TY - PAT
T1 - Anti-cancer Lead Molecule
AU - Sagar, Sunil
AU - Kaur, Mandeep
AU - Esau, Luke E.
N1 - KAUST Repository Item: Exported on 2019-02-13
PY - 2014/4/17
Y1 - 2014/4/17
N2 - Derivatives of plumbagin can be selectively cytotoxic to breast cancer cells. Derivative `A` (Acetyl Plumbagin) has emerged as a lead molecule for testing against estrogen positive breast cancer and has shown low hepatotoxicity as well as overall lower toxicity in nude mice model. The toxicity of derivative `A` was determined to be even lower than vehicle control (ALT and AST markers). The possible mechanism of action identified based on the microarray experiments and pathway mapping shows that derivative `A` could be acting by altering the cholesterol-related mechanisms. The low toxicity profile of derivative `A` highlights its possible role as future anti-cancer drug and/or as an adjuvant drug to reduce the toxicity of highly toxic chemotherapeutic drugs
AB - Derivatives of plumbagin can be selectively cytotoxic to breast cancer cells. Derivative `A` (Acetyl Plumbagin) has emerged as a lead molecule for testing against estrogen positive breast cancer and has shown low hepatotoxicity as well as overall lower toxicity in nude mice model. The toxicity of derivative `A` was determined to be even lower than vehicle control (ALT and AST markers). The possible mechanism of action identified based on the microarray experiments and pathway mapping shows that derivative `A` could be acting by altering the cholesterol-related mechanisms. The low toxicity profile of derivative `A` highlights its possible role as future anti-cancer drug and/or as an adjuvant drug to reduce the toxicity of highly toxic chemotherapeutic drugs
UR - http://hdl.handle.net/10754/594844
UR - http://appft.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220140107196%22.PGNR.&OS=DN/20140107196&RS=DN/20140107196
UR - http://assignment.uspto.gov/#/search?adv=publNum:20140107196
UR - http://www.google.com/patents/US20140107196
UR - http://worldwide.espacenet.com/publicationDetails/biblio?CC=US&NR=2014107196A1&KC=A1&FT=D
M3 - Patent
M1 - US9890106B2
ER -