Crystalline forms of ras inhibitors, compositions containing the same, and methods of use thereof
US-2024352036-A1 · Oct 24, 2024 · US
US2016289244A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016289244-A1 |
| Application number | US-201415100985-A |
| Country | US |
| Kind code | A1 |
| Filing date | Dec 2, 2014 |
| Priority date | Dec 2, 2013 |
| Publication date | Oct 6, 2016 |
| Grant date | — |
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This invention provides maytansinoids having improved tumor inhibition activity, in particular, the present invention provides a method of treatment of cancer, in particular colon cancer, using maytansinoid compounds having two fused macrocyclic rings.
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1 . A compound having a structure of: wherein R 1 , R 2 , and R 3 are independently selected from the group consisting of hydrogen and an group having 1 to 6 carbon atoms. 2 . The compound of claim 1 , wherein the compound having a structure of 3 . A compound having a structure of: wherein R is a substituted or non-substituted chain alkyl group having at least 3 carbon atoms and no more than 8 carbon atoms. 4 . The compound of claim 3 , wherein R is CH 2 CH 2 CH 3 . 5 . A method of treating cancer, comprising: administering an effective dose of the compound according to claim 1 daily. 6 . The method according to claim 5 , wherein the effective dosage is at least 1.6 μg/kg per patient body weight. 7 . The method according to claim 5 , wherein the effective dosage is about 3.2 μg/kg per patient body weight. 8 . The method according to claim 5 , wherein the effective dosage is about 0.004 mg/kg per patient body weight. 9 . The method according to claim 5 , wherein the effective dosage is about 20 μg/kg per patient body weight. 10 . The method according to claim 5 , wherein the effective dosage is about 40 μg/kg per patient body weight. 11 . The method according to claim 5 , wherein the effective dosage is about 0.05 mg/kg per patient body weight. 12 . The method according to claim 5 , wherein the cancer treated is colon carcinoma. 13 . The method according to claim 5 , wherein the cancer treated is oral epidermoid carcinoma. 14 . The method according to claim 5 , wherein the cancer treated is promyelocytic leukemia. 15 . The method according to claim 5 , wherein the cancer treated is prostate carcinoma. 16 . The method according to claim 5 , wherein the cancer treated is breast carcinoma. 17 . The method accordion to claim 5 , wherein the cancer treated is lure carcinoma. 18 . A method of treating cancer comprising administering an effective dose of the compound according to claim 3 daily.
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