U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C23H28N8O4
Molecular Weight 480.5196
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of COPANLISIB

SMILES

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

InChI

InChIKey=PZBCKZWLPGJMAO-UHFFFAOYSA-N
InChI=1S/C23H28N8O4/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)

HIDE SMILES / InChI

Description
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/27310202 https://www.cancer.gov/publications/dictionaries/cancer-drug?cdrid=653981 http://www.selleckchem.com/products/bay80-6946.html

Copanlisib, developed by Bayer, is a phosphoinositide 3-kinase (PI3K) inhibitor with potential antineoplastic activity. Copanlisib inhibits the activation of the PI3K signaling pathway, which may result in inhibition of tumor cell growth and survival in susceptible tumor cell populations. Activation of the PI3K signaling pathway is frequently associated with tumorigenesis and dysregulated PI3K signaling may contribute to tumor resistance to a variety of antineoplastic agents. Copanlisib is currently under Phase II/III clinical trials for the treatment of non-Hodgkin lymphoma and chronic lymphocytic leukemia.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
ALIQOPA

Approved Use

ALIQOPA is indicated for the treatment of adult patients with relapsed follicular lymphoma (FL) who have received at least two prior systemic therapies. Accelerated approval was granted for this indication based on overall response rate. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial.

Launch Date

1.50526086E12
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
463 ng/mL
60 mg 1 times / week steady-state, intravenous
dose: 60 mg
route of administration: Intravenous
experiment type: STEADY-STATE
co-administered:
COPANLISIB plasma
Homo sapiens
population: UNKNOWN
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
447 μg/L
0.8 mg/kg 1 times / week multiple, intravenous
dose: 0.8 mg/kg
route of administration: Intravenous
experiment type: MULTIPLE
co-administered:
COPANLISIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
1570 ng × h/mL
60 mg 1 times / week steady-state, intravenous
dose: 60 mg
route of administration: Intravenous
experiment type: STEADY-STATE
co-administered:
COPANLISIB plasma
Homo sapiens
population: UNKNOWN
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
1280 μg × h/L
0.8 mg/kg 1 times / week multiple, intravenous
dose: 0.8 mg/kg
route of administration: Intravenous
experiment type: MULTIPLE
co-administered:
COPANLISIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
39.1 h
60 mg 1 times / week steady-state, intravenous
dose: 60 mg
route of administration: Intravenous
experiment type: STEADY-STATE
co-administered:
COPANLISIB plasma
Homo sapiens
population: UNKNOWN
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
35.6 h
0.8 mg/kg 1 times / week multiple, intravenous
dose: 0.8 mg/kg
route of administration: Intravenous
experiment type: MULTIPLE
co-administered:
COPANLISIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FED
Doses

Doses

DosePopulationAdverse events​
1.2 mg/kg 3 times / month steady, intravenous
Highest studied dose
Dose: 1.2 mg/kg, 3 times / month
Route: intravenous
Route: steady
Dose: 1.2 mg/kg, 3 times / month
Sources:
unhealthy, 62 years (range: 35–86 years)
n = 3
Health Status: unhealthy
Age Group: 62 years (range: 35–86 years)
Sex: M+F
Population Size: 3
Sources:
DLT: Alanine aminotransferase increased, Aspartate aminotransferase increased...
Dose limiting toxicities:
Alanine aminotransferase increased (grade 3, 1 patient)
Aspartate aminotransferase increased (grade 4, 1 patient)
Acidosis lactic (grade 4, 1 patient)
Anion gap (grade 4, 1 patient)
Ketonaemia (grade 4, 1 patient)
Left ventricular systolic dysfunction (grade 3, 1 patient)
Sources:
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources:
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources:
Disc. AE: Hyperglycemia, Neutropenia...
AEs leading to
discontinuation/dose reduction:
Hyperglycemia (7%)
Neutropenia (5%)
Hypertension (5%)
Pneumonitis (2%)
Hyperglycemia (2%)
Sources:
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources: Page: зю 99
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources: Page: зю 99
Disc. AE: Thrombocytopenia, Neutropenia...
AEs leading to
discontinuation/dose reduction:
Thrombocytopenia (3%)
Neutropenia (1.8%)
Anemia (1.2%)
Nausea (1.2%)
Fatigue (2.4%)
Hypercalcemia (1.2%)
Acute kidney injury (1.6%)
Pneumonitis (3.6%)
Febrile neutropenia (1.8%)
Diarrhea (2.4%)
Pyrexia (5.4%)
Sepsis (1.8%)
Hyperglycemia (4.8%)
Pneumonitis (6%)
Sources: Page: зю 99
AEs

AEs

AESignificanceDosePopulation
Alanine aminotransferase increased grade 3, 1 patient
DLT, Disc. AE
1.2 mg/kg 3 times / month steady, intravenous
Highest studied dose
Dose: 1.2 mg/kg, 3 times / month
Route: intravenous
Route: steady
Dose: 1.2 mg/kg, 3 times / month
Sources:
unhealthy, 62 years (range: 35–86 years)
n = 3
Health Status: unhealthy
Age Group: 62 years (range: 35–86 years)
Sex: M+F
Population Size: 3
Sources:
Left ventricular systolic dysfunction grade 3, 1 patient
DLT, Disc. AE
1.2 mg/kg 3 times / month steady, intravenous
Highest studied dose
Dose: 1.2 mg/kg, 3 times / month
Route: intravenous
Route: steady
Dose: 1.2 mg/kg, 3 times / month
Sources:
unhealthy, 62 years (range: 35–86 years)
n = 3
Health Status: unhealthy
Age Group: 62 years (range: 35–86 years)
Sex: M+F
Population Size: 3
Sources:
Acidosis lactic grade 4, 1 patient
DLT, Disc. AE
1.2 mg/kg 3 times / month steady, intravenous
Highest studied dose
Dose: 1.2 mg/kg, 3 times / month
Route: intravenous
Route: steady
Dose: 1.2 mg/kg, 3 times / month
Sources:
unhealthy, 62 years (range: 35–86 years)
n = 3
Health Status: unhealthy
Age Group: 62 years (range: 35–86 years)
Sex: M+F
Population Size: 3
Sources:
Anion gap grade 4, 1 patient
DLT, Disc. AE
1.2 mg/kg 3 times / month steady, intravenous
Highest studied dose
Dose: 1.2 mg/kg, 3 times / month
Route: intravenous
Route: steady
Dose: 1.2 mg/kg, 3 times / month
Sources:
unhealthy, 62 years (range: 35–86 years)
n = 3
Health Status: unhealthy
Age Group: 62 years (range: 35–86 years)
Sex: M+F
Population Size: 3
Sources:
Aspartate aminotransferase increased grade 4, 1 patient
DLT, Disc. AE
1.2 mg/kg 3 times / month steady, intravenous
Highest studied dose
Dose: 1.2 mg/kg, 3 times / month
Route: intravenous
Route: steady
Dose: 1.2 mg/kg, 3 times / month
Sources:
unhealthy, 62 years (range: 35–86 years)
n = 3
Health Status: unhealthy
Age Group: 62 years (range: 35–86 years)
Sex: M+F
Population Size: 3
Sources:
Ketonaemia grade 4, 1 patient
DLT, Disc. AE
1.2 mg/kg 3 times / month steady, intravenous
Highest studied dose
Dose: 1.2 mg/kg, 3 times / month
Route: intravenous
Route: steady
Dose: 1.2 mg/kg, 3 times / month
Sources:
unhealthy, 62 years (range: 35–86 years)
n = 3
Health Status: unhealthy
Age Group: 62 years (range: 35–86 years)
Sex: M+F
Population Size: 3
Sources:
Hyperglycemia 2%
Disc. AE
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources:
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources:
Pneumonitis 2%
Disc. AE
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources:
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources:
Hypertension 5%
Disc. AE
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources:
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources:
Neutropenia 5%
Disc. AE
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources:
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources:
Hyperglycemia 7%
Disc. AE
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources:
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources:
Anemia 1.2%
Disc. AE
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources: Page: зю 99
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources: Page: зю 99
Hypercalcemia 1.2%
Disc. AE
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources: Page: зю 99
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources: Page: зю 99
Nausea 1.2%
Disc. AE
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources: Page: зю 99
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources: Page: зю 99
Acute kidney injury 1.6%
Disc. AE
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources: Page: зю 99
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources: Page: зю 99
Febrile neutropenia 1.8%
Disc. AE
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources: Page: зю 99
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources: Page: зю 99
Neutropenia 1.8%
Disc. AE
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources: Page: зю 99
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources: Page: зю 99
Sepsis 1.8%
Disc. AE
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources: Page: зю 99
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources: Page: зю 99
Diarrhea 2.4%
Disc. AE
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources: Page: зю 99
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources: Page: зю 99
Fatigue 2.4%
Disc. AE
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources: Page: зю 99
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources: Page: зю 99
Thrombocytopenia 3%
Disc. AE
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources: Page: зю 99
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources: Page: зю 99
Pneumonitis 3.6%
Disc. AE
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources: Page: зю 99
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources: Page: зю 99
Hyperglycemia 4.8%
Disc. AE
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources: Page: зю 99
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources: Page: зю 99
Pyrexia 5.4%
Disc. AE
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources: Page: зю 99
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources: Page: зю 99
Pneumonitis 6%
Disc. AE
60 mg 3 times / month steady, intravenous
Recommended|MTD
Dose: 60 mg, 3 times / month
Route: intravenous
Route: steady
Dose: 60 mg, 3 times / month
Sources: Page: зю 99
unhealthy, adult
n = 168
Health Status: unhealthy
Condition: hematologic malignancies
Age Group: adult
Sex: M+F
Population Size: 168
Sources: Page: зю 99
Overview

Overview

Drug as perpetrator​

Drug as perpetrator​

TargetModalityActivityMetaboliteClinical evidence
no
no
no
no
no
no
no
no
no
no
no
no
no
no
no
no
no
no
yes [IC50 0.09 uM]
yes [IC50 10.8 uM]
yes [IC50 11.5 uM]
yes [IC50 7 uM]
Drug as victim

Drug as victim

TargetModalityActivityMetaboliteClinical evidence
yes
yes
yes
yes (co-administration study)
Comment: ole, a strong CYP3A inhibitor which is also with inhibitory activity against human transporter P-glycoprotein (P-gp) and Breast Cancer Resistance Protein (BCRP), administered at a dose of 200 mg once daily for 10 days increased the mean AUC of a single IV dose of 60 mg ALIQOPA 53% with no effect on Cmax in patients with cancer
Page: 65.0
Tox targets

Tox targets

Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Preliminary results of a phase II study of single agent Bay 80-6946, a Novel PI3K inhibitor, in patients with relapsed/refractory, indolent or aggressive lymphoma.
2014 Feb
Patents

Sample Use Guides

60 mg in solution administered intravenously on Days 1, 8 and 15 of each 28-day treatment cycle
Route of Administration: Oral
Several breast cancer, endometrial cancer, and hematologic tumor cell lines were particularly sensitive to Copanlisib, with IC50 values less than 10nmol/L
Name Type Language
COPANLISIB
INN   USAN   WHO-DD  
USAN   INN  
Official 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
Common Name English
COPANLISIB [MI]
Common Name English
BAY-80-6946
Code English
2-AMINO-N-(7-METHOXY-8-(3-MORPHOLIN-4-YLPROPOXY)-2,3-DIHYDROIMIDAZO(1,2-C)QUINAZOLIN-5-YL)PYRIMIDINE-5-CARBOXAMIDE
Systematic Name English
BAY80-6946
Code English
copanlisib [INN]
Common Name English
5-PYRIMIDINECARBOXAMIDE, 2-AMINO-N-(2,3-DIHYDRO-7-METHOXY-8-(3-(4-MORPHOLINYL)PROPOXY)IMIDAZO(1,2-C)QUINAZOLIN-5-YL)-
Systematic Name English
BAY 80-6946
Code English
COPANLISIB [USAN]
Common Name English
Copanlisib [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C129825
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
FDA ORPHAN DRUG 463314
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
WHO-ATC L01XX61
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
FDA ORPHAN DRUG 811321
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
FDA ORPHAN DRUG 552416
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
NCI_THESAURUS C2152
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
FDA ORPHAN DRUG 811421
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
FDA ORPHAN DRUG 552616
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
NDF-RT N0000175605
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
FDA ORPHAN DRUG 552516
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
EU-Orphan Drug EU/3/18/2064
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
Code System Code Type Description
SMS_ID
100000170809
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
PRIMARY
NCI_THESAURUS
C96796
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
PRIMARY
PUBCHEM
24989044
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
PRIMARY
MERCK INDEX
m12036
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
PRIMARY
WIKIPEDIA
Copanlisib
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
PRIMARY
EVMPD
SUB184952
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
PRIMARY
RXCUI
1945077
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
PRIMARY
DRUG CENTRAL
5256
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
PRIMARY
ChEMBL
CHEMBL3218576
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
PRIMARY
FDA UNII
WI6V529FZ9
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
PRIMARY
CAS
1032568-63-0
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
PRIMARY
DAILYMED
WI6V529FZ9
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
PRIMARY
LACTMED
Copanlisib
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
PRIMARY
USAN
CD-71
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
PRIMARY
INN
9726
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
PRIMARY
DRUG BANK
DB12483
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
PRIMARY
CHEBI
173077
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
PRIMARY
EPA CompTox
DTXSID00145728
Created by admin on Fri Dec 15 17:26:49 UTC 2023 , Edited by admin on Fri Dec 15 17:26:49 UTC 2023
PRIMARY