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Condensed pyrimidines as inhibitors of the p97 complex
专利权人:
Cleave Biosciences; Inc.
发明人:
ZHOU, Han-Jie,PARLATI, Francesco,WUSTROW, David
申请号:
ES13745937
公开号:
ES2667726T3
申请日:
2013.07.19
申请国别(地区):
ES
年份:
2018
代理人:
摘要:
A condensed pyrimidine compound of formula I ** Formula ** in which: A is CH2, NR1, O or S; m is an integer of 1-3; n is 0 or an integer of 1-2; the ring containing A is a ring of five or six members such that the sum of m + n is 1 or 2; Y is selected from the group consisting of hydrogen, halogen, Rc, ORc, CN, CO2H, CON (Rc) 2, C (NRc) N (Rc) 2, CH2N (Rc) 2, SO2N (Rc) 2 and SO2Rc in which each Rc is independently selected from the group consisting of hydrogen, alkyl, fluoroalkyl, aryl, aralkyl, heterocyclylalkyl, heteroaryl and any combination thereof; Z is selected from the group consisting of halogen, unsubstituted alkyl of 1 to 6 carbons, alkyl or substituted alkenyl of 1 to 4 carbons, and substituted alkoxy of 1 to 4 carbons; wherein the substituted alkyl or alkenyl group is substituted with ORa, SRa, OC (O) Ra, C (O) Ra, C (O) ORa, OC (O) N (Ra) 2, C (O) N ( Ra) 2, N (Ra) C (O) ORa, N (Ra) C (O) R8, N (Ra) C (O) N (Ra) 2, N (Ra) C (NRa) N (Ra) 2, N (Ra) S (O) tRa, S (O) tORa, S (O) tN (Ra) 2, N (Ra) 2 or PO3 (Ra) 2 in which each Ra is independently hydrogen, alkyl, fluoroalkyl, aryl, aralkyl, heterocyclylalkyl, heteroaryl or any combination thereof; and, the substituted alkoxy group is substituted with ORb, Rb, OC (O) Rb, N (Rb) 2, C (O) Rb, C (O) ORb, OC (O) N (Rb) 2, C (O ) N (Rb) 2, N (Rb) C (O) ORb, N (Rb) C (O) Rb, N (Rb) C (O) N (Rb) 2, N (Rb) C (NRb) N (Rb) 2, N (Rb) S (O) tRb, S (O) tORb, S (O) tN (Rb) 2, N (Rb) 2 or PO3 (Rb) 2 in which each Rb is independently hydrogen , alkyl, fluoroalkyl, aryl, aralkyl, heterocyclylalkyl, heteroaryl, or any combination thereof; R1 is selected from a group consisting of hydrogen, unsubstituted alkyl of 1 to 6 carbons, substituted alkyl of 1 to 4 carbons and -C (O) Rd; wherein, the substituted alkyl is substituted with ORd, SRd, OC (O) Rd, C (O) Rd, C (O) ORd, -OC (O) N (Rd) 2, C (O) N (Rd ) 2, N (Rd) C (O) ORd, N (Rd) C (O) Rd, N (Rd) C (O) N (Rd) 2, N (Rd) C (NRd) N (Rd) 2 , N (Rd) S (O) tRd, S (O) tORd, S (O) tN (R
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