WO1987000180A1

WO1987000180A1 - Pentapeptides with cell growth regulatory effects and a process for the preparation thereof

Info

Publication number: WO1987000180A1
Application number: PCT/NO1986/000041
Authority: WO
Inventors: Kjell Elgjo; Karl-Ludvig Reichelt
Original assignee: Bio Tech AS
Current assignee: Bio Tech AS
Priority date: 1985-06-26
Filing date: 1986-06-18
Publication date: 1987-01-15
Anticipated expiration: 1987-12-26
Also published as: DE3662198D1; FI86861C; AU5964286A; JPS62503170A; DK96987A; US4794169A; FI86861B; FI870811A0; NO860752L; FI870811A7; JP2577730B2; AU584438B2; DK96987D0; EP0228404B1; CA1298435C; EP0228404A1

Abstract

New pentapeptide of formula (I), in which X1 and X2 are the same or different and are OH or NH2, Y is H or OH, X3 is CO or CH2, one of the groups Z1 and Z2 is H and the other is H or CH3, all the amino acid units being in L-configuration, with the exception that the C-terminal amino acid unit is in D-configuration when Z2 is methyl, and the C-terminal carboxyl group may be reduced to -CH2-OH or be in amide form, and cation complexes and salts thereof. The pentapeptide may be prepared by subjecting a protected derivative thereof to deprotection. The pentapeptide has cell growth regulatory activity.

Description

Pentapeptides with cell growth regulatory effects and a process for the preparation thereof.

The present invention relates to new pentapeptides which reversibly inhibit cell proliferation in squamous epithelia, and a process for preparing such pentapeptides.

Many skin disorders are characterized by an abnormally fast rate of cell proliferation in the epidermis. In this, category of skin diseases, psoriasis is the one which has been best investigated. Here, cell proliferation takes place very rapidly, and the cells do not have sufficient time to mature normally and are shed from the surface still containing the cell nucleus. In many other skin diseases the cell prolifer¬ ation rate is markedly increased, but none of these have been subjected to such extensive studies as has psoriasis. High mitotic activity is also found in most benign and malignant skin tumors of epidermal origin.

Cell division (mitosis) in the normal epidermis is con¬ fined to the lowermost cell layer (the basal cell layer) facing the underlying layer of connective tissue (the der is) . After a basal cell has divided into two daughter cells, one of the daughter cells - on average - remains in the basal cell layer, while the other gradually matures (keratinizes) as it migrates through the various layers of the epidermis. It reaches the surface as a fully keratinized cell without a nucleus, and is eventually shed. In the adult epidermis the number of cells lost from the surface in a given time is exactly balanced by the production of new cells in the basal cell layer. It is only in this manner that a constant thickness of the epidermis can be maintained. If a large number of epidermal cells are suddenly lost, e.g. after injury, the rate of cell division in the basal cell layer increases after a short lag time. After a period of time which depends on the degree of cell loss, the epidermis regains its former, normal, thickness. Large series of experi¬ ments have indicated that the balance between cell loss and cell renewal in the epidermis is biologically regulated accord¬ ing to the negative feedback principle. In such a system, the maturing cells continuously produce an inhibitor which diffuses down to the basal cell layer where it inhibits the rate of cell proliferation. The concentration of inhibitor in the basal cell layer is dependent on the number of mature, or maturing cells. Thus, when mature cells are lost from the surface, the concentration of inhibitor decreases, allowing the basal cells to divide at a faster rate. This regulatory mechanism seems to be active to a certain extent even in malignant tumors.

We have now discovered that the keratinizing cells produce an inhibitor (or a group of inhibitors) which is of peptide nature. We have also been able to isolate and determine the structure of such compounds. In particular we have purified, identified and chemically synthesized pentapeptides which, when tested for biological activity in vivo, reversibly inhibit the rate of cell proliferation in the basal cell layer, e.g. upon administration to mice. Furthermore, _in vitro experiments have demonstrated that cells of an established cell line are inhibited by these pentapeptides at very low concentrations. This cell line originates from mouse epidermis treated with a skin carcinogen (DMBA = dimethylbenzanthracene) . Continuous treatment jLn vitro will arrest cell proliferation completely for a period of several days in normal keratinizing epithelial cells, while transformed cells are only partially inhibited. In both cases the inhibition is completely reversible when the treatment is terminated. In vitro experiments have also demon¬ strated that both normal and transformed cells mature (kerati- nize) at a faster rate after a 24-hour treatment with one of the new pentapeptides. No toxic effects have been observed either jLn vivo or _in. vitro at the concentrations tested.

According to the invention there is provided a pentapeptide of the formula

wherein X 1 and X2 are the same or different and are OH or NH-,

Y is H or OH,

X³ is CO or CH-, one of the groups Z 1 and Z2 is H and the other H or CH_, all amino acid units being in the L-configuration, with the exception that the C-terminal amino acid unit is in the D-

2 configuration when Z is methyl, and the C-terminal carboxyl group may be reduced to -CH--OH or in amide form, and cation complexes and salts thereof.

Suitable cation complexes are particularly complexes with

++ ++ ++ ++ Zn , Ca , Mg and Mn . Suitable salts are acid addition salts, such as hydrochlorides and alkali, alkaline earth and a ine salts which are physiologically acceptable. Thus, the following amino acid units may be included in the pentapeptide, counted from the C-terminal end:

1) Glycine (Gly) [Z¹ = Z² = H]

D-Alanine (D-Ala) [Z¹ = H, Z² = CH-]

1 2 ^3' Sarcosine [Z = CH₃, Z = H]

2) Alanine (Ala) [Y = H] Serine (Ser) [Y = OH]

3) Aspartic acid (Asp) [X² = OH]

2 Asparagine (Asn) [X = NH-]

4) Glutamic acid (Glu) [X¹ = OH]

Gluta ine (Gin) [X² = NH-]

^"_

5) Pyroglutamic acid (pGlu) [X = CO]

Proline (Pro) [X³ = CH-]

In the following Table 1 _in vivo results (change in mouse epidermal mitotic rate) have been described as example for four different new pentapeptides. The epidermal mitotic rate was measured for the first three hours after intraperitoneal injec¬ tion of the new pentapeptides. Mitotic rate was determined by means of "Colcemid" (Demecolcine) . A reduced rate was deter¬ mined as a percentage in comparison with control animals from the same cage. TABLE I

The new pentapeptide may, in a per se known manner, be incorporated in pharmaceutical compositions, e.g. as tablets, injection solutions, nose-spray compositions or suppositories.

The compounds of formula I may be prepared by subjecting a compound of formula I wherein carboxyl groups, amino groups and hydroxyl groups optionally present have been protected, to a treatment to remove the protective grou (s) .

During the synthesis of the pentapeptide it is e.g. possi¬ ble to use one of the classical coupling methods published in the comprehensive and well known peptide literature. In general any reactive group (e.g. amino, hydroxyl and/or carboxyl) which shall not participate in a peptide bond, should be kept protected during the entire synthesis, and the last step will accordingly be a deprotection of a completely pro¬ tected derivative of the desired final product. For the coup¬ ling steps in which the individual protected amino acids are bound together, several different known methods may be used, and these have been described in detail in the comprehensive literature regarding peptide synthesis. However, it is prefer¬ able here to prepare the different peptides by means of the so- called solid phase method, which is considered to be suitable for the preparation of oligopeptides and their analogues in a rapid manner and with good yields. In this method, which was first introduced by R.B. Merrifield in 1963, the growing peptide chain is kept attached to a solid polymer support, and the synthesis starts by binding the C-terminal amino acid to the polymer. The most common amino acids attached to a polymer support are today commercially available. The next amino acid is then coupled to this polymer-bound amino acid by a repeated cycle with deprotection, washing and coupling. In this manner the entire peptide is built up in a polymer- bound form, and in the last step the final product is split off from the polymer by means of a suitable reagent (usually hydrofluoric acid, HF) . In the following a typical example of a solid phase peptide synthesis is described.

Polymer support:

As solid carrier the following may, for example be used - either chloromethylated polystyrene, cross-linked with 2% divinyl benzene, "mesh" size 200-400 with chloro substitution of 0.3 - 1.5 meq./g, or

- benzhydrylamine resin, also cross-linked with 2% divinylbenzene, "mesh" size 200-400 with NH- substitution of 0.3-1.5 meq./g.

In the following example a commercially available chloro¬ methylated polymer to which amino group protected glycine has already been attached, is used.

Example: Synthesis of pGlu-Glu-Asp-Ala-Gly.

2 mmoles of Boc-Gly-Rx were used as starting material, and the following amino acids were added according to the usual principles for solid peptide synthesis:

Boc-Ala 1.13 g

Boc-Asp(OcHex) 1.80 g

Boc-Glu(OcHex) 1.90 g pGlu 0,90 g

The following cycle was used:

Wash 3 times with methylene chloride (1 min.) Wash once with 40% TFA (1 min.) Deprotect with 40% TFA (30 min.)

Wash once with me hylene chloride (1 min.)

Wash once with ethanol (1 min.)

Wash twice with methylene chloride (1 min.)

Wash once with 10% TEA (1 min.)

Neutralize with 10% TEA (10 min.)

Wash 3 times with methylene chlorid (1 min.)

Add 3 molar excess of Boc-amino acid and DCC

Couple 3 hours.

In the last cycle the pyroglutamic acid was washed for 30 minutes with 10% TFA instead of with 40% since deprotection was not necessary.

Abbreviations: TFA trifluoroacetic acid

TEA triethylamine

Boc t-butoxy carbonyl

DCCf dicyclohexyl carbodiimide

Rx polymer support

OcHex cyclohexyloxy.

Hydrogen fluoride treatmentϊ

3,8 g of dried resin with pentapeptides attached thereto were placed in a Kel-F reaction vessel and wetted with approxi¬ mately 10 ml of anisole. The reaction vessel was cooled by means of dry-ice/acetone, and 40 ml of HF were distilled over into the reaction vessel. The polymer with pentapeptide attached thereto was then stirred at 0 for 45 minutes, where¬ after HF was removed by evaporation. The polymer was then washed with ether and extracted with 10% acetic acid, and the extract was lyophilized.

All the pentapeptides described herein have been prepared from the appropriate protected amino acids in a similar way. In Table II the physical-chemical data for six of these novel peptides are given. «-.

TABLE II - Synthesized peptides - physical-chemical data

Legend to Table II

Thin layer chromatography (TLC) - Systems SI: ^" Silica: n-BuOH:EtOAc:HOAc:H₂0 (1:1:1:1)

Detection: o-tolidine S2: Silica Fm: n-BuOH:Pyr:HOAc:H₂0(6:6:1,2:4,8)

Detection: o-tolidine S3: Silica F: n-BuOH:PyrHOAc:H₂0(15:10:3:12)

Detection: o-tolidine

1-4: See table I

5: pGlu-Glu-Asp-Ser-Gly(NH₂) 6: pGlu-Glu-Asp-Ser-D-Ala

Electrophoresis-system

Whatman 3MM: Pyridine: acetic acid, pH 6.4, 1500V, 1 hour Detection: o-tolidine

Spot migrating towards the anode

Rf value with reference to arginine a) Rf value with reference to picric acid.

High performance liquid chromatography (HCLC) - systems

51 : Column C-18

Flow rate: 1 ml/min.

Solvent : A-O.1% TFA, B-60% CH₃C in A Gradient : linear, 0 to 100% B in 40 min. Detector : UV 210 nm.

52 : Column: C-18

Flow rate: 1 ml/min.

Solvent : A-0.05 M aH₂P0₄, B-60% CH₃CN in A

Gradient : linear, 0 to 100% B in 40 min.

Detector : UV 210 nm

Retention time (RT) in min.

Claims

P A T E N T C L A I M S

1. New pentapeptide, c h a r a c t e r i z e d b y the formula

m which X 1 and X2 are the same or different and are OH or

NH₂, Y is H or OH,

X³ is CO or CH-, one of the groups Z 1 and Z2 i.s H and the other is H or CH-,, all the amino acid units being in L-configuration, with the exception that the C-terminal amino acid unit is in D-configu-

2 ration when Z is methyl, and the C-terminal carboxyl group may be reduced to -CH--OH or be in amide form -CO-NH-, and cation complexes and salts thereof.

2. Pentapeptide according to claim 1, c h a r a c t e r i z e d i n that it has formula I in wwhhiicchh χl is OH, X² is OH, X³ is CO, Y is OH, Z¹ is H and Z² is H.

3. Pentapeptide according to claim 1, c h a r a c t e r i z e d i n that it has formula I in which χl is H₂, X² is OH, X³ is CO, Y is OH, Z¹ is H and Z² is H.

4. Pentapeptide according to claim 1, c h a r a c t e r i z e d i n that it has formula I in which χl is OH, X² is OH, X³ is CO, Y is H, Z¹ is H and Z² is H.

5. Process for the preparation of a compound of formula I of claim 1, c h a r a c t e r i z e d i n that a protected derivative of said compound is subjected to deprotection.

6. Process according to claim 5, c h a r a c t e r i z e d i n that the pentapeptide, optionally in protected form, is built up by means of solid phase peptide synthesis in which the C-terminal amino acid is first attached to solid support and then the other amino acids in the desired order.