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Details

Stereochemistry ACHIRAL
Molecular Formula C11H12N4O2.ClH.H2O
Molecular Weight 286.715
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TODRALAZINE HYDROCHLORIDE MONOHYDRATE

SMILES

O.Cl.CCOC(=O)NNC1=C2C=CC=CC2=CN=N1

InChI

InChIKey=YALNFCRINZHFMY-UHFFFAOYSA-N
InChI=1S/C11H12N4O2.ClH.H2O/c1-2-17-11(16)15-14-10-9-6-4-3-5-8(9)7-12-13-10;;/h3-7H,2H2,1H3,(H,13,14)(H,15,16);1H;1H2

HIDE SMILES / InChI

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

Molecular Formula C11H12N4O2
Molecular Weight 232.2386
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula H2O
Molecular Weight 18.0153
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Sources: www.drugfuture.com/mt/tocoferil-nicotinate.pdf
Curator's Comment: description was created based on several sources, including: http://www.ncbi.nlm.nih.gov/pubmed/6425526 http://www.naoru.com/Apiracohl.html http://www.ncbi.nlm.nih.gov/pubmed/9412993

Todralazine is a hydralazinophthalazine-derived drug currently used in the treatment of arterial hypertension. As vasodilator, it might be used in combination with isosorbide dinitrate. Side effects and drug toxicity were uncommon in such vasodilator therapy.

Approval Year

Targets

Targets

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Todralazine is used as an antihypertensive agent
PubMed

PubMed

TitleDatePubMed
Patents

Patents

Sample Use Guides

40 – 120 mg in 3 doses per day
Route of Administration: Oral
In Vitro Use Guide
Todralazine (TDR) decreased the free radical level in granulocyte samples. At the highest of the tested TDR concentrations (80 μg/ml), the free radical level was lower by ~40% in the samples where only TDR was present than in the control samples (spontaneous release, without TDR).
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:01:01 GMT 2023
Edited
by admin
on Fri Dec 15 19:01:01 GMT 2023
Record UNII
5998D60YO0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TODRALAZINE HYDROCHLORIDE MONOHYDRATE
Common Name English
TODRALAZINE HYDROCHLORIDE HYDRATE [JAN]
Common Name English
APERDOR
Brand Name English
TODRALAZINE HYDROCHLORIDE
MART.  
Common Name English
ETHYL 3-(PHTHALAZIN-1-YL)CARBAZATE HYDROCHLORIDE MONOHYDRATE
Systematic Name English
APRIDE
Brand Name English
ATAPREN
Brand Name English
TODRALAZINE HYDROCHLORIDE HYDRATE
JAN  
Common Name English
ILLCUT
Brand Name English
HYDRAZINECARBOXYLIC ACID, 2-(1-PHTHALAZINYL)-, ETHYL ESTER, HYDROCHLORIDE, HYDRATE (1:1:1)
Common Name English
BT-621
Code English
TODRALAZINE HYDROCHLORIDE [MART.]
Common Name English
BINAZIN
Brand Name English
APIRACOHL
Brand Name English
PROPAT
Brand Name English
Code System Code Type Description
CAS
56387-60-1
Created by admin on Fri Dec 15 19:01:01 GMT 2023 , Edited by admin on Fri Dec 15 19:01:01 GMT 2023
PRIMARY
EVMPD
SUB04903MIG
Created by admin on Fri Dec 15 19:01:01 GMT 2023 , Edited by admin on Fri Dec 15 19:01:01 GMT 2023
PRIMARY
PUBCHEM
23724962
Created by admin on Fri Dec 15 19:01:01 GMT 2023 , Edited by admin on Fri Dec 15 19:01:01 GMT 2023
PRIMARY
SMS_ID
100000092665
Created by admin on Fri Dec 15 19:01:01 GMT 2023 , Edited by admin on Fri Dec 15 19:01:01 GMT 2023
PRIMARY
ChEMBL
CHEMBL1079787
Created by admin on Fri Dec 15 19:01:01 GMT 2023 , Edited by admin on Fri Dec 15 19:01:01 GMT 2023
PRIMARY
FDA UNII
5998D60YO0
Created by admin on Fri Dec 15 19:01:01 GMT 2023 , Edited by admin on Fri Dec 15 19:01:01 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
ANHYDROUS->SOLVATE
Related Record Type Details
ACTIVE MOIETY