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Details

Stereochemistry ACHIRAL
Molecular Formula C27H36N6O3
Molecular Weight 492.6131
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CPG-52364

SMILES

COC1=C(OC)C=C2C(NCCN3CCOCC3)=NC(=NC2=C1)C4=CC=C(C=C4)N5CCN(C)CC5

InChI

InChIKey=TUOZJWZCVIRDKO-UHFFFAOYSA-N
InChI=1S/C27H36N6O3/c1-31-10-12-33(13-11-31)21-6-4-20(5-7-21)26-29-23-19-25(35-3)24(34-2)18-22(23)27(30-26)28-8-9-32-14-16-36-17-15-32/h4-7,18-19H,8-17H2,1-3H3,(H,28,29,30)

HIDE SMILES / InChI

Molecular Formula C27H36N6O3
Molecular Weight 492.6131
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 11:36:40 UTC 2023
Edited
by admin
on Sat Dec 16 11:36:40 UTC 2023
Record UNII
5TVM84YK6F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CPG-52364
Common Name English
6,7-DIMETHOXY-2-(4-(4-METHYLPIPERAZIN-1-YL)PHENYL)-N-(2-MORPHOLINOETHYL)QUINAZOLIN-4-AMINE
Systematic Name English
4-QUINAZOLINAMINE, 6,7-DIMETHOXY-2-(4-(4-METHYL-1-PIPERAZINYL)PHENYL)-N-(2-(4-MORPHOLINYL)ETHYL)-
Systematic Name English
Code System Code Type Description
FDA UNII
5TVM84YK6F
Created by admin on Sat Dec 16 11:36:40 UTC 2023 , Edited by admin on Sat Dec 16 11:36:40 UTC 2023
PRIMARY
MANUFACTURER PRODUCT INFORMATION
CPG-52364
Created by admin on Sat Dec 16 11:36:40 UTC 2023 , Edited by admin on Sat Dec 16 11:36:40 UTC 2023
PRIMARY Description: CPG-52364 a small molecule TLR7/8/9 antagonist, has recently completed phase 1 clinical trial for SLE therapy. Toll-like receptors (TLRs) are a family of type I transmembrane receptors and the central components of the innate immune system. Human TLR3, TLR7, TLR8, and TLR9 are expressed on endosomal membranes in the cells and recognize pathogenderived nucleic acid molecular patterns.5 However, recognition of endogenous immune complexes containing self-nucleic acids as PAMPs or DAMPs contributes to certain autoimmune diseases, such as systemic lupus erythematosus (SLE), psoriasis,7 arthritis, and multiple sclerosis.8 Therefore, inhibition of these recognition signals is expected to have therapeutic value. (last updated: 11/11/2015).
PUBCHEM
25105690
Created by admin on Sat Dec 16 11:36:40 UTC 2023 , Edited by admin on Sat Dec 16 11:36:40 UTC 2023
PRIMARY
CAS
1093135-60-4
Created by admin on Sat Dec 16 11:36:40 UTC 2023 , Edited by admin on Sat Dec 16 11:36:40 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
TARGET -> INHIBITOR
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY
Originator: Coley Pharmaceutical Group; Class: Small molecule; Mechanism of Action: Toll-like receptor 7 antagonist, Toll-like receptor 8 antagonist, Toll-like receptor 9 antagonist; Highest Development Phase: Discontinued for Systemic lupus erythematosus; Most Recent Events: 27 Jan 2010 Discontinued - Phase-I for Systemic lupus erythematosus in USA (PO), 27 Jan 2010 Discontinued - Phase-I for Systemic lupus erythematosus in USA (PO), 29 Oct 2007 Phase-I clinical trials in Systemic lupus erythematosus in USA (PO)