemia P388 cell line or other appropriate cell lines in vitro to determine which compounds will be most effective against each type of tumor cell. As in the tubulin polymerization assays, the para methoxy substituent of the 3-aroyl phenyl group was very important in producing cytotoxic activity against P388 leukemia cells. Significantly, the compounds that failed to inhibit tubulin polymerization, the 3,5-dimethoxybenzoyl, 2,6-dimethoxybenzoyl and the dimethoxy-4-hydroxybenzoyl compounds also failed to show measurable activity against the leukemia cells. Another significant finding was that 3-(3',4',5'-trimethoxybenzoyl)- 2 4 methoxyphenyl)-6-methoxybenzo[b]thiophene had a smaller ED 50 value than a nitrogen derivative of combretastatin, 5-[(Z)-2-(3',4',5'-trimethoxyphenyl)ethenyl]-2-methoxy-.N-bis- (phenylmethyl)aniline. The in vitro activities of 3-(3',4',5'-trimethoxybenzoyl)- 2 4 methoxyphenyl)-6-methoxybenzo[b]thiophene against other cell lines are listed in Table 1 of Example 4 below.

As will be obvious to one of skill in the art, tubulin polymerization plays a role in diseases other than cancer. Chagas' disease, for example, is caused by 7Trpanosoma crui,. a flagellate protozoa which has a substantial protein composition containing tubulin both as a component of the subpcllicular microtubule system and the flagellum (De Souza). Chagas' disease is characterized by lesions in the heart, alimentary tract and nervous system. The disease currently affects approximately 16-18 million people and is the leading cause of myocarditis in the Americas (WHO). Inhibition of tubulin polymerization, crucial to the parasite's mobility, would provide an effective treatment. Indeed, the use of agents that selectively affect tubulin polymerization has precedence in the therapy of other parasitic diseases. The benzimidazoles are very effective anti-helmenthic drugs (Katiyar, et and the dinitroanilines have shown promise against Leishmania, a parasite closely related to Trypanosoma (Chan and Gong). Currently, only two drugs exist for the treatment of Chagas'disease: benznidazole and nifurtimox. Both of these compounds are nitroheterocycles that are converted into nitro anion radicals that then interfere with macromolecular synthesis. These drugs have several adverse effects, including thrombocytopenic purpura and polyneropathy. These compounds may also cause genotoxicity in children (Marr el al., De Castro). A suitable assay for determining the tubulin polymerization inhibitors ability to treat parasites is described by Maldonado et al.

For their use in treating disease, the tubulin polymerization inhibitors may be present as part of pharmacologically active compositions suitable for the treatment of animals, particularly humans. The tubulin polymerization inhibitor or tubulin polymerization inhibitor-containing composition must then contact the tubulin-containing system wherein tubulin polymerization needs to be inhibited, for example, the tumor cells or the cells of the flagellate parasite.

Pharmacologically active compositions of the tubulin polymerization inhibitors can be introduced via intravenous injection or orally in solid formulations such as tablets, chewable tablets or capsules. The preparation may also be a parenteral preparation for injection directly at the site of the tumor or parasitic infection.

The preferred dosage of the active ingredient inhibitor compound will vary depending upon the size and type of tumor or degree of parasitic infection, the patient's weight and age, and the exact identity of the tubulin polymerization inhibitor employed. The number of administrations of the pharmaceutically active composition will also vary according to the response of the individual patient to the treatment. For the treatment of cancer, suitable dosages of the tubulin polymerization inhibitors occur in amounts between 0.5 mg/kg of body, weight to 100 mg'kg of body weight per day, preferably of between 1.0 mg/kg of body weight to about mg/kg of body weight. It is contemplated that a similar dosage range would be suitable for the treatment of parasitic infections. Moreover, tubulin inhibition assays can also provide one of skill in the art with the appropriate concentrations of inhibitors that must reach the tubulincontaining cells, and the appropriate dosage can be calculated from that information.

The preparations of tubulin polymerization inhibitors may require the use of suitable phamaceutically acceptable carriers. As used herein. "pharmaceutically acceptable carrier" includes any and all solvents, dispersion media, coatings, antibacterial and antifungal agents and isotonic agents and the like. The use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active ingredient, its use in the therapeutic composition is contemplated.

Supplementary active ingredients can also be incorporated into the compositions. The phrase 'pharmaceutically acceptable" also refers to molecular entities and compositions that do not produce an allergic or similar untoward reaction when administered to an animal or a human.

The following examples are included to demonstrate preferred embodiments and best modes of the invention. It should be appreciated by those of skill in the art that the techniques disclosed in the examples which follow represent techniques discovered by the inventor to function well in the practice of the invention, and thus can be considered to constitute preferred modes for its practice. However, those of skill in the art should, in light of the present disclosure, appreciate that many changes can be made in the specific embodiments which are disclosed and still obtain a like or similar result without departing from the spirit and scope of the invention.

EXAMPLE 1 BENZOIbhTHIOPHENES Synthesis of 3-(.4'5'-trimethoxvbcnzovl)-2-(4-methoxhen-6-metho eno[thiohene (Compound 1 and 1A) 2-(4'-methoxyphenyl)-6-methoxybcnzo[]thiophne was prepared according to the procedure of Kost et al. To a well-stirred solution of 5 0.500 g. 1.85 mmol) and 3,4.5trimethoxybenzoyl chloride (0.640 g. 2.77 mmol) in CHCI, (20 ml). was added AICI 3 (0.123 g.

0.925 mmol) portion-wise over a 15 minute period. After 5 hours (total reaction time), water was added, and the product was isolated initially by extraction with CI1,Cl and subsequently by extraction with ethyl acetate (EtOAc). The organic layers were separately washed with brine and then combined and dried over MgSO,. Purification by flash chromatography (silica gel, 60:40 EtOAc/hexane) afforded 3-(3'.4'.5'-trimethoxycnzoy I -(4'-methoxyphcnyl)-6methoxyben.o[hlthiophene (0.537 g. 1.16 mmol. 63%) as an off-white solid. Recrystallization (hexane/ethanol) afforded a highly pure crystalline sample of the compound with mp 131-133"C.

'H-NMR (CDCI 3 360 Mhz): 8 7.66 J= 8.9 Hz, 1H. ArH), 7.32 J= 2.4 Hz. 1H, ArH), 7.31 J= 8.8 Hz, 2H, ArH), 7.07 2H. ArH), 7.01 (dd, J= 8.9, 2.4 Hz, 1H. ArH), 6.75 J 8.8 Hz. 2H, ArH), 3.89 3H, 3.83 3H, -OCH 3 3.74 3H, -OCH 3 3.73 6H,

-OCH

3 'C-NMR (CDC13, 90 Mhz): 8 192.9, 159.9, 157.7, 152.7, 143.7, 142.6, 140.1, 133.9, 132.3, 130.3, 129.9, 126.1, 124.2, 114.9, 114.1, 107.5, 104.4, 60.8, 56.1, 55.6, 55.2. HRMS (EI) M+ calcd for C2 6

H

2 4 0 6 S 464.1294, found 464.1294. Anal. Calcd for C 26

H

24 0 6 S: C, 67.23; H, 5.21; S, 6.90. Found: C, 67.20; H, 5.26; S, 6.88.

*Synthesis of 3M- 6 6-dimethoxybenzov)2(4-methoxyphenyl)6methoxybe!nzorblthiophene To a well-stirred solution of 2-(4'-methoxyphenyl) 6-methoxybenzo[b]thiophefle (0.500 g, 1.85 mmol) and 2,6-dimethoxybelzoyl chloride (1.11 g, 5.56 mmnol) in CH 2

CI

2 (40 mL) was added AICl 3 (0.986 g, 7.40 mmol) portion-wise over a 15 minute period. After 6 hours, water was added, and the product was isolated initially by extraction with CH 2

CI

2 and subsequently by extraction with EtOAc. The organic layers were separately washed with brine and then combined and dried over MgSO 4 Purification by flash chromatography (silica gel, 60:40 EtOAc/hexane) afforded the title compound (0.484 g, 1.11 mmol, 60%) as an off-white solid.

Recrystallization (hexane/ethanol) afforded a highly pure, crystalline sample with mp 146 152 OC 1-1-NMR (CDCI 3 360 Mhz): 8 8.54 (dd, J 0.3 Hz, iIH. ArH), 7.25 J 2.1 Hz, IlH, ArHj), 7.12 J =8.8 Hz. 21-1, ArH), 7. 10 (dd. J= 9.0. 2.5 Hz, IlH. Arfi), 6.98 J= 8.4 Hz.

I H, ArH 6.58 (d,1J 8.8 Hz, 211I, Art!), 6.,20 J =8.4 Hz. 2H, ArH), 3.88 3H1. -0C11 3 3.73 3H, -OCH3), 3.60 6H, -0C11 3 1 3 C-NMR (CDCI 3 90 Mhz): 8 190.3, 159.5, 157.5, 157.3, 151.3, 139.3, 132.9, 131.9. 130.8, 130.5, 126.4, 125.7, 120.3 115.0, 112.6. 103.9, 103.6, 55.6, 55.5. 55.3. FIRMS (El) M' calcd fo r C,1 5 14 2 0 5 S 434.1188, found 434.1188. Anal. Calcd for C 25

H

22 0 5 S: C. 69.11; H, 5.10; S, 7.38. Found: C. 69.19; H, 5.18; S, 7.28.

Synthesis of 34- 3. 5' dimethoxvhenzovl )-2-(4'-methoxvphelvl)-6-methoxvhenzofhlthio]2hene To a well-stirred solution of 2-(4'-rnethoxyphenyl) 6-methoxybenzo[blthiophefle (0.615 g, 2.27 mmol) and 3,5-dimcthoxybenzoyl chloride (1.37 g, 6.83 mmol) in CH 2 CI (45 mL) was added AIC1 3 (1.21 g, 9.09 mmol) pontion-wise over a 15 minute period. After 17 hours. water wa added, and the product was isolated initially by extraction with CHCl, and subsequently by extraction with EtOAc. The organic layers werc separately washed with brine and then combined and dried over MgSO 4 Purification by flash chromatography (silica gel. 60:40 EtOAc/hexane) afforded the title compound (0.475 g. 1.09 mmol, 48%) as an off-white solid.

Recrystallization (hexane/ethanol) afforded a highly pure, crystalline sample with mp 114-120 0 C: I H-NMR (CDCl 3 360 Mhz): 8 7.59 J 8.9 Hz, IlH, ArH), 7.32 J =8.5 Hz, 2H, Arfi), 7.32 J =2.4 Hz, I H, ArH), 6.98 (dd, J 9.0, 2.4 Hz. 1 H, ArH), 6.94 J 2.1 Hz, 2H, ArH 6.76 J 8.7 Hz, 2H, AMl), 6.52 J 2.4 Hz, I1H, ArHD, 3.89 3H, -OCH3), 3.76 (s, 3 H, 3.71 6H, -OCH 3 1 3 C-NMR (CDCl 3 90 Mhz): 8 194.0, 160.5, 159.8, 157.7, 143.9, 140.0, 139.3, 133.8, 130.3, 130.1, 126.0, 124.1, 114.9, 114.0, 107.6, 106.1, 104.4, 55.6, 55.5, 55.2. HRMS (EI) M calcd for C 25

H

22 0 5 S 434.1188, found 434.1245. Anal. Calcd. for

C

25

H

22 0 5 S: C, 69.11; H, 5.10; S, 7.38. Found: C, 69.00; H, 5.16; S, 7.34.

Synthesis of 4 '-dimethoxvbenzovl)-2-(4'-methoxhenyl)-6-methoxybenzorb1thiophene To a well stirred solution of 2-(4'-methoxyphenyl)-6-methoxybenzo[b]thiophene (0.327g, 1.21 mmol) and 3,4-dimethoxybenzoyl chloride (0.557 g, 2.77 mmol) in CH 2 Cl 2 (20 ml) was added AICI 3 (0.616 g, 4.62 mmol) portion-wise over a 15 minute period. After 7 hours, water was added, and the product was isolated initially by extraction with CH 2

CI

2 and subsequently by extraction with EtOAc. The organic layers were separately washed with brine and then combined and dried over MgSO,. Purification by flash chromatography (silica gel, 60:40 Et20/hexanes) afforded the title compound (0.402 g, 0.92 mmol, 76%) as a pale yellow solid.

Synthesis of 3 .(4'-methoxvbenzovl)-2-(4'-methoxyphenvl)-6-methoxvbenzorbl-thiophene To a well stirred solution of 2-(4'-methoxyphenyl)-6-methoxybenzo[b]thiophene (0.305 g, 1.13 mmol) and 4-methoxybenzoyl chloride (0.378 g. 2.22 mmol) in CH2C, (45 ml) was added AICI 3 (0.550 g, 4.12 mmol) portion-wise over a 15 minute period. After 1.3 hours, water was added, and the product was isolated initially by extraction with CHCI1 and subsequently by extraction with EtOAc. The organic layers were separately washed with brine and then combined and dried over MgSO 4 Purification by flash chromatography (silica gel, 70:30 EtOAc/hexanes) afforded the title compound (0.3576 g, 0.88 mmol, 78%) as a pale yellow solid.

Recrystallization (EtOAc/hexanes) afforded a highly pure, crystalline sample with mp 119 120 'H-NMR(CDCI 3 360 MHz): 5 7.77 J= 9.0 Hz 2H. ArH), 7.52 J= 8.9 Hz, 1H.

ArH). 7.35 J 8.9 Hz. 2H. ArH), 7.31 J 2.3 lz. 1 H. Arl). 6.95 (dd. J= 8.9, 2.4 Hz. IH.

ArI). 6.76 J 9.0. 211. ArH). 6.75 J 8.9. 211. ArH), 3.87 3H. -OCHU). 3.79 3H. OCH 3.74 311. -OCH 3 3 C-NMR (CDCI. 90 MHz): 8 193.2. 193,7, 159.7, 157.6, 142.4. 140.0. 134.0, 132.2, 130.5, 130.4. 130.2. 126.0, 124.0, 114.7. 114.0. 113.6, 104.5. 55.6.

55.4, 55.2. HRMS (El) M' calcd for C 24

H

20 0 4 S, 404.1082, found 404.1059. Anal. Calcd for

C

24 1-1 20 4 S: C, 71.27; H, 4.98; S, 7.93. Found: C, 71.39; H, 4.98; S, 7.90.

Synthesis of 3-(4'-ethoxvbenzovl)-2-(4'-methoxvhenyl)-6-methoxvbenzo[bl-thiophene To a well stirred solution of 2-(4'-methoxyphenyl)-6-methoxybenzo[b]thiophene (0.300 g, 1.11 mmol) and 4-ethoxybenzoyl chloride (0.555 g, 3.01 mmol) in CH 2

CI

2 (45 ml) was added AIC13 (0.502 g, 3.76 mmol) portion-wise over a 15 minute period. After 45 minutes, water was added, and the product was isolated initially by extraction with CH 2 Cl 2 and subsequently by extraction with EtOAc. The organic layers were separately washed with brine and then combined and dried over MgSO 4 Purification by flash chromatography (silica gel, 70:30 EtOAc/hexanes) afforded the title compound (0.389 g, 0.93 mmol, 84%) as a white solid.

Recrystallization (EtOAc/hexanes) afforded a highly pure, crystalline sample with mp 124 125 'H-NMR (CDC 3 360 MHz): 8 7.77 J= 8.9 Hz, 2H, ArH), 7.52 J= 8.9 Hz, 1H, ArH), 7.35 J= 8.8 Hz, 2H, ArH), 7.31 J= 2.4 Hz, 1H, ArH), 6.95 (dd, J= 8.9, 2.4 Hz, 1H, ArH), 6.76 J 8.8 Hz, 2H, ArH), 6.75 J 8.9 Hz, 2H, ArH), 4.01 J 7.0 Hz, 2H,

CH

2 3.88 3H, 3.74 3H, -OCH 3 1.39 J= 7.0, 3H, CH 3 3 C-NMR (CDCI 3 90 Mhz): 6 193.1, 163.1, 159.7, 157.6, 142.3, 140.0, 134.0, 132.3, 130.6, 130.2. 126, 124.0, 114.7, 114.0. 114.0, 104.3, 63.7. 55.6, 55.2. 14.6. HRMS (EI) M' calcd for C- 5

H

22 0 4

S

418.1239, found 418.1241. Anal. Calcd for C, 5 H2 2 0 4 S: C. 71.75; H, 5.30; S, 7.66. Found: C, 71.68; H, 5.30; S, 7.61.

Synthesis of 4' 5'-triethoxvbenzovl)-2-(4'-methoxvphenvl)-6-methoxybenzo[blthiophene To a well stirred solution of 2-(4'-methoxyphenyl)-6-methoxybcnzo[b]thiophene (0.501g, 1.85 mmol) and 3,4,5-triethoxybenzoyl chloride (1.00 g. 3.66 mmol) in CHCI, (45 ml) was added AIC1, (0.870 g, 6.52 mmol) portion-wise over a 15 minute period. After 30 minutes.

water was added, and the product was isolated initially by extraction with CH 2

CI

2 and subsequently by extraction with EtOAc. The organic layers were separately washed with brine and then combined and dried over MgSO,. Purification by flash chromatography (silica gel, 70:30 EtOAc/hexanes) afforded the title compound (0.827 g, 1.63 mmol. 88%) as a pale yellow solid. Recrystallization (EtOAc/hexanes) afforded a highly pure. crystalline sample with mp 108-110 0 C. 'H-NMR (CDCI 3 360 Mhz): 6 7.64 J= 8.9 1-1z 1I. ArH 7.32 J= 2.3Hz, 111. ArH), 7.29 (d J= 8.7 Hz. 211, ArH). 7.02(s, 2H. ArH), 6.99 (dd. J 9.0. 2.4 Hz. I1H.

ArH), 6.73 J= 8.7, 1H, ArH), 4.06 J =7.1 Hz, 2H. 3.91 J= 7.0, 4H, CH2), 3.89 3H, -OCH 3 3.74 3H, -OCH 3 1.34 J 7.0 Hz, 6H, 1.28 J 7.1 Hz, 3H. CH3); 3 C-NMR (CDCI 3 90 MHz): 8 193.2, 159.8, 157.7, 152.5, 143.6, 142.6, 140.0, 133.9. 132.3, 130.3, 130.1, 126.0, 124.2, 114.8, 114.0, 108.9, 104.4, 68.8, 64.6, 55.6, 55.2, 15.4, 14.7. HRMS (EI) M calcd for C 29

H

30 0 6 S 506.1763, found 506.1777. Anal. Calcd for C 29

H

30 0 6 S: C, 68.75; H, 5.97; S, 6.33. Found: C, 68.67; H, 5.97; S, 6.27.

Synthesis of 5" trimethoxyphenvl)propionvl]-2-(4'-methoxyphenyl)- 6 methoxvbenzorblthiophene To a well-stirred solution of 2-(4'-methoxyphenyl) 6-methoxybenzo[b]thiophene (0.206 g, 0.762 mmol) and 5'-trimethoxyphenyl)propionyl chloride (0.390 g, 1.51 mmol) in

CH

2

CI

2 (50 mL) was added AIC13 (0.520 g, 3.89 mmol) portion-wise over a 15 minute period.

After 18 hours (total reaction time), water was added, and the product was isolated initially by extraction with CH 2 C12 and subsequently by extraction with EtOAc. The organic layers were separately washed sequentially with NaHCO 3 (sat) and brine and then combined and dried over MgSO 4 Purification by flash chromatography (silica gel, 70:30 EtOAc/hexane) afforded the title compound as an off-white solid. 'H-NMR (CDCl,, 360 Mhz): 6 7.92 J= 8.9 Hz, 1H.

ArH). 7.35 J= 8.7 Hz, 2H. ArH), 7.25 1H, ArH), 7.04 (dd, J= 8.9, 2.4 Hz. 1H. ArH), 6.93 8.7 Hz, 2H. ArH). 6.15 2H. ArH) 3.88 3H, -OCH 3 3.85 3H. -OCH 3 3.78 3H. -OCH 3 3.72 6H. -OCH3), 3.80 2H. CH2), 3.70 2H, CH 2 TUBULIN POLVMERIZATION

ASSAY

IC

50 values for tubulin polymerization were determined according to the procedure described in Bai et al. Purified tubulin is obtained from bovine brain cells as described in Hamel and Lin Various amounts of inhibitor were preincubated for 15 minutes at 37 0 C with purified tubulin. After the incubation period, the reaction was cooled and GTP was added to induce tubulin polymerization. Polymerization was then monitored in a Gilford spectrophotometer at 350 nm. The final reaction mixtures (0.25 ml) contained 1.5 mg/ml tubulin. 0.6 mg/ml microtubule-associated proteins (MAPs). 0.5 mM GTP. 0.5 mM MgCI 2 4% DMSO and 0.1 M 4-morpholinccthanesulfonatc buffer (MES. pH IC,, is the amount of inhibitor needed to inhibit tubulin polymerization 50% with respect to the amount of inhibition that occurs in the absence of inhibitor. The ICo value determined for 3-(3',4'.5'-Trimethoxybenzoyl)-2-(4'methoxyphenyl)-6-methoxybenzo[b]thiophene was 1.5 2.5 p.M.

CYTOTOXIC ASSAY WITH P388 LEUKEMIA CELLS Some of the newly prepared compounds were evaluated for cytotoxic activity against P388 leukemia cells using an assay system similar to the National Institutes of Cancer procedure described below and in Monks et al. The EDso value (defined as the effective dosage required to inhibit 50% of cell growth) of 3-(3',4',5'-trimethoxybenzoyl)-2-(4'-methoxyphenyl)-6methoxybenzo[b]thiophene was found to be 22.2 pg/ml. The EDso values of dimethoxybenzoyl, 2,6-dimethoxybenzoyl and 3,5-dimethoxy-4-hydroxybenzoyl derivatives of 2-(4-methoxyphenyl)-6-methoxybenzo-[b]thiophene compounds were estimated as greater than 100 ug/ml. The ED 50 value of a nitrogen derivative of combretastatin, trimethoxyphenyl)ethenyl]-2-methoxy-N, N-bis-(phenylmethyl)aniline was 33.9 itg/ml.

GROWTH INHIBITORY ACTIVITY AGAINST OTHER CANCER CELL LINES 3-(3',4',5'-Trimethoxybenzoyl)-2-(4'-methoxyphenyl)-6-methoxybenzo[b]-thiophene was evaluated in terms of growth inhibitory activity against several human cancer cell lines, including ovarian CNS, renal, lung, colon and melanoma lines. The assay used is described in Monks et al. Briefly, the cell suspensions, diluted according to the particular cell type and the expected target cell density (5,000 40,000 cells per well based on cell growth characteristics), were added by pipet (100 il) to 96-well microtiter plates. Inoculates were allowed a preincubation time of 24 28 hours at 37 0 C for stabilization. Incubation with the inhibitor compounds lasted for 48 hours in 5% CO, atmosphere and 100% humidity. Determination of cell growth was done by in situ fixation of cells, followed by staining with a protein-binding dye, sulforhodamine B (SRB), which binds to the basic amino acids of cellular macromolecules. The solubilized stain was measured spectrophotometrically. The results of these assays are shown in Table 1. Gs1 5 is defined as the dosage required to inhibit tumor cell growth by TABLE 1 Activity of 3-(3',4',5'-Trimethoxyphenyl)-2-(4'-methoxyphenyl)- 6 methoxybenzoblthiophene Against Human Cancer Cell Lines Cell Type Cell-Line GIso (g/ml) Ovarian OVCAR-3 1.9 x CNS SF-295 2.0 x Renal A498 4.6 x Lung-NSC NCI-H460 1.3 x Colon KM20L2 4.9 x 10' 2 Melanoma SK-MEL-5 4.8 x EXAMPLE 1A Improved Benzo[blthiophene Derivative Syntheses Experimental procedures for certain of the following compounds are described in Example 1. The biological activity presented in Example 1 (other than with P388 cells) related to compound 1 (and 1A) 5'-trimethoxybenzoyl)-2-(4'-methoxyphenyl)- 6 methoxybenzo[b]thiophene). The information for compound 1 is now updated. The inventors now report the IC 50 for inhibition of tubulin polymerization as an inhibition of the rate (Compound 1A and 10A) rather than a final "steady-state" number (all other compounds).

Compound IA Isame as compound 1 in Example 1] trimethoxybenzoyl)-2-(4'-methoxyphenyl)-6-methoxybenzoib]thiophene (see FIG. 2A, FIG.

2B and FIG. was retested for various activities.

Inhibition of tubulin polymerization with compound 1A gave 50% inhibition of the maximum tubulin assembly rate at 1.1 pM. The same assay with combretastatin A-4 gave a maximum rate of 0.73 tim. Electron microscopy failed to demonstrate any morphological difference in polymer formed in the presence or absence of compound IA. In both cases a mixture of microtubules and ribbons composed of parallel protofilaments was observed.

The human Burkitt lymphoma line CA46 was treated with varying concentrations of compound 1A, and a 50% growth inhibition occurred at 2 pM. Cells treated with a 10 pM concentration had a marked increase in the mitotic index, from 3% to 30%. Such an antimitotic effect. when combined with the tubulin assembly data. is strong evidence that tubulin is the intracellular target of compound 1A.

Modest inhibition of the binding of 3 H]colchicine to tubulin was observed with pM compound I A. as compared with the total inhibition caused by combrctastatin A-4.

Increasing the concentration of compound IA to 50 pM resulted in little additional inhibition.

Compound 2A 6'-dimcthoxybcnzoyl)-2-(4'-mcthoxyphenyl)-6methoxybenzolblthiophene (see FIG. 5) was found only mildly active with P388 cells as shown in Table 2.

Table 2 P388 Leukemia Data (Compound 2A) Cell Type Cell Line EDo 5 (pg/ml) Mouse Leukemia P388 >100 Compound 3A 5' dimethoxybenzoyl)-2-(4'-metoxypheflyl)- 6 methoxybcnzotblthiophefle (see FIG. 6) was also only mildly active with the P388 cell line as shown in Table 3.

Table 3 P388 Leukemia Data (Compound 3A) Cell Type Cell Line

ED

50 (pig/ml) Mouse Leukemia P388 >100 Compound 4A 4'-dimethoxybenzoyl)-2-(4'-mthoxylphefyl).

6 methoxybenzolblthiophefle (see FIG. 7) was synthesized and tested anew. The improved experimental as compared to that in Example 1 is included (immediately below) for compound 4A, found better than that in Example 1.

To a well stirred solution of methoxypheny l)-6-methoxybenzo~ib]thiophene (0.327 g, 1.21 mmol) and 3,4-dimethoxybenzoyl chloride (0.557 g. 2.77 mmol) in CH- 2 Cl 2 (20 ml) was added AIC1 3 (0.6 16 g, 4.62 mmol) portion-wise over a 15 min period. After 7 h, water was added, and the product was isolated initially by extraction with CH 2

,CI

2 and subsequently by extraction with EtOAc. The organic layers were separately washed with brine, combined and dried over Mg SO 4 Purification by flash chromatography (silica gel, 60:40 Et 2 O/hexanes) afforded 5 (0.402 g, 0.92 mmol. 76%) as a pale yellow solid. H-NMR (CDCI 3 360 MHz) d 7.54 J 8.9 Hz, I1H. Affl), 7.50 J 1.9 Hz. 1Hr 1u), 7.34 J =8.9 Hz. 21-1, ArH). 7.33 (in. 41-1. Arl-). 6.96 (dd. J 2.4 Hz. Ill1. Arl_1). 6.75 J 211. ArHl). 6.66 J Ill. Arli), 3.88 31-1. -OC L- 1 3.85 611. -OCIL 1 3.74 311, -0CI Compound 4A. 4'-dimcthoxy'bcnzoyl -methoxyphcnyl)-6methoxybenzolb]thiophcnC. had biological activity as shownm in Tablcs 4 and Compound 4A gave inhibition of tubulin polymerization with an IC 50 40 4M.

Table 4 P388 Leukemia Data (Compound 4A) Cell Type Cell Line

ED

50 (pg/mI) Mouse Leukemia P388 23 Table Human Cancer Cell Line Studies (Compound 4A) Cell Type Cell Line G1 50 (ltglml) Pancreas adn BXPC-3 5.2 Neuroblast SK-N-SH 3.2 Thyroid ca SW1736 Lung-NSC NCI-H-460 4.6 Pharynx-sqan FADU 4.7 Prostate DU-145 Compound 5A 3-(4'-mcthoxvbeflzoyl)2(4'l1Cthoxyphenyl)- 6 methoxybenzoilbthiophefle (see FIG. as shown in Table 6 and 7, had certain biological activity.

Table 6 P388 Leukemia Data (Compound Cell Type Cell Line

ED

50 (pg/mi) Mouse Leukemnia P388 >100 Table 7 Human Cancer Cell Line Studies (Compound Cell Type Cell Line Gl,(Pg/mI) Pancreas adn I3XPC-3 8.9 Mclanoma RPN-11-7951 CNS U251 Lung-NSC NCI-H460 Pharynx-sqam FADU Prostate DU-145 Compound 6A 3-(4'-ethoxyben~zoyl)-2-(4'-methoxyphenyl)- 6 methoxybenzolblthiophefle (see FIG. 9) has notable biological activity as seen in Tables 8 and 9.

Table 8 P388 Leukemia Data (Compound 6A) Cell Type Mouse Leukemnia Cell Line E- 50 qLwinl) ?~iVU P388 >1UV Cell Type Pancreas adn Melanoma

CNS

Lung-NSC Pharynx-sqam, Prostate Table 9 Human Cancer Cell Line Studies (Compound 6A) Cell Line G1 50 (4g/ml) BXPC-3 0.65 RPMI-7951 3.2 U251 0.43 NCI-H460 2.4 FADU 0.48 DU-145 3.9 Compound 7A 5'-triethoxybnzoyl)-2-(4'-methoxyphenyl)- 6 methoxybenzofblthiophefle (see FIG. 10) is described in Example 1.

Compound 7A was found to be mildly active in the cell toxicity tests as shown in Tables 10 andl11.

Table P388 Leukemia Data (Compound 7A) Cell Line P388 Cell Type Mouse Leukemia

ED,,

0 (pg/ml) >100 Table 11 Human Cancer -Cell Line Studies (Compound 7A) Cell Type Cell Line G1 50 (jig/ml) Pancreas adn BXPC-3 Melanoma RPMI-7951 CNS U251 Lung-NSC NCI-H460 Pharynx-sqam FADU Prostate DU-145 Compound 8A 5-t ri met hoxy phenyl)p ro piofylI]2-(4'-m ethoxy phny)- 6-mcthoxybcnizolbithiophene (see FIG. 11) was synthesizcd as follows (an improved synthesis is compared to that in Example 1).

To a well stirred solution of 2-(4'-methoxyphcn)l )-6-methoxybenzolbl thiophene (0.500 g, 1.85 mrnol) and 3'-(3',4',5'trirrethoxyphenyl) propionyl chloride (1.43 g, 5.55 rnmol) in CHCl, (50 ml) was added AIC1 3 (1.00 g, 7.50 mimol) portion-wise over a 15 min period. After 18 h, water was added, and the product was isolated initially by extraction with CH 2

CI

2 and subsequently by extraction with EtOAc. The organic layers were separately wvashed with NaHCO3 (sat) and brine, and then combined and dried over Mg SO 4 Purification by flash chromatography (silica gel. 70:30 hcxane/EtOAc) afforded 4 (0.089 g. 0. 18 mm-ol. as an off-white solid. Recrystallization (cihanolfhexane) yielded a highly pure. crystalline sample with an mp =127-128'C. I I 44MR (CDCI 3 360 Mllz) d 7.92 J= 8.91 z. 11. ArHj). 7.35 J= 8.7 Hlz. 211. ArFI), 7.25 J =2.4 Hz7- 1ll. ArHl). 7.04 8.9 1lIz. 2.4 liz. Ill1. ArH). 6.93 d. J 8.7 Hiz. 21-1. 3.88 311. -OCH 3 .5(.31 -OCLI 3.78 3 H. -OCHi.). 3.72 (s.

6H, -OCH13). 3.8 J =7.5Hz. 211, 3.7 J 7.45 2H. 13 C-NMR(CDCI,. 200.8. 160.5. 157.8, 153.0, 146.0, 140.0, 136.5. 136.2. 132.5. 132.3. 130.8. 126.2. 124.7, 115.1.

114.3, 105.2-, 104.3, 60.8, 55.9, 55.6, 55.3, 44.8. 31.1. HRMS (El) M+ calc d for C 28

H

2 g0 6

S

492.1607. found 492.2337. Anal. Caled for C 2 8H 28

O

6 S: C, 68.27; Hl, 5.73; S, 6.51. Found: C, 68. 17; H, 5.80; S, 6.50.

Compound 8A, 5' trmtoyhnlpoinll2('mtoyhnl,6 methoxybenzo[bthiophele (see FIG. 11), had biological activity as shown in Tables 12 and 13.

Table 12 P388 Leukemia Data (Compound 8A) Cell Line P388 Cell Type Mouse Leukemia

ED

50 (jig/mi) Cell Type Pancreas adn Melanoma

CNS

Lung-NSC Pharynx-sqam Prostate Table 13 Human Cancer Cell Line Studies (Compound 8A Cell Line G1 50 (jig/mi) BXPC-3 RPMI-7951 U251 NCI-H460 3.8 FADU 9.1 DU-145 Compound 9A 3-(3',4',5'-trithoxybcnzovi)-2-(4'-cthoxypheflyl)- 6 cthoxybenzolbithiophefle (see FIG. 12) was synthesizcd as follows.

To a well-stirred solution of 2-(4'ethoxypheny1)-6-ethoxybenzo[h]thophele (0.087 g, 0.291 mmol) and 3, 4, 5-triethoxybenzoyl chloride (0.200 g, 0.733 mnrol) in CH 2 C1 2 (30ml) was added AICl.I 126 g, 0.942 mmol) portionwise over a 5 min period. After 24 h, water was added. and the product was isolated initially by extraction with CHCl 2 and subsequently by extraction with EtOAc. The organic layers were washed separately with brine and then combined and dried over Mg S0O. Purification by flash chromatography (silica gel. 80:20 hexane/EtOAc) affordcd a highly pure sample of the desired product (0.043 g. 28%) as a white solid with mp 126-128-C. 'I-I -NMR (CDC1 3 360MHz) d 7.64 =8.9 Hiz. I1. ArH). 7.31 (d.

J 2.3 Hz. 1 H. ArH), 7.27 J 9.3 Hz. 211. ArH), 7.02 2H, ArH), 6.99 (dd, J 2.3 Hz.

I H. ArH), 6.71 J =8.7 Hz, 211,. ArH), 4.11 J= 6.9 Hz, 2H, -OCHU3), 4.06 J 7.1 HZ- 2H, OCI-l,), 3.95 J =3.9H-z, 2H, -OCH2), 3.91 J 6.96Hz, 4H, -OCj1 2 1 .46 J 3H, CH3), 1.37 J1 7.0Hz, 3H, CU- 3 1.34 J 7.0Hz, 6H, CH3), 1.28 J 7.0Hz, 3H, CHj); 1 3 C-NMR (CDC1 3 90 MHz) d 193.3, 159.2, 157.0, 152.5, 143.6, 143.3, 140.0, 133.9, 132.3, 130.3, 130.1, 126.0, 124.2, 115.3, 114.5, 109.0, 105.3, 68.9, 64.7, 63.9, 63.4, 15.5, 14.8, 14.8, 14.7. HRMS (El) M-calc for C 31

H

34 0 6 S 534.753, found 534.2185. Anal calcd for

C

31

H

34 0 6 S: C, 69.64; H,6.41; S, 5.99. Found: C, 69.45; H, 6.50; S, 5.94.

Compound 9A was tested for biological activity as shown in Tables 14 and Table 14 P388 Leukemia Data (Compound 9A) Cell Type Cell Line

ED

50 (jig/mi) Mouse Leukemia P388 Table Human Cancer Cell Line Studies (Compound 9A) Cell Type Cell Line G1 50 (jig/mi) Pancreas adn BXPC-3 Melanoma RPMI-7951 CNS U251 Lung-NSC NCI-H460 Pharvnx-sqamn FADU Prostate DU-145 Compound IJOA 3-(4'-cthoxy-3', 5'-dimethoxybcnzol)-2-(4'-mcthoxyphcnyl)- 6 mcthoxyhenzolblthiophene (see FIG. 13) was sy'nthesized as follows.

To a well stirred solution of Nal (0.04 9 g. 2.041 mmoli and 34(3. 4'hydroxy-bcnzol)-'2(4'-mcthoxYlphcflNl)-6-mcthox\ hcniolhjthophcne (0.105 g, 0.233 mmol) in TI IF (30 ml). cooled in ice wvas added ethyltrifluoromethanc sulfonate 1 mi. 0. 137 g.

0.771 mmol). After 30 min. water w~as added and the product wa isolated antially by extraction with CHC1 2 and subsequently by extraction with EtOAc. The organic layers were washed with NaHCO3 followed by brine and then the combined organic layers were dried over MgSO 4 Purification by flash chromatography (silica gel, 70:30 hexane/EtOAc) afforded the desired product as a white solid (0.037g, 0.077 mmol, 35%) with mp 138-139'C. 'H -NN4R (CDCI 3 360MHz) d 7.69 J 8.9 Hz, 1 H, Arli) 7.33 J 2.3 Hz, 1 H, ArH) 7.29 J 8.7Hz, 2H, ArH), 7.05 2H, ArH), 7.01 (dd, J 8.9, 2.4 Hz, I1H, ArH), 6.74 J= 8.7 Hz, 2H, ArH), 4.05 J 7.1 Hz, 2H, -OCH 2 3.90 3H, OCjj 3 3.74 3H, -OCjj3), 3.71 6H, -0CHi 3 1.29 J= 7.0, 3H, CHj); HRMS (EI) M+ calcd for C 27

H

26 0 6 S 478.1450, found 478.1434.

Compound I OA behaves very similarly to compound 1IA. It demonstrates clear inhibition of tubulin polymerization of rate, but not of plateau. The polymerization curves obtained with 4, and 40 utM of compound I OA were nearly identical. Biological activity of compound IlOA is shown in Table 16.

Table 16 Human Cancer Cell Line Studies (Compound Cell Type Cell Line

GI

50 igml) Pancreas adn BXPC-3 0.22 Melanoma SK-N-SH 0.17 Thyroid ca SW1736 0.31 Lung-NSC NCI-H460 0.32 Pharynx-sqamn FADU 0.31 Prostate DU-145 0.35 Compound I1I A 3-(4'-N,N-dimethlamilobeflzoyl)2(4'-methoxyphen)'l)- 6 methoxybenizojbithiophefle (see FIG. 14) was synthesized as follows.

To a well stirred solution of 2-(4'-methoxyphelyl)-6-methoxybenzo[b] thiophene (0.501 g, 1.85 mnmol) and 4-N,N-dimethylamiflobenzoyl chloride (1.43 g, 5.55 mmol) in CH 2

CI

2 mL) was added AIC1 3 (1.147 g, 8.60 mmol) portion-wise over a 15 min period. After 24 h, the rcaction mixture was refluxed for 2 h and then quenched with water. The product was isolated initially by extraction with CHCI 2 and subsequently by extraction with EtOAc. The organic layers were separately washed with saturated NaHCO 3 and then with brine. They were then combined and dried over MgSO 4 Purification by flash chromatography (silica gel. 70:30 hexane/EtOAc) afforded 6 (0.408 g, 0.98 mmul. 53%) as an pale yellow solid. Recrystallization (cthanol/exane/CHC12 yielded a highly pure. crystalline sample of 6 with an mp 163-164*C.

H -NMR (CDC1 3 360 MHz) d 7.74 (dt, J 9. 1, Hz, 2H, ArH), 7.45 J 8.7Hz, 11H. ArH), 7.42 (dt, J 8.9, 2.2 Hz, 2H, Arli), 7.31 J 2.3 Hz, I1H, ArH), 6.92 (dd, J 2.4 Hz.

I H, ArH), 6.75 (dt, J 8.9, 2.2 Hz, 2HI ArH), 6.51 (dt, J Hz, 2H, Arll), 3.87 3H, OCHJ), 3.75 3H, -OCHj), 3.01 6H, -N(CIL) 2 3

C-NMR(CDCI

3 90MHz) HRMS (El) M caled for C 25

H

23 0 3 NS 417.1400, found4l7.1390. Anal. Caled for C 25

H

23 0 3 NS: C, 71.92; H, 5.81; N, 3.36; S, 7.68. Found C, 71.81; H, 5.55; N, 3.38; S, 7.68.

Compound I IlA showed an inhibition of tubulin polymerization with an IC 5 0 40 pM.

Further biological activity of compound 1. I A is shown in Table 17.

Table 17 Human Cancer Cell Line Studies (Compound I A) Cell Type Cell Line G150 (jig/mI) Pancreas adn BXPC-3 Neuroblast SK-N-SH Thyroid ca SW1736 Lung-NSC NCI-H460 Pharynx-sqarn FADU Prostate DU-145 Compound 12A 5'-trifluorobnzoyl)2(4'-mlethoxypheflyl)4methoxybenzolbithiophcfle (see FIG. 15) was synthesized as follows: To a well stirred solution of -methoxyphenyl )-4-methoxybenzo~bIlthiophene (0.201g, 0.74 mmol) and 3,4.5-trifluorobenzoyl chloride (0.288g, 1 .48 mmol) in CH 2 CI_' (7 mL) was added AIC1 3 (0.304g, 2.22mmol) portion-wise over a 15 minute period. After 18h, water was added, and the product was isolated initially with CH 2 C1, and subsequently by extraction with EtOAc. The organic layers were separately washed sequentially with NaHCO 3 and brine and then dried over MgSO 4 Purification by flash chromatography (silica gel. 80:20 hexane/EtOAc) afforded bcnzofbllthiophefle (0.032g. 0.O8mxnol. 10%) as a white solid. Recrystallization (Ethanol1/hcxancCI1 2 CI1 2 yielded a highly pure crystal line sample. 'H-NMR(CDCI 3 360 M1z) 57.74 J=8.9Hz. 2H. ArHD, 7.70 J--9.3 I z. Ill., ArH), 7.68 I 11, AriD. 7.43 (dd. 6.61 z. 211 Ad-i). 7.00 J=8.9 1-z. 211. Aril). 6.83 J=8.4 I z. Il11. ArH). 4.09 3 H. 0C1 3 (S 31. 'C-NMR (CDCI 3 90MHz) 190.5. 160.1, 159.1. 152.3. 150.0.

146.6, 141.3, 134.4. 132.9, 132.1, 127.9, 126.9, 122.4, 114.5. 114.1, 114.1, 114.0, 113.9, 113.8.

56.0. 55.4. HRMS (El) M" calcd for C 23

H

15

F

3 0 3 S 428.0694 found 428.0620. Compound 12A shows an inhibition of tubulin polymerization 40 jiM. Biological activity of compound 12A is shown in Table 18.

Table 18 Human Cancer Cell Line Studies (Compound 12A) Cell Type Cell Line G1 50 (tg/iml) Pancreas adn BXPC-3 Neuroblast SK-N-SH Thyroid ca SW1736. Lung-NSC NCI-H460 Pharynx-sqarn FADU 6.7 D cJtJ3UL DU-145 I %J Compound 13A 5'-trimethoxybenzoyl)-2-( 4 -methoxyphenyl)- 4 methoxybeflzolblthiophefle (see FIG. 16) are synthesizcd as follows: To a well stirred solution of -methoxyphenyl)-4-methoxy'befZO[b~thiophene (0.200g, 0.74mrnol) and 3,4,5-trimethoxybenzoyl chloride 1 84g, 0.74mmol) in CH_2C1 2 (7mL) was added AIC1 3 (0.200g, 1 .48mmoI) portion-wise over a 15 minute period. After 1 8h, water was added, and the product was isolated initially with CHI 2 Cl 2 and subsequently by extraction with EtOAc. The organic layers were separately washed sequentially with NaHCO 3 and brine and then dried over MgSO 4 Purification by flash chromatography (silica gel, 70:30 hexane/EtOAc) afforded benzo[b]thiophene (0.023g' 0.05mrnol, as a white solid. Recrystallization (Ethanol/hexane/CH 2

CI

2 yielded a highly pure crystalline sample. I H-NMR (CDCI 3 360 MHz) 57.80 .1=8.4Hz. I H. ArH), 7.73 .1=8.8Hz. 2'H. Arjj). 7.66 I H. ArH). 7.02 2H, ArHl), 6.96 J=8.8Hz.. 2H-. ArH), 6.70 .1=8.3Hz. 1 H. ariD., 4.08 3H. -OCI± 3 3.95 3H.

-OCH

3 3.91 611. -OCIL). 3.87 R1], -OC HRMS (El) M* calcd for C,,1-1 24 0,S 464.1294. found 464.13 10. Anal. Calcd for C 26

H

24 0 6 S: C, 67.23; H, 5.21:- S. 6.90. Found C.

67.19; H, 5.26; S, 6.87. Compound 13A shows an inhibition of tubulin polymerization pM. Biological activity of compound 13A is shown in Table 19.

Nei Th: Ph 1 Prc Table 19 Human Cancer Cell Line Studies (Compound 13A) Cell Type Cell Line Gl 50 (jiglml) icreas adn BXPC-3 uroblast SK-N-SH. yroid ca SW1736 ng-NSC NCI-H460 arynx-sqarn FADU 7.8 )state DU-145 Compound 14A 5'-trifluorobenzoyI)-2-(4'-methoxyphenyl)- 6 methoxybenzoiblthiophcfle (see FIG. 17) was synthesized as follows.

To a well-stirred solution of 2-(4'methoxyphenyl)-6-methoxybeIzo[b]thiophene 112 g, 0.4 14 mmol) and 3, 4, 5-trifluorobenzoyl chloride (0.437 g, 2.271 rnrol) in CH- 2 C1 2 (40 ml) was added AIC1 3 (0.471 g, 3.532 mmnol) portionwise over a 15 min period under reflux conditions.

After 30 h, water was added, and the product was isolated initially by extraction with CMCI, and subsequently by extraction with EtOAc. The organic layers were washed separately with brine and then combined and dried over MgSO 4 Purification by flash chromatography (silica gel, first with hexanes then with 95:5 hexane/EtOAc) afforded a yellow liquid (0.068 g, 'H -NMR (CDC1 3 360MHz) d 7.69 J =8.9 Hz, 1lH, Aiji), 7.37 (d,J 6.7 Hz, 1H, ArH), 7.35 (d,J= 6.7 Hz7. IlH, ArH), 7.33 J= 2.4 Hz. lH, 7.26 J 8.8 Hz. 2H, NH), 7.04 (dd. J 8.9.

2.4 Hz. I H. ArU), 6.77 J =8.8 Hz. 211, Arl!), 3.90 3H-. OCHR), 3.77 3H. -OCji3).

Compound 14A showed inhibition of tubulin polymerization with an IC 50 40 tiM.

Biological activity of compound 1 4A is shown in Table Table Human Cancer Cell Line Studies (Compound 14A) Cell Type Cell Line G150 (4.g/ml) Pancreas adn BXPC-3 Neuroblast SK-N-SH Thyroid ca .SW1736 Lung-NSC NCI-H460 Pharynx-sqam FADU 13.6 Prostate DU- 145 Compound 15A 6'-pentafluorobeflzoyl)2(4'-methoxyphenyl)- 6 mcthoxybenzolbltbiophefle (see FIG. 18) was synthesized as follows.

To a well-stirred solution of 2-(4Pmehoxyphenyl)-6-methoxyberLzotb]thiophene (0.538 g, 1.989 mmol) and 2, 3, 4,5, 6-pentafluoro benzoyl chloride (1.000 g, 4.338 mmol) in CH 2

CI

2 ml) was added AlC1 3 (2.147 g, 16.103 mmol) portionwise over a 5 min period. After 4.5 h, water was added, and the product was isolated initially by extraction with CH 2

CI

2 and subsequently by extraction with EtOAc. The organic layers were washed separately with brine and then combined and dried over MgSO 4 Purification by flash chromatography (silica gel, 90:10 hexane/EtOAc then with 80:20 hexane/EtOAc) afforded the desired product (0.5086 g, 60%) as a yellow colored solid. Recrystallization with ethylacetate/hexane mixture, gave highly pure product (0.206g). I H-NMR (CDCI3. 360MHz) d 8.47 J =9.0 Hz, I1H, Ari±), 7.30 J =2.4 1 Iz, -1H, ArH). 7.24 J =8.8 Hz, 2H. ArH), 7.16 (dd, J 2.2 Hz. I H. ArH), 6.77 J 211. ArH), 3.91 3 H, -OCI 3.78, 3 H. OCLI H RMS (El) M* calc for

C

23 11 13 0 3 SF, 464.0537. found 464.0506.

Compound 15A shows an inhibition of tubulin polymerization with an IC 50 40 1 iM.

Biological activity of compound 15A is shown in Table 21.

Table 21 Human -Cancer Cell Line Studies (Compound Cell Type Cell Line GISO (jig/mI) Pancreas adn BXPC-3 5.9 Neuroblast SK-N-SH 1.4 Thyroid ca SW1736 Lung-NSC NCI-H460 7.9 Pharynx-sqam FADU 1.3 Prostate DU-145 Compound 16A 5'-trimethoxybeflzoyl)2(4'-methoxyphenyl)benzolblthiophcfle (see FIG. 19) was synthesized as follows: To a well-stirred solution of 2-(4 '-methoxyphenyl)beflzo[b~thiophefle (0.081 g, 0.32 mmol) and 3,4,5-trimethoxybeflzoyl chloride 148 g. 0.64 mmol) in CHCl 2 (15 mL) was addcd AIC1 3 (0.144g, 1.08 mnmol) portion-wise over a 5 minute period. After 3h 20min, water was added, and the product was isolated initially by extraction with CHC1 2 and subsequently bN extraction with EtOAc. The organic layers were separately washed with brine and then combined and dried over MgSO 4 Purification by flash chromatography (silica gel, 90:10 hexane/EtOAc then with 80:20 hexane/EtOAc) afforded desired benzo[bljthiophene (0.035 g, 26%) as white solid. 'H-NMR (CDCI,. 360 MHz) 8 7.87 I1-I. ArH), 7.78 (in, I H. ArH.), 7.37 (mn. 41-1. ArH). 7.07 2H. Art!). 6.76 J=6.7, 2H. ArhJ., 3.84 3H. -0db3), 3.75 3H.

-OCH9., 3.73 611. -0CH1) Compound 16A shows an inhibition of tubulin polymerization with an IC,, 40 jiM.

Biological activity of compound 16A is shown in Table2.

Table 22 Human Cancer Cell Line Studies (Compound 16A) Cell Type Cell Line G150 (pg/mI) Pancreas adn BXPC-3 1.7 Neuroblast SK-N-SH 0.83 Thyroid ca SW1736 4.6 Lung-NSC NCI-H460 2.7 Pharynx-sqamn FADU 0.63 Prostate DU-145 4.8 Compound 17A 5'-trimethoxyphenyl)ciflfamoylV- 2 4 mcthoxypheny)-6-mlcthoxybenzobIthiophene (see FIG. 20) was synthesized as follows.

To a well stirred solution of 2-4-ehxpey)6mtoyez~~hohn (1.006 g, 3.721 mmol) and 3-(3',4',5'trimethoxy)cilfaloyl chloride (1.834 g, 7.146 mmol) in CH,C1 2 mL) was added AIC1 3 (2.093 g, 15.697 mrnol) portion-wise over a 15S min period. After 4 h, water was added, and the product was isolated initially by extraction with CH.CI 2 and subsequently by extraction with EtOAc. The organic layers were separately washcd with saturated NaHCO 3 And then with brine. They were then combined and dried over MgSO 4 Purification by flash chromatography (silica gel, 60:40 hexane/EtOAc) afforded the desired product (0.586g, 1.20 mmol, 32. as a pale yellow solid. Recrystallization (ethanol/hexane) yielded a highly pure, crystalline sample with an mp 154-1 55-C. 'I I -NMR (CDCI 3 360 MHz) d 8.18 J 9.0 Hz. I H.ArH). 7.5 J =15 Hz. I11. ArLW. 7.49 (dt, J 8.9. 2.2 Hz. 2H.

ArI). 7.30 J =2.3Hz7. 1 H. ArH). 7.08 (dd. J 2.5 Hz, I H. ArH). 6.95 (dt, J 8.8. 2.1 Hz, 211, ArH), 6.55 J 15.7 11z- 111. ArID, 6.41 2H1. Arij., 3.90 311. OCH3), 3.84 (s, 3H. OCH3), 3.80 3H, OCH3), 3.77 6H-, 0C113); 'C-NMR (CDCI,, 9OMHz).HRMS (El) M+ calcd for C 28

H

26

O

6 S 490.1450, found 490.1300. Anal. Calcd for C 28

H

26 0 6 S: C, 68.55; H.

5.30; S, 6.54. Found C, 68.57; H, 5.39; S, 6.52.

Compound 17A showed an inhibition of tubulin polymerization with an Ic 50 40 PM.

Biological activity of compound 17A is shown in Table 23.

Table 23 Human Cancer-Cell Line Studies (Compound 17A)~ Cell Type Cell Line

GI

5 o .ig/ml) Pancreas adn BXPC-3 2.3 Neuroblast SK-N-SH 1.3 Thyroid ca SW1 736 5.2 Lung-NSC NCI-H460 3.9 Pharynx-sqam FADU 1.8 Prostate DU-145 Compound 18A 5'-trimethoxybeflzoyl)2(4'-CthoxYphenvl)- 6 ctboxybcnzolblthiophefle (see FIG. 21 was synthesized as follows.

To a well-stirred solution of 2-(4 ethoxyphenyl)-6-ethoxvbeflzo[b~thiophene (0.095 g, 0.32 mmol) and 3,4,5-trimethoxybenzoyl chloride 159 g, 0.69 mmol) in CH 2 CI, (15 mL) was added AIC1 3 (0.139g, 1 .04 mmol) portion-wise over a 5 minute period. After 30 min.. water was addcd. and the product was isolated initially by extraction with CHCI 2 and subsequently by extraction with EtOAc. The organic layers were separately washed with brine and then combined and dried over MgSO 4 Purification by flash chromatography (silica gel, 80:20 hexane/EtOAc) afforded benzo[blthiophefle 110 g, 0.2 minol, 69%) as an off-white solid.

'H-NMR (CDCI,, 360 Mhz) 5 7.65 J 8.9 Hz. 1 H. ArKj). 7.32 J 2. 3 HZ. I H. Arjj), 7.29 J 8.8 H~z_ 2H, ArHi), 7.06 21H, Arn!). 7.00 (dd. J 2.4 Hz. I1H. ArK]). 6.73 J 8.7 Hz. 211. ArH). 4.12 J =7.0 1lz. 2H-. 3.97 J 6.9 Hiz. 2H. -Cl 3.83 3H.

-O-Cjj). 3.73 6H. -OCIj 3 1.47 J 6.9 1lIz- 3f11, -CRI). 1.37 J =7.0 Hz. 3H. -CR).

Compound 18A showed an inhibition of tubulin polymerization with an IC 50 40 1 Biological activity of compound 18A is shown in Table 24.

Table 24 Human Cancer Cell Line Studies (Compound 18A)~ Cell Type Cell Line

GI

50 (pg/m1) Pancreas adn BXPC-3 1.6 Neuroblast SK-N-SH 0.33 Thyroid ca SW1736 2.3 Lung-NSC NCI-H460 1.4 Pharynx-sqam FADU 0.60 Prostate DU-145 3.6 Compound 19A 3-(4'-bydroxy -3',5'-dimethoxybflzoyl)2(4'-methoxyphenyl)- 6 methoxy benzoibithiophefle (see FIG. 22) was synthesized as follows.

To a well-stirred solution of 2-4-ehxpey)6mtoyez~~hohn (0.250 g, 0.925 rnmol) and 3,4,5-trimethoxybenzoyl chloride (0.320 g, 1.39 mmol) in CH 2

CI

2 (20 mL) was added AIC1 3 (0.925 g, 6.94 mmol) portion-wise over a 15 min period. After 20 h, water was addcd. and the product was isolated initially by extraction with CH 2 CI, and subsequently by extraction with EtOAc. The organic layers were separately washed with brine and then combined and dried over MgSO 4 Purification by flash chromatography (silica gel, 60:40 EtOAc/hexane) followed by recrystallization (hexane/ethanol) afforded a highly pure, crystalline sample of 2 (0.018 g, 0.040 mmol) with mp 142 1431C. 'H -NMR (CDCl 3 360 MHz) d 7.62 (dd, J 0.3 Hz, I H, 7.33 J =8.9 Hz. 2H, Arjj), 7.33 J =2.5 Hz, IRH. ArH), 7.12 211. Ar~j) 7.00 (dd, J 8.9. 2.4 Hz, I H. ArH), 6.76 J =8.9 Hz, 2H. ArH), 5.90 I H. 011). 3.89 3H. -OCH3). 3.77 6[I. OCj-l). 3.76 3H, -OCIL). "C-NMR (CDC1 3 MHz) d 192.7. 159.9.,157.8, 146.6.142.9.140.2, 139.9. 134.1, 130.3, 130.1. 128.7. 126.2. 124.2.

114.9, 114.2, 107.5, 104.5. 56.4, 55.7, 55.3. H-RMS (El) M' calcd for C,SH22O 6 S 450.1137.

found 450.1139. Anal. Calcd for C 2 5

H

2 2 0 6 S: C, 66.65; H, 4.92; S, 7.12. Found: C, 66.52; H, 5.01; S, 6.97.

Table 25 shows biological activity of compound 19A.

37 Table P388 Leukemia Data (Compound 19A) Cell Type Cell Line ED 5 0 (pg/ml) Mouse Leukemia P388 >100 Compound 20A 3-(phenylacctyl)-2-(4'-methoxyphenyl)-6methoxybenzo[blthiophene (see FIG. 23) was synthesized as follows.

To a well stirred solution of2-(4'-methoxyphenyl)-6-methoxybenzo[b]thiophene (0.452 g, 1.67 mmol) and phenylacetyl chloride (0.52 g, 3.34 mmol) in CH 2 Cl 2 (50 mL) was added AIC1 3 (0.670 g, 5.02 mmol) portion-wise over a 15 min period. After I h (total reaction time), water was added, and the product was isolated initially by extraction with CHC1l and subsequently by extraction with EtOAc. The organic layers were separately washed sequentially with NaHCO 3 and brine and then dried over MgSO 4 Purification by flash chromatography (silica gel, 70:30 hexane/EtOAc) afforded benzo[b]thiophene 2 (0.11 g, 0.29 mmol, 17.1%) as a white solid. Recrystallization (Ethanol/hexane) yielded a highly pure, crystalline sample. 'H NMR (CDCI 3 360 MHz) d 7.87 J= 9 Hz, 1H. ArH), 7.45 (td, J= 8.82, 2.16 Hz, 2H. ArH), 7.2 4H, ArH), 7.0 5H, ArH), 3.88 3H, -OCHj), 3.86 3H. -OCH3), 3.73 2H, Cf 2 Tables 26 and 27 show biological activity of compound Table 26 P388 Leukemia Data (Compound Cell Type Cell Line EDso (pg/ml) Mouse Leukemia P388 Table 27 Human Cancer Cell Line Studies (Compound Cell Type Cell Line G1 50 (j9g/Ml) Pancreas adn BXPC-3 Melanoma RPMI-7951 GNS U251 Lung-NSC NCI-H1460 Pharynx-s'qam FADU 9.2 Prostate DU-145 Compound 21A 5'-tri meth oxy)p henv la cetyI)2(4'-met hoxyp hen 1)- 6 methoxybenzolblthiophefle (see FIG. 24) was synthesized as follows.

To a well stirred solution of 2-(4'-methoxyphenyl)-6-nmethoxybenzo[b]thiophene (0.302 g, 1.12 mnmol) and 3',4',5'trimethoxypheflyl acetyl chloride (0.541 g, 2.21 mmol) in CH 2 Cl, mL) was added AIC1 3 (0.600 g, 4.50 mmnol) portion-wise over a 15 min period. After h, water was added, and the product was isolated initially by extraction with CH 2

CI

2 and subsequently by extraction with EtOAc. The organic layers were separately washed with NaHCO 3 (sat) and brine, and then combined and dried over MgSO 4 Purification by flash chromatography (silica gel, 60:40 hexane/EtOAc) afforded benzo[blthiophene 3 (0.470 g, 0.99 mmol, 88.7%) as a white solid. Recrystallization (ethanol/hexane) yielded a highly pure, crystalline solid with an mp 1 17-118 0

C.

'H-NMR (CDCI 3 360 MHz) d 7.89 (d,J 9 Hz, 11. Arjj), 7.43 (td, J =8.82, 2.16 Hz, 211. ArH). 7.25 J =2.3 Hz, I H. Arh!), 7.0 (in. 3H. Arjj), 6.15 2H. Art!). 3.88 3H. OCHj 3 3.87 3H, -OCH.

3 3.77 311, -0C1 3 3.72 6H-. -00CH), 3.66 211, CL! 2 3

C

NN4R(CDCI 3 90 Mhz) 198.9. 160.6, 157.8, 153.0, 145.6. 140.0,, 132.8,, 130,9, 129.8. 126. 1, 124.5, 115.2, 114.5, 106.4, 104.2, 60.8, 56.0, 55.6, 55.4, 49.9. HR'MS (El) M' calcd for

C

27

H

26 0 6 S 478.1450, found 478.1609. Anal. Calcd for C 27

H

26 0 6 S: C, 67.77; H, 4.48; S, S. 6.70.

Found C, 67.85; H, 5.55; S, 6.73.

Tables 28 and 29 show biological activity of compound 21 A.

Table 28 P388 Leukemia Data (Compound 21AI Cell Type Cell Line

ED

50 (ltg/ml) Mouse Leukemia P388 Table 29 Human Cancer Cell Line Studies (Compound 21A) Cell Type Cell Line G1 5 0 (44I) Pancreas adn BXPC-3 9.8 Melanoma RPMI-7951 CNS U251 Lung-NSC NCI-H460 Pharynx-sqamn FADU 7.9 Prostate DU-145 EXAMPLE 2 DIARYL-ETHER benzolbltionhene

DERIVATIVES

The following two compounds have been prepared by chemical synthesis and one of them has been evaluated in termns of its biological efficacy. The biological results on the other derivative are forthcoming.

Compound 22B 3 -(3',4',5I-trimethoxy-pheox)2-(4'-mthoxYlphcn)I)- 6 mctho~ybcnzojbjthiophefle S-oxide (see FIG. 25) was sNvnthsizcd as follows.

To a well stirred solution of 3.4.5-trimethox)yphflol (0.08 1g. 0.44 mmol) in DMF (5 ml) was added NaH (0.020 g, 0.84 mmol) and stirred at room temperature for 15 min followed by thc addition of a mixture of 3 ,7-dibromo and 3-bromo -2-(4'-methoxyphenyl methoxybenzolb]thiophefle-S-oxide (0.lS0g, 0.35 mxol). After 2 h the reaction mixture is partitioned between 10% ethanol -ethylacetate mixture and water. The aqueous phase was extracted 3x with 10% ethanol solution. Washing the organic layer with water (5x) followed by brine, drying over MgSO 4 and evaporation of the solvent gave a dark colored oil. Trituration of the residue with ether and hexane mixture resulted in desired products as a yellow fluffy solid.

'l--NMR (CDC1 3 300 MHz) 857.65 J1 8.9 Hz, 2H, ArH), 7.34 J =2.3 Hz, I H, ArH), 7.22 J 8.5 Hz, I H, ArH), 6.99 (dd, J 2.4 Hz, I H, Mjj), 6.86 J 2H, AI), 6.29 2H, Arli), 3.89 3H, -OCij 3 3.79 3H, -OC 3.76 3H, -OCH 3 3.75 6H, OCH3).

Compound 23B ,4',5?-trimetboxyphefloxy)2(4'-methoxyphenyI)- 6 inetboxybenzolbiophene (see FIG. 26) was synthesized as follows.

To an ice cooled, well stirred solution of mixture of 3-(3',4',5'-trimethoxyphenoxy)- 2 4 methoxyphenyl)-6-methoxybezo [b]thiophefle S-oxide and 7-bromo-3 trimethoxyphenoxy)2(4'-methoxyphenyl)6methoxybenzo[b]tiophene S-oxides 183 g, 0.34 mmol) in THF (10 ml) was added lithium aluminum hydride (0.028 g, 0.72 mmol). After 1.5 h, the reaction was quenched with water followed by usual work up with ethyl acetate, brine and dried over MgSO 4 Removal of the solvent followed by purification by flash chromatography (80:20 hexanes: ethyl acetate) resulted in desired product (0.011 g, 0.025 mxnmol) as a white colorless solid with an mp 129-13 1 0 C. I H-NMR (CDC1 3 300 Mhz) 8 7.66 J= 8.9 Hz, 2H, Ar~j), 7.31 J =8.7 Hz, I H. ArH), 7.25 J 2.2 Hz, IRH. ArH), 6.91 J 9.0 H~z, 2H, AriD), 6.90 (dd, J 2.3 Hz, I H. ArH), 6.21 2H, ArH, 3.88 3H, -OCH3), 3.82 3H, -OCfl) .8 s H -OCHi,37 s H -OCH 3 HRMS (El) M cald for C.

2 5 i-1 24 0 6

S

452.1248, found 452, 1294. Anal. Calcd for C, 5

H-

2 4 0 6 S: C, 66.36; H, 5.35; S, 7.08. Found: C, 65.12; H, 5.39; S, 6.96.

HRMS (El) M calcd for C 2 5

H

24 0 6 S 452.1248, found 452.1294. Anal. Calcd for C2,H 2 4

O

6 S: C. 66.36; H, 5.35, S, 7.08. Found: C, 65.12; H, 5.39; 5, 6.96.

The biological activity of compound 23B was measured as seen in Tables 30 and 3 1. The inhibition of tubulin polymerization by compound 23 B gave an ICS 50 1.4 P.M.

TABLE P388 Lukmia Data (Compound 23B) Cell Type Cell Line

ED,,

0 ig/ml) Mouse Leukemia P388 3.09 TABLE 31 Human Cancer Cell Line Studies (In Vitro) (Compound 23B Cell Type Cell Line GI 5 0 (pg/ml) Pancreas adn BXPC-3 0.23 Neuroblast SK-N-SH 0.063 Thyroid ca SW1736 0.73 Lung-NSC NC1-H460 0.31 Pharynx-sqam FADU 0.098 Prostate DU-145 0.42 Significant biological activity is expected for the as yet untested compound based on the prevalence of such activity for compounds 23B and the compounds described in other Examples.

It will be apparent to anyone skilled in the art that the experimental procedures used to prepare the benzo[b]thiophene derivatives (Example 1 and 1A) can be suitably modified to incorporate a wide-variety of alkoxy groups and substitution patterns.

In addition, the availability of the vinyl bromide used as a precursor in the preparation of diaryl ether derivatives (22B and 23B Example 2) provides a myriad of reaction possibilities for the preparation of related derivatives. For example, the vinylbromide may undergo halogenmetal exchange to form a very nucleophilic vinyl-metal species which will prove very reactive with a wide variety ofelectrophiles (most notably carbonyl groups). The vinylbromide may also be subject to direct attack by organocuprate reagents which upon 1.4 addition and subsequent elimination of bromide, will render new compounds which are substituted at the 3-position of the bcnzo[h]thiophene core structure. This should be especially useful for installing aryl groups (both substituted and unfunctionalized) directly on the 3-position of the bcnzo[b]thiophenc core structure.

EXAMPLE 3 BENZOFURAN

DERIVATIVES

Compound 24C 3-(3',4',5'-trimethoxybenzoyl)-2-(4'-methoxyphenyl)-6methoxybenzolblfuran (see FIG. 27) was prepared as follows.

To a well-stirred solution of 2-(4'mehoxyphenyl)-6-methoxybenzo[b]furan (1.104 g, 0.409 mmol) and 3, 4, 5-trimethoxybenzoyl chloride (0.195 g, 0.846 mmol) in CH 2 Cl 2 (25 ml) was added AIC1 3 (0.169 g, 1.270 mmol) portionwise over a 5 min period. After 3 h, water was added, and the product was isolated initially by extraction with CH 2 Cl 2 and subsequently by extraction with EtOAc. The organic layers were washed separately with brine and then combined and dried over MgSO 4 Purification by flash chromatography (silica gel, 90:10 hexane/EtOAc then with 80:20 hexane/EtOAc) afforded a highly pure sample of the desired product (0.045 g, 25%) as a yellow colored liquid. 'H-NMR (CDC1 3 360MHz) d 7.58 J= 8.8.

Hz, 1H, ArH), 7.39 J= 8.9 Hz, 2H, ArH), 7.12 2H, ArH), 7.10 J= 2.2 Hz, 1H, ArH_), 6.98 (dd, J= 8.8, 2.2 Hz, 1H, ArH), 6.89 J= 8.9 Hz, 2H, ArH), 3.91 3H, -OCH3), 3.87 (s, 3H. OCH 3 3.81 3H, -OCH3), 3.79 3H, -OCH3). 1 3 C-NMR (CDCl 3 90 MHz) 5 184.2, 161.1, 159.6, 156.1, 152.6, 146.3, 141.9, 132.5, 131.2, 129.7, 123.4, 122.8. 121.4, 114.2, 113.8, 107.3. 95.4, 60.9, 56.1, 55.8, 55.3. HRMS (El) M'calc for C 26

H

24 0 7 448.1522. found 448.1522.

Anal. Calcd for C 2 6

H

24 0 7 C, 69.63; H. 5.39. Found: C, 69.56: H. 5.33.

Compound 24C had the biological activity shown in Table 32. Compound 24C showed inhibition oftubulin polymerization with an IC 5 2.1 iM (totally flat at 4 pM).

TABLE 32 Human Cancer Cell Line Studies (Compound 31C) Cell Type Cell Line Glso (pg/ml) Pancreas adn BXPC-3 0.038 Neuroblast SK-N-SH 0.025 Thyroid ca SW1736 0.047 Lung-NSC NCI-H460 0.041 Pharynx-sqam FADU 0.035 Prostate DU-145 0.062 EXAMPLE 4 DIHYDRONAPHTHALENE

DERIVATIVES

Compound 25D 1-(bydroxymethyl-3',4',5'-trimethoxyphenyl)-6-methoxy-3,4dihydronaphthalene (see FIG. 28), was prepared as follows.

To a well stirred solution of tetramethylethylenediamine (20 mL) and BuLi (4.6 mL of M solution in hexane, 11.500 mmol) cooled to -500C in dry ice/acetone bath was added 6methoxy-3,4-dihydro- (2H)-naphthalene p-toluenesulfonylhydrazone (1.008 g, 2.927 mmol) and stirred at that temperature for 30 min. It was then allowed to warm to room temperature and stirred at room temperature for 30 min. The reaction mixture was cooled to 0°C in ice water, followed by the addition of 3,4,5-trimethoxybenzaldehyde (2.279 g, 11.616 mmol). After 1 h of stirring at 0°C, the reaction was quenched with water, extracted with ethylacetate. The organic layer was washed with aqueous copper sulfate solution followed by brine and dried over MgSO 4 Purification of the compound by flash chromatography yielded the desired product as thick yellow oil (0.2897 mg, 0.8128 mmol) in 28% yield which solidified upon keeping it in the refrigerator. 'H-NMR (CDC 3 360 MHz) d 7.19 J= 8.6 Hz, 1H, ArH), 6.72 J= 2.65, 1H, ArH), 6.68 2H, ArH), 6.6 (dd, J= 2.7, 8.5 Hz, 1H, ArH), 6.02 J 4.7Hz, 1H, CH), 5.67 (s, 1H, CH), 3.84 6H, OCH 3 3.83 3H, OCH 3 3.78 3H, OCH 3 2.75 J= 7.7 Hz, 2H, CH2), 2.34 2H, CH 2 13C-NMR (CDCI 3 90 MHz) d 157.9, 152.7, 138.2, 138.1, 137.6, 136.7, 125.8, 124.6, 124.4, 113.4, 110.4, 103.6, 73.7, 60.3, 55.6, 54.7, 28.3, 22.6. HRMS (EI) M'calc for C,,H 24 0 5 356.4, found mp 89-92 0

C.

Certain biological activity of compound 25D is shown in Table 33. Compound showed inhibition of tubulin polymerization with an IC 5 0 40 .M.

Table 33 Human Cancer Cell Line Studies (Compound Cell Type Cell Line Glso (pg/ml) Pancreas adn BXPC-3 0.53 Neuroblast SK-N-SH 0.30 Thyroid ca SW1736 2.1 Lung-NSC NCI-H460 Pharynx-sqam FADU 0.51 Prostate DU-145 2.6 Compound 26D 1-(3',4',5'-trimethoxybenzoyl)-6-methoxy-3,4dihydronaphthalene (see FIG. 29) was prepared as follows.

To a well stirred solution of Dess-martin reagent (0.313g. 0.736 mmol) in CH 2 C1 2 (10 ml) was added 6-methoxy-3,4-dihydronaphthyl-3,4,5-trimethoxyphenyl-methanol (0.050 g, 0.140 mmol). After 2 h water was added and the suspension was partitoned between 1.3 M NaOH mL) and CH 2 C12 (50 mL) and the organic layer was washed with more of NaOH (20 mL, 1.3 M) followed by many times with water, once with brine and dried over MgSO 4 Purification by flash chromatography (silica gel, 80:20 hexane/EtOAc) afforded a highly pure sample of the desired product (0.0495g, 99.6%) as an yellow colored solid. 'H-NMR (CDCl 3 360MHz) d 7.19 J= 8.5 Hz, 1H, ArH), 7.15 2H, ArH), 6.77 J= 2.5 Hz, 1H, ArH), 6.70 (dd, J= 2.6, Hz, 1H, ArH), 6.35 J 4.7Hz, 1H, ArH), 3.92 3H, OCH 3 3.86 6H, OCH,), 3.81 (s, 3H, OCH 3 2.86 J 7.8 Hz, 2H, CH 2 2.49 2H, CH 2 3 C-NMR (CDCI 3 90 MHz) d 196.1, 159.2, 152.9, 142.5, 138.3, 137.6, 133.0, 132.9, 126.9, 125.2, 114.0,111.3, 107.6,60.9, 56.3, 55.2, 28.1, 23.1. HRMS (El) M calc for C, 2

H

22 05 354.1467, found 354.0859.

Certain biological activity of compound 26D is shown in Table 34. Compound 26D showed inhibition of tubulin polymerization with.an IC 50 1.7 4M (total flat at 4 pM).

Table 34 Human Cancer Cell Line Studies (Compound 26D) Cell Type Cell Line G1 50 (lg/ml) Pancreas adn BXPC-3 0.003 Neuroblast SK-N-SH <0.001 Thyroid ca SW1736 0.0048 Lung-NSC NCI-H460 0.0033 Pharynx-sqam FADU 0.0013 Prostate DU-145 0.0038 It will be apparent to anyone skilled in the art that the experimental procedures used to prepare the dihydronaphthalene derivatives 25D and 26D (Example 4) can be readily modified by appropriate substrate choice to prepare a wide variety of 3,4-dihydronaphthalene derivatives.

For example, treating the vinyl-lithium intermediate (generated in situ) with 3,4.5tricthoxybcnzaldehyde (instead of 3.4,5-trimcthoxybcnzaldchyde) will result in the preparation of ethoxylated ligands. This example can similarly be applied to the preparation of numerous other alkoxy dihydronaphthalene derivatives.

In addition, oxidation of the secondary alcohol to a ketone moiety (as in the conversion of to 26D) renders a molecule (like 26D) which contains an cx,p-unsaturated ketone will readily undergo 1,4 addition by organocuprate reagents to generate new tetralin compounds which are substituted at both the 1 and 2-positions. This establishes the requisite protocol to install a wide variety of groups (alkyl, vinyl, aryl) both substituted with alkoxy or halogen moieties, and unfunctionalized. These 1,2-disubstituted tetralins can also be treated with organoselenium reagents followed by oxidation and elimination to regenerate the 3,4dihydronaphthalene core structure (with substituents now at both the 1 and 2 positions).

EXAMPLE NITROGEN ANALOGS OF COMBRETASTATIN Combretastatins are seen in U.S. Patents 5,409,953 (Pettit et 5,561,122 (Pettit), 4,996,237 (Pettit et and 4,940,726 (Pettit et Related compounds are seen in U.S. Patent 5,430,062 (Cushman et al.).

Compounds 27E and 28E (E/Z)-l-(3'-methoxy-4'-nitrophenyl)- 2 3 4 trimethoxyphenyl) ethene (see FIG. 30 and FIG. 31), isomeric compounds, were prepared as follows.

A solution of 3,4,5-trimethoxybenzyltriphenylphosphonium bromide 1 (1.50 g, 2.86 mmol) and 3-methoxy-4-nitrobenzaldehyde 2 (0.518 g, 2.86 mmol) in CH,C1 2 (50 mL) was stirred under a nitrogen atmosphere. After 30 min, NaH (0.412 g, 17.16 mmol) was added.

After 16 h, water was added and the product was isolated by extraction with CH 2

CI

2 The organic phase was washed with brine and dried over MgSO,. The solvent was removed under reduced pressure to afford ethene 3 as a mixture of isomcrs 1.46/1.00 as determined by careful integration of 'H-NMR signals).

Purification and characterization of(Z) isomer, compound 27E, was done as follows.

Purification by flash chromatography (silica gel, 70:30 hexanes:ethyl acetate) afforded ethene 27E (0.319 g, 0.923 mmol. 32%) as a bright yellow solid. Recrystallization (hexanes/CHCl,) afforded an analytically pure sample of ethene 27E. mp 83-85 0 C. 'H-NMR

(CDCL

3 360 MHz) d 7.80 J 8.4 lIz I. Arij). 6.98 J 1.3 Hz. Il ArlI), 6.95(dd. J =8.6 Hz. 1.4 Hz. IH, ArH). 6.72 J= 12.1. 11. inyl Cl). 6.54 J= 12.1. 11H. vinyl CH).

6.46 2H. ArH), 3.84 311. OCH 3 3.77 3H. OCH1). 3.71 61-. OCH1 3

C-NMR

(CDCL

3 90 MHz)d 153.2, 153.0, 143.9, 138.0. 137.9, 133.5, 131.6, 127.9, 125.9. 121.1, 113.8.

106.0, 60.9, 56.3, 56.1. HRMS (El) M' calcd for CIgH, 9

NO

6 345.1212, found 345.1229. Anal.

Calcd for CsH, 9 NO: C, 62.60; H, 5.55; N, 4.06. Found: C, 62.68; H, 5.58; N. 4.05.

Compound 27E showed inhibition of tubulin polymerization with an ICs, 40 u.M and biological activity as seen in Table Table Human Cancer Cell Line Studies (Compound 27E) Cell Type Cell Line G1 50 ±g/mI) Pancreas adn BXPC-3 1.9 Neuroblast SK-N-SH 2.1 Thyroid ca SW1736 3.3 Lung-NSC NCI-H460 2.3 Pharynx-sqamn FADU 1.1 Prostate DU-145 2.6 Purification and characterization of isomer, compound 28E, was done as follows.

Purification by flash chromatography (silica gel, 70:30 hexanes:ethyl acetate) afforded ethene 28E (0.274 g, 0.793 mmuol, 28%) as a bright yellow solid. Recrystallization (hexanes/CH2

ICI

2 gave an analytically pure sample of (E )ethene 28E. mp 187-1 88 0 C. I'H- NMvR (CDCL 3 360 MHz) d 7.92 J =8.6 Hz, 1 H, ArH), 7.16 (in, 2H, Ad-I), 7.15 J =16.4 Hz, I H, vinyl ClH), 6.99 J =16.4 Hz, I1H, vinyl ClH), 6.77 2H. ArH), 4.03 3H, 0CH 3 3.93 6H, OCH 3 3.89 3H, 0CH 3 1 3 C-NMR (CDCL 3 90 MHz) d 153.7, 153.5, 143.8, 138.9, 138.0, 132.9, 131.8, 126.6, 125.9. 117.9, 111.0, 104.1, 61.0, 56.5, 56.2. HR'MS (El) M.

calcd for C, 8 HjqN0 6 345.1212, found 345.1220. Anal. Calcd for C, 8 H,gN0 6 C, 62.60; H, 5.55; N. 4.06. Found: C. 62.5 1; H, 5.53, N. 3.95.

Compound 29E (Z)-1-(4'amino-3'-methoxYpbhlyl)2(3"A'",5S trimet hoxypbenv l)ctbefe (see FIG. 32), wa preparcd as follows.

-cthene 27E (0.454 g, 1.31 mmol) was dissolved in a mixture acetone (10 mnL) and water (5 mL) and heated at 50 C. After 30 min. Na,S'0 4 (4.57 g. 26.28 mmol) wa added slowly. After I h of reflux at 50 0 C the mixture was cooled to room temperature and water was added. The product was rinsed with NaHCO 3 and then it was isolated by extraction with ethyl acetate. The organic layer was dried over Na 2

SO

4 The solvent was removed under reduced pressure. and the crude product (0.302 g, 0.956 mimol, 73%) obtained was also usable in azide formation.

Compound 30E (Z)-I-(4'azido-3'-methoxyphefyl)2( 3 41 trimethoxyphenyl)ethene (see FIG. 33) was prepared as follows.

(Z)-amino ethene 29E 166 g, 0.526 nimol) was dissolved in acetone (7.5 mL) in the dark, and cooled to 0 0 C, then HIi (0.22 M, 7.5 ml) was added. After 10 min of stirring under a nitrogen atmosphere, NaNO 2 (0.160 g, 2.31 mmol) was added. After 30 min, NaN 3 (0.427 g, 6.58 mmol) was added. After 15 min. at 0 0 C, dry ether(7.5 mL) was layered in. After 45 min, water was added and the product was isolated by extraction with ether. The organic layer was extracted with brine and dried over MgSO 4 The solvent was removed under reduced pressure and purified by flash chromatophy (silica gel, 70:30 hexanes:ethyl acetate). -compound was obtained as a white solid (0.077 g, 0.226 mmol, 43%) with mp 61-630 C. I H-NMR

(CDCI

3 360 MHz), d 6.89 2H, AriD), 6.81 IH, Arli), 6.54 J 12.1 Hz,lH. vinyl CHj), 6.50 2H, ArHD, 6.49 J =12.1 HzIH, vinyl CHi), 3.83 3H, OCij 3 3.71 6H, OCH 3 3.67 3H. OCH 3 1 3 C-NMR (CDCL 3 90 MHz) d 153.0, 151.3, 137.3, 134.7, 132.5. 130.2, 129.1, 127.1, 122.3. 119.8, 112.5, 105.9, 60.8, 55.9, 55.7. HRMS (El) M+ calcd for C 18

H

19

N

3 0 4 341.1376. found 341.1360. Anal. Calcd. for C 18

H

19

N

3 0 4 C, 63.33; H, 5.62; N, 12.31. Found: C. 63.23. H, 5.62; N, 12.21.

Compound 30E showed inhibition of tubulin polymerization with an IC, 0 1.5 PM.

Certain biological activity of compound 30E, (Z)-1-(4'azido-3n1mcthoxypheflyI)- 2 3 trimethoxyphenyl)cthenc, is shown in Table 36.

Pancrcas Neuroblas Thyroid c Lung-NS4 Pharyvnx-~ Prostate Table 36 Human Cancer Cell Line Studies (Compound ell Type Cell Line Cl 50 (pg/mi) idn BXPC-3 0.30 .1 SK-N-SH 0.24 a SW1736 0.45 C NCI-11460 0.35 ;qam FADU 0.42 DU-145 0.70 Compounds 31E and 32E (EZ--4-ehx-"nirpey)2('4,' trimethoxypbenyl)cthefle (see FIG. 34 and FIG. 35), isomeric compounds, were prepared as follows.

3,4,5-Trimethoxybenzaldehyde (1.17 g, 5.98 inmol) and 3-rnethoxy-4-, nitrobenzyltriphelphosphoniurn bromide 6 (3.01 g, 5.92 mmol) were dissolved in CH 2

CI

2 mL) and stirred under a nitrogen atmosphere. After 30 min, NaH (0.7 10 g, 29.6 mmol) was added. After 14 h, water was added carefu~lly and the product was isolated by extraction with

CH

2

CI

2 The organic phase was washed with brine and dried over MgSO 4 to afford a mixture of ethenes compound 3 2E and 3W1 (ZIE 2.9/ Purification and characterization of (Z)-ethene (compound 31E) was done as follows.

Purification by flash chromatography (silica gel, 70:30 hexanes:ethyl acetate) afforded ethene 3 1E (1 .44 g, 4.16 mmol, 73%) as a light yellow solid. Recrystallyzation (hexanes/ CH,C1 2 afforded an analytically pure sample of ethene 3 1E, mp 1 19-12 1 C. I'H-NMR

(CDCI

3 360 MHz) d 7.80 J =2.2 Hz, I H. Arli), 7.43 (dd, J 2.2 Hz, I1H. ArH), 6.94 (d, J =8.6 Hz, 114I, ArH), 6.58 J =12.2 Hz. I1H, vinyl CH), 6.45 J =13.3 Hz. I1H. vinyl CH), 6.47 2H, ArH), 3.94 3H, OC 3 3.85 3H. OCHj 3 3.72 6H, OCR 3 3

C-NMR

(CDCL

3 90 MHz) d 153.2, 151.7, 139.5, 137.7, 134.6, 131.8, 131.3, 129.7. 126.8, 125.9, 113. 1, 105.9, 60.9, 56.5, 56.0. HRMS (El) M' calcd for C 18

H

19 ,N0 6 345.1212. found 345.1191. Anal.

CalcdforC, 8 H~qNO 6 62.60; H, 5.55, N, 4.06. Found: C, 62.53; H. 5.61; N, 3.97.

Compound 3 1 E, I -(4"-methoxy-3 "-nitrophenyl ).2-(3',4'.5S-trimethoxypheflyl )ethene, showed certain biological activity as seen in Tables 37 and 38.

Table 37 P388 Leukemia Data (Compound 31F) Cell Type Cell Linc EDm (p.g/ml) Mouse Leukemia P388 Table 38 Human Cancer Cell Line Studies (ComDound 31E) Cell Type Cell Line G1 50 (jig/ml) Pancreas ad BXPC-3 0.037 Neuroblast SK-N-SH Thyroid ca SW1736 0.056 Lung-NSC NCI-H460 0.043 Pharynx-sqamn FADU 2.6 Prostate DU-145 0.046 Purification and characterization of (E)-ethene 32E was done as follows. Purification by flash chromatography (silica gel, 70:30 hexanes:ethyl acetate) afforded ethene 32E (0.541 g, 1.57 mmol, 27%) as a bright yellow solid. Recrystalyzation (hexanes/CHCI 2 afforded an analytically pure sample, mp =147-148 0 C. I H-NMR (CDC1 3 3 60 M4Hz) d 8.01 J =2.2 Hz.

I H, ArH), 7.65 (dd, J 2.3 Hz. I H. AriD), 7.15 J =8.7 Hz, I H, ArIA), 7.00 J =16.2 Hz, I H, vinyl C11), 6.93 =16.2 Hz, I H, vinyl CH), 6.73 2H, ArH), 3.99 3H. OCH 3 3.92 6H, OCH 3 3.88 3H. OCH 3 1 3 C-NMR (CDCl 3 90 MHz) d 153.5, 150.2, 140.0, 138.5, 132.4, 131.8, 130.4, 129.6, 125.2. 123.1, 113.8, 103.8, 61.0, 56.7, 56.2. HRMS (EI) M' calcd for C 18

H,

9 N0 6 345.1212, found 345.1206. Anal. Calcd for C 1 8

H

19 N0 6 C, 62.60; H. 5.55; N. 4.06. Found: C. 62.60; H, 5.60; N. 3.97.

Compound 33E -(3'-amino-4'-mcthoxypbenl~l)- 2 3 4 5 trimachoxypbelyl)Cthefle (see FIG. 36) was prepared as follows.

Ethene 3 1E 1.24 g, 3.5 8 mnmol) was dissolved in a mixture of acetone (40 mL) and water (20 mL) and heated at 50 0 C. After 30 min. Na,S10 4 (12.47 g, 71.61 mnmol) was added slowly. After 30 min of reflux at 50 0 C the mixture was cooled to room temperature and water was added. The product was isolated by extraction with ethyl acetate. The organic layer was -dried over. Na 2

SO

4 The solvent was removed under reduced pressure and the product was purified by flash chromatography (70:30, hexanes:ethyl acetate) to afford a pure sample of arylam-ine (0.423 g, 1.34 mmol, 37%) 33E, mp 64-660 C. I H-NMR (CDCL 3 360 MHz) d 6.71 (s,IH, ArH), 6.68 2H,ArH), 6.55 2H, ArH), 6.46 J=12..2 Hz, 1H, vinyl CHi), 6.37 J1 12.0 Hz, I1H, vinyl C11), 3.84 3H, OCR 3 3.83 3H, OCH 3 3.71 6H, 0'C11); 1 3

C_

NMR (CDCI 3 90MHz) d 152.9, 146.7, 137.2, 135.8, 133.0, 130.2, 130.0, 128.4, 119.5, 115.3, 110. 1, 106.2, 60.9, 56.0, 5 5.5. 1-RMS (El) M+ calcd for C 1 8

H

2 IN0 4 315.147 1, found 315.1466 Compound 33E showed inhibition of tubulin polymerization with an IC 50 =1.7 PtM.

Compound 33 E, 1-(3 '-arino-4'-methoxyphenyl)- 2 3 -trimethoxyphenyl)ethene, had certain biological activity as shown in Table 39.

Pa Nc Th

L.

Pr Table 39 Human Cancer Cell Line Studies (Compound 33E) Cell Type Cell Line G1 50 (pg/ml) ncreas adn BXPC-3 0.00 13 ~uroblast SK-N-SH <0.00 iyroid ca SW1736 <0.00 ig-NSC NCI-H460 0.00068 iarynx-sqamn FADU <0.0010 DU-145 0.00096 U3 L42 L%.

Compound 34E (Z)-1-(3'azido-4'-methoxYpheflyl)-2(3",4",iS" trimethoxyphenyl)cthefle (see FIG. 37) was prepared as follows.

(7)-amino etherie 33E (0.327g, 1.04 mmol) was dissolved in acetone (15 mL) and cooled to 0 0 C, then HCI (0.22 M, 15 mL) was added. After 10 min of stirrng under a nitrogen atmosphere, the NaNO 2 (0.316 g, 4.58 mmol) was added. After 30 min, NaN 3 (0.852 g, 13.10 mnrol) was added. After 15 min. at 0 0 C, dry ether (17 mL) was layered in. After 45 min of stirring the mixture was extracted with brine. the product was dried over MgSO 4 The solvent was removed under reduced pressure and purified by flash column chromatography (70:30 hexanes:ethyl acetate). The product obtained was a yellow oil 163 g, 0.478 mmol, 1 Fl- NMR (CDCL 3 360 MHz) d 7.03 (dd, J =8.4 Hz, 2.1 Hz, 1 H, ArH), 6.97 J =2.1 Hz, 11-I, ArH), 6.76 J 8.4 Hz, 1 H, AriD, 6.49 2H. ArH), 6.49 J 11.9 Hz, I H. vinyl CHD, 6.43 J =12.2 Hz, I H,vinyl CHJ), 3.84 6 H, 0Ct1 3 3.71 6 H, 0C11 3 1 3 C-NMR (CDCI 3 MHz) d 152.9, 150.7, 137.3, 132.4, 130.3, 129.6, 128.3, 127.8, 126.5, 120.4, 111.5, 105.8, 60.8, 5S5.8. Anal. Calcd for C 18 H I 9

N

3 :0 4 C, 63.3 3; H, 5.61 N, 12.3 1. Found: C, 63.3 8; H, 5.64; N, 12.28.

Compound 34E, (Z)-1-(3'azido-4'-methoxyphenyl)- 2 3 had certain biological activity as shown in Tables 40 and 41. Compound 34E showed inhibition of tubulin polymerization with an IC 5 0 1.3 pM.

Table P388 Leukemia Data(Compound 34E) Cell Type Cell Line EDso (pg/ml) Mouse Leukemia P388 0.0384 Table 41 Human Cancer Cell Line Studies (Compound 34E) Cell Type Cell Line G1 5 o (pg/ml) Pancreas adn BXPC-3 0.0050 Neuroblast SK-N-SH 0.0033 Thyroid ca SW1736 1.2 Lung-NSC NCI-H460 0.0056 Pharynx-sqam FADU 0.0076 Prostate DU-145 0.0091 Functionalization of the nitrogen analogs of combretastatin is as follows. The amino analogs of combretastatin described in this application may be suitably modified through amide linkages to incorporate short peptide oligomcrs. The new compounds prepared in this fashion may have improved bioavailability (especially in terms of water solubility) and enhanced molecular recognition for the selective colchicine binding site on P-tubulin. A wide variety of amino acid residues may be attached to the nitrogen atom in an analogous fashion. A typical experimental procedure (in this case for the attachment of a serine residue) is described below.

To a well-stirred solution of serine and amino-combretastatin in diethyl ether was added diisopropylcarbodiimide (DIC). After stirring for 12 hours, the solvent was removed under reduced pressure and the amide product was purified by flash chromatography and recrystallization.

It should be clear to anyone skilled in the art that this general procedure may be employed to prepare amides incorporating many amino acid residues (both naturally occurring and synthetic) and may be used to prepare short, medium, or large oligomers.

P:AOPER\MKRSPECI\7654 I8-div.doc-18/12/03 -52- In addition, functionalization of the amino analogs of combretastatin to include the taxol side-chain through an amide linkage may result in combretastatin-taxol hybrid drugs of enhanced cytotoxicity and selectivity. The taxol side chain may be incorporated through direct reaction with the ojima 3-lactam (Ojima et al., Nicolaou et al.).

All of the compositions and methods disclosed and claimed herein can be made and executed without undue experimentation in light of the present disclosure. While the compositions and methods of this invention have been described in terms of preferred embodiments, it will be apparent to those of skill in the art that variations may be applied to the compositions and/or methods and in the steps or in the sequence of steps of the method described herein without departing from the concept, spirit and scope of the invention. More specifically, it will be apparent that certain agents which are both chemically and physiologically related may be substituted for the agents described herein while the same or similar results would be achieved. All such similar substitutes and modifications apparent to those skilled in the art are deemed to be within the spirit, scope and concept of the invention as defined by the appended claims.

The reference to any prior art in this specification is not, and should not be taken as, an acknowledgment or any form of suggestion that that prior art forms part of the common general knowledge in Australia.

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Claims (41)

1. A compound of the structure: R1 Z-Y-Ar' R2 Ar X R3 R4 wherein X is chosen from the group consisting of O, NH, and CH 2 RI-R 4 are independently chosen from the group consisting of H, OH and Ci-C alkoxy, Z is chosen from the group consisting of C=O, CH 2 C 2 H 2 CHOH, and CHOCH 3 Y is chosen from the group consisting of a covalent bond, CH 2 and CH 2 CH 2 and Ar and Ar' are aryl moieties chosen from the group consisting of phenyl and napthyl, further substituted with at least one Ci-C 5 alkoxy group, at least one of which has at least two CI-C 5 alkoxy groups, wherein Ar' is 3,4,5-trimethoxyphenyl, Z is C=O, Y is a covalent bond, R 3 is methoxy, Ri, R 2 and R 4 are H, and Ar is substituted with a methoxy group.

2. The compound of claim 1, wherein Z is C=O.

3. The compound of claim 1 wherein Ar' is chosen from the group consisting of 3,4,5-trimethoxyphenyl, 3,4-dimethoxyphenyl, 3,4-diethoxyphenyl and 3,4,5- triethoxyphenyl.

4. The compound of claim 1 wherein Ar is 4-methoxyphenyl.

5. The compound of claim 1 wherein R 3 is OCH 3 P:\OPERMKR\SPECI\765418 div.doc.1812/03 -57-

6. A method for inhibiting tubulin polymerization by contacting a tubulin-containing system with an effective amount of a compound having the structure: RI 1 SZ-Y-Ar' R2 Ar R3 R4 wherein X is chosen from the group consisting of S, NH, CH 2 and 0, RI-R 4 are independently chosen from the group consisting of H, OH and Ci-C alkoxy, Z is chosen from the group consisting of C=O, CH 2 C 2 H 2 CHOH, and CHOCH 3 Y is chosen from the group consisting of a covalent bond, CH 2 and CH 2 CH 2 and Ar and Ar' are aryl substituents chosen from the group consisting of phenyl and napthyl, further substituted with at least one Ci-C 5 alkoxy group.

7. The method of claim 6, wherein said system is in a flagellate parasite.

8. The method of claim 6, wherein said system is in a tumor cell.

9. The method of claim 6, wherein the contacted system is located in a patient.

10. The method of claim 6, wherein said compound is 3-(3',4',5'-trimethoxybenzoyl)- 2-(4'-methoxyphenyl)-6-methoxybenzo[b]thiophene.

11. The method of claim 6, wherein the effective amount of the compound is between AM and 10 tM. P;\OPER\M KR\SPECI\765418-div.doc-18/12/03 -58-

12. The method of claim 6 wherein the effective amount of the compound is between 2 tM and 6 /M.

13. A method for inhibiting the growth of tumor cells comprising contacting the tumor cells with an effective amount of a tubulin polymerization inhibitor, said inhibitor having the structure: R, Z-Y-Ar' R2 Ar X R3 R4 wherein X is chosen from the group consisting of S, NH, CH 2 and O, Ri-R 4 are independently chosen from the group consisting of H, OH and Ci-C alkoxy, Z is chosen from the group consisting of C=O, CH 2 C 2 H 2 CHOH, and CHOCH 3 Y is chosen from the group consisting of a covalent bond, CH 2 and CH 2 CH 2 and Ar and Ar' are aryl substituents chosen from the group consisting of phenyl and napthyl, further substituted with at least one C 1 -C 5 alkoxy group.

14. The method of claim 13 wherein X is S. The method of claim 13 wherein Z is C=O.

16. The method of claim 13 wherein Ar' is chosen from the group consisting of 3,4,5- trimethoxyphenyl, 3,4-dimethoxyphenyl, 4-methoxyphenyl, 4-ethoxyphenyl, 3,4- diethoxyphenyl and 3,4,5-triethoxyphenyl.

17. The method of claim 13 wherein Ar is 4-methoxyphenyl. P:\OPER\MKR\SPECI\765418div.doc-18I2/03 -59-

18. The method of claim 13 wherein said tubulin polymerization inhibitor is selected from the group consisting of 3-(3',4'-dimethoxybenzoyl)-2-(4'-methoxyphenyl)-6- methoxybenzo[b]thiophene, 3-(4'-ethoxy-benzoyl)-2-(4'-methoxyphenyl)-6- methoxybenzo[b]thiophene, 3-(3',4',5'-triethoxy-benzoyl)-2-(4'-methoxyphenyl)-6- methoxybenzo[b]-thiophene, and 3-[3'-(3",4",5"-trimethoxyphenyl)propanoyl]-2-(4'- methoxyphenyl)-6-methoxybenzo[b]thiophene.

19. The method of claim 13 wherein said tubulin polymerization inhibitor is 3- (3',4',5'-trimethoxybenzoyl)-2-(4'-methoxyphenyl)-6-methoxybenzo[b]thiophene. The method of claim 13 wherein said tubulin polymerization inhibitor is methoxybenzoyl)-2-(4-methoxyphenyl)-6-mehtoxybenzo[b]thiophene.

21. The method of claim 13 wherein said tumor cells are located in a patient.

22. The method of claim 13 wherein the effective dosage is between 0.5 mg/kg body weight/day and 100 mg/kg body weight/day.

23. The method of claim 13 wherein the effective dosage is between 1.0 mg/kg body weight/day and 20 mg/kg body weight/day.

24. The method of claim 13 for treating cancer, wherein said cancer is chosen from the group consisting of melanomas, leukemias, lung cancers, ovarian cancers, CNS cancers, renal cancers, thyroid, pharyngeal, pancreatic and prostate cancers. The method of claim 13 for treating colon cancer.

26. A method of inhibiting tumor cell growth comprising administering a therapeutically effective amount of the structure P:AOPER\MKR\SPEC[\7654 8-div.doc-18/12/03 CH 3 C CH 3 O' where X is CHOH or C=0.

27. A compound of the structure CH 3 0 where RI and R 2 are independently CH30, NO 2 NH 2 or N 3 and CH 3 0; and C 2 H 2 is in the E or Z configuration; with the proviso that one of R 1 and R 2 is CH 3 0 and the other is NO 2 NH 2 or N 3

28. The compound of claim 27 where C 2 H 2 is E C 2 H 2 R 1 is CH30 and R 2 is NH2.

29. A method of inhibiting tumor cell growth comprising administering a therapeutically effective amount of the compound of claim 28.

30. The compound of claim 27 where C 2 H 2 is E C 2 H 2 Ri is NH 2 and R 2 is

31. A method of inhibiting tumor cell growth comprising administering a therapeutically effective amount of the compound of claim

32. The compound of claim 27 where C 2 H 2 is Z C 2 H 5 Ri is CH30 and R 2 is NH 2 P:\OPER\M KR\SPECI\765418-div do- 18/12/03 -61-

33. A method of inhibiting tumor cell growth comprising administering a therapeutically effective amount of the compound of claim 32.

34. The compound of claim 27 where C 2 H 2 is Z C 2 H 2 Ri is NH 2 and R 2 is CH 3 O. A method of inhibiting tumor cell growth comprising administering a therapeutically effective amount of the compound of claim 34.

36. The compound of claim 27 where C 2 H 2 is E C 2 H 2 R 1 is CH30 and R 2 is NO 2

37. The compound of claim 27 where C 2 H 2 is E C 2 H 2 R 1 is NO 2 and R 2 is CH 3 O.

38. The compound of claim 27 where C 2 H 2 is Z C 2 H 5 R 1 is CH30 and R 2 is NO 2

39. The compound of claim 27 where C 2 H 2 is Z C 2 H 2 Ri is NO 2 and R 2 is CH 3 0. The compound of claim 27 where C 2 H 2 is E C 2 H 2 R 1 is CH 3 0 and R 2 is N 3

41. A method of inhibiting tumor cell growth comprising administering a therapeutically effective amount of the compound of claim

42. The compound of claim 27 where C 2 H 2 is E C 2 H 2 Ri is N 3 and R 2 is CH 3 0. P:\OPER\MKR\SPECI\765418-div.doc- 8/12/03 -62-

43. A method of inhibiting tumor cell growth comprising administering a therapeutically effective amount of the compound of claim 42.

44. The compound of claim 27 where C 2 H 2 is Z C 2 H 5 R 1 is CH30 and R 2 is N 3 A method of inhibiting tumor cell growth comprising administering a therapeutically effective amount of the compound of claim 44.

46. The compound of claim 27 where C 2 H 2 is Z C 2 H 2 RI is N 3 and R 2 is CH 3 0.

47. A method of inhibiting tumor cell growth comprising administering a therapeutically effective amount of the compound of claim 46. DATED this 15th day of December, 2003 Baylor University AND Arizona Disease Control By DAVIES COLLISON CAVE Patent Attorneys for the Applicant