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Details

Stereochemistry ACHIRAL
Molecular Formula C11H23N7
Molecular Weight 253.3472
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MELADRAZINE

SMILES

CCN(CC)C1=NC(=NN)N=C(N1)N(CC)CC

InChI

InChIKey=IRQOBYXMACIFKD-UHFFFAOYSA-N
InChI=1S/C11H23N7/c1-5-17(6-2)10-13-9(16-12)14-11(15-10)18(7-3)8-4/h5-8,12H2,1-4H3,(H,13,14,15,16)

HIDE SMILES / InChI

Molecular Formula C11H23N7
Molecular Weight 253.3472
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Meladrazine is a drug used in urology as an antispasmodic. Meladrazine acts on the central nervous system as a polysynaptic inhibitor. Its usefulness in treating spasticity in patients with multiple sclerosis is well known. As many of these patients have bladder problems, a coincidental beneficial effect on uninhibited bladders has been discovered. Meladrazine caused a high incidence of side effects; therefore, treatment with terodiline separately is recommended for geriatric patients who have severe motor urge incontinence.

Approval Year

PubMed

PubMed

TitleDatePubMed
N,N,N,N-Tetra-ethyl-6-{2-[(E)-1-(4-nitro-phen-yl)ethyl-idene]hydrazino}-1,3,5-triazine-2,4-diamine.
2009 Jul 11
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:23:29 UTC 2023
Edited
by admin
on Fri Dec 15 16:23:29 UTC 2023
Record UNII
2V6Z0JG2X0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MELADRAZINE
INN   WHO-DD  
INN  
Official Name English
meladrazine [INN]
Common Name English
Meladrazine [WHO-DD]
Common Name English
2,4-BIS(DIETHYLAMINO)-6-HYDRAZINO-S-TRIAZINE
Systematic Name English
BA 13155 FREE BASE
Code English
HYDRAMITRAZINE [MI]
Common Name English
NSC-99857
Code English
BA-13155 FREE BASE
Code English
Classification Tree Code System Code
NCI_THESAURUS C29698
Created by admin on Fri Dec 15 16:23:29 UTC 2023 , Edited by admin on Fri Dec 15 16:23:29 UTC 2023
WHO-VATC QG04BD03
Created by admin on Fri Dec 15 16:23:29 UTC 2023 , Edited by admin on Fri Dec 15 16:23:29 UTC 2023
WHO-ATC G04BD03
Created by admin on Fri Dec 15 16:23:29 UTC 2023 , Edited by admin on Fri Dec 15 16:23:29 UTC 2023
Code System Code Type Description
FDA UNII
2V6Z0JG2X0
Created by admin on Fri Dec 15 16:23:29 UTC 2023 , Edited by admin on Fri Dec 15 16:23:29 UTC 2023
PRIMARY
EPA CompTox
DTXSID20161107
Created by admin on Fri Dec 15 16:23:29 UTC 2023 , Edited by admin on Fri Dec 15 16:23:29 UTC 2023
PRIMARY
PUBCHEM
71679
Created by admin on Fri Dec 15 16:23:29 UTC 2023 , Edited by admin on Fri Dec 15 16:23:29 UTC 2023
PRIMARY
NSC
99857
Created by admin on Fri Dec 15 16:23:29 UTC 2023 , Edited by admin on Fri Dec 15 16:23:29 UTC 2023
PRIMARY
SMS_ID
100000081444
Created by admin on Fri Dec 15 16:23:29 UTC 2023 , Edited by admin on Fri Dec 15 16:23:29 UTC 2023
PRIMARY
DRUG BANK
DB13272
Created by admin on Fri Dec 15 16:23:29 UTC 2023 , Edited by admin on Fri Dec 15 16:23:29 UTC 2023
PRIMARY
DRUG CENTRAL
3756
Created by admin on Fri Dec 15 16:23:29 UTC 2023 , Edited by admin on Fri Dec 15 16:23:29 UTC 2023
PRIMARY
ECHA (EC/EINECS)
237-736-9
Created by admin on Fri Dec 15 16:23:29 UTC 2023 , Edited by admin on Fri Dec 15 16:23:29 UTC 2023
PRIMARY
WIKIPEDIA
MELADRAZINE
Created by admin on Fri Dec 15 16:23:29 UTC 2023 , Edited by admin on Fri Dec 15 16:23:29 UTC 2023
PRIMARY
MERCK INDEX
m238
Created by admin on Fri Dec 15 16:23:29 UTC 2023 , Edited by admin on Fri Dec 15 16:23:29 UTC 2023
PRIMARY Merck Index
CAS
13957-36-3
Created by admin on Fri Dec 15 16:23:29 UTC 2023 , Edited by admin on Fri Dec 15 16:23:29 UTC 2023
PRIMARY
NCI_THESAURUS
C66076
Created by admin on Fri Dec 15 16:23:29 UTC 2023 , Edited by admin on Fri Dec 15 16:23:29 UTC 2023
PRIMARY
EVMPD
SUB08717MIG
Created by admin on Fri Dec 15 16:23:29 UTC 2023 , Edited by admin on Fri Dec 15 16:23:29 UTC 2023
PRIMARY
INN
1798
Created by admin on Fri Dec 15 16:23:29 UTC 2023 , Edited by admin on Fri Dec 15 16:23:29 UTC 2023
PRIMARY
MESH
C005040
Created by admin on Fri Dec 15 16:23:29 UTC 2023 , Edited by admin on Fri Dec 15 16:23:29 UTC 2023
PRIMARY
ChEMBL
CHEMBL2105242
Created by admin on Fri Dec 15 16:23:29 UTC 2023 , Edited by admin on Fri Dec 15 16:23:29 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY