US2016287555A1PendingUtilityA1
Substituted chroman derivatives, medicaments and use in therapy
Est. expirySep 21, 2024(expired)· nominal 20-yr term from priority
A23L 2/52A23V 2002/00A61P 35/00A61K 45/06A23L 33/10A61K 31/085A61K 31/353C07D 311/38C07D 311/58
73
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Claims
Claims
exact text as granted — not AI-modified1 . A composition comprising a compound of formula (I-b):
or a pharmaceutically acceptable salt thereof wherein:
R 1 is hydroxy, halo, C 1-6 alkoxy or C 1-6 alkyl;
the drawing “ ” and R 2 together represent a double bond or the drawing “ ” represents a single bond and R 2 is hydrogen or hydroxy,
R 3 , R 4 and R 5 are independently hydrogen, hydroxy, halo, NR 10 R 11 , C 1-6 alkoxy, C 1-6 fluoroalkyl or C 1-6 alkyl;
R 6 is hydrogen, hydroxy, halo, C 1-6 alkoxy or C 1-6 alkyl;
R 7 is hydroxy or C 1-6 alkoxy;
R 8 and R 9 are independently hydrogen, hydroxy, halo, NR 10 R 11 , C 1-6 alkoxy, C 1-6 fluoroalkyl or C 1-6 alkyl; and
R 10 and R 11 are independently hydrogen, C 1-6 alkyl or trialkyl silyl;
and an anti-cancer agent,
wherein said composition is optionally in association with one or more pharmaceutical carriers, excipients, auxiliaries and/or diluents.
2 . The composition of claim 1 , wherein the anti-cancer agent is cisplatin, dehydroequol or paclitaxel.
3 . The composition of claim 1 , wherein the compound of formula (I-b) is selected from compound Nos. 1 to 9 and 42 as set forth below:
4 . The composition of claim 2 , wherein the compound of formula (I-b) is:
5 . The composition of claim 3 , wherein the anti-cancer agent is dehydroequol.
6 . The composition of claim 4 , wherein the anti-cancer agent is dehydroequol.
7 . A method for the treatment, prevention or amelioration of cancer or a tumour mass, which comprises administering to a subject in need thereof a therapeutically effective amount of a compound of formula (I-b) as defined in claim 1 .
8 . The method of claim 7 , wherein the compound of formula (I-b) is selected from compound Nos. 1 to 9 and 42.
9 . The method of claim 7 , wherein the cancer or tumour mass is of epithelial origin, of mesenchymal origin or of neural origin.
10 . The method of claim 9 , wherein the cancer or tumour mass of epithelial origin is prostate, ovarian, cervical, breast, gall-bladder, pancreatic, colorectal, renal or non-small lung cancer.
11 . The method of claim 9 , wherein the cancer or tumour mass of mesenchymal origin is melanoma, mesothelioma or sarcoma cancer.
12 . The method of claim 9 , wherein the cancer or tumour mass of neural origin is glioma.
13 . The method of claim 7 , wherein the compound is simultaneously administered with an anti-cancer agent.
14 . The method of claim 7 , wherein the compound is sequentially administered with an anti-cancer agent.
15 . The method of claim 13 , wherein the anti-cancer agent is cisplatin, dehydroequol or paclitaxel.
16 . The method of claim 14 , wherein the anti-cancer agent is cisplatin, dehydroequol or paclitaxel.
17 . The method of claim 13 , wherein the compound of formula (I-b) is:
said anti-cancer agent is dehydroequol, and said subject is afflicted with ovarian or pancreatic cancer.
18 . The method of claim 14 , wherein the compound of formula (I-b) is:
said anti-cancer agent is dehydroequol, and said subject is afflicted with ovarian or pancreatic cancer.
19 . The method of claim 7 , wherein the compound acts as a radiosensitising agent.
20 . The method of claim 7 , wherein the compound acts as a chemosensitising agent.Cited by (0)
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