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Details

Stereochemistry ACHIRAL
Molecular Formula C23H28N8O4.2ClH
Molecular Weight 553.442
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of COPANLISIB HYDROCHLORIDE

SMILES

Cl.Cl.COC1=C(OCCCN2CCOCC2)C=CC3=C1N=C(NC(=O)C4=CN=C(N)N=C4)N5CCN=C35

InChI

InChIKey=STGQPVQAAFJJFX-UHFFFAOYSA-N
InChI=1S/C23H28N8O4.2ClH/c1-33-19-17(35-10-2-6-30-8-11-34-12-9-30)4-3-16-18(19)28-23(31-7-5-25-20(16)31)29-21(32)15-13-26-22(24)27-14-15;;/h3-4,13-14H,2,5-12H2,1H3,(H2,24,26,27)(H,28,29,32);2*1H

HIDE SMILES / InChI

Molecular Formula C23H28N8O4
Molecular Weight 480.5196
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Molecular Formula ClH
Molecular Weight 36.461
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 Fri Dec 15 16:01:45 UTC 2023
Edited
by admin
on Fri Dec 15 16:01:45 UTC 2023
Record UNII
03ZI7RZ52O
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
COPANLISIB HYDROCHLORIDE
USAN   WHO-DD  
USAN  
Official Name English
BAY-80-6946 DIHYDROCHLORIDE
Code English
COPANLISIB DIHYDROCHLORIDE
Common Name English
BAY-84-1236
Code English
BAY 84-1236
Code English
5-PYRIMIDINECARBOXAMIDE, 2-AMINO-N-(2,3-DIHYDRO-7-METHOXY-8-(3-(4-MORPHOLINYL)PROPOXY)IMIDAZO(1,2-C)QUINAZOLIN-5-YL)-, HYDROCHLORIDE (1:2)
Systematic Name English
BAY 80-6946 DIHYDROCHLORIDE
Code English
COPANLISIB HYDROCHLORIDE [USAN]
Common Name English
2-Amino-N-{7-methoxy-8-[3-(morpholin-4-yl)propoxy]-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl}pyrimidine-5-carboxamide dihydrochloride
Systematic Name English
COPANLISIB HYDROCHLORIDE ANHYDROUS
Common Name English
COPANLISIB DIHYDROCHLORIDE [ORANGE BOOK]
Common Name English
Copanlisib hydrochloride [WHO-DD]
Common Name English
COPANLISIB HYDROCHLORIDE [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C129825
Created by admin on Fri Dec 15 16:01:45 UTC 2023 , Edited by admin on Fri Dec 15 16:01:45 UTC 2023
NCI_THESAURUS C2152
Created by admin on Fri Dec 15 16:01:45 UTC 2023 , Edited by admin on Fri Dec 15 16:01:45 UTC 2023
Code System Code Type Description
FDA UNII
03ZI7RZ52O
Created by admin on Fri Dec 15 16:01:45 UTC 2023 , Edited by admin on Fri Dec 15 16:01:45 UTC 2023
PRIMARY
CHEBI
173081
Created by admin on Fri Dec 15 16:01:45 UTC 2023 , Edited by admin on Fri Dec 15 16:01:45 UTC 2023
PRIMARY
NCI_THESAURUS
C138994
Created by admin on Fri Dec 15 16:01:45 UTC 2023 , Edited by admin on Fri Dec 15 16:01:45 UTC 2023
PRIMARY
PUBCHEM
66562429
Created by admin on Fri Dec 15 16:01:45 UTC 2023 , Edited by admin on Fri Dec 15 16:01:45 UTC 2023
PRIMARY
EPA CompTox
DTXSID301027642
Created by admin on Fri Dec 15 16:01:45 UTC 2023 , Edited by admin on Fri Dec 15 16:01:45 UTC 2023
PRIMARY
SMS_ID
100000170810
Created by admin on Fri Dec 15 16:01:45 UTC 2023 , Edited by admin on Fri Dec 15 16:01:45 UTC 2023
PRIMARY
USAN
CD-72
Created by admin on Fri Dec 15 16:01:45 UTC 2023 , Edited by admin on Fri Dec 15 16:01:45 UTC 2023
PRIMARY
DRUG BANK
DBSALT002581
Created by admin on Fri Dec 15 16:01:45 UTC 2023 , Edited by admin on Fri Dec 15 16:01:45 UTC 2023
PRIMARY
ChEMBL
CHEMBL3218576
Created by admin on Fri Dec 15 16:01:45 UTC 2023 , Edited by admin on Fri Dec 15 16:01:45 UTC 2023
PRIMARY
CAS
1402152-13-9
Created by admin on Fri Dec 15 16:01:45 UTC 2023 , Edited by admin on Fri Dec 15 16:01:45 UTC 2023
PRIMARY
EVMPD
SUB184953
Created by admin on Fri Dec 15 16:01:45 UTC 2023 , Edited by admin on Fri Dec 15 16:01:45 UTC 2023
PRIMARY
MERCK INDEX
m12036
Created by admin on Fri Dec 15 16:01:45 UTC 2023 , Edited by admin on Fri Dec 15 16:01:45 UTC 2023
PRIMARY
Related Record Type Details
SOLVATE->ANHYDROUS
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY