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Details

Stereochemistry ACHIRAL
Molecular Formula C25H21N8O2.C5H14NO
Molecular Weight 569.6574
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of TOTROMBOPAG CHOLINE

SMILES

C[N+](C)(C)CCO.CC1=NN(C(O)=C1\N=N\C2=C([O-])C(=CC=C2)C3=CC=CC(=C3)C4=NN=NN4)C5=CC=C(C)C(C)=C5

InChI

InChIKey=XVCUREWYXITPSI-JGUILPGDSA-M
InChI=1S/C25H22N8O2.C5H14NO/c1-14-10-11-19(12-15(14)2)33-25(35)22(16(3)30-33)27-26-21-9-5-8-20(23(21)34)17-6-4-7-18(13-17)24-28-31-32-29-24;1-6(2,3)4-5-7/h4-13,34-35H,1-3H3,(H,28,29,31,32);7H,4-5H2,1-3H3/q;+1/p-1/b27-26+;

HIDE SMILES / InChI

Molecular Formula C25H22N8O2
Molecular Weight 466.4946
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Molecular Formula C5H13NO
Molecular Weight 103.1628
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Totrombopag is an orally bioavailable, nonpeptide, small-molecule thrombopoietin receptor agonist. It induces proliferation and differentiation of megakaryocytes and progenitor cells, ultimately increasing the production of platelets. Totrombopag has been investigated in healthy volunteers in a phase 1, single-blind, randomized fashion to cause a dosedependent increase in platelet count with demonstrated safety. There were no serious adverse events, no significant changes in laboratory or cardiovascular safety parameters and there was no observed relationship between the incidence or severity of adverse events and dose. Most adverse events were mild in intensity and self-limiting. Totrombopag was developed for the treatment of immune thrombocytopenic purpura.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
170.0 nM [IC50]
PubMed

PubMed

TitleDatePubMed
Novel thrombopoietic agents.
2007
Emerging drugs for idiopathic thrombocytopenic purpura in adults.
2008 Jun

Sample Use Guides

Once-daily at doses of 160 to 640 mg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:02:05 UTC 2023
Edited
by admin
on Fri Dec 15 16:02:05 UTC 2023
Record UNII
IRH58115R1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TOTROMBOPAG CHOLINE
USAN  
USAN  
Official Name English
SB-559448-AAA
Code English
ETHANAMINIUM, 2-HYDROXY-N,N,N-TRIMETHYL-, SALT WITH 2-(3,4-DIMETHYLPHENYL)-2,4-DIHYDRO-4-((2-HYDROXY-3'-(1H-TETRAZOL-5-YL)(1,1'-BIPHENYL)-3-YL)AZO)-5-METHYL-3H-PYRAZOL-3-ONE (1:1)
Common Name English
TOTROMBOPAG CHOLINE [USAN]
Common Name English
2-HYDROXY-N,N,N-TRIMETHYLETHANAMINIUM 5-(3'-((2Z)-2-(1-(3,4-DIMETHYLPHENYL)-3-METHYL-5-OXO-1,5-DIHYDRO-4H-PYRAZOL-4-YLIDENE)DIAZANYL)-2'-HYDROXYBIPHENYL-3-YL)TETRAZOLIDE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C2459
Created by admin on Fri Dec 15 16:02:05 UTC 2023 , Edited by admin on Fri Dec 15 16:02:05 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C76603
Created by admin on Fri Dec 15 16:02:05 UTC 2023 , Edited by admin on Fri Dec 15 16:02:05 UTC 2023
PRIMARY
USAN
SS-104
Created by admin on Fri Dec 15 16:02:05 UTC 2023 , Edited by admin on Fri Dec 15 16:02:05 UTC 2023
PRIMARY
FDA UNII
IRH58115R1
Created by admin on Fri Dec 15 16:02:05 UTC 2023 , Edited by admin on Fri Dec 15 16:02:05 UTC 2023
PRIMARY
CAS
851606-62-7
Created by admin on Fri Dec 15 16:02:05 UTC 2023 , Edited by admin on Fri Dec 15 16:02:05 UTC 2023
PRIMARY
ChEMBL
CHEMBL3545303
Created by admin on Fri Dec 15 16:02:05 UTC 2023 , Edited by admin on Fri Dec 15 16:02:05 UTC 2023
PRIMARY
SMS_ID
300000044616
Created by admin on Fri Dec 15 16:02:05 UTC 2023 , Edited by admin on Fri Dec 15 16:02:05 UTC 2023
PRIMARY
PUBCHEM
46174137
Created by admin on Fri Dec 15 16:02:05 UTC 2023 , Edited by admin on Fri Dec 15 16:02:05 UTC 2023
PRIMARY
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PARENT -> SALT/SOLVATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY