IP Library Patent Application 17601055
Patent Application
App. No. 17/601,055

A Camptothecin Drug and Its Antibody Conjugate Thereof

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Quick Facts
Patent No.
US None
App. No.
17/601,055
Abstract

The present application discloses a camptothecin drug and its antibody conjugate. Based on a comprehensive understanding of ADC drugs, the inventor designed a series of active anti-tumor exatecan-derivatives. The designed anti-tumor molecular compound showed good anti-tumor activity in the experiment.

Claims (33)

1 . A camptothecin compound having the general formula I or its pharmaceutically acceptable salts thereof:

wherein

R 1 and R 2 each is independently selected from the group consisting of C 1 -C 3 alkyl or substituted alkyl, —H, —CF 3 , aryl, substituted aryl or heteroaryl; or R 1 and R 2 together with the carbon atoms to which they are attached form cyclobutane, cyclopentane or cyclohexane; and R 1 and R 2 are not hydrogen at the same time.

2 . The camptothecin compound or its pharmaceutically acceptable salts thereof according to claim 1 , having a formula selected from the following formulae (a), (b), or (c):

wherein

R 1 is hydrogen, R 2 is C 1 -C 3 alkyl, —CF 3 , aryl, substituted aryl or heteroaryl as in formula (a); or

R 1 and R 2 are C 1 -C 3 alkyl, —CF 3 , aryl, heteroaryl or substituted aryl as in formula (b); or

R 1 and R 2 together with the carbon atoms to which they are connected form cyclobutane, cyclopentane or cyclohexane;

wherein

in formula (a), R 2 is independently selected from —(CH 2 )n 1 -CH 3 , —CF 3 , aryl, heteroaryl, substituted aryl, where n 1 =0, 1 or 2;

in formula (b), R 1 and R 2 are independently selected from —(CH 2 )n 1 -CH 3 , —CF 3 , aryl, heteroaryl, substituted aryl, where n 1 =0, 1 or 2; and

In formula (c), R 1 and R 2 , together with the carbon atoms to which they are connected form cyclobutane, cyclopentane, or cyclohexane, and n 2 =1, 2 or 3.

3 . The camptothecin compound or pharmaceutically acceptable salts thereof according to claim 2 , having a formula selected from the following formulae (a-1) or (a-2):

wherein

R 1 is hydrogen, R 2 is independently selected from —(CH 2 )n 1 -CH 3 , —CF 3 , aryl, heteroaryl or substituted aryl, where n 1 =0, 1 or 2;

wherein

the carbon connected to R 2 has two configurations: R or S;

in formula (a-1), the carbon to which R 2 is attached is in the R configuration; and

in formula (a-2), the carbon to which R 2 is attached is in the S configuration.

4 . The camptothecin compound or its pharmaceutically acceptable salts thereof according to claim 1 , wherein the substituted aryl comprises aryl groups having substituents selected from the group consisting of halogen, hydrocarbyl, alkoxy, hydroxyl, nitro, amino, hydroxyl and cyano.

5 . The camptothecin compound or its pharmaceutically acceptable salts thereof according to claim 1 , having a formula selected from the following formulae:

6 . An antitumor drug for treating a solid tumor or a blood tumor, comprising the camptothecin compound or its pharmaceutically acceptable salts thereof according to claim 1 , wherein the solid tumor or blood tumor comprises lung cancer, kidney cancer, urethral cancer, colon cancer, rectal cancer, prostate cancer, glioma multiforme, ovarian cancer, pancreatic cancer, breast cancer, melanoma, liver cancer, bladder cancer, gastric cancer, lung cancer or esophageal cancers.

7 . An antibody-drug conjugate having a formula as shown in formula II,

wherein

Ab is an antibody moiety comprising an antibody, an antibody fragment or a protein;

L is a linker connecting the Ab at one end to the drug moiety (D) at the other end;

D is a drug moiety selected from the camptothecin compounds or its pharmaceutically acceptable salts thereof according to any of claims 1 - 6 , wherein D is connected to L through a hydroxyl group on the D; and

m is an integer ranging from 1-20; and

wherein the antibody-drug conjugate is configured to exert its drug effect by releasing a drug moiety (D) after reaching at a target cell

8 . The antibody-drug conjugate according to claim 7 , wherein the connecting unit

L is selected from the group consisting of —O—, —N(R)n 1 -, —CH 2 —, —CH(R)n 1 -, amide, ester bond, —S—, and -(PEG)n 2 -, wherein n 1 is an integer ranging from 1-3, n 2 is an integer ranging from 1-20.

9 . The antibody-drug conjugate according to claim 7 , wherein the antibody moiety has a binding specificity to a target cell of cancer or an autoimmune disease.

10 . A pharmaceutical composition for treating a solid tumor or a blood tumor, comprising the antibody-drug conjugate according to any of claim 7 , wherein the solid tumor or blood tumor comprises lung cancer, kidney cancer, urethral cancer, colon cancer, rectal cancer, prostate cancer, glioma multiforme, ovarian cancer, pancreatic cancer, breast cancer, melanoma, liver cancer, bladder cancer, gastric cancer, or esophageal cancer.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2024
From: BAILI-BIO (CHENGDU) PHARMACEUTICAL CO., LTD.
To: SYSTIMMUNE, INC.
Reel/Frame 066938/0800 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 14, 2022
From: SICHUAN BAILI PHARMACEUTICAL CO. LTD.
To: BAILI-BIO (CHENGDU) PHARMACEUTICAL CO., LTD.
Reel/Frame 059907/0297 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 2, 2021
From: ZHU, YI; WAN, WEILI; QIN, WENFANG; ZHANG, YONG; ZHUO, SHI
To: SICHUAN BAILI PHARMACEUTICAL CO., LTD
Reel/Frame 057679/0789 →