U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS
This repository is under review for potential modification in compliance with Administration directives.

Details

Stereochemistry ACHIRAL
Molecular Formula C31H42N6O4.H2O4S
Molecular Weight 660.781
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TANDUTINIB SULFATE

SMILES

OS(O)(=O)=O.COC1=CC2=C(C=C1OCCCN3CCCCC3)N=CN=C2N4CCN(CC4)C(=O)NC5=CC=C(OC(C)C)C=C5

InChI

InChIKey=FXCQXNUGIYMXAR-UHFFFAOYSA-N
InChI=1S/C31H42N6O4.H2O4S/c1-23(2)41-25-10-8-24(9-11-25)34-31(38)37-17-15-36(16-18-37)30-26-20-28(39-3)29(21-27(26)32-22-33-30)40-19-7-14-35-12-5-4-6-13-35;1-5(2,3)4/h8-11,20-23H,4-7,12-19H2,1-3H3,(H,34,38);(H2,1,2,3,4)

HIDE SMILES / InChI

Molecular Formula C31H42N6O4
Molecular Weight 562.703
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula H2O4S
Molecular Weight 98.078
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: Description was created based on several sources, including https://www.drugbank.ca/drugs/DB05465

Millennium Pharmaceuticals Inc's tandutinib (MLN-518), a piperazinyl derivative of quinazoline, is an orally active inhibitor of FLT3 kinase and family members PDGFR beta and c-Kit. Tandutinib inhibited FLT3 phosphorylation, downstream signaling and malignant growth in vitro and in animal models. The drug exhibited limited activity as a single agent in phase I and II clinical trials in patients with AML and myelodysplastic syndrome, but displayed promising antileukemic activity (90% complete remissions) in a phase I/II trial in patients with newly diagnosed AML when administered in combination with cytarabine and daunorubicin. Phase II clinical trials for tandutinib in patients with Glioblastoma have being discontinued. The use of tandutinib to treat AML has been granted fast-track status by the U.S. Food and Drug Administration. Phase II trials were underway., but later withwrawn.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
576 ng/mL
525 mg 2 times / day multiple, oral
dose: 525 mg
route of administration: Oral
experiment type: MULTIPLE
co-administered:
TANDUTINIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
1285 ng/mL
700 mg 2 times / day steady-state, oral
dose: 700 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
TANDUTINIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
486 ng/mL
600 mg 2 times / day steady-state, oral
dose: 600 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
TANDUTINIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
689 ng × day/mL
525 mg 2 times / day multiple, oral
dose: 525 mg
route of administration: Oral
experiment type: MULTIPLE
co-administered:
TANDUTINIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
8193 ng × h/mL
700 mg 2 times / day steady-state, oral
dose: 700 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
TANDUTINIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
4659 ng × h/mL
600 mg 2 times / day steady-state, oral
dose: 600 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
TANDUTINIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
1.06 day
525 mg 2 times / day multiple, oral
dose: 525 mg
route of administration: Oral
experiment type: MULTIPLE
co-administered:
TANDUTINIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
13.2 h
700 mg 2 times / day steady-state, oral
dose: 700 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
TANDUTINIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
10.4 h
600 mg 2 times / day steady-state, oral
dose: 600 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
TANDUTINIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
Doses

Doses

DosePopulationAdverse events​
700 mg 2 times / day multiple, oral
Highest studied dose
Dose: 700 mg, 2 times / day
Route: oral
Route: multiple
Dose: 700 mg, 2 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: FASTED
Sources:
DLT: Muscular weakness, Diarrhea...
Dose limiting toxicities:
Muscular weakness (grade 3-4, 66.7%)
Diarrhea (grade 3, 33.3%)
Sources:
700 mg 2 times / day multiple, oral
Highest studied dose
Dose: 700 mg, 2 times / day
Route: oral
Route: multiple
Dose: 700 mg, 2 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
DLT: Fatigue, Weakness...
Dose limiting toxicities:
Fatigue (grade 3, 33.3%)
Weakness (grade 3, 33.3%)
Sources:
525 mg 2 times / day multiple, oral
MTD
Dose: 525 mg, 2 times / day
Route: oral
Route: multiple
Dose: 525 mg, 2 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: FASTED
Sources:
DLT: Muscular weakness, Fatigue...
Dose limiting toxicities:
Muscular weakness (grade 3, 16.7%)
Fatigue (grade 3, 16.7%)
Sources:
600 mg 2 times / day multiple, oral
MTD
Dose: 600 mg, 2 times / day
Route: oral
Route: multiple
Dose: 600 mg, 2 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
DLT: Blood phosphorus abnormal...
Dose limiting toxicities:
Blood phosphorus abnormal (grade 3, 16.7%)
Sources:
AEs

AEs

AESignificanceDosePopulation
Diarrhea grade 3, 33.3%
DLT
700 mg 2 times / day multiple, oral
Highest studied dose
Dose: 700 mg, 2 times / day
Route: oral
Route: multiple
Dose: 700 mg, 2 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: FASTED
Sources:
Muscular weakness grade 3-4, 66.7%
DLT, Disc. AE
700 mg 2 times / day multiple, oral
Highest studied dose
Dose: 700 mg, 2 times / day
Route: oral
Route: multiple
Dose: 700 mg, 2 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: FASTED
Sources:
Fatigue grade 3, 33.3%
DLT
700 mg 2 times / day multiple, oral
Highest studied dose
Dose: 700 mg, 2 times / day
Route: oral
Route: multiple
Dose: 700 mg, 2 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Weakness grade 3, 33.3%
DLT
700 mg 2 times / day multiple, oral
Highest studied dose
Dose: 700 mg, 2 times / day
Route: oral
Route: multiple
Dose: 700 mg, 2 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Fatigue grade 3, 16.7%
DLT, Disc. AE
525 mg 2 times / day multiple, oral
MTD
Dose: 525 mg, 2 times / day
Route: oral
Route: multiple
Dose: 525 mg, 2 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: FASTED
Sources:
Muscular weakness grade 3, 16.7%
DLT, Disc. AE
525 mg 2 times / day multiple, oral
MTD
Dose: 525 mg, 2 times / day
Route: oral
Route: multiple
Dose: 525 mg, 2 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: FASTED
Sources:
Blood phosphorus abnormal grade 3, 16.7%
DLT
600 mg 2 times / day multiple, oral
MTD
Dose: 600 mg, 2 times / day
Route: oral
Route: multiple
Dose: 600 mg, 2 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Detection of FLT3 oncogene mutations in acute myeloid leukemia using conformation sensitive gel electrophoresis.
2008 Nov
N-(4-Isopropoxyphen-yl)acetamide.
2009 Apr 10
The FLT3 inhibitor tandutinib (formerly MLN518) has sequence-independent synergistic effects with cytarabine and daunorubicin.
2009 Aug 15
ABT-869, a promising multi-targeted tyrosine kinase inhibitor: from bench to bedside.
2009 Jul 30
Patient-derived acute myeloid leukemia (AML) bone marrow cells display distinct intracellular kinase phosphorylation patterns.
2009 May 15
AC220 is a uniquely potent and selective inhibitor of FLT3 for the treatment of acute myeloid leukemia (AML).
2009 Oct 1
Patents

Sample Use Guides

oral tandutinib 500 mg twice daily on days 1-28. Treatment repeats every 28 days in the absence of disease progression or unacceptable toxicity.
Route of Administration: Oral
Tandutinib inhibited IL-3-independent cell growth and FLT3-ITD autophosphorylation with an IC(50) of 10-100 nM.
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:59:52 GMT 2025
Edited
by admin
on Mon Mar 31 17:59:52 GMT 2025
Record UNII
T7Q9I8CGQ7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TANDUTINIB SULFATE
Common Name English
CT-53518 SULFATE
Preferred Name English
CT-53518 SULPHATE
Common Name English
1-PIPERAZINECARBOXAMIDE, 4-(6-METHOXY-7-(3-(1-PIPERIDINYL)PROPOXY)-4-QUINAZOLINYL)-N-(4-(1-METHYLETHOXY)PHENYL)-, SULFATE (1:1)
Systematic Name English
TANDUTINIB SULPHATE
Common Name English
Code System Code Type Description
CAS
387867-14-3
Created by admin on Mon Mar 31 17:59:52 GMT 2025 , Edited by admin on Mon Mar 31 17:59:52 GMT 2025
PRIMARY
PUBCHEM
12002085
Created by admin on Mon Mar 31 17:59:52 GMT 2025 , Edited by admin on Mon Mar 31 17:59:52 GMT 2025
PRIMARY
FDA UNII
T7Q9I8CGQ7
Created by admin on Mon Mar 31 17:59:52 GMT 2025 , Edited by admin on Mon Mar 31 17:59:52 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY