US20010041733A1

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Publication number: US20010041733A1
Application number: US09/879,888
Authority: US
Inventors: Joseph Steiner; Gregory Hamilton
Original assignee: GPI Nil Holdings Inc
Current assignee: Gliamed Inc
Priority date: 1998-06-03
Filing date: 2001-06-14
Publication date: 2001-11-15
Also published as: US6274617B1; AU770459B2; JP2002516843A; CA2334204A1; WO1999062487A1; AU7717098A; EP1085853A1

Abstract

This invention relates to pharmaceutical compositions and methods for treating alopecia and promoting hair growth using heterocyclic esters or amides.

Description

This application is a continuation-in-part of U.S. patent application No. 08/869,426, filed on Jun. 4, 1997, the entire contents of which are herein incorporated by reference.[0001]

BACKGROUND OF THE INVENTION

1. Field of Invention[0002]

This invention relates to pharmaceutical compositions and methods for treating alopecia and promoting hair growth using low molecular weight, small molecular heterocyclic esters or amides.[0003]

2. Description of Related Art[0004]

Hair loss occurs in a variety of situations. These situations include male pattern alopecia, alopecia senilis, alopecia areata, diseases accompanied by basic skin lesions or tumors, and hair loss are very complicated, but in some instances can he attributed to aging, genetic disposition, the activation of male hormones, the loss of blood supply to hair follicles, and scalp abnormalities.[0005]

The immunosuppressant drugs FK506, rapamycin and cyclosporin are well known as potent T-cell specific immunosuppressants, and are effective against graft rejection after organ transplantation. It has been reported that topical, but not oral, application of FK506 (Yamamoto et al., J. Invest. Dermatol., 1994, 102, 160-164; Jiang et al., J. Invest. Dermatol. 1995, 104, 523-525) and cyclosporin (Iwabuchi et al., J. Dermatol. Sci. 1995, 9, 64-69) stimulates hair growth in a dose-dependent manner. One form of hair loss, alopecia areata, is known to be associated with autoimmune activities; hence, topically administered immunomodulatory compounds are expected to demonstrate efficacy for treating that type of hair loss. The hair growth stimulating effects of FK506 have been the subject of an international patent filing covering stimulation (Honbo et al.,[0006]EP 0 423 714 A2). Honbo et al. discloses the use of relatively large tricyclic compounds, known for the immunosuppressive effects, as hair revitalizing agents.

The hair growth and revitalization effects of FK506 and related agents are disclosed in many U.S. patents (Goulet et al., U.S. Pat. No. 5,258,389; Luly et al., U.S. Pat. No. 5,457,111; Goulet et al., U.S. Pat. No. 5,532,248; Goulet et al., U.S. Pat. No. 5,189,042; and Ok et a U.S. Pat. No. 5,208,241; Rupprecht et al. U.S. Pat. No. 5,284,840; Organ et al., U.S. Pat. No. 5,284,877). These patents claim FK506 related compounds. Although they do not claim methods of hair revitalization, they disclose the known use of FK506 for effecting hair growth. Similar to FK506 (and the claimed variations in the Honbo et al. patent), the compounds claimed in these patents are relatively large. Further, the cited patents relate to immunomodulatory compounds for use in autoimmune related diseases, for which FK506's efficacy is well known.[0007]

Other U.S. patents disclose the use of cyclosporin and related compounds for hair revitalization (Hauer et al., U.S. Pat. No. 5,342,625; Eberle, U.S. Pat. No. 5,284,826; Hewitt et al., U.S. Pat. No. 4,996,193). These patents also relate to compounds useful treating autoimmune diseases and cite the known use of cyclosporin and related immunosuppressive compounds for hair growth.[0008]

However, immunosuppressive compounds by definition suppress the immune system and also exhibit other toxic side effects. Accordingly, there is a need for non-immunosuppressant, small molecule compounds which are useful as hair revitalizing compounds.[0009]

Hamilton and Steiner disclose in U.S. Pat. No. 5,614,547 novel pyrrolidine carboxylate compounds which bind to the immunophilin FKBP12 and stimulate nerve growth, but which lack immunosuppressive effects. Unexpectedly, it has been discovered that these non-immunosuppressant compounds promote hair growth with an efficacy similar to FK506. Yet their novel small molecule structure and non-immunosuppressive properties differentiate them from FK506 and related immunosuppressive compounds found in the prior art.[0010]

SUMMARY OF THE INVENTION

The present invention relates to a method for treating alopecia or promoting hair growth in an animal, which comprises administering to said animal an effective amount of a heterocyclic ester or amide.[0011]

The present invention further relates to a pharmaceutical composition which comprises:[0012]

(i) an effective amount of a heterocyclic ester or amide for treating alopecia or promoting hair growth in an animal; and[0013]

(ii) a pharmaceutically acceptable carrier.[0014]

The heterocyclic esters and amides used in the inventive methods and pharmaceutical compositions have an affinity for FKBP-type immunophilins and do not exert any significant immunosuppressive activity.[0015]

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a photogragh of C57 Black 6 mice before being shaved for the hair regeneration experiment.[0016]

FIG. 2 is a photograph of mice treated with a vehicle a six weeks. FIG. 2 shows that less than 3% of the shaved area is covered with new hair growth when the vehicle (control) is administered.[0017]

FIG. 3 is a photograph of mice treated with 10 μM of GPI 1046, a related non-immunosuppressive neuroimmunophilin FKBP ligand, after six weeks. FIG. 3 shows the remarkable effects of neuroimmunophilin FKBP ligands, wherein 90% of the shaved area is covered with new hair growth.[0018]

FIG. 4 is a photograph of mice treated with 30 μM of GPI 1046, a related non-immunosuppressive neuroimmunophilin FKBP ligand, after six weeks. FIG. 4 shows the remarkable ability of neuroimmunophilin FKBP ligands to achieve, essentially, complete hair regrowth in the shaved area.[0019]

FIG. 5 is a bar graph depicting the relative hair growth indices for C57 Black 6 mice treated with a vehicle, FK506, and various non-immunosuppressive neuroimmunophilin FKBP ligands, including GPI 1572, 14 days after treatment with each identified compound. FIG. 5 demonstrates the remarkable early hair growth neuroimmunophilin FKBP ligands.[0020]

DETAILED DESCRIPTION OF THE INVENTIONDefinitions

“Alopecia” refers to deficient hair growth and partial or complete loss of hair, including without limitation androgenic alopecia (male pattern baldness) , toxic alopecia, alopecia senilis, alopecia areata, alopecia pelada and trichotillomania. Alopecia results when the pilar cycle is disturbed. The most frequent phenomenon is a shortening of the hair growth or anagen phase due to cessation of cell proliferation. This results in an early onset of the catagen phase, and consequently a large number of hairs in the telogen chase during which the follicles are detached from the dermal papillae, and the hairs fall out. Alopecia has a number of etiologies, including genetic factors, aging, local and systemic diseases, febrile conditions, mental stresses, hormonal problems, and secondary effects of drugs.[0021]

“GPI 1605” refers to a compound of formula[0022]
“GPI 1046” refers to 3-(3-pyridyl)-1-propyl (2s-1-(3,3-dimethyl-1,2-dioxopentyl)-2-pyrrolidine-carboxylate, a compound of formula[0023]
“GPI 1312” refers to a compound of formula[0024]
“GPI 1572” refers to a compound of formula[0025]
“GPI 1389” refers to a compound of formula[0026]
“GPI 1511” refers to a compound of formula[0027]
“GPI 1234” refers to a compound of formula[0028]
“Isomers” refer to different compounds that have the same molecular formula. “Stereoisomers” are isomers that differ only in the way the atoms are arranged in space, “Enantiomers” are a pair of stereoisomers that are non-superimposable mirror images of each other. “Diastereoisomers” are stereoisomers which are not mirror images of each other. “Racemic mixture” means a mixture containing equal parts of individual enantiomers. “Non-racemic mixture” is a mixture containing unequal parts or individual enantiomers or stereoisomers.[0029]
“Pharmaceutically acceptable salt, ester, or solvate” refers to a salt, ester, or solvate or a subject compound which possesses the desired pharmacolocical activity and which is neither biologically nor otherwise undesirable. A salt, ester, or solvate can be formed with inorganic acids such as acetate, adipate, alginate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, citrate, camphorate, camphorsulfonate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, fumarate, glucoheptanoate, gluconate, glycerophosphate, hemisulfate, heptanoate, hexanoate, hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethanesulfonate, lactate, maleate, methanesulfonate, naphthylate, 2-naphthalenesulfonate, nicotinate, oxalate, sulfate, thiocyanate, tosylate and undecanoate. Examples of base salts, esters, or solvates include ammonium salts; alkali metal salts, such as sodium and potassium salts; alkaline earth metal salts, such as calcium and magnesium salts; salts with organic bases, such as dicyclohexylamine salts; N-methyl-D-glucamine; and salts with amino acids, such as arginine, lysine, and so forth. Also, the basic nitrogen-containing groups can be quarternized with such agents as lower alkyl halides, such as methyl, ethyl, propyl, and butyl chlorides, bromides, and iodides; dialkyl sulfates, such as dimethyl, diethyl, dibutyl, and diamyl sulfates; long stearyl chlorides, bromides, and iodides; aralkyl halides such as benzyl and phenethyl bromides, and others. Water or oil-soluble or dispersible products are thereby obtained.[0030]
“Pilar cycle” refers to the life cycle of hair follicles, and includes three phases:[0031]
(1) the anagen phase, the period of active hair growth which, insofar as scalp hair is concerned, lasts about three to five years;[0032]
(2) the catagen phase, the period when growth stops and the follicle atrophies which, insofar as scalp hair is concerned, lasts about one to two weeks; and[0033]
(3) the telogen phase, the rest period when hair progressively separates and finally falls out: which, insofar as scalp hair is concerned, lasts about three to four months.[0034]
Normally 80 to 90 percent of the follicles are in the anagen phase, less than 1 percent being in the catagen phase, and the rest being in the telogen phase. In the telogen phase, hair is uniform in diameter with a slightly bulbous, non-pigmented root. By contrast, in the anagen phase, hair has a large colored bulb at its root.[0035]
“Promoting hair growth” refers to maintaining, inducing, stimulating, accelerating, or revitalizing the germination of hair.[0036]
“Treating alopecia” refers to:[0037]
(i) preventing alopecia in an animal which may be predisposed to alopecia; and/or[0038]
(ii) inhibiting, retarding or reducing alopecia; and/or[0039]
(iii) promoting hair growth; and/or[0040]
(iv) prolonging the anagen phase of the hair cycle; and/or[0041]
(v) converting vellus hair to growth as terminal hair. Terminal hair is coarse, pigmented, long hair in which the bulb of the hair follicle is seated deep in the dermis. Vellus hair, on the other hand, is fine, thin, non-pigmented short hair in which the hair bulb is located superficially in the dermis. As alopecia progresses, the hairs change from the terminal to the vellus type.[0042]

Methods of the Present Invention

The present invention relates to a method for treating alopecia or promoting hair growth in an animal, which comprises administering to said animal an effective amount of a heterocyclic ester or amide.[0043]

The inventive method is particularly useful for treating male pattern alopecia, alopecia senilis, alopecia areata, alopecia resulting from skin lesions or tumors, alopecia resulting from cancer therapy such as chemotherapy and radiation, and alopecia resulting from systematic disorders such as nutritional disorders and internal secretion disorders.[0044]

Pharmaceutical Compositions of the Present Invention[0045]

The present invention also relates to a pharmaceutical composition comprising:[0046]

(i) an effective amount of a heterocyclic ester or amide for treating alopecia or promoting hair growth in an animal; and[0047]

(ii) a pharmaceutically acceptable carrier.[0048]

HETEROCYCLIC ESTERS AND AMIDES

The heterocyclic esters and amides used in the methods and pharmaceutical compositions of the present invention are low molecular weight, small molecule compounds having an affinity for an FKBP-type immunophilin, such as FKBP12. When a heterocyclic ester or amide binds to an FKBP-type immunophilin, it has been found to inhibit the prolyl-peptidyl cis-trans isomerase, or rotamase, activity of the binding protein. Unexpectedly, the compounds have also been found to stimulate hair growth. The compounds are devoid of any significant immunosuppressive activity.[0049]

FORMULA I

The heterocyclic ester or amide may be a compound of formula I[0050]
or a pharmaceutically acceptable salt, ester, or solvate thereof, wherein:[0051]
A and B, together with the nitrogen and carbon atoms to which they are respectively attached, form a 5-7 membered saturated or unsaturated heterocyclic ring containing, in addition to the nitrogen atom, one or more additional O, S, SO, SO[0052]₂, N, NH or NR₁heteroatom(s);
X is O or S;[0053]
Z is O, NH or NR;[0054]
W and Y are independently O, S, CH[0055]₂, or H2;
R[0056]₁is C₁-C₆straight or branched chain alkyl or C₂-C₆straight or branched chain alkyl, which is substituted with one or more sustituent(s) independently selected from the group consisting of (Ar₁)_n, C₃-C₆straight or branched chain alkyl or C₂-C₆straight or branched chain alkenyl substituted with (Ar₁)_n, C₃-C₉cycloalkyl, C₁-C₆straight or branched chain alkyl or C₂-C₆, straight or branched chain alkenyl substituted with C₃-C₈cycloalkyl, and Ar₂;
n is 1 or 2;[0057]
R[0058]₂is either C₁-C₉straight or branched chain alkyl, C₂-C₉straight or branched chain or alkenyl, C₃-C₉cycloalkyl, C₅-C₇cycloalkenyl, or Ar₁, wherein said alkyl, alkenyl, cycloalkyl or cycloalkenyl is either unsubstituted or substituted with one or more substituent(s) independently selected from the group consisting of C₁-C₄straight or branched chain alkyl, C₂-C₄straight or branched chain alkenyl, and hydroxyl; and
Ar[0059]₁and Ar₂are independently an alicyclic or aromatic, mono-, bi- or tricyclic, carbo- or heterocyclic ring, wherein the ring is either unsubstituted or substituted with one or more substituent(s) independently selected from the group consisting of halo, hydroxyl, nitro, trifluoromethyl, C₁-C₆straight or branched chain alkyl, C₂-C₆straight or branched chain alkenyl, C₁-C₄alkoxy, C₂-C₄alkenloxy, phenoxy, benzyloxy, and amino; wherein the individual ring size is 5-6members; and wherein the heterocyclic ring contains 7-6 heteroatom(s) independently selected from the group consisting of O, N, and S.
Suitable carbo- and heterocyclic rings include without limitation naphthyl, indolyl, furyl, thiazolyl, thienyl, pyridyl, quinolinyl, isoquinolinyl, fluorenyl and phenyl.[0060]

FORMULA II

Additionally, the heterocyclic ester or amide may be a compound of formula II[0061]
or a pharmaceutically acceptable salt, ester, or solvate thereof, wherein:[0062]
A, B and C are independently CH[0063]₂, O, S, SO, SO₂, NH or NR₁;
R[0064]₁is C₁-C₅straight or branched chain alkyl or C₂-C₅straight or branched chain alkenyl, which is substituted with one or more substituent(s) independently selected from the group consisting of (Ar₁)_nand C₁-C₆straight or branched chain alkyl or C₂-C₆straight or branched chain alkenyl substituted with (Ar₁)_n;
n is 1 or 2;[0065]
R[0066]₂is either C₁-C₉straight or branched chain alkyl, C₂-C₉straight or branched chain alkenyl, C₁-C₉cycloalkyl, C₅-C₇cycloalkenyl, or Ar₁; and
Ar[0067]₁is an alicyclic or aromatic, mono-, bi- or tricyclic, carbo- or heterocyclic ring, wherein the ring is either unsubstituted or substituted with one or more substituent(s) independently selected from the group consisting of halo, hydroxyl, nitro, trifluoromethyl, C₁-C₄straight or branched chain alkyl, C₂-C₆straight or branched chain alkenyl, C₁-C₄alkoxy, C₂-C₄alkenyloxy, phenoxy, benzyloxy, and amino; wherein the individual ring size is 5-6 members; and wherein the heterocyclic ring contains 1-6 heteroatom(s) independently selected from the group consisting of O, N, and S.
In a preferred embodiment of the compounds of formula I, the heterocyclic ester or amide is the compound GPI 1572, of the formula[0068]
In a particularly preferred embodiment of formula compounds:[0069]
A is CH[0070]₂;
B is CH[0071]₂or S;
C is CH[0072]₂or NH;
R[0073]₁is selected from the group consisting of 3-phenylpropyl and 3-(3-pyridyl)propyl; and
R[0074]₂is selected from the group consisting of 1,1-dimethylpropyl cyclohexl, and tert-butyl.

Specific examples of this embodiment are presented in TABLE I.[0075]

TABLE I


No.	A	B	C	R₁	R₂

1	CH₂	S	CH₂	3-phenylpropyl	1,1-dimethylpropyl
2	CH₂	S	CH₂	3-(3-pyridyl)propyl	1,1-dimethylpropyl
3	CH₂	S	CH₂	3-phenylpropyl	cyclohexyl
4	CH₂	S	CH₂	3-phenylpropyl	tert-butyl
5	CH₂	CH₂	NH	3-phenylpropyl	1,1-dimethylpropyl
6	CH₂	CH₂	NH	3-phenylpropyl	cyclohexyl
7	CH₂	CH₂	NH	3-phenylpropyl	tert-butyl

FORMULA III

The heterocyclic ester or amide may also be a compound of formula III[0076]
or a pharmaceutically acceptable salt, ester, or solvate thereof, wherein:[0077]
A, B, C and D are independently CH[0078]₂, O, S, SO, SO₂, NH or NR₁;
R[0079]₁is C₁-C₅straight or branched chain alkyl or C₂-C₅straight or branched chain alkenyl, which is substituted with one or more substituent(s) independently selected from the group consisting of (Ar₁)_nand C₁-C₆straight or branched chain alkyl or C₂-C₆straight or branched chain alkenyl substituted with (Ar₁)_n;
n is 1 or 2;[0080]
R[0081]₂is either C₁-C₉straight or branched chain alkyl, C₂-C₉straight or branched chain alkenyl, C₃-C₉. cycloalkyl, C₅-C₇cycloalkenyl, or Ar₁; and
Ar[0082]₁is an alicyclic or aromatic, mono-, bi- or tricyclic, carbo- or heterocyclic ring, wherein the ring is either unsubstituted or substituted with one or more substituent(s) independently selected from the group consisting of halo, hydroxyl, nitro, trifluoromethyl, C₁-C₆straight or branched chain alkyl, C₂-C₆straight or branched chain alkenyl, C₁-C₄alkoxy, C₂-C₄alkenyloxy, phenoxy, benzyloxy, and amino; wherein the individual ring size is 5-6 members; and wherein the heterocyclic ring contains 1-6 heteroatom(s) independently selected from the group consisting of O, N, and S.
In a particularly preferred embodiment of formula III compounds:[0083]
A is CH[0084]₂;
B is CH[0085]₂;
C is S, O, or NH;[0086]
D is CH[0087]₂;
R[0088]₁is selected from the group consisting of 3-phenylpropyl and (3,4,5-trimethoxy)phenylpropyl; and
R[0089]₂is selected from the group consisting of 1,1-dimethylpropyl, cyclohexyl, tert-butyl, phenyl, and 3,4,5-trimethoxyphenyl.

Specific examples of this embodiment are presented in TABLE II.[0090]

TABLE II


No.	A	B	C	D	R₁	R₂

8	CH₂	CH₂	S	CH₂	3-phenylpropyl	1,1-dimethylpropyl
9	CH₂	CH₂	O	CH₂	3-phenylpropyl	1,1-dimethylpropyl
10	CH₂	CH₂	S	CH₂	3-phenylpropyl	cyclohexyl
11	CH₂	CH₂	O	CH₂	3-phenylpropyl	cyclohexyl
12	CH₂	CH₂	S	CH₂	3-phenylpropyl	phenyl
13	CH₂	CH₂	O	CH₂	3-phenylpropyl	phenyl
14	CH₂	CH₂	NH	CH₂	3-phenylpropyl	1,1-dimethylpropyl
15	CH₂	CH₂	NH	CH₂	3-phenylpropyl	phenyl

FORMULA IV

The heterocyclic ester or amide may also be a compound of formula IV[0091]
or a pharmaceutically acceptable salt, ester, or solvate thereof, wherein:[0092]
V is C, N, or S;[0093]
A and B, taken together with V and the carbon atom to which they are respectively attached, form a 5-7 membered saturated or unsaturated heterocyclic ring containing, in addition to V, one or more heteroatom(s) independently selected from the group consisting of O, S, SO, SO[0094]₂, N, NH;, and N;
R is either C[0095]₁-C₉straight or branched chain alkyl, C₂-C₉straight or branched chain alkenyl, C₁-C₉cycloalkyl, C₅-C₇cycloalkenyl, or Ar₃, wherein R is either unsubstituted or substituted with one or more substituent(s) independently selected from the group consisting of halo, haloalkyl, carbonyl, carboxy, hydroxy, nitro, trifluoromethyl, C₁-C₆straight or branched chain alkyl, C₂-C₆straight or branched chain alkenyl, C₁-C₄alkoxy, C₁-C₄alkenyloxy, phenoxy, benzyloxy, thioalkyl, alkylthio, sulfhydryl, amino, alkylamino, aminoalkyl, aminocarboxyl, and Ar₄;
Ar[0096]₃and Ar₄are independently an alicyclic or aromatic, mono-, bi- or tricyclic, carbo- or heterocyclic ring; wherein the individual ring size is 5-8 members; wherein said heterocyclic ring contains 1-6 heteroatom(s) independently selected from the group consisting of O, N, and S; and
R[0097]₁, R₂, W, X, Y, and Z are as defined in Formula I above.
All the compounds of Formulas I-IV posses asymmetric centers and thus can be produced as mixtures of stereoisomers or as individual R- and S- stereoisomers. The individual stereoisomers may be obtained by using an optically active starting material, by resolving a racemic or non-racemic mixture of an intermediate at some appropriate stage of the synthesis, or by resolving t he compounds of Formulas I-IV. It is understood that the compounds of Formulas I-IV encompass individual stereoisomers as well as mixtures (racemic and non-racemic) of stereoisomers. Preferably, S-stereoisomers are used in the pharmaceutical compositions and methods of the present invention.[0098]

Affinity for FKBP12

The compounds used in the inventive methods and pharmaceutical compositions have an affinity for the inhibition of the prolyl peptidyl cis-trans isomerase activity of FKBP may be measured as an indicator of this affinity.[0099]

K₁Test Procedure

Inhibition of the peptidyl-prolyl isomerase (rotamase) activity of the compounds used in the inventive methods and pharmaceutical compositions can be evaluated by known methods described in the literature (Harding et al.,[0100]Nature,1939, 341:758-760; Holt et al.J. Am. Chem. Soc.,115:9923-9938). These values are obtained as apparent K₁'s and are presented for representative compounds in TABLE III.

The cis-trans isomerization of an alanine-proline bond in a model substrate, N-succinyl-Ala-Ala-Pro-Phe-p-nitroanilide, is monitored spectrophotometrically in a chymotrypsin-coupled assay, which releases para-nitroanilide from the trans form of the substrate. The inhibition of this reaction caused by the addition of different concentrations of inhibitor is determined, and the data is analyzed as a change in first-order rate constant as a function of inhibitor concentration to yield the apparerent K[0101]₁, values.

In a plastic cuvette are added 950 mL of ice cold assay buffer (25 mM HEPES, pH: 7.8, 100 mM NaCl), 10 mL of FKBP (2.5 mM in 10 mM Tris-Cl pH 7.5, 100 mM NaCl, 1 mM dithiothreitol), 25 mL of chymotrypsin (50 mg/ml in 1 mM HCl) and 10 mL of test compound at various concentrations in dimethyl sulfoxide. The reaction is initiated by the addition of 5 mL of substrate in 2.35 mM LiCl in trifluoroethanol).[0102]

The absorbance at 390 nm versus time is monitored for 90 seconds using a spectrophotometer and the rate constants are determined from the absorbance versus time data files.[0103]

TABLE III


In Vitro Test Results - Formulas I to IV

	Compound	K_i(nM)

	1	215
	2	638

Route of Administration

To effectively treat alopecia or promote hair growth, the compounds used in the inventive methods and pharmaceutical compositions must readily affect the targeted areas. For these purposes, the compounds are preferably administered topically to the skin.[0104]

For topical application to the skin, the compounds can be formulated into suitable ointments containing the compounds suspended or dissolved in, for example, mixtures with one or more of the following: mineral oil, liquid petrolatum, white petrolatum, propylene glycol, polyoxyethylene polyoxypropylene compound, emulsifying wax and water. Alternatively, the compounds can be formulated into suitable lotions or creams containing the active compound suspended or dissolved in, for example, a mixture of one or more of the following mineral oil, sorbitan monostearate, polysorbate 60, cetyl ester wax, cetearyl alcohol, 2-octyldodecanol, benzyl alcohol and water.[0105]

Other routes of administration known in the pharmaceutical art are also contemplated by this invention.[0106]

Dosage

Dosage levels on the order of about 0.mg to about 10,000 mg of the active ingredient compound are useful in the treatment of the above conditions, with preferred levels of about 0.1 mg to about 1,000 mg. The specific dose level for any particular patient will vary depending upon a variety of factors, including the activity of the specific compound employed; the age, body weight, general health, sex and diet of the patient; the time of administration; the rate of excretion; drug combination; the severity of the particular disease being treated; and the form of administration. Typically, in vitro dosage-effect results provide useful guidance on the proper doses for patient administration. Studies in animal models are also helpful. The considerations for determining the proper dose levels are well known in the art.[0107]

The compounds can be administered with other hair revitalizing agents. Specific dose levels for the other hair revitalizing agents will depend upon the factors previously stated and the effectiveness of the drug combination.[0108]

EXAMPLES

The following example are illustrations of the present invention and are not intended to be limitations thereon. Unless otherwise indicated, all percentages are based upon 100% by weight of the final composition.[0109]

Example 1Synthesis of 3-phenyl-1-propyl (2S)-1-(3,3-dimethyl-1,2-dioxopentyl)-2-(4-thiazolidine)carboxylate (1) 1-(1,2-dioxo-2-methoxyethyl)2-(4-thiazolidine)-carboxylate

A solution of L-thioproline (1.51 g; 11.34 mmol) in 40 mL of dry methylene chloride was cooled to 0° C. and treated with 3.3 mL (2.41 g; 23,81 mmol) of triethylamine. After stirring this mixture for 30 minutes, a solution of methyl oxalyl chloride (1.81 g; 14.74 mmol) was added dropwise. The resulting mixture was stirred at 0° C. for 1.5 hours, filtered through Celite to remove solids, dried and concentrated. The crude material was purified on a silic gel column, 2.0 g of this oxamate as ar. orange-yellow solid.[0110]

3-phenyl-1-propyl (2S) -1-(1,2-dioxo-2-methoxyethyl)2-(4-thiazolidine)carboxylate

1-(1,2,-dioxo-2-methoxyethyl)2-(4-thiazolidine)-carboxylate (500 mg; 2.25 mmol) 3-phenyl-1-propanol 3.65 mmol), 4-dimethylaminopyridine (95 mg; 0.75 mmol) and camphorsulfonic: acid (175 mg; 0.75 mmol) in 30 mL of methylene chloride were stirred together overnight. The mixture was filtered through Celite to remove solids and chromatographed (25% ethyl acetate/hexane) to obtain 690 mg of material.[0111]¹H NMR (CDCl₃, 300 MHz); δ1.92-2.01 (m, 2H)); 2.61-2.69 (m, 2H); 3.34 (m, 1H) 4.11-4.25 (m, 2H) ; 4.73 (m, 1H) ; 5.34 (m1H); 7.12 (m, 3H) ; 7.23 (m, 2H).

3-phenyl-1-propyl (2S)-1- (3,3-dimethyl-1,2-dioxopentyl) -2-(4-thiazolidine) carboxylate (1)

A solution of 3-phenyl-1-propyl(2S)-1-(1,2-dioxo-2-methoxyethyl)2-(4-thiazolidine)carboxylate (670 mg; 1.98 mmol) in tetrahydrofuran (10 mL) was cooled to—78° C. and treated with 2.3 mL of a 1.0 M solution of 1.1-dimethylpropylmagnesium chloride in ether. After stirring the mixture for 3 hours, it was poured into saturated ammonium chloride, extracted into ethyl acetate, and the organic phase was washed with water, dried and concentrated. The crude material was purified on a silica gel column, eluting with 25% ethyl acetate in hexane, to obtain 380 mg of the compound of Example 1 as a yellow oil.[0112]¹H NMR (CDCl₃, 300 MHz): d 0.86 (t, 3H); 1.21 (s, 3H); 1.26 (s, 3H); 1.62-1.91 (m, 3H); 2.01 (m, 2H); 2.71 (m, 2H); 3.26-3.33 (m, 2H) 4.19 (m 2H); 4.58 (m, 1H); 7.190 (m, 3H); 7.30 (m, 2H). Analysis calculated for C₂₀H₂₇NO₄S:C C, 63.63; H, 7.23 N, 3.71. Found: C, 64.29; H, 7.39; N, 3.46.

Example 2Synthesis of 3-(3-pyridyl)-1-propyl (2S)-1-(3,3-dimethyl-1,2-dioxopentyl)-2-(4-thiazolidine)carboxylate (2)

The compound of Example 2 was prepared according to the procedure of Example 1, using 3-(3-pyridyl)-1-propanol in the final step, to yield 3-(3-pyridyl)-1-propyl(2S)-1-(3,3-dimethyl-1,2-dioxopentyl)-2-(4-thiazolidine)carboxylate.[0113]¹H NMR (CDCl₃, 300 MHz): δ 0.89 (t, 3H, J=7.3); 1.25 (s, 3H); 1.28 (s, 3H); 1.77 (q, 2H, J=7.3); 2.03 (tt, 2H, J=6.4, 7.5); 2.72 (t, 2H, J=7.5); 3.20 (dd, 1H, J=4.0, 11.8); 3.23 (dd, 1H, J=7.0, 11.8); 4.23 (t, 2H, J=6.4); 4.55 (d, 2H, J=8.9); 5.08 (dd, 1H, J=4.0, 7.0); 7.24 (m, 1H); 8.48 (m, 2H). Analysis calculated for C₁₉H₂₆N₂O₄S—0.5H₂O: C, 58.89; H, 7.02; N, 7.23. Found: C, 58.83; H, 7.05; N, 7.19.

Example 3In Vivo Hair Generation Tests With C57 Black 6 Mice

Experiment A: C57 black 6 mice were used to demonstrate the hair revitalizing properties of a low molecular weight, small molecule, non-immunosuppressive neuroimmunophilin FKBP ligand, GPT 1046, which is related to heterocyclic esters and amides. Referring now to FIGS. 1 and 2 of the drawings, C57 black 6 mice, approximately 7 weeks old, had an area of about 2 inches by 2 inches on their hindquarters shaved to remove all existing hair. Care was taken not to nick or cause abrasion to the underlaying dermal layers. The animals were in anagen growth phase, as indicated by the pinkish color of the skin. Referring now to FIGS. 2, 3 and[0114]4, four animals per group were treated by topical administration with 20% propylene glycol vehicle (FIG. 2), 10 μM GPI 1046 (FIG. 3) or 30 μM GPI 1046 (FIG. 4) dissolved in the vehicle. The animals were treated with vehicle or GPI 1046 every 48 hours (3 applications total over the course of 5 days) and the hair growth was allowed to proceed for 6 weeks. Hair growth was quantitated by the percent of shaved area covered by new hair growth during this time period.

FIG. 2 shows that animals treated with vehicle exhibited only a small amount of hair growth in patches or tufts, with less than 3% of the shaved area covered with new growth. In contrast, FIG. 3 shows dramatic hair growth, covering greater than 90% of the shaved area in all animals. Further, FIG. 4 shows that mice treated with 30 μM GPI 1046 exhibited essentially complete hair regrowth and their shaved areas were indistinguishable from unshaven C57 black 6 mice.[0115]

Experiment B: C57 black 6 mice were used to demonstrate the hair revitalizing properties of a variety of low molecular weight, small molecule, non-immunosuppressive neuroimmunophilin FKBP ligands, including GPI 1572. CS57 Black 6 mice, 55 to 75 days old, had an area of about 2 inches by 2 inches on their hindquarters shaved to remove all existing hair. Care was taken not to nick or cause abrasion to the underlying dermal layers. The animals were in a anagen growth phase when shaved. Five animals per group were treated by topical administration with vehicle, FK506, or one of the low molecular weight, small molecule, non-immunosuppressive neuroimmunophilin FK506 ligands (GPI1605, 1046, 1312, 1572, 1389, 1511, and 1234) at a concentration of one micromole per milliliter to the shaved area. The animals were treated three times per week, and hair growth was evaluated 14 days after initiation of treatment. Hair growth was quantitated by the percent of shaved area covered by new hair growth, as scored by a blinded observer, on a scale of 0 (no growth) to five (complete hair regrowth in shaved area).[0116]

FIG. 5 shows that after 14 days, the animals treated with vehicle exhibited the beginning of growth in small tufts. In contrast, animals treated with one of the low molecular weight, small molecule, non-immunosuppressive neuroimmunophilin FKBP ligands, including GPI 1572, exhibited dramatic hair growth.[0117]

Example 4

A lotion comprising the following composition may be prepared.[0118]



	(%)

	95% Ethanol	80.0
	a heterocyclic ester or amide as defined	10.0
	above
	α-Tocopherol acetate	0.01
	Ethylene oxide (40 mole) adducts of hardened	0.5
	castor oil
	purified water	9.0
	perfume and dye	q.s.

Into 95% ethanol are added a heterocyclic ester or amide, α-tocopherol acetate, ethylene oxide (40 mole) adducts of hardened castor oil, perfume and a dye. The resulting mixture is stirred and dissolved, and purified water is added to the mixture to obtain a transparent liquid lotion.[0119]

5 ml of the lotion may be applied once or twice per day to a site having marked baldness or alopecia.[0120]

Example 5

A lotion comprising the following composition shown may be prepared.[0121]



	(%)

	95% Ethanol	80.0
	a heterocyclic ester or amide as defined	0.005
	above
	Hinokitol	0.01
	Ethylene oxide (40 mole) adducts of hardened	0.5
	castor oil
	Purified water	19.0
	Perfume and dye	q.s.

Into 95% ethanol are added a heterocyclic ester or amide, hinokitol, ethylene oxide (40 mole) adducts of hardened castor oil, perfume, and a dye. The resulting mixture is stirred, and purified water is added to the mixture to obtain a transparent liquid lotion.[0122]

The lotion may be applied by spraying once to 4 times per day to a site having marked baldness or alopecia.[0123]

Example 6

An emulsion may be prepared from A phase and B phase having the following compositions.[0124]



	(%)

	(A phase)
	Whale wax	0.5
	Cetanol	2.0
	Petrolatum	5.0
	Squalane	10.0
	Polyoxyethylene (10 mole) monostearate	2.0
	Sorbitan monocleate	1.0
	a heterocyclic ester or amide as defined	0.01
	above
	(B phase)
	Glycerine	10.0
	Purified water	69.0
	Perfume, dye, and preservative	q.s.

The A phase and the B phase are respectively heated and melted and maintained at 80° C. Both phased are then mixed and cooled under stirring to normal temperature to obtain an emulsion.[0125]

The emulsion may be applied by spraying once to four times per day to a site having marked baldness or alopecia.[0126]

Example 7

A cream may be prepared from A phase and B phase having the following compositions.[0127]



	(%)

	(A Phase)
	Fluid paraffin	5.0
	Cetostearyl alcohol	5.5
	Petrolatum	5.5
	Glycerine monostearate	33.0
	Polyoxyethylene (20 mole) 2-octyldodecyl	3.0
	ether
	Propylparaben	0.3
	(B Phase)
	a heterocyclic ester or amide as defined	0.8
	above
	Glycerine	7.0
	Dipropylene glycol	20.0
	Polyethylene glycol 4000	5.0
	Sodium Hexametaphosphate	0.005
	Purified water	44.895

The A phase is heated and melted, and maintained at 70° C. The B phase is added into the A phase and the mixture is stirred to obtain an emulsion. The emulsion is then cooled to obtain a cream.[0128]

The cream may be applied once to 4 times per day to a site having marked baldness or alopecia.[0129]

Example 8

A liquid comprising the following composition may be prepared.[0130]



	(%)

	Polyoxyethylene butyl ether	20.0
	Ethanol	50.0
	a heterocyclic ester or amide as defined	0.001
	above
	Propylene glycol	5.0
	Polyoxyethylene hardened castor oil	0.4
	derivative (ethylene oxide 80 mole adducts)
	Perfume	q.s.
	Purified water	q.s.

Into ethanol are added polyoxypropylene butyl ether, propylene glycol, polyoxyethylene hardened castor oil, a heterocyclic ester or amide, and perfume. The resulting mixture is stirred, and purified water is added to the mixture to obtain a liquid.[0131]

The liquid may be applied once to 4 times per day to a site having marked baldness or alopecia.[0132]

Example 9

A shampoo comprising the following composition may be prepared.[0133]



	(%)

	Sodium laurylsulfate	5.0
	Triethanolamine laurylsulfate	5.0
	Betaine lauryldimethylaminoacetate	6.0
	Ethylene glycol distearate	2.0
	Polyethylene glycol	5.0
	a heterocyclic ester or amide as defined	5.0
	above
	Ethanol	2.0
	Perfume	0.3
	Purified water	69.7

Into 69.7 of purified water are added 5.0 g of sodium laurylsulfate, 5.0 g triethanolamine laurylsulfate, 6.0 g of betaine lauryldimethyl-aminoacetate. Then a mixture obtained by adding 5.0 g of a heterocyclic ester or amide, 5.0 g of polyethylene glycol, and 2.0 g of ethylene glycol distearate to 2.0 g of ethanol, followed by stirring, and 0.3 g of perfume are successively added. The resulting mixture is heated and subsequently cooled to obtain a shampoo.[0134]

The shampoo may be used on the scalp once or twice per day.[0135]

Example 10

A patient is suffering from alopecia senilis. A heterocyclic ester or amide as identified above, or a pharmaceutical composition comprising the same, may be administered to the patient. Increased hair growth is expected to occur following treatment.[0136]

Example 11

A patient is suffering from male pattern alopecia. A heterocyclic ester or amide as identified above, or a pharmaceutical composition comprising the same, may be administered to the patient. Increased hair growth is expected to occur following treatment.[0137]

Example 12

A patient is suffering from alopecia areata. A heterocyclic ester or amide as identified above, or a pharmaceutical composition comprising the same, may be administered to the patient. Increased hair growth is expected to occur following treatment.[0138]

Example 13

A patient is suffering from hair loss caused by skin lesions. A heterocyclic ester or amide as identified above, or a pharmaceutical composition comprising the same, may be administered to the patient. Increased hair growth is expected to occur following treatment.[0139]

Example 14

A patient is suffering from hair loss caused by tumors. A heterocyclic ester or amide as identified above, or a pharmaceutical composition comprising the same, may be administered to the patient. Increased hair growth is expected to occur following treatment.[0140]

Example 15

A patient is suffering from hair loss caused by a systematic disorder, such as a nutritional disorder or an internal secretion disorder. A heterocyclic ester or amide as identified above, or a pharmaceutical composition comprising the same, may be administered to the patient. Increased hair growth is expected to occur following treatment.[0141]

Example 15

A patient is suffering from hair loss caused by chemotherapy. A heterocyclic ester or amide as identified above, or a pharmaceutical composition comprising the same, may be administered to the patient. Increased hair growth is expected to occur following treatment.[0142]

Example17

A patient is suffering from hair loss caused by radiation. A heterocyclic ester or amide as identified above, or a pharmaceutical composition comprising the same, may be administered to the patient. Increased hair growth is expected to occur following treatment.[0143]

The invention being thus described, it will be obvious that the same may be varied in many ways. Such variations are not to be regarded as a departure from the spirit and scope of the invention and all such modifications are intended to be included within the scope of the following claims.[0144]