US4743590A
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US
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In vitro and in vivo treatment of cancer cells and treatment of viruses with a tripeptide compound
Assignee: Individual
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Filing: 1986-03-24
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Granted: 1988-05-10
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Expires: 2006-03-24
Abstract
Abstract The cancericidal activity of all the permutations of a tripeptide compound formed from dichlorodiethylaminophenylalanine, parafluorophenylalanine and methionine bonded together with peptide links was demonstrated using seven in vitro tumor cell lines. The viabilities of each of the tumor cell lines were significantly reduced by treatment for 1 to 24 hours with 1 to 50 ug of the tripeptide per ml of carrier solvent. A pulse exposure to the tripeptide demonstrated that the reductions in tumor cell was comparable to continuous exposure. Other in vitro tests were all conducted on AKR mice. Methods of treating virus by exposing the virus to one of the noted tripeptide compounds is also contemplated. Methods of treating tumor cells with the tripeptides dissolved in a solvent consisting of dimethylacetamide, propylene glycol and absolute ethanol are also contemplated by the present invention. Methods of treating tumor cells resistant to other chemotherapeutic agents is contemplated by this invention.
Inventors
- 👤 Augusto DeBarbieri
- 👤 Julius G. Bekesi
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-09 04:00
CPC Classifications
C; C07; C07H; C07H13/00; C07H13/02; C07H13/04; C07H15/00; C07H15/02; C07H15/04; C07K; C07K5/00; C07K5/04; C07K5/06; C07K5/06008; C07K5/06078; C07K5/08; C07K5/0802; C07K5/0812; C07K5/0827
Claims Analysis
Total Claims: 18
Claim 1
Independent Claim
64 words
The method of treating tumor cells comprising: culturing the tumor cells with L-PAM, methotrexate, or cisplatin whereby the tumor cells become resistant to L-PAM, methotrexate, or cisplatin; administering to the tumor cells in vitro at a therapeutically effective dose for treating tumor cells a tripeptide compound, selected from the group consisting of: (a) 3-(p-fluorophenyl)-L-alanyl-3-[m-bis(2-chloroethyl)-aminophenyl]-L-alanyl-L-methionine (b) 3-[m-bis(2-chloroethyl)aminophenyl]-L-alanyl-3-(p-fluorophenyl)-L-alanyl-L-methionine (c) 3-(p-fluoropheny)-L-alanyl-L-methionyl-3-[m-bis(2-chloroethyl)aminophenyl]-L-alanine (d) 3-[m-bis(2-chloroethyl)aminophenyl]-L-alanyl-L-methionyl-3-(p-fluorophenyl)-L-alanine (e) L-methionyl-3-(p-fluorophenyl)-L-alanyl-3-[m-bis(2-chloroethyl)aminophenyl]-L-alanine (f) L-methionyl-3[m-bis(2-chloroethyl)aminophenyl]-L-alanyl-3-(p-fluorophenyl)-L-alanine.
Claim 2
Independent Claim
64 words
The method of treating tumor cells comprising: culturing the tumor cells with L-PAM, methotrexate, or cisplatin whereby the tumor cells become resistant to L-PAM, methotrexate, or cisplatin; administering to the tumor cells in vitro at a therapeutically effective dose for treating tumor cells a tripeptide compound, selected from the group consisting of: (a) 3-(p-fluorophenyl)-L-alanyl-3-[m-bis(2-chloroethyl)-aminophenyl]-L-alanyl-L-methionine (b) 3-[m-bis(2-chloroethyl)aminophenyl]-L-alanyl-3-(p-fluorophenyl)-L-alanyl-L-methionine (c) 3-(p-fluoropheny)-L-alanyl-L-methionyl-3-[m-bis(2-chloroethyl)aminophenyl]-L-alanine (d) 3-[m-bis(2-chloroethyl)aminophenyl]-L-alanyl-L-methionyl-3-(p-fluorophenyl)-L-alanine (e) L-methionyl-3-(p-fluorophenyl)-L-alanyl-3-[m-bis(2-chloroethyl)aminophenyl]-L-alanine (f) L-methionyl-3[m-bis(2-chloroethyl)aminophenyl]-L-alanyl-3-(p-fluorophenyl)-L-alanine.
Claim 3
Dependent Claim
14 words
The method of claim 1, wherein the tripeptide compound is 3-(p-fluorophenyl)-L-alanyl-3-[m-bis(2-chloroethyl)aminophenyl]-L-alanyl-L-methionine ethyl ester hydrochloride.
Claim 4
Dependent Claim
89 words
The method of claim 2, wherein 10 mg of the tripeptide is first dissolved in a solution of 0.25 ml of N-N-dimethylacetamide, 0.25 ml of absolute ethanol and 0.5 ml of propylene glycol; preparing a stock solution by further diluting the dissolved drug in an aqueous solution of 50% propylene glycol to a concentration of 1 to 2 mg per ml; and administering the tripeptide compound at concentrations ranging from 0.5 to 50 ug per ml of the tumor cells for 15 minutes to 24 hours at 37° C.
Claim 5
Dependent Claim
92 words
The method of claim 2, wherein 10 mg of the tripeptide is first dissolved in a solution of 0.25 ml of N,N-dimethylacetamide, 0.25 ml of pure ethanol, and 0.5 ml of propylene glycol; preparing the solution by further diluting the dissolved drug in an aqueous solution of 50% propylene glycol so that the stock solutions are concentrated in a range of 1 to 2 mg per ml; exposing the tumor cells to 0.5 to 50 ug of the tripeptide compound per ml of solvent for pulse exposure from 0.25 to 4 hours.
Claim 6
Dependent Claim
26 words
The method of claim 2, wherein the tumor cells are a member selected from a group consisting of MJY-alpha murine mammary cells and B-16 melanoma cells.
Claim 7
Dependent Claim
24 words
The method of claim 5, wherein the tumor cells are in a layer density of approximately 2×10 5 cells per sq. cm. of well.
Claim 8
Dependent Claim
27 words
The method of claim 2, wherein the tumor cells are a member selected from the group consisting of murine L-1210 leukemia cells and primary human leukemia cells.
Claim 9
Dependent Claim
17 words
The method of claim 7, wherein the tumor cells are at cell concentrations of 6-10×10 5 cells/ml.
Claim 10
Independent Claim
57 words
A method of treating tumor cells resistant to L-PAM, methotrexate or cisplatin comprising: (a) preparing a therapeutic quantity of a tripeptide compound in a pharmaceutical vehicle, said tripeptide compound being 3-(p-fluorophenyl)-L-alanyl-3-[m-bis-(2-chloroethyl)aminophenyl]-L-alanyl-L-methionine ethyl ester hydrochloride; (b) administering in a repetitive dosing regimen said pharmaceutical vehicle containing said tripeptide compound to a malignant tissue containing said resistant tumor cells.
Claim 11
Independent Claim
57 words
A method of treating tumor cells resistant to L-PAM, methotrexate or cisplatin comprising: (a) preparing a therapeutic quantity of a tripeptide compound in a pharmaceutical vehicle, said tripeptide compound being 3-(p-fluorophenyl)-L-alanyl-3-[m-bis-(2-chloroethyl)aminophenyl]-L-alanyl-L-methionine ethyl ester hydrochloride; (b) administering in a repetitive dosing regimen said pharmaceutical vehicle containing said tripeptide compound to a malignant tissue containing said resistant tumor cells.
Claim 12
Dependent Claim
31 words
The method of claim 9, wherein said therapeutic amount is between about 3.75 uM to about 15 uM for an exposure time of between about 15 minutes to about 60 minutes.
Claim 13
Dependent Claim
29 words
The method of claim 10, wherein said repetative dosing regimen for administering said therapeutic amount of said tripeptide compound for said exposure time is about a 24 hour period.
Claim 14
Dependent Claim
16 words
The method of claim 9, wherein said malignant tissue is treated in an in vitro condition.
Claim 15
Dependent Claim
16 words
The method of claim 9, wherein said malignant tissue is treated in an in vivo condition.
Claim 16
Dependent Claim
28 words
The method of claim 9 wherein said resistant tumor cells are a member selected from the group consisting of murine L1210 leukemia cells and primary human leukemia cells.
Claim 17
Dependent Claim
14 words
The method of claim 9, wherein said resistant tumor cells are primary human leukemias.
Claim 18
Dependent Claim
29 words
The method of claim 7, wherein said primary human leukemia is a member selected from the group consisting of human AMML leukemia, human ALL leukemia, and hairy cell leukemia.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1991-05-10 | 1991-11-09 | 1992-05-10 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1995-05-10 | 1995-11-09 | 1996-05-10 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1999-05-10 | 1999-11-09 | 2000-05-10 | $7700.00 | Window Closed / Lapsed |